TY - JOUR
T1 - Reducing duplicate genetic testing in inpatient and outpatient settings across a large safety-net system
AU - Alarcon Manchego, Peter
AU - Krouss, Mona
AU - Alaiev, Daniel
AU - Talledo, Joseph
AU - Zaurova, Milana
AU - Chandra, Komal
AU - Tsega, Surafel
AU - Garcia, Mariely
AU - Ford, Kenra
AU - Apfelroth, Stephen
AU - Bajaj, Komal
AU - Shin, Dawi
AU - Cho, Hyung J.
N1 - Publisher Copyright:
© 2023 The Author(s). Published by Oxford University Press on behalf of American Society for Clinical Pathology. All rights reserved.
PY - 2023/9/1
Y1 - 2023/9/1
N2 - Objectives: To develop a system-wide electronic health record (EHR) intervention at a large safety-net hospital system to reduce wasteful duplicate genetic testing. Methods: This project was initiated at a large urban public health care system. An EHR alert was designed to be triggered when a clinician attempted to order any of 16 specified genetic tests for which a previous result existed within the EHR system. Measurements included the proportion of completed genetic tests that were duplicates and alerts per 1,000 tests. Data were stratified by clinician type, specialty, and inpatient vs ambulatory setting. Results: Across all settings, the rate of duplicate genetic testing decreased from 2.35% (1,050 of 44,592 tests) to 0.09% (21 of 22,323 tests) (96% relative reduction, P <. 001). The alert rate per 1,000 tests was 277 for inpatient orders and 64 for ambulatory orders. Among clinician types, residents had the highest alert rate per 1,000 tests at 166 and midwives the lowest at 51 (P <. 01). Among clinician specialties, internal medicine had the highest alert rate per 1,000 tests at 245 and obstetrics and gynecology the lowest at 56 (P <. 01). Conclusions: The EHR intervention successfully reduced duplicate genetic testing by 96% across a large safety-net setting.
AB - Objectives: To develop a system-wide electronic health record (EHR) intervention at a large safety-net hospital system to reduce wasteful duplicate genetic testing. Methods: This project was initiated at a large urban public health care system. An EHR alert was designed to be triggered when a clinician attempted to order any of 16 specified genetic tests for which a previous result existed within the EHR system. Measurements included the proportion of completed genetic tests that were duplicates and alerts per 1,000 tests. Data were stratified by clinician type, specialty, and inpatient vs ambulatory setting. Results: Across all settings, the rate of duplicate genetic testing decreased from 2.35% (1,050 of 44,592 tests) to 0.09% (21 of 22,323 tests) (96% relative reduction, P <. 001). The alert rate per 1,000 tests was 277 for inpatient orders and 64 for ambulatory orders. Among clinician types, residents had the highest alert rate per 1,000 tests at 166 and midwives the lowest at 51 (P <. 01). Among clinician specialties, internal medicine had the highest alert rate per 1,000 tests at 245 and obstetrics and gynecology the lowest at 56 (P <. 01). Conclusions: The EHR intervention successfully reduced duplicate genetic testing by 96% across a large safety-net setting.
KW - duplicate testing
KW - genetic testing
KW - high-value care
KW - quality improvement
KW - safety net
UR - https://www.scopus.com/pages/publications/85171983922
U2 - 10.1093/ajcp/aqad052
DO - 10.1093/ajcp/aqad052
M3 - Article
C2 - 37202882
AN - SCOPUS:85171983922
SN - 0002-9173
VL - 160
SP - 292
EP - 296
JO - American Journal of Clinical Pathology
JF - American Journal of Clinical Pathology
IS - 3
ER -