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1.
authorea preprints; 2024.
Preprint in English | PREPRINT-AUTHOREA PREPRINTS | ID: ppzbmed-10.22541.au.170670045.55494016.v1

ABSTRACT

Objective: to investigate a possible bi-directional association between gestational diabetes (GDM) and the SARS-CoV-2 infection during pregnancy. Design: case-control study with prospective data collection for the case group and 1:2 matching with historical controls Setting: University Hospital of Bern, Switzerland Population: 224 pregnant women: 75 cases with SARS-CoV-2 infection during pregnancy, matched 1:2 with controls based on parity, BMI and ethnicity. Methods: SARS-CoV-2 infection was diagnosed by RT-PCR. Screening for GDM was performed by 75mg oral glucose tolerance test at 26 weeks’ gestation in all women. Main Outcomes: Prevalence of GDM was calculated in both groups. Multivariate binary logistic regression analysis was performed to assess risk factors for GDM and inpatient COVID-19 management. Results: 34.6% of the patients in the case group suffered from GDM, vs. 16.1% in the control group (p=0.002). 35.7% patients were diagnosed with GDM after the SARS-CoV-2 infection, vs. 33.3% diagnosed before infection (OR(95%CI) 1.11(0.40-3.08), p=0.84), with no correlation between the time-point of infection and GDM diagnosis. SARS-CoV-2 (OR(95%CI) 2.79 (1.42, 5.47), p=0.003) and BMI (OR(95%CI) 1.12 (1.05, 1.19), p=0.001) were significant independent risk factors for GDM. Conclusions: The significantly higher rate of GDM among women with SARS-CoV-2 infection during pregnancy, as compared to matching controls, suggests that GDM increases the risk of infection. On the other hand, SARS-CoV-2 during pregnancy might increase the risk of developing GDM. Vaccination and caution in using protective measures should be recommended to pregnant women, particularly those with co-morbidities. Funding: none Keywords: SARS-CoV-2, gestational diabetes, COVID-19


Subject(s)
COVID-19 , Diabetes Mellitus , Diabetes, Gestational
2.
Manon Vouga; Guillaume Favre; Oscar Martinez Perez; Leo Pomar; Laura Forcen Acebal; Alejandra Abascal; Maria Rosa Vila Hernandez; Najeh Hcini; Véronique Lambert; Gabriel Carles; Joanna Sichitiu; Laurent Salomon; Julien Stiremann; Yves Ville; Begoña Martinez de Tejada; Anna Goncé; Ameth Hawkins-Villareal; Karen Castillo; Eduard Gratacos Solsona; Lucas Trigo; Brian Cleary; Michael Geary; Helena Bartels; Feras Al-Kharouf; Fergal Malone; Mary Higgins; Niamh Keating; Susan Knowles; Christophe Poncelet; Carolina Carvalho; Fernanda Ribeiro-do-Valle; Garanhani Surita; Amanda Dantas-Silva; Carolina Borrelli; Adriana Gomes Luz; Javiera Fuenzalida; Jorge Carvajal; Manuel Guerra Canales; Olivia Hernandez; Olga Grechukhina; Albert Ko; Uma Reddy; Rita Figueiredo; Marina Moucho; Pedro Viana Pinto; Carmen De Luca; Marco De Santis; Diogo Ayres de Campos; Charles Garabedian; Damien Subtil; Betania Bohrer; Maria Lucia Da Rocha Oppermann; Maria Celeste; Osorio Wender; Lavinia Schuler-Faccini; Maria Teresa Vieira Sanseverino; Camila Giugliani; Luciana Friedrich; Mariana Horn Scherer; Nicolas Mottet; Guillaume Ducarme; Helene Pelerin; Chloe Moreau; Bénédicte Breton; Thibaud Quibel; Patrick Rozenberg; Doris Mueller; Cristina Granado; Irene Hoesli; Cécile Monod; Dirk Bassler; Sandra Heldstab; Nicole Ochsenbein Kölble; Loïc Sentilhes; Melissa Charvet; Jan Deprest; Jute Richter; Lennart Van der Veeken; Béatrice Eggel-Hort; Gaetan Plantefeve; Mohamed Derouich; Albaro José Nieto Calvache; Maria Camila Lopez-Giron; Juan Manuel Burgos-Luna; Maria Fernanda Escobar-Vidarte; Kurt Hecher; Ann-Christin Tallarek; Eran Hadar; Karina Krajden Haratz; Gustavo Malinger; Ron Maymon; Yariv Yogev; Leonhard Schäffer; Arnaud Toussaint; Marie-Claude Rossier; Renato Augusto Moreira de sa; Claudia Grawe; Karoline Aebi-Popp; Anda-Petronela Radan; Luigi Raio; Daniel Surbek; Paul Böckenhoff; Brigitte Strizek; Martin Kaufmann; Andrea Bloch; Michel Boulvain; Silke Johann; Sandra Andrea Heldstab; Monya Todesco Bernasconi; Gaston Grant; Anis Feki; Anne-Claude Muller Brochut; Marylene Giral; Lucie Sedille; Andrea Papadia; Romina Capoccia Brugger; Brigitte Weber; Tina Fischer; Christian Kahlert; Karin Nielsen Saines; Mary Cambou; Panagiotis Kanellos; Xiang Chen; Mingzhu Yin; Annina Haessig; David Baud; Alice Panchaud.
ssrn; 2020.
Preprint in English | PREPRINT-SSRN | ID: ppzbmed-10.2139.ssrn.3724278

ABSTRACT

Background: Recent evidence suggests that pregnant women might be at higher risk of severe disease associated with the emerging pandemic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), while exposed fetuses/newborns could suffer from preterm birth, growth restriction and neonatal infections. The magnitude of this increased risk and specific risk factors for severity remains unclear.Methods: We performed a case control study comparing pregnant women with severe coronavirus disease 19 (case) to pregnant women with a milder form (controls) enrolled in COVI-Preg international registry cohort between from March 24 to July 26, 2020. Risk factors for severity, obstetrical, fetal and neonatal outcomes were assessed.Findings: A total of 926 pregnant women with a positive test for SARS-CoV-2 were included, among which 92 (9.9%) presented a severe COVID-19 disease. Risk factors for severe maternal outcomes were pulmonary comorbidities [aOR 4.3, 95% CI 1.9-9.5], hypertensive disorders [aOR 2.7, 95% CI 1.0-7.0] and diabetes [aOR2.2, 95% CI 1.1-4.5]. Pregnant women with severe maternal outcomes were at higher risk of cesarean sections [70.7% (n=53/75)], preterm deliveries [62.7% (n= 32/51)] and newborns requiring admission to the neonatal intensive care unit [41.3% (n=31/75)].Interpretation: Pregnant women, particularly those with associated comorbidities, seem to be at higher risk of severe complications of SARS-CoV-2 infection. Obstetrical and neonatal outcomes appear to be influenced by the severity of maternal disease; complications include cesarean sections, prematurity and neonatal admission to the intensive care unit.Funding Statement: None.Declaration of Interests: The authors declare that they have no conflicts of interest.Ethics Approval Statement: The study was approved by both the Swiss Ethical Board (CER-VD- 2020-00548) and the local ethics boards at each participating center.


Subject(s)
COVID-19 , Coronavirus Infections , Diabetes Mellitus , Hypertension
3.
Manon Vouga; Guillaume Favre; Oscar Martinez Perez; Leo Pomar; Laura Forcen Acebal; Alejandra Abascal; Maria Rosa Vila Hernandez; Najeh Hcini; Véronique Lambert; Gabriel Carles; Joanna Sichitiu; Laurent Salomon; Julien Stiremann; Yves Ville; Begoña Martinez de Tejada; Anna Goncé; Ameth Hawkins-Villareal; Karen Castillo; Eduard Gratacos Solsona; Lucas Trigo; Brian Cleary; Michael Geary; Helena Bartels; Feras Al-Kharouf; Fergal Malone; Mary Higgins; Niamh Keating; Susan Knowles; Christophe Poncelet; Carolina Carvalho; Fernanda Ribeiro-do-Valle; Garanhani Surita; Amanda Dantas-Silva; Carolina Borrelli; Adriana Gomes Luz; Javiera Fuenzalida; Manuel Guerra Canales; Olivia Hernandez; Olga Grechukhina; Albert Ko; Uma Reddy; Rita Figueiredo; Marina Moucho; Pedro Viana Pinto; Carmen De Luca; Marco De Santis; Diogo Ayres de Campos; Charles Garabedian; Damien Subtil; Betania Bohrer; Maria Lucia Da Rocha Oppermann; Maria Celeste; Osorio Wender; Lavinia Schuler-Faccini; Maria Teresa Vieira Sanseverino; Camila Giugliani; Luciana Friedrich; Mariana Horn Scherer; Nicolas Mottet; Guillaume Ducarme; Helene Pelerin; Chloe Moreau; Bénédicte Breton; Thibaud Quibel; Patrick Rozenberg; Doris Mueller; Cristina Granado; Irene Hoesli; Cécile Monod; Dirk Bassler; Sandra Heldstab; Nicole Ochsenbein Kölble; Loïc Sentilhes; Melissa Charvet; Jan Deprest; Jute Richter; Lennart Van der Veeken; Béatrice Eggel-Hort; Gaetan Plantefeve; Mohamed Derouich; Albaro José Nieto Calvache; Maria Camila Lopez-Giron; Juan Manuel Burgos-Luna; Maria Fernanda Escobar-Vidarte; Kurt Hecher; Ann-Christin Tallarek; Eran Hadar; Karina Krajden Haratz; Gustavo Malinger; Ron Maymon; Yariv Yogev; Leonhard Schäffer; Arnaud Toussaint; Marie-Claude Rossier; Renato Augusto Moreira de sa; Claudia Grawe; Karoline Aebi-Popp; Anda-Petronela Radan; Luigi Raio; Daniel Surbek; Paul Böckenhoff; Brigitte Strizek; Martin Kaufmann; Andrea Bloch; Michel Boulvain; Silke Johann; Monya Todesco Bernasconi; Gaston Grant; Anis Feki; Anne-Claude Muller Brochut; Marylene Giral; Lucie Sedille; Andrea Papadia; Romina Capoccia Brugger; Brigitte Weber; Tina Fischer; Christian Kahlert; Karin Nielsen Saines; Mary Cambou; Panagiotis Kanellos; Xiang Chen; Mingzhu Yin; Annina Haessig; David Baud; Alice Panchaud.
ssrn; 2020.
Preprint in English | PREPRINT-SSRN | ID: ppzbmed-10.2139.ssrn.3684424

ABSTRACT

Background: Pregnant women represent a vulnerable population at higher risk of complications of infectious diseases. Data regarding the consequences of the emerging pandemic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) during pregnancy are scarce. Recent evidence suggests that pregnant women might be at higher risk of severe disease, while exposed fetuses and newborns could suffer from preterm birth, growth restriction and neonatal infections.Methods: We developed an international web registry to allow structured data collection. Pregnant women at any stage during gestation tested for SARS-CoV-2 infection were enrolled. Maternal, obstetrical and neonatal outcomes were recorded.Findings: 1033 pregnant women tested for SARS-CoV-2 were included, among which 926 tested positive and 107 tested negative. Positive pregnant women were at higher risk of severe maternal outcomes compared to negative women [aRR 5.6, 95% CI 1.4-22.7]. Risk factors for severe maternal outcomes among positive women were pulmonary comorbidities [aOR 4.3, 95% CI 1.9-9.5], hypertensive disorders [aOR 2.7, 95% CI 1.0-7.0] and diabetes [aOR2.2, 95% CI 1.1-4.5]. No difference in term of obstetrical and neonatal outcomes were observed between positive and negative women. Positive pregnant women with severe maternal outcomes were at higher risk of cesarean sections [70.7% (n=53/75)], preterm deliveries [62.7% (n= 32/51)] and newborns requiring admission to the neonatal intensive care unit [41.3% (n=31/75)]. A positive neonatal SARS-CoV-2 test was observed in 2.9% (n=11/384) of newborns with an available test at birth.Interpretation: Pregnant women, particularly those with associated comorbidities, seem to be at higher risk of severe complications of SARS-CoV-2 infection. Preliminary data regarding obstetrical and neonatal outcomes among women with a mild disease are reassuring.Funding Statement: None.Declaration of Interests: The authors declare that we have no conflicts of interest.Ethics Approval Statement: The study was approved by both the Swiss Ethical Board (CER-VD-2020-00548) and the local ethics boards at each participating center.


Subject(s)
Coronavirus Infections , Diabetes Mellitus , Communicable Diseases , Hypertension , COVID-19
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