# No Emergence of Colistin Resistance in the Respiratory Tract of Lung Transplant Patients Treated With Inhaled Colistin

**Authors:** Nathalie Grall, Maksud Assadi, Marina Esposito-Farese, Brice Lortat-Jacob, Sébastien Tanaka, Enora Atchade, Jonathan Messika, Vincent Bunel, Hervé Mal, Pierre Mordant, Yves Castier, Bastien Garnier, Signara Gueye, Marie Petitjean, Erick Denamur, Laurence Armand-Lefevre, Charles Burdet, Philippe Montravers, Alexy Tran-Dinh

PMC · DOI: 10.3389/ti.2024.13545 · Transplant International · 2025-01-23

## TL;DR

Inhaled colistin used to prevent pneumonia after lung transplants does not increase the risk of colistin-resistant bacteria in the respiratory tract.

## Contribution

This study provides evidence that inhaled colistin does not promote colistin resistance in lung transplant patients.

## Key findings

- Inhaled colistin did not lead to the emergence of colistin-resistant bacteria in respiratory samples.
- The incidence-rate ratio for natural and acquired resistance was not statistically significant.
- No association was found between inhaled colistin and increased colistin resistance within 90 days post-transplant.

## Abstract

Secondary prophylaxis using inhaled colistin (IC) was implemented to prevent recurrences of Pseudomonas aeruginosa or extended-spectrum β-lactamase-producing Enterobacterales (ESBL-PE) pneumonia during the postoperative intensive care unit (ICU) stay after lung transplantation (LT). We evaluated the risk of emergence of colistin resistance in the respiratory tract during secondary IC prophylaxis. We conducted a prospective, single-centre, observational study of all adult patients who underwent LT between 1 July 2018 and 30 June 2019. IC was started and continued for at least 90 days for P. aeruginosa or ESBL-PE pneumonia. During the 90 days following LT, all respiratory samples were routinely tested for the presence of GNB of reduced susceptibility to colistin. Twenty-seven (38.6%) of the 70 included patients received IC. Among the 867 respiratory samples tested, IC did not promote the emergence of bacterial species with natural or acquired resistance to colistin (incidence-rate ratio of 0.21 [0.03–1.58], p = 0.13 and 1.68 [0.55–5.12], p = 0.37, respectively). Our study suggests no association between the use of IC and an increased risk of colistin resistance in the respiratory tract within 90 days of LT.

## Linked entities

- **Chemicals:** colistin (PubChem CID 5311054)
- **Diseases:** pneumonia (MONDO:0005249)
- **Species:** Pseudomonas aeruginosa (taxon 287), Enterobacterales (taxon 91347)

## Full-text entities

- **Diseases:** PE pneumonia (MESH:D011014)
- **Species:** Enterobacterales (order) [taxon 91347], Homo sapiens (human, species) [taxon 9606], Pseudomonas aeruginosa (species) [taxon 287]

## Full text

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## Figures

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## References

61 references — full list in the complete paper: https://tomesphere.com/paper/PMC11799951/full.md

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Source: https://tomesphere.com/paper/PMC11799951