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Hypervirulent Klebsiella pneumoniae linked to higher abscess risk and longer hospital stays in bloodstream infections

Hypervirulent Klebsiella pneumoniae linked to higher abscess risk and longer hospital stays in blood…
Photo by Bioscience Image Library by Fayette Reynolds / Unsplash
Key Takeaway
Consider hvKp in K. pneumoniae bloodstream infections for higher abscess risk and longer stays, but note mortality data are limited.

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.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedApr 2026
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.
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