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Author Notes:

Correspondence: Anna Grodzinsky, 4401 Wornall Road, SLNI CV Research #5603, Kansas City, MO 64111, Phone: 913-932-5475, Fax: 816-932-5613.

Disclosures: Dr. Kosiborod has received research grants from the American Heart Association, Genentech, Sanofi-Aventis, Gilead, Medtronic Minimed, Glumetrics, Maquet, Eisai and consultant honoraria from Genentech, Gilead, F Hoffmann LaRoche, AstraZeneca, Regeneron, Edwards Lifesciences, Eli Lilly, Amgen, Takeda.

Dr. McGuire has received consultant honoraria from Takeda, Janssen, Merck, Regeneron, Boehringer Ingelheim and clinical trial leadership honoraria from Boehringer Ingelheim, Takeda, Orexigen, Genentech, Roche, AstraZeneca, Bristol Myers Squibb, Eli Lilly, Daiichi Sankyo, Merck, Eisai, Omthera, Lexicon, Novo Nordisk, GlaxoSmithKline, Janssen.

Dr. Spertus owns the copyrights to the Seattle Angina Questionnaire.

He has received research grants from the NHLBI, AHA, ACCF, Gilead, Lilly, EvaHeart, Amorcyte and consultant honoraria from United Healthcare, Genentech, Amgen and SEI Research support from Takeda and consultant honoraria from Boehringer Ingelheim, Bristol Myers Squibb, Merck; DMC member and Novo-Nordisk.

Dr. Bhatt has received research grants from Amgen, Astra Zeneca, Bristol Myers Squibb, Cardax Chiesi, Eisai, and royalties from Elsevier Practice Update, Ischemix, Pfizer, Regado Biosciences, Sanofi Aventis, Slack Publications/Cardiology, WebMD

Dr. Arnold has received advisory board income from Novartis.

The other authors report no conflicts of interest.

Subject:

Research Funding:

The Outcomes of PCI Study (OPS) was supported by an American Heart Association Outcomes Research Center grant (0875149N) and the Personalized Risk Information Services Manager™ (PRISM) study was supported by a grant from the National Heart Lung and Blood Institute (R01-HL096624).

Dr. Grodzinsky is supported by a T32 training grant from the NHLBI (HL110837).

The funding agencies had no role in data collection, analysis, interpretation or the decision to submit the results.

The content is solely the responsibility of the authors and does not necessarily represent the official views of the funding agencies.

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Cardiac & Cardiovascular Systems
  • Cardiovascular System & Cardiology
  • coronary artery disease
  • diabetes mellitus
  • myocardial ischemia
  • percutaneous coronary intervention
  • risk
  • SILENT-MYOCARDIAL-ISCHEMIA
  • QUALITY-OF-LIFE
  • CHRONIC STABLE ANGINA
  • PROSPECTIVE COHORT
  • DISEASE
  • TRIAL
  • QUESTIONNAIRE
  • RANOLAZINE
  • INFARCTION
  • OUTCOMES

Residual Angina After Elective Percutaneous Coronary Intervention in Patients With Diabetes Mellitus

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Journal Title:

Circulation: Cardiovascular Quality and Outcomes

Volume:

Volume 10, Number 9

Publisher:

, Pages e003553-e003553

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Background-Previous studies suggest that among patients with stable coronary artery disease, patients with diabetes mellitus (DM) have less angina and more silent ischemia when compared with those without DM. However, the burden of angina in diabetic versus nondiabetic patients after elective percutaneous coronary intervention (PCI) has not been recently examined. Methods and Results-In a 10-site US PCI registry, we assessed angina before and at 1, 6, and 12 months after elective PCI with the Seattle Angina Questionnaire angina frequency score (range, 0-100, higher=better). We also examined the rates of antianginal medication prescriptions at discharge. A multivariable, repeated-measures Poisson model was used to examine the independent association of DM with angina over the year after treatment. Among 1080 elective PCI patients (mean age, 65 years; 74.7% men), 34.0% had DM. At baseline and at each follow-up, patients with DM had similar angina prevalence and severity as those without DM. Patients with DM were more commonly prescribed calcium channel blockers and long-Acting nitrates at discharge (DM versus not: 27.9% versus 20.9% [P=0.01] and 32.8% versus 25.5% [P=0.01], respectively), whereas β-blockers and ranolazine were prescribed at similar rates. In the multivariable, repeated-measures model, the risk of angina was similar over the year after PCI in patients with versus without DM (relative risk, 1.04; range, 0.80-1.36). Conclusions-Patients with stable coronary artery disease and DM exhibit a burden of angina that is at least as high as those without DM despite more antianginal prescriptions at discharge. These findings contradict the conventional teachings that patients with DM experience less angina because of silent ischemia.

Copyright information:

© 2017 American Heart Association, Inc.

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