Knowledge Systems for Sustainable Development

PNAS – Proceedings of the National Academy of Sciences of the United States
of America

(Accessed 22 January 2012)
http://www.pnas.org/content/early/recent

Knowledge Systems for Sustainable Development Special Feature Sackler Colloquium – Social Sciences – Sustainability Science
Lorrae van Kerkhoff and Nicole A. Szlezák

Abstract http://www.pnas.org/content/early/2012/01/13/0900541107.abstract
It is becoming increasingly recognized that our collective ability to tackle complex problems will require the development of new, adaptive, and innovative institutional arrangements that can deal with rapidly changing knowledge and have effective learning capabilities. In this paper, we applied a knowledge-systems perspective to examine how institutional innovations can affect the generation, sharing, and application of scientific and technical knowledge. We report on a case study that examined the effects that one large innovative organization, The Global Fund to Fight AIDS, Tuberculosis, and Malaria, is having on the knowledge dimensions of decision-making in global health. The case study shows that the organization created demand for new knowledge from a range of actors, but it did not incorporate strategies for meeting this demand into their own rules, incentives, or procedures. This made it difficult for some applicants to meet the organization’s dual aims of scientific soundness and national ownership of projects. It also highlighted that scientific knowledge needed to be integrated with managerial and situational knowledge for success. More generally, the study illustrates that institutional change targeting implementation can also significantly affect the dynamics of knowledge creation (learning), access, distribution, and use. Recognizing how action-oriented institutions can affect these dynamics across their knowledge system can help institutional designers build more efficient and effective institutions for sustainable development.

Particle-based adjuvants for subunit vaccines

Proceedings of the National Academy of Sciences of the United States
of America

(Accessed 22 January 2012)
http://www.pnas.org/content/early/recent

Commentary: Reorienting our view of particle-based adjuvants for subunit vaccines
Steven R. Little
PNAS 2012 ; published ahead of print January 17, 2012, doi:10.1073/pnas.1120993109

[No abstract] http://www.pnas.org/content/early/2012/01/09/1120993109.full.pdf+html

Evidence-based medical guidelines: LMIC countries

Tropical Medicine & International Health
February 2012  Volume 17, Issue 2  Pages 143–261
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-3156/currentissue

Medical Guidelines
Transfer of evidence-based medical guidelines to low- and middle-income countries (pages 144–146)
Stephan Ehrhardt and Christian G. Meyer
Article first published online: 21 OCT 2011 | DOI: 10.1111/j.1365-3156.2011.02910.x

[No abstract; Free full text]

Infectious diseases among refugees and immigrants compared to native Danes

Tropical Medicine & International Health
February 2012  Volume 17, Issue 2  Pages 143–261
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-3156/currentissue

Migrant Health
Mortality from infectious diseases among refugees and immigrants compared to native Danes: a historical prospective cohort study (pages 223–230)
M. Norredam, M. Olsbjerg, J. H. Petersen, I. Bygbjerg and A. Krasnik
Article first published online: 27 OCT 2011 | DOI: 10.1111/j.1365-3156.2011.02901.x

Summary
Objectives Refugees and immigrants are likely to be vulnerable to mortality from infectious diseases as a result of high prevalences in their countries of origin and barriers in access to healthcare in the recipient countries. Consequently, we aimed to compare and investigate differences in mortality from infectious diseases among refugees and immigrants and native Danes.

Methods A register-based, historical prospective cohort design. All refugees (n = 29 139) and family-reunited immigrants (n = 27 134) who, between 1 January1993 and 31 December1999, were granted the right to reside in Denmark were included and matched 1:4 on age and sex with native Danes. Civil registration numbers were cross-linked to the Register of Causes of Death, and fatalities owing to infectious diseases (based on ICD-10 diagnosis) were identified. Mortality ratios were estimated separately for men and women by migrant status and region of birth; adjusting for age and income; using a Cox regression model, after a mean follow-up of 10–12 years after arrival.

Results Female [hazard ratio (HR) = 4.15; 95% CI: 2.38, 7.25] and male (HR = 2.05; 95% CI: 1.27, 3.33) refugees experienced significantly higher mortality risks from infectious diseases than did native Danes, as was the case for male immigrants (HR = 2.39; 95% CI: 1.20, 4.76) but less so for female immigrants (HR = 1.23; 95% CI: 0. 50-3.01). Mortality by region of origin was notably higher for individuals from North Africa and sub-Saharan Africa.

Conclusions Higher mortality among refugees and immigrants than among the native population should lead to reflections on medical reception systems in recipient countries and subsequent possibilities of access to specialised diagnostic and curative healthcare.

Modeling Effects of H1N1 Vaccine Distribution in the U.S.

Value in Health
January 2012, Vol. 15, No. 1
http://www.valueinhealthjournal.com/home

CLINICAL OUTCOMES ASSESSMENT
Modeling the Effects of H1N1 Influenza Vaccine Distribution in the U.S.

Richard C. Larson, Anna Teytelman

Abstract
Objective
We analyzed the effects of the timing of vaccine distribution in 11 US states during the 2009 H1N1 influenza pandemic.

Methods
By using reported data on the fraction of patients presenting with flu-related symptoms, we developed a transformation that allowed estimation of the state-specific temporal flu wave curve, representing the number of new infections during each week. We also utilized data describing the weekly numbers of vaccine doses delivered and administered. By using a simple difference equations model of flu progression, we developed two influenza wave curves: first, an “observable” curve that included the beneficial effects of vaccinations, and second, an unobservable curve that depicted how the flu would have progressed with no vaccine administered. We fit the observable curve to match the estimated epidemic curve and early exponential growth associated with R0, the reproductive number. By comparing the number of infections in each scenario, we estimated the infections averted by the administration of vaccine.

Results
Southern states experienced peak infection several weeks before northern states, and most of the vaccine was delivered well after the peak of the southern flu wave. Our models suggest that the vaccine had minimal ameliorative impact in the southern states and measurable positive impact in the northern states. Vaccine delivery after peak also results in a smaller fraction of the population’s seeking the vaccine.

Conclusions
Our analysis suggests that current Centers for Disease Control and Prevention policy of allocating flu vaccine over time in direct proportion to states’ populations may not be best in terms of averting nationally the maximum possible number of infections.

India records full year without new polio cases

   India recorded a full year without new polio cases. A WHO report noted that India “appears to have interrupted wild poliovirus transmission, completing one year without polio since its last case, in a 2-year-old girl in the state of West Bengal, on 13 January 2011.” WHO noted that India was once recognized as the world’s epicentre of polio. If all pending laboratory investigations return negative, in the coming weeks India will officially be deemed to have stopped indigenous transmission of wild poliovirus. The number of polio-endemic countries, those which have never stopped indigenous wild poliovirus transmission, will then be reduced to a historical low of three: Afghanistan, Nigeria and Pakistan.

The WHO announcement noted that “global health leaders paid tribute to the Government of India for its leadership and financial commitment to the polio eradication effort, and to the millions of vaccinators, community mobilizers, Rotarians, parents and caregivers who have supported polio eradication for more than a decade. The scale of the eradication effort in India is mind-boggling: each year, more than 170 million children under the age of 5 are vaccinated in two national immunization campaigns, with up to 70 million children in the highest-risk areas vaccinated multiple times in additional special campaigns; the whole effort requires nearly a billion doses of oral polio vaccine annually.”

WHO Director-General Margaret Chan said, “India’s success is arguably its greatest public health achievement and has provided a global opportunity to push for the end of polio. The Global Polio Eradication Initiative is in full emergency mode and focused on using this momentum to close this crippling disease down. Stopping polio in India required creativity, perseverance and professionalism – many of the innovations in polio eradication were sparked by the challenges in India. The lessons from India must now be adapted and implemented through emergency actions to finish polio everywhere.”

India is described as one of the largest donors to polio eradication, largely self-financing its immunization efforts. By 2013, India will have contributed US$2 billion for its polio campaigns.

http://www.who.int/mediacentre/news/releases/2012/polio_20120113/en/index.html

Global Network for Neglected Tropical Diseases launches END7 Campaign

    The Global Network for Neglected Tropical Diseases, an initiative of the Sabin Vaccine Institute, launched the END7 Campaign, “dedicated to eliminating seven major neglected tropical diseases (NTDs) as a public health threat to poor communities by the end of 2020.” The campaign noted that NTDs infect one in six people worldwide, including 500 million children, carry a higher health burden than malaria and tuberculosis, and that treatment for NTDs is one of the most cost-effective health programs available today. Pills to treat the seven leading NTDs are donated by pharmaceutical companies and many programs use existing infrastructure, such as schools and community centers, to administer the treatments. The END7 campaign “raises the public awareness and funding required to cover the costs of distributing medicine and setting up treatment programs in impoverished communities.” The annual cost works out to approximately 50 cents to treat and protect one person for a whole year against all seven diseases. The announcement said that the UK and U.S. governments, as well as major pharmaceutical companies, have already made significant contributions. END7 works with global partners such as the World Health Organization and the Bill & Melinda Gates Foundation. The campaign will be managed through a Facebook hub “to promote campaign videos, photographs, success stories and other content —including a real-time donation ticker.”  http://www.prnewswire.com/news-releases/major-campaign-launched-to-eliminate-seven-diseases-by-2020-136999458.html

SAGE publishes November 2011 meeting report

WHO’s Strategic Advisory Group of Experts (SAGE) on immunization published the report of its November 2011 meeting. The announcement noted that SAGE “recommended…that to eradicate polio there must be accountability and consequences at all levels for individuals, institutions and governments who fail to deliver on their mandates. SAGE stated unequivocally that the risk of failure to finish global polio eradication constitutes a programmatic emergency of global proportions for public health and is not acceptable under any circumstances. Moreover, the country reports produced by the Global Polio Eradication Initiative Independent Monitoring Board must identify the root causes why some infected countries are failing to interrupt transmission and hold appropriate individuals, agencies and authorities responsible. Failure, SAGE warned, would lead to a resurgence of the disease and would be seen as the most expensive public health failure in history.

“SAGE welcomed the Decade of Vaccines collaboration as a new initiative to create a global coalition to fully realize the potential of immunization in saving lives. SAGE reviewed the draft Decade of Vaccines global action plan and although the expert group supported the overall direction, it was agreed that the plan needed to be more exciting and innovative, extending the benefits of immunization beyond childhood. SAGE requested the planning teams to identify a few major “game-changers” which if implemented would have a significant impact.

“Other topics were also discussed during the meeting such as: the negotiations around the legally binding instrument on mercury and thiomersal containing vaccines; monitoring national immunization coverage and reinforcing surveillance; optimizing immunization schedules for conjugate pneumococcal vaccines; use of hepatitis A vaccines; and progress of tuberculosis vaccine candidate trials.”

Full report of the SAGE November 2011 meetingpdf, 869kb

Background documents and presentations

Agenda, list of participants and declarations of interests

http://www.who.int/immunization/newsroom/newsstory_sage_nov_2011_report/en/index.html

DoVC opens online consultation on draft Global Vaccine Action Plan (GVAP)

 The Decade of Vaccines Collaboration (DoVC) initiated an online consultation capability seeking feedback on the draft Global Vaccine Action Plan (GVAP) via its website. The consultation, which complements ongoing meetings with a range of civil society organizations, governments and other stakeholders, runs 16 January – 1 February 2012. Participants are invited to register for the consultation at http://www.dovcollaboration.org/consultation/?login which leads to a password-protected area of the website where the GVAP draft is made available and an online survey is provided. The survey is focused to four questions about the GVAP draft:

– Do you feel the Global Vaccine Action Plan accurately reflects what is needed over the next decade? If not, can you provide suggestions to improve the document?

– What are the top five most transformational changes you could see in the next 10 years that would truly be “game changing?” Are they captured in the document?

– Do you feel that your stakeholder group is sufficiently and appropriately represented in the document? If not, can you provide suggestions to improve the document?

– Do you have any other comments or suggestions?

The GVAP draft will continue to evolve and will be submitted in March 2012 for World Health Assembly action when WHA meets in May, 2012.

PhRMA Report: 282 medicines in development for children and adolescents

The Pharmaceutical Research and Manufacturers of America (PhRMA), in a new report, said that America’s biopharmaceutical companies are researching 282 medicines currently in clinical trials or under review by the FDA “to help meet the unique health care needs of children and adolescents.” The reviews these medicines noting:

– 54 for cancer which, despite significant progress, is still the leading cause of death by disease among American children,

– 49 for infectious diseases, resulting in more than 164 million missed school days annually in American public schools due to the spread of infectious diseases,

– 48 for genetic disorders, including medicines for cystic fibrosis, which affects 30,000 American children and adults,

– 25 for neurologic disorders, including medicines for epilepsy, which affects more than 300,000 school children under age 14 in the United States.

The report is available here: http://bit.ly/xRAVhd

http://www.phrma.org/media/releases/nearly-300-medicines-development-meet-unique-needs-children

Twitter Watch to 15 January 2012

Twitter Watch 
Items of interest from a variety of twitter feeds associated with immunization, vaccines and global public health. This capture is highly selective and is by no means intended to be exhaustive.

GAVIAlliance GAVI Alliance
Learn more about #GAVI ‘s pneumococcal AMC! Step by step guide to the method behind the AMC mechanism- ht.ly/8u1St #globalhealth
2 hours ago

UNDP UN Development
Be involved: @WorldBank asks for input on Global Partnership For Enhanced Social Accountability on.undp.org/wcH7h5
3 hours ago

MSF_USA Doctors w/o Borders
Two years after the EQ, the health care system in Port-au-Prince and surrounding areas is still in disarray. bit.ly/xeDXMZ #Haiti
5 hours ago

GAVIAlliance GAVI Alliance
Rigorous monitoring and the bivalent oral #polio vaccine are main factors in India’s 1 year Polio-free success -http://ht.ly/8tsS5 @Rotary
14 Jan

historyvaccines History of Vaccines
Dr. Hotez gives Hilleman Lecture at CHOP: Innovations in neglected tropical diseases bit.ly/wgsVPj #vaccine #NTD
12 Jan

globalfundnews The Global Fund
We’re reading: ‘French Government Defends Global AIDS Fund’ bit.ly/zTUb8B
13 Jan

WHO WHO
Congratulations to #India for 12 months without #polio – a remarkable milestone bit.ly/wV2c06
12 Jan

GAVIAlliance GAVI Alliance
Good news in the fight against measles! China’s #measles incidence hits record low in 2011- ht.ly/8q7sr #globalhealth
11 Jan

NIAIDNews NIAID News
Healthy volunteers needed for NIAID #clinicaltrials testing #vaccines to prevent #malaria, #HIV and more go.usa.gov/RXz
11 Jan

sabinvaccine Sabin Vaccine Inst.
Water and sanitation is a human right- Dr Roses @pahowho #StopCholera
11 Jan

Evaluation: Functioning of the International Health Regulations (IHR)

Globalization and Health
[Accessed 15 January 2012]
http://www.globalizationandhealth.com/

Research
Descriptive Review and Evaluation of the Functioning of the International Health Regulations (IHR) Annex 2
Anema A, Druyts E, Hollmeyer HG, Hardiman MC and Wilson K Globalization and Health 2012, 8:1 (10 January 2012)
Open Access

Abstract (provisional)
Background
The International Health Regulations (IHRs) (2005) was developed with the aim of governing international responses to public health risks and emergencies. The document requires all 194 World Health Organization (WHO) Member States to detect, assess, notify and report any potential public health emergency of international concern (PHEIC) under specific timelines. Annex 2 of the IHR outlines decision-making criteria for State-appointed National Focal Points (NFP) to report potential PHEICs to the WHO, and is a critical component to the effective functioning of the IHRs.

Methods
The aim of the study was to review and evaluate the functioning of Annex 2 across WHO-reporting States Parties. Specific objectives were to ascertain NFP awareness and knowledge of Annex 2, practical use of the tool, activities taken to implement it, its perceived usefulness and user-friendliness. Qualitative telephone interviews, followed by a quantitative online survey, were administered to NFPs between October, 2009 and February, 2010.

Results
A total of 29 and 133 NFPs participated in the qualitative and quantitative studies, respectively. Qualitative interviews found most NFPs had a strong working knowledge of Annex 2; perceived the tool to be relevant and useful for guiding decisions; and had institutionalized management, legislation and communication systems to support it. NFPs also perceived Annex 2 as human and disease-centric, and emphasized its reduced applicability to potential PHEICs involving bioterrorist attacks, infectious diseases among animals, radio-nuclear and chemical spills, and water- or food-borne contamination. Among quantitative survey respondents, 88% reported having excellent/good knowledge of Annex 2; 77% reported always/usually using Annex 2 for assessing potential PHEICs; 76% indicated their country had some legal, regulatory or administrative provisions for using Annex 2; 95% indicated Annex 2 was always/usually useful for facilitating decisions regarding notifiability of potential PHEICs.

Conclusion
This evaluation, including a large sample of WHO-reporting States Parties, found that the IHR’s Annex 2 is perceived as useful for guiding decisions about notifiability of potential PHEICs. There is scope for the WHO to expand training and guidance on application of the IHR’s Annex 2 to specific contexts. Continued monitoring and evaluation of the functioning of the IHR is imperative to promoting global health security.

Confronting The Urgent Challenge Of Diabetes

Health Affairs
January 2012; Volume 31, Issue 1
http://content.healthaffairs.org/content/current

Issue Theme: Confronting The Growing Diabetes Crisis [23 articles covering a range of issue relevant to this theme]
Overview Of The Crisis
Confronting The Urgent Challenge Of Diabetes: An Overview
Judith E. Fradkin
Health Aff January 2012 31:12-19; doi:10.1377/hlthaff.2011.1150

Abstract
The rising tide of diabetes has an unacceptable human and societal toll. Rates of all major forms of diabetes are increasing at enormous individual and societal cost: 8.3 percent of the US population is afflicted today, and financial costs reached $174 billion for 2007. A major cause of blindness, renal failure, amputation, and cardiovascular disease, diabetes also increases the risk of cancer and dementia and more than doubles individual health care costs. Control of glucose, blood pressure, and lipids improves outcomes. Yet diabetes management is nonetheless suboptimal, particularly in disproportionately affected poor and minority populations. Safer, less burdensome, and more personalized approaches to therapy are needed. People at high risk for type 2 diabetes must be identified if society is to realize the benefits of therapies proven to delay or prevent the disease. We have many of the tools we need to address this challenge, and we must apply them now.

Use Of 13 Disease Registries In 5 Countries and Health Care Value

Health Affairs
January 2012; Volume 31, Issue 1
http://content.healthaffairs.org/content/current

Web first
Use Of 13 Disease Registries In 5 Countries Demonstrates The Potential To Use Outcome Data To Improve Health Care’s Value
Stefan Larsson, Peter Lawyer, Göran Garellick, Bertil Lindahl, and Mats Lundström
Health Aff January 2012 31:220-227; published ahead of print December 7, 2011, doi:10.1377/hlthaff.2011.0762

Abstract
As health care systems worldwide struggle with rising costs, a consensus is emerging to refocus reform efforts on value, as determined by the evaluation of patient outcomes relative to costs. One method of using outcome data to improve health care value is the disease registry. An international study of thirteen registries in five countries (Australia, Denmark, Sweden, the United Kingdom, and the United States) suggests that by making outcome data transparent to both practitioners and the public, well-managed registries enable medical professionals to engage in continuous learning and to identify and share best clinical practices. The apparent result: improved health outcomes, often at lower cost. For example, we calculate that if the United States had a registry for hip replacement surgery comparable to one in Sweden that enabled reductions in the rates at which these surgeries are performed a second time to replace or repair hip prostheses, the United States would avoid $2 billion of an expected $24 billion in total costs for these surgeries in 2015.

Global Financial Crisis and Health Funding In Developing Countries

Health Affairs
January 2012; Volume 31, Issue 1
http://content.healthaffairs.org/content/current

Web first
The Global Financial Crisis Has Led To A Slowdown In Growth Of Funding To Improve Health In Many Developing Countries
Katherine Leach-Kemon, David P. Chou, Matthew T. Schneider, Annette Tardif, Joseph L. Dieleman, Benjamin P.C. Brooks, Michael Hanlon, and Christopher J.L. Murray
Health Aff January 2012 31:228-235; published ahead of print December 14, 2011, doi:10.1377/hlthaff.2011.1154

Abstract
How has funding to developing countries for health improvement changed in the wake of the global financial crisis? The question is vital for policy making, planning, and advocacy purposes in donor and recipient countries alike. We measured the total amount of financial and in-kind assistance that flowed from both public and private channels to improve health in developing countries during the period 1990–2011. The data for the years 1990–2009 reflect disbursements, while the numbers for 2010 and 2011 are preliminary estimates. Development assistance for health continued to grow in 2011, but the rate of growth was low. We estimate that assistance for health grew by 4 percent each year from 2009 to 2011, reaching a total of $27.73 billion. This growth was largely driven by the World Bank’s International Bank for Reconstruction and Development and appeared to be a deliberate strategy in response to the global economic crisis. Assistance for health from bilateral agencies grew by only 4 percent, or $444.08 million, largely because the United States slowed its development assistance for health. Health funding through UN agencies stagnated, and the Global Fund to Fight AIDS, Tuberculosis, and Malaria announced that it would make no new grants for the next two years because of declines in funding. Given the international community’s focus on meeting the Millennium Development Goals by 2015 and persistent economic hardship in donor countries, continued measurement of development assistance for health is essential for policy making.

Influenza-Associated Pneumococcal Pneumonia (H1N1)

Journal of Infectious Diseases
Volume 205 Issue 3 February 1, 2012
http://www.journals.uchicago.edu/toc/jid/current

Editorial Commentaries
Carlos G. Grijalva and Marie R. Griffin
Unveiling the Burden of Influenza-Associated Pneumococcal Pneumonia
J Infect Dis. (2012) 205(3): 355-357 doi:10.1093/infdis/jir753

Extract
In the United States alone, seasonal (interpandemic) influenza is responsible for an average of 226 000 hospitalizations and >23 000 deaths per year [1, 2]. Although all age groups are susceptible to influenza virus infections, children experience the highest disease incidence, whereas older adults suffer the most serious disease-related complications and mortality. Many of these events are secondary bacterial pneumonias, most of which are thought to be caused by Streptococcus pneumoniae (the pneumococcus). Although several observations have suggested that influenza plays an important role in the pneumococcal pneumonia incidence, its contribution has been difficult to appreciate. In this issue of the Journal, Weinberger and colleagues present an elegant assessment that helps to clarify the contribution of influenza virus infections to pneumococcal pneumonia hospitalizations during the 2009 influenza pandemic [3].

Several lines of evidence indirectly support an interaction between influenza virus and the pneumococcus: First, pneumococcal nasopharyngeal acquisition patterns mirror the seasonal patterns of influenza outbreaks [4]. Second, increases in pneumococcal pneumonias during previous influenza pandemics have been documented [5, 6]. Third, concurrent influenza infections and pneumococcal pneumonias have been described [7, 8], and prevention of these pneumonias has been demonstrated in an efficacy trial of a 9-valent pneumococcal conjugate vaccine in South African children. In that randomized study, vaccination with pneumococcal conjugate vaccine reduced the incidence of influenza-associated pneumonia (ie, pneumococcal pneumonia with concurrent influenza infection) by 45% compared with controls [9]. This decline, however, was seen only in human immunodeficiency virus–infected children, and significant reductions were also observed for concurrent infections with parainfluenza viruses and human metapneumovirus [9 …

VIRUSES
Daniel M. Weinberger, Lone Simonsen, Richard Jordan, Claudia Steiner, Mark Miller, and Cécile Viboud
Impact of the 2009 Influenza Pandemic on Pneumococcal Pneumonia Hospitalizations in the United States
J Infect Dis. (2012) 205(3): 458-465 doi:10.1093/infdis/jir749

Abstract
Background. Infection with influenza virus increases the risk for developing pneumococcal disease. The A/H1N1 influenza pandemic in autumn 2009 provided a unique opportunity to evaluate this relationship.

Methods. Using weekly age-, state-, and cause-specific hospitalizations from the US State Inpatient Databases of the Healthcare Cost and Utilization Project 2003–2009, we quantified the increase in pneumococcal pneumonia hospitalization rates above a seasonal baseline during the pandemic period.

Results. We found a significant increase in pneumococcal hospitalizations from late August to mid-December 2009, which corresponded to the timing of highest pandemic influenza activity. Individuals aged 5–19 years, who have a low baseline level of pneumococcal disease, experienced the largest relative increase in pneumococcal hospitalizations (ratio, 1.6 [95% confidence interval {CI}, 1.4–1.7]), whereas the largest absolute increase was observed among individuals aged 40–64 years. In contrast, there was no excess disease in the elderly. Geographical variation in the timing of excess pneumococcal hospitalizations matched geographical patterns for the fall pandemic influenza wave.

Conclusions. The 2009 influenza pandemic had a significant impact on the rate of pneumococcal pneumonia hospitalizations, with the magnitude  of this effect varying between age groups and states, mirroring observed variations in influenza activity.

Editorial: WHO and Margaret Chan – the next 5 years

The Lancet  
Jan 14, 2012  Volume 379  Number 9811 p93 – 192  e5 – 11
http://www.thelancet.com/journals/lancet/issue/current

Editorial
WHO and Margaret Chan: the next 5 years
The Lancet

WHO is in the process of appointing a Director-General whose tenure will run from June, 2012, to June, 2017. Margaret Chan, the current incumbent, is the only candidate standing. WHO’s Executive Board will consider her appointment when they meet later this month, and the World Health Assembly will ratify the Board’s decision in May. It is certain that Dr Chan will win a second term.

Her renewed appointment comes at a perilous moment for WHO. As a letter we publish online this week from Oxfam reveals, WHO is in crisis. Rescue is needed. But is this predicament a fair reflection of the Director-General’s performance? No, it is not.  When Dr Chan was elected she made a promise—namely, that she wanted her term to be judged by progress on health for Africa and for women. WHO’s leadership of Every Woman, Every Child, the UN Secretary-General’s Global Strategy on Women’s and Children’s Health, has been her great success these past 5 years. Add to that the remarkable achievement in September, 2011, of a political declaration on non-communicable diseases, together with her refashioning of a failing health systems agenda around universal coverage, and you have a record that is a surprising success for an agency in the vortex of a financial emergency.

One cannot judge Dr Chan’s legacy without recalling that her first priority 5 years ago was to deliver the initiatives begun by her predecessor, Dr Lee Jong-wook, who tragically died during his first term as Director-General. The most important project left unfinished was the Commission on Social Determinants of Health. Initially sceptical, Dr Chan not only saw this important report through to completion, but also became a significant champion of the social determinants agenda. Also recall that Dr Chan deftly led communications with the media and public during the 2009 influenza A H1N1 pandemic.

None of this is to say that there have not been disappointments. Her leadership team has not been a success. Only recently have the right people been selected for crucial portfolios. Several regional offices of WHO remain lacklustre backwaters. And sometimes one wishes for a sharper message, a stronger articulation of what WHO is for in the 21st century. These matters can be addressed during a second term. But that term will depend on proper financing of WHO by its donors. And here Dr Chan faces her greatest test of all.

Online First
Correspondence
Jan 13, 2012
Action to preserve WHO’s core functions cannot wait for organisational reform
Mohga M Kamal-Yanni

Preview
While WHO undergoes a wide-ranging reform sparked by a US$300 million budget shortfall, the agency is facing an exodus of qualified staff that is affecting its ability to work.1 The Executive Board is due to meet on Jan 16 to agree long-term principles and priorities for the organisation; it must ensure, in particular, that core functions are accorded the priority they merit. Oxfam is especially concerned that inadequate funding will severely diminish the WHO Essential Medicines Department, which for more than three decades has had an indispensable role in enabling developing countries to access affordable medicines.

Global movement for health equity: from Santiago to Rio and beyond

The Lancet  
Jan 14, 2012  Volume 379  Number 9811 p93 – 192  e5 – 11
http://www.thelancet.com/journals/lancet/issue/current

Health Policy
Building of the global movement for health equity: from Santiago to Rio and beyond
Michael Marmot, Jessica Allen, Ruth Bell, Peter Goldblatt

Summary
Health inequalities are present throughout the world, both within and between countries. The Commission on Social Determinants of Health drew attention to dramatic social gradients in health within most countries and made proposals for action. These inequalities are not inevitable. The purpose of this article is to report on activity that has taken place worldwide after the report by the Commission on Social Determinants of Health. First, we summarise the global situation. Second, we summarise an interim report of the emerging findings from an independent review of social determinants and the health divide, which was commissioned by the WHO European region. The world conference on social determinants of health will be held in Rio de Janeiro, Brazil, in October, 2011. This summit provides an opportunity to galvanise support, prioritise action, and respond to the call by the Commission on Social Determinants of Health for social justice as a route to a fair distribution of health.

Opinion: Controlling H5N1 mutation data

Nature  
Volume 481 Number 7380 pp113-230  12 January 2012
http://www.nature.com/nature/current_issue.html

World View
Don’t censor life-saving science
Controlling who is allowed access to information about mutations in the H5N1 bird flu virus is unacceptable, says Peter Palese.
11 January 2012

The recent arguments over the creation of a transmissible form of the bird flu virus (H5N1) feel very familiar. My colleagues and I were at the centre of a similar controversy in 2005, when we reconstructed the 1918 flu virus, which had killed up to 50 million people worldwide. News stories around the globe debated the merits of our research and television pundits argued opposing viewpoints. Naturally, the US government was concerned — as it is now. Yet our research was published in full. So why are similar concerns being used now to demand unacceptable censorship of the H5N1 scientific papers?

I have spent my career studying potentially dangerous pathogens — 20 years ago, my lab developed the technique that has enabled the H5N1 researchers to insert the mutations that render the virus more easily transmissible. In the 1990s, researchers discovered degraded samples of the 1918 virus in lung tissue from US soldiers who had died from the ‘Spanish flu’. Using polymerase chain reaction technology, they amplified and sequenced the virus’s RNA. We then took an existing influenza virus and, one by one, swapped its genes with those from the 1918 virus, eventually recreating a live version.

As we prepared our results for publication, the US government convened the National Science Advisory Board for Biosecurity (NSABB), which advises the community about research using agents that pose threats to national security or public health. Our experiments had made some people nervous.

During our discussions with members of the NSABB, we explained the importance of bringing such a deadly pathogen back to life. Although these experiments may seem dangerously foolhardy, they are actually the exact opposite. They gave us the opportunity to make the world safer, allowing us to learn what makes the virus dangerous and how it can be disabled. Thankfully, the discussions were largely constructive — within a week, the NSABB recommended that we continue to study the virus under biocontainment conditions, and publish the results so that other scientists could participate in the research. After we published our full paper in 2005 (T. M. Tumpey et al. Science 310, 77–80; 2005), researchers poured into the field who probably would not otherwise have done, leading to hundreds of papers about the 1918 virus. As a result, we now know that the virus is sensitive to the seasonal flu vaccine, as well as to the common flu drugs amantadine (Symmetrel) and oseltamivir (Tamiflu). Had we not reconstructed the virus and shared our results with the community, we would still be in fear that a nefarious scientist would recreate the Spanish flu and release it on an unprotected world. We now know such a worst-case scenario is no longer possible.

This experience has made the NSABB’s latest recommendation — that the H5N1 researchers not reveal the mutations behind the virus’s transmissibility — all the more frustrating. I make the same argument today that we made in 2005 — publishing those experiments without the details is akin to censorship, and counter to science, progress and public health. Why did the (different) members of the committee come to a different conclusion in this case? I can only hope that they take a more sensible stance and change their minds, or that the scientific community at large convinces them to do so. Certainly, the authors of the papers, as well as the journals considering them for publication (including this one), should resist the committee’s unworkable compromise that the full information should be released only to approved experts, and insist on full disclosure.

Giving the full details to vetted scientists is neither practical nor sufficient. Once 20–30 laboratories with postdoctoral fellows and students have such information available, it will be impossible to keep the details secret. Even more troublesome, however, is the question of who should decide which scientists are allowed to have the information. We need more people to study this potentially dangerous pathogen, but who will want to enter a field in which you can’t publish your most scientifically interesting results?

“Who will want to enter a field in which you can’t publish your most scientifically interesting results?”

Knowing which mutations render the virus more dangerous could help on a public-health level — if an outbreak of bird flu occurs in Taiwan, for instance, and researchers sequence the virus and see those mutations, we would know to ramp up the production of appropriate vaccines and antiviral drugs.

Incidentally, I believe that the risk of future outbreaks in humans is low: H5N1 has had the opportunity to cause widespread pandemics for many, many decades, yet it has not done so. Although we know the virus is transmissible between ferrets, little is known about how it will behave in other animals, including humans.

The more danger a pathogen poses, the more important it is to study it (under appropriate containment conditions), and to share the results with the scientific community. Slowing down the scientific enterprise will not ‘protect’ the public — it only makes us more vulnerable.

Vaccination Timing and the A(H1N1) Pandemic in Norway

PLoS One
[Accessed 15 January 2012]
http://www.plosone.org/article/browse.action;jsessionid=577FD8B9E1F322DAA533C413369CD6F3.ambra01?field=date

Effect of Vaccines and Antivirals during the Major 2009 A(H1N1) Pandemic Wave in Norway – And the Influence of Vaccination Timing
Birgitte Freiesleben de Blasio, Bjørn G. Iversen, Gianpaolo Scalia Tomba
PLoS ONE: Research Article, published 10 Jan 2012 10.1371/journal.pone.0030018

Abstract
To evaluate the impact of mass vaccination with adjuvanted vaccines (eventually 40% population coverage) and antivirals during the 2009 influenza pandemic in Norway, we fitted an age-structured SEIR model using data on vaccinations and sales of antivirals in 2009/10 in Norway to Norwegian ILI surveillance data from 5 October 2009 to 4 January 2010. We estimate a clinical attack rate of approximately 30% (28.7–29.8%), with highest disease rates among children 0–14 years (43–44%). Vaccination started in week 43 and came too late to have a strong influence on the pandemic in Norway. Our results indicate that the countermeasures prevented approximately 11–12% of potential cases relative to an unmitigated pandemic. Vaccination was found responsible for roughly 3 in 4 of the avoided infections. An estimated 50% reduction in the clinical attack rate would have resulted from vaccination alone, had the campaign started 6 weeks earlier. Had vaccination been prioritized for children first, the intervention should have commenced approximately 5 weeks earlier in order to achieve the same 50% reduction. In comparison, we estimate that a non-adjuvanted vaccination program should have started 8 weeks earlier to lower the clinical attack rate by 50%.

In conclusion, vaccination timing was a critical factor in relation to the spread of the 2009 A(H1N1) influenza. Our results also corroborate the central role of children for the transmission of A(H1N1) pandemic influenza.

Compulsory Licensing of Pharmaceuticals Since the Doha Declaration

PLoS Medicine
(Accessed 15 January 2012)
http://www.plosmedicine.org/article/browse.action?field=date

Trends in Compulsory Licensing of Pharmaceuticals Since the Doha Declaration: A Database Analysis
Reed Beall, Randall Kuhn
Research Article, published 10 Jan 2012
doi:10.1371/journal.pmed.1001154

Abstract 
Background
It is now a decade since the World Trade Organization (WTO) adopted the “Declaration on the TRIPS Agreement and Public Health” at its 4th Ministerial Conference in Doha. Many anticipated that these actions would lead nations to claim compulsory licenses (CLs) for pharmaceutical products with greater regularity. A CL is the use of a patented innovation that has been licensed by a state without the permission of the patent title holder. Skeptics doubted that many CLs would occur, given political pressure against CL activity and continued health system weakness in poor countries. The subsequent decade has seen little systematic assessment of the Doha Declaration’s impact.

Methods and Findings
We assembled a database of all episodes in which a CL was publically entertained or announced by a WTO member state since 1995. Broad searches of CL activity were conducted using media, academic, and legal databases, yielding 34 potential CL episodes in 26 countries. Country- and product-specific searches were used to verify government participation, resulting in a final database of 24 verified CLs in 17 nations. We coded CL episodes in terms of outcome, national income, and disease group over three distinct periods of CL activity. Most CL episodes occurred between 2003 and 2005, involved drugs for HIV/AIDS, and occurred in upper-middle-income countries (UMICs). Aside from HIV/AIDS, few CL episodes involved communicable disease, and none occurred in least-developed or low-income countries.

Conclusions
Given skepticism about the Doha Declaration’s likely impact, we note the relatively high occurrence of CLs, yet CL activity has diminished markedly since 2006. While UMICs have high CL activity and strong incentives to use CLs compared to other countries, we note considerable countervailing pressures against CL use even in UMICs. We conclude that there is a low probability of continued CL activity. We highlight the need for further systematic evaluation of global health governance actions.

Editors’ Summary 
Background
The development of a new drug is a time-consuming and expensive process. To stimulate investment in drug development, the creators of new drugs (including the pharmaceutical companies that undertake the development and testing that is needed before any drug can be used in patients) can apply for “intellectual property rights” (a patent). Intellectual property rights protect the investments made by companies during drug development by preventing other companies from making the new drug for a fixed period of time and by providing a means by which creators of new drugs can negotiate payment from other companies for the use of their creation. Until recently, the extent and enforcement of intellectual property rights varied widely around the world. Then, in 1995, the World Trade Organization (WTO) was established. By providing a set of ground rules for trade among nations, the WTO aims to ensure that trade flows as smoothly, predictably, and freely as possible around the world. One of the founding documents of the WTO is the Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS Agreement), which attempts to bring the protection of intellectual property rights (including patents) under common international rules.

Why Was This Study Done?
Unfortunately, patent protection for drugs (pharmaceuticals) means that many medicines are too expensive for use in developing countries. While maintaining incentives for drug development, the TRIPS Agreement allows governments to license the use of patented inventions to someone else without the consent of the patent owner. Such “compulsory licensing” normally occurs only after negotiations for a voluntary license have failed, and the patent owner still receives an appropriate payment. It soon became clear that some governments were unsure of their right to use compulsory licensing and other flexibilities in the TRIPS Agreement, a situation likely to affect public health in poor countries by hindering universal access to medicines. Consequently, the WTO issued the “Declaration on the TRIPS Agreement and Public Health” at its 4th Ministerial Conference in Doha in November 2001. Reaction to the Doha Declaration, which reaffirms that the “TRIPS Agreement does not and should not prevent members from taking measures to protect public health,” has been mixed. Some experts predicted that it would increase compulsory licensing of pharmaceuticals, but others suggested that political pressure against compulsory licensing and health system weaknesses in poor countries would limit claims for compulsory licenses. In this database analysis, the researchers systematically assess the impact of the Doha Declaration on the compulsory licensing of pharmaceuticals.

What Did the Researchers Do and Find?
By systematically searching media archives for reports of WTO member states considering or announcing compulsory licensing of pharmaceuticals, the researchers identified 24 verified compulsory licensing episodes in 17 nations that occurred between January 1995 and June 2011. Half of these episodes ended with an announcement of a compulsory license, and the majority ended in a price reduction for a specific pharmaceutical product for the potential issuing nation through a compulsory license, a voluntary license, or a negotiated discount. Sixteen of the compulsory licensing episodes involved drugs for HIV/AIDS, four involved drugs for other communicable diseases, and four involved drugs for non-communicable diseases such as cancer. More than half the compulsory licensing episodes occurred in upper-middle-income countries (including Brazil and Thailand). Finally, most compulsory licensing episodes occurred between 2003 and 2005. There was a smaller peak of activity in the months leading up to the Doha conference, but after 2006 activity declined substantially.

What Do These Findings Mean?
Given these findings, the researchers suggest that the Doha Declaration is unlikely to have an important long-term impact on the use of compulsory licensing or on access to pharmaceuticals for communicable diseases other than HIV/AIDS in developing and low-income countries. Most notably, the researchers found no evidence of a spike in compulsory licensing episodes immediately after the Doha Declaration, and they note that the lagged spike that occurred between 2003 and 2005 could have resulted in large part from the global antiretroviral advocacy campaign. Moreover, compulsory licensing activity has diminished greatly since 2006. Thus, the researchers conclude, health advocates who pushed for the Doha Declaration reforms have had little success in engaging trade as a positive, proactive force for addressing health gaps.

Dr. Christian Loucq inaugurated Director General at International Vaccine Institute (IVI)

    Dr. Christian Loucq was inaugurated as the new head of the International Vaccine Institute (IVI) based in Seoul, South Korea. Dr. Loucq will serve an initial four-year term to build upon the Institute’s successes achieved under the leadership of his predecessor Dr. John Clemens, IVI said.  Dr. Loucq commented, “I am humbled, honored, and very enthusiastic to be joining the IVI team as Director-General. Since its establishment in 1997, IVI has been a pioneering organization in many aspects of vaccinology – from R&D to epidemiology and from local manufacturing to access – aimed at preventing infectious diseases among the world’s poorest children. As the new Director-General, I will strive to increase IVI’s impact in the fight against infectious diseases in developing countries, based on its scientific contributions to the research, development and optimal use of new and improved vaccines.”

http://www.ivi.org/event_news/news_view.asp?enid=127

Nigeria Immunization Challenge update

The Gates Foundation said that Nigeria’s 36 Executive Governors and the Federal Capital Territory have signed up to the Nigeria Immunization Challenge launched by the foundation last year. Gates Foundation CEO Jeff Raikes said, “Renewed political resolve and accountability are critical to stopping polio in Nigeria and we find it encouraging to witness both through the support expressed by every Executive Governor across the country for this initiative. By collectively signing up to this challenge, they are sending a very clear message about their commitment to lead the fight to eliminate polio in Nigeria.” The Nigeria Immunization Challenge “sets specific objectives that need to be met during each quarter of 2012. If met, Nigeria will significantly improve its chances of stopping polio and protecting more children against vaccine-preventable diseases such as measles and whooping cough…The Nigerian states that meet all the necessary threshold criteria by the end of 2012 will be awarded a $500,000 grant from the Bill & Melinda Gates Foundation to support their top health priorities.” The foundation announcement noted that as of December 30, 2011, 51 cases of wild poliovirus had been reported in eight Nigerian states, compared with 21 cases in 2010. http://www.gatesfoundation.org/press-releases/Pages/immunization-leadership-challenge-120105.aspx

CHOP launches new HPV-related website

   The Children’s Hospital of Philadelphia Vaccine Education Center launched a new HPV-related websitewww.prevent-hpv.com. The site “features a video by Dr. Paul Offit as well videos of families discussing their decision to get the HPV vaccine. There are also links to additional information, questions and answers, and opportunities to share via social media.”

AMA Virtual Mentor (January, 2012): Vaccines and Ethics

   The AMA said it published a new issue of Virtual Mentor (January, 2012) focused on Vaccines and Ethics at (www.virtualmentor.org) which includes:

– A clinical case concerning HPV vaccine

– A consideration of how American society has handled its vaccine controversies, co-authored by Art Caplan

– Ethical implications of current research into a possible stress vaccine

– A contribution from researchers at the Jenner Institute, Oxford, about vaccine research ethics

– A look at residents’ role in adult immunizations on the “front lines” by Jay Jacobson, MD

MMWR Weekly for January 6, 2012

The MMWR Weekly for January 6, 2012 / Vol. 60 / Nos. 51 & 52 includes:
Severe Influenza Among Children and Young Adults with Neurologic and Neurodevelopmental Conditions — Ohio, 2011

Imported Human Rabies — New Jersey, 2011

Receipt of A(H1N1)pdm09 Vaccine by Prisons and Jails — United States, 2009–10 Influenza Season

Update: Influenza A (H3N2)v Transmission and Guidelines — Five States, 2011

Twitter Watch to 8 January 2012

Twitter Watch 
Items of interest from a variety of twitter feeds associated with immunization, vaccines and global public health. This capture is highly selective and is by no means intended to be exhaustive.

GAVIAlliance GAVI Alliance
MenAfriVac #vaccine could prevent 150,000 deaths by 2015 in Africa’s “meningitis belt”- ht.ly/8lQeS
11 hours ago

gatesfoundation Gates Foundation
Op-Ed: It’s part of our social responsibility to get our children vaccinated: gates.ly/wOuLs2 #vaccines
6 Jan

bmj_latest BMJ
BBC News – Hepatitis C vaccine: Oxford researchers’ trial ‘promising’ bbc.in/w7UWRx
5 Jan

HHSGov HHSGov
#HHS releases 1st Global Health Strategy. Sec Sebelius talks about building a healthier, safer planet: 1.usa.gov/zlWRDG
6 Jan

CDCgov CDCgov
Read about Dr. Claire Huang & her team at #CDC247, who have developed a dengue vaccine candidate, now in human trials. go.usa.gov/RYU
6 Jan

ArthurCaplan Arthur Caplan
outcome of bachmann hpv challenge gifts put to good use prevent-hpv.com
4 Jan

DofVC DoV Collaboration
Keen to know the status of the Global #Vaccine Action Plan? Check out our new post on GVAP progress: bit.ly/wDK63G
3 Jan

The Anthrax Attacks 10 Years Later

Annals of Internal Medicine
January 3, 2012; 156 (1 Part 1)
http://www.annals.org/content/current

Ideas and Opinions
The Anthrax Attacks 10 Years Later
Larry M. Bush and Maria T. Perez
Ann Intern Med January 3, 2012 156:41-44; published ahead of print October 3, 2011,

Abstract
Ten years ago, just weeks after the September 11 attacks, the United States experienced a deliberate act of bioterrorism. Through use of the postal service, anthrax spores were widely disseminated, including to homes, the Senate, and major newsrooms, resulting in morbidity and mortality and effectively disrupting our way of life and revealing our vulnerability. Even though such attacks had been the subject of much writing and had been planned for, detection of and the appropriate response to an attack with an agent from the so-called “Category ‘A’ List” had only been considered in theoretical terms. What transpired during the following difficult weeks, including how public health and federal government agencies performed, has been both praised and criticized. An intertwined epidemiologic and criminal investigation of such magnitude was unprecedented in U.S. history. To address the question of whether we as a nation are now better prepared for future threats involving biologic agents, it is important to learn from the lessons of the 2001 anthrax attacks, including the critical role of clinicians in surveillance. As physicians involved in diagnosing anthrax in the index case and alerting authorities, we offer our perspective on these events a decade after their occurrence

Managing scarce health resources in developing countries

British Medical Journal
07 January 2012 (Vol 344, Issue 7838)
http://www.bmj.com/content/current

Analysis
Twenty criteria to make the best of scarce health resources in developing countries
BMJ 2011; 343 doi: 10.1136/bmj.d7023 (Published 25 November 2011)
James D Shelton, science adviser

Extract
The needs of developing countries are so great and potential interventions so numerous that priorities are essential. James D Shelton suggests a simple checklist for deciding on priorities and improving implementation

It is difficult to exaggerate the health needs of developing countries. Consider the formidable core list of priorities in President Obama’s Global Health Initiative: maternal health, diarrhoea, pneumonia, routine immunisable diseases, family planning, nutrition, sanitation, malaria, HIV, tuberculosis, and priority neglected tropical diseases—and each has multiple interventions. Yet, numerous other worthy health conditions clamour for attention. These include infectious diseases such as influenza, meningitis, cholera, and emerging zoonoses but also injuries, mental illness, surgery, palliative care, and chronic diseases. The immense needs dwarf the available resources and fragile overloaded systems. Even basic infrastructure is often lacking—for example, national service provision assessments from Uganda and Tanzania indicate that only 24% and 35%, respectively, of health facilities have regular electricity and only 31% and 34%, respectively, have regular water supply.1 2 Health worker shortages and related system dysfunctions have been described as a “slow-burning crisis.”3 Health workers can perform only a limited number of tasks, and organisational system structures are fragile as well. Accordingly, many effective public health approaches such as water and sanitation, food fortification, or alcohol taxation bypass clinical services entirely.

So what is the best use of resources? Much of the advocacy for health interventions stresses the importance of a particular health problem and the clinical efficacy of proposed interventions. However, true success on a large scale in resource constrained environments requires much more. To help a more systematic approach, I suggest some key criteria that should help both to inform priorities and to improve interventions

European Health Systems: Comparative Research

Health Economics, Policy and Law 
Volume 7 – Special Issue 01 – January 2012
http://journals.cambridge.org/action/displayIssue?jid=HEP&tab=currentissue

Special Focus Issue
Back to the future: 10 years of European health reforms
Anna Dixon and Emmi Poteliakhoff
Health Economics, Policy and Law / Volume 7 / Special Issue 01, pp 1 – 10
Copyright © Cambridge University Press 2012
Published online: 05 January 2012
DOI:10.1017/S1744133111000247

Abstract
The challenges facing European health systems have changed little over 30 years but the responses to them have. Policy ideas that emerged in some countries spread to others; however, the way policies were implemented and the impact they have had has been shaped by specific national contexts. Comparative policy analysis has evolved in response to this, moving away from simple classifications of health systems and crude rankings to studies that try and understand more deeply what works, where and why. For policymakers interested in how other countries have dealt with common challenges, it is important that they avoid the naïve transplantation of policy solutions but understand the need to translate policies to fit the institutional context of a particular country. Policies that cross borders will necessarily be shaped by the social and political institutions of a country. These dimensions should not be ignored in comparative research. The next decade will require health systems to deliver improved care for people with complex needs while at the same time delivering greater value. Policymakers will benefit from looking backwards as well as to their neighbours in order to develop appropriate policy solutions.

Observations
The role of comparative health studies for policy learning
Richard B. Saltman

The folly of cross-country ranking exercises
Adam Oliver

The unwritten rules of cross-national policy analysis
Theodore Marmor

Shall we dance? The intricate project of comparison in the study of health policy
Carolyn H. Tuohy

Articles
Reflections on the evolution of health technology assessment in Europe
Corinna Sorenson and Kalipso Chalkidou

Choice policies in Northern European health systems
Karsten Vrangbaek, Ruth Robertson, Ulrika Winblad, Hester Van de Bovenkamp and Anna Dixon

Paying for hospital care: the experience with implementing activity-based funding in five European countries
Jacqueline O’Reilly, Reinhard Busse, Unto Häkkinen, Zeynep Or, Andrew Street and Miriam Wiley

The rise of the regulatory state in health care: a comparative analysis of the Netherlands, England and Italy
Jan-Kees Helderman, Gwyn Bevan and George France

Overcoming fragmentation in health care: chronic care in Austria, Germany and the Netherlands
Ellen Nolte, Cécile Knai, Maria Hofmarcher, Annalijn Conklin, Antje Erler, Arianne Elissen, Maria Flamm, Brigit Fullerton, Andreas Sönnichsen and Hubertus J. M. Vrijhoef

Human Vaccines Special Issue: Influenza Vaccines

Human Vaccines & Immunotherapeutics (formerly Human Vaccines)
Volume 8, Issue 1  January 2012
http://www.landesbioscience.com/journals/vaccines/toc/volume/7/issue/12/

Editor’s Corner
Special Focus: Influenza Vaccines
Susanna Esposito

We have been living with influenza for many years, and have become so used to it becoming a part of our lives to which we usually do not pay much attention. After the excitement of the initial discovery of influenza viruses in 1933 and the development of the first vaccines in the 1940s, relatively little happened in the field during the rest of the 20th century except for the development of the first serological assays, the definition of some correlates of protection, and the expansion of worldwide production capacity.

However, the coming of the 21st century brought new epidemiological data and technological innovations in the production of vaccines. The epidemiological studies showed that influenza viruses are underestimated global killers; they cause annual epidemics and occasional pandemics that have claimed the lives of millions, and the emergence of new strains continues to challenge public health authorities and scientific communities. The real-time monitoring of the evolution of influenza viruses has improved our understanding of the factors leading to viral pathogenicity and/or transmissibility, and the development of new vaccines will be critical for controlling future outbreaks of the disease. The correlates of protection continue to rely on serum antibodies, but live attenuated vaccines also employ another mechanism of protection, and the use of adjuvants and intradermal vaccination has improved the effectiveness of inactivated vaccines. Furthermore, alternatives to eggs have become available, and reverse genetics has allowed us to navigate new horizons. All of these findings have had a significant impact on public health policies and the recommendations for influenza vaccination in different age groups.

The aim of this special issue is to provide a comprehensive update of the state-of-the-art concerning influenza and its prevention. It begins with an overview of influenza viruses that also covers influenza in birds and animals, moves on to deal with the epidemiological, clinical and diagnostic aspects of the disease in different age groups, and finally discusses the various issues associated with its prevention. There are chapters on newly available influenza vaccines, the new technologies used to prepare them, and why there is a need for a quadrivalent vaccine. The recommendations concerning vaccination in children, adults and the elderly are described in detail, and the differences between countries are explained and discussed. The reasons for the low vaccination coverage rate even in high-risk categories are critically reviewed, and there is a discussion of the economic value of vaccination and its impact on public health. Finally, consideration is given to the use of influenza vaccination in special situations such as pregnancy, and there is a summary of the lessons learned from the last pandemic.

I hope that these articles by representative highly experienced authors will make this issue useful to experts in pediatrics, infectious diseases, public health and internal medicine, and believe they can make a significant contribution to our fight against influenza.

Special Focus Review
Economic value of influenza vaccination
Volume 8, Issue 1   January 2012
Chiara de Waure, Maria Assunta Veneziano, Chiara Cadeddu, Silvio Capizzi, Maria Lucia Specchia, Stefano Capri and Walter Ricciardi

Extract
Influenza epidemics are responsible for high mortality and morbidity rates in particular among elderly and high risk groups. This review is aimed at assessing the economic value of vaccination in these groups. A search of full economic evaluations of influenza vaccination in comparison with no interventions was performed on PubMed from January 1990 to May 2011. Only economic evaluations dealing with elderly and high risk groups were considered. The quality of selected articles was assessed through Drummond’s checklist. Sixteen cost-effectiveness analyses and four cost-benefit analyses were included: overall, the quality of studies was fairly good. The vaccination was demonstrated to be cost-effective or cost-saving in almost all studies, independently by the perspective and the type of analysis. Influenza vaccination is a worthwhile intervention from the pharmacoeconomic view-point, anyway a standardization of methods should be desirable in order to guarantee the comparability and transferability of results.

Herpes Simplex Vaccine: Trial Efficacy Results

New England Journal of Medicine
January 5, 2012  Vol. 366 No. 1
http://content.nejm.org/current.shtml

Original Articles
Efficacy Results of a Trial of a Herpes Simplex Vaccine
R.B. Belshe and Others

Background
Two previous studies of a herpes simplex virus type 2 (HSV-2) subunit vaccine containing glycoprotein D in HSV-discordant couples revealed 73% and 74% efficacy against genital disease in women who were negative for both HSV type 1 (HSV-1) and HSV-2 antibodies. Efficacy was not observed in men or HSV-1 seropositive women.

Methods
We conducted a randomized, double-blind efficacy field trial involving 8323 women 18 to 30 years of age who were negative for antibodies to HSV-1 and HSV-2. At months 0, 1, and 6, some subjects received the investigational vaccine, consisting of 20 μg of glycoprotein D from HSV-2 with alum and 3-O-deacylated monophosphoryl lipid A as an adjuvant; control subjects received the hepatitis A vaccine, at a dose of 720 enzyme-linked immunosorbent assay (ELISA) units. The primary end point was occurrence of genital herpes disease due to either HSV-1 or HSV-2 from month 2 (1 month after dose 2) through month 20.

Results
The HSV vaccine was associated with an increased risk of local reactions as compared with the control vaccine, and it elicited ELISA and neutralizing antibodies to HSV-2. Overall, the vaccine was not efficacious; vaccine efficacy was 20% (95% confidence interval [CI], −29 to 50) against genital herpes disease. However, efficacy against HSV-1 genital disease was 58% (95% CI, 12 to 80). Vaccine efficacy against HSV-1 infection (with or without disease) was 35% (95% CI, 13 to 52), but efficacy against HSV-2 infection was not observed (−8%; 95% CI, −59 to 26).

Conclusions
In a study population that was representative of the general population of HSV-1– and HSV-2–seronegative women, the investigational vaccine was effective in preventing HSV-1 genital disease and infection but not in preventing HSV-2 disease or infection. (Funded by the National Institute of Allergy and Infectious Diseases and GlaxoSmithKline; ClinicalTrials.gov number, NCT00057330.)

Risk Factors for Nonreceipt of Hepatitis B Vaccine in the Newborn Nursery

The Pediatric Infectious Disease Journal
January 2012 – Volume 31 – Issue 1  pp: A11-A12,1-9,e1-e36
http://journals.lww.com/pidj/pages/currenttoc.aspx

Original Studies
Maternal Characteristics and Hospital Policies as Risk Factors for Nonreceipt of Hepatitis B Vaccine in the Newborn Nursery
O’Leary, Sean T.; Nelson, Christina; Duran, Julie
Pediatric Infectious Disease Journal. 31(1):1-4, January 2012.
doi: 10.1097/INF.0b013e3182345995

Abstract:
Background: A birth dose of hepatitis B vaccine (HBV) is a primary focus of the Advisory Committee on Immunization Practices’ strategy to eliminate transmission of hepatitis B virus in the United States. We sought to assess the impact of maternal characteristics and hospital policy on the receipt of a birth dose of HBV.

Methods: A retrospective cohort study was performed using data from the 2008 Colorado birth registry. Hospital policy was assessed by state health department personnel. Univariate and multivariate logistic regression analyses were used to examine the association of maternal characteristics and hospital policy with nonreceipt of HBV.

Results: A total of 64,425 infants were identified in the birth cohort, of whom 61.6% received a birth dose of HBV. Higher maternal education and income were associated with nonreceipt of HBV (master’s degree vs. eighth grade or less: adjusted odds ratio [OR] = 1.66, 95% confidence interval [CI] = 1.49–1.85; >$75,000 vs. <$15,000: adjusted OR = 1.21, 95% CI = 1.13–1.30). Lack of a hospital policy stipulating a universal birth dose strongly predicted nonreceipt of a birth dose of HBV (policy with no birth dose vs. policy with a birth dose: adjusted OR = 2.21, 95% CI = 2.13–2.30).

Conclusions: Maternal characteristics such as higher education and income are associated with nonreceipt of the HBV during the perinatal period. To effectively reduce risk of perinatal hepatitis B transmission, hospitals should stipulate that all infants are offered HBV and ensure that these policies are implemented and followed.

Prioritization of Zoonoses in Canada: A Stakeholder-Informed Approach

PLoS One
[Accessed 8 January 2012]
http://www.plosone.org/article/browse.action;jsessionid=577FD8B9E1F322DAA533C413369CD6F3.ambra01?field=date

A Stakeholder-Informed Approach to the Identification of Criteria for the Prioritization of Zoonoses in Canada
Victoria Ng, Jan M. Sargeant
PLoS ONE: Research Article, published 06 Jan 2012 10.1371/journal.pone.0029752

Abstract 
Background
Zoonotic diseases account for over 60% of all communicable diseases causing illness in humans and 75% of recently emerging infectious diseases. As limited resources are available for the control and prevention of zoonotic diseases, it is necessary to prioritize diseases in order to direct resources into those with the greatest needs. The selection of criteria for prioritization has traditionally been on the basis of expert opinion; however, details of the methods used to identify criteria from expert opinion often are not published and a full range of criteria may not be captured by expert opinion.

Methodology/Principal Findings
This study used six focus groups to identify criteria for the prioritization of zoonotic diseases in Canada. Focus groups included people from the public, animal health professionals and human health professionals. A total of 59 criteria were identified for prioritizing zoonotic diseases. Human-related criteria accounted for the highest proportion of criteria identified (55%), followed by animal-related criteria (26%) then pathogen/disease-related criteria (19%).

Similarities and differences were observed in the identification and scoring of criteria for disease prioritization between groups; the public groups were strongly influenced by the individual-level of disease burden, the responsibility of the scientific community in disease prioritization and the experiences of recent events while the professional groups were influenced by the societal- and population-level of disease burden and political and public pressure.

Conclusions/Significance
This was the first study to describe a mixed semi-quantitative and qualitative approach to deriving criteria for disease prioritization. This was also the first study to involve the opinion of the general public regarding disease prioritization. The number of criteria identified highlights the difficulty in prioritizing zoonotic diseases. The method presented in this paper has formulated a comprehensive list of criteria that can be used to inform future disease prioritization studies.

Genetic Variation in Susceptibility to Infectious Diseases in Humans

PLoS One
[Accessed 8 January 2012]
http://www.plosone.org/article/browse.action;jsessionid=577FD8B9E1F322DAA533C413369CD6F3.ambra01?field=date

Evolutionary Determinants of Genetic Variation in Susceptibility to Infectious Diseases in Humans
Christi Baker, Janis
PLoS ONE: Research Article, published 05 Jan 2012 10.1371/journal.pone.0029089

Abstract 
Although genetic variation among humans in their susceptibility to infectious diseases has long been appreciated, little focus has been devoted to identifying patterns in levels of variation in susceptibility to different diseases. Levels of genetic variation in susceptibility associated with 40 human infectious diseases were assessed by a survey of studies on both pedigree-based quantitative variation, as well as studies on different classes of marker alleles. These estimates were correlated with pathogen traits, epidemiological characteristics, and effectiveness of the human immune response. The strongest predictors of levels of genetic variation in susceptibility were disease characteristics negatively associated with immune effectiveness. High levels of genetic variation were associated with diseases with long infectious periods and for which vaccine development attempts have been unsuccessful. These findings are consistent with predictions based on theoretical models incorporating fitness costs associated with the different types of resistance mechanisms. An appreciation of these observed patterns will be a valuable tool in directing future research given that genetic variation in disease susceptibility has large implications for vaccine development and epidemiology.

Hepatitis C virus vaccine: chimpanzee-derived adenovirus vector

Science Translational Medicine
4 January 2012 vol 4, issue 115
http://stm.scienceag.org/content/mcurrent

Focus: Hepatitis C Virus
Chimp Virus Makes a Savvy Vaccine Vector
Michael Houghton
4 January 2012: 115fs1
Abstract
A hepatitis C virus vaccine delivered by a chimpanzee-derived adenovirus vector produces strong T cell immune responses in healthy human volunteers.

Research Articles
Hepatitis C
Novel Adenovirus-Based Vaccines Induce Broad and Sustained T Cell Responses to HCV in Man
Eleanor Barnes, Antonella Folgori, Stefania Capone, Leo Swadling, Stephen Aston, Ayako Kurioka, Joel Meyer, Rachel Huddart, Kira Smith, Rachel Townsend, Anthony Brown, Richard Antrobus, Virginia Ammendola, Mariarosaria Naddeo, Geraldine O’Hara, Chris Willberg, Abby Harrison, Fabiana Grazioli, Maria Luisa Esposito, Loredana Siani, Cinzia Traboni, Ye Oo, David Adams, Adrian Hill, Stefano Colloca, Alfredo Nicosia, Riccardo Cortese, and Paul Klenerman
4 January 2012: 115ra1
An adenoviral HCV vaccine induces antiviral T cell responses in human volunteers.

Gene therapy
Vaccine Vectors Derived from a Large Collection of Simian Adenoviruses Induce Potent Cellular Immunity Across Multiple Species
Stefano Colloca, Eleanor Barnes, Antonella Folgori, Virginia Ammendola, Stefania Apone, Agostino Cirillo, Loredana Siani, Mariarosaria Naddeo, Fabiana Grazioli, Maria Luisa Esposito, Maria Ambrosio, Angela Sparacino, Marta Bartiromo, Annalisa Meola, Kira Smith, Ayako Kurioka, Geraldine A. O’Hara, Katie J. Ewer, Nicholas Anagnostou, Carly Bliss, Adrian V. S. Hill, Cinzia Traboni, Paul Klenerman, Riccardo Cortese, and Alfredo Nicosia
4 January 2012: 115ra2
Simian adenoviruses screened from wild-derived candidates can prime T cell responses in man and may serve as new vaccine vector candidates.

Influenza vaccination among HCP after H1N1

Vaccine
http://www.sciencedirect.com/science/journal/0264410X
Volume 30, Issue 5  pp. 821-982 (20 January 2012)

Regular Papers
Influenza vaccination among healthcare personnel after pandemic influenza H1N1
Original Research Article
Pages 911-915
José Sánchez-Payá, Ignacio Hernández-García, Vicente García-Román, Robert Camargo-Angeles, Julio Barrenengoa-Sañudo, Cesar O. Villanueva-Ruiz, Hector R. Martínez, María González-Hernández

Abstract
The purpose of this study was to evaluate the coverage rates for influenza vaccination among health-care personnel (HCP), and if the reasons for accepting influenza vaccine by HCP and the frequency of vaccine-related adverse events (AEs) in 2010–2011 were different compared to 2009–2010. The AEs were detected by telephoning the worker one week after the vaccination. The coverage for seasonal vaccination in 2009–2010 was 31.0%, whereas that for 2009 pandemic influenza (H1NI) was 22.2% and 24.4% (p < 0.05) in 2010–2011. The most frequent reason for being vaccinated during the three campaigns was to “protect my health”. Over 80.5% of the HCP reported 2009 pandemic influenza (H1N1) vaccine-related AEs compared to the 25.3% and 25.4% reporting seasonal vaccine-related AEs in 2009–2010 and 2010–2011 respectively (p < 0.05). None of the AEs were severe. Specific measures should be implemented in our country to recover and improve poor vaccination coverage.

Pandemic influenza vaccination lessons: Latin America and the Caribbean

Vaccine
http://www.sciencedirect.com/science/journal/0264410X
Volume 30, Issue 5  pp. 821-982 (20 January 2012)

Regular Papers
Pandemic influenza vaccination: Lessons learned from Latin America and the Caribbean
Original Research Article
Pages 916-921
Alba María Ropero-Álvarez, Alvaro Whittembury, Hannah Jane Kurtis, Thais dos Santos, M. Carolina Danovaro-Holliday, Cuauhtémoc Ruiz-Matus

Abstract
In April 2009, the World Health Organization (WHO) reported the emergence of a new influenza (H1N1) virus which led to the first pandemic declaration of the 21st century. Most countries in Latin America and the Caribbean (LAC) had a national preparedness plan in place at this time; however, the vaccination component of such plans was largely undeveloped. Nevertheless, countries were able to capitalize on the infrastructure of their immunization programs and widespread experience utilizing the seasonal influenza vaccine to prepare rapidly, developing H1N1 vaccination plans targeting individuals with chronic disease, pregnant women and health care workers, among others. In LAC vaccine was acquired through three mechanisms: the Pan American Health Organization’s Revolving Fund, direct manufacturer purchase, and WHO donations. Vaccine access was not equitable both in quantity of vaccine available and timeless of vaccine availability. As of December 2010, an estimated 145 million doses had been administered in LAC. Despite high regional coverage, there were large variations in coverage at the national level; pregnant women had the lowest coverage, despite their high risk for morbidity and mortality. The number of severe adverse events reported in LAC was similar to those expected with the seasonal influenza vaccine. Risk communication was one of the key challenges countries faced, mainly due to concerns and misinformation spread regarding vaccine safety. Countries and the international community need to learn from the experiences gained during H1N1 vaccination in order to be better prepared for the next pandemic.

Effects of nationwide Hib vaccine shortage in U.S.

Vaccine
http://www.sciencedirect.com/science/journal/0264410X
Volume 30, Issue 5  pp. 821-982 (20 January 2012)

Regular Papers
Effects of a nationwide Hib vaccine shortage on vaccination coverage in the United States
Original Research Article
Pages 941-947
Tammy A. Santibanez, Abigail Shefer, Elizabeth C. Briere, Amanda C. Cohn, Amy V. Groom

Abstract
Background
A shortage of Haemophilus influenzae type b (Hib) vaccine that occurred in the United States during December 2007 to September 2009 resulted in an interim recommendation to defer the booster dose, but to continue to vaccinate as recommended with the primary series during the first year of life.

Objectives
To quantify effects of the Hib shortage on vaccination coverage and to determine if any demographic subgroups were disproportionately affected.

Methods
Data from the 2009 National Immunization Survey (NIS) were divided based on child’s age at the onset of the shortage. Comparisons were made in primary series coverage by 9 months between children <7 months versus ≥7 months at the start of the shortage. Comparisons in primary series plus booster dose completion by 19 months were made between children who were <12 months versus ≥12 months at the start of the shortage.

Results
Nationally, there was a difference in Hib primary series completion by 9 months among children age <7 months versus ≥7 months at the start of the shortage (73.9% versus 81.2%, P < 0.001). There was a large difference in the percentage of children fully vaccinated with the primary series plus booster dose by 19 months among children age <12 months versus ≥12 months at the start of the shortage (39.5% versus 66.0%, P<0.001). There were differential effects of the shortage on primary series coverage among states and for some demographic characteristics.

Conclusions
As expected booster dose coverage was reduced consistent with interim recommendations, but primary series coverage was also reduced by 7 percentage points nationally.

Maternal determinants of complete child immunization: Nigeria

Vaccine
Volume 30, Issue 4  pp. 685-820 (17 January 2012)
Regular Papers

Maternal determinants of complete child immunization among children aged 12–23 months in a southern district of Nigeria
Original Research Article
Pages 730-736
Akinola Ayoola Fatiregun, Anselm O. Okoro

Abstract
This study was conducted to identify determinants of complete immunization status among children aged 12–23 months in a southern district of Nigeria. The World Health Organization cluster survey was used to evaluate immunization coverage of infants. Mothers of 525 children selected by the two-stage sampling method and interviewed using an adapted questionnaire responded. Completion of the immunization schedule was verified by an immunization card or by reported history indicating that the child had received full doses of four of the antigens included in the Nigeria routine immunization schedule. Multivariate logistic regression was used to identify factors associated with completion of immunization. Only 32.4% of children had completed the immunization schedule. Determinants of complete immunization status included a maternal age less than 30 years (AOR = 2.26, 95% CI:1.27–4.03), availability of an immunization card at first contact (AOR = 7.72, 95% CI:4.43–13.44), fewer than three children (AOR = 2.22, 95% CI:11.1–4.42), completion of post secondary education (AOR = 2.34, 95% CI:1.12–4.47) and maternal unemployment (AOR = 1.71, 95% CI:1.01–2.89). Identifying mothers whose children are at risk of not completing the immunization schedule and educating them is an important strategy to improve antigen coverage and prevent early childhood deaths from diseases like tuberculosis, poliomyelitis, tetanus, diphtheria, pertussis and measles.

Report: 20 cases of wild poliovirus type 1 in China

Report: Outbreak of wild poliovirus type 1 in China: 20 cases reported
20 December 2011
WHO Europe website

As of 14 December 2011, China has reported 20 cases of wild poliovirus since the outbreak began in August 2011. Of the 20 cases, 11 cases are in adults 19-53 years of age and 9 cases are in children under 3-years-old. The latest case had an onset date of 9 October 2011, and all cases are from the Xinjiang Uygur Autonomous Region of western China.

The Ministry of Health of China has responded to the outbreak by conducting supplementary immunization activities (SIAs) on 8-12 September 2011, which targeted children under 15 years of age and reached a total of 4,065,033 children. A second round, also targeting children age 15 and under was carried out on 8-12 October and reached 4,150,575 children. Vaccination rounds targeting individuals age 15-39 have taken place in a number of prefectures since September 13 and more than 4 million people have been immunized.

Most recently, a third immunization round targeting both children under 15 and adults 15-39 took place on 15-22 November. External WHO and UNICEF monitors reported high coverage, as experienced in previous immunization rounds. The next round of polio SIAs is planned for March 2012.

The Regional Commission for the Certification of Poliomyelitis Eradication in the Western Pacific Region (RCC) met on 14-19 December 2011 in Ha Noi, Viet Nam. At this meeting, the RCC commended China for its efforts to investigate and respond to the polio outbreak, but it concluded that it was too early to determine whether the outbreak is coming under control. In order for the Region to retain its polio-free certification, 12 months must elapse following the most recent polio case or wild poliovirus isolate (i.e. including the high transmission season of 2012), with surveillance indicators meeting all sensitivity criteria.

WHO notes that wild poliovirus transmission could persist during the low transmission season. Therefore it recommends that the Ministry of Health in China should consider implementing a non-selective, universal mOPV1 vaccination policy for all children younger than 15 years of age during measles SIAs planned for December. Updates about the polio situation in China can be viewed at the WHO Western Pacific Region web site (see link at right).

As in the past, WHO/Europe urges all Member States to remain vigilant and ensure enhanced polio surveillance for wild poliovirus importations and to maintain high coverage with polio vaccine. This is of particular importance for countries with intensive travel and trade routes with China. All those traveling to and from countries or areas reporting wild poliovirus should be vaccinated as per WHO’s international travel and health recommendations.

http://www.euro.who.int/en/what-we-do/health-topics/disease-prevention/vaccines-and-immunization/news/news/2011/12/outbreak-of-wild-poliovirus-type-1-in-china-20-cases-reported

H5N1 Transmissable Research: Key Documents at 1 Jan 2012

[Editor’s Note: We present three key statements involving the continuing debate around publication of recent H5N1 research on transmissible strains and related biosecurity concerns: The NSABB statement, a WHO statement of concern, and a Washington Post editorial]

Press Statement: National Science Advisory Board for Biosecurity (NSABB) Review of H5N1 Research
The U.S. government remains concerned about the threat of influenza, for the risks it poses seasonally, as well as its potential to cause a pandemic. Our domestic and global influenza surveillance efforts have become increasingly capable, along with expanded vaccine manufacturing capacity and assistance to other countries in their efforts to detect and respond to a pandemic. To enhance the detection of and response to influenza outbreaks, the U.S. government supports a broad range of domestic and global preparedness and response efforts that include research on better diagnostics, vaccines, and therapeutics.

Currently, H5N1 avian influenza virus — the strain commonly referred to as “bird flu” — rarely infects humans and does not spread easily from person to person. However, many scientists and public health officials are concerned that the virus could evolve in nature into a form that is transmissible among humans — an event that could potentially make this deadly virus an extremely serious global public health threat. Thus research on factors that can affect the transmissibility of the H5N1 virus is critically important to international efforts to prepare and prevent threats to public health.

While the public health benefits of such research can be important, certain information obtained through such studies has the potential to be misused for harmful purposes. The National Science Advisory Board for Biosecurity (NSABB) — an independent expert committee that advises the Department of Health and Human Services (HHS) and other Federal departments and agencies on matters of biosecurity — completed a review of two unpublished manuscripts describing NIH-funded research on the transmissibility of H5N1. These manuscripts — which describe laboratory experiments that resulted in viruses with enhanced transmissibility in mammals – concluded that the H5N1 virus has greater potential than previously believed to gain a dangerous capacity to be transmitted among mammals, including perhaps humans, and describe some of the genetic changes that appear to correlate with this potential.

Following its review, the NSABB decided to recommend that HHS ask the authors of the reports and the editors of the journals that were considering publishing the reports to make changes in the manuscripts. Due to the importance of the findings to the public health and research communities, the NSABB recommended that the general conclusions highlighting the novel outcome be published, but that the manuscripts not include the methodological and other details that could enable replication of the experiments by those who would seek to do harm.

The NSABB also recommended that language be added to the manuscripts to explain better the goals and potential public health benefits of the research, and to detail the extensive safety and security measures taken to protect laboratory workers and the public.

HHS agreed with this assessment and provided these non-binding recommendations to the authors and journal editors.

Recognizing the significant potential benefit of the information about the experimental details to the global influenza surveillance and research communities, the U.S. government is working to establish a mechanism to allow secure access to the information to those with a legitimate need in order to achieve important public health goals. The U.S. government is also developing a proposed oversight policy that would augment existing approaches to evaluating research that has the potential to be misused for harmful purposes.

The NSABB supports the overall goals of the National Institutes of Health, in conducting safe, ethical and informative research to enhance health, lengthen life, and reduce the burdens of illness and disability. http://www.nih.gov/news/health/dec2011/od-20.htm

Statement: WHO concerned that new H5N1 influenza research could undermine the 2011 Pandemic Influenza Preparedness Framework
30 December 2011
The World Health Organization (WHO) takes note that studies undertaken by several institutions on whether changes in the H5N1 influenza virus can make it more transmissible between humans have raised concern about the possible risks and misuses associated with this research. WHO is also deeply concerned about the potential negative consequences. However, WHO also notes that studies conducted under appropriate conditions must continue to take place so that critical scientific knowledge needed to reduce the risks posed by the H5N1 virus continues to increase.

H5N1 influenza viruses are a significant health risk to people for several reasons.  Although this type of influenza does not infect humans often, when it does, approximately 60% of those infected die. In addition, because these viruses can cause such severe illness in people, scientists are especially concerned that this type of influenza could one day mutate so it spreads easily between people and causes a very serious influenza pandemic.

Research which can improve the understanding of these viruses and can reduce the public health risk is a scientific and public health imperative. In order to enable those public health gains, countries where these viruses occur should share their influenza viruses for public health purposes while countries and organizations receiving these viruses should share benefits resulting from the virus sharing. Both types of sharing are on equal footing and equally important parts of the collective global actions needed to protect public health.

While it is clear that conducting research to gain such knowledge must continue, it is also clear that certain research, and especially that which can generate more dangerous forms of the virus than those which already exist, has risks. Therefore such research should be done only after all important public health risks and benefits have been identified and reviewed, and it is certain that the necessary protections to minimize the potential for negative consequences are in place.

In May 2011, the new Pandemic Influenza Preparedness (PIP) Framework came into effect. This Framework was adopted by all WHO Member States as a guide to the sharing of influenza viruses with pandemic potential and the resulting benefits. One specific requirement of this Framework, which pertains to influenza viruses of pandemic potential, and is in keeping with best scientific practice, is for laboratories receiving them through WHO’s Global Influenza Surveillance and Response System (GISRS) to collaborate with, and appropriately acknowledge, scientists in countries where the virus originated when initiating research.

WHO recognizes that the scientists who led the work of the new studies received their virus samples from the WHO Global Influenza Surveillance Network (GISN), which preceded GISRS, and before negotiations on the new PIP Framework began. However, now that the Framework has been adopted by all WHO Member States, WHO considers it critically important that scientists who undertake research with influenza viruses with pandemic potential samples fully abide by the new requirements.

Since the PIP Framework represents a major step forward and was agreed upon only after several years of difficult negotiations, WHO stresses that this H5N1 research must not undermine this major public health achievement. WHO will work with Member States and other key parties to ensure scientists understand the new requirements that have been agreed to with the Framework.

 

Editorial: A flu virus risk worth taking
Washington Post
30 Dec 2011
By Anthony S. Fauci, Gary J. Nabel and Francis S. Collins
Anthony Fauci is director of the National Institute of Allergy and Infectious Diseases (NIAID), Gary Nabel works in the virology laboratory at the NIAID and Francis Collins is director of the National Institutes of Health.

A deadly influenza virus has circulated widely in birds in recent years, decimating flocks but rarely spreading to humans. Nonetheless, because of its persistence in bird flocks, this highly pathogenic virus has loomed as a major public health threat. Seasonal influenza kills less than 1 percent of the people it infects. In contrast, human infections with the H5N1 virus, though exceedingly rare, are fatal in most cases. Should this virus mutate in a way that allows it to be transmitted as efficiently among people as seasonal influenza viruses are, it could take an unprecedented toll on human life.

A number of important scientific and public health questions regarding this virus remain unanswered, including the likelihood of such mutations arising and the mechanisms by which they may occur. Two recent studies co-funded by the National Institutes of Health have shed light on how this potentially grave human health threat could become a reality. Working carefully with influenza viruses they have engineered in isolated laboratories, scientists in Europe and the United States have identified several mechanisms by which the virus might evolve to transmit efficiently in the ferret, the best animal model for human influenza infection. This research has allowed identification of genetic pathways by which such a virus could be better adapted to transmission among people. This laboratory virus does not exist in nature. There is, however, considerable concern that such a virus could evolve naturally. We cannot predict whether it or something similar will arise naturally, nor when or where it might appear.

Despite these uncertainties, much good can come from generating a potentially dangerous virus in the laboratory. We have to consider the unpredictable and explosive nature of influenza epidemics.

While the World Health Organization and the Centers for Disease Control and Prevention (CDC) provide excellent public health surveillance for novel influenza strains, influenza outbreaks still occur suddenly and in unexpected places. The recent H1N1 pandemic exemplifies the problem: In 2009, a new influenza virus emerged. It was shown to have originated from an animal reservoir, and it spread so rapidly that it strained the pharmaceutical industry’s capacity to prepare vaccines fast enough to blunt its spread.

Moreover, we do not fully understand the underlying factors that allow influenza viruses to be transmitted efficiently in humans after they emerge from different species.  The ferret transmission studies were intended in part to fill these important gaps in knowledge.

Understanding the biology of influenza virus transmission has implications for outbreak prediction, prevention and treatment. In defining the mutations required for mammalian transmission, public health officials are provided with genetic signatures that, like fingerprints, could help scientists more readily identify newly emergent, potentially harmful viruses, track their spread and detect threatening outbreaks. The ability to identify such viruses even a few months faster than by conventional surveillance provides critical time to slow or stop an outbreak. The CDC provides this health security by implementing public health protective measures, preparing vaccines and stockpiling antiviral drugs. Identifying threatening viruses can also facilitate the early stages of manufacturing vaccines that protect against such a virus in advance of an outbreak.

In addition, determining the molecular Achilles’ heel of these viruses can allow scientists to identify novel antiviral-drug targets that could be used to prevent infection in those at risk or to better treat those who become infected. Decades of experience tell us that disseminating information gained through biomedical research to legitimate scientists and health officials provides a critical foundation for generating appropriate countermeasures and, ultimately, protecting public health.

The underlying question, of course, is whether the benefits of such research outweigh the risks. The answer is not simple. A highly pathogenic avian influenza virus transmissible in humans could arise in ways not predicted by laboratory studies. And it is not clear whether the laboratory virus would behave in humans as it does in ferrets. Nonetheless, new data can provide valuable insights that would inform influenza preparedness and help delineate the principles of influenza virus transmission between species.

Along with support for this research comes a responsibility to ensure that the information is used for good. Safeguarding against the potential accidental release or deliberate misuse of laboratory pathogens is imperative. The engineered viruses developed in the ferret experiments are maintained in high-security laboratories. The scientists, journal editors and funding agencies involved are working together to ensure that access to specific information that could be used to create dangerous pathogens will be limited to those with an established and legitimate need to know.

http://www.washingtonpost.com/opinions/a-flu-virus-risk-worth-taking/2011/12/30/gIQAM9sNRP_story.html

GAVI announces fresh support from Sweden, U.S.

 GAVI announced new support from the Swedish Ministry of Foreign Affairs which will contribute US$55.5 million to support its 2012 immunisation programmes.  The contribution includes an additional US$18.5 million from Sweden’s initial commitment, which was announced at the GAVI pledging conference on 13 June 2011. Sweden is the first GAVI donor to further increase its contribution following the conference. GAVI also expressed “its deep appreciation” to the U.S. for an increase in funding secured in the Fiscal Year 2012 omnibus spending bill passed by the US Congress on 17 December. The omnibus bill recommends that GAVI receive US$100 million, an increase of US$10.2 million over the US$89.8 million appropriated in FY2011. Seth Berkley, CEO of the GAVI Alliance, commented, “Working with our partners, including USAID, we aim to immunise a quarter of a billion children by 2015. We are grateful, that despite significant fiscal constraints, Congress has approved funding that will allow us to continue this important work and build on the measurable results we’ve achieved over more than a decade.”

http://www.gavialliance.org/library/news/press-releases/2011/sweden-increases-funding-for-immunisation/
http://www.gavialliance.org/library/news/statements/2011/gavi-appreciation-for-fy2012-appropriations-passed-by-us-congress/

Meeting Documentation: 130th WHO Executive Board – January 2012; GVAP draft

Meeting: 130th WHO Executive Board session
Date: 16–23 January 2012
Location: Geneva, Switzerland
Provisional Agenda: http://apps.who.int/gb/ebwha/pdf_files/EB130/B130_1-en.pdf

[Editor’s Note: The provisional agenda includes a number of issues relating to global immunization and vaccines supported in part by the documents highlighted just below. We note with interest the agenda item “Draft global vaccine action plan: update  EB130/21 associated with the on-going Decade of Vaccine Collaboration (DoVC) and include initial paragraphs and the closing requested action by the WHO Executive Board.
   Further below we note the availability and selected items from the provisional agenda for the World Health Assembly meeting to be held in May 2012, which also includes treatment of the Global Vaccine Action Plan (GVAP).]

EB130/13
Monitoring of the achievement of the health-related Millennium Development Goals
Progress in the achievement of the health-related Millennium Development Goals and global health goals after 2015

EB130/16
Implementation of the International Health Regulations (2005)

EB130/17
Global mass gatherings: implications and opportunities for global health security

EB130/18
Pandemic influenza preparedness: sharing of influenza viruses and access to vaccines and other benefits: report of the Advisory Group

EB130/19
Poliomyelitis: intensification of the global eradication initiative

EB130/21
Draft global vaccine action plan: update
Report by the Secretariat
[Initial paragraphs and closing action request; full document (6 pages) available at http://apps.who.int/gb/ebwha/pdf_files/EB130/B130_21-en.pdf ]

1. This document summarizes progress in the development of the global vaccine action plan that was initially discussed by the Sixty-fourth World Health Assembly in 2011 as part of the progress report on the implementation of the Global Immunization Vision and Strategy.1 The final version of the action plan will be presented to the Sixty-fifth World Health Assembly in May 2012.

THE GLOBAL VACCINE ACTION PLAN – AN IMMUNIZATION AGENDA FOR THE DECADE OF VACCINES
2. The Decade of Vaccines (2011–2020) envisages a world in which all individuals and communities enjoy lives that are free from vaccine-preventable diseases. Its purpose is to extend, by 2020 and beyond, the full benefits of immunization to all people, regardless of where they are born, who they are, or where they live.

3. In May 2011, the Sixty-fourth World Health Assembly noted the report on the Global Immunization Vision and Strategy 2006–2015, the first 10-year strategic framework to realize the potential of immunization in addressing morbidity and mortality from vaccine-preventable diseases. It has been a global rallying point, enabled the design of regional strategies, and guided the development of comprehensive, fully costed, multi-year national plans for immunization. The report to the Health Assembly included a description of the start of the collaborative process to develop a global vaccine action plan that builds on the success of the Global Immunization Vision and Strategy. The action plan aims to go further, integrating all aspects of immunization, including research and development, delivery, access to quality vaccines that are affordable, and public and political support. The action plan will also include projections of financial resource availability and requirements, and a clear process to define an accountability framework, arrived at through a comprehensive global, regional, and in-country consultation process…

ACTION BY THE EXECUTIVE BOARD
29. The Executive Board is invited to take note of the report and provide further guidance to support the preparation of the final draft of the global vaccine action plan.
1: Document A64/14.

Provisional Agenda for the Sixty-fifth World Health Assembly (May 2012) EB130/33: http://apps.who.int/gb/ebwha/pdf_files/EB130/B130_33-en.pdf The agenda includes the following items of special interest regarding immunization and vaccines issues:

13. Technical and health matters
13.9 Pandemic influenza preparedness: sharing of influenza viruses and access to vaccines and other benefits: report on the work of the Advisory Group
13.10 Poliomyelitis: intensification of the global eradication initiative
13.11 Elimination of schistosomiasis
13.12 Draft global vaccine action plan
13.16 Progress reports
   Disease eradication, prevention and control
D. Smallpox eradication: destruction of variola virus stocks (resolution WHA60.1)
E. Eradication of dracunculiasis (resolution WHA64.16)
F. Chagas disease: control and elimination (resolution WHA63.20)
G. Viral hepatitis (resolution WHA63.18)
H. Prevention and control of multidrug-resistant tuberculosis and extensively drug resistant tuberculosis (resolution WHA62.15)
I. Cholera: mechanisms for control and prevention (resolution WHA64.15)
J. Control of human African trypanosomiasis (resolution WHA57.2)
K. Global health sector strategy on HIV/AIDS, 2011–2015 (resolution WHA64.14)
L. Prevention and control of sexually transmitted infections: global strategy (resolution WHA59.19)