Department of Obstetrics and Gynecology, Sancaktepe Sehit Prof Dr Ilhan Varank Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.
Fetal Medicine Unit, St George's University Hospitals NHS Foundation Trust, University of London, London, UK.
Ultrasound Obstet Gynecol. 2022 Jul;60(1):96-102. doi: 10.1002/uog.24916.
There is little evidence related to the effects of the Omicron severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variant on pregnancy outcomes, particularly in unvaccinated women. This study aimed to compare pregnancy outcomes of unvaccinated women infected with SARS-CoV-2 during the pre-Delta, Delta and Omicron waves.
This was a retrospective cohort study conducted at two tertiary care facilities: Sancaktepe Training and Research Hospital, Istanbul, Turkey, and St George's University Hospitals NHS Foundation Trust, London, UK. Included were women who tested positive for SARS-CoV-2 by real-time reverse-transcription polymerase chain reaction (RT-PCR) during pregnancy, between 1 April 2020 and 14 February 2022. The cohort was divided into three periods according to the date of their positive RT-PCR test: (i) pre-Delta (1 April 2020 to 8 June 2021 in Turkey, and 1 April 2020 to 31 July 2021 in the UK), (ii) Delta (9 June 2021 to 27 December 2021 in Turkey, and 1 August 2021 to 27 December 2021 in the UK) and (iii) Omicron (after 27 December 2021 in both Turkey and the UK). Baseline data collected included maternal age, parity, body mass index, gestational age at diagnosis and comorbidities. The primary outcome was the need for oxygen supplementation, classified as oxygen support via nasal cannula or breather mask, non-invasive mechanical ventilation with continuous positive airway pressure (CPAP) or high-flow oxygen, mechanical ventilation with intubation, or extracorporeal membrane oxygenation (ECMO). Inferences were made after balancing of confounders, using an evolutionary search algorithm. Selected confounders were maternal age, body mass index and gestational age at diagnosis of infection.
During the study period, 1286 unvaccinated pregnant women with RT-PCR-proven SARS-CoV-2 infection were identified, comprising 870 cases during the pre-Delta period, 339 during the Delta wave and 77 during the Omicron wave. In the confounder-balanced cohort, infection during the Delta wave vs during the pre-Delta period was associated with increased need for nasal oxygen support (risk ratio (RR), 2.53 (95% CI, 1.75-3.65); P < 0.001), CPAP or high-flow oxygen (RR, 2.50 (95% CI, 1.37-4.56); P = 0.002), mechanical ventilation (RR, 4.20 (95% CI, 1.60-11.0); P = 0.003) and ECMO (RR, 11.0 (95% CI, 1.43-84.7); P = 0.021). The maternal mortality rate was 3.6-fold higher during the Delta wave compared to the pre-Delta period (5.3% vs 1.5%, P = 0.010). Infection during the Omicron wave was associated with a similar need for nasal oxygen support (RR, 0.62 (95% CI, 0.25-1.55); P = 0.251), CPAP or high-flow oxygen (RR, 1.07 (95% CI, 0.36-3.12); P = 0.906) and mechanical ventilation (RR, 0.44 (95% CI, 0.06-3.45); P = 0.438) with that in the pre-Delta period. The maternal mortality rate was similar during the Omicron wave and the pre-Delta period (1.3% vs 1.3%, P = 0.999). The need for nasal oxygen support during the Omicron wave was significantly lower compared to the Delta wave (RR, 0.26 (95% CI, 0.11-0.64); P = 0.003). Perinatal outcomes were available for a subset of the confounder-balanced cohort. Preterm birth before 34 weeks' gestation was significantly increased during the Delta wave compared with the pre-Delta period (15.4% vs 4.9%, P < 0.001).
Among unvaccinated pregnant women, SARS-CoV-2 infection during the Delta wave, in comparison to the pre-Delta period, was associated with increased requirement for oxygen support (including ECMO) and higher maternal mortality. Disease severity and pregnancy complications were similar between the Omicron wave and pre-Delta period. SARS-CoV-2 infection of unvaccinated pregnant women carries considerable risks of morbidity and mortality regardless of variant, and vaccination remains key. Miscommunication of the risks of Omicron infection may impact adversely vaccination uptake among pregnant women, who are at increased risk of complications related to SARS-CoV-2. © 2022 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.
关于奥密克戎变异株对妊娠结局的影响,尤其是对未接种疫苗的女性的影响,相关证据有限。本研究旨在比较在德尔塔和奥密克戎波之前、期间和之后感染 SARS-CoV-2 的未接种疫苗的女性的妊娠结局。
这是一项在两家三级保健机构进行的回顾性队列研究:土耳其伊斯坦布尔 Sancaktepe 培训和研究医院和英国伦敦圣乔治大学医院 NHS 基金会信托。纳入的是在妊娠期间通过实时逆转录聚合酶链反应(RT-PCR)检测到 SARS-CoV-2 阳性的女性,时间在 2020 年 4 月 1 日至 2022 年 2 月 14 日之间。该队列根据其阳性 RT-PCR 测试日期分为三个时期:(i)德尔塔之前(2021 年 6 月 9 日至 2021 年 12 月 27 日在土耳其,2021 年 7 月 31 日至 2021 年 12 月 27 日在英国),(ii)德尔塔(2021 年 8 月 1 日至 2021 年 12 月 27 日在土耳其,2021 年 12 月 27 日在英国)和(iii)奥密克戎(2021 年 12 月 27 日之后在土耳其和英国)。收集的基线数据包括母亲年龄、产次、体重指数、诊断时的孕龄和合并症。主要结局是需要氧疗支持,分为经鼻导管或呼吸面罩吸氧、持续气道正压通气(CPAP)或高流量吸氧、经气管插管机械通气或体外膜氧合(ECMO)。使用进化搜索算法在平衡混杂因素后进行推断。选择的混杂因素为母亲年龄、体重指数和感染时的孕龄。
在研究期间,确定了 1286 名未接种疫苗的孕妇经 RT-PCR 证实感染 SARS-CoV-2,其中 870 例发生在德尔塔波之前、339 例发生在德尔塔波、77 例发生在奥密克戎波。在混杂因素平衡的队列中,与德尔塔波相比,感染发生在德尔塔波之前与需要经鼻吸氧支持增加有关(风险比(RR),2.53(95%CI,1.75-3.65);P<0.001)、CPAP 或高流量吸氧(RR,2.50(95%CI,1.37-4.56);P=0.002)、机械通气(RR,4.20(95%CI,1.60-11.0);P=0.003)和 ECMO(RR,11.0(95%CI,1.43-84.7);P=0.021)。与德尔塔波相比,奥密克戎波的孕产妇死亡率高 3.6 倍(5.3%比 1.5%,P=0.010)。与德尔塔波相比,奥密克戎波感染需要经鼻吸氧支持(RR,0.62(95%CI,0.25-1.55);P=0.251)、CPAP 或高流量吸氧(RR,1.07(95%CI,0.36-3.12);P=0.906)和机械通气(RR,0.44(95%CI,0.06-3.45);P=0.438)相似。奥密克戎波和德尔塔波的孕产妇死亡率相似(1.3%比 1.3%,P=0.999)。与德尔塔波相比,奥密克戎波需要经鼻吸氧支持的比例显著降低(RR,0.26(95%CI,0.11-0.64);P=0.003)。在混杂因素平衡的队列中,有一部分可获得围产期结局。与德尔塔波之前相比,34 周前早产的比例在德尔塔波显著增加(15.4%比 4.9%,P<0.001)。
在未接种疫苗的孕妇中,与德尔塔波之前相比,感染 SARS-CoV-2 在德尔塔波与需要氧疗支持(包括 ECMO)增加和更高的孕产妇死亡率相关。奥密克戎波与德尔塔波之前相比,疾病严重程度和妊娠并发症相似。无论变异如何,SARS-CoV-2 感染未接种疫苗的孕妇都有相当大的发病率和死亡率风险,疫苗接种仍然是关键。奥密克戎感染风险的沟通不畅可能会对孕妇的疫苗接种率产生不利影响,而孕妇与 SARS-CoV-2 相关的并发症风险增加。