WHO IVR: Dengue vaccine research – update

WHO: Initiative for Vaccine Research (IVR)
Dengue vaccine research
Dengue is a mosquito-borne flavivirus disease that has spread to most tropical and many subtropical areas. The disease is caused by four closely related viruses, the Dengue viruses 1-4. There are no specific dengue therapeutics and prevention is currently limited to vector control measures. A dengue vaccine would therefore represent a major advance in the control of the disease.

Status of vaccine development
While no licensed dengue vaccine is available, several vaccine candidates are currently being evaluated in clinical studies.

The candidate currently at the most advanced clinical development stage, a live-attenuated tetravalent vaccine based on chimeric yellow fever-dengue virus (CYD-TDV), has progressed to phase III efficacy studies. Results from a phase IIb efficacy study in Thailand have been published in September 2012.
More information on the phase IIb study of CYD-TDV (September 2012)
pdf, 55kb

Several other live-attenuated vaccines, as well as subunit, DNA and purified inactivated vaccine candidates, are at earlier stages of clinical development. Additional technological approaches, such as virus-vectored and VLP-based vaccines, are under evaluation in preclinical studies…

http://www.who.int/vaccine_research/diseases/dengue/dengue_vaccines/en/index.html

WHO Epidemiological Brief 26: Measles, rubella and polio update

WHO Europe: WHO Epidemiological Brief 26: Measles, rubella and polio update
“This issue provides an overview of selected epidemiological characteristics of measles and rubella in the WHO European Region for the first seven months of 2012. The analysis is based on cases with disease onset dates during this period. The report also provides information on acute flaccid paralysis (AFP) surveillance.”

http://www.euro.who.int/__data/assets/pdf_file/0017/173060/EpiBrief-Issue-26-Sept-2012.pdf

SHEA Guidance Statement – The Use of Live Attenuated Influenza Vaccine (LAIV) in Healthcare Personnel (HCP) (Sep 2012)

SHEA Guidance Statement

Infection Control and Hospital Epidemiology
Vol. 33, No. 10, October 2012
http://www.jstor.org/stable/10.1086/667772

The Use of Live Attenuated Influenza Vaccine (LAIV) in Healthcare Personnel (HCP): Guidance from the Society for Healthcare Epidemiology of America (SHEA)
Thomas R. Talbot, MD, MPH,1 Hilary Babcock, MD, MPH,2 Deborah Cotton, MD, MPH,3,4 Lisa L. Maragakis, MD, MPH,5 Gregory A. Poland, MD,6 Edward J. Septimus, MD,7,8 Michael L. Tapper, MD,9 David J. Weber, MD, MPH,10 and writing as the SHEA Task Force on Healthcare Personnel Influenza Vaccination

[Editor’s Extract]
“…SHEA endorses the use of LAIV as an alternative to the inactivated influenza vaccine, particularly for those HCP who avoid an annual influenza vaccination because of fear of needle injections. SHEA also agrees with the restriction of LAIV from those HCP who, in the week following vaccination, have frequent contact with patients who reside in a protective environment (eg, HCP in a bone marrow transplantation unit), but it notes that this recommendation is made as a result of an abundance of caution. Those HCP who have frequent contact with patients in protective environments but who will not care for such patients in the week following vaccination may still receive LAIV. HCP who have the potential for infrequent contact with patients in protective environments (ie, when the majority of patients contacted do not reside in a protective environment, such as a radiology technologist performing a chest radiograph or an emergency department physician during the initial patient evaluation) should not be excluded from vaccination with LAIV. Finally, HCP who provide care to other immunosuppressed populations (eg, neonatal and burn unit patients and oncologic patients undergoing chemotherapy but not requiring a formal protective environment) may still receive LAIV…”

Meeting: IOM – Improving Health, Health Systems, and Health Policy Around the World – September 24, 2012

Meeting: IOM – Improving Health, Health Systems, and Health Policy Around the World
September 24, 2012
The Conference Center at The New York Academy of Medicine (Library Reading Room) • 1216 Fifth Avenue, New York, NY 10029 Map

The Institute of Medicine’s Roundtable on Health Literacy will host its next workshop on September 24, 2012 at The Conference Center at The New York Academy of Medicine. International Approaches to Health Literacy is the topic of the workshop. Experts will present material on the subject to the Roundtable. The workshop is free and open to the public.  If you would like to register to attend, please do so under “attend this meeting”. Please see the posted agenda for a schedule of the day.
http://www.iom.edu/Activities/PublicHealth/HealthLiteracy/2012-SEP-24.aspx?utm_medium=etmail&utm_source=Institute%20of%20Medicine&utm_campaign=09.11.12+Meeting+Alert&utm_content=Meetings%20&%20Events&utm_term=Academic

IOM Report: How Far Have We Come in Reducing Health Disparities? Progress Since 2000

IOM Report: How Far Have We Come in Reducing Health Disparities?  Progress Since 2000 – Workshop Summary
https://download.nap.edu/login.php?record_id=13383&page=%2Fcatalog.php%3Frecord_id%3D13383
Released: September 12, 2012

At the turn of the 21st century, several important reports and events designed to raise awareness of health disparities and to describe initial efforts to reduce health disparities took place. The Surgeon General’s office released several reports that showed dramatic disparities, for example, in tobacco use and access to mental health services by race and ethnicity. Second, the first real legislation focused on reducing health disparities was signed into law, creating the National Center for Minority Health and Health Disparities within the NIH. In 2001, the IOM released its landmark report, Crossing the Quality Chasm: A New Health System for the 21st Century, highlighting the importance of a focus on health care quality rather than a focus on only access and cost issues. Building upon these reports and events, the IOM held a workshop on April 8, 2010, that discussed progress to address health disparities and focused on the success of various federal initiatives to reduce health disparities. This document summarizes the workshop.

Book: Genome-Based Therapeutics: Targeted Drug Discovery and Development: Workshop Summary

Book: Genome-Based Therapeutics: Targeted Drug Discovery and Development: Workshop Summary
Authors:
Adam C. Berger and Steve Olson, Rapporteurs; Roundtable on Translating Genomic-Based Research for Health; Board on Health Sciences Policy; Institute of Medicine
IOM
September 5, 2012
http://iom.edu/Reports/2012/Genome-Based-Therapeutics-Targeted-Drug-Discovery-and-Development.aspx?utm_medium=etmail&utm_source=Institute%20of%20Medicine&utm_campaign=09.05.12+Report+-+Genomics+Therapeutics&utm_content=New%20Reports&utm_term=Academic

Description
Genome-Based Therapeutics summarizes a workshop that was held on March 21, 2012, titled New Paradigms in Drug Discovery: How Genomic Data Are Being Used to Revolutionize the Drug Discovery and Development Process. At this workshop the goal was to examine the general approaches being used to apply successes achieved so far, and the challenges ahead.

Genome-Based Therapeutics explains that new technologies have the potential to open up avenues of development and to identify new drug targets to pursue. Specifically, improved validation of gene-disease associations through genomics research has the potential to revolutionize drug production and lower development costs. Genetic information has helped developers by increasing their understanding of the mechanisms of disease as well as individual patients’ reactions to their medications. There is a need to identify the success factors for the various models that are being developed, whether they are industry-led, academia-led, or collaborations between the two.

Directory: Developing World Health Partnerships (IFPMA)

Directory: Developing World Health Partnerships
The International Federation of Pharmaceutical Manufacturers & Associations (IFPMA)
September 2012

Now totaling 220 and reaching people in more than 160 countries, these health partnerships highlight the commitment of research-based pharmaceutical industry and its many partners including governments, intergovernmental organizations, nongovernmental organizations, private sector companies and universities to improve health around the world.

The launch of this directory coincides with the release of an independent review of the contributions these health partnerships’ make to the health of people in low- and middle-income countries. This review was conducted by BSR, a global business network and consultancy focused on sustainability.

“Global health issues are complex, and solutions often require a range of organizations working together,” said Eduardo Pisani, IFPMA Director General. “Understanding the value of partnerships, our industry and partners have increased these programs dramatically in recent years as highlighted in our directory. This year, we are pleased that BSR analyzed these programs and made suggestions for increasing the benefit people in developing countries.”

The industry-led health partnerships catalogued in the IFPMA’s Developing World Health Partnerships Directory focus on a wide range of activities from developing new treatments and improving their availability to strengthening health systems, raising awareness, prevention and training. They also cover various types of diseases such as HIV/AIDS, neglected tropical diseases, malaria, non-communicable diseases and more cross-cutting challenges such as women and children’s health.

Developing World Health Partnerships Directory or BSR’s review can be found at: http://partnerships.ifpma.org/

http://www.ifpma.org/fileadmin/content/News/2012/FINAL_IFPMA_press_release_-_partnerships_-_11_September_2012.pdf

Editorial: WHO’s ambitious new European health strategy

British Medical Journal
14 September 2012 (Vol 345, Issue 7874)
http://www.bmj.com/content/345/7874

Editorial
WHO’s ambitious new European health strategy
BMJ 2012; 345 doi: 10.1136/bmj.e5928 (Published 5 September 2012)
Cite this as: BMJ 2012;345:e5928
David J Hunter, professor of health policy and management

[Extract]
Political will must be galvanised for Health 2020 to succeed

It may seem the wrong moment to launch an ambitious European health policy framework and strategy and invite governments to adopt it, as the World Health Organization’s Regional Office for Europe is asking its 53 member states to do. However, the architects of Health 2020,1 2 WHO’s flagship strategy that has been in preparation for almost two years and will be launched at the 62nd Regional Committee in Malta, 10-14 September 2012, regard the timing as propitious. They insist that, although the economic and fiscal crises facing Europe present major challenges, they also present opportunities to renew efforts to improve the health of European people. The argument that lies at the heart of Health 2020 is that “good health is essential for economic and social development.” It echoes Derek Wanless’s recommendation a decade ago to the UK government that it should emphasise public health more strongly to ensure the survival of the NHS.3

WHO issues its European health report every three years. The 2012 report provides the context that explains why the Health 2020 strategy needs to be taken seriously.4 Although people across Europe are generally living longer, often in better health, these improvements are not being shared equally. Substantial health inequalities persist between and within countries and are increasing in some cases, as set out in WHO’s European review of social determinants of health …

Health requirements for pilgrims attending the Hajj in Mecca, Kingdom of Saudi Arabia, 24–29 October 2012

Eurosurveillance
Volume 17, Issue 37, 13 September 2012
http://www.eurosurveillance.org/Public/Articles/Archives.aspx?PublicationId=11678

News
Health requirements for pilgrims attending the Hajj in Mecca, Kingdom of Saudi Arabia, 24–29 October 2012
Eurosurveillance editorial team
European Centre for Disease Prevention and Control (ECDC), Stockholm, Sweden

Hajj is the annual pilgrimage to Mecca, the Kingdom of Saudi Arabia (KSA). The 2012 Hajj is expected to gather over two million Muslims from more than 180 countries across the globe between 24 and 29 October and is by far the largest mass gathering in the world. With the Hajj approaching, the Ministry of Health of Saudi Arabia has issued information in Arabic and English about health requirements and recommendations on its website [1].
A publication in the Weekly Epidemiological Record informs visitors in English and French of the full requirements for entry into Saudi Arabia and information is also available in English from The National Travel Health Network and Centre (NaTHNaC) website [2,3].
Special requirements for visitors to the Hajj concern vaccinations against meningococcal meningitis, polio and yellow fever.
Health authorities in countries of origin are required to provide information to pilgrims on infectious diseases symptoms, methods of transmission, complications and means of prevention. In an attempt to prevent the spread of foodborne infections Hajj performers are not allowed to bring fresh food to Saudi Arabia. Only properly canned or sealed food or food stored in containers with easy access for inspection is allowed in small quantities, sufficient for one person for the duration of his or her trip.
The KSA provides free healthcare to all visiting pilgrims during the Hajj, with the KSA Ministry of Health as one of the main contributors.

References
– Saudi Ministry of Health Requirements and Health Matters. Riyadh: Ministry of Hajj. Kingdom of Saudi Arabia. [Accessed 13 Sep 2012]. Available from: http://www.hajinformation.com/main/t20.htm

– Health conditions for travellers to Saudi Arabia for the pilgrimage to Mecca (Hajj). Wkly Epidemiol Rec. 2012;87(30):277-80.

– National Travel Health Network and Centre. Advice for Pilgrims for the Hajj and Umrah Season of 1433 (2012).  London: Health protection Agency. [accessed 13 Sep 2012]. Available from: http://www.nathnac.org/pro/factsheets/pdfs/Hajj_Umrah.pdf

Comment – Treatment of tuberculosis: have we turned the corner?

The Lancet  
Sep 15, 2012  Volume 380  Number 9846  p949 – 1030  e2 – 6
http://www.thelancet.com/journals/lancet/issue/current

Comment
Treatment of tuberculosis: have we turned the corner?
Giovanni Battista Migliori, Giovanni Sotgiu

Preview
The number of multidrug-resistant (MDR) tuberculosis cases officially reported to WHO increased from 29 000 to 53 000 between 2008 and 2010,1 still representing only 18% of the estimated 290 000 patients potentially identifiable if drug susceptibility testing was done in all notified cases of tuberculosis.1 A recent study done in Belarus2 showed a new global record for prevalence of MDR tuberculosis with 35·3% of new patients and 76·5% of previously treated patients diagnosed with the disease. This finding clearly shows how far case mismanagement can affect the chances to control (and eventually eliminate) the disease.

Effect of intermittent preventive treatment for malaria during infancy on serological responses to measles and other EPI vaccines

The Lancet  
Sep 15, 2012  Volume 380  Number 9846  p949 – 1030  e2 – 6
http://www.thelancet.com/journals/lancet/issue/current

Articles
Effect of intermittent preventive treatment for malaria during infancy on serological responses to measles and other vaccines used in the Expanded Programme on Immunization: results from five randomised controlled trials
Jane Crawley, Charalambos Sismanidis, Tracey Goodman, Paul Milligan, WHO Advisory Committee on serological responses to vaccines used in the Expanded Programme on Immunization in infants receiving Intermittent Preventive Treatment for malaria

Preview
IPTi with sulfadoxine-pyrimethamine does not affect serological responses to EPI vaccines. This analysis, therefore, supports the WHO recommendation for coadministration of IPTi with sulfadoxine-pyrimethamine to infants at the time of the second and third doses of DTP and measles vaccination, in areas of sub-Saharan Africa with moderate to high malaria transmission and where malaria parasites are sensitive to these drugs. It also suggests that treatment of clinical malaria at or around the time of vaccination does not compromise vaccine responsiveness.

WHO European review of social determinants of health and the health divide

The Lancet  
Sep 15, 2012  Volume 380  Number 9846  p949 – 1030  e2 – 6
http://www.thelancet.com/journals/lancet/issue/current

Review
WHO European review of social determinants of health and the health divide
Michael Marmot, Jessica Allen, Ruth Bell, Ellen Bloomer, Peter Goldblatt, on behalf of the Consortium for the European Review of Social Determinants of Health and the Health Divide

Summary
The European region has seen remarkable heath gains in those populations that have experienced progressive improvements in the conditions in which people are born, grow, live, and work. However, inequities, both between and within countries, persist. The review reported here, of inequities in health between and within countries across the 53 Member States of the WHO European region, was commissioned to support the development of the new health policy framework for Europe: Health 2020. Much more is understood now about the extent, and social causes, of these inequities, particularly since the publication in 2008 of the report of the Commission on Social Determinants of Health. The European review builds on the global evidence and recommends policies to ensure that progress can be made in reducing health inequities and the health divide across all countries, including those with low incomes. Action is needed—on the social determinants of health, across the life course, and in wider social and economic spheres—to achieve greater health equity and protect future generations

Waning Protection after Fifth Dose of Acellular Pertussis Vaccine in Children

New England Journal of Medicine
September 13, 2012  Vol. 367 No. 11
http://content.nejm.org/current.shtml

Original Article
Waning Protection after Fifth Dose of Acellular Pertussis Vaccine in Children
Nicola P. Klein, M.D., Ph.D., Joan Bartlett, M.P.H., M.P.P., Ali Rowhani-Rahbar, M.D., M.P.H., Ph.D., Bruce Fireman, M.A., and Roger Baxter, M.D.
N Engl J Med 2012; 367:1012-1019 September 13, 2012

Background
In the United States, children receive five doses of diphtheria, tetanus, and acellular pertussis (DTaP) vaccine before 7 years of age. The duration of protection after five doses of DTaP is unknown.

Methods
We assessed the risk of pertussis in children in California relative to the time since the fifth dose of DTaP from 2006 to 2011. This period included a large outbreak in 2010. We conducted a case–control study involving members of Kaiser Permanente Northern California who were vaccinated with DTaP at 47 to 84 months of age. We compared children with pertussis confirmed by a positive polymerase-chain-reaction (PCR) assay with two sets of controls: those who were PCR-negative for pertussis and closely matched controls from the general population of health-plan members. We used logistic regression to examine the risk of pertussis in relation to the duration of time since the fifth DTaP dose. Children who received whole-cell pertussis vaccine during infancy or who received any pertussis-containing vaccine after their fifth dose of DTaP were excluded.

Results
We compared 277 children, 4 to 12 years of age, who were PCR-positive for pertussis with 3318 PCR-negative controls and 6086 matched controls. PCR-positive children were more likely to have received the fifth DTaP dose earlier than PCR-negative controls (P<0.001) or matched controls (P=0.005). Comparison with PCR-negative controls yielded an odds ratio of 1.42 (95% confidence interval, 1.21 to 1.66), indicating that after the fifth dose of DTaP, the odds of acquiring pertussis increased by an average of 42% per year.

Conclusions
Protection against pertussis waned during the 5 years after the fifth dose of DTaP. (Funded by Kaiser Permanente).

Drs. Klein and Baxter report receiving grant support to their institution from Sanofi Pasteur, GlaxoSmithKline, Novartis, Merck, and Pfizer. No other potential conflict of interest relevant to this article was reported.

Addressing Health Inequalities in the Delivery of the HPV Vaccination Programme: Examining the Role of the School Nurse

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

Addressing Health Inequalities in the Delivery of the Human Papillomavirus Vaccination Programme: Examining the Role of the School Nurse
Tammy Boyce, Alison Holmes
PLoS ONE: Research Article, published 13 Sep 2012 10.1371/journal.pone.0043416

Abstract 
Background
HPV immunisation of adolescent girls is expected to have a significant impact in the reduction of cervical cancer. UK The HPV immunisation programme is primarily delivered by school nurses. We examine the role of school nurses in delivering the HPV immunisation programme and their impact on minimising health inequalities in vaccine uptake.

Methods and Findings
A rapid evidence assessment (REA) and semi-structured interviews with health professionals were conducted and analysed using thematic analysis. 80 health professionals from across the UK are interviewed, primarily school nurses and HPV immunisation programme coordinators. The REA identified 2,795 articles and after analysis and hand searches, 34 relevant articles were identified and analysed. Interviews revealed that health inequalities in HPV vaccination uptake were mainly related to income and other social factors in contrast to published research which emphasises potential inequalities related to ethnicity and/or religion. Most school nurses interviewed understood local health inequalities and made particular efforts to target girls who did not attend or missed doses. Interviews also revealed maintaining accurate and consistent records influenced both school nurses’ understanding and efforts to target inequalities in HPV vaccination uptake.

Conclusions
Despite high uptake in the UK, some girls remain at risk of not being vaccinated with all three doses. School nurses played a key role in reducing health inequalities in the delivery of the HPV programme. Other studies identified religious beliefs and ethnicity as potentially influencing HPV vaccination uptake but interviews for this research found this appeared not to have occurred. Instead school nurses stated girls who were more likely to be missed were those not in education. Improving understanding of the delivery processes of immunisation programmes and this impact on health inequalities can help to inform solutions to increase uptake and address health inequalities in childhood and adolescent vaccination programmes

Editorial: The Dual-Use Conundrum

Science        
14 September 2012 vol 337, issue 6100, pages 1265-1424
http://www.sciencemag.org/current.dtl

Editorial
The Dual-Use Conundrum
Paul Berg
Paul Berg is the Cahill Professor of Biochemistry, Emeritus, at the Stanford University School of Medicine, Palo Alto, CA. He received the Nobel Prize in Chemistry in 1980 and was an organizer of the Asilomar conference on recombinant DNA in 1975.

Summary
Scientists are increasingly able to create genetically modified microorganisms whose properties are perceived as being beneficial as well as potentially useful for malevolent purposes. In 2004, a committee of the U.S. National Academy of Sciences adopted the term “dual use” for instances in which genetic or biosynthetic manipulations create new microorganisms, which, although valuable scientifically, are susceptible to misuse.* The premise was that the prospects for malevolent outcomes derive from deliberate actions to inflict specific or widespread harm. But in those and subsequent discussions, too little attention was given to the likelihood of an accidental laboratory release of modified agents that would allow them to spread in susceptible human populations. Recent research with a highly pathogenic influenza virus has highlighted the importance of this issue. Reviews of the influenza research concluded that given “the risk of accidental or malicious release,” the benefits of such studies must be well justified.† Thus, specific guidelines must be enforced to thwart not only intentionally harmful outcomes but accidental releases as well.

Review: Rinderpest Eradication: Appropriate Technology and Social Innovations

Science        
14 September 2012 vol 337, issue 6100, pages 1265-1424
http://www.sciencemag.org/current.dtl

Review
Rinderpest Eradication: Appropriate Technology and Social Innovations
Jeffrey C. Mariner, James A. House, Charles A. Mebus, Albert E. Sollod, Dickens Chibeu, Bryony A. Jones, Peter L. Roeder, Berhanu Admassu, and Gijs G. M. van ’t Klooster

Abstract
Rinderpest is only the second infectious disease to have been globally eradicated. In the final stages of eradication, the virus was entrenched in pastoral areas of the Greater Horn of Africa, a region with weak governance, poor security, and little infrastructure that presented profound challenges to conventional control methods. Although the eradication process was a development activity rather than scientific research, its success owed much to several seminal research efforts in vaccine development and epidemiology and showed what scientific decision-making and management could accomplish with limited resources. The keys to success were the development of a thermostable vaccine and the application of participatory epidemiological techniques that allowed veterinary personnel to interact at a grassroots level with cattle herders to more effectively target control measures.

Measles, mumps, and rubella virus vaccine (M–M–RII): A review of 32 years of clinical and postmarketing experience

Vaccine
http://www.sciencedirect.com/science/journal/

Measles, mumps, and rubella virus vaccine (M–M–R™II): A review of 32 years of clinical and postmarketing experience
Available online 6 September 2012
In Press, Uncorrected ProofNote to users
Fabio Lievanoa, Susan A. Galeaa, Michele Thornton, Richard T. Wiedmanna, Susan Manoffa, Trung N. Trana, Manisha A. Amina, Margaret M. Seminacka, Kristen A. Vagiea,
Adrian Danaa, Stanley A. Plotkin

Abstract
M–M–RII (measles, mumps, and rubella virus vaccine live; Merck & Co., Inc.) is indicated for simultaneous vaccination against measles, mumps, and rubella in individuals ≥12 months of age. Before the vaccine era, these viruses infected most exposed individuals, with subsequent morbidity and mortality. One of the greatest achievements of public health has been to eliminate these 3 diseases in large geographic areas.

The safety profile of M–M–RII is described using data from routine global postmarketing surveillance. Postmarketing surveillance has limitations (including incomplete reporting of case data), but allows collection of real-world information on large numbers of individuals, who may have concurrent medical problems excluding them from clinical trials. It can also identify rare adverse experiences (AEs).

Over its 32-year history, 575 million doses of M–M–RII have been distributed worldwide, with 17,536 AEs voluntarily reported for an overall rate of 30.5 AEs/1,000,000 doses distributed. This review provides evidence that the vaccine is safe and well-tolerated.

A Human-Powered Refrigeration System To Save Lives In Developing Countries (Vaccines)

Scientific American
http://www.scientificamerican.com/
10 September 2012

A Human-Powered Refrigeration System To Save Lives In Developing Countries
Ariel Schwartz
It’s a big enough feat to ship much-needed vaccines to rural areas of the developing world. Finding a way to keep those vaccines refrigerated in places that have spotty access to electricity?
http://www.scientificamerican.com/article.cfm?id=a-human-powered-refrigeration-syste-2012-09

Twitter Watch [accessed 15 September 2012 15:08]

Twitter Watch  [accessed 15 September 2012  15:08]
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.

PAHO/WHO @pahowho
New regional agency will enhance joint action for public health in the Caribbean @carpha1 #carpha #caricom http://new.paho.org/hq/index.php?option=com_content&view=article&id=7180%3Anew-regional-agency-will-enhance-joint-action-for-public-health-in-the-caribbean&catid=1443%3Anews-front-page-items&lang=en&Itemid=1926#.UFTUZLp55C0.twitter …
12:18 PM – 15 Sep 12

Mirta Roses Periago ‏@mirtaroses
#CARPHA will become operational in Jan 2013 & merges the operations of 5 regional health institutions.Learn which here: http://psc28.wordpress.com/2012/09/14/third-caribbean-public-health-agency-carpha-international-partners-event/#more-204 …
Retweeted by PAHO/WHO
2:28 PM – 14 Sep 12

Partners In Health ‏@PIH
Sign the @HereIAmCampaign petition & urge world leaders to support a fully funded Global Fund to fight #AIDS #TB http://ow.ly/dJ55H 
9:01 AM – 15 Sep 12

Sabin Vaccine Inst.  ‏@sabinvaccine
Read about how @EmoryUniversity receives $6M #AIDS research grant from #GatesFoundation http://bit.ly/U7UMMJ 
1:11 PM – 14 Sep 12

HIVVaccineEnterprise ‏@HIVEnterprise
#AIDSVax2012 wraps up. Thanks to @HarvardCFAR and #Ragon Institute. Check our the webcasts, http://aidsvac.capitalreach.com/ . pic.twitter.com/pGBnvetK
Retweeted by IAVI
1:04 PM – 12 Sep 12

WHO ‏@WHO
WHO has deployed epidemiologists and logisticians from @WHOAFRO and HQ to support the #Ebola response in DR Congo http://goo.gl/PQ0rk 
5:44 AM – 14 Sep 12

World Bank @WorldBank
Free! Download the Global #Financial Development Report now: http://bit.ly/Q5rnBL 
12:07 PM – 13 Sep 12

Amanda Glassman @glassmanamanda
Where Will the World’s Poor Live? Updated Data on the Distribution of Global Poverty – http://www.cgdev.org/content/publications/detail/1426481/ … via @CGDev
8:21 AM – 13 Sep 12

GAVI Alliance ‏@GAVIAlliance
China ready to expand collaboration with @GAVIAlliance! Learn more on @GAVISeth 1st high-level visit to Beijing: http://ht.ly/dGyRx 
7:35 AM – 13 Sep 12

WHO ‏@WHO
Half of all children under-five deaths occurred in India, Nigeria, Democratic Republic of Congo, Pakistan and China http://goo.gl/ZJMx6 
10:51 PM – 12 Sep 12

Vaccines: The Week in Review 8 September 2012

Editor’s Notes:

Email Summary: Vaccines: The Week in Review is available as a weekly email summary: please send your request to david.r.curry@centerforvaccineethicsandpolicy.org.

pdf version: A pdf of the current issues is available here: Vaccines_The Week in Review_8 September 2012

Twitter: Readers can also follow developments on twitter: @vaxethicspolicy.

Support: If you would like to join the growing list of individuals who support this service and its contribution to their roles in public health, clinical practice, government, IGOs/NGOs, research, industry and academia, please visit this page at The Wistar Institute, our co-founder and fiduciary. Thank you…

ECDC updates guidance on HPV vaccines in Europe – continuing focus on immunising all girls/defers on boys

The European Centre for Disease Prevention and Control (ECDC) published an update to its 2008 guidance on human papillomavirus (HPV) vaccines in Europe “in light of the introduction of vaccination programmes in 19 European countries and new evidence from research studies in the past four years.” Randomised trials and observations from the field have demonstrated good safety profiles and efficacy against cervical cancer precursors. In spite of this, and that most of these countries are providing the vaccine for free, vaccination rates are lower than expected.

Vaccinating girls is shown to be more cost-effective than vaccinating boys. ECDC’s guidance is that public health initiatives should continue to focus on vaccinating girls.

Among the deterring factors for the slow uptake are the cost of the vaccine and the regime of three doses in six months. Routine vaccination targets girls between ages 10 to 14 years as the vaccines are clinically proven to be most effective when administered before the onset of sexual activity. These girls require parental permission to be vaccinated therefore the role of parents and healthcare workers is of utmost importance.

Nineteen countries out of the 29 EU/EEA countries have introduced HPV vaccination programmes following the authorisation of the vaccines but vaccination rates in EU countries range from only 17% to 84%. In 2010, only Portugal and the United Kingdom had full vaccination coverage rates above 80% for the target groups out of the seven countries reporting this data.

ECDC Director Marc Sprenger said: “We, public health authorities, frontline healthcare workers and parents alike, have a shared responsibility to protect thousands of women from cervical cancer. We need to work together to ensure that all girls between 10 and 14 years of age are vaccinated. European countries may need to examine why HPV vaccination coverage rates in their countries are not higher and strengthen their vaccination campaigns accordingly.”

Since its introduction by some European countries in 2006 the inclusion of boys in HPV vaccination programmes has been an open question. Only the quadrivalent HPV vaccine has been evaluated for men but current data shows that it gives the same, if not better, levels of efficacy for boys as girls of the same age groups. But the personal benefit of the vaccine for men in terms of cancer prevention is very low, most likely resulting in few boys being vaccinated and low vaccination coverage rates.

Marc Sprenger said “ECDC’s conclusion is that including boys in the current HPV vaccination programmes is unlikely to be cost-effective. A better investment of public resources is to focus on immunising all girls. This issue can be re-assessed when vaccination costs are significantly reduced.”

http://www.ecdc.europa.eu/en/press/Press%20Releases/20120905_pressrelease_HPVGuidanceUpdate%20(2).pdf

WHO DG Addresses Regional Committee for South-East Asia, Sixty-fifth Session – polio

Speech: WHO Director-General Address to the Regional Committee for South-East Asia, Sixty-fifth Session
Dr Margaret Chan
Director-General of the World Health Organization
Yogyakarta, Indonesia
5 September 2012
http://www.who.int/dg/speeches/2012/searo_20120905/en/index.html

Excerpt:
“…Let me begin with some well-deserved praise. On present trends, this region is set to be declared polio-free in January 2014.

India, the skeptics said it could not be done. But you did it. You stopped wild poliovirus transmission dead in its tracks. You have silenced the critics.

You have provided definitive proof that eradication is technically feasible, and you have done so in what was arguably the most challenging of all the remaining strongholds of this virus.

This is what your experience tells the world. The poliovirus is not permanently entrenched. It is not destined to remain a perpetual threat to each new generation of children. It can indeed be driven out of existence.

I fully agree with the assessment of the Independent Monitoring Board. This is a “magnificent” achievement. The Indian government succeeded because of its passionate engagement in a mission to protect its people from a vicious disease.

I appreciate, too, the specific lessons from the Indian experience set out in your report on polio eradication.

The most critical factor for success is ownership of the programme, from the local to the national level. The Indian government owned this programme, operating as the principal source of staff and funds. Other lessons include the importance of tight-knit partnerships, constant innovation, and a relentless drive to improve quality and accountability.

The May World Health Assembly elevated polio eradication to the level of a global public health emergency. This region has the expertise, bolstered by success, to lead the world in such an emergency response.

Medical officers from India, Bangladesh, and Nepal are now directly assisting countries that are still battling polio. I urge you to continue this leadership role. We can and must win.

As the IMB report noted, polio is now at its lowest level worldwide since records began.

Public health faces some heavy challenges, some bad trouble heading our way. Any longstanding problem that can be solved, once and for all, will free much-needed capacity and resources…”

http://www.who.int/csr/don/2012_09_08/en/index.html

Government of Japan commits US$9.07 million to GAVI

GAVI reported that the Government of Japan “underlined its commitment to protecting millions of children from vaccine-preventable diseases today by renewing its funding support for the GAVI Alliance.” Kimihiro Ishikane, Ambassador Extraordinary and Plenipotentiary Mission of Japan to the Association of Southeast Asian Nations, speaking at the Asia Pacific Development Summit, said, “For the fiscal year 2012, I am hereby happy to announce that Japan will make a contribution of US$9.07 million. Japan is also ready to make due contribution accordingly from the year 2013 onwards.”

http://www.gavialliance.org/library/news/press-releases/2012/japan-funds-life-saving-vaccines-for-developing-countries/

Weekly Epidemiological Record (WER) for 7 September 2012

The Weekly Epidemiological Record (WER) for 7 September 2012, vol. 87, 36 (pp. 337–344) includes:
Outbreak news
– Cholera, Sierra Leone
– Ebola haemorrhagic fever, Democratic Republic of the Congo
– Ebola haemorrhagic fever, Uganda
Performance of acute flaccid paralysis (AFP) surveillance and incidence of poliomyelitis, 2012

http://www.who.int/entity/wer/2012/wer8736.pdf

Update: Polio this week – As of 05 Sep 2012

Update: Polio this week – As of 05 Sep 2012
Global Polio Eradication Initiative

–          The outbreak in Katsina, northern Nigeria, is continuing, with four new wild poliovirus (WPV) type 1 cases reported this week. Katsina has reported 16 cases of WPV1 since May, more than any other state in the country. Katsina now accounts for 40% of all WPV1 cases in Nigeria since May. Upwards of one-third of children remain under-immunized in the state. During the most recent supplementary immunization activity (SIA), nearly one-third of children were missed in Katsina city (the most populous part of the state and location of the bulk of cases).

–          The Strategic Advisory Group of Experts on immunization (SAGE) Polio Working Group met this week in Geneva, Switzerland. Among other topics, the SAGE Polio Working Group discussed concrete ways to more effectively manage the short- and long-term implications of vaccine-derived polioviruses (VDPVs), including a potential switch from trivalent oral polio vaccine (OPV) to bivalent OPV even before the interruption of the remaining strains of WPV type 1 and WPV type 3. This approach had previously been endorsed in principle by SAGE. In May, the World Health Assembly (WHA) had requested the development of a comprehensive polio eradication and endgame strategy, to feature the potential timing of such a switch. The outcomes of the discussions from the SAGE Polio Working Group, and with continued guidance from SAGE and the WHA, will help inform a comprehensive Polio Eradication and Endgame Strategy 2014-2018.

http://www.polioeradication.org/Dataandmonitoring/Poliothisweek.aspx

Conference: AIDS Vaccine – BOSTON 9-12 SEPTEMBER 2012

Conference: AIDS Vaccine
BOSTON 9-12 SEPTEMBER 2012
“…the largest and most diverse international meeting of researchers, advocates, clinicians, private sector partners and public health experts working collaboratively to advance HIV vaccine science. With a focus on new minds and new ideas, AIDS Vaccine 2012 will make a special effort to welcome the most promising young- and early-career researchers to share and debate cutting-edge ideas and approaches to HIV vaccine research and development with their colleagues from around the world”

http://vaccineenterprise.org/conference/2012/

Symposium: Health and Human Security in the Americas Lima, Peru – 6-9 September 2012

Symposium: Health and Human Security in the Americas
PAHO, Japan Center for International Exchange (JCIE)
Lima, Peru, 6-9 September, 2012.

Preliminary Agenda:
http://new.paho.org/per/images/stories/FtPage/2012/20120905_agenda_eng.pdf

“PAHO/WHO and the Japan Center for International Exchange (JCIE) are co-hosting a Regional Meeting on Health and Human Security to be held in Lima, Peru, 6-9 September, 2012. The event will open on September 6th with a Symposium on Health and Human Security in the Americas.”
http://new.paho.org/per/index.php?option=com_content&task=view&id=1864&Itemid=724

Analysis: No more disease silos for sub-Saharan Africa

British Medical Journal
08 September 2012 (Vol 345, Issue 7873)
http://www.bmj.com/content/345/7873

Analysis
No more disease silos for sub-Saharan Africa
BMJ 2012; 345 doi: 10.1136/bmj.e5812 (Published 31 August 2012)
Cite this as: BMJ 2012;345:e5812
Patricio V Marquez, lead health specialist, Eastern and Southern Africa Region1, Jill L Farrington, honorary senior lecturer2

Extract
Countries in sub-Saharan Africa are facing a double burden of communicable and non-communicable disease. Patricio Marquez and Jill Farrington argue that knowledge of their common determinants and the links between diseases should be used to spur development of coordinated programmes to prevent and treat both

While much of the health focus in sub-Saharan Africa, has been directed at communicable diseases (particularly HIV/AIDS, tuberculosis, and malaria), non-communicable diseases are a growing problem for the region, causing almost one third of total deaths.1 The May 2012 World Health Assembly resolution on setting a global target for reducing non-communicable diseases2 and the pronouncements made at the 19th International AIDS Conference in July remind us of the similar challenges faced by these two sets of disease and the potential shared solutions. The theme of the AIDS conference “turning the tide together” seems apt and should give pause for thought in the lead-up to further debate about non-communicable diseases at the UN and other international forums.

The approach to preventing and treating HIV/AIDS—exemplified by an intention to build on lessons learnt, take account of recent scientific advances, and demonstrable ability to scale-up key interventions—seems particularly relevant to non-communicable diseases. But how should sub-Saharan Africa, well represented at the AIDS conference, gear up to the challenge of non-communicable diseases in a way that avoids creating new vertical programmes in competition for scarce resources?

What is the essence of the problem?

Although communicable diseases have traditionally been leading causes of disease and mortality in sub-Saharan Africa, rapid urbanisation, changes in dietary patterns, behavioural and biological factors, and major improvements in the prevention and treatment of communicable diseases, particularly AIDS, that are helping raise life expectancy, are all contributing to a shift in disease patterns. For some countries, such as Mauritius and Seychelles, and some populations, such as people aged over 45 years, …

http://www.bmj.com/content/345/bmj.e5812

A report on the large measles outbreak in Lyon, France, 2010 to 2011

Eurosurveillance
Volume 17, Issue 36, 06 September 2012
http://www.eurosurveillance.org/Public/Articles/Archives.aspx?PublicationId=11678

Surveillance and outbreak reports
A report on the large measles outbreak in Lyon, France, 2010 to 2011
by C Huoi, JS Casalegno, T Bénet, A Neuraz, G Billaud, D Eibach, Y Mekki, R Rudigoz, J Massardier, C Huissoud, M Massoud, P Gaucherand, O Claris, Y Gillet, D Floret, B Lina, P Vanhems

[Summary]
In 2010 and 2011, the city of Lyon, located in the Rhône-Alpes region (France), has experienced one of the highest incidences of measles in Europe. We describe a measles outbreak in the Lyon area, where cases were diagnosed at Lyon University hospitals (LUH) between 2010 and mid-2011. Data were collected from the mandatory notification system of the regional public health agency, and from the virology department of the LUH. All patients and healthcare workers who had contracted measles were included. Overall, 407 cases were diagnosed, with children of less than one year of age accounting for the highest proportion (n=129, 32%), followed by individuals between 17 and 29 years-old (n=126, 31%). Of the total cases, 72 (18%) had complications. The proportions of patients and healthcare workers who were not immune to measles were higher among those aged up to 30 years. Consequently, women of childbearing age constituted a specific population at high risk to contract measles and during this outbreak, 13 cases of measles, seven under 30 years-old, were identified among pregnant women. This study highlights the importance of being vaccinated with two doses of measles vaccine, the only measure which could prevent and allow elimination of the disease.

Incentives, health promotion and equality

Health Economics, Policy and Law 
Volume 7 – Issue 03 – July 2012
http://journals.cambridge.org/action/displayIssue?jid=HEP&tab=currentissue

Articles
Incentives, health promotion and equality
Kristin Voigt

Abstract
The use of incentives to encourage individuals to adopt ‘healthier’ behaviours is an increasingly popular instrument in health policy. Much of the literature has been critical of ‘negative’ incentives, often due to concerns about equality; ‘positive’ incentives, however, have largely been welcomed as an instrument for the improvement of population health and possibly the reduction of health inequalities. The aim of this paper is to provide a more systematic assessment of the use of incentives from the perspective of equality. The paper begins with an overview of existing and proposed incentive schemes. I then suggest that the distinction between ‘positive’ and ‘negative’ incentives – or ‘carrots’ and ‘sticks’ – is of limited use in distinguishing those incentive schemes that raise concerns of equality from those that do not. The paper assesses incentive schemes with respect to two important considerations of equality: equality of access and equality of outcomes. While our assessment of incentive schemes will, ultimately, depend on various empirical facts, the paper aims to advance the debate by identifying some of the empirical questions we need to ask. The paper concludes by considering a number of trade-offs and caveats relevant to the assessment of incentive schemes.

Varicella vaccine uptake in Shandong province, China

Human Vaccines & Immunotherapeutics(formerly Human Vaccines)
Volume 8, Issue 9  September 2012
http://www.landesbioscience.com/journals/vaccines/toc/volume/8/issue/8/

Short Report
Varicella vaccine uptake in Shandong province, China
http://dx.doi.org/10.4161/hv.20722
Authors: Aiqiang Xu, Qing Xu, Xueqiang Fang, Stephanie Bialek and Chengbin Wang

Abstract:
Varicella vaccine has been licensed in China for decade to be used as single dose in children aged ≥ 12 mo of age in private sector. Little data were available on varicella uptake to date in China yet. A cross-sectional study was conducted in Shandong Province in May 2011 to examine varicella vaccination coverage among children aged 16–40 mo and examine factors associated with varicella vaccine uptake. The overall coverage among children eligible for varicella vaccine was 62% (range 16.7–94.7% by county), much lower than the coverage of the eight vaccines included in the national immunization program (all above 97%). Though proximity to immunization services (< 5 km) was linked with higher vaccine uptake (62.6 vs. 37.4%, p = 0.02), county-level economic development (77.8, 61.0 and 47.1% for developed, sub-developed and developing regions, respectively, p < 0.001) played an even more important role in varicella vaccination. Moreover, there was little variation in coverage of vaccines included in the national immunization program along with county-level economic development. Even though varicella vaccine uptake is relatively high for use on a private basis, the vaccination coverage is not high enough to prevent epidemiology shift to adolescents and adults who are more prone to develop severe outcomes to varicella.    Further enhancement on varicella vaccination coverage is necessary and inclusion to national immunization program seems to be a promising option for achieving and maintaining high coverage.

Social and cultural determinants of oral cholera vaccine uptake in Zanzibar

Human Vaccines & Immunotherapeutics(formerly Human Vaccines)
Volume 8, Issue 9  September 2012
http://www.landesbioscience.com/journals/vaccines/toc/volume/8/issue/8/

Research Paper
Social and cultural determinants of oral cholera vaccine uptake in Zanzibar
http://dx.doi.org/10.4161/hv.20901
Authors: Christian Schaetti, Said M. Ali, Raymond Hutubessy, Ahmed M. Khatib, Claire-Lise Chaignat and Mitchell G. Weiss

Abstract:
Effectiveness of mass cholera vaccination campaigns requires not only technical and financial capacity but also consideration of social and cultural factors affecting vaccine acceptance. This study examined the influence of local community views of cholera on oral cholera vaccine (OCV) uptake in a mass vaccination campaign in 2009 in peri-urban and rural areas of Zanzibar. It used data from interviews conducted before the campaign and followed previous research assessing determinants of anticipated OCV acceptance. OCV uptake was lower than the reported anticipated acceptance. Less than half of the 356 adult respondents (49.7%) drank the required two doses of OCV. Variables referring to socio-cultural features of diarrheal illness that respondents identified with a cholera case vignette explained uptake better than analysis only of socio-demographic characteristics. Somatic features of illness not specific for cholera were negative determinants. Recognition of unconsciousness as a serious sign of dehydration and concern that cholera outbreaks would overwhelm the local healthcare system in the rural area were positive determinants of acceptance. Female gender, rural residence and older age were also positive determinants of OCV uptake. For further vaccine action with OCVs, cholera as a cause of severe dehydration should be distinguished from other causes of diarrhea. Planning should acknowledge rural concern about the relationship of limited capacity of the healthcare system to cope with cholera outbreaks and the priority of a cholera vaccine. Findings recommend particular efforts to increase cholera immunization coverage among young adults, in peri-urban areas and for men.

Individualism, acceptance and differentiation as attitude traits in the public’s response to vaccination

Human Vaccines & Immunotherapeutics(formerly Human Vaccines)
Volume 8, Issue 9  September 2012
http://www.landesbioscience.com/journals/vaccines/toc/volume/8/issue/8/

Research Paper
Individualism, acceptance and differentiation as attitude traits in the public’s response to vaccination
http://dx.doi.org/10.4161/hv.21183
Authors: Baruch Velan, Valentina Boyko, Liat Lerner-Geva, Arnona Ziv, Yaakov Yagar and Giora Kaplan

Abstract:
The attitude of the general public to vaccination was evaluated through a survey conducted on a representative sample of the Israeli population (n = 2,018), in which interviewees were requested to express their standpoints regarding five different vaccination programs. These included: pandemic influenza vaccination, seasonal influenza vaccination, travel vaccines, Human Papilloma Virus vaccine and childhood vaccinations. Analysis of the responses reveal three major attitude traits: a) acceptance, characterized by the opinion that targets should be vaccinated; b) individualism, characterized by the opinion that vaccination should be left to personal choice; and c) differentiation, characterized by the tendency to express different attitudes when addressing different vaccination programs. Interestingly, direct opposition to vaccination was found to be a minor attitude trait in this survey. Groups within the population could be defined according to their tendency to assume these different attitudes as Acceptors, Judicious-acceptors, Differentiators, Soft-individualists, and Hard-individualists. These groups expressed different standpoints on all five vaccination programs as well as on other health recommendations, such as screening for early detection of cancer. Attitude traits could be also correlated, to a certain extent, with actual compliance with vaccination programs. Interestingly, attitudes to vaccination were not correlated with social profiles related to income or education, although younger individuals exhibited higher degrees of individualism and differentiation. Taken together, all this is in accordance with the current social settings, underlining the individual’s tendency for critical evaluation and self-stirring. This should be taken into consideration by health authorities involved in vaccination programs.

Modeling the economic value of a Chagas’ disease therapeutic vaccine

Human Vaccines & Immunotherapeutics(formerly Human Vaccines)
Volume 8, Issue 9  September 2012
http://www.landesbioscience.com/journals/vaccines/toc/volume/8/issue/8/

Research Paper
Modeling the economic value of a Chagas’ disease therapeutic vaccine
http://dx.doi.org/10.4161/hv.20966
Authors: Bruce Y. Lee, Kristina M. Bacon, Angela R. Wateska, Maria Elena Bottazzi, Eric Dumonteil and Peter J. Hotez

Abstract:
The health burden of Chagas’ disease (resulting from Trypanosoma cruzi infection) in Latin America (estimated to outweigh that of malaria by 5-fold and affect 2–6 million people in Mexico alone) has motivated development of therapeutic vaccines to prevent infection progression to severe disease. Our economic model for a Chagas’ therapeutic vaccine in Mexico suggests that a vaccine would be highly cost-effective and in many cases economically dominant (providing both cost savings and health benefits) throughout a range of protection durations, severe adverse event risk, and dosing regimens and would be most likely to provide a positive return on investment if the vaccine prevented (rather than delayed) the onset of cardiomyopath

Cancer Vaccines/Immunotherapy – Commentary Series

Human Vaccines & Immunotherapeutics(formerly Human Vaccines)
Volume 8, Issue 9  September 2012
http://www.landesbioscience.com/journals/vaccines/toc/volume/8/issue/8/

Special Focus: Cancer Commentary Series Guest Editors: Michael G. Hanna and Alex Kudrin

Cancer Commentary Series
SPECIAL FOCUS REVIEW

Reimbursement challenges with cancer immunotherapeutics
Alex Kudrin
http://dx.doi.org/10.4161/hv.20550
Abstract |

SPECIAL FOCUS COMMENTARIES
Overview of cancer vaccines: Considerations for development
Alex Kudrin
http://dx.doi.org/10.4161/hv.20518
Abstract |

Cancer immunotherapy products: Regulatory aspects in the European Union
Jorge Camarero and Sol Ruiz
http://dx.doi.org/10.4161/hv.21142
Abstract |

Cancer vaccines and immunotherapeutics: Challenges for pricing, reimbursement and market access
Bengt Jönsson and Nils Wilking
Abstract |

Viewpoint: Ethical Challenges of Preexposure Prophylaxis for HIV

JAMA   
September 05, 2012, Vol 308, No. 9
http://jama.ama-assn.org/current.dtl

Viewpoint | September 5, 2012 ONLINE FIRST
Ethical Challenges of Preexposure Prophylaxis for HIV
Jonathan S. Jay, JD, MA; Lawrence O. Gostin, JD
JAMA. 2012;308(9):867-868. doi:10.1001/2012.jama.10158

Extract
On July 16, 2012, emtricitabine/tenofovir (Truvada; Gilead Sciences) became the first drug approved by the US Food and Drug Administration (FDA) for preexposure prophylaxis (PrEP) of human immunodeficiency virus (HIV) for adults at high risk. Clinical trials have demonstrated that daily use of oral antiretroviral drugs can reduce the risk of HIV acquisition through sexual intercourse. With 50 000 new HIV infections per year in the United States1 and 2 million per year worldwide,2 PrEP could become a major component of “combination prevention” along with condoms, counseling, testing, and treatment…

…EQUITY AND JUSTICE
Despite empowering patients and promoting the public’s health, PrEP could exacerbate health care inequalities. High cost and intense medical monitoring could exclude individuals with low income, unstable housing, drug dependence, or mental illness. This challenge is even greater in low-income countries with limited resources and infrastructure.

Early PrEP adopters are likely to include gay and bisexual men and heterosexual serodiscordant couples with greater education and resources. Extending PrEP to other groups will require effective public health governance, along with research and innovation. Fortunately, a blueprint exists: antiretroviral strategies for both HIV treatment and preventing mother-to-child transmission have relied on advances in science, financing, access, and health care to achieve remarkable success globally.

Underserved Populations. Reaching populations with disproportionate HIV incidence, including young black men who engage in male-to-male sexual contact, is crucial to reduce HIV burdens and promote equity. Although the Affordable Care Act will expand coverage, it cannot ensure testing and PrEP for all vulnerable individuals. Prevention programs should explore synergies with HIV testing campaigns, which currently link to treatment, but they could also link to PrEP for HIV-negative, high-risk individuals.

Women. The FDA approval includes at-risk women, despite mixed evidence of PrEP effectiveness but clear need: 25% of new HIV infections in the United States1 and half worldwide2 occur in women. PrEP addresses the need for a female-controlled prevention mechanism that can be used without a male partner’s consent. The efficacy of oral PrEP remains less certain for women than for men, although the results of the VOICE study (clinicaltrials.gov NCT00705679) are expected in 2013 and could alleviate concerns raised by the FEM-PrEP study, which closed early due to futility.7 A female-specific prevention method such as vaginal microbicide could enhance the effectiveness of chemoprophylaxis among women. The CAPRISA 004 trial found that topical tenofovir gel, used before and after sexual contact, reduced HIV acquisition by 39%.8

Generalized Epidemics. Most new HIV infections worldwide occur in developing countries experiencing generalized epidemics. Although the United States is the only country to have approved a PrEP indication, others may soon follow. PrEP rollout represents a vital test for governments, global health programs (eg, PEPFAR and the Global Fund to Fight AIDS, Tuberculosis and Malaria), and normative bodies (World Health Organization). Cost and health care infrastructure could represent major barriers to widespread PrEP availability. Planning for regulatory review, financing, and implementation must therefore continue.

Ethical Resource Allocation. Thousands of Americans with HIV are currently on waiting lists for drug treatment, even though effective treatment significantly reduces the risk of transmission.9 Given scarce resources, what are the relative priorities between PrEP for healthy individuals and treatment for currently infected individuals? Although these 2 uses may appear to entail inescapable trade-offs, expanding treatment for all infected individuals (which is now recommended),10 while selectively offering PrEP to high-risk individuals, is the best public health strategy and could lower health care costs in the long term.

Ethical Research. The FDA’s approval of PrEP will trigger scrutiny of HIV prevention trials using placebo controls. Beneficence requires researchers to minimize risks to study participants—and while regulatory approval alone does not determine the appropriate standard of care, it signals a strong evidence base and shifting clinical norms. Offering PrEP to study participants, however, presents scientific and logistical research challenges, with no consensus on how to balance conflicting obligations. Multistakeholder deliberations should proceed on this topic.

Viewpoint: Clinical Trial Data as a Public Good

JAMA   
September 05, 2012, Vol 308, No. 9
http://jama.ama-assn.org/current.dtl

Viewpoint | September 5, 2012
Clinical Trial Data as a Public Good
Marc A. Rodwin, JD, PhD; John D. Abramson, MD, MS
JAMA. 2012;308(9):871-872. doi:10.1001/jama.2012.9661

Extract
Knowledge of the benefits and risks of prescription drugs is based mainly on published reports of clinical trials, yet the medical literature may present an incomplete and potentially biased sample of clinical trials.1 Trials with positive results generally are published more frequently than studies that conclude that a new drug poses greater risks or is no more effective than standard therapy or a placebo. Furthermore, some articles may distort trial findings by omitting important data or by modifying prespecified outcome measures. Lack of access to detailed information about clinical trials can undermine the integrity of medical knowledge…

Medical Exemptions to School Immunization Requirements [U.S.]

Journal of Infectious Diseases
Volume 206 Issue 7 October 1, 2012
http://www.journals.uchicago.edu/toc/jid/current

EDITORIAL COMMENTARY
Keeping the M in Medical Exemptions: Protecting Our Most Vulnerable Children
Daniel A. Salmon and Neal A. Halsey

(See the brief report by Stadlin et al, on pages 989–92.)

In this issue of the journal, Stadlin et al report that, although the rates of medical exemptions to school immunization requirements are rather modest, easier processes for offering medical exemptions were associated with higher rates of medical exemptions [1]. This finding is consistent with previous studies that found that the ease of obtaining nonmedical religious or philosophical exemptions was associated with higher rates of exemptions [2, 3]. Interestingly, states with more difficult procedures for nonmedical exemptions had higher rates of medical exemptions, suggesting that some parents may be opting for medical exemptions when it is difficult to obtain nonmedical exemptions. This observation is consistent with our unpublished …

MAJOR ARTICLES AND BRIEF REPORTS
PUBLIC POLICY
Stephanie Stadlin, Robert A. Bednarczyk, and Saad B. Omer
Editor’s choice: Medical Exemptions to School Immunization Requirements in the United States—Association of State Policies With Medical Exemption Rates (2004–2011)
J Infect Dis. (2012) 206(7): 989-992 doi:10.1093/infdis/jis436

Abstract
All 50 US states allow medical exemptions from school entry immunization requirements. The extent to which medical exemptions are granted and the relationship with ease of obtaining these exemptions has not previously been examined in detail. We evaluated counts and rates of state-level medical exemptions to kindergarten entry requirements over 7 school years (2004–2005 through 2010–2011). During this period, 0.26%–0.41% of enrolled children received medical exemptions. In states with easier medical exemption criteria, medical exemption rates were significantly higher (adjusted incidence rate ratio: 6.4 [95% confidence interval: 2.7–15.6]). Routine evaluation of medical exemption rates is needed to ensure their appropriate use.

Re-emergence of cholera in the Americas: Risks, susceptibility, and ecology

Journal of Global Infectious Diseases (JGID) July-September 2012
Volume 4 | Issue 3   Page Nos. 139-186
http://www.jgid.org/currentissue.asp?sabs=n

ORIGINAL ARTICLE
Re-emergence of cholera in the Americas: Risks, susceptibility, and ecology
Mathieu JP Poirier1, Ricardo Izurieta1, Sharad S Malavade1, Michael D McDonald2
USA DOI: 10.4103/0974-777X.100576

Background: The re-emergence of cholera in Haiti has established a new reservoir for the seventh cholera pandemic which threatens to spread to other countries in the Americas. Materials and Methods: Statistics from this new epidemic are compared to the 1991 Peru epidemic, which demonstrated the speed and complexity with which this disease can spread from country to country. Environmental factors implicated in the spread of Vibrio cholerae such as ocean currents and temperatures, as well as biotic factors from zooplankton to waterfowl pose a risk for many countries in the Americas. Results: The movement of people and goods from Hispaniola are mostly destined for North America, but occur to some degree throughout the Americas. These modes of transmission, and the probability of uncontrolled community spread beyond Hispaniola, however, are completely dependent upon risk factors within these countries such as water quality and availability of sanitation. Although North America has excellent coverage of these deterrents to the spread of infectious gastrointestinal diseases, many countries throughout Latin America and the Caribbean lack these basic services and infrastructures. Conclusions : In order to curb the immediate spread of cholera in Hispaniola, treatment availability should be expanded to all parts of the island and phase II epidemic management initiatives must be developed.

It is the lifetime that matters: public preferences over maximising health and reducing inequalities in health

Journal of Medical Ethics
September 2012, Volume 38, Issue 9
http://jme.bmj.com/content/current

Brief report
It is the lifetime that matters: public preferences over maximising health and reducing inequalities in health
Paul Dolan1, Akil Tsuchiya2
Received 8 September 2011
Revised 10 February 2012
Accepted 3 March 2012
Published Online First 6 April 2012

Abstract
Scarce healthcare resources can be allocated in many ways. The National Institute for Health and Clinical Excellence in the UK focuses on the size of the benefit relative to costs, yet we know that there is support among clinicians and the general public for reducing inequalities in health. This paper shows how the UK general public trade-off these sometimes competing objectives, and the data we gather allow us to show the weight given to different population groups, for example, 1 extra year of life in full health to someone who would otherwise die at the age of 60 years is worth more than twice as much as an additional year of life to someone who would otherwise die at the age of 70 years. Such data can help inform the rationing decisions faced by all healthcare systems around the world.

Lancet: Universal Health Coverage – Editorial, Commrent, Series

The Lancet  
Sep 08, 2012  Volume 380  Number 9845  p859 – 948
http://www.thelancet.com/journals/lancet/issue/current

Editorial
The struggle for universal health coverage
The Lancet
Preview
Certain concepts resonate so naturally with the innate sense of dignity and justice within the hearts of men and women that they seem an insuppressible right. That health care should be accessible to all is surely one such concept. Yet in the past, this notion has struggled against barriers of self-interest and poor understanding. Building on several previous Lancet Series that have examined health and health systems in Mexico, China, India, southeast Asia, Brazil, and Japan, today we try to challenge those barriers with a collection of papers that make the ethical, political, economic, and health arguments in favour of universal health coverage (UHC), and which will be presented in New York on Sept 26, to coincide with the UN General Assembly.

Comment
Universal health coverage: the third global health transition?
Judith Rodin, David de Ferranti

Universal health coverage: good health, good economics
Julio Frenk, David de Ferranti

Universal health coverage is a development issue
David B Evans, Robert Marten, Carissa Etienne

Profile
Margaret Chan: committed to universal health coverage
David Holmes
Extract
Margaret Chan is a woman who needs little introduction. As WHO Director-General, her face is a fixture on news bulletins whenever there is a serious disease outbreak, drug safety issue, or food scare. But it was the less sensational—although some would argue more important—work that Chan and WHO are doing to promote universal health coverage that she was keen to talk about when she spoke to The Lancet.

Universal health coverage is, Chan says, “part of her DNA”, and has become an important part of WHO’s agenda under her stewardship. After her appointment for a second 5-year term as Director-General in May this year, Chan used her speech to the World Health Assembly to issue a stern rebuke to those “bitter observers” who say that the financial crisis “derailed the best chance ever to alleviate poverty and give this lopsided world greater fairness and balance”. Instead, Chan argued that “the best days for health are ahead of us, not behind us”, in large part because of the critical momentum that has built behind the move towards universal health coverage.

The launch in 2010 of WHO’s Health Systems Financing: the Path to Universal Coverage led to “more than 60 middle-income and low-income countries requesting technical assistance and advice to move towards universal health coverage”, Chan told The Lancet. She points to the “amazing achievement” of Mexico as a measure of what progress can be made. Universal health coverage is, Chan says, “the most powerful unifying single concept that public health has to offer, because you can realise the dream and the aspiration of health for every person irrespective of what class you belong to, whether you are a woman, or whether you are poor”.

Chan’s commitment to universal health coverage has been shaped by personal experience. Born in 1947 and brought up in Hong Kong under British rule, Chan says she “benefited from a similar system to the National Health Service in the UK”. Her mother, she says, was very “liberal minded”, and always told her to “follow her heart”, but it was following her “childhood sweetheart” (now her husband, David) that led her into medicine. After working as a teacher, Chan followed David to Canada and the University of Western Ontario in the early 1970s, where he was to study medicine. There, Chan was delighted to win a place to train in a Canadian health system already on the last leg of its journey towards universal health coverage…

Series
Universal Health Coverage
Does progress towards universal health coverage improve population health?
Rodrigo Moreno-Serra, Peter C Smith
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Universal Health Coverage
Political and economic aspects of the transition to universal health coverage
William D Savedoff, David de Ferranti, Amy L Smith, Victoria Fan
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Universal Health Coverage
Moving towards universal health coverage: health insurance reforms in nine developing countries in Africa and Asia
Gina Lagomarsino, Alice Garabrant, Atikah Adyas, Richard Muga, Nathaniel Otoo
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Viewpoint
Achieving universal health coverage in low-income settings
Jeffrey D Sachs
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The goal of universal health coverage is deeply embedded in politics, ethics, and international law. Article 25 of the 1948 Universal Declaration of Human Rights states that everyone has the right to a standard of living adequate for health, including medical care, and the right to security in the event of sickness or disability.1 Motherhood and childhood are to be afforded special care and assistance. In the same year, the Constitution of the World Health Organization came into force, declaring that “The enjoyment of the highest attainable standard of health is one of the fundamental rights of every human

Nature Editorial: Accountable and transparent (biomedical COI)

Nature  
Volume 489 Number 7414 pp5-170  6 September 2012
http://www.nature.com/nature/current_issue.html
Nature 489, 5  (06 September 2012)
doi:10.1038/489005a
Published online
05 September 2012

The US government has changed how biomedical scientists disclose their financial interests. The revised rules are welcome, but Internet access to the identified conflicts should be a requirement.

Toughened rules for how US biomedical scientists report financial interests came into force last month. The changes, which affect scientists who receive grants from the government, are welcome — although in one respect they do not go far enough.

About 38,000 researchers, most of them recipients of grants from the US National Institutes of Health (NIH), the world’s largest medical-research funder, will need to comply with the beefed-up rules. The changes update regulations put in place in 1995 to ensure that investigator bias doesn’t sway the design, conduct or reporting of research.

There are several important changes. First, investigators must now disclose to their institutions every “significant financial interest” belonging to themselves or their immediate family that is related to any of their institutional responsibilities — from teaching and seeing patients to lab research and service on ethics committees. This requirement appropriately casts a broader net than the previous rules, which generally asked for disclosure on only a project-specific basis.

The change ends ambiguity that, for instance, might have allowed a researcher to conclude that paid service on the board of a major pharmaceutical company drew only on clinical expertise, and therefore was not relevant to a government-funded research project that used one of the company’s experimental compounds. Under the updated rules, there will be no question that such income must be disclosed, and institutions will have a more complete picture of their scientists’ potentially relevant financial interests.

   “Public trust in the medical enterprise is at risk and must be built, not undermined.”

It takes only one example to drive home the significance of this change. Between January 2000 and January 2006, high-profile psychiatrist Charles Nemeroff, then at Emory University in Atlanta, Georgia, received more than US$800,000 in payments from drug-maker GlaxoSmithKline for over 250 speeches that he gave to psychiatrists. He failed to disclose this income to Emory administrators. After being discovered, Nemeroff argued that the rules on whether such income was reportable were ambiguous.

The tougher rules, crucially, give institutions prime responsibility for determining whether a given financial interest — company-paid speaking honoraria, consulting fees, paid authorship, travel reimbursements and stock ownership all qualify — is related to a government-funded grant, and whether it constitutes a conflict. Under the old regime, the scientist was charged with deciding whether a given interest was related to the research and thus whether it was reportable. That arrangement did not inspire confidence — a problem in an era in which public trust in the medical enterprise is at risk and must be built, not undermined.

The updated rules also lower the threshold at which an interest is defined as significant, from $10,000 under the old rules to $5,000. In a moribund economy with many US taxpayers struggling to make ends meet, this is fitting.

The rules have also been strengthened in other important ways. For instance, far more detail will now be reported by institutions to the NIH about each identified conflict, including the approximate dollar value of the interest and the measures being taken to manage or eliminate the conflict. There is also, importantly, an explicit exception to the disclosure requirements for income that scientists earn from universities or government agencies for teaching, serving on advisory or review panels and giving seminars or lectures.

The new rules fall down, however, in one significant regard. When it first published the proposed changes, the NIH described what it called “an important and significant new requirement to…underscore our commitment to fostering transparency, accountability, and public trust”.

That requirement was that institutions would post details of their investigators’ financial conflicts of interest on a publicly accessible website that was updated every year. In the final iteration of the new rules, the website has been made optional, and institutions faced with requests for information may instead respond in writing, within five business days. This is an outdated approach to transparency. It will not advance the public’s faith in timely, comprehensive and truly accessible disclosure, at a time when the boundary between academia and industry has become ever more porous, and when the average citizen’s trust in government-funded medical research is ever more crucial.   The NIH should revise the rules again to make the website mandatory. It is within the agency’s power to insist on this standard, and it is the right thing to do.

Tuberculosis, Drug Resistance, and the History of Modern Medicine

New England Journal of Medicine
September 6, 2012  Vol. 367 No. 10
http://content.nejm.org/current.shtml

Review Article
200th Anniversary Article
Tuberculosis, Drug Resistance, and the History of Modern Medicine
Salmaan Keshavjee, M.D., Ph.D., and Paul E. Farmer, M.D., Ph.D.
N Engl J Med 2012; 367:931-936September 6, 2012

Extract
Tuberculosis is a treatable airborne infectious disease that kills almost 2 million people every year. Multidrug-resistant (MDR) tuberculosis — by convention, a disease caused by strains of Mycobacterium tuberculosis that are resistant to isoniazid and rifampin, the backbone of first-line antituberculosis treatment — afflicts an estimated 500,000 new patients annually. Resistance to antituberculosis agents has been studied since the 1940s; blueprints for containing MDR tuberculosis were laid out in the clinical literature and in practice, in several settings, more than 20 years ago.1,2 Yet today, barely 0.5% of persons with newly diagnosed MDR tuberculosis worldwide receive treatment that is considered the standard of care in the United States.3 Those who have not received appropriate treatment continue to fuel a global pandemic that now includes strains resistant to most — and by some accounts all — classes of drugs tested. 4,5 Despite the enormity of the threat, investments to contain the epidemic and to cure infected patients have been halting and meager when compared, for example, with those made to address the acquired immunodeficiency syndrome (AIDS) pandemic. In this essay we seek to elucidate the reasons for the anemic response to drug-resistant tuberculosis by examining the recent history of tuberculosis policy…

Ethical Considerations in Studying Drug Safety — The Institute of Medicine Report

New England Journal of Medicine
September 6, 2012  Vol. 367 No. 10
http://content.nejm.org/current.shtml

Health Law, Ethics, and Human Rights
Ethical Considerations in Studying Drug Safety — The Institute of Medicine Report
Michelle M. Mello, J.D., Ph.D., Steven N. Goodman, M.D., M.H.S., Ph.D., and Ruth R. Faden, Ph.D., M.P.H.
N Engl J Med 2012; 367:959-964September 6, 2012

Extract
The tumult arising from revelations of serious safety risks associated with widely prescribed drugs, including rosiglitazone (Avandia, GlaxoSmithKline), rofecoxib (Vioxx, Merck), and celecoxib (Celebrex, Pfizer), has led to widespread recognition that improvement is needed in our national system of ensuring drug safety. Notwithstanding federal legislation in 2007 that strengthened the authority of the Food and Drug Administration (FDA) in the postmarketing period,1 critical weaknesses in the national system persist.

Central to these weaknesses are dilemmas surrounding not only the science but also the ethics of drug-safety research,2 many of which came to the fore in the heated public debate about the Thiazolidinedione Intervention with Vitamin D Evaluation (TIDE) trial, which compared the cardiovascular outcomes of long-term treatment with rosiglitazone with those of pioglitazone (Actos, Takeda) in patients with type 2 diabetes.3 At the request of the FDA, an Institute of Medicine (IOM) committee, on which we served, was convened to examine the ethics and science of FDA-required postmarketing safety research. In this article, we review the key ethics findings from the committee’s May 1, 2012, report4 and offer some reflections on the challenges ahead…

Is Universal HBV Vaccination of Healthcare Workers a Relevant Strategy in Developing Endemic Countries? [Niger]

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

Is Universal HBV Vaccination of Healthcare Workers a Relevant Strategy in Developing Endemic Countries? The Case of a University Hospital in Niger
Gérard Pellissier, Yazdan Yazdanpanah, Eric Adehossi, William Tosini, Boubacar Madougou, Kaza Ibrahima, Isabelle Lolom, Sylvie Legac, Elisabeth Rouveix, Karen Champenois, Christian Rabaud, Elisabeth Bouvet
PLoS ONE: Research Article, published 07 Sep 2012 10.1371/journal.pone.0044442

Abstract 
Background
Exposure to hepatitis B virus (HBV) remains a serious risk to healthcare workers (HCWs) in endemic developing countries owing to the strong prevalence of HBV in the general and hospital populations, and to the high rate of occupational blood exposure. Routine HBV vaccination programs targeted to high-risk groups and especially to HCWs are generally considered as a key element of prevention strategies. However, the high rate of natural immunization among adults in such countries where most infections occur perinatally or during early childhood must be taken into account.

Methodology/Principal Findings
We conducted a cross sectional study in 207 personnel of 4 occupational groups (medical, paramedical, cleaning staff, and administrative) in Niamey’s National Hospital, Niger, in order to assess the prevalence of HBV markers, to evaluate susceptibility to HBV infection, and to identify personnel who might benefit from vaccination. The proportion of those who declared a history of occupational blood exposure ranged from 18.9% in the administrative staff to 46.9% in paramedical staff. Only 7.2% had a history of vaccination against HBV with at least 3 injections. Ninety two percent were anti-HBc positive. When we focused on170 HCWs, only 12 (7.1%) showed no biological HBV contact. Twenty six were HBsAg positive (15,3%; 95% confidence interval: 9.9%–20.7%) of whom 8 (32%) had a viral load >2000 IU/ml.

Conclusions/Significance
The very small proportion of HCWs susceptible to HBV infection in our study and other studies suggests that in a global approach to prevent occupational infection by bloodborne pathogens, a universal hepatitis B vaccination of HCWs is not priority in these settings. The greatest impact on the risk will most likely be achieved by focusing efforts on primary prevention strategies to reduce occupational blood exposure. HBV screening in HCWs and treatment of those with chronic HBV infection should be however considered

Point-of-Care Testing for Infectious Diseases: Diversity, Complexity, and Barriers in Low- And Middle-Income Countries

PLoS Medicine
(Accessed 8 September 2012)
http://www.plosmedicine.org/article/browse.action?field=date

Point-of-Care Testing for Infectious Diseases: Diversity, Complexity, and Barriers in Low- And Middle-Income Countries
Nitika Pant Pai, Caroline Vadnais, Claudia Denkinger, Nora Engel, Madhukar Pai Policy Forum, published 04 Sep 2012
doi:10.1371/journal.pmed.1001306

Summary Points

– Enthusiasm and hope are increasing around point-of-care (POC) diagnostics for diseases of global health importance.

– The mere availability of rapid or simple tests does not automatically ensure their adoption or scale-up. A range of barriers prevent the successful use of POC testing—economic, regulatory, and policy-related, as well as user/provider perceptions and cultural barriers.

– Technology as such does not define a POC test. Rather, it is the successful use at the POC that defines a diagnostic process as POC testing. Thus, the focus must be on POC testing programs, rather than POC technologies.

– We discuss a framework that envisions POC testing as a spectrum of technologies (simplest to more sophisticated), users (lay persons to highly trained), and settings (homes, communities, clinics, peripheral laboratories, and hospitals).

– A deeper appreciation of this diversity in target product profiles, and likely barriers in each setting, might help test developers and public health managers to identify the most impactful product and delivery model.

Cost-effectiveness of tick-borne encephalitis vaccination in Slovenian adults

Vaccine
Volume 30, Issue 44, Pages 6225-6340 (28 September 2012)
http://www.sciencedirect.com/science/journal/0264410X/30/44

Cost-effectiveness of tick-borne encephalitis vaccination in Slovenian adults
Original Research Article
Pages 6301-6306
Renata Šmit

Abstract
Background
Slovenia is an endemic country with a high incidence rate of tick-borne encephalitis (TBE) and low vaccination coverage. TBE causes high costs for the health care insurances as well as the society due to hospitalization and frequent long term or permanent neurological sequelae. Vaccination is effective and a safe prophylaxis against TBE.

Objective
The purpose of this study was to evaluate the incremental cost-effectiveness ratio (ICER) between vaccination and no vaccination in Slovenia. The results are shown as cost per quality-adjusted life year (QALY) gained from the view of the health care payer and the society.

Methods
Based on the natural course of the disease, the Markov model was used for comparing the economic and health outcomes of vaccinated and unvaccinated groups from 18 to 80 years of age.

Results
The incremental cost-effectiveness ratio from the current Slovenian vaccination programme for FSME-Immun® compared to no vaccination amounts to €15,128 per QALY gained and for Encepur® €20,099 per QALY gained from the view of the health care payer. From the view of the society vaccination is cost saving, mainly due to avoiding the high indirect costs.

Conclusions
According to the cost-effectiveness threshold as proposed by the Slovenian Health Council, the current Slovenian vaccination programme against TBE is cost-effective from the health care payer’s perspective and also economical from the society’s perspective