Pelin Meryem, Sert Havva
Faculty of Health Sciences, Internal Medicine Nursing Department, Sakarya University, Sakarya, Turkey.
BMC Nurs. 2025 Feb 7;24(1):143. doi: 10.1186/s12912-025-02793-8.
This study carried out to examine the effects of nursing care given to coronary intensive care patients according to their circadian rhythms on sleep quality, pain, anxiety, and delirium.
This study was designed as a randomised controlled, clinical investigation. The study population consisted of patients treated in the coronary care unit of a training and research hospital between September 2022 and February 2023. Total of 44 participants were included. The included participants were followed up for 3 days in the coronary intensive care unit. Data were collected using "Patient Information Form, Sleep Quality Scale in Coronary Intensive Care Patients (SQ-CC), Visual Analogue Scale (VAS), Morningness-Eveningness Questionnaire (MEQ), Hospital Anxiety and Depression Scale (HADS), Intensive Care Delirium Screening Checklist (ICDSC)." In addition, melatonin and cortisol measurements were made, and sleep data were taken with a smartwatch. Patients with intermediate chronotype, delirium, on ventilator support, or using sedative drugs were excluded. The chronotypes of the participants were determined, and the patients in the intervention group were given nursing care by their circadian rhythms. No intervention was made to the control group, and their routine care was continued in accordance with intensive care unit functioning. Frequency distribution, dependent and independent sample t-test, Wilcoxon test, repeated measures analysis of variance, Mann Whitney U, and chi-square analysis were used to evaluate the data. The study has been registered in ClinicalTrials.gov (Identifiers: NCT04934436). During statistical analysis, the groups were coded as Group A and Group B, ensuring blinding for the statistician.
The intervention group's sleep quality increased compared to the control group (post-test SQ-CC total scores: intervention group 22.41 ± 6.67 vs. control group 50.45 ± 10.63, p < 0.001). Although no significant difference was found between the groups as a result of the study, there was a significant decrease in the pain score in the intervention group (VAS pre-test: 1.55 ± 2.15, post-test: 0.68 ± 2.21, p = 0.036). The anxiety of the intervention group decreased significantly compared to the control group (post-test HADS-Anxiety scores: intervention group 3.18 ± 3.29 vs. control group 8.50 ± 5.66, p = 0.001). The post-test delirium score was higher in the control group compared to the intervention group (post-test ICDSC scores: intervention group 0.32 ± 0.48 vs. control group 1.18 ± 0.50, p < 0.001). Melatonin increased and cortisol decreased in both groups without statistically significant differences between them (melatonin and cortisol levels: p > 0.05). Considering the sound levels in the environment, the first-night decibel mean was significantly higher in the intervention group than in the control group (first-night decibel mean: intervention group 56.58 ± 2.43 dB vs. control group 54.51 ± 2.41 dB, p < 0.05). Finally, the smartwatch data show no significant difference in sleep times between groups (p < 0.05), but the intervention group had more deep and total sleep, while the control group had less deep sleep.
Nursing care given in accordance with the circadian rhythm increases sleep quality and reduces the risk of delirium and anxiety in patients followed up with acute coronary syndrome in the coronary intensive care unit.
本研究旨在探讨根据冠心病重症监护患者的昼夜节律提供护理对其睡眠质量、疼痛、焦虑和谵妄的影响。
本研究设计为一项随机对照临床研究。研究对象为2022年9月至2023年2月在一家培训和研究医院的冠心病监护病房接受治疗的患者。共纳入44名参与者。纳入的参与者在冠心病重症监护病房进行了3天的随访。使用“患者信息表、冠心病重症监护患者睡眠质量量表(SQ - CC)、视觉模拟量表(VAS)、晨型 - 夜型问卷(MEQ)、医院焦虑抑郁量表(HADS)、重症监护谵妄筛查清单(ICDSC)”收集数据。此外,还进行了褪黑素和皮质醇测量,并使用智能手表获取睡眠数据。排除中间型昼夜节律、谵妄、使用呼吸机支持或使用镇静药物的患者。确定参与者的昼夜节律类型,干预组患者根据其昼夜节律接受护理。对照组不进行干预,按照重症监护病房的常规功能继续进行常规护理。采用频率分布、独立样本和相关样本t检验、Wilcoxon检验、重复测量方差分析、Mann - Whitney U检验和卡方分析来评估数据。该研究已在ClinicalTrials.gov注册(标识符:NCT04934436)。在统计分析过程中,将两组编码为A组和B组,确保统计人员处于盲态。
与对照组相比,干预组的睡眠质量有所提高(测试后SQ - CC总分:干预组22.41±6.67,对照组50.45±10.63,p < 0.001)。尽管研究结果显示两组之间无显著差异,但干预组的疼痛评分有显著下降(VAS测试前:1.55±2.15,测试后:0.68±2.21,p = 0.036)。与对照组相比,干预组的焦虑显著降低(测试后HADS - 焦虑评分:干预组3.18±3.29,对照组8.50±5.66,p = 0.001)。测试后,对照组的谵妄评分高于干预组(测试后ICDSC评分:干预组0.32±0.48,对照组1.18±0.50,p < 0.001)。两组的褪黑素均升高,皮质醇均降低,但两组之间无统计学显著差异(褪黑素和皮质醇水平:p > 0.05)。考虑到环境中的声音水平,干预组第一晚的分贝平均值显著高于对照组(第一晚分贝平均值:干预组56.58±2.43 dB,对照组54.51±2.41 dB,p < 0.05)。最后,智能手表数据显示两组之间的睡眠时间无显著差异(p < 0.05),但干预组的深度睡眠和总睡眠时间更多,而对照组的深度睡眠较少。
在冠心病重症监护病房,根据昼夜节律提供护理可提高急性冠脉综合征患者的睡眠质量,并降低谵妄和焦虑风险。