A cross-sectional evaluation of five warfarin anticoagulation services in Uganda and South Africa.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 02 09 2019
accepted: 18 12 2019
entrez: 30 1 2020
pubmed: 30 1 2020
medline: 14 4 2020
Statut: epublish

Résumé

Warfarin is the most commonly prescribed oral anticoagulant in sub-Saharan Africa and requires ongoing monitoring. The burden of both infectious diseases and non-communicable diseases is high and medicines used to treat comorbidities may interact with warfarin. We describe service provision, patient characteristics, and anticoagulation control at selected anticoagulation clinics in Uganda and South Africa. We evaluated two outpatient anticoagulation services in Kampala, Uganda and three in Cape Town, South Africa between 1 January and 31 July 2018. We collected information from key staff members about the clinics' service provision and extracted demographic and clinical data from a sample of patients' clinic records. We calculated time in therapeutic range (TTR) over the most recent 3-month period using the Rosendaal interpolation method. We included three tertiary level, one secondary level and one primary level anticoagulation service, seeing between 30 and 800 patients per month. Care was rendered by nurses, medical officers, and specialists. All healthcare facilities had on-site pharmacies; laboratory INR testing was off-site at two. Three clinics used warfarin dose-adjustment protocols; these were not validated for local use. We reviewed 229 patient clinical records. Most common indications for warfarin were venous thrombo-embolism in 112/229 (49%), atrial fibrillation in 74/229 (32%) and valvular heart disease in 30/229 (13%). Patients were generally followed up monthly. HIV prevalence was 20% and 5% at Ugandan and South African clinics respectively. Cardiovascular comorbidity predominated. Furosemide, paracetamol, enalapril, simvastatin, and tramadol were the most common concomitant drugs. Anticoagulation control was poor at all included clinics with median TTR of 41% (interquartile range 14% to 69%). TTR was suboptimal at all included sites, despite frequent patient follow-up. Strategies to improve INR control in sub-Saharan patients taking warfarin are needed. Locally validated warfarin dosing algorithms in Uganda and South Africa may improve INR control.

Identifiants

pubmed: 31995565
doi: 10.1371/journal.pone.0227458
pii: PONE-D-19-22709
pmc: PMC6988943
doi:

Substances chimiques

Anticoagulants 0
Warfarin 5Q7ZVV76EI

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0227458

Subventions

Organisme : Department of Health
ID : 16/137/101
Pays : United Kingdom

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Jerome Roy Semakula (JR)

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

Johannes P Mouton (JP)

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

Andrea Jorgensen (A)

Department of Biostatistics, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.

Claire Hutchinson (C)

Department of Molecular and Clinical Pharmacology, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.

Shaazia Allie (S)

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

Lynn Semakula (L)

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

Neil French (N)

Department of Molecular and Clinical Pharmacology, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.

Mohammed Lamorde (M)

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

Cheng-Hock Toh (CH)

Institute of Infection and Global Health, University of Liverpool, Liverpool, United Kingdom.

Marc Blockman (M)

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

Christine Sekaggya-Wiltshire (C)

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

Catriona Waitt (C)

Infectious Diseases Institute, College of Health Sciences Makerere University, Kampala, Uganda.
Department of Molecular and Clinical Pharmacology, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.

Munir Pirmohamed (M)

Wolfson Centre for Personalised Medicine, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.

Karen Cohen (K)

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

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Classifications MeSH