Araştırma Makalesi

Factors affecting colistin nephrotoxicity in intensive care units

Sayı: 1 8 Mayıs 2026
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Factors affecting colistin nephrotoxicity in intensive care units

Öz

Aim: Colistin is frequently used for the treatment of multidrug-resistant gram-negative infections in intensive care units; however, nephrotoxicity remains a major limitation of its clinical use. The incidence and risk factors of colistin-associated renal toxicity vary across studies, particularly in critically ill populations. This study aimed to evaluate the incidence of renal toxicity and associated risk factors in intensive care unit patients receiving intravenous colistin therapy. Material and Methods: This retrospective observational cohort study included 59 critically ill patients who received intravenous colistin therapy between 2013 and 2015. Nephrotoxicity was defined according to the Acute Kidney Injury Network criteria. Clinical and laboratory data were analyzed. Variables associated with nephrotoxicity were assessed using appropriate statistical tests, and multivariate analysis was performed to identify independent predictors. Results: Nephrotoxicity developed in 67.8% of patients. Older age, coronary artery disease and higher baseline blood urea nitrogen were associated with toxicity in unadjusted analyses. After adjustment, only elevated baseline blood urea nitrogen remained independently associated with nephrotoxicity. Renal impairment most commonly occurred within the first week of therapy, and 8.5% of patients required renal replacement therapy. Colistin dose was not independently associated with nephrotoxicity. Conclusion: Colistin-associated nephrotoxicity was common and typically developed early in critically ill patients. Reduced baseline renal functional reserve, particularly reflected by elevated blood urea nitrogen levels, appears to increase susceptibility to toxicity. Close renal monitoring and early risk assessment are essential during colistin therapy. Keywords: colistin, nephrotoxicity, intensive care, risk factors, acute kidney injury

Anahtar Kelimeler

Destekleyen Kurum

Bu çalışma herhangi bir kurum veya kuruluş tarafından maddi olarak desteklenmemiştir.

Etik Beyan

Etik kurul onayı İzmir Katip Çelebi Üniversitesi Girişimsel Olmayan Klinik Araştırmalar Etik Kurulu’ndan alınmış olup, belge ek olarak sunulmuştur. Çalışma retrospektif olarak gerçekleştirilmiş ve Helsinki Bildirgesi ilkelerine uygun olarak yürütülmüştür.

Teşekkür

Bu makale, İzmir Kâtip Çelebi Üniversitesi Anesteziyoloji ve Reanimasyon uzmanlık eğitimi kapsamında hazırlanan tez çalışmasına dayanmaktadır. Bu çalışma için herhangi bir finansal destek alınmamıştır. Yazarlar arasında çıkar çatışması bulunmamaktadır.

Kaynakça

  1. Ning Y, Chu Y, Wu Y, Huang Y, Wang C, Jiang L. Case Report: Respiratory paralysis associated with polymyxin B therapy. Front Pharmacol 2022; 13: 963140.
  2. Falagas ME, Kasiakou SK. Colistin: the revival of polymyxins for the management of multidrug-resistant gram-negative bacterial infections. Clin Infect Dis 2005; 40: 1333-41.
  3. Ayoub Moubareck C. Polymyxins and Bacterial Membranes: A Review of Antibacterial Activity and Mechanisms of Resistance. Membranes (Basel) 2020; 10: 181.
  4. Niu B, Vater J, Rueckert C, Blom J, Lehmann M, Ru JJ et al. Polymyxin P is the active principle in suppressing phytopathogenic Erwinia spp. by the biocontrol rhizobacterium Paenibacillus polymyxa M-1. BMC Microbiol 2013; 13: 137.
  5. Yang S, Wang H, Zhao D, Zhang S, Hu C. Polymyxins: recent advances and challenges. Front Pharmacol 2024; 15: 1424765.
  6. El-Sayed Ahmed MAE, Zhong LL, Shen C, Yang Y, Doi Y, Tian GB. Colistin and its role in the Era of antibiotic resistance: an extended review (2000-2019). Emerg Microbes Infect 2020; 9: 868-85.
  7. Nikaido H. Molecular basis of bacterial outer membrane permeability revisited. Microbiol Mol Biol Rev 2003; 67: 593-656.
  8. Pogue JM, Lee J, Marchaim D, Yee V, Zhao JJ, Chopra T et al. Incidence of and risk factors for colistin-associated nephrotoxicity in a large academic health system. Clin Infect Dis 2011; 53: 879-84.

Ayrıntılar

Birincil Dil

İngilizce

Konular

Yoğun Bakım

Bölüm

Araştırma Makalesi

Yayımlanma Tarihi

8 Mayıs 2026

Gönderilme Tarihi

26 Ekim 2025

Kabul Tarihi

26 Şubat 2026

Yayımlandığı Sayı

Yıl 2026 Sayı: 1

Kaynak Göster

APA
Yıldırım, T., & Savacı, H. S. (2026). Factors affecting colistin nephrotoxicity in intensive care units. Turkish Journal of Clinics and Laboratory, 1. https://doi.org/10.18663/tjcl.1811166
AMA
1.Yıldırım T, Savacı HS. Factors affecting colistin nephrotoxicity in intensive care units. TJCL. 2026;(1). doi:10.18663/tjcl.1811166
Chicago
Yıldırım, Tuğba, ve Hüseyin Serdar Savacı. 2026. “Factors affecting colistin nephrotoxicity in intensive care units”. Turkish Journal of Clinics and Laboratory, sy 1. https://doi.org/10.18663/tjcl.1811166.
EndNote
Yıldırım T, Savacı HS (01 Mayıs 2026) Factors affecting colistin nephrotoxicity in intensive care units. Turkish Journal of Clinics and Laboratory 1
IEEE
[1]T. Yıldırım ve H. S. Savacı, “Factors affecting colistin nephrotoxicity in intensive care units”, TJCL, sy 1, May. 2026, doi: 10.18663/tjcl.1811166.
ISNAD
Yıldırım, Tuğba - Savacı, Hüseyin Serdar. “Factors affecting colistin nephrotoxicity in intensive care units”. Turkish Journal of Clinics and Laboratory. 1 (01 Mayıs 2026). https://doi.org/10.18663/tjcl.1811166.
JAMA
1.Yıldırım T, Savacı HS. Factors affecting colistin nephrotoxicity in intensive care units. TJCL. 2026. doi:10.18663/tjcl.1811166.
MLA
Yıldırım, Tuğba, ve Hüseyin Serdar Savacı. “Factors affecting colistin nephrotoxicity in intensive care units”. Turkish Journal of Clinics and Laboratory, sy 1, Mayıs 2026, doi:10.18663/tjcl.1811166.
Vancouver
1.Tuğba Yıldırım, Hüseyin Serdar Savacı. Factors affecting colistin nephrotoxicity in intensive care units. TJCL. 01 Mayıs 2026;(1). doi:10.18663/tjcl.1811166


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