Twice-daily versus once-daily lisinopril and losartan for hypertension: Real-world effectiveness and safety.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 27 08 2020
accepted: 19 11 2020
entrez: 3 12 2020
pubmed: 4 12 2020
medline: 26 1 2021
Statut: epublish

Résumé

Lisinopril and losartan manufacturer labels recommend twice-daily dosing (BID) if once-daily (QDay) is insufficient to lower blood pressure (BP). Retrospective cohort study of patients taking QDay lisinopril and losartan who experienced a dose-doubling (index date). A text-processing tool categorized BID and QDay groups at the index date based on administration instructions. We excluded: pregnant/hospice, regimens other than BID/QDay, and without BP measurements -6 months/+12 months of the index date. The most proximal BP measurements -6 months and +2 weeks to 12 months of the index date were used to evaluate BP differences. Propensity scores were generated, and differences in BP and adverse events (angioedema, acute kidney injury, hyperkalemia) between BID/QDay groups were analyzed within dosing cohorts using inverse propensity of treatment-weighted regression models. Of 11,210 and 6,051 patients who met all criteria for lisinopril and losartan, 784 (7.0%) and 453 (7.5%) were taking BID, respectively. BID patients were older and had higher comorbidity and medication burdens. There were no differences in systolic/diastolic BP between BID and QDay, with absolute differences in mean systolic BP ranging from -1.8 to 0.7 mmHg and diastolic BP ranging from -1.1 to 0.1 mmHg (all 95% confidence intervals [CI] cross 0). Lisinopril 10mg BID was associated with an increased odds of angioedema compared to lisinopril 20mg QDay (odds ratio 2.27, 95%CI 1.13-4.58). Adjusted models do not support improved effectiveness or safety of BID lisinopril and losartan.

Sections du résumé

BACKGROUND
Lisinopril and losartan manufacturer labels recommend twice-daily dosing (BID) if once-daily (QDay) is insufficient to lower blood pressure (BP).
METHODS AND RESULTS
Retrospective cohort study of patients taking QDay lisinopril and losartan who experienced a dose-doubling (index date). A text-processing tool categorized BID and QDay groups at the index date based on administration instructions. We excluded: pregnant/hospice, regimens other than BID/QDay, and without BP measurements -6 months/+12 months of the index date. The most proximal BP measurements -6 months and +2 weeks to 12 months of the index date were used to evaluate BP differences. Propensity scores were generated, and differences in BP and adverse events (angioedema, acute kidney injury, hyperkalemia) between BID/QDay groups were analyzed within dosing cohorts using inverse propensity of treatment-weighted regression models. Of 11,210 and 6,051 patients who met all criteria for lisinopril and losartan, 784 (7.0%) and 453 (7.5%) were taking BID, respectively. BID patients were older and had higher comorbidity and medication burdens. There were no differences in systolic/diastolic BP between BID and QDay, with absolute differences in mean systolic BP ranging from -1.8 to 0.7 mmHg and diastolic BP ranging from -1.1 to 0.1 mmHg (all 95% confidence intervals [CI] cross 0). Lisinopril 10mg BID was associated with an increased odds of angioedema compared to lisinopril 20mg QDay (odds ratio 2.27, 95%CI 1.13-4.58).
CONCLUSIONS
Adjusted models do not support improved effectiveness or safety of BID lisinopril and losartan.

Identifiants

pubmed: 33270787
doi: 10.1371/journal.pone.0243371
pii: PONE-D-20-26973
pmc: PMC7714357
doi:

Substances chimiques

Antihypertensive Agents 0
Lisinopril E7199S1YWR
Losartan JMS50MPO89

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0243371

Subventions

Organisme : American Heart Association-American Stroke Association
ID : 19POST34380226
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002535
Pays : United States

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Catherine G Derington (CG)

Department of Population Health Sciences, School of Medicine, University of Utah, Salt Lake City, UT, United States of America.

Jordan B King (JB)

Department of Population Health Sciences, School of Medicine, University of Utah, Salt Lake City, UT, United States of America.
Institute for Health Research, Kaiser Permanente Colorado, Aurora, CO, United States of America.

Thomas Delate (T)

University of Colorado Skaggs School of Pharmacy and Pharmaceutical Sciences, Aurora, CO, United States of America.
Drug Use Management, Kaiser Permanente National Pharmacy, Aurora, CO, United States of America.

Sheila R Botts (SR)

Department of Pharmacy, Kaiser Permanente Colorado, Aurora, CO, United States of America.

Miranda Kroehl (M)

Colorado School of Public Health, Aurora, CO, United States of America.

David P Kao (DP)

Cardiac and Vascular Center, University of Colorado Health, Aurora, CO, United States of America.
School of Medicine, University of Colorado, Aurora, CO, United States of America.

Katy E Trinkley (KE)

University of Colorado Skaggs School of Pharmacy and Pharmaceutical Sciences, Aurora, CO, United States of America.
School of Medicine, University of Colorado, Aurora, CO, United States of America.

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