This retrospective cohort study analyzed 207 K. pneumoniae bloodstream infection episodes (with 164 isolates sequenced) at a tertiary hospital in Japan. It compared five-biomarker-defined hypervirulent Klebsiella pneumoniae (hvKp) to classical K. pneumoniae (cKp), assessing outcomes including abscess complications, length of stay, antibiotic duration, and 30-day mortality. Main results showed hvKp was associated with higher abscess complications: 17 of 28 (61%) in hvKp versus 23 of 174 (13%) in cKp, with an adjusted odds ratio of 10.7 (95% CI, 4.36-26.2). Length of stay was 28 days in hvKp versus 14 days in cKp (adjusted ratio 1.60; 95% CI, 1.18-2.16), and antibiotic duration was 43 days in hvKp versus 14 days in cKp (adjusted ratio 2.13; 95% CI, 1.64-2.77). For 30-day mortality, no significant difference was observed, with effect size, absolute numbers, p-value or CI, and direction not reported. Multidrug resistance was 11% in hvKp strains versus 30% in cKp strains (P = .040), and abscess rates across lineages varied, e.g., 9 of 10 in ST23 versus 1 of 4 in ST412. Safety and tolerability data were not reported. Key limitations include that the study was underpowered for 30-day mortality, and associations were attenuated after adjusting for abscess-related complications. In practice, diagnostic tools distinguishing hvKp and cKp subgroups may aid abscess evaluation and source control, but these findings are observational and require confirmation.
View Original Abstract ↓
Background Five-biomarker-defined hypervirulent Klebsiella pneumoniae (hvKp) causes invasive infections, but its burden in bloodstream infections versus classical K. pneumoniae (cKp) is unclear. Methods This retrospective cohort study at a tertiary hospital in Japan included K. pneumoniae bloodstream infection episodes from January 2022-December 2024. hvKp was defined by the presence of all 5 genotypic biomarkers (rmpA, rmpA2, iucA, iroB, and peg-344). The primary outcome was abscess complications, and secondary outcomes were length of stay and antibiotic duration. Whole-genome sequencing was performed for 164 isolates. Results Among the 207 episodes, 28 (14%) were of hvKp. Abscess complication occurred in 17 (61%) hvKp versus 23 (13%) cKp episodes (adjusted odds ratio 10.7; 95% CI, 4.36-26.2). Median length of stay in hvKp versus cKp was 28 versus 14 days (adjusted ratio 1.60; 95% CI, 1.18-2.16) and median antibiotic duration was 43 versus 14 days (adjusted ratio 2.13; 95% CI, 1.64-2.77). These associations were attenuated after adjusting for abscess-related complications. No significant difference in 30-day mortality was observed, although the study was underpowered. Multidrug resistance was less frequent in hvKp strains than in cKp strains (11% vs. 30%; P = .040). Among the sequenced hvKp episodes, abscess rates varied across lineages, from 9 of 10 in ST23 to 1 of 4 in ST412. Conclusions Five biomarker-defined hvKp strains delineated a bloodstream infection subgroup with frequent abscess complications and prolonged care. hvKp and cKp present distinct clinical challenges; diagnostic tools distinguishing these subgroups may aid abscess evaluation and source control.