Pregnancy outcomes and vaccine effectiveness during the period of omicron as the variant of concern, INTERCOVID-2022: a multinational, observational study.


Journal

Lancet (London, England)
ISSN: 1474-547X
Titre abrégé: Lancet
Pays: England
ID NLM: 2985213R

Informations de publication

Date de publication:
11 02 2023
Historique:
received: 11 08 2022
revised: 22 11 2022
accepted: 24 11 2022
pubmed: 21 1 2023
medline: 15 2 2023
entrez: 20 1 2023
Statut: ppublish

Résumé

In 2021, we showed an increased risk associated with COVID-19 in pregnancy. Since then, the SARS-CoV-2 virus has undergone genetic mutations. We aimed to examine the effects on maternal and perinatal outcomes of COVID-19 during pregnancy, and evaluate vaccine effectiveness, when omicron (B.1.1.529) was the variant of concern. INTERCOVID-2022 is a large, prospective, observational study, involving 41 hospitals across 18 countries. Each woman with real-time PCR or rapid test, laboratory-confirmed COVID-19 in pregnancy was compared with two unmatched women without a COVID-19 diagnosis who were recruited concomitantly and consecutively in pregnancy or at delivery. Mother and neonate dyads were followed until hospital discharge. Primary outcomes were maternal morbidity and mortality index (MMMI), severe neonatal morbidity index (SNMI), and severe perinatal morbidity and mortality index (SPMMI). Vaccine effectiveness was estimated, adjusted by maternal risk profile. We enrolled 4618 pregnant women from Nov 27, 2021 (the day after WHO declared omicron a variant of concern), to June 30, 2022: 1545 (33%) women had a COVID-19 diagnosis (median gestation 36·7 weeks [IQR 29·0-38·9]) and 3073 (67%) women, with similar demographic characteristics, did not have a COVID-19 diagnosis. Overall, women with a diagnosis had an increased risk for MMMI (relative risk [RR] 1·16 [95% CI 1·03-1·31]) and SPMMI (RR 1·21 [95% CI 1·00-1·46]). Women with a diagnosis, compared with those without a diagnosis, also had increased risks of SNMI (RR 1·23 [95% CI 0·88-1·71]), although the lower bounds of the 95% CI crossed unity. Unvaccinated women with a COVID-19 diagnosis had a greater risk of MMMI (RR 1·36 [95% CI 1·12-1·65]). Severe COVID-19 symptoms in the total sample increased the risk of severe maternal complications (RR 2·51 [95% CI 1·84-3·43]), perinatal complications (RR 1·84 [95% CI 1·02-3·34]), and referral, intensive care unit (ICU) admission, or death (RR 11·83 [95% CI 6·67-20·97]). Severe COVID-19 symptoms in unvaccinated women increased the risk of MMMI (RR 2·88 [95% CI 2·02-4·12]) and referral, ICU admission, or death (RR 20·82 [95% CI 10·44-41·54]). 2886 (63%) of 4618 total participants had at least a single dose of any vaccine, and 2476 (54%) of 4618 had either complete or booster doses. Vaccine effectiveness (all vaccines combined) for severe complications of COVID-19 for all women with a complete regimen was 48% (95% CI 22-65) and 76% (47-89) after a booster dose. For women with a COVID-19 diagnosis, vaccine effectiveness of all vaccines combined for women with a complete regimen was 74% (95% CI 48-87) and 91% (65-98) after a booster dose. COVID-19 in pregnancy, during the first 6 months of omicron as the variant of concern, was associated with increased risk of severe maternal morbidity and mortality, especially among symptomatic and unvaccinated women. Women with complete or boosted vaccine doses had reduced risk for severe symptoms, complications, and death. Vaccination coverage among pregnant women remains a priority. None.

Sections du résumé

BACKGROUND
In 2021, we showed an increased risk associated with COVID-19 in pregnancy. Since then, the SARS-CoV-2 virus has undergone genetic mutations. We aimed to examine the effects on maternal and perinatal outcomes of COVID-19 during pregnancy, and evaluate vaccine effectiveness, when omicron (B.1.1.529) was the variant of concern.
METHODS
INTERCOVID-2022 is a large, prospective, observational study, involving 41 hospitals across 18 countries. Each woman with real-time PCR or rapid test, laboratory-confirmed COVID-19 in pregnancy was compared with two unmatched women without a COVID-19 diagnosis who were recruited concomitantly and consecutively in pregnancy or at delivery. Mother and neonate dyads were followed until hospital discharge. Primary outcomes were maternal morbidity and mortality index (MMMI), severe neonatal morbidity index (SNMI), and severe perinatal morbidity and mortality index (SPMMI). Vaccine effectiveness was estimated, adjusted by maternal risk profile.
FINDINGS
We enrolled 4618 pregnant women from Nov 27, 2021 (the day after WHO declared omicron a variant of concern), to June 30, 2022: 1545 (33%) women had a COVID-19 diagnosis (median gestation 36·7 weeks [IQR 29·0-38·9]) and 3073 (67%) women, with similar demographic characteristics, did not have a COVID-19 diagnosis. Overall, women with a diagnosis had an increased risk for MMMI (relative risk [RR] 1·16 [95% CI 1·03-1·31]) and SPMMI (RR 1·21 [95% CI 1·00-1·46]). Women with a diagnosis, compared with those without a diagnosis, also had increased risks of SNMI (RR 1·23 [95% CI 0·88-1·71]), although the lower bounds of the 95% CI crossed unity. Unvaccinated women with a COVID-19 diagnosis had a greater risk of MMMI (RR 1·36 [95% CI 1·12-1·65]). Severe COVID-19 symptoms in the total sample increased the risk of severe maternal complications (RR 2·51 [95% CI 1·84-3·43]), perinatal complications (RR 1·84 [95% CI 1·02-3·34]), and referral, intensive care unit (ICU) admission, or death (RR 11·83 [95% CI 6·67-20·97]). Severe COVID-19 symptoms in unvaccinated women increased the risk of MMMI (RR 2·88 [95% CI 2·02-4·12]) and referral, ICU admission, or death (RR 20·82 [95% CI 10·44-41·54]). 2886 (63%) of 4618 total participants had at least a single dose of any vaccine, and 2476 (54%) of 4618 had either complete or booster doses. Vaccine effectiveness (all vaccines combined) for severe complications of COVID-19 for all women with a complete regimen was 48% (95% CI 22-65) and 76% (47-89) after a booster dose. For women with a COVID-19 diagnosis, vaccine effectiveness of all vaccines combined for women with a complete regimen was 74% (95% CI 48-87) and 91% (65-98) after a booster dose.
INTERPRETATION
COVID-19 in pregnancy, during the first 6 months of omicron as the variant of concern, was associated with increased risk of severe maternal morbidity and mortality, especially among symptomatic and unvaccinated women. Women with complete or boosted vaccine doses had reduced risk for severe symptoms, complications, and death. Vaccination coverage among pregnant women remains a priority.
FUNDING
None.

Identifiants

pubmed: 36669520
pii: S0140-6736(22)02467-9
doi: 10.1016/S0140-6736(22)02467-9
pmc: PMC9910845
pii:
doi:

Types de publication

Observational Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

447-457

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests LS has been a consultant for Dilafor and Ferring Pharmaceuticals and has received payment in the past for presentations and educational events from Bayer, GlaxoSmithKline, Ferring Pharmaceuticals, and Sigvaris. BMdT received a research grant from the General Health Direction of Geneva, has participated on an advisory board of Effik and Pierre Favre, and has received medical equipment from Pregnolia, Hologic, and PeriLynx. All other authors declare no competing interests.

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Auteurs

Jose Villar (J)

Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, UK; Oxford Maternal and Perinatal Health Institute, Green Templeton College, University of Oxford, Oxford, UK.

Constanza P Soto Conti (CP)

Division Neonatología, Hospital Materno Infantil Ramón Sarda, Buenos Aires, Argentina.

Robert B Gunier (RB)

Center for Environmental Research and Community Health (CERCH), School of Public Health, University of California, Berkeley, CA, USA.

Shabina Ariff (S)

Department of Paediatrics and Child Health, The Aga Khan University Hospital, Karachi, Pakistan.

Rachel Craik (R)

Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, UK.

Paolo I Cavoretto (PI)

Vita-Salute San Raffaele University and IRCCS San Raffaele Scientific Institute, Obstetrics and Gynaecology Department, Milan, Italy.

Stephen Rauch (S)

Center for Environmental Research and Community Health (CERCH), School of Public Health, University of California, Berkeley, CA, USA.

Serena Gandino (S)

Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, UK.

Ricardo Nieto (R)

Division Neonatología, Hospital Materno Infantil Ramón Sarda, Buenos Aires, Argentina.

Adele Winsey (A)

Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, UK.

Camilla Menis (C)

Department of Clinical Sciences and Community Health, University of Milan, NICU, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Gabriel B Rodriguez (GB)

Oxford Maternal and Perinatal Health Institute, Green Templeton College, University of Oxford, Oxford, UK.

Valeria Savasi (V)

Unit of Obstetrics and Gynecology, L- Sacco Hospital ASST Fatebenefratelli Sacco, Department of Biological and Clinical Sciences, University of Milan, Milan, Italy.

Niyazi Tug (N)

Department of Obstetrics and Gynecology, Sancaktepe Sehit Prof Dr Ilhan Varank Training and Research Hospital, University of Health Sciences, Istanbul, Türkiye.

Sonia Deantoni (S)

Neonatal Care Unit, Department of Public Health and Pediatrics, School of Medicine, University of Turin, Turin, Italy.

Marta Fabre (M)

Instituto de Investigación Sanitario de Aragón (IIS Aragon), Hospital Clínico Universitario Lozano Blesa Zaragoza, Zaragoza, Spain.

Begoña Martinez de Tejada (B)

Department of Pediatrics, Gynecology & Obstetrics, Hôpitaux Universitaires de Genève, Geneva, Switzerland.

Maria Jose Rodriguez-Sibaja (MJ)

Instituto Nacional de Perinatología Isidro Espinosa de los Reyes, Mexico City, Mexico.

Stefania Livio (S)

Children's Hospital V Buzzi, ASST Fatebenefratelli Sacco, Milan, Italy.

Raffaele Napolitano (R)

Elizabeth Garrett Anderson Institute for Women's Health, University College London, London, UK; Fetal Medicine Unit, University College London Hospitals NHS Foundation Trust, London, UK.

Nerea Maiz (N)

Maternal-Fetal Medicine Unit, Department of Obstetrics and Gynecology, Hospital Universitari Vall d'Hebron, Vall d'Hebron, Barcelona Hospital Campus, Universitat Autonoma de Barcelona, Barcelona, Spain.

Helena Sobrero (H)

Centro Hospitalario Pereira Rossell, Montevideo, Uruguay.

Ashley Peterson (A)

Tufts Medical Center, Boston, MA, USA.

Philippe Deruelle (P)

Department of Obstetrics and Gynecology, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.

Carolina Giudice (C)

Servicio de Neonatologia, Hospital Italiano de Buenos Aires, Instituto Universitario Hospital Italiano, Buenos Aires, Argentina.

Jagjit S Teji (JS)

Ann and Robert H Lurie Children's Hospital of Chicago, Chicago, IL, USA.

Roberto A Casale (RA)

Maternal and Child Department, Hospital Nacional Profesor Alejandro Posadas, Buenos Aires, Argentina.

Laurent J Salomon (LJ)

Hôpital Universitaire Necker-Enfants Malades, Paris, France.

Federico Prefumo (F)

Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy.

Leila Cheikh Ismail (L)

Department of Clinical Nutrition and Dietetics, College of Health Sciences, University of Sharjah, Sharjah, United Arab Emirates.

Michael G Gravett (MG)

Department of Obstetrics and Gynecology and Department of Global Health, University of Washington, Seattle, WA, USA.

Marynéa Vale (M)

Hospital Universitário da Universidade Federal do Maranhão, São Luís, Maranhão, Brazil.

Valeria Hernández (V)

Facultad de Ciencias Médicas, Universidad Nacional de Córdoba, Córdoba, Argentina.

Loïc Sentilhes (L)

Department of Obstetrics and Gynecology, Bordeaux University Hospital, Bordeaux, France.

Sarah R Easter (SR)

Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Carola Capelli (C)

Servicio de Neonatología del Departamento Materno Infantil, Hospital Universitario Austral, Buenos Aires, Argentina.

Emily Marler (E)

St George's University Hospitals NHS Foundation Trust, London, UK.

Daniela M Cáceres (DM)

Hospital Julio C Perrando, Resistencia, Chaco, Argentina.

Guadalupe Albornoz Crespo (G)

Clínica y Maternidad Suizo Argentina, Buenos Aires, Argentina.

Ernawati Ernawati (E)

Medical Faculty Universitas Airlangga - Dr Soetomo General Academic Hospital, Surabaya, Indonesia.

Michal Lipschuetz (M)

Obstetrics and Gynecology Division- Hadassah Medical Center Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.

Ken Takahashi (K)

Department of Obstetrics and Gynecology, The Jikei University School of Medicine, Tokyo, Japan.

Carmen Vecchiarelli (C)

Sanatorio Otamendi, Buenos Aires, Argentina.

Teresa Hubka (T)

Ascension-Resurrection Medical Center, Chicago, Illinois, USA.

Satoru Ikenoue (S)

Department of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo, Japan.

Gabriela Tavchioska (G)

General Hospital With Extended Activity Prilep, Prilep, North Macedonia.

Babagana Bako (B)

Department of Obstetrics and Gynaecology, College of Medical Sciences, Gombe State University, Gombe, Nigeria.

Adejumoke I Ayede (AI)

College of Medicine, University of Ibadan and University College Hospital, Ibadan, Nigeria.

Brenda Eskenazi (B)

Center for Environmental Research and Community Health (CERCH), School of Public Health, University of California, Berkeley, CA, USA.

Jim G Thornton (JG)

University of Nottingham Medical School, University of Nottingham, Nottingham, UK.

Zulfiqar A Bhutta (ZA)

Department of Paediatrics and Child Health, The Aga Khan University Hospital, Karachi, Pakistan; Center for Global Child Health, Hospital for Sick Children, Toronto, ON, Canada.

Stephen H Kennedy (SH)

Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, UK; Oxford Maternal and Perinatal Health Institute, Green Templeton College, University of Oxford, Oxford, UK.

Aris T Papageorghiou (AT)

Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, UK; Oxford Maternal and Perinatal Health Institute, Green Templeton College, University of Oxford, Oxford, UK; St George's University Hospitals NHS Foundation Trust, London, UK. Electronic address: aris.papageorghiou@wrh.ox.ac.uk.

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