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Invasive Pulmonary Aspergillosis in Acute-on-Chronic Liver Failure Patients: Short-Term Outcomes and Antifungal Options
INTRODUCTION: Acute-on-chronic liver failure (ACLF) patients are susceptible to invasive fungal infections. We evaluated the prognosis and antifungal options in ACLF patients with invasive pulmonary aspergillosis (IPA). METHODS: ACLF patients with IPA from 15 hospitals were retrospectively screened...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Healthcare
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8572893/ https://www.ncbi.nlm.nih.gov/pubmed/34468963 http://dx.doi.org/10.1007/s40121-021-00524-5 |
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author | Chen, Danli Qian, Zhiping Su, Haibin Meng, Zhongji Lv, Jun Huang, Yan Gao, Yanhang Liu, Jingyuan Zhao, Caiyan Gao, Hongbo Chen, Yu Xia, Jie Peng, Liang Han, Tao Li, Hai Zheng, Xin Wang, Xianbo Lu, Xiaobo Shi, Yu Hu, Jinhua Chen, Jinjun |
author_facet | Chen, Danli Qian, Zhiping Su, Haibin Meng, Zhongji Lv, Jun Huang, Yan Gao, Yanhang Liu, Jingyuan Zhao, Caiyan Gao, Hongbo Chen, Yu Xia, Jie Peng, Liang Han, Tao Li, Hai Zheng, Xin Wang, Xianbo Lu, Xiaobo Shi, Yu Hu, Jinhua Chen, Jinjun |
author_sort | Chen, Danli |
collection | PubMed |
description | INTRODUCTION: Acute-on-chronic liver failure (ACLF) patients are susceptible to invasive fungal infections. We evaluated the prognosis and antifungal options in ACLF patients with invasive pulmonary aspergillosis (IPA). METHODS: ACLF patients with IPA from 15 hospitals were retrospectively screened from 2011 to 2018, and 383 ACLF patients without lung infections were included from a prospective cohort (NCT02457637). Demographic, laboratory, clinical data, and 28-day outcomes were documented in the two cohorts. RESULTS: ACLF patients with probable IPA (n = 145) had greater 28-day mortality (33.6% vs. 15.7%, p < 0.001) than those without (n = 383). The respiratory failure-associated 28-day mortality was greater in ACLF patients with IPA than in those without before (17.1% vs. 0.3%, p < 0.001) and after (16.0% vs. 0.0%, p < 0.001) propensity score matching in 116 pairs. IPA patients with lung injury had greater 28-day all-cause mortality (66.5% vs. 24.2%, p < 0.001) and IPA-associated mortality (45.8% vs. 8.1%, p < 0.001) than patients without lung injury (PaO2/FiO2 ≥ 400 mmHg). Antifungal therapy was prescribed to 139 of 145 patients, and 102 patients were treated with voriconazole alone (n = 59) or sequential/combined therapy (n = 43) with varying loading doses (100–800 mg) and daily maintenance doses (0–800 mg). A proposed optimal voriconazole regimen (loading dose, 200 mg twice daily; daily maintenance dose, 100 mg) achieved comparable short-term survival and optimal trough drug concentrations (1–5 μg/mL) on therapeutic drug monitoring in 26 patients. CONCLUSION: Presence of IPA increases the short-term mortality of ACLF patients mainly due to respiratory failure. An optimal voriconazole regimen is needed for such critical patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40121-021-00524-5. |
format | Online Article Text |
id | pubmed-8572893 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-85728932021-11-15 Invasive Pulmonary Aspergillosis in Acute-on-Chronic Liver Failure Patients: Short-Term Outcomes and Antifungal Options Chen, Danli Qian, Zhiping Su, Haibin Meng, Zhongji Lv, Jun Huang, Yan Gao, Yanhang Liu, Jingyuan Zhao, Caiyan Gao, Hongbo Chen, Yu Xia, Jie Peng, Liang Han, Tao Li, Hai Zheng, Xin Wang, Xianbo Lu, Xiaobo Shi, Yu Hu, Jinhua Chen, Jinjun Infect Dis Ther Original Research INTRODUCTION: Acute-on-chronic liver failure (ACLF) patients are susceptible to invasive fungal infections. We evaluated the prognosis and antifungal options in ACLF patients with invasive pulmonary aspergillosis (IPA). METHODS: ACLF patients with IPA from 15 hospitals were retrospectively screened from 2011 to 2018, and 383 ACLF patients without lung infections were included from a prospective cohort (NCT02457637). Demographic, laboratory, clinical data, and 28-day outcomes were documented in the two cohorts. RESULTS: ACLF patients with probable IPA (n = 145) had greater 28-day mortality (33.6% vs. 15.7%, p < 0.001) than those without (n = 383). The respiratory failure-associated 28-day mortality was greater in ACLF patients with IPA than in those without before (17.1% vs. 0.3%, p < 0.001) and after (16.0% vs. 0.0%, p < 0.001) propensity score matching in 116 pairs. IPA patients with lung injury had greater 28-day all-cause mortality (66.5% vs. 24.2%, p < 0.001) and IPA-associated mortality (45.8% vs. 8.1%, p < 0.001) than patients without lung injury (PaO2/FiO2 ≥ 400 mmHg). Antifungal therapy was prescribed to 139 of 145 patients, and 102 patients were treated with voriconazole alone (n = 59) or sequential/combined therapy (n = 43) with varying loading doses (100–800 mg) and daily maintenance doses (0–800 mg). A proposed optimal voriconazole regimen (loading dose, 200 mg twice daily; daily maintenance dose, 100 mg) achieved comparable short-term survival and optimal trough drug concentrations (1–5 μg/mL) on therapeutic drug monitoring in 26 patients. CONCLUSION: Presence of IPA increases the short-term mortality of ACLF patients mainly due to respiratory failure. An optimal voriconazole regimen is needed for such critical patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40121-021-00524-5. Springer Healthcare 2021-09-01 2021-12 /pmc/articles/PMC8572893/ /pubmed/34468963 http://dx.doi.org/10.1007/s40121-021-00524-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Original Research Chen, Danli Qian, Zhiping Su, Haibin Meng, Zhongji Lv, Jun Huang, Yan Gao, Yanhang Liu, Jingyuan Zhao, Caiyan Gao, Hongbo Chen, Yu Xia, Jie Peng, Liang Han, Tao Li, Hai Zheng, Xin Wang, Xianbo Lu, Xiaobo Shi, Yu Hu, Jinhua Chen, Jinjun Invasive Pulmonary Aspergillosis in Acute-on-Chronic Liver Failure Patients: Short-Term Outcomes and Antifungal Options |
title | Invasive Pulmonary Aspergillosis in Acute-on-Chronic Liver Failure Patients: Short-Term Outcomes and Antifungal Options |
title_full | Invasive Pulmonary Aspergillosis in Acute-on-Chronic Liver Failure Patients: Short-Term Outcomes and Antifungal Options |
title_fullStr | Invasive Pulmonary Aspergillosis in Acute-on-Chronic Liver Failure Patients: Short-Term Outcomes and Antifungal Options |
title_full_unstemmed | Invasive Pulmonary Aspergillosis in Acute-on-Chronic Liver Failure Patients: Short-Term Outcomes and Antifungal Options |
title_short | Invasive Pulmonary Aspergillosis in Acute-on-Chronic Liver Failure Patients: Short-Term Outcomes and Antifungal Options |
title_sort | invasive pulmonary aspergillosis in acute-on-chronic liver failure patients: short-term outcomes and antifungal options |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8572893/ https://www.ncbi.nlm.nih.gov/pubmed/34468963 http://dx.doi.org/10.1007/s40121-021-00524-5 |
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