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Once Versus Thrice Daily Colistin in Critically Ill Ptients with Multi-Drug Resistant Infections
Monireh Ghazaeian1, Majid Mokhtari2, Mehran Kouchek2
1Department of Clinical Pharmacy, Faculty of pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Abstract:
The aim of this study was to evaluate the procalcitonin (PCT) changes in two different high-dose colistin regimens in the treatment of multi-drug resistant MDR gram negative infections in ICU patients. This is a prospective study of adult ICU patients with bacteremia and ventilator associated pneumonia (VAP) caused by MDR gram negative pathogens. Patients were assigned to two colistin administration groups. Group A received 9 and group B received 3 million international units every 24 and 8 h respectively. Baseline characteristics and measurements of PCT concentrations at the start, the 3rd and the 5th day of the antibiotic therapy and their trends between the two groups were recorded and compared. of 40 patients enrolled, 34 completed the study protocol, of whom 30 (88.2%) had (VAP) and 4 (11.8%) had bacteremia. There were no statistically significant differences in the baseline characteristics between the two groups. The mean PCT levels in two study groups were; 2.34, 1.24, and 0.95 in group A and 5.89, 1.24 and 0.8 in group B at the baseline, 3rd and 5th day of colistin administration respectively (P=0.47). The ICU length of stay (LOS) in days and ICU mortality were; 31.31, 35.3% and 32.06, 22.2% in groups A and B (P=0.39, 0.87), respectively.
Conclusion:
We did not find any statistically significant differences in the serum PCT levels, ICU LOS or ICU mortality, between the two groups, who received maximum recommended dose of CMS with 2 different intervals of every 8 or 24 h.
Insights
This study found no significant differences in procalcitonin (PCT) levels, ICU length of stay, or mortality between high-dose colistin regimens for multi-drug resistant gram-negative infections. Both 8-hourly and 24-hourly dosing showed similar outcomes in ICU patients.
Area of Science:
- Infectious Diseases
- Critical Care Medicine
- Pharmacology
Background:
- Multi-drug resistant (MDR) gram-negative infections pose a significant threat in intensive care units (ICUs).
- Colistin is a crucial antibiotic for treating these infections, but optimal dosing strategies are still debated.
- Procalcitonin (PCT) is a biomarker used to monitor bacterial infections and response to antibiotic therapy.
Purpose of the Study:
- To compare procalcitonin (PCT) changes in patients with MDR gram-negative infections treated with two different high-dose colistin regimens.
- To evaluate the impact of these regimens on clinical outcomes, including ICU length of stay (LOS) and mortality.
Main Methods:
- A prospective study involving adult ICU patients with bacteremia or ventilator-associated pneumonia (VAP) caused by MDR gram-negative pathogens.
- Patients were randomized into two groups: Group A received 9 million international units (MIU) of colistin every 24 hours, and Group B received 3 MIU every 8 hours.
- PCT levels were measured at baseline, day 3, and day 5. ICU LOS and mortality were recorded.
Main Results:
- A total of 34 patients completed the study; 30 had VAP and 4 had bacteremia.
- No statistically significant differences were observed in baseline characteristics between the groups.
- Mean PCT levels, ICU LOS, and ICU mortality showed no significant differences between the colistin regimens (P > 0.05 for all).
Conclusions:
- High-dose colistin administration, whether every 8 or 24 hours, did not result in statistically significant differences in serum PCT levels, ICU LOS, or ICU mortality.
- These findings suggest that both dosing intervals may be comparable in managing severe MDR gram-negative infections in the ICU setting.
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