<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>21(4)</volume><submitter>Coiffard B</submitter><pubmed_abstract>It is unknown if solid organ transplant recipients are at higher risk for severe COVID-19. The management of a lung transplantation (LTx) program and the therapeutic strategies to adapt the immunosuppressive regimen and antiviral measures is a major issue in the COVID-19 era, but little is known about worldwide practice. We sent out to 180 LTx centers worldwide in June 2020 a survey with 63 questions, both regarding the management of a LTx program in the COVID-19 era and the therapeutic strategies to treat COVID-19 LTx recipients. We received a total of 78 responses from 15 countries. Among participants, 81% declared a reduction of the activity and 47% restricted LTx for urgent cases only. Sixteen centers observed deaths on waiting listed patients and eight centers performed LTx for COVID-19 disease. In 62% of the centers, COVID-19 was diagnosed in LTx recipients, most of them not severe cases. The most common immunosuppressive management included a decreased dose or pausing of the cell cycle inhibitors. Remdesivir, hydroxychloroquine, and azithromycin were the most proposed antiviral strategies. Most of the centers have been affected by the COVID-19 pandemic and proposed an active therapeutic strategy to treat LTx recipients with COVID-19.</pubmed_abstract><journal>American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons</journal><pagination>1586-1596</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9906357</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Management of lung transplantation in the COVID-19 era-An international survey.</pubmed_title><pmcid>PMC9906357</pmcid><pubmed_authors>Thomas PA</pubmed_authors><pubmed_authors>Langer F</pubmed_authors><pubmed_authors>Schafers HJ</pubmed_authors><pubmed_authors>Hraiech S</pubmed_authors><pubmed_authors>Papazian L</pubmed_authors><pubmed_authors>Seiler F</pubmed_authors><pubmed_authors>Coiffard B</pubmed_authors><pubmed_authors>Bals R</pubmed_authors><pubmed_authors>Lepper PM</pubmed_authors><pubmed_authors>Wilkens H</pubmed_authors><pubmed_authors>Reynaud-Gaubert M</pubmed_authors><pubmed_authors>Daviet F</pubmed_authors><pubmed_authors>Cassir N</pubmed_authors><pubmed_authors>Prud'Homme E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Management of lung transplantation in the COVID-19 era-An international survey.</name><description>It is unknown if solid organ transplant recipients are at higher risk for severe COVID-19. The management of a lung transplantation (LTx) program and the therapeutic strategies to adapt the immunosuppressive regimen and antiviral measures is a major issue in the COVID-19 era, but little is known about worldwide practice. We sent out to 180 LTx centers worldwide in June 2020 a survey with 63 questions, both regarding the management of a LTx program in the COVID-19 era and the therapeutic strategies to treat COVID-19 LTx recipients. We received a total of 78 responses from 15 countries. Among participants, 81% declared a reduction of the activity and 47% restricted LTx for urgent cases only. Sixteen centers observed deaths on waiting listed patients and eight centers performed LTx for COVID-19 disease. In 62% of the centers, COVID-19 was diagnosed in LTx recipients, most of them not severe cases. The most common immunosuppressive management included a decreased dose or pausing of the cell cycle inhibitors. Remdesivir, hydroxychloroquine, and azithromycin were the most proposed antiviral strategies. Most of the centers have been affected by the COVID-19 pandemic and proposed an active therapeutic strategy to treat LTx recipients with COVID-19.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2025-04-18T14:25:44.311Z</modification><creation>2025-04-07T00:34:54.909Z</creation></dates><accession>S-EPMC9906357</accession><cross_references><pubmed>33084144</pubmed><doi>10.1111/ajt.16368</doi></cross_references></HashMap>