Achieving optimal adherence to medical therapy by telehealth: Findings from the ORBITA medication adherence sub-study.


Journal

Pharmacology research & perspectives
ISSN: 2052-1707
Titre abrégé: Pharmacol Res Perspect
Pays: United States
ID NLM: 101626369

Informations de publication

Date de publication:
02 2021
Historique:
received: 06 10 2020
revised: 25 11 2020
accepted: 07 12 2020
entrez: 11 2 2021
pubmed: 12 2 2021
medline: 12 11 2021
Statut: ppublish

Résumé

The ORBITA trial of percutaneous coronary intervention (PCI) versus a placebo procedure for patients with stable angina was conducted across six sites in the United Kingdom via home monitoring and telephone consultations. Patients underwent detailed assessment of medication adherence which allowed us to measure the efficacy of the implementation of the optimization protocol and interpretation of the main trial endpoints. Prescribing data were collected throughout the trial. Self-reported adherence was assessed, and urine samples collected at pre-randomization and at follow-up for direct assessment of adherence using high-performance liquid chromatography with tandem mass spectrometry (HPLC MS/MS). Self-reported adherence was >96% for all drugs in both treatment groups at both stages. The percentage of samples in which drug was detected at pre-randomization and at follow-up in the PCI versus placebo groups respectively was: clopidogrel, 96% versus 90% and 98% versus 94%; atorvastatin, 95% versus 92% and 92% versus 91%; perindopril, 95% versus 97% and 85% versus 100%; bisoprolol, 98% versus 99% and 96% versus 97%; amlodipine, 99% versus 99% and 94% versus 96%; nicorandil, 98% versus 96% and 94% versus 92%; ivabradine, 100% versus 100% and 100% versus 100%; and ranolazine, 100% versus 100% and 100% versus 100%. Adherence levels were high throughout the study when quantified by self-reporting methods and similarly high proportions of drug were detected by urinary assay. The results indicate successful implementation of the optimization protocol delivered by telephone, an approach that could serve as a model for treatment of chronic conditions, particularly as consultations are increasingly conducted online.

Identifiants

pubmed: 33570248
doi: 10.1002/prp2.710
pmc: PMC7876856
doi:

Substances chimiques

Calcium Channel Blockers 0
Cardiovascular Agents 0
Hydroxymethylglutaryl-CoA Reductase Inhibitors 0
Platelet Aggregation Inhibitors 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e00710

Subventions

Organisme : British Heart Foundation
ID : FS/17/16/32560
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/V001620/1
Pays : United Kingdom
Organisme : Department of Health
Pays : United Kingdom

Investigateurs

Sayan Sen (S)
Ricardo Petraco (R)
Christopher Cook (C)
Yousif Ahmad (Y)
James Howard (J)
Matthew Shun-Shin (M)
Jamil Mayet (J)
Jaspal Kooner (J)
Ramzi Khamis (R)
Kare Tang (K)
John Davies (J)
Thomas Keeble (T)
Raffi Kaprielian (R)
Iqbal Malik (I)
Sukhjinder Nijjer (S)
Amarjit Sethi (A)
Christopher Baker (C)
Punit Ramrakha (P)
Ravi Assomull (R)
Rodney Foale (R)
Nearchos Hadjiloizou (N)
Masood Khan (M)
Michael Bellamy (M)
Ghada Mikhail (G)
Piers Clifford (P)
Andrew Sharp (A)
Robert Gerber (R)
Suneel Talwar (S)
Peter O'Kane (P)
Terry Levy (T)
Rosie Swallow (R)
Roland Wensel (R)

Informations de copyright

© 2021 The Authors. Pharmacology Research & Perspectives published by John Wiley & Sons Ltd, British Pharmacological Society and American Society for Pharmacology and Experimental Therapeutics.

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Auteurs

David Thompson (D)

National Heart and Lung Institute, Imperial College London, London, UK.
Institute of Cardiovascular Science, University College London, London, UK.

Rasha Al-Lamee (R)

National Heart and Lung Institute, Imperial College London, London, UK.

Michael Foley (M)

National Heart and Lung Institute, Imperial College London, London, UK.

Hakim M Dehbi (HM)

Comprehensive Clinical Trials Unit at UCL, University College London, London, UK.

Simon Thom (S)

National Heart and Lung Institute, Imperial College London, London, UK.

Justin E Davies (JE)

National Heart and Lung Institute, Imperial College London, London, UK.

Darrel P Francis (DP)

National Heart and Lung Institute, Imperial College London, London, UK.

Prashanth Patel (P)

Department of Chemical Pathology and Metabolic Diseases, University Hospitals of Leicester, Leicester, UK.
Department of Cardiovascular Sciences, University of Leicester, Leicester, UK.
NIHR Leicester Biomedical Research Unit in Cardiovascular Disease, Leicester, UK.

Pankaj Gupta (P)

Department of Chemical Pathology and Metabolic Diseases, University Hospitals of Leicester, Leicester, UK.
Department of Cardiovascular Sciences, University of Leicester, Leicester, UK.
NIHR Leicester Biomedical Research Unit in Cardiovascular Disease, Leicester, UK.

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