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

Abstract

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.

Keywords: Aerosol; Colistin; Intravenous; Nephrotoxicity; Ventilator-associated pneumonia.

Figures

Fig. 1

Patients’ flowchart. VAP ventilator-acquired pneumonia, CPIS Clinical Pulmonary Infection Score, AS aerosolised, IV intravenous, COS colistin-only susceptible. *The order of randomization was as follows: Block 1: AS, AS, IV, IV; Block 2: AS, IV, AS, IV; Block 3: IV, IV, AS, AS; Block 4: IV, AS, IV, AS. Details of combination are displayed in Table 1

Fig. 2

Microorganism’s distribution in study groups

Fig. 3

Cure rates between the study groups. The cure rates were shown when colistin was prescribed in monotherapy, in combination or both

Fig. 4

a Evolution of P/F ratio in both groups. b Evolution of positivity rate of bacteriological samples in both groups. c Time to bacterial eradication (TBE) between groups

Fig. 5

a Incidence of acute renal failure (ARF) and necessity of replacement renal therapy (RRT) in both groups. b Mean time to ARF onset in both groups

Fig. 6

Survival analysis in study groups

Fig. 7

Duration of mechanical ventilation in study groups

Fig. 8

Post-therapy assessment of Clinical Pulmonary Infection Score (CPIS) in study groups