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Comparison of quality of life and treatment efficacy in patients with chronic low back pain syndrome

机译:慢性下腰痛综合征患者生活质量和疗效比较

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AIM: To test use of quality of life (QL) parameters for assessing treatment efficacy in patients with chronic low back pain syndrome (CLBPS). MATERIAL AND METHODS: Clinical, device examinations, questionnaire survey were made in 100 patients, most of them females (77%) with CLBPS due to spinal osteochondrosis. Mean age of the patients was 45.69 +/- 7.61 years, mean duration of the disease 10.20 +/- 6.01 years, duration of the exacerbation 4.04 +/- 1.75 months. Most of the examinees had CLBPS x-ray stage II. QL was evaluated by questionning (general SF-36, HAQ and special Oswestry low back pain disability (OLBPD) questionnaires). RESULTS: The patients were divided into two groups by clinical and device findings and responses to the questionnaires. Group I patients had significant improvement of all the parameters studied, patients of group 2 had no improvement. A strong correlation was found between OLBPD responses and the patients' appraisal of the treatment efficacy. The effect value, standardized significance rates and factors intensity reflected high informative value of the questionnaire by assessment of efficacy of CLBPS treatment. CONCLUSION: SF-36 and OLBPD are recommended as adequate general and special questionnaires respectively, to estimate QL in patients with CLBPS. The treatment is effective if total parameters of physical and mental health by SF-36 rise significantly while vital activity disorders by OLBPD reduce more than 2-fold.
机译:目的:测试生活质量(QL)参数在评估慢性下背痛综合征(CLBPS)患者中的疗效。材料与方法:对100例患者进行了临床,设备检查,问卷调查,其中女性(77%)是由于脊柱骨软骨病导致的CLBPS。患者的平均年龄为45.69 +/- 7.61岁,平均病程为10.20 +/- 6.01年,病情恶化的持续时间为4.04 +/- 1.75个月。大多数考生患有CLBPS X射线II期检查。通过提问(一般SF-36,HAQ和Oswestry特殊的腰背痛残疾(OLBPD)问卷)对QL进行评估。结果:根据临床和设备发现以及对问卷的回答,将患者分为两组。第一组患者的所有研究参数均明显改善,第二组患者无任何改善。发现OLBPD反应与患者对治疗效果的评估之间存在很强的相关性。通过评估CLBPS治疗的疗效,效果值,标准化显着率和因子强度反映了问卷的高信息价值。结论:推荐SF-36和OLBPD分别作为适当的一般和特殊问卷,以评估CLBPS患者的QL。如果SF-36的身体和精神健康的总体参数显着提高,而OLBPD的生命活动障碍降低了2倍以上,则该治疗有效。

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