Journal List > Tuberc Respir Dis > v.64(2) > 1001192

Kim, Kim, Kang, Choi, Lee, Hwang, Shin, Park, Park, Lee, Jang, Kim, Mo, Lee, Hyun, Jung, Choi, and Lee: A Trial of Aerosolized Colistin for the Treatment of Nosocomial Pneumonia due to Multidrug-resistant Acinetobacter baumannii

Abstract

Background:

Recently, multidrug-resistant (MDR) A. baumannii has been implicated for a significant proportion of nosocominal pneumonia in many intensive care units (ICUs), and its acquisition may increase mortality and the length of stay in the ICU. Aerosolized colistin has been successfully used in patients with cystic fibrosis, but there is a lack of data regarding the use of aerosolized colistin in patients with nosocomial pneumonia.

Methods:

We conducted the present study to assess the effectiveness of aerosolized colistin for the treatment of MDR A. baumannii nosocomial pneumonia. We retrospectively reviewed the medical records of 10 patients who had been hospitalized in the medical ICU and had received aerosolized colistin as a therapy for MDR A. baumannii pneumonia.

Results:

The mean duration of aerosolized colistin therapy was 12.7±2.4 days. Nine (90%) of 10 patients showed a favorable response to the therapy. Follow-up cultures were available for all patients, and the responsible pathogen was completely eradicated. One patient suffered from bronchospasm, which resolved after treatment with nebulized salbutamol.

Conclusion:

Our results corroborate previous reports that aerosolized colistin may be an effective and safe choice for the treatment of nosocomial pneumonia caused by MDR A. baumannii. Larger prospective controlled clinical studies are warranted to validate further the effectiveness and safety of aerosolized colistin therapy. (Tuberc Respir

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Table 1.
Demographic and clinical characteristics of patients
No. Sex Age Diagnosis at ICU admission Comorbidities ICU stay Hospital stay Isolation days IV antibiotics§
1 M 71 Pneumonia, ARDS CMV pneumonia 88 136 32 Ganciclovir
2 F 50 Pneumonia, ARDS Intestinal obstruction, Spontaneous pneumothorax 69 147 14 Tazocin, Aztreonam
3 M 71 Aspiration pneumonia CBD & colon cancer, Intraabdominal abscess, ARF, Drug induced eosinophilic pneumonia l 54 132 6 Teicoplanin, Imipenem
4 F 82 Pulmonary TB DM, ARF, acalculous cholecystitis, Renal tubular acidosis, Toxic hepatitis, Sacral sore, Dementia 129 135 15 Antituberculous agents
5 F 65 Pulmonary TB DM, Toxic hepatitis, Dermatomyositis Sacral sore s, 71 96 5 Antituberculous agents
6 M 52 Pneumonia, ARDS DM, ARF, Alcoholic liver disease 63 63 8 Teicoplanin, Metronidazole
7 F 70 Pulmonary TB Interstitial lung disease, DM, CIP 89 102 12 Antituberculous agents
8 M 38 Severe CAP End stage renal disease, CMV pneumonia, CIP 74 74 5 Ganciclovir, Teicoplanin, Meropenem, Moxifloxacin
9 M 78 Severe CAP COPD, Liver cirrhosis, CRF, Heart failure, Atrial fibrillation 21 21 5 Teicoplanin, meropenem
10 M 41 Pneumonia, ARDS Small bowel perforation, Peritonitis, Dieulafoy's ulcer 26 37 6 Teicoplanin, meropenem
AVR   61.8     68.4 94.3 3 10.8  

ICU: Intensive Care Unit; IV: Intravenous; ARDS: Acute Respiratory Distress Syndrome; CMV: Cytomegalovirus; CBD: Common Bile Duct; ARF: Acute Renal Failure; TB: Tuberculosis; DM: Diabetes Mellitus; CIP: Critical Illness Polyneuropathy; CAP: Community-Acquired Pneumonia; COPD: Chronic Obstructive Pulmonary Disease; CRF: Chronic Renal Failure; AVR: Average.

Duration of ICU stay (days),

Duration of hospitalization (days),

Time from ICU admission to first isolation of A. baumannii from tracheal secretions of patients (days),

§ Concomitant intravenous antibiotic treatment with aerosolized colistin.

Table 2.
Clinical outcomes of patients treated with aerosolized colistin
No. Sex Age Treatment days Dosage Follow-up culture Outcome Clinical course Adverse effect
1 M 71 13 75 mg 8 hrs Pseudomonas aeruginosa Cure Discharge  
2 F 50 7 75 mg 8 hrs Stenotrophomonas maltophilia Cure Discharge  
3 M 71 11 75 mg 8 hrs No bacteria Cure Death (Intraabdominal infection)  
4 F 82 14 75 mg 8 hrs No bacteria Improvement Discharge§  
5 F 65 14 1 150 mg 8 hrs No bacteria Cure Discharge  
6 M 52 13 1 150 mg 8 hrs Pseudomonas aeruginosa Improvement Death (MRSA pneumonia)  
7 F 70 14 75 mg 8 hrs Stenotrophomonas maltophilia Improvement Hospitalization Bronchospasm
8 M 38 16 75 mg 8 hrs No bacteria Improvement Hospitalization  
9 M 78 12 75 mg 8 hrs MRSA Deterioration Death (MRSA pneumonia)  
10 M 41 13 75 mg 8 hrs No bacteria Improvement Death (Intraabdominal infection)  
AVR     12.7          

Duration of aerosolized colistin (days),

Dosage of aerosolized colistin per day,

Posttreatment isolated organism from trachea secretions of patients,

§ She was transferred to the ICU of another hospital, so her clinical outcome was classified as improvement

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