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. Early Enzymatic Burn Debridement: Results of the DETECT Multicenter Randomized Controlled Trial. JOURNAL OF BURN CARE & RESEARCH. OXFORD: OXFORD UNIV PRESS, 2024, 11 pp. ISSN 1559-047X. Available from: https://dx.doi.org/10.1093/jbcr/irad142.
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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
Original language English
Type of outcome Article in a journal
Field of Study 30212 Surgery
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 1.400 in 2022
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1093/jbcr/irad142
UT WoS 001077735400001
Keywords in English burns; enzymatic debridement; eschar; surgery; excision; grafting
Tags 14110229
Tags International impact, Reviewed
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 4/3/2024 10:41.
Abstract
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.
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