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. 2014 May 8:348:g2866.
doi: 10.1136/bmj.g2866.

Influence of healthy candidate bias in assessing clinical effectiveness for implantable cardioverter-defibrillators: cohort study of older patients with heart failure

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Influence of healthy candidate bias in assessing clinical effectiveness for implantable cardioverter-defibrillators: cohort study of older patients with heart failure

Soko Setoguchi et al. BMJ. .

Abstract

Objective: To assess the potential contribution of unmeasured general health status to patient selection in assessments of the clinical effectiveness of implantable cardioverter-defibrillator (ICD) therapy.

Design: Retrospective cohort study.

Setting: Linked data from an ICD registry, heart failure registry, and Medicare claims data for ICDs implanted in 2005 through 2009.

Participants: 29,426 patients admitted to hospital with heart failure aged 66 years or older and eligible for ICD therapy for primary prevention.

Main outcome measures: Non-traumatic hip fracture, admission to a skilled nursing facility, and 30 day mortality-outcomes unlikely to be improved by ICD therapy.

Results: Compared with 17,853 patients without ICD therapy, 11,573 patients with ICD therapy were younger and had lower ejection fraction and more cardiac admissions to hospital but fewer non-cardiac admissions to hospital and comorbid conditions. Patients with ICD therapy had greater freedom from unrelated events after adjusting for age and sex: hip fracture (hazard ratio 0.77, 95% confidence interval 0.64 to 0.92), skilled nursing facility admission (0.53, 0.50 to 0.55), and 30 day mortality (0.12, 0.10 to 0.15).

Conclusions: Lower risks of measured outcomes likely reflect unmeasured differences in comorbidity and frailty. The findings highlight potential pitfalls of observational comparative effectiveness research and support physician consideration of general health status in selecting patients for ICD therapy.

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Conflict of interest statement

Competing interests: All authors have completed the ICMJE uniform disclosure form at www.icmje.org/coi_disclosure.pdf (available on request from the corresponding author). SS reported receiving grants from Agency for Healthcare Research and Quality and from the Center for Medicare and Medicaid Services during the conduct of the study. She has made available online a detailed listing of financial disclosures (www.dcri.duke.edu/about-us/conflict-of-interest/). DLB reported receiving grants from Amarin, AstraZeneca, Bristol-Myers Squibb, Eisai, Ethicon, Medtronic, Roche, Sanofi Aventis, and The Medicines Company; conducting unfunded research for FlowCo, PLx Pharma, and Takeda; receiving personal fees from the Duke Clinical Research Institute, the Mayo Clinic, the Population Health Research Institute, the American College of Cardiology, Belvoir Publications, Slack Publications, WebMD, and Elsevier Practice Update Cardiology; serving on advisory boards for Elsevier Practice Update Cardiology, Medscape Cardiology, and Regado Biosciences; serving on the board of directors of the Boston VA Research Institute and the Society of Cardiovascular Patient Care; receiving non-financial support from the Society of Cardiovascular Patient Care and the American Heart Association; and serving as editor for the Journal of Invasive Cardiology, outside of the submitted work. AEE reported receiving honorariums from Biotronik, Boston Scientific, Medtronic, and St Jude Medical; receiving research funding from Biotronik, Boston Scientific, Medtronic, and St Jude Medical; and receiving fellowship program support from Biotronik, Boston Scientific, Medtronic, and St Jude Medical.

Figures

None
Fig 1 Conceptual relation of data sources and schematic presentation of cohort 1 (implantable converter-defibrillator (ICD)+heart failure registry population) and cohort 2 (heart failure registry population). Cohort 1 consists of patients receiving ICD therapy from overlapping area between ICD registry and Medicare data (area A+B) and patients not receiving ICD therapy from overlapping area between heart failure registry and Medicare data but no overlap with ICD registry (area C). Cohort 2 consists of patients receiving ICD therapy from overlapping area between the heart failure registry, ICD registry, and Medicare data (area B) and patients not receiving ICD therapy from area C
None
Fig 2 Crude survival curves of patients receiving and not receiving implantable converter-defibrillator (ICD) therapy in cohort 1 for admissions for non-traumatic hip fracture, admissions to a skilled nursing home, and 30 day all cause mortality

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