Stable warfarin dose prediction in sub-Saharan African patients: A machine-learning approach and external validation of a clinical dose-initiation algorithm.


Journal

CPT: pharmacometrics & systems pharmacology
ISSN: 2163-8306
Titre abrégé: CPT Pharmacometrics Syst Pharmacol
Pays: United States
ID NLM: 101580011

Informations de publication

Date de publication:
01 2022
Historique:
revised: 24 09 2021
received: 06 08 2021
accepted: 27 10 2021
pubmed: 11 12 2021
medline: 23 3 2022
entrez: 10 12 2021
Statut: ppublish

Résumé

Warfarin remains the most widely prescribed oral anticoagulant in sub-Saharan Africa. However, because of its narrow therapeutic index, dosing can be challenging. We have therefore (a) evaluated and compared the performance of 21 machine-learning techniques in predicting stable warfarin dose in sub-Saharan Black-African patients and (b) externally validated a previously developed Warfarin Anticoagulation in Patients in Sub-Saharan Africa (War-PATH) clinical dose-initiation algorithm. The development cohort included 364 patients recruited from eight outpatient clinics and hospital departments in Uganda and South Africa (June 2018-July 2019). Validation was conducted using an external validation cohort (270 patients recruited from August 2019 to March 2020 in 12 outpatient clinics and hospital departments). Based on the mean absolute error (MAE; mean of absolute differences between the actual and predicted doses), random forest regression (12.07 mg/week; 95% confidence interval [CI], 10.39-13.76) was the best performing machine-learning technique in the external validation cohort, whereas the worst performing technique was model trees (17.59 mg/week; 95% CI, 15.75-19.43). By comparison, the simple, commonly used regression technique (ordinary least squares) performed similarly to more complex supervised machine-learning techniques and achieved an MAE of 13.01 mg/week (95% CI, 11.45-14.58). In summary, we have demonstrated that simpler regression techniques perform similarly to more complex supervised machine-learning techniques. We have also externally validated our previously developed clinical dose-initiation algorithm, which is being prospectively tested for clinical utility.

Identifiants

pubmed: 34889080
doi: 10.1002/psp4.12740
pmc: PMC8752108
doi:

Substances chimiques

Anticoagulants 0
Warfarin 5Q7ZVV76EI
Simvastatin AGG2FN16EV

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

20-29

Subventions

Organisme : Medical Research Council
ID : MR/L006758/1
Pays : United Kingdom
Organisme : National Institute for Health Research (NIHR)
ID : 16/137/101
Organisme : Wellcome Trust
ID : 222075/Z/20/Z
Pays : United Kingdom

Informations de copyright

© 2021 The Authors. CPT: Pharmacometrics & Systems Pharmacology published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics.

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Auteurs

Innocent G Asiimwe (IG)

Department of Pharmacology and Therapeutics, The Wolfson Centre for Personalized Medicine, Medical Research Council Centre for Drug Safety Science, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, UK.

Marc Blockman (M)

Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa.

Karen Cohen (K)

Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa.

Clint Cupido (C)

Victoria Hospital Internal Medicine Research Initiative, Victoria Hospital Wynberg, Cape Town, South Africa.
Department of Medicine, University of Cape Town, Cape Town, South Africa.

Claire Hutchinson (C)

Department of Pharmacology and Therapeutics, The Wolfson Centre for Personalized Medicine, Medical Research Council Centre for Drug Safety Science, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, UK.

Barry Jacobson (B)

Department of Molecular Medicine and Haematology, University of the Witwatersrand, Johannesburg, South Africa.

Mohammed Lamorde (M)

Infectious Diseases Institute, Makerere University College of Health Sciences, Kampala, Uganda.

Jennie Morgan (J)

Metro District Health Services, Western Cape Department of Health, Cape Town, South Africa.

Johannes P Mouton (JP)

Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa.

Doreen Nakagaayi (D)

Uganda Heart Institute, Kampala, Uganda.

Emmy Okello (E)

Uganda Heart Institute, Kampala, Uganda.

Elise Schapkaitz (E)

Department of Molecular Medicine and Hematology, Charlotte Maxeke Johannesburg Academic Hospital National Health Laboratory System Complex and University of Witwatersrand, Johannesburg, South Africa.

Christine Sekaggya-Wiltshire (C)

Infectious Diseases Institute, Makerere University College of Health Sciences, Kampala, Uganda.

Jerome R Semakula (JR)

Infectious Diseases Institute, Makerere University College of Health Sciences, Kampala, Uganda.

Catriona Waitt (C)

Department of Pharmacology and Therapeutics, The Wolfson Centre for Personalized Medicine, Medical Research Council Centre for Drug Safety Science, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, UK.
Infectious Diseases Institute, Makerere University College of Health Sciences, Kampala, Uganda.

Eunice J Zhang (EJ)

Department of Pharmacology and Therapeutics, The Wolfson Centre for Personalized Medicine, Medical Research Council Centre for Drug Safety Science, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, UK.

Andrea L Jorgensen (AL)

Department of Health Data Science, Institute of Population Health Sciences, University of Liverpool, Liverpool, UK.

Munir Pirmohamed (M)

Department of Pharmacology and Therapeutics, The Wolfson Centre for Personalized Medicine, Medical Research Council Centre for Drug Safety Science, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, UK.

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