Changing epidemiology of bloodstream infection in a 25-years hematopoietic stem cell transplant program: current challenges and pitfalls on empiric antibiotic treatment impacting outcomes

2019 ◽  
Vol 55 (3) ◽  
pp. 603-612 ◽  
Author(s):  
Pedro Puerta-Alcalde ◽  
Celia Cardozo ◽  
Francesc Marco ◽  
Maria Suárez-Lledó ◽  
Estela Moreno ◽  
...  
2003 ◽  
Vol 110 (4) ◽  
pp. 179-183 ◽  
Author(s):  
Guillermo J. Ruiz-Argüelles ◽  
David Gómez-Rangel ◽  
Guillermo J. Ruiz-Delgado ◽  
Alejandro Ruiz-Argüelles ◽  
Beatriz Pérez-Romano ◽  
...  

2021 ◽  
pp. 107815522110014
Author(s):  
Eris Tollkuci ◽  
Rebecca Myers

Introduction Citrobacter bacteria are gram-negative anaerobic bacilli commonly found in water, soil, food, and the intestinal tracts of animals and humans. Patients at highest risk of these nosocomial infections include neonates and adults who are ≥65 years of age, debilitated, or immunocompromised. Citrobacter braakii ( C. braakii), specifically, has been reported to cause sepsis in immunocompromised patients. Herein, we describe a case of an allogeneic stem cell transplant (SCT) adult patient with C. braakii bloodstream infection. Case Report We report our experience managing a central line-associated bloodstream infection (CLABSI) due to C. braakii in an allogeneic SCT patient. Management and Outcomes: Our patient was initially managed with cefepime. The central venous catheter (CVC) was removed. Blood cultures cleared 24 hours after antibiotic initiation. Therapy was transitioned to oral levofloxacin once susceptibilities resulted. Discussion The course of this patient highlights the important relationship between an unusual pathogen, C. braakii, in an immunocompromised allogeneic SCT patient. In our case, the source of the bacteremia was most likely a CLABSI given the positive catheter tip cultures. Although this report describes the successful utilization of cefepime and levofloxacin in the treatment of C. braakii infection, caution should be exercised when choosing empiric antimicrobial therapy as AmpC resistance. This clinical scenario can aid health care providers in making informed treatment decisions when faced with patients diagnosed with this relatively uncommon pathogen. Further reports should be published to determine C. braakii bacteremia management in hematopoietic stem cell transplant patients.


2019 ◽  
Author(s):  
Jessica Fernandes Ramos ◽  
Gleice Cristina Leite ◽  
Roberta Cristina Ruedas Martins ◽  
Camila Rizek ◽  
Sabri Saeed Al Sanabani ◽  
...  

Abstract Summary Bloodstream infection (BSI) caused by Pseudomonas aeruginosa has high mortality in hematopoietic stem cell transplant (HSCT) recipients. Objectives: To evaluate clinical, in vitro synergy and molecular features of 30 BSI caused by carbapenems-resistant P. aeruginosa (CRPA) in HSCT patients. Methods: Demographic and clinical data including treatment were collected and a database was built using EPIINFO, bivariate and multivariate analysis were run to assess outcome using SPSS. In vitro synergy using time-kill assays, pulsed-field electrophoresis (PFGE) and PCR for carbapenemases and virulence genes were performed for all isolates. Whole genome sequence (WGS) of main clones was done by Nextera XT, using Illumina MiSeq technology. Results: Mortality was 71%; most patients who died were allogeneic HSCT (78%) (p=0.02). Clinical isolates showed a high resistance level to meropenem: 50% had a MIC of 512 µg/mL; two thirds were susceptible to amikacin (MIC 2-512 µg/mL) and 100% to colistin. Many (17/30) isolates achieved synergistic effect with meropenem plus colistin but not with amikacin. None antagonism was observed. The presence of synergy by time-kill between colistin and meropenem showed a tendency towards a better outcome (HR 0.68 95%CI 0.02-1.02; p=0.06). The most frequent carbapenemase gene identified was blaSPM, and six co-harboured both blaKPC and blaSPM. Isolates presented genes related with virulence factors such as toxA, exoS and more patients with BSI caused by P. aeruginosa harbouring gene lasB evolved to death. The WGS showed that all five clones harboured SPM-1, Tn4371 and belonged to ST277; however, the resistance and virulence genes differ among the clones. Conclusion: CRPA BSI showed high mortality in HSCT patients. All clones carried SPM-1, Tn4371 and belonged to ST277. Synergy by time-kill between colistin and meropenem showed a tendency towards a better outcome


2018 ◽  
Vol 54 (6) ◽  
pp. 828-838 ◽  
Author(s):  
José Carlos Jaime-Pérez ◽  
Lorena Salazar-Cavazos ◽  
Patrizia Aguilar-Calderón ◽  
José Luis Herrera-Garza ◽  
César Homero Gutiérrez-Aguirre ◽  
...  

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