Evidence map›Paper›PMID 31729588›Full record

ArticleCardiovascular drugs and therapy2019

Trends for and Clinical Factors Associated with Choice of Oral P2Y

Nishank Jain, Suzanne L Hunt, Huizhong Cui, Milind A Phadnis, Jonathan D Mahnken, Theresa I Shireman, Junqiang Dai, Jawahar L Mehta, Rafia S Rasu

Open access · hybridAbstract read
In one paragraph

Article in Cardiovascular drugs and therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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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

9 authors at 5 institutions in 1 country.

Nishank JainDepartment of Internal Medicine, University of Arkansas for Medical Sciences, 4301 W. Markham St, Slot 501, Little Rock, AR, 72205, USA. NJain2@uams.edu.
Suzanne L HuntDepartment of Biostatistics, University of Kansas School of Medicine, Kansas City, KS, USA.
Huizhong CuiDepartment of Biostatistics, University of Kansas School of Medicine, Kansas City, KS, USA.
Milind A PhadnisDepartment of Biostatistics, University of Kansas School of Medicine, Kansas City, KS, USA.
Jonathan D MahnkenDepartment of Biostatistics, University of Kansas School of Medicine, Kansas City, KS, USA.
Theresa I ShiremanDepartment of Health Services, Policy and Practice, School of Public Health, Brown University, Providence, RI, USA.
Junqiang DaiDepartment of Biostatistics, University of Kansas School of Medicine, Kansas City, KS, USA.
Jawahar L MehtaDepartment of Internal Medicine, University of Arkansas for Medical Sciences, 4301 W. Markham St, Slot 501, Little Rock, AR, 72205, USA.
Rafia S RasuDepartment of Pharmacy Practice, School of Pharmacy, University of North Texas, Fort Worth, TX, USA.
University of Kansas · USBrown University · USCentral Arkansas Veterans Healthcare System · USUniversity of Arkansas for Medical Sciences · USUniversity of North Texas Health Science Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTrends and clinical factors associated with prescribing choices for oral P2Y12 inhibitors (P2Y12-I) remain unknown for patients on chronic dialysis, i.e., with end-stage renal disease (ESRD).

methodsFrom 2011-2014 U.S. Renal Data System registry, we identified 36,542 ESRD patients who received new prescriptions for P2Y12-I (median age 64.0 years and 54% males). Of the cohort, 93% were receiving hemodialysis and 7% on peritoneal dialysis. We analyzed trends and investigated clinical factors associated with specific P2Y12-I prescribed.

resultsClopidogrel was prescribed for 95%, prasugrel for 3%, and ticagrelor for 2%. Clopidogrel was favored for those ≥75 years (18% of cohort). Compared to Caucasians, African Americans (36% of cohort) and Hispanics (19% of cohort) were less likely to receive prasugrel and ticagrelor (P<0.05). Patients receiving hemodialysis versus peritoneal dialysis were less likely to receive prasugrel over clopidogrel, adjusted odds ratio (aOR) 0.67 (0.55-0.82). Each additional year of dialysis decreased the odds of receiving prasugrel over clopidogrel, aOR 0.91 (0.85-0.98). History of atrial fibrillation reduced the odds of receiving ticagrelor or prasugrel over clopidogrel, aOR 0.69 (0.54-0.89) and 0.73 (0.60-0.89), respectively. Concomitant oral anticoagulant use was not associated with choice of P2Y12-I. Occurrence of non-ST segment elevation myocardial infarction or percutaneous coronary intervention within the 6-month period prior to the index date favored ticagrelor over prasugrel, aOR 1.31 (1.06-1.62) and 1.29 (1.01-1.66), respectively. However, prescribing trends favoring ticagrelor over prasugrel were not observed for deployment of drug-eluting, or multiple coronary stents.

conclusionBetween 2011 and 2014, clopidogrel remained the most common P2Y12-I whereas ticagrelor and prasugrel remained underutilized in ESRD patients. Prescribing practices for these drugs were based upon clinically approved indication for their use in the general population as well as perceived complexity of an ESRD patient including demographics, dialysis-related factors and comorbidities. Comparative effectiveness studies involving ESRD patients are needed to prove that ticagrelor and prasugrel are just as safe and effective as clopidogrel before clinicians can make informed decisions for choice of P2Y12-I in this patient population.

Indexed as

Renal DialysisAdministration, OralAdolescentAdultAgedCardiovascular DiseasesClinical Decision-MakingClopidogrelDrug PrescriptionsDrug UtilizationFemaleHumansKidney Failure, ChronicMaleMiddle AgedPatient SelectionClopidogrelPlatelet Aggregation InhibitorsPrasugrel HydrochloridePurinergic P2Y Receptor AntagonistsTicagrelorcardiovascular,chronic dialysis,clopidogrel,oral P2Y12 inhibitors,prasugrelticagrelor

Identifiers

PMID31729588
PMCPMC6904390
OpenAlexW2983333735

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.