Effect estimate: OR 1.73 (95% CI 1.07-2.79)
p-value: p=0.02
Novel device therapies targeting cardiac remodeling may offer next steps for heart failure patients who remain symptomatic despite guideline-directed medical therapy.
May support device evaluation in symptomatic HF on GDMT; leaves open confirmation in prospective trials.
Heart failure (HF) is clinical syndrome that develops and progresses as a result of the overexpression of biologically active molecules that are sufficient to cause deleterious effects on the heart and circulation. Over the past 2 decades the adherence to practice guidelines for treating HF, including the use of angiotensin-converting enzyme inhibitors/angiotensin-receptor antagonists and beta-blockers, has resulted in improved survival for patients. However, despite the use of these evidence-based strategies that block the deleterious effects of neurohormonal activation, the overall mortality for HF remains unacceptably high. Unfortunately, when patients remain symptomatic despite having their medical and/or device therapies optimized, the "next steps" to improving patient morbidity are not at all clear. Thus, there remains an unmet need with respect to the treatment of HF patients. The concept that cardiac remodeling represents an important mechanism for disease progression in HF is reviewed, as well as discussion of several novel treatment strategies with respect to devices that are intended to prevent worsening cardiac remodeling.
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Misra et al. (2008) conducted a review in Heart Failure (n=300). CorCap cardiac support device vs. Optimal medical therapy alone or mitral valve surgery alone was evaluated on Composite ordinal endpoint of vital status, major cardiac procedure for progression of HF, and change in NYHA classification (OR 1.73, 95% CI 1.07-2.79, p=0.02). The CorCap cardiac support device significantly improved the clinical composite outcome of vital status, need for major cardiac procedures, and NYHA class compared to control in patients with heart failure.
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