Julie Milbak

and 11 more

Objective: To evaluate if SARS-CoV-2 is detectable in vaginal swabs and whether antibodies against SARS-CoV-2 are present in maternal and umbilical cord blood of pregnant women with COVID-19. Design: Prospective cohort study. Setting: Department of Obstetrics and Gynaecology, Copenhagen University Hospital – North Zealand, Denmark. Population: Pregnant women tested positive for SARS-CoV-2 in a pharyngeal swab between August 20th, 2020 and March 1st, 2021 who gave birth during the same period. Methods: Maternal blood sample and vaginal swabs were collected at inclusion. If included during pregnancy, these samples were repeated at delivery in addition to an umbilical cord blood sample. Swabs were analysed for SARS-CoV-2 and blood samples for SARS-CoV-2 total antibodies. Placental and neonatal swabs were performed on clinical indications. Main outcome measures: SARS-CoV-2 in vaginal swabs and SARS-CoV-2 total antibodies in maternal and umbilical cord blood. Results: We included 28 women, hereof 4 serious maternal or fetal outcomes including 1 neonatal death. Within the first eight days after a maternal positive pharyngeal swab, SARS-CoV-2 was detectable in two vaginal (2/28) and two placental swabs (2/4), whereas SARS-CoV-2 antibodies were detected in 1/13 women. After eight days, SARS-CoV-2 was not detectable in vaginal swabs and SARS-CoV-2 antibodies were observed in 19/21 of women. Antibodies in cord blood of seropositive mothers appeared after 16 days. Conclusion: Vertical transmission of SARS-CoV-2 seems plausible since SARS-CoV-2 is detectable in the vagina up to eight days after a positive pharyngeal swab at which time the neonate is not yet protected by antibodies.

Nina Nathan

and 8 more

Objective: To develop a prediction model for labour dystocia, suitable for risk stratification at onset of labour. Design: A cohort-based registry design was employed using data from the Copenhagen Pregnancy Cohort and the Danish Medical Birth Registry. Setting: The study was conducted at Copenhagen University Hospital – Rigshospitalet, Denmark Population: Nulliparous women with a singleton pregnancy and cephalic presentation in spontaneous labour at term from 2014 to 2020. Methods: Logistic regression analysis was employed to construct the prediction model. Candidate predictors were pre-selected based on clinical reasoning and existing evidence. These were maternal age, pre-pregnancy body mass index, height, gestational age, physical activity, self-reported medical condition, WHO-5 score, and fertility treatment. Main outcome measures: The candidate predictors ability to predict labour dystocia. For model performance, we calculated the area under the receiver operating characteristics curve (AUC) for discriminative capacity and Brier score for model calibration. Results: A total of 12,445 women involving 5,525 events of labour dystocia (44%) were included. All candidate predictors were retained in the final model, which demonstrated moderate discriminative ability with AUC was 62.3% (95% CI:60.7-64.0) and Brier score of 0.24. Conclusions: Our model represents an initial advancement in the prediction of labour dystocia utilizing readily available information obtainable upon admission in active labour. As means of facilitating risk stratification the development of a user-friendly online tool for clinicians is a logical next step. Nevertheless, further model development and external testing across other populations is warranted.