Affiliation:
1. Department of Obstetrics and Gynecology The Ohio State University Columbus Ohio USA
2. Department of Obstetrics and Gynecology Duke University Durham North Carolina USA
3. Department of Obstetrics and Gynecology Christiana Care Newark Delaware USA
4. Department of Obstetrics and Gynecology WakeMed Health and Hospitals Raleigh North Carolina USA
5. Department of Obstetrics and Gynecology Columbia University New York New York USA
6. Department of Obstetrics and Gynecology University of North Carolina Chapel Hill North Carolina USA
7. Department of Obstetrics and Gynecology Wake Forest University Winston‐Salem North Carolina USA
Abstract
AbstractObjectiveTo develop a model for predicting postpartum readmission for hypertension and pre‐eclampsia at delivery discharge and assess external validation or model transportability across clinical sites.DesignPrediction model using data available in the electronic health record from two clinical sites.SettingTwo tertiary care health systems from the Southern (2014–2015) and Northeastern USA (2017–2019).PopulationA total of 28 201 postpartum individuals: 10 100 in the South and 18 101 in the Northeast.MethodsAn internal‐external cross validation (IECV) approach was used to assess external validation or model transportability across the two sites. In IECV, data from each health system were first used to develop and internally validate a prediction model; each model was then externally validated using the other health system. Models were fit using penalised logistic regression, and accuracy was estimated using discrimination (concordance index), calibration curves and decision curves. Internal validation was performed using bootstrapping with bias‐corrected performance measures. Decision curve analysis was used to display potential cut points where the model provided net benefit for clinical decision‐making.Main outcome measuresThe outcome was postpartum readmission for either hypertension or pre‐eclampsia <6 weeks after delivery.ResultsThe postpartum readmission rate for hypertension and pre‐eclampsia overall was 0.9% (0.3% and 1.2% by site, respectively). The final model included six variables: age, parity, maximum postpartum diastolic blood pressure, birthweight, pre‐eclampsia before discharge and delivery mode (and interaction between pre‐eclampsia × delivery mode). Discrimination was adequate at both health systems on internal validation (c‐statistic South: 0.88; 95% confidence interval [CI] 0.87–0.89; Northeast: 0.74; 95% CI 0.74–0.74). In IECV, discrimination was inconsistent across sites, with improved discrimination for the Northeastern model on the Southern cohort (c‐statistic 0.61 and 0.86, respectively), but calibration was not adequate. Next, model updating was performed using the combined dataset to develop a new model. This final model had adequate discrimination (c‐statistic: 0.80, 95% CI 0.80–0.80), moderate calibration (intercept −0.153, slope 0.960, Emax 0.042) and provided superior net benefit at clinical decision‐making thresholds between 1% and 7% for interventions preventing readmission. An online calculator is provided here.ConclusionsPostpartum readmission for hypertension and pre‐eclampsia may be accurately predicted but further model validation is needed. Model updating using data from multiple sites will be needed before use across clinical settings.
Funder
National Center for Advancing Translational Sciences
National Institutes of Health
Subject
Obstetrics and Gynecology
Cited by
1 articles.
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