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在资源有限环境下开展孕期药物警戒国际研究的操作经验教训:世界卫生组织全球疫苗安全多国合作项目

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.

作者信息

Sharan Apoorva, Jahagirdar Shubhashri, Stuurman Anke L, Elango Varalakshmi, Riera-Montes Margarita, Kumar Kashyap Neeraj, Kumar Arora Narendra, Mathai Mathews, Mangtani Punam, Devlieger Hugo, Anderson Steven, Whitaker Barbee, Wong Hui-Lee, Cutland Clare L, Guillard Maure Christine

机构信息

The INCLEN Trust International, New Delhi, India.

Swiss Tropical and Public Health Institute (Swiss TPH), Basel, Switzerland.

出版信息

Vaccine X. 2022 Aug;11:100160. doi: 10.1016/j.jvacx.2022.100160. Epub 2022 Apr 9.

Abstract

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.

摘要

世界卫生组织全球疫苗安全多国合作组织开展的孕期安全性研究旨在估计选定围产期和新生儿结局的最低可检测风险,并评估标准化病例定义在低收入和中等收入国家(LMICs)用于研究结局和孕产妇免疫的适用性。本文记录了该研究获得的操作经验教训。在七个国家的21家医院开展了一项前瞻性观察性研究。对各研究地点发生的所有分娩进行筛查,以确定2019年5月至2020年8月期间选定的围产期和新生儿结局。每个结局招募多达100例病例,以评估标准化病例定义的适用性。实施了一项多方面的研究质量保证计划。还评估了新冠疫情对研究地点运作和项目实施的影响。多层伦理和行政审批、临床记录有限、难以确定需要住院随访的结局以及网络连接质量差成为研究实施的重要障碍。使用电子平台、应用严格的质量保证计划以及中央团队与研究地点团队之间频繁互动有助于提高数据质量。在一些研究地点,新冠疫情使数据收集中断长达6周。我们的研究成功建立了一个基于医院的国际监测网络,用于在地理分布不同、基础设施水平、临床和卫生利用实践各异的地点,使用共同的研究方案和程序评估围产期和新生儿结局。参与研究地点监测能力的增强将有助于支持未来针对孕期干预措施的药物警戒工作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fdc/9065890/933201a75108/gr1.jpg

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