National Trends in Drug Payments for HIV Preexposure Prophylaxis in the United States, 2014 to 2018

Annals of Internal Medicine
17 November 2020 Volume 173, Issue 10
http://annals.org/aim/issue

 

Original Research
National Trends in Drug Payments for HIV Preexposure Prophylaxis in the United States, 2014 to 2018
A Retrospective Cohort Study
Nathan W. Furukawa, MD, MPH, Weiming Zhu, MD, PhD, Ya-Lin A. Huang, PhD, … et al.
Improving uptake of preexposure prophylaxis (PrEP) for people at risk for HIV is a priority of the National HIV/AIDS Federal Action Plan. This analysis estimates the distribution of PrEP costs in the United States between 2014 and 2018.

The Moral Imperative to Include Pregnant Women in Clinical Trials of Interventions for COVID-19

Annals of Internal Medicine
17 November 2020 Volume 173, Issue 10
http://annals.org/aim/issue

 

Ideas and Opinions
The Moral Imperative to Include Pregnant Women in Clinical Trials of Interventions for COVID-19
FREE
Isabelle Malhamé, MD, MSc, Rohan D’Souza, MD, PhD, and Matthew P. Cheng, MDCM
Although the number of clinical trials of interventions for COVID-19 is increasing, many exclude pregnant women or do not address pregnancy. This commentary discusses why pregnant women should be included in these trials.

Payments for Preexposure Prophylaxis in the United States: Too Much for Too Few

Annals of Internal Medicine
17 November 2020 Volume 173, Issue 10
http://annals.org/aim/issue

 

Editorials
Payments for Preexposure Prophylaxis in the United States: Too Much for Too Few

Kevin L. Ard, MD, MPH and
Rochelle P. Walensky, MD, MPH
Furukawa and colleagues provided a detailed analysis suggesting that costs are a fundamental reason why PrEP uptake is low. The editorialists discuss strategies to increase use of PrEP to prevent HIV infection.

Explanation in AI and law: Past, present and future

Artificial Intelligence – An International Journal
Volume 289, December 2020
https://www.sciencedirect.com/journal/artificial-intelligence/vol/289/suppl/C

 

Research article Abstract only
Explanation in AI and law: Past, present and future
Katie Atkinson, Trevor Bench-Capon, Danushka Bollegala
Article 103387
Abstract
Explanation has been a central feature of AI systems for legal reasoning since their inception. Recently, the topic of explanation of decisions has taken on a new urgency, throughout AI in general, with the increasing deployment of AI tools and the need for lay users to be able to place trust in the decisions that the support tools are recommending. This paper provides a comprehensive review of the variety of techniques for explanation that have been developed in AI and Law. We summarise the early contributions and how these have since developed. We describe a number of notable current methods for automated explanation of legal reasoning and we also highlight gaps that must be addressed by future systems to ensure that accurate, trustworthy, unbiased decision support can be provided to legal professionals. We believe that insights from AI and Law, where explanation has long been a concern, may provide useful pointers for future development of explainable AI.

Acceptability of on-site rapid HIV/HBV/HCV testing and HBV vaccination among three at-risk populations in distinct community-healthcare outreach centres: the ANRS-SHS 154 CUBE study

BMC Infectious Diseases
http://www.biomedcentral.com/bmcinfectdis/content
(Accessed 21 Nov 2020)

 

Acceptability of on-site rapid HIV/HBV/HCV testing and HBV vaccination among three at-risk populations in distinct community-healthcare outreach centres: the ANRS-SHS 154 CUBE study
HIV, HBV and HCV infections continue to represent major health concerns, especially among key at-risk populations such as men who have sex with men (MSM), people who inject drugs (PWIDs), transgender women (TG…
Authors: Ruxandra Calin, Véronique Massari, Gilles Pialoux, Nelly Reydellet, Eve Plenel, Carole Chauvin, Marie Jauffret-Roustide, Nesrine Day, Georges Kreplak, Anaenza Freire Maresca, Nicolas Derche, Sandra Louis, Stanislas Pol, Véronique Doré, Christine Rouzioux and Pierre Chauvin
Citation: BMC Infectious Diseases 2020 20:851
Content type: Research article
Published on: 16 November 2020

Impact of HPV-16/18 AS04-adjuvanted vaccine on preventing subsequent infection and disease after excision treatment: post-hoc analysis from a randomized controlled trial

BMC Infectious Diseases
http://www.biomedcentral.com/bmcinfectdis/content
(Accessed 21 Nov 2020)

 

Impact of HPV-16/18 AS04-adjuvanted vaccine on preventing subsequent infection and disease after excision treatment: post-hoc analysis from a randomized controlled trial
It is widely acknowledged that HPV prophylactic vaccine could prevent new infections and their associated lesions among women who are predominantly HPV-naive at vaccination. Yet there still remains uncertainty…
Authors: Shuang Zhao, Shangying Hu, Xiaoqian Xu, Xun Zhang, Qinjing Pan, Feng Chen and Fanghui Zhao
Citation: BMC Infectious Diseases 2020 20:846
Content type: Research article
Published on: 16 November 2020

Sharing genomic data from clinical testing with researchers: public survey of expectations of clinical genomic data management in Queensland, Australia

BMC Medical Ethics
http://www.biomedcentral.com/bmcmedethics/content
(Accessed 21 Nov 2020)

 

Sharing genomic data from clinical testing with researchers: public survey of expectations of clinical genomic data management in Queensland, Australia
Authors: Miranda E. Vidgen, Sid Kaladharan, Eva Malacova, Cameron Hurst and Nicola Waddell
Content type: Research article
19 November 2020

Ethics framework for treatment use of investigational drugs

BMC Medical Ethics
http://www.biomedcentral.com/bmcmedethics/content
(Accessed 21 Nov 2020)

 

Ethics framework for treatment use of investigational drugs
Authors: Jan Borysowski and Andrzej Górski
Content type: Debate
18 November 2020
Abstract
Background
Expanded access is the use of investigational drugs (IDs) outside of clinical trials. Generally it is performed in patients with serious and life-threatening diseases who cannot be treated satisfactorily with authorized drugs. Legal regulations of expanded access to IDs have been introduced among others in the USA, the European Union (EU), Canada and Australia. In addition, in the USA an alternative to expanded access is treatment under the Right-to-Try law. However, the treatment use of IDs is inherently associated with a number of ethically relevant problems.
Main text
The objective of this article is to present a coherent framework made up of eight requirements which have to be met for any treatment use of an ID to be ethical. These include a justified need for the use of an ID, no threat to clinical development of the ID, adequate scientific evidence to support the treatment, patient’s benefit as the primary goal of the use of an ID, informed decision of a patient, fair access of patients to IDs, independent review, as well as the dissemination of treatment results.
Conclusions
While this framework is essentially consistent with the legal regulations of expanded access of the USA, the EU, Canada and Australia, it is substantially wider in scope because it addresses some important issues that are not covered by the regulations. Overall, the framework that we developed minimizes the risks and threats, and maximizes potential benefits to each of the four key stakeholders involved in the treatment use of IDs including patients, doctors, drug manufacturers, and society at large.

Clinical Ethics Committees in Africa: lost in the shadow of RECs/IRBs?

BMC Medical Ethics
http://www.biomedcentral.com/bmcmedethics/content
(Accessed 21 Nov 2020)

 

Clinical Ethics Committees in Africa: lost in the shadow of RECs/IRBs?
Clinical Ethics Committees (CECs) are well established at healthcare institutions in resource-rich countries. However, there is limited information on established CECs in resource poor countries, especially in Africa. This study aimed to establish baseline data regarding existing formal CECs in Africa to raise awareness of and to encourage the establishment of CECs or Clinical Ethics Consultation Services (CESs) on the continent.
Authors: Keymanthri Moodley, Siti Mukaumbya Kabanda, Leza Soldaat, Anita Kleinsmidt, Adetayo Emmanuel Obasa and Sharon Kling
Citation: BMC Medical Ethics 2020 21:115
Content type: Research article
Published on: 18 November 2020

Selecting appropriate endpoints for assessing treatment effects in comparative clinical studies for COVID-19

Contemporary Clinical Trials
Volume 97 October 2020
https://www.sciencedirect.com/journal/contemporary-clinical-trials/vol/97/suppl/C

 

Research article Full text access
Selecting appropriate endpoints for assessing treatment effects in comparative clinical studies for COVID-19
Zachary R. McCaw, Lu Tian, Kevin N. Sheth, Wan-Ting Hsu, … Lee-Jen Wei
Article 106145
Abstract
To evaluate the efficacy and safety of a new treatment for COVID-19 vs. standard care, certain key endpoints are related to the duration of a specific event, such as hospitalization, ICU stay, or receipt of supplemental oxygen. However, since patients may die in the hospital during study follow-up, using, for example, the duration of hospitalization to assess treatment efficacy can be misleading. If the treatment tends to prolong patients’ survival compared with standard care, patients in the new treatment group may spend more time in hospital. This can lead to a “survival bias” issue, where a treatment that is effective for preventing death appears to prolong an undesirable outcome. On the other hand, by using hospital-free survival time as the endpoint, we can circumvent the survival bias issue. In this article, we use reconstructed data from a recent, large clinical trial for COVID-19 to illustrate the advantages of this approach. For the analysis of ICU stay or oxygen usage, where the initiating event is potentially an outcome of treatment, standard survival analysis techniques may not be appropriate. We also discuss issues with analyzing the durations of such events.

Long-term durability of immunogenicity induced by standard and triple-dose hepatitis B vaccine in patients receiving methadone maintenance treatment

Expert Review of Vaccines
Vol 19 (9) 2020
https://www.tandfonline.com/toc/ierv20/current

 

Case Report
Long-term durability of immunogenicity induced by standard and triple-dose hepatitis B vaccine in patients receiving methadone maintenance treatment
Tian Yao , Yuanting Wu , Shuang Dong , Linying Gao , Shan Shi , Zhihong Shao , Lina Wu , Dan Feng , Jing Shi , Yawei Zhang , Yongliang Feng , Xiaofeng Liang & Suping Wang
Pages: 785-794
Published online: 14 Sep 2020

Transparency, trust, and community welfare: towards a precision public health ethics framework for the genomics era

Genome Medicine
https://genomemedicine.biomedcentral.com/articles
[Accessed 21 Nov 2020]

 

Comment
Transparency, trust, and community welfare: towards a precision public health ethics framework for the genomics era
Authors: Eric T. Juengst and Annelies Van Rie
Citation: Genome Medicine 2020 12:98
Published on: 20 November 2020
Abstract
Infectious disease control is experiencing a paradigm shift, as pathogen sequencing technologies and digital applications are increasingly implemented for control of diseases such as tuberculosis, Ebola, and COVID-19. A new ethical framework should be a critical part of this emerging paradigm to ensure that the benefit of precision public health interventions based on advances in genomics research is not outweighed by the risks they pose to individuals, families, and vulnerable segments of the population. We suggest that the ethical framework guiding practice in this domain combines standard precepts from public health ethics with emerging ethics principles from precision medicine.

Establishment of COVID-19 testing laboratory in resource-limited settings: challenges and prospects reported from Ethiopia

Global Health Action
Volume 13, Issue 1 (2020)
https://www.tandfonline.com/toc/zgha20/current?nav=tocList

 

Article
Establishment of COVID-19 testing laboratory in resource-limited settings: challenges and prospects reported from Ethiopia
Adugna Abera , Habtamu Belay , Aboma Zewude , Bokretsion Gidey , Desalegn Nega , Boja Dufera , Abnet Abebe , Tujuba Endriyas , Birhanu Getachew , Henok Birhanu , Hailemariam Difabachew , Bacha Mekonnen , Helina Legesse , Firdawek Bekele , Kalkidan Mekete , Seble Seifu , Heven Sime , Nebiyou Yemanebrhan , Mesfin Tefera , Hiwot Amare , Berhane Beyene , Estifanos Tsige , Adisu Kebede , Geremew Tasew , Getachew Tollera , Ebba Abate , Adugna Woyessa & Ashenafi Assefa
Article: 1841963
Published online: 17 Nov 2020

Universal access to essential medicines as part of the right to health: a cross-national comparison of national laws, medicines policies, and health system indicators

Global Health Action
Volume 13, Issue 1 (2020)
https://www.tandfonline.com/toc/zgha20/current?nav=tocList

 

Article
Universal access to essential medicines as part of the right to health: a cross-national comparison of national laws, medicines policies, and health system indicators
Katrina Perehudoff
Article: 1699342
Published online: 02 Nov 2020
ABSTRACT
Background
Access to essential medicines for the world’s poor and vulnerable has made little progress since 2000, except for a few specific medicines such as antiretrovirals for HIV/AIDS. Human rights principles written into national law can create a supportive environment for universal access to medicines; however, systematic research and policy guidance on this topic is lacking.
Objective
To examine how international human rights law and WHO’s essential medicines policies are embedded in national law for medicines affordability and financing, and interpreted and implemented in practice to promote universal access to essential medicines.
Methods
This thesis consists of (1) a cross-national content analysis of 192 national constitutions, 71 national medicines policies, and legislation for universal health coverage (UHC) from 16 mostly low- and middle-income countries; (2) a case study of medicines litigation in Uruguay, and (3) a follow-up report of eight right to health indicators for access to medicines from 195 countries.
Results
Some, but not all, of the 12 principles from human rights law and WHO’s policy are embedded in national UHC law and medicines policies (part 1). Even the most rights-compliant legislation for access to medicines is subject to the unique and inconsistent interpretation of domestic courts, which may be inconsistent with the right to health in international law (part 2). Many national health systems for which data were available still fail to meet the official targets for eight indicators of access to medicines (part 3).
Conclusions
International human rights law and WHO policy are embedded in national law for essential medicines and practically implemented in national health systems. Law makers can use these findings and the example texts in this thesis as a starting point for writing and monitoring governments’ rights-based legal commitments for access to medicines. Future research should study the effect of national law on access to medicines and population health.

Factors contributing to the uptake of childhood vaccination in Galkayo District, Puntland, Somalia

Global Health Action
Volume 13, Issue 1 (2020)
https://www.tandfonline.com/toc/zgha20/current?nav=tocList

 

Article
Factors contributing to the uptake of childhood vaccination in Galkayo District, Puntland, Somalia
Mohamed Farah Abdullahi , Jennifer Stewart Williams , Klas-Göran Sahlèn , Khalif Bile & John Kinsman
Article: 1803543
Published online: 27 Aug 2020

Applying systems thinking to knowledge mobilisation in public health

Health Research Policy and Systems
http://www.health-policy-systems.com/content
[Accessed 21 Nov 2020]

 

Commentary
Applying systems thinking to knowledge mobilisation in public health
Knowledge mobilisation (KM) is a vital strategy in efforts to improve public health policy and practice. Linear models describing knowledge transfer and translation have moved towards multi-directional and complexity-attuned approaches where knowledge is produced and becomes meaningful through social processes. There are calls for systems approaches to KM but little guidance on how this can be operationalised. This paper describes the contribution that systems thinking can make to KM and provides guidance about how to put it into action.
Authors: Abby Haynes, Lucie Rychetnik, Diane Finegood, Michelle Irving, Louise Freebairn and Penelope Hawe
17 November 2020

Disability inclusion in humanitarian action

Humanitarian Exchange Magazine
Number 78, October 2020
https://odihpn.org/magazine/inclusion-of-persons-with-disabilities-in-humanitarian-action-what-now/

 

Disability inclusion in humanitarian action
by HPN October 2020
The theme of this edition of Humanitarian Exchange, co-edited with Sherin Alsheikh Ahmed from Islamic Relief Worldwide, is disability inclusion in humanitarian action. Persons with disabilities are not only disproportionately impacted by conflicts, disasters and other emergencies, but also face barriers to accessing humanitarian assistance. At the same time, global commitments and standards and the IASC Guidelines on the inclusion of persons with disabilities in humanitarian action all emphasise how persons with disabilities are also active agents of change. Disability and age-focused organisations have led on testing and demonstrating how inclusion can be done better. Yet despite this progress, challenges to effective inclusion remain.

As Kirstin Lange notes in the lead article, chief among these challenges is humanitarian agencies’ lack of engagement with organisations of persons with disabilities. Simione Bula, Elizabeth Morgan and Teresa Thomson look at disability inclusion in humanitarian response in the Pacific, and Kathy Al Jubeh and Alradi Abdalla argue for a ‘participation revolution’, building on learning from the gender movement. Tchaurea Fleury and Sulayman AbdulMumuni Ujah outline how the Bridge Article 11 training initiative is encouraging constructive exchange between humanitarian and disability actors. The lack of good, disaggregated data is highlighted by Sarah Collinson; Frances Hill, Jim Cranshaw and Carys Hughes emphasise the need for training resources in local languages and accessible formats; and Sophie Van Eetvelt and colleagues report on a review of the evidence on inclusion of people with disabilities and older people.

Rebecca Molyneux and co-authors analyse the findings of a review of a DFID programme in north-east Nigeria, while Carolin Funke highlights the importance of strategic partnerships between disability-focused organisations, drawing on her research in Cox’s Bazar. Sherin Alsheikh Ahmed describes Islamic Relief Worldwide’s approach to mainstreaming protection and inclusion, while Pauline Thivillier and Valentina Shafina outline IRC’s Client Responsive Programming. The edition ends with reflections by Mirela Turcanu and Yves Ngunzi Kahashi on CAFOD’s SADI approach.

A cross sectional study on immunization status among children 12 to 24 months of age in urban field practice area of tertiary health care centre, Hyderabad

International Journal of Community Medicine and Public Health
Vol 7, No 11 (2020) November 2020
https://www.ijcmph.com/index.php/ijcmph/issue/view/68

 

Table of Contents
A cross sectional study on immunization status among children 12 to 24 months of age in urban field practice area of tertiary health care centre, Hyderabad
Arundhathi Baaki, Lavanya Katta, Sreelatha Panuganti, B. Kiranmai
DOI: 10.18203/2394

Vaccine hesitancy in India-the challenges: a review

International Journal of Community Medicine and Public Health
Vol 7, No 11 (2020) November 2020
https://www.ijcmph.com/index.php/ijcmph/issue/view/68

 

Review Articles
Vaccine hesitancy in India-the challenges: a review
Gopalakrishnan S., Sujitha P.
DOI: 10.18203/2394-6040.ijcmph20204768
Abstract
Immunization is the most cost-effective scientific method of reducing childhood morbidity and mortality. In India the national immunization programme has not been able to attain complete coverage of the eligible children and hence mortality due to vaccine preventable diseases is approximately 5 lakhs annually.  Every year, 89 lakhs children are at risk to develop vaccine preventable diseases due to lack of immunization. While most people vaccinate according to the recommended schedule, this success is challenged by individuals and groups who delay, hesitant or refuse vaccines due to various reasons. Despite the realization of compulsory scheduling of vaccines, there are an alarming number of parents who do not permit the vaccination of their children as scheduled. Vaccine hesitancy refers to a delay in acceptance or refusal of vaccines despite the availability of vaccination services. WHO in 2019 listed vaccine hesitancy as one of the ten global health threats. The recent vaccination coverage evaluation studies have shown that there is a perceptible drop in the vaccine coverage in most parts of India and also that the disparity in the urban-rural coverage is also widening. Hence an evaluation of the reasons for vaccine hesitancy is vital at present to strengthen the universal immunization program. The authors are trying to trace the present status and reasons for vaccine hesitancy reported in recent times, which can lead to outbreaks of already controlled vaccine preventable diseases and to identify strategies which are being implemented to overcome the vaccine hesitancy.

Financial Penalties Imposed on Large Pharmaceutical Firms for Illegal Activities

JAMA
November 17, 2020, Vol 324, No. 19, Pages 1925-2006
https://jamanetwork.com/journals/jama/currentissue

 

Research Letter
Financial Penalties Imposed on Large Pharmaceutical Firms for Illegal Activities
Denis G. Arnold, PhD; Oscar Jerome Stewart, PhD; Tammy Beck, PhD
JAMA. 2020;324(19):1995-1997. doi:10.1001/jama.2020.18740
This study describes financial penalties levied on pharmaceutical companies for illegal activities by type of activity and dollar value between 2003 and 2016.

Preventing the Spread of SARS-CoV-2 With Masks and Other “Low-tech” Interventions

JAMA
November 17, 2020, Vol 324, No. 19, Pages 1925-2006
https://jamanetwork.com/journals/jama/currentissue

 

Viewpoint
Preventing the Spread of SARS-CoV-2 With Masks and Other “Low-tech” Interventions
Andrea M. Lerner, MD, MS; Gregory K. Folkers, MS, MPH; Anthony S. Fauci, MD
free access has active quiz has multimedia has audio
JAMA. 2020;324(19):1935-1936. doi:10.1001/jama.2020.21946
In this Viewpoint, Anthony Fauci and colleagues at NIAID emphasize the continued importance of low-tech public health practices, such as wearing masks, limiting large gatherings, hand washing, and physical distancing, to help control the COVID-19 pandemic even after safe and effective vaccines become available until distribution and uptake of vaccines confer herd immunity on a population level.

Postapproval Vaccine Safety Surveillance for COVID-19 Vaccines in the US

JAMA
November 17, 2020, Vol 324, No. 19, Pages 1925-2006
https://jamanetwork.com/journals/jama/currentissue

 

Postapproval Vaccine Safety Surveillance for COVID-19 Vaccines in the US
Grace M. Lee, MD, MPH; José R. Romero, MD; Beth P. Bell, MD, MPH
free access has active quiz
JAMA. 2020;324(19):1937-1938. doi:10.1001/jama.2020.19692
This Viewpoint reviews systems in place to monitor postlicensure vaccine safety, and recommends harmonizing end points and protocols across vaccine trials and surveillance systems to enable timely identification and reliable evaluation of potential adverse events.

Postlicensure Evaluation of COVID-19 Vaccines

JAMA
November 17, 2020, Vol 324, No. 19, Pages 1925-2006
https://jamanetwork.com/journals/jama/currentissue

 

Postlicensure Evaluation of COVID-19 Vaccines
Manish M. Patel, MD; Michael L. Jackson, PhD; Jill Ferdinands, PhD
free access has active quiz
JAMA. 2020;324(19):1939-1940. doi:10.1001/jama.2020.19328
This Viewpoint explains the “test-negative” modified case-control design commonly used for evaluating vaccine effectiveness, describes why it may be lead to biased estimates of COVID-19 vaccine effectiveness in patients with severe illness more likely to test negative, and proposes potential approaches to correcting the bias, including incorporation of clinical assessment of cases.

Heritable Human Genome EditingThe International Commission Report

JAMA
November 17, 2020, Vol 324, No. 19, Pages 1925-2006
https://jamanetwork.com/journals/jama/currentissue

 

Heritable Human Genome EditingThe International Commission Report
Eli Y. Adashi, MD, MS; I. Glenn Cohen, JD
has audio
JAMA. 2020;324(19):1941-1942. doi:10.1001/jama.2020.19059
This Viewpoint summarizes the report of the International Commission on the Clinical Use of Human Germline Genome Editing sponsored by the US National Academy of Medicine and the UK Royal Society, enumerating technical, regulatory, and ethical standards that need to be met before HHGE can be used on human embryos.

Bioinformatics, Sequencing Accuracy, and the Credibility of Clinical Genomics

JAMA
November 17, 2020, Vol 324, No. 19, Pages 1925-2006
https://jamanetwork.com/journals/jama/currentissue

 

Editorial
Bioinformatics, Sequencing Accuracy, and the Credibility of Clinical Genomics
W. Gregory Feero, MD, PhD
Abstract
JAMA. 2020;324(19):1945-1947. doi:10.1001/jama.2020.19939
The adoption of clinical exome and whole-genome sequencing based on next-generation sequencing technologies has increased rapidly over the last decade; this has been accelerated by increasing coverage of these services by private and public insurers.1,2 Examples of use include tumor and germline sequencing in patients with cancer, rapid turn-around sequencing of the genomes of critically ill neonates to diagnose mendelian conditions, and noninvasive prenatal testing for reproductive decision-making. The accuracy of sequencing results is of paramount importance to patients, clinicians, and those paying for testing services; inaccuracy can affect not only the tested individual, but their extended biological family.3 Understanding what accuracy means in the context of genome sequencing is a challenge. In the genomics community accuracy is often described using 2 terms: analytic validity, eg, does the sequencing process reliably detect variations that are present in an individual’s genome; and clinical validity, eg, are the variants detected reliably related to health outcomes.

Self-efficacy and HPV Vaccine Attitudes Mediate the Relationship Between Social Norms and Intentions to Receive the HPV Vaccine Among College Students

Journal of Community Health
Volume 45, issue 6, December 2020
https://link.springer.com/journal/10900/volumes-and-issues/45-6

 

Articles
Self-efficacy and HPV Vaccine Attitudes Mediate the Relationship Between Social Norms and Intentions to Receive the HPV Vaccine Among College Students
Authors (first, second and last of 5)
Madison E. Stout, Shannon M. Christy, Catherine E. Mosher
Content type: Original Paper
Published: 16 May 2020
Pages: 1187 – 1195

Identifying Associations Between Influenza Vaccination Status and Access, Beliefs, and Sociodemographic Factors Among the Uninsured Population in Suffolk County, NY

Journal of Community Health
Volume 45, issue 6, December 2020
https://link.springer.com/journal/10900/volumes-and-issues/45-6

 

Identifying Associations Between Influenza Vaccination Status and Access, Beliefs, and Sociodemographic Factors Among the Uninsured Population in Suffolk County, NY
Authors (first, second and last of 4)
George Chen, Masooma Kazmi, Jedan Phillips
Content type: Original Paper
Published: 30 June 2020
Pages: 1236 – 1241

COVID-19 vaccines: no time for complacency

The Lancet
Nov 21, 2020 Volume 396 Number 10263 p1607-1702, e89
https://www.thelancet.com/journals/lancet/issue/current

 

Editorial
COVID-19 vaccines: no time for complacency
The Lancet
“Yes. Yes. Yes.” That was the response of John Bell, Regius Professor of Medicine at the University of Oxford, when asked whether we could be confident that life will be returning to normal by spring. He was being interviewed by the BBC shortly after the announcement last week by Pfizer and BioNTech that their COVID-19 vaccine candidate had 90% efficacy in clinical trials. Similar announcements about the Russian Sputnik V and Moderna vaccines followed soon after. The prospect of preventing illness and death, and avoiding the harm and misery of extended restrictions, is a cause for optimism. But although it is right to be hopeful and encouraged, we are far from ending COVID-19 as a public health issue.

Unfortunately, the trials’ results were announced via press releases, leaving many scientific uncertainties that will dictate how the vaccines will affect the course of the pandemic. Little safety data are available. How well the vaccines work in older people or those with underlying conditions and their efficacy in preventing severe disease are still unclear. Peer-reviewed publication should resolve these issues, but other questions will not be answerable for some time. For one, the duration of protection is unknown and will have a huge bearing on the practicalities and logistics of immunisation (will boosters be needed? How often?).

Whether the vaccines prevent transmission of SARS-CoV-2 or mainly just protect against illness is largely unknown too. If the latter, achieving herd immunity through immunisation becomes a difficult prospect. Pfizer and Moderna together project that there will be enough vaccine for 35 million individuals in 2020, and perhaps up to 1 billion in 2021. As a result, many millions of people at high risk of disease will not be immunised any time soon, necessitating the continued use of non-pharmaceutical interventions. There is a danger that the public might become complacent following the news of promising vaccines, but how much more difficult will it be to ensure adherence to guidance and restrictions when a vaccine is available to many but others remain unprotected? Vaccine hesitancy is also a clear threat to COVID-19 control. New data show that willingness to take a COVID-19 vaccine is far from universal. When even wearing a face mask can be painted as a political act rather than a public health measure, responsible leadership and careful public communications will be essential.

These concerns will be irrelevant in places where a vaccine is unavailable entirely. Leaving aside the huge logistical challenges of manufacturing and roll-out (including onerous cold-chain requirements for some candidates), vaccine nationalism remains a major threat to equitable access. COVAX, the GAVI-led financing mechanism to provide COVID vaccines to low-income and middle-income countries, has raised US$2 billion, but needs $5 billion more for 2021. Pfizer and Moderna have not yet reached agreements with COVAX to supply vaccines; Pfizer has issued an expression of interest. By contrast, a handful of high-income countries have already secured the option to buy hundreds of millions of doses. Although some vaccine developers have promised to limit profits from the COVID-19 pandemic, Pfizer and Moderna have made no such commitments.

What does the long-term future look like? Will SARS-CoV-2 become endemic, in a post-pandemic phase? It is likely, but it is too early to be sure what form this endemicity will take. Vaccines will be just one determinant. Reinfections are another: they appear rare so far, but the pandemic is still young. The nature and length of immune responses, and the characteristics of the virus and infection play a role too. Can infection provide sterilising immunity? How quickly does protective immunity wane? How severe might reinfection be? How does immunity vary by sex, ethnicity, and age? Will we have annual seasonal outbreaks? Or longer spells of quiescence punctuated by re-emergence? And how will health systems have to adapt accordingly? These issues and many others will determine the continuing impacts of COVID-19 on health and all are still poorly understood.

2020 has been a year of incredible scientific achievement. In less than 12 months, researchers have characterised a novel illness, sequenced a new virus’s genome, developed diagnostics, produced treatment protocols, and established the efficacy of drugs and vaccines in randomised controlled trials. Many people are feeling hopeful for the first time in a long time. But there is still much to learn and many barriers to overcome. On Nov 14, 5 days after the announcement by Pfizer, 663  772 new cases of COVID-19 were recorded, the largest number in a single day. It is a dangerous moment to be complacent.

Emerging mental health challenges, strategies, and opportunities in the context of the COVID-19 pandemic: Perspectives from South American decision-makers

Revista Panamericana de Salud Pública/Pan American Journal of Public Health (RPSP/PAJPH)
https://www.paho.org/journal/en

20 Nov 2020
Emerging mental health challenges, strategies, and opportunities in the context of the COVID-19 pandemic: Perspectives from South American decision-makers
Current topic | English |

Vaccines to prevent COVID-19: a protocol for a living systematic review with network meta-analysis including individual patient data (The LIVING VACCINE Project)

Systematic Reviews
https://systematicreviewsjournal.biomedcentral.com/articles
[Accessed 21 Nov 2020]

 

https://stm.sciencemag.org/
Vaccines to prevent COVID-19: a protocol for a living systematic review with network meta-analysis including individual patient data (The LIVING VACCINE Project)
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes coronavirus disease 2019 (COVID-19) which has rapidly spread worldwide. Several human randomized clinical trials assessing potential vaccines…
Authors: Steven Kwasi Korang, Sophie Juul, Emil Eik Nielsen, Joshua Feinberg, Faiza Siddiqui, Giok Ong, Sarah Klingenberg, Areti Angeliki Veroniki, Fanlong Bu, Lehana Thabane, Allan Randrup Thomsen, Janus C. Jakobsen and Christian Gluud
Citation: Systematic Reviews 2020 9:262
Content type: Protocol
Published on: 20 November 2020

A clinical perspective of the U.S. anti-vaccination epidemic: Considering marginal costs and benefits, CDC best practices guidelines, free riders, and herd immunity

Vaccine
Volume 38, Issue 50 Pages 7877-8054 (25 November 2020)
https://www.sciencedirect.com/journal/vaccine/vol/38/issue/50

 

Discussion Abstract only
A clinical perspective of the U.S. anti-vaccination epidemic: Considering marginal costs and benefits, CDC best practices guidelines, free riders, and herd immunity
Michael G. Anderson, Eric A. Ballinger, David Benjamin, Lawrence D. Frenkel, … Karin W. Zucker
Pages 7877-7879

Cost-effectiveness of HPV vaccination for adults through age 45 years in the United States: Estimates from a simplified transmission model

Vaccine
Volume 38, Issue 50 Pages 7877-8054 (25 November 2020)
https://www.sciencedirect.com/journal/vaccine/vol/38/issue/50

 

Research article Abstract only
Cost-effectiveness of HPV vaccination for adults through age 45 years in the United States: Estimates from a simplified transmission model
Harrell W. Chesson, Elissa Meites, Donatus U. Ekwueme, Mona Saraiya, Lauri E. Markowitz
Pages 8032-8039

Does education about local vaccination rates and the importance of herd immunity change US parents’ concern about measles?

Vaccine
Volume 38, Issue 50 Pages 7877-8054 (25 November 2020)
https://www.sciencedirect.com/journal/vaccine/vol/38/issue/50

 

Research article Open access
Does education about local vaccination rates and the importance of herd immunity change US parents’ concern about measles?
Bridget C. Griffith, Angela K. Ulrich, Andy B. Becker, Dawn Nederhoff, … Nicole E. Basta
Pages 8040-8048

Effect of a vaccine information statement (VIS) on immunization status and parental knowledge, attitudes, and beliefs regarding infant immunization in Japan

Vaccine
Volume 38, Issue 50 Pages 7877-8054 (25 November 2020)
https://www.sciencedirect.com/journal/vaccine/vol/38/issue/50

 

Japanese Society for Vaccinology paper
Research article Abstract only
Effect of a vaccine information statement (VIS) on immunization status and parental knowledge, attitudes, and beliefs regarding infant immunization in Japan
Aya Saitoh, Akihiko Saitoh, Tomohiro Katsuta, Mahito Mine, … Kenji Okada
Pages 8049-8054

Vaccination Attitude and Communication in Early Settings: An Exploratory Study

Vaccines — Open Access Journal
http://www.mdpi.com/journal/vaccines
(Accessed 21 Nov 2020)

 

Open Access Article
Vaccination Attitude and Communication in Early Settings: An Exploratory Study
by Noemi Mereu et al
Vaccines 2020, 8(4), 701; https://doi.org/10.3390/vaccines8040701 – 20 Nov 2020
Abstract
Background: This study assesses attitudes towards vaccination in mothers of new-born babies and explores its association with different exposures to communication. Methods: Data were collected through questionnaires administered by means of interviews. Results: Data highlighted that 20% of mothers showed an orientation towards […

Strategies to Improve Coverage of Typhoid Conjugate Vaccine (TCV) Immunization Campaign in Karachi, Pakistan

Vaccines — Open Access Journal
http://www.mdpi.com/journal/vaccines
(Accessed 21 Nov 2020)

 

Open Access Article
Strategies to Improve Coverage of Typhoid Conjugate Vaccine (TCV) Immunization Campaign in Karachi, Pakistan
by Farah Naz Qamalar et al
Vaccines 2020, 8(4), 697; https://doi.org/10.3390/vaccines8040697 – 19 Nov 2020
Abstract
The emergence and spread of extensively drug-resistant (XDR) typhoid in Karachi, Pakistan led to an outbreak response in Lyari Town, Karachi utilizing a mass immunization campaign with typhoid conjugate vaccine (TCV), Typbar TCV®. The mass immunization campaign, targeted Lyari Town, Karachi, one of […]

Open Access Article
Understanding How Adolescents Think about the HPV Vaccine
by Robyn A. Pennella et al
Vaccines 2020, 8(4), 693; https://doi.org/10.3390/vaccines8040693 – 18 Nov 2020
Abstract
Despite educational efforts, Tennessee human papillomavirus (HPV) vaccination rates are 43%, among the lowest in the United States. This study examined how adolescents think about the HPV vaccine to identify patterns and misconceptions to enhance educational efforts. Adolescents (ages 11–12) (N = […]