Bloodstream Infections Caused by Serratia marcescens: Have a High Prevalence of ESBL and Carbapenemase Production in Pediatric Patients

et al. Bloodstream infections caused by Serratia marcescens : Have a high prevalence of esbl and carbapenemase production in pediatric patients. J Pediatr Inf 2022;16(3):e173-e178. mevcut-Abstract Objective: In this study, it was aimed to present a cohort study conduct-ed retrospectively in order to examine the unexpected Serratia marcescens bacteremia prevalence in a children’s hospital in Türkiye. Material and Methods: S. marcescens was isolated in the blood cultures of 45 patients at a 20-month period. Demographic features and clinical findings of the 45 patients including age, sex, underlying diseases, white blood cell (WBC), C-reactive protein (CRP), serum albumin level, length of hospital stay and length of pediatric intensive care unit stay, portal of entry, duration of central venous catheter, results of antimicrobial susceptibility testing and 28-day all-cause mortality were examined. BSI. Definitions used to characterize antimicrobial resistant bacteria were classified as multidrug-resistant (MDR), extensively drug-resistant (XDR) and pandrug-resistant (PDR). Results: Twelve patients (26.9%) had a malignancy. Mean hospitalization duration was 42.7 ± 41.4 (3-171) days. Central venous catheters (CVCs), including chemo-ports and Hickman catheters, were present in 43 patients during episodes of BSI. Twenty-four patients had primary BSI while 21 patients had catheter-related BSI. Mean length of CVC presence be-Available direnç fore catheter-related BSI was 46.02 ± 50.96 (1-200) days. During bacteremia episodes, 24 catheters (55.8%) were removed. Four patients (8.9%) died during the bacteremia episode. Laboratory findings of the deceased patients were as follows: mean WBC was 17.200/mm³; mean serum CRP level was 147.2 mg/L; and mean serum albumin level was 2.43 g/dL. Among all cases, 57.8% of the S. marcescens isolates produced ESBL and 40% produced carbapenemase. We classified these isolates as non-MDR (42.2%), MDR (31.1%), XDR (24.4%) and PDR (2.2%). The most common regimes received for XDR isolates were high-dose prolonged meropenem, amikacin, levofloxacin, and tigecycline. Conclusion: It is a great concern that S. marcescens isolates are intrinsi-cally resistant to polymyxins and produce ESBL and carbapenemase. Our mortality rate was reduced by high-dose prolonged-infusion of meropenem and early catheter removal.

[1]  Yunsong Yu,et al.  Molecular Characterization of Carbapenem-Resistant Serratia marcescens Clinical Isolates in a Tertiary Hospital in Hangzhou, China , 2020, Infection and drug resistance.

[2]  J. Lipman,et al.  A review of -multidrug-resistant Enterobacteriaceae in a neonatal unit in Johannesburg, South Africa , 2019, BMC Pediatrics.

[3]  Saiping Jiang,et al.  Clinical outcomes of prolonged infusion (extended infusion or continuous infusion) versus intermittent bolus of meropenem in severe infection: A meta-analysis , 2018, PloS one.

[4]  H. Abdel-Hady,et al.  Conventional Versus Prolonged Infusion of Meropenem in Neonates With Gram-negative Late-onset Sepsis: A Randomized Controlled Trial , 2017, The Pediatric infectious disease journal.

[5]  M. Souli,et al.  Double-carbapenem combination as salvage therapy for untreatable infections by KPC-2-producing Klebsiella pneumoniae , 2017, European Journal of Clinical Microbiology & Infectious Diseases.

[6]  J. Rolain,et al.  Outbreak of Serratia marcescens Coproducing ArmA and CTX-M-15 Mediated High Levels of Resistance to Aminoglycoside and Extended-Spectrum Beta-Lactamases, Algeria. , 2015, Microbial drug resistance.

[7]  Sharon Calaman,et al.  Pharmacokinetics of Continuous‐Infusion Meropenem for the Treatment of Serratia marcescens Ventriculitis in a Pediatric Patient , 2015, Pharmacotherapy.

[8]  Min Hyung Kim,et al.  Risk Factors for Mortality in Patients with Serratia marcescens Bacteremia , 2015, Yonsei medical journal.

[9]  Katherine E Henson,et al.  Risk of Suicide After Cancer Diagnosis in England , 2018, JAMA psychiatry.

[10]  M. Falagas,et al.  Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. , 2012, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases.

[11]  Thierry Naas,et al.  Global Spread of Carbapenemase-producing Enterobacteriaceae , 2011, Emerging infectious diseases.

[12]  J. D. Bard,et al.  Carbapenemase-Producing Serratia marcescens: the Treatment Conundrum , 2010 .

[13]  S. Bouchillon Antibiotic Profile of 55 Carbapenem-Resistant Serratia marcescens (CRSm) - T.E.S.T. Program , 2009 .

[14]  D. Warren,et al.  Clinical practice guidelines for the diagnosis and management of intravascular catheter-related infection: 2009 Update by the Infectious Diseases Society of America. , 2009, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[15]  Y. Chuang,et al.  Clinical experiences of the infections caused by extended-spectrum beta-lactamase-producing Serratia marcescens at a medical center in Taiwan. , 2006, Japanese journal of infectious diseases.

[16]  W. Ko,et al.  Serratia marcescens bacteremia at a medical center in southern Taiwan: high prevalence of cefotaxime resistance. , 2005, Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi.

[17]  Tae Hyong Kim,et al.  Serratia Bacteremia in a Large University Hospital: Trends in Antibiotic Resistance During 10 Years and Implications for Antibiotic Use , 2002, Infection Control & Hospital Epidemiology.

[18]  Daniel J Sexton,et al.  Health CareAssociated Bloodstream Infections in Adults: A Reason To Change the Accepted Definition of Community-Acquired Infections , 2002, Annals of Internal Medicine.

[19]  W. L. Yu,et al.  Serratia marcescens bacteremia: clinical features and antimicrobial susceptibilities of the isolates. , 1998, Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi.

[20]  B. Yangco,et al.  CDC definitions for nosocomial infections. , 1989, American journal of infection control.

[21]  J M Hughes,et al.  CDC definitions for nosocomial infections, 1988. , 1988, American journal of infection control.

[22]  L. Saiman,et al.  Population pharmacokinetics of meropenem administered as a prolonged infusion in children with cystic fibrosis. , 2016, The Journal of antimicrobial chemotherapy.

[23]  J. Cherry,et al.  Feigin and Cherry's textbook of pediatric infectious diseases , 2013 .

[24]  M. Ferraro Performance standards for antimicrobial susceptibility testing , 2001 .