Department of Obstetrics and Gynecology, Brigham and Women's Hospital, and Harvard Medical School, Boston, Massachusetts.
Obstet Gynecol. 2024 Feb 1;143(2):273-276. doi: 10.1097/AOG.0000000000005471. Epub 2023 Nov 14.
We conducted a retrospective cohort study of pregnant patients who tested positive for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection by RNA polymerase chain reaction test or home test who were counseled about taking nirmatrelvir-ritonavir if they were within 5 days of symptom onset. Obstetric and coronavirus disease 2019 (COVID-19) outcomes were compared between patients who did and did not take the medication. Overall, 114 individuals took nirmatrelvir-ritonavir and 323 did not. The cohorts were comparable, including high rates of vaccination in both groups. Nirmatrelvir-ritonavir was well-tolerated, with no patients discontinuing medication due to side effects. There were no intensive care unit admissions in either group. Most obstetric and medical outcomes were similar between those taking and not taking nirmatrelvir-ritonavir. Patients taking nirmatrelvir-ritonavir had significantly higher rates of surgical site infection (3 [2.7%] vs 0 [0%], P =.02) and preeclampsia (11 [9.6%] vs 12 [3.7%], P =.02). Outcome event numbers were too small for multivariable modeling. These preliminary data may be reassuring to clinicians and patients who would like to use nirmatrelvir-ritonavir in pregnancy.
我们对通过 RNA 聚合酶链反应检测或家庭检测呈严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2) 感染阳性且在症状出现后 5 天内接受过利托那韦-奈玛特韦咨询的孕妇进行了回顾性队列研究。比较了服用和未服用该药的患者的产科和 2019 冠状病毒病 (COVID-19) 结局。总体而言,114 人服用了利托那韦-奈玛特韦,323 人未服用。两组患者具有可比性,两组的疫苗接种率均较高。利托那韦-奈玛特韦耐受良好,无因副作用而停药的患者。两组均无人入住重症监护病房。服用和未服用利托那韦-奈玛特韦的患者大多数产科和医疗结局相似。服用利托那韦-奈玛特韦的患者手术部位感染率明显更高(3 [2.7%] 比 0 [0%],P =.02)和子痫前期发生率更高(11 [9.6%] 比 12 [3.7%],P =.02)。由于事件数量较少,无法进行多变量建模。这些初步数据可能会让想要在怀孕期间使用利托那韦-奈玛特韦的临床医生和患者感到放心。