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Preeclampsia prediction with blood pressure measurements: A global external validation of the ALSPAC models.
de Kat, Annelien C; Hirst, Jane E; Woodward, Mark; Barros, Fernando C; Barsosio, Hellen C; Berkley, James A; Carvalho, Maria; Cheikh Ismail, Leila; McGready, Rose; Norris, Shane A; Nosten, Francois; Ohuma, Eric; Tshivuila-Matala, Chrystelle O O; Stones, William; Staines Urias, Eleonora; Clara Restrepo-Mendez, Maria; Lambert, Ann; Munim, Shama; Winsey, Adele; Papageorghiou, Aris T; Bhutta, Zulfiqar A; Villar, Jose; Kennedy, Stephen H; Peters, Sanne A E.
Afiliação
  • de Kat AC; The George Institute for Global Health, School of Public Health, Imperial College, London, United Kingdom; Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, United Kingdom.
  • Hirst JE; The George Institute for Global Health, School of Public Health, Imperial College, London, United Kingdom; Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, United Kingdom.
  • Woodward M; The George Institute for Global Health, School of Public Health, Imperial College, London, United Kingdom; School of Public Health, Imperial College, London, United Kingdom.
  • Barros FC; Programa de Pós-Graduação em Saúde e Comportamento, Universidade Católica de Pelotas, Pelotas, Rio Grande do Sul, Brazil.
  • Barsosio HC; KEMRI-Coast Centre for Geographical Medicine and Research, Kilifi, Kenya.
  • Berkley JA; KEMRI-Coast Centre for Geographical Medicine and Research, Kilifi, Kenya; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine Research, Oxford, United Kingdom.
  • Carvalho M; Faculty of Health Sciences, Aga Khan University, Nairobi, Kenya.
  • Cheikh Ismail L; Clinical Nutrition and Dietetics Department, University of Sharjah, Sharjah, United Arab Emirates.
  • McGready R; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine Research, Oxford, United Kingdom; Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Mae Sot, Thailand.
  • Norris SA; SAMRC Developmental Pathways for Health Research Unit, Department of Paediatrics & Child Health, University of the Witwatersrand, Johannesburg, South Africa.
  • Nosten F; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine Research, Oxford, United Kingdom; Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Mae Sot, Thailand.
  • Ohuma E; Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, United Kingdom; Maternal, Adolescent, Reproductive & Child Health (MARCH) Centre, London School of Hygiene and Tropical Medicine (LSHTM), London, United Kingdom.
  • Tshivuila-Matala COO; Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, United Kingdom; SAMRC Developmental Pathways for Health Research Unit, Department of Paediatrics & Child Health, University of the Witwatersrand, Johannesburg, South Africa.
  • Stones W; Faculty of Health Sciences, Aga Khan University, Nairobi, Kenya.
  • Staines Urias E; Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, United Kingdom.
  • Clara Restrepo-Mendez M; Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, United Kingdom.
  • Lambert A; Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, United Kingdom.
  • Munim S; Department of Obstetrics and Gynaecology, Division of Women and Child Health, Aga Khan University, Karachi, Pakistan.
  • Winsey A; Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, United Kingdom.
  • Papageorghiou AT; Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, United Kingdom; Oxford Maternal and Perinatal Health Institute (OMPHI), Green Templeton College, University of Oxford, Oxford, United Kingdom.
  • Bhutta ZA; Center for Global Child Health, Hospital for Sick Children, Toronto, Canada.
  • Villar J; Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, United Kingdom; Oxford Maternal and Perinatal Health Institute (OMPHI), Green Templeton College, University of Oxford, Oxford, United Kingdom.
  • Kennedy SH; Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, United Kingdom; Oxford Maternal and Perinatal Health Institute (OMPHI), Green Templeton College, University of Oxford, Oxford, United Kingdom.
  • Peters SAE; The George Institute for Global Health, School of Public Health, Imperial College, London, United Kingdom; Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Pregnancy Hypertens ; 30: 124-129, 2022 Dec.
Article em En | MEDLINE | ID: mdl-36179538
OBJECTIVE: The prediction of preeclampsia in pregnancy has resulted in a plethora of prognostic models. Yet, very few make it past the development stage and most fail to influence clinical practice. The timely identification of high-risk pregnant women could deliver a tailored antenatal care regimen, particularly in low-resource settings. This study externally validated and calibrated previously published models that predicted the risk of preeclampsia, based on blood pressure (BP) at multiple time points in pregnancy, in a geographically diverse population. METHODS: The prospective INTERBIO-21st Fetal Study included 3,391 singleton pregnancies from Brazil, Kenya, Pakistan, South Africa, Thailand and the UK, 2012-2018. Preeclampsia prediction was based on baseline characteristics, BP and deviation from the expected BP trajectory at multiple time points in pregnancy. The prediction rules from the Avon Longitudinal Study of Parents and Children (ALSPAC) were implemented in the INTERBIO-21st cohort. RESULTS: Model discrimination was similar to the development cohort. Performance was best with baseline characteristics and a BP measurement at 34 weeks' gestation (AUC 0.85, 95 % CI 0.80-0.90). The ALSPAC models largely overestimated the true risk of preeclampsia incidence in the INTERBIO-21st cohort. CONCLUSIONS: After recalibration, these prediction models could potentially serve as a risk stratifying tool to help identify women who might benefit from increased surveillance during pregnancy.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pré-Eclâmpsia Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pré-Eclâmpsia Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido