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dc.contributor.authorGonzález, Raquel
dc.contributor.authorGoncé, Anna
dc.contributor.authorGil Mira, María del Mar 
dc.contributor.authorMazarico, Edurne
dc.contributor.authorFerriols-Pérez, Elena
dc.contributor.authorToro, Paloma
dc.contributor.authorLlurba, Elisa
dc.contributor.authorSaéz, Elisa
dc.contributor.authorRodríguez-Zambrano, Miguel Ángel
dc.contributor.authorGarcía-Otero, Laura
dc.contributor.authorLópez, Marta
dc.contributor.authorSantacruz Martín, Belén 
dc.contributor.authorRomán, Mª. Ángeles
dc.contributor.authorPayà, Antoni
dc.contributor.authorAlonso, Sofia
dc.contributor.authorCruz-Lemini, Mónica
dc.contributor.authorPons-Duran, Clara
dc.contributor.authorBernardo Herrera, Luis
dc.contributor.authorChen, Haily
dc.contributor.authorBardají, Azucena
dc.contributor.authorQuintó, Llorenç
dc.contributor.authorMenendez, Clara
dc.date.accessioned2024-02-12T14:08:53Z
dc.date.available2024-02-12T14:08:53Z
dc.date.issued2023
dc.identifier.issn0001-6349spa
dc.identifier.urihttps://hdl.handle.net/10641/3957
dc.description.abstractIntroduction Pregnant women have an increased risk of severe COVID-19. Evaluation of drugs with a safety reproductive toxicity profile is a priority. At the beginning of the pandemic, hydroxychloroquine (HCQ) was recommended for COVID-19 treatment. Material and methods A randomized, double-blind, placebo-controlled clinical trial was conducted in eight teaching hospitals in Spain to evaluate the safety and efficacy of HCQ in reducing viral shedding and preventing COVID-19 progression. Pregnant and postpartum women with a positive SARS-CoV-2 PCR (with or without mild COVID-19 signs/symptoms) and a normal electrocardiogram were randomized to receive either HCQ orally (400 mg/day for 3 days and 200 mg/day for 11 days) or placebo. PCR and electrocardiogram were repeated at day 21 after treatment start. Enrollment was stopped before reaching the target sample due to low recruitment rate. Trial registration EudraCT #: 2020-001587-29, on April 2, 2020. Clinical trials.gov # NCT04410562, registered on June 1, 2020. Results A total of 116 women (75 pregnant and 41 post-partum) were enrolled from May 2020 to June 2021. The proportion of women with a positive SARS-CoV-2 PCR at day 21 was lower in the HCQ group (21.8%, 12/55) than in the placebo group (31.6%, 18/57), although the difference was not statistically significant (P = 0.499). No differences were observed in COVID-19 progression, adverse events, median change in QTc, hospital admissions, preeclampsia or poor pregnancy and perinatal outcomes between groups. Conclusions HCQ was found to be safe in pregnant and postpartum women with asymptomatic or mild SARS-CoV-2 infection. Although the prevalence of infection was decreased in the HCQ group, the statistical power was insufficient to confirm the potential beneficial effect of HCQ for COVID-19 treatment.spa
dc.language.isoengspa
dc.publisherActa Obstetricia et Gynecologica Scandinavicaspa
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subjectCOVID-19spa
dc.subjectHydroxychloroquinespa
dc.subjectPregnancyspa
dc.subjectRandomized controlled trialspa
dc.subjectWomenspa
dc.subjectSARS-CoV-2spa
dc.titleEfficacy and safety of hydroxychloroquine for treatment of mild SARS-CoV-2 infection and prevention of COVID-19 severity in pregnant and postpartum women: A randomized, double-blind, placebo-controlled trial.spa
dc.typejournal articlespa
dc.type.hasVersionAMspa
dc.rights.accessRightsopen accessspa
dc.description.extent1101 KBspa
dc.identifier.doi10.1111/aogs.14745spa
dc.relation.publisherversionhttps://obgyn.onlinelibrary.wiley.com/doi/full/10.1111/aogs.14745spa


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