Impact of a clinical decision support system in an electronic health record to enhance detection of α₁-antitrypsin deficiency.

BACKGROUND Because α(1)-antitrypsin deficiency (AATD) is underrecognized, strategies to enhance guideline-based diagnostic testing are warranted. METHODS We studied the impact of issuing a guideline-based alert within an electronic health record (EHR) to test for AATD on the rate of testing for and detection of AATD. For patients at the Cleveland Clinic whose physician-ordered pulmonary function test results showed airflow obstruction, the rates of testing for and detection of AATD were determined during a baseline (prealert) period and again after implementing the alert. RESULTS During the baseline period, among 979 eligible subjects, 4.7% were tested; 8.9% of those who had phenotype testing performed were found to have AATD (serum levels < 100 mg/dL), of whom 3.2% had the PI*ZZ genotype. After the alert, among the 624 eligible subjects, the rate of testing increased severalfold (15.1%, P < .001), though neither the rate of detecting AATD (5.3%) nor PI*ZZ (2.6%) differed from the rates during the baseline period. Having an alternate diagnosis (other than asthma) that could explain airflow obstruction (eg, congestive heart failure, sarcoidosis, Langerhans cell histiocytosis) was associated with a lower rate of testing (P = .041), while carrying a diagnosis of asthma tended to increase the testing frequency (P = .15). Multivariate analysis showed that younger age and a smoking history were associated with being tested. CONCLUSIONS Issuing an alert within an EHR was associated with a severalfold increase in the frequency of testing for α(1)-antitrypsin without a higher rate of diagnosing severe AATD. While the lack of more frequent diagnosis of AATD may reflect a high rate of baseline detection, these results prompt consideration of additional strategies to enhance detection of AATD.