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

Author:

Devine Joshua W.1ORCID,Tadrous Mina23ORCID,Hernandez Inmaculada4ORCID,Callaway Kim Katherine56ORCID,Rothenberger Scott D.5,Mukhopadhyay Nandita7ORCID,Gellad Walid F.58,Suda Katie J.58ORCID

Affiliation:

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

2. Leslie Dan Faculty of Pharmacy University of Toronto Ontario Canada

3. Institute for Health System Solutions and Virtual Care Women’s College Hospital Toronto Ontario Canada

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

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

6. Department of Health Policy and Management University of Pittsburgh School of Public Health Pittsburgh PA USA

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

8. Center for Health Equity Research and Promotion VA Pittsburgh Healthcare System Pittsburgh PA USA

Abstract

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 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 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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

Reference39 articles.

1. 2017 ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ASPC/NMA/PCNA Guideline for the Prevention, Detection, Evaluation, and Management of High Blood Pressure in Adults: Executive Summary: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines

2. 2020 International Society of Hypertension Global Hypertension Practice Guidelines

3. FDA updates and press announcements on angiotensin II receptor blocker (ARB) recalls (valsartan losartan and irbesartan). US Food and Drug Administration. July 13 2018. Updated November 13 2019. Accessed July 2 2023. https://www.fda.gov/drugs/drug‐safety‐and‐availability/fda‐updates‐and‐press‐announcements‐angiotensin‐ii‐receptor‐blocker‐arb‐recalls‐valsartan‐losartan

4. Hypertension Hot Potato — Anatomy of the Angiotensin-Receptor Blocker Recalls

5. Reflections of the Angiotensin Receptor Blocker Recall by the FDA and Repercussions on Healthcare

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