Reinitiation and Subsequent Discontinuation of Angiotensin-Converting Enzyme Inhibitors and Angiotensin Receptor Blockers among New and Prevalent Users Aged 65 Years or More with Peripheral Arterial Disease.
antiplatelet agents
ischemic stroke
myocardial infarction
new user
non-persistence
peripheral arterial disease
reinitiation
statins
Journal
Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304
Informations de publication
Date de publication:
26 Jan 2023
26 Jan 2023
Historique:
received:
18
12
2022
revised:
11
01
2023
accepted:
23
01
2023
entrez:
25
2
2023
pubmed:
26
2
2023
medline:
26
2
2023
Statut:
epublish
Résumé
Angiotensin-converting enzyme inhibitors (ACEIs) or angiotensin-receptor blockers (ARBs) are recommended in the treatment of arterial hypertension in patients with peripheral arterial disease (PAD). The aims of our study were: (a) to analyse the extent of reinitiation and subsequent discontinuation in older hypertensive PAD patients non-persistent with ACEIs/ARBs; (b) to determine patient and medication factors associated with reinitiation and subsequent discontinuation; and (c) to compare these factors between prevalent and new users. The analysis of reinitiation was performed on a sample of 1642 non-persistent patients aged ≥65 years with PAD newly diagnosed in 2012. Patients reinitiating ACEIs/ARBs were used for the analysis of subsequent discontinuation identified according to the treatment gap period of at least 6 months without any prescription of ACEI/ARB. In the group of non-persistent patients, 875 (53.3%) patients reinitiated ACEIs/ARBs during a follow-up (24.8 months on average). Within this group, subsequent discontinuation was identified in 414 (47.3%) patients. Being a new user was associated with subsequent discontinuation, but not with reinitiation. Myocardial infarction during non-persistence and after reinitiation was associated with reinitiation and lower likelihood of subsequent discontinuation, respectively. Being a prevalent or a new user is associated with the use of medication also after initial discontinuation.
Identifiants
pubmed: 36830904
pii: biomedicines11020368
doi: 10.3390/biomedicines11020368
pmc: PMC9953445
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : Scientific Grant Agency of the Ministry of Education, Science, Research and Sport of the Slovak Republic
ID : VEGA 1/0024/21
Références
Annu Rev Pharmacol Toxicol. 2012;52:275-301
pubmed: 21942628
Circulation. 2017 Mar 21;135(12):e726-e779
pubmed: 27840333
Lancet Glob Health. 2019 Aug;7(8):e1020-e1030
pubmed: 31303293
Biomedicines. 2022 Jun 22;10(7):
pubmed: 35884784
Lancet. 2013 Oct 19;382(9901):1329-40
pubmed: 23915883
J Am Board Fam Med. 2007 Jan-Feb;20(1):72-80
pubmed: 17204738
Vasc Health Risk Manag. 2007;3(2):229-34
pubmed: 17580733
PLoS One. 2019 Nov 15;14(11):e0225390
pubmed: 31730627
Ann Intern Med. 2018 Jul 3;169(1):30-35
pubmed: 29946690
J Hypertens. 2018 Oct;36(10):1953-2041
pubmed: 30234752
Br J Clin Pharmacol. 2018 Oct;84(10):2365-2372
pubmed: 29943849
J Manag Care Pharm. 2003 Sep-Oct;9(5):424-9
pubmed: 14613440
Eur Heart J. 2018 Mar 1;39(9):763-816
pubmed: 28886620
Eur Heart J. 2018 Jan 7;39(2):119-177
pubmed: 28886621
Pharmacoepidemiol Drug Saf. 2019 Jun;28(6):788-795
pubmed: 30784140
Br J Clin Pharmacol. 2012 May;73(5):691-705
pubmed: 22486599
Am Fam Physician. 2019 Mar 15;99(6):362-369
pubmed: 30874413
BMJ. 2016 Jun 28;353:i3305
pubmed: 27353261
J Hypertens. 2007 Mar;25(3):689-97
pubmed: 17278986
Arterioscler Thromb Vasc Biol. 2020 Mar;40(3):541-553
pubmed: 31996023