Mataro I, Giudice G, D'Alessio R, Maggio G, Vestita M
Department of Emergency and Reception, Plastic Surgery and Burn Centre Units, Hospital A. Cardarelli, Naples, Italy.
Department of Emergency and Organ Transplantation, Unit of Plastic, Aesthetic and Reconstructive Surgery and Burn Centre, Bari, Italy.
Ann Burns Fire Disasters. 2018 Jun 30;31(2):109-112.
Nexobrid is a highly selective enzymatic debriding agent used in the acute management of burns to perform escharectomy. From October 2016 to April 2017, we treated 6 patients affected with lower limb chronic ulcers of different etiologies with Nexobrid in order to perform eschar removal by enzymatic debridement. For all patients, a dosage of Nexobrid, calculated as 2gr per 1% TBSA, was applied in a 2-3 mm thick uniform layer on the ulcer eschar and fibrin tissue and left for 4 hours, covered with an occlusive dressing. Patients were assessed in terms of ulcer cleansing 24 hours and 7 days post Nexobrid debridement, by wound bed score (WBS) and % of remaining necrotic tissue. A patient pain VAS was also recorded at 24 hours and 7 days post debridement. Adverse events at these time points were also noted. The results documented a complete removal of necrotic tissue in a time frame of 4 hours. At 24 hours, all lesions were completely debrided. At 7 days, there was a partial recurrence of necrotic tissue, as also documented by decreased WBS. All patients reported none to mild pain, and no adverse events were noted, except for mild erythema along the edges of the lesion on healthy skin in one case. This is a preliminary observation. Optimal dosage and application of Nexobrid in this indication needs to be validated by further controlled data.
Nexobrid是一种高选择性酶促清创剂,用于烧伤的急性处理以进行焦痂切除。2016年10月至2017年4月,我们用Nexobrid治疗了6例不同病因的下肢慢性溃疡患者,以便通过酶促清创去除焦痂。对于所有患者,以每1%体表面积2克计算的Nexobrid剂量,以2 - 3毫米厚的均匀层涂抹在溃疡焦痂和纤维蛋白组织上,留置4小时,并用封闭敷料覆盖。在Nexobrid清创后24小时和7天,通过创面床评分(WBS)和剩余坏死组织百分比对患者进行溃疡清洁情况评估。在清创后24小时和7天还记录了患者的疼痛视觉模拟评分(VAS)。同时也记录了这些时间点的不良事件。结果表明在4小时内坏死组织被完全清除。在24小时时,所有创面均已完全清创。在7天时,坏死组织出现部分复发,WBS降低也证实了这一点。所有患者均报告无疼痛至轻度疼痛,除1例在健康皮肤病变边缘出现轻度红斑外,未观察到不良事件。这是一项初步观察。Nexobrid在此适应症中的最佳剂量和应用需要通过进一步的对照数据进行验证。