The Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
Division of Cardiovascular Medicine and Surgery, Tzafon Medical Center, Tiberias, Israel; School of Graduate Studies, The Academic Center Levinsky-Wingate, Wingate Institute, Netanya, Israel.
Pain Manag Nurs. 2023 Aug;24(4):e18-e25. doi: 10.1016/j.pmn.2023.02.003. Epub 2023 Mar 21.
There is minimal research on the effect of individualized preoperative education on postoperative pain and postoperative pain medication intake.
The study objective was to assess the effect of individually tailored preoperative education on postoperative pain severity, number of pain breakthroughs, and use of pain medication in participants receiving the intervention compared to controls.
A pilot study with 200 participants was conducted. The experimental group received an informational booklet and discussed their ideas surrounding pain and pain medication with the researcher. Controls received no intervention. Postoperative pain severity was measured by a Numerical Rating System (NRS), which was divided into mild (NRS 1-3), moderate (NRS 4-6), and severe (NRS 7-10).
In the participant cohort, 68.8% of participants were male, and the average age was 60.48±10.7. Average postoperative 48-hour cumulative pain scores were lower in those who received the intervention compared to controls; 50.0 (IQR 35.8-60.0) vs. 65 (IQR 51.0-73.0; p < .01) participants who received the intervention had less frequent pain breakthroughs when compared to controls (3.0 [IQR 2.0-5.0] vs. 6.0 [IQR 4.0-8.0; p < .01]). There was no significant difference in the amount of pain medication taken by either group.
Participants who receive individualized preoperative pain education are more likely to have decreased postoperative pain.
关于个体化术前教育对术后疼痛和术后止痛药摄入的影响的研究甚少。
本研究旨在评估个体化术前教育对接受干预组与对照组患者术后疼痛严重程度、疼痛发作次数和止痛药使用的影响。
对 200 名参与者进行了一项试点研究。实验组接受了一本信息手册,并与研究人员讨论了他们对疼痛和止痛药的想法。对照组未接受干预。术后疼痛严重程度采用数字评分系统(NRS)进行测量,分为轻度(NRS 1-3)、中度(NRS 4-6)和重度(NRS 7-10)。
在参与者队列中,68.8%的参与者为男性,平均年龄为 60.48±10.7 岁。与对照组相比,接受干预的患者术后 48 小时累积疼痛评分较低;接受干预的 50.0(IQR 35.8-60.0)名参与者与对照组相比,疼痛发作次数较少(3.0 [IQR 2.0-5.0] vs. 6.0 [IQR 4.0-8.0; p <.01])。两组止痛药的使用量均无显著差异。
接受个体化术前疼痛教育的患者术后疼痛更轻。