Dara Torres1, Miriam L González2, Adriana Loera1, Marco Aguilera1, George Relyea3, Paula Aristizabal4, Miguela A Caniza5. 1. Department of Hematology/Oncology, Hospital General de Tijuana, Tijuana, Mexico; Department of Pediatrics, Division of Pediatric Hematology/Oncology, University of California San Diego-Rady Children's Hospital, San Diego, CA. 2. Department of Infectious Diseases, St Jude Children's Research Hospital, Memphis, TN. 3. School of Public Health, University of Memphis, Memphis, TN. 4. Department of Pediatrics, Division of Pediatric Hematology/Oncology, University of California San Diego-Rady Children's Hospital, San Diego, CA. 5. Department of Infectious Diseases, St Jude Children's Research Hospital, Memphis, TN; International Outreach Program, St Jude Children's Research Hospital, Memphis, TN. Electronic address: miguela.caniza@stjude.org.
Abstract
BACKGROUND: The US National Healthcare Safety Network has provided a definition of mucosal barrier injury-associated, laboratory-confirmed bloodstream infection (MBI-LCBI) to improve infection surveillance. To date there is little information about its influence in pediatric oncology centers in low- to middle-income countries. OBJECTIVES: To determine the influence of the definition on the rate of central line-associated bloodstream infection (CLABSI) and compare the clinical characteristics of MBI versus non-MBI LCBI cases. METHODS: We retrospectively applied the National Healthcare Safety Network definition to all CLABSIs recorded at a pediatric oncology center in Tijuana, Mexico, from January 2011 through December 2014. CLABSI events were reclassified according to the MBI-LCBI definition. Clinical characteristics and outcomes of MBI and non-MBI CLABSIs were compared. RESULTS: Of 55 CLABSI events, 44% (24 out of 55) qualified as MBI-LCBIs; all were MBI-LCBI subcategory 1 (intestinal flora pathogens). After the number of MBI-LCBI cases was removed from the numerator, the CLABSI rate during the study period decreased from 5.72-3.22 infections per 1,000 central line days. Patients with MBI-LCBI were significantly younger than non-MBI-LCBI patients (P = .029) and had a significantly greater frequency of neutropenia (100% vs 39%; P = .001) and chemotherapy exposure (87% vs 58%; P = .020) and significantly longer median hospitalization (34 vs 23 days; P = .008). CONCLUSION: A substantial proportion of CLABSI events at our pediatric cancer center met the MBI-LCBI criteria. Our results support separate monitoring and reporting of MBI and non-MBI-LCBIs in low- to middle-income countries to allow accurate detection and tracking of preventable (non-MBI) bloodstream infections.
BACKGROUND: The US National Healthcare Safety Network has provided a definition of mucosal barrier injury-associated, laboratory-confirmed bloodstream infection (MBI-LCBI) to improve infection surveillance. To date there is little information about its influence in pediatric oncology centers in low- to middle-income countries. OBJECTIVES: To determine the influence of the definition on the rate of central line-associated bloodstream infection (CLABSI) and compare the clinical characteristics of MBI versus non-MBI LCBI cases. METHODS: We retrospectively applied the National Healthcare Safety Network definition to all CLABSIs recorded at a pediatric oncology center in Tijuana, Mexico, from January 2011 through December 2014. CLABSI events were reclassified according to the MBI-LCBI definition. Clinical characteristics and outcomes of MBI and non-MBI CLABSIs were compared. RESULTS: Of 55 CLABSI events, 44% (24 out of 55) qualified as MBI-LCBIs; all were MBI-LCBI subcategory 1 (intestinal flora pathogens). After the number of MBI-LCBI cases was removed from the numerator, the CLABSI rate during the study period decreased from 5.72-3.22 infections per 1,000 central line days. Patients with MBI-LCBI were significantly younger than non-MBI-LCBIpatients (P = .029) and had a significantly greater frequency of neutropenia (100% vs 39%; P = .001) and chemotherapy exposure (87% vs 58%; P = .020) and significantly longer median hospitalization (34 vs 23 days; P = .008). CONCLUSION: A substantial proportion of CLABSI events at our pediatric cancer center met the MBI-LCBI criteria. Our results support separate monitoring and reporting of MBI and non-MBI-LCBIs in low- to middle-income countries to allow accurate detection and tracking of preventable (non-MBI) bloodstream infections.
Authors: Miguela A Caniza; Gabriela Maron; Jonathan McCullers; Wilfrido A Clara; Rafael Cedillos; Lourdes Dueñas; Sandra Arnold; Bonnie F Williams; Elaine I Tuomanen Journal: Infect Control Hosp Epidemiol Date: 2007-10-22 Impact factor: 3.254
Authors: Peggy Ann Hazamy; Valerie B Haley; Boldtsetseg Tserenpuntsag; Marie Tsivitis; Rosalie Giardina; Robin Knab; Emily Lutterloh Journal: Am J Infect Control Date: 2014-12-30 Impact factor: 2.918
Authors: Kristen E Metzger; Yvonne Rucker; Mary Callaghan; Michelle Churchill; Borko D Jovanovic; Teresa R Zembower; Maureen K Bolon Journal: Infect Control Hosp Epidemiol Date: 2015-02 Impact factor: 3.254
Authors: Victor D Rosenthal; Hu Bijie; Dennis G Maki; Yatin Mehta; Anucha Apisarnthanarak; Eduardo A Medeiros; Hakan Leblebicioglu; Dale Fisher; Carlos Álvarez-Moreno; Ilham Abu Khader; Marisela Del Rocío González Martínez; Luis E Cuellar; Josephine Anne Navoa-Ng; Rédouane Abouqal; Humberto Guanche Garcell; Zan Mitrev; María Catalina Pirez García; Asma Hamdi; Lourdes Dueñas; Elsie Cancel; Vaidotas Gurskis; Ossama Rasslan; Altaf Ahmed; Souha S Kanj; Olber Chavarría Ugalde; Trudell Mapp; Lul Raka; Cheong Yuet Meng; Le Thi Anh Thu; Sameeh Ghazal; Achilleas Gikas; Leonardo Pazmiño Narváez; Nepomuceno Mejía; Nassya Hadjieva; May Osman Gamar Elanbya; María Eugenia Guzmán Siritt; Kushlani Jayatilleke Journal: Am J Infect Control Date: 2011-09-10 Impact factor: 2.918
Authors: Víctor Daniel Rosenthal; Dennis George Maki; Yatin Mehta; Hakan Leblebicioglu; Ziad Ahmed Memish; Haifaa Hassan Al-Mousa; Hanan Balkhy; Bijie Hu; Carlos Alvarez-Moreno; Eduardo Alexandrino Medeiros; Anucha Apisarnthanarak; Lul Raka; Luis E Cuellar; Altaf Ahmed; Josephine Anne Navoa-Ng; Amani Ali El-Kholy; Souha Sami Kanj; Ider Bat-Erdene; Wieslawa Duszynska; Nguyen Van Truong; Leonardo N Pazmino; Lucy Chai See-Lum; Rosalia Fernández-Hidalgo; Gabriela Di-Silvestre; Farid Zand; Sona Hlinkova; Vladislav Belskiy; Hussain Al-Rahma; Marco Tulio Luque-Torres; Nesil Bayraktar; Zan Mitrev; Vaidotas Gurskis; Dale Fisher; Ilham Bulos Abu-Khader; Kamal Berechid; Arnaldo Rodríguez-Sánchez; Florin George Horhat; Osiel Requejo-Pino; Nassya Hadjieva; Nejla Ben-Jaballah; Elías García-Mayorca; Luis Kushner-Dávalos; Srdjan Pasic; Luis E Pedrozo-Ortiz; Eleni Apostolopoulou; Nepomuceno Mejía; May Osman Gamar-Elanbya; Kushlani Jayatilleke; Miriam de Lourdes-Dueñas; Guadalupe Aguirre-Avalos Journal: Am J Infect Control Date: 2014-09 Impact factor: 2.918
Authors: Margaret A Dudeck; Lindsey M Weiner; Katherine Allen-Bridson; Paul J Malpiedi; Kelly D Peterson; Daniel A Pollock; Dawn M Sievert; Jonathan R Edwards Journal: Am J Infect Control Date: 2013-12 Impact factor: 2.918
Authors: Arne Simon; Roland A Ammann; Udo Bode; Gudrun Fleischhack; Hans-Martin Wenchel; Dorothee Schwamborn; Chara Gravou; Paul-Gerhardt Schlegel; Stefan Rutkowski; Claudia Dannenberg; Dieter Körholz; Hans Jürgen Laws; Michael H Kramer Journal: BMC Infect Dis Date: 2008-05-23 Impact factor: 3.090
Authors: Paula Aristizabal; Spencer Fuller; Rebeca Rivera-Gomez; Mario Ornelas; Laura Nuno; Carlos Rodriguez-Galindo; Raul Ribeiro; William Roberts Journal: Pediatr Blood Cancer Date: 2016-12-21 Impact factor: 3.167
Authors: Miriam L Gonzalez; Paula Aristizabal; Adriana Loera-Reyna; Dara Torres; Mario Ornelas-Sánchez; Laura Nuño-Vázquez; Marco Aguilera; Alicia Sánchez; Mitzy Romano; Rebeca Rivera-Gómez; George Relyea; Paola Friedrich; Miguela A Caniza Journal: JCO Glob Oncol Date: 2021-05