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Clinical Therapeutics

Validation of a Community-Acquired Pneumonia Score To Improve Empiric Antibiotic Selection at an Academic Medical Center

Meredith B. Oliver, Karen Fong, Laura Certain, Emily S. Spivak, Tristan T. Timbrook
Meredith B. Oliver
aDepartment of Pharmacy, University of Minnesota Masonic Children’s Hospital, Minneapolis, Minnesota, USA
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Karen Fong
bDepartment of Pharmacy Services, University of Utah Health, Salt Lake City, Utah, USA
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Laura Certain
cDepartment of Medicine, Division of Infectious Diseases, University of Utah School of Medicine, Salt Lake City, Utah, USA
dVeterans Affairs Medical Center, Salt Lake City, Utah, USA
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Emily S. Spivak
cDepartment of Medicine, Division of Infectious Diseases, University of Utah School of Medicine, Salt Lake City, Utah, USA
dVeterans Affairs Medical Center, Salt Lake City, Utah, USA
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Tristan T. Timbrook
eBiofire Diagnostics, Salt Lake City, Utah, USA
fCollege of Pharmacy, University of Utah Health, Salt Lake City, Utah, USA
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  • ORCID record for Tristan T. Timbrook
DOI: 10.1128/AAC.01482-20
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ABSTRACT

The 2019 American Thoracic Society and the Infectious Diseases Society of America community-acquired pneumonia (CAP) guidelines recommend that drug-resistant pathogens (DRP) be empirically covered if locally validated risk factors are present. This retrospective case-control validation study evaluated the performance of the drug resistance in pneumonia (DRIP) clinical prediction score. Two hundred seventeen adult patients with ICD-10 (https://www.who.int/classifications/classification-of-diseases) pneumonia diagnosis, positive confirmed microbiologic data, and clinical signs and symptoms were included. A DRIP score of ≥4 was used to assess model performance. Logistic regression was used to select for significant predictors and create a modified DRIP score, which was evaluated to define clinical application. The DRIP score predicted pneumonia due to a DRP with a sensitivity of 67% and specificity of 73%. The area under the receiver operating characteristic (AUROC) curve was 0.76 (95% confidence interval [CI], 0.69 to 0.82). From regression analysis, prior infection with a DRP and antibiotics in the last 60 days, yielding scores of 2 points and 1 point, respectively, remained local risk factors in predicting drug-resistant pneumonia. Sensitivity (47%) and specificity (94%) were maximized at a threshold of ≥2 in the modified DRIP model. Therefore, prior infection with a DRP remained the only clinically relevant predictor for drug-resistant pneumonia. The original DRIP score demonstrated a decreased performance in our patient population and behaved similarly to other clinical prediction models. Empiric CAP therapy without anti-methicillin-resistant Staphylococcus aureus and antipseudomonal coverage should be considered for noncritically ill patients without a drug resistant pathogen infection in the past year. Our data support the necessity of local validation to authenticate clinical risk predictors for drug-resistant pneumonia.

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Validation of a Community-Acquired Pneumonia Score To Improve Empiric Antibiotic Selection at an Academic Medical Center
Meredith B. Oliver, Karen Fong, Laura Certain, Emily S. Spivak, Tristan T. Timbrook
Antimicrobial Agents and Chemotherapy Jan 2021, 65 (2) e01482-20; DOI: 10.1128/AAC.01482-20

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Validation of a Community-Acquired Pneumonia Score To Improve Empiric Antibiotic Selection at an Academic Medical Center
Meredith B. Oliver, Karen Fong, Laura Certain, Emily S. Spivak, Tristan T. Timbrook
Antimicrobial Agents and Chemotherapy Jan 2021, 65 (2) e01482-20; DOI: 10.1128/AAC.01482-20
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KEYWORDS

pneumonia
bacterial
drug resistance
antimicrobial stewardship
validation study

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