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. 2020 Nov 2;3(11):e2025127.
doi: 10.1001/jamanetworkopen.2020.25127.

Association of Race/Ethnicity-Specific Changes in Antihypertensive Medication Classes Initiated Among Medicare Beneficiaries With the Eighth Joint National Committee Panel Member Report

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Association of Race/Ethnicity-Specific Changes in Antihypertensive Medication Classes Initiated Among Medicare Beneficiaries With the Eighth Joint National Committee Panel Member Report

Calvin L Colvin et al. JAMA Netw Open. .

Abstract

Importance: In December 2013, the panel members appointed to the Eighth Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC8) published a recommendation that non-Black adults initiate antihypertensive medication with a thiazide-type diuretic, calcium channel blocker, angiotensin-converting enzyme inhibitor (ACEI), or angiotensin receptor blocker (ARB), whereas Black adults initiate treatment with a thiazide-type diuretic or calcium channel blocker. β-Blockers were not recommended as first-line therapy.

Objective: To assess changes in antihypertensive medication classes initiated by race/ethnicity from before to after publication of the JNC8 panel member report.

Design, setting, and participants: This serial cross-sectional analysis assessed a 5% sample of Medicare beneficiaries aged 66 years or older who initiated antihypertensive medication between 2011 and 2018, were Black (n = 3303 [8.0%]), White (n = 34 943 [84.5%]), or of other (n = 3094 [7.5%]) race/ethnicity, and did not have compelling indications for specific antihypertensive medication classes.

Exposures: Calendar year and period after vs before publication of the JNC8 panel member report.

Main outcomes and measures: The proportion of beneficiaries initiating ACEIs or ARBs and, separately, β-blockers vs other antihypertensive medication classes.

Results: In total, 41 340 Medicare beneficiaries (65% women; mean [SD] age, 75.7 [7.6] years) of Black, White, or other races/ethnicities initiated antihypertensive medication and met the inclusion criteria for the present study. In 2011, 25.2% of Black beneficiaries initiating antihypertensive monotherapy did so with an ACEI or ARB compared with 23.7% in 2018 (P = .47 for trend). Among beneficiaries initiating monotherapy, the proportion filling a β-blocker was 20.1% in 2011 and 15.4% in 2018 for White beneficiaries (P < .001 for trend), 14.2% in 2011 and 11.1% in 2018 for Black beneficiaries (P = .08 for trend), and 11.3% in 2011 and 15.0% in 2018 for beneficiaries of other race/ethnicity (P = .40 for trend). After multivariable adjustment and among beneficiaries initiating monotherapy, there was no evidence of a change in the proportion filling an ACEI or ARB before to after publication of the JNC8 panel member report overall (prevalence ratio, 1.00; 95% CI, 0.97-1.03) or in Black vs White beneficiaries (prevalence ratio, 0.96; 95% CI, 0.83-1.12; P = .60 for interaction). Among beneficiaries initiating monotherapy, the proportion filling a β-blocker decreased from before to after publication of the JNC8 panel member report (prevalence ratio, 0.89; 95% CI, 0.84-0.93) with no differences across race/ethnicity groups (P > .10 for interaction).

Conclusions and relevance: A substantial proportion of older US adults who initiate antihypertensive medication do so with non-guideline-recommended classes of medication.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr King reported receiving research funding to his institution from Novartis and Amgen unrelated to the current project; and receiving consulting fees from MedStar Health on a project funded by Amarin unrelated to the current project. Dr Oparil reported receiving personal fees from 98point6 Inc; receiving personal fees and serving as a member of the scientific advisory board for CinCor Pharma Inc; receiving grants and personal fees from ROX Medical Inc; receiving grants from Bayer and Idorsia Pharmaceuticals Ltd; receiving personal fees, receiving nonfinancial support, and serving as Chief Medical Officer for Preventric Diagnostics outside the submitted work; being Editor-in-Chief and receiving an annual stipend from Current Hypertension Reports; and serving as co-chair for the Eighth Joint National Committee, “2014 Evidence-Based Guideline for the Management of High Blood Pressure in Adults: Report From the Panel Members Appointed to the Eighth Joint National Committee.” Dr Wright reported receiving funding from the National Institutes of Health and the Ohio department of Medicaid. Dr Hess reported serving on a Data and Safety Monitoring Board for Astellas Pharmaceutical related to a product being tested for vasomotor symptoms. Dr Muntner reported receiving a research grant and consulting funds from Amgen unrelated to the current work. Dr Bress reported receiving research funding to his institution from Amgen and from Amarin Corporation unrelated to the current manuscript. No other disclosures were reported.

Figures

Figure 1.
Figure 1.. Proportion of Medicare Beneficiaries of Black, White, and Other Races/Ethnicities Initiating Monotherapy With an Angiotensin-Converting Enzyme Inhibitor (ACEI) or Angiotensin Receptor Blocker (ARB), β-Blocker, Thiazide-Type Diuretic, or Calcium Channel Blocker, by Calendar Year
Figure 2.
Figure 2.. Proportion of Medicare Beneficiaries of Black, White, and Other Races/Ethnicities Initiating Combination Therapy With an Angiotensin-Converting-Enzyme Inhibitor (ACEI) or Angiotensin Receptor Blocker (ARB), β-Blocker, Thiazide-Type Diuretic, or Calcium Channel Blocker, by Calendar Year

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References

    1. James PA, Oparil S, Carter BL, et al. . 2014 Evidence-based guideline for the management of high blood pressure in adults: report from the panel members appointed to the Eighth Joint National Committee (JNC 8). JAMA. 2014;311(5):507-520. doi:10.1001/jama.2013.284427 - DOI - PubMed
    1. Chobanian AV, Bakris GL, Black HR, et al. ; National Heart, Lung, and Blood Institute Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure; National High Blood Pressure Education Program Coordinating Committee . The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure: the JNC 7 report. JAMA. 2003;289(19):2560-2572. doi:10.1001/jama.289.19.2560 - DOI - PubMed
    1. Officers A; ALLHAT Officers and Coordinators for the ALLHAT Collaborative Research Group. The Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial . Major outcomes in high-risk hypertensive patients randomized to angiotensin-converting enzyme inhibitor or calcium channel blocker vs diuretic: the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT). JAMA. 2002;288(23):2981-2997. doi:10.1001/jama.288.23.2981 - DOI - PubMed
    1. Leenen FHH, Nwachuku CE, Black HR, et al. ; Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial Collaborative Research Group . Clinical events in high-risk hypertensive patients randomly assigned to calcium channel blocker versus angiotensin-converting enzyme inhibitor in the antihypertensive and lipid-lowering treatment to prevent heart attack trial. Hypertension. 2006;48(3):374-384. doi:10.1161/01.HYP.0000231662.77359.de - DOI - PubMed
    1. Dahlöf B, Devereux RB, Kjeldsen SE, et al. ; LIFE Study Group . Cardiovascular morbidity and mortality in the Losartan Intervention for Endpoint Reduction in Hypertension Study (LIFE): a randomised trial against atenolol. Lancet. 2002;359(9311):995-1003. doi:10.1016/S0140-6736(02)08089-3 - DOI - PubMed

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