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儿童急性烧伤负压伤口治疗辅助治疗研究(SONATA in C):一项随机对照试验方案

Study of negative pressure wound therapy as an adjunct treatment for acute burns in children (SONATA in C): protocol for a randomised controlled trial.

作者信息

Frear Cody C, Griffin Bronwyn, Cuttle Leila, McPhail Steven M, Kimble Roy

机构信息

Centre for Children's Burns and Trauma Research, Level 7, Children's Health Research Center, The University of Queensland, 62 Graham St., South Brisbane, QLD, 4101, Australia.

The Pegg Leditschke Children's Burns Centre, Queensland Children's Hospital, Lvl. 5, 501 Stanley St., South Brisbane, QLD, 4101, Australia.

出版信息

Trials. 2019 Feb 13;20(1):130. doi: 10.1186/s13063-019-3223-9.

Abstract

BACKGROUND

Although negative pressure wound therapy (NPWT) is widely used in the management of several wound types, its efficacy as a primary therapy for acute burns has not yet been adequately investigated, with research in the paediatric population particularly lacking. There is limited evidence, however, that NPWT might benefit children with burns, amongst whom scar formation, wound progression and pain continue to present major management challenges. The purpose of this trial is to determine whether NPWT in conjunction with standard therapy accelerates healing, reduces wound progression and decreases pain more effectively than standard treatment alone.

METHODS/DESIGN: A total of 104 children will be recruited for this trial. To be eligible, candidates must be under 17 years of age and present to the participating children's hospital within 7 days of their injury with a thermal burn covering <5% of their total body surface area. Facial and trivial burns will be excluded. Following a randomised controlled parallel design, participants will be allocated to either an active control or intervention group. The former will receive standard therapy consisting of Acticoat™ and Mepitel™. The intervention arm will be treated with silver-impregnated dressings in addition to NPWT via the RENASYS TOUCH™ vacuum pump. Participants' dressings will be changed every 3 to 5 days until their wounds are fully re-epithelialised. Time to re-epithelialisation will be studied as the primary outcome. Secondary outcomes will include pain, pruritus, wound progression, health-care-resource use (and costs), ease of management, treatment satisfaction and adverse events. Wound fluid collected during NPWT will also be analysed to generate a proteomic profile of the burn microenvironment.

DISCUSSION

The study will be the first randomised controlled trial to explore the clinical effects of NPWT on paediatric burns, with the aim of determining whether the therapy warrants implementation as an adjunct to standard burns management.

TRIAL REGISTRATION

Australian New Zealand Clinical Trials Registry, ACTRN12618000256279 . Registered on 16 February 2018.

摘要

背景

尽管负压伤口治疗(NPWT)广泛应用于多种伤口类型的处理,但其作为急性烧伤的主要治疗方法的疗效尚未得到充分研究,尤其是在儿科人群中缺乏相关研究。然而,有有限的证据表明NPWT可能对烧伤儿童有益,在这些儿童中,瘢痕形成、伤口进展和疼痛仍然是主要的管理挑战。本试验的目的是确定NPWT联合标准治疗是否比单纯标准治疗更有效地加速愈合、减少伤口进展并减轻疼痛。

方法/设计:本试验共招募104名儿童。符合条件的候选人必须年龄在17岁以下,在受伤后7天内到参与试验的儿童医院就诊,热烧伤面积占全身表面积的比例小于5%。面部烧伤和轻微烧伤将被排除。采用随机对照平行设计,参与者将被分配到活性对照组或干预组。前者将接受由Acticoat™和Mepitel™组成的标准治疗。干预组除了通过RENASYS TOUCH™真空泵进行NPWT外,还将使用含银敷料进行治疗。参与者的敷料每3至5天更换一次,直到伤口完全重新上皮化。重新上皮化的时间将作为主要结局进行研究。次要结局将包括疼痛、瘙痒、伤口进展、医疗资源使用(及成本)、管理的难易程度、治疗满意度和不良事件。在NPWT期间收集的伤口渗出液也将进行分析,以生成烧伤微环境的蛋白质组图谱。

讨论

本研究将是第一项探索NPWT对儿童烧伤临床效果的随机对照试验,目的是确定该治疗方法是否值得作为标准烧伤管理的辅助手段实施。

试验注册

澳大利亚新西兰临床试验注册中心,ACTRN12618000256279。于2018年2月16日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdeb/6374905/ab6d943b90b3/13063_2019_3223_Fig1_HTML.jpg

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