PLoS Currents: Outbreaks (Accessed 6 February 2016)

PLoS Currents: Outbreaks
http://currents.plos.org/outbreaks/
(Accessed 6 February 2016)

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Residency Training at the Front of the West African Ebola Outbreak: Adapting for a Rare Opportunity
February 2, 2016 · Discussion
Medical trainees face multiple barriers to participation in major outbreak responses such as that required for Ebola Virus Disease through 2014-2015 in West Africa. Hurdles include fear of contracting and importing the disease, residency requirements, scheduling conflicts, family obligations and lack of experience and maturity. We describe the successful four-week deployment to Liberia of a first year infectious diseases trainee through the mechanism of the Global Outbreak Alert and Response Network of the World Health Organization. The posting received prospective approval from the residency supervisory committees and employing hospital management and was designed with components fulfilling the Accreditation Council for Graduate Medical Education (ACGME) core competencies. It mirrored conventional training with regards to learning objectives, supervisory framework and assessment methods. Together with Centers for Disease Control and Prevention and many other partners, the team joined the infection prevention and control efforts in Monrovia. Contributions were made to a ‘ring fencing’ infection control approach that was being introduced, including enhancement of triage, training and providing supplies in high priority health-care facilities in the capital and border zones. In addition the fellow produced an electronic database that enabled monitoring infection control standards in health facilities. This successful elective posting illustrates that quality training can be achieved, even in the most challenging environments, with support from the pedagogic and sponsoring institutions. Such experiential learning opportunities benefit both the outbreak response and the trainee, and if scaled up would contribute towards building a global health emergency workforce. More should be done from residency accreditation bodies in facilitating postings in outbreak settings.

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Epidemiology of Chikungunya Virus in Bahia, Brazil, 2014-2015
February 1, 2016 · Discussion
Chikungunya is an emerging arbovirus that is characterized into four lineages. One of these, the Asian genotype, has spread rapidly in the Americas after its introduction in the Saint Martin island in October 2013. Unexpectedly, a new lineage, the East-Central-South African genotype, was introduced from Angola in the end of May 2014 in Feira de Santana (FSA), the second largest city in Bahia state, Brazil, where over 5,500 cases have now been reported. Number weekly cases of clinically confirmed CHIKV in FSA were analysed alongside with urban district of residence of CHIKV cases reported between June 2014 and October collected from the municipality’s surveillance network. The number of cases per week from June 2014 until September 2015 reveals two distinct transmission waves. The first wave ignited in June and transmission ceased by December 2014. However, a second transmission wave started in January and peaked in May 2015, 8 months after the first wave peak, and this time in phase with Dengue virus and Zika virus transmission, which ceased when minimum temperature dropped to approximately 15°C. We find that shorter travelling times from the district where the outbreak first emerged to other urban districts of FSA were strongly associated with incidence in each district in 2014 (R2).

Systems vaccinology informs influenza vaccine immunogenicity

PNAS – Proceedings of the National Academy of Sciences of the United States of America
http://www.pnas.org/content/early/
(Accessed 6 February 2016)

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Commentary
Systems vaccinology informs influenza vaccine immunogenicity
Adolfo García-Sastrea,1
Author Affiliations
Extract
Vaccines are the most efficient way to control and eradicate infectious diseases. The smallpox vaccine has led to the eradication of variola virus, which has been the cause of a high number of human casualties for many years in the not so distant past. Other viral vaccines that have not yet led to eradication, but have remarkably reduced the burden of viral infections, are the poliovirus, measles virus, mump virus, rubella virus, and yellow fever virus vaccines. More recently, the development of hepatitis B virus, chicken pox, zoster, rotavirus, and human papilloma virus vaccines have highlighted the impact of modern vaccines in controlling viral infections, including those involved in cancer development. Nevertheless, there is room for the improvement of several existing viral vaccines, such as the influenza and dengue virus vaccines, and challenges in the generation of effective vaccines against some specific viruses, including respiratory syncytial virus, several herpesviruses, and HIV. It also might be possible to generate effective vaccines against emergent viral infections, including chikungunya, Hendra, Nipah, Zika, and ebolaviruses, but difficulties include the need for large and costly studies to assess vaccine efficacy and the unpredictability of where the next human infections with such emerging pathogens will occur. Another major scientific challenge in the development of novel and improved virus vaccines is that, despite the previous successes in vaccine development, based on studies assessing whether a vaccine is safe and efficacious, no definitive studies have exposed the immunological mechanisms associated with vaccine efficacy. Thus, we still do not know for the most part how vaccines work. Challenges include limitations associated with animal models and difficulties to access informative human samples from multiple tissues. In this respect, the application of systems biology tools to the study of human vaccines (so-called “systems vaccinology”) gives new hope for the elucidation of the mechanistic details associated with vaccine safety and efficacy. In PNAS, Nakaya et al. (1) use systems vaccinology to find new clues on the immunogenic and transcriptional networks that are associated with robust influenza vaccine responses correlated with protection.

Prehospital & Disaster Medicine Volume 31 – Issue 01 – February 2016

Prehospital & Disaster Medicine
Volume 31 – Issue 01 – February 2016
https://journals.cambridge.org/action/displayIssue?jid=PDM&tab=currentissue

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Original Research
Developing a Performance Assessment Framework and Indicators for Communicable Disease Management in Natural Disasters
Javad Babaie, Ali Ardalan, Hasan Vatandoost, Mohammad Mehdi Goya and Ali Akbarisari
Prehospital and Disaster Medicine / Volume 31 / Issue 01 / February 2016, pp 27 – 35
Abstract
Introduction
Communicable disease management (CDM) is an important component of disaster public health response operations. However, there is a lack of any performance assessment (PA) framework and related indicators for the PA. This study aimed to develop a PA framework and indicators in CDM in disasters.
Methods
In this study, a series of methods were used. First, a systematic literature review (SLR) was performed in order to extract the existing PA frameworks and indicators. Then, using a qualitative approach, some interviews with purposively selected experts were conducted and used in developing the PA framework and indicators. Finally, the analytical hierarchy process (AHP) was used for weighting of the developed indicators.
Results
The input, process, products, and outcomes (IPPO) framework was found to be an appropriate framework for CDM PA. Seven main functions were revealed to CDM during disasters. Forty PA indicators were developed for the four categories.
Conclusion
There is a lack of any existing PA framework in CDM in disasters. Thus, in this study, a PA framework (IPPO framework) was developed for the PA of CDM in disasters through a series of methods. It can be an appropriate framework and its indicators could measure the performance of CDM in disasters.

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Special Reports
Protecting the Health and Well-being of Populations from Disasters: Health and Health Care in The Sendai Framework for Disaster Risk Reduction 2015-2030
Amina Aitsi-Selmi and Virginia Murray
Prehospital and Disaster Medicine / Volume 31 / Issue 01 / February 2016, pp 74 – 78
DOI: http://dx.doi.org/10.1017/S1049023X15005531 Published online: 17 December 2015
Abstract
The Sendai Framework for Disaster Risk Reduction (DRR) 2015-2030 is the first of three United Nations (UN) landmark agreements this year (the other two being the Sustainable Development Goals due in September 2015 and the climate change agreements due in December 2015). It represents a step in the direction of global policy coherence with explicit reference to health, economic development, and climate change. The multiple efforts of the health community in the policy development process, including campaigning for safe schools and hospitals, helped to put people’s mental and physical health, resilience, and well-being higher up the DRR agenda compared with its predecessor, the 2005 Hyogo Framework for Action. This report reflects on these policy developments and their implications and reviews the range of health impacts from disasters; summarizes the widened remit of DRR in the post-2015 world; and finally, presents the science and health calls of the Sendai Framework to be implemented over the next 15 years to reduce disaster losses in lives and livelihoods.

Public Health Reports – Volume 131 , Issue Number 1 January/February 2016

Public Health Reports
Volume 131 , Issue Number 1 January/February 2016
http://www.publichealthreports.org/issuecontents.cfm?Volume=131&Issue=1

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[Feature Article]
A Call for Greater Consideration for the Role of Vaccines in National Strategies to Combat Antibiotic-Resistant Bacteria: Recommendations from the National Vaccine Advisory Committee
National Vaccine Advisory Committee

Overcoming Barriers to Low HPV Vaccine Uptake in the United States: Recommendations from the National Vaccine Advisory Committee
National Vaccine Advisory Committee

The race for a Zika vaccine is on

Science
05 February 2016 Vol 351, Issue 6273
http://www.sciencemag.org/current.dtl

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In Depth
Infectious Disease
The race for a Zika vaccine is on
Jon Cohen
Science 05 Feb 2016:
Vol. 351, Issue 6273, pp. 543-544
DOI: 10.1126/science.351.6273.543
Summary
Scientists first isolated Zika virus in 1947, but the disease it caused in humans was considered mild: It did nothing to 80% of the people it infected, and the ones who had symptoms only had temporary fevers and rashes. But last year, a high number of cases of brain-damaging microcephaly in newborns began to surface in Brazil in lockstep with the arrival of the Zika virus, which is spread by mosquitoes. The World Health Organization on 1 February declared these clusters of disease a “public health emergency of international concern,” and a rush of vaccinemakers has jumped into the race to develop a preventive. Vaccines exist against several other flaviviruses, the family Zika belongs to, and experts predict that this won’t be a major scientific challenge. They also say it may be possible to piggyback on the other flavivirus vaccines, like ones made for dengue and yellow fever. Then again, vaccine R&D takes time, and because this effort is starting from scratch, researchers say it will take at least a few years before a vaccine can prove itself safe and effective in large human efficacy studies.

Understanding the role of Indigenous community participation in Indigenous prenatal and infant-toddler health promotion programs in Canada: A realist review

Social Science & Medicine
Volume 150, Pages 1-290 (February 2016)
http://www.sciencedirect.com/science/journal/02779536/150

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Review article
Understanding the role of Indigenous community participation in Indigenous prenatal and infant-toddler health promotion programs in Canada: A realist review
Pages 128-143
Janet Smylie, Maritt Kirst, Kelly McShane, Michelle Firestone, Sara Wolfe, Patricia O’Campo
Abstract
Purpose
Striking disparities in Indigenous maternal-child health outcomes persist in relatively affluent nations such as Canada, despite significant health promotion investments. The aims of this review were two-fold: 1. To identify Indigenous prenatal and infant-toddler health promotion programs in Canada that demonstrate positive impacts on prenatal or child health outcomes. 2. To understand how, why, for which outcomes, and in what contexts Indigenous prenatal and infant-toddler health promotion programs in Canada positively impact Indigenous health and wellbeing.
Methods
We systematically searched computerized databases and identified non-indexed reports using key informants. Included literature evaluated a prenatal or child health promoting program intervention in an Indigenous population in Canada. We used realist methods to investigate how, for whom, and in what circumstances programs worked. We developed and appraised the evidence for a middle range theory of Indigenous community investment-ownership-activation as an explanation for program success.
Findings
Seventeen articles and six reports describing twenty programs met final inclusion criteria. Program evidence of local Indigenous community investment, community perception of the program as intrinsic (mechanism of community ownership) and high levels of sustained community participation and leadership (community activation) was linked to positive program change across a diverse range of outcomes including: birth outcomes; access to pre- and postnatal care; prenatal street drug use; breast-feeding; dental health; infant nutrition; child development; and child exposure to Indigenous languages and culture.
Conclusions
These findings demonstrate Indigenous community investment-ownership-activation as an important pathway for success in Indigenous prenatal and infant-toddler health programs.

Comparison of immune responses to a killed bivalent whole cell oral cholera vaccine between endemic and less endemic settings

Tropical Medicine & International Health
February 2016 Volume 21, Issue 2 Pages 157–291
http://onlinelibrary.wiley.com/doi/10.1111/tmi.2016.21.issue-2/issuetoc

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Original Article
Comparison of immune responses to a killed bivalent whole cell oral cholera vaccine between endemic and less endemic settings
Sachin N. Desai1,*, Zenebe Akalu2, Mekonnen Teferi2, Byomkesh Manna3, Samuel Teshome1,
Ju Yeon Park1, Jae Seung Yang1, Deok Ryun Kim1, Suman Kanungo3 and Laura Digilio1
Article first published online: 18 DEC 2015
DOI: 10.1111/tmi.12641
Summary
Studies on safety, immunogenicity and efficacy of the killed, bivalent whole cell oral cholera vaccine (Shanchol) have been conducted in historically endemic settings of Asia. Recent cholera vaccination campaigns in Haiti and Guinea have also demonstrated favourable immunogenicity and effectiveness in nonendemic outbreak settings. We performed a secondary analysis, comparing immune responses of Shanchol from two randomised controlled trials performed in an endemic and a less endemic area (Addis Ababa) during a nonoutbreak setting. While Shanchol may offer some degree of immediate protection in primed populations living in cholera endemic areas, as well as being highly immunogenic in less endemic settings, understanding the characteristics of immune responses in each of these areas is vital in determining ideal dosing strategies that offer the greatest public health impact to populations from areas with varying degrees of cholera endemicity.

Can thermostable vaccines help address cold-chain challenges? Results from stakeholder interviews in six low- and middle-income countries

Vaccine
Volume 34, Issue 7, Pages 875-994 (10 February 2016)
http://www.sciencedirect.com/science/journal/0264410X/34/7
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Original Research Article
Can thermostable vaccines help address cold-chain challenges? Results from stakeholder interviews in six low- and middle-income countries
Pages 899-904
Debra D. Kristensen, Tina Lorenson, Kate Bartholomew, Shirley Villadiego
Abstract
Introduction
This study captures the perspectives of stakeholders at multiple levels of the vaccine supply chain regarding their assessment of challenges with storing vaccines within recommended temperature ranges and their perceptions on the benefits of having vaccines with improved stability, including the potential short-term storage and transport of vaccines in a controlled-temperature chain.
Methods
Semi-structured interviews were undertaken with 158 immunization stakeholders in six countries. Interviewees included national decision-makers and advisors involved in vaccine purchasing decisions, national Expanded Programme on Immunization managers, and health and logistics personnel at national, subnational, and health facility levels.
Results
Challenges with both heat and freeze-exposure of vaccines were recognized in all countries, with heat-exposure being a greater concern. Conditions leading to freeze-exposure including ice build-up due to poor refrigerator performance and improper icepack conditioning were reported by 53% and 28% of participants, respectively. Respondents were interested in vaccine products with improved heat/freeze-stability characteristics. The majority of those involved in vaccine purchasing indicated they would be willing to pay a US$0.05 premium per dose for a freeze-stable pentavalent vaccine (68%) or a heat-stable rotavirus vaccine (59%), although most (53%) preferred not to pay the premium for a heat-stable pentavalent vaccine if the increased stability required changing from a liquid to a lyophilized product. Most respondents (73%) were also interested in vaccines labeled for short-term use in a controlled-temperature chain. The majority (115/158) recognized the flexibility this would provide during outreach or should cold-chain breaks occur. Respondents were also aware that possible confusion might arise and additional training would be required if handling conditions were changed for some, but not all vaccines.
Conclusion
Participating immunization stakeholders recognized the benefits of vaccine products with improved stability characteristics and of labeling vaccines for controlled-temperature chain use as a means to help address cold-chain issues in their immunization programs.

Infant vaccination timing: Beyond traditional coverage metrics for maximizing impact of vaccine programs, an example from southern Nepal

Vaccine
Volume 34, Issue 7, Pages 875-994 (10 February 2016)
http://www.sciencedirect.com/science/journal/0264410X/34/7
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Infant vaccination timing: Beyond traditional coverage metrics for maximizing impact of vaccine programs, an example from southern Nepal
Original Research Article
Pages 933-941
Michelle M. Hughes, Joanne Katz, Janet A. Englund, Subarna K. Khatry, Laxman Shrestha, Steven C. LeClerq, Mark Steinhoff, James M. Tielsch
Abstract
Background
Immunization programs currently measure coverage by assessing the proportion of children 12–24 months who have been immunized but this does not address the important question of when the scheduled vaccines were administered. Data capturing the timing of vaccination in first 6 months, when severe disease is most likely to occur, are limited.
Objective
To estimate the time to Bacillus Calmette–Guérin (BCG) (recommended at birth), diphtheria-tetanus-pertussis-H, influenza b-hepatitis B (DTP-Hib-HepB), and oral polio vaccine (OPV) (recommended at 6, 10, and 14 weeks) vaccinations and risk factors for vaccination delay in infants <6 months of age in a district in southern Nepal where traditional coverage metrics are high.
Design/methods
Infants enrolled in a randomized controlled trial of maternal influenza vaccination were visited weekly at home from birth through age 6 months to ascertain if any vaccinations had been given in the prior week. Infant, maternal, and household characteristics were recorded. BCG, DTP-Hib-HepB, and OPV vaccination coverage at 4 and 6 months was estimated. Time to vaccination was estimated through Kaplan–Meier curves; Cox-proportional hazards models were used to examine risk factors for delay for the first vaccine.
Results
The median age of BCG, first OPV and DTP-Hib-HepB receipt was 22, 21, and 18 weeks, respectively. Almost half of infants received no BCG by age 6 months. Only 8% and 7% of infants had received three doses of OPV and DTP-Hib-HepB, respectively, by age 6 months.
Conclusion
A significant delay in receipt of infant vaccines was found in a prospective, population-based, cohort in southern Nepal despite traditional coverage metrics being high. Immunization programs should consider measuring time to receipt relative to the official schedule in order to maximize benefits for disease control and child health.

Burden of four vaccine preventable diseases in older adults

Vaccine
Volume 34, Issue 7, Pages 875-994 (10 February 2016)
http://www.sciencedirect.com/science/journal/0264410X/34/7
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Burden of four vaccine preventable diseases in older adults
Original Research Article
Pages 942-949
Maartje Kristensen, Alies van Lier, Renske Eilers, Scott A. McDonald, Wim Opstelten, Nicoline van der Maas, Wim van der Hoek, Mirjam E. Kretzschmar, Mark M. Nielen, Hester E. de Melker
Abstract
Background
Implementation of additional targeted vaccinations to prevent infectious diseases in the older adults is under discussion in different countries. When considering the added value of such preventive measures, insight into the current disease burden will assist in prioritization. The aim of this study was derive the first estimates of the disease burden in adults aged 50 years or over in the Netherlands for influenza, pertussis, pneumococcal disease and herpes zoster.
Methods
The average annual disease burden for these four diseases in the Netherlands was calculated for the period 2010–2013 using the disability-adjusted life years (DALY) measure. Disease models and parameters were obtained from previous research. Where possible we adapted these models specifically for older adults and applied age-specific parameters derived from literature. The disease burden based on these adapted models and parameters was compared with the disease burden based on the general population models.
Results
The estimated average annual disease burden was from high to low: pneumococcal disease (37,223 DALYs/year), influenza (7941 DALYs/year), herpes zoster (942 DALYs/year), and pertussis (812 DALYs/year). The adaptation of models and parameters specifically for the elderly resulted in a higher disease burden compared to the use of general population models.
Conclusions
Among older adults, the disease burden in the period 2010–2013 was highest for pneumococcal disease, mostly because of high mortality, followed by influenza. Disease burden of herpes zoster and pertussis was relatively low and consisted mostly of years lived with disability. Better information on the course of infectious diseases and long-term consequences would enable more accurate estimation of disease burden in older adults.

Maternal Tdap vaccination: Coverage and acute safety outcomes in the vaccine safety datalink, 2007–2013

Vaccine
Volume 34, Issue 7, Pages 875-994 (10 February 2016)
http://www.sciencedirect.com/science/journal/0264410X/34/7
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Maternal Tdap vaccination: Coverage and acute safety outcomes in the vaccine safety datalink, 2007–2013
Original Research Article
Pages 968-973
Elyse Olshen Kharbanda, Gabriela Vazquez-Benitez, Heather S. Lipkind, Nicola P. Klein, T. Craig Cheetham, Allison L. Naleway, Grace M. Lee, Simon Hambidge, Michael L. Jackson, Saad B. Omer, Natalie McCarthy, James D. Nordin
Abstract
Introduction
Since October 2012, the combined tetanus toxoid, reduced diphtheria toxoid, acellular pertussis vaccine (Tdap) has been recommended in the United States during every pregnancy.
Methods
In this observational study from the Vaccine Safety Datalink, we describe receipt of Tdap during pregnancy among insured women with live births across seven health systems. Using a retrospective matched cohort, we evaluated risks for selected medically attended adverse events in pregnant women, occurring within 42 days of vaccination. Using a generalized estimating equation, we calculated adjusted incident rate ratios (AIRR).
Results
Our vaccine coverage cohort included 438,487 live births between January 1, 2007 and November 15, 2013. Across the coverage cohort, 14% received Tdap during pregnancy. By 2013, Tdap was administered during pregnancy in 41.7% of live births, primarily in the 3rd trimester. Our vaccine safety cohort included 53,885 vaccinated and 109,253 matched unvaccinated pregnant women. There was no increased risk for a composite outcome of medically attended acute adverse events within 3 days of vaccination. Similarly, across the safety cohort, over a 42 day window, incident neurologic events, thrombotic events, and new onset proteinuria did not differ by maternal receipt of Tdap. Among women receiving Tdap at 20 weeks gestation or later, as compared to their matched controls, there was no increased risk for gestational diabetes or cardiac events while venous thromboembolic events and thrombocytopenia were diagnosed within 42 days of vaccination at slightly decreased rates.
Conclusion
Tdap coverage during pregnancy increased from 2007 through 2013, but was still below 50%. No acute maternal safety signals were detected in this large cohort.

Media/Policy Watch [to 6 February 2016)

Media/Policy Watch  [to 6 February 2016)
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 6 February 2016
Is It Time To Ditch Tdap As A Routinely Recommended Teen Vaccination?
The Tdap vaccine wanes so quickly against pertussis that researchers question whether it makes sense for preteens and teens to receive the booster routinely. Strategic vaccination during outbreaks may make more sense, they suggest.
Tara Haelle, Contributor Feb 05, 2016

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Foreign Policy
http://foreignpolicy.com/
Accessed 6 February 2016
The Ebola Rape Epidemic No One’s Talking About
When the outbreak hit West Africa, fevers spiked – and so did rates of teenage pregnancy…
2 February 2016
Outbreaks of infectious diseases often leave girls and women vulnerable to violence and rape — a result of the civil unrest and instability that epidemics leave in their wake. “This wouldn’t come as a surprise if we thought of epidemics like any other disaster,” said Monica Onyango, a clinical assistant professor of global health at Boston University. “Epidemics are just like a conflict situation. You have a loss of governance; you have chaos and instability; and all of that leaves women vulnerable to gender-based violence.”

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New York Times
http://www.nytimes.com/
Accessed 6 February 2016
Growing Support Among Experts for Zika Advice to Delay Pregnancy
February 09, 2016 – By DONALD G. McNEIL Jr ”

More Than 3,100 Pregnant Women in Colombia Have Zika Virus: Government
February 06, 2016 – By REUTERS –

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Washington Post
http://www.washingtonpost.com/
Accessed 6 February 2016
Brazil considers reforming biosecurity law amid criticism
Brazilian officials will soon decide whether to amend the South American nation’s rigid procedures for sharing Zika samples, the Cabinet chief’s spokeswoman said Friday, as officials announced that they were sending a set of samples to U.S. researchers amid complaints of hoarding.
Jenny Barchfield and Mauricio Savarese | AP | Foreign | Feb 5, 2016

WHO statement on the first meeting of the International Health Regulations (2005) (IHR 2005) Emergency Committee on Zika virus and observed increase in neurological disorders and neonatal malformations

WHO statement on the first meeting of the International Health Regulations (2005) (IHR 2005) Emergency Committee on Zika virus and observed increase in neurological disorders and neonatal malformations
WHO statement
1 February 2016

The first meeting of the Emergency Committee (EC) convened by the Director-General under the International Health Regulations (2005) (IHR 2005) regarding clusters of microcephaly cases and other neurologic disorders in some areas affected by Zika virus was held by teleconference on 1 February 2016, from 13:10 to 16:55 Central European Time.

The WHO Secretariat briefed the Committee on the clusters of microcephaly and Guillain-Barré Syndrome (GBS) that have been temporally associated with Zika virus transmission in some settings. The Committee was provided with additional data on the current understanding of the history of Zika virus, its spread, clinical presentation and epidemiology.

The following States Parties provided information on a potential association between microcephaly and/or neurological disorders and Zika virus disease: Brazil, France, United States of America, and El Salvador.

The Committee advised that the recent cluster of microcephaly cases and other neurologic disorders reported in Brazil, following a similar cluster in French Polynesia in 2014, constitutes a Public Health Emergency of International Concern (PHEIC).

The Committee provided the following advice to the Director-General for her consideration to address the PHEIC (clusters of microcephaly and neurologic disorders) and their possible association with Zika virus, in accordance with IHR (2005).

Microcephaly and neurologic disorders
:: Surveillance for microcephaly and GBS should be standardized and enhanced, particularly in areas of known Zika virus transmission and areas at risk of such transmission.
:: Research into the etiology of new clusters of microcephaly and neurologic disorders should be intensified to determine whether there is a causative link to Zika virus and/or other factors or co-factors.

As these clusters have occurred in areas newly infected with Zika virus, and in keeping with good public health practice and the absence of another explanation for these clusters, the Committee highlights the importance of aggressive measures to reduce infection with Zika virus, particularly among pregnant women and women of childbearing age.

As a precautionary measure, the Committee made the following additional recommendations:
Zika virus transmission
:: Surveillance for Zika virus infection should be enhanced, with the dissemination of standard case definitions and diagnostics to at-risk areas.
:: The development of new diagnostics for Zika virus infection should be prioritized to facilitate surveillance and control measures.
:: Risk communications should be enhanced in countries with Zika virus transmission to address population concerns, enhance community engagement, improve reporting, and ensure application of vector control and personal protective measures.
:: Vector control measures and appropriate personal protective measures should be aggressively promoted and implemented to reduce the risk of exposure to Zika virus.
:: Attention should be given to ensuring women of childbearing age and particularly pregnant women have the necessary information and materials to reduce risk of exposure.
:: Pregnant women who have been exposed to Zika virus should be counselled and followed for birth outcomes based on the best available information and national practice and policies.

Longer-term measures
:: Appropriate research and development efforts should be intensified for Zika virus vaccines, therapeutics and diagnostics.
:: In areas of known Zika virus transmission health services should be prepared for potential increases in neurological syndromes and/or congenital malformations.

Travel measures
:: There should be no restrictions on travel or trade with countries, areas and/or territories with Zika virus transmission.
:: Travellers to areas with Zika virus transmission should be provided with up to date advice on potential risks and appropriate measures to reduce the possibility of exposure to mosquito bites.
:: Standard WHO recommendations regarding disinsection of aircraft and airports should be implemented.

Data sharing
:: National authorities should ensure the rapid and timely reporting and sharing of information of public health importance relevant to this PHEIC.
:: Clinical, virologic and epidemiologic data related to the increased rates of microcephaly and/or GBS, and Zika virus transmission, should be rapidly shared with WHO to facilitate international understanding of the these events, to guide international support for control efforts, and to prioritize further research and product development.

Based on this advice the Director-General declared a Public Health Emergency of International Concern (PHEIC) on 1 February 2016. The Director-General endorsed the Committee’s advice and issued them as Temporary Recommendations under IHR (2005). The Director-General thanked the Committee Members and Advisors for their advice.

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List of Members of, and Advisers to, the International Health Regulations (2005) Emergency Committee on Zika virus and observed increase in neurological disorders and neonatal malformations

Vaccines and Global Health: The Week in Review 30 January 2016

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_30 January 2016

blog edition: comprised of the approx. 35+ entries posted below on 3 February 2016.

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 30 January 2016]

EBOLA/EVD [to 30 January 2016]
Public Health Emergency of International Concern (PHEIC); “Threat to international peace and security” (UN Security Council)

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WHO Director-General addresses the Executive Board
Report by the Director-General to the Executive Board at its 138th Session
Geneva, Switzerland
25 January 2016
[Initial text]
Madam Chair, distinguished members of the Executive Board, Excellencies, colleagues in the UN system, ladies and gentlemen,

Fifteen months ago, Guinea, Liberia, and Sierra Leone were together reporting more than 950 cases of Ebola every week. Today, the three countries have interrupted all chains of transmission from the original outbreak that began more than two years ago.

This is a monumental achievement that needs to be acknowledged. Please join me in honouring the leadership of the three governments, the heroic sacrifices of health care workers and communities, and the unwavering support from a host of partners.

However, WHO has not yet declared the outbreak in West Africa over. As we now know, the virus can hide in the bodies of fully recovered survivors for as long as a year.

Since March of last year, WHO has documented 11 small flare-ups of infection following reintroduction of the virus from survivors. All were rapidly detected and quickly contained.

On 14 January, WHO declared that the outbreak in Liberia, the last country reporting cases, was over, but warned that the risk of further flare-ups would persist. The warning was well-founded. The next day, Sierra Leone confirmed its first new case since September of last year.

Let me put this setback in perspective.
First, these countries promptly report new cases. Vigilance is intense. Our view of the situation is sharp and transparent.

Second, these countries have the world’s largest pool of expertise in responding to Ebola. They know exactly what to do.

Third, I still have more than 1000 staff in West Africa to assist in detecting and responding to flare-ups like this one. I thank them for their skill and dedication.

Finally, thanks to a WHO-led clinical trial, we have a vaccine that can be used to confer a back-up ring of protection.

The Ebola virus is stubborn. I have no doubt that further flare-ups will occur. I have no doubt that all will be quickly contained.

The outbreak lingers in a second sense as well. Well over 10,000 survivors face persistent health problems together with continuing stigmatization. They need care.

Ebola delivered an extremely severe and shattering blow to societies and economies. Recovery will take some time.
While the job is by no means finished, no one anticipates that the situation will return to what we were seeing 15 months ago.

The determination is fierce. International solidarity has been extraordinary. The many steps taken at national and international levels have had a decisive impact.

No one will let this virus take off and run away again….

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Report – Science in emergencies: UK lessons from Ebola
Second Report of Session 2015–16 HC 469
UK House of Commons
Science and Technology Committee
Published on 25 January 2016 :: 50 pages
Introduction
Ebola is a rare and deadly disease. It is spread through direct contact with the bodily fluids of infected people and with objects and materials contaminated with these fluids. Since late 2013, West Africa has experienced the largest Ebola outbreak ever recorded. It was, first and foremost, a human tragedy. We pay tribute to all those who worked tirelessly to tackle this outbreak, some of whom gave evidence to this inquiry, and many of whom continue working to avert similar crises in the future. We also commend the Government on its leading contribution to the fight against Ebola, and the financial, and personnel, commitments that it made, from constructing and staffing Ebola treatment centres in Sierra Leone to deploying troops, helicopters, aircrew and an aviation support ship to provide much needed logistical support.

Examples of UK successes in tackling Ebola, however, must not allow complacency to set in. Despite this impressive deployment of resources to combat Ebola in Sierra Leone, the UK response—like the international response—was undermined by systemic delay. The biggest lesson that must be learnt from this outbreak of Ebola is that even minor delays in responding cost lives. Rapid reaction is essential for any hope of success in containing an outbreak. Yet delays were evident at every stage of our response, from escalating Public Health England’s disease surveillance data to those with the capacity to act, to convening a Scientific Advisory Group for Emergencies—the main mechanism for channelling scientific advice to Government in an emergency—which failed to be established until October 2014, three months after ‘Cobra’, the Government’s emergency response committee, first met. In the absence of established mechanisms, ad hoc approaches emerged to fill the gaps. Inevitably, these were not as effective, or as targeted, as they should have been.

We recognise the enormous efforts made by governments, universities, regulatory bodies, humanitarian agencies, pharmaceutical companies and others to ensure that clinical trials for Ebola vaccines, treatments and diagnostics were launched in record time. But such efforts do not obscure the fact that the UK and other countries were not ‘research ready’ when the outbreak began, prompting a less than optimal and uncoordinated research response. The failure to conduct therapeutic trials earlier in the outbreak was a serious missed opportunity that will not only have cost lives in this epidemic but will impact our ability to respond to similar events in the future.

Research during an outbreak must be initiated rapidly, while still being designed and conducted to the highest possible standards. While we recognise the difficulties that arose in this outbreak, they are inherent to all epidemics; therefore, if we want to improve our response, we must address the weaknesses in our research readiness that this epidemic exposed. We are not convinced, however, that the Government has looked ahead and considered how a more timely, co-ordinated and robust response could be achieved when the next epidemic emerges.

Rapid and reliable communication is integral to delivering an effective response to a disease emergency. And yet, throughout the Ebola outbreak, we saw that systems to share advice, expertise, epidemiological and clinical data—particularly between the UK and Sierra Leone—were inadequate. We were concerned that this had harmful repercussions including a failure to undertake basic, yet important, research about the efficacy of Ebola treatments, as well as undermining the robustness of transmission modelling work. We recommend that the Chief Medical Officer urgently establishes new processes and protocols to ensure that knowledge and data are communicated effectively throughout an outbreak and that research is embedded into an emergency response from the outset.

The Government’s communications on Ebola with the UK public were accurate and balanced, making it all the more disappointing that the Government failed to explain why it went against guidance from the World Health Organization and Public Health England and introduced screening for Ebola at UK ports of entry. We recommend that when interventions like screening are instigated during an emergency, the Government makes the evidential basis for the intervention explicit.

Ebola also highlighted structural weaknesses in the UK’s capacity to absorb and withstand shocks to the system arising from emergencies. Despite hosting world-leading experts in immunology, epidemiology and tropical medicine in the UK, there are currently no licenced treatments for, and vaccinations against, Ebola. This situation has arisen, in part, due to a long-term market failure to invest in interventions for rare but potentially catastrophic epidemics. While we welcome the Government’s recent announcements of much needed research funds in this area, we recommend that it works with leading experts to publish an emerging infectious disease strategy, setting out the ‘priority threats’ the UK wishes to address, so that these funds can be effectively targeted and their benefits maximised.

We are also concerned that, in the unlikely but possible event of a domestic outbreak, the UK lacks the capability to go further and manufacture enough vaccines to vaccinate UK citizens in an emergency. Existing facilities are degraded and new plant will take years to build, leaving the UK in a vulnerable position. There is a need for the Government to do more than simply encourage inward investment in advanced manufacturing. We recommend that it acts now and negotiates with vaccine manufacturers to establish pre-agreed access to manufacturing capabilities that can be called upon quickly in an emergency.

The willingness of Government agencies, third sector organisations, health and aid workers, universities, and pharmaceutical companies to go above and beyond to help tackle the outbreak was phenomenal. The swift pace at which clinical trials were approved and conducted particularly stood out. The Defence Science and Technology Laboratory’s rapid diagnostic test for Ebola—which was developed, manufactured and latterly trialled on patients in Sierra Leone by January 2015—exemplifies the game-changing innovations that can be achieved by Government research and development facilities collaborating with private partners and clinicians. We were therefore dismayed to learn that, despite the promise shown by this test, and the production of 10,000 testing kits, it was not released for general use by the Government. Instead, we received different explanations, from different Government departments and agencies, about why the test was not operationalised. We are concerned that this is indicative of a worrying lack of cross-Government co-ordination, as well as an accountability deficit, for key aspects of the UK Ebola response. We ask the Government to clarify urgently why the rapid diagnostic test for Ebola was not released for use.

Prior to the Ebola outbreak, the Government had remained largely silent on its policy towards global health since it published its Health is Global framework in 2011. While we hope that the world will never experience an Ebola outbreak of this magnitude again, it would be naïve to assume that epidemics with the potential to cause death and devastation, and cross national borders, can be consigned to the past. Our global health policy will have a profound impact on the lives of people in the UK and beyond. It is therefore vital that the Government clearly sets out what would trigger an in-country response to a disease emergency and what capability the UK should be able to deploy readily overseas.
European Medicines Agency [to 30 January 2016]
http://www.ema.europa.eu/
29/01/2016
Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 25-28 January 2016
…Update on Ebola
The CHMP has adopted a final scientific opinion following its review of experimental Ebola treatments. The final report includes information on nine experimental medicines intended for the treatment of people infected with the Ebola virus: BCX4430, Brincidofovir, Favipiravir, TKM-Ebola, AVI-7537, ZMapp, Anti-Ebola F(ab’)2, GS-5734 and Ebotab. The assessment report for this review will be published shortly…

POLIO [to 30 January 2016]

POLIO [to 30 January 2016]
Public Health Emergency of International Concern (PHEIC)

Polio this week as of 27 January 2016
:: There are eleven weeks to go until the globally synchronized switch from the trivalent to bivalent oral polio vaccine, an important milestone in achieving a polio-free world. Read more here.
:: The WHO Executive Board is meeting this week, reviewing the report on polio eradication.
:: On 21 January, Syria passed two years without a reported case of polio despite the conflict which has affected the delivery of health services, including childhood vaccinations.
No new polio cases are reported in active country-level reports
Circulating vaccine-derived poliovirus – Lao People’s Democratic Republic
WHO – Disease outbreak news
29 January 2016
On 17 January 2016, the National IHR Focal Point (NFP) of Lao People’s Democratic Republic (PDR) notified WHO of 2 additional cases of vaccine-derived poliovirus type 1 (VDPV1). Both cases are from Longsane district, Xaisomboun Province…

Public health response
Since the detection of the first confirmed cVDPV1 in Lao PDR, outbreak response activities have been conducted nationwide, including the national round in December and the affected provinces (Bolikhamxay and Xaisomboun) and a neighbouring province (Xiengkhuang). The national Emergency Operations Centre has been activated to coordinate response efforts and a polio outbreak response plan was drafted. Enhanced surveillance is occurring throughout the country, including daily zero-reporting of AFP cases. Active case finding is ongoing in high risk districts, including retrospective review of hospital and health centre records.

Six rounds with trivalent OPV vaccine have been planned from October 2015 to March 2016 (4 sub-national and 2 national) with approximately 10 million doses to be administered to children younger than 15 years…

MERS-CoV [to 30 January 2016]

MERS-CoV [to 30 January 2016]

Thailand confirms MERS CoV in traveler, WHO cautions against continued risk of importation
SEAR/PR/1618
New Delhi, 24 January 2016: Thailand today confirmed Middle East respiratory syndrome coronavirus (MERS CoV) disease in a traveler, the second such case in the country in the last seven months, as WHO cautioned other member states in its South-East Asia Region against the continuing risks and the need to remain vigilant.

“The new case of MERS CoV is a reminder of the continued risk of importation of the disease from countries where it still persists. All countries need to further enhance surveillance for severe acute respiratory infections, focus on early diagnosis, and step up infection prevention and control procedures in health-care facilities to rapidly detect any case of importation and effectively prevent its spread,” Dr Poonam Khetrapal Singh, Regional Director, WHO South-East Asia Region, said…

WHO & Regionals [to 30 January 2016]

WHO & Regionals [to 30 January 2016]

Increased breastfeeding could save 800,000 children and US$ 300 billion
29 January 2016 — New studies find that despite strong health and economic benefits from breastfeeding, few children are exclusively breastfed until 6 months, as recommended by WHO. Globally, an estimated 1 in 3 infants under 6 months are exclusively breastfed – a rate that has not improved in 2 decades.

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Libya conflict leaves nearly 2 million in need of health care
January 2016 — Peace talks have stalled in Libya, leaving millions of people in urgent need of health care. A total of US$ 50 million is required to meet critical health needs.

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Weekly Epidemiological Record (WER) 29 January 2016, vol. 91, 4 (pp. 33–52) –
Contents:
33 Malaria vaccine: WHO position paper – January 2016

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Disease Outbreak News (DONs)
:: 29 January 2016 – Zika virus infection – United States of America – United States Virgin Islands
:: 29 January 2016 – Circulating vaccine-derived poliovirus – Lao People’s Democratic Republic
:: 29 January 2016 – Middle East respiratory syndrome coronavirus (MERS-CoV) – Thailand
:: 27 January 2016 – Lassa Fever – Nigeria
:: 27 January 2016 – Zika virus infection – Dominican Republic
:: 26 January 2016 – Middle East respiratory syndrome coronavirus (MERS-CoV) – Saudi Arabia
:: 26 January 2016 – Middle East respiratory syndrome coronavirus (MERS-CoV) – United Arab Emirates
:: 26 January 2016 – Human infection with avian influenza A(H5N6) virus – China

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:: WHO Regional Offices
WHO African Region AFRO
:: Workshop on Exchange of Best Practices to Reaching Every District/Community, equity and integration of child survival interventions in ESA commences
Cape Town, 25 January 2016 – A historic five-day workshop organized jointly by WHO, UNICEF and JSI, MCSP/USAID on Exchange of Best Practices to Reaching Every District/Community (REC), equity and integration of child survival interventions in East and Southern African (ESA) kicked off on Monday 25 January, 2016 in Cape Town, South Africa.

WHO Region of the Americas PAHO
:: New evidence in The Lancet shows more benefits of breastfeeding (01/30/2016)
:: PAHO urges governments to implement public policies that can prevent more than one-third of cancers (01/29/2016)
:: PAHO Director briefs global health authorities on Zika virus in the Americas (01/28/2016)

WHO South-East Asia Region SEARO
:: Thailand confirms MERS CoV in traveler, WHO cautions against continued risk of importation 24 January 2016:

WHO European Region EURO
:: Zika virus: risk of importation increases, but risk of spread in Europe remains extremely low during winter 29-01-2016
:: Food marketing, children’s rights and Professor Cyrus Cooper on the life-course approach in the latest Public Health Panorama 28-01-2016
:: Statement – After causing the 2009 pandemic, A(H1N1) circulates as a seasonal human influenza virus. The influenza vaccine will protect against it 26-01-2016
:: Global recommendations to stop childhood obesity launched 25-01-2016

WHO Eastern Mediterranean Region EMRO
:: Optimism on Pakistan’s progress on polio 30 January 2016
:: WHO acknowledges Saudi progress in control of Middle East respiratory syndrome 26 January 2016

WHO Western Pacific Region
No new digest content identified.

CDC/ACIP [to 30 January 2016]

CDC/ACIP [to 30 January 2016]
http://www.cdc.gov/media/index.html

[see Zika coverage above which includes CDC briefing content above]

MMWR Weekly – January 29, 2016 / Vol. 65 / No. 3
http://www.cdc.gov/mmwr/index2015.html
:: Active Monitoring of Travelers Arriving from Ebola-Affected Countries — New York City, October 2014–April 2015
:: Zika Virus Spreads to New Areas — Region of the Americas, May 2015–January 2016
:: Possible Association Between Zika Virus Infection and Microcephaly — Brazil, 2015
:: Interim Guidelines for the Evaluation and Testing of Infants with Possible Congenital Zika Virus Infection — United States, 2016
:: Notes from the Field: Ongoing Cholera Outbreak — Kenya, 2014–2016
:: Announcement: Fifty Years of Global Immunization at CDC — 1966–2015

NCI-designated Cancer Centers Urge HPV Vaccination for the Prevention of Cancer

NCI-designated Cancer Centers Urge HPV Vaccination for the Prevention of Cancer
Jan. 27, 2016
Approximately 79 million people in the United States are currently infected with a human papillomavirus (HPV) according to the Centers for Disease Control and Prevention (CDC), and 14 million new infections occur each year. Several types of high-risk HPV are responsible for the vast majority of cervical, anal, oropharyngeal (middle throat) and other genital cancers. The CDC also reports that each year in the U.S., 27,000 men and women are diagnosed with an HPV-related cancer, which amounts to a new case every 20 minutes. Even though many of these HPV-related cancers are preventable with a safe and effective vaccine, HPV vaccination rates across the U.S. remain low.

Together we, a group of the National Cancer Institute (NCI)-designated Cancer Centers, recognize these low rates of HPV vaccination as a serious public health threat. HPV vaccination represents a rare opportunity to prevent many cases of cancer that is tragically underused. As national leaders in cancer research and clinical care, we are compelled to jointly issue this call to action.

According to a 2015 CDC report, only 40 percent of girls and 21 percent of boys in the U.S. are receiving the recommended three doses of the HPV vaccine. This falls far short of the goal of 80 percent by the end of this decade, set forth by the U.S. Department of Health and Human Service’s Healthy People 2020 mission. Furthermore, U.S. rates are significantly lower than those of countries such as Australia (75 percent), the United Kingdom (84-92 percent) and Rwanda (93 percent), which have shown that high vaccination rates are currently achievable.

The HPV vaccines, like all vaccines used in the U.S., passed extensive safety testing before and after being approved by the U.S. Food and Drug Administration (FDA). The vaccines have a safety profile similar to that of other vaccines approved for adolescents in the U.S. Internationally, the safety of HPV vaccines has been tested and approved by the World Health Organization’s Global Advisory Committee on Vaccine Safety.

CDC recommends that boys and girls receive three doses of HPV vaccine at ages 11 or 12 years. The HPV vaccine series can be started in preteens as early as age 9 and should be completed before the 13th birthday. The HPV vaccine is more effective the earlier it is given; however, it is also recommended for young women until age 26 and young men until age 21.

The low vaccination rates are alarming given our current ability to safely and effectively save lives by preventing HPV infection and its associated cancers. Therefore, we urge parents and health care providers to protect the health of our children through a number of actions:
We encourage all parents and guardians to have their sons and daughters complete the 3-dose HPV vaccine series before the 13th birthday, and complete the series as soon as possible in children aged 13 to 17. Parents and guardians should talk to their health care provider to learn more about HPV vaccines and their benefits.

We encourage young men (up to age 21) and young women (up to age 26), who were not vaccinated as preteens or teens, to complete the 3-dose HPV vaccine series to protect themselves against HPV.

We encourage all health care providers to be advocates for cancer prevention by making strong recommendations for childhood HPV vaccination. We ask providers to join forces to educate parents/guardians and colleagues about the importance and benefits of HPV vaccination.

HPV vaccination is our best defense in stopping HPV infection in our youth and preventing HPV-related cancers in our communities. The HPV vaccine is CANCER PREVENTION.

Apollo Therapeutics: Consortium of World-Leading UK Universities and Global Pharmaceutical Companies Launch £40 Million Fund to Drive Therapeutic Innovation

Apollo Therapeutics: Consortium of World-Leading UK Universities and Global Pharmaceutical Companies Launch £40 Million Fund to Drive Therapeutic Innovation
:: Unique collaboration between AstraZeneca, GlaxoSmithKline, Johnson & Johnson Innovation and the technology transfer offices of Imperial College London, UCL (University College London) and the University of Cambridge, to drive forward therapeutic innovation
:: £40 million Apollo Therapeutics Fund aims to significantly improve the speed and potential of university research being translated into novel medicines
:: First time global pharmaceutical companies and world-leading universities* have created this type of fund
January 25, 2016
LONDON–(BUSINESS WIRE)–Three global pharmaceutical companies (AstraZeneca, GlaxoSmithKline, Johnson & Johnson Innovation) and the technology transfer offices of three world-leading universities (Imperial College London, University College London and the University of Cambridge) have joined forces with a combined £40 million to create the Apollo Therapeutics Fund (‘Apollo’). This pioneering new joint venture will support the translation of ground-breaking academic science from within these universities into innovative new medicines for a broad range of diseases.

“Collaboration is one of our most powerful tools in the pursuit of new medicines. Working with experts outside our own laboratories exposes us to differing expertise and innovation and means we can jointly shoulder risk – which in turn enables us to pursue some really exciting, ambitious science.”

Each of the three industry partner companies (AstraZeneca UK Limited, Glaxo Group Limited and Johnson & Johnson Innovation-JJDC, Inc.) will contribute £10 million over 6 years to the venture. The technology transfer offices (TTOs) of the three university partners – Imperial Innovations Group plc, Cambridge Enterprise Ltd Limited and UCL Business PLC – will each contribute a further £3.3 million. The aim of Apollo is to advance academic preclinical research from these universities to a stage at which it can either be taken forward by one of the industry partners following an internal bidding process or be out-licensed. The three industry partners will also provide R&D expertise and additional resources to assist with the commercial evaluation and development of projects.

Drug development is extremely complex, costly and lengthy; currently only around 10 percent of therapies entering clinical trials reach patients as medicines. By combining funding for promising early-stage therapeutics from leading UK universities with a breadth of industry expertise, Apollo aims to share the risk and accelerate the development of important new treatments, while also reducing the cost.

Dr Ian Tomlinson, former Senior Vice President, Worldwide Business Development and Biopharmaceuticals R&D, for GSK and founder & Chief Scientific Officer of Domantis Limited has been appointed Chairman of the Apollo Therapeutics Investment Committee (AIC). Comprising representatives from the six partners, the AIC will make all investment decisions.

The AIC will be advised by an independent Drug Discovery Team (DDT) of ex-industry scientists who will be employed by Apollo to work with the universities and their TTOs to identify and shape projects to bring forward for development. All therapy areas and modalities, including small molecules, peptides, proteins, antibodies, cell and gene therapies will be considered.

Apollo will be based at Stevenage Bioscience Catalyst. Once funded, projects will be progressed by the DDT alongside the university investigators, with other external resources and also in-kind resources from the industry partners as appropriate. For successful projects, the originating university and TTO will receive a percentage of future commercial revenues or out-licensing fees and the remainder will be divided amongst all the Apollo partners.

Dr Ian Tomlinson, Chairman of the Apollo Therapeutics Investment Committee commented:
“This is the first time that three global pharmaceutical companies and the TTOs of three of the world’s top ten universities have come together to form a joint enterprise of this nature, making the Apollo Therapeutics Fund a truly innovative venture.

Apollo provides an additional source of early stage funding that will allow more therapeutics projects within the three universities to realise their full potential. The active participation of the industry partners will also mean that projects will be shaped at a very early stage to optimise their suitability for further development…

MSF/Médecins Sans Frontières [to 30 January 2016]

MSF/Médecins Sans Frontières [to 30 January 2016]
http://www.doctorswithoutborders.org/news-stories/press/press-releases

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Press Releases
MSF Alert: Five Epidemics to Watch
January 25, 2016
GENEVA/NEW YORK—Five diseases with the potential to become epidemics in 2016 are being highlighted by the international medical humanitarian organization Doctors Without Borders/Médecins Sans Frontières (MSF), as the World Health Organization’s executive board meets in Geneva this week.

Without proper investment in preventing and responding to outbreaks of cholera, malaria, measles, meningitis and a group of often-overlooked diseases spread by viruses and parasites, they are likely to pose an ever greater threat to people’s health in the year ahead.

“We know that thousands of lives will be at risk in the year to come, although the means exist to prevent these deaths,” said Monica Rull, operational health advisor for MSF. “Epidemics of cholera, malaria, measles and meningitis take place every year, incapacitating and killing many—and this needs to stop. At the same time, the threat posed by emerging and re-emerging virus and parasite-spread diseases—such as dengue fever, Zika, Ebola and Kala Azar—needs to be faced.”…

Partners In Health [to 30 January 2016]

Partners In Health [to 30 January 2016]
http://www.pih.org/blog

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Jan 29, 2016
Cervical Cancer Program Expands in Haiti
Cervical cancer is the most common cancer in women in Haiti, and the second leading cause of cancer deaths among the same group, according to the ICO Information Centre on HPV and Cancer, a data clearinghouse.

This is true in a day and age when cervical cancer can largely be prevented and treated through timely vaccinations and regular gynecological exams. There is no reason that can’t be true in Haiti.

In November, Zanmi Lasante, as Partners In Health is known in Haiti, launched a two-year program that will dramatically increase its capacity to vaccinate young girls and screen and treat women for cervical cancer. Over the next 24 months, staff will vaccinate 20,000 girls in St. Marc, Mirebalais, and Belladère against human papillomavirus (HPV), a disease that causes virtually all cervical cancer. They will also screen 20,000 more women for cervical cancer in St. Marc and the surrounding area, while boosting efforts to screen and treat women in Mirebalais and Belladère.

Additional staff will be hired and equipment and materials will be purchased to meet increased demand for these gynecological services, most of which will be provided at St. Nicholas Hospital in St. Marc. Pap smears, biopsies, and colposcopy—a procedure used to closely examine the cervix—will also be available for women whose initial tests indicate they may have cancer…

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Jan 28, 2016
Need to Know: Zika Virus
The Zika virus has been reported in 23 countries and territories so far, including Haiti and Mexico, where Partners In Health has thousands of staff and serves thousands more patients on a daily basis. Dr. Joia Mukherjee, PIH’s chief medical officer and an infectious disease expert, answers key questions about the virus. .

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Jan 27, 2016
Study Finds Poverty Spread Ebola
A study quantifies how poor areas of Monrovia increased transmission of Ebola in 2014.

Global Fund [to 30 January 2016]

Global Fund [to 30 January 2016]
http://www.theglobalfund.org/en/news/

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News
Dutch Postcode Lottery Supports TB Programs for Syrian Refugees
28 January 2016
AMSTERDAM – The Dutch Postcode Lottery announced a contribution of €2.5 million to the Global Fund to support the fight against tuberculosis among Syrian refugees in Lebanon, Jordan and Iraq.

The Bill & Melinda Gates Foundation will match the contribution from the Dutch Postcode Lottery.

“Partnerships like this allow us to better focus on leaving no one behind, regardless of their status, circumstance, or ethnic and religious background,” said Mark Dybul, Executive Director of the Global Fund. “TB is a serious challenge, and collective efforts to reduce it are ultimately connected with achieving quality access to health care by all.”

Marieke van Schaik, Managing Director of the Dutch Postcode Lottery, said: “We are honored to grant this award to the Global Fund to support the work that the organization is doing in emergency situations.”

The Global Fund partnership, through the Emergency Fund special initiative, provides access to funds in emergency situations connected with HIV, TB or malaria. The Emergency Fund currently supports the provision and continuity of essential TB prevention, diagnosis and treatment services in Lebanon and Jordan, and will be expanded to Iraq.

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News
Global Fund Hails New Malaria Investment
25 January 2016
GENEVA – The Global Fund welcomes a significant new investment against malaria by the United Kingdom and the Bill & Melinda Gates Foundation.

Announced today in Liverpool by George Osborne, Chancellor of the Exchequer, and Bill Gates, co-chair of the Bill & Melinda Gates Foundation, the funding of £3 billion over the next five years will support research and other efforts to eliminate malaria.

The new fund will accelerate gains made against the mosquito-borne disease. Global efforts have already achieved a 60 percent decline in deaths since 2000, when malaria killed one million people, mostly young children. Yet today’s announcement underscored the need to expand efforts to eliminate this preventable disease.

The fund will receive £500 million a year from Britain’s overseas aid budget for the next five years, as well as US$200 million a year from the Gates Foundation to support research and development and accelerate malaria elimination efforts…

Cost effectiveness analysis of Year 2 of an elementary school-located influenza vaccination program–Results from a randomized controlled trial

BMC Health Services Research

(Accessed 30 January 2016)

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Research article
Cost effectiveness analysis of Year 2 of an elementary school-located influenza vaccination program–Results from a randomized controlled trial
Byung-Kwang Yoo, Sharon G. Humiston, Peter G. Szilagyi, Stanley J. Schaffer, Christine Long and Maureen Kolasa
BMC Health Services Research201515:511
DOI: 10.1186/s12913-015-1169-5
Abstract
Background
School-located vaccination against influenza (SLV-I) has the potential to improve current suboptimal influenza immunization coverage for U.S. school-aged children. However, little is known about SLV-I’s cost-effectiveness. The objective of this study is to establish the cost-effectiveness of SLV-I based on a two-year community-based randomized controlled trial (Year 1: 2009–2010 vaccination season, an unusual H1N1 pandemic influenza season, and Year 2: 2010–2011, a more typical influenza season).
Methods
We performed a cost-effectiveness analysis on a two-year randomized controlled trial of a Western New York SLV-I program. SLV-I clinics were offered in 21 intervention elementary schools (Year 1 n = 9,027; Year 2 n = 9,145 children) with standard-of-care (no SLV-I) in control schools (Year 1 n = 4,534 (10 schools); Year 2 n  = 4,796 children (11 schools)). We estimated the cost-per-vaccinated child, by dividing the incremental cost of the intervention by the incremental effectiveness (i.e., the number of additionally vaccinated students in intervention schools compared to control schools).
Results
In Years 1 and 2, respectively, the effectiveness measure (proportion of children vaccinated) was 11.2 and 12.0 percentage points higher in intervention (40.7 % and 40.4 %) than control schools. In year 2, the cost-per-vaccinated child excluding vaccine purchase ($59.88 in 2010 US $) consisted of three component costs: (A) the school costs ($8.25); (B) the project coordination costs ($32.33); and (C) the vendor costs excluding vaccine purchase ($16.68), summed through Monte Carlo simulation. Compared to Year 1, the two component costs (A) and (C) decreased, while the component cost (B) increased in Year 2. The cost-per-vaccinated child, excluding vaccine purchase, was $59.73 (Year 1) and $59.88 (Year 2, statistically indistinguishable from Year 1), higher than the published cost of providing influenza vaccination in medical practices ($39.54). However, taking indirect costs (e.g., averted parental costs to visit medical practices) into account, vaccination was less costly in SLV-I ($23.96 in Year 1, $24.07 in Year 2) than in medical practices.
Conclusions
Our two-year trial’s findings reinforced the evidence to support SLV-I as a potentially favorable system to increase childhood influenza vaccination rates in a cost-efficient way. Increased efficiencies in SLV-I are needed for a sustainable and scalable SLV-I program

Adult pertussis is unrecognized public health problem in Thailand

BMC Infectious Diseases
http://www.biomedcentral.com/bmcinfectdis/content
(Accessed 30 January 2016)

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Research article
Adult pertussis is unrecognized public health problem in Thailand
Nirada Siriyakorn, Pornvimol Leethong, Terapong Tantawichien, Saowalak Sripakdee, Anusak Kerdsin, Surang Dejsirilert and Leilani Paitoonpong
BMC Infectious Diseases 2016 16:25
Published on: 25 January 2016
Abstract
Background
Although pertussis has been considered a disease of childhood, it is also recognized as an important respiratory tract infection in adolescents and adults. However, in countries with routine vaccination against pertussis with high coverage, pertussis is not usually taken into consideration for the etiology of prolonged cough in adults. Previous studies in a variety of populations in developed countries have documented that pertussis is quite common, ranging from 2.9 to 32 % of adolescents and adults with prolonged cough. The anticipation and early recognition of this change in the epidemiology is important because the affected adolescents and adults act as reservoirs of the disease and source of infection to the vulnerable population of infants, for whom the disease can be life threatening. We conducted a prospective study to determine the prevalence of pertussis in Thai adults with prolonged cough.
Methods
Seventy-six adult patients with a cough lasting for more than 2 weeks (range, 14–180 days) were included in the present study. The data regarding medical history and physical examination were carefully analyzed. Nasopharyngeal swabs from all patients were obtained for the detection of deoxyribonucleic acid of Bordetella pertussis by the polymerase chain reaction (PCR) method. Paired serum samples were collected and tested for IgG antibody against pertussis toxin by using an ELISA method.
Results
Of 76 adult patients, 14 patients (18.4 %) with the mean age of 59 (range, 28–85) years and the mean duration of cough of 34 (range, 14–120) days had laboratory evidence of acute pertussis infection. One patient was diagnosed by the PCR method, while the rest had serological diagnosis. Whooping cough is a significantly associated symptom of patients with chronic cough who had laboratory evidence of pertussis. (p < .05, odds ratio 3.75, 95 % confidence interval: 1.00,14.06)
Conclusion
Pertussis is being increasingly recognized as a cause of prolonged, distressing cough among adults in Thailand. This result addresses the need of pertussis vaccination in Thai adults for preventing transmission to a high risk group such as newborn infants.

Economic evaluations of interventions to reduce neonatal morbidity and mortality: a review of the evidence in LMICs and its implications for South Africa

Cost Effectiveness and Resource Allocation
http://www.resource-allocation.com/
(Accessed 30 January 2016)

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Review
Economic evaluations of interventions to reduce neonatal morbidity and mortality: a review of the evidence in LMICs and its implications for South Africa
Mandy Maredza, Lumbwe Chola and Karen Hofman
Abstract
Background
Newborn mortality, comprising a third of all under-5 deaths, has hardly changed in low and middle income countries (LMICs) including South Africa over the past decade. To attain the MDG 4 target, greater emphasis must be placed on wide-scale implementation of proven, cost-effective interventions. This paper reviews economic evidence on effective neonatal health interventions in LMICs from 2000–2013; documents lessons for South African policy on neonatal health; and identifies gaps and areas for future research.
Methods
A narrative review was performed in leading public health databases for full economic evaluations conducted between 2000 and 2013. Data extraction from the articles included in the review was guided by the Consolidated Health Economic Evaluation Reporting Standards (CHEERS) checklist, and the quality of the included economic evaluations was assessed using the Quality of Health Economics Studies Instrument (QHES).
Results
Twenty-seven economic evaluations were identified, from South East Asia and sub-Saharan Africa, with those from sub-Saharan Africa primarily focused on HIV/AIDS. Packages of care to prevent neonatal mortality were more cost-effective than vertical interventions. A wide variability in methodological approaches challenges the comparability of study results between countries. In South Africa, there is limited cost-effectiveness evidence for the interventions proposed by the National Perinatal Morbidity and Mortality Committee.
Conclusions
Neonatal strategies have a strong health system focus but this review suggests that strengthening community care could be an additional component for averting neonatal deaths. While some evidence exists, having a more complete understanding of how to most effectively deploy scarce resources for neonatal health in South Africa in the post-2015 era is essential.

Systematic review on tuberculosis transmission on aircraft…

Eurosurveillance
Volume 21, Issue 4, 28 January 2016
http://www.eurosurveillance.org/Public/Articles/Archives.aspx?PublicationId=11678

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Review articles
Systematic review on tuberculosis transmission on aircraft and update of the European Centre for Disease Prevention and Control risk assessment guidelines for tuberculosis transmitted on aircraft (RAGIDA-TB)
by S Kotila, L Payne Hallström, N Jansen, P Helbling, I Abubakar
Abstract
As a setting for potential tuberculosis (TB) transmission and contact tracing, aircraft pose specific challenges. Evidence-based guidelines are needed to support the related-risk assessment and contact-tracing efforts. In this study evidence of TB transmission on aircraft was identified to update the Risk Assessment Guidelines for TB Transmitted on Aircraft (RAGIDA-TB) of the European Centre for Disease Prevention and Control (ECDC). Electronic searches were undertaken from Medline (Pubmed), Embase and Cochrane Library until 19 July 2013. Eligible records were identified by a two-stage screening process and data on flight and index case characteristics as well as contact tracing strategies extracted. The systematic literature review retrieved 21 records. Ten of these records were available only after the previous version of the RAGIDA guidelines (2009) and World Health Organization guidelines on TB and air travel (2008) were published. Seven of the 21 records presented some evidence of possible in-flight transmission, but only one record provided substantial evidence of TB transmission on an aircraft. The data indicate that overall risk of TB transmission on aircraft is very low. The updated ECDC guidelines for TB transmission on aircraft have global implications due to inevitable need for international collaboration in contract tracing and risk assessment.

Global Public Health – Volume 11, Issue 3, 2016

Global Public Health
Volume 11, Issue 3, 2016
http://www.tandfonline.com/toc/rgph20/current

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Articles
Developing collaborative approaches to international research: Perspectives of new global health researchers
Paula Godoy-Ruiz, Donald C. Cole, Lindsey Lenters & Kwame McKenzie
pages 253-275
Open access
DOI:10.1080/17441692.2014.999814
Abstract
Within a global context of growing health inequities, the fostering of partnerships and collaborative research have been promoted as playing a critical role in tackling health inequities and health system problems worldwide. Since 2004, the Canadian Coalition for Global Health Research (CCGHR) has facilitated annual Summer Institutes for new global health researchers aimed at strengthening global health research competencies and partnerships among participants. We sought to explore CCGHR Summer Institute alumni perspectives on the Summer Institute experience, particularly on the individual research pairings of Canadian and low- and middle-income countries researchers that have characterised the program. The results reveal that the Summer Institute offered an enriching learning opportunity for participants and worked to further their collaborative projects through providing dedicated one-on-one time with their international research partner, feedback from colleagues from around the world and mentorship by more senior researchers. Positive individual relationships among researchers, as well as the existence of institutional collaborations, employer and funding support, and agendas of local and national politicians were factors that have influenced the ongoing collaboration of partners. There is a need to more fully examine the interplay between individual and institutional-level collaborations, as well as their social and political contexts.

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Articles
Alternative accounting in maternal and infant global health
Vincanne Adams, Sienna R. Craig & Arlene Samen
DOI:10.1080/17441692.2015.1021364
pages 276-294
Abstract
Efforts to augment accountability through the use of metrics, and especially randomised controlled trial or other statistical methods place an increased burden on small nongovernmental organisations (NGOs) doing global health. In this paper, we explore how one small NGO works to generate forms of accountability and evidence that may not conform to new metrics trends but nevertheless deserve attention and scrutiny for being effective, practical and reliable in the area of maternal and infant health. Through an analysis of one NGO and, in particular, its organisational and ethical principles for creating a network of safety for maternal and child health, we argue that alternative forms of (ac)counting like these might provide useful evidence of another kind of successful global health work

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Vaccine procurement during an influenza pandemic and the role of Advance Purchase Agreements: Lessons from 2009-H1N1
Mark Turner
pages 322-335
DOI:10.1080/17441692.2015.1043743
Abstract
Vaccines are hugely important tools in minimising the effect pandemic influenza could have on a population. The reforms introduced by the Pandemic Influenza Preparedness Framework are ill-suited to providing sufficient levels of access to vaccines to meet the needs of developing states, and as such developing states will continue to be reliant upon the traditional methods of vaccine procurement to procure the majority of the vaccines they required. Using procurement during 2009-H1N1 as a case study, this paper examines the methods of procurement utilised by states in order to determine if the procurement tools available to developing states are sufficient to procure adequate levels of pandemic influenza vaccines. Particular focus is given to the role Advance Purchase Agreements (APAs) play in the procurement process. By exploring this case study it is possible to argue that these procurement methods are ineffective for developing states, and when the next influenza pandemic occurs, demand will once again outstrip supply globally, due to supply of vaccines being dominated by the developed states with APAs in place.

HPV Vaccine Awareness, Barriers, Intentions, and Uptake in Latina Women

Journal of Immigrant and Minority Health
Volume 18, Issue 1, February 2016
http://link.springer.com/journal/10903/18/1/page/1

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Original paper
HPV Vaccine Awareness, Barriers, Intentions, and Uptake in Latina Women
Julia Lechuga, Lina Vera-Cala…
Abstract
Latina women are at heightened risk of cervical cancer incidence and mortality. The human papillomavirus (HPV) is the principal cause of the majority of cervical cancer cases. A vaccine that protects against HPV was licensed in 2006. Eight years post-licensure, mixed research findings exist regarding the factors that predict vaccine uptake in Latinas. We conducted a population-based phone survey with a random sample of 296 Latinas living in a Midwestern U.S. City. Intention to vaccinate was significantly associated with health care provider recommendations, worry about side effects, knowing other parents have vaccinated, perceived severity of HPV, and worry that daughter may become sexually active following vaccination. Worry that daughter may become sexually active was the only factor related to vaccine uptake. Findings suggest that training providers to discuss the low risk of severe side effects, consequences of persistent HPV, and sexuality related concerns with Latino women may encourage vaccination.

Journal of the Royal Society – Interface :: 01 January 2016

Journal of the Royal Society – Interface
01 January 2016; volume 13, issue 114
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Research Articles
Self-enforcing regional vaccination agreements
Petra Klepac, Itamar Megiddo, Bryan T. Grenfell, Ramanan Laxminarayan
J. R. Soc. Interface 2016 13 20150907; DOI: 10.1098/rsif.2015.0907. Published 20 January 2016
Abstract
In a highly interconnected world, immunizing infections are a transboundary problem, and their control and elimination require international cooperation and coordination. In the absence of a global or regional body that can impose a universal vaccination strategy, each individual country sets its own strategy. Mobility of populations across borders can promote free-riding, because a country can benefit from the vaccination efforts of its neighbours, which can result in vaccination coverage lower than the global optimum. Here we explore whether voluntary coalitions that reward countries that join by cooperatively increasing vaccination coverage can solve this problem. We use dynamic epidemiological models embedded in a game-theoretic framework in order to identify conditions in which coalitions are self-enforcing and therefore stable, and thus successful at promoting a cooperative vaccination strategy. We find that countries can achieve significantly greater vaccination coverage at a lower cost by forming coalitions than when acting independently, provided a coalition has the tools to deter free-riding. Furthermore, when economically or epidemiologically asymmetric countries form coalitions, realized coverage is regionally more consistent than in the absence of coalitions.

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Research Articles
Role of vaccination-induced immunity and antigenic distance in the transmission dynamics of highly pathogenic avian influenza H5N1
Ioannis Sitaras, Xanthoula Rousou, Donata Kalthoff, Martin Beer, Ben Peeters, Mart C. M. de Jong
J. R. Soc. Interface 2016 13 20150976; DOI: 10.1098/rsif.2015.0976. Published 13 January 2016
Abstract
Highly pathogenic avian influenza (HPAI) H5N1 epidemics in poultry cause huge economic losses as well as sporadic human morbidity and mortality. Vaccination in poultry has often been reported as being ineffective in preventing transmission and as a potential driving force in the selection of immune escape mutants. We conducted transmission experiments to evaluate the transmission dynamics of HPAI H5N1 strains in chickens vaccinated with high and low doses of immune escape mutants we have previously selected, and analysed the data using mathematical models. Remarkably, we demonstrate that the effect of antigenic distances between the vaccine and challenge strains used in this study is too small to influence the transmission dynamics of the strains used. This is because the effect of a sufficient vaccine dose on antibody levels against the challenge viruses is large enough to compensate for any decrease in antibody titres due to antigenic differences between vaccine and challenge strains. Our results show that at least under experimental conditions, vaccination will remain effective even after antigenic changes as may be caused by the initial selection in vaccinated birds.

The Lancet – Jan 30, 2016

The Lancet
Jan 30, 2016 Volume 387 Number 10017 p403-504
http://www.thelancet.com/journals/lancet/issue/current

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Editorial
Ebola’s legacy: UK deficits and their global lessons
The Lancet
Summary
A devastating report on the UK’s lessons from Ebola was published this week by the House of Commons Science and Technology Committee. Much of the blame for the world’s lacklustre response to Ebola has been laid at the door of WHO. But the committee also found surprising weaknesses in the UK’s application of science to global health emergencies. It makes important recommendations for corrective action. Although targeted towards the UK, the committee’s findings will also likely apply to other high-income countries involved in the response to Ebola.

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Articles
Global, regional, and national levels and trends in maternal mortality between 1990 and 2015, with scenario-based projections to 2030: a systematic analysis by the UN Maternal Mortality Estimation Inter-Agency Group
Leontine Alkema, Doris Chou, Daniel Hogan, Sanqian Zhang, Ann-Beth Moller, Alison Gemmill, Doris Ma Fat, Ties Boerma, Marleen Temmerman, Colin Mathers, Lale Say, United Nations Maternal Mortality Estimation Inter-Agency Group collaborators, technical advisory group
Summary
Background
Millennium Development Goal 5 calls for a 75% reduction in the maternal mortality ratio (MMR) between 1990 and 2015. We estimated levels and trends in maternal mortality for 183 countries to assess progress made. Based on MMR estimates for 2015, we constructed projections to show the requirements for the Sustainable Development Goal (SDG) of less than 70 maternal deaths per 100 000 livebirths globally by 2030.
Methods
We updated the UN Maternal Mortality Estimation Inter-Agency Group (MMEIG) database with more than 200 additional records (vital statistics from civil registration systems, surveys, studies, or reports). We generated estimates of maternal mortality and related indicators with 80% uncertainty intervals (UIs) using a Bayesian model. The model combines the rate of change implied by a multilevel regression model with a time-series model to capture data-driven changes in country-specific MMRs, and includes a data model to adjust for systematic and random errors associated with different data sources.
Results
We had data for 171 of 183 countries. The global MMR fell from 385 deaths per 100 000 livebirths (80% UI 359–427) in 1990, to 216 (207–249) in 2015, corresponding to a relative decline of 43·9% (34·0–48·7), with 303 000 (291 000–349 000) maternal deaths worldwide in 2015. Regional progress in reducing the MMR since 1990 ranged from an annual rate of reduction of 1·8% (0·0–3·1) in the Caribbean to 5·0% (4·0–6·0) in eastern Asia. Regional MMRs for 2015 ranged from 12 deaths per 100 000 livebirths (11–14) for high-income regions to 546 (511–652) for sub-Saharan Africa. Accelerated progress will be needed to achieve the SDG goal; countries will need to reduce their MMRs at an annual rate of reduction of at least 7·5%.
Interpretation
Despite global progress in reducing maternal mortality, immediate action is needed to meet the ambitious SDG 2030 target, and ultimately eliminate preventable maternal mortality. Although the rates of reduction that are needed to achieve country-specific SDG targets are ambitious for most high mortality countries, countries that made a concerted effort to reduce maternal mortality between 2000 and 2010 provide inspiration and guidance on how to accomplish the acceleration necessary to substantially reduce preventable maternal deaths.
Funding
National University of Singapore, National Institute of Child Health and Human Development, USAID, and the UNDP/UNFPA/UNICEF/WHO/World Bank Special Programme of Research, Development and Research Training in Human Reproduction.

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Series
Breastfeeding
Breastfeeding in the 21st century: epidemiology, mechanisms, and lifelong effect
Cesar G Victora, Rajiv Bahl, Aluísio J D Barros, Giovanny V A França, Susan Horton, Julia Krasevec, Simon Murch, Mari Jeeva Sankar, Neff Walker, Nigel C Rollins, The Lancet Breastfeeding Series Group

Breastfeeding
Why invest, and what it will take to improve breastfeeding practices?
Nigel C Rollins, Nita Bhandari, Nemat Hajeebhoy, Susan Horton, Chessa K Lutter, Jose C Martines, Ellen G Piwoz, Linda M Richter, Cesar G Victora, The Lancet Breastfeeding Series Group

Sharing Clinical Trial Data — A Proposal from the International Committee of Medical Journal Editors

New England Journal of Medicine
January 28, 2016 Vol. 374 No. 4
http://www.nejm.org/toc/nejm/medical-journal

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Editorial
Sharing Clinical Trial Data — A Proposal from the International Committee of Medical Journal Editors
Darren B. Taichman, M.D., Ph.D., Joyce Backus, M.S.L.S., Christopher Baethge, M.D., Howard Bauchner, M.D., Peter W. de Leeuw, M.D., Jeffrey M. Drazen, M.D., John Fletcher, M.B., B.Chir., M.P.H., Frank A. Frizelle, M.B., Ch.B., F.R.A.C.S., Trish Groves, M.B., B.S., M.R.C.Psych., Abraham Haileamlak, M.D., Astrid James, M.B., B.S., Christine Laine, M.D., M.P.H., Larry Peiperl, M.D., Anja Pinborg, M.D., Peush Sahni, M.B., B.S., M.S., Ph.D., and Sinan Wu, M.D.
N Engl J Med 2016; 374:384-386
January 28, 2016
DOI: 10.1056/NEJMe1515172

The International Committee of Medical Journal Editors (ICMJE) believes that there is an ethical obligation to responsibly share data generated by interventional clinical trials because participants have put themselves at risk. In a growing consensus, many funders around the world — foundations, government agencies, and industry — now mandate data sharing. Here we outline the ICMJE’s proposed requirements to help meet this obligation. We encourage feedback on the proposed requirements. Anyone can provide feedback at http://www.icmje.org by 18 April 2016.

The ICMJE defines a clinical trial as any research project that prospectively assigns people or a group of people to an intervention, with or without concurrent comparison or control groups, to study the cause-and-effect relationship between a health-related intervention and a health outcome. Further details may be found in the Recommendations for the Conduct, Reporting, Editing and Publication of Scholarly Work in Medical Journals at http://www.icmje.org.

As a condition of consideration for publication of a clinical trial report in our member journals, the ICMJE proposes to require authors to share with others the deidentified individual-patient data (IPD) underlying the results presented in the article (including tables, figures, and appendices or supplementary material) no later than 6 months after publication. The data underlying the results are defined as the IPD required to reproduce the article’s findings, including necessary metadata. This requirement will go into effect for clinical trials that begin to enroll participants beginning 1 year after the ICMJE adopts its data-sharing requirements. (The ICMJE plans to adopt data-sharing requirements after considering feedback received to the proposals made here.)

Enabling responsible data sharing is a major endeavor that will affect the fabric of how clinical trials are planned and conducted and how their data are used. By changing the requirements of the manuscripts we will consider for publication in our journals, editors can help foster this endeavor. As editors, our direct influence is logically, and practically, limited to those data underpinning the results and analyses we publish in our journals.

The ICMJE also proposes to require that authors include a plan for data sharing as a component of clinical trial registration. This plan must include where the researchers will house the data and, if not in a public repository, the mechanism by which they will provide others access to the data, as well as other data-sharing plan elements outlined in the 2015 Institute of Medicine Report (e.g., whether data will be freely available to anyone upon request or only after application to and approval by a learned intermediary, whether a data use agreement will be required).1 ClinicalTrials.gov has added an element to its registration platform to collect data-sharing plans. We encourage other trial registries to similarly incorporate mechanisms for the registration of data-sharing plans. Trialists who want to publish in ICMJE member journals (or nonmember journals that choose to follow these recommendations) should choose a registry that includes a data-sharing plan element as a specified registry item or allows for its entry as a free-text statement in a miscellaneous registry field. As a condition of consideration for publication in our member journals, authors will be required to include a description of the data-sharing plan in the submitted manuscript. Authors may choose to share the deidentified IPD underlying the results presented in the article under less restrictive, but not more restrictive, conditions than were indicated in the registered data-sharing plan.

The ICMJE already requires the prospective registration of all clinical trials prior to enrollment of the first participant. This requirement aims, in part, to prevent selective publication and selective reporting of research outcomes, and to prevent unnecessary duplication of research effort. Including a commitment to a data-sharing plan is a logical addition to trial registration that will further each of these goals. Prospective trial registration currently includes documenting the planned primary and major secondary end points to be assessed, which enables identification of incomplete reporting as well as post hoc analyses. Declaring the plan for sharing data prior to their collection will further enhance transparency in the conduct and reporting of clinical trials by exposing when data availability following trial completion differs from prior commitments.

Sharing clinical trial data, including deidentified IPD, requires planning to ensure appropriate ethics committee or institutional review board approval and the informed consent of study participants. Accordingly, we will defer these requirements for 1 year to allow investigators, trial sponsors, and regulatory bodies time to plan for their implementation.

Just as the confidentiality of trial participants must be protected (through the deidentification of IPD), and the needs of those reasonably requesting data met (through the provision of useable data), the reasonable rights of investigators and trial sponsors must also be protected. The ICMJE proposes the following to safeguard these rights. First, ICMJE editors will not consider the deposition of data in a registry to constitute prior publication. Second, authors of secondary analyses using these shared data must attest that their use was in accordance with the terms (if any) agreed to upon their receipt. Third, they must reference the source of the data using a unique identifier of a clinical trial’s data set to provide appropriate credit to those who generated it and allow searching for the studies it has supported. Fourth, authors of secondary analyses must explain completely how theirs differ from previous analyses. In addition, those who generate and then share clinical trial data sets deserve substantial credit for their efforts. Those using data collected by others should seek collaboration with those who collected the data. However, because collaboration will not always be possible, practical, or desired, an alternative means of providing appropriate credit needs to be developed and recognized in the academic community. We welcome ideas about how to provide such credit.

Data sharing is a shared responsibility. Editors of individual journals can help foster data sharing by changing the requirements of the manuscripts they will consider for publication in their journals. Funders and sponsors of clinical trials are in a position to support and ensure adherence to IPD-sharing obligations. If journal editors become aware that IPD-sharing obligations are not being met, they may choose to request additional information; to publish an expression of concern; to notify the sponsors, funders, or institutions; or in certain cases, to retract the publication.

In the rare situation in which compliance with these requirements is impossible, editors may consider authors’ requests for exceptions. If an exception is made, the reason(s) must be explained in the publication.

Sharing data will increase confidence and trust in the conclusions drawn from clinical trials. It will enable the independent confirmation of results, an essential tenet of the scientific process. It will foster the development and testing of new hypotheses. Done well, sharing clinical trial data should also make progress more efficient by making the most of what may be learned from each trial and by avoiding unwarranted repetition. It will help to fulfill our moral obligation to study participants, and we believe it will benefit patients, investigators, sponsors, and society.

Historical Parallels, Ebola Virus Disease and Cholera: Understanding Community Distrust and Social Violence with Epidemics

PLoS Currents: Outbreaks
http://currents.plos.org/outbreaks/
(Accessed 30 January 2016)

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Historical Parallels, Ebola Virus Disease and Cholera: Understanding Community Distrust and Social Violence with Epidemics
January 26, 2016 · Discussion
In the three West African countries most affected by the recent Ebola virus disease (EVD) outbreak, resistance to public health measures contributed to the startling speed and persistence of this epidemic in the region. But how do we explain this resistance, and how have people in these communities understood their actions? By comparing these recent events to historical precedents during Cholera outbreaks in Europe in the 19th century we show that these events have not been new to history or unique to Africa. Community resistance must be analysed in context and go beyond simple single-variable determinants. Knowledge and respect of the cultures and beliefs of the afflicted is essential for dealing with threatening disease outbreaks and their potential social violence.

Strategies to Prevent Cholera Introduction during International Personnel Deployments: A Computational Modeling Analysis Based on the 2010 Haiti Outbreak

PLoS Medicine
http://www.plosmedicine.org/
(Accessed 30 January 2016)

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Editorial
Can Data Sharing Become the Path of Least Resistance?
The PLOS Medicine Editors
Published: January 26, 2016
DOI: 10.1371/journal.pmed.1001949
Initial text
The year 2016 could be the year when medical research converges on data sharing as a universal standard, if recent events, reflected in several PLOS Medicine articles this month, are a good indication. Attaining that standard, however, may take a little longer…

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Strategies to Prevent Cholera Introduction during International Personnel Deployments: A Computational Modeling Analysis Based on the 2010 Haiti Outbreak
Joseph A. Lewnard, Marina Antillón, Gregg Gonsalves, Alice M. Miller, Albert I. Ko, Virginia E. Pitzer
Research Article | published 26 Jan 2016 | PLOS Medicine
10.1371/journal.pmed.1001947
Abstract
Background
Introduction of Vibrio cholerae to Haiti during the deployment of United Nations (UN) peacekeepers in 2010 resulted in one of the largest cholera epidemics of the modern era. Following the outbreak, a UN-commissioned independent panel recommended three pre-deployment intervention strategies to minimize the risk of cholera introduction in future peacekeeping operations: screening for V. cholerae carriage, administering prophylactic antimicrobial chemotherapies, or immunizing with oral cholera vaccines. However, uncertainty regarding the effectiveness of these approaches has forestalled their implementation by the UN. We assessed how the interventions would have impacted the likelihood of the Haiti cholera epidemic.
Methods and Findings
We developed a stochastic model for cholera importation and transmission, fitted to reported cases during the first weeks of the 2010 outbreak in Haiti. Using this model, we estimated that diagnostic screening reduces the probability of cases occurring by 82% (95% credible interval: 75%, 85%); however, false-positive test outcomes may hamper this approach. Antimicrobial chemoprophylaxis at time of departure and oral cholera vaccination reduce the probability of cases by 50% (41%, 57%) and by up to 61% (58%, 63%), respectively. Chemoprophylaxis beginning 1 wk before departure confers a 91% (78%, 96%) reduction independently, and up to a 98% reduction (94%, 99%) if coupled with vaccination. These results are not sensitive to assumptions about the background cholera incidence rate in the endemic troop-sending country. Further research is needed to (1) validate the sensitivity and specificity of rapid test approaches for detecting asymptomatic carriage, (2) compare prophylactic efficacy across antimicrobial regimens, and (3) quantify the impact of oral cholera vaccine on transmission from asymptomatic carriers.
Conclusions
Screening, chemoprophylaxis, and vaccination are all effective strategies to prevent cholera introduction during large-scale personnel deployments such as that precipitating the 2010 Haiti outbreak. Antimicrobial chemoprophylaxis was estimated to provide the greatest protection at the lowest cost among the approaches recently evaluated by the UN.

Assessing Progress towards Public Health, Human Rights, and International Development Goals Using Frontier Analysi

PLoS One
http://www.plosone.org/
[Accessed 30 January 2016]

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Assessing Progress towards Public Health, Human Rights, and International Development Goals Using Frontier Analysis
Jeanne Luh, Ryan Cronk, Jamie Bartram
Research Article | published 26 Jan 2016 | PLOS ONE
10.1371/journal.pone.0147663
71/journal.pone.0145548
Abstract
Indicators to measure progress towards achieving public health, human rights, and international development targets, such as 100% access to improved drinking water or zero maternal mortality ratio, generally focus on status (i.e., level of attainment or coverage) or trends in status (i.e., rates of change). However, these indicators do not account for different levels of development that countries experience, thus making it difficult to compare progress between countries. We describe a recently developed new use of frontier analysis and apply this method to calculate country performance indices in three areas: maternal mortality ratio, poverty headcount ratio, and primary school completion rate. Frontier analysis is used to identify the maximum achievable rates of change, defined by the historically best-performing countries, as a function of coverage level. Performance indices are calculated by comparing a country’s rate of change against the maximum achievable rate at the same coverage level. A country’s performance can be positive or negative, corresponding to progression or regression, respectively. The calculated performance indices allow countries to be compared against each other regardless of whether they have only begun to make progress or whether they have almost achieved the target. This paper is the first to use frontier analysis to determine the maximum achievable rates as a function of coverage level and to calculate performance indices for public health, human rights, and international development indicators. The method can be applied to multiple fields and settings, for example health targets such as cessation in smoking or specific vaccine immunizations, and offers both a new approach to analyze existing data and a new data source for consideration when assessing progress achieved.

Cervical Cancer Screening in Partly HPV Vaccinated Cohorts – A Cost-Effectiveness Analysis

PLoS One
http://www.plosone.org/
[Accessed 30 January 2016]

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Cervical Cancer Screening in Partly HPV Vaccinated Cohorts – A Cost-Effectiveness Analysis
Steffie K. Naber, Suzette M. Matthijsse, Kirsten Rozemeijer, Corine Penning, Inge M. C. M. de Kok, Marjolein van Ballegooijen
Research Article | published 29 Jan 2016 | PLOS ONE
10.13
Abstract
Background
Vaccination against the oncogenic human papillomavirus (HPV) types 16 and 18 will reduce the prevalence of these types, thereby also reducing cervical cancer risk in unvaccinated women. This (measurable) herd effect will be limited at first, but is expected to increase over time. At a certain herd immunity level, tailoring screening to vaccination status may no longer be worth the additional effort. Moreover, uniform screening may be the only viable option. We therefore investigated at what level of herd immunity it is cost-effective to also reduce screening intensity in unvaccinated women.
Methods
We used the MISCAN-Cervix model to determine the optimal screening strategy for a pre-vaccination population and for vaccinated women (~80% decreased risk), assuming a willingness-to-pay of €50,000 per quality-adjusted life year gained. We considered HPV testing, cytology testing and co-testing and varied the start age of screening, the screening interval and the number of lifetime screens. We then calculated the incremental cost-effectiveness ratio (ICER) of screening unvaccinated women with the strategy optimized to the pre-vaccination population as compared to with the strategy optimized to vaccinated women, assuming different herd immunity levels.
Results
Primary HPV screening with cytology triage was the optimal strategy, with 8 lifetime screens for the pre-vaccination population and 3 for vaccinated women. The ICER of screening unvaccinated women 8 times instead of 3 was €28,085 in the absence of herd immunity. At around 50% herd immunity, the ICER reached €50,000.
Conclusion
From a herd immunity level of 50% onwards, screening intensity based on the pre-vaccination risk level becomes cost-ineffective for unvaccinated women. Reducing the screening intensity of uniform screening may then be considered.

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Science – 29 January 2016

Science
29 January 2016 Vol 351, Issue 6272
http://www.sciencemag.org/current.dtl

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EDITORIAL
Global science engagement
Geraldine Richmond
Summary
In rural Laos, more than 50% of newborns will be stunted by age 2 due to chronic malnourishment. Worldwide, 161 million children under the age of 5, many of them in Africa and Asia, suffered irreversible stunting as of 2013. The developed world is not immune. As recently as 2010, stunting affected 8 to 9% of babies enrolled in U.S. federal food-subsidy programs. Next week in Washington, DC, the American Association for the Advancement of Science (AAAS is the publisher of Science) will convene its annual meeting (11 to 15 February), where world leaders will discuss food security and other major challenges that lie ahead in both the science and international policy arenas.

WHO Director-General addresses the Executive Board

WHO Director-General addresses the Executive Board
Report by the Director-General to the Executive Board at its 138th Session
Geneva, Switzerland
25 January 2016
Madam Chair, distinguished members of the Executive Board, Excellencies, colleagues in the UN system, ladies and gentlemen,
Fifteen months ago, Guinea, Liberia, and Sierra Leone were together reporting more than 950 cases of Ebola every week. Today, the three countries have interrupted all chains of transmission from the original outbreak that began more than two years ago.
This is a monumental achievement that needs to be acknowledged. Please join me in honouring the leadership of the three governments, the heroic sacrifices of health care workers and communities, and the unwavering support from a host of partners.
However, WHO has not yet declared the outbreak in West Africa over. As we now know, the virus can hide in the bodies of fully recovered survivors for as long as a year.
Since March of last year, WHO has documented 11 small flare-ups of infection following reintroduction of the virus from survivors. All were rapidly detected and quickly contained.
On 14 January, WHO declared that the outbreak in Liberia, the last country reporting cases, was over, but warned that the risk of further flare-ups would persist. The warning was well-founded. The next day, Sierra Leone confirmed its first new case since September of last year.

Let me put this setback in perspective.
First, these countries promptly report new cases. Vigilance is intense. Our view of the situation is sharp and transparent.
Second, these countries have the world’s largest pool of expertise in responding to Ebola. They know exactly what to do.
Third, I still have more than 1000 staff in West Africa to assist in detecting and responding to flare-ups like this one. I thank them for their skill and dedication.
Finally, thanks to a WHO-led clinical trial, we have a vaccine that can be used to confer a back-up ring of protection.
The Ebola virus is stubborn. I have no doubt that further flare-ups will occur. I have no doubt that all will be quickly contained.
The outbreak lingers in a second sense as well. Well over 10,000 survivors face persistent health problems together with continuing stigmatization. They need care.
Ebola delivered an extremely severe and shattering blow to societies and economies. Recovery will take some time.
While the job is by no means finished, no one anticipates that the situation will return to what we were seeing 15 months ago.
The determination is fierce. International solidarity has been extraordinary. The many steps taken at national and international levels have had a decisive impact.
No one will let this virus take off and run away again….

In the wake of Ebola, health officials are more alert to alarming signals coming from the microbial world.
Last year’s MERS outbreak in the Republic of Korea showed the devastation a new disease can cause, even in a country with an advanced health system.
The explosive spread of Zika virus to new geographical areas, with little population immunity, is another cause for concern, especially given the possible link between infection during pregnancy and babies born with small heads.
Although a causal link between Zika infection in pregnancy and microcephaly has not been established, the circumstantial evidence is suggestive and extremely worrisome. An increased occurrence of neurological syndromes, noted in some countries coincident with arrival of the virus, adds to the concern.
I thank all newly affected countries for detecting the virus quickly, and promptly and transparently notifying WHO in line with the International Health Regulations.
I have asked Dr Carissa Etienne to brief the Board later this week on the current Zika situation and our response.

Yet another alarming signal was China’s detection last year, in animal and human samples, of a mechanism of drug resistance, involving the mcr-1 gene, that is easily transferred from one bacterial strain to others, including some with epidemic potential.
That finding, which raised the spectre of bacteria that are resistant to nearly all antibiotics, has since been replicated in several other countries.

Ladies and gentlemen,
In my address to last year’s Health Assembly, I announced my intention to create a new programme for responding to outbreaks and humanitarian emergencies.
I expressed my desire to design the programme for effectiveness, speed, flexibility, and rapid impact, with administrative procedures and business processes fit to support its operational platform.
In July, I appointed a group of very senior experts to advise me on the programme’s functions, structure, administration, and lines of managerial accountability. The advisory group provided this guidance with great diligence, and in great detail. The group was frank, critical, and thorough.
The experts looked at all independent assessments of the Ebola response issued to date and analysed the experiences of some effective emergency operations, like those run by the World Food Programme and UNICEF.
The group held eight meetings, beginning in July, and delivered its final report to me last week.
The experts in the advisory group called for profound transformational changes in the way we respond to outbreaks and emergencies.
This is what was needed. This is what I wanted. This is what is widely regarded as the right direction to take.
Let me reassure you, our Member States that the Regional Directors and I are determined to change the way we respond to outbreaks and emergencies. The lessons from Ebola must be applied.
We are committed to implementing a single programme, with a single line of accountability, a single budget, a single set of business processes, a single cadre of staff, and a single set of performance benchmarks that cut across all three levels of WHO.
These changes will make WHO much stronger, at all levels, in supporting countries and building national and global capacity to prevent, detect, and respond to emergencies with health consequences.
The new programme for health emergency management will have an operational arm, complementing WHO’s established functions in setting norms and standards.

As with outbreaks, the complexity of humanitarian emergencies underscores the need for transformational changes in our response capacity.
Ongoing armed conflicts and protracted crises have left an unprecedented 77 million people in urgent need of essential health care. Some 60 million of these people have been uprooted from their homes, the largest number since the Second World War.
Their health expectations are not high. They just want to survive.
I join others in deploring the attacks on health care workers and facilities that are becoming almost routine in the Middle East, including the recent bombing of a polio vaccination centre in Pakistan.
I join others, including the UN Secretary-General, in deploring the use of siege tactics as a method of warfare. Such tactics target civilians and violate international humanitarian law.
Has the world lost its moral compass? Even wars have laws. Forcing civilians to starve to death breaks those laws.
On the positive side, the world showed its solidarity before a shared threat last December in Paris, when 195 countries adopted a climate treaty. But more needs to be done to address the root causes of other crises that profoundly threaten health.
It is easier to deliver humanitarian assistance than to work out political solutions to the root causes of protracted conflict, violent extremism, terrorism, and the forced displacement of millions.
The world has rallied in support, delivering unprecedented levels of humanitarian assistance. But the costs of doing so are unsustainable.

Ebola taught the world that an outbreak in any part of the world can have global repercussions. The refugee crisis in Europe taught the world that wars in faraway places will not stay remote.
In a profoundly interconnected world, there is no such thing as a local outbreak. There is no such thing as a faraway war. As some assessments of the Ebola response have concluded, having strong public health infrastructures and capabilities in place in vulnerable countries is the first line of defence against the infectious disease threat.

Universal health coverage, based on the principles of primary health care, is an instrument for improving the resilience of health systems and the resilience of communities. It tackles the root causes of conditions that let outbreaks hide undetected for months and run out of control.
Universal health coverage is also the most efficient way to respond to the rise of noncommunicable diseases. It is a pillar of sustainable development that supports multiple goals and targets in the 2030 development agenda.
Development that is inclusive and sustainable is by far the best way to build resilience to the shocks our world keeps delivering with ever-greater force.

Ladies and gentlemen,
The Sustainable Development Goals, the SDGs, respect the way that all dimensions of life on this planet shape human health. The agenda is unprecedented in its scope and breath-taking in its ambition.
Health is the focus of goal three, but multiple other goals and targets address the social, economic, and environmental determinants of health.
The thirteen targets under the health goal continue the unfinished business of the Millennium Development Goals and respond to some additional health threats, namely NCDs and mental health, substance abuse, road traffic crashes, and hazardous environmental chemicals.
The inclusion of universal health coverage is the target that underpins all others and is key to their achievement. Health benefits greatly from the agenda’s broad and integrated approach, especially when it comes to the target set for NCDs.
The SDGs easily accommodate recent global strategies and plans of action approved by our Member States. In fact, all 13 health targets are reflected in your agenda for this EB session.
However, the new agenda has profound implications for the way WHO operates, not supplying health services but delivering what countries and their people need and expect.
The SDGs call for stronger country offices, a firm emphasis on innovation, and greater collaboration with partners and multiple sectors of government.
Our programmes that contributed so much to the MDGs for reducing maternal and child mortality, and turning around the epidemics of HIV, tuberculosis, malaria, and the neglected tropical diseases are mature.
They are well-placed to support even more ambitious targets, aligned with the SDG principles of integrated and inclusive approaches that deliver country-level results.
The culture of measurement and accountability, introduced during the MDG era, will continue. Determination to address the health needs of women and adolescents is strong.
Initiatives for the eradication of polio and guinea worm disease have moved forward greatly over the past year. These efforts must continue.

Ladies and gentlemen,
The future is clouded by some major threats to health that encircle the globe. They define some top priorities for urgent and collaborative action in the months ahead.
The volatile microbial world is an ever-present threat. As underscored during last year’s Health Assembly, too many countries lack the core capacities needed to implement the International Health Regulations.
This must change. These countries must be supported to build IHR core capacities to prevent, detect, and respond to outbreaks.
The Global Policy Group has endorsed the Joint External Evaluation tool for the assessment of gaps so that technical support to the countries, from WHO and partners, can be provided.
Noncommunicable diseases are a growing threat with major risk factors that can be modified.

Later today, the Commission on Ending Childhood Obesity will present its final report to me.
The report uses the latest cutting-edge science to deliver a series of policy recommendations with teeth. Implementing the recommendations will take political will, and courage, as some go against the interests of powerful economic operators.
Antimicrobial resistance is a danger of the utmost urgency. This year will be a pivotal one, culminating in a UN high level meeting on AMR later this year. We have a global action plan. What we need now is the action.
A top priority is to fully engage ministers responsible for agriculture and food. We will explore ways to do so during next month’s European Union ministerial conference on antimicrobial resistance in Amsterdam.
Climate change is another defining issue for health. While the Paris climate accord is a most welcome step forward, it will not prevent a number of immediate and severe health consequences.
We need to sharpen our programmes for dealing with these consequences, like outbreaks of cholera and dengue, the disruptions in food security that follow droughts and floods, the ill health linked to indoor and outdoor pollution, and the need for emergency assistance following extreme weather events.
The priority dearest to my heart is, of course, universal health coverage. Packed into that commitment are a host of issues that are important for you and all Member States: like access to safe and effective medicines, an adequate health workforce, finding ways to make health products more affordable, and the challenge of caring for ageing populations, especially people with dementia.
By stressing people instead of diseases, universal health coverage provides a much needed, compassionate, and more responsive platform for delivering coherent and integrated health services. By honouring the human right to health, and providing protection against financial ruin, it helps alleviate the root cause of significant human misery.
It embodies that commitment to fairness that I believe is at the heart of what WHO does best.
We must always remember the people. People seeing their families and communities devastated by an outbreak. Children trapped in obesogenic environments.
People with a common infection whose doctors say, “Sorry, there is nothing I can do.” People forced to leave their homes by war or weather.
People driven into poverty by the costs of a disease like cancer or a car crash.
These are the people, and their needs, that must drive our commitment.
Thank you.