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芬兰新确诊慢性幼年特发性关节炎患者第一年疾病修正药物的使用情况。

First-year purchases of disease-modifying drugs of incident patients with chronic juvenile arthritis in Finland.

机构信息

Department of paediatrics, Päijät-Häme Central Hospital, Lahti, Finland.

出版信息

Clin Exp Rheumatol. 2011 Sep-Oct;29(5):878-81. Epub 2011 Oct 31.

Abstract

OBJECTIVES

To establish a nationwide overview on drug treatment of juvenile idiopathic arthritis (JIA), which is the most frequent form of chronic arthritis (JA) in children and adolescents. The emphasis is on the first 12 months after diagnosis, and any changes in medication practices during the early years of the present millennium are registered.

METHODS

The Social Insurance Institution (SII) in Finland keeps a national register on individuals granted with a special reimbursement for medication of defined chronic diseases. From that register, we identified by the ICD-code of M08 all JA patients aged 16 years or under with an index day from 2000 through 2007. The prescription register of the SII showed the medication purchased for the patients. The register does not cover infused medications given in hospitals. We evaluated the first disease year's medication and the treatment strategy of the very first three months.

RESULTS

Within our study period 2000-2007, the proportion of patients using methotrexate during the first year of treatment increased from 54 to 72% (p<0.001). The combination of two or more DMARDs became more popular (increased from 16 to 21%) as the initial treatment strategy. These changes parallel a decrease in per oral glucocorticoids. The proportion of JA patients receiving TNFα-blockers during the first year after diagnose reached the level of about 5% during the years 2004 to 007.

CONCLUSIONS

The drug treatment of patients with recent onset JA has become more intensive during the course of the new millennium in Finland, a fact expected to improve the disease outcome.

摘要

目的

建立一个关于儿童青少年特发性关节炎(JIA)药物治疗的全国性概述,这是儿童慢性关节炎(JA)最常见的形式。重点是诊断后 12 个月,登记本千年早期药物治疗实践的任何变化。

方法

芬兰社会保险机构(SII)保存了一份关于获得特定慢性病药物报销个人的国家登记册。从该登记册中,我们根据 M08 ICD 代码确定了所有年龄在 16 岁及以下的 JA 患者,索引日为 2000 年至 2007 年。SII 的处方登记册显示了为患者购买的药物。该登记册不包括在医院输注的药物。我们评估了第一年的用药情况和最初三个月的治疗策略。

结果

在我们的研究期间(2000-2007 年),第一年治疗中使用甲氨蝶呤的患者比例从 54%增加到 72%(p<0.001)。作为初始治疗策略,两种或更多种 DMARD 联合使用的比例增加(从 16%增加到 21%)。这些变化与口服糖皮质激素的减少平行。在诊断后第一年接受 TNFα 阻滞剂治疗的 JA 患者比例在 2004 年至 007 年期间达到了约 5%。

结论

在本千年期间,芬兰新发病例 JA 患者的药物治疗变得更加密集,预计这将改善疾病结局。

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