Centre of Vascular and Miniinvasive Surgery, Hospital Agel, Trinec Podlesi, The Czech Republic; Salvatella Ltd., Centre of Non-healing Wounds Treatment, Podiatric Outpatients' Department, Trinec, The Czech Republic.
Military hospital, Olomouc, The Czech Republic.
J Wound Care. 2023 Aug 2;32(8):480-491. doi: 10.12968/jowc.2023.32.8.480.
This study was conducted to provide comparative data on the clinical efficacy and safety of a novel hard-to-heal wound dressing (Sorelex; Contipro a.s., Czech Republic) that combines octenidine and hyaluronan, compared with a silver-based dressing.
This multicentre, open-label, randomised, post-market, clinical follow-up study provides a comparison of a octenidine and hyaluronan combination with a standard-of-care (SoC) silver-containing dressing. The investigators evaluated the management of infection in the hard-to-heal wounds based on recorded changes in the appearance of the wound bed tissue and the presence of clinical signs of infection after three weeks of treatment. Other relevant assessed parameters of wound healing were: wound size; exudation level; wound pain level; and surrounding skin appearance.
The study cohort included 48 patients in the Sorelex arm and 39 patients in the SoC arm. Both products evinced numerous parameters of wound infection management: reductions in the wound bed slough; marked decreases in wound size; the formation of re-epithelialisation and granulation tissue; and improved pain management. Sorelex significantly improved the condition of surrounding skin after three weeks of treatment, unlike SoC. Sorelex reduced wound area significantly more than SoC (p=0.04). No statistically significant differences were detected in other assessed parameters between the two study arms. All the participating investigators expressed their satisfaction with both products. No adverse reactions to Sorelex were recorded over the mean treatment period of 53 days.
The octenidine and hyaluronan combination provides a new alternative choice of dressing for the treatment of infected hard-to-heal wounds when compared with a silver-based product.
本研究旨在提供一种新型难愈伤口敷料(Sorelex;Contipro a.s.,捷克共和国)的临床疗效和安全性的对比数据,该敷料结合了奥替尼啶和透明质酸,与基于银的敷料相比。
这项多中心、开放性、随机、上市后、临床随访研究比较了奥替尼啶和透明质酸的组合与标准护理(SoC)含银敷料。研究者根据治疗 3 周后伤口床组织外观的变化和感染的临床体征评估难愈伤口感染的管理情况。其他评估伤口愈合的相关参数包括:伤口大小;渗出水平;伤口疼痛水平;和周围皮肤外观。
Sorelex 组纳入 48 例患者,SoC 组纳入 39 例患者。两种产品均在伤口感染管理的多个参数上表现出疗效:减少伤口床的坏死组织;明显减少伤口大小;形成再上皮化和肉芽组织;以及改善疼痛管理。与 SoC 不同,Sorelex 在治疗 3 周后显著改善了周围皮肤的状况。Sorelex 显著减少了伤口面积,与 SoC 相比有统计学意义(p=0.04)。在两个研究组之间,其他评估参数没有检测到统计学上的显著差异。所有参与的研究者都对两种产品表示满意。在 53 天的平均治疗期间,没有记录到 Sorelex 的不良反应。
与基于银的产品相比,奥替尼啶和透明质酸的组合为治疗感染性难愈伤口提供了一种新的替代敷料选择。