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Clinical efficacy and safety of Guipi decoction combined with escitalopram oxalate tablets in patients with depression 被引量:1
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作者 Jia Yu Feng-Quan Xu 《World Journal of Clinical Cases》 SCIE 2023年第29期7017-7025,共9页
BACKGROUND Depression is a widespread mental health condition that requires effective treatment.In the treatment of depression,traditional Chinese medicine(TCM)offers obvious advantages,fewer adverse reactions,and a l... BACKGROUND Depression is a widespread mental health condition that requires effective treatment.In the treatment of depression,traditional Chinese medicine(TCM)offers obvious advantages,fewer adverse reactions,and a lower recurrence rate.AIM To evaluate the clinical benefits of Guipi decoction combined with escitalopram oxalate tablets for individuals with depression.METHODS In total,80 patients diagnosed as having depression were enrolled in the study and divided into either an experimental group or a control group.All of the patients were orally administered escitalopram oxalate tablets.Additionally,the experimental group received Jiajian Guipi decoction and reduced Governor vessel fumigation over 4 wk.TCM syndrome scores,Hamilton depression rating scale(HAM-D)scores,self-rating depression scale(SDS)scores,and Pittsburgh sleep quality index scores were measured for the two groups and compared before and after the treatment.The two groups were monitored for any adverse reactions.RESULTS After 4 wk of treatment,both groups exhibited a significant reduction in TCM syndrome scores compared with their pre-treatment scores(P<0.05).However,the experimental group exhibited significantly lower TCM syndrome scores than the control group(P<0.05).Similarly,the post-treatment SDS and HAM-D-24 scores were significantly lower in both groups than the pre-treatment scores(P<0.05),with the experimental group exhibiting lower scores than the control group(P<0.05).The total treatment efficiency was significantly better in the experimental group(97.14%)than in the control group(77.78%)(P<0.05).Furthermore,after 4 wk of treatment,the Pittsburgh sleep quality index scores for both groups were significantly lower than those before the treatment(P<0.05),with the experimental group exhibiting lower scores than the control group(P<0.05).The incidence of adverse reactions was significantly lower in the experimental group than in the control group(P<0.05).CONCLUSION The combination of Guipi decoction and escitalopram oxalate tablets was found to be an effective and safe treatment for depression.This combination could reduce TCM syndrome scores,improve depressive symptoms,and enhance sleep quality. 展开更多
关键词 Jiajian Guipi decoction escitalopram oxalate tablets Depressive disorder Sleep quality Traditional Chinese medicine syndromes
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Pumpkin seed ethanolic extract protects against escitalopram-induced reproductive toxicity in male mice
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作者 Agrawal Karuna Shahani Lata Bhatnagar Pradeep 《Asian pacific Journal of Reproduction》 2023年第2期71-80,共10页
Objective:To investigate the protective role of pumpkin seed ethanolic extract against escitalopram-induced reproductive toxicity in male mice.Methods:Swiss albino male mice were randomly divided into five groups with... Objective:To investigate the protective role of pumpkin seed ethanolic extract against escitalopram-induced reproductive toxicity in male mice.Methods:Swiss albino male mice were randomly divided into five groups with six mice in each group.Group Ⅰreceived normal water orally,Group Ⅱ,Ⅲ,Ⅳand Ⅴreceived escitalopram oxalate(10 mg/kg),pumpkin seed extract(300 mg/kg)plus escitalopram oxalate(10 mg/kg),escitalopram oxalate(20 mg/kg),and pumpkin seed extract(300 mg/kg)plus escitalopram oxalate(20 mg/kg),respectively.All test doses were continuously administered orally once daily per animal body weight for 30 days and 60 days.Body weight and sexual organ weight were evaluated on day 31 and 61.Effects of pumpkin seed extract on sperm parameters,biochemical parameters and histology of testis were also investigated.Results:Escitalopram 10 or 20 mg/kg caused reproductive toxicity in male mice after 30 and 60 days of treatment.However,simultaneous administration of escitalopram oxalate(10 or 20 mg/kg)with pumpkin seed extract(300 mg/kg)attenuated escitalopram-induced testicular toxicity.Significant increase in the body weight and relative organ weight was observed.Sperm count,sperm motility and viability significantly increased(P<0.05).The histopathological alterations caused by escitalopram was also ameliorated.Conclusions:Ethanolic extract of pumpkin seeds(300 mg/kg body weight)protects again reproductive toxicity induced by escitalopram.Therefore,dietary intake of pumpkin seed extract might be useful for male patients who expose to antidepressant drug due to depression. 展开更多
关键词 escitalopram oxalate Pumpkin seeds Testicular toxicity Sperm parameters Male Swiss albino mice
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Pilot study of genome-wide DNA methylation and gene expression for treatment response to escitalopram in panic disorder
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作者 Zhi-Li Zou Yuan Zhang +3 位作者 Yu-Lan Huang Jin-Yu Wang Bo Zhou Hua-Fu Chen 《World Journal of Psychiatry》 SCIE 2023年第8期524-532,共9页
BACKGROUND Antidepressants,particularly selective serotonin reuptake inhibitors,are currently considered the first-line treatment for panic disorder(PD).However,little is known about the relationship between the bioma... BACKGROUND Antidepressants,particularly selective serotonin reuptake inhibitors,are currently considered the first-line treatment for panic disorder(PD).However,little is known about the relationship between the biomarkers that may predict better treatment.AIM To compare genome-wide methylation and gene expression patterns between responsive and non-responsive patients with PD after 4 wk of escitalopram treatment.METHODS Thirty patients with PD were enrolled in this study(responders=13;nonresponders=17).All patients were assessed using the PD Severity Scale-Chinese version before and after treatment.The Illumina Infinium MethylationEPIC(850k)BeadChip for genome-wide methylation screening and mRNA sequencing was used in all patients with PD.RESULTS A total of 701 differentially methylated positions(DMPs)were found between responders and non-responders(|Δβ|≥0.06,q<0.05),and the hyper-and hypomethylated CpG sites were 511(72.9%)and 190(27.1%),respectively.Relative to non-responders,there were 59 differential transcripts,of which 20 were downregulated and 39 were upregulated(q<0.05).However,no differen tially expressed genes were identified by mRNA sequencing after correcting for multiple testing(|log2(FC)|>1,q>0.05).CONCLUSION This preliminary study showed that DMPs might be associated with the treatment response to escitalopram in PD;however,these DMPs need to be verified in large samples. 展开更多
关键词 Panic disorder METHYLATION Expression profiling escitalopram
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Neuroprotective Effect of Escitalopram Oxalate in Rats with Chronic Hypoperfusion 被引量:5
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作者 马莉 卢祖能 +1 位作者 胡沛 姚长江 《Journal of Huazhong University of Science and Technology(Medical Sciences)》 SCIE CAS 2015年第4期514-518,共5页
Summary: The neuroproteetive effects of escitalopram oxalate in rats with chronic hypoperfusion and the possible mechanism were explored. Chronic hypoperfusion (2-VO) model was prepared and given escitalopram oxala... Summary: The neuroproteetive effects of escitalopram oxalate in rats with chronic hypoperfusion and the possible mechanism were explored. Chronic hypoperfusion (2-VO) model was prepared and given escitalopram oxalate (experimental group) or PBS (control group) after 6 weeks. Eight weeks after the operation, Morris water maze test was carried out to evaluate the learning and memory ability of the rats. The cell proliferation, three-dimensional vascular distribution, cell morphological changes in ischemic area and the plasma vascular endothelial growth factor (VEGF) were detected to explore the possible mechanisms. (1) Morris water maze test showed that the escape latency in the experimental group was significantly shorter than in the control group, while the first quadrant swimming time in the experi- mental group was significantly longer than the control group (both P〈0.01). (2) Cerebrovascular confo- cal detection results showed that the inside diameter of capillaries was significantly less in the experi- mental group than in the control group; the vascular density was significantly increased in the experi- mental group and the total area of capillaries was also significantly increased in the experimental group as compared with the control group. (3) There was statistically significant difference in BrdU-positive cells in the ischemic brain tissue between the experimental group and the control group (P=0.003〈0.01). (4) VEGF concentrations in the plasma and the ischemic area were higher in the experimental group than in the control group (P〈0.05). It was concluded that escitalopram oxalate could significantly im- prove the learning and memory ability of the rats with chronic cerebral ischemia probably by the VEGF-mediated angiogenesis. 展开更多
关键词 escitalopram oxalate chronic hypoperfusion NEUROPROTECTION MECHANISM vascular endo- thelial growth factor
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Escitalopram-induced liver injury: A case report and review of literature 被引量:3
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作者 Qin Xiang Ng Christl Suet Kwan Yong +2 位作者 Wayren Loke Wee Song Yeo Alex Yu Sen Soh 《World Journal of Hepatology》 CAS 2019年第10期719-724,共6页
BACKGROUND Depression is a growing public health problem that affects over 350 million people globally and accounts for approximately 7.5%of healthy years lost due to disability.Escitalopram,one of the first-line medi... BACKGROUND Depression is a growing public health problem that affects over 350 million people globally and accounts for approximately 7.5%of healthy years lost due to disability.Escitalopram,one of the first-line medications for the treatment of depression,is a selective serotonin reuptake inhibitor and one of the most commonly prescribed antidepressant medications worldwide.Although thought to be generally safe and with minimal drug-drug interactions,we herein present an unusual case of cholestatic liver injury,likely secondary to escitalopram initiation.CASE SUMMARY A 56-year-old Chinese lady presented with fever and cholestatic liver injury two weeks after initiation of escitalopram for the treatment of psychotic depression.Physical examination was unremarkable.Further investigations,including a computed tomography scan of the abdomen and pelvis and tests for hepatitis A,B and C and for autoimmune liver disease were unyielding.Hence,a diagnosis of escitalopram-induced liver injury was made.Upon stopping escitalopram,repeat liver function tests showed downtrending liver enzymes with eventual normalization of serum aspartate aminotransferase and alanine aminotransferase one-week post-discharge.CONCLUSION Clinicians should be aware of the possibility of escitalopram-induced liver injury when initiating depressed patients on antidepressant treatment.This requires extra vigilance as most patients may remain asymptomatic.Measurement of liver function tests could be considered after initiation of antidepressant treatment,especially in patients with pre-existing liver disease. 展开更多
关键词 DEPRESSION ANTIDEPRESSANT escitalopram LIVER INJURY DRUG-INDUCED Druginduced LIVER INJURY
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Effect of escitalopram on cognitive function in depressionA mismatch negativity potentials study
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作者 Zhenhe Zhou Guozhen Yuan Jianjun Yao Zaohuo Cheng 《Neural Regeneration Research》 SCIE CAS CSCD 2011年第31期2441-2445,共5页
We detected the event-related potential mismatch negativity (MMN) of 30 depression patients and compared to 30 age,gender,and education-matched healthy controls.Results showed that amplitudes of frequency and durati... We detected the event-related potential mismatch negativity (MMN) of 30 depression patients and compared to 30 age,gender,and education-matched healthy controls.Results showed that amplitudes of frequency and duration MMN were lower in depression patients compared with control patients,indicating abnormality in auditory processing (i.e.,cognitive impairment).Following escitalopram treatment for 8 weeks,the amplitudes of frequency and duration MMN were significantly increased and Hamilton Rating Scale for Depression scores were significantly decreased in depression patients.These data suggest that escitalopram can improve cognitive function of patients with depression.Further,MMN may be a useful tool for evaluating cognitive function and treatment effects. 展开更多
关键词 DEPRESSION event-related potentials mismatch negativity cognitive function escitalopram
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The Efficacy of Escitalopram Combined with Olanzapine in Depression:A Systematic Review and Meta-analysis 被引量:1
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作者 SUN Xuan WANG Zhe +8 位作者 MIAO Tian-de WANG Dong-jun GUAN Yuan-yuan TIAN Zhi-kui TIAN Chun-ying ZHU Qing-qing ZHOU Zong-hui BU Huai-en WANG Hong-wu 《World Journal of Integrated Traditional and Western Medicine》 2021年第5期24-35,共12页
Background:Depression will become the second most common disease after coronary heart disease(CHD).Escitalopram and olanzapine are commonly used to treat depression.Some studies indicated that escitalopram combined wi... Background:Depression will become the second most common disease after coronary heart disease(CHD).Escitalopram and olanzapine are commonly used to treat depression.Some studies indicated that escitalopram combined with olanzapine is effective in treating depression,however,there is no evidence to support these results.Our objective was to study the efficacy of escitalopram combined with olanzapine on depression by conducting a systematic review and meta analysis,and to provide reference for doctors.Methods:Relevant evidence were searched from PubMed,SinoMed,the Cochrane Library,Web of Science,Embase,China Knowledge Resource Integrated(CNKI),Wanfang Data Knowledge Service Platform databases(WANFANG)and VIP dating from inception to July 2020.The randomized controlled trials(RCTs)of escitalopram and olanzapine for the treatment of depression was obtained.According to inclusion and exclusion criteria,two researches(Sun Wu and Wang Zhe)independently screened the literature,extracted data,and evaluated the quality of included studies.Rev Man 5.3 software was used to conduct statistical analyze.Results:A total of 39 studies involving 3,267 patients were identified.These studies were finally included into the meta-analysis.Pooled results showed that there was a significant difference in efficiency(RR=1.18,95%CI:1.14 to 1.12,P<0.00001),HAMD(MD=-4.54,95%CI:-5.09 to-3.99,P<0.00001),and HAMA(MD=-3.94,95%CI:-5.57 to-2.12,P<0.0001).There was no significant difference in adverse reactions(MD=0.07,95%CI-0.03 to 0.17,P=0.19).Heterogeneity test showed that due to the high heterogeneity of HAMD(P<0.00001,12=86%)and HAMA(P<0.00001,I2=91%),after removing the items with high heterogeneity,there were also statistically significant in HAMD(MD=-5.22,95%CI:-5.53 to-4.91,P<0.00001)and HAMA(MD=-5.46,95%CI:-6.15 to-4.77,P<0.00001).Conclusion:Based on this study,the combination of escitalopram and olanzapine was more effective in treating depression than the control group.It is suggested that clinical and scientific researchers carry out more high-quality,large-sample,multi-center RCTs to provide more evidence-based medical evidence for the future study of escitalopram combined with olanzapine in the treatment of depression. 展开更多
关键词 escitalopram OLANZAPINE DEPRESSION META-ANALYSIS Randomized controlled trials
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Relief of hot flashes with escitalopram in non-depressed menopausal women in Japan: Results of a retrospective analysis
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作者 Chikako Mori Atsushi Imai 《Health》 2012年第10期893-896,共4页
Purpose: Hormone therapy (estrogen with or without progestin) remains the gold standard treatment for hot flashes in menopausal women, but concerns for the risk of hormone therapy have resulted in its decline and a de... Purpose: Hormone therapy (estrogen with or without progestin) remains the gold standard treatment for hot flashes in menopausal women, but concerns for the risk of hormone therapy have resulted in its decline and a demand for nonhormonal treatments with demonstrated efficacy for hot flashes. Aim of this study was to examine the efficacy of selective serotonin reuptake inhibitor escitalopram on hot flashes in a healthy sample of non-depressant menopausal women in Japan. Methods: We retrospectively analyzed the medical records of 11 menopausal patients with hot flashes, who received escitalopram (10 mg daily) for 2 weeks between March and August 2012. Hot flashes severities and scores were recorded on a scale of 0 to 10 points, at beginning and end of 2 weeks treatment. Results: At 2 weeks of therapy, 9 of 11 patients reported significant decreases in hot flash frequency and severity, but the remission of the symptom was not observed in 2 patients. Speed of relief from hot flashes was rapid (within one week). Conclusions: Escitalopram 10 mg/day may be a prompt and effective option for treating hot flashes in menopausal women who do not want to use hormone replacement therapy. 展开更多
关键词 Hot FLASHES escitalopram Selective SEROTONIN REUPTAKE Inhibitors MENOPAUSE
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Escitalopram-induced hepatitis:A case report
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作者 Guillaume Wabont Laurie Ferret +3 位作者 Nicolas Houdre Antoine Lepied Johana Bene Etienne Cousein 《World Journal of Clinical Cases》 SCIE 2022年第8期2468-2473,共6页
BACKGROUND The antidepressant escitalopram is widely prescribed for the treatment of depression.It is generally well-tolerated,and cholestasis is not mentioned in its summary of product characteristics(Sm PC).We prese... BACKGROUND The antidepressant escitalopram is widely prescribed for the treatment of depression.It is generally well-tolerated,and cholestasis is not mentioned in its summary of product characteristics(Sm PC).We present a case of cholestatic and cytolysis liver injury due to escitalopram and a Vigi Base?study.CASE SUMMARY A 68-year-old man was admitted to our emergency unit due to clinical jaundice associated with hepatitis,pruritus and dark urine.We tested the patient for the most common etiologies of jaundice,including hemolysis,viral hepatitis,cirrhosis,carcinoma,cholangitis,cholelithiasis and intrahepatic or extrahepatic obstruction.The etiological study was negative,and an adverse drug reaction was the sole possible explanation.The patient was receiving treatment with escitalopram.Two days after its withdrawal,pruritus was resolved.Ten days after withdrawal,clinical jaundice disappeared.It took a month and three weeks after withdrawal for the patient to have normalized liver function tests.To our knowledge,this is the first reported case of cholestasis where treatment with escitalopram was the only possible cause,with a highly probable causality.In addition,we determined whether escitalopram is associated with hepatotoxicity and cholestasis by performing a disproportionality analysis.All cases of hepatobiliary disorders induced by escitalopram and reported in the World Health Organization pharmacovigilance database(Vigi Base?)were analyzed to characterize this toxicity.We found that patients treated with escitalopram had an increased risk of hepatitis[odds ratio(OR)=1.938(1.186-3.166)]and cholestasis[OR=1.866(1.279-2.724)][OR(95%confidence interval)].The median duration between the introduction of escitalopram and the occurrence of acute hepatitis and/or cholestasis was ten days+/-seven days.CONCLUSION Although extremely rare,this case report,the review of the literature and the pharmacovigilance update confirm that escitalopram can cause drug-induced hepatotoxicity and cholestasis,generally within a week after initiation.Thus,escitalopram should be withdrawn immediately if an iatrogenic cause cannot be excluded.If its responsibility is ascertained,escitalopram should be consequently contraindicated.In addition,serotoninergic antidepressants in patients with nonsevere depression are ineffective and harmful.Finally,the Sm PC of escitalopram should be updated to alert for this risk and give clear clinical guidelines. 展开更多
关键词 escitalopram HEPATITIS CHOLESTASIS PHARMACOVIGILANCE Case report
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坦索罗辛联合艾司西酞普兰治疗慢性骨盆疼痛综合征的疗效观察
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作者 孙景存 陈维 +1 位作者 王江静 张洪亮 《河北医药》 CAS 2024年第16期2462-2465,共4页
目的分析坦索罗辛联合艾司西酞普兰治疗慢性骨盆疼痛综合征的临床疗效、症状改善和炎症水平的影响。方法选取2022年1月至2023年1月收治的慢性骨盆疼痛患者120例作为研究对象(参考Kendall样本量估计方法,样本量:观察变量的10~20倍,预计... 目的分析坦索罗辛联合艾司西酞普兰治疗慢性骨盆疼痛综合征的临床疗效、症状改善和炎症水平的影响。方法选取2022年1月至2023年1月收治的慢性骨盆疼痛患者120例作为研究对象(参考Kendall样本量估计方法,样本量:观察变量的10~20倍,预计估算量:60~120个),随机数表法分为对照组和观察组,每组60例。对照组给予坦索罗辛治疗,观察组给予坦索罗辛联合艾司西酞普兰治疗,疗程均为2个月。比较2组患者治疗前、后的排尿症状、炎性因子水平、临床指标和症状积分变化情况,对比2组患者的不良反应发生情况。结果观察组患者的尿频尿急、尿后滴沥、排尿疼痛评分和总积分均低于对照组(P<0.05);观察组治愈率显著高于对照组(P<0.05);观察组白细胞计数(WBC)、白介素-1β(IL-1β)、干扰素-α(INF-α)均低于对照组,平均尿流率(AFR)、白细胞介素-2(IL-2)均高于对照组(P<0.05);2组不良反应发生率差异无统计学意义(P>0.05)。结论坦索罗辛联合艾司西酞普兰治疗慢性骨盆疼痛综合征有助于改善临床症状和临床指标、抑制炎性反应,临床疗效较好。 展开更多
关键词 坦索罗辛 艾司西酞普兰 慢性骨盆疼痛综合征 治疗结果
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基于临床症状和生物学特征预测电针抗抑郁临床疗效的探索性分析
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作者 胡凌娟 赵冰骢 +3 位作者 李晶 图娅 杨昕婧 郭卓 《辽宁中医杂志》 CAS 北大核心 2024年第11期1-5,共5页
目的探索影响轻中度抑郁症患者对电针、药物和针药联合3种不同干预措施应答的关键因素。方法将61例轻中度抑郁症患者随机分为电针组(20例,脱落1例)、药物组(20例,脱落4例)和针药联合组(21例,脱落1例)。电针治疗选取主穴百会、印堂并接电... 目的探索影响轻中度抑郁症患者对电针、药物和针药联合3种不同干预措施应答的关键因素。方法将61例轻中度抑郁症患者随机分为电针组(20例,脱落1例)、药物组(20例,脱落4例)和针药联合组(21例,脱落1例)。电针治疗选取主穴百会、印堂并接电,每次30 min,每周3次;药物治疗口服草酸艾司西酞普兰,5~10 mg/d;针药联合组的患者同时接受电针和药物治疗,治疗均持续6周。观察患者抑郁严重程度、生活质量等临床表现,ELISA法检测3组患者血清相关指标表达水平。结果治疗后,3组患者,24项汉密尔顿抑郁量在(24-item Hamilton depression scale,HAMD-24)评分均显著下降(P<0.05),3组患者,健康状况调查问卷(short form 36 health survey,SF-36)评分均显著提高(P<0.05)。3组患者的HAMD-24应答率、缓解率、SSRS、SF-36评分差异无统计学意义(P>0.05)。结合临床症状和分子生物学指标模拟的模型较为可靠。结论适合不同干预措施的轻、中度抑郁症患者人群基本特征有所不同。对伴随较严重睡眠障碍的抑郁症患者,选择针药联合治疗更有可能取得较好的临床疗效。 展开更多
关键词 电针 草酸艾司西酞普兰 抑郁症 疗效预测 睡眠障碍
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艾司西酞普兰联合焦点解决短程治疗对青少年抑郁患者负性情绪、认知功能的影响
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作者 李梅 巫江丽 +1 位作者 周国岭 丁凯景 《浙江医学》 CAS 2024年第11期1192-1196,共5页
目的分析艾司西酞普兰联合焦点解决短程治疗对青少年抑郁患者负性情绪、认知功能的影响。方法选取2021年12月至2023年6月在杭州市第七人民医院就诊的60例抑郁症青少年患者,根据随机数字表法分为观察组(30例)和对照组(30例)。对照组使用... 目的分析艾司西酞普兰联合焦点解决短程治疗对青少年抑郁患者负性情绪、认知功能的影响。方法选取2021年12月至2023年6月在杭州市第七人民医院就诊的60例抑郁症青少年患者,根据随机数字表法分为观察组(30例)和对照组(30例)。对照组使用艾司西酞普兰治疗,观察组在对照组治疗的基础上联合焦点解决短程治疗。对比两组患者的临床疗效、负性情绪、认知功能、不良反应。结果治疗后2~6周两组患者健康问卷评分均降低,观察组较对照组更优(均P<0.05);两组的汉密尔顿抑郁量表评分、广泛性焦虑自评量表评分均降低,观察组较对照组更低(均P<0.05);两组的精神状态评定量表评分均上升,观察组较对照组的认知功能更优(均P<0.05)。与对照组相比,观察组的不良反应总发生率更低(P<0.05)。结论艾司西酞普兰联合焦点解决短程治疗不仅可缓解青少年抑郁患者的焦虑和负面情绪,还能提高患者的认知功能,降低不良反应发生率,值得在临床推广应用。 展开更多
关键词 艾司西酞普兰 焦点解决短程治疗 抑郁 负性情绪 认知功能
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艾司西酞普兰联合支持性心理治疗在抑郁障碍中的效果分析
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作者 李哲 武文煜 +1 位作者 贾荣 曾淑娥 《中国社区医师》 2024年第23期32-34,共3页
目的:探讨艾司西酞普兰联合支持性心理治疗在抑郁障碍中的效果。方法:选取2021年1月—2022年1月在云南省精神病医院住院治疗的60例抑郁障碍患者进行研究,基于随机双盲法分为对照组和观察组,各30例。两组均应用艾司西酞普兰治疗,观察组... 目的:探讨艾司西酞普兰联合支持性心理治疗在抑郁障碍中的效果。方法:选取2021年1月—2022年1月在云南省精神病医院住院治疗的60例抑郁障碍患者进行研究,基于随机双盲法分为对照组和观察组,各30例。两组均应用艾司西酞普兰治疗,观察组在此基础上进行支持性心理治疗。比较两组患者抑郁、日常行为能力及临床疗效情况。结果:两组患者治疗4周、8周后汉密尔顿抑郁量表(HAMD-24)、抑郁自评量表(SDS)评分均低于治疗前,且治疗8周后HAMD-24、SDS评分低于治疗4周后,差异有统计学意义(P<0.05);观察组患者治疗4周、8周后HAMD-24、SDS评分低于对照组,差异有统计学意义(P<0.05)。两组患者治疗4周、8周后日常生活能力量表(ADL)评分均高于治疗前,且治疗8周后ADL评分高于治疗4周后,差异有统计学意义(P<0.05);观察组患者治疗4周、8周后ADL评分高于对照组,差异有统计学意义(P<0.05)。两组总有效率比较,差异无统计学意义(P>0.05)。结论:艾司西酞普兰联合支持性心理治疗对抑郁障碍患者有明显疗效,效果优于单用艾司西酞普兰。 展开更多
关键词 抑郁障碍 艾司西酞普兰 支持性心理治疗
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艾司西酞普兰联合运动方案对苯二氮[艹卓]类药物依赖焦虑症患者睡眠质量的影响
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作者 王惠强 王哲伟 《世界睡眠医学杂志》 2024年第2期454-457,共4页
目的:探讨艾司西酞普兰联合运动方案对苯二氮[艹卓]类(BDZ)药物依赖焦虑症患者睡眠质量的影响。方法:选取2021年9月至2023年2月泉州市第三医院收治的BDZ类药物依赖焦虑症患者120例作为研究对象,按照抛掷法随机分为对照组(n=58)和观察组(... 目的:探讨艾司西酞普兰联合运动方案对苯二氮[艹卓]类(BDZ)药物依赖焦虑症患者睡眠质量的影响。方法:选取2021年9月至2023年2月泉州市第三医院收治的BDZ类药物依赖焦虑症患者120例作为研究对象,按照抛掷法随机分为对照组(n=58)和观察组(n=62)。对照组仅予以艾司西酞普兰治疗,观察组予以艾司西酞普兰联合运动方案治疗。比较2组睡眠质量、失眠程度、负性情绪以及生命质量。结果:治疗后,观察组匹兹堡睡眠质量指数(PSQI)中主观睡眠质量、入睡时间、睡眠效率、睡眠障碍、日间功能5个维度评分及总分均低于对照组,差异均有统计学意义(均P<0.05),失眠严重程度指数(ISI)评分低于对照组,差异有统计学意义(P<0.05);观察组汉密尔顿焦虑抑郁量表(HADS)评分均较对照组低,差异有统计学意义(P<0.05),健康调查简表(SF-36)评分较对照组高,差异有统计学意义(P<0.05)。结论:艾司西酞普兰联合运动方案能明显提高BDZ类药物依赖焦虑症患者的睡眠质量,改善失眠症状,缓解负性情绪,提高生命质量。 展开更多
关键词 艾司西酞普兰 运动方案 苯二氮[艹卓]类 药物依赖 睡眠质量
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草酸艾司西酞普兰联合复方解郁汤治疗青少年抑郁症的临床疗效分析
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作者 周俊 丁虎 《辽宁中医杂志》 CAS 北大核心 2024年第7期80-84,共5页
目的 探讨草酸艾司西酞普兰联合复方解郁汤治疗青少年抑郁症的临床疗效。方法 选择该院2021年12月—2022年12月期间精神科收治青少年抑郁症患者86例,按照随机数字表法分试验组(43例)和对照组(43例)。所有患者均予以认知行为疗法治疗,对... 目的 探讨草酸艾司西酞普兰联合复方解郁汤治疗青少年抑郁症的临床疗效。方法 选择该院2021年12月—2022年12月期间精神科收治青少年抑郁症患者86例,按照随机数字表法分试验组(43例)和对照组(43例)。所有患者均予以认知行为疗法治疗,对照组予以草酸艾司西酞普兰片,试验组在对照组的基础上联用复方解郁汤治疗。两组均以4周为1个疗程,共治疗2个疗程。对比两组治疗前后脑源性神经营养因子水平、血清炎症因子水平、单胺类神经递质水平、抑郁情况评分、睡眠质量评分、自杀态度评分,观察并评估两组治疗效果及治疗期间不良反应。结果 与治疗前比,治疗后两组BDNF水平较高,IL-1β、IL-6、TNF-α水平降低;与对照组比,治疗后试验组BDNF水平较高,IL-1β、IL-6、TNF-α水平较低(P<0.05)。与治疗前比,治疗后两组NE、5-HT、DA水平升高;与对照组比,治疗后试验组NE、5-HT、DA水平较高(P<0.05)。与治疗前比,治疗后两组HAMA及PSQI评分降低;与对照组比,治疗后试验组HAMA及PSQI评分较低(P<0.05)。试验组临床总有效率较对照组高,差异有统计学意义(P<0.05)。与治疗前比,治疗后两组自杀意念QSA评分较高;与对照组比,治疗后试验组自杀意念QSA评分较高(P<0.05)。两组均未出现严重不良反应,比较差异无统计学意义(P>0.05)。结论 草酸艾司西酞普兰联合复方解郁汤对青少年抑郁症患者的治疗效果显著,能上调脑源性神经营养因子及单胺类神经递质水平,降低血清炎症因子水平,改善睡眠质量及自杀意念,不良反应较少,是一种安全有效的治疗方案。 展开更多
关键词 草酸艾司西酞普兰 复方解郁汤 青少年抑郁症 临床疗效
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Shugan Jieyu capsule effects on peripheral blood micro-124, micro- 132, and brain-derived neurotrophic factor in patients with mild to moderate depression
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作者 Xian Zhang Yang Liu +6 位作者 Hua-Fei Tang Feng Jiang Chun-Liang Chen Ting-Ting Wang Hui-Zhong Gu Qiang Zhao Rui Ma 《World Journal of Psychiatry》 SCIE 2024年第9期1354-1363,共10页
BACKGROUND To assess the effectiveness of Shugan Jieyu capsules on peripheral blood miR-124,miR-132,and brain-derived neurotrophic factor(BDNF)levels in patients with mild to moderate depression following coronary art... BACKGROUND To assess the effectiveness of Shugan Jieyu capsules on peripheral blood miR-124,miR-132,and brain-derived neurotrophic factor(BDNF)levels in patients with mild to moderate depression following coronary artery intervention[percuta-neous coronary intervention(PCI)]for coronary heart disease.Patients with mild-to-moderate depression of the liver-qi stagnation type after PCI for coronary heart disease at the 305th Hospital of the People’s Liberation Army were enrolled from June 2022 to November 2023 and randomly assigned to two groups:Experimental(treated with Shugan Jieyu capsules)and control(tr-eated with escitalopram oxalate tablets).This study compared the antidepressant effects of these treatments using 17-item Hamilton Rating Scale for Depression(HAMD-17)scores,metabolic equivalents,low-density lipoprotein cholesterol,BDNF,high-sensitivity C-reactive protein levels,miR-124 and miR-132 levels,distribution of immune-related lymphocyte subsets,and traditional Chinese me-dicine syndrome scores before and after 6 weeks of treatment.RESULTS No significant difference was observed in any index between the two groups before treatment(P>0.05).After treatment,the total efficacy rates were 93.33%and 90.00%in the experimental and control groups,respectively.Experimental group had significantly lower scores for the main and secondary syndromes compared to the control group(P<0.05).No significant difference was observed in the metabolic equivalents between the two groups be-fore and after treatment(P>0.05).The levels of low-density lipoprotein cholesterol,high-sensitivity C-reactive pro-tein,and miR-132 were significantly lower,whereas those of miR-124,BDNF,CD3+T lymphocytes,CD3+CD4+T helper lymphocytes,and CD3+CD4+/CD3+CD8+cells were significantly higher in the experimental group com-pared to the control group(P<0.05).The incidence of adverse reactions during experimental group was signi-ficantly lower than that in control group(P<0.05).CONCLUSION Shugan Jieyu capsules have good efficacy in patients with mild-to-moderate depression after PCI,and its me-chanism may contribute to the regulation of miR-124,miR-132,BDNF levels,and lymphoid immune cells. 展开更多
关键词 Shugan Jieyu capsule Coronary heart disease DEPRESSION escitalopram oxalate tablet Micro-124 Micro-132 Brain-derived neurotrophic factor
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舒肝解郁胶囊联合艾司西酞普兰对脑梗死后抑郁症的影响
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作者 董海花 王霆 吴建峰 《临床研究》 2024年第9期110-113,共4页
目的探究舒肝解郁胶囊联合艾司西酞普兰用于脑梗死后抑郁症的疗效及对血5-羟色胺(5-HT)和神经递质功率的影响。方法将2020年6月至2023年6月河南省济源市人民医院收治的脑梗死后抑郁症患者进行中医辩证分型,选取96例症属肝郁脾虚者纳入... 目的探究舒肝解郁胶囊联合艾司西酞普兰用于脑梗死后抑郁症的疗效及对血5-羟色胺(5-HT)和神经递质功率的影响。方法将2020年6月至2023年6月河南省济源市人民医院收治的脑梗死后抑郁症患者进行中医辩证分型,选取96例症属肝郁脾虚者纳入研究对象,以随机数字表法分为两组展开前瞻性研究,各48例,96例患者均接受常规治疗,对照组予以艾司西酞普兰实施治疗,观察组则基于对照组联用舒肝解郁胶囊实施治疗,比较两组治疗前后汉密尔顿抑郁量表(HAMD)评分、汉密尔顿焦虑量表(HAMA)评分、美国国立卫生研究院卒中量表(NIHSS)评分、5-HT水平、神经递质功率、疗效及不良反应。结果治疗后,观察组HAMD、HAMA与NIHSS评分均显著低于对照组,差异均有统计学意义(P<0.05);治疗后,两组5-HT浓度均上升,且观察组5-HT浓度显著高于对照组,差异均有统计学意义(P<0.05);治疗后,观察组谷氨酸(Glu)、γ-氨基丁酸(GABA)、多巴胺(DA)、乙酰胆碱(Ach)等神经递质功率亦显著高于对照组,差异均有统计学意义(P<0.05);治疗后,观察组治疗有效率(95.83%)高于对照组(79.17%),差异具有统计学意义(P<0.05);治疗后,两组不良反应情况差异无统计学意义(P>0.05)。结论联合舒肝解郁胶囊与艾司西酞普兰治疗脑梗死后抑郁症患者疗效较好,能有效提升血浆5-HT水平及神经递质功率,降低抑郁焦虑程度,促进神经功能损伤快速康复,具有较高用药安全性。 展开更多
关键词 舒肝解郁胶囊 艾司西酞普兰 脑梗死后抑郁症 5-羟色胺 神经递质功率
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阿戈美拉汀与草酸艾司西酞普兰联合治疗对抑郁症患者症状及睡眠质量的影响
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作者 杨晓江 《中外医疗》 2024年第12期117-120,共4页
目的研究阿戈美拉汀与草酸艾司西酞普兰联合治疗对抑郁症患者症状及睡眠质量的影响。方法单纯选取2022年10月—2023年8月泉州市第三医院收治的100例抑郁症患者作为研究对象,采用随机数表法分为两组,每组50例。对照组给予草酸艾司西酞普... 目的研究阿戈美拉汀与草酸艾司西酞普兰联合治疗对抑郁症患者症状及睡眠质量的影响。方法单纯选取2022年10月—2023年8月泉州市第三医院收治的100例抑郁症患者作为研究对象,采用随机数表法分为两组,每组50例。对照组给予草酸艾司西酞普兰治疗,观察组给予阿戈美拉汀与草酸艾司西酞普兰治疗。对比两组患者不同治疗时间的抑郁症状程度、睡眠质量以及药物不良反应。结果治疗4、8周后,观察组的汉密尔顿抑郁量表(Hamilton Depression Scale,HAMD)评分均低于对照组,差异有统计学意义(P均<0.05)。治疗8周后,观察组匹兹堡睡眠质量指数(Pittsburgh Sleep Quality Index,PSQI)中各个项目(日间功能障碍、催眠药物、入睡时间、睡眠时间、睡眠质量、睡眠效率及睡眠障碍)评分均低于对照组,差异有统计学意义(P均<0.05)。两组患者药物不良反应总发生率比较(12.00%vs 8.00%),差异无统计学意义(χ^(2)=0.444,P=0.504)。结论阿戈美拉汀与草酸艾司西酞普兰联合治疗可更有效减轻抑郁症患者的症状程度,改善患者的睡眠质量,且不会明显造成药物不良反应的发生,安全性相对有保障。 展开更多
关键词 抑郁症 阿戈美拉汀 草酸艾司西酞普兰 症状程度 睡眠质量
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艾司西酞普兰联合团体正念减压治疗与团体认知行为治疗对广泛性焦虑障碍患者的影响 被引量:1
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作者 段登艾 王维 +2 位作者 张勇辉 张志雄 陆香秀 《临床精神医学杂志》 CAS 2024年第2期109-112,共4页
目的:探讨艾司西酞普兰联合团体正念减压治疗(mindfulness based stress reduction,MBSR)及团体认知行为治疗(cognitive behavior therapy,CBT)对广泛性焦虑障碍(generalized anxiety disorder,GAD)患者的焦虑、抑郁症状的效果。方法:纳... 目的:探讨艾司西酞普兰联合团体正念减压治疗(mindfulness based stress reduction,MBSR)及团体认知行为治疗(cognitive behavior therapy,CBT)对广泛性焦虑障碍(generalized anxiety disorder,GAD)患者的焦虑、抑郁症状的效果。方法:纳入2019年10月至2021年10月本院收治的GAD患者78例,依编号随机法分为MBSR组(43例)和CBT组(35例)。MBSR组给予口服艾司西酞普兰联合团体MBSR;CBT组给予口服艾司西酞普兰联合团体CBT。分别于基线时(T0)、8周末(T1)、干预结束3个月后(T2)用汉密尔顿焦虑量表(Hamilton anxiety scale,HAMA)、汉密尔顿抑郁量表(Hamilton depression scale,HAMD)测评2组患者的焦虑、抑郁情况,并进行分析。结果:两组共完成63例(MBSR组36例,CBT组27例)。T0时,2组患者的HAMA、HAMD评分差异无统计学意义;T1、T2时,2组HAMA、HAMD评分均显著降低(P均<0.05);2组间评分差异无统计学意义。结论:艾司西酞普兰联合团体正念减压治疗或团体认知行为治疗均能明显改善GAD患者的焦虑、抑郁水平,且持续有效。 展开更多
关键词 广泛性焦虑障碍 团体正念减压治疗 团体认知行为治疗 艾司西酞普兰
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