Department of Clinical Immunology and Rheumatology, Kalinga Institute of Medical Sciences (KIMS), KIIT University, Bhubaneswar, 751024, India.
Department of Clinical Immunology & Rheumatology, Sanjay Gandhi Postgraduate Institute of Medical Sciences (SGPGIMS), Lucknow, 226014, India.
Rheumatol Int. 2019 Aug;39(8):1397-1403. doi: 10.1007/s00296-019-04323-7. Epub 2019 May 17.
The American College of Rheumatology (ACR) 2016 criteria for fibromyalgia (FM) is recommended for use in primary and referral setting. However, neither the ACR 2016 nor its predecessor ACR 2010 criteria have been validated in a referral setting. We hypothesized that the presence of higher comorbidities in the referral care setting may affect the performance of the ACR 2016. All patients referred to a tertiary care hospital with widespread pain for more than 3 months were screened using (1) the ACR 2016 criteria and (2) by a blinded expert physician (using ACR 1990 criteria). Using the ACR 1990 as reference standard, the sensitivity and specificity were calculated. Also, concomitant depression (BPHQ: Brief Patient Health Questionnaire), anxiety disorder (GAD7: Generalized Anxiety Disorder-7) and alexithymia (TAS-20: Toronto Alexithymia Scale-20) were screened for using standardized instruments. Other central sensitization syndromes were also screened clinically. Of 147 patients (132 females; median age 36 [30-45] years, median symptom duration 4 [1-6] years), 112 met the ACR 1990 criteria while 93 met the ACR 2016 criteria. There was disagreement between the two criteria in 47 patients. The sensitivity and specificity of ACR 2016 were 71% and 60%, respectively. Patients diagnosed by ACR 2016 criteria alone, had higher GAD7 scores than those diagnosed by the ACR 1990 alone. However, BPHQ and TAS-20 did not differ between the groups. Patients diagnosed by the ACR 2016 criteria had a greater odds (OR 5.2 CI 1.3-21.7, p = 0.022) of having concomitant restless leg syndrome or post-traumatic stress disorder or chronic fatigue syndrome. The sensitivity/specificity of the ACR 2016 in tertiary settings matched those found in previous primary care-based studies. Thus, the ACR 2016 criteria are valid for use in the tertiary setting. However, patients diagnosed by only the ACR 2016 criteria (and not by the ACR 1990) have high probability of having another concomitant comorbidity.
美国风湿病学会 (ACR) 2016 年纤维肌痛 (FM) 标准推荐用于初级和转诊环境。然而,ACR 2016 年标准及其前身 ACR 2010 年标准均未在转诊环境中得到验证。我们假设在转诊护理环境中存在更高的合并症可能会影响 ACR 2016 年标准的性能。所有因广泛疼痛超过 3 个月而被转诊至三级保健医院的患者均使用 (1) ACR 2016 年标准和 (2) 由一位盲法专家医师 (使用 ACR 1990 年标准) 进行筛查。使用 ACR 1990 年标准作为参考标准,计算敏感性和特异性。此外,还使用标准化工具筛查同时存在的抑郁 (BPHQ:简短患者健康问卷)、焦虑障碍 (GAD7:广泛性焦虑障碍-7) 和躯体化障碍 (TAS-20:多伦多躯体化障碍量表-20)。还进行了其他中枢敏化综合征的临床筛查。在 147 名患者 (132 名女性;中位年龄 36 [30-45] 岁,中位症状持续时间 4 [1-6] 年) 中,112 名符合 ACR 1990 年标准,93 名符合 ACR 2016 年标准。两项标准之间存在 47 名患者的分歧。ACR 2016 年标准的敏感性和特异性分别为 71%和 60%。仅根据 ACR 2016 年标准诊断的患者的 GAD7 评分高于仅根据 ACR 1990 年标准诊断的患者。然而,两组之间的 BPHQ 和 TAS-20 没有差异。根据 ACR 2016 年标准诊断的患者发生伴有不安腿综合征或创伤后应激障碍或慢性疲劳综合征的可能性更大 (OR 5.2 CI 1.3-21.7,p = 0.022)。在三级环境中,ACR 2016 年标准的敏感性/特异性与之前在初级保健为基础的研究中发现的标准相匹配。因此,ACR 2016 年标准可在三级环境中使用。然而,仅根据 ACR 2016 年标准诊断的患者 (而不是根据 ACR 1990 年标准诊断的患者) 有很高的可能性同时存在另一种合并症。