Alexis Elward
Washington University in St. Louis
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Critical Care Medicine | 2006
David K. Warren; Wasim W. Quadir; Alexis Elward; Michael J. Cox; Victoria J. Fraser
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 (
The New England Journal of Medicine | 2008
David B. Blossom; Priti R. Patel; Alexis Elward; Luke N. Robinson; Ganpan Gao; Robert Langer; Kiran M. Perkins; Jennifer L. Jaeger; Katie M. Kurkjian; Marilyn Jones; Sarah Schillie; Nadine Shehab; Daniel Ketterer; Ganesh Venkataraman; Takashi Kei Kishimoto; Zachary Shriver; Ann W. McMahon; K. Frank Austen; Steven Kozlowski; Arjun Srinivasan; George Turabelidze; Carolyn V. Gould; Matthew J. Arduino; Ram Sasisekharan
83,544 vs.
Clinical Microbiology Reviews | 2007
Elizabeth Foglia; Mary Dawn Meier; Alexis Elward
23,803, p < .001). Controlling for other factors that may affect costs and lengths of stay, catheter-associated bloodstream infections resulted in an attributable cost of
Pediatrics | 2005
Alexis Elward; David K. Warren; Victoria J. Fraser
11,971 (95% confidence interval,
The Lancet | 2013
Aaron M. Milstone; Alexis Elward; Xiaoyan Song; Danielle M. Zerr; Rachel Orscheln; Kathleen Speck; Daniel Obeng; Nicholas G. Reich; Susan E. Coffin; Trish M. Perl
6,732–
Clinical Infectious Diseases | 2001
David K. Warren; Jeanne E. Zack; Alexis Elward; Michael J. Cox; Victoria J. Fraser
18,352), ICU length of stay of 2.41 days (95% confidence interval, 0.08–3.09 days), and hospital length of stay of 7.54 days (95% confidence interval, 3.99–11.09 days). Conclusions:Patients with catheter-associated bloodstream infection had significantly longer ICU and hospital lengths of stay, with higher unadjusted total mortality rate and hospital cost compared with uninfected patients. After adjusting for underlying severity of illness, the attributable cost of catheter-associated bloodstream infection was approximately
Pediatrics | 2008
Stephanie A. Fritz; Jane Garbutt; Alexis Elward; William D. Shannon; Gregory A. Storch
11,971.
Infection Control and Hospital Epidemiology | 2006
Alexis Elward; Victoria J. Fraser
BACKGROUND In January 2008, the Centers for Disease Control and Prevention began a nationwide investigation of severe adverse reactions that were first detected in a single hemodialysis facility. Preliminary findings suggested that heparin was a possible cause of the reactions. METHODS Information on clinical manifestations and on exposure was collected for patients who had signs and symptoms that were consistent with an allergic-type reaction after November 1, 2007. Twenty-one dialysis facilities that reported reactions and 23 facilities that reported no reactions were included in a case-control study to identify facility-level risk factors. Unopened heparin vials from facilities that reported reactions were tested for contaminants. RESULTS A total of 152 adverse reactions associated with heparin were identified in 113 patients from 13 states from November 19, 2007, through January 31, 2008. The use of heparin manufactured by Baxter Healthcare was the factor most strongly associated with reactions (present in 100.0% of case facilities vs. 4.3% of control facilities, P<0.001). Vials of heparin manufactured by Baxter from facilities that reported reactions contained a contaminant identified as oversulfated chondroitin sulfate (OSCS). Adverse reactions to the OSCS-contaminated heparin were often characterized by hypotension, nausea, and shortness of breath occurring within 30 minutes after administration. Of 130 reactions for which information on the heparin lot was available, 128 (98.5%) occurred in a facility that had OSCS-contaminated heparin on the premises. Of 54 reactions for which the lot number of administered heparin was known, 52 (96.3%) occurred after the administration of OSCS-contaminated heparin. CONCLUSIONS Heparin contaminated with OSCS was epidemiologically linked to adverse reactions in this nationwide outbreak. The reported clinical features of many of the cases further support the conclusion that contamination of heparin with OSCS was the cause of the outbreak.
Infection Control and Hospital Epidemiology | 2004
Allison M. Kennedy; Alexis Elward; Victoria J. Fraser
SUMMARY Ventilator-associated pneumonia (VAP) is the second most common hospital-acquired infection among pediatric intensive care unit (ICU) patients. Empiric therapy for VAP accounts for approximately 50% of antibiotic use in pediatric ICUs. VAP is associated with an excess of 3 days of mechanical ventilation among pediatric cardiothoracic surgery patients. The attributable mortality and excess length of ICU stay for patients with VAP have not been defined in matched case control studies. VAP is associated with an estimated
Infection Control and Hospital Epidemiology | 2007
Bs Elizabeth E. Foglia; Victoria J. Fraser; Alexis Elward
30,000 in attributable cost. Surveillance for VAP is complex and usually performed using clinical definitions established by the CDC. Invasive testing via bronchoalveolar lavage increases the sensitivity and specificity of the diagnosis. The pathogenesis in children is poorly understood, but several prospective cohort studies suggest that aspiration and immunodeficiency are risk factors. Educational interventions and efforts to improve adherence to hand hygiene for children have been associated with decreased VAP rates. Studies of antibiotic cycling in pediatric patients have not consistently shown this measure to prevent colonization with multidrug-resistant gram-negative rods. More consistent and precise approaches to the diagnosis of pediatric VAP are needed to better define the attributable morbidity and mortality, pathophysiology, and appropriate interventions to prevent this disease.