Vousden Nicola, Ramakrishnan Rema, Bunch Kathryn, Morris Eddie, Simpson Nigel A B, Gale Christopher, O'Brien Patrick, Quigley Maria, Brocklehurst Peter, Kurinczuk Jennifer J, Knight Marian
National Perinatal Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Royal College of Obstetricians and Gynaecologists, London, UK.
BMJ Med. 2022 Feb 28;1(1):e000053. doi: 10.1136/bmjmed-2021-000053. eCollection 2022.
To compare the severity of maternal infection and perinatal outcomes during periods in which wildtype, alpha variant, and delta variant of SARS-CoV-2 were dominant in the UK.
Prospective cohort study.
194 obstetric units across the UK, during the following periods: between 1 March and 30 November 2020 (wildtype dominance), between 1 December 2020 and 15 May 2021 (alpha variant dominance), and between 16 May and 31 October 2021 (delta variant dominance).
4436 pregnant women admitted to hospital with covid-19 related symptoms.
Moderate to severe maternal SARS-CoV-2 infection (indicated by any of the following: oxygen saturation <95% on admission, need for oxygen treatment, evidence of pneumonia on imaging, admission to intensive care, or maternal death), and pregnancy and perinatal outcomes (including mode and gestation of birth, stillbirth, live birth, admission to neonatal intensive care, and neonatal death).
1387, 1613, and 1436 pregnant women were admitted to hospital with covid-19 related symptoms during the wildtype, alpha, and delta dominance periods, respectively; of these women, 340, 585, and 614 had moderate to severe infection, respectively. The proportion of pregnant women admitted with moderate to severe infection increased during the subsequent alpha and delta dominance periods, compared with the wildtype dominance period (wildtype 24.5% alpha 36.2% (adjusted odds ratio 1.98, 95% confidence interval 1.66% to 2.37%); wildtype 24.5% delta 42.8% (2.66, 2.21 to 3.20)). Compared with the wildtype dominance period, women admitted during the alpha dominance period were significantly more likely to have pneumonia, require respiratory support, and be admitted to intensive care; these three risks were even greater during the delta dominance period (wildtype delta: pneumonia, adjusted odds ratio 2.52, 95% confidence interval 2.06 to 3.09; respiratory support, 1.90, 1.52 to 2.37; and intensive care, 2.71, 2.06 to 3.56). Of 1761 women whose vaccination status was known, 38 (2.2%) had one dose and 16 (1%) had two doses before their diagnosis (of whom 14 (88%) had mild infection). The proportion of women receiving drug treatment for SARS-CoV-2 management was low, but did increase between the wildtype dominance period and the alpha and delta dominance periods (10.4% wildtype 14.9% alpha (2.74, 2.08 to 3.60); 10.4% wildtype 13.6% delta (2.54, 1.90 to 3.38)).
While limited by the absence of variant sequencing data, these findings suggest that during the periods when the alpha and delta variants of SARS-CoV-2 were dominant, covid-19 was associated with more severe maternal infection and worse pregnancy outcomes than during the wildtype dominance period. Most women admitted with SARS-CoV-2 related symptoms were unvaccinated. Urgent action to prioritise vaccine uptake in pregnancy is essential.
ISRCTN40092247.
比较在英国新冠病毒野生型、α变异株和δ变异株占主导期间孕产妇感染的严重程度及围产期结局。
前瞻性队列研究。
英国194个产科单位,研究时段如下:2020年3月1日至11月30日(野生型占主导)、2020年12月1日至2021年5月15日(α变异株占主导)、2021年5月16日至10月31日(δ变异株占主导)。
4436名因新冠相关症状入院的孕妇。
孕产妇中重度新冠病毒感染(以下任何一项指征:入院时血氧饱和度<95%、需吸氧治疗、影像学显示肺炎、入住重症监护室或孕产妇死亡),以及妊娠和围产期结局(包括分娩方式和孕周、死产、活产、入住新生儿重症监护室及新生儿死亡)。
在野生型、α变异株和δ变异株占主导期间,分别有1387名、1613名和1436名因新冠相关症状入院的孕妇;其中,分别有340名、585名和614名发生中重度感染。与野生型占主导期间相比,在随后的α变异株和δ变异株占主导期间,入院时中重度感染的孕妇比例增加(野生型24.5%,α变异株36.2%(调整比值比1.98,95%置信区间1.66%至2.37%);野生型24.5%,δ变异株42.8%(2.66,2.21至3.20))。与野生型占主导期间相比,α变异株占主导期间入院的女性发生肺炎、需要呼吸支持和入住重症监护室的可能性显著更高;在δ变异株占主导期间,这三种风险更高(野生型与δ变异株相比:肺炎,调整比值比2.52,95%置信区间2.06至3.09;呼吸支持,1.90,1.52至2.37;重症监护,2.71,2.06至3.56)。在已知疫苗接种状况的1761名女性中,38名(2.2%)在诊断前接种了一剂疫苗,16名(1%)接种了两剂疫苗(其中14名(88%)为轻症感染)。接受新冠病毒治疗药物治疗的女性比例较低,但在野生型占主导期间与α变异株和δ变异株占主导期间之间确实有所增加(野生型10.4%,α变异株14.9%(2.74,2.08至3.60);野生型10.4%,δ变异株13.6%(2.54,1.90至3.38))。
尽管因缺乏变异株测序数据而受到限制,但这些发现表明,在新冠病毒α变异株和δ变异株占主导期间,与野生型占主导期间相比,新冠与更严重的孕产妇感染及更差的妊娠结局相关。大多数因新冠相关症状入院的女性未接种疫苗。迫切需要采取行动优先推动孕期接种疫苗。
ISRCTN40092247