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Development and validation of a prediction model for gestational hypertension in a Ghanaian cohort

OBJECTIVE: To develop and validate a prediction model for identifying women at increased risk of developing gestational hypertension (GH) in Ghana. DESIGN: A prospective study. We used frequencies for descriptive analysis, χ(2) test for associations and logistic regression to derive the prediction m...

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Autores principales: Antwi, Edward, Groenwold, Rolf H H, Browne, Joyce L, Franx, Arie, Agyepong, Irene A, Koram, Kwadwo A, Klipstein-Grobusch, Kerstin, Grobbee, Diederick E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5253568/
https://www.ncbi.nlm.nih.gov/pubmed/28093430
http://dx.doi.org/10.1136/bmjopen-2016-012670
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author Antwi, Edward
Groenwold, Rolf H H
Browne, Joyce L
Franx, Arie
Agyepong, Irene A
Koram, Kwadwo A
Klipstein-Grobusch, Kerstin
Grobbee, Diederick E
author_facet Antwi, Edward
Groenwold, Rolf H H
Browne, Joyce L
Franx, Arie
Agyepong, Irene A
Koram, Kwadwo A
Klipstein-Grobusch, Kerstin
Grobbee, Diederick E
author_sort Antwi, Edward
collection PubMed
description OBJECTIVE: To develop and validate a prediction model for identifying women at increased risk of developing gestational hypertension (GH) in Ghana. DESIGN: A prospective study. We used frequencies for descriptive analysis, χ(2) test for associations and logistic regression to derive the prediction model. Discrimination was estimated by the c-statistic. Calibration was assessed by calibration plot of actual versus predicted probability. SETTING: Primary care antenatal clinics in Ghana. PARTICIPANTS: 2529 pregnant women in the development cohort and 647 pregnant women in the validation cohort. Inclusion criterion was women without chronic hypertension. PRIMARY OUTCOME: Gestational hypertension. RESULTS: Predictors of GH were diastolic blood pressure, family history of hypertension in parents, history of GH in a previous pregnancy, parity, height and weight. The c-statistic of the original model was 0.70 (95% CI 0.67–0.74) and 0.68 (0.60 to 0.77) in the validation cohort. Calibration was good in both cohorts. The negative predictive value of women in the development cohort at high risk of GH was 92.0% compared to 94.0% in the validation cohort. CONCLUSIONS: The prediction model showed adequate performance after validation in an independent cohort and can be used to classify women into high, moderate or low risk of developing GH. It contributes to efforts to provide clinical decision-making support to improve maternal health and birth outcomes.
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spelling pubmed-52535682017-01-25 Development and validation of a prediction model for gestational hypertension in a Ghanaian cohort Antwi, Edward Groenwold, Rolf H H Browne, Joyce L Franx, Arie Agyepong, Irene A Koram, Kwadwo A Klipstein-Grobusch, Kerstin Grobbee, Diederick E BMJ Open Epidemiology OBJECTIVE: To develop and validate a prediction model for identifying women at increased risk of developing gestational hypertension (GH) in Ghana. DESIGN: A prospective study. We used frequencies for descriptive analysis, χ(2) test for associations and logistic regression to derive the prediction model. Discrimination was estimated by the c-statistic. Calibration was assessed by calibration plot of actual versus predicted probability. SETTING: Primary care antenatal clinics in Ghana. PARTICIPANTS: 2529 pregnant women in the development cohort and 647 pregnant women in the validation cohort. Inclusion criterion was women without chronic hypertension. PRIMARY OUTCOME: Gestational hypertension. RESULTS: Predictors of GH were diastolic blood pressure, family history of hypertension in parents, history of GH in a previous pregnancy, parity, height and weight. The c-statistic of the original model was 0.70 (95% CI 0.67–0.74) and 0.68 (0.60 to 0.77) in the validation cohort. Calibration was good in both cohorts. The negative predictive value of women in the development cohort at high risk of GH was 92.0% compared to 94.0% in the validation cohort. CONCLUSIONS: The prediction model showed adequate performance after validation in an independent cohort and can be used to classify women into high, moderate or low risk of developing GH. It contributes to efforts to provide clinical decision-making support to improve maternal health and birth outcomes. BMJ Publishing Group 2017-01-16 /pmc/articles/PMC5253568/ /pubmed/28093430 http://dx.doi.org/10.1136/bmjopen-2016-012670 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Epidemiology
Antwi, Edward
Groenwold, Rolf H H
Browne, Joyce L
Franx, Arie
Agyepong, Irene A
Koram, Kwadwo A
Klipstein-Grobusch, Kerstin
Grobbee, Diederick E
Development and validation of a prediction model for gestational hypertension in a Ghanaian cohort
title Development and validation of a prediction model for gestational hypertension in a Ghanaian cohort
title_full Development and validation of a prediction model for gestational hypertension in a Ghanaian cohort
title_fullStr Development and validation of a prediction model for gestational hypertension in a Ghanaian cohort
title_full_unstemmed Development and validation of a prediction model for gestational hypertension in a Ghanaian cohort
title_short Development and validation of a prediction model for gestational hypertension in a Ghanaian cohort
title_sort development and validation of a prediction model for gestational hypertension in a ghanaian cohort
topic Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5253568/
https://www.ncbi.nlm.nih.gov/pubmed/28093430
http://dx.doi.org/10.1136/bmjopen-2016-012670
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