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首页> 外文期刊>Scandinavian journal of pain >Patient reported outcomes and neuropsychological testing in patients with chronic non-cancer pain in long-term opioid therapy: a pilot study
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Patient reported outcomes and neuropsychological testing in patients with chronic non-cancer pain in long-term opioid therapy: a pilot study

机译:患者报告长期阿片类药物治疗慢性非癌症疼痛患者的结果和神经心理学检测:试点研究

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摘要

Background and aims: Opioid consumption has increased dramatically in patients with chronic non-cancer pain (CNCP), but long-term consequences are still unclear. The aim of this study is to investigate the effects of long-term opioid treatment on pain, cognition, mood, sleep and quality of life in CNCP patients. Methods: In this cross-sectional pilot study, two groups of patients with CNCP treated in a multidisciplinary pain center were selected: (1) opioid group: >30 mg morphine equivalent/day for >4 weeks, and (2) control group: no opioid consumption for >4 weeks. Socio-demographic data, alcohol consumption, smoking habits and body mass index (BMI) were registered and pain (brief pain inventory), mood (Hospital Anxiety and Depression Scale), sleep (Pittsburgh Sleep Quality Index) and quality of life (RAND 36-Item Health Survey) were assessed. Continuous Reaction Time and the Digit Span Test were used to evaluate cognitive function. Data was analyzed with a Fisher’s exact test and Wilcoxon two-sample test. Results: Forty-two patients with CNCP were included (21 in each group). No differences regarding sociodemographics, smoking/alcohol habits and duration, type, or intensity of pain were found. More patients in the opioid group had significantly higher BMI (62% above BMI 25 vs. 33.3%, p = 0.042). Consequently, the subsequent data analyses were controlled for BMI. The two groups did not differ in pain, cognition, anxiety, depression, sleep or quality of life but both showed lower values than the normal standards. Further, the opioid group presented a tendency to lower ratings regarding pain and social function and performed below the normal cut off in the continuous reaction time. Conclusions: No significant differences between the two groups were found regarding any of the above-mentioned variables. Interestingly, the patients assessed, regardless of taking opioids or not, could be classified with moderate pain intensity, anxiety and low quality of sleep and life compared to norm standards. Implications: The findings of this pilot study suggested that long-term opioid treatment may influence pain and quality of life among CNCP patients. A larger cohort is needed to verify these findings.
机译:背景和目的:慢性非癌症疼痛(CNCP)的患者,阿片类药物急剧增加,但长期后果仍然不清楚。本研究的目的是探讨长期阿片类药物治疗CNCP患者患者疼痛,认知,情绪,睡眠和生活质量的影响。方法:在这种横断面试验研究中,选择了两组患有在多学科疼痛中心的CNCP患者:(1)阿片类药物组:> 4周的30毫克吗啡等当天,和(2)对照组:没有表阿片消耗> 4周。社会人口统计数据,酒精消费,吸烟习惯和体重指数(BMI)是注册和疼痛(简短的疼痛库存),情绪(医院焦虑和抑郁级),睡眠(匹兹堡睡眠质量指数)和生活质量(兰德36 - 评估了卫生调查。连续反应时间和数字跨度试验用于评估认知功能。通过Fisher的确切测试和Wilcoxon两种样品测试分析了数据。结果:包括42例CNCP患者(每组21例)。没有关于社会碘目,吸烟/酒精习惯和持续时间,类型或疼痛强度的差异。阿片类药物中的更多患者的BMI显着高于BMI(62%以上BMI 25 vs.33.3%,P = 0.042)。因此,将随后的数据分析控制为BMI。两组疼痛,认知,焦虑,抑郁,睡眠或生活质量没有差异,但两者都表现出比正常标准更低的值。此外,阿片类药物呈现出对疼痛和社会功能的额定额率的趋势,并在连续反应时间的正常切断以下进行。结论:发现两组之间的任何关于上述变量的显着差异。有趣的是,患者评估,无论服用阿片类药物,是否可以按照规范标准进行中度疼痛强度,焦虑和低睡眠和生活质量归类。含义:该试点研究的结果表明,长期阿片类药物治疗可能会影响中共患者的痛苦和生活质量。需要更大的群组来验证这些发现。

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