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Tapentadol Prolonged Release Reduces the Severe Chronic Ischaemic Pain and Improves the Quality of Life in Patients with Type 2 Diabetes

机译:他喷他多的延长释放减少了2型糖尿病患者的严重慢性缺血性疼痛并改善了生活质量

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摘要

This study has been performed in diabetic type 2 patients with pain due to peripheral artery disease (PAD) in order to evaluate the efficacy and tolerability of tapentadol prolonged release (PR). Methods. 25 patients with type 2 diabetes (13 F and 12 M) were admitted in the study. The evaluation of the analgesic efficacy of tapentadol PR was based on both the assessment of the intensity of the pain (NRS scale from 0 to 10) and the nature of the pain (DN4 questionnaire) and on assessment of the patient's quality of life and state of health (SF-12 Health Survey). Study duration was 3 months: a baseline visit and follow-up included visits after 1 week, 1 month, 2 months, and 3 months. Results. At the beginning of the study, the mean intensity of the pain was 7.88 ± 1.17 on the NRS scale and at visit 2 it reduced in a statistically significant way; at the end of the treatment with tapentadol PR, the mean intensity was 2.84 points on the NRS scale. Conclusion. In type 2 diabetic patients with chronic severe pain due to PAD, tapentadol PR reduced pain intensity, improving the quality of life.
机译:为了评估他喷他多缓释(PR)的疗效和耐受性,本研究已在2型糖尿病伴有外周动脉疾病(PAD)疼痛的患者中进行。方法。该研究纳入了25位2型糖尿病患者(13 F和12 M)。他喷他多PR的镇痛效果评估基于对疼痛强度的评估(NRS评分从0到10)和疼痛性质(DN4问卷),以及对患者生活质量和状态的评估健康状况(SF-12健康调查)。研究持续时间为3个月:基线随访和随访包括1周,1个月,2个月和3个月后的随访。结果。在研究开始时,平均疼痛强度在NRS量表上为7.88±1.17,在第2次就诊时,其疼痛程度有统计学意义的减轻;在他喷他多PR治疗结束时,NRS量表的平均强度为2.84点。结论。在患有PAD引起的慢性严重疼痛的2型糖尿病患者中,他喷他多PR降低了疼痛强度,改善了生活质量。

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