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Research Journal of Pharmacy and Technology
Year : 2022, Volume : 15, Issue : 3
First page : ( 1059) Last page : ( 1063)
Print ISSN : 0974-3618. Online ISSN : 0974-360X.
Article DOI : 10.52711/0974-360X.2022.00177

Efficacy and safety of colistin-imipenem/cilastatin combination therapy for multidrug-resistant gram-negative bacteria infections in critically ill pediatric patients

Ahmed S. Mancy1,*, Shaheen Sara2, Albaghdady Ayman3, Sabri Nagwa A.2

1Department of Pharmacy Practice, Faculty of Pharmacy, Heliopolis University, Cairo, Egypt

2Department of Clinical Pharmacy, Faculty of Pharmacy, Ain-Shams University, Cairo, Egypt

3Department of Pediatric Surgery, Faculty of Medicine, Ain Shams University, Cairo, Egypt

*Corresponding Author E-mail: ahmed.mancy17@gmail.com, ahmed.mancy@hu.edu.eg

Online published on 14 June, 2022.

Abstract

Purpose

The aim of this study was to ensure the safety and efficacy of intravenous administration of colistin-imipenem/cilastatin combination to critically ill pediatrics suffering from multidrug-resistant gram-negative sepsis.

Patients and methods

The study was designed to give sixty patients in Al-Demerdash hospital pediatric intensive care units (PICU), Ain Shams University, Cairo, Egypt, either imipenem/cilastatin as a monotherapy (thirty patients) or colistin-imipenem/cilastatin intravenously as a combination (thirty patients). The interventional prospective randomized study was performed with focusing on patients’ hemodynamic parameters, vital signs, sepsis markers and microbiological response.

Results

Thirty patients received intravenous colistin-imipenem/cilastatin combination; with median age of 8.5 months (range: 1–36 months). The isolated bacteria were Acinetobacter baumannii, Klebsiella pneumoniae, Pseudomonas aeruginosa and Escherichia coli. Klebsiella pneumoniae was the most common isolate (51.7%) of the overall examined sixty patients. Patient who received the combination therapy, was associated with improving in vital signs and hemodynamic parameters with significant p = 0.001, and microbiological responses were represented by the recorded cultures. No patients were defined by renal impairment or neurological toxicity as a side effect to colistin therapy. However, nonsignificant differences in fatality was found among the two groups with p = 0.108.

Conclusion

Colistin combination therapy resulted in better clinical outcomes of PICU patients, which were represented by eradication of the multidrug-resistant gram-negative bacteria without noticeable nephrotoxicity.

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Keywords

Imipenem/Cilastatin, Colistin, Pediatrics, Combination therapy, MDR.

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