Key result
The CardioBBEAT trial enrolled 621 patients with chronic heart failure, revealing clinically relevant baseline imbalances between the telemonitoring and usual care groups that required adjustments to the statistical analysis plan.
Why the study?
Does home telemonitoring added to usual care improve the Incremental Cost-Effectiveness Ratio and clinical outcomes in patients with chronic heart failure?
RCT (n=621)
Open-label
Centralized stacked randomization
Yes
Does home telemonitoring added to usual care improve the Incremental Cost-Effectiveness Ratio and clinical outcomes in patients with chronic heart failure?
The CardioBBEAT trial is designed to evaluate the health economic and clinical impact of home telemonitoring in patients with chronic heart failure, though baseline imbalances will require adjusted analyses.
Baseline imbalances require adjusted analyses before interpreting telemonitoring benefits; leaves open its cost-effectiveness in chronic HF.
BACKGROUND: Evidence that home telemonitoring for patients with chronic heart failure (CHF) offers clinical benefit over usual care is controversial as is evidence of a health economic advantage. METHODS: Between January 2010 and June 2013, patients with a confirmed diagnosis of CHF were enrolled and randomly assigned to 2 study groups comprising usual care with and without an interactive bi-directional remote monitoring system (Motiva®). The primary endpoint in CardioBBEAT is the Incremental Cost-Effectiveness Ratio (ICER) established by the groups' difference in total cost and in the combined clinical endpoint "days alive and not in hospital nor inpatient care per potential days in study" within the follow-up of 12 months. RESULTS: A total of 621 predominantly male patients were enrolled, whereof 302 patients were assigned to the intervention group and 319 to the control group. Ischemic cardiomyopathy was the leading cause of heart failure. Despite randomization, subjects of the control group were more often in NYHA functional class III-IV, and exhibited peripheral edema and renal dysfunction more often. Additionally, the control and intervention groups differed in heart rhythm disorders. No differences existed regarding risk factor profile, comorbidities, echocardiographic parameters, especially left ventricular and diastolic diameter and ejection fraction, as well as functional test results, medication and quality of life. While the observed baseline differences may well be a play of chance, they are of clinical relevance. Therefore, the statistical analysis plan was extended to include adjusted analyses with respect to the baseline imbalances. CONCLUSIONS: CardioBBEAT provides prospective outcome data on both, clinical and health economic impact of home telemonitoring in CHF. The study differs by the use of a high evidence level randomized controlled trial (RCT) design along with actual cost data obtained from health insurance companies. Its results are conducive to informed political and economic decision-making with regard to home telemonitoring solutions as an option for health care. Overall, it contributes to developing advanced health economic evaluation instruments to be deployed within the specific context of the German Health Care System. TRIAL REGISTRATION: ClinicalTrials.gov NCT02293252 ; date of registration: 10 November 2014.
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Hofmann et al. (2015) conducted an RCT in Chronic heart failure (n=621). Home telemonitoring (Motiva®) vs. Usual care was evaluated on Incremental Cost-Effectiveness Ratio (ICER) established by the difference in total cost and the combined clinical endpoint 'days alive and not in hospital nor inpatient care per potential days in study'. The CardioBBEAT trial enrolled 621 patients with chronic heart failure, revealing clinically relevant baseline imbalances between the telemonitoring and usual care groups that required adjustments to the statistical analysis plan.
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