Nonadherence in Hypertension: How to Develop and Implement Chemical Adherence Testing.


Journal

Hypertension (Dallas, Tex. : 1979)
ISSN: 1524-4563
Titre abrégé: Hypertension
Pays: United States
ID NLM: 7906255

Informations de publication

Date de publication:
01 2022
Historique:
pubmed: 6 11 2021
medline: 19 1 2022
entrez: 5 11 2021
Statut: ppublish

Résumé

Nonadherence to antihypertensive medication is common, especially in those with apparent treatment-resistant hypertension (true treatment-resistant hypertension requires exclusion of nonadherence), and its routine detection is supported by clinical guidelines. Chemical adherence testing is a reliable and valid method to detect adherence, yet methods are unstandardized and are not ubiquitous. This article describes the principles of chemical adherence testing for hypertensive patients and provides a set of recommendations for centers wishing to develop the test. We recommend testing should be done in either of two instances: (1) in those who have resistant hypertension or (2) in those on 2 antihypertensives who have a less than 10 mm Hg drop in systolic blood pressure on addition of the second antihypertensive medication. Furthermore, we recommend that verbal consent is secured before undertaking the test, and the results should be discussed with the patient. Based on medications prescribed in United Kingdom, European Union, and United States, we list top 20 to 24 drugs that cover >95% of hypertension prescriptions which may be included in the testing panel. Information required to identify these medications on mass spectrometry platforms is likewise provided. We discuss issues related to ethics, sample collection, transport, stability, urine versus blood samples, qualitative versus quantitative testing, pharmacokinetics, instrumentation, validation, quality assurance, and gaps in knowledge. We consider how to best present, interpret, and discuss chemical adherence test results with the patient. In summary, this guidance should help clinicians and their laboratories in the development of chemical adherence testing of prescribed antihypertensive drugs.

Identifiants

pubmed: 34739765
doi: 10.1161/HYPERTENSIONAHA.121.17596
doi:

Substances chimiques

Antihypertensive Agents 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

12-23

Subventions

Organisme : British Heart Foundation
ID : CS/17/3/32799
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/19/16/34270
Pays : United Kingdom

Auteurs

Dan Lane (D)

The Department of Chemical Pathology and Metabolic Diseases, Level 4, Sandringham Building, Leicester Royal Infirmary, United Kingdom (D.L., P.P., P.G.).
Leicester Diabetes Centre, University of Leicester, Leicester General Hospital, Leicester, United Kingdom (D.L., K.K.).

Alexander Lawson (A)

Department of Clinical Chemistry, Immunology and Toxicology, Heartlands Hospital University Hospitals Birmingham, United Kingdom (A.L.).

Angela Burns (A)

Department of Clinical Biochemistry, Queen Elizabeth University Hospital, Glasgow, United Kingdom (A.B.).

Michel Azizi (M)

Université de Paris, Inserm CIC1418, Paris, France (M.A.).
APHP, Hypertension Unit, Hôpital Européen Georges Pompidou, Paris, France (M.A.).

Michel Burnier (M)

Service of Nephrology and Hypertension, University Hospital, Lausanne, Switzerland (M.B.).

Donald J L Jones (DJL)

Department of Cardiovascular Sciences, University of Leicester, Cardiovascular Research Centre, Glenfield Hospital, Leicester, United Kingdom (D.J.L.J., P.P., P.G.).

Benjamin Kably (B)

Université de Paris, France (B.K.).
APHP, Pharmacology Unit, Hôpital Européen Georges Pompidou, Paris, France (B.K.).

Kamlesh Khunti (K)

Leicester Diabetes Centre, University of Leicester, Leicester General Hospital, Leicester, United Kingdom (D.L., K.K.).

Reinhold Kreutz (R)

Charité - Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Institut für Klinische Pharmakologie und Toxikologie, Germany (R.K.).

Prashanth Patel (P)

The Department of Chemical Pathology and Metabolic Diseases, Level 4, Sandringham Building, Leicester Royal Infirmary, United Kingdom (D.L., P.P., P.G.).
Department of Cardiovascular Sciences, University of Leicester, Cardiovascular Research Centre, Glenfield Hospital, Leicester, United Kingdom (D.J.L.J., P.P., P.G.).

Alexandre Persu (A)

Division of Cardiology, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium/Pole of Cardiovascular Research, Institut de Recherche Expérimentale et Clinique, Université Catholique de Louvain (A.P.).

Wilko Spiering (W)

Department of Vascular Medicine, University Medical Center Utrecht, Utrecht University, the Netherlands (W.S.).

Stefan W Toennes (SW)

Institute of Legal Medicine, Department of Forensic Toxicology, University Hospital, Goethe University, Frankfurt, Germany (S.W.T.).

Maciej Tomaszewski (M)

Division of Cardiovascular Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, University of Manchester, United Kingdom (M.T.).
Manchester Heart Centre, Manchester University National Health Service Foundation Trust, United Kingdom (M.T.).

Bryan Williams (B)

Department of Cardiovascular Sciences, University College London, United Kingdom (B.W.).

Pankaj Gupta (P)

The Department of Chemical Pathology and Metabolic Diseases, Level 4, Sandringham Building, Leicester Royal Infirmary, United Kingdom (D.L., P.P., P.G.).
Department of Cardiovascular Sciences, University of Leicester, Cardiovascular Research Centre, Glenfield Hospital, Leicester, United Kingdom (D.J.L.J., P.P., P.G.).

Indranil Dasgupta (I)

Renal Unit, Heartlands Hospital, Birmingham and Warwick Medical School, University of Warwick, Coventry, United Kingdom (I.D.).

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