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Early filiform needle acupuncture for poststroke depression: a meta-analysis of 17 randomized controlled clinical trials 被引量:12
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作者 Jiping Zhang Jing Chen +4 位作者 Junqi Chen Xiaohui Li Xueyan Lai Shaoqun Zhang Shengxu Wang 《Neural Regeneration Research》 SCIE CAS CSCD 2014年第7期773-784,共12页
OBJECTIVE: To evaluate the effectiveness and safety of filiform needle acupuncture for poststroke depression, and to compare acupuncture with the therapeutic efficacy of antidepressant drugs. DATA RETRIEVAL: We retr... OBJECTIVE: To evaluate the effectiveness and safety of filiform needle acupuncture for poststroke depression, and to compare acupuncture with the therapeutic efficacy of antidepressant drugs. DATA RETRIEVAL: We retrieved data from the Chinese National Knowledge Infrastructure (1979-2012), Wanfang (1980-2012), VIP (1989-2012), Chinese Biomedical Literature (1975- 2012), PubMed (1966-2012), Ovid Lww (-2012), and Cochrane Library (-2012) Database using the internet. SELECTION CRITERIA: Randomized controlled trials on filiform needle acupuncture versus antidepressant drugs for treatment of poststroke depression were included. Moreover, the in- cluded articles scored at least 4 points on the Jadad scale. Exclusion criteria: other acupuncture therapies as treatment group, not stroke-induced depression patients, score 〈 4 points, non-ran- domized controlled trials, or animal trials. MAIN OUTCOME MEASURES: These were the Hamilton Depression Scale scores, clinical ef- fective rate, Self-Rating Depression Scale scores, Side Effect Rating Scale scores, and incidence of adverse reaction and events. RESULTS: A total of 17 randomized controlled clinical trials were included. Meta-analysis results displayed that after 4 weeks of treatment, clinical effective rate was better in patients treated with fill- form needle acupuncture than those treated with simple antidepressant drugs [relative risk = 1.11, 95% confidence interval (C/): 1.03-1.21, P = 0.01]. At 6 weeks, clinical effective rate was similar between filiform needle acupuncture and antidepressant drug groups. At 2 weeks after filiform needle acupuncture, Hamilton Depression Scale (17 items) scores were lower than in the antide- pressant drug group (mean difference = -2.34, 95%CI: -3.46 to -1.22, P 〈 0.000,1). At 4 weeks, Hamilton Depression Scale (24 items) scores were similar between filiform needle acupuncture and antidepressant drug groups. Self-Rating Depression Scale scores were lower in filiform needle acupuncture group than in the antidepressant drug group. Side Effect Rating Scale was used in only two articles, and no meta-analysis was conducted. Safety evaluation of the 17 arti- cles showed that gastrointestinal tract reactions such as nausea and vomiting were very common in the antidepressant drug group. Incidence of adverse reaction and events was very low in the filiform needle acupuncture group. CONCLUSION: Early filiform needle acupuncture for poststroke depression can perfectly con- trol depression. Filiform needle acupuncture is safe and reliable. Therapeutic effects of filiform needle acupuncture were better than those of antidepressant drugs. 展开更多
关键词 nerve regeneration poststroke depression filiform needle acupuncture antidepressantdrugs randomized controlled trials clinical effective rate SAFETY META-ANALYSIS the GuangdongProvincial "211 Engineering" Stage-III Key Disciplines Construction Project neural regeneration
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Clinical Observation of Huatanjieyu Granule in the Treatment of Post-stroke Depression 被引量:2
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作者 Xi WANG Chunqi AI +2 位作者 Lizhu LIU Dongyu XIA Qin GONG 《Medicinal Plant》 CAS 2020年第3期87-89,共3页
[Objectives]To observe the clinical effect of Huatanjieyu granule on patients with post-stroke depression.[Methods]Total 76 patients with confirmed post-stroke depression were randomly divided into two groups(treatmen... [Objectives]To observe the clinical effect of Huatanjieyu granule on patients with post-stroke depression.[Methods]Total 76 patients with confirmed post-stroke depression were randomly divided into two groups(treatment group and control group)according to the double-blind principle.The treatment group(38 cases)was treated with Huatanjieyu granule combined with escitalopram,and the control group(38 cases)was treated with escitalopram alone.The course of treatment was 6 weeks.Through clinical efficacy,Hamilton Depression Scale(HAMD)and Treatment Emergent Symptom Scale(TESS)scores were compared,and blood,liver function,renal function and electrocardiogram were examined.[Results]The scores of HAMD and TESS in patients with post-stroke depression were significantly decreased by Huatanjieyu granule,and there were no obvious side effects.The total effective rate was 92.1%in the treatment group and 76.3%in the control group.There was significant difference between the two groups(P<0.01).[Conclusions]Huatanjieyu granule was effective in the treatment of post-stroke depression with little side effects and was easy to be accepted by patients. 展开更多
关键词 Traditional Chinese medicine Huatanjieyu granule post-stroke depression clinical observation
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Lavender aromatherapy on anxiety and depression in patients with Acute Coronary Syndrome: a single-blind randomized clinical trial 被引量:1
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作者 Mohammad Nategh Mohammad Reza Heidari +3 位作者 Abbas Ebadi Reza Norouzadeh Zahra Mohebbinia Bahman Aghaie 《Frontiers of Nursing》 2022年第2期233-239,共7页
Objective:In cardiovascular disease,a patient’s anxiety and depression can increase cardiac rehabilitation duration and recovery.Lavender aromatherapy as a non-pharmacological intervention effective in other contexts... Objective:In cardiovascular disease,a patient’s anxiety and depression can increase cardiac rehabilitation duration and recovery.Lavender aromatherapy as a non-pharmacological intervention effective in other contexts may be an efficient intervention to alleviating anxiety and depression in patients with Acute Coronary Syndrome(ACS).Methods:In this study,110 ACS patients were randomly assigned to two intervention and control groups.Inhalation of the lavender fragrance was prescribed for the intervention group and the drop of aromatic almond for the control group for 3 days.Results:The first-day anxiety and depression were significantly different in the two groups at 1 h and 9 h after the intervention.The’morning’s difference before the intervention was not significant,but it was substantial 1 h after the intervention.On the third morning of the intervention,this difference was confirmed.Conclusions:This study confirmed the effectiveness of lavender aromatherapy in reducing anxiety and depression in ACS patients.This’study’s results enable intensive care nurses to use aromatherapy with lavender oil as a non-pharmacological and cost-effective intervention to reduce their psychological tensions and increase patient satisfaction during hospitalization in the cardiac care units(CCU). 展开更多
关键词 ANXIETY AROMATHERAPY Acute Coronary Syndrome depression LAVENDER randomized clinical trial
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Progress of Traditional Chinese Medicine in the Treatment of Post-stroke Depression
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作者 Shanbei ZHONG 《Medicinal Plant》 CAS 2022年第3期92-95,共4页
The patients with post-stroke depression often form a negative evaluation of themselves,and even have the idea of suicide in serious cases.Therefore,post-stroke depression has become one of the most common complicatio... The patients with post-stroke depression often form a negative evaluation of themselves,and even have the idea of suicide in serious cases.Therefore,post-stroke depression has become one of the most common complications of mental illness after stroke,which seriously hinders the normal rehabilitation of the central nervous system,thus increasing the disability rate,early recurrence rate and mortality rate of patients.Therefore,the active treatment of post-stroke depression is very necessary.Western medicine uses antidepressant drugs for this kind of patients,but because the side effects of antidepressants are relatively large,the compliance of patients is not good,it is not easy to see the effect,while traditional Chinese medicine(TCM)has many ways to deal with post-stroke depression with obvious advantages,the side effects are relatively small,and there is more compliance in patients.This paper focuses on several TCM treatment methods,hoping to provide a reference for the treatment of post-stroke depression. 展开更多
关键词 post-stroke depression TCM treatment clinical progress
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Efficacy of Lycium barbarum polysaccharide in adolescents with subthreshold depression: interim analysis of a randomized controlled study 被引量:7
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作者 Xiaoyue Li Xuan Mo +5 位作者 Tao Liu Robin Shao Kayla Teopiz Roger S.McIntyre Kwok-Fai So Kangguang Lin 《Neural Regeneration Research》 SCIE CAS CSCD 2022年第7期1582-1587,共6页
Subthreshold depression is a highly prevalent condition in adolescents who are at high risk for developing major depressive disorder.In preclinical models of neurological and psychiatric diseases,Lycium barbarum polys... Subthreshold depression is a highly prevalent condition in adolescents who are at high risk for developing major depressive disorder.In preclinical models of neurological and psychiatric diseases,Lycium barbarum polysaccharide(LBP)extracted from Goji berries had antidepressant effects including but not limited to anti-oxidative and anti-inflammatory properties.However,the effect of LBP on subthreshold depression is unclear.To investigate the clinical efficacy and safety of LBP for treating subthreshold depression in adolescents,we conducted a randomized,double-blind,placebo-controlled trial(RCT)with 29 adolescents with subthreshold depression recruited at The Fifth Affiliated Hospital of Guangzhou Medical University.The participants were randomly assigned to groups where they received either 300 mg LBP(LBP group,n=15,3 boys and 12 girls aged 15.13±2.17 years)or a placebo(placebo group,n=14,2 boys and 12 girls aged 15±1.71 years)for 6 successive weeks.Interim analyses revealed that the LBP group exhibited a greater change in Hamilton Depression Scale(HAMD-24)scores relative to the baseline and a higher remission rate(HAMD-24 total score≤7)at 6 weeks compared with the placebo group.Scores on the Beck Depression Inventory-II(BDI-II),Pittsburgh Sleep Quality Index(PSQI),Kessler Psychological Distress Scale(Kessler),and Screen for Child Anxiety-Related Emotional Disorders(SCARED)were similar between the LBP and placebo groups.No side effects related to the intervention were reported in either group.These results indicate that LBP administration reduced depressive symptoms in adolescents with subthreshold depression.Furthermore,LBP was well tolerated with no treatment-limiting adverse events.Clinical trials involving a larger sample size are needed to further confirm the anti-depressive effects of LBP in adolescents with subthreshold depression.This study was approved by the Medical Ethics Committee of the Fifth Affiliated Hospital of Guangzhou Medical University(Guangzhou,China;approval No.L2019-08)on April 4,2019 and was registered on ClinicalTrials.gov(identifier:NCT04032795)on July 25,2019. 展开更多
关键词 adolescents EFFICACY Goji berry Lycium barbarum polysaccharide randomized clinical trial SAFETY subthreshold depression TOLERANCE
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Efficacy and safety of Di-Tan Decoction for treating post-stroke neurological disorders:a systematic review and Meta-analysis of randomized clinical trials 被引量:2
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作者 Kwon Hyuk-Ku Zhang Ting +2 位作者 Wu Xuan Gao Qiu Jing Yi Park Sunmin 《Chinese Journal of Natural Medicines》 SCIE CAS CSCD 2021年第5期339-350,共12页
The management of post-stroke complications plays an important role in the quality of life.Di-Tan Decoction(DTD;涤痰汤)is a widely used traditional Chinese medicine.This study incorporated systematic review and meta-a... The management of post-stroke complications plays an important role in the quality of life.Di-Tan Decoction(DTD;涤痰汤)is a widely used traditional Chinese medicine.This study incorporated systematic review and meta-analysis to evaluate the efficacy of DTD in post-stroke neurological disorders.Randomized clinical trials(RCTs)were searched from English,Chinese and Korean electronic medical databases,by including the keywords"Di-Tan Tang","Di-Tan Decoction","Scour Phlegm Decoction","stroke",and"RCT.Each RCT included control(placebo,conventional therapy,or Western medicine)and experimental(DTD treatment)groups.For patients inflicted with stroke for 1-6 weeks,the outcomes of post-stroke neurological disorders were measured by scales for post-stroke symptoms and were classified as"completely healed","markedly effective","effective"and"ineffective".Totally,11 RCTs(n=490 controls and n=502 DTD subjects)were selected from 210 articles identified in the initial search.A metaanalysis of evaluation criteria in post-stroke symptoms revealed that the overall odds ratio(ORs)for alleviating post-stroke neurological disorders were 0.30-fold lower(95%CI=0.21-0.43)in the DTD group than the control(Western medicine)group(P<0.00001).Moreover,regardless of the type of stroke diagnostic scale applied(including NFA,HDS,and NIHSS),the overall post-stroke symptoms determined were less severe in the DTD group(n=219)than the control group(n=217).No adverse effects of DTD were observed in the 11 RCTs reviewed.All 11 studies used an appropriate method for randomization of subjects to evaluate the risk of bias(ROB),and 7 studies included allocation concealment as well as blinding of patients and practitioners.High-risk ROB was included in6 RCTs.No significant publication bias was derived from the funnel plot.Our results indicate that the administration of DTD alone,and DTD in combination with Western medicine,exert greater efficacy for post-stroke complication therapy,than Western medicine administered alone.More rigorous and regulated studies are required to confirm the therapeutic efficacy of DTD for post-stroke neurological disorders.disorders. 展开更多
关键词 Di-Tan Decoction post-stroke Adverse effects Randomized clinical trials Risk of bias
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Effect of Tiaoshen Kaiqiao acupuncture in the treatment of ischemic post-stroke depression:a randomized controlled trial 被引量:12
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作者 Li Menghan Zhang Bo +4 位作者 Meng Zhihong Sha Tao Han Yuhui Zhao Hong Zhang Chunhong 《Journal of Traditional Chinese Medicine》 SCIE CAS CSCD 2017年第2期171-178,共8页
OBJECTIVE:To observe the effect of Tiaoshen Kaiqiao acupuncture in the treatment of ischemic post-stroke depression.METHODS:This research was a single-blind, positive-controlled trial done in a single entity.Totally58... OBJECTIVE:To observe the effect of Tiaoshen Kaiqiao acupuncture in the treatment of ischemic post-stroke depression.METHODS:This research was a single-blind, positive-controlled trial done in a single entity.Totally58 patients with ischemic post-stroke depression were randomly divided into two groups.The acupuncture group was given Tiaoshen Kaiqiao acupuncture therapy and placebo starch tablets treatment,while the control group was treated with fluoxetine tablets and body acupuncture treatment.Evaluated the clinical efficacy of the two groups with Hamilton Depression Scale(HAMD),Anti Depression Drug Side Effects Rating Scale(SERS), Clinical Global Impression Scale(CGI) respectively before treatment, the fourth weekend of treatment, the eighth weekend of treatment,the twelfth weekend of treatment.The adverse reactions in two groups were observed and documented.RESULTS:The HAMD scale scores of the two groups in different treatment period were significantly decreased compared with that before treatment(P < 0.05); the score reduction of HAMD scale between the two groups had no significant differences(P > 0.05).There was significant difference between the SERS scores of two groups(P < 0.05); the control group had more adverse reactions, and the score would be increased with the extension of treatment time.Effect index(EI) of CGI in the acupuncture group is better than that of control group(P < 0.05).CONCLUSION:The effects of Tiaoshen Kaiqiao acupuncture and fluoxetine in the treatment of ischemic post-stroke depression were similar, but the former had no obvious adverse reaction and side effects. 展开更多
关键词 post-stroke depression ACUPUNCTURE FLUOXETINE Randomized controlled trial
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中医药治疗抑郁症临床试验注册现况分析
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作者 张乃金 马炳旭 +4 位作者 崔淮星 田家祺 曾仙月 孙璇 王泓午 《世界中医药》 CAS 北大核心 2024年第6期864-870,共7页
目的:基于中国临床试验注册中心(ChiCTR)和美国临床试验注册平台(ClinicalTrials.gov),分析中医药治疗抑郁症相关临床试验注册的热点及现状。方法:检索建库至2022年7月31日于中国临床试验注册中心和美国临床试验注册平台注册的中医药治... 目的:基于中国临床试验注册中心(ChiCTR)和美国临床试验注册平台(ClinicalTrials.gov),分析中医药治疗抑郁症相关临床试验注册的热点及现状。方法:检索建库至2022年7月31日于中国临床试验注册中心和美国临床试验注册平台注册的中医药治疗抑郁症的临床试验,提取相关资料并汇总分析。结果:纳入临床试验298项,共来自17个国家,涉及我国22个省级行政区的118家注册机构,其中注册数量前3的地域分别为北京市、广东省和上海市;纳入试验以单中心试验为主,研究类型以干预性研究为主,其中主要为随机对照试验;使用频率最高的随机方法为简单随机化方法,共118项随机对照试验明确说明应用了盲法;研究对象以卒中后抑郁症最多,干预措施以针灸最多,结局性指标以评分量表为主,使用次数最多的量表为汉密尔顿抑郁量表(HAMD)。结论:近年来相关学者对中医药治疗抑郁症临床试验注册重视程度有所提高,同时也存在试验注册地区分布不平衡、研究者在试验设计方面水平不足,对中医药临床试验特色挖掘不够等问题。 展开更多
关键词 抑郁症 中医药 临床试验 注册登记 中国临床试验注册中心 随机对照试验 分析
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Impacts of acupuncture and moxibustion on outcome indices of depression patients' subjective reports 被引量:3
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作者 樊凌 符文彬 +4 位作者 许能贵 刘健华 李滋平 欧爱华 WANG You-jing 《World Journal of Acupuncture-Moxibustion》 2013年第2期22-28,共7页
Objective To assess the clinical efficacy of acupuncture and moxibustion on depression based on the outcome indexes of the patient subjective reports. Methods One hundred and sixty-three cases of depression conformed ... Objective To assess the clinical efficacy of acupuncture and moxibustion on depression based on the outcome indexes of the patient subjective reports. Methods One hundred and sixty-three cases of depression conformed to the inclusive standards were randomized into a soothing liver and regulating mind group (group A), an acupoint shallow puncturing group (group B) and a non- acupoint shallow puncturing group (group C). In group A, the conventional acupuncture was applied to the four gate points [Hegu (合谷 LI 4) and Taichong (太冲 LR 3)], Baihui (百会 GV 20) and Yintang (印堂 GV 29), direct moxibustion with moxa cone was applied to the four flower points [Geshu (膈俞 BL 17), Danshu (胆俞 BL 19)]. Finally, intradermal needling was used at Xinshu (心俞 BL 15) and Ganshu (肝俞 BL 18). In group 13, the acupoints selected were same as those in the soothing liver and regulating mind group, with a shallower needling depth and a shorter duration of moxibustion. In group C, the spots selected were located at 10 mm lateral to the acupoints selected in group A, with same manipulation method as that in group 13. In all the three groups, the treatment was given twice a week, for 12 weeks. Before treatment, 1 month and 3 months after treatment, the scores of symptoms were respectively assessed with the symptom checklist 90 (SCL 90), and the corresponding short- term, mid-term and long-term efficacies of the acupuncture and moxibustion program for soothing the liver and regulating mind were investigated. Results At each time point after treatment, the scores of somatization, compulsion, depression, anxiety, hostility, extremeness, psychotic behavior and other 8 dimensionalit-ies were significantly different between group A and group C (all P〈0.05). In the scores of depression, anxiety and hostility there were significant differences between the group A and the group C (all P〈0.05). Conclusion Acupuncture and moxibustion can improve the scores of SCL 90 for the patients with depression, and the outcome indexes of the patient subjective reports can accurately assess the clinical efficacy. 展开更多
关键词 acupuncture moxibustion depression patient report outcome SCL 90 scale clinical trial
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帕罗西汀合用喹硫平治疗双重抑郁症的随机开放试验 被引量:37
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作者 王新法 吴焕 娄涛 《中国心理卫生杂志》 CSSCI CSCD 北大核心 2011年第3期196-199,共4页
目的:评价帕罗西汀合用喹硫平治疗双重抑郁症的疗效和安全性。方法:将符合中国精神障碍分类与诊断标准第三版(Chinese classification and diagnostic criteria of mental disorders,CCMD-3)双重抑郁症诊断标准的66例门诊及住院患者随... 目的:评价帕罗西汀合用喹硫平治疗双重抑郁症的疗效和安全性。方法:将符合中国精神障碍分类与诊断标准第三版(Chinese classification and diagnostic criteria of mental disorders,CCMD-3)双重抑郁症诊断标准的66例门诊及住院患者随机分为两组,研究组(n=34)给予帕罗西汀合用喹硫平治疗,对照组(n=32)给予帕罗西汀治疗,疗程12周。于治疗前和治疗后2、4、6、8、12周分别使用汉密顿抑郁量表(Hanmilton Depression Scale,HAMD)、汉密顿焦虑量表(Hanmilton Anxiety Scale,HAMA)、临床总体印象疗效总评量表的病情严重程度(Clinical Global Impression,CGI)、不良反应量表(Treatment E-mergent Symptom Scale,TESS)评定疗效和不良反应。HAMD总分≤7分为痊愈;HAMD总分>7分,减分率≥50%为好转,痊愈和好转合称有效。结果:治疗前研究组和对照组HAMD、HAMA评分差异无统计学意义(P>0.05)。治疗12周后,研究组和对照组的HAMD、HAMA评分均低于治疗前(Ps<0.05);研究组6、8、12周HAMD、HAMA评分均低于对照组(Ps<0.05);研究组有效率高于对照组(P<0.05);两组间不良反应发生率差异无统计学意义(P>0.05)。结论:帕罗西汀合用喹硫平治疗双重抑郁症疗效较好,安全性高。 展开更多
关键词 帕罗西汀 喹硫平 双重抑郁症 临床试验
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消痰解郁方治疗消化系统癌症并发抑郁症随机对照临床研究 被引量:9
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作者 杨玉兴 魏品康 +3 位作者 修丽娟 矫建鹏 孙大志 燕忠生 《中国中医药信息杂志》 CAS CSCD 2013年第2期12-16,共5页
目的评价消痰解郁方治疗消化系统癌症并发抑郁症的有效性与安全性。方法采用前瞻性、完全随机、平行对照方法,将120例消化系统癌症并发抑郁症患者分为治疗组(消痰解郁方,60例)、中药对照组(逍遥丸,30例)和西药对照组(盐酸氟西汀,30例),... 目的评价消痰解郁方治疗消化系统癌症并发抑郁症的有效性与安全性。方法采用前瞻性、完全随机、平行对照方法,将120例消化系统癌症并发抑郁症患者分为治疗组(消痰解郁方,60例)、中药对照组(逍遥丸,30例)和西药对照组(盐酸氟西汀,30例),治疗6周,治疗前后测评患者KPS评分、抑郁自评量表(SDS)、汉密顿抑郁量表(HAMD),并检测血清T细胞亚群及NK细胞水平。结果消痰解郁方可以改善患者的临床症状、提高KPS评分,降低SDS和HAMD分值;升高血清NK细胞、CD3和CD4/CD8,降低CD8,差异有统计学意义(P<0.05,P<0.01),总有效率为82.46%(47/60),优于中药和西药对照组(P<0.05,P<0.01),且无不良反应。结论消痰解郁方治疗消化系统癌症并发抑郁症安全有效。 展开更多
关键词 消化系统癌症 抑郁症 消痰解郁方 临床随机对照试验
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国产安非他酮缓释片治疗抑郁症的Ⅱ期临床研究 被引量:5
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作者 姜荣环 张鸿燕 +4 位作者 舒良 杜波 李华芳 马崔 刘忠纯 《中国新药杂志》 CAS CSCD 北大核心 2006年第2期128-131,共4页
目的:评价安非他酮治疗抑郁症的疗效和安全性。方法:采用随机、双盲、多中心、平行对照研究。共入组抑郁症患者237例,其中试验组119例,对照组118例,分别口服安非他酮150~450 mg·d-1,氟西汀10~30 mg·d-1。疗程均为6周。用汉... 目的:评价安非他酮治疗抑郁症的疗效和安全性。方法:采用随机、双盲、多中心、平行对照研究。共入组抑郁症患者237例,其中试验组119例,对照组118例,分别口服安非他酮150~450 mg·d-1,氟西汀10~30 mg·d-1。疗程均为6周。用汉密尔顿抑郁量表(HAMD)和临床总体印象量表(CGI)评定疗效,药物不良反应量表(TESS)评定安全性。结果:治疗6周后两组患者HAMD评分较基线均显著降低(P<0.05),总有效率安非他酮组70.69%,氟西汀组74.14%。组间差异无显著性(P>0.05)。不良反应发生率安非他酮组41.4%,氟西汀组44.8%,组间差异无显著性(P>0.05)。结论:安非他酮治疗抑郁症安全有效。 展开更多
关键词 安非他酮 氟西汀 抑郁症 Ⅱ期临床试验
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心理干预对肺癌患者焦虑抑郁症状影响的Meta分析 被引量:41
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作者 王丽娟 刘威 《中国全科医学》 CAS CSCD 北大核心 2013年第7期808-810,共3页
目的采用Meta分析的方法探讨心理干预对肺癌患者焦虑抑郁症状的影响。方法计算机检索万方、维普、CNKI及中国生物医学等中文数据库,全面收集有关心理干预对肺癌患者焦虑抑郁症状影响的临床对照试验,汇总数据采用RevMan 5.1.6和Stata 12.... 目的采用Meta分析的方法探讨心理干预对肺癌患者焦虑抑郁症状的影响。方法计算机检索万方、维普、CNKI及中国生物医学等中文数据库,全面收集有关心理干预对肺癌患者焦虑抑郁症状影响的临床对照试验,汇总数据采用RevMan 5.1.6和Stata 12.0进行分析,两组之间差异采用标准均数差(SMD)或OR及其95%CI描述。结果根据纳入和排除标准最终纳入8个临床对照试验,包括608例肺癌患者,其中观察组349例,对照组259例。Meta分析结果表明:治疗前,心理干预组与对照组患者抑郁自评量表(SDS)评分〔SMD=0.61,95%CI(-0.63,1.86),P=0.33〕和焦虑自评量表(SAS)评分〔SMD=-0.01,95%CI(-1.08,1.05),P=0.98〕差异均无统计学意义(P>0.05);治疗后,心理干预组患者SDS评分〔SMD=-1.03,95%CI(-1.64,-0.43),P=0.0007〕和SAS评分〔SMD=-1.11,95%CI(-2.24,0.02),P=0.05〕低于对照组患者,两组之间差异有统计学意义(P≤0.05)。结论现有证据表明,心理干预可有效地改善肺癌患者的焦虑抑郁症状,改善患者生活质量。由于纳入研究质量及数量有限,本研究结论尚需大样本高质量临床研究进行证实。 展开更多
关键词 心理干预 肺肿瘤 焦虑 抑郁 临床对照研究 META分析
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中药治疗中风后抑郁症用药规律探讨 被引量:25
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作者 段艳霞 李洁 史美育 《中华中医药学刊》 CAS 2011年第6期1419-1421,共3页
目的:总结历年来发表的中药治疗中风后抑郁症(PSD)临床研究文献中的常用方药,以期为PSD的中药治疗与研究提供可信的参考依据。方法:计算机检索中国生物医学文献数据库(CBMd isc 1979 to 4/2008)、中国知网中国期刊全文数据库(CNK I 1994... 目的:总结历年来发表的中药治疗中风后抑郁症(PSD)临床研究文献中的常用方药,以期为PSD的中药治疗与研究提供可信的参考依据。方法:计算机检索中国生物医学文献数据库(CBMd isc 1979 to 4/2008)、中国知网中国期刊全文数据库(CNK I 1994 to 4/2008)、重庆维普中文科技期刊数据库(VIP 1989 to 4/2008)中文数据库和Pubm ed、EMbase英文数据库,并手工检索相关杂志,收集发表的关于中药治疗PSD的随机对照试验(RCT)和临床对照试验(CCT)的临床文献。应用频次和构成比统计有效中药的种类和药物,分析其用药规律。结果:75篇文献纳入研究,有70篇提供了基本方,应用频次居前10位的药物种类依次为补益药、活血化瘀药、理气药、安神药、解表药、化痰止咳平喘药、清热药、开窍药、利水渗湿药和平肝熄风药;应用频次居前10位的单味中药依次为柴胡、郁金、菖蒲、当归、甘草、白芍、川芎、远志、香附、茯苓。结论:中医药治疗中风后抑郁症,多以活血化瘀、疏肝理气和补益正气、养心安神为最基本方法,同时配合应用化痰、祛湿、调理脾胃、滋养肝肾等多种治法和药物,标本兼治,方能收到良好的治疗效果。 展开更多
关键词 中药 中风后抑郁症 临床试验 用药规律
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心理干预对糖尿病患者焦虑抑郁症状及血糖控制影响的Meta分析 被引量:54
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作者 付明媚 董雅娟 《中国全科医学》 CAS CSCD 北大核心 2013年第4期436-439,共4页
目的采用Meta分析的方法探讨心理干预对我国糖尿病患者焦虑抑郁症状及血糖控制的影响。方法计算机检索万方、维普、CNKI及中国生物医学等中文数据库,全面收集有关心理干预对糖尿病患者焦虑抑郁症状及血糖控制影响的临床对照试验,汇总... 目的采用Meta分析的方法探讨心理干预对我国糖尿病患者焦虑抑郁症状及血糖控制的影响。方法计算机检索万方、维普、CNKI及中国生物医学等中文数据库,全面收集有关心理干预对糖尿病患者焦虑抑郁症状及血糖控制影响的临床对照试验,汇总数据采用RevMan5.1.6和Stata12.0进行分析,两组之间差异采用SMD或OR及其95%c,描述。结果根据纳入和排除标准最终纳入25个临床对照试验,包括2417例糖尿病患者,其中心理干预组1239例,对照组1178例。Meta分析结果表明:治疗前,心理干预组与对照组患者抑郁自评量表(SDS)评分和焦虑自评量表(SAS)评分差异均无统计学意义(P〉0.05);治疗后,两组之间SDS评分[SMD=-1.32,95%CI(-1.74,-0.90),P〈0.00001]和SAS评分[SMD=-1.06,95%CI(-1.62,-0.50),P=0.0002]差异均有统计学意义。此外,治疗后两组之间空腹血糖[sMD=-1.18,95%CI(-1.56,-0.81),P〈0.00001]、餐后2h血糖[SMD=-0.62,95%CI(-0.74,-0.50),P〈0.00001]及糖化血红蛋白水平[sMD=-1.35,95%c,(-2.02,-O.68),P〈0.0001]差异亦有统计学意义,而治疗前差异无统计学意义(P〉0.05)。结论现有证据表明,心理干预可有效地改善糖尿病患者的抑郁和焦虑症状,并可较好地控制血糖水平,显著降低空腹血糖、餐后2小时血糖及糖化血红蛋白水平。由于纳入研究质量及数量有限,本研究结论尚需大样本高质量临床研究进行证实。 展开更多
关键词 心理干预 糖尿病 焦虑 抑郁 临床对照研究 META分析
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认知行为疗法和帕罗西汀治疗对轻型抑郁障碍的临床对照研究 被引量:5
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作者 桑文华 张迪然 +4 位作者 田国庆 于雪竹 刘建丛 杨老虎 张彦恒 《中国循证医学杂志》 CSCD 2007年第10期711-714,共4页
目的比较认知行为疗法和帕罗西汀对轻型抑郁障碍患者的临床疗效及预后差异。方法制定一套适用于轻型抑郁障碍的认知行为治疗操作手册。将64例符合DSM-Ⅳ诊断标准的轻型抑郁障碍患者分为认知行为治疗组和帕罗汀治疗组各32例,治疗6周,用... 目的比较认知行为疗法和帕罗西汀对轻型抑郁障碍患者的临床疗效及预后差异。方法制定一套适用于轻型抑郁障碍的认知行为治疗操作手册。将64例符合DSM-Ⅳ诊断标准的轻型抑郁障碍患者分为认知行为治疗组和帕罗汀治疗组各32例,治疗6周,用汉密顿抑郁量表评定两组治疗前和治疗后第2、4、6周末的减分值、6周后疗效及6个月随访时的复发/再燃率及其副作用。结果①治疗有第6周末两组减分值差异有统计学意义(F=8.3,P=0);②帕罗汀治疗组和认知行为治疗组在第6周末两组疗效差异无统计学意义(u=316.5,P=0.06),其中帕罗汀治疗组痊愈率为20.7%,显效率为48.3%,认知行为治疗组痊愈率为10.0%,显效率为36.7%。③随访时6个月时,帕罗汀组复发(包括再燃率)高于认知行为治疗组(u=106.5,P=0.04)。结论单纯认知行为治疗与帕罗汀治疗在一定程度上疗效相当,所制定的手册针对轻型抑郁障碍患者的特点,对于轻型抑郁障碍有一定的治疗效果,可在临床推广试用。 展开更多
关键词 心理学 认知行为疗法 帕罗西汀 抑郁障碍 临床对照研究
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吗氯贝胺与米帕明治疗抑郁症多中心双盲对照试验 被引量:3
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作者 周沫 刘平 +7 位作者 舒良 谭春香 老洪尧 郑洪波 顾世芬 范俭雄 宣妙珍 李永远 《中国心理卫生杂志》 CSSCI CSCD 北大核心 2002年第10期714-716,共3页
目的 :以经典抗抑郁药物米帕明为阳性对照药采用随机双盲双模拟方法对吗氯贝胺和米帕明治疗抑郁症的疗效和安全性进行研究。方法 :共纳入病人 2 0 0例 ,分别口服吗氯贝胺 3 0 0 -60 0mg d或米帕明75 -2 5 0mg d。结果 :两组病人Hamilto... 目的 :以经典抗抑郁药物米帕明为阳性对照药采用随机双盲双模拟方法对吗氯贝胺和米帕明治疗抑郁症的疗效和安全性进行研究。方法 :共纳入病人 2 0 0例 ,分别口服吗氯贝胺 3 0 0 -60 0mg d或米帕明75 -2 5 0mg d。结果 :两组病人Hamilton抑郁量表 (HAMD)以及Hamilton焦虑量表 (HAMA)总分在治疗结束时均显著下降 (P <0 0 0 1)。两组之间疗效无显著差异 (p >0 0 5 )。治疗结束时HAMD减分率分别为吗氯贝胺组 0 74± 0 2 4,米帕明组 0 74± 0 2 4(P >0 0 5 ) ;有效率吗氯贝胺组 79 4% ,米帕明组 85 4% (P >0 0 5 )。吗氯贝胺组有 10种不良反应发生频率显著低于米帕明组 ,主要是抗胆碱能、中枢神经系统及心血管系统不良反应。吗氯贝胺的疗效指数也显著高于米帕明组。结论 展开更多
关键词 吗氯贝胺 米帕明 抑郁症 临床试验 疗效 安全性
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军队老年人群抑郁症状与体质相关关系调查 被引量:8
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作者 吕全江 封颖璐 +1 位作者 顾伟 方凡夫 《解放军医院管理杂志》 2013年第5期476-478,共3页
目的了解军队老年人群抑郁症状发生情况,掌握该群体抑郁患者的中医体质分型及特点,为从体质着手防治抑郁症状提供依据。方法采取横断面现场调查填写老年人生活质量调查表和老年抑郁短量表,并复核干休所个人医疗档案相结合的方法。结果... 目的了解军队老年人群抑郁症状发生情况,掌握该群体抑郁患者的中医体质分型及特点,为从体质着手防治抑郁症状提供依据。方法采取横断面现场调查填写老年人生活质量调查表和老年抑郁短量表,并复核干休所个人医疗档案相结合的方法。结果军队老年人群抑郁症状发生率为19.5%,三个年龄段抑郁症状发生率无明显差异(P>0.05);在抑郁人群中,位于前3位的体质分别为气郁质、气虚质和阴虚质;非抑郁人群中,位于前3位的体质分别是平和质、气虚质和痰湿质,两组人群的体质构成分布不同(P<0.05)。与轻度症状组相比,中、重度症状人群中气虚质比例分别达到43.8%和30.5%(P=0.00,P=0.005),阴虚质比例分别为16%和15%(P=0.016,P=0.016);轻度抑郁症状者气郁质明显高于其它两组(P=0.02);重度抑郁人群中湿热质占16.6%,明显高于轻度抑郁症状者(P=0.003)。结论军队老年人群抑郁症状发生率为19.5%;气虚质、气郁质和阴虚质是抑郁人群常见的体质类型;抑郁和非抑郁人群的体质构成分布不同;抑郁症状程度与体质类型有密切关系。 展开更多
关键词 老年人 抑郁症状 体质 临床试验 横断面研究
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刺五加联合碳酸锂对青少年双相障碍抑郁发作的疗效观察 被引量:3
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作者 唐记华 王高华 +4 位作者 白雪光 王晓萍 翁深宏 刘忠纯 刘浩 《中国心理卫生杂志》 CSSCI CSCD 北大核心 2005年第7期480-482,共3页
目的:探讨刺五加联合碳酸锂对青少年双相障碍抑郁发作的疗效及不良反应。方法:连续收集门诊及住院的12-17岁双相障碍抑郁发作患者65例,采用随机双盲对照试验设计,将入选对象分为A组刺五加联合碳酸锂治疗组,B组氟西汀联合碳酸锂治疗组,疗... 目的:探讨刺五加联合碳酸锂对青少年双相障碍抑郁发作的疗效及不良反应。方法:连续收集门诊及住院的12-17岁双相障碍抑郁发作患者65例,采用随机双盲对照试验设计,将入选对象分为A组刺五加联合碳酸锂治疗组,B组氟西汀联合碳酸锂治疗组,疗程6周,以汉密尔顿抑郁量表(HAMD)减分情况评定疗效,不良反应症状量表(TESS)评定不良反应。结果:研究结束后有效病例63例(A组32例,B组31 例),脱落2例(均为B组)。进行意向(ITT)分析A组32例,B组33例,按符合方案(PP)分析前者32例, 后者31例。两组治疗后各周HAMD评分均较疗前有显著降低(P<0.001),治疗后各周A、B两组之间HAMD减分t检验,差异亦无显著性(P>0.05),疗程结束时两组显效率和有效率差异无显著性(P>0.05)。B组有2例治疗过程中出现病情转相,但转躁率两组之间无显著差异。结论:刺五加联合碳酸锂治疗青少年双相障碍抑郁发作有明显的效果,且无转躁发生,是安全有效的治疗方案。 展开更多
关键词 双相障碍 抑郁发作 临床试验 刺五加
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文拉法辛缓释剂治疗伴或不伴高血压的老年期抑郁症对照研究 被引量:7
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作者 袁勇贵 李海林 《中国心理卫生杂志》 CSSCI CSCD 北大核心 2006年第5期339-341,共3页
目的:探讨文拉法辛缓释剂对伴有高血压的老年期抑郁症的疗效和安全性。方法:使用文拉法辛缓释剂对30例伴有高血压的老年期抑郁症和30例无高血压的老年期抑郁症患者进行为期6周的对照治疗,在治疗前及治疗后第1、2、4、6周末评定汉密尔顿... 目的:探讨文拉法辛缓释剂对伴有高血压的老年期抑郁症的疗效和安全性。方法:使用文拉法辛缓释剂对30例伴有高血压的老年期抑郁症和30例无高血压的老年期抑郁症患者进行为期6周的对照治疗,在治疗前及治疗后第1、2、4、6周末评定汉密尔顿抑郁量表(HAMD 17项),并进行临床疗效评定, 监测血压,记录不良反应。结果:高血压组和非高血压组患者的HAMD评分均从第1周末起明显下降(P< 0.05或P<0.01),且一直持续至治疗第6周末。两组6周末的有效率和临床治愈率差异无显著性(P> 0.05)。高血压组患者使用文拉法辛缓释剂治疗后第2周末收缩压变化值显著高于非高血压患者(0.9±0.4, 0.6±0.5,P=0.01)。两组间的不良反应发生率差异无统计学意义(P>0.05)。结论:文拉法辛缓释剂治疗老年期抑郁症疗效肯定,不良反应少,对血压无明显影响。 展开更多
关键词 抑郁症 老年 开放性临床试验 高血压 文拉法辛
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