Aerosolized colistin for the treatment of nosocomial pneumonia due to multidrug-resistant Gram-negative bacteria in patients without cystic fibrosis

Nosocomial pneumonia due to multidrug-resistant Gram-negative bacteria, such as certain Pseudomonas aeruginosa and Acinetobacter baumannii strains, is among the most serious complications that occur in the intensive care unit (ICU) setting. Mortality, morbidity and health care costs are substantially increased by this type of infection [1‐3]. Increasing rates of resistance among Gram-negative bacteria to most classes of antimicrobial agents have frequently led to clinical failure of currently employed therapies. Lack of development and introduction into clinical practice of new antibiotics to combat multiresistant Gram-negative bacteria have stimulated renewed interest in the use of the older antibiotic colistin.

Outcomes in patients with ventilator-associated pneumonia (VAP) due to multidrug-resistant Gram-negative bacteria are poor [1]. Intravenous colistin was recently used to treat such infections. Notably, a recent study [4] compared intravenous colistin (21 patients) with imipenem (14 patients) in the treatment of VAP due to multidrug-resistant A baumannii. Mortality rates were similar: 61.9% among patients treated with intravenous colistin and 64.2% among patients treated with imipenem. In patients with cystic fibrosis, aerosolized colistin has successfully been used to treat acute pulmonary exacerbations of infection or initial colonization with P aeruginosa strains [5, 6]. However, there is a lack of data regarding the use of aerosolized colistin in patients without cystic fibrosis. A few reports have indicated that aerosolized colistin may be a beneficial additional therapeutic intervention in the management of nosocomial pneumonia (whether ventilator associated or not) [7‐10]. In addition, a few old reports of the use of aerosolized polymyxin B yielded controversial results. Feeley and coworkers [11] reported that use of polymyxin B aerosol in seriously ill patients is associated with increased incidence of pneumonia due to polymyxin-resistant organisms. However, Klastersky and colleagues [12] found endotracheal administration of polymyxin B plus aminosidin to be a useful alternative regimen to endotracheal gentamicin for the prevention of lung infections.

We present data from our recent experience with aerosolized colistin for the treatment of pneumonia due to multidrug-resistant Gram-negative bacteria in eight ICU patients.

From 1 October 2000 through 31 January 2004, 152 patients received treatment with intravenous colistin for infections with multidrug-resistant Gram-negative bacteria. Eight out of 152 patients were identified as having received aerosolized colistin for the management of Gram-negative nosocomial pneumonia. Table 1 describes the demographic and clinical features of these patients, including comorbidities, responsible pathogen(s) and susceptibility of the pathogen(s) to commonly tested antimicrobial agents, as well as the outcome of the infection and of the patient.

The mean age of the patients was 59.6 years and most of them were male (six out of eight). All patients had been admitted to the ICU, with a mean Acute Physiology and Chronic Health Evaluation II scores on the day of ICU admission and on day 1 of aerosolized colistin administration of 14.6 and 17.1, respectively. During the preceding 3 months, three patients had been hospitalized in the same or another unit. All patients had received other antimicrobial regimens before aerosolized colistin was initiated. In addition, three patients received immunosuppressive treatment (steroids) and four received immunoglobulin therapy during their hospitalization.

The responsible pathogens in the eight cases of nosocomial pneumonia were Acinetobacter baumannii (seven out of eight) and P aeruginosa (one out of eight) strains. Only in one case was a second strain isolated from the same culture specimen, and it was found to be methicillin-resistant Staphylococcus aureus. Half of the isolated pathogens were sensitive only to colistin; the rest were multidrug-resistant strains.

All patients received mechanical ventilatory support for a mean of 19.4 days. Colistin was prepared for nebulization; 1 or 2 million IU colistin was diluted in 2 or 4 ml sterile normal saline 0.9%, respectively. In patients undergoing mechanical ventilation aerosolized colistin was delivered by means of the Siemens Servo Ventilator 300 (Siemens-Elma AB, Solna, Sweden). In spontaneously breathing patients colistin was administered as follows: 1,000,000 IU were added to 4 ml normal saline and the solution was nebulized with 8 l/min oxygen flow and inhaled via a face mask. This technique of administration of aerosolized medication is commonly used worldwide for the administration of bronchodilators in nebulized form. The daily dose of aerosolized colistin ranged from 1.5 to 6 million IU divided into three or four doses, and the duration of administration ranged from 3 to 32 days (mean 10.5 days). No strictly uniform dosing strategy for aerosolized colistin was applied, and differences in regimen reflect the differing approaches of the individual attending physicians. In addition, seven out of eight patients received concomitant intravenous treatment with colistin or other antimicrobial agents with activity against Gram-negative bacteria, such as β lactams, quinolones and aminoglycosides. Only one patient received aerosolized colistin as monotherapy; she had received intravenous colistin therapy before aerosolized colistin for 7 days and continued to receive the intravenous therapy after the end of aerosolized therapy (for 32 days).

The pneumonia was observed to respond to treatment in seven out of eight patients who received supplemental therapy with aerosolized colistin. Four episodes of pneumonia were cured and three were improved at the end of treatment. Only one out of the eight patients who received aerosolized colistin for the treatment of multidrug-resistant Gram-negative pneumonia deteriorated and finally died. He was a 50-year-old multiple trauma patient, who was admitted to the ICU with fractures located at C4–C5, haemothorax and functional dissection of the spinal cord due to a car accident. His past medical history was noteworthy for arterial hypertension, Wolff–Parkinson–White syndrome, chronic renal insufficiency due to polycystic kidney disease and ankylosing spondylitis, for which he was receiving steroid therapy. During his prolonged hospitalization in the ICU, the patient developed pneumonia due to multidrug-resistant A baumannii, requiring intubation. His clinical condition became complicated by sepsis syndrome due to an infection caused by a colistin-only sensitive P aeruginosa strain, which was unresponsive to administered antimicrobial treatment. On day 95 of his hospitalization in the ICU, he died from septic shock and multiple organ failure.

Follow-up cultures were available for five out of eight patients. In four of them the responsible pathogen was eradicated, and in one case the pathogen persisted in repeated specimen cultures; this patient died. Superinfection with Gram-positive micro-organisms or yeasts was not observed. No Gram-negative bacterium developed resistance to colistin in subsequent specimen cultures during or at the end of aerosolized treatment.

Administration of aerosolized colistin was well tolerated by all patients. During treatment, all patients were closely monitored for possible respiratory adverse reactions, but none of them experienced chest tightness, bronchoconstriction, or apnoea. Only two patients, who had history of chronic obstructive pulmonary disease, received concurrent treatment with inhaled β₂ agonist. Only in the patient who died did renal function worsen (baseline serum creatinine increased by 1.4 mg/dl) during aerosolized colistin treatment. This patient, as mentioned above, had a history of polycystic kidney disease and chronic renal failure, and died from septic shock and multiple organ failure. No deterioration in renal function was observed in the other seven patients during colistin treatment. One patient had baseline serum creatinine levels of 5.4 mg/dl, and at the end of colistin treatment serum creatinine had decreased to 4.5 mg/dl. That particular patient was already receiving haemodialysis treatment before the initiation of intravenous or aerosolized colistin.

Of 152 patients who received treatment with intravenous colistin for infections with multidrug-resistant Gram-negative bacteria during the period of study, 55 had received less than 72 hours of intravenous colistin and were excluded from all analyses. Medical records were not available for three patients; in addition, one patient was in the hospital during data collection. Thus, 93 patients were further analyzed. Forty-five of these patients received intravenous colistin for the treatment of nosocomial pneumonia due to Gram-negative bacteria. Survival and clinical cure rates for the infection were better, although not statistically significantly so, in patients with pneumonia who received additional aerosolized colistin than in patients who received only intravenous colistin treatment (survival: 7/8 patients [87.5%] versus 34/45 patients [75.6%], P = 0.41; clinical cure: 7/8 patients [87.5%] versus 30/45 patients [66.7%], P = 0.67).

Aerosolized colistin may be an effective adjunctive intervention for the treatment of nosocomial pneumonia due to multidrug-resistant Gram-negative bacteria in patients without cystic fibrosis. Colistin and polymyxin E are old antibiotics; colistin was almost abandoned for many years because of its reported nephrotoxicity and neurotoxicity. This medication was reintroduced into clinical practice just a few years ago, and this resulted mainly from increased resistance rates among Gram-negative bacteria, especially in the ICU setting, and the absence of new and effective alternative therapeutic options [16‐18].

The idea of using colistin or polymyxin B (which belongs to the same group of antibiotics, and has similar antimicrobial spectrum, usage indications and toxicities as colistin) in the nebulized form for the management of pneumonia due to Gram-negative bacteria is not new. In 1963, Pino and coworkers [19] used aerosolized colistin in patients with pulmonary suppurations. A few years later, Marschke and Sarauw [20] reported two cases of pneumonia due to P aeruginosa strains in patients with underlying bronchiectasis and chronic bronchitis, in which polymyxin B was given by inhalation. Both patients experienced dyspnoea due to airway obstruction. Recently, aerosolized colistin was used successfully to treat and prevent pneumonia caused by P aeruginosa in patients with human immunodeficiency syndrome and in patients with nosocomial pneumonia and tracheobronchitis [21‐23].

There is extensive experience with administration of aerosolized colistin to patients with cystic fibrosis, in whom this type of treatment is used to prevent or treat lung infections with P aeruginosa strains. Notably, studies found that nebulized colistin reduced the number of relapses of lung infections and subsequently the decline in lung function among patients with cystic fibrosis [24‐27].

The pharmacokinetic properties and dosing strategies of aerosolized colistin are not well defined. Whether the various forms of colistin used for inhalation therapy (e.g. dry powder formulation for inhalation, colistin solutions for nebulization) or the different types of nebulizing systems influence the effectiveness and safety of colistin remains to be determined [28‐31].

Adverse effects of aerosolized colistin or polymyxin B are a major concern; potential adverse effects include bronchoconstriction, chest tightness and apnoea due to neuromuscular blockade. One study conducted in 58 children with cystic fibrosis who received nebulized colistin for the treatment of lung infections [32] reported that 20 of them experienced a decrease in forced expiratory volume in 1 s by greater than 10% from baseline. In addition, another study [33] found that 35 out of 46 adult patients with cystic fibrosis who also received nebulized colistin for lung infection developed chest tightness. However, treatment with inhaled β₂ agonists before the initiation of aerosolized colistin was able to prevent the development of such side effects in the respiratory system. Another significant concern regarding the use of aerosolized colistin for the treatment of nosocomial pneumonia is dissemination of multidrug-resistant bacteria through nebulizer devices [34, 35]. However, this potential problem could be eliminated by strict use of appropriate infection control guidelines by medical and nursing hospital staff.

Our study is not without limitations. It is a small case series and is of a retrospective design. In addition, there is no control group of patients receiving treatment with only intravenous antimicrobial agents. Furthermore, some of the patients also received intravenous treatment with other antimicrobial agents, which might have influenced the outcomes.

Two major risks are arising from the wide use of colistin: the emergence of Gram-negative bacteria, such as P aeruginosa and A baumannii, resistant to colistin; and an increase of infections due to Gram-positive and Gram-negative pathogens, such as Proteus and Serratia spp., inherently resistant to colistin. Consequently, there is an urgent need to restrict the use of colistin use in order to minimize these risks.