Duke University, Durham, North Carolina.
University of Michigan, Ann Arbor.
Arthritis Care Res (Hoboken). 2018 Feb;70(2):268-274. doi: 10.1002/acr.23273.
To compare practice patterns and prescribing differences for juvenile idiopathic arthritis (JIA) between adult rheumatologists (ARs) and pediatric rheumatologists (PRs), the perceived educational needs, and factors that enhance or impede co-management.
Two parallel, cross-sectional surveys focusing on JIA were administered in 2009 to a random sample of 193 PRs and 500 ARs using the American College of Rheumatology membership file. Bivariate analysis was conducted for common items.
The response rate was 62.1% for ARs (n = 306) and 72.3% for PRs (n = 138). Only 23% of responding ARs (n = 69) reported caring for children with JIA. Of these, 94% strongly agreed/agreed feeling comfortable diagnosing JIA; however, only 76% felt comfortable treating JIA. Clinical vignettes highlighted several prescribing differences. Forty-eight percent of ARs and 31% of PRs felt medications to treat JIA did not have clear dosing guidelines. Though PRs initiated disease-modifying antirheumatic drugs and biologic agents earlier, treatments were similar after 3 months. To enhance co-management, 74% of pediatric respondents endorsed shared medical records.
Nearly one-quarter of surveyed ARs care for children with JIA, with most limiting their practice to older children. There was more discomfort in treating JIA than diagnosing it, and there were significant prescribing differences. Both provider types identified the need for better dosing and treatment resources. Updated management guidelines along with exposure to pediatric rheumatology in fellowship could reduce treatment differences and enhance the care of children with JIA. Shared medical records and improvement in reimbursement may optimize co-management.
比较成人类风湿学家(ARs)和儿科风湿病学家(PRs)在治疗青少年特发性关节炎(JIA)方面的实践模式和处方差异,以及他们对教育需求的认知,同时还探讨了促进或阻碍共同管理的因素。
2009 年,我们使用美国风湿病学会(ACR)的会员档案,对随机抽取的 193 名 PRs 和 500 名 ARs 进行了两项平行的、针对 JIA 的横断面调查。对常见项目进行了双变量分析。
ARs 的回复率为 62.1%(n=306),PRs 的回复率为 72.3%(n=138)。只有 23%的回复 ARs(n=69)报告说照顾患有 JIA 的儿童。其中,94%强烈同意/同意他们能够诊断 JIA;然而,只有 76%的人认为自己能够治疗 JIA。临床病例突显了一些处方差异。48%的 ARs 和 31%的 PRs 认为治疗 JIA 的药物没有明确的剂量指南。尽管 PRs 更早地开始使用疾病修饰抗风湿药物和生物制剂,但在 3 个月后,治疗方法相似。为了加强共同管理,74%的儿科受访者支持共享医疗记录。
近四分之一接受调查的 ARs 会照顾患有 JIA 的儿童,但大多数 ARs 将其治疗范围限制在年龄较大的儿童。在治疗 JIA 方面,他们比诊断 JIA 感到更多的不适,并且存在显著的处方差异。这两种类型的提供者都认为需要更好的剂量和治疗资源。通过 fellowship接触儿科风湿病学以及更新管理指南可以减少治疗差异,从而优化对患有 JIA 的儿童的护理。共享医疗记录和改善报销可能会优化共同管理。