Curtis Jeffrey R, Harrold Leslie R, Asgari Maryam M, Deodhar Atul, Salman Craig, Gelfand Joel M, Wu Jashin J, Herrinton Lisa J
Professor of Medicine in the Department of Clinical Immunology and Rheumatology at the University of Alabama at Birmingham.
Associate Professor at the Meyers Primary Care Institute and Fallon Clinic at the University of Massachusetts Medical School.
Perm J. 2016 Fall;20(4):15-151. doi: 10.7812/TPP/15-151. Epub 2016 Jul 29.
Few studies have assessed the prevalence and features of axial spondyloarthritis (axSpA) and ankylosing spondylitis in diverse, population-based, community settings.
We used computerized diagnoses to estimate the prevalence of axSpA and ankylosing spondylitis in Kaiser Permanente Northern California (KPNC).
We identified persons aged 18 years or older with 1 or more International Classification of Diseases, Ninth Revision (ICD-9) diagnosis Code 720.X (ankylosing spondylitis and other inflammatory spondylopathies) in clinical encounter data from 1996 through 2009 to estimate the prevalence of axSpA and ankylosing spondylitis. We reviewed medical records to confirm the diagnosis in a random sample and estimated the positive predictive value of computerized data to identify confirmed cases using various case definitions.
In the computerized data, 5568 adults had diagnostic codes indicating axSpA. On the basis of our case-finding approach using a single physician diagnosis code for ICD-9 720.X, the point prevalence of these conditions, standardized to the 2000 US Census, was 2.26 per 1000 persons for axSpA and 1.07 per 1000 for ankylosing spondylitis. Less than half of suspected cases saw a rheumatologist. The most specific algorithm for confirmed ankylosing spondylitis required 2 or more computerized diagnoses assigned by a rheumatologist, with 67% sensitivity (95% confidence interval, 64%-69%) and 81% positive predictive value (95% confidence interval, 79%-83%).
Observed prevalence in the KPNC population, compared with national estimates for axSpA and ankylosing spondylitis, suggests there is substantial underrecognition of these conditions in routine clinical practice. However, use of computerized data is able to identify true cases of ankylosing spondylitis, facilitating population-based research.
很少有研究在不同的、基于人群的社区环境中评估轴向型脊柱关节炎(axSpA)和强直性脊柱炎的患病率及特征。
我们使用计算机化诊断来估计北加利福尼亚州凯撒医疗集团(KPNC)中axSpA和强直性脊柱炎的患病率。
我们在1996年至2009年的临床诊疗数据中,识别出年龄在18岁及以上、有1个或更多国际疾病分类第九版(ICD - 9)诊断代码720.X(强直性脊柱炎和其他炎性脊柱病)的患者,以估计axSpA和强直性脊柱炎的患病率。我们查阅病历以在随机样本中确认诊断,并使用各种病例定义估计计算机化数据识别确诊病例的阳性预测值。
在计算机化数据中,5568名成年人有诊断代码表明患有axSpA。基于我们使用针对ICD - 9 720.X的单一医生诊断代码的病例发现方法,按照2000年美国人口普查进行标准化后,这些疾病的点患病率为axSpA每1000人中有2.26例,强直性脊柱炎每1000人中有1.07例。不到一半的疑似病例看过风湿病专科医生。确诊强直性脊柱炎最特异的算法需要风湿病专科医生给出2个或更多计算机化诊断,其敏感性为67%(95%置信区间,64% - 69%),阳性预测值为81%(95%置信区间,79% - 83%)。
与全国axSpA和强直性脊柱炎的估计患病率相比,KPNC人群中的观察患病率表明在常规临床实践中对这些疾病的认识严重不足。然而,使用计算机化数据能够识别强直性脊柱炎的真正病例,有助于开展基于人群的研究。