David K. Warren
Washington University in St. Louis
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by David K. Warren.
Clinical Infectious Diseases | 2009
Leonard A. Mermel; Michael Allon; Emilio Bouza; Donald E. Craven; Patricia M. Flynn; Issam Raad; Bart J. A. Rijnders; Robert J. Sherertz; David K. Warren; North Carolina
These updated guidelines replace the previous management guidelines published in 2001. The guidelines are intended for use by health care providers who care for patients who either have these infections or may be at risk for them.
Critical Care Medicine | 2003
David K. Warren; Sunita J. Shukla; Margaret A. Olsen; Marin H. Kollef; Michael J. Cox; Max M. Cohen; Victoria J. Fraser
ObjectiveTo determine the attributable cost of ventilator-associated pneumonia from a hospital-based cost perspective, after adjusting for potential confounders. DesignPatients admitted between January 19, 1998, and December 31, 1999, were followed prospectively for the occurrence of ventilator-associated pneumonia. Hospital costs were defined by using the hospital cost accounting database. SettingThe medical and surgical intensive care units at a suburban, tertiary care hospital. PatientsPatients requiring >24 hrs of mechanical ventilation. InterventionsNone. Measurements and Main ResultsWe measured occurrence of ventilator-associated pneumonia, in-hospital mortality rate, total intensive care unit (ICU) and hospital lengths of stay (LOS), and total hospital cost per patient. Ventilator-associated pneumonia occurred in 127 of 819 patients (15.5%). Compared with uninfected, ventilated patients, patients with ventilator-associated pneumonia had a higher Acute Physiology and Chronic Health Evaluation II score on admission (p < .001) and were more likely to require multiple intubations (p < .001), hemodialysis (p < .001), tracheostomy (p < .001), central venous catheters (p < .001), and corticosteroids (p < .001). Patients with ventilator-associated pneumonia were more likely to be bacteremic during their ICU stay (36 [28%] vs. 22 [3%];p < .001). Patients with ventilator-associated pneumonia had significantly higher unadjusted ICU LOS (26 vs. 4 days;p < .001), hospital LOS (38 vs. 13 days;p < .001), mortality rate (64 [50%] vs. 237 [34%];p < .001), and hospital costs (
The New England Journal of Medicine | 2013
Michael W. Climo; Deborah S. Yokoe; David K. Warren; Trish M. Perl; Maureen K. Bolon; Loreen A. Herwaldt; Robert A. Weinstein; Kent A. Sepkowitz; John A. Jernigan; Kakotan Sanogo; Edward S. Wong
70,568 vs.
Critical Care Medicine | 2006
David K. Warren; Wasim W. Quadir; Alexis Elward; Michael J. Cox; Victoria J. Fraser
21,620, p < .001). Multiple linear regression, controlling for other factors that may affect costs, estimated the attributable cost of ventilator-associated pneumonia to be
Critical Care Medicine | 2009
Michael W. Climo; Kent A. Sepkowitz; Gianna Zuccotti; Victoria J. Fraser; David K. Warren; Trish M. Perl; Kathleen Speck; John A. Jernigan; Jaime R. Robles; Edward S. Wong
11,897 (95% confidence interval =
Journal of Clinical Microbiology | 2004
David K. Warren; Robert S. Liao; Liana R. Merz; Michael Eveland; W. Michael Dunne
5,265–
Pediatrics | 2005
Alexis Elward; David K. Warren; Victoria J. Fraser
26,214;p < .001). ConclusionsPatients with ventilator-associated pneumonia had significantly longer ICU and hospital LOS, with higher crude hospital cost and mortality rate compared with uninfected patients. After we adjusted for underlying severity of illness, the attributable cost of ventilator-associated pneumonia was approximately
Infection Control and Hospital Epidemiology | 2006
David K. Warren; Sara E. Cosgrove; Daniel J. Diekema; Gianna Zuccotti; Michael W. Climo; Maureen K. Bolon; Jerome I. Tokars; Gary A. Noskin; Edward S. Wong; Kent A. Sepkowitz; Loreen A. Herwaldt; Trish M. Perl; Steven L. Solomon; Victoria J. Fraser
11,897.
Clinical Infectious Diseases | 2007
Jeffrey C. Jones; Theodore J. Rogers; Peter Brookmeyer; William Michael Dunne; Gregory A. Storch; Craig M. Coopersmith; Victoria J. Fraser; David K. Warren
BACKGROUND Results of previous single-center, observational studies suggest that daily bathing of patients with chlorhexidine may prevent hospital-acquired bloodstream infections and the acquisition of multidrug-resistant organisms (MDROs). METHODS We conducted a multicenter, cluster-randomized, nonblinded crossover trial to evaluate the effect of daily bathing with chlorhexidine-impregnated washcloths on the acquisition of MDROs and the incidence of hospital-acquired bloodstream infections. Nine intensive care and bone marrow transplantation units in six hospitals were randomly assigned to bathe patients either with no-rinse 2% chlorhexidine-impregnated washcloths or with nonantimicrobial washcloths for a 6-month period, exchanged for the alternate product during the subsequent 6 months. The incidence rates of acquisition of MDROs and the rates of hospital-acquired bloodstream infections were compared between the two periods by means of Poisson regression analysis. RESULTS A total of 7727 patients were enrolled during the study. The overall rate of MDRO acquisition was 5.10 cases per 1000 patient-days with chlorhexidine bathing versus 6.60 cases per 1000 patient-days with nonantimicrobial washcloths (P=0.03), the equivalent of a 23% lower rate with chlorhexidine bathing. The overall rate of hospital-acquired bloodstream infections was 4.78 cases per 1000 patient-days with chlorhexidine bathing versus 6.60 cases per 1000 patient-days with nonantimicrobial washcloths (P=0.007), a 28% lower rate with chlorhexidine-impregnated washcloths. No serious skin reactions were noted during either study period. CONCLUSIONS Daily bathing with chlorhexidine-impregnated washcloths significantly reduced the risks of acquisition of MDROs and development of hospital-acquired bloodstream infections. (Funded by the Centers for Disease Control and Prevention and Sage Products; ClinicalTrials.gov number, NCT00502476.).
The American Journal of Medicine | 2010
Hitoshi Honda; Melissa J. Krauss; Jeffrey C. Jones; Margaret A. Olsen; David K. Warren
Objective:To determine the attributable cost and length of stay of intensive care unit (ICU)–acquired, catheter-associated bloodstream infections from a hospital-based cost perspective, after adjusting for potential confounders. Design:Patients admitted to the ICU between January 19, 1998, and July 31, 2000, were observed prospectively for the occurrence of catheter-associated bloodstream infections. Hospital costs were obtained from the hospital cost accounting database. Setting:The medical and surgical ICUs at a 500-bed suburban, tertiary care hospital. Patients:Patients requiring central venous catheterization while in the ICU. Interventions:None. Measurements and Main Results:We measured occurrence of catheter-associated bloodstream infection, in-hospital mortality rate, total ICU and hospital lengths of stay, and total hospital costs. Catheter-associated bloodstream infection occurred in 41 of 1,132 patients (3.6 cases per 1000 catheter days). Patients with catheter-associated bloodstream infection had significantly higher unadjusted ICU length of stay (median, 24 vs. 5 days; p < .001), hospital length of stay (median, 45 vs. 11 days; p < .001), mortality rate (21 [51%] vs. 301 [28%], p = .001), and total hospital costs (