Detailed Information on Publication Record
2024
Early Enzymatic Burn Debridement: Results of the DETECT Multicenter Randomized Controlled Trial
SHOHAM, Yaron, Lior ROSENBERG, William HICKERSON, Jeremy GOVERMAN, Narayan IYER et. al.Basic information
Original name
Early Enzymatic Burn Debridement: Results of the DETECT Multicenter Randomized Controlled Trial
Authors
SHOHAM, Yaron, Lior ROSENBERG, William HICKERSON, Jeremy GOVERMAN, Narayan IYER, Julio BARRERA-ORO, Břetislav LIPOVÝ, Stan MONSTREY, Sigrid BLOME-EBERWEIN, Lucy A WIBBENMEYER, Martin SCHARPENBERG and Adam J SINGER
Edition
JOURNAL OF BURN CARE & RESEARCH, OXFORD, OXFORD UNIV PRESS, 2024, 1559-047X
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30212 Surgery
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 1.400 in 2022
Organization unit
Faculty of Medicine
UT WoS
001077735400001
Keywords in English
burns; enzymatic debridement; eschar; surgery; excision; grafting
Tags
Tags
International impact, Reviewed
Změněno: 19/8/2024 10:23, Mgr. Tereza Miškechová
Abstract
V originále
Since 1970 surgeons have managed deep burns by surgical debridement and autografting. We tested the hypothesis that enzymatic debridement with NexoBrid would remove the eschar reducing surgery and achieve comparable long-term outcomes as standard of care (SOC). In this Phase 3 trial, we randomly assigned adults with deep burns (covering 3-30% of total body surface area [TBSA]) to NexoBrid, surgical or nonsurgical SOC, or placebo Gel Vehicle (GV) in a 3:3:1 ratio. The primary endpoint was complete eschar removal (ER) at the end of the debridement phase. Secondary outcomes were need for surgery, time to complete ER, and blood loss. Safety endpoints included wound closure and 12 and 24-months cosmesis on the Modified Vancouver Scar Scale. Patients were randomized to NexoBrid (n = 75), SOC (n = 75), and GV (n = 25). Complete ER was higher in the NexoBrid versus the GV group (93% vs 4%; P < .001). Surgical excision was lower in the NexoBrid vs the SOC group (4% vs 72%; P < .001). Median time to ER was 1.2 and 3.9 days for the NexoBrid and SOC respectively (P < .001). ER blood loss was lower in the NexoBrid than the SOC group (14 +/- 512 mL vs 814 +/- 1020 mL, respectively; P < .0001). MVSS scores at 12 and 24 months were noninferior in the NexoBrid versus SOC groups (3.7 +/- 2.1 vs 5.0 +/- 3.1 for the 12 months and 3.04 +/- 2.2 vs 3.30 +/- 2.76 for the 24 months). NexoBrid resulted in early complete ER in >90% of burn patients, reduced surgery and blood loss. NexoBrid was safe and well tolerated without deleterious effects on wound closure and scarring.