ArticleInfection2026
Aztreonam/avibactam during continuous venovenous haemodiafiltration in a critically ill patient with NDM-producing Klebsiella pneumoniae: a case report and review of the literature.
Article in Infection, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
purposeAztreonam/avibactam represents a valuable therapeutic option for infections caused by metallo-β-lactamase-producing Enterobacterales, but data on its use during continuous renal replacement therapy (CRRT) are scarce and largely limited to a single pharmacokinetic report. Here, we describe the clinical course of a 76-year-old woman with end-stage renal disease who received aztreonam/avibactam while undergoing continuous venovenous haemodiafiltration (CVVHDF) during a critical illness secondary to a presumed invasive infection by NDM-producing Klebsiella pneumoniae.
methodsCeftazidime/avibactam plus aztreonam was started empirically for fever, pyuria and a urinary NDM-producing K. pneumoniae isolate, then switched to co-formulated aztreonam/avibactam after surgery and ICU transfer (intermittent-haemodialysis phase: loading 1 g/0.333 g, then 0.675/0.225 g every 12 h as a 3-h infusion). When CVVHDF was started for worsening sepsis, the regimen was changed to a 2 g/0.667 g loading dose followed by 1 g/0.333 g every 8 h given as an uninterrupted continuous infusion, replicating the only previously reported CVVHDF regimen.
resultsThe course was confounded by vancomycin-resistant Enterococcus faecium bacteraemia, bowel ischaemia with perforation, stercoral peritonitis and polymicrobial intra-abdominal infection. No microbiologically documented recurrence of the NDM-producing organism occurred after treatment, although rectal colonization persisted.
conclusionsThe case demonstrates the practical feasibility of continuous-infusion aztreonam/avibactam during CVVHDF. Efficacy and PK/PD target attainment cannot be confirmed, as susceptibility testing for the index strain and therapeutic drug monitoring were unavailable.
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