中国神经精神疾病杂志
中國神經精神疾病雜誌
중국신경정신질병잡지
CHINESE JOURNAL OF NERVOUS AND MENTAL DISEASES
2015年
5期
288-292
,共5页
张俊%崔明%吴延海%宋红梅%翟长平%邓家佩%王守虎%骆祥芬%王升
張俊%崔明%吳延海%宋紅梅%翟長平%鄧傢珮%王守虎%駱祥芬%王升
장준%최명%오연해%송홍매%적장평%산가패%왕수호%락상분%왕승
重复经颅磁刺激%度洛西汀%抑郁障碍
重複經顱磁刺激%度洛西汀%抑鬱障礙
중복경로자자격%도락서정%억욱장애
Repetitive transcranial magnetic stimulation%Duloxetine%Depression
目的:探讨低频重复经颅磁刺激(repetitive transcranial magnetic stimulation,rTMS)联合度洛西汀治疗抑郁障碍的临床疗效和安全性。方法将69例抑郁障碍患者随机分为研究组(35例)和对照组(34例),研究组给予6周度洛西汀联合1 Hz rTMS治疗,rTMS作用于右侧前额叶背外侧皮质区域,对照组给予6周度洛西汀联合伪rTMS治疗。两组分别于治疗前和治疗2、4、6周采用汉密尔顿抑郁量表(Hamilton depression rating scale-24,HAMD-24)评估抑郁症状,并按量表减分情况划分疗效等级;治疗2、4、6周采用治疗时出现的症状量表(treatment emergent symptom scale,TESS)评定不良反应。结果两组各脱落2例患者。HAMD评分经重复测量方差分析,时间主效应(P<0.001)、分组主效应(P=0.029)及时间与分组交互效应(P<0.001)均有统计学意义。疗效评估表明,治疗2、4、6周时研究组的临床疗效均优于对照组(P<0.001)。对照组1例患者因不能耐受胃肠道不良反应而退组,两组其他不良反应均较轻微,未出现严重不良反应。结论1 Hz rTMS联合度洛西汀改善抑郁症状作用显著,疗效优于单一用药,且较为安全,值得临床推广应用。
目的:探討低頻重複經顱磁刺激(repetitive transcranial magnetic stimulation,rTMS)聯閤度洛西汀治療抑鬱障礙的臨床療效和安全性。方法將69例抑鬱障礙患者隨機分為研究組(35例)和對照組(34例),研究組給予6週度洛西汀聯閤1 Hz rTMS治療,rTMS作用于右側前額葉揹外側皮質區域,對照組給予6週度洛西汀聯閤偽rTMS治療。兩組分彆于治療前和治療2、4、6週採用漢密爾頓抑鬱量錶(Hamilton depression rating scale-24,HAMD-24)評估抑鬱癥狀,併按量錶減分情況劃分療效等級;治療2、4、6週採用治療時齣現的癥狀量錶(treatment emergent symptom scale,TESS)評定不良反應。結果兩組各脫落2例患者。HAMD評分經重複測量方差分析,時間主效應(P<0.001)、分組主效應(P=0.029)及時間與分組交互效應(P<0.001)均有統計學意義。療效評估錶明,治療2、4、6週時研究組的臨床療效均優于對照組(P<0.001)。對照組1例患者因不能耐受胃腸道不良反應而退組,兩組其他不良反應均較輕微,未齣現嚴重不良反應。結論1 Hz rTMS聯閤度洛西汀改善抑鬱癥狀作用顯著,療效優于單一用藥,且較為安全,值得臨床推廣應用。
목적:탐토저빈중복경로자자격(repetitive transcranial magnetic stimulation,rTMS)연합도락서정치료억욱장애적림상료효화안전성。방법장69례억욱장애환자수궤분위연구조(35례)화대조조(34례),연구조급여6주도락서정연합1 Hz rTMS치료,rTMS작용우우측전액협배외측피질구역,대조조급여6주도락서정연합위rTMS치료。량조분별우치료전화치료2、4、6주채용한밀이돈억욱량표(Hamilton depression rating scale-24,HAMD-24)평고억욱증상,병안량표감분정황화분료효등급;치료2、4、6주채용치료시출현적증상량표(treatment emergent symptom scale,TESS)평정불량반응。결과량조각탈락2례환자。HAMD평분경중복측량방차분석,시간주효응(P<0.001)、분조주효응(P=0.029)급시간여분조교호효응(P<0.001)균유통계학의의。료효평고표명,치료2、4、6주시연구조적림상료효균우우대조조(P<0.001)。대조조1례환자인불능내수위장도불량반응이퇴조,량조기타불량반응균교경미,미출현엄중불량반응。결론1 Hz rTMS연합도락서정개선억욱증상작용현저,료효우우단일용약,차교위안전,치득림상추엄응용。
Objective To investigate the clinical efficacy and safety of repetitive transcranial magnetic stimulation combined with duloxetine in treatment of depression. Methods Sixty-nine cases of depression were randomly divided in?to study group (n=35 patients) and control group (n=34 patients). The study group received duloxetine combined with 1Hz rTMS treatment on the right dorsolateral prefrontal cortex area for 6 weeks whereas the control group received duloxetine combined with pseudo-rTMS treatment for 6 weeks. The Hamilton Depression Rating Scale (HAMD-24) and Treatment Emergent Symptom Scale (TESS) were used to assess the clinical efficacy and the adverse reactions before, 2, 4 and 6 weeks after the treatment, respectively. Results Four patients (two from each group) dropped out of the study. The main effects of time (P<0.001) and groups (P=0.029) were significant and so was the interactive effect of time and group (P<0.001). The clinical curative effect of the study group were significantly better compared with the control group at the 2, 4, 6 weeks following treatment (P<0.001). The adverse reactions were mild in these two groups. Conclusions The combi?nation of 1 Hz rTMS with duloxetine is superior to either medication alone for the treatment depression.