Optimized oral cholera vaccine distribution strategies to minimize disease incidence: A mixed integer programming model and analysis of a Bangladesh scenario

Vaccine
Volume 33, Issue 46, Pages 6135-6370 (17 November 2015)
http://www.sciencedirect.com/science/journal/0264410X/33/46
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Optimized oral cholera vaccine distribution strategies to minimize disease incidence: A mixed integer programming model and analysis of a Bangladesh scenario
Original Research Article
Pages 6218-6223
Hannah K. Smalley, Pinar Keskinocak, Julie Swann, Alan Hinman
Abstract
In addition to improved sanitation, hygiene, and better access to safe water, oral cholera vaccines can help to control the spread of cholera in the short term. However, there is currently no systematic method for determining the best allocation of oral cholera vaccines to minimize disease incidence in a population where the disease is endemic and resources are limited. We present a mathematical model for optimally allocating vaccines in a region under varying levels of demographic and incidence data availability. The model addresses the questions of where, when, and how many doses of vaccines to send. Considering vaccine efficacies (which may vary based on age and the number of years since vaccination), we analyze distribution strategies which allocate vaccines over multiple years. Results indicate that, given appropriate surveillance data, targeting age groups and regions with the highest disease incidence should be the first priority, followed by other groups primarily in order of disease incidence, as this approach is the most life-saving and cost-effective. A lack of detailed incidence data results in distribution strategies which are not cost-effective and can lead to thousands more deaths from the disease. The mathematical model allows for what-if analysis for various vaccine distribution strategies by providing the ability to easily vary parameters such as numbers and sizes of regions and age groups, risk levels, vaccine price, vaccine efficacy, production capacity and budget.

I Immunise: An evaluation of a values-based campaign to change attitudes and beliefs

Vaccine
Volume 33, Issue 46, Pages 6135-6370 (17 November 2015)
http://www.sciencedirect.com/science/journal/0264410X/33/46
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I Immunise: An evaluation of a values-based campaign to change attitudes and beliefs
Original Research Article
Pages 6235-6240
Katie Attwell, Melanie Freeman
Abstract
This paper presents results of a study determining the efficacy of a values based approach to changing vaccination attitudes. It reports an evaluation survey of the “I Immunise” campaign, conducted in Fremantle, Western Australia, in 2014. “I Immunise” explicitly engaged with values and identity; formulated by locals in a community known for its alternative lifestyles and lower-than-national vaccine coverage rates. Data was collected from 304 online respondents. The campaign polarised attitudes towards vaccination and led some to feel more negatively. However, it had an overall positive response with 77% of participants. Despite the campaign only resonating positively with a third of parents who had refused or doubted vaccines, it demonstrates an important in-road into this hard-to-reach group.

MMR vaccination status of children exempted from school-entry immunization mandates

Vaccine
Volume 33, Issue 46, Pages 6135-6370 (17 November 2015)
http://www.sciencedirect.com/science/journal/0264410X/33/46
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MMR vaccination status of children exempted from school-entry immunization mandates
Original Research Article
Pages 6250-6256
Alison M. Buttenheim, Karthik Sethuraman, Saad B. Omer, Alexandra L. Hanlon, Michael Z. Levy, Daniel Salmon
Abstract
Background
Child immunizations are one of the most successful public health interventions of the past century. Still, parental vaccine hesitancy is widespread and increasing. One manifestation of this are rising rates of nonmedical or “personal beliefs” exemptions (PBEs) from school-entry immunization mandates. Exemptions have been shown to be associated with increased risk of disease outbreak, but the strength of this association depends critically on the true vaccination status of exempted children, which has not been assessed.
Objective
To estimate the true measles-mumps-rubella (MMR) vaccination status of children with PBEs.
Methods
We use administrative data collected by the California Department of Public Health in 2009 and imputation to estimate the MMR vaccination status of children with PBEs under varying scenarios.
Results
Results from 2009 surveillance data indicate MMR1/MMR2 coverage of 18–47% among children with PBEs at typical schools and 11–34% among children with PBEs at schools with high PBE rates. Imputation scenarios point to much higher coverage (64–92% for MMR1 and 25–58% for MMR2 at typical schools; 49–90% for MMR1 and 16–63% for MMR2 at high PBE schools) but still below levels needed to maintain herd immunity against measles.
Conclusions
These coverage estimates suggest that prior analyses of the relative risk of measles associated with vaccine refusal underestimate that risk by an order of magnitude of 2–10 times.

Intellectual property rights and challenges for development of affordable human papillomavirus, rotavirus and pneumococcal vaccines: Patent landscaping and perspectives of developing country vaccine manufacturers

Vaccine
Volume 33, Issue 46, Pages 6135-6370 (17 November 2015)
http://www.sciencedirect.com/science/journal/0264410X/33/46
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Intellectual property rights and challenges for development of affordable human papillomavirus, rotavirus and pneumococcal vaccines: Patent landscaping and perspectives of developing country vaccine manufacturers
Original Research Article
Pages 6366-6370
Subhashini Chandrasekharan, Tahir Amin, Joyce Kim, Eliane Furrer, Anna-Carin Matterson, Nina Schwalbe, Aurélia Nguyen
Abstract
The success of Gavi, the Vaccine Alliance depends on the vaccine markets providing appropriate, affordable vaccines at sufficient and reliable quantities. Gavi’s current supplier base for new and underutilized vaccines, such as the human papillomavirus (HPV), rotavirus, and the pneumococcal conjugate vaccine is very small. There is growing concern that following globalization of laws on intellectual property rights (IPRs) through trade agreements, IPRs are impeding new manufacturers from entering the market with competing vaccines. This article examines the extent to which IPRs, specifically patents, can create such obstacles, in particular for developing country vaccine manufacturers (DCVMs). Through building patent landscapes in Brazil, China, and India and interviews with manufacturers and experts in the field, we found intense patenting activity for the HPV and pneumococcal vaccines that could potentially delay the entry of new manufacturers. Increased transparency around patenting of vaccine technologies, stricter patentability criteria suited for local development needs and strengthening of IPRs management capabilities where relevant, may help reduce impediments to market entry for new manufacturers and ensure a competitive supplier base for quality vaccines at sustainably low prices.

Vaccines and Global Health: The Week in Review 7 November 2015

Vaccines and Global Health: The Week in Review is a weekly digest  summarizing news, events, announcements, peer-reviewed articles and research in the global vaccine ethics and policy space. Content is aggregated from key governmental, NGO, international organization and industry sources, key peer-reviewed journals, and other media channels. This summary proceeds from the broad base of themes and issues monitored by the Center for Vaccine Ethics & Policy in its work: it is not intended to be exhaustive in its coverage. You are viewing the blog version of our weekly digest, typically comprised of between 30 and 40 posts below all dated with the current issue date

.Request an Email Summary: Vaccines and Global Health : The Week in Review is published as a single email summary, scheduled for release each Saturday evening before midnight (EDT in the U.S.). If you would like to receive the email version, please send your request to david.r.curry@centerforvaccineethicsandpolicy.org.

pdf version A pdf of the current issue is available here:  Vaccines and Global Health_The Week in Review_7 November 2015

blog edition: comprised of the approx. 35+ entries posted below on 13 September 2015..

Twitter:  Readers can also follow developments on twitter: @vaxethicspolicy.
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Links:  We endeavor to test each link as we incorporate it into any post, but recognize that some links may become “stale” as publications and websites reorganize content over time. We apologize in advance for any links that may not be operative. We believe the contextual information in a given post should allow retrieval, but please contact us as above for assistance if necessary.

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David R. Curry, MS
Executive Director
Center for Vaccine Ethics and Policy
a program of the
– Division of Medical Ethics, NYU Medical School
– Children’s Hospital of Philadelphia Vaccine Education Center
Associate Faculty, Division of Medical Ethics, NYU Medical School

EBOLA/EVD [to 7 November 2015]

EBOLA/EVD [to 7 November 2015]
Public Health Emergency of International Concern (PHEIC); “Threat to international peace and security” (UN Security Council)

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Ebola Situation Report – 4 November 2015
[Excerpt]
SUMMARY
:: One new confirmed case of Ebola virus disease (EVD) was reported from Guinea in the week to 1 November. The case is the newborn child of a 25-year-old woman who was confirmed as a case in the prefecture of Forecariah during the previous week. The child was delivered in an Ebola treatment centre (ETC) in Conakry, and is currently undergoing treatment. The mother died after giving birth. Her other two young children were also confirmed as cases during the previous week and are receiving treatment. The 3 confirmed cases reported the previous week generated a large number of high-risk contacts in Forecariah who are now entering the second week of their 21-day post-exposure follow-up period. On 1 November there were 382 contacts under follow-up in Guinea (compared with 364 the previous week), 141 of whom are high-risk. Therefore there remains a near-term risk of further cases among both registered and untraced contacts. Sierra Leone reported zero cases for a seventh consecutive week, and will be declared free of EVD transmission on 7 November if no further cases are reported.

:: Case incidence has remained at 5 confirmed cases or fewer per week for 14 consecutive weeks. Over the same period, transmission of the virus has been geographically confined to several small areas in western Guinea and Sierra Leone, marking a transition to a distinct, third phase of the epidemic. The phase-3 response coordinated by the Interagency Collaboration on Ebola builds on existing measures to drive case incidence to zero, and ensure a sustained end to EVD transmission. Enhanced capacity to rapidly identify a reintroduction (either from an area of active transmission or from an animal reservoir), or re-emergence of virus from a survivor, and capacity for testing and counselling as part of a comprehensive package to safeguard the welfare of survivors are central to the phase-3 response framework…

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Statement on the end of the Ebola outbreak in Sierra Leone
Delivered by Dr Anders Nordström, WHO Representative in Sierra Leone

Today, 7 November 2015, the World Health Organization declares the end of the Ebola outbreak in Sierra Leone.

Since Sierra Leone recorded the first Ebola case on 24 May 2014, a total number of 8,704 people were infected and 3,589 have died. From those who tragically lost their lives, 221 of them were healthcare workers. We remember them all today.

We are now moving into a new phase of 90 days enhanced surveillance which will run until 5 February 2016. This new phase is critical as our goal is to ensure a resilient zero and that we can detect and respond to any potential Ebola flare ups. This period is about ensuring that we can consolidate the gains of existing systems to manage future risks.
The World Health Organization commends the Government of Sierra Leone and the people of Sierra Leone for the significant achievement of ending this Ebola outbreak.

The world had never faced an Ebola outbreak of this scale and magnitude and the world has neither seen a nation mobilizing its people and resources as Sierra Leone did. The power of the people of Sierra Leone is the reason why we could put an end to this outbreak today.

This power of the people and the foundation now in place needs to be further nurtured and supported in order to build a strong and resilient public health system which stands ready to contain the next outbreak of a disease, Ebola or any other public health threat.

Under the leadership of the Sierra Leonean Government, an effective response was initiated to manage the outbreak. The use of rapid response teams and strong community involvement to identify new cases early and quickly stop any Ebola virus transmission should continue to be the cornerstone of the national response strategy.
WHO will maintain an enhanced staff presence in Sierra Leone as the response transitions from outbreak control, to support enhanced vigilance and to the recovery of essential health services.

The Ebola outbreak has decimated families, the health system, the economy and social structures. All need to recover and heal.

WHO is confident that the Government of Sierra Leone together with its national and international partners will use the foundation already in place; dedicated and trained health workers; systems for alerts and information management; community engagement and care for people – to deal with other priority health problems, child mortality topping the list.

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CDC/MMWR/ACIP Watch [to 7 November 2015]
http://www.cdc.gov/media/index.html

World Health Organization Declares Sierra Leone Free of Ebola Virus Transmission
On November 7, 2015, the World Health Organization (WHO) declared Sierra Leone free of Ebola virus transmission. This date marked 42 days (two 21-day incubation periods) from the release of the last known patient with Ebola from a Sierra Leone Ebola treatment unit (ETU).

The Centers for Disease Control and Prevention (CDC) celebrates the extraordinary efforts of those in Sierra Leone whose hard work, commitment and dedication to stopping Ebola transmission has brought the country this far. CDC’s work in Sierra Leone will continue even after the Ebola outbreak is considered over.

With the support of CDC and many other partners, Sierra Leone has a stronger disease surveillance and response system in place for suspected Ebola cases, and the country remains vigilant in its efforts to stay at zero cases. CDC and U.S. government partners will continue to support Sierra Leone in assisting survivors and rebuilding the country’s public health infrastructure.

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UNICEF [to 7 November 2015]
http://www.unicef.org/media/media_78364.html

UNICEF welcomes end of Ebola outbreak in Sierra Leone, calls for more support to 11,500+ affected children
FREETOWN, Sierra Leone, 7 November 2015 – The WHO declaration marking the end of the Ebola outbreak in Sierra Leone today is welcomed by UNICEF as a major victory for the large-scale and coordinated 18-month response. But enhanced surveillance must continue so that the country is ready for any possible future outbreaks, and work must also intensify to support those affected by the outbreak and to build a resilient recovery.

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World Bank [to 7 November 2015]
http://www.worldbank.org/en/news/all

Statement by World Bank Group President on Declaration of End of Ebola Transmission in Sierra Leone
WASHINGTON, November 7, 2015 –World Bank Group President Jim Yong Kim issued the following statement on today’s announcement declaring the end of Ebola transmission in Sierra Leone.

“My colleagues and I at the World Bank Group congratulate the government and people of Sierra Leone for their tireless efforts to reach this critical milestone in the long fight against Ebola.

“Still, we are also mindful of the staggering human and economic costs of the Ebola epidemic, as well as the need for continued vigilance as some cases remain in the region. We remember the nearly 4,000 people – including more than 220 heroic health workers – in Sierra Leone who lost their lives, those who lost their loved ones, and the many survivors still in need of support.

“The World Bank Group remains committed to supporting Sierra Leone, Liberia and Guinea as they work to bring this deadly epidemic to a final end, to recover and rebound. We will do everything we can to help these countries and the world prevent another deadly pandemic.”

About the World Bank Group Response to Ebola
The World Bank Group has mobilized US$1.62 billion in financing for Ebola response and recovery efforts. This total includes US$1.17 billion from IDA, the World Bank Group’s fund for the poorest countries and at least US$450 million from IFC, a member of the World Bank Group, to enable trade, investment and employment. In Sierra Leone, the WBG’s IDA financing totaling US$318 million includes support for more than 9,000 Ebola survivors.

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WHO Director-General addresses Princeton – Fung Global Forum on lessons learned from the Ebola crisis
Dr Margaret Chan, Director-General of the World Health Organization
Keynote address at the Princeton – Fung Global Forum, Dublin, Ireland
2 November 2015

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WHO “Stories from Countries”
Ebola: Then and Now – Rick Brennan 3 November 2015
Ebola: Then and Now – Saffea Gborie 3 November 2015
Ebola: Then and Now – David Nabarro 3 November 2015
Ebola: Then and Now – Suvi Peltoniemi 3 November 2015
Ebola: Then and Now – Bruce Aylward 1 November 2015

POLIO [to 7 November 2015]

POLIO [to 7 November 2015]
Public Health Emergency of International Concern (PHEIC)

GPEI Update: [Anticipated weekly update as of 4 November 2015 not posted on GPEI website]

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Inactivated polio vaccine introduced in routine immunization programme in Yemen
Sana’a, 3 November 2015— Inactivated polio vaccine (IPV) was formally introduced into the routine immunization programme today in Sana’a, Yemen for all children under the age of one. The introduction, which is supported by GAVI – the Vaccine Alliance, WHO and UNICEF, came as a significant step towards eradicating polio and enhancing Yemen’s immunization programme. Currently, there are no cases of polio in Yemen.

“This is a significant step in eradicating polio as part of the Global Polio Endgame strategic Plan,” says Dr Ahmed Shadoul, WHO Representative for Yemen. “It’s a huge achievement to introduce this vaccine, given the major security, political and economic challenges facing Yemen today.”

The planned introduction of IPV for polio eradication represents the fastest global introduction of any new vaccine in low- and middle-income countries in recent history. Yemen is one of 126 countries that are introducing the vaccine in 2014–2015.

“Yemen is committed to eradicating polio so the national immunization programme has made every effort to introduce the vaccine,” said Dr Ghada Al-Haboob, Director of the Expanded Programme on Immunization. “We are doing our best to ensure that every child receives this vaccine in order to maintain the advances made in the field of immunization…

 

WHO & Regionals [to 7 November 2015]

WHO & Regionals [to 7 November 2015]
SAGE: Call for nominations
2 November 2015
Application deadline: 15 January 2016
The World Health Organization (WHO) is soliciting proposals for nominations for current and future vacancies on its Strategic Advisory Group of Experts (SAGE) on immunization. Nominations are solicited from all regions and are required to be submitted no later than 15 January 2016. Nominations will then be carefully reviewed by the SAGE membership selection panel, which will propose the selection of nominees to the WHO Director-General for appointment.
SAGE is the principal advisory group to WHO for vaccines and immunization. SAGE reports directly to the Director-General and is charged with advising WHO on overall global policies and strategies, ranging from vaccine and technology research and development, to delivery of immunization and its linkages with other health interventions. Its remit is not restricted to childhood vaccines and immunization but extends to all vaccine-preventable diseases as well as all age groups…

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GIN October 2015 pdf, 1.73Mb
3 November 2015

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Weekly Epidemiological Record (WER) 6 November 2015, vol. 90, 45 (pp. 609–616) includes:
609 Zika virus outbreaks in the Americas
610 Malaria situation, 2015

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:: WHO Regional Offices
WHO African Region AFRO
:: Statement on the end of the Ebola outbreak in Sierra Leone
Delivered by Dr Anders Nordström, WHO Representative in Sierra Leone. Today, 7 November 2015

WHO Region of the Americas PAHO
:: Country efforts lead the way toward malaria elimination in the Americas (11/05/2015)
:: Regional Dengue Symposium Addresses Today’s Challenges in Dengue Control (11/03/2015)

WHO South-East Asia Region SEARO
No new digest content identified.

WHO European Region EURO
:: Engaging people in every step: patients and carers explain the benefits of people-centred health care 05-11-2015

WHO Eastern Mediterranean Region EMRO
:: Health needs in conflict zones must be addressed by Dr Ala Alwan
5 November 2015
:: Inactivated polio vaccine introduced in routine immunization programme in Yemen
3 November 2015
:: WHO reaches besieged Dar’a and vulnerable Hama with 290 000 life-saving treatments
2 November 2015

WHO Western Pacific Region
No new digest content identified.

Gavi [to 7 November 2015]

Gavi [to 7 November 2015]
http://www.gavialliance.org/library/news/press-releases/

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Afghanistan ensures safe passage of life-saving vaccines
02 November 2015
Afghan health ministry shows commitment to immunisation by opening critical storage facility at central airport
Kabul, Afghanistan, 27 October 2015 – As humanitarian organisations responded to Afghanistan’s earthquake this week, the Government underlined its commitment to ensuring no interruptions in the flow of life-saving vaccines by inaugurating a special storage facility at Kabul airport.

The new facility, which guarantees safekeeping of vaccines before they are transported to a network of immunisation centres, represents a critical step in the Health Ministry’s plans to strengthen cold chain management across Afghanistan.

Kabul airport represents the main point of entry for the 10 types of vaccines that Afghanistan purchases overseas, but new consignments are often held up – either because of customs clearance or security issues at their final destination.

Equipped with standard cold equipment to keep vaccines at the right temperature and a back-up generator in case of power shortages, the new storage facility ensures a two-three month supply of routine vaccines can remain in transit at the airport at any one time.

“This is a crucial first step for ensuring quality of vaccines once the vaccine shipments arrive in the country,” said Afghan Health Minister, Dr. Ferozudin Feroz, speaking at the facility’s inauguration…

HIV scientists launch 23 million euro project to develop vaccine

HIV scientists launch 23 million euro project to develop vaccine
2nd November 2015
A new 23 million euro initiative to accelerate the search for an effective HIV vaccine begins today.

Financed by the European Commission, the European AIDS Vaccine Initiative (EAVI2020) brings together leading HIV researchers from public organisations and biotech companies from across Europe, Australia, Canada and the USA in a focused effort to develop protective and therapeutic HIV vaccines.

According to the World Health Organisation, around 35 million people were living with HIV at the end of 2013. Over two million people are newly infected every year, and it is estimated that around 22 billion US dollars is spent yearly on HIV treatment and care. An effective vaccine remains the best hope of ending the epidemic.

Although researchers have been working on developing a vaccine for 30 years, recent advances are helping to speed up their quest. Scientists have isolated antibodies that are able to block HIV infection in preclinical models, and there have been new developments in using synthetic biology to design better vaccines.

The EAVI2020 consortium, which is led by Imperial College London, unites scientists from 22 institutions, pooling their knowledge and expertise to develop novel candidate vaccines that can be taken through to human trials within five years. EAVI2020 is funded with an EU-grant under the health program of Horizon 2020 for research and innovation.

Professor Robin Shattock, Coordinator of EAVI2020, from the Department of Medicine at Imperial College London, said: “Creating an effective vaccine against HIV represents one of the greatest biological challenges of a generation. This project creates an unique opportunity for us to build on the enormous scientific progress gleaned over the last few years, providing an unprecedented insight into the nature of protective antibodies and anti-viral cellular response that will be needed for an effective vaccine. We now understand much more about how humans make protective immune responses and how to structure vaccine candidates. We have a level of understanding at a molecular level that was not previously available.

“But it is impossible for one group or institution to create an HIV vaccine on its own. This new project should enable us to move much more quickly. It brings together a multidisciplinary team of molecular biologists, immunologists, virologists, biotechnologists and clinicians, providing the breadth of expertise needed to take the latest discoveries in the lab and rapidly advance them through preclinical testing and manufacture, into early human trials.”…

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IAVI International AIDS Vaccine Initiative [to 7 November 2015]
http://www.iavi.org/press-releases/2015

IAVI Supports New EU-Funded AIDS Vaccine Research Consortium
November 2, 2015
NEW YORK – The International AIDS Vaccine Initiative (IAVI) will provide product development expertise and laboratory assessment support to a new research consortium announced today called the European AIDS Vaccine Initiative (EAVI2020).
Funded by a European Union grant under the Horizon 2020 health program, the consortium unites 22 public organizations and biotech companies across Europe, Australia, Canada and the United States to develop preventive and therapeutic HIV vaccines. The project aims to develop novel candidate vaccines that can be taken into human trials within five years…

Sabin Vaccine Institute [to 7 November 2015]

Sabin Vaccine Institute [to 7 November 2015]
http://www.sabin.org/updates/pressreleases

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Regional Dengue Symposium Addresses Today’s Challenges in Dengue Control
PAHO, DVI and Sabin provide an open forum to discuss the future of dengue
RIO DE JANEIRO, BRAZIL — November 3, 2015 — More than one hundred public health experts and stakeholders gathered today in Rio de Janeiro, Brazil, for the First Regional Dengue Symposium, led by the Pan American Health Organization (PAHO), the Sabin Vaccine Institute (Sabin) and the Dengue Vaccine Initiative (DVI)…

European Medicines Agency [to 7 November 2015]

European Medicines Agency [to 7 November 2015]
http://www.ema.europa.eu/

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:: Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 3-5 November 2015
06/11/2015
Review concludes evidence does not support that HPV vaccines cause CRPS or POTS
The PRAC has completed a detailed scientific review of the evidence surrounding reports of two syndromes, complex regional pain syndrome (CRPS) and postural orthostatic tachycardia syndrome (POTS) in young women given human papillomavirus (HPV) vaccines. These vaccines are given to protect them from cervical cancer and other HPV-related cancers and pre-cancerous conditions. This review concluded that the evidence does not support a causal link between the vaccines (Cervarix, Gardasil/Silgard and Gardasil-9) and development of CRPS or POTS. Therefore there is no reason to change the way the vaccines are used or amend the current product information. More information is included in the table below.

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:: Supporting better use of medicines
06/11/2015
EMA releases guidance on methods to be used in the design and conduct of post authorisation efficacy studies
The European Medicines Agency (EMA) has released a draft scientific guideline that outlines how post-authorisation efficacy studies (PAES) should be designed by companies to support regulatory decision making in the European Union (EU). In addition, a guidance that describes the regulatory aspects for the fulfilment of imposed PAES is also published.

GHIT Fund [to 7 November 2015]

GHIT Fund [to 7 November 2015]
https://www.ghitfund.org/
GHIT was set up in 2012 with the aim of developing new tools to tackle infectious diseases that devastate the world’s poorest people. Other funders include six Japanese pharmaceutical companies, the Japanese Government and the Bill & Melinda Gates Foundation.

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Press Room 2015.11.05
From a Phase 2 TB Vaccine Trial, to Early Work to Neutralize Drug-Resistant Malaria, $10.7 Million in New Investments from GHIT Fund Escalates and Diversifies Japan’s Global Health Commitments
Projects advance product development partnerships with Japanese pharma, Kickstart GHIT’s Grand Challenges; New funds also target dengue, leishmaniasis

The Global Health Innovative Technology Fund (GHIT Fund), which in the last two years has invested US$43 million to develop innovative tools for fighting diseases worldwide, today announced it is investing $10.7 million* at multiple points in the product development pipeline to seek new interventions for malaria, tuberculosis (TB), leishmaniasis and dengue.

FIVE-YEAR GLOBAL INITIATIVE TO PROTECT ALL WOMEN AND GIRLS FROM CERVICAL CANCER KICKS OFF IN LONDON

FIVE-YEAR GLOBAL INITIATIVE TO PROTECT ALL WOMEN AND GIRLS FROM CERVICAL CANCER KICKS OFF IN LONDON
Wide ranging commitments to bring cervical cancer prevention to the women who need it most

London, 4 November, 2015— Cervical Cancer Action (CCA), a coalition of global health advocates, hosted leaders from governments in Africa, Latin American and Asia, along with representatives from the World Health Organization, United Nations Agencies, global philanthropies, international not-for-profit organizations and vaccine and medical diagnostic companies in London today to launch a global initiative to tackle the growing burden of cervical cancer in low- and lower-middle income countries.

Taking Cervical Cancer Prevention to Scale: Protecting All Women and Girls is a landmark initiative that aims to increase collaboration, commitment and investment to ensure that all women and girls are protected within ten years. It is focused on expanding and aligning global efforts to ensure that all girls are vaccinated against HPV, the virus that causes cervical cancer, and all women receive screening…

…During the meeting, new data on the cost of action to prevent cervical cancer in low-income and lower-middle income countries was released by the American Cancer Society in partnership with a team at Harvard University. “We know what to do, we have the tools, and with the evidence presented at this meeting we also know what it will cost to act,” said Ambassador Sally Cowal, Senior Vice President, Global Cancer Control at the American Cancer Society. US$3.65 billion are required over the next ten years to vaccinate all 10-year-old girls and provide screening and preventive treatment to women at highest risk for cervical cancer in low-income and low-middle income countries.

Cervical Cancer Action, The London School of Hygiene & Tropical Medicine, Cancer Research UK, Union for International Cancer Control, American Cancer Society, PATH, Grounds for Health, Jhpiego, International Federation of Gynecology and Obstetrics (FIGO), International Planned Parenthood Federation, UNAIDS and Women Deliver are among the initial partners…

Fondation Merieux [to 7 November 2015]

Fondation Merieux [to 7 November 2015]
http://www.fondation-merieux.org/news
Mission: Contribute to global health by strengthening local capacities of developing countries to reduce the impact of infectious diseases on vulnerable populations.

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Demand side interventions to increase and sustain vaccination uptake meeting
13 October 2015, Les Pensieres, Annecy (France)
Fondation Mérieux organized the Demand side interventions to increase and sustain vaccination uptake Meeting on September 28-30 at Les Pensières conference center, Veyrier-du-lac, France.

Report: I am Here, I Belong: the Urgent Need to End Childhood Statelessness – UNHCR

Report: I am Here, I Belong: the Urgent Need to End Childhood Statelessness
UNHCR
November 2015 [Release] :: 28 pages
http://www.unhcr.org/ibelong/wp-content/uploads/2015-10-StatelessReport_ENG15-web.pdf

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Overview from Report Preface
Stateless children are born into a world in which they will face a lifetime of discrimination; their status profoundly affects their ability to learn and grow, and to fulfil their ambitions and dreams for the future.

With a stateless child being born somewhere in the world at least every 10 minutes, this is a problem that is growing. In countries hosting the 20 largest stateless populations, at least 70,000 stateless children are born each year.

The effects of being born stateless are severe. In more than 30 countries, children need nationality documentation to receive medical care. In at least 20 countries, stateless children cannot be legally vaccinated.

This report aims to go beyond these statistics, providing direct testimony of children and young people and how being stateless affects them.

In July and August 2015, UNHCR spoke with more than 250 children and youth,1 and their parents and guardians, in seven countries around the world about their experiences of childhood statelessness.

This is the first geographically diverse survey of the views of stateless children and youth. Many of the children and young people had never spoken to anyone about what it was like to be stateless.

The report highlights how not being recognized as a national of any country can create insurmountable barriers to education and adequate health care and stifle job prospects. It reveals the devastating psychological toll of statelessness and its serious ramifications not only for young people, whose whole futures are before them, but also for their families, communities and countries. It powerfully demonstrates the urgency of ending and preventing childhood
statelessness.

OECD – Healthcare improving too slowly to meet rising strain of chronic diseases

OECD – Healthcare improving too slowly to meet rising strain of chronic diseases
4/11/2015 –

Too many lives are still lost in OECD countries because healthcare quality is improving too slowly to cope with ageing populations and the growing number of people with one or more chronic diseases, according to a new OECD report.

Health at a Glance 2015 shows that overall health expenditure continues to grow slowly in many OECD countries in line with GDP growth, although health spending fell in 2013 for a third consecutive year in Italy and Portugal and a fourth in Greece.

The new edition of Health at a Glance provides a set of dashboards allowing readers to visualise the relative performance of different OECD countries on selected indicators. These dashboards show that all countries have wide scope for improving the quality of health care and tackling unhealthy lifestyles, such as obesity and harmful alcohol consumption.
No country consistently performs at the top of the country ranking on key indicators of quality of care, even those that spend the most on health. There is room for improvement in all countries in the prevention, early diagnosis and treatment of different health problems.

The United States, for example, is doing well in providing acute care for people having a heart attack or a stroke and preventing them from dying, but is not performing well in preventing avoidable hospital admissions for people with chronic conditions such as asthma and diabetes. The reverse is true in Portugal, Spain and Switzerland, which have relatively low rates of hospital admissions for certain chronic conditions, but relatively high rates of mortality for patients admitted to hospital for a heart attack or stroke.

Finland and Sweden do relatively well in saving the lives of people following diagnosis for cervical, breast or colorectal cancer, but the survival rates for these types of cancer is lower in Chile, Poland, the Czech Republic, the United Kingdom and Ireland…

Capacity building in national influenza laboratories – use of laboratory assessments to drive progress

BMC Infectious Diseases
http://www.biomedcentral.com/bmcinfectdis/content
(Accessed 7 November 2015)

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Research article
Capacity building in national influenza laboratories – use of laboratory assessments to drive progress
Lucinda Johnson, Sarah Muir-Paulik, Pam Kennedy, Steven Lindstrom, Amanda Balish, Tricia Aden, Ann Moen BMC Infectious Diseases 2015, 15:501 (6 November 2015)

Knowledge, attitudes and perceptions towards polio immunization among residents of two highly affected regions of Pakistan

BMC Public Health
http://www.biomedcentral.com/bmcpublichealth/content
(Accessed 7 November 2015)

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Research article
Counting the cost of child mortality in the World Health Organization African region
Joses Kirigia, Rosenabi Muthuri, Juliet Nabyonga-Orem, Doris Kirigia BMC Public Health 2015, 15:1103 (6 November 2015)

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Research article
Knowledge, attitudes and perceptions towards polio immunization among residents of two highly affected regions of Pakistan
Muhammad Khan, Akram Ahmad, Talieha Aqeel, Saad Salman, Qamer Ibrahim, Jawaria Idrees, Muhammad Khan BMC Public Health 2015, 15:1100 (5 November 2015)
Abstract
Background
Despite the efforts of national and international organizations, polio has not been eradicated from Pakistan. The prevalence of polio in Pakistan is exceptional in global context. Quetta and Peshawar divisions are amongst the most affected regions hit by polio in Pakistan. This study was carried out to assess the knowledge, attitudes and perceptions towards polio immunization among residents of Quetta and Peshawar divisions in Pakistan.
Methods
A descriptive, cross-sectional study involving 768 participants was conducted from August to December, 2014 in Quetta and Peshawar divisions in Pakistan. Multistage sampling technique was used to draw a sample of residents from each division. A pre-tested, self-administered questionnaire was used to collect the data from eligible participants. Descriptive and logistic regression analyses were used to express the results.
Results
A total of 38.8 % participants exhibited good knowledge about polio. Mean knowledge score of the participants was 7.35 ± 2.54 (based on 15 knowledge questions). Older age (p < 0.001), low qualification (p < 0.05), rural locality (p < 0.05) and Quetta division (p < 0.001) were significantly associated with poor knowledge of polio. A large proportion of participants displayed negative attitudes towards polio immunization (84.8 %), with a mean score of 19.19 ± 2.39 (based on 8 attitude statements). Lack of education (p < 0.001) and rural residence (p < 0.001) were significantly associated with the negative attitudes of participants towards polio immunization. False religious beliefs (39.06 %), lack of knowledge (33.7 %), fear of infertility by polio vaccines (32.16 %) and security issues (29.42 %) were reported by the participants as the main barriers towards polio immunization.
Conclusion
The findings of this study showed poor knowledge and negative attitudes of participants towards polio immunizations. Religious beliefs and lack of knowledge about polio immunization were reported as the major barriers towards polio immunization.

Rapid Evidence Assessment of the Literature (REAL © ): streamlining the systematic review process and creating utility for evidence-based health care

BMC Research Notes
http://www.biomedcentral.com/bmcresnotes/content
(Accessed 7 November 2015)

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Research article
Rapid Evidence Assessment of the Literature (REAL © ): streamlining the systematic review process and creating utility for evidence-based health care
Cindy Crawford, Courtney Boyd, Shamini Jain, Raheleh Khorsan, Wayne Jonas BMC Research Notes 2015, 8:631
Abstract
Background
Systematic reviews (SRs) are widely recognized as the best means of synthesizing clinical research. However, traditional approaches can be costly and time-consuming and can be subject to selection and judgment bias. It can also be difficult to interpret the results of a SR in a meaningful way in order to make research recommendations, clinical or policy decisions, or practice guidelines. Samueli Institute has developed the Rapid Evidence Assessment of the Literature (REAL) SR process to address these issues. REAL provides up-to-date, rigorous, high quality SR information on health care practices, products, or programs in a streamlined, efficient and reliable manner. This process is a component of the Scientific Evaluation and Review of Claims in Health Care (SEaRCH™) program developed by Samueli Institute, which aims at answering the question of “What works?” in health care.
Methods/design
The REAL process (1) tailors a standardized search strategy to a specific and relevant research question developed with various stakeholders to survey the available literature; (2) evaluates the quantity and quality of the literature using structured tools and rulebooks to ensure objectivity, reliability and reproducibility of reviewer ratings in an independent fashion and; (3) obtains formalized, balanced input from trained subject matter experts on the implications of the evidence for future research and current practice.
Results
Online tools and quality assurance processes are utilized for each step of the review to ensure a rapid, rigorous, reliable, transparent and reproducible SR process.
Conclusions
The REAL is a rapid SR process developed to streamline and aid in the rigorous and reliable evaluation and review of claims in health care in order to make evidence-based, informed decisions, and has been used by a variety of organizations aiming to gain insight into “what works” in health care. Using the REAL system allows for the facilitation of recommendations on appropriate next steps in policy, funding, and research and for making clinical and field decisions in a timely, transparent, and cost-effective manner.

Child health in Syria: recognising the lasting effects of warfare on health

Conflict and Health
http://www.conflictandhealth.com/
[Accessed 7 November 2015]

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Review
Child health in Syria: recognising the lasting effects of warfare on health
Devakumar D, Birch M, Rubenstein LS, Osrin D, Sondorp E and Wells JCK Conflict and Health 2015, 9:34 (3 November 2015)
Abstract
The war in Syria, now in its fourth year, is one of the bloodiest in recent times. The legacy of war includes damage to the health of children that can last for decades and affect future generations. In this article we discuss the effects of the war on Syria’s children, highlighting the less documented longer-term effects. In addition to their present suffering, these children, and their own children, are likely to face further challenges as a result of the current conflict. This is essential to understand both for effective interventions and for ethical reasons.

Developing World Bioethics – December 2015

Developing World Bioethics
December 2015 Volume 15, Issue 3 Pages iii–iii, 115–275
http://onlinelibrary.wiley.com/doi/10.1111/dewb.2015.15.issue-2/issuetoc

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Considerations for a Human Rights Impact Assessment of a Population Wide Treatment for HIV Prevention Intervention (pages 115–124)
Johanna Hanefeld, Virginia Bond, Janet Seeley, Shelley Lees and Nicola Desmond
Article first published online: 8 NOV 2013 | DOI: 10.1111/dewb.12038
Abstract
Increasing attention is being paid to the potential of anti-retroviral treatment (ART) for HIV prevention. The possibility of eliminating HIV from a population through a universal test and treat intervention, where all people within a population are tested for HIV and all positive people immediately initiated on ART, as part of a wider prevention intervention, was first proposed in 2009. Several clinical trials testing this idea are now in inception phase. An intervention which relies on universally testing the entire population for HIV will pose challenges to human rights, including obtaining genuine consent to testing and treatment. It also requires a context in which people can live free from fear of stigma, discrimination and violence, and can access services they require. These challenges are distinct from the field of medical ethics which has traditionally governed clinical trials and focuses primarily on patient researcher relationship. This paper sets out the potential impact of a population wide treatment as prevention intervention on human rights. It identifies five human right principles of particular relevance: participation, accountability, the right to health, non-discrimination and equality, and consent and confidentiality. The paper proposes that explicit attention to human rights can strengthen a treatment as prevention intervention, contribute to mediating likely health systems challenges and offer insights on how to reach all sections of the population.

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Perceived Quality of Informed Refusal Process: A Cross-Sectional Study from Iranian Patients’ Perspectives (pages 172–178)
Mehrdad Farzandipour, Abbas Sheikhtaheri and Monireh Sadeqi Jabali
Article first published online: 11 APR 2014 | DOI: 10.1111/dewb.12054
Abstract
Patients have the right to refuse their treatment; however, this refusal should be informed. We evaluated the quality of the informed refusal process in Iranian hospitals from patients’ viewpoints. To this end, we developed a questionnaire that covered four key aspects of the informed refusal process including; information disclosure, voluntariness, comprehension, and provider-patient relationship. A total of 284 patients who refused their treatment from 12 teaching hospitals in the Isfahan Province, Iran, were recruited and surveyed to produce a convenience sample. Patients’ perceptions about the informed refusal process were scored and the mean scores of the four components were calculated. The findings showed that the practice of information disclosure (9.6 ± 6.4 out of 22 points) was perceived to be moderate, however, comprehension (2.3 ± 1.4 out of 4 points), voluntariness (8.7 ± 1.5 out of 12 points) and provider–patient relationship (10.2 ±  5.2 out of 16 points) were perceived to be relatively good. We found that patients, who refused their care before any treatment had commenced, reported a lower quality of information disclosure and voluntariness. Patients informed by nurses and those who had not had a previous related admission, reported lower scores for comprehension and relationship. In conclusion, the process of obtaining informed refusal was relatively satisfactory except for levels of information disclosure. To improve current practices, Iranian patients need to be better informed about; different treatment options, consequences of treatment refusal, costs of not continuing treatment and follow-ups after refusal. Developing more informative refusal forms is needed.

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Enhancing Research Ethics Review Systems in Egypt: The Focus of an International Training Program Informed by an Ecological Developmental Approach to Enhancing Research Ethics Capacity (pages 199–207)
Hillary Anne Edwards, Tamer Hifnawy and Henry Silverman
Article first published online: 3 JUN 2014 | DOI: 10.1111/dewb.12062
Abstract
Recently, training programs in research ethics have been established to enhance individual and institutional capacity in research ethics in the developing world. However, commentators have expressed concern that the efforts of these training programs have placed ‘too great an emphasis on guidelines and research ethics review’, which will have limited effect on ensuring ethical conduct in research. What is needed instead is a culture of ethical conduct supported by national and institutional commitment to ethical practices that are reinforced by upstream enabling conditions (strong civil society, public accountability, and trust in basic transactional processes), which are in turn influenced by developmental conditions (basic freedoms of political freedoms, economic facilities, social opportunities, transparency guarantees, and protective security). Examining this more inclusive understanding of the determinants of ethical conduct enhances at once both an appreciation of the limitations of current efforts of training programs in research ethics and an understanding of what additional training elements are needed to enable trainees to facilitate national and institutional policy changes that enhance research practices. We apply this developmental model to a training program focused in Egypt to describe examples of such additional training activities.

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Improving the Quality of Host Country Ethical Oversight of International Research: The Use of a Collaborative ‘Pre-Review’ Mechanism for a Study of Fexinidazole for Human African Trypanosomiasis (pages 241–247)
Carl H. Coleman, Chantal Ardiot, Séverine Blesson, Yves Bonnin, Francois Bompart, Pierre Colonna, Ames Dhai, Julius Ecuru, Andrew Edielu, Christian Hervé, François Hirsch, Bocar Kouyaté, Marie-France Mamzer-Bruneel, Dionko Maoundé, Eric Martinent, Honoré Ntsiba, Gérard Pelé, Gilles Quéva, Marie-Christine Reinmund, Samba Cor Sarr, Abdoulaye Sepou, Antoine Tarral, Djetodjide Tetimian, Olaf Valverde, Simon Van Nieuwenhove and Nathalie Strub-Wourgaft
Article first published online: 14 JUL 2014 | DOI: 10.1111/dewb.12068
Abstract
Developing countries face numerous barriers to conducting effective and efficient ethics reviews of international collaborative research. In addition to potentially overlooking important scientific and ethical considerations, inadequate or insufficiently trained ethics committees may insist on unwarranted changes to protocols that can impair a study’s scientific or ethical validity. Moreover, poorly functioning review systems can impose substantial delays on the commencement of research, which needlessly undermine the development of new interventions for urgent medical needs. In response to these concerns, the Drugs for Neglected Diseases Initiative (DNDi), an independent nonprofit organization founded by a coalition of public sector and international organizations, developed a mechanism to facilitate more effective and efficient host country ethics review for a study of the use of fexinidazole for the treatment of late stage African Trypanosomiasis (HAT). The project involved the implementation of a novel ‘pre-review’ process of ethical oversight, conducted by an ad hoc committee of ethics committee representatives from African and European countries, in collaboration with internationally recognized scientific experts. This article examines the process and outcomes of this collaborative process.

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To What did They Consent? Understanding Consent Among Low Literacy Participants in a Microbicide Feasibility Study in Mazabuka, Zambia (pages 248–256)
Esther Munalula-Nkandu, Paul Ndebele, Seter Siziya and JC Munthali
Article first published online: 1 AUG 2014 | DOI: 10.1111/dewb.12069

We conducted a study to review the consenting process in a vaginal Microbicide feasibility study conducted in Mazabuka, Zambia. Participants were drawn from those participating in the microbicide study. A questionnaire and focus group discussion were used to collect information on participants understanding of study aims, risks and benefits. Altogether, 200 participants took part in this study. The results of the study showed that while all participants signed or endorsed their thumbprints to the consent forms, full informed consent was not attained from most of the participants since 77% (n = 154) of the participants had numerous questions about the study and 34% (n = 68) did not know who to get in touch with concerning the study. Study objectives were not fully understood by over 61% of the participants. Sixty four percent of the participants were not sure of the risks of taking part in the microbicide study. A significant number thought the study was all about determining their HIV status. Some participants were concerned that their partners were not on the trial as they were convinced that being on the study meant that that they had a lifetime protection from HIV infection. The process of obtaining consent was inadequate as various phases of the study were not fully understood. We recommend the need for researchers to reinforce the consenting process in all studies and more so when studies are conducted in low literacy populations.

Epidemiology and Infection :: Volume 143 – Issue 16 – December 2015

Epidemiology and Infection
Volume 143 – Issue 16 – December 2015
http://journals.cambridge.org/action/displayIssue?jid=HYG&tab=currentissue

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The pandemic potential of avian influenza A(H7N9) virus: a review
W. D. TANNER, D. J. A. TOTH and A. V. GUNDLAPALLI
pp 3359 – 3374
Summary
In March 2013 the first cases of human avian influenza A(H7N9) were reported to the World Health Organization. Since that time, over 650 cases have been reported. Infections are associated with considerable morbidity and mortality, particularly within certain demographic groups. This rapid increase in cases over a brief time period is alarming and has raised concerns about the pandemic potential of the H7N9 virus. Three major factors influence the pandemic potential of an influenza virus: (1) its ability to cause human disease, (2) the immunity of the population to the virus, and (3) the transmission potential of the virus. This paper reviews what is currently known about each of these factors with respect to avian influenza A(H7N9). Currently, sustained human-to-human transmission of H7N9 has not been reported; however, population immunity to the virus is considered very low, and the virus has significant ability to cause human disease. Several statistical and geographical modelling studies have estimated and predicted the spread of the H7N9 virus in humans and avian species, and some have identified potential risk factors associated with disease transmission. Additionally, assessment tools have been developed to evaluate the pandemic potential of H7N9 and other influenza viruses. These tools could also hypothetically be used to monitor changes in the pandemic potential of a particular virus over time.

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Age-specific measles mortality during the late 19th–early 20th centuries
G. D. SHANKS, M. WALLER, H. BRIEM and M. GOTTFREDSSON
pp 3434 – 3441
SUMMARY
Measles mortality fell prior to the introduction of vaccines or antibiotics. By examining historical mortality reports we sought to determine how much measles mortality was due to epidemiological factors such as isolation from major population centres or increased age at time of infection. Age-specific records were available from Aberdeen; Scotland; New Zealand and the states of Australia at the end of the 19th and beginning of the 20th centuries. Despite the relative isolation of Australia, measles mortality was concentrated in very young children similar to Aberdeen. In the more isolated states of Tasmania, Western Australia and Queensland adults made up 14–15% of measles deaths as opposed to 8–9% in Victoria, South Australia and New South Wales. Mortality in Iceland and Faroe Islands during the 1846 measles epidemic was used as an example of islands isolated from respiratory pathogens. The transition from crisis mortality across all ages to deaths concentrated in young children occurred prior to the earliest age-specific mortality data collected. Factors in addition to adult age of infection and epidemiological isolation such as nutritional status and viral virulence may have contributed to measles mortality outcomes a century ago.

Eurosurveillance – Volume 20, Issue 44, 05 November 2015

Eurosurveillance
Volume 20, Issue 44, 05 November 2015
http://www.eurosurveillance.org/Public/Articles/Archives.aspx?PublicationId=11678

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Research Articles
Dealing with Ebola virus disease in Spain: epidemiological inquiries received by the Department of Public Health Alerts, April to December 2014
by V Blaya-Nováková, Mía Ángeles Lópaz-Pérez, I Méndez-Navas, Mía F Domínguez-Berjón, J Astray-Mochales

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Development and deployment of a rapid recombinase polymerase amplification Ebola virus detection assay in Guinea in 2015
by O Faye, O Faye, Bé Soropogui, P Patel, AA El Wahed, C Loucoubar, G Fall, D Kiory, N’F Magassouba, S Keita, MK Kondé, AA Diallo, L Koivogui, H Karlberg, A Mirazimi, O Nentwich, O Piepenburg, M Niedrig, M Weidmann, AA Sall
Abstract
In the absence of a vaccine or specific treatments for Ebola virus disease (EVD), early identification of cases is crucial for the control of EVD epidemics. We evaluated a new extraction kit (SpeedXtract (SE), Qiagen) on sera and swabs in combination with an improved diagnostic reverse transcription recombinase polymerase amplification assay for the detection of Ebola virus (EBOV-RT-RPA). The performance of combined extraction and detection was best for swabs. Sensitivity and specificity of the combined SE and EBOV-RT-RPA were tested in a mobile laboratory consisting of a mobile glovebox and a Diagnostics-in-a-Suitcase powered by a battery and solar panel, deployed to Matoto Conakry, Guinea as part of the reinforced surveillance strategy in April 2015 to reach the goal of zero cases. The EBOV-RT-RPA was evaluated in comparison to two real-time PCR assays. Of 928 post-mortem swabs, 120 tested positive, and the combined SE and EBOV-RT-RPA yielded a sensitivity and specificity of 100% in reference to one real-time RT-PCR assay. Another widely used real-time RT-PCR was much less sensitive than expected. Results were provided very fast within 30 to 60 min, and the field deployment of the mobile laboratory helped improve burial management and community engagement.
Perspectives

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Preparing for imported Ebola cases in Israel, 2014 to 2015
by T Brosh-Nissimov, L Poles, M Kassirer, R Singer, E Kaliner, DD Shriki, E Anis, I Fogel, D Engelhard, I Grotto

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Public health challenges and legacies of Japan’s response to the Ebola virus disease outbreak in West Africa 2014 to 2015
by T Saito

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Mobile diagnostics in outbreak response, not only for Ebola: a blueprint for a modular and robust field laboratory
by R Wölfel, K Stoecker, E Fleischmann, B Gramsamer, M Wagner, P Molkenthin, A Di Caro, S Günther, S Ibrahim, GH Genzel, AJ Ozin-Hofsäss, P Formenty, L Zöller

Food Insecurity And Health Outcomes

Health Affairs
November 2015; Volume 34, Issue 11
http://content.healthaffairs.org/content/current

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Food & Health
Food Insecurity And Health Outcomes
Craig Gundersen1,* and James P. Ziliak2
Author Affiliations
1Craig Gundersen (cggunder@illinois.edu) is the Soybean Industry Endowed Professor in Agricultural Strategy in the Department of Agricultural and Consumer Economics, University of Illinois, in Urbana.
2James P. Ziliak is the Carol Martin Gatton Endowed Chair in Microeconomics in the Department of Economics, University of Kentucky, in Lexington.
Abstract
Almost fifty million people are food insecure in the United States, which makes food insecurity one of the nation’s leading health and nutrition issues. We examine recent research evidence of the health consequences of food insecurity for children, nonsenior adults, and seniors in the United States. For context, we first provide an overview of how food insecurity is measured in the country, followed by a presentation of recent trends in the prevalence of food insecurity. Then we present a survey of selected recent research that examined the association between food insecurity and health outcomes. We show that the literature has consistently found food insecurity to be negatively associated with health. For example, after confounding risk factors were controlled for, studies found that food-insecure children are at least twice as likely to report being in fair or poor health and at least 1.4 times more likely to have asthma, compared to food-secure children; and food-insecure seniors have limitations in activities of daily living comparable to those of food-secure seniors fourteen years older. The Supplemental Nutrition Assistance Program (SNAP) substantially reduces the prevalence of food insecurity and thus is critical to reducing negative health outcomes.

Health Policy and Planning – Volume 30, Issue 10, December 2015

Health Policy and Planning
Volume 30 Issue 10 December 2015
http://heapol.oxfordjournals.org/content/current

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Assessing the pro-poor effect of different contracting schemes for health services on health facilities in rural Afghanistan
Olakunle Alonge1,*, Shivam Gupta1, Cyrus Engineer1, Ahmad Shah Salehi2 and David H Peters1
Author Affiliations
1Department of International Health, Johns Hopkins Bloomberg School of Public Health, Suite E8622, 615 N Wolfe Street, Baltimore, MD 21205, USA and
2Department of Health Economics and Finance, Afghanistan Ministry of Public Health, Kabul, Afghanistan
Accepted October 30, 2014.
Abstract
Background Despite progress in improving health outcomes in Afghanistan by contracting public health services through non-governmental organizations (NGOs), inequity in access persists between the poor and non-poor. This study examined the distributive effect of different contracting types on primary health services provision between the poor and non-poor in rural Afghanistan.
Method Contracts to NGOs were made to deliver a common set of primary care services in each province, with the funding agencies determining contract terms. The contracting approaches could be classified into three contracting out types (CO-1, CO-2 and CO-3) and a contracting-in (CI) approach based on the contract terms, design and implementation. Exit interviews of patients attending randomly sampled primary health facilities were collected through systematic sampling across 28 provinces at two time points. The outcome, the odds that a client attending a health facility is poor, was modelled using logistic regression with a robust variance estimator, and the effect of contracting was estimated using the difference-in-difference approach combined with stratified analyses.
Results The sample covered 5960 interviews from 306 health facilities in 2005 and 2008. The adjusted odds of a poor client attending a health facility over time increased significantly for facilities under CO-1 and CO-2, with odds ratio of 2.82 (1.49, 5.36) P-value 0.001 and 2.00 (1.33, 3.02) P-value 0.001, respectively. The odds ratios for those under CO-3 and CI were not statistically significantly different over time. When compared with the non-contracting facilities, the adjusted ratio of odds ratios of poor status among clients was significantly higher for only those under CO-1, ratio of 2.50 (1.32, 4.74) P-value 0.005.
Conclusions CO-1 arrangement which allows contractors to decide on how funds are allocated within a fixed lump sum with non-negotiable deliverables, and actively managed through an independent government agency, is effective in improving equity of health services provision.

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Use of health care among febrile children from urban poor households in Senegal: does the neighbourhood have an impact?
Georges Karna Kone1,*, Richard Lalou2, Martine Audibert3, Hervé Lafarge4, Stéphanie Dos Santos2, Alphousseyni Ndonky2 and Jean-Yves Le Hesran5
Author Affiliations
1Centre de Recherche du Centre Hospitalier de l’Université de Montréal (CR CHUM) et Université de Daloa (Cote d’ivoire), 850 rue saint Denis Montréal, Canada,
2UMR 151 IRD/AMU, Laboratoire Population–Environnement–Développement, Aix-Marseille Université, centre Saint-Charles, Case 10, 3, place Victor-Hugo, 13331 Marseille cedex 3, France,
3CERDI, CNRS, 65 Boulevard François Mitterrand, 63000 Clermont-Ferrand, France,
4University of Paris Dauphine 32, avenue Henri Varagnat 93143 Bondy cedex, France
Accepted December 31, 2014.
Abstract
Urban malaria is considered a major public health problem in Africa. The malaria vector is well adapted in urban settings and autochthonous malaria has increased. Antimalarial treatments prescribed presumptively or after rapid diagnostic tests are also highly used in urban settings. Furthermore, health care strategies for urban malaria must comply with heterogeneous neighbourhood ecosystems where health-related risks and opportunities are spatially varied. This article aims to assess the capacity of the urban living environment to mitigate or increase individual or household vulnerabilities that influence the use of health services. The data are drawn from a survey on urban malaria conducted between 2008 and 2009. The study sample was selected using a two-stage randomized sampling. The questionnaire survey covered 2952 households that reported a case of fever episode in children below 10 years during the month before the survey.
Self-medication is a widespread practice for children, particularly among the poorest households in Dakar. For rich households, self-medication for children is more a transitional practice enabling families to avoid opportunity costs related to visits to health facilities. For the poorest, it is a forced choice and often the only treatment option. However, the poor that live in well-equipped neighbourhoods inhabited by wealthy residents tend to behave as their rich neighbours. They grasp the opportunities provided by the area and adjust their behaviours accordingly. Though health care for children is strongly influenced by household socio-economic characteristics, neighbourhood resources (facilities and social networks) will promote health care among the poorest and reduce access inequalities. Without being a key factor, the neighbourhood of residence—when it provides resources—may be of some help to overcome the financial hurdle. Findings suggest that the neighbourhood (local setting) is a relevant scale for health programmes in African cities.

Humanitarian Exchange Magazine – Number 65, November 2015

Humanitarian Exchange Magazine
Number 65 November 2015
http://odihpn.org/wp-content/uploads/2015/10/HE_65_web.pdf
The crisis in Iraq

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Human trafficking in crises: a neglected protection concern
by Laura Lungarotti, Sarah Craggs and Agnes Tillinac

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Connecting humanitarian actors and displaced communities: the IDP call centre in Iraq
by Gemma Woods and Sarah Mace

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Unleashing the multi-purpose power of cash
by Su’ad Jarbawi
Iraq is an upper middle-income country with high literacy rates, sound infrastructure, functioning markets and a comprehensive hawala cash transfer network covering all 18 governorates, making it an appropriate context for cash transfer programmes. Despite this, cash transfers have been on the periphery of the Iraq humanitarian response. As of the last Humanitarian Response Plan in June 2015, cash transfer programmes (both conditional and unconditional) constituted only 3% of the total funding appeal of $497.9 million

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Hello, money: the impact of technology and e-money in the Nepal earthquake response
by Erik Johnson, Glenn Hughson and Alesh Brown
On 30 April 2015, five days after the massive earthquake in Nepal, the UN Office for the Coordination of Humanitarian Affairs (OCHA) hosted humanitarian agencies in the UN com-pound to start what came to be known as the Cash Coordination Group (CCG). Four working groups were established, focusing on geographical mapping of which agencies were doing cash and where; market analysis; analysis and comparison of financial service providers; and standardising transfer amounts. This article, written by three members of the CCG, highlights learning on market analysis through the use of a mobile application, the identification and use of financial service providers and e-cash.

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Using participatory tools to assess remittances in disasters
by Loic Le De, J. C. Gaillard and Wardlow Friesen
In many low-income countries, remittances help to sustain people’s livelihoods and reduce their vulnerability to disasters. However, most studies on this topic are short-term and rely on econometric methods and analysis. Research suggests that aid agencies are aware of the importance of remittances in disasters, but rarely consider them within their relief actions and recovery programmes since their understanding of such mechanisms is generally very limited. Drawing on fieldwork in Samoa, this article concludes that participatory methods, despite some limitations and challenges, contribute to a better understanding of the complexity of remittances and their importance in people’s livelihoods following disaster.

Knowledge, Behavioral, and Sociocultural Factors Related to Human Papillomavirus Infection and Cervical Cancer Screening Among Inner-City Women in Panama

Journal of Community Health
Volume 40, Issue 6, December 2015
http://link.springer.com/journal/10900/40/4/page/1

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Original Paper
Knowledge, Behavioral, and Sociocultural Factors Related to Human Papillomavirus Infection and Cervical Cancer Screening Among Inner-City Women in Panama
Cheryl A. Vamos, Arlene E. Calvo, Ellen M. Daley…

Journal of Epidemiology & Community Health November 2015

Journal of Epidemiology & Community Health
November 2015, Volume 69, Issue 11
http://jech.bmj.com/content/current

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Editorial
Transnational research partnerships: leveraging big data to enhance US health
Casey Crump1, Kristina Sundquist2,3, Marilyn A Winkleby3
Author Affiliations
1Department of Medicine, Stanford University, Stanford, California, USA
2Center for Primary Health Care Research, Lund University, Malmö, Sweden
3Stanford Prevention Research Center, Stanford University, Stanford, California, USA
Published Online First 12 March 2015
Extract
In the current era of big data and small research budgets, new strategies are needed for more cost-effective leveraging of big data to enhance our nation’s health. One strategy is to promote transnational partnerships to tap into the rich, extensive databases available in other countries, particularly in Europe. The National Institutes of Health (NIH) has increasingly recognised that new collaborations that bring together multiple data sources will play a critical role in advancing our knowledge of disease causation, improving patient care, and promoting healthier communities. However, given cuts in research funding and fierce competition for US grants, some question whether US dollars should be diverted to fund ‘foreign’ studies. In this commentary, we argue that transnational research partnerships offer significant advantages for enhancing the health of the US population as well as the broader global community.

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Contextual socioeconomic factors associated with childhood mortality in Nigeria: a multilevel analysis
Victor T Adekanmbi1,2, Ngianga-Bakwin Kandala1,3, Saverio Stranges1,4, Olalekan A Uthman5,6
Author Affiliations
1Division of Health Sciences, University of Warwick Medical School, Coventry, UK
2Center for Evidence-based Global Health, Ilorin, Nigeria
3Division of Epidemiology and Biostatistics, University of Witwatersrand, School of Public Health, Johannesburg, South Africa
4Department of Population Health, Luxembourg Institute of Health (LIH), Luxembourg
5Division of Health Sciences, Warwick-Centre for Applied Health Research and Delivery (WCAHRD), University of Warwick Medical School, Coventry, UK
6International Health Group, Liverpool School of Tropical Medicine, Liverpool, UK
Published Online First 10 June 2015
Abstract
Background Childhood mortality is a well-known public health issue, particularly in the low and middle income countries. The overarching aim of this study was to examine whether neighbourhood socioeconomic disadvantage is associated with childhood mortality beyond individual-level measures of socioeconomic status in Nigeria.
Methods Multilevel logistic regression models were applied to data on 31 482 under-five children whether alive or dead (level 1) nested within 896 neighbourhoods (level 2) from the 37 states in Nigeria (level 3) using the most recent 2013 Nigeria Demographic and Health Survey (DHS).
Results More than 1 of every 10 children studied had died before reaching the age of 5 years (130/1000 live births). The following factors independently increased the odds of childhood mortality: male sex, mother’s age at 15–24 years, uneducated mother or low maternal education attainment, decreasing household wealth index at individual level (level 1), residing in rural area and neighbourhoods with high poverty rate at level 2. There were significant neighbourhoods and states clustering in childhood mortality in Nigeria.
Conclusions The study provides evidence that individual-level and neighbourhood-level socioeconomic conditions are important correlates of childhood mortality in Nigeria. The findings of this study also highlight the need to implement public health prevention strategies at the individual level, as well as at the area/neighbourhood level. These strategies include the establishment of an effective publicly funded healthcare system, as well as health education and poverty alleviation programmes.

Ethical challenges of containing Ebola: the Nigerian experience

Journal of Medical Ethics
November 2015, Volume 41, Issue 11
http://jme.bmj.com/content/current

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Viewpoint
Ethical challenges of containing Ebola: the Nigerian experience
Omosivie Maduka1, Osaretin Odia2
Abstract
Responding effectively to an outbreak of disease often requires routine processes to be set aside in favour of unconventional approaches. Consequently, an emergency response situation usually generates ethical dilemmas. The emergence of the Ebola virus in the densely populated cities of Lagos and Port Harcourt in Nigeria brought bleak warnings of a rapidly expanding epidemic. However, these fears never materialised largely due to the swift reaction of emergency response and incident management organisations, and the WHO has now declared Nigeria free of Ebola. However, numerous ethical issues arose in relation to the response to the outbreak. This paper discusses some of these ethical challenges and the vital lessons learned. Ethical challenges relating to confidentiality, the dignity of persons, non-maleficence, stigma and the ethical obligations of health workers are examined. Interventions implemented to ensure that confidentiality and the dignity of persons improved and stigma was reduced, included community meetings, knowledge communication and the training of media personnel in the ethical reporting of Ebola issues. In addition, training in infection prevention and control helped to allay the fears of health workers. A potential disaster was also averted when the use of an experimental medicine was reconsidered. Other countries currently battling the epidemic can learn a lot from the Nigerian experience

The Lancet – Nov 07, 2015

The Lancet
Nov 07, 2015 Volume 386 Number 10006 p1795-1916 e27-e36
http://www.thelancet.com/journals/lancet/issue/current

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Comment
Providing incentives to share data early in health emergencies: the role of journal editors
Christopher J M Whitty, Trevor Mundel, Jeremy Farrar, David L Heymann, Sally C Davies, Mark J Walport
DOI: http://dx.doi.org/10.1016/S0140-6736(15)00758-8
Summary
The recent epidemic of Ebola virus disease in west Africa showed the power of data generated and analysed by the responder and academic communities to help shape and improve the public health response in international health emergencies. The swift response of clinical, public health, and academic professionals from diverse backgrounds was exemplary. Data and insights from many sciences, especially in peer-reviewed papers and online data, were crucial to planning the immediate and medium-term strategy.

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The Lancet Commissions
Health and climate change: policy responses to protect public health
Nick Watts, W Neil Adger, Paolo Agnolucci, Jason Blackstock, Peter Byass, Wenjia Cai, Sarah Chaytor, Tim Colbourn, Mat Collins, Adam Cooper, Peter M Cox, Joanna Depledge, Paul Drummond, Paul Ekins, Victor Galaz, Delia Grace, Hilary Graham, Michael Grubb, Andy Haines, Ian Hamilton, Alasdair Hunter, Xujia Jiang, Moxuan Li, Ilan Kelman, Lu Liang, Melissa Lott, Robert Lowe, Yong Luo, Georgina Mace, Mark Maslin, Maria Nilsson, Tadj Oreszczyn, Steve Pye, Tara Quinn, My Svensdotter, Sergey Venevsky, Koko Warner, Bing Xu, Jun Yang, Yongyuan Yin, Chaoqing Yu, Qiang Zhang, Peng Gong, Hugh Montgomery, Anthony Costello
Summary
The 2015 Lancet Commission on Health and Climate Change has been formed to map out the impacts of climate change, and the necessary policy responses, in order to ensure the highest attainable standards of health for populations worldwide. This Commission is multidisciplinary and international in nature, with strong collaboration between academic centres in Europe and China.

Nature Medicine | Editorial – Sharing data to save lives

Nature Medicine
November 2015, Volume 21 No 11 pp1235-1371
http://www.nature.com/nm/journal/v21/n11/index.html

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Nature Medicine | Editorial
Sharing data to save lives
Published online 05 November 2015
Journals can and should ensure that they erect no barriers to fast and wide sharing of critical data during major public health emergencies. But funders and scientists must also play a part.
On 1–2 September in Geneva, the World Health Organization (WHO) gathered a group of public health experts, scientists, funders, editors, industry and government representatives for a consultation related to the sharing of data during public health emergencies. Many attendees were directly involved in pathogen genome sequencing and in generating or using clinical, epidemiological and observational data during the 2014 Ebola epidemic in West Africa. Their experiences illustrate that improvements to the norms and process of data sharing in such scenarios are urgently needed.

A notable example was the way in which pathogen genome sequence data was handled. Although two batches of Ebola genome sequences obtained from patient samples were released in April and July 2014, no additional virus genome sequences were released until November that same year. Although restricted availability of patient samples hampered the sequencing of genomes, it is acknowledged that some viral genome sequence data were generated but not publicly released during this interval.

These viral genome sequences would remain useful to investigators seeking to understand the molecular features of virus evolution no matter when they are released. However, their utility to those seeking to trace the chain of transmission (e.g., human-to-human or animal-to-human), to determine whether a pathogen is genetically stable or rapidly mutating, and to track new pathogen variants entering the population, wanes days to weeks after the sequences are generated. Moreover, this ‘real-time’ utility is not restricted to pathogen genome sequence data; clinical trial and observational studies of the efficacy—or lack thereof—of candidate therapies can also enable clinicians to adapt in real-time. Waiting to release these data months after their generation during a public health emergency risks allowing medical workers to repeatedly test therapies that other clinicians had determined were ineffective.

Why are such data not rapidly and widely released in a systematic manner? Many barriers to data sharing were identified during the meeting in Geneva, including patient privacy concerns, government restrictions on the export of patient samples, lack of access to advanced technology in limited resource settings, and lack of personnel and time.
As editors, we wish to address another concern, which a consensus felt was a formidable barrier to early data release: the perception that public release of data will have a negative effect on later scientific publication of the same data. More specifically, many data producers worry that if they publicly release their data prior to submitting a manuscript to a peer-reviewed journal, the editors of the journal may consider the released data no longer novel and reject their manuscript for that reason. In addition, especially when data producers are on the ground working to stem an outbreak and are thus occupied with tasks more important than writing manuscripts, other scientists may analyze the released data, submit the resulting manuscript, and ultimately ‘scoop’ the data-producing lab.

Allaying the first concern is the responsibility of scientific journals. Encouragingly, all editors in attendance emphatically declared that their journals do not wish to hinder real-time sharing of data that could have a clinical impact during public health emergencies. Reflecting this sentiment, the WHO summary released after the consultation states, “It was unequivocally agreed by representatives from leading biomedical journals that public disclosure of important information of potential relevance to public health emergencies should not be delayed by publication timelines, and that pre-publication disclosure must not and will not prejudice journal publication.” The Nature journals agree with this statement; it is consistent with our long-standing policy of not penalizing authors for posting most data on preprint servers. Moving forward, although we already require that all data be available to editors and referees at the time of submission—and freely available to all at the time of publication—when we feel that the data in a submitted manuscript may be useful more broadly to agencies working to stem a public health emergency, we will encourage authors to publicly release the data immediately. We will use editorial discretion in defining major public health emergencies and the relevance of the data in question. To regularly remind readers of these principles, we will ask authors of papers that present data that were released prior to submission or publication to add a sentence to the final published paper explicitly stating this fact.

But these steps address just one part of the problem. Scientists, funders and governments must work to solve the rest. For instance, journals become aware of the existence of data when it is submitted for consideration for publication; yet this could be months after it was initially generated. Only scientists, with the cooperation of governments, can ensure that the data are broadly released as quickly as possible. Scientists are also responsible for ensuring that data users are aware of any limitations of rapidly released potentially preliminary data.

Just as crucially, journals cannot allay concerns about scientists scooping each other. Communities of data producers and users must agree on guidelines for the etiquette of data sharing and data use. Useful precedents might be found in guidelines crafted by other communities that successfully grappled with similar challenges, such as the 2006 Global Initiative on Sharing Avian Influenza Data. Once data producers and users coalesce around a set of guidelines, funders can create policies to ensure that they are followed as often as possible, and that data producers remain incentivized to quickly share their results.

Attendees at the WHO consultation agreed on a list of practical steps that can be taken to remove all identified barriers to data sharing. A list of these steps was submitted to the WHO emergency R&D preparedness blueprint Advisory Group, and it awaits endorsement by the WHO and its partners.

The Nature journals’ commitment to enable rather than hinder data sharing in major public health emergencies is effective immediately.

Pediatrics – November 2015

Pediatrics
November 2015, VOLUME 136 / ISSUE 5 http://pediatrics.aappublications.org/content/136/5?current-issue=y

Effectiveness and Cost of Bidirectional Text Messaging for Adolescent Vaccines and Well Care
Sean T. O’Leary, Michelle Lee, Steven Lockhart, Sheri Eisert, Anna Furniss, Juliana Barnard, Doron Shmueli, Shannon Stokley, L. Miriam Dickinson, Allison Kempe

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Deferred Consent for Randomized Controlled Trials in Emergency Care Settings
Katie Harron, Kerry Woolfall, Kerry Dwan, Carrol Gamble, Quen Mok, Padmanabhan Ramnarayan, Ruth Gilbert
Abstract
BACKGROUND: There is limited experience in using deferred consent for studies involving children, which was legalized in the United Kingdom in 2008. We aimed to inform future studies by evaluating consent rates and reasons for nonconsent in a large randomized controlled trial in pediatric intensive care.
METHODS: In the CATCH trial, eligible children from 14 PICUs in England and Wales were randomly assigned to 3 types of central venous catheters. To avoid delay in treatment, children admitted on an emergency basis were first randomly assigned to a trial central venous catheter, and we deferred seeking consent to use already collected data and blood samples until after stabilization.
RESULTS: Consent was obtained for 984/1358 (72%) of children admitted on an emergency basis. Failure to obtain consent resulted mainly from a lack of opportunity (early discharge or transfer) for survivors and difficulties in seeking consent for children who died. For admissions where there was an opportunity to approach (n = 1298), inclusion rates differed according to survival status: 93/984 (9%) of consented patients died, compared with 58/314 (18%) of nonconsented patients. For children admitted on an emergency basis whose families were approached, 984/1178 (84%) provided deferred consent (n = 15 sites), compared with 441/641 (69%) of children admitted on an elective basis who were approached for prospective consent (n = 9 sites).
CONCLUSIONS: Design of emergency randomized controlled trials should balance the potential burden that seeking consent in difficult situations may cause against risk of bias by disproportionately excluding children who die or are transferred. Ethics committees could consider approving the use of already collected data when best efforts to obtain deferred consent are unsuccessful.

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HPV Vaccination Coverage of Male Adolescents in the United States
Peng-jun Lu, David Yankey, Jenny Jeyarajah, Alissa O’Halloran, Laurie D. Elam-Evans, Philip J. Smith, Shannon Stokley, James A. Singleton, Eileen F. Dunne

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Promoting HPV Vaccination in Safety-Net Clinics: A Randomized Trial
Jasmin A. Tiro, Joanne M Sanders, Sandi L. Pruitt, Clare Frey Stevens, Celette Sugg Skinner, Wendy P. Bishop, Sobha Fuller, Donna Persaud

Who Is Worst Off? Developing a Severity-scoring Model of Complex Emergency Affected Countries in Order to Ensure Needs Based Funding

PLOS Currents: Disasters
http://currents.plos.org/disasters/
[Accessed 7 November 2015]

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Who Is Worst Off? Developing a Severity-scoring Model of Complex Emergency Affected Countries in Order to Ensure Needs Based Funding
November 3, 2015 · Research article
Background: Disasters affect close to 400 million people each year. Complex Emergencies (CE) are a category of disaster that affects nearly half of the 400 million and often last for several years. To support the people affected by CE, humanitarian assistance is provided with the aim of saving lives and alleviating suffering. It is widely agreed that funding for this assistance should be needs-based. However, to date, there is no model or set of indicators that quantify and compare needs from one CE to another. In an effort to support needs-based and transparent funding of humanitarian assistance, the aim of this study is to develop a model that distinguishes between levels of severity among countries affected by CE.
Methods: In this study, severity serves as a predictor for level of need. The study focuses on two components of severity: vulnerability and exposure. In a literature and Internet search we identified indicators that characterize vulnerability and exposure to CE. Among the more than 100 indicators identified, a core set of six was selected in an expert ratings exercise. Selection was made based on indicator availability and their ability to characterize preexisting or underlying vulnerabilities (four indicators) or to quantify exposure to a CE (two indicators). CE from 50 countries were then scored using a 3-tiered score (Low-Moderate, High, Critical).
Results: The developed model builds on the logic of the Utstein template. It scores severity based on the readily available value of four vulnerability and four exposure indicators. These are 1) GNI per capita, PPP, 2) Under-five mortality rate, per 1 000 live births, 3) Adult literacy rate, % of people ages 15 and above, 4) Underweight, % of population under 5 years, and 5) number of persons and proportion of population affected, and 6) number of uprooted persons and proportion of population uprooted.
Conclusion: The model can be used to derive support for transparent, needs-based funding of humanitarian assistance. Further research is needed to determine its validity, the robustness of indicators and to what extent levels of scoring relate to CE outcome.

Editorial – Eradicating polio

Science
6 November 2015 vol 350, issue 6261, pages 597-712
http://www.sciencemag.org/current.dtl

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Editorial
Eradicating polio
Anthony Adams1,*, David M. Salisbury2,
1Anthony Adams is a former professor of public health at the Australian National University and the former Chief Medical Officer of Australia.
2David M. Salisbury is an associate fellow at the Centre for Global Health Security, Chatham House, London, UK.

On 20 September 2015, the Global Commission for the Certification of Poliomyelitis Eradication (GCC) declared that type 2 wild poliovirus had been eradicated. The GCC examined reports from 189 of 195 countries around the world and studied separate data [held by the World Health Organization (WHO)] from the remaining countries. According to WHO, nearly 2 million appropriate clinical samples had been tested, and no type 2 wild polioviruses were found. The announcement is the first step toward eradicating all three wild poliovirus types. But this landmark will only be declared when the GCC is confident that there have been no wild virus cases of any type for 3 years.

The last case of type 3 wild poliovirus occurred in northern Nigeria 3 years ago. In theory, declaration of its eradication could happen now. However, the polio programs from 18 African countries have not yet been scrutinized by the African Regional Certification Commission to ensure that no cases have been missed. This assessment will happen 3 years after each country’s last case of any wild poliovirus. By the end of 2017, all African countries must have gone successfully through their regional commission’s scrutiny, and no wild virus cases must have occurred. If that happens, all countries in the world will submit their data to the GCC and type 3 wild poliovirus eradication can be declared.

That will leave just the type 1 poliovirus, which is still circulating in Pakistan and Afghanistan. To date, the 51 cases of 2015 are far fewer than the 334 cases reported in 2014. This is probably the result of improved access to vaccination in key regions. But there are always fewer cases the year after high numbers are reported, because natural infection reduces the numbers of children susceptible to polio in the following year. The polio programs in both countries must further accelerate their activities. If transmission is interrupted by the end of 2016, then the world can be declared polio-free in 2019.

One underappreciated consequence of the path toward eradication is that all polioviruses (wild and vaccine strains) in laboratory, research, and manufacturing facilities will have to be destroyed or securely contained. Last month, the WHO Strategic Advisory Group of Experts on immunization reaffirmed April 2016 as the date for the globally synchronized withdrawal of type 2 oral poliovirus vaccine. This first step toward the eventual phased removal of all three vaccine types brings urgency to completing the destruction, and securing the containment, of type 2 wild polioviruses in all facilities. The fewer the places that hold either polioviruses or specimens that could contain polioviruses, the more certain we can be that they will not be released inadvertently. This means that the vaccine industry will have to comply with high levels of assurance of containment in their manufacturing processes. Researchers and institutions holding samples collected from places where there could have been polioviruses must ensure that these are destroyed or secured under appropriate biocontainment levels. Countries will need to submit inventories of all laboratories to the GCC for review, and manufacturers and laboratories planning to retain type 2 polioviruses will need to be inspected for compliance with containment guidelines.

In 1980, smallpox was declared eradicated after a global immunization campaign led by WHO. But 2 years earlier, a year after the last natural smallpox case (in Somalia), there was an inadvertent release of smallpox virus from a research lab in the United Kingdom, from which one person died. While we wait for Pakistan and Afghanistan to stop the spread of type 1, we must prepare to safely and securely contain all polioviruses. A second human virus may soon be consigned to history. Until then, the whole world, especially countries with fragile health systems, remains at risk of this disease.
A.A. and D.M.S. are writing on behalf of the GCC: Anthony Adams (Chair), Supamit Chunsuttiwat, Arlene King, Rose Gana F. Leke, Yagob Al Mazrou, and David M. Salisbury.

Evidence gaps and ethical review of multicenter studies

Science
6 November 2015 vol 350, issue 6261, pages 597-712
http://www.sciencemag.org/current.dtl

Policy Forum
Research Ethics
Evidence gaps and ethical review of multicenter studies
Ann-Margret Ervin1,*, Holly A. Taylor1,2, Curtis L. Meinert1, Stephan Ehrhardt1
Author Affiliations
1Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
2Johns Hopkins Berman Institute of Bioethics, Baltimore, MD, USA.

Large, multicenter clinical studies are the backbone of evidence-based prevention and health care. Ethical review of multicenter research is usually conducted by the institutional review board (IRB) of each participating institution. However, variation in interpretation of regulations by IRBs is common and can have ethical and scientific implications (1, 2). Recent mandates in the United States aim to reduce the administrative burden and to expedite multicenter research by conducting ethical review with a single, central IRB of record (CIRB). Yet the quality of ethical review must not suffer. We characterize current models of ethical review in the United States and identify research gaps that must be addressed before such policies are instituted.

Review: From Antigen Delivery System to Adjuvanticy: The Board Application of Nanoparticles in Vaccinology

Vaccines — Open Access Journal
http://www.mdpi.com/journal/vaccines
(Accessed 7 November 2015)

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Review: From Antigen Delivery System to Adjuvanticy: The Board Application of Nanoparticles in Vaccinology
by Diana Boraschi and Paola Italiani
Vaccines 2015, 3(4), 930-939; doi:10.3390/vaccines3040930 – published 5 November 2015
Abstract
In the last years, nanotechnologies have raised great interest because of the potential applications of engineered nanoparticles in nanomedicine (i.e., in vaccination, in diagnostic imaging procedures, and as therapeutic drug delivery systems). The use of nanoparticles in medicine has brought about the issue of their interaction with the immune system for two main reasons: first, understanding how long nanomedicines could persist in the organism and exert their beneficial effects before being recognized and eliminated by our defensive systems; second, understanding how the immune responses can be modulated by nanoparticles in order to obtain optimal effects. This issue is crucial in vaccine formulations based on the use of nanoparticles, which can operate both as a delivery system to enhance antigen processing and as an immunostimulatory adjuvant to induce and amplify protective immunity, in part because of their ability to activate the inflammasome and induce the maturation of interleukin 1β. Nanoparticles can be excellent adjuvants due to their biocompatibility and their physicochemical properties (e.g., size, shape, and surface charge), which can be tailored to obtain different immunological effects. This review provides an overview of recent strategies for the use of nanoparticles as promising/attractive adjuvants for novel prophylactic and therapeutic vaccines. The use of nanovaccines, with their practically infinite possibilities of specific design, could open the way to precision vaccinology, i.e., vaccine formulations tailored on the individual immune reactivity status.

Lesbian Adolescent and Young Adult Initiation of HPV Vaccine

American Academy of Pediatrics – AAP Grand Rounds
November 2015, VOLUME 34 / ISSUE 5
Lesbian Adolescent and Young Adult Initiation of HPV Vaccine
Agenor M, Peitzmeier S, Gordon A, et al.
Investigators from multiple institutions assessed the awareness and initiation of the human papillomavirus (HPV) vaccine series among US women and girls based on sexual orientation. Data from the 2006–2010 National Survey of Family Growth (NSFG), a national probability sample of 15- to 44-year-old women, were abstracted for the study. Primary outcomes were self-reported awareness and initiation of the HPV vaccine. Sexual orientation identity was the primary predictor.

The time-course of protection of the RTS,S vaccine against malaria infections and clinical disease

Malaria Journal
4 November 2015
Research
The time-course of protection of the RTS,S vaccine against malaria infections and clinical disease
Melissa A. Penny12*, Peter Pemberton-Ross12 and Thomas A. Smith12
1 Department of Epidemiology and Public Health, Swiss Tropical and Public Health Institute, Basel, 4051, Switzerland
2 University of Basel, Petersplatz 1, Basel, Switzerland
doi:10.1186/s12936-015-0969-8
Abstract
Background
Recent publications have reported follow-up of the RTS,S/AS01 malaria vaccine candidate Phase III trials at 11 African sites for 32 months (or longer). This includes site- and time-specific estimates of incidence and efficacy against clinical disease with four different vaccination schedules. These data allow estimation of the time-course of protection against infection associated with two different ages of vaccination, both with and without a booster dose.
Methods
Using an ensemble of individual-based stochastic models, each trial cohort in the Phase III trial was simulated assuming many different hypothetical profiles for the vaccine efficacy against infection in time, for both the primary course and boosting dose and including the potential for either exponential or non-exponential decay. The underlying profile of protection was determined by Bayesian fitting of these model predictions to the site- and time-specific incidence of clinical malaria over 32 months (or longer) of follow-up. Using the same stochastic models, projections of clinical efficacy in each of the sites were modelled and compared to available observed trial data.
Results
The initial protection of RTS,S immediately following three doses is estimated as providing an efficacy against infection of 65 % (when immunizing infants aged 6–12 weeks old) and 91 % (immunizing children aged 5–17 months old at first vaccination). This protection decays relatively rapidly, with an approximately exponential decay for the 6–12 weeks old cohort (with a half-life of 7.2 months); for the 5–17 months old cohort a biphasic decay with a similar half-life is predicted, with an initial rapid decay followed by a slower decay. The boosting dose was estimated to return protection to an efficacy against infection of 50–55 % for both cohorts. Estimates of clinical efficacy by trial site are consistent with those reported in the trial for all cohorts.
Conclusions
The site- and time-specific clinical observations from the RTS,S/AS01 trial data allowed a reasonably precise estimation of the underlying vaccine protection against infection which is consistent with common underlying efficacy and decay rates across the trial sites. This calibration suggests that the decay in efficacy against clinical disease is more rapid than that against infection because of age-shifts in the incidence of disease. The dynamical models predict that clinical effectiveness will continue to decay and that likely effects beyond the time-scale of the trial will be small.

Media/Policy Watch [to 7 November 2015]

Media/Policy Watch
This section is intended to alert readers to substantive news, analysis and opinion from the general media on vaccines, immunization, global; public health and related themes. Media Watch is not intended to be exhaustive, but indicative of themes and issues CVEP is actively tracking. This section will grow from an initial base of newspapers, magazines and blog sources, and is segregated from Journal Watch above which scans the peer-reviewed journal ecology.

We acknowledge the Western/Northern bias in this initial selection of titles and invite suggestions for expanded coverage. We are conservative in our outlook in adding news sources which largely report on primary content we are already covering above. Many electronic media sources have tiered, fee-based subscription models for access. We will provide full-text where content is published without restriction, but most publications require registration and some subscription level.

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Forbes
http://www.forbes.com/
Accessed 7 November 2015
What Kind Of Doctor Fires Vaccine-Refusing Patients?
A number of stories published in the midst of the Disneyland measles outbreak last winter looked at the trend of doctors, particularly pediatricians, “firing” families that refused vaccines for their children. The practice remains controversial among pediatricians but relevant enough that a recent session at the American Academy of Pediatrics […]
Tara Haelle, Contributor Nov 02, 2015

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Foreign Policy
http://foreignpolicy.com/
Accessed 7 November 2015
Cholera Is Coming
An outbreak of the deadly disease is sweeping across Iraq. But El Niño, climate change, and Middle Eastern instability could make the crisis much bigger.
Laurie Garrett | November 2, 2015

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New York Times
http://www.nytimes.com/
Accessed 7 November 2015
The Last Place on Earth With Ebola: Getting Guinea to Zero
Workers from aid groups have descended on the villages where the virus is still spreading, a promising experimental vaccine is being given to adults who have been in contact with a victim, and government officials, once
November 07, 2015 – By DIONNE SEARCEY

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Reuters
http://www.reuters.com/
Accessed 7 November 2015
Cholera spreads from Iraq to Syria, Kuwait, Bahrain: UNICEF
ERBIL, Iraq | By Isabel Coles
A cholera outbreak in Iraq has spread to neighboring Syria, Kuwait and Bahrain, and risks turning into a region-wide epidemic as millions of pilgrims prepare to visit the country, UNICEF’s Iraq director said.

The disease, which can lead to death by dehydration and kidney failure within hours if left untreated, was detected west of Baghdad in September and has since infected at least 2,200 people in Iraq and has killed six.

“It (the outbreak) already has a regional dynamic and the risk of that can only be increased by people from all over the region coming into Iraq,” UNICEF country director, Peter Hawkins, said on Thursday. “Kuwait, Bahrain and Syria have already had confirmed cases.”

Millions of Shi’ite Muslims are due to visit Iraq in December for Arbaeen, a religious ritual marking the end of an annual mourning period for the Prophet Mohammad’s grandson Hussein, whose death in 680 AD entrenched the schism between Shi’ites and Sunnis.

Hawkins said UNICEF was working with clerics in the Shi’ite shrine cities of Najaf and Kerbala to convey information about how to guard against cholera, which is endemic in Iraq and the wider region…

Vaccines and Global Health_The Week in Review_31 October 2015

Vaccines and Global Health: The Week in Review is a weekly digest  summarizing news, events, announcements, peer-reviewed articles and research in the global vaccine ethics and policy space. Content is aggregated from key governmental, NGO, international organization and industry sources, key peer-reviewed journals, and other media channels. This summary proceeds from the broad base of themes and issues monitored by the Center for Vaccine Ethics & Policy in its work: it is not intended to be exhaustive in its coverage. You are viewing the blog version of our weekly digest, typically comprised of between 30 and 40 posts below all dated with the current issue date

.Request an Email Summary: Vaccines and Global Health : The Week in Review is published as a single email summary, scheduled for release each Saturday evening before midnight (EDT in the U.S.). If you would like to receive the email version, please send your request to david.r.curry@centerforvaccineethicsandpolicy.org.

pdf version A pdf of the current issue is available here:  Vaccines and Global Health_The Week in Review_31 October 2015a

blog edition: comprised of the approx. 35+ entries posted below on 13 September 2015..

Twitter:  Readers can also follow developments on twitter: @vaxethicspolicy.
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Links:  We endeavor to test each link as we incorporate it into any post, but recognize that some links may become “stale” as publications and websites reorganize content over time. We apologize in advance for any links that may not be operative. We believe the contextual information in a given post should allow retrieval, but please contact us as above for assistance if necessary.

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David R. Curry, MS
Executive Director
Center for Vaccine Ethics and Policy
a program of the
– Division of Medical Ethics, NYU Medical School
– Children’s Hospital of Philadelphia Vaccine Education Center
Associate Faculty, Division of Medical Ethics, NYU Medical School

TB

TB

Global tuberculosis report 2015
WHO
20th Edition October 2015 :: 204 pages
ISBN 978 92 4 156505 9
Overview
This is the twentieth global report on tuberculosis (TB) published by WHO in a series that started in 1997. It provides a comprehensive and up-to-date assessment of the TB epidemic and progress in implementing and financing TB prevention, care, control and research at global, regional and country levels using data reported by over 200 countries that account for more than 99% of the world’s TB cases. In this 2015 edition, particular attention is given to assessment of whether 2015 global TB targets set in the context of the Millennium Development Goals were achieved worldwide and at regional and country levels.
The four annexes of the report include an explanation of how to access and use the online global TB database, one-page profiles for 22 high TB-burden countries, one page regional profiles for WHO’s six regions, and tables that show estimates and data for key indicators for all countries for the latest year…

Executive summary [excerpt]
Background
The year 2015 is a watershed moment in the battle against tuberculosis (TB). It marks the deadline for global TB targets set in the context of the Millennium Development Goals (MDGs), and is a year of transitions: from the MDGs to a new era of Sustainable Development Goals (SDGs), and from the Stop TB Strategy to the End TB Strategy. It is also two decades since WHO established a global TB monitoring system; since that time, 20 annual rounds of data collection have been completed.

Using data from 205 countries and territories, which account for more than 99% of the world’s population, this global TB report documents advances in prevention, diagnosis and treatment of the disease. It also identifies areas where efforts can be strengthened.

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Main findings and messages
The advances are major: TB mortality has fallen 47% since 1990, with nearly all of that improvement taking place since 2000, when the MDGs were set.
In all, effective diagnosis and treatment of TB saved an estimated 43 million lives between 2000 and 2014.

The MDG target to halt and reverse TB incidence has been achieved on a worldwide basis, in each of the six WHO regions and in 16 of the 22 high-burden countries that collectively account for 80% of TB cases. Globally, TB incidence has fallen by an average of 1.5% per year since 2000 and is now 18% lower than the level of 2000.

This year’s report describes higher global totals for new TB cases than in previous years, but these reflect increased and improved national data rather than any increase in the spread of the disease.

Despite these advances and despite the fact that nearly all cases can be cured, TB remains one of the world’s biggest threats.

In 2014, TB killed 1.5 million people (1.1 million HIV-negative and 0.4 million HIV-positive). The toll comprised 890,000 men, 480,000 women and 140 000 children.
TB now ranks alongside HIV as a leading cause of death worldwide. HIV’s death toll in 2014 was estimated at 1.2 million, which included the 0.4 million TB deaths among HIV-positive people.1

Worldwide, 9.6 million people are estimated to have fallen ill with TB in 2014: 5.4 million men, 3.2 million women and 1.0 million children. Globally, 12% of the 9.6 million new TB cases in 2014 were HIV-positive.

To reduce this burden, detection and treatment gaps must be addressed, funding gaps closed and new tools developed.

In 2014, 6 million new cases of TB were reported to WHO, fewer than two-thirds (63%) of the 9.6 million people estimated to have fallen sick with the disease. This means that worldwide, 37% of new cases went undiagnosed or were not reported. The quality of care for people in the latter category is unknown.

Of the 480,000 cases of multidrug-resistant TB (MDR-TB) estimated to have occurred in 2014, only about a quarter of these – 123,000 – were detected and reported.

Although the number of HIV-positive TB patients on antiretroviral therapy (ART) improved in 2014 to 392,000 people (equivalent to 77% of notified TB patients known to be co-infected with HIV), this number was only one third of the estimated 1.2 million people living with HIV who developed TB in 2014. All HIV-positive TB cases are eligible for ART.

Funding gaps amounted to US$ 1.4 billion for implementation of existing interventions in 2015. The most recent estimate of the annual funding gap for research and development is similar, at about US$ 1.3 billion.

From 2016, the goal is to end the global TB epidemic by implementing the End TB Strategy. Adopted by the World Health Assembly in May 2014 and with targets linked to the newly adopted SDGs, the strategy serves as a blueprint for countries to reduce the number of TB deaths by 90% by 2030 (compared with 2015 levels), cut new cases by 80% and ensure that no family is burdened with catastrophic costs due to TB…

[Report excerpt p.112]
8.3 New vaccines to prevent TB
The slow decline in TB incidence globally (Chapter 2) and the persistent threat of MDR-TB both highlight the critical need for new effective TB vaccines. It is estimated that at least US$ 8 billion is required each year for TB diagnosis and treatment using currently available interventions (Chapter 7).

A recent modelling study showed that developing at least one new TB vaccine over the next 10–15 years would cost about US$ 0.8–1 billion, approximately 1% of diagnosis and treatment costs, and that an adolescent and adult vaccine with 60% efficacy delivered to 20% of the population-at-risk could avert as many as 30–50 million new cases of TB by 2050.1

Recent modelling also indicates that targeting adolescents will prevent morbidity and mortality in infants and young children, and is a more effective strategy to protect them from TB than direct vaccination of infants with a similar vaccine.2

The potential for an adult/adolescent vaccine to have a meaningful impact on the global TB epidemic, compared with the limited impact of an infant vaccine, has shifted the focus of TB vaccine development. The new paradigm emphasises the development of a diverse pipeline of new TB vaccine candidates that target the prevention of active TB in these older age groups.

Scientific advances have also enabled the pursuit of more sophisticated approaches to vaccine design. The global pipeline of TB vaccine candidates in clinical trials is more robust than at any previous period in history, now including recombinant BCGs, attenuated M. tuberculosis strains, recombinant viral-vectored platforms, protein/adjuvant combinations, and mycobacterial extracts.

The status of the pipeline for new vaccines in August 2015 is shown in Figure 8.4. These vaccines aim either to prevent infection (pre-exposure) or to prevent primary progression to disease or reactivation of latent TB (post-exposure). Further details are provided below…
1 Aeras, TB Vaccine Research and Development: A Business Case for Investment.
Rockville: Aeras; 2014. Available at: http://bit.ly/1EodJBj
2 White, R. Indirect effects in infants on the force of TB disease from vaccinating
adolescents and adults. London: TB Modelling Group, TB Centre, Centre
for the Mathematical Modelling of Infectious Diseases; 2015.

::::::

Aeras [to 31 October 2015]
http://www.aeras.org/pressreleases
Aeras Responds to the WHO’s Report on Threat of TB Epidemic
Rockville, MD, October 28, 2015 – The World Health Organization (WHO) released its Global Tuberculosis Report 2015 today, announcing that tuberculosis (TB) caused 1.5 million deaths in 2014, and HIV/AIDS caused 1.2 million deaths last year1.

“While we applaud the progress made to date, with an estimated 9.6 million people fighting active disease and 1.5 million people dying from TB in 2014, it is essential that the appropriate resources are invested in research and development to create the new drugs, diagnostics, and vaccines we desperately need to arrest this global epidemic,” said Aeras CEO Jacqueline E. Shea, Ph.D. “Governments and other funders must dramatically increase the level of resources available for this urgent research.” According to the WHO, there is a $1.3 billion yearly funding gap for TB research and development2.

The WHO’s report also points to the serious threat of dangerous strains of multidrug-resistant (MDR) and extensively drug-resistant (XDR) TB. In 2014, nearly half a million people developed MDR-TB2. Extensively drug-resistant TB has been reported in 105 countries, representing almost 10 percent of all MDR-TB cases2. Today’s report underscores the urgency of increased funding for TB R&D, warns Dr. Shea. “A new, effective vaccine is essential to ending the TB epidemic,” she adds. “There are so many scientific avenues worthy of further exploration that could be pursued with the appropriate resources, including new vaccine approaches; shorter, faster drug regimens; and improved diagnostics.”

The WHO’s announcement follows the End TB Strategy adopted by the World Health Assembly in 2014 and the United Nations’ recently affirmed Sustainable Development Goals, which include a target to reduce the number of TB deaths by 90% by 2030. “This simply cannot be achieved with the current tools we have to fight this epidemic,” Dr. Shea cautions. “Now is the time for global R&D funders to prioritize TB R&D.”

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PATH [to 31 October 2015]
http://www.path.org/news/index.php
Announcement | October 29, 2015
PATH scientist: new tools can better detect tuberculosis
Report calls for faster validation
Last week, UNITAID released its Tuberculosis Diagnostics Technology and Market Landscape report, co-authored by PATH scientist Dr. David Boyle, who oversees the PATH Diagnostics Program Tuberculosis (TB) Portfolio. The report, now in its fourth edition, reviews current and potential technologies and critical market challenges to improved access to better TB diagnostics.

Malaria Vaccine+

Malaria Vaccine+

Global Fund [to 31 October 2015]
http://www.theglobalfund.org/en/news/
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World Health Organisation right to be wary about first malaria vaccine
By Seth Berkley and Mark Dybul in Voices on 29 October 2015
Mosquirix is one of the most widely anticipated vaccines to have been developed. It is the first vaccine for malaria – a disease that kills more than 1,200 children every day– and has been clinically proven to provide protection against the disease. So, given that it has passed the toughest regulatory hurdles required of it, why is it only being made available in a handful of countries?

Demand for the vaccine is likely to be high. With more than 200m cases a year, malaria is endemic in almost every country in sub-Saharan Africa, as well as large parts of Asia and Latin America. Last week, two advisory bodies to the World Health Organisation, the strategic advisory group of experts on immunisation and the malaria policy advisory committee, recommended against its immediate widespread use, and many people may have been left wondering why.

But it was a smart call. While there is a potential to save many lives with this vaccine, we have reason to tread carefully. Rather than being a simple solution, Mosquirix comes with complex caveats and some outstanding questions that the clinical studies were not able to address. While some may argue that any delay in getting the vaccine out to people could end up costing lives, experts first want certainty that, in a real-life setting, it indeed brings the benefits we expect, based on what was shown in the trials.

Clinical trials found Mosquirix to be both safe and effective, providing 39% efficacy at preventing clinical cases of malaria over the course of a four-year trial. While this is low for a vaccine, it is worth remembering that given the large number of people at risk, providing protection in just four out of 10 cases could still go a very long way. Moreover, since there can be more than one episode per child, the trials found that the vaccine prevented on average 1,774 cases of malaria per 1,000 children.

However, what happens during the controlled setting of a clinical trial does not necessarily translate into a real-world situation, and here lies the concern.

To begin with, Mosquirix requires four doses. That’s a lot for a vaccine. What’s more, trials suggest that its already low efficacy is further reduced if the fourth dose is not administered, down to about 28% protection against clinical malaria and reducing its impact on severe cases of malaria to nearly zero. That is worrying because, typically, the more doses required of a vaccine the higher the dropout rate.

It then becomes a question of how reliably the vaccine can be administered – and, again, Mosquirix presents challenges. To achieve maximum effect, it should be given to children from five months, with the fourth dose given around the age of two. This is out of sync with the typical immunisation schedule for children in poorer countries, who are brought in for routine vaccination when they are six to 14 weeks old.

Delivering the vaccine will require unprecedented efforts to inform and mobilise people to bring their children to health clinics at the prescribed time to complete all four doses. But, with many of the countries in question already struggling to improve routine immunisation rates, it remains to be seen how reliably four doses of Mosquirix can be deployed.

That doesn’t mean it can’t be done. In light of how big a priority malaria is for these countries they may well indeed make it work. After all, we have seen this happen with the human papillomavirus (HPV) vaccine, another much sought after vaccine for developing countries, which is given to school-age girls to prevent cervical cancer.

But even if high coverage can be achieved, there is still a danger that news of the vaccine will give people a false sense of security and lead to a reduction in the use of other malaria interventions, which would be tragic. Insecticide treated bednets and anti-malarial medicine have already led to a 37% global decrease in malaria cases since 2000, and a 60% decline in the malaria mortality rate.

Mosquirix is no magic bullet and at best may prove to be a useful complementary tool in reducing malaria, but only one of many already being used.

All this combined is why the WHO has been so cautious, recommending that we proceed with just a few demonstration projects in three to five settings, and involving around 1 million children. This is a sensible approach; it is due diligence. With so many lives at stake, it is critical that we shed more light on these unknowns, so that we fully understand the impact of this vaccine before, or even if, we should make it more widely available.

EBOLA/EVD [to 31 October 2015]

EBOLA/EVD [to 31 October 2015]
Public Health Emergency of International Concern (PHEIC); “Threat to international peace and security” (UN Security Council)

Ebola Situation Report – 28 October 2015
[Excerpts]
SUMMARY
:: Three new confirmed cases of Ebola virus disease (EVD) were reported in the week to 25 October, all of which were reported in Guinea. The country also reported 3 cases the previous week. All 3 new cases are from the same household in the subprefecture of Kaliah, Forecariah, and are registered high-risk contacts linked to a case from the same area last week. There are currently 364 contacts under follow-up in Guinea (an increase from 246 the previous week), 141 of whom are high-risk. An additional 233 contacts identified during the past 42 days remain untraced. Therefore there remains a near-term risk of further cases among both registered and untraced contacts. Sierra Leone reported zero cases for a sixth consecutive week, and will be declared free of EVD transmission on 7 November if no further cases are reported.

:: Case incidence has remained at 5 confirmed cases or fewer per week for 13 consecutive weeks. Over the same period, transmission of the virus has been geographically confined to several small areas in western Guinea and Sierra Leone, marking a transition to a distinct, third phase of the epidemic. The phase-3 response coordinated by the Interagency Collaboration on Ebola builds on existing measures to drive case incidence to zero, and ensure a sustained end to EVD transmission. Enhanced capacity to rapidly identify a reintroduction (either from an area of active transmission or from an animal reservoir), or re-emergence of virus from a survivor, and capacity for testing and counselling as part of a comprehensive package to safeguard the welfare of survivors are central to the phase-3 response framework…

POLIO [to 31 October 2015]

POLIO [to 31 October 2015]
Public Health Emergency of International Concern (PHEIC)

GPEI Update: Polio this week as of 28 October 2015
Global Polio Eradication Initiative
Full report link: http://www.polioeradication.org/Dataandmonitoring/Poliothisweek.aspx
:: On 20 October, the Strategic Advisory Group of Experts on immunization (SAGE) confirmed that the globally coordinated withdrawal of the type 2 component in oral polio vaccine (OPV) should occur in April 2016, specifically in a window from 17 April to 1 May. Countries should intensify their preparatory efforts to switch from trivalent OPV to bivalent OPV to meet this timeline.
:: Withdrawing OPV type 2 is a crucial part of the polio endgame strategy, in order to eliminate the very rare cases of vaccine associated paralytic polio (VAPP) or circulating vaccine derived polioviruses (cVDPVs). The type 2 component of OPV accounts for 40% of VAPP cases, and upwards of 90% of cVDPV cases. By contrast, wild poliovirus type 2 has not been detected anywhere since 1999 and the Global Commission for the Certification of Poliomyelitis Eradication (GCC) declared this strain globally eradicated at its meeting in September 2015.
:: SAGE cautioned, however, that more work needs to be implemented ahead of the April 2016 switch date. It is critical that countries meet established deadlines to protect populations by moving the world towards destruction of wild poliovirus type 2 stocks or their appropriate containment in designated ‘poliovirus essential’ facilities. Ongoing cVDPV2 outbreaks needed to be fully stopped. And a global supply constraint of inactivated polio vaccine needed to be carefully managed in the lead-up to the switch, with available supply prioritized to highest risk areas. More
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[Selected Country Update Information]
Afghanistan
:: One new positive environmental sample was reported in the past week, in Hilmand province, with collection date of 19 September.
:: Urgent efforts are underway to strengthen the implementation of the national emergency action plan in the country. Focus is on:
.. Improving governance and coordination of the Emergency Operations Centre
.. Improving SIA quality by focusing resources on low-performing districts, and clearly identifying and targeting persistently missed children
.. Maximizing the impact of front-line health workers through more systematic vaccinator selection, training and supervision
.. Ensuring closer cross-border coordination in border areas with Pakistan
.. Further strengthening surveillance
::National Immunization Days (NIDs) will take place on 1 – 3 November using trivalent OPV and Subnational Immunization Days (SNIDs) are planned from 29 November to 1 December in the south and east of the country using bivalent OPV. Additional campaigns with inactivated polio vaccine are also planned for November (exact dates to be confirmed).
Madagascar
:: One new case of circulating vaccine-derived poliovirus type 1 (cVDPV1) was reported in the past week, with onset of paralysis on 22 August from Sud-Ouest province. The total number of cVDPV1 cases for 2015 is ten.
::: The 2015 cases are genetically linked to the case reported in September 2014, indicating prolonged and widespread circulation of the virus. Learn more about vaccine derived polioviruses here.
:: The emergency outbreak response continues to be intensified. A fourth round of National Immunization Days targeting an expanded age group will be held in November.

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SAGE confirms global polio vaccine switch date as April 2016
Monday, October 26, 2015
Landmark decision paves way for worldwide trivalent to bivalent OPV switch
Convening in Geneva, Switzerland, on 20 October 2015, the Strategic Advisory Group of Experts on immunization (SAGE) confirmed that the globally coordinated withdrawal of the type 2 component in the oral poliovirus vaccine (OPV) should occur in April 2016, specifically in a window from 17 April to 1 May 2016. Countries should soon begin to intensify their preparatory efforts to switch from trivalent oral polio vaccine (tOPV) to bivalent OPV (bOPV) to meet this timeline.

SAGE’s landmark decision follows the endorsement by the World Health Assembly (WHA) in May 2015, when Ministers of Health from 194 member states adopted a resolution on the global effort to eradicate polio, paving the way for a world free of polio.

SAGE concluded that significant progress had been made since its last meeting in April 2015, with no cases in Africa since August and over a year having passed since the last case in the Middle East was seen, strengthened surveillance and more children being reached with vaccines in key areas of Pakistan and Afghanistan. As a result of these steps, all countries and the partners of the Global Polio Eradication Initiative (GPEI) should plan for April 2016 as the definitive date for the global withdrawal of OPV type 2 (OPV2).

Withdrawing OPV type 2 is a crucial part of the polio endgame strategy, in order to eliminate the very rare cases of vaccine associated paralytic polio (VAPP) or circulating vaccine derived polioviruses (cVDPVs). The type 2 component of OPV accounts for 40% of VAPP cases, and upwards of 90% of cVDPV cases. By contrast, wild poliovirus type 2 has not been detected anywhere since 1999 and the Global Commission for the Certification of Poliomyelitis Eradication (GCC) declared this strain globally eradicated at its meeting in September 2015.

SAGE cautioned, however, that more work needs to be implemented ahead of the April 2016 switch date. It is critical that countries meet established deadlines to protect populations by moving the world towards destruction of wild poliovirus type 2 stocks or their appropriate containment in designated ‘poliovirus essential’ facilities. Ongoing cVDPV2 outbreaks in Guinea and South Sudan needed to be fully stopped. And a global supply constraint of inactivated polio vaccine needed to be carefully managed in the lead-up to the switch. The level of commitment from countries to meet the deadline to introduce IPV ahead of the switch has been exceptional, however due to technical challenges in scaling up manufacturing, short term supply constraints mean that some countries that are at low risk of cVDPV2 emergence and circulation are expected to experience slight delays in deliveries. The available supply must be prioritized to highest risk areas and stocks set aside for use as part of a response to detection of a type 2 poliovirus after OPV2 withdrawal.

The withdrawal of type 2 OPV will ultimately eliminate the risk of emergence of new cVDPV2s in the future, and will also prevent upwards of 200 cases of VAPP that currently occur each year as a result of the type 2 component in trivalent OPV. This globally synchronised switch will therefore be of great significance for the polio eradication programme with tremendous public health benefits.

WHO & Regionals [to 31 October2015]

WHO & Regionals [to 31 October2015]

WHO mobilizes 510,000 doses of oral cholera vaccine in Iraq
27 October 2015 – Iraq declared an outbreak of cholera on 15 September 2015. The current number of laboratory confirmed cases is 2055. As an integrated part of the current outbreak response strategy oral cholera vaccines (OCV) have been mobilized through the international coordination group based in Geneva. Based on a public health risk assessment, it has been determined that a number of displacement camps housing Syrian refugees and internally displaced Iraqis are at high risk for further spread of the cholera outbreak.

In addition to current prevention and control measures, WHO is working with the Ministry of Health to provide OCV in an immunization campaign for vulnerable populations in 62 refugee camps for internally displaced persons and collective centres throughout the country, targeting approximately 249,319 people. This is the first time Iraq will introduce the OCV Shanchol vaccine.

2 doses of vaccine are required for an individual to be protected. The campaign begins with an initial round of vaccinations followed by – after a required, minimum 14 days interval – a second round of doses, which will complete the vaccination. For such a campaign to be effective, it is vital that a second dose is administered. The first round is scheduled to take place on 31 October.

Targeted social mobilization, campaign logistics and health education are key components to ensure the successful implementation of OCV. In order to achieve herd immunity all members of a family above 1 year of age must be vaccinated.

Additional staff from WHO and health cluster partners have been deployed to Iraq in order to support the cholera response measures, facilitate the logistics and preparation of the campaign in select locations to ensure as many people as possible are protected.

The provision of safe water, sanitation and personal hygiene will continue to be the critical cholera prevention and control measures. Cholera vaccination is a safe and effective additional tool that can be used under the right conditions to supplement existing priority cholera control measures, not to replace them, and prevention and control measures must be accelerated before, during and after the 2 successive rounds.

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Weekly Epidemiological Record (WER) 30 October 2015, vol. 90, 44 (pp. 589–608) includes:
589 Maternal and neonatal tetanus elimination: validation survey in 4 States and 2 union territories in India, May 2015

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WHO call for stronger parliamentary engagement on health
29 OCTOBER 2015
IPU – Inter-Parliamentary Union
World Health Organization (WHO) Director General Dr Margaret Chan has urged MPs around the world to step up their efforts to improve the health of their citizens, stressing the importance of political solutions in a new generation of complex challenges. In her first address to an IPU assembly, Dr Chan stressed the vital role of MPs in a wide range of strategies including delivering universal health coverage, taxing tobacco, improving food labelling and fighting tax, trade and insurance policies which impacted on the poor. She warned of new threats including drug-resistant pathogens, the globalized marketing of unhealthy products, and the growing rates of chronic non-communicable diseases such as heart disease, cancer and diabetes – which have overtaken infectious diseases as the world’s biggest killers. Dr Chan also offered to strengthen WHO’s collaboration with IPU through structured technical support to IPU’s advisory bodies and confirmed a new role for parliamentarians in jointly organized side events at WHO assemblies, the organization’s supreme decision-making body. Her address builds on the existing cooperation between WHO and IPU in fields including women’s and children’s health, family planning, violence against women and girls and harmful traditional practices.

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World Antibiotic Awareness Week
30 October 2015 — The first World Antibiotic Awareness Week 16 to 22 November 2015 encourages best practices among the general public, health workers, policy-makers and the agriculture sector to avoid further emergence and spread of antibiotic resistance. The campaign urges people to “handle antibiotics with care”, because when antibiotics are misused or over prescribed bacteria become resistant to their effects, making some infectious diseases difficult – sometimes impossible – to treat

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Typhoon-affected communities in the Philippines vulnerable to disease outbreaks
October 2015 — WHO and partners are assisting the Government of the Philippines by providing targeted support using in-country resources. WHO has assisted with logistics, information management, provision of emergency kits, disease surveillance and is set to deploy more national experts and medical supplies.

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Earthquake response in Afghanistan and Pakistan
October 2015 — An earthquake with magnitude 7.7 occurred in north-eastern Afghanistan on 26 October, 2015 affecting both Afghanistan and Pakistan. WHO is assessing the public health impact of the earthquake and responding to the region’s health needs.

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Globally, an estimated two-thirds of the population under 50 are infected with herpes simplex virus type 1
28 October 2015

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Request for proposals: MICs Task Force Consultant
23 October 2015
Terms of referencepdf, 135kb
Deadline for application: 20 November 2015

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:: WHO Regional Offices
WHO African Region AFRO
No new digest content identified.

WHO Region of the Americas PAHO
:: Wider access to ultrasound would save maternal and neonatal lives in Latin America and the Caribbean (10/29/2015)

WHO South-East Asia Region SEARO
:: Reconstruction of health systems should remain top priority in Nepal
Media statement from Dr Poonam Khetrapal Singh, Regional Director, WHO South-East Asia Region on six month anniversary of the Nepal earthquake
[undated]

WHO European Region EURO
:: Statement – The challenges of migration require migrant-sensitive health systems for today and for the future 29-10-2015
:: “No” to influenza vaccination costs thousands of lives 28-10-2015
:: WHO/Europe and the Ministry of Health of Hungary conduct a joint assessment of refugee and migrant health in Hungary 27-10-2015
:: Good prison health involves empowering prisoners 26-10-2015

WHO Eastern Mediterranean Region EMRO
:: WHO pre-positions emergency supplies in Somalia in preparation for El Niño
30 October 2015, Mogadishu – WHO is working closely with the Federal Ministry of Health of Somalia in order to prepare for any possible health emergencies resulting from the El Niño climate phenomenon expected to hit some countries of the Region in 2015, including Somalia. WHO and partner United Nations agencies have developed contingency plans and are scaling up preparedness activities, including pre-positioning of aid supplies in areas most likely to be affected by flooding

WHO Western Pacific Region
No new digest content identified.

CDC/MMWR/ACIP Watch [to 31 October2015]

CDC/MMWR/ACIP Watch [to 31 October2015]
http://www.cdc.gov/media/index.html

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CDC resumes weekly flu activity reports
FRIDAY, OCTOBER 30, 2015
Information about influenza activity in the United States is collected, compiled and analyzed by the Centers for Disease Control and Prevention (CDC) and published in a report called FluView. CDC…
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MMWR October 30, 2015 / No. 42/ No. 42/ Vol. 64
:: Human Papillomavirus Vaccination Coverage Among Female Adolescents in Managed Care Plans — United States, 2013
OCTOBER 30, 2015
Human papillomavirus (HPV) vaccination is an effective primary prevention strategy that can reduce many of the HPV infections that lead to cancer, and is routinely recommended for persons aged 11–12 years. To determine whether the recommended HPV vaccination series is currently being administered to adolescents with health insurance, CDC and the National Committee for Quality Assurance assessed 2013 data from the Healthcare Effectiveness Data and Information Set. This report summarizes that assessment.

[Report excerpt]
…Most female adolescents in commercial and Medicaid health plans are currently not receiving the recommended doses of HPV vaccine by age 13 years. The HEDIS HPV vaccination measure was publicly reported for the first time in 2013, approximately 7 years after the quadrivalent HPV vaccine was licensed in the United States and recommended by the Advisory Committee on Immunization Practices (ACIP) for use in female adolescents (4), allowing health care providers time to adapt to the recommendations. Despite this, results from this study indicate that health plans are performing poorly overall with regard to HPV vaccination rates in female adolescents aged 13 years…

European Vaccine Initiative [to 31 October2015]

European Vaccine Initiative [to 31 October2015]
http://www.euvaccine.eu/news-events
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:: Search for a placental malaria vaccine leads to breakthrough in cancer research
30 October 2015
A placental malaria vaccine research and development project at the Faculty of Medical Health and Science of the University of Copenhagen leads to an encouraging discovery in the fight against cancer.
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:: EVI letter published in latest edition of The Economist
30 October 2015
A letter sent by EVI to The Economist pointing out misleading figures in the article in the 10 October edition “Breaking the fever”, has been published in the latest edition in the Letters section under Science v malaria.
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:: Recent article to emerge from the PAMCPH project in PLoS ONE
28 October 2015
The full article, entitled “The Influence of Sub-Unit Composition and Expression System on the Functional Antibody Response in the Development of a VAR2CSA Based Plasmodium falciparum Placental Malaria Vaccine”, can be accessed via this link

ICH announces organisational changes as it marks 25 years of successful harmonisation

ICH announces organisational changes as it marks 25 years of successful harmonisation
26 October 2015
The International Council for Harmonisation (ICH), formerly the International Conference on Harmonisation (ICH) held the inaugural meetings of its new Assembly [and Management Committee] on 23 October 2015.

The reforms build on a 25-year track record of successful delivery of harmonised guidelines for global pharmaceutical development, and their regulation. The changes announced today build on that success and will reinforce the foundations of ICH to make it better-equipped to face the challenges of global pharmaceutical development and regulation.

The reforms will mean that ICH is a truly global initiative, expanding beyond the current ICH members. More involvement from regulators around the world is welcomed and expected, as they will be invited to join counterparts from Europe, Japan, USA, Canada and Switzerland as ICH regulatory members. This is matched by the possibility of wider inclusion of global industry sectors affected by ICH harmonisation. The reforms strengthen ICH as the leading platform for global pharmaceutical regulatory harmonisation, and one that brings together in a transparent manner all key regulatory authorities and industry stakeholders.

The changes give ICH a more stable operating structure through the establishment of an ICH association, a legal entity under Swiss law. The association establishes the new Assembly as the over-arching governing body that will be instrumental in facilitating future growth through the participation of new members.

At the end of the inaugural meeting, ICH Assembly members declared “The fundamentals of what the ICH parties are trying to achieve are not changed, but the reforms to the process and organisation were needed to adapt to changes in how medicines are developed and regulated. These changes mark an exciting moment for us to help harmonise and streamline the global drug development process for the benefit of patients around the world.”