Evidence map›Paper›PMID 33206191›Full record

ArticleJAMA network open2020

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, Jordan B King, Suzanne Oparil, Jackson T Wright, Gbenga Ogedegbe, April Mohanty, Shakia T Hardy, Lei Huang, Rachel Hess, Paul Muntner and 1 more

Open access · goldAbstract read
In one paragraph

Article in JAMA network open, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 19 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 1 country.

Calvin L ColvinDepartment of Epidemiology, University of Alabama at Birmingham, Birmingham.
Jordan B KingDepartment of Population Health Sciences, University of Utah School of Medicine, Salt Lake City.
Suzanne OparilDivision of Cardiovascular, Disease, Department of Medicine, University of Alabama at Birmingham, Birmingham.
Jackson T WrightDivision of Nephrology and Hypertension, Case Western Reserve University, University Hospitals Cleveland Medical Center, Cleveland, Ohio.
Gbenga OgedegbeNew York University Grossman School of Medicine, New York.
April MohantyIDEAS Center of Innovation, Veterans Affairs Salt Lake City Health Care System, Salt Lake City, Utah.
Shakia T HardyDepartment of Epidemiology, University of Alabama at Birmingham, Birmingham.
Lei HuangDepartment of Epidemiology, University of Alabama at Birmingham, Birmingham.
Rachel HessDepartment of Population Health Sciences, University of Utah School of Medicine, Salt Lake City.
Paul MuntnerDepartment of Epidemiology, University of Alabama at Birmingham, Birmingham.
Adam BressDepartment of Population Health Sciences, University of Utah School of Medicine, Salt Lake City.
University of Alabama at Birmingham · USUniversity of Utah · USCase Western Reserve University · USKaiser Permanente · USNew York University · US

Funding

Utah Center for Clinical and Translational ScienceUL1TR002538 · NCATS · UNIVERSITY OF UTAH · PI HESS, RACHEL, MAJERSIK, JENNIFER JUHL · 2018 to 2022
$26.0M
Evaluating novel approaches for estimating awake and sleep blood pressureR01HL139716 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LEVITAN, EMILY B, SHIMBO, DAICHI · 2018 to 2021
$3.4M
Genetic ancestry and antihypertensive medication responses in African AmericansK01HL133468 · NHLBI · UNIVERSITY OF UTAH · PI BRESS, ADAM P · 2016 to 2020
$787k
NCATS NIH HHS UL1 TR002538NHLBI NIH HHS K01 HL133468NHLBI NIH HHS R01 HL139716
6 · The paper itself

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.

Indexed as

Practice Guidelines as TopicAdrenergic beta-AntagonistsAgedAged, 80 and overAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsAntihypertensive AgentsBlack or African AmericanCalcium Channel BlockersEthnicityFemaleGuideline AdherenceHumansHypertensionMaleMedicareAdrenergic beta-AntagonistsAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsAntihypertensive AgentsCalcium Channel BlockersSodium Chloride Symporter Inhibitors

Identifiers

PMID33206191
PMCPMC7675104
OpenAlexW3101869035

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.