Faculty of Health Sciences, Artvin Çoruh University, Artvin, Turkey.
Faculty of Health Sciences, Kırklareli University, Kırklareli, Turkey.
J Tissue Viability. 2024 May;33(2):220-224. doi: 10.1016/j.jtv.2024.02.007. Epub 2024 Feb 13.
This study aimed to determine the incidence, severity and characteristics of medical device-related pressure injuries in intensive care units.
This is a cross-sectional study. Data were collected from 187 patients admitted to the Anaesthesia and Reanimation intensive care unit of a university hospital between January and May 2023. The skin of the patients enrolled in the study was assessed for the presence of medical device-related pressure injuries, and all medical devices used were recorded. Data were collected using the Patient Identification Form, the Medical Device-Related Pressure Injury Follow-up Form, and the Braden Scale for Predicting Pressure Ulcer Risk.
It was found that 30.6% of the patients developed medical device-related pressure injuries; of these, 73.7% had stage I pressure injuries. We found that 36.8% of the patients were diagnosed with medical device-related pressure injuries within 8-11 days. The results showed that endotracheal tube (61.4%), non-invasive ventilation/oxygen mask (52.6%), Foley catheter (49.1%), and nasogastric tube (36.8%) devices were the most common causes of the development of medical device-related pressure injuries. Patients' demographic characteristics were found to have a significant effect on the development of medical device-related pressure injuries (p < .05).
The study found that the incidence of medical device-related pressure injuries was relatively high and that a relationship was observed between the patients' demographic characteristics and medical device-related pressure injuries. It is crucial that ICU nurses, who are more likely to encounter medical device-related pressure injuries, consider these factors when caring for their patients and take appropriate preventive measures to reduce the incidence of these injuries.
本研究旨在确定重症监护病房医疗器械相关性压力损伤的发生率、严重程度和特征。
这是一项横断面研究。数据收集于 2023 年 1 月至 5 月期间在一所大学附属医院麻醉和复苏重症监护病房收治的 187 名患者。对纳入研究的患者的皮肤进行医疗器械相关性压力损伤评估,并记录所有使用的医疗器械。使用患者识别表、医疗器械相关性压力损伤随访表和布雷登压疮风险预测量表收集数据。
发现 30.6%的患者发生医疗器械相关性压力损伤;其中 73.7%为 1 期压力损伤。我们发现 36.8%的患者在 8-11 天内被诊断为医疗器械相关性压力损伤。结果表明,气管内导管(61.4%)、无创通气/氧气面罩(52.6%)、 Foley 导管(49.1%)和鼻胃管(36.8%)是导致医疗器械相关性压力损伤最常见的原因。患者的人口统计学特征被发现对医疗器械相关性压力损伤的发生有显著影响(p<.05)。
研究发现医疗器械相关性压力损伤的发生率相对较高,且患者的人口统计学特征与医疗器械相关性压力损伤之间存在关联。对于更有可能遇到医疗器械相关性压力损伤的 ICU 护士来说,在护理患者时考虑这些因素并采取适当的预防措施以降低这些损伤的发生率至关重要。