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柳氮磺胺吡啶、金制剂或青霉胺长期治疗的临床和实验室效应:病程对治疗反应的影响。

Clinical and laboratory effects of prolonged therapy with sulfasalazine, gold or penicillamine: the effects of disease duration on treatment response.

作者信息

Situnayake R D, McConkey B

机构信息

Department of Medicine and Rheumatology, Dudley Road Hospital, Birmingham, UK.

出版信息

J Rheumatol. 1990 Oct;17(10):1268-73.

PMID:1979349
Abstract

Serial observations for up to 5 years of clinical score (a subjective global assessment), serum C-reactive protein (CRP) and the erythrocyte sedimentation rate (ESR) were analyzed in 3 groups of patients with active rheumatoid arthritis (RA) requiring treatment with a second line drug. The groups comprised 315 patients (243 women, 72 men) who had sulfasalazine (SAS); 203 patients (141 women, 62 men) who had sodium aurothiomalate (gold) and 163 patients (131 women, 32 men) who had penicillamine. The groups matched in most respects but the gold group had a smaller proportion of women, a shorter median disease duration and a higher median CRP than the remaining 2 groups. The penicillamine group contained a higher proportion of seropositive patients. In each group there were significant improvements in clinical score, CRP and ESR for all time points from 6 to 30 months; these improvements were maintained for longer (up to 60 months for SAS) in the SAS and gold groups but the differences between the drugs after 30 months were probably a consequence of falling number of patients, not differing drug potencies. The mean ESR and CRP levels fell to about 30 mm/h and 20-30 mg/l, respectively. Response was defined as (1) treatment duration greater than 6 months, (2) clinical score improvement greater than 4 by 6 months, (3) ESR fall to less than 30 mm/h by 6 months. By these criteria 142 of 681 patients (20.9%) responded; the response rates were SAS 20.3%, gold 24.1%, penicillamine 17.8%.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对3组需要二线药物治疗的活动性类风湿性关节炎(RA)患者进行了长达5年的临床评分(主观整体评估)、血清C反应蛋白(CRP)和红细胞沉降率(ESR)的系列观察。这3组患者包括:315例服用柳氮磺胺吡啶(SAS)的患者(243名女性,72名男性);203例服用硫代苹果酸金钠(金制剂)的患者(141名女性,62名男性);以及163例服用青霉胺的患者(131名女性,32名男性)。这些组在大多数方面相匹配,但金制剂组女性比例较小,疾病持续时间中位数较短,且CRP中位数高于其余两组。青霉胺组血清阳性患者比例较高。在每组中,从6个月到30个月的所有时间点,临床评分、CRP和ESR均有显著改善;在SAS组和金制剂组中,这些改善持续时间更长(SAS组长达60个月),但30个月后药物之间的差异可能是患者数量减少的结果,而非药物效力不同。ESR和CRP的平均水平分别降至约30mm/h和20 - 30mg/l。反应定义为:(1)治疗持续时间大于6个月;(2)6个月时临床评分改善大于4;(3)6个月时ESR降至小于30mm/h。根据这些标准,681例患者中有142例(20.9%)有反应;反应率分别为:SAS组20.3%,金制剂组24.1%,青霉胺组17.8%。(摘要截取自250字)

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