Evidence map›Paper›PMID 33849572›Full record

ArticleMalaria journal2021

Are malaria transmission-blocking vaccines acceptable to high burden communities? Results from a mixed methods study in Bo, Sierra Leone.

Kaci D McCoy, Caroline T Weldon, Rashid Ansumana, Joseph M Lamin, David A Stenger, Sadie J Ryan, Kevin Bardosh, Kathryn H Jacobsen, Rhoel R Dinglasan

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 3 pooled it
4.7field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 3 syntheses or guidelines pooled it, 31 citations in OpenAlex.

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  16. Monoclonal antibodies for malaria prevention.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 6 institutions in 3 countries.

Kaci D McCoy *CDC Southeastern Center of Excellence in Vector Borne Diseases, Gainesville, FL, USA.
Caroline T Weldon *CDC Southeastern Center of Excellence in Vector Borne Diseases, Gainesville, FL, USA.
Rashid AnsumanaMercy Hospital Research Laboratory, Bo, Sierra Leone.
Joseph M LaminMercy Hospital Research Laboratory, Bo, Sierra Leone.
David A StengerCenter for Bio/Molecular Science and Engineering, Naval Research Laboratory, Washington, DC, USA.
Sadie J RyanCDC Southeastern Center of Excellence in Vector Borne Diseases, Gainesville, FL, USA.
Kevin BardoshCenter for One Health Research, School of Public Health, University of Washington, Seattle, WA, USA.
Kathryn H JacobsenDepartment of Global and Community Health, College of Health and Human Services, George Mason University, Fairfax, VA, USA.
Rhoel R DinglasanCDC Southeastern Center of Excellence in Vector Borne Diseases, Gainesville, FL, USA. rdinglasan@epi.ufl.edu.ORCID http://orcid.org/0000-0001-5433-8179
University of Florida · USGeorge Mason University · USNjala University · SLSoutheastern Health · USUnited States Naval Research Laboratory · USUniversity of Washington · US

Funding

Wellcome Trust
6 · The paper itself

Abstract

backgroundMalaria transmission-blocking vaccines (TBVs) could help break the cycle of malaria transmission by conferring community rather than individual protection. When introducing new intervention strategies, uptake is dependent on acceptability, not just efficacy. In this exploratory study on acceptability of TBVs in Sierra Leone, it was hypothesized that TBVs would be largely acceptable to adults and health workers in areas with relatively few ongoing malaria interventions, and that (i) knowledge of malaria and vaccines, (ii) health behaviours associated with malaria and vaccines, and (iii) attitudes towards different vaccines types could lead to greater TBV acceptability.

methodsThis study used a mixed methods approach in Bo, Sierra Leone, to understand community knowledge, attitudes, and practices related to malaria and vaccination in general. This included: (i) a population-based cross-sectional survey (n=615 adults), (ii) 6 focus group discussions with parents, and (iii) 20 key informant interviews. The concept of a TBV was explained to participants before they were asked about their willingness to accept this vaccine modality as part of an integrated malaria elimination programme.

resultsThis study found that most adults would be willing to receive a TBV vaccine. Respondents noted mostly positive past experiences with adult and childhood vaccinations for other infectious diseases and high levels of engagement in other malaria prevention behaviors such as bed nets. Perceived barriers to TBV acceptance were largely focused on general community-level distribution of a vaccine, including personal fears of vaccination and possible costs. After an explanation of the TBV mechanism, nearly all focus group and interview participants believed that community members would accept the vaccine as part of an integrated malaria control approach. Both parents and health workers offered insight on how to successfully roll-out a future TBV vaccination programme.

conclusionsThe willingness of community members in Bo, Sierra Leone to accept a TBV as part of an integrated anti-malarial strategy suggests that the atypical mechanism of TBV action might not be an obstacle to future clinical trials. This study's findings suggests that perceived general barriers to vaccination implementation, such as perceived personal fears and vaccine cost, must be addressed in future clinical and implementation research studies.

Indexed as

Health Knowledge, Attitudes, PracticeAdultAgedCross-Sectional StudiesFemaleFocus GroupsHumansMalariaMalaria VaccinesMaleMiddle AgedPatient Acceptance of Health CareSierra LeoneVaccinationYoung AdultMalaria VaccinesAcceptabilityBoMalariaSierra LeoneTransmission-blocking vaccine (TBV)

Identifiers

PMID33849572
PMCPMC8045381
OpenAlexW3155242576

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.