# Real-world outcomes and safety of colistin therapy in children with multidrug-resistant gram-negative infections: a nine-year experience

**Authors:** Nesli Ağralı Eröz, Zümrüt Şahbudak Bal, Kübra Cebeci, Gülizar Turan, Nihal Karadaş, Deniz Yılmaz Karapınar, Ezgi Kıran Taşçı, Miray Karakoyun, Gökçen Kartal Öztürk, Gülcihan Özek, Coskun Ekemen, Asli Arslan, Melike Yaşar Duman, Feriha Çilli, Gülhadiye Avcu

PMC · DOI: 10.1007/s00431-026-06863-0 · European Journal of Pediatrics · 2026-03-20

## TL;DR

This study examines the use and safety of colistin in treating drug-resistant bacterial infections in children over nine years, finding that treatment outcomes depend more on disease severity than antibiotic combinations.

## Contribution

The study provides long-term real-world pediatric data on colistin use for multidrug-resistant Gram-negative infections.

## Key findings

- Colistin was used in combination regimens for 117 treatment episodes in children with multidrug-resistant Gram-negative infections.
- Endotracheal intubation was the strongest independent predictor of mortality in these patients.
- Microbiological eradication was achieved in 70% of culture-confirmed episodes, but nephrotoxicity occurred in 12.8% of patients.

## Abstract

Antimicrobial resistance (AMR) among Gram-negative (GN) pathogens has emerged as a critical global threat, particularly in low- and middle-income countries where access to novel antimicrobials is limited. In Türkiye, colistin (CST) remains a last-resort therapy against multidrug-resistant (MDR) and carbapenem-resistant Gram-negative bacteria (CR-GNB) despite its nephrotoxic potential. This study aimed to evaluate the clinical characteristics, microbiological outcomes, and adverse events associated with CST therapy in pediatric patients over a nine-year period. We conducted a single-center retrospective cohort study including pediatric patients treated with CST for nosocomial MDR-GN infections at a tertiary university hospital between January 2016 and March 2025. Demographic, clinical, microbiological, and treatment-related data were collected. Univariable comparisons and multivariable logistic regression analyses were performed to identify factors associated with nephrotoxicity, treatment failure, and mortality. A total of 117 treatment episodes were identified among 112 patients (mean age: 75.9 ± 69.5 months; 65% male). The predominant pathogens were Klebsiella pneumoniae (39.7%), Pseudomonas aeruginosa (26.4%), and Acinetobacter baumannii (22.0%). CST was used in combination regimens in all episodes, most commonly with carbapenems (73.5%). Microbiological eradication was achieved in 70% of culture-confirmed episodes. The overall sepsis-related mortality rate was 18.8%. Nephrotoxicity occurred in 12.8% of patients and was associated with mortality and severity indicators in univariable analyses. In multivariable analysis, endotracheal intubation remained the only independent predictor of mortality (adjusted OR 23.98, 95% CI 4.47–128.52).

Conclusions: CST remains a last-resort agent for MDR and CR-GNB infections in pediatric settings with limited access to novel antimicrobials. Although microbiological eradication was achieved in most cases, treatment outcomes were primarily driven by disease severity and host-related factors rather than antimicrobial combinations. Endotracheal intubation emerged as the strongest independent predictor of mortality.
What is Known – What is New•CST is widely used as a last-resort option for pediatric MDR-GN infections.•Nephrotoxicity and variable clinical outcomes remain major concerns.•This study provides long-term real-world pediatric data on CST use.• Disease severity and host-related factors were the main determinants of treatment failure and mortality.

What is Known – What is New

•CST is widely used as a last-resort option for pediatric MDR-GN infections.

•Nephrotoxicity and variable clinical outcomes remain major concerns.

•This study provides long-term real-world pediatric data on CST use.

• Disease severity and host-related factors were the main determinants of treatment failure and mortality.

The online version contains supplementary material available at 10.1007/s00431-026-06863-0.

## Linked entities

- **Chemicals:** colistin (PubChem CID 5311054)
- **Species:** Klebsiella pneumoniae (taxon 573), Pseudomonas aeruginosa (taxon 287), Acinetobacter baumannii (taxon 470)

## Full-text entities

- **Genes:** CST12P (cystatin 12, pseudogene) [NCBI Gene 106478911] {aka Cst, Ctes4, E2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, UROD (uroporphyrinogen decarboxylase) [NCBI Gene 7389] {aka PCT, UPD}
- **Diseases:** HAP (MESH:D000077299), metabolic disorders (MESH:D008659), Urinary tract infection (MESH:D014552), multiorgan dysfunction (MESH:D009102), malignancy (MESH:D009369), BSI (MESH:D018805), meningitis (MESH:D008580), chronic pulmonary diseases (MESH:D002908), CRAB (MESH:D000151), urticaria (MESH:D014581), fever (MESH:D005334), Nosocomial infections (MESH:D003428), Infectious Diseases (MESH:D003141), inflammation (MESH:D007249), seizures (MESH:D012640), hypersensitivity (MESH:D004342), genetic syndromes (MESH:D030342), CR-GNB (MESH:D016905), altered consciousness (MESH:D003244), intra-abdominal infections (MESH:D059413), MDR (MESH:D018088), GNB infections (MESH:D007239), Superinfection (MESH:D015163), leukocytosis (MESH:D007964), DTR (MESH:D019553), neuromuscular blockade (MESH:D020879), bacterial infection (MESH:D001424), Kidney Disease (MESH:D007674), Mortality (MESH:D003643), pneumonia (MESH:D011014), fungal (MESH:D009181), primary immunodeficiency (MESH:D000081207), Pseudomonas aeruginosa (MESH:D011552), neurotoxicity (MESH:D020258), Neutropenia (MESH:D009503), associated (MESH:D018886), inflammatory response (MESH:D018746), system (MESH:D015619), cardiovascular diseases (MESH:D002318), leukopenia (MESH:D007970), critically ill (MESH:D016638), AMR (MESH:D060467), pulmonary (MESH:D008171), neurological diseases (MESH:D020271), MV (MESH:D053717), central nervous system (CNS) infections (MESH:D002494)
- **Chemicals:** creatinine (MESH:D003404), cephalosporins (MESH:D002511), glycopeptide (MESH:D006020), CIP (MESH:D002939), piperacillin-tazobactam (MESH:D000077725), aminoglycoside (MESH:D000617), ganciclovir (MESH:D015774), IPM (MESH:D015378), penicillins (MESH:D010406), vancomycin (MESH:D014640), fluoroquinolones (MESH:D024841), aztreonam (MESH:D001398), ceftazidime-avibactam (MESH:C000595613), TGC (MESH:D000078304), LVX (MESH:D064704), urea (MESH:D014508), cyclosporine (MESH:D016572), gentamicin (MESH:D005839), TMP-SMX (MESH:D015662), ampicillin/sulbactam (MESH:C035444), CBA (-), MEM (MESH:D000077731), FEP (MESH:D011138), acyclovir (MESH:D000212), AMK (MESH:D000583), CRO (MESH:D002443), Carbapenem (MESH:D015780), beta-lactam (MESH:D047090), AmB (MESH:D000666), cefepime (MESH:D000077723)
- **Species:** Acinetobacter baumannii (species) [taxon 470], Candida tropicalis (species) [taxon 5482], Pseudomonas aeruginosa (species) [taxon 287], Pneumocystis jirovecii (species) [taxon 42068], Achromobacter xylosoxidans (species) [taxon 85698], Elizabethkingia (genus) [taxon 308865], Escherichia coli (E. coli, species) [taxon 562], Klebsiella pneumoniae (species) [taxon 573], Enterobacterales (order) [taxon 91347], Lodderomyces parapsilosis (species) [taxon 5480], Homo sapiens (human, species) [taxon 9606], Candida albicans (species) [taxon 5476]

## Full text

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## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC13002681/full.md

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Source: https://tomesphere.com/paper/PMC13002681