Operational lessons learned in conducting an international study on pharmacovigilance in pregnancy in resource-constrained settings: The WHO Global Vaccine safety Multi-Country collaboration project.

Maternal health Multi-country Studies Neonatal health Pharmacovigilance Surveillance Vaccine Safety

Journal

Vaccine: X
ISSN: 2590-1362
Titre abrégé: Vaccine X
Pays: England
ID NLM: 101748769

Informations de publication

Date de publication:
Aug 2022
Historique:
received: 23 09 2021
revised: 03 02 2022
accepted: 04 04 2022
pubmed: 19 4 2022
medline: 19 4 2022
entrez: 18 4 2022
Statut: ppublish

Résumé

The WHO Global Vaccine Safety Multi-Country Collaboration study on safety in pregnancy aims to estimate the minimum detectable risk for selected perinatal and neonatal outcomes and assess the applicability of standardized case definitions for study outcomes and maternal immunization in low- and middle-income countries (LMICs). This paper documents the operational lessons learned from the study. A prospective observational study was conducted across 21 hospitals in seven countries. All births occurring at sites were screened to identify select perinatal and neonatal outcomes from May 2019 to August 2020. Up to 100 cases per outcome were recruited to assess the applicability of standardized case definitions. A multi-pronged study quality assurance plan was implemented. The impact of the COVID-19 pandemic on site functioning and project implementation was also assessed. Multi-layered ethics and administrative approvals, limited clinical documentation, difficulty in identifying outcomes requiring in-hospital follow-up, and poor quality internet connectivity emerged as important barriers to study implementation. Use of electronic platforms, application of a rigorous quality assurance plan with frequent interaction between the central and site teams helped improve data quality. The COVID-19 pandemic disrupted data collection for up to 6 weeks in some sites. Our study succeeded in establishing an international hospital-based surveillance network for evaluating perinatal and neonatal outcomes using common study protocol and procedures in geographically diverse sites with differing levels of infrastructure, clinical and health-utilization practices. The enhanced surveillance capacity of participating sites shall help support future pharmacovigilance efforts for pregnancy interventions.

Identifiants

pubmed: 35434599
doi: 10.1016/j.jvacx.2022.100160
pii: S2590-1362(22)00020-1
pmc: PMC8993756
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100160

Subventions

Organisme : World Health Organization
ID : 001
Pays : International

Informations de copyright

© 2022 The Author(s).

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Apoorva Sharan (A)

The INCLEN Trust International, New Delhi, India.
Swiss Tropical and Public Health Institute (Swiss TPH), Basel, Switzerland.
University of Basel, Basel, Switzerland.

Shubhashri Jahagirdar (S)

The INCLEN Trust International, New Delhi, India.

Anke L Stuurman (AL)

P95 Pharmacovigilance and Epidemiology, Leuven, Belgium.

Varalakshmi Elango (V)

P95 Pharmacovigilance and Epidemiology, Leuven, Belgium.

Margarita Riera-Montes (M)

P95 Pharmacovigilance and Epidemiology, Leuven, Belgium.

Neeraj Kumar Kashyap (N)

The INCLEN Trust International, New Delhi, India.

Narendra Kumar Arora (N)

The INCLEN Trust International, New Delhi, India.

Mathews Mathai (M)

Centre for Maternal and Newborn Health, Liverpool School of Tropical Medicine, Liverpool, UK.

Punam Mangtani (P)

Department of Infectious Disease Epidemiology, London School of Tropical Medicine, London, UK.

Hugo Devlieger (H)

Universitair Ziekenhuis, Leuven, Belgium.

Steven Anderson (S)

Center for Biologics Evaluation and Research (CBER), U.S. Food and Drug Administration (FDA), Silver Spring, MD, USA.

Barbee Whitaker (B)

Center for Biologics Evaluation and Research (CBER), U.S. Food and Drug Administration (FDA), Silver Spring, MD, USA.

Hui-Lee Wong (HL)

Center for Biologics Evaluation and Research (CBER), U.S. Food and Drug Administration (FDA), Silver Spring, MD, USA.

Clare L Cutland (CL)

African Leadership in Vaccinology Expertise (Alive), Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Christine Guillard Maure (C)

Department of Regulation and Prequalification, World Health Organization, Geneva, Switzerland.

Classifications MeSH