دورية أكاديمية

Efficacy and toxicity of aerosolised colistin in ventilator-associated pneumonia: a prospective, randomised trial.

التفاصيل البيبلوغرافية
العنوان: Efficacy and toxicity of aerosolised colistin in ventilator-associated pneumonia: a prospective, randomised trial.
المؤلفون: Abdellatif, Sami1 abdellatifsamy@gmail.com, Trifi, Ahlem1 ahlem.ahurabta@gmail.com, Daly, Foued1 dalyfouad@gmail.com, Mahjoub, Khaoula1 khaoulamahjoub@yahoo.fr, Nasri, Rochdi1 rochdinasri@yahoo.fr, Ben Lakhal, Salah1 benlakhal.salah@gmail.com
المصدر: Annals of Intensive Care. 3/31/2016, Vol. 6 Issue 1, p1-11. 11p.
مصطلحات موضوعية: *COLISTIN, *DRUG toxicity, *DRUG efficacy, *MECHANICAL ventilators, *PNEUMONIA, *ACINETOBACTER baumannii, *PSEUDOMONAS aeruginosa infections, *NOSOCOMIAL infections, *INFECTIOUS disease transmission, *THERAPEUTICS
مستخلص: Background: Cases of ventilator-associated pneumonia (VAP) due to multidrug-resistant (MDR) gram-negative bacilli (GNB) mainly Acinetobacter baumannii, Pseudomonas aeruginosa and enterobacteria are common in hospitalised patients of Tunisian intensive care units (ICUs). Parenteral colistin has been used for the therapy of VAP caused by MDR GNB at Tunisian hospitals over the past few years with a favourable clinical response. However, its use fell out of favour because of the reported drug-related nephrotoxicity and neurotoxicity. Objectives: To determine whether aerosolised (AS) colistin was beneficial and safe in therapy of gram-negative VAP. Methods: This was a randomised, single-blind study, in 149 critically ill adults who developed gram-negative VAP. Included patients were divided into two groups whether they received AS colistin (intervention group; n = 73) or intravenous (IV) colistin (control group; n = 76). AS colistin was given as 4 million units (MU) by nebulisation three times per 24 h. IV colistin was given as a loading dose of 9 MU followed by 4.5 MU two times per 24 h. Patients were followed during 28 days. Primary outcome was cure of VAP assessed at day 14 of therapy and defined as resolution of clinical signs of VAP and bacteriological eradication. Secondary outcomes were incidence of acute renal failure (ARF), mechanical ventilation length, ICU length of stay and 28-day mortality. Results were analysed based on intention-to-treat concept. Results: The patient's baseline characteristics and distribution of pathogens VAP in both groups were similar. The clinical cure rate was 67.1 % in AS group and 72 % in IV group ( p = 0.59). When administered in monotherapy or in combination, the AS regimen was as effective as IV regimen. Patients in AS group had significantly lower incidence of ARF (17.8 vs 39.4 %, p = 0.004), more favourable improvement of P/ F ratio (349 vs 316 at day 14, p = 0.012), shortened time to bacterial eradication (TBE) (9.89 vs 11.26 days, p = 0.023) and earlier weaning from ventilator in ICU survivors with a mean gain in ventilator-free days of 5 days. No difference was shown in the length of stay and the 28-day mortality. Conclusion: Aerosolised colistin seems to be beneficial. It provided a therapeutic effectiveness non-inferior to parenteral colistin in therapy of MDR bacilli VAP with a lower nephrotoxicity, a better improvement of P/ F ratio, a shortened bacterial eradication time and earlier weaning from ventilator in ICU survivors. Trial registration ClinicalTrials.gov Identifier: NCT02683603 [ABSTRACT FROM AUTHOR]
قاعدة البيانات: Academic Search Index
الوصف
تدمد:21105820
DOI:10.1186/s13613-016-0127-7