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用吡罗昔康治疗骨关节炎。

Treatment of osteoarthritis with piroxicam.

出版信息

Eur J Rheumatol Inflamm. 1983;6(1):73-83.

PMID:6345167
Abstract

A large scale multicentre study was carried out in 757 patients with osteoarthritis in hospital clinics and general practice. It was intended to compare the efficacy and tolerance of piroxicam and placebo, and to compare morning administration of piroxicam with evening administration. Piroxicam in a single daily dose of 20 mg was shown to be superior to placebo. In the first two weeks of treatment the incidence of side-effects with piroxicam was similar to placebo. Piroxicam was equally effective when administered in the morning or at night, evidence for the view that a single daily dose relieves symptoms for at least 24 hours. There was a suggestion that the side-effects with piroxicam, particularly gastrointestinal were less frequent when the medication was taken at night. Responses were similar in hospital and general practice patients and in those under or over the age of 70. A good or fair response to piroxicam was achieved in 81% of patients. Sixty seven per cent reported piroxicam as better than their previous therapy, and the same percentage elected to continue treatment with the drug at the end of the study. About half of all side effects were thought to be drug related and about half were gastrointestinal. Side effects led to withdrawal of treatment in 8% of all patients receiving piroxicam. There were 5 cases of haematemesis or melaena (0.7%). There were 30 reports of oedema or weight gain an incidence of 4%. Side-effects of all types were similar in patients under and over the age of 70. This study confirms the efficacy and good toleration of piroxicam in the treatment of osteoarthritis predicted by earlier clinical trial experience.

摘要

一项针对757例骨关节炎患者的大规模多中心研究在医院门诊和普通诊所开展。该研究旨在比较吡罗昔康与安慰剂的疗效及耐受性,并比较吡罗昔康早晨给药与晚上给药的效果。结果显示,每日单次服用20毫克吡罗昔康的效果优于安慰剂。在治疗的前两周,吡罗昔康的副作用发生率与安慰剂相似。吡罗昔康早晨给药或晚上给药效果相同,这证明了每日单次给药可缓解症状至少24小时的观点。有迹象表明,晚上服用吡罗昔康时,其副作用,尤其是胃肠道副作用的发生频率较低。医院患者和普通诊所患者以及70岁以下或70岁以上患者的反应相似。81%的患者对吡罗昔康有良好或尚可的反应。67%的患者报告吡罗昔康比他们之前的治疗方法更好,并且在研究结束时,相同比例的患者选择继续使用该药治疗。所有副作用中约一半被认为与药物有关,约一半为胃肠道副作用。副作用导致接受吡罗昔康治疗的所有患者中有8%停药。有5例呕血或黑便(0.7%)。有30例水肿或体重增加的报告(发生率为4%)。70岁以下和70岁以上患者的各类副作用相似。这项研究证实了吡罗昔康在治疗骨关节炎方面的疗效和良好耐受性,这与早期临床试验经验所预测的一致。

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