Evidence map›Paper›PMID 37403107›Full record

ArticleBMC medicine2023

Informing a target product profile for rapid tests to identify HBV-infected pregnant women with high viral loads: a discrete choice experiment with African healthcare workers.

Yasir Shitu Isa, Jonathan Sicsic, Henry Njuguna, John Ward, Mohamed Chakroun, Mohamed El-Kassas, Rado Ramanampamonjy, Salim Chalal, Jeanne Perpétue Vincent, Monique Andersson and 17 more

Open access · goldAbstract read
In one paragraph

Article in BMC medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 2 pooled it
2.3field-weighted citation impact, top 8% 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

3 citing papers in PubMed, 2 syntheses or guidelines pooled it, 4 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
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

27 authors at 20 institutions in 15 countries.

Yasir Shitu IsaInstitut Pasteur, Université Paris Cité, Unité d'Épidémiologie Des Maladies Émergentes, 25-28 Rue du Dr Roux, 75015, Paris, France.
Jonathan SicsicUniversité Paris Cité, LIRAES F-75006, Paris, France.
Henry NjugunaCoalition for Global Hepatitis Elimination, Decatur, GA, USA.
John WardCoalition for Global Hepatitis Elimination, Decatur, GA, USA.
Mohamed ChakrounInfectious Disease Department, Fattouma Bourguiba Hospital, Monastir, Tunisia.
Mohamed El-KassasEndemic Medicine Department, Faculty of Medicine, Helwan University, Cairo, Egypt.
Rado RamanampamonjyUnité de Gastro-Entérologie, Hôpital Joseph Raseta Befelatanana, Antananarivo, Madagascar.
Salim ChalalInstitut Pasteur, Université Paris Cité, Unité d'Épidémiologie Des Maladies Émergentes, 25-28 Rue du Dr Roux, 75015, Paris, France.
Jeanne Perpétue VincentInstitut Pasteur, Université Paris Cité, Unité d'Épidémiologie Des Maladies Émergentes, 25-28 Rue du Dr Roux, 75015, Paris, France.
Monique AnderssonDivision of Medical Virology, Stellenbosch University, Faculty of Medicine and Health Sciences, Cape Town, South Africa.
Hailemichael DesalegnMedical Department, St. Paul's Hospital Millennium Medical College, Addis Ababa, Ethiopia.
Fatou FallDepartment of Hepatology and Gastroenterology, Hopital Principal de Dakar, Dakar, Senegal.
Asgeir JohannessenDepartment of Infectious Diseases, Vestfold Hospital, Tønsberg, Norway.
Philippa C MatthewsThe Francis Crick Institute, London, UK.
Gibril NdowMedical Research Council Unit The Gambia, London School of Hygiene & Tropical Medicine, Fajara, The Gambia.
Edith OkekeFaculty of Medical Sciences, University of Jos, Jos, Nigeria.
Nicholas RichesDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
Moussa SeydiService de Maladies Infectieuses Et Tropicales, Centre Hospitalier National Universitaire de Fann, Dakar, Senegal.
Edford SinkalaDepartment of Internal Medicine, University of Zambia, Lusaka, Zambia.
C Wendy SpearmanDivision of Hepatology, Department of Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Alexander StockdaleDepartment of Clinical Infection, Microbiology and Immunology, Institute of Infection, University of Liverpool, Liverpool, UK.
Michael J VinikoorDepartment of Internal Medicine, University of Zambia, Lusaka, Zambia.
Gilles WandelerDepartment of Infectious Diseases, Bern University Hospital, University of Bern, Bern, Switzerland.
Roger SombiéService d'Hépato-Gastroentérologie, Centre Hospitalier Universitaire Yalgado Ouédraogo, Ouagadougou, Burkina Faso.
Maud LemoineMedical Research Council Unit The Gambia, London School of Hygiene & Tropical Medicine, Fajara, The Gambia.
Judith E MuellerInstitut Pasteur, Université Paris Cité, Unité d'Épidémiologie Des Maladies Émergentes, 25-28 Rue du Dr Roux, 75015, Paris, France.
Yusuke ShimakawaInstitut Pasteur, Université Paris Cité, Unité d'Épidémiologie Des Maladies Émergentes, 25-28 Rue du Dr Roux, 75015, Paris, France. yusuke.shimakawa@gmail.com.ORCID 0000-0002-4198-4785
Institut Pasteur · FRHepatitis B Foundation · USMRC Unit the Gambia · GMCentre Hospitalier National Universitaire de Fann · SNCentre Hospitalier Universitaire Yalgado Ouédraogo · BFHelwan University · EGHôpital Principal de Dakar · SNHospital Fatuma Bourguiba Monastir · TNLiverpool School of Tropical Medicine · GBStellenbosch University · ZASt. Paul's Hospital Millennium Medical College · ETUniversité Paris Cité · FRUniversity College Hospital · GBUniversity of Alabama at Birmingham · USUniversity of Bern · CHUniversity of Cape Town · ZAUniversity of Jos · NGUniversity of Liverpool · GBUniversity of Oslo · NOUniversity of Zambia · ZM

Funding

Mechanisms of HBV Functional Cure During Tenofovir-based ART in HIV/HBV CoinfectionR01AI147727 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Michael Jeffrey Vinikoor · 2019 to 2026
$3.9M
Department of HealthNIAID NIH HHS R01 AI147727Wellcome TrustWellcome Trust 110110/Z/15/Z
6 · The paper itself

Abstract

backgroundElimination of mother-to-child transmission of hepatitis B virus (HBV) requires infant immunoprophylaxis and antiviral prophylaxis for pregnant women with high viral loads. Since real-time polymerase chain reaction (RT-PCR), a gold standard for assessing antiviral eligibility, is neither accessible nor affordable for women living in low-income and middle-income countries (LMICs), rapid diagnostic tests (RDTs) detecting alternative HBV markers may be needed. To inform future development of the target product profile (TPP) for RDTs to identify highly viremic women, we used a discrete choice experiment (DCE) and elicited preference and trade-off of healthcare workers (HCW) in Africa between the following four attributes of fictional RDTs: price, time-to-result, diagnostic sensitivity, and specificity.

methodsThrough an online questionnaire survey, we asked participants to indicate their preferred test from a set of two RDTs in seven choice tasks with varying levels of the four attributes. We used mixed multinomial logit models to quantify the utility gain or loss generated by each attribute. We attempted to define minimal and optimal criteria for test attributes that can satisfy ≥ 70% and ≥ 90% of HCWs, respectively, as an alternative to RT-PCR.

resultsA total of 555 HCWs from 41 African countries participated. Increases in sensitivity and specificity generated significant utility and increases in cost and time-to-result generated significant disutility. The size of the coefficients for the highest attribute levels relative to the reference levels were in the following order: sensitivity (β = 3.749), cost (β = -2.550), specificity (β = 1.134), and time-to-result (β = -0.284). Doctors cared most about test sensitivity, while public health practitioners cared about cost and midwives about time-to-result. For an RDT with 95% specificity, costing 1 US$, and yielding results in 20 min, the minimally acceptable test sensitivity would be 82.5% and the optimally acceptable sensitivity would be 87.5%.

conclusionsAfrican HCWs would prefer an RDT with the following order of priority: higher sensitivity, lower cost, higher specificity, and shorter time-to-result. The development and optimization of RDTs that can meet the criteria are urgently needed to scale up the prevention of HBV mother-to-child transmission in LMICs.

Indexed as

Hepatitis B virusPregnant PeopleAntiviral AgentsFemaleHealth PersonnelHumansInfantInfectious Disease Transmission, VerticalPregnancySensitivity and SpecificityViral LoadAntiviral AgentsAfricaDiscrete choice experimentEliminationHepatitis BMother-to-child transmissionPreferencesRapid diagnostic testTarget product profile

Identifiers

PMID37403107
PMCPMC10320875
OpenAlexW4383069231

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.