Abstract

BackgroundThis study aimed to investigate the epidemiology, microbiology, and risk factors associated with mortality and multi-drug resistance bacterial bloodstream infections (BSIs) among adult cancer patients in Shiraz, Iran. We also report a four-year trend of antimicrobial resistance patterns of BSIs.MethodsWe conducted a retrospective study at a referral oncology hospital from July 2015 to August 2019, which included all adults with confirmed BSI.Results2393 blood cultures tested during the four-year study period; 414 positive cultures were included. The mean age of our patients was 47.57 ± 17.46 years old. Central Line-Associated BSI (CLABSI) was more common in solid tumors than patients with hematological malignancies. Gram-negative (GN) bacteria were more detected (63.3%, 262) than gram-positive bacteria (36.7%, 152). Escherichia coli was the most common gram-negative organism (123/262, 47%), followed by Pseudomonas spp. (82/262, 31%) and Klebsiella pneumoniae (38/262, 14.5%). Coagulase-negative staphylococci (CoNS) was the most frequently isolated pathogen among gram-positive bacteria (83/152, 54.6%). Acinetobacter spp., Pseudomonas spp., E. coli, and K. pneumoniae were the most common Extended-Spectrum Beta-Lactamase (ESBL) producers (100, 96.2, 66.7%, and 60.7, respectively). Acinetobacter spp., Pseudomonas spp., Enterobacter spp., E. coli, and K. pneumoniae were the most common carbapenem-resistant (CR) isolates (77.8, 70.7, 33.3, 24.4, and 13.2%, respectively). Out of 257 Enterobacterales and non-fermenter gram-negative BSIs, 39.3% (101/257) were carbapenem-resistant. Although the incidence of multi-drug resistance (MDR) gram-negative BSI increased annually during 2015–2018, the mortality rate of gram-negative BSI remains unchanged at about 20% (p-value = 0.55); however, the mortality rate was significantly greater (35.4%) in those with resistant gram-positive BSI (p-value = 0.001). The overall mortality rate was 21.5%. Early (7-day mortality) and late mortality rate (30-day mortality) were 10 and 3.4%, respectively.ConclusionsThe emergence of MDR gram-negative BSI is a significant healthcare problem in oncology centers. The high proportion of the most frequently isolated pathogens were CR and ESBL-producing Enterobacterales and Pseudomonas spp. We have few effective choices against MDRGN BSI, especially in high-risk cancer patients, which necessitate newer treatment options.

Highlights

  • This study aimed to investigate the epidemiology, microbiology, and risk factors associated with mortality and multi-drug resistance bacterial bloodstream infections (BSIs) among adult cancer patients in Shiraz, Iran

  • Clinical and laboratory features The mean of white blood cell (WBC), erythrocyte sedimentation rate (ESR), and C-reactive protein (CRP) were (6.94 ± 11.28) X 109 /L, (71.68 ± 37.26) mm/hour, (82.59 ± 41.44) mg/dl, respectively

  • Given the emergence of Carbapenem-resistant gram-negative (CRGN) bacteria isolated in blood culture of patients with BSI during 2015–2018 and the high proportion of CR isolates in non-fermenters and in Enterobacterales, we investigated the odds of different possible risk factors for carbapenemresistant BSI by logistic regression model (Table 4)

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Summary

Introduction

This study aimed to investigate the epidemiology, microbiology, and risk factors associated with mortality and multi-drug resistance bacterial bloodstream infections (BSIs) among adult cancer patients in Shiraz, Iran. We report a four-year trend of antimicrobial resistance patterns of BSIs. Bacterial bloodstream infection (BSI) is one of the most common complications of chemotherapy-induced neutropenia in patients with hematologic malignancies and solid organ tumors [1,2,3], which is associated with high mortality and morbidity [4,5,6,7,8]. While proper diagnosis and treatment are essential to decrease BSI-associated complications, inappropriate empiric antimicrobial therapy increases mortality [11]. Surveillance of antimicrobial resistance is one of ASP’s critical aspects and guides clinicians for appropriate empiric antimicrobial therapy [13, 14]

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