Automated identification of an aspirin-exacerbated respiratory disease cohort

被引:35
作者
Cahill, Katherine N. [1 ,2 ]
Johns, Christina B. [2 ]
Cui, Jing [1 ,2 ]
Wickner, Paige [1 ,2 ]
Bates, David W. [1 ,3 ]
Laidlaw, Tanya M. [1 ,2 ]
Beeler, Patrick E. [1 ,3 ,4 ,5 ]
机构
[1] Harvard Med Sch, Dept Med, Boston, MA USA
[2] Brigham & Womens Hosp, Div Rheumatol Immunol & Allergy, 75 Francis St, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Div Gen Internal Med & Primary Care, 75 Francis St, Boston, MA 02115 USA
[4] Univ Zurich Hosp, Res Ctr Med Informat, Zurich, Switzerland
[5] Univ Zurich, Zurich, Switzerland
基金
瑞士国家科学基金会; 美国国家卫生研究院;
关键词
Aspirin-exacerbated respiratory disease; electronic health record; asthma; nasal polyps; nonsteroidal anti-inflammatory drugs; chronic rhinosinusitis; structured query language; clinical decision support; RHINOSINUSITIS-ASTHMA; DESENSITIZATION; ALGORITHM; VALIDATION; SAFETY;
D O I
10.1016/j.jaci.2016.05.048
中图分类号
R392 [医学免疫学];
学科分类号
100108 [医学免疫学];
摘要
Background: Aspirin-exacerbated respiratory disease (AERD) is characterized by 3 clinical features: asthma, nasal polyposis, and respiratory reactions to cyclooxygenase-1 inhibitors (nonsteroidal anti-inflammatory drugs). Electronic health records (EHRs) contain information on each feature of this triad. Objective: We sought to determine whether an informatics algorithm applied to the EHR could electronically identify patients with AERD. Methods: We developed an informatics algorithm to search the EHRs of patients aged 18 years and older from the Partners Healthcare system over a 10-year period (2004-2014). Charts with search terms for asthma, nasal polyps, and record of respiratory (cohort A) or unspecified (cohort B) reactions to nonsteroidal anti-inflammatory drugs were identified as "possible AERD.'' Two clinical experts reviewed all charts to confirm a diagnosis of "clinical AERD'' and classify cases as "diagnosed AERD'' or "undiagnosed AERD'' on the basis of physician-documented AERD-specific terms in patient notes. Results: Our algorithm identified 731" possible AERD'' cases, of which 638 were not in our AERD patient registry. Chart review of cohorts A (n 5 511) and B (n 5 127) demonstrated a positive predictive value of 78.4% for "clinical AERD,'' which rose to 88.7% when unspecified reactions were excluded. Of those with clinical AERD, 12.4% had no mention of AERD by any treating caregiver and were classified as "undiagnosed AERD.'' "Undiagnosed AERD'' cases were less likely than "diagnosed AERD'' cases to have been seen by an allergist/immunologist (38.7% vs 93.2%; P <.0001). Conclusions: An informatics algorithm can successfully identify both known and previously undiagnosed cases of AERD with a high positive predictive value. Involvement of an allergist/immunologist significantly increases the likelihood of an AERD diagnosis.
引用
收藏
页码:819 / +
页数:13
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