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Updated: Jan 30, 2026

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Azithromycin and early allograft function after lung transplantation: A randomized, controlled trial
Anke Van Herck1, Anna E Frick2, Veronique Schaevers1
1Lung Transplant Unit, Department of Chronic Diseases, Metabolism & Ageing.
Summary
Azithromycin treatment before and after lung transplantation did not improve early lung function. However, it did reduce airway inflammation, confirming its anti-inflammatory effects in lung allograft recipients.
Area of Science:
- Pulmonology
- Transplantation Medicine
- Pharmacology
Background:
- Chronic lung allograft dysfunction (CLAD) is a primary limitation to long-term survival after lung transplantation (LTx).
- Azithromycin has demonstrated benefits in improving CLAD-free and long-term survival post-LTx.
- The impact of azithromycin on early lung allograft function remains unclear.
Purpose of the Study:
- To evaluate the effect of pre-transplant and prompt post-transplant azithromycin on early lung allograft function.
- To assess secondary outcomes including airway inflammation, rejection, infection, and survival rates.
Main Methods:
- A prospective, randomized, double-blind, placebo-controlled trial involving 68 patients undergoing LTx.
- Azithromycin or placebo administered pre-transplant and daily for 31 days post-transplant.
- Primary outcome: 15% improvement in FEV1 within 3 months post-LTx; secondary outcomes included inflammation markers and survival.
Main Results:
- No significant difference in FEV1 between azithromycin and placebo groups at 3 months post-LTx (p=0.41).
- Azithromycin group showed reduced airway inflammation, evidenced by lower bronchoalveolar lavage (BAL) neutrophilia and IL-8 levels at Days 30 and 90.
- No significant differences observed in other secondary outcomes between the groups.
Conclusions:
- Pre- and post-transplant azithromycin did not enhance early lung allograft function.
- The study confirmed the anti-inflammatory properties of azithromycin in the context of LTx.
- Further research may explore alternative azithromycin regimens or patient populations for potential benefits.
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