Publication | Closed Access
Multicenter Postapproval Clinical Trial of Integra® Dermal Regeneration Template for Burn Treatment
345
Citations
31
References
2003
Year
Limb ReconstructionBurn Injury PatientsWound AssessmentSurgeryDermatologySkin RegenerationRegenerative MedicineWound CareBurn TreatmentInvasive InfectionBurn Care FacilitiesSkin SubstituteScar PreventionBurn ManagementWound InfectionBurn Scar PreventionPatient SafetyLower Extremity WoundReconstructive SurgeryWound HealingMedicineDermatological Surgery
The study evaluated the safety and effectiveness of Integra® Dermal Regeneration Template in 216 burn patients across 13 U.S. burn centers. Integra® was applied to surgically excised wounds, regenerated a dermal layer within 2–3 weeks, and was then covered with a thin epidermal autograft.
Abstract The safety and effectiveness of Integra® Dermal Regeneration Template was evaluated in a postapproval study involving 216 burn injury patients who were treated at 13 burn care facilities in the United States. The mean total body surface area burned was 36.5% (range, 1–95%). Integra® was applied to fresh, clean, surgically excised burn wounds. Within 2 to 3 weeks, the dermal layer regenerated, and a thin epidermal autograft was placed. The incidence of invasive infection at Integra®-treated sites was 3.1% (95% confidence interval, 2.0–4.5%) and that of superficial infection 13.2% (95% confidence interval, 11.0–15.7%). Mean take rate of Integra® was 76.2%; the median take rate was 95%. The mean take rate of epidermal autograft was 87.7%; the median take rate was 98%. This postapproval study further supports the conclusion that Integra® is a safe and effective treatment modality in the hands of properly trained clinicians under conditions of routine clinical use at burn centers.
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