Melinda Hohrein
BJC HealthCare
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Featured researches published by Melinda Hohrein.
Infection Control and Hospital Epidemiology | 2008
Galit Holzmann-Pazgal; D. Hopkins-Broyles; Angela Recktenwald; Melinda Hohrein; Patricia Kieffer; Charles B. Huddleston; Sharma Anshuman; Victoria J. Fraser
A retrospective case-control study was performed to determine the risks and outcomes associated with pediatric cardiothoracic surgical site infection. Undergoing more than 1 cardiothoracic operative procedure, having preoperative infection, and undergoing surgery on a Monday were significant risk factors. Cardiothoracic surgical site infection increased hospital and pediatric intensive care unit length of stay. Deep surgical site infection significantly increased mortality.
Pediatric Infectious Disease Journal | 2015
Alexis Elward; Jeanne Yegge; Angela Recktenwald; Louise Jadwisiak; Patti Kieffer; Melinda Hohrein; D. Hopkins-Broyles; Keith F. Woeltje
Background: Surgical site infections (SSIs) occur in approximately 700 pediatric patients annually and are associated with increased morbidity, mortality and cost. The aim of this study is to determine risk factors for SSI among pediatric patients undergoing craniotomy and spinal fusion. Methods: This is a retrospective case-control study. Cases were craniotomy or spinal fusion patients with SSI as defined by Centers for Disease Control and Prevention criteria with surgery performed from January 1, 2008 to July 31, 2009. For each case patient, 3 uninfected controls were randomly selected among patients who underwent the same procedure as the case patient within 1 month. We performed analyses of risk factors for craniotomy and spinal fusion SSI separately and as a combined outcome variable. Results: Underweight body mass index, increased time at lowest body temperature, increased interval to antibiotic redosing, the combination of vancomycin and cefazolin for prophylaxis, longer preoperative and postoperative intensive care unit stay and anticoagulant use at 2 weeks postoperatively were associated with an increased risk of SSI in the combined analysis of craniotomy and spinal fusion. Forty-seven percent of cases and 27% of controls received preoperative antibiotic doses that were inappropriately low because of their weight. Conclusions: We identified modifiable risk factors for SSI including antibiotic dosing and body temperature during surgery. Preoperative antibiotic administration is likely to benefit from standard processes. Further studies of risk benefit for prolonged low body temperature during procedures are needed to determine the optimal balance between neuroprotection and potential immunosuppression associated with low body temperature.
American Journal of Infection Control | 2014
Carole Leone; Kathleen Gase; Jeanne Yegge; Raya Khoury; Joshua A. Doherty; Melinda Hohrein; Hilary M. Babcock
ISSUE: Our 28 bed Hematology Oncology (Heme-Onc) unit has had an unacceptably high central line assosciated bloodstream infection (CLABSI) rate. This patient population with various hematologic malignancies, including stem cell transplants, is at high risk for neutropenia, mucositis and graft-versus-host disease. Despite aggressive prevention efforts with implementation of multiple evidence-based CLABSI interventions over a 3 year period, no significant reduction in the CLABSI rate was achieved. PROJECT: Applying the new January 2013 National Healthcare Safety Network (NHSN) mucosal barrier injury laboratoryconfirmed bloodstream infection (MBI-LCBSI) definition, we identified that 80% of the CLABSIs on our Heme-Onc unit met the MBI-LCBSI definition for the first quarter of 2013. To determine if this finding was new, all CLABSIs from 2012 on this Heme-Onc unit were retrospectively reviewed applying the 2013 NSHN MBILCBI definition. Tracking of the CLABSI rate excluding the MBI-LCBSIs continued in 2013. Chi square tests were performed to determine if the overall CLABSI rate was significantly different than the CLABSI rate excluding MBI-LCBIs for both 2012 and 2013. RESULTS: The overall CLABSI rate in 2012 was 4.07 BSI/1,000 device days. 67.6% of the CLABSIs in 2012met the definition for MBI-LCBSI. The CLABSI rate, excluding MBI-LCBSIs, was 1.32 BSI/1,000 device days. For the first eleven months of 2013, the overall CLABSI rate was 3.6 BSI/1,000 device days. 77.8 % of the CLABSIs met the MBI-LCBSI definition in 2013. The CLABSI rate, excluding the MBI-LCBIs, was 0.8 BSI/1,000 device days. There was a significant difference between the rates in 2012, (c2 (1) 1⁄4 11.72, p < .01) as well as in 2013, (c2 (1) 1⁄4 13.33, p < .01).
/data/revues/01966553/v43i6sS/S0196655315003247/ | 2015
Kathleen Gase; Hui Xu; Melinda Hohrein; Carol O'Donnell; Carole Leone; Joshua A. Doherty; Jeanne Yegge; Hilary M. Babcock
/data/revues/01966553/v43i6sS/S0196655315003247/ | 2015
Kathleen Gase; Hui Xu; Melinda Hohrein; Carol O'Donnell; Carole Leone; Joshua A. Doherty; Jeanne Yegge; Hilary M. Babcock
/data/revues/01966553/v43i6sS/S0196655315002849/ | 2015
Kathleen Gase; Laura Kelly; Melinda Hohrein; Kristen Siebels; Hilary M. Babcock
American Journal of Infection Control | 2014
Jeanne A. Yegge; Kathleen Gase; Melinda Hohrein; Hui Xu; Raya Khoury; Hilary M. Babcock
/data/revues/01966553/v42i6sS/S0196655314005537/ | 2014
Raya Khoury; Richard Lumor; Jeanne Yegge; Kathleen Gase; Melinda Hohrein; Hilary M. Babcock
/data/revues/01966553/v42i6sS/S0196655314002715/ | 2014
Jeanne Yegge; Kathleen Gase; Melinda Hohrein; Raya Khoury; Hilary M. Babcock