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阿米替林治疗颞下颌关节紊乱症患者的慢性疼痛。

Amitriptyline treatment of chronic pain in patients with temporomandibular disorders.

作者信息

Plesh O, Curtis D, Levine J, McCall W D

机构信息

Department of Restorative Dentistry, School of Dentistry, University of California, San Francisco 94143-0758, USA.

出版信息

J Oral Rehabil. 2000 Oct;27(10):834-41. doi: 10.1046/j.1365-2842.2000.00572.x.

Abstract

Randomized clinical trials of amitriptyline will require data from pilot studies to be used for sample size estimates, but such data are lacking. This study investigated the 6-week and 1-year effectiveness of low dose amitriptyline (10-30 mg) for the treatment of patients with chronic temporomandibular disorder (TMD) pain. Based on clinical examination, patients were divided into two groups: myofascial and mixed (myofascial and temporomandibular joint disorders). Baseline pain was assessed by a Visual Analogue Scale (VAS) for pain intensity and by the McGill Pain Questionnaire (MPQ). Depression was assessed by the Beck Depression Inventory (BDI) short form. Patient assessment of global treatment effectiveness was obtained after 6 weeks and 1 year of treatment by using a five-point ordinal scale: (1) worse, (2) unchanged, (3) minimally improved, (4) moderately improved, (5) markedly improved. The results showed a significant reduction for all pain scores after 6 weeks and 1 year post-treatment. The depression scores changed in depressed but not in non-depressed patients. Global treatment effectiveness showed significant improvement 6 weeks and 1 year post-treatment. However, pain and global treatment effectiveness were less improved at 1 year than at 6 weeks.

摘要

阿米替林的随机临床试验需要来自前期研究的数据来进行样本量估计,但目前缺乏此类数据。本研究调查了低剂量阿米替林(10 - 30毫克)治疗慢性颞下颌关节紊乱病(TMD)疼痛患者6周和1年的疗效。根据临床检查,患者被分为两组:肌筋膜型和混合型(肌筋膜型和颞下颌关节紊乱型)。通过视觉模拟量表(VAS)评估疼痛强度基线,并通过麦吉尔疼痛问卷(MPQ)进行评估。使用贝克抑郁量表(BDI)简表评估抑郁情况。在治疗6周和1年后,采用五点序数量表对患者的整体治疗效果进行评估:(1)更差,(2)无变化,(3)略有改善,(4)中度改善,(5)显著改善。结果显示,治疗后6周和1年时,所有疼痛评分均显著降低。抑郁评分在抑郁患者中发生了变化,但在非抑郁患者中未发生变化。治疗后6周和1年时,整体治疗效果显示出显著改善。然而,1年时的疼痛和整体治疗效果改善程度低于6周时。

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