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一项关于非关节性风湿性疾病及其对萘普生钠治疗反应的研究。

A study of non-articular rheumatic disorders and their response to treatment with naproxen sodium.

作者信息

Wheatley D

出版信息

Curr Med Res Opin. 1979;6(3):229-35. doi: 10.1185/03007997909109428.

Abstract

A group of 85 patients suffering from non-articular rheumatic disorders was studied in an open trial of naproxen sodium in general practice. Patients were assessed and then treated for 7 days with naproxen sodium at a dosage of 275 mg 3 or 4-times daily depending on the severity of pain. Patients were asked to keep a daily record of symptoms and were re-assessed by the doctor after 7 days and, in some cases, after 14 days. Pain and limitation of movement were the predominant symptoms at admission. Patients' daily records showed statistically significant reductions in pain from Day 1 and significant reductions of limitation of movement from Day 2 of the study. At the 7-day follow-up, 27 were cured, 35 improved, 19 not changed or worse, and 4 were not assessed. Thirty patients were given a second weeks' therapy and at the end of this period 24 were cured or improved. Indigestion was the most common side-effect, but only 1 patient withdrew from the trial because of this. One patient developed a rash and was withdrawn from the trial. Both patients were taking the lower dose.

摘要

在一项关于萘普生钠的全科医疗开放试验中,对85名患有非关节性风湿性疾病的患者进行了研究。对患者进行评估后,根据疼痛的严重程度,给予萘普生钠每日3或4次、每次275毫克的剂量治疗7天。要求患者每天记录症状,并在7天后由医生重新评估,在某些情况下,在14天后重新评估。入院时,疼痛和活动受限是主要症状。患者的每日记录显示,从研究第1天起疼痛有统计学意义的减轻,从第2天起活动受限有显著减轻。在7天的随访中,27例治愈,35例好转,19例无变化或恶化,4例未评估。30名患者接受了第二周的治疗,在此阶段结束时,24例治愈或好转。消化不良是最常见的副作用,但只有1例患者因此退出试验。1例患者出现皮疹并退出试验。两名患者均服用较低剂量。

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