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Improvement of non-adherence and reduction of BP values in patients with difficult-to-treat hypertension: the ATHAN clinical trial.
Oliveras, Anna; Vázquez, Susana; Vega, María Victoria; Camps, Carme; Illana, Francisco J; Armario, Pedro; Crespo, Marta; de la Sierra, Alejandro.
Afiliação
  • Oliveras A; Hypertension Unit, Nephrology Dpt, Hospital del Mar, Barcelona, Spain. aoliveras@hospitaldelmar.cat.
  • Vázquez S; IMIM (Hospital del Mar Medical Research Institute), Universitat Pompeu Fabra, Barcelona, Spain. aoliveras@hospitaldelmar.cat.
  • Vega MV; Hypertension Unit, Nephrology Dpt, Hospital del Mar, Barcelona, Spain.
  • Camps C; IMIM (Hospital del Mar Medical Research Institute), Universitat Pompeu Fabra, Barcelona, Spain.
  • Illana FJ; Laboratori de Referència de Catalunya, Barcelona, Spain.
  • Armario P; Hypertension Unit, Nephrology Dpt, Hospital del Mar, Barcelona, Spain.
  • Crespo M; Biochemistry Department, Hospital de la Santa Creu i Sant Pau, IIB Sant Pau, Barcelona, Spain.
  • de la Sierra A; Cardiovascular Risk Area, Complex Hospitalari Universitari Moisès Broggi, University of Barcelona, Barcelona, Spain.
Hypertens Res ; 47(10): 2864-2873, 2024 Oct.
Article em En | MEDLINE | ID: mdl-39085464
ABSTRACT
Hypertension treatment and blood pressure (BP) control reduce cardiovascular disease burden. However, prevalence of controlled BP is overall insufficient and lack of adherence to treatment is a suggested major contributor. This prospective, randomized clinical trial was designed to evaluate whether a specific 3-month (m) action plan to improve therapeutic adherence results in a decrease in BP. Patients with ambulatory 24 h-BP ≥ 130/80 mmHg despite receiving ≥2 antihypertensive drugs and with therapeutic non-compliance confirmed by antihypertensive drugs analyzed in urine were randomized (11) to receive a specific 3 m program to improve adherence (INT = intervention) or routine follow-up (C = control). Antihypertensive treatment was not modified and knowledge of non-adherence was only notified to patients randomized to the intervention group. Before randomization and at 3 m all patients underwent urinary screening for antihypertensive drugs and 24 h-ambulatory-BP monitoring. Forty-five patients (36% women, mean age 58 ± 13 yr) were randomized. At 3 m, mean (95% CI) BP differences (INT vs. C) were 12.2 mmHg (4.3-20.8), adjusted-p = 0.032 and 8.7 mmHg (2.5-14.8), adjusted-p = 0.018 for 24 h-systolic and 24 h-diastolic BP, respectively. Differences (INT vs. C) for office SBP and DBP were 18.4 mmHg (6.8-30.1), adjusted-p = 0.005 and 15.7 mmHg (7.2-24.2), adjusted-p < 0.001. Non-detected antihypertensive drugs were median [IQR] 40% [25-100] and 0% [0-20] at baseline and 3 m, respectively, in the INT group, and 33.3% [25-63.7] and 33.3% [23.8-57.9], in the C group (p < 0.001 for the 3-month between-group comparison). A combined action plan of notifying knowledge of non-adherence plus a 3-month specific nursing intervention to improve therapeutic adherence results in BP reduction in patients with inadequate therapeutic compliance.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pressão Sanguínea / Monitorização Ambulatorial da Pressão Arterial / Adesão à Medicação / Hipertensão / Anti-Hipertensivos Idioma: En Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Espanha

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pressão Sanguínea / Monitorização Ambulatorial da Pressão Arterial / Adesão à Medicação / Hipertensão / Anti-Hipertensivos Idioma: En Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Espanha