The interim analysis from the ongoing MASTRR Registry is the largest prospective study of its kind in in-patient soft tissue reconstruction. Researchers evaluated the Myriad Matrix and Myriad Morcells products within a cohort where 59% of patients were classified as ASA Class III or IV. The population included individuals with diabetes, vascular disease, and nicotine use, further complicated by the fact that 89% of treated defects were categorized as clean-contaminated or contaminated.
Despite the clinical difficulty, no adverse events were linked to the Myriad products over a median follow-up of 27 weeks. The study authors highlighted that these results compare favorably against resorbable synthetic bioscaffolds, which have historically reported infection rates between 16% and 25% in similar meta-analyses. CEO Brian Ward noted that the data underscores the product's performance in challenging real-world scenarios, potentially offering a way to mitigate the significant hospital costs and recovery delays associated with post-operative surgical site infections.

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