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Derivation and Validation of a Clinical Prediction Rule for Nosocomial Pneumonia after Coronary Artery Bypass Graft Surgery
Laura M. Kinlin, Cheryl Kirchner, Huiling Zhang, Jennifer Daley and David N. Fisman
Clinical Infectious Diseases
Vol. 50, No. 4 (15 February 2010), pp. 493-501
Published by: Oxford University Press
Stable URL: http://www.jstor.org/stable/27799610
Page Count: 9
You can always find the topics here!Topics: Pneumonia, Coronary artery bypass, Disease risk, Infections, Predisposing factors, Surgical specialties, Percutaneous transluminal coronary angioplasty, Mortality, Blood transfusion, Health care industry
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Background. Nosocomial pneumonia is an important cause of morbidity and mortality among surgical patients in the United States. The emergence of effective but potentially costly or risky preventive interventions makes perioperative risk stratification desirable. We sought to develop a prediction rule for pneumonia after coronary artery bypass grafting (CABG), a common surgical procedure. Methods. Data on individuals undergoing CABG at 32 hospitals in 6 states were extracted from Tenet Healthcare's Quality and Resource Management System. A logistic regression-based prediction rule was developed in half of the study sample and validated in the remaining patients. Results. Of 17,143 individuals undergoing CABG from January 1999 through February 2004, 361 (2%) developed pneumonia without a known aspiration etiology. Thirteen independent predictors of pneumonia were identified in the derivation subset of the sample: body mass index <18.5 (defined as the weight in kilograms divided by the square of the height in meters), smoking history, admission from a nonresidential setting, cancer history, chronic obstructive pulmonary disease, Canadian Cardiovascular Society score ≥3, prior internal mammary artery CABG, emergency status, serum creatinine level >1.2 mg/dL, percutaneous transluminal coronary angioplasty, blood transfusion, preoperative vancomycin administration, and receipt of mechanical ventilation for >1 day. The model-based rule was well calibrated (Hosmer-Lemeshow X2 = 5.51; P = .70) and demonstrated good discrimination (area under the receiver-operating characteristic curve [ROC AUC], 0.78) in the derivation group. Discriminatory ability was also reasonable in the validation cohort (ROC AUC, 0.75; P = .18, for difference in ROC AUC between groups). Conclusions. Using a large cohort of patients treated at community and teaching hospitals, we derived and validated a prediction rule for pneumonia after CABG. This index may prove to be useful in prioritizing receipt of preventive interventions.
Clinical Infectious Diseases © 2010 Oxford University Press