Clinical outcomes of nirmatrelvir-ritonavir use in pregnant women during the Omicron wave of the coronavirus disease 2019 pandemic

被引:3
|
作者
Lin, Chih-Wei [1 ]
Liang, Yu-Ling [1 ]
Chuang, Ming-Ta [1 ]
Tseng, Chun-Han [1 ]
Tsai, Pei-Yin [1 ]
Su, Mei-Tsz [1 ]
机构
[1] Natl Cheng Kung Univ, Coll Med, Natl Cheng Kung Univ Hosp, Dept Obstet & Gynecol, 138 Sheng Li Rd, Tainan, Taiwan
关键词
Antiviral agents; COVID-19; Nirmatrelvir-ritonavir drug combination; Pregnancy; Safety;
D O I
10.1016/j.jiph.2023.10.007
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: Paxlovid is an oral drug composed of nirmatrelvir and ritonavir that has been demonstrated to be effective in decreasing the risk of severe coronavirus disease 2019 (COVID-19). Here, we report the use of paxlovid in pregnant women with COVID-19. Methods: Pregnant women attending a tertiary referral hospital in Taiwan from 29 April to 30 July 2022 were enrolled in the study. We compared baseline characteristics, clinical manifestations, and adverse events between paxlovid-treated women and those without paxlovid use. Maternal and neonatal outcomes were analysed in women who delivered during the study period. Results: A total of 30 paxlovid-treated pregnant women and 55 women without paxlovid use were included in the analysis. The mean duration of COVID-19-associated symptoms in the paxlovid-treated women was shorter than that in the control group (10.10 days versus 15.59 days, p = 0.04). No severe adverse events due to paxlovid use were observed. Dysgeusia and diarrhoea were the most common adverse effects. Thirteen paxlovid-treated and 28 untreated women delivered during the study period. More pregnant women in the paxlovid group who delivered during the study period underwent caesarean delivery compared to the group without antiviral treatment (10 of 13 [76.92%] versus 12 of 28 [42.86%], p = 0.042), and insignificantly more newborns were born small for gestational age in the paxlovid group compared to the control group (3 of 13 [23.08%] versus 1 of 28 [3.57%], p = 0.086). Conclusion: Our study showed that paxlovid was effective and safe for pregnant women during the Omicron wave of the COVID-19 pandemic. A higher proportion of caesarean delivery rates was observed among paxlovid-treated women. Long-term follow-up of pregnant women exposed to paxlovid and their offspring is needed. (c) 2023 The Author(s). Published by Elsevier Ltd on behalf of King Saud Bin Abdulaziz University for Health Sciences. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:1942 / 1946
页数:5
相关论文
共 50 条
  • [1] Oral Nirmatrelvir-Ritonavir Use and Clinical Outcomes in Pregnant Patients With Coronavirus Disease 2019 (COVID-19)
    Toure, Bineta B.
    Panakam, Aisvarya
    Johns, Sarah L.
    Butler, Sharlay K.
    Tuomala, Ruth E.
    Diouf, Khady
    OBSTETRICS AND GYNECOLOGY, 2024, 143 (02): : 273 - 276
  • [2] Molnupiravir and Nirmatrelvir-Ritonavir: Oral Coronavirus Disease 2019 Antiviral Drugs
    Saravolatz, Louis D.
    Depcinski, Shawn
    Sharma, Mamta
    CLINICAL INFECTIOUS DISEASES, 2023, 76 (01) : 165 - 171
  • [3] Combined Protection of Vaccination and Nirmatrelvir-Ritonavir Against Hospitalization in Adults With Coronavirus Disease 2019
    Shah, Melisa M.
    Joyce, Brendan
    Plumb, Ian D.
    Sahakian, Sam
    Feldstein, Leora R.
    Barkley, Eric
    Paccione, Mason
    Deckert, Joseph
    Sandmann, Danessa
    Hagen, Melissa Briggs
    Gerhart, Jacqueline L.
    CLINICAL INFECTIOUS DISEASES, 2024, 79 (01) : 108 - 110
  • [4] Nirmatrelvir-Ritonavir (Paxlovid) for Mild Coronavirus Disease 2019 (COVID-19) in Pregnancy and Lactation
    Lin, Christine Y.
    Cassidy, Arianna G.
    Li, Lin
    Prahl, Mary K.
    Golan, Yarden
    Gaw, Stephanie L.
    OBSTETRICS AND GYNECOLOGY, 2023, 141 (05): : 957 - 960
  • [5] Predicting the Public Health Impact of Bivalent Vaccines and Nirmatrelvir-Ritonavir Against Coronavirus Disease 2019
    Park, Hailey J.
    Tan, Sophia T.
    Leon, Tomas M.
    Jain, Seema
    Schechter, Robert
    Lo, Nathan C.
    OPEN FORUM INFECTIOUS DISEASES, 2023, 10 (09):
  • [6] Safety Profile and Clinical and Virological Outcomes of Nirmatrelvir-Ritonavir Treatment in Patients With Advanced Chronic Kidney Disease and Coronavirus Disease 2019 (COVID-19)
    Chan, Gordon Chun Kau
    Lui, Grace Chung Yan
    Wong, Candy Ngai Sze
    Yip, Sindy Sin Ting
    Li, Timothy Chun Man
    Cheung, Catherine Siu King
    Sze, Ryan Kin Ho
    Szeto, Cheuk Chun
    Chow, Kai Ming
    CLINICAL INFECTIOUS DISEASES, 2023, 77 (10) : 1406 - 1412
  • [7] In outpatients with COVID-19 during Omicron variant circulation, molnupiravir and nirmatrelvir-ritonavir improved outcomes
    Chagla, Zain
    ANNALS OF INTERNAL MEDICINE, 2024, 177 (01) : JC7 - JC7
  • [8] Characterization of Virologic Rebound Following Nirmatrelvir-Ritonavir Treatment for Coronavirus Disease 2019 (COVID-19)
    Boucau, Julie
    Uddin, Rockib
    Marino, Caitlin
    Regan, James
    Flynn, James P.
    Choudhary, Manish C.
    Chen, Geoffrey
    Stuckwisch, Ashley M.
    Mathews, Josh
    Liew, May Y.
    Singh, Arshdeep
    Reynolds, Zahra
    Iyer, Surabhi L.
    Chamberlin, Grace C.
    Vyas, Tammy D.
    Vyas, Jatin M.
    Turbett, Sarah E.
    Li, Jonathan Z.
    Lemieux, Jacob E.
    Barczak, Amy K.
    Siedner, Mark J.
    CLINICAL INFECTIOUS DISEASES, 2023, 76 (03) : E526 - E529
  • [9] The Impacts of Nirmatrelvir-Ritonavir on Myocardial Injury and Long-Term Cardiovascular Outcomes in Hospitalized Patients with COVID-19 amid the Omicron Wave of the Pandemic
    Gu, Jun
    Han, Zhi-Hua
    Wang, Chang-qian
    Zhang, Jun-feng
    CARDIOVASCULAR DRUGS AND THERAPY, 2024,
  • [10] National survey study of nirmatrelvir-ritonavir prescribing processes and access barriers during the severe acute respiratory coronavirus virus 2 (SARS-CoV-2) omicron surge of the coronavirus disease 2019 (COVID-19) pandemic
    Wang, Rebecca
    Calderwood, Michael S.
    Worby, Craig P.
    Mercado, Jose R.
    Kim, Justin J.
    INFECTION CONTROL & HOSPITAL EPIDEMIOLOGY, 2023, 44 (11) : 1881 - 1883