Pillemer S R, Matteson E L, Jacobsson L T, Martens P B, Melton L J, O'Fallon W M, Fox P C
National Institute of Dental and Craniofacial Research, National Institutes of Health, Gene Therapy and Therapeutics Branch, Bethesda, MD 20892, USA.
Mayo Clin Proc. 2001 Jun;76(6):593-9. doi: 10.4065/76.6.593.
To estimate the incidence of physician-diagnosed primary Sjögren syndrome (SS) among residents of Olmsted County, Minnesota, in the setting of usual medical care and to determine how often objective criteria are available in the medical records of such patients.
We reviewed all medical records of residents in Olmsted County with physician-diagnosed SS from 1976 to 1992 to determine whether they had undergone objective tests for keratoconjunctivitis sicca, salivary dysfunction, or serologic abnormality. Confounding illnesses were excluded. To identify misclassified cases, all records from patients with xerostomia or keratoconjunctivitis sicca were also reviewed. The average annual SS incidence rates were calculated by considering the entire population to be at risk.
Of 75 patients with onset of SS during the study period, 53 had primary SS. All patients were white, 51 (96.2%) were women, and the mean +/- SD age was 59+/-15.8 years. The age- and sex-adjusted annual incidence was 3.9 per 100,000 population (95% confidence interval, 2.8-4.9) for patients with primary SS. Eleven patients (20.8%) with physician-diagnosed SS had no documentation of objective eye, mouth, or laboratory abnormalities. Objective evaluations performed most frequently were laboratory and ocular tests and least often were investigations of xerostomia.
The average annual incidence rate for physician-diagnosed primary SS in Olmsted County is about 4 cases per 100,000 population. These data probably underestimate the true incidence because they are based on usual medical care of patients with SS in a community setting, rather than on a case-detection survey. In the future, a true incidence may be possible with a higher index of suspicion, greater attention to objective tests, and increased awareness of new classification criteria for SS. For epidemiological studies based on existing data, application of current criteria may not be feasible, and consensus on criteria for such studies would be useful.
在常规医疗环境下,评估明尼苏达州奥尔姆斯特德县居民中经医生诊断的原发性干燥综合征(SS)的发病率,并确定此类患者的病历中客观标准的可用频率。
我们回顾了1976年至1992年奥尔姆斯特德县经医生诊断为SS的居民的所有病历,以确定他们是否接受了针对干燥性角结膜炎、唾液功能障碍或血清学异常的客观检查。排除混杂疾病。为识别分类错误的病例,还查阅了口干或干燥性角结膜炎患者的所有病历。通过将整个人口视为有风险人群来计算年平均SS发病率。
在研究期间发病的75例SS患者中,53例为原发性SS。所有患者均为白人,51例(96.2%)为女性,平均年龄±标准差为59±15.8岁。原发性SS患者经年龄和性别调整后的年发病率为每10万人3.9例(95%置信区间,2.8 - 4.9)。11例(20.8%)经医生诊断为SS的患者没有客观眼部、口腔或实验室异常的记录。最常进行的客观评估是实验室和眼部检查,而对口干的检查最少。
奥尔姆斯特德县经医生诊断的原发性SS的年平均发病率约为每10万人4例。这些数据可能低估了真实发病率,因为它们基于社区环境中SS患者的常规医疗,而非病例检测调查。未来,通过更高的怀疑指数、对客观检查的更多关注以及对SS新分类标准的更高认识,可能得出真实发病率。对于基于现有数据的流行病学研究,应用当前标准可能不可行,对此类研究的标准达成共识将是有用的。