Cuttle Leila, Naidu Sanjeev, Mill Julie, Hoskins Wendy, Das Karina, Kimble Roy M
Royal Children's Hospital Burns Research Group, University of Queensland, Department of Paediatrics and Child Health, Royal Children's Hospital, Herston, Queensland 4029, Australia.
Burns. 2007 Sep;33(6):701-7. doi: 10.1016/j.burns.2007.02.012. Epub 2007 Jul 17.
We wished to determine whether changing our centre's practice of using Acticoat instead of Silvazine as our first-line burns dressing provided a better standard of care in terms of efficacy, cost and ease of use. A retrospective cohort study was performed examining 328 Silvazine treated patients from January 2000 to June 2001 and 241 Acticoat treated patients from July 2002 to July 2003. During those periods the respective dressings were used exclusively. There was no significant difference in age, %BSA and mechanism of burn between the groups. In the Silvazine group, 25.6% of children required grafting compared to 15.4% in the Acticoat group (p=0.001). When patients requiring grafting were excluded, the time taken for re-epithelialisation in the Acticoat group (14.9 days) was significantly less than that for the Silvazine group (18.3 days), p=0.047. There were more wounds requiring long term scar management in the Silvazine group (32.6%) compared to the Acticoat group (29.5%), however this was not significant. There was only one positive blood culture in each group, indicating that both Silvazine and Acticoat are potent antimicrobial agents. The use of Acticoat as our primary burns dressing has dramatically changed our clinical practice. Inpatients are now only 18% of the total admissions, with the vast majority of patients treated on an outpatient basis. In terms of cost, Acticoat was demonstrated to be less expensive over the treatment period than Silvazine . We have concluded that Acticoat is a safe, cost-effective, efficacious dressing that reduces the time for re-epithelialisation and the requirement for grafting and long term scar management, compared to Silvazine.
我们希望确定,将我们中心的一线烧伤敷料从水凝胶银离子抗菌敷料(Silvazine)改为纳米银抗菌敷料(Acticoat),在疗效、成本和易用性方面是否能提供更好的护理标准。我们进行了一项回顾性队列研究,调查了2000年1月至2001年6月期间接受水凝胶银离子抗菌敷料治疗的328例患者,以及2002年7月至2003年7月期间接受纳米银抗菌敷料治疗的241例患者。在这些时间段内,分别仅使用了相应的敷料。两组患者在年龄、烧伤面积百分比和烧伤机制方面没有显著差异。在水凝胶银离子抗菌敷料组中,25.6%的儿童需要进行植皮,而纳米银抗菌敷料组为15.4%(p = 0.001)。排除需要植皮的患者后,纳米银抗菌敷料组的上皮再形成时间(14.9天)显著短于水凝胶银离子抗菌敷料组(18.3天),p = 0.047。与纳米银抗菌敷料组(29.5%)相比,水凝胶银离子抗菌敷料组中需要长期瘢痕管理的伤口更多(32.6%),但这并不显著。每组仅出现1例阳性血培养结果,表明水凝胶银离子抗菌敷料和纳米银抗菌敷料都是有效的抗菌剂。将纳米银抗菌敷料用作我们的主要烧伤敷料极大地改变了我们的临床实践。现在住院患者仅占总入院人数的18%,绝大多数患者在门诊接受治疗。在成本方面,纳米银抗菌敷料在治疗期间被证明比水凝胶银离子抗菌敷料更便宜。我们得出结论,与水凝胶银离子抗菌敷料相比,纳米银抗菌敷料是一种安全、经济高效、有效的敷料,可减少上皮再形成时间以及植皮和长期瘢痕管理的需求。