Abbott dissolving heart stent succeeds in pivotal U.S. trial: study
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A novel dissolving heart stent developed by Abbott Laboratories proved comparably safe and effective as its market-leading Xience stent in a large, late-stage trial that will be used to seek U.S. approval of the device, according to data presented at a medical meeting on Monday.
The bioabsorbable Absorb stent succeeded in demonstrating non-inferiority to Xience up to one year after implantation in the 2,008-patient study called Absorb III, researchers at the Transcatheter Cardiovascular Therapeutics meeting in San Francisco reported.
The primary data point measuring target lesion failure, a combination of heart disease-related death, heart attacks associated with the treated blood vessel and need for repeat procedures in the treated area, occurred in 7.8 percent of Absorb patients versus 6.1 percent for Xience. The difference was not deemed statistically significant, researchers said.
On a variety of secondary measures, Xience also appeared to be numerically better at one year, but with no statistically significant differences.
The bioabsorbable Absorb stent succeeded in demonstrating non-inferiority to Xience up to one year after implantation in the 2,008-patient study called Absorb III, researchers at the Transcatheter Cardiovascular Therapeutics meeting in San Francisco reported.
The primary data point measuring target lesion failure, a combination of heart disease-related death, heart attacks associated with the treated blood vessel and need for repeat procedures in the treated area, occurred in 7.8 percent of Absorb patients versus 6.1 percent for Xience. The difference was not deemed statistically significant, researchers said.
On a variety of secondary measures, Xience also appeared to be numerically better at one year, but with no statistically significant differences.
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