PLoS Neglected Tropical Diseases (Accessed 23 August 2014)

PLoS Neglected Tropical Diseases
(Accessed 23 August 2014)
http://www.plosntds.org/

Vaccine Strategies for the Control and Prevention of Japanese Encephalitis in Mainland China, 1951–2011
Xiaoyan Gao, Xiaolong Li, Minghua Li, Shihong Fu, Huanyu Wang, Zhi Lu, Yuxi Cao, Ying He, Wuyang Zhu, Tingting Zhang, Ernest A. Gould, Guodong Liang Review | published 14 Aug 2014 | PLOS Neglected Tropical Diseases 10.1371/journal.pntd.0003015

Editorial
Outbreak of Ebola Virus Disease in Guinea: Where Ecology Meets Economy
Daniel G. Bausch mail, Lara Schwarz
Published: July 31, 2014
DOI: 10.1371/journal.pntd.0003056
Initial text
Ebola virus is back, this time in West Africa, with over 350 cases and a 69% case fatality ratio at the time of this writing [1]. The culprit is the Zaire ebolavirus species, the most lethal Ebola virus known, with case fatality ratios up to 90%. The epicenter and site of first introduction is the region of Guéckédou in Guinea’s remote southeastern forest region, spilling over into various other regions of Guinea as well as to neighboring Liberia and Sierra Leone (Figure 1). News of this outbreak engenders three basic questions: (1) What in the world is Zaire ebolavirus doing in West Africa, far from its usual haunts in Central Africa? (2) Why Guinea, where no Ebola virus has ever been seen before? (3) Why now? We’ll have to wait for the outbreak to conclude and more data analysis to occur to answer these questions in detail, and even then we may never know, but some educated speculation may be illustrative…

PNAS 100th Anniversary – Vaccines Special Feature

PNAS – Proceedings of the National Academy of Sciences of the United States of America
(Accessed 23 August 2014)
http://www.pnas.org/content/early/

Vaccines PNAS 100th Anniversary Special Feature – Introduction
Rino Rappuoli
PNAS 2014 ; published ahead of print August 19, 2014, doi:10.1073/pnas.1413559111
Full Text (PDF)
Excerpt
The special issue of the centenary of PNAS provides an opportunity to review the history of vaccines, the most exciting features of vaccine science, and to contemplate the future. The picture that emerges is intriguing: The history of vaccines confirms that vaccines have been the medical intervention with the greatest beneficial impact on human health and longevity (3). Vaccines dramatically reduced the incidence of infectious diseases that historically killed hundreds of millions, and made a substantial contribution to life expectancy that during the last century in developed countries increased from ∼47–80 y (4). During the last 30 y, improvements in our understanding of immunology and technological progress involving recombinant DNA, conjugation technology, and genomics provided vaccines against diseases, which could not be conquered by conventional vaccine technologies.

Finally, new, emerging, more powerful technologies, including rationally designed adjuvants and systems biology (4–6), raise the possibility of new and better vaccines that may allow better control of existing diseases and extend the benefits of vaccination to newly emerging infectious diseases and to noncommunicable diseases as well.
In the next few decades vaccines have the potential to continue to be the most powerful tool for advancing global health and contributing to human well-being by (i) extending the benefits of vaccination beyond childhood and especially among pregnant women and the elderly; (ii) providing tools to prevent and control emerging infections, such as pandemic influenza and HIV; (iii) preventing and controlling noncommunicable diseases, such as cancer, neurodegenerative, autoimmune, and metabolic disorders that are the leading causes of morbidity and mortality in modern society; (iv) extending the benefits of vaccination to low-income countries so that during the next two decades we can close the health and longevity gap between poor and rich countries (4, 7); and (v) controlling most of the existing, and reducing the emergence of, antibiotic-resistant bacteria (8).

The bitter truth is that although vaccines keep people healthy and save money, fewer and fewer pharmaceutical companies invest in the development of new vaccines. Rather, their investment dollars are channeled disproportionately to new drug therapies in areas such as oncology, immunology, inflammation, and cardiovascular, metabolic, and neurodegenerative diseases, for which the return on investment tends to be higher and more predictable than for vaccines….

History of vaccination
Stanley Plotkin1
Author Affiliations
Edited by Rino Rappuoli, Novartis Vaccines, Siena, Italy, and approved February 5, 2014 (received for review January 13, 2014)
Abstract
Vaccines have a history that started late in the 18th century. From the late 19th century, vaccines could be developed in the laboratory. However, in the 20th century, it became possible to develop vaccines based on immunologic markers. In the 21st century, molecular biology permits vaccine development that was not possible before.

Valuing vaccination
Till Bärnighausena,b, David E. Blooma,1, Elizabeth T. Cafiero-Fonsecaa, and Jennifer Carroll O’Briena
Author Affiliations
Edited by Rino Rappuoli, Novartis Vaccines, Siena, Italy, and approved July 18, 2014 (received for review March 20, 2014)
Abstract
Vaccination has led to remarkable health gains over the last century. However, large coverage gaps remain, which will require significant financial resources and political will to address. In recent years, a compelling line of inquiry has established the economic benefits of health, at both the individual and aggregate levels. Most existing economic evaluations of particular health interventions fail to account for this new research, leading to potentially sizable undervaluation of those interventions. In line with this new research, we set forth a framework for conceptualizing the full benefits of vaccination, including avoided medical care costs, outcome-related productivity gains, behavior-related productivity gains, community health externalities, community economic externalities, and the value of risk reduction and pure health gains. We also review literature highlighting the magnitude of these sources of benefit for different vaccinations. Finally, we outline the steps that need to be taken to implement a broad-approach economic evaluation and discuss the implications of this work for research, policy, and resource allocation for vaccine development and delivery.

Vaccines, new opportunities for a new society
Rino Rappuoli1, Mariagrazia Pizza, Giuseppe Del Giudice, and Ennio De Gregorio
Author Affiliations
Edited by Rafi Ahmed, Emory University, Atlanta, GA, and approved May 27, 2014 (received for review February 18, 2014)
Abstract
Vaccination is the most effective medical intervention ever introduced and, together with clean water and sanitation, it has eliminated a large part of the infectious diseases that once killed millions of people. A recent study concluded that since 1924 in the United States alone, vaccines have prevented 40 million cases of diphtheria, 35 million cases of measles, and a total of 103 million cases of childhood diseases. A report from the World Health Organization states that today vaccines prevent 2.5 million deaths per year: Every minute five lives are saved by vaccines worldwide. Overall, vaccines have done and continue to do an excellent job in eliminating or reducing the impact of childhood diseases. Furthermore, thanks to new technologies, vaccines now have the potential to make an enormous contribution to the health of modern society by preventing and treating not only communicable diseases in all ages, but also noncommunicable diseases such as cancer and neurodegenerative disorders. The achievement of these results requires the development of novel technologies and health economic models able to capture not only the mere cost–benefit of vaccination, but also the value of health per se.

Systems vaccinology: Probing humanity’s diverse immune systems with vaccines
Bali Pulendran1
Author Affiliations
Edited by Rino Rappuoli, Novartis Vaccines, Siena, Italy, and approved May 21, 2014 (received for review March 10, 2014)
Abstract
Homo sapiens are genetically diverse, but dramatic demographic and socioeconomic changes during the past century have created further diversification with respect to age, nutritional status, and the incidence of associated chronic inflammatory disorders and chronic infections. These shifting demographics pose new challenges for vaccination, as emerging evidence suggests that age, the metabolic state, and chronic infections can exert major influences on the immune system. Thus, a key public health challenge is learning how to reprogram suboptimal immune systems to induce effective vaccine immunity. Recent advances have applied systems biological analysis to define molecular signatures induced early after vaccination that correlate with and predict the later adaptive immune responses in humans. Such “systems vaccinology” approaches offer an integrated picture of the molecular networks driving vaccine immunity, and are beginning to yield novel insights about the immune system. Here we discuss the promise of systems vaccinology in probing humanity’s diverse immune systems, and in delineating the impact of genes, the environment, and the microbiome on protective immunity induced by vaccination. Such insights will be critical in reengineering suboptimal immune systems in immunocompromised populations.

Vaccines against poverty
Calman A. MacLennana,b,1 and Allan Saula
Author Affiliations
Edited by Inder M. Verma, The Salk Institute for Biological Studies, La Jolla, CA, and approved April 2, 2014 (received for review February 14, 2014)
Abstract
With the 2010s declared the Decade of Vaccines, and Millennium Development Goals 4 and 5 focused on reducing diseases that are potentially vaccine preventable, now is an exciting time for vaccines against poverty, that is, vaccines against diseases that disproportionately affect low- and middle-income countries (LMICs). The Global Burden of Disease Study 2010 has helped better understand which vaccines are most needed. In 2012, US$1.3 billion was spent on research and development for new vaccines for neglected infectious diseases. However, the majority of this went to three diseases: HIV/AIDS, malaria, and tuberculosis, and not neglected diseases. Much of it went to basic research rather than development, with an ongoing decline in funding for product development partnerships. Further investment in vaccines against diarrheal diseases, hepatitis C, and group A Streptococcus could lead to a major health impact in LMICs, along with vaccines to prevent sepsis, particularly among mothers and neonates. The Advanced Market Commitment strategy of the Global Alliance for Vaccines and Immunisation (GAVI) Alliance is helping to implement vaccines against rotavirus and pneumococcus in LMICs, and the roll out of the MenAfriVac meningococcal A vaccine in the African Meningitis Belt represents a paradigm shift in vaccines against poverty: the development of a vaccine primarily targeted at LMICs. Global health vaccine institutes and increasing capacity of vaccine manufacturers in emerging economies are helping drive forward new vaccines for LMICs. Above all, partnership is needed between those developing and manufacturing LMIC vaccines and the scientists, health care professionals, and policy makers in LMICs where such vaccines will be implemented.

Pan American Journal of Public Health (RPSP/PAJPH) July 2014

Revista Panamericana de Salud Pública/Pan American Journal of Public Health (RPSP/PAJPH)
July 2014 Vol. 36, No. 1
http://www.paho.org/journal/index.php?option=com_content&view=article&id=148&Itemid=261&lang=en

ORIGINAL RESEARCH ARTICLES
Factors associated with use of maternal health services in Haiti: a multilevel analysis [Factores asociados con la utilización de los servicios de salud materna en Haití: un análisis de varios niveles]
Stella O. Babalola

SPECIAL REPORTS
Building alliances for improving newborn health in Latin America and the Caribbean [Alianzas para mejorar la salud de los recién nacidos en América Latina y el Caribe]
Molly K. Miller-Petrie, Goldy Mazia, Magdalena Serpa,
Bertha Pooley, Margaret Marshall, Carlos Meléndez, and Marisol Vicuña

SPECIAL SECTION
Efectos combinados de la ampliación de la atención primaria de salud y de las transferencias condicionadas de dinero en efectivo sobre la mortalidad infantil en Brasil, 1998–2010 [The combined effects of the expansion of primary health care and conditional cash transfers on infant mortality in Brazil, 1998–2010]
Federico C. Guanais

Efficacy of inactivated poliovirus vaccine in India

Science
22 August 2014 vol 345, issue 6199, pages 845-976
http://www.sciencemag.org/current.dtl
Report
Efficacy of inactivated poliovirus vaccine in India
[free full text]
Hamid Jafari1,* Jagadish M. Deshpande2, Roland W. Sutter3, Sunil Bahl1, Harish Verma3, Mohammad Ahmad1, Abhishek Kunwar1, Rakesh Vishwakarma1, Ashutosh Agarwal1, Shilpi Jain4, Concepcion Estivariz5, Raman Sethi1, Natalie A. Molodecky3, Nicholas C. Grassly6, Mark A. Pallansch5, Arani Chatterjee4, R. Bruce Aylward3
Abstract
Inactivated poliovirus vaccine (IPV) is efficacious against paralytic disease, but its effect on mucosal immunity is debated. We assessed the efficacy of IPV in boosting mucosal immunity. Participants received IPV, bivalent 1 and 3 oral poliovirus vaccine (bOPV), or no vaccine. A bOPV challenge was administered 4 weeks later, and excretion was assessed 3, 7, and 14 days later. Nine hundred and fifty-four participants completed the study. Any fecal shedding of poliovirus type 1 was 8.8, 9.1, and 13.5% in the IPV group and 14.4, 24.1, and 52.4% in the control group by 6- to 11-month, 5-year, and 10-year groups, respectively (IPV versus control: Fisher’s exact test P < 0.001). IPV reduced excretion for poliovirus types 1 and 3 between 38.9 and 74.2% and 52.8 and 75.7%, respectively. Thus, IPV in OPV-vaccinated individuals boosts intestinal mucosal immunity.
Editor’s Summary
Two vaccines together are better than one alone
Polio is proving difficult to eradicate. Making the choice between administering a live attenuated vaccine orally (Sabin) or an inactivated vaccine (Salk) by injection has been highly controversial. Patients prefer the Sabin vaccine, but it requires many doses to offer immunity. Jafari et al. tested the two vaccines together in northern India. The injected vaccine significantly reduced virus shedding and boosted intestinal mucosal immunity in children already given the oral vaccine. Thus, using both vaccines could help speed the eventual global demise of polio.

Debate erupts on ‘repurposed’ drugs for Ebola

Science
15 August 2014 vol 345, issue 6198, pages 709-844
http://www.sciencemag.org/content/345/6198.toc
Special Issue: Parenting

Infectious Diseases
Debate erupts on ‘repurposed’ drugs for Ebola
Martin Enserink
With the outbreak of Ebola in West Africa escalating, some scientists think they can save lives by using existing, approved drugs that weren’t developed for Ebola but that might nonetheless help patients. Among the proposals being floated are interferon α and statins. The advantage of such existing drugs is that they have been tested for safety, and they are cheap and widely available. But some Ebola scientists oppose trying anything that has not been shown to reduce mortality from Ebola in nonhuman primates. They say that some of the drugs might make the disease worse, and even if they just aren’t effective, they might hamper the prospects for the long-term future of more promising drugs developed specifically for Ebola. So far, the World Health Organization appears to be skeptical as well.

Relative cost-effectiveness of a norovirus vaccine in the deployed military setting compared to a vaccine against Campylobacter sp., ETEC, and Shigella sp.

Vaccine
Volume 32, Issue 40, Pages 5145-5258 (8 September 2014)
http://www.sciencedirect.com/science/journal/0264410X/32/40
Relative cost-effectiveness of a norovirus vaccine in the deployed military setting compared to a vaccine against Campylobacter sp., ETEC, and Shigella sp.
Original Research Article
Pages 5156-5162
Aaron Tallant, Chad K. Porter, Shannon D. Putnam, David R. Tribble, Tomoko I. Hooper, Mark S. Riddle
Abstract
Norovirus (NoV) has been identified as a significant cause of acute gastrointestinal illness among deployed military troops. We conducted a cost-effectiveness analysis for the use of a NoV vaccine in the military using a previously developed model that evaluated vaccines for ETEC, Campylobacter, and Shigella for prevention of non-outbreak associated travelers’ diarrhea. Under conservative assumptions, acquisition of a NoV vaccine by the Department of Defense is estimated to result in a cost-effectiveness ratio per duty day lost to illness (CERDDL) of $1344 compared to a CERDDL of $776, $800, and $1275 for ETEC, Campylobacter sp., and Shigella sp., respectively compared to current management strategies. The absolute value of avoiding a duty day lost is likely to vary under different scenarios, and further study is needed to evaluate how improved diagnostics and prevention of outbreaks may impact the relative value of this vaccine. Overall, this study demonstrates the utility of a previously established evidence-based decision tool for prioritization of vaccine acquisition in an important target population.

Human papillomavirus (HPV) vaccination and subsequent sexual behaviour: Evidence from a large survey of Nordic women

Vaccine
Volume 32, Issue 39, Pages 4881-5144 (3 September 2014)
http://www.sciencedirect.com/science/journal/0264410X/32/39

Human papillomavirus (HPV) vaccination and subsequent sexual behaviour: Evidence from a large survey of Nordic women
Original Research Article
Pages 4945-4953
Bo T. Hansen, Susanne K. Kjær, Lisen Arnheim-Dahlström, Kai-Li Liaw, Kirsten E. Jensen, Louise T. Thomsen, Christian Munk, Mari Nygård
Abstract
Objective
To assess whether recipients and non-recipients of the human papillomavirus (HPV) vaccine subsequently differ in terms of sexual risk taking behaviour.
Design
Cross-sectional survey. Sequential analyses constructed from self-reported age at vaccination, age at first intercourse and age at response.
Setting
A random selection of women aged 18–46 years living in Denmark, Norway and Sweden in 2011–2012, eligible for opportunistic or organized catch-up HPV vaccination.
Participants
A total of 3805 women reported to have received the HPV vaccine and 40,247 reported not to have received it. Among vaccinees, 1539 received the HPV vaccine before or at the same age as sexual debut, of which 476 and 1063 were eligible for organized catch-up and opportunistic vaccination, respectively.
Main outcome measures
Self-reported sexual behaviour, compared by hazard ratios and odds ratios for women who received the HPV vaccine before or at the same age as sexual debut versus women who did not receive the HPV vaccine.
Results
HPV vaccination did not result in younger age at first intercourse. Women who received the HPV vaccine before or at the same age as sexual debut did not have more sexual partners than did non-vaccinees. Non-use of contraception during first intercourse was more common among non-vaccinees than among HPV vaccinees. The results were similar for organized catch-up and opportunistic vaccinees.
Conclusion
Women who received the HPV vaccine before or at the same age as sexual debut did not subsequently engage more in sexual risk taking behaviour than women who did not receive the HPV vaccine.

Duration of post-vaccination immunity against yellow fever in adults

Vaccine
Volume 32, Issue 39, Pages 4881-5144 (3 September 2014)
http://www.sciencedirect.com/science/journal/0264410X/32/39

Duration of post-vaccination immunity against yellow fever in adults
Original Research Article
Pages 4977-4984
Collaborative group for studies on yellow fever vaccines
Abstract
Introduction
Available scientific evidence to recommend or to advise against booster doses of yellow fever vaccine (YFV) is inconclusive. A study to estimate the seropositivity rate and geometric mean titres (GMT) of adults with varied times of vaccination was aimed to provide elements to revise the need and the timing of revaccination.
Methods
Adults from the cities of Rio de Janeiro and Alfenas located in non-endemic areas in the Southeast of Brazil, who had one dose of YFV, were tested for YF neutralising antibodies and dengue IgG. Time (in years) since vaccination was based on immunisation cards and other reliable records.
Results
From 2011 to 2012 we recruited 691 subjects (73% males), aged 18–83 years. Time since vaccination ranged from 30 days to 18 years. Seropositivity rates (95%C.I.) and GMT (International Units/mL; 95%C.I.) decreased with time since vaccination: 93% (88–96%), 8.8 (7.0–10.9) IU/mL for newly vaccinated; 94% (88–97), 3.0 (2.5–3.6) IU/mL after 1–4 years; 83% (74–90), 2.2 (1.7–2.8) IU/mL after 5–9 years; 76% (68–83), 1.7 (1.4–2.0) IU/mL after 10–11 years; and 85% (80–90), 2.1 (1.7–2.5) IU/mL after 12 years or more. YF seropositivity rates were not affected by previous dengue infection.
Conclusions
Even though serological correlates of protection for yellow fever are unknown, seronegativity in vaccinated subjects may indicate primary immunisation failure, or waning of immunity to levels below the protection threshold. Immunogenicity of YFV under routine conditions of immunisation services is likely to be lower than in controlled studies. Moreover, infants and toddlers, who comprise the main target group in YF endemic regions, and populations with high HIV infection rates, respond to YFV with lower antibody levels. In those settings one booster dose, preferably sooner than currently recommended, seems to be necessary to ensure longer protection for all vaccinees.

Valuing vaccines using value of statistical life measures

Vaccine
Volume 32, Issue 39, Pages 4881-5144 (3 September 2014)
http://www.sciencedirect.com/science/journal/0264410X/32/39

Valuing vaccines using value of statistical life measures
Original Research Article
Pages 5065-5070
Ramanan Laxminarayan, Dean T. Jamison, Alan J. Krupnick, Ole F. Norheim
Abstract
Vaccines are effective tools to improve human health, but resources to pursue all vaccine-related investments are lacking. Benefit–cost and cost-effectiveness analysis are the two major methodological approaches used to assess the impact, efficiency, and distributional consequences of disease interventions, including those related to vaccinations. Childhood vaccinations can have important non-health consequences for productivity and economic well-being through multiple channels, including school attendance, physical growth, and cognitive ability. Benefit–cost analysis would capture such non-health benefits; cost-effectiveness analysis does not. Standard cost-effectiveness analysis may grossly underestimate the benefits of vaccines.
A specific willingness-to-pay measure is based on the notion of the value of a statistical life (VSL), derived from trade-offs people are willing to make between fatality risk and wealth. Such methods have been used widely in the environmental and health literature to capture the broader economic benefits of improving health, but reservations remain about their acceptability. These reservations remain mainly because the methods may reflect ability to pay, and hence be discriminatory against the poor. However, willingness-to-pay methods can be made sensitive to income distribution by using appropriate income-sensitive distributional weights.
Here, we describe the pros and cons of these methods and how they compare against standard cost-effectiveness analysis using pure health metrics, such as quality-adjusted life years (QALYs) and disability-adjusted life years (DALYs), in the context of vaccine priorities. We conclude that if appropriately used, willingness-to-pay methods will not discriminate against the poor, and they can capture important non-health benefits such as financial risk protection, productivity gains, and economic wellbeing.

Parents’ preferences for seasonal influenza vaccine for their children in Japan

Vaccine
Volume 32, Issue 39, Pages 4881-5144 (3 September 2014)
http://www.sciencedirect.com/science/journal/0264410X/32/39

Parents’ preferences for seasonal influenza vaccine for their children in Japan
Original Research Article
Pages 5071-5076
Aiko Shono, Masahide Kondo
Abstract
In Japan, trivalent inactivated influenza vaccine is the only approved influenza vaccine. It is typically administrated by hypodermic injection, and children under 13 years of age are recommended to be vaccinated two times during each winter season. Live-attenuated influenza vaccine (LAIV) is administered by a thimerosal-free nasal spray. If LAIV is approved in the future in Japan, parents will have an alternative type of influenza vaccine for their children. This study investigated parents’ preference for the type of seasonal influenza vaccine for their children if alternatives are available. The marginal willingness to pay for vaccine benefits was also evaluated.
We conducted a discrete choice experiment, a quantitative approach that is often used in healthcare studies, in January 2013. Respondents were recruited from a registered online survey panel, and parents with at least one child under 13 years of age were offered questionnaires.
This study showed that for seasonal influenza vaccines for their children, parents are more likely to value safety, including thimerosal-free vaccines and those with a lower risk of adverse events, instead of avoiding the momentary pain from an injection. If LAIV is released in Japan, the fact that it is thimerosal-free could be an advantage. However, for parents to choose LAIV, they would need to accept the slightly higher risk of minor adverse events from LAIV.

Vaccination coverage and susceptibility against vaccine-preventable diseases of healthcare students in Athens, Greece

Vaccine
Volume 32, Issue 39, Pages 4881-5144 (3 September 2014)
http://www.sciencedirect.com/science/journal/0264410X/32/39

Vaccination coverage and susceptibility against vaccine-preventable diseases of healthcare students in Athens, Greece
Original Research Article
Pages 5083-5086
Katerina Karageorgou, Panos Katerelos, Andreas Efstathiou, Maria Theodoridou, Helena C. Maltezou
Abstract
Background
Vaccination of healthcare students is important to protect them from acquiring and transmitting vaccine-preventable diseases (VPDs) to high-risk patients and other healthcare workers (HCWs). The aim of the current study was to estimate the vaccination coverage, the susceptibility against VPDs, the knowledge and attitudes toward vaccinations of healthcare students studying at the Athens Technological Educational Institute.
Methods
The study was conducted during the academic year 2012–2013 using a standardized questionnaire.
Results
The mean knowledge score (correct answers) of healthcare students about the vaccines that are recommended by the Greek Ministry of Health for HCWs was 41%. Completed vaccination rates range from 19.6% for varicella to 80.2% for tetanus-diphtheria. A history of measles, mumps, rubella, varicella, hepatitis A, hepatitis B, or pertussis was reported by 8.2%, 4%, 5.4%, 70.4%, 1.5%, 0%, and 3% of students, respectively. Susceptibility rates were 20.5% against measles, 26.4% against mumps, 13.9% against rubella, 15.7% against varicella, 47.8% against hepatitis A, 17.3% against hepatitis B, and 19.8% against tetanus–diphtheria. Mandatory vaccination of HCWs was supported by 145 (96.7%) students.
Conclusions
There are significant immunity gaps against all VPDs among healthcare students in Athens. A system to easily identify non-immune students should be established in association with efficient reminder systems. Education of healthcare students about VPDs and vaccines will improve their attitudes toward vaccinations and their vaccination coverage. Mandatory vaccinations should be considered for HCWs in order to promote safety within healthcare facilities.

Examining Ontario’s universal influenza immunization program with a multi-strain dynamic model

Vaccine
Volume 32, Issue 39, Pages 4881-5144 (3 September 2014)
http://www.sciencedirect.com/science/journal/0264410X/32/39

Examining Ontario’s universal influenza immunization program with a multi-strain dynamic model
Original Research Article
Pages 5098-5117
E.W. Thommes, A. Chit, G.C. Meier, C.T. Bauch
Abstract
Seasonal influenza imposes a significant worldwide health burden each year. Mathematical models help us to understand how changes in vaccination affect this burden. Here, we develop a new dynamic transmission model which directly tracks the four dominant seasonal influenza strains/lineages, and use it to retrospectively examine the impact of the switch from a targeted to a universal influenza immunization program (UIIP) in the Canadian province of Ontario in 2000. According to our model results, averaged over the first four seasons post-UIIP, the rates of influenza-associated health outcomes in Ontario were reduced to about half of their pre-UIIP values. This is conservative compared to the results of a study estimating the UIIP impact from administrative data, though that study finds age-specific trends similar to those presented here. The strain interaction in our model, together with its flexible parameter calibration scheme, make it readily extensible to studying scenarios beyond the one explored here.

Vaccine – Special Issue: Vaccine-preventable Diseases and Vaccinations Among Health-care Workers

Vaccine
Volume 32, Issue 38, Pages 4813-4880 (27 August 2014)
http://www.sciencedirect.com/science/journal/0264410X/32/38
Special Issue: Vaccine-preventable Diseases and Vaccinations Among Health-care Workers
Edited by Helena C. Maltezou and Gregory A. Poland
Immunization of healthcare providers: A critical step toward patient safety
Page 4813
Helena C. Maltezou, G.A. Poland
Healthcare providers as sources of vaccine-preventable diseases
Review Article
Pages 4814-4822
Emily Sydnor, Trish M. Perl
A global perspective of vaccination of healthcare personnel against measles: Systematic review
Review Article
Pages 4823-4839
Amy Parker Fiebelkorn, Jane F. Seward, Walter A. Orenstein
Vaccination of health care workers against pertussis: Meeting the need for safety within hospitals
Original Research Article
Pages 4840-4843
U. Heininger
Vaccination of health care workers against influenza: Is it time to think about a mandatory policy in Europe?
Original Research Article
Pages 4844-4848
Sabine Wicker, Georg Marckmann
Incentives and barriers regarding immunization against influenza and hepatitis of health care workers
Pages 4849-4854
David FitzSimons, Greet Hendrickx, Tinne Lernout, Selim Badur, Alex Vorsters, Pierre Van Damme
Vaccinations among medical and nursing students: Coverage and opportunities
Original Research Article
Pages 4855-4859
Pierre Loulergue, Odile Launay
Addressing the anti-vaccination movement and the role of HCWs
Original Research Article
Pages 4860-4865
S. Tafuri, M.S. Gallone, M.G. Cappelli, D. Martinelli, R. Prato, C. Germinario
Professional and ethical responsibilities of health-care workers in regard to vaccinations
Original Research Article
Pages 4866-4868
Maria Theodoridou
Update on immunizations for healthcare personnel in the United States
Original Research Article
Pages 4869-4875
Thomas R. Talbot
Vaccination policies for healthcare workers in Europe
Original Research Article
Pages 4876-4880
Helena C. Maltezou, Gregory A. Poland

From Google Scholar+ [to 23 August 2014]

From Google Scholar & other sources: Selected Journal Articles, Newsletters, Dissertations, Theses, Commentary

Procedia in Vaccinology
Volume 8, 2014, Pages 68–76
7th Vaccine & ISV Annual Global Congress
Primary Cervical Cancer Prevention in Morocco: HPV Vaccine Awareness and Acceptability among Parents
M. Mouallifa, H. Bowyerb, S. Festalic, A. Albertd, Y. Filalie, S. Gueninf, P. Delvennef, J. Wallerb,
M. Ennajic
DOI: 10.1016/j.provac.2014.07.012
Abstract
Cervical cancer is a major public health concern in Morocco where it represents the second most common and lethal cancer in women. Human papillomavirus (HPV) vaccines have been licensed in Morocco since 2008 but there is no available data on their acceptability. This study aimed to assess awareness of HPV and the vaccine, and to identify factors associated with acceptability of the vaccine among parents in Morocco. A questionnaire-based survey using face-to-face interviews was conducted in a sample of 852 parents (670 mothers and 182 fathers) with at least one unmarried daughter ≤26 years. The study took place within public and private health centres and clinics in four regions in Morocco between July and August 2012. The main outcome measure was willingness to consider vaccinating a daughter against HPV. Responses revealed very low awareness of HPV infection (5%) and the HPV vaccine (14%). None of the participants had vaccinated their daughters against HPV and only 35% (32% of mothers and 45% of fathers) were willing to consider doing so in the future. Higher education and income, previous awareness of the HPV vaccine and endorsement of the belief that a recommendation from the ministry of health or a doctor to have the vaccine would be encouraging, were associated with mothers’ HPV vaccine acceptance. Non-acceptance among mothers was associated with having more than two daughters, believing the vaccine was expensive and lack of information. The only factor associated with the fathers’ acceptance of the vaccine was the cost. Increasing HPV and HPV vaccine awareness through educational campaigns, along with active recommendation by physicians and a publically funded vaccination programme could increase parental acceptance of the vaccine in Morocco.

Pediatrics
Published online August 18, 2014
doi: 10.1542/peds.2013-4077
Vaccine Message Framing and Parents’ Intent to Immunize Their Infants for MMR
Kristin S. Hendrix, PhDa,b, S. Maria E. Finnell, MD, MSa,b,c, Gregory D. Zimet, PhDa, Lynne A. Sturm, PhDa, Kathleen A. Lane, MSd, and Stephen M. Downs, MD, MSa,b
Author Affiliations
aDepartments of Pediatrics, and
dBiostatistics, Indiana University School of Medicine, Indianapolis, Indiana;
bRegenstrief Institute, Inc, Indianapolis, Indiana; and
cRyan White Center for Pediatric Infectious Disease, Riley Hospital for Children, Indianapolis, Indiana
Abstract
BACKGROUND AND OBJECTIVE: Emphasizing societal benefits of vaccines has been linked to increased vaccination intentions in adults. It is unclear if this pattern holds for parents deciding whether to vaccinate their children. The objective was to determine whether emphasizing the benefits of measles-mumps-rubella (MMR) vaccination directly to the vaccine recipient or to society differentially impacts parents’ vaccine intentions for their infants.
METHODS: In a national online survey, parents (N = 802) of infants CONCLUSION: This study concludes that despite the high level of awareness about tetanus and tetanus immunisation, there is a low coverage rate of tetanus immunisation among women of child bearing age in Ojodu LCDA of Lagos State. Women of child bearing age should also be targeted at the community level in tetanus immunisation campaign programme.

The Nigerian Postgraduate Medical Journal
2014, 21(2):107-114
Awareness, perception and coverage of tetanus immunisation in women of child bearing age in an urban district of Lagos, Nigeria.
Sule SS, Nkem-Uchendu C, Onajole AT, Ogunowo BE
National Postgraduate Medical College of Nigeria, Km 26 Lagos-Badagry Expressway, Ijanikin, Lagos. Nigeria.
Abstract
AIMS AND OBJECTIVES: This study assessed the level of awareness and perception of women of child bearing age to tetanus immunisation and determines the coverage rate in Ojodu Local Council Development Area (LCDA) of Lagos State, Nigeria.
SUBJECTS AND METHODS: This is a descriptive cross-sectional study of 288 women of child bearing age selected using multistage sampling technique. Information was obtained using structured close-ended questionnaire. Data analysis was done using Epi-InfoTM software, version 3.5.1.
RESULTS: There was high level of awareness of tetanus immunisation among respondents (89%) and as a method of prevention of tetanus (76%). There was a positive association between the level of awareness and respondents’ educational level and occupation (p < 0.05). However, there is a low level of awareness regarding the number of doses of the vaccine required in pregnancy(14.4%) and for life protection (19.5%). Those who ever received the vaccine, got it post-injury (48.9%) and in pregnancy (45.2%). Age, occupation and parity were positively associated with receiving the vaccine (p < 0.05), while parity and marital status were positively associated with number of dose of vaccine received (p < 0.05). Only about 20% of the respondents had received two or more doses of the vaccine.
CONCLUSION: This study concludes that despite the high level of awareness about tetanus and tetanus immunisation, there is a low coverage rate of tetanus immunisation among women of child bearing age in Ojodu LCDA of Lagos State. Women of child bearing age should also be targeted at the community level in tetanus immunisation campaign programme.

Epidemiology & Infection
2014 Aug 14:1-10. [Epub ahead of print]
http://journals.cambridge.org/action/displayIssue?jid=HYG&tab=currentissue
Transport networks and inequities in vaccination: remoteness shapes measles vaccine coverage and prospects for elimination across Africa.
Metcalf CJ1, Tatem A2, Bjornstad ON3, Lessler J4, O’Reilly K5, Takahashi S6, Cutts F7, Grenfell BT2.
Abstract
SUMMARY Measles vaccination is estimated to have averted 13•8 million deaths between 2000 and 2012. Persisting heterogeneity in coverage is a major contributor to continued measles mortality, and a barrier to measles elimination and introduction of rubella-containing vaccine. Our objective is to identify determinants of inequities in coverage, and how vaccine delivery must change to achieve elimination goals, which is a focus of the WHO Decade of Vaccines. We combined estimates of travel time to the nearest urban centre (⩾50 000 people) with vaccination data from Demographic Health Surveys to assess how remoteness affects coverage in 26 African countries. Building on a statistical mapping of coverage against age and geographical isolation, we quantified how modifying the rate and age range of vaccine delivery affects national coverage. Our scenario analysis considers increasing the rate of delivery of routine vaccination, increasing the target age range of routine vaccination, and enhanced delivery to remote areas. Geographical isolation plays a key role in defining vaccine inequity, with greater inequity in countries with lower measles vaccine coverage. Eliminating geographical inequities alone will not achieve thresholds for herd immunity, indicating that changes in delivery rate or age range of routine vaccination will be required. Measles vaccine coverage remains far below targets for herd immunity in many countries on the African continent and is likely to be inadequate for achieving rubella elimination. The impact of strategies such as increasing the upper age range eligible for routine vaccination should be considered.

Special Focus Newsletters
RotaFlash [PATH]
August 19, 2014
Headline: Rotavirus vaccines now in Niger and Eritrea
Dual launch in Niger means more children’s lives saved more quickly

Confidence Commentary from Dr Heidi Larson
Distrust and fear fuel two International Public Health Emergencies in 2014
The Vaccine Confidence Project
London School of Hygiene and Tropical Medicine

Ebola [to 23 August 2014]

Forbes
http://www.forbes.com/
Accessed 23 August 2014
As Ebola Outbreak Expands, These Experimental Drugs Could See Action
Scott Gottlieb Contributor
…There are at least three vaccines in development for Ebola that are garnering attention….

Foreign Policy
http://www.foreignpolicy.com/
Accessed 23 August 2014
The Race to Develop an Ebola Vaccine
BY Siddhartha Mahanta 12 August 2014

New Yorker
http://www.newyorker.com/
Ebolanomics
The Economics of Ebola Drugs
By James Surowiecki
August 25, 2014
The deadly hemorrhagic fever Ebola was first discovered in 1976, and it has haunted the public imagination for twenty years, ever since the publication of Richard Preston’s “The Hot Zone.” Yet, in all that time, no drug has ever been approved to treat the disease. Now the deadliest outbreak yet is raging in West Africa, and there are no real tools to stop it. (Supplies of the experimental drug administered to two American patients have already run out.) The lack of an Ebola treatment is disturbing. But, given the way drug development is funded, it’s also predictable…
Ebola and the Fiction of Quarantine
By Geoff Manaugh and Nicola Twilley
August 11, 2014
Excerpts
Amid heated debate, the Ebola virus came to the United States on Saturday, August 2, 2014, aboard a Gulfstream jet chartered by the Centers for Disease Control and Prevention. The virus was carried in the bloodstream of Doctor Kent Brantly, who travelled within an Aeromedical Biological Containment System—a hermetically sealed, transparent plastic tent that isolated the patient from the flight crew…
…Medical quarantine has its own architecture: levels of separation and isolation, nests inside of nests. The structure’s first level, according to Jonathan Richmond, a biosecurity consultant who spent thirty-five years at the C.D.C., consists of “not much of anything at all, except simple behavioral guidelines like, ‘Don’t stick things in your mouth.’ ” Biosafety levels three and four are typically reserved for airborne diseases. Ones that only spread through contact, like the Ebola virus, normally call for level-two containment. But because Ebola has no proven vaccine or cure, Brantly, who was transported to Emory Hospital in Atlanta, has been under level-four containment—a protocol that requires what Richmond calls “extraordinary engineering controls.”…

Reuters
http://www.reuters.com/
Accessed 23 August 2014
Experimental Ebola drugs needed for “up to 30,000 people”
Wed Aug 20, 2014 1:00pm EDT
:: Scientists estimate need for drugs, vaccines in West Africa
:: Study shows dilemma after WHO backs use of untested drugs
:: Only tiny quantities of experimental medicines available
:: 17 drugs and 12 vaccines in pipeline, but progress slow

Vaccines and Global Health: The Week in Review 9 August 2014

Vaccines and Global Health: The Week in Review will resume publication on 23 August following a short annual leave for the Editor]

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

.Request an Email Summary: Vaccines and Global health : The Week in Review is published as a single email summary, scheduled for release each Saturday evening before midnight (EDT in the U.S.). If you would like to receive the email version, please send your request to david.r.curry@centerforvaccineethicsandpolicy.org.
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pdf versionA pdf of the current issues is available here: Vaccines and Global Health_The Week in Review_9 August 2014

Twitter:  Readers can also follow developments on twitter: @vaxethicspolicy.
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Links:  We endeavor to test each link as we incorporate it into any post, but recognize that some links may become “stale” as publications and websites reorganize content over time. We apologize in advance for any links that may not be operative. We believe the contextual information in a given post should allow retrieval, but please contact us as above for assistance if necessary.
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David R. Curry, MS
Executive Director
Center for Vaccine Ethics and Policy
a program of the
– Division of Medical Ethics, NYU Medical School
– The Wistar Institute Vaccine Center
– Children’s Hospital of Philadelphia Vaccine Education Center
Associate Faculty, Division of Medical Ethics, NYU Medical School

WHO Statement on the Meeting of the International Health Regulations Emergency Committee Regarding the 2014 Ebola Outbreak in West Africa

Ebola outbreak in west Africa: Meeting of the International Health Regulations Emergency Committee
8 August 2014 — The first meeting of the Emergency Committee convened by the Director-General under the International Health Regulations (2005) regarding the 2014 Ebola Virus Disease outbreak in West Africa was held by teleconference on 6-7 August 2014. The Director-General accepted the Committee’s assessment and on 8 August 2014 declared the Ebola outbreak in West Africa a Public Health Emergency of International Concern.

WHO Statement on the Meeting of the International Health Regulations Emergency Committee Regarding the 2014 Ebola Outbreak in West Africa
WHO statement
8 August 2014
[full text]
The first meeting of the Emergency Committee convened by the Director-General under the International Health Regulations (2005) [IHR (2005)] regarding the 2014 Ebola Virus Disease (EVD, or “Ebola”) outbreak in West Africa was held by teleconference on Wednesday, 6 August 2014 from 13:00 to 17:30 and on Thursday, 7 August 2014 from 13:00 to 18:30 Geneva time (CET).

Members and advisors of the Emergency Committee met by teleconference on both days of the meeting1. The following IHR (2005) States Parties participated in the informational session of the meeting on Wednesday, 6 August 2014: Guinea, Liberia, Sierra Leone, and Nigeria.

During the informational session, the WHO Secretariat provided an update on and assessment of the Ebola outbreak in West Africa. The above-referenced States Parties presented on recent developments in their countries, including measures taken to implement rapid control strategies, and existing gaps and challenges in the outbreak response.

After discussion and deliberation on the information provided, the Committee advised that:
:: the Ebola outbreak in West Africa constitutes an ‘extraordinary event’ and a public health risk to other States;
:: the possible consequences of further international spread are particularly serious in view of the virulence of the virus, the intensive community and health facility transmission patterns, and the weak health systems in the currently affected and most at-risk countries.
:: a coordinated international response is deemed essential to stop and reverse the international spread of Ebola.

It was the unanimous view of the Committee that the conditions for a Public Health Emergency of International Concern (PHEIC) have been met.

The current EVD outbreak began in Guinea in December 2013. This outbreak now involves transmission in Guinea, Liberia, Nigeria, and Sierra Leone. As of 4 August 2014, countries have reported 1 711 cases (1 070 confirmed, 436 probable, 205 suspect), including 932 deaths. This is currently the largest EVD outbreak ever recorded. In response to the outbreak, a number of unaffected countries have made a range of travel related advice or recommendations.

In light of States Parties’ presentations and subsequent Committee discussions, several challenges were noted for the affected countries:
:: their health systems are fragile with significant deficits in human, financial and material resources, resulting in compromised ability to mount an adequate Ebola outbreak control response;
:: inexperience in dealing with Ebola outbreaks; misperceptions of the disease, including how the disease is transmitted, are common and continue to be a major challenge in some communities;
:: high mobility of populations and several instances of cross-border movement of travellers with infection;
:: several generations of transmission have occurred in the three capital cities of Conakry (Guinea); Monrovia (Liberia); and Freetown (Sierra Leone); and
:: a high number of infections have been identified among health-care workers, highlighting inadequate infection control practices in many facilities.
The Committee provided the following advice to the Director-General for her consideration to address the Ebola outbreak in accordance with IHR (2005).
::
States with Ebola transmission
:: The Head of State should declare a national emergency; personally address the nation to provide information on the situation, the steps being taken to address the outbreak and the critical role of the community in ensuring its rapid control; provide immediate access to emergency financing to initiate and sustain response operations; and ensure all necessary measures are taken to mobilize and remunerate the necessary health care workforce.
:: Health Ministers and other health leaders should assume a prominent leadership role in coordinating and implementing emergency Ebola response measures, a fundamental aspect of which should be to meet regularly with affected communities and to make site visits to treatment centres.
:: States should activate their national disaster/emergency management mechanisms and establish an emergency operation centre, under the authority of the Head of State, to coordinate support across all partners, and across the information, security, finance and other relevant sectors, to ensure efficient and effective implementation and monitoring of comprehensive Ebola control measures. These measures must include infection prevention and control (IPC), community awareness, surveillance, accurate laboratory diagnostic testing, contact tracing and monitoring, case management, and communication of timely and accurate information among countries. For all infected and high risks areas, similar mechanisms should be established at the state/province and local levels to ensure close coordination across all levels.
:: States should ensure that there is a large-scale and sustained effort to fully engage the community – through local, religious and traditional leaders and healers – so communities play a central role in case identification, contact tracing and risk education; the population should be made fully aware of the benefits of early treatment.
:: It is essential that a strong supply pipeline be established to ensure that sufficient medical commodities, especially personal protective equipment (PPE), are available to those who appropriately need them, including health care workers, laboratory technicians, cleaning staff, burial personnel and others that may come in contact with infected persons or contaminated materials.
:: In areas of intense transmission (e.g. the cross border area of Sierra Leone, Guinea, Liberia), the provision of quality clinical care, and material and psychosocial support for the affected populations should be used as the primary basis for reducing the movement of people, but extraordinary supplemental measures such as quarantine should be used as considered necessary.
:: States should ensure health care workers receive: adequate security measures for their safety and protection; timely payment of salaries and, as appropriate, hazard pay; and appropriate education and training on IPC, including the proper use of PPEs.
:: States should ensure that: treatment centres and reliable diagnostic laboratories are situated as closely as possible to areas of transmission; that these facilities have adequate numbers of trained staff, and sufficient equipment and supplies relative to the caseload; that sufficient security is provided to ensure both the safety of staff and to minimize the risk of premature removal of patients from treatment centres; and that staff are regularly reminded and monitored to ensure compliance with IPC.
:: States should conduct exit screening of all persons at international airports, seaports and major land crossings, for unexplained febrile illness consistent with potential Ebola infection. The exit screening should consist of, at a minimum, a questionnaire, a temperature measurement and, if there is a fever, an assessment of the risk that the fever is caused by EVD. Any person with an illness consistent with EVD should not be allowed to travel unless the travel is part of an appropriate medical evacuation.
:: There should be no international travel of Ebola contacts or cases, unless the travel is part of an appropriate medical evacuation. To minimize the risk of international spread of EVD:
– Confirmed cases should immediately be isolated and treated in an Ebola Treatment Centre with no national or international travel until 2 Ebola-specific diagnostic tests conducted at least 48 hours apart are negative;
– Contacts (which do not include properly protected health workers and laboratory staff who have had no unprotected exposure) should be monitored daily, with restricted national travel and no international travel until 21 days after exposure;
– Probable and suspect cases should immediately be isolated and their travel should be restricted in accordance with their classification as either a confirmed case or contact.
:: States should ensure funerals and burials are conducted by well-trained personnel, with provision made for the presence of the family and cultural practices, and in accordance with national health regulations, to reduce the risk of Ebola infection. The cross-border movement of the human remains of deceased suspect, probable or confirmed EVD cases should be prohibited unless authorized in accordance with recognized international biosafety provisions.
:: States should ensure that appropriate medical care is available for the crews and staff of airlines operating in the country, and work with the airlines to facilitate and harmonize communications and management regarding symptomatic passengers under the IHR (2005), mechanisms for contact tracing if required and the use of passenger locator records where appropriate.
:: States with EVD transmission should consider postponing mass gatherings until EVD transmission is interrupted.
::
States with a potential or confirmed Ebola Case, and unaffected States with land borders with affected States
:: Unaffected States with land borders adjoining States with Ebola transmission should urgently establish surveillance for clusters of unexplained fever or deaths due to febrile illness; establish access to a qualified diagnostic laboratory for EVD; ensure that health workers are aware of and trained in appropriate IPC procedures; and establish rapid response teams with the capacity to investigate and manage EVD cases and their contacts.
:: Any State newly detecting a suspect or confirmed Ebola case or contact, or clusters of unexplained deaths due to febrile illness, should treat this as a health emergency, take immediate steps in the first 24 hours to investigate and stop a potential Ebola outbreak by instituting case management, establishing a definitive diagnosis, and undertaking contact tracing and monitoring.
:: If Ebola transmission is confirmed to be occurring in the State, the full recommendations for States with Ebola Transmission should be implemented, on either a national or subnational level, depending on the epidemiologic and risk context.
::
All States
:: There should be no general ban on international travel or trade; restrictions outlined in these recommendations regarding the travel of EVD cases and contacts should be implemented.
:: States should provide travelers to Ebola affected and at-risk areas with relevant information on risks, measures to minimize those risks, and advice for managing a potential exposure.
:: States should be prepared to detect, investigate, and manage Ebola cases; this should include assured access to a qualified diagnostic laboratory for EVD and, where appropriate, the capacity to manage travelers originating from known Ebola-infected areas who arrive at international airports or major land crossing points with unexplained febrile illness.
:: The general public should be provided with accurate and relevant information on the Ebola outbreak and measures to reduce the risk of exposure.
:: States should be prepared to facilitate the evacuation and repatriation of nationals (e.g. health workers) who have been exposed to Ebola.
The Committee emphasized the importance of continued support by WHO and other national and international partners towards the effective implementation and monitoring of these recommendations.
Based on this advice, the reports made by affected States Parties and the currently available information, the Director-General accepted the Committee’s assessment and on 8 August 2014 declared the Ebola outbreak in West Africa a Public Health Emergency of International Concern (PHEIC). The Director-General endorsed the Committee’s advice and issued them as Temporary Recommendations under IHR (2005) to reduce the international spread of Ebola, effective 8 August 2014. The Director-General thanked the Committee Members and Advisors for their advice and requested their reassessment of this situation within 3 months.

Ebola – West Africa (to 9 August 2014)

WHO to convene ethical review of experimental treatment for Ebola
WHO statement
6 August 2014
Early next week, WHO will convene a panel of medical ethicists to explore the use of experimental treatment in the ongoing Ebola outbreak in West Africa. Currently there is no registered medicine or vaccine against the virus, but there are several experimental options under development.
The recent treatment of two health workers from Samaritan’s Purse with experimental medicine has raised questions about whether medicine that has never been tested and shown to be safe in people should be used in the outbreak and, given the extremely limited amount of medicine available, if it is used, who should receive it.
“We are in an unusual situation in this outbreak. We have a disease with a high fatality rate without any proven treatment or vaccine,” says Dr Marie-Paule Kieny, Assistant Director-General at the World Health Organization. “We need to ask the medical ethicists to give us guidance on what the responsible thing to do is.”
The gold standard for assessing new medicine involves a series of trials in humans, starting small to make sure the medicine is safe to use. Then, the studies are expanded to more people to see how effective it is, and how best to use it.
The guiding principle with use of any new medicine is ‘do no harm’. Safety is always the main concern.

WHO: Global Alert and Response (GAR) – Disease Outbreak News [to 9 August 2014]
http://www.who.int/csr/don/en/
:: Ebola virus disease update – West Africa 8 August 2014

CDC/MMWR Watch [to 9 August 2014]
http://www.cdc.gov/mmwr/mmwr_wk.html
:: CDC’s surge response to West African Ebola Outbreak – Press Release
August 6, 2014
The Centers for Disease Control and Prevention (CDC) is rapidly increasing its ongoing efforts to curb the expanding West African Ebola outbreak and deploying staff to four African nations currently affected: Guinea, Sierra Leone, Liberia, and Nigeria.
MMWR Weekly – August 8, 2014 / Vol. 63 / No. 31
No new digest content identified.

Ebola: World Bank Group Mobilizes Emergency Funding to Fight Epidemic in West Africa
WASHINGTON, August 4, 2014 – With the latest death toll from the West Africa Ebola epidemic now at 887, the World Bank Group today pledged as much as US $200 million in emergency funding to help Guinea, Liberia, and Sierra Leone contain the spread of Ebola infections, help their communities cope with the economic impact of the crisis, and improve public health systems throughout West Africa

WHO statement on the second meeting of the International Health Regulations Emergency Committee concerning the international spread of wild poliovirus

WHO statement on the second meeting of the International Health Regulations Emergency Committee concerning the international spread of wild poliovirus
WHO statement
3 August 2014
[full text; Editor’s text bolding]

On 5 May 2014 the Director-General declared the international spread of wild poliovirus in 2014 a Public Health Emergency of International Concern (PHEIC) under the International Health Regulations [IHR 2005], issued Temporary Recommendations to reduce the international spread of wild poliovirus, and requested a reassessment of this situation by the Emergency Committee in 3 months. The 2nd meeting of the Emergency Committee was held by teleconference on Thursday 31 July 2014 from 13:00 to 17:15 Geneva time (CET) 1.

The affected States Parties that met the criteria for ‘States currently exporting wild poliovirus’ participated in the informational session of the meeting and were as follows: Cameroon, Equatorial Guinea, Pakistan and the Syrian Arab Republic.

During the informational session the WHO Secretariat updated the Committee on wild poliovirus transmission and international spread since 5 May 2014. The above affected States Parties presented information on the implementation of the Temporary Recommendations issued on 5 May 2014, including the national declaration of a public health emergency and recommendations for travellers, and recent developments in the intensification of national polio eradication strategies.

Using the criteria applied to the declaration of the PHEIC in May, the Committee considered whether the conditions for a PHEIC still apply. After discussion of the information provided, the Committee advised that the international spread of polio in 2014 continues to constitute an extraordinary event and a public health risk to other States for which a coordinated international response continues to be essential.

Since 5 May 2014, and the onset of the high transmission season for polio, there has been new international spread of wild poliovirus in central Asia (from Pakistan to Afghanistan as recently as June 2014) and a poliovirus originating in Central Africa (Equatorial Guinea) was reported from the Americas. The latter had been detected in a single sewage sample that was collected in Brazil in March 2014 at a site that covered an international airport in the state of Sao Paolo. Equatorial Guinea was consequently confirmed as a ‘State currently exporting wild poliovirus’ and informed of the need to implement the relevant Temporary Recommendations, bringing to four the total number of ‘States currently exporting wild poliovirus’. Two of the ‘States currently exporting wild poliovirus’, Pakistan and Cameroon, have had additional cases and geographic expansion of the infected area within each country since 5 May 2014. The possible consequences of international spread have worsened since the declaration of the PHEIC, as susceptible populations living in polio-free but conflict-torn States and areas have increased, with further deterioration of their routine immunization services.

The international spread of poliovirus in 2014 continues to threaten the ongoing effort to eradicate globally one of the world’s most serious vaccine preventable diseases. It was the unanimous view of the Committee that the conditions for a Public Health Emergency of International Concern (PHEIC) continue to be met.

All four ‘States currently exporting wild poliovirus’ had initiated implementation of the Temporary Recommendations issued by the Director-General on 5 May 2014, and further intensified national eradication efforts. While recognizing and appreciating these efforts, the Committee noted that the application of the Temporary Recommendations by affected States Parties remains incomplete. Additional efforts are required to declare and/or operationalize national emergency procedures, to improve vaccination coverage of international travellers and to ensure eradication strategies are fully implemented to international standards in all infected and high risk areas.

The Committee reiterated that the over-riding priority for all polio-infected States must be to interrupt wild poliovirus transmission within their borders as rapidly as possible through high quality application in all geographic areas of the polio eradication strategies. The Committee reinforced the need for a coordinated regional approach to accelerate interruption of virus transmission in each epidemiologic zone.
The Committee provided the following advice to the Director-General for her consideration to reduce the international spread of wild poliovirus.
:: States Currently Exporting Wild Poliovirus: Pakistan, Cameroon, Equatorial Guinea and the Syrian Arab Republic continue to meet the criteria for such States and pose the highest risk for further wild poliovirus exportations in 2014. The Temporary Recommendations issued by the Director-General on 5 May 2014 for such States should continue to be implemented.
:: States Infected with Wild Poliovirus but Not Currently Exporting: Afghanistan, Ethiopia, Iraq, Israel, Nigeria, and Somalia continue to meet the criteria for such States and pose an ongoing risk for new wild poliovirus exportations in 2014. The Temporary Recommendations issued by the Director-General on 5 May 2014 for such States should continue to be implemented.
The Committee reaffirmed that any polio-free State which becomes infected with wild poliovirus should immediately implement the advice for ‘States infected with wild poliovirus but not currently exporting’. In the event of new international spread from an infected State, that State should immediately implement the requirements for ‘States currently exporting wild poliovirus’. The Committee noted that although a single wild poliovirus of Equatorial Guinea origin had been detected in Brazil in March 2014, Brazil was not considered polio-infected in the context of the global eradication initiative, as there was no evidence that this poliovirus exposure had resulted in transmission2. The Committee stressed the importance of surveillance in all polio-infected and polio-free countries.
The Committee acknowledged the efforts that Affected States have made to address the Temporary Recommendations, and recognised the challenges experienced by Affected States in their implementation. However, cognizant of the grave implications of any new international spread of poliovirus for the global eradication effort, the Committee considered whether additional Temporary Recommendations were needed at this time to further mitigate this risk. The Committee decided that additional time is first required to fully gauge the impact of the existing Temporary Recommendations in reducing the international spread of wild poliovirus. The Committee recommended, however, that this situation be reviewed again after 3 months.
Noting the challenges, both material and technical, that States had reported in implementing the Temporary Recommendations, the Committee emphasized the importance of continued support by WHO and the Global Polio Eradication Initiative partners towards the effective implementation and monitoring of these recommendations.
Based on this advice and the reports made by affected States Parties, the Director-General accepted the Committee’s assessment and declared that the international spread of wild poliovirus in 2014 continued to constitute a Public Health Emergency of International Concern (PHEIC). The Director-General thanked the Committee Members and Advisors for their advice, requested their reassessment of this situation in 3 months and extended the following Temporary Recommendations under the IHR (2005), effective 3 August 2014:
::
States currently exporting wild poliovirus
These States should:
:: officially declare, if not already done, at the level of head of state or government, that the interruption of poliovirus transmission is a national public health emergency;
:: ensure that all residents and long-term visitors (i.e. > 4 weeks) receive a dose of OPV or inactivated poliovirus vaccine (IPV) between 4 weeks and 12 months prior to international travel;
:: ensure that those undertaking urgent travel (i.e. within 4 weeks), who have not received a dose of OPV or IPV in the previous 4 weeks to 12 months, receive a dose of polio vaccine at least by the time of departure as this will still provide benefit, particularly for frequent travellers;
:: ensure that such travellers are provided with an International Certificate of Vaccination or Prophylaxis in the form specified in Annex 6 of the International Health Regulations (2005) to record their polio vaccination and serve as proof of vaccination;
:: maintain these measures until the following criteria have been met: (i) at least 6 months have passed without new exportations and (ii) there is documentation of full application of high quality eradication activities in all infected and high risk areas; in the absence of such documentation these measures should be maintained until at least 12 months have passed without new exportations.
::
States infected with wild poliovirus but not currently exporting
These States should:
:: officially declare, if not already done, at the level of head of state or government, that the interruption of poliovirus transmission is a national public health emergency;
:: encourage residents and long-term visitors to receive a dose of OPV or IPV 4 weeks to 12 months prior to international travel; those undertaking urgent travel (i.e. within 4 weeks) should be encouraged to receive a dose at least by the time of departure;
:: ensure that travellers who receive such vaccination have access to an appropriate document to record their polio vaccination status;
:: maintain these measures until the following criteria have been met: (i) at least 6 months have passed without the detection of wild poliovirus transmission in the country from any source, and (ii) there is documentation of full application of high quality eradication activities in all infected and high risk areas; in the absence of such documentation these measures should be maintained until at least 12 months without evidence of transmission.

GPEI Update: Polio this week – As of 6 August 2014

GPEI Update: Polio this week – As of 6 August 2014
Global Polio Eradication Initiative
Editor’s Excerpt and text bolding
Full report: http://www.polioeradication.org/Dataandmonitoring/Poliothisweek.aspx
:: On 31 July, the second meeting of the International Health Regulations (IHR) Emergency Committee on polio was held by teleconference, to reassess the situation and examine the actions that countries have taken since the declaration of the ‘public health emergency of international concern’ (PHEIC) in May. The Director-General of WHO accepted the advice of the Committee and has declared that the international spread of polio in 2014 continues to constitute a PHEIC. She has extended the Temporary Recommendations, effective 3 August, and requested the Committee to reassess the situation in a further 3 months. Of note, the Committee had expressed concern that application of the existing Temporary Recommendations remains incomplete. For more, including the full report of the Committee, please click here.
:: The United Arab Emirates (UAE) have produced a short film to sensitize migrant workers to the importance of vaccinating their children against polio. The three-minute film will be shown on Etihad Airways flights from Lahore, Islamabad, Peshawar and Karachi, Pakistan, throughout August. Special public screenings in high-risk neighbourhoods will also be organized. To view the short film, please click here.
Pakistan
:: Two new WPV1 cases were reported in the past week, from Khyber Agency, Federally Administered Tribal Areas (FATA) and Peshawar, Khyber Pakhtunkhwa (KP), bringing the total number of WPV1 cases for 2014 to 104. The most recent WPV1 case in the country had onset of paralysis on 9 July, from South Waziristan, FATA
Central Africa
:: Two new WPV1 cases were reported from Cameroon (from Est province, with onset of paralysis on 1 July and 9 July). In 2014, ten cases were reported in central Africa: five in Cameroon and five in Equatorial Guinea.
:: The two cases are from a refugee camp in the east of the country, among refugees from Central African Republic (CAR). Coordination with NGOs and organizations such as UNHCR is being strengthened.
:: Given the new cases detected in Est region, Cameroon is developing a rapid response plan.
:: Efforts are also ongoing to improve immunity levels and surveillance sensitivity in neighbouring CAR. With evidence of declining surveillance and immunity levels, coupled with large-scale population movements, the risk of spread of polio into CAR is high. Coordination with NGOs and other health organizations on the ground is strong. Plans are under discussion to conduct polio campaigns. As part of this, active searches for acute flaccid paralysis (AFP) will be conducted, and communities and health centres sensitized on the need for immunization and detection of AFP cases.
:: Equatorial Guinea has conducted three national campaigns using bivalent OPV. Two more national activities are planned for all children aged less than 15 years in August (7-10 and 28-31). In addition, two more activities are planned (20-23 September for <5s, and in November – exact dates and age group to be confirmed). A house-to-house search for AFP cases will be conducted during the campaign; a similar search is currently taking place in Gabon. Countries across central Africa are conducting campaigns.

Weekly Epidemiological Record (WER) 8 August 201

The Weekly Epidemiological Record (WER) 8 August 2014, vol. 89, 32/33 (pp. 357–368)
includes:
:: Health conditions for travellers to Saudi Arabia for the pilgrimage to Mecca (Hajj), 2014
:: Global Polio Eradication Initiative: 10th meeting of the Independent Monitoring Board
:: Monthly report on dracunculiasis cases, January– June 2014
http://www.who.int/entity/wer/2014/wer8932_33.pdf?ua=1

WHO: Humanitarian Health Action [to 9 August 2014]

WHO: Humanitarian Health Action [to 9 August 2014]

:: Gaza Conflict 6 August 2014
Hospitals are treating a constant influx of casualties in already overcrowded facilities and with vastly reduced supply of electricity. More than 17,000 patients utilized UNRWA’s 13 open clinics on 2-3 August, higher than the pre-war average of 14,000 patients a day. Currently more than 30% of clinic patients are displaced persons staying in shelters. The public health needs are: fuel, electricity and medical supplies; follow up care for the injured; health care for the displaced people; mental health interventions for patients, their family members and support to children; elective surgeries for patients whose surgeries were postponed.
:: Read the health situation report from the Regional Office website

GAVI Watch [to 9 August 2014]

GAVI Watch [to 9 August 2014]
http://www.gavialliance.org/library/news/press-releases/

:: Niger tackles its two biggest child killers with GAVI Alliance support 05 August 2014

:: South Sudan’s Introduction of Pentavalent Vaccine: A Historic Moment as the Vaccine Has Now Reached All 73 GAVI Countries August 4, 2014
South Sudan’s recent launch of pentavalent vaccine (on 16 July 2014) marked a historic milestone in the global fight against vaccine-preventable diseases. This is not only a major accomplishment for the country and its children, but also for the international community, as pentavalent (DTP-HepB-Hib) vaccine is now available in all 73 GAVI countries, accounting for more than half of the world’s children. Although available for nearly three decades in high-income countries, Haemophilus influenzae type B (Hib) vaccine was not accessible in low-income countries until the late 1990s. With a steady rollout of Hib-containing pentavalent vaccine, all children living in low-income countries will now have protection against meningitis and severe pneumonia, as well as diphtheria, tetanus, pertussis, and Hepatitis B…

Governance for health in the 21st century

Governance for health in the 21st century
By Ilona Kickbusch and David Gleicher
2012, xv + 107 pages
ISBN 978 92 890 0274 5 :: Order no. 13400121
English (PDF, 2.3 MB)
Overview
Governance for health describes the attempts of governments and other actors to steer communities, whole countries or even groups of countries in the pursuit of health as integral to well-being. This study tracks recent governance innovations to address the priority determinants of health and categorizes them into five strategic approaches to smart governance for health. It relates the emergence of joint action by the health sector and non-health sectors, by public and private actors and by citizens, all of whom have an increasing role to play in achieving seminal changes in 21st-century societies.
This study was commissioned to provide the evidence base for the new European health policy, Health 2020. Calling for a health-in-all-policies, whole-of-government and whole-of-society approach, Health 2020 uses governance as a “lens” through which to view all technical areas of health.

American Journal of Tropical Medicine and Hygiene – August 2014

American Journal of Tropical Medicine and Hygiene
August 2014; 91 (2)
http://www.ajtmh.org/content/current

Editorial
The Impact of the Fogarty International Clinical Scholars and Fellows Program Extends Beyond Borders
Catherine P. Benziger and Robert H. Gilman
Am J Trop Med Hyg 2014 91:211-212; Published online June 2, 2014, doi:10.4269/ajtmh.14-0265
[No abstract; free full text]

Doctors and Vampires in Sub-Saharan Africa: Ethical Challenges in Clinical Trial Research
Koen Peeters Grietens*, Joan Muela Ribera, Annette Erhart, Sarah Hoibak, Raffaella M. avinetto,
Charlotte Gryseels, Susan Dierickx, Sarah O’Neill, Susanna Hausmann Muela and Umberto D’Alessandro
Author Affiliations
Department of Public Health, Institute of Tropical Medicine, Antwerp, Belgium; School of International Health Development, Nagasaki University; Partners for Applied Social Sciences (PASS) International, Tessenderlo, Belgium; Department of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium; Global Fund to Fight AIDS, Tuberculosis and Malaria, Geneva, Switzerland; Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium; Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Belgium; Medical Research Council, Fajara, The Gambia; London School of Tropical Medicine and Hygiene, London, United Kingdom
Abstract.
Collecting blood samples from individuals recruited into clinical research projects in sub-Saharan Africa can be challenging. Strikingly, one of the reasons for participant reticence is the occurrence of local rumors surrounding “blood stealing” or “blood selling.” Such fears can potentially have dire effects on the success of research projects—for example, high dropout rates that would invalidate the trial’s results—and have ethical implications related to cultural sensitivity and informed consent. Though commonly considered as a manifestation of the local population’s ignorance, these rumors represent a social diagnosis and a logical attempt to make sense of sickness and health. Born from historical antecedents, they reflect implicit contemporary structural inequalities and the social distance between communities and public health institutions. We aim at illustrating the underlying logic governing patients’ fear and argue that the management of these beliefs should become an intrinsic component of clinical research.

Decline in severe diarrhea hospitalizations after the introduction of rotavirus vaccination in Ghana: a prevalence study

BMC Infectious Diseases
(Accessed 9 August 2014)
http://www.biomedcentral.com/bmcinfectdis/content

Research article
Decline in severe diarrhea hospitalizations after the introduction of rotavirus vaccination in Ghana: a prevalence study
Christabel C Enweronu-Laryea, Isaac Boamah, Eric Sifah, Stanley K Diamenu and George Armah
Author Affiliations
BMC Infectious Diseases 2014, 14:431 doi:10.1186/1471-2334-14-431
Published: 6 August 2014
Abstract (provisional)
Background
Almost all diarrhea deaths in young children occur in developing countries. Immunization against rotavirus, the leading cause of childhood severe dehydrating acute diarrhea may reduce the burden of severe diarrhea in developing countries. Ghana introduced rotavirus and pneumococcal vaccination in the national expanded program on immunization in May 2012.
Methods
Review of all-cause diarrheal hospitalization data for children aged 59?months and younger at 2 pediatric referral hospitals in southern Ghana from 2008 to 2014. The proportion of acute diarrhea (defined as 3 or more watery, non-bloody stools within 24?hours that has lasted for less than 7?days) cases caused by rotavirus was determined. Temporal trend and age group distribution of all-cause diarrhea and rotavirus gastroenteritis before and after introduction of the new vaccines were compared.
Results
Of the 5847 children hospitalized with all-cause diarrhea during the 74 months (January 2008 – February 2014), 3963 (67.8%) children were recruited for rotavirus surveillance and stool specimens were tested for rotavirus in 3160/3963 (79.7%). Median monthly hospitalization for all-cause diarrhea reduced from 84 [interquartile range (IQR) 62 – 105] during the 52 months pre-vaccination introduction to 46 (IQR 42 – 57) in the 22 months after implementation of vaccination. Significant decline in all-cause diarrhea hospitalization occurred in children aged 0 – 11 months: 56.3% (2711/4817) vs. 47.2% 486/1030 [p=0.0001, 95% confidence interval (CI) 0.77 – 0.88] and there was significant reduction of rotavirus gastroenteritis hospitalization: 49.7% (1246/2505) vs. 27.8% (182/655) [p=0.0001, 95% CI 0.32 – 0.47] before and after vaccine introduction respectively.
Conclusions
Implementation of rotavirus vaccination program may have resulted in significant reduction of severe diarrhea hospitalization even though this observational study could not exclude the effect of other confounding factors. Continued surveillance is recommended to monitor the progress of this program.

What makes public health studies ethical? Dissolving the boundary between research and practice

BMC Medical Ethics
(Accessed 9 August 2014)
http://www.biomedcentral.com/bmcmedethics/content

Debate
What makes public health studies ethical? Dissolving the boundary between research and practice
Donald J Willison, Nancy Ondrusek, Angus Dawson, Claudia Emerson, Lorraine E Ferris, Raphael Saginur, Heather Sampson and Ross Upshur
Author Affiliations
BMC Medical Ethics 2014, 15:61 doi:10.1186/1472-6939-15-61
Published: 8 August 2014
Abstract (provisional)
Background
The generation of evidence is integral to the work of public health and health service providers. Traditionally, ethics has been addressed differently in research projects, compared with other forms of evidence generation, such as quality improvement, program evaluation, and surveillance, with review of non-research activities falling outside the purview of the research ethics board. However, the boundaries between research and these other evaluative activities are not distinct. Efforts to delineate a boundary – whether on grounds of primary purpose, temporality, underlying legal authority, departure from usual practice, or direct benefits to participants – have been unsatisfactory.
Public Health Ontario has eschewed this distinction between research and other evaluative activities, choosing to adopt a common framework and process to guide ethical reflection on all public health evaluative projects throughout their lifecycle – from initial planning through to knowledge exchange.
Discussion
The Public Health Ontario framework was developed by a working group of public health and ethics professionals and scholars, in consultation with individuals representing a wide range of public health roles. The first part of the framework interprets the existing Canadian research ethics policy statement (commonly known as the TCPS 2) through a public health lens. The second part consists of ten questions that guide the investigator in the application of the core ethical principles to public health initiatives.
The framework is intended for use by those designing and executing public health evaluations, as well as those charged with ethics review of projects. The goal is to move toward a culture of ethical integrity among investigators, reviewers and decision-makers, rather than mere compliance with rules. The framework is consonant with the perspective of the learning organization and is generalizable to other public health organizations, to health services organizations, and beyond.
Summary
Public Health Ontario has developed an ethics framework that is applicable to any evidence-generating activity, regardless of whether it is labelled research. While developed in a public health context, it is readily adaptable to other health services organizations and beyond.

BMC Public Health (Accessed 9 August 2014)

BMC Public Health
(Accessed 9 August 2014)
http://www.biomedcentral.com/bmcpublichealth/content

Research article
Factors associated with hepatitis B vaccine series completion in a randomized trial for injection drug users reached through syringe exchange programs in three US cities
Sarah Bowman, Lauretta E Grau, Merrill Singer, Greg Scott, Robert Heimer BMC Public Health 2014, 14:820 (9 August 2014)
Provisional PDF

Commentary
Costs and benefits of influenza vaccination: more evidence, same challenges
Bruno Christian Ciancio and Giovanni Rezza
BMC Public Health 2014, 14:818 doi:10.1186/1471-2458-14-818
Published: 8 August 2014
Abstract (provisional)
Seasonal influenza vaccination coverage in most EU/EEA remains suboptimal. Providers’ and users’ confidence in influenza vaccines is undermined by reports of moderate to low vaccine effectiveness and by the lack of solid evidence on disease burden. A study from Preaud and co. indicates that even with current levels of vaccine effectiveness, increasing vaccination coverage would significantly reduce disease burden and health cost. The results of the study should be interpreted cautiously because some of the assumptions are not generalizable or are imprecise, especially those on vaccine coverage, disease burden and health cost. Increasing vaccination coverage in EU/EEA countries is very challenging. Multifaceted approaches and country specific strategies are needed to address vaccine hesitancy in health care workers and in the population, and to manage organisational and financial obstacles. One key element for increasing vaccination coverage is the development of better influenza vaccines, e.g. vaccines that are more effective, provide longer lasting immunity and do not require annual administration. Vaccine producers should consider this as the highest research priority in the field of influenza vaccine development..

Research article
Annual public health and economic benefits of seasonal influenza vaccination: a European estimate
Emmanuelle Preaud, Laure Durand, Bérengère Macabeo, Norbert Farkas, Brigitte Sloesen, Abraham Palache, Francis Shupo, Sandrine I Samson
BMC Public Health 2014, 14:813 (7 August 2014)
Provisional PDF

Effect of BCG vaccination against Mycobacterium tuberculosis infection in children: systematic review and meta-analysis

British Medical Journal
09 August 2014(vol 349, issue 7970)
http://www.bmj.com/content/349/7970

Research
Effect of BCG vaccination against Mycobacterium tuberculosis infection in children: systematic review and meta-analysis
A Roy, senior scientist1, M Eisenhut, consultant paediatrician2, R J Harris, statistician1, L C Rodrigues, professor of epidemiology3, S Sridhar, research associate4, S Habermann, junior doctor2, L Snell, junior doctor2, P Mangtani, senior lecturer3, I Adetifa, paediatrician and medical epidemiologist5, A Lalvani, professor of infectious disease4, I Abubakar, professor of infectious disease epidemiology16
Author affiliations
BMJ 2014; 349 doi: http://dx.doi.org/10.1136/bmj.g4643 (Published 05 August 2014) Cite this as: BMJ 2014;349:g4643
Accepted 11 July 2014
Abstract
Objectives
To determine whether BCG vaccination protects against Mycobacterium tuberculosis infection as assessed by interferon γ release assays (IGRA) in children.
Design
Systematic review and meta-analysis. Searches of electronic databases 1950 to November 2013, checking of reference lists, hand searching of journals, and contact with experts.
Setting
Community congregate settings and households.
Inclusion criteria Vaccinated and unvaccinated children aged under 16 with known recent exposure to patients with pulmonary tuberculosis. Children were screened for infection with M tuberculosis with interferon γ release assays.
Data extraction
Study results relating to diagnostic accuracy were extracted and risk estimates were combined with random effects meta-analysis.
Results
The primary analysis included 14 studies and 3855 participants. The estimated overall risk ratio was 0.81 (95% confidence interval 0.71 to 0.92), indicating a protective efficacy of 19% against infection among vaccinated children after exposure compared with unvaccinated children. The observed protection was similar when estimated with the two types of interferon γ release assays (ELISpot or QuantiFERON). Restriction of the analysis to the six studies (n=1745) with information on progression to active tuberculosis at the time of screening showed protection against infection of 27% (risk ratio 0.73, 0.61 to 0.87) compared with 71% (0.29, 0.15 to 0.58) against active tuberculosis. Among those infected, protection against progression to disease was 58% (0.42, 0.23 to 0.77).
Conclusions B
CG protects against M tuberculosis infection as well as progression from infection to disease.
Trial registration PROSPERO registration No CRD42011001698 (www.crd.york.ac.uk/prospero/).

Feature Infectious Diseases
Ebola: an opportunity for a clinical trial?
BMJ 2014; 349 doi: http://dx.doi.org/10.1136/bmj.g4997 (Published 06 August 2014) Cite this as: BMJ 2014;349:g4997
As the largest outbreak of Ebola virus has forced hitherto neglected tropical diseases on to the public agenda, debate is growing over whether affected patients should have the chance to try experimental drugs. Sophie Arie reports

Measles Vaccination in the Presence or Absence of Maternal Measles Antibody: Impact on Child Survival

Clinical Infectious Diseases (CID)
Volume 59 Issue 4 August 15, 2014
http://cid.oxfordjournals.org/content/current

Measles Vaccination in the Presence or Absence of Maternal Measles Antibody: Impact on Child Survival
Peter Aaby1,2, Cesário L. Martins1, May-Lill Garly1, Andreas Andersen1,2, Ane B. Fisker1, Mogens H. Claesson3, Henrik Ravn2, Amabelia Rodrigues1, Hilton C. Whittle4, and Christine S. Benn1,2
Author Affiliations
1Bandim Health Project, Indepth Network, Bissau, Guinea-Bissau
2Research Centre for Vitamins and Vaccines, Bandim Health Project, Statens Serum Institut, Copenhagen
3Institute of International Health, Immunology and Microbiology, Faculty of Health Sciences, University of Copenhagen, Denmark
4London School of Hygiene and Tropical Medicine, United Kingdom
Abstract
Background. Measles vaccine (MV) has a greater effect on child survival when administered in early infancy, when maternal antibody may still be present.
Methods. To test whether MV has a greater effect on overall survival if given in the presence of maternal measles antibody, we reanalyzed data from 2 previously published randomized trials of a 2-dose schedule with MV given at 4–6 months and at 9 months of age. In both trials antibody levels had been measured before early measles vaccination.
Results. In trial I (1993–1995), the mortality rate was 0.0 per 1000 person-years among children vaccinated with MV in the presence of maternal antibody and 32.3 per 1000 person-years without maternal antibody (mortality rate ratio [MRR], 0.0; 95% confidence interval [CI], 0–.52). In trial II (2003–2007), the mortality rate was 4.2 per 1000 person-years among children vaccinated in presence of maternal measles antibody and 14.5 per 1000 person-years without measles antibody (MRR, 0.29; 95% CI, .09–.91). Possible confounding factors did not explain the difference. In a combined analysis, children who had measles antibody detected when they received their first dose of MV at 4–6 months of age had lower mortality than children with no maternal antibody, the MRR being 0.22 (95% CI, .07–.64) between 4–6 months and 5 years.
Conclusions.  Child mortality in low-income countries may be reduced by vaccinating against measles in the presence of maternal antibody, using a 2-dose schedule with the first dose at 4–6 months (earlier than currently recommended) and a booster dose at 9–12 months of age.
Clinical Trials Registration. NCT00168558.

Maternal Immunization

Clinical Infectious Diseases (CID)
Volume 59 Issue 4 August 15, 2014
http://cid.oxfordjournals.org/content/current

Maternal Immunization
Stanley A. Plotkin, Section Editor, Helen Y. Chu1 and Janet A. Englund2
Author Affiliations
1Department of Medicine, Division of Allergy and Infectious Diseases, University of Washington
2Department of Pediatrics, Division of Infectious Diseases, Seattle Children’s Hospital, Washington
Abstract
Maternal immunization has the potential to protect the pregnant woman, fetus, and infant from vaccine-preventable diseases. Maternal immunoglobulin G is actively transported across the placenta, providing passive immunity to the neonate and infant prior to the infant’s ability to respond to vaccines. Currently inactivated influenza, tetanus toxoid, and acellular pertussis vaccines are recommended during pregnancy. Several other vaccines have been studied in pregnancy and found to be safe and immunogenic and to provide antibody to infants. These include pneumococcus, group B Streptococcus, Haemophilus influenzae type b, and meningococcus vaccines. Other vaccines in development for potential maternal immunization include respiratory syncytial virus, herpes simplex virus, and cytomegalovirus vaccines.

Need of surveillance response systems to combat Ebola outbreaks and other emerging infectious diseases in African countries

Infectious Diseases of Poverty
[Accessed 9 August 2014]
http://www.idpjournal.com/content

Letter to the Editor
Need of surveillance response systems to combat Ebola outbreaks and other emerging infectious diseases in African countries
Ernest Tambo, Emmanuel Chidiebere Ugwu and Jeane Yonkeu Ngogang
Author Affiliations
Infectious Diseases of Poverty 2014, 3:29 doi:10.1186/2049-9957-3-29
Published: 5 August 2014
Abstract (provisional)
There is growing concern in Sub-Saharan Africa about the spread of the Ebola virus disease (EVD), formerly known as Ebola haemorrhagic fever, and the public health burden that it ensues. Since 1976, there have been 884,955 suspected and laboratory confirmed cases of EVD and the disease has claimed 2,309 lives including 729 lives in West Africa. There are certain requirements that must be met when responding to EVD outbreaks and this process could incur certain challenges. For the purposes of this paper, five have been identified: (i) the deficiency in the development and implementation of surveillance response systems against Ebola and others infectious disease outbreaks in Africa; (ii) the lack of education and knowledge resulting in an EVD outbreak triggering panic, anxiety, psychosocial trauma, isolation and dignity impounding, stigmatisation, community ostracism and resistance to associated socio-ecological and public health consequences; (iii) limited financial resources, human technical capacity and weak community and national health system operational plans for prevention and control responses, practices and management; (iv) inadequate leadership and coordination; and (v) the lack of development of new strategies, tools and approaches, such as improved diagnostics and novel therapies including vaccines which can assist in preventing, controlling and containing Ebola outbreaks as well as the spread of the disease. Hence, there is an urgent need to develop and implement an active early warning alert and surveillance response system for outbreak response and control of emerging infectious diseases. Understanding the unending risks of transmission dynamics and resurgence is essential in implementing rapid effective response interventions tailored to specific local settings and contexts. Therefore, the following actions are recommended: (i) national and regional inter-sectorial and trans-disciplinary surveillance response systems that include early warnings, as well as critical human resources development, must be quickly adopted by allied ministries and organisations in African countries in epidemic and pandemic responses; (ii) harnessing all stakeholders commitment and advocacy in sustained funding, collaboration, communication and networking including community participation to enhance a coordinated responses, as well as tracking and prompt case management to combat challenges; (iii) more research and development in new drug discovery and vaccines; and (iv) understanding the involvement of global health to promote the establishment of public health surveillance response systems with functions of early warning, as well as monitoring and evaluation in upholding research-action programmes and innovative interventions.

Naturally Acquired Immunity Against Human Papillomavirus (HPV): Why It Matters in the HPV Vaccine Era

Journal of Infectious Diseases
Volume 210 Issue 4 August 15, 2014
http://jid.oxfordjournals.org/content/curren

Naturally Acquired Immunity Against Human Papillomavirus (HPV): Why It Matters in the HPV Vaccine Era
Silvia Franceschi and Iacopo Baussano
Author Affiliations
International Agency for Research on Cancer, Lyon, France
(See the major article by Castellsagué et al on pages 517–34.)
Extract
Scientists do not know precisely which elements of the immune system are important in preventing or resolving human papillomavirus (HPV) infections in unvaccinated women. HPV has a battery of immune-evasion mechanisms that include hiding within the host mucosal cells, low-level production of late (L) proteins, and inhibition of innate immunity and cell-mediated response by early proteins [1].
HPV vaccine trials show that sufficiently high levels of neutralizing antibodies against viral capsid strongly protect women who are negative for vaccine types at baseline against homologous (same-type) HPV infection. The measurement of HPV antibodies is also important for identifying unvaccinated women who have mounted an antibody response following previous exposure to HPV infection and may, therefore, be naturally protected. However, only approximately half of women seroconvert within 18 months after HPV infection [2]. The interpretation of HPV serology is additionally complicated by substantial differences across assays used in different studies (eg, detection ranges, targeted HPV types, and epitopes) [3–5]. Despite these limitations, seroprevalence studies have been essential in understanding HPV exposure [6] and infection trends [7], and have more recently started providing prospective estimates of naturally acquired immunity after HPV infection [4].
In this issue of The Journal of Infectious Diseases, Castellsagué and colleagues [8] report on the association of HPV types 16 and 18 antibody levels …

Risk of Newly Detected Infections and Cervical Abnormalities in Women Seropositive for Naturally Acquired Human Papillomavirus Type 16/18 Antibodies: Analysis of the Control Arm of PATRICIA

Journal of Infectious Diseases
Volume 210 Issue 4 August 15, 2014
http://jid.oxfordjournals.org/content/current

Risk of Newly Detected Infections and Cervical Abnormalities in Women Seropositive for Naturally Acquired Human Papillomavirus Type 16/18 Antibodies: Analysis of the Control Arm of PATRICIA
Xavier Castellsagué, Paulo Naud, Song-Nan Chow, Cosette M. Wheeler, Maria Julieta V. Germar,
Matti Lehtinen, Jorma Paavonen, Unnop Jaisamrarn, Suzanne M. Garland, Jorge Salmerón, Dan Apter, Henry Kitchener, Julio C. Teixeira, S. Rachel Skinner, Genara Limson, Anne Szarewski, Barbara Romanowski, Fred Y. Aoki, Tino F. Schwarz, Willy A. J. Poppe, F. Xavier Bosch, Newton S. de Carvalho, Klaus Peters, Wiebren A. A. Tjalma, Mahboobeh Safaeian, Alice Raillard, Dominique Descamps, Frank Struyf, Gary Dubin, Dominique Rosillon, and Laurence Baril
J Infect Dis. (2014) 210 (4): 517-534 doi:10.1093/infdis/jiu139
Free Full Text (HTML)

Relative Efficacy of AS03-Adjuvanted Pandemic Influenza A(H1N1) Vaccine in Children: Results of a Controlled, Randomized Efficacy Trial

Journal of Infectious Diseases
Volume 210 Issue 4 August 15, 2014
http://jid.oxfordjournals.org/content/current

Relative Efficacy of AS03-Adjuvanted Pandemic Influenza A(H1N1) Vaccine in Children: Results of a Controlled, Randomized Efficacy Trial
Terry Nolan1,2,a, Sumita Roy-Ghanta3,a, May Montellano5, Lily Weckx8, Rolando Ulloa-Gutierrez11, Eduardo Lazcano-Ponce12, Angkool Kerdpanich16, Marco Aurélio Palazzi afadi9,10,
Aurelio Cruz-Valdez12, Sandra Litao6, Fong Seng Lim18, Abiel Mascareñas de Los Santos13, Miguel Angel Rodriguez Weber14, Juan-Carlos Tinoco15, Marcela Hernandez-de Mezerville11, Idis Faingezicht11, Pensri Kosuwon17, Pio Lopez19, Charissa Borja-Tabora7, Ping Li3, Serge Durviaux20, Louis Fries4, Gary Dubin3, Thomas Breuer20, Bruce L. Innis3 and David W. Vaughn21
Abstract
Background. The vaccine efficacy (VE) of 1 or 2 doses of AS03-adjuvanted influenza A(H1N1) vaccine relative to that of 2 doses of nonadjuvanted influenza A(H1N1) vaccine in children 6 months to Methods. A total of 6145 children were randomly assigned at a ratio of 1:1:1 to receive 2 injections 21 days apart of A/CNCT00alifornia/7/2009(H1N1)-AS03 vaccine at dose 1 and saline placebo at dose 2, 2 doses 21 days apart of A/California/7/2009(H1N1)-AS03 vaccine (the Ad2 group), or 2 doses 21 days apart of nonadjuvanted A/California/7/2009(H1N1) vaccine (the NAd2 group). Active surveillance for influenza-like illnesses continued from days 14 to 385. Nose and throat samples obtained during influenza-like illnesses were tested for A/California/7/2009(H1N1), using reverse-transcriptase polymerase chain reaction. Immunogenicity, reactogenicity, and safety were assessed.
Results. There were 23 cases of confirmed 2009 pandemic influenza A(H1N1) (A[H1N1]pdm09) infection for the primary relative VE analysis. The VE in the Ad2 group relative to that in the NAd2 group was 76.8% (95% confidence interval, 18.5%–93.4%). The benefit of the AS03 adjuvant was demonstrated in terms of the greater immunogenicity observed in the Ad2 group, compared with the NAd2 group.
Conclusion. The 4–8-fold antigen-sparing adjuvanted pandemic influenza vaccine demonstrated superior and clinically important prevention of A(H1N1)pdm09 infection, compared with nonadjuvanted vaccine, with no observed increase in medically attended or serious adverse events. These data support the use of adjuvanted influenza vaccines during influenza pandemics.
Clinical Trials Registration. NCT01051661.

Incremental Benefits of Male HPV Vaccination: Accounting for Inequality in Population Uptake

PLoS One
[Accessed 9 August 2014]
http://www.plosone.org/
Research Article
Incremental Benefits of Male HPV Vaccination: Accounting for Inequality in Population Uptake
Megan A. Smith mail, Karen Canfell
Abstract
Background
Vaccines against HPV16/18 are approved for use in females and males but most countries currently have female-only programs. Cultural and geographic factors associated with HPV vaccine uptake might also influence sexual partner choice; this might impact post-vaccination outcomes. Our aims were to examine the population-level impact of adding males to HPV vaccination programs if factors influencing vaccine uptake also influence partner choice, and additionally to quantify how this changes the post-vaccination distribution of disease between subgroups, using incident infections as the outcome measure.
Methods
A dynamic model simulated vaccination of pre-adolescents in two scenarios: 1) vaccine uptake was correlated with factors which also affect sexual partner choice (“correlated”); 2) vaccine uptake was unrelated to these factors (“unrelated”). Coverage and degree of heterogeneity in uptake were informed by observed data from Australia and the USA. Population impact was examined via the effect on incident HPV16 infections. The rate ratio for post-vaccination incident HPV16 in the lowest compared to the highest coverage subgroup (RRL) was calculated to quantify between-group differences in outcomes.
Results
The population-level incremental impact of adding males was lower if vaccine uptake was “correlated”, however the difference in population-level impact was extremely small (<1%) in the Australia and USA scenarios, even under the conservative and extreme assumption that subgroups according to coverage did not mix at all sexually. At the subgroup level, “correlated” female-only vaccination resulted in RRL = 1.9 (Australia) and 1.5 (USA) in females, and RRL = 1.5 and 1.3 in males. “Correlated” both-sex vaccination increased RRL to 4.2 and 2.1 in females and 3.9 and 2.0 in males in the Australia and USA scenarios respectively.
Conclusions
The population-level incremental impact of male vaccination is unlikely to be substantially impacted by feasible levels of heterogeneity in uptake. However, these findings emphasize the continuing importance of prioritizing high coverage across all groups in HPV vaccination programs in terms of achieving equality of outcomes.

From Intense Rejection to Advocacy: How Muslim Clerics Were Engaged in a Polio Eradication Initiative in Northern Nigeria

PLoS Medicine
(Accessed 9 August 2014)
http://www.plosmedicine.org/
Health in Action
From Intense Rejection to Advocacy: How Muslim Clerics Were Engaged in a Polio Eradication Initiative in Northern Nigeria
Sani-Gwarzo Nasir, Gambo Aliyu mail, Inuwa Ya’u, Muktar Gadanya, Muktar Mohammad, Mahmud Zubair, Samer S. El-Kamary
Published: August 05, 2014
DOI: 10.1371/journal.pmed.1001687
Summary Points
:: Of the several setbacks suffered by the polio eradication initiative in Nigeria, vaccination rejection by Muslim clerics (imams) is perhaps the most profound.
:: Anti-polio propaganda, misconceptions, and violence against vaccinators at the community level present huge challenges to polio eradication in Nigeria and globally.
:: However, the intense opposition to polio vaccination is systematically being reversed by the active engagement of imams to promote uptake of polio vaccination in areas worst hit by the disease.
:: A coalition campaign involving imams, Islamic school teachers, traditional rulers, doctors, journalists, and polio survivors is gradually turning the tide against polio vaccine rejection in northern Nigeria.
:: Innovative engagement and the coalition campaign at the community level should be part of the focus of the polio eradication initiative in Nigeria.

From Google Scholar [to 9 August 2014]

From Google Scholar & other sources: Selected Journal Articles, Newsletters, Dissertations, Theses, Commentary

Expert Review of Vaccines
Volume 13, Number 8 (August 2014)
http://informahealthcare.com/toc/erv/current
Special Focus: Pertussis – Review
Waning vaccine immunity in teenagers primed with whole cell and acellular pertussis vaccine: recent epidemiology
Posted online on August 5, 2014. (doi:10.1586/14760584.2014.944167)
Sarah L Sheridan1,2, Katie Frith3, Thomas L Snelling4,5, Keith Grimwood1,6, Peter B McIntyre7 and Stephen B Lambert *1,8
Abstract
The recent epidemics of pertussis (whooping cough) in parts of the USA and Australia have led to the largest numbers of annual cases reported in over half a century. These epidemics demonstrated a new pattern, with particularly high rates of disease among pre-adolescents and early adolescents. These high rates of pertussis coincided with the first cohorts vaccinated with purely acellular pertussis vaccine, which replaced whole-cell pertussis (wP) vaccine in the later 1990s in the USA and Australia. Studies undertaken during these epidemics provide new evidence of more rapid waning of acellular pertussis-containing vaccines and longer-term protection from effective wP-containing vaccines. There is evidence that receiving wP as at least the first dose of pertussis-containing vaccine provides greater and more long-lived protection, irrespective of the nature of subsequent doses. This evidence will be reviewed together with the immunobiology associated with both vaccines, and the implications for pertussis control discussed.

Special Focus Newsletters
RotaFlash (PATH)
August 4, 2014
Headline: Rotavirus technical experts meet to prioritize intussusception research agenda

Special Request Posting
Cell Host & Microbe
2014 Jun 11;15(6):729-40. doi: 10.1016/j.chom.2014.05.009.
http://www.cell.com/cell-host-microbe/current
The classical lancefield antigen of group a Streptococcus is a virulence determinant with implications for vaccine design.
van Sorge NM1, Cole JN2, Kuipers K3, Henningham A2, Aziz RK4, Kasirer-Friede A5, Lin L3, Berends ET6, Davies MR7, Dougan G8, Zhang F9, Dahesh S3, Shaw L3, Gin J10, Cunningham M11, Merriman JA12, Hütter J13, Lepenies B13, Rooijakkers SH6, Malley R9, Walker MJ14, Shattil SJ5, Schlievert PM12, Choudhury B15, Nizet V16.
Author information
Abstract
Group A Streptococcus (GAS) is a leading cause of infection-related mortality in humans. All GAS serotypes express the Lancefield group A carbohydrate (GAC), comprising a polyrhamnose backbone with an immunodominant N-acetylglucosamine (GlcNAc) side chain, which is the basis of rapid diagnostic tests. No biological function has been attributed to this conserved antigen. Here we identify and characterize the GAC biosynthesis genes, gacA through gacL. An isogenic mutant of the glycosyltransferase gacI, which is defective for GlcNAc side-chain addition, is attenuated for virulence in two infection models, in association with increased sensitivity to neutrophil killing, platelet-derived antimicrobials in serum, and the cathelicidin antimicrobial peptide LL-37. Antibodies to GAC lacking the GlcNAc side chain and containing only polyrhamnose promoted opsonophagocytic killing of multiple GAS serotypes and protected against systemic GAS challenge after passive immunization. Thus, the Lancefield antigen plays a functional role in GAS pathogenesis, and a deeper understanding of this unique polysaccharide has implications for vaccine development.

Media Watch: Ebola Covergae

Al Jazeera
http://www.aljazeera.com/Services/Search/?q=vaccine
Accessed 9 August 2014
Experts: Give new US Ebola drug to Africans
World’s top Ebola specialists question why only US aid workers given experimental drug, but firm says little available

The Atlantic
http://www.theatlantic.com/magazine/
Accessed 9 August 2014
An Ebola Vaccine Is Not the Answer
Instead, we need a treatment and better quarantine measures.
Olga Khazan
5 August 2014
In a widely shared Onion article from a few days ago, scientists “announced” that an Ebola vaccine was still 50 white people away. This was a jab at pharmaceutical companies, who, cynics think, will only set their R&D wheels in motion if there’s money on the horizon….

Council on Foreign Relations
http://www.cfr.org/
Accessed 9 August 2014
Transcript : The Ebola Outbreak
with John Campbell, Laurie Garrett, Robert McMahon August 5, 2014
CFR fellows discuss the recent Ebola outbreak in western Africa and its effect on the region.

Forbes
http://www.forbes.com/
Accessed 9 August 2014
BioWar Lab Helping To Develop Treatment For Ebola
Paul Rodgers, Contributor Aug 04, 2014
A top U.S. biological-warfare unit is developing a treatment for the deadly Ebola virus and could have it in the field within two years. The virus, which has killed more than 800 people in West Africa as of August 4, is a “Category A Bioterrorism Agent” along with anthrax, botulism, bubonic…

The Guardian
http://www.guardiannews.com/
Accessed 9 August 2014
Ebola rages in Africa as west agonises over ethics of vaccine and drug testing
31 July 2014
In 2002, scientists writing in a leading American medical journal discussed the possibility that the Ebola virus could be used in a biochemical weapon. It would be technically difficult and unlikely to cause mass destruction because those infected quickly die and the virus is not as transmissible as many assume. But, the scientists warned, if it could be done, there would be no protection. No vaccine or drug treatment exists…

New Yorker
http://www.newyorker.com/
Accessed 9 August 2014
After Ebola – The New Yorker
Jul 31, 2014 … There are several vaccines under development; in early animal tests, more than one has shown promise. But it will be years before they are …

New York Times
http://www.nytimes.com/
Accessed 9 August 2014
Ebola Drug Could Save a Few Lives. But Whose?
By ANDREW POLLACK AUG. 8, 2014
With hundreds of Africans dying from the outbreak of Ebola, some activists have said it is wrong that extremely scarce supplies of an experimental drug went to two white American aid workers.
But others wonder: What if the first doses of the drug — which had never been used in people and had not even finished the typical animal safety testing — had been given to African patients instead?
“It would have been the front-page screaming headline: ‘Africans used as guinea pigs for American drug company’s medicine,’ ” said Dr. Salim S. Abdool Karim, director of Caprisa, an AIDS research center in South Africa.
A history of controversy about drug testing in Africa is just one of the complexities facing public health authorities as they wrestle with whether and how to bring that drug and possibly other experimental ones to the countries afflicted with Ebola. Who should get such a scarce supply of medicine? Health workers? Children? The newly infected who are not yet as sick?
There are virtually no remaining supplies of the drug, called ZMapp, that was used to treat the two Americans, United States officials say. And even a few months from now, according to various estimates, there may be no more than a few hundred doses….
Inside Hospital’s Ebola Battle
August 9, 2014
At the government hospital in Kenema, Sierra Leone, health care workers struggle to contain the Ebola epidemic, which has killed almost 1,000 people across West Africa.

Vaccines and Global Health: The Week in Review 2 August 2014

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

.Request an Email Summary: Vaccines and Global health : The Week in Review is published as a single email summary, scheduled for release each Saturday evening before midnight (EDT in the U.S.). If you would like to receive the email version, please send your request to david.r.curry@centerforvaccineethicsandpolicy.org.
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pdf versionA pdf of the current issues is available here: Vaccines and Global Health_The Week in Review_2 August 2014

Twitter:  Readers can also follow developments on twitter: @vaxethicspolicy.
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Links:  We endeavor to test each link as we incorporate it into any post, but recognize that some links may become “stale” as publications and websites reorganize content over time. We apologize in advance for any links that may not be operative. We believe the contextual information in a given post should allow retrieval, but please contact us as above for assistance if necessary.
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David R. Curry, MS
Executive Director
Center for Vaccine Ethics and Policy
a program of the
– Division of Medical Ethics, NYU Medical School
– The Wistar Institute Vaccine Center
– Children’s Hospital of Philadelphia Vaccine Education Center
Associate Faculty, Division of Medical Ethics, NYU Medical School

Ebola [to 2 August 2014]

WHO: Global Alert and Response (GAR) – Disease Outbreak News [to 2 August 2014]
http://www.who.int/csr/don/en/
:: Ebola virus disease, West Africa – update 31 July 2014

Briefing: WHO Director-General assesses the Ebola outbreak with three West African presidents
Overview of the Ebola situation delivered to the Presidents of Guinea, Liberia, and Sierra Leone
Conakry, Guinea
1 August 2014
Dr Margaret Chan briefed the presidents on the Ebola situation in Conakry, Guinea. She underscored the many unprecedented dimensions of the outbreak, the extraordinary challenges that have emerged, and the need for a turning point in the international response. She announced that on 6-7 August, WHO will convene an Emergency Committee meeting in order to ascertain whether the ongoing Ebola outbreak in West Africa constitutes a “public health emergency of international concern” (PHEIC) and, if it does, to recommend appropriate action.
:: Ebola Virus Disease Outbreak Response Plan in West Africa July – December 2014
:: Ebola outbreak response update pdf, 793kb 28 July 2014

CDC/MMWR Watch [to 2 August 2014]
http://www.cdc.gov/mmwr/mmwr_wk.html
:: CDC Telebriefing on Ebola outbreak in West Africa – Transcript July 31, 2014
CDC hosted a media telebriefing to discuss the on-going outbreak of Ebola in West Africa.
:: As West Africa Ebola outbreak worsens, CDC issues Level 3 Travel Warning – Press Release July 31, 2014
The Centers for Disease Control and Prevention (CDC) today issued a warning to avoid nonessential travel to the West African nations of Guinea, Liberia, and Sierra Leone. This Level 3 travel warning is a reflection of the worsening Ebola outbreak in this region.
MMWR Weekly – August 1, 2014 / Vol. 63 / No. 30
:: Notes from the Field: Outbreak of Pertussis in a School and Religious Community Averse to Health Care and Vaccinations — Columbia County, Florida, 2013

POLIO [to 2 August 2014]

POLIO [to 2 August 2014]
GPEI Update: Polio this week – As of 31 July 2014
Global Polio Eradication Initiative
Editor’s Excerpt and text bolding
Full report: http://www.polioeradication.org/Dataandmonitoring/Poliothisweek.aspx
:: In Pakistan, three new cases have been reported, including one from Balochistan. It is the first case in this province since October 2012. However, four positive environmental samples were collected in 2014 from Quetta, Balochistan, the most recent of which on 20 June. This case is linked to these positive environmental samples, suggesting local circulation of WPV1 this year in this area.
:: In Nigeria, more cases due to circulating vaccine-derived poliovirus type 2 (cVDPV2) have been reported this year (18) than those due to wild poliovirus type 1 (5 WPV1). Four new cVDPV2 cases were reported this week alone.
Nigeria
:: Four new cVDPV2 cases were reported in the past week, three from Kano and one from Borno. The total number of cVDPV2 cases for 2014 is now 18. The most recent cVDPV2 case had onset of paralysis on 22 June, from Kano.
:: Mop-up vaccination activities took place in parts of four northern Nigerian states from 12-15 July. Larger subnational activities are planned for the country’s north during 9-12 August (trivalent OPV), as part of urgent efforts to address the spread of cVDPV2, and 20-23 September (bivalent OPV).
Pakistan
:: Three new WPV1 cases were reported in the past week, from Federally Administered Tribal Areas (FATA – from Khyber Agency and South Waziristan), and from Balochistan (Killa Abdullah), bringing the total number of WPV1 cases for 2014 to 102. The case from South Waziristan is the most recent in the country, with onset of paralysis on 9 July.

Editorial: Polio eradication: placing health before conflict
The Lancet
Aug 02, 2014 Volume 384 Number 9941 p377 – 468 e30 – 31

Taliban In Pakistan Derail World Polio Eradication
NPR | 28 July 2014
Excerpt
…Today the militant group continues to threaten to kill not only vaccinators but also parents who get their children immunized. That threat has had a chilling effect on anti-polio efforts nationwide. And it completely halted vaccination drives in some Taliban-controlled areas. It’s in these places that the crippling virus has come roaring back — and threatened to stymie global efforts to wipe out polio. The worldwide campaign to eradicate polio has been going on for more than two decades. It has cost more than $10 billion. Now the success of the campaign hinges on whether Pakistan can control the virus…..

GAVI Watch [to 2 August 2014]

GAVI Watch [to 2 August 2014]
http://www.gavialliance.org/library/news/press-releases/

:: 5-in-1 vaccine now in all 73 poorest countries
30 July 2014
The five-in-one pentavalent vaccine is now being used in all GAVI Alliance-supported countries – now the race is on to increase coverage of the vaccine which protects children against five life-threatening diseases.
Pentavalent, which protects against diphtheria, tetanus and pertussis (DTP) as well as Hepatitis B (HepB) and Haemophilus influenza type B (Hib), was first introduced with GAVI support in Kenya in 2001. South Sudan became the 73rd and final GAVI-supported country to introduce the vaccine on 16th July 2014…

Global Fund Welcomes Germany’s Increased Contribution

Global Fund Welcomes Germany’s Increased Contribution
31 July 2014
Excerpt
GENEVA – The Global Fund to Fight AIDS, Tuberculosis and Malaria warmly welcomed a decision by the German parliament to increase Germany’s contribution to €245 million for 2014 in the budget for this year, reaffirming a strong commitment to global health.

At the launch of the Global Fund’s Fourth Replenishment last December, Germany had already announced a pledge of €200 million for this year as part of a total commitment of €600 million for the 2014-2016 period. By signing a Multi-Year Contribution Agreement that same month, Germany was able to provide the Global Fund with a predictable flow of resources to fight the three diseases.

With the 2014 budget now taking effect after its passage by parliament and signed into law by Federal President Joachim Gauck, the additional sum of €45 million can be added to the overall German contribution, representing an increase of more than 20 percent for 2014.
On top of that, the German contribution unlocks about US$30 million in additional contribution from the United States, which devised its pledge in a way that partially matches additional contributions by other donors…

Pfizer Enters Into Agreement to Acquire Baxter’s Portfolio of Marketed Vaccines

Pfizer Enters Into Agreement to Acquire Baxter’s Portfolio of Marketed Vaccines
July 30, 2014
Excerpt
Pfizer announced that it has entered into a definitive agreement to acquire Baxter International Inc.’s portfolio of marketed vaccines for US$635 million. As part of the transaction, Pfizer will also acquire a portion of Baxter’s facility in Orth, Austria, where these vaccines are manufactured…
…Baxter’s portfolio of marketed vaccines consists of NeisVac-C and FSME-IMMUN/TicoVac. NeisVac-C is a vaccine that helps protect against meningitis caused by group C meningococcal meningitis (MenC)…FSME-IMMUN/TicoVac is a vaccine that helps protect against tick-borne encephalitis (TBE), an infection of the brain, which is transmitted by the bite of ticks infected with the TBE-virus….
…“Vaccines make a tremendous and valuable impact on public health around the world. They have significantly reduced the threat of widespread and often fatal diseases and every day people of all ages benefit from safe and effective vaccines,” said Susan Silbermann, Pfizer Vaccines President. “For over a decade Pfizer has been the global leader in pneumococcal disease prevention. We are working hard to bring innovative vaccines to market that prevent and treat serious diseases. Through this acquisition, we will add two high-quality and life-saving vaccines that bring scale and depth to our portfolio.”…

American Journal of Infection Control – Volume 42, Issue 8, p819-940 August 2014

American Journal of Infection Control
Volume 42, Issue 8, p819-940 August 2014
http://www.ajicjournal.org/current

Health care workers—part of the system or part of the public? Ambivalent risk perception in health care workers
Anat Gesser-Edelsburg, PhD, Nathan Walter, MA, Manfred S. Green, MSc, MBChB, MPH, PhD
Published Online: June 14, 2014
DOI: http://dx.doi.org/10.1016/j.ajic.2014.04.012
Abstract
Background
The emergence of the avian influenza A (H7N9) in China during 2013 illustrates the importance of health care professionals as a mediating channel between health agencies and the public. Our study examined health care professionals’ risk perceptions considering their unique position as representing the health care system and yet also being part of the public, hence a risk group. Recent studies have examined the role of health professionals’ personal risk perceptions and attitudes regarding compliance of the general public with vaccination. Our study examined how risk perception affects their risk analysis.
Methods
We employed an online survey of Israeli health care professionals and the general public in Israel (N = 240).
Results
When risk perception is relatively low, health care professionals tend to base their attitudes toward vaccines on analytical knowledge (Rc = 0.315; P < .05), whereas in situations with high risk perception, the results did not indicate any significant difference between Israeli health professionals and the Israeli general public, hence both groups base their attitudes more on emotions and personal experience than on analytical knowledge. Conclusions Public health organizations must consider the fact that health professionals are a group that cannot be automatically treated as an extension of the organization. When the risk is tangible and relevant, health care workers behave and act like everybody else. Our study contributes to understanding health care professionals’ perceptions about vaccines and the thinking processes underlying such perceptions.

Varicella seroprevalence among health care workers in Korea: Validity of self-reported history and cost-effectiveness of prevaccination screening
Ji-Hea Kang, RN1, Yoon Soo Park, MD1, Shin Young Park, RN, Sae Bom Kim, RN, Kwang-Pil Ko, MD, Yiel-Hea Seo, MD 1These authors contributed equally to this work. DOI: http://dx.doi.org/10.1016/j.ajic.2014.05.013
Abstract
Background The validity of self-reported varicella history and cost-effectiveness of a prevaccination screening strategy have not been examined among health care workers (HCWs) living in Korea.
Methods We investigated varicella-zoster virus immunity of all HCWs in high-risk departments. To determine the history of varicella, all applicants completed a standardized questionnaire at the time of blood sampling for serologic testing.
Results Of the 550 HCWs, 526 (96%) were varicella seropositive. Although self-reported history was highly predictive of seropositivity (≥96%) among all age groups, the negative predictive value was extremely low (4%-5%) among all age groups. The prevaccination screening strategy was cheaper than vaccination without antibody screening if the varicella seroprevalence was >28%.
Conclusion
Seroprevalence was high (≥95%) among HCWs born in Korea before 1988. The self-reported varicella history did not accurately predict immunity, especially for individuals who have negative or uncertain varicella history. Given the high seroprevalence of varicella in Korean HCWs, serologic screening before vaccination was more cost-effective than universal vaccination.

Analysis of prices paid by low-income countries – how price sensitive is government demand for medicines?

BMC Public Health
(Accessed 2 August 2014)
http://www.biomedcentral.com/bmcpublichealth/content

Research article
Analysis of prices paid by low-income countries – how price sensitive is government demand for medicines?
Divya Srivastava and Alistair McGuire
Author Affiliations
BMC Public Health 2014, 14:767 doi:10.1186/1471-2458-14-767
Published: 30 July 2014
Abstract (provisional)
Background
Access to medicines is an important health policy issue. This paper considers demand structures in a selection of low-income countries from the perspective of public authorities as the evidence base is limited. Analysis of the demand for medicines in low-income countries is critical for effective pharmaceutical policy where regulation is less developed, health systems are cash constrained and medicines are not typically subsidised by a public health insurance system
Methods
This study analyses the demand for medicines in low-income countries from the perspective of the prices paid by public authorities. The analysis draws on a unique dataset from World Health Organization (WHO) and Health Action International (HAI) using 2003 data on procurement prices of medicines across 16 low-income countries covering 48 branded drugs and 18 therapeutic categories. Variation in prices, the mark-ups over marginal costs and estimation of price elasticities allows assessment of whether these elasticities are correlated with a country’s national income.
Results
Using the Ramsey pricing rule, the study’s findings suggest that substantial cross-country variation in prices and mark-ups exist, with price elasticities ranging from -1 to -2, which are weakly correlated with national income.
Conclusions
Government demand for medicines thus appears to be price elastic, raising important policy implications aimed at improving access to medicines for patients in low-income countries.

HPV vaccination – What about the boys?

British Medical Journal
02 August 2014(vol 349, issue 7969)
http://www.bmj.com/content/349/7969

Editorials
HPV vaccination – What about the boys?
Margaret Stanley, professor 1,
Colm O’Mahony, consultant in sexual health and HIV2, Simon Barton, clinical director HIV/genitourinary medicine and dermatology3
Author affiliations
BMJ 2014; 349 doi: http://dx.doi.org/10.1136/bmj.g4783 (Published 29 July 2014) Cite this as: BMJ 2014;349:g4783
Excerpt
A year ago an editorial in The BMJ highlighted the limitations of HPV vaccination in the UK1 and called for decisive action to maximise the public health benefits by thinking about vaccinating boys and some men. Similarly, a recent review by Stanley concluded, after consideration of cost effectiveness, that “failure to implement male vaccination looks like a missed public health opportunity.”2 We therefore share the disappointment expressed by the Royal College of Surgeons’ cancer services committee about the lack of response to its concerns about the inequity of vaccinating only girls against HPV in the UK.3
To summarise, the UK vaccination programme initially opted for Cervarix, a bivalent vaccine against HPV types 16 and 18, which are associated with cervical cancer. The programme switched to the quadrivalent Gardasil (which also protects against genital warts caused by HPV types 6 and 11) in September 2012 but still vaccinates only 12-13 year old girls. Interestingly, new data show that at that age the immune response to these vaccines is excellent and that only two doses of either vaccine is sufficient for long lasting immunity, rather than the three required at older ages…
…The only sensible answer to these dilemmas is a gender neutral vaccination strategy in schools that gives two doses of the vaccine to all 12-13 year old boys and girls. Anything else is discriminatory, inequitable, less effective, and difficult to explain. Can the UK afford to do it? If the price is right, we can’t afford not to.

Views and Reviews
Vaccinate boys as well as girls against HPV: it works, and it may be cost effective
BMJ 2014;349:g4834 (Published 29 July 2014)

Bulletin of the World Health Organization – Volume 92, Number 7, July 2014

Bulletin of the World Health Organization
Volume 92, Number 7, July 2014, 465-544
http://www.who.int/bulletin/volumes/92/7/en/

Varicella and herpes zoster hospitalizations before and after implementation of one-dose varicella vaccination in Australia: an ecological study
Anita E Heywood, Han Wang, Kristine K Macartney & Peter McIntyre
Objective
To examine trends in varicella and herpes zoster (HZ) hospitalization following the availability and subsequent National Immunization Programme funding of one-dose varicella vaccination in Australia.
Methods
Varicella vaccination coverage for children born between 2001 and 2009 was obtained from the Australian Childhood Immunization Register. Principal or any coded varicella or HZ hospitalizations were retrieved from the national hospital morbidity database from 1998 to 2010. Trends in hospitalization rates in different age groups and indigenous status were assessed. Incidence rate ratios (IRR) were calculated between periods before and after implementation of immunization programme funding.
Findings
In the first year of the funded immunization programme, varicella vaccine coverage reached 75% in children aged 24 months and more than 80% in children aged 60 months. Compared with the pre-vaccine period, varicella hospitalization rates during the funded programme were significantly lower for age groups younger than 40 years; with the greatest reduction in children aged 18–59 months (IRR: 0.25; 95% confidence interval, CI: 0.22–0.29). Indigenous children had a higher varicella hospitalization rate compared with non-indigenous children before vaccine implementation (IRR: 1.9; 95% CI: 1.4–2.7), but afterwards reached equivalence (IRR: 1.1; 95% CI: 0.7–1.6). The age-standardized HZ hospitalization rate declined between the periods (IRR: 0.95; 95% CI: 0.92–0.97).
Conclusion
Rapid attainment of high coverage reduced varicella hospitalizations in the targeted age group, particularly for indigenous children, but also in non-targeted age groups, with no increase in HZ hospitalizations. This suggests high one-dose varicella vaccine coverage can have a substantial impact on severe disease.

A prospective study of maternal, fetal and neonatal deaths in low- and middle-income countries
Sarah Saleem, Elizabeth M McClure, Shivaprasad S Goudar, Archana Patel, Fabian Esamai, Ana Garces, Elwyn Chomba, Fernando Althabe, Janet Moore, Bhalachandra Kodkany, Omrana Pasha, Jose Belizan, Albert Mayansyan, Richard J Derman, Patricia L Hibberd, Edward A Liechty, Nancy F Krebs, K Michael Hambidge, Pierre Buekens, Waldemar A Carlo, Linda L Wright, Marion Koso-Thomas, Alan H Jobe, Robert L Goldenberg & on behalf of the Global Network Maternal Newborn Health Registry Study Investigators
Objective
To quantify maternal, fetal and neonatal mortality in low- and middle-income countries, to identify when deaths occur and to identify relationships between maternal deaths and stillbirths and neonatal deaths.
Methods
A prospective study of pregnancy outcomes was performed in 106 communities at seven sites in Argentina, Guatemala, India, Kenya, Pakistan and Zambia. Pregnant women were enrolled and followed until six weeks postpartum.
Findings
Between 2010 and 2012, 214 070 of 220 235 enrolled women (97.2%) completed follow-up. The maternal mortality ratio was 168 per 100 000 live births, ranging from 69 per 100 000 in Argentina to 316 per 100 000 in Pakistan. Overall, 29% (98/336) of maternal deaths occurred around the time of delivery: most were attributed to haemorrhage (86/336), pre-eclampsia or eclampsia (55/336) or sepsis (39/336). Around 70% (4349/6213) of stillbirths were probably intrapartum; 34% (1804/5230) of neonates died on the day of delivery and 14% (755/5230) died the day after. Stillbirths were more common in women who died than in those alive six weeks postpartum (risk ratio, RR: 9.48; 95% confidence interval, CI: 7.97–11.27), as were perinatal deaths (RR: 4.30; 95% CI: 3.26–5.67) and 7-day (RR: 3.94; 95% CI: 2.74–5.65) and 28-day neonatal deaths (RR: 7.36; 95% CI: 5.54–9.77).
Conclusion
Most maternal, fetal and neonatal deaths occurred at or around delivery and were attributed to preventable causes. Maternal death increased the risk of perinatal and neonatal death. Improving obstetric and neonatal care around the time of birth offers the greatest chance of reducing mortality.