A Retrospective Cohort Study of the 2018 Angiotensin Receptor Blocker Recalls and Subsequent Drug Shortages in Patients With Hypertension.

drug recall drug shortages hypertension valsartan

Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
29 Dec 2023
Historique:
medline: 29 12 2023
pubmed: 29 12 2023
entrez: 29 12 2023
Statut: aheadofprint

Résumé

Valsartan was recalled by the US Food and Drug Administration in July 2018 for carcinogenic impurities, resulting in a drug shortage and management challenges for valsartan users. The influence of the valsartan recall on clinical outcomes is unknown. We compared the risk of adverse events between hypertensive patients using valsartan and a propensity score-matched group using nonrecalled angiotensin receptor blockers and angiotensin-converting enzyme inhibitors. We used Optum's deidentified Clinformatics Datamart (July 2017-January 2019). Hypertensive patients who received valsartan or nonrecalled angiotensin receptor blockers/angiotensin-converting enzyme inhibitors for 1 year before and on the recall date were compared. Primary outcomes were measured in the 6 months following the recall and included: (1) a composite measure of all-cause hospitalization, all-cause emergency department visit, and all-cause urgent care visit, and (2) a composite cardiac event measure of hospitalizations for acute myocardial infarction and hospitalizations/emergency department visits/urgent care visits for stroke/transient ischemic attack, heart failure, or hypertension. We compared the risk of outcomes between treatment groups using Cox proportional hazard models. Of the hypertensive patients, 76 934 received valsartan, and 509 472 received a nonrecalled angiotensin receptor blocker/angiotensin-converting enzyme inhibitor. Valsartan use at the time of recall was associated with a higher risk of all-cause hospitalization, emergency department use, or urgent care use (hazard ratio [HR], 1.02 [95% CI, 1.00-1.04]) and the composite of cardiac events (HR, 1.22 [95% CI, 1.15-1.29]) within 6 months after the recall. The valsartan recall and shortage affected hypertensive patients. Local- and national-level systems need to be enhanced to protect patients from drug shortages by providing safe and reliable medication alternatives.

Sections du résumé

BACKGROUND BACKGROUND
Valsartan was recalled by the US Food and Drug Administration in July 2018 for carcinogenic impurities, resulting in a drug shortage and management challenges for valsartan users. The influence of the valsartan recall on clinical outcomes is unknown. We compared the risk of adverse events between hypertensive patients using valsartan and a propensity score-matched group using nonrecalled angiotensin receptor blockers and angiotensin-converting enzyme inhibitors.
METHODS AND RESULTS RESULTS
We used Optum's deidentified Clinformatics Datamart (July 2017-January 2019). Hypertensive patients who received valsartan or nonrecalled angiotensin receptor blockers/angiotensin-converting enzyme inhibitors for 1 year before and on the recall date were compared. Primary outcomes were measured in the 6 months following the recall and included: (1) a composite measure of all-cause hospitalization, all-cause emergency department visit, and all-cause urgent care visit, and (2) a composite cardiac event measure of hospitalizations for acute myocardial infarction and hospitalizations/emergency department visits/urgent care visits for stroke/transient ischemic attack, heart failure, or hypertension. We compared the risk of outcomes between treatment groups using Cox proportional hazard models. Of the hypertensive patients, 76 934 received valsartan, and 509 472 received a nonrecalled angiotensin receptor blocker/angiotensin-converting enzyme inhibitor. Valsartan use at the time of recall was associated with a higher risk of all-cause hospitalization, emergency department use, or urgent care use (hazard ratio [HR], 1.02 [95% CI, 1.00-1.04]) and the composite of cardiac events (HR, 1.22 [95% CI, 1.15-1.29]) within 6 months after the recall.
CONCLUSIONS CONCLUSIONS
The valsartan recall and shortage affected hypertensive patients. Local- and national-level systems need to be enhanced to protect patients from drug shortages by providing safe and reliable medication alternatives.

Identifiants

pubmed: 38156554
doi: 10.1161/JAHA.123.032266
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e032266

Auteurs

Joshua W Devine (JW)

Des Moines University Department of Public Health Des Moines IA USA.

Mina Tadrous (M)

Leslie Dan Faculty of Pharmacy University of Toronto Ontario Canada.
Institute for Health System Solutions and Virtual Care Women's College Hospital Toronto Ontario Canada.

Inmaculada Hernandez (I)

University of California San Diego School of Pharmacy and Pharmaceutical Sciences La Jolla CA USA.

Katherine Callaway Kim (K)

Division of General Internal Medicine, Department of Medicine University of Pittsburgh School of Medicine Pittsburgh PA USA.
Department of Health Policy and Management University of Pittsburgh School of Public Health Pittsburgh PA USA.

Scott D Rothenberger (SD)

Division of General Internal Medicine, Department of Medicine University of Pittsburgh School of Medicine Pittsburgh PA USA.

Nandita Mukhopadhyay (N)

University of Pittsburgh School of Dental Medicine Department of Oral and Craniofacial Sciences, Center for Craniofacial and Dental Genetics Pittsburgh PA USA.

Walid F Gellad (WF)

Division of General Internal Medicine, Department of Medicine University of Pittsburgh School of Medicine Pittsburgh PA USA.
Center for Health Equity Research and Promotion VA Pittsburgh Healthcare System Pittsburgh PA USA.

Katie J Suda (KJ)

Division of General Internal Medicine, Department of Medicine University of Pittsburgh School of Medicine Pittsburgh PA USA.
Center for Health Equity Research and Promotion VA Pittsburgh Healthcare System Pittsburgh PA USA.

Classifications MeSH