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一项关于吡罗昔康治疗急性肌肉骨骼疾病的双盲、安慰剂对照研究。

A double blind, placebo controlled study of piroxicam in the management of acute musculoskeletal disorders.

作者信息

Lacey P H, Dodd G D, Shannon D J

出版信息

Eur J Rheumatol Inflamm. 1984;7(3):95-104.

PMID:6443759
Abstract

General Practitioners from the United Kingdom produced data on 1,282 patients with acute soft tissue injury treated with either piroxicam (Feldene) or matching placebo for a period of up to two weeks. The dosage of piroxicam was 40 mg for the first 2 days and 20 mg daily thereafter. Clinical assessment included pain, swelling, limitation of active and passive movement and overall assessment of efficacy and toleration. Piroxicam was significantly better than placebo in improving patient signs and symptoms, and in its overall efficacy (P less than 0.001); 87% of piroxicam treated patients had excellent or good responses, compared to 53% of placebo treated patients. On analysis of four of the most commonly occurring diagnoses (injuries of ankle, knee, shoulder, back) patients with moderate or severe pain showed a significant improvement on treatment with piroxicam. Physicians' overall assessment of toleration showed no evidence of differences between treatments. Over 90% of patients in both treatment groups had good or excellent toleration. Withdrawals due to side effects were 3% and 2.5% respectively for piroxicam and placebo treated patients.

摘要

来自英国的全科医生提供了1282例急性软组织损伤患者的数据,这些患者接受了吡罗昔康( Feldene)或匹配的安慰剂治疗,为期两周。吡罗昔康的剂量在前两天为40毫克,此后每天20毫克。临床评估包括疼痛、肿胀、主动和被动活动受限以及疗效和耐受性的总体评估。在改善患者体征和症状以及总体疗效方面,吡罗昔康明显优于安慰剂(P小于0.001);接受吡罗昔康治疗的患者中有87%有优秀或良好的反应,而接受安慰剂治疗的患者中这一比例为53%。对四种最常见诊断(脚踝、膝盖、肩膀、背部损伤)进行分析时,中度或重度疼痛的患者在接受吡罗昔康治疗后有显著改善。医生对耐受性的总体评估显示,两种治疗之间没有差异的迹象。两个治疗组中超过90%的患者耐受性良好或优秀。接受吡罗昔康和安慰剂治疗的患者因副作用而停药的比例分别为3%和2.5%。

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