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本文引用的文献

1
Device-related pressure ulcers: SECURE prevention.与设备相关的压疮:安全预防。
J Wound Care. 2020 Feb 1;29(Sup2a):S1-S52. doi: 10.12968/jowc.2020.29.Sup2a.S1.
2
Introduction of a pilot study.一项试点研究的介绍。
Korean J Anesthesiol. 2017 Dec;70(6):601-605. doi: 10.4097/kjae.2017.70.6.601. Epub 2017 Nov 14.
3
Medical device-related pressure injuries: An exploratory descriptive study in an acute tertiary hospital in Australia.医疗器械相关压力性损伤:澳大利亚一家急性三级医院的探索性描述性研究。
J Tissue Viability. 2017 Nov;26(4):246-253. doi: 10.1016/j.jtv.2017.09.008. Epub 2017 Oct 4.
4
Pressure injury prevalence in intensive care versus non-intensive care patients: A state-wide comparison.重症监护与非重症监护患者的压疮发生率:全州范围比较。
Aust Crit Care. 2017 Sep;30(5):244-250. doi: 10.1016/j.aucc.2016.12.003. Epub 2017 Jan 4.
5
CONSORT 2010 statement: extension to randomised pilot and feasibility trials.《CONSORT 2010声明:随机试点和可行性试验的扩展》
BMJ. 2016 Oct 24;355:i5239. doi: 10.1136/bmj.i5239.
6
Revised National Pressure Ulcer Advisory Panel Pressure Injury Staging System: Revised Pressure Injury Staging System.修订后的国家压疮咨询委员会压力性损伤分期系统:修订后的压力性损伤分期系统。
J Wound Ostomy Continence Nurs. 2016 Nov/Dec;43(6):585-597. doi: 10.1097/WON.0000000000000281.
7
A Prospective, Descriptive Study to Determine the Rate and Characteristics of and Risk Factors for the Development of Medical Device-related Pressure Ulcers in Intensive Care Units.一项前瞻性描述性研究,以确定重症监护病房中与医疗器械相关压疮的发生率、特征及发生风险因素。
Ostomy Wound Manage. 2016 Feb;62(2):12-22.
8
Premature Discontinuation of Randomized Trials in Critical and Emergency Care: A Retrospective Cohort Study.危重症与急诊护理中随机试验的提前终止:一项回顾性队列研究
Crit Care Med. 2016 Jan;44(1):130-7. doi: 10.1097/CCM.0000000000001369.
9
Reducing pressure injuries in critically ill patients by using a patient skin integrity care bundle (InSPiRE).通过使用患者皮肤完整性护理包(InSPiRE)减少重症患者的压疮
Am J Crit Care. 2015 May;24(3):199-209. doi: 10.4037/ajcc2015930.
10
Better reporting of interventions: template for intervention description and replication (TIDieR) checklist and guide.更好的干预措施报告:干预描述和复制(TIDieR)清单和指南模板。
BMJ. 2014 Mar 7;348:g1687. doi: 10.1136/bmj.g1687.

重症监护病房预防器械相关压力性损伤的固定:一项随机对照可行性研究。

Securement to prevent device-related pressure injuries in the intensive care unit: A randomised controlled feasibility study.

机构信息

Joint appointment Intensive Care Services, Royal Brisbane and Women's Hospital and School of Nursing, Queensland University of Technology, Australia.

Institute of Skin Integrity and Infection Prevention, University of Huddersfield, Huddersfield, UK.

出版信息

Int Wound J. 2020 Dec;17(6):1566-1577. doi: 10.1111/iwj.13432. Epub 2020 Jun 28.

DOI:10.1111/iwj.13432
PMID:32596937
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7948617/
Abstract

Medical device-related pressure injuries are the most common cause of pressure injuries within the intensive care unit, in particular those caused by nasogastric tubes and endotracheal tubes. There are several known methods, which can alleviate the pressure of these devices on the skin surface to reduce the rate of these injuries. To determine the feasibility of conducting a larger, adequately powered trial testing, several clinically effective interventions to reduce the incidence of medical device-related pressure injuries caused by these devices. Patients were recruited into both study arms and received one of three different methods of skin protection for both arms. Outcome measures included fidelity to the processes of care protocol, recruitment potential, and the number of medical device-related pressure injuries. Recruitment (n = 87) was slower than expected with less than 10% of screened potential patients available for enrolment. Fidelity to the process of care for each subgroup was variable with better adherence in the nasogastric tube arm compared to the endotracheal tube arm. This feasibility study has revealed concerns about the intervention designs and effectiveness as well as challenges for the adherence of the nursing staff to the protocol.

摘要

医疗器械相关性压力损伤是重症监护病房中最常见的压力损伤原因,特别是由鼻胃管和气管内管引起的压力损伤。有几种已知的方法可以减轻这些设备对皮肤表面的压力,从而降低这些损伤的发生率。为了确定进行更大规模、充分有力的试验测试的可行性,研究人员采用了几种临床有效的干预措施来降低这些设备引起的医疗器械相关性压力损伤的发生率。将患者招募到两个研究组中,并对双臂使用三种不同的皮肤保护方法。结果测量包括护理协议流程的忠实程度、招募潜力和医疗器械相关性压力损伤的数量。与预期相比,招募速度较慢,只有不到 10%的筛选出的潜在患者可入组。每个亚组的护理流程忠实程度各不相同,与气管内管组相比,鼻胃管组的依从性更好。这项可行性研究揭示了对干预设计和效果的关注,以及护理人员遵守方案的挑战。