TY - JOUR
T1 - Electronic sniffer systems to identify the acute respiratory distress syndrome
AU - Wayne, Max T.
AU - Valley, Thomas S.
AU - Cooke, Colin R.
AU - Sjoding, Michael W.
N1 - Publisher Copyright:
© 2019 by the American Thoracic Society.
PY - 2019/4
Y1 - 2019/4
N2 - Background: The acute respiratory distress syndrome (ARDS) results in substantial mortality but remains underdiagnosed in clinical practice. Automated ARDS "sniffer" systems, tools that can automatically analyze electronic medical record data, have been developed to improve recognition of ARDS in clinical practice. Objectives: To perform a systematic review examining the evidence underlying automated sniffer systems for ARDS detection. Data Sources: MEDLINE and Scopus databases through November 2018 to identify studies of tools using routinely available clinical data to detect patients with ARDS. Data Extraction: Study design, tool description, and diagnostic performance were extracted by two reviewers. The Quality Assessment of Diagnostic Accuracy Studies-2 was used to evaluate each study for risk of bias in four domains: patient selection, index test, reference standard, and study flow and timing. Synthesis: Among 480 studies identified, 9 met inclusion criteria, and they evaluated six unique ARDS sniffer tools. Eight studies had derivation and/or temporal validation designs, with one also evaluating the effects of implementing a tool in clinical practice. A single study performed an external validation of previously published ARDS sniffer tools. Studies reported a wide range of sensitivities (43-98%) and positive predictive values (26-90%) for detection of ARDS. Most studies had potential for high risk of bias identified in their study design, including patient selection (five of nine), reference standard (four of nine), and flow and timing (three of nine). In the single external validation without any perceived risks of biases, the performance of ARDS sniffer tools was worse. Conclusions: Sniffer systems developed to detect ARDS had moderate to high predictive value in their derivation cohorts, although most studies had the potential for high risks of bias in study design. Methodological issues may explain some of the variability in tool performance. There remains an ongoing need for robust evaluation of ARDS sniffer systems and their impact on clinical practice.
AB - Background: The acute respiratory distress syndrome (ARDS) results in substantial mortality but remains underdiagnosed in clinical practice. Automated ARDS "sniffer" systems, tools that can automatically analyze electronic medical record data, have been developed to improve recognition of ARDS in clinical practice. Objectives: To perform a systematic review examining the evidence underlying automated sniffer systems for ARDS detection. Data Sources: MEDLINE and Scopus databases through November 2018 to identify studies of tools using routinely available clinical data to detect patients with ARDS. Data Extraction: Study design, tool description, and diagnostic performance were extracted by two reviewers. The Quality Assessment of Diagnostic Accuracy Studies-2 was used to evaluate each study for risk of bias in four domains: patient selection, index test, reference standard, and study flow and timing. Synthesis: Among 480 studies identified, 9 met inclusion criteria, and they evaluated six unique ARDS sniffer tools. Eight studies had derivation and/or temporal validation designs, with one also evaluating the effects of implementing a tool in clinical practice. A single study performed an external validation of previously published ARDS sniffer tools. Studies reported a wide range of sensitivities (43-98%) and positive predictive values (26-90%) for detection of ARDS. Most studies had potential for high risk of bias identified in their study design, including patient selection (five of nine), reference standard (four of nine), and flow and timing (three of nine). In the single external validation without any perceived risks of biases, the performance of ARDS sniffer tools was worse. Conclusions: Sniffer systems developed to detect ARDS had moderate to high predictive value in their derivation cohorts, although most studies had the potential for high risks of bias in study design. Methodological issues may explain some of the variability in tool performance. There remains an ongoing need for robust evaluation of ARDS sniffer systems and their impact on clinical practice.
KW - Acute lung injury
KW - Acute respiratory distress syndrome
KW - Diagnostic tool
KW - Identification
KW - Systematic review
UR - http://www.scopus.com/inward/record.url?scp=85063727849&partnerID=8YFLogxK
U2 - 10.1513/AnnalsATS.201810-715OC
DO - 10.1513/AnnalsATS.201810-715OC
M3 - Review article
C2 - 30521765
AN - SCOPUS:85063727849
SN - 2325-6621
VL - 16
SP - 488
EP - 495
JO - Annals of the American Thoracic Society
JF - Annals of the American Thoracic Society
IS - 4
ER -