Davies Hannah G, Thorley Emma V, Al-Bahadili Rossul, Sutton Natalina, Burt Jessica, Hookham Lauren, Karampatsas Kostas, Lambach Philipp, Muñoz Flor, Cutland Clare L, Omer Saad, Le Doare Kirsty
Centre for Neonatal and Paediatric Infection, Institute of Infection & Immunity, St George's, University of London, Cranmer Terrace, Tooting, London, United Kingdom.
MRC, UVRI & LSHTM Uganda Research Centre, Entebbe, Uganda.
Vaccine X. 2024 Feb 23;18:100464. doi: 10.1016/j.jvacx.2024.100464. eCollection 2024 Jun.
The GAIA (Global Alignment on Immunisation Safety Assessment in Pregnancy) consortium was established in 2014 with the aim of creating a standardised, globally coordinated approach to monitoring the safety of vaccines administered in pregnancy. The consortium developed twenty-six standardised definitions for classifying obstetric and infant adverse events. This systematic review sought to evaluate the current state of adverse event reporting in maternal vaccine trials following the publication of the case definitions by GAIA, and the extent to which these case definitions have been adopted in maternal vaccine safety research.
A comprehensive search of published literature was undertaken to identify maternal vaccine research studies. PubMed, EMBASE, Web of Science, and Cochrane were searched using a combination of MeSH terms and keyword searches to identify observational or interventional studies that examined vaccine safety in pregnant women with a comparator group. A two-reviewer screening process was undertaken, and a narrative synthesis of the results presented.
14,737 titles were identified from database searches, 435 titles were selected as potentially relevant, 256 were excluded, the remaining 116 papers were included. Influenza vaccine was the most studied (25.0%), followed by TDaP (20.7%) and SARS-CoV-2 (12.9%).Ninety-one studies (78.4%) were conducted in high-income settings. Forty-eight (41.4%) utilised electronic health-records. The majority focused on reporting adverse events of special interest (AESI) in pregnancy (65.0%) alone or in addition to reactogenicity (27.6%). The most frequently reported AESI were preterm birth, small for gestational age and hypertensive disorders. Fewer than 10 studies reported use of GAIA definitions. Gestational age assessment was poorly described; of 39 studies reporting stillbirths 30.8% provided no description of the gestational age threshold.
Low-income settings remain under-represented in comparative maternal vaccine safety research. There has been poor uptake of GAIA case definitions. A lack of harmonisation and standardisation persists limiting comparability of the generated safety data.
GAIA(孕期免疫接种安全性评估全球协作组织)于2014年成立,旨在创建一种标准化、全球协调的方法来监测孕期接种疫苗的安全性。该协作组织制定了26项用于分类产科和婴儿不良事件的标准化定义。本系统评价旨在评估GAIA病例定义发布后,孕产妇疫苗试验中不良事件报告的现状,以及这些病例定义在孕产妇疫苗安全性研究中的采用程度。
对已发表文献进行全面检索,以识别孕产妇疫苗研究。使用医学主题词(MeSH)和关键词搜索相结合的方式在PubMed、EMBASE、科学网和Cochrane中进行检索,以识别观察性或干预性研究,这些研究在有对照的情况下研究孕妇的疫苗安全性。进行了双审筛选过程,并对结果进行了叙述性综合分析。
从数据库搜索中识别出14737个标题,435个标题被选为可能相关,256个被排除,其余116篇论文被纳入。流感疫苗是研究最多的(25.0%),其次是破伤风、白喉、无细胞百日咳疫苗(TDaP,20.7%)和严重急性呼吸综合征冠状病毒2(SARS-CoV-2,12.9%)。91项研究(78.4%)在高收入环境中进行。48项(41.4%)使用了电子健康记录。大多数研究仅关注报告孕期特殊关注的不良事件(AESI,65.0%)或除反应原性外还关注AESI(27.6%)。最常报告的AESI是早产、小于胎龄儿和高血压疾病。报告使用GAIA定义的研究不到10项。孕周评估描述不佳;在报告死产的39项研究中,30.8%未提供孕周阈值的描述。
在比较孕产妇疫苗安全性研究中,低收入环境的代表性仍然不足。GAIA病例定义的采用情况不佳。缺乏协调性和标准化仍然限制了所生成安全数据的可比性。