Department of Rheumatology & Clinical Immunology, University Medical Center Utrecht, Utrecht.
Department of Rheumatology, Northwest Clinics, Alkmaar and Den Helder, Amersfoort, The Netherlands.
Rheumatology (Oxford). 2020 Apr 1;59(4):845-851. doi: 10.1093/rheumatology/kez391.
To establish the performance of (subsets of) the 2015 ACR/EULAR gout classification criteria in patients with unclassified arthritis, and to determine the value of dual-energy CT (DECT) herein. Reference was the MSU crystal detection result in SF at polarization microscopy.
We included subjects with acute, unclassified mono or oligoarthritis, who underwent SF analysis and DECT. Performance was assessed by calculating area under the receiver operating characteristic curve of (i) the clinical criteria subset, (ii) the clinical+serum urate subset and (iii) the full set (including DECT).
Of the 89 subjects enrolled, 40 met the clinical+serum urate subset criteria, and 49 (55%) subjects did not. Of these 49, 30 had a negative microscopy result, of whom 15 had positive DECT; of these 15, 14 met the full set criteria only after adding the positive DECT result. For the clinical-only subset, the areas under the curves (AUCs) were 0.68 and 0.69 without and with DECT result, respectively, and for the clinical+serum urate subset without and with DECT, AUCs were 0.81 and 0.81, respectively (results not significant).
Adding the serum urate results to the clinical subset improves the performance, but adding the DECT result does not, neither does adding the DECT results to the clinical+serum urate subset. However, DECT seems to have an additive value in gout classification, especially when microscopy of SF is negative; 14/89 of patients (16%) only met the classification criteria with the use of DECT.
ClinicalTrials.gov, http://clinicaltrials.gov, NCT03038386.
在未分类关节炎患者中建立(2015 年 ACR/EULAR 痛风分类标准的子集)的性能,并确定双能 CT(DECT)在此的价值。参考标准是偏振显微镜下 SF 中 MSU 晶体检测结果。
我们纳入了患有急性、未分类单关节炎或寡关节炎的患者,这些患者接受了 SF 分析和 DECT。通过计算(i)临床标准子集、(ii)临床+血清尿酸子集和(iii)全套标准(包括 DECT)的接收者操作特征曲线下面积来评估性能。
在纳入的 89 名受试者中,40 名符合临床+血清尿酸子集标准,49 名(55%)受试者不符合。在这 49 名受试者中,30 名显微镜检查结果为阴性,其中 15 名 DECT 检查结果为阳性;在这 15 名受试者中,只有在添加阳性 DECT 结果后,14 名才符合全套标准。对于仅临床子集,没有和有 DECT 结果的曲线下面积(AUCs)分别为 0.68 和 0.69,对于临床+血清尿酸子集,没有和有 DECT 的 AUCs 分别为 0.81 和 0.81(无显著差异)。
将血清尿酸结果添加到临床亚集中可提高性能,但添加 DECT 结果则不能,将 DECT 结果添加到临床+血清尿酸亚集中也不能。然而,DECT 在痛风分类中似乎具有附加价值,尤其是在 SF 显微镜检查为阴性时;14/89 名患者(16%)仅在使用 DECT 时才符合分类标准。
ClinicalTrials.gov,http://clinicaltrials.gov,NCT03038386。