AIM: To evaluate disease-specific quality of life (QOL) in liver cirrhosis patients and to compare it with those of a healthy population. Also an important objective was to assess whether QOL in liver cirrhosis patien...AIM: To evaluate disease-specific quality of life (QOL) in liver cirrhosis patients and to compare it with those of a healthy population. Also an important objective was to assess whether QOL in liver cirrhosis patients differs by age and gender, by type and severity of disease. METHODS: The case group of 131 liver cirrhosis patients was selected. The control group of 262 was enrolled from a healthy population according to the scheme of case-control study. Clinical, demographic, laboratory data were collected. QOL was measured with a specific chronic liver disease questionnaire (CLDQ), which was translated and validated in Lithuanian. QOL scores were compared between groups by age, gender, type and severity of disease. Cronbach’s alpha statistics calculation was used for evaluation of internal consistency reliability. Student’s t test or ANOVA were used for evaluation hypothesis about probability equation. RESULTS: QOL was significantly lower in liver cirrhosis patients than in healthy population (59.5 ± 18.3 vs 85.3 ± 12.3, P < 0.001). The significant QOL differences between case and control groups were observed in domains of worry and abdominal symptoms, the smaller differences-in emotional functions and systematic symptom domains. Significantly worse QOL was in observed patients with increased clinical severity of the disease measured by Child-Pugh class. Age, gender and etiology of disease had an insignificant effect on QOL in cirrhotic patients. CONCLUSION: QOL was significantly impaired in all CLDQ domains in liver cirrhosis patients. Increase in severity of disease was the major factor associated with poorer QOL.展开更多
Objective: To compare the quality of life (QOL) for gynecologic cancer patients with different cancer sites and to assess the impact of patients’ characteristics, disease parameters, and treatments on the subscale an...Objective: To compare the quality of life (QOL) for gynecologic cancer patients with different cancer sites and to assess the impact of patients’ characteristics, disease parameters, and treatments on the subscale and overall QOL. Methods: A prospective study was conducted including 146 gynecologic cancer patients. QOL data were collected using the general Functional Assessment of Cancer Therapy (FACT- G) QOL questionnaire. Results: Advanced stage patients showed significantly poor physical well-being, emotional well-being, and functional well-being, as compared with early stage patients. QOL was reported higher in older patients (P=0.03), patients above high school education (P=0.004), and patients with help at home (P=0.009). Conclusion: Patients with later stage, multi- modality therapy, poor education, and little social support have the most significant impairments and need more support.展开更多
Rationale: Most cancer patients require a totally-implanted Central Venous Catheter (CVC) for their treatment. We develop and validate a French-language questionnaire dubbed QASICC (Questionnaire for Acceptance of and...Rationale: Most cancer patients require a totally-implanted Central Venous Catheter (CVC) for their treatment. We develop and validate a French-language questionnaire dubbed QASICC (Questionnaire for Acceptance of and Satisfaction with Implanted Central Venous Catheter) assessing patient satisfaction with and acceptance of their CVC.?Method: The construction and first validation of the questionnaire was made using validated methodology consisting in four phases. Phase 1 aimed at collecting a comprehensive list of relevant items. Phase 2 consisted in converting items into questions followed by a first item selection procedure. Phase 3 tested the acceptance of the provisional module to a small number of patients. Phase 4 involved a first validation on patients to determine its psychometric characteristics.?Results: Responses to the questionnaire were collected from 215 patients. The final tool included 27 questions assessing seven dimensions: pain, contribution to the comfort of the treatment, esthetics and privacy, impact on professional activities, social and sports, impact on daily activities, local discomfort and overall satisfaction.Conclusions: This first statistical validation seems very promising and allows us to confirm the structure and the psychometric properties of the tool. Further validation studies are required on standard and specific populations in order to confirm these first results.展开更多
OBJECTIVE: To evaluate the development of health outcomes assessment instruments in Chinese medicine. METHODS: A comprehensive literature search for all published articles in China National Knowledge Infrastructure ...OBJECTIVE: To evaluate the development of health outcomes assessment instruments in Chinese medicine. METHODS: A comprehensive literature search for all published articles in China National Knowledge Infrastructure Database, Chongqing VIP Database and WANFANG Data was conducted. The studies that met the inclusion and exclusion criteria were used to extract information according to a predesigned assessment instrument. RESULTS: A total of 97 instruments for health outcome assessment in Chinese medicine were identified. Of these questionnaires, 7 were generic, 12 were condition-specific and 78 were disease-specific. All instruments were suitable for adults, children, and both men and women. These instruments aimed to evaluate the health-related quality of life, signs and symptoms as well as patient satisfaction and doctor-reported outcome. However, the descriptions were poorly constructed for some of the most basic parameters, such as the domains and items, administrative mode, response options, memory recall periods, burden evaluation, format, copyright, content validity, and other properties. CONCLUSION: The instrument development for health outcomes assessment in Chinese medicine is increasing rapidly; however, there are many limitations in current methodologies and standards, and further studies are needed.展开更多
OBJECTIVE: To evaluate the application of health assessment instruments in Chinese medicine. METHODS: According to a pre-defined search strategy, a comprehensive literature search for all articles published in China...OBJECTIVE: To evaluate the application of health assessment instruments in Chinese medicine. METHODS: According to a pre-defined search strategy, a comprehensive literature search for all articles published in China National Knowledge Infrastructure databases was conducted. The resulting articles that met the defined inclusion and exclusion criteria were used for analysis. RESULTS: A total of 97 instruments for health outcome assessment in Chinese medicine have been used in fundamental and theoretical research, and 14 of these were also used in 29 clinical trials that were randomized controlled trials, or descriptive or cross-sectional studies. In 2 152 Chinese medicine-based studies that used instruments in their methodology, more than 150 questionnaires were identified. Among the identified questionnaires, 51 were used in more than 10 articles (0.5%). Most of these instruments were developed in Western countries and few studies (4%) used the instrument as the primary evidence for their conclusions. CONCLUSION: Usage of instruments for health outcome assessment in Chinese medicine is increasing rapidly; however, current limitations include selection rationale, result interpretation and standardization, which must be addressed accordingly.展开更多
Objective:To measure the prevalence of depression in patients with psoriasis and to evaluate the relationship between the severity of psoriasis and depression and its effect on patients’quality of life.Methods:A tota...Objective:To measure the prevalence of depression in patients with psoriasis and to evaluate the relationship between the severity of psoriasis and depression and its effect on patients’quality of life.Methods:A total of 154 patients with a confirmed diagnosis of psoriasis were assessed to determine the severity of psoriasis based on the psoriasis area and severity index score,presence,and severity of depression using the patient health questionnaire 9,and quality of life using the dermatology life quality index 10.Pearson correlation coefficient was used to demonstrate the relationship between continuous variables with 95%confidence intervals(CIs);P<0.00001 was taken to indicate statistical significance.Results:The severity of psoriasis was mild in 36.36%of patients,moderate in 25.97%,severe in 32.47%,and very severe in 5.20%.Of the 154 patients,139(90.3%)had depression;the severity of depression was mild in most affected patients(46.7%)and severe in 2.6%of patients.Psoriasis had a moderate effect on the quality of life in 37.01%of patients and a very large effect in 33.77%of patients.The severity of psoriasis was positively correlated with depression(Pearson correlation coefficient,r=0.42,P<0.00001,95%CI:0.28–0.54)and quality of life(r=0.43,P<0.00001,95%CI:0.29–0.55).Conclusion:Depression is a common comorbidity in patients with psoriasis.The severity of psoriasis is positively correlated with the severity of depression and is associated with poor quality of life.展开更多
目的运用抑郁症状群筛选工具,调查综合医院神经内科门诊患者抑郁症状群的检出率;探讨神经内科门诊伴有抑郁症状群患者的生活质量。方法使用中文版患者健康问卷(patient health questionnaire,PHQ)的抑郁症状群分量表(PHQ-9)及健康状况...目的运用抑郁症状群筛选工具,调查综合医院神经内科门诊患者抑郁症状群的检出率;探讨神经内科门诊伴有抑郁症状群患者的生活质量。方法使用中文版患者健康问卷(patient health questionnaire,PHQ)的抑郁症状群分量表(PHQ-9)及健康状况调查问卷(the short form-36 health survey,SF-36)对综合医院神经内科门诊患者进行调查。共收集有效问卷306份。分析了患者抑郁症状群与生活质量的相关性。结果存在抑郁症状群患者有149例(占受调查人群的48.7%)。具有抑郁症状群的神经内科门诊患者SF-36各维度评分低于不伴有抑郁症状群患者。SF-36各维度评分与PHQ-9评分呈负相关,具有统计学意义(r值:-0.182~-0.839,P≤0.001)。结论在综合医院神经内科门诊就诊者中,抑郁症状群检出率较高,这类患者生活质量较差。展开更多
目的:通过问卷调查评估正颌患者治疗过程中健康相关生命质量指数的变化,初步探讨正颌外科治疗对正颌患者健康相关生命质量状况的影响,为今后正颌治疗提供一定的参考依据。方法:于正颌外科治疗安放矫治器前(T1)-正颌外科手术前1周(T2)-...目的:通过问卷调查评估正颌患者治疗过程中健康相关生命质量指数的变化,初步探讨正颌外科治疗对正颌患者健康相关生命质量状况的影响,为今后正颌治疗提供一定的参考依据。方法:于正颌外科治疗安放矫治器前(T1)-正颌外科手术前1周(T2)-正颌外科术后正畸完成后1周(T3),采用改良的正颌患者生命质量问卷(Health-related quality of life,HRQOL)对58例正颌患者进行问卷调查,PEMS3.1软件包对正颌治疗三阶段四因子分及HRQOL总分进行统计分析。结果:HRQOL总分及颜面、口颌功能、社交因子分T3阶段明显低于T1、T2(P<0.01),正颌治疗后患者HRQOL改善明显,但自我关注因子分改变未见统计学差异;T1~T2,各因子未见统计学差异。结论:正颌外科治疗能明显改善正颌患者的健康相关生命质量水平,但患者自我关注水平不随身体、心理和社交生活质量的改善而降低,在临床治疗中要合理引导患者的审美观和心理状态,以达到更好的治疗结果。展开更多
目的:引进简明幸福与生活质量满意度问卷(Quality of Life Enjoyment and Satisfaction Ques-tionnaire,Short Form,Q-LES-Q-SF),评估其在中国精神障碍患者中的信效度和适用性。方法:在山东省精神卫生中心2007年7月-2008年1月的门诊和...目的:引进简明幸福与生活质量满意度问卷(Quality of Life Enjoyment and Satisfaction Ques-tionnaire,Short Form,Q-LES-Q-SF),评估其在中国精神障碍患者中的信效度和适用性。方法:在山东省精神卫生中心2007年7月-2008年1月的门诊和住院患者中,按照就诊或住院的先后顺序,选取385例符合《ICD-10精神与行为障碍分类》诊断标准的精神分裂症(n=193)和心境障碍患者(n=192);按1∶2的比例选取与其相匹配的健康对照者196例。对所有对象进行Q-LES-Q-SF初次测评,30天后进行重测,对原始测评结果进行信度分析。以世界卫生组织生活质量量表(World Health Organization Quality of Life,WHO-QOL-100)为效标变量评价患者和健康对照者效标效度并进行区分效度分析。结果:信度分析显示量表的Cronbacnα系数为0.920,重测信度为0.785。总量表评分与WHOQOL-100总分及6个领域和24个方面均具有较高的相关性(心境障碍,r=0.22~0.71;精神分裂症,r=0.24~0.70;健康对照,r=0.17~0.73;Ps<0.01)。精神分裂症组和心境障碍组患者的幸福与生活质量满意度总分及各条目分均低于健康对照组[如总分,(46.42±8.36)vs.(54.34±8.11),(46.20±10.12)vs.(54.34±8.11),Ps<0.01]。结论:简明幸福与生活质量满意度问卷在中国精神障碍患者中有较好的信效度,适用于精神障碍患者生活质量的量化评估。展开更多
目的观察养阴润肠方治疗慢性传输型便秘临床疗效。方法符合纳入标准的32例慢性传输型便秘患者,使用养阴润肠方治疗3个疗程,每个疗程7d,分别记录治疗前、2个疗程后、3个疗程后、停药1个月后便秘患者生活质量自评量表(patient assessment ...目的观察养阴润肠方治疗慢性传输型便秘临床疗效。方法符合纳入标准的32例慢性传输型便秘患者,使用养阴润肠方治疗3个疗程,每个疗程7d,分别记录治疗前、2个疗程后、3个疗程后、停药1个月后便秘患者生活质量自评量表(patient assessment of constipation quality of life questionnaire,PAC-QOL)评分及Cleveland便秘评分。结果治疗结束时治愈17例,显效8例,有效4例,无效3例,总有效率为90.6%。治疗前后PAC-QOL比较,在治疗2个疗程后、3个疗程后、停药1个月后,生理积分、担忧度积分、满意度积分、总分均显著减少(P<0.01);3个疗程后、停药1个月后,心理积分显著减少(P<0.01);与治疗前比较,治疗2个疗程后、3个疗程后、停药1个月后Cleveland评分均显著减少(P<0.01)。结论养阴润肠方治疗慢性传输型便秘在全身整体性调节和提高生活质量等方面疗效确切。展开更多
文摘AIM: To evaluate disease-specific quality of life (QOL) in liver cirrhosis patients and to compare it with those of a healthy population. Also an important objective was to assess whether QOL in liver cirrhosis patients differs by age and gender, by type and severity of disease. METHODS: The case group of 131 liver cirrhosis patients was selected. The control group of 262 was enrolled from a healthy population according to the scheme of case-control study. Clinical, demographic, laboratory data were collected. QOL was measured with a specific chronic liver disease questionnaire (CLDQ), which was translated and validated in Lithuanian. QOL scores were compared between groups by age, gender, type and severity of disease. Cronbach’s alpha statistics calculation was used for evaluation of internal consistency reliability. Student’s t test or ANOVA were used for evaluation hypothesis about probability equation. RESULTS: QOL was significantly lower in liver cirrhosis patients than in healthy population (59.5 ± 18.3 vs 85.3 ± 12.3, P < 0.001). The significant QOL differences between case and control groups were observed in domains of worry and abdominal symptoms, the smaller differences-in emotional functions and systematic symptom domains. Significantly worse QOL was in observed patients with increased clinical severity of the disease measured by Child-Pugh class. Age, gender and etiology of disease had an insignificant effect on QOL in cirrhotic patients. CONCLUSION: QOL was significantly impaired in all CLDQ domains in liver cirrhosis patients. Increase in severity of disease was the major factor associated with poorer QOL.
文摘Objective: To compare the quality of life (QOL) for gynecologic cancer patients with different cancer sites and to assess the impact of patients’ characteristics, disease parameters, and treatments on the subscale and overall QOL. Methods: A prospective study was conducted including 146 gynecologic cancer patients. QOL data were collected using the general Functional Assessment of Cancer Therapy (FACT- G) QOL questionnaire. Results: Advanced stage patients showed significantly poor physical well-being, emotional well-being, and functional well-being, as compared with early stage patients. QOL was reported higher in older patients (P=0.03), patients above high school education (P=0.004), and patients with help at home (P=0.009). Conclusion: Patients with later stage, multi- modality therapy, poor education, and little social support have the most significant impairments and need more support.
文摘Rationale: Most cancer patients require a totally-implanted Central Venous Catheter (CVC) for their treatment. We develop and validate a French-language questionnaire dubbed QASICC (Questionnaire for Acceptance of and Satisfaction with Implanted Central Venous Catheter) assessing patient satisfaction with and acceptance of their CVC.?Method: The construction and first validation of the questionnaire was made using validated methodology consisting in four phases. Phase 1 aimed at collecting a comprehensive list of relevant items. Phase 2 consisted in converting items into questions followed by a first item selection procedure. Phase 3 tested the acceptance of the provisional module to a small number of patients. Phase 4 involved a first validation on patients to determine its psychometric characteristics.?Results: Responses to the questionnaire were collected from 215 patients. The final tool included 27 questions assessing seven dimensions: pain, contribution to the comfort of the treatment, esthetics and privacy, impact on professional activities, social and sports, impact on daily activities, local discomfort and overall satisfaction.Conclusions: This first statistical validation seems very promising and allows us to confirm the structure and the psychometric properties of the tool. Further validation studies are required on standard and specific populations in order to confirm these first results.
基金supported by the National Natural Science Foundation of China (Project Grant No. 81073163)
文摘OBJECTIVE: To evaluate the development of health outcomes assessment instruments in Chinese medicine. METHODS: A comprehensive literature search for all published articles in China National Knowledge Infrastructure Database, Chongqing VIP Database and WANFANG Data was conducted. The studies that met the inclusion and exclusion criteria were used to extract information according to a predesigned assessment instrument. RESULTS: A total of 97 instruments for health outcome assessment in Chinese medicine were identified. Of these questionnaires, 7 were generic, 12 were condition-specific and 78 were disease-specific. All instruments were suitable for adults, children, and both men and women. These instruments aimed to evaluate the health-related quality of life, signs and symptoms as well as patient satisfaction and doctor-reported outcome. However, the descriptions were poorly constructed for some of the most basic parameters, such as the domains and items, administrative mode, response options, memory recall periods, burden evaluation, format, copyright, content validity, and other properties. CONCLUSION: The instrument development for health outcomes assessment in Chinese medicine is increasing rapidly; however, there are many limitations in current methodologies and standards, and further studies are needed.
基金supported by the National Natural Science Foundation of China(No.81073163)
文摘OBJECTIVE: To evaluate the application of health assessment instruments in Chinese medicine. METHODS: According to a pre-defined search strategy, a comprehensive literature search for all articles published in China National Knowledge Infrastructure databases was conducted. The resulting articles that met the defined inclusion and exclusion criteria were used for analysis. RESULTS: A total of 97 instruments for health outcome assessment in Chinese medicine have been used in fundamental and theoretical research, and 14 of these were also used in 29 clinical trials that were randomized controlled trials, or descriptive or cross-sectional studies. In 2 152 Chinese medicine-based studies that used instruments in their methodology, more than 150 questionnaires were identified. Among the identified questionnaires, 51 were used in more than 10 articles (0.5%). Most of these instruments were developed in Western countries and few studies (4%) used the instrument as the primary evidence for their conclusions. CONCLUSION: Usage of instruments for health outcome assessment in Chinese medicine is increasing rapidly; however, current limitations include selection rationale, result interpretation and standardization, which must be addressed accordingly.
文摘Objective:To measure the prevalence of depression in patients with psoriasis and to evaluate the relationship between the severity of psoriasis and depression and its effect on patients’quality of life.Methods:A total of 154 patients with a confirmed diagnosis of psoriasis were assessed to determine the severity of psoriasis based on the psoriasis area and severity index score,presence,and severity of depression using the patient health questionnaire 9,and quality of life using the dermatology life quality index 10.Pearson correlation coefficient was used to demonstrate the relationship between continuous variables with 95%confidence intervals(CIs);P<0.00001 was taken to indicate statistical significance.Results:The severity of psoriasis was mild in 36.36%of patients,moderate in 25.97%,severe in 32.47%,and very severe in 5.20%.Of the 154 patients,139(90.3%)had depression;the severity of depression was mild in most affected patients(46.7%)and severe in 2.6%of patients.Psoriasis had a moderate effect on the quality of life in 37.01%of patients and a very large effect in 33.77%of patients.The severity of psoriasis was positively correlated with depression(Pearson correlation coefficient,r=0.42,P<0.00001,95%CI:0.28–0.54)and quality of life(r=0.43,P<0.00001,95%CI:0.29–0.55).Conclusion:Depression is a common comorbidity in patients with psoriasis.The severity of psoriasis is positively correlated with the severity of depression and is associated with poor quality of life.
文摘目的运用抑郁症状群筛选工具,调查综合医院神经内科门诊患者抑郁症状群的检出率;探讨神经内科门诊伴有抑郁症状群患者的生活质量。方法使用中文版患者健康问卷(patient health questionnaire,PHQ)的抑郁症状群分量表(PHQ-9)及健康状况调查问卷(the short form-36 health survey,SF-36)对综合医院神经内科门诊患者进行调查。共收集有效问卷306份。分析了患者抑郁症状群与生活质量的相关性。结果存在抑郁症状群患者有149例(占受调查人群的48.7%)。具有抑郁症状群的神经内科门诊患者SF-36各维度评分低于不伴有抑郁症状群患者。SF-36各维度评分与PHQ-9评分呈负相关,具有统计学意义(r值:-0.182~-0.839,P≤0.001)。结论在综合医院神经内科门诊就诊者中,抑郁症状群检出率较高,这类患者生活质量较差。
文摘目的:通过问卷调查评估正颌患者治疗过程中健康相关生命质量指数的变化,初步探讨正颌外科治疗对正颌患者健康相关生命质量状况的影响,为今后正颌治疗提供一定的参考依据。方法:于正颌外科治疗安放矫治器前(T1)-正颌外科手术前1周(T2)-正颌外科术后正畸完成后1周(T3),采用改良的正颌患者生命质量问卷(Health-related quality of life,HRQOL)对58例正颌患者进行问卷调查,PEMS3.1软件包对正颌治疗三阶段四因子分及HRQOL总分进行统计分析。结果:HRQOL总分及颜面、口颌功能、社交因子分T3阶段明显低于T1、T2(P<0.01),正颌治疗后患者HRQOL改善明显,但自我关注因子分改变未见统计学差异;T1~T2,各因子未见统计学差异。结论:正颌外科治疗能明显改善正颌患者的健康相关生命质量水平,但患者自我关注水平不随身体、心理和社交生活质量的改善而降低,在临床治疗中要合理引导患者的审美观和心理状态,以达到更好的治疗结果。
文摘目的:引进简明幸福与生活质量满意度问卷(Quality of Life Enjoyment and Satisfaction Ques-tionnaire,Short Form,Q-LES-Q-SF),评估其在中国精神障碍患者中的信效度和适用性。方法:在山东省精神卫生中心2007年7月-2008年1月的门诊和住院患者中,按照就诊或住院的先后顺序,选取385例符合《ICD-10精神与行为障碍分类》诊断标准的精神分裂症(n=193)和心境障碍患者(n=192);按1∶2的比例选取与其相匹配的健康对照者196例。对所有对象进行Q-LES-Q-SF初次测评,30天后进行重测,对原始测评结果进行信度分析。以世界卫生组织生活质量量表(World Health Organization Quality of Life,WHO-QOL-100)为效标变量评价患者和健康对照者效标效度并进行区分效度分析。结果:信度分析显示量表的Cronbacnα系数为0.920,重测信度为0.785。总量表评分与WHOQOL-100总分及6个领域和24个方面均具有较高的相关性(心境障碍,r=0.22~0.71;精神分裂症,r=0.24~0.70;健康对照,r=0.17~0.73;Ps<0.01)。精神分裂症组和心境障碍组患者的幸福与生活质量满意度总分及各条目分均低于健康对照组[如总分,(46.42±8.36)vs.(54.34±8.11),(46.20±10.12)vs.(54.34±8.11),Ps<0.01]。结论:简明幸福与生活质量满意度问卷在中国精神障碍患者中有较好的信效度,适用于精神障碍患者生活质量的量化评估。
文摘目的观察养阴润肠方治疗慢性传输型便秘临床疗效。方法符合纳入标准的32例慢性传输型便秘患者,使用养阴润肠方治疗3个疗程,每个疗程7d,分别记录治疗前、2个疗程后、3个疗程后、停药1个月后便秘患者生活质量自评量表(patient assessment of constipation quality of life questionnaire,PAC-QOL)评分及Cleveland便秘评分。结果治疗结束时治愈17例,显效8例,有效4例,无效3例,总有效率为90.6%。治疗前后PAC-QOL比较,在治疗2个疗程后、3个疗程后、停药1个月后,生理积分、担忧度积分、满意度积分、总分均显著减少(P<0.01);3个疗程后、停药1个月后,心理积分显著减少(P<0.01);与治疗前比较,治疗2个疗程后、3个疗程后、停药1个月后Cleveland评分均显著减少(P<0.01)。结论养阴润肠方治疗慢性传输型便秘在全身整体性调节和提高生活质量等方面疗效确切。