Emerging Resistance Trends in Viridans Group Streptococci Bloodstream Infections Among Immunocompromised Children Receiving Levofloxacin Prophylaxis

• Published in: Journal of the Pediatric Infectious Diseases Society Vol. 12; no. 7; pp. 381 - 391
• Main Authors: Quintero, Ana M, Cruz Vidal, Diego A, Klamer, Brett G, Ardura, Monica I, Oyeniran, Sophonie J
• Format: Journal Article
• Language: English
• Published: US Oxford University Press 31.07.2023
• Subjects: Anti-Bacterial Agents - pharmacology; Anti-Bacterial Agents - therapeutic use; Bacteremia - drug therapy; Bacteremia - prevention & control; Child; Humans; Levofloxacin - pharmacology; Levofloxacin - therapeutic use; Microbial Sensitivity Tests; Streptococcal Infections - drug therapy; Streptococcal Infections - prevention & control; Viridans Streptococci; viridans group streptococci; immunocompromised children; levofloxacin prophylaxis; fluoroquinolone resistance; bacteremia
• ISSN: 2048-7207; 2048-7207
• DOI: 10.1093/jpids/piad041

Abstract Background Levofloxacin prophylaxis (LVXp) is often used for patients with underlying leukemia and severe neutropenia to reduce the risk of fever and bacteremia. This study evaluated trends in viridans group streptococci (VGS) antibiotic susceptibilities over time and clinical outcomes of children with VGS bloodstream infections (BSIs) during institutional adoption of LVXp. Methods VGS blood culture isolates between 1/1/2010 and 12/31/2021 with susceptibility testing reported were included. Available isolates were re-identified to the species level and additional susceptibility testing was performed. Demographic and clinical data were abstracted from medical records. Results A total of 264 VGS BSI isolates were identified in immunocompromised (IC, n = 125) and non-immunocompromised subjects, (non-IC, n = 139). IC subjects had lower rates of VGS isolates susceptible (S) to LVX and higher minimum inhibitory concentration (MICs) to LVX (p = 0.004) and ciprofloxacin (p = 0.0005) compared with non-IC subjects. No other evaluated antibiotic had increased MICs in either group. Fifteen of 19 (74%) LVX not susceptible (NS) isolates occurred in IC subjects, 13 represented breakthrough infections. IC subjects had higher rates of VGS-related shock (p = 0.012), need for pressor support (p = 0.039), and longer duration of hospitalization than non-IC subjects (p < 0.001). Clinical outcomes were comparable between subjects with LVX S and NS VGS BSI isolates. Conclusions VGS with reduced susceptibility to LVX emerged during institutional adoption of LVXp in high-risk children with immunocompromising conditions, but did not result in significant differences in clinical outcomes. Ongoing surveillance and susceptibility testing are critical in weighing the utility of LVXp against emerging antimicrobial resistance in this high-risk population. Implementation of levofloxacin (LVX) prophylaxis among high-risk children with underlying malignancy led to reduced rates of fluoroquinolone susceptible VGS bloodstream isolates over time, without significant differences in clinical outcomes when compared to subjects with LVX susceptible BSI isolates.