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Published on: August 4, 2021
Colistin inhalation monotherapy for ventilator-associated pneumonia of Acinetobacter baumannii in prematurity
Chia-Hao Kang1, Chih-Min Tsai, Tin-Hsin Wu
1Department of Pediatrics, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
Insights
Inhaled colistin effectively treated ventilator-associated pneumonia (VAP) in premature infants caused by Acinetobacter baumannii. This treatment showed no adverse events, suggesting its potential for VAP management in neonates.
Area of Science:
- Neonatal intensive care
- Infectious disease management
- Pediatric pulmonology
Background:
- Ventilator-associated pneumonia (VAP) in neonates caused by Acinetobacter baumannii presents a growing challenge with high mortality.
- Limited data exists on inhaled colistin monotherapy for VAP in preterm infants.
Purpose of the Study:
- To evaluate the efficacy and safety of aerosolized colistin as monotherapy for VAP caused by Acinetobacter baumannii in preterm infants.
Main Methods:
- Retrospective evaluation of eight preterm infants (25-36 weeks gestation) with VAP due to Acinetobacter baumannii.
- Treatment involved inhaled colistin (1,000,000 IU twice daily) for an average of 9.1 days.
- Five isolates were multi-drug resistant Acinetobacter baumannii (MDR-AB), all sensitive to colistin.
Main Results:
- Complete cure achieved in all preterm infants, with successful eradication of Acinetobacter baumannii from airway secretions.
- No clinical or laboratory adverse events were observed during colistin treatment.
Conclusions:
- Aerosolized colistin monotherapy is a viable treatment option for VAP caused by Acinetobacter baumannii in preterm infants.
- Further controlled studies are recommended to confirm these findings and establish definitive treatment guidelines.
Background:
Ventilator-associated pneumonia (VAP) caused by Acinetobacter baumannii is increasing. It has a high mortality rate but experience in using inhaled colistin as monotherapy for VAP in children, especially pre-term infants, is limited. This study presents experiences using aerosolized colistin as monotherapy for VAP due to A. baumannii infection in pre-term infants.
Methods:
Eight pre-term infants (gestational age 25-36 weeks) admitted to the neonatal intensive care unit (NICU) of Kaohsiung Chang Gung Memorial Hospital in Taiwan from January 2006 to December 2010 who received inhaled colistin as monotherapy for VAP due to A. baumannii infection were retrospectively evaluated. Of the isolated microorganisms, five were multi-drug resistant strains of A. baumannii (MDR-AB) but all were sensitive to colistin. All patients received inhaled colistin at a dose of 1,000,000 IU (33.4 mg) twice daily for an average of 9.1 days (range, 4-22 days).
Results:
All pre-term infants were cured, with A. baumannii eradicated from airway secretions. There were no clinical or laboratory adverse events related to colistin use.
Conclusions:
Aerosolized colistin may be used as monotherapy for VAP due to A. baumannii infection in pre-term infants. A larger controlled study is warranted to corroborate the findings.
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