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2001年,大多数接受类风湿性关节炎常规治疗的患者不符合大多数近期临床试验的纳入标准或美国风湿病学会的缓解标准。

Most patients receiving routine care for rheumatoid arthritis in 2001 did not meet inclusion criteria for most recent clinical trials or american college of rheumatology criteria for remission.

作者信息

Sokka Tuulikki, Pincus Theodore

机构信息

Division of Rheumatology and Immunology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, USA.

出版信息

J Rheumatol. 2003 Jun;30(6):1138-46.

Abstract

OBJECTIVE

To determine the proportion of 2 cohorts of patients with rheumatoid arthritis (RA) in Nashville, Tennessee, who met 4 common criteria for inclusion in clinical trials: > or = 6 swollen joints, > or = 6 tender joints, erythrocyte sedimentation rate > or = 28 mm/h, and/or morning stiffness > or = 45 min.

METHODS

Two cohorts of patients with RA, all of whom had met American Rheumatism Association (ARA) [now American College of Rheumatology (ACR)] criteria for RA at some time, were studied. Cohort L (late) included 146 consecutive patients whose mean disease duration was 14.0 years and who had been under care at a weekly academic rheumatology clinic for a mean of 6.2 years when seen in 1998-2001. Cohort E (early) included 232 patients of 5 private practice rheumatologists whose symptoms began in 1998 or later and whose mean disease duration was 1.8 years when seen in 2001. Patients were reviewed for the 4 inclusion criteria as well as 6 ARA remission criteria.

RESULTS

In Cohort L, on a 28 joint count, 42.5% of patients had > or = 6 swollen joints, 25.3% had > or = 6 tender joints, 19.9% had both > or = 6 swollen and > or = 6 tender joints, 25.0% had ESR > or = 28, and 45.9% had morning stiffness > or = 45 min. In Cohort E, on a 42 joint count, 63.4% of patients had > or = 6 swollen joints, 50.4% had > or = 6 tender joints, 38.8% had both > or = 6 swollen and > or = 6 tender joints, 49.3% had ESR > or = 28, and 50.9% had morning stiffness > or = 45 min. Overall, 15.3% of Cohort L and 34.1% of Cohort E patients had > or = 6 swollen and tender joints, as well as an ESR > or = 28 or morning stiffness > or = 45 min. Only 4.1% of Cohort L and no patient in Cohort E met ARA criteria for remission.

CONCLUSION

The majority of patients seen in routine care in these 2 cohorts did not meet criteria for inclusion in most contemporary RA clinical trials, including clinical trials sponsored by pharmaceutical companies to introduce new drugs or biological agents. Few of these patients met ARA criteria for remission. Controlled trial data are not available concerning results of treatment with new biological agents or disease modifying antirheumatic drugs in a large proportion, if not a majority, of patients with RA at this time.

摘要

目的

确定田纳西州纳什维尔市两个类风湿关节炎(RA)患者队列中符合临床试验4项常见纳入标准的患者比例,这4项标准为:≥6个肿胀关节、≥6个压痛关节、红细胞沉降率≥28 mm/h和/或晨僵≥45分钟。

方法

对两个RA患者队列进行研究,所有患者均曾在某一时刻符合美国风湿病协会(ARA)[现为美国风湿病学会(ACR)]的RA标准。队列L(晚期)包括146例连续患者,其平均病程为14.0年,1998 - 2001年就诊时在每周一次的学术风湿病诊所接受治疗的平均时间为6.2年。队列E(早期)包括5位私人执业风湿病医生的232例患者,其症状始于1998年或之后,2001年就诊时平均病程为1.8年。对患者进行这4项纳入标准以及6项ARA缓解标准的评估。

结果

在队列L中,以28个关节计数,42.5%的患者有≥6个肿胀关节,25.3%有≥6个压痛关节,19.9%有≥6个肿胀关节且≥6个压痛关节,25.0%红细胞沉降率≥28,45.9%晨僵≥45分钟。在队列E中,以42个关节计数,63.4%的患者有≥6个肿胀关节,50.4%有≥6个压痛关节,38.8%有≥6个肿胀关节且≥6个压痛关节,49.3%红细胞沉降率≥28,50.9%晨僵≥45分钟。总体而言,队列L中15.3%的患者以及队列E中34.1%的患者有≥6个肿胀和压痛关节,且红细胞沉降率≥28或晨僵≥45分钟。队列L中只有4.1%的患者符合ARA缓解标准,队列E中无患者符合。

结论

这两个队列中接受常规治疗的大多数患者不符合大多数当代RA临床试验的纳入标准,包括制药公司为引入新药或生物制剂而开展的临床试验。这些患者中很少有人符合ARA缓解标准。目前尚无关于大多数(即便不是全部)RA患者使用新生物制剂或改善病情抗风湿药治疗结果的对照试验数据。

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