A Retrospective Case Series Analysis of Pregnancy and COVID-19 Based on a Global Postmarketing COVID-19 Surveillance Program

IF 3.2 4区 医学 Q2 PHARMACOLOGY & PHARMACY Clinical therapeutics Pub Date : 2024-07-01 DOI:10.1016/j.clinthera.2024.06.012
Elena Beyzarov PharmD, Yan Chen MD, PhD, Patrick Caubel MD, PhD
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Abstract

Purpose

To document and characterize COVID-19 cases involving pregnancy in the context of exposure to pharmaceutical products.

Methods

This retrospective case series analysis leveraged the Pfizer safety database containing worldwide adverse event data related to use of Pfizer products between October 1, 2019 and November 3, 2022. Selected Medical Dictionary for Drug Regulatory Activities (Version 25.0) Preferred Terms and subsequent clinical review were used to identify COVID-19 cases involving female patients who received Pfizer products during pregnancy and infants with intrauterine exposure to Pfizer products.

Findings

As of November 3, 2022, 504 pregnancy cases (426 maternal; 78 infants) were identified. Most maternal cases reported COVID-19 during the third trimester, and (when known) 52% of cases involved presentation or progression of severe COVID-19 with associated complications requiring hospitalization, and often intensive management (eg, mechanical ventilation, oxygen support) and emergent delivery. Twenty-three maternal cases were fatal; patients developed severe COVID-19 disease involving multisystem deterioration (eg, cardiopulmonary injury/decompensation, coagulopathies, septic/hemorrhagic shock) and frequently required risk-benefit decisions regarding maintaining/prolonging pregnancies to improve fetal viability while attempting to improve or stabilize maternal conditions or electing to either terminate pregnancies or induce emergent deliveries. Approximately 40% of maternal cases reported medical history involving at least one underlying condition (eg, diabetes, respiratory disorders, renal/hepatic disease, cardiac disease, obesity, autoimmune conditions) considered potentially associated with susceptibility to infection/adverse outcome of infection, or twin/triplet pregnancy, which may further complicate COVID-19 disease. Most cases with known fetal outcomes reported normal newborns including preterm/low birth weight infants, which occurred in many cases involving emergent preterm delivery due to deteriorating maternal conditions. The remaining smaller proportion of cases involved abnormal newborn/perinatal/postperinatal complications (eg, premature births, respiratory distress, alveolar damage, meconium aspiration with hypoxic-ischemic encephalopathy), intrauterine/neonatal death (due to multiple concurrent complications such as neonatal sepsis, hypoxemia/acute respiratory distress, potential cardiac damage, mucormycosis) and congenital anomaly (eg, intrauterine growth restriction in association with contracting COVID-19). Among infants tested within our dataset, 28 cases involved reference to infants who tested positive for COVID-19 infection at birth or shortly thereafter, with vertical transmission suspected only in 2 infants.

Implication

This large retrospective case series provides additional perspectives regarding potential impact of COVID-19 on pregnancy outcomes, and its characterization of this case volume may contribute to the current information landscape related to COVID-19 in pregnancy. Further studies may be warranted to confirm the generalizability of our findings to the general pregnant patient population infected with COVID-19.

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基于全球 COVID-19 上市后监测计划的妊娠与 COVID-19 的回顾性病例系列分析。
目的:记录和描述因接触药品而导致妊娠的COVID-19病例:这项回顾性病例系列分析利用了辉瑞安全数据库,其中包含与2019年10月1日至2022年11月3日期间使用辉瑞产品相关的全球不良事件数据。利用《药品监管活动医学词典(25.0 版)首选术语选编》和随后的临床审查来确定 COVID-19 病例,这些病例涉及在怀孕期间接受辉瑞产品治疗的女性患者以及宫内暴露于辉瑞产品的婴儿:截至2022年11月3日,共发现504例妊娠病例(426例孕妇;78例婴儿)。大多数孕产妇在怀孕三个月时报告了COVID-19,52%的病例(如果已知)出现或发展为严重的COVID-19,并伴有相关并发症,需要住院治疗,通常需要加强管理(如机械通气、氧气支持)和紧急分娩。23例产妇死亡;患者出现了严重的COVID-19疾病,涉及多系统恶化(如心肺损伤/失代偿、凝血功能障碍、脓毒症/失血性休克),经常需要在风险与收益之间做出抉择:维持/延长妊娠以提高胎儿存活率,同时尝试改善或稳定产妇病情,或者选择终止妊娠或紧急分娩。约 40% 的孕产妇病例报告了至少一种潜在疾病(如糖尿病、呼吸系统疾病、肝肾疾病、心脏病、肥胖、自身免疫性疾病)的病史,这些疾病被认为可能与感染易感性/感染的不良后果或双胎/三胎妊娠有关,这可能会使 COVID-19 疾病进一步复杂化。大多数已知胎儿结局的病例均报告新生儿正常,包括早产/低出生体重儿,其中许多病例是由于产妇病情恶化而紧急早产。其余较小比例的病例涉及异常新生儿/围产期/围产期后并发症(如早产、呼吸窘迫、肺泡损伤、胎粪吸入缺氧缺血性脑病)、宫内/新生儿死亡(由于多种并发症,如新生儿败血症、低氧血症/急性呼吸窘迫、潜在的心脏损伤、粘液瘤病)和先天性异常(如与感染 COVID-19 相关的宫内生长受限)。在我们数据集中接受检测的婴儿中,有 28 例病例涉及出生时或出生后不久 COVID-19 感染检测呈阳性的婴儿,仅有 2 例婴儿被怀疑为垂直传播:这一大型回顾性病例系列提供了有关 COVID-19 对妊娠结局潜在影响的更多视角,其对这一病例量的描述可能有助于了解目前与妊娠期 COVID-19 相关的信息。可能有必要开展进一步研究,以确认我们的研究结果是否适用于感染 COVID-19 的一般妊娠患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical therapeutics
Clinical therapeutics 医学-药学
CiteScore
6.00
自引率
3.10%
发文量
154
审稿时长
9 weeks
期刊介绍: Clinical Therapeutics provides peer-reviewed, rapid publication of recent developments in drug and other therapies as well as in diagnostics, pharmacoeconomics, health policy, treatment outcomes, and innovations in drug and biologics research. In addition Clinical Therapeutics features updates on specific topics collated by expert Topic Editors. Clinical Therapeutics is read by a large international audience of scientists and clinicians in a variety of research, academic, and clinical practice settings. Articles are indexed by all major biomedical abstracting databases.
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