High non-adherence rates to secondary prevention by chemical adherence testing in patients with TIA.


Journal

Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association
ISSN: 1532-8511
Titre abrégé: J Stroke Cerebrovasc Dis
Pays: United States
ID NLM: 9111633

Informations de publication

Date de publication:
Sep 2022
Historique:
received: 01 06 2022
revised: 14 07 2022
accepted: 17 07 2022
pubmed: 29 7 2022
medline: 25 8 2022
entrez: 28 7 2022
Statut: ppublish

Résumé

Transient ischaemic attack (TIA) clinics are important for secondary prevention of fatal or disabling stroke. Non-adherence to prescribed medications is an important reason for treatment failure but difficult to diagnose. This study ascertained the utility of a novel biochemical tool in the objective biochemical diagnosis of non-adherence. One-hundred consecutive urine samples collected from patients attending the TIA clinic, at a tertiary centre, were analysed for presence or absence of prescribed cardiovascular medications using liquid chromatography-mass spectrometry (LC-MS/MS). Patients were classified as adherent or non-adherent, respectively. Demographic and clinical characteristics were compared between the two cohorts. Univariate regression analyses were performed for individual variables and model fitting was undertaken for significant variables. The mean duration of follow-up from the index event was 31 days [standard deviation (SD): 18.9]. The overall rate of non-adherence for at least one medication was 24%. In univariate analysis, the number of comorbidities [3.4 (SD: 1.9) vs. 2.5 (1.9), P = 0.032] and total number of all prescribed medications [6.0 (3.3) vs 4.4 (2.1), P = 0.032] were higher in the non-adherent group. On multivariate analysis, the total number of medications prescribed correlated with increased non-adherence (odds ratio: 1.27, 95% Confidence Intervals: 1.1-1.5, P = 0.01). LC-MS/MS is a clinically useful tool for the diagnosis of non-adherence. Nearly a quarter of TIA patients were non-adherent to their cardiovascular medications Addressing non-adherence early may reduce the risk of future disabling cardiovascular events.

Identifiants

pubmed: 35901588
pii: S1052-3057(22)00359-7
doi: 10.1016/j.jstrokecerebrovasdis.2022.106665
pii:
doi:

Substances chimiques

Cardiovascular Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106665

Informations de copyright

Crown Copyright © 2022. Published by Elsevier Inc. All rights reserved.

Auteurs

Dan Lane (D)

Department of Metabolic Diseases and Chemical Pathology, University Hospitals of Leicester NHS Trust, Level 4, Sandringham Building, Leicester Royal Infirmary, Leicester LE1 5WW, United Kingdom.

Lucy Beishon (L)

Department of Cardiovascular Sciences, University of Leicester, United Kingdom.

Vinoda Sharma (V)

Department of Cardiology, Sandwell and West Birmingham Hospitals NHS Trust, United Kingdom.

Farah Salim (F)

Department of Cardiovascular Sciences, University of Leicester, United Kingdom.

Shirley Sze (S)

Department of Cardiovascular Sciences, University of Leicester, United Kingdom.

Matthew A Timmins (MA)

Department of Metabolic Diseases and Chemical Pathology, University Hospitals of Leicester NHS Trust, Level 4, Sandringham Building, Leicester Royal Infirmary, Leicester LE1 5WW, United Kingdom.

Thompson Robinson (T)

Department of Cardiovascular Sciences, University of Leicester, United Kingdom; Department of Stroke Medicine, University Hospitals of Leicester NHS Trust, United Kingdom; National Institute for Health Research Leicester Biomedical Research Centre, University of Leicester, United Kingdom.

David Eveson (D)

Department of Stroke Medicine, University Hospitals of Leicester NHS Trust, United Kingdom.

Amit Mistri (A)

Department of Stroke Medicine, University Hospitals of Leicester NHS Trust, United Kingdom.

Prashanth Patel (P)

Department of Metabolic Diseases and Chemical Pathology, University Hospitals of Leicester NHS Trust, Level 4, Sandringham Building, Leicester Royal Infirmary, Leicester LE1 5WW, United Kingdom; Department of Cardiovascular Sciences, University of Leicester, United Kingdom.

Pankaj Gupta (P)

Department of Metabolic Diseases and Chemical Pathology, University Hospitals of Leicester NHS Trust, Level 4, Sandringham Building, Leicester Royal Infirmary, Leicester LE1 5WW, United Kingdom; Department of Cardiovascular Sciences, University of Leicester, United Kingdom. Electronic address: Pankaj.gupta@uhl-tr.nhs.uk.

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