# Ceftazidime–Avibactam in Multidrug-Resistant Klebsiella spp. Infections: Is Monotherapy as Effective as Combination Therapy?

**Authors:** Rukiyye Bulut, İbrahim Erayman, Bahar Kandemir, Pınar Belviranlı Keskin

PMC · DOI: 10.3390/antibiotics15020116 · Antibiotics · 2026-01-25

## TL;DR

This study shows that ceftazidime–avibactam is effective for treating severe Klebsiella infections, with no major difference between using it alone or with other drugs.

## Contribution

Demonstrates real-world effectiveness of ceftazidime–avibactam monotherapy versus combination therapy for CRK infections.

## Key findings

- Ceftazidime–avibactam achieved 76.8% treatment success in CRK infections.
- Monotherapy and combination therapy showed no significant difference in clinical outcomes.
- Treatment duration was the only factor significantly affecting clinical outcomes.

## Abstract

Background/Objectives: Carbapenem-resistant Klebsiella spp. (CRK) causes healthcare-associated infections with high mortality. This study evaluated the clinical outcomes of ceftazidime–avibactam (CZA) therapy in CRK infections. Methods: Patients hospitalized in a tertiary care hospital in Türkiye between June 2021 and December 2022 with CRK-positive cultures, CZA susceptibility, and ≥72 h of CZA treatment were retrospectively analyzed. Results: Ninety-nine patients (61.6% male; mean age 63.7 ± 17.5 years) were included, 89.9% of whom were treated in the intensive care unit (ICU). Hypertension (29.3%), diabetes (28.3%), and malignancy (26.3%) were the most frequent comorbidities. The main infection types were bloodstream infection (56.6%) and ventilator-associated pneumonia (29.3%). CZA was used as monotherapy in 49.5%, and in combination in 50.5% of cases. The mean treatment duration was 13.2 ± 6.3 days. Clinical improvement occurred at 3.4 ± 1.2 days and microbiological eradication at 4.7 ± 2.1 days. Treatment success was achieved in 76.8% of patients, while 30- and 90-day mortality rates were 48.5% and 72.7%, respectively. Only treatment duration significantly affected clinical outcome (p < 0.001). Conclusions: CZA demonstrates favorable outcomes in CRK infections, with no significant difference between monotherapy and combination therapy. These findings support the use of CZA as an effective treatment option for severe CRK infections in real-world clinical settings and may help guide antimicrobial stewardship strategies in high-risk hospitalized patients.

## Linked entities

- **Chemicals:** ceftazidime–avibactam (PubChem CID 90643431)
- **Diseases:** diabetes (MONDO:0005015), malignancy (MONDO:0004992)

## Full-text entities

- **Genes:** ALPP (alkaline phosphatase, placental) [NCBI Gene 250] {aka ALP, PALP, PLAP, PLAP-1}, GGTLC5P (gamma-glutamyltransferase light chain 5 pseudogene) [NCBI Gene 653590] {aka GGT}, GGT1 (gamma-glutamyltransferase 1) [NCBI Gene 2678] {aka CD224, D22S672, D22S732, GGT, GGT 1, GGTD}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, CRK (CRK proto-oncogene, adaptor protein) [NCBI Gene 1398] {aka CRKII, p38}
- **Diseases:** Stevens-Johnson syndrome (MESH:D013262), pyelonephritis (MESH:D011704), hematological malignancy (MESH:D019337), VAP (MESH:D053717), pneumonia (MESH:D011014), acute kidney injury (MESH:D058186), Diarrhea (MESH:D003967), cerebrovascular accident (MESH:D020521), COPD (MESH:D029424), Chest Diseases (MESH:D002637), multiple organ dysfunction syndrome (MESH:D009102), AIDS (MESH:D000163), respiratory failure (MESH:D012131), rashes (MESH:D005076), meningitis (MESH:D008580), CKD (MESH:D051436), malignancy (MESH:D009369), intra-abdominal infections (MESH:D059413), DM (MESH:D003920), CRK infection (MESH:D007710), neurotoxicity (MESH:D020258), critically ill (MESH:D016638), injury to (MESH:D014947), skin and soft tissue infections (MESH:D018461), respiratory tract infection (MESH:D012141), Infectious Diseases (MESH:D003141), BSI (MESH:D018805), fungal (MESH:D009181), CRE (MESH:D004756), coronary artery disease (MESH:D003324), Gram-negative bacterial infections (MESH:D016905), hepatocellular injury (MESH:D056486), renal impairment (MESH:D007674), thrombocytosis (MESH:D013922), nosocomial pneumonia (MESH:D000077299), toxicity (MESH:D064420), urinary tract infections (MESH:D014552), Cerebrovascular event (MESH:D002561), gastrointestinal intolerance (MESH:D005767), cholestasis (MESH:D002779), COVID-19 (MESH:D000086382), bacteremia (MESH:D016470), Infection (MESH:D007239), Mortality (MESH:D003643), immunodeficiency (MESH:D007153), neutropenia (MESH:D009503), Hypertension (MESH:D006973), encephalopathy (MESH:D001927), altered consciousness (MESH:D003244), Healthcare-Associated Infections (MESH:D003428), Clostridioides difficile infections (MESH:D003015)
- **Chemicals:** gentamicin (MESH:D005839), meropenem (MESH:D000077731), ceftazidime (MESH:D002442), vancomycin (MESH:D014640), Carbapenem (MESH:D015780), avibactam (MESH:C543519), ertapenem (MESH:D000077727), tigecycline (MESH:D000078304), metronidazole (MESH:D008795), bilirubin (MESH:D001663), aminoglycoside (MESH:D000617), teicoplanin (MESH:D017334), caspofungin (MESH:D000077336), creatinine (MESH:D003404), beta-lactam (MESH:D047090), imipenem (MESH:D015378), quinolone (MESH:D015363), urea (MESH:D014508), cephalosporin (MESH:D002511), NDM (MESH:C052821), fosfomycin (MESH:D005578), CZA (MESH:C000595613), -lactamase (-)
- **Species:** Enterobacterales (order) [taxon 91347], Klebsiella [taxon 2885105], Pseudomonas aeruginosa (species) [taxon 287], Enterobacteriaceae (enterobacteria, family) [taxon 543], Homo sapiens (human, species) [taxon 9606], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395]

## Full text

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## References

22 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937278/full.md

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Source: https://tomesphere.com/paper/PMC12937278