Jang Young-Jin, Choi Haemi, Han Tae Sun, Sung Dajung, Woo Jae Yeon, Kim Tae-Hyeong, Park Min-Hyeon
Department of Psychiatry, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Department of Psychiatry, Eunpyeong St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Psychiatry Investig. 2022 Sep;19(9):738-747. doi: 10.30773/pi.2022.0117. Epub 2022 Sep 22.
We aimed to investigate the improvement in sleep quantity and quality when clonidine was used in children and adolescents with insomnia. We also examined how sociodemographic characteristics such as age, sex, underlying psychological problems, and levels of depression and anxiety affected the effect of clonidine.
We retrospectively reviewed outpatients aged 6 to 24 who took clonidine due to insomnia from September 2019 to September 2021 at the Department of Psychiatry at Eunpyeong St. Mary's Hospital of Catholic University. We used the Pittsburgh Sleep Quality Index (PSQI), Children's Depression Inventory (CDI), and State-Trait Anxiety Inventory (STAI) for our study.
A total of 62 participants were included in our study (34 females, mean age 13.94±4.94 years). After using clonidine, there was a significant decrease in PSQI components 1, 2, and 5, especially PSQI component 2. There was a greater decrease in sleep latency when clonidine was used in females, those aged between 13 and 24, those with mood/anxiety disorder or attention-deficit/hyperactivity disorder, those whose sleep latency exceeded 60 minutes at baseline, and those who used clonidine for more than 14 days. Those with higher STAI-Trait scores and CDI scores at baseline showed less improvement in total PSQI scores.
Considering that there are currently no Food and Drug Administration-approved sleep drugs for children and adolescents and no apparent difference in efficacy and safety among sleep drugs, we demonstrated that treatment with clonidine might be a good approach to improve sleep quality and quantity for children and adolescents.
我们旨在研究可乐定用于治疗儿童和青少年失眠时对睡眠数量和质量的改善情况。我们还考察了年龄、性别、潜在心理问题以及抑郁和焦虑水平等社会人口学特征如何影响可乐定的疗效。
我们回顾性分析了2019年9月至2021年9月在天主教大学恩平圣母医院精神科因失眠服用可乐定的6至24岁门诊患者。我们在研究中使用了匹兹堡睡眠质量指数(PSQI)、儿童抑郁量表(CDI)和状态-特质焦虑量表(STAI)。
我们的研究共纳入62名参与者(34名女性,平均年龄13.94±4.94岁)。使用可乐定后,PSQI的第1、2和5项成分显著降低,尤其是PSQI的第2项成分。女性、年龄在13至24岁之间、患有情绪/焦虑障碍或注意力缺陷多动障碍、基线睡眠潜伏期超过60分钟以及使用可乐定超过14天的患者,使用可乐定后睡眠潜伏期的降低幅度更大。基线时STAI-特质得分和CDI得分较高的患者,PSQI总分的改善程度较小。
鉴于目前美国食品药品监督管理局尚未批准用于儿童和青少年的助眠药物,且助眠药物之间在疗效和安全性方面无明显差异,我们证明可乐定治疗可能是改善儿童和青少年睡眠质量和数量的一种良好方法。