DCB cost-effective for treatment of femoropopliteal disease
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LAS VEGAS — Treatment with a drug-coated balloon was cost-effective and perhaps economically dominant compared with a standard balloon in patients with femoropopliteal disease, according to data presented at VIVA 15.
David J. Cohen, MD, MSc, and colleagues conducted a prospective economic study alongside the IN.PACT SFA II trial of a drug-coated balloon (DCB; IN.PACT Admiral, Medtronic) compared with standard percutaneous transluminal angioplasty (PTA) in 181 patients with symptomatic femoropopliteal disease over 24 months.
David J. Cohen
The researchers assessed cost-effectiveness by cost per quality-adjusted life year (QALY).
Patients who received DCB had average initial hospital costs that were $1,129 higher than for patients assigned PTA, mostly because the DCB is more expensive than the standard balloon, according to Cohen.
“There was a reduction in the need for provisional stenting in the DCB group, probably not because of the angiographic results, but reflecting the operators’ comfort with that approach,” Cohen, from Saint-Luke’s Mid America Heart Institute, Kansas City, Missouri, said during a press conference.
However, follow-up costs related to the target limb were $1,211 less in the DCB group compared with the PTA group, Cohen, said, noting that a reduction in hospitalizations for repeat revascularization were the main driver.
Therefore, he said, total costs for both groups were almost identical (DCB group, $11,277; PTA group, $11,359; P = .97). When adjustment was made to account for one extreme outlier from the DCB group, DCB were lower in total costs by approximately $700, he said.
On the basis of these findings, Cohen said DCB were economically dominant — lower costs and better outcomes — compared with standard balloons. Using a threshold of $50,000 per QALY gained (a common threshold in the United States), the probability of DCB being economically attractive was approximately 69%, and using a threshold of $150,000 per QALY gained, the probability was approximately 80%, he noted.
“Based on these findings, we conclude that for patients similar to those enrolled in the IN.PACT SFA II trial, the IN.PACT Admiral DCB appears to be economically attractive (i.e., cost-effective) compared to standard PTA based on current U.S. standards, Cohen concluded. ˗ by Erik Swain
Reference:
Cohen D. Late-Breaking Clinical Trials. Presented at: VIVA 15; Nov. 2-5, 2015; Las Vegas.