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Survival Analysis of Transplant-Associated Thrombotic Microangiopathy Under Different Diagnostic Criteria and Efficacy of Plasma Exchange

BACKGROUND: Transplant-associated thrombotic microangiopathy (TA-TMA) is a serious complication of hematopoietic stem cell transplantation (HSCT). The efficacy and survival of plasma exchange (PE) for TA-TM have not been fully clarified. In addition, there is a lack of consensus on diagnostic criter...

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Autores principales: Xu, Yifan, Wei, Yan, Wang, Lijun, Lu, Ning, Wu, Yongli, Dou, Liping, Liu, Daihong, Li, Meng, Gao, Chunji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290434/
https://www.ncbi.nlm.nih.gov/pubmed/37337423
http://dx.doi.org/10.12659/AOT.939890
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author Xu, Yifan
Wei, Yan
Wang, Lijun
Lu, Ning
Wu, Yongli
Dou, Liping
Liu, Daihong
Li, Meng
Gao, Chunji
author_facet Xu, Yifan
Wei, Yan
Wang, Lijun
Lu, Ning
Wu, Yongli
Dou, Liping
Liu, Daihong
Li, Meng
Gao, Chunji
author_sort Xu, Yifan
collection PubMed
description BACKGROUND: Transplant-associated thrombotic microangiopathy (TA-TMA) is a serious complication of hematopoietic stem cell transplantation (HSCT). The efficacy and survival of plasma exchange (PE) for TA-TM have not been fully clarified. In addition, there is a lack of consensus on diagnostic criteria for TA-TMA. MATERIAL/METHODS: We retrospectively analyzed 32 patients diagnosed with TA-TMA by different diagnostic criteria from January 2018 to February 2022 at the First Medical Center of the PLA General Hospital. RESULTS: (1) The patients with TA-TMA treated with PE in this study had a remission rate of 42.8%, a 100-day OS of 47.6%, and a 6-month OS of 38.1%. The only factor affecting the response to PE treatment was the number of PE sessions (P=0.047). (2) III–IV aGVHD prior to TA-TMA diagnosis (P=0.002), renal or neurological dysfunction (P=0.021), and the time to onset of TA-TMA (P=0.002) were independent risk factors for overall survival with TA-TMA. (3) Probable TA-TMA had the highest survival rate, but the Jodele criteria are expected to diagnose earlier and provide the greatest benefit to patients. CONCLUSIONS: PE can temporarily alleviate TA-TMA patients’ clinical symptoms and laboratory indicators. It does not, however, significantly increase overall survival. In addition, probable TA-TMA improved survival prognosis through early detection of patients with TA-TMA. There is a need for further large prospective trials to identify the population more suitable for PE treatment of TA-TMA and more valid diagnostic criteria.
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spelling pubmed-102904342023-06-25 Survival Analysis of Transplant-Associated Thrombotic Microangiopathy Under Different Diagnostic Criteria and Efficacy of Plasma Exchange Xu, Yifan Wei, Yan Wang, Lijun Lu, Ning Wu, Yongli Dou, Liping Liu, Daihong Li, Meng Gao, Chunji Ann Transplant Original Paper BACKGROUND: Transplant-associated thrombotic microangiopathy (TA-TMA) is a serious complication of hematopoietic stem cell transplantation (HSCT). The efficacy and survival of plasma exchange (PE) for TA-TM have not been fully clarified. In addition, there is a lack of consensus on diagnostic criteria for TA-TMA. MATERIAL/METHODS: We retrospectively analyzed 32 patients diagnosed with TA-TMA by different diagnostic criteria from January 2018 to February 2022 at the First Medical Center of the PLA General Hospital. RESULTS: (1) The patients with TA-TMA treated with PE in this study had a remission rate of 42.8%, a 100-day OS of 47.6%, and a 6-month OS of 38.1%. The only factor affecting the response to PE treatment was the number of PE sessions (P=0.047). (2) III–IV aGVHD prior to TA-TMA diagnosis (P=0.002), renal or neurological dysfunction (P=0.021), and the time to onset of TA-TMA (P=0.002) were independent risk factors for overall survival with TA-TMA. (3) Probable TA-TMA had the highest survival rate, but the Jodele criteria are expected to diagnose earlier and provide the greatest benefit to patients. CONCLUSIONS: PE can temporarily alleviate TA-TMA patients’ clinical symptoms and laboratory indicators. It does not, however, significantly increase overall survival. In addition, probable TA-TMA improved survival prognosis through early detection of patients with TA-TMA. There is a need for further large prospective trials to identify the population more suitable for PE treatment of TA-TMA and more valid diagnostic criteria. International Scientific Literature, Inc. 2023-06-20 /pmc/articles/PMC10290434/ /pubmed/37337423 http://dx.doi.org/10.12659/AOT.939890 Text en © Ann Transplant, 2023 https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Original Paper
Xu, Yifan
Wei, Yan
Wang, Lijun
Lu, Ning
Wu, Yongli
Dou, Liping
Liu, Daihong
Li, Meng
Gao, Chunji
Survival Analysis of Transplant-Associated Thrombotic Microangiopathy Under Different Diagnostic Criteria and Efficacy of Plasma Exchange
title Survival Analysis of Transplant-Associated Thrombotic Microangiopathy Under Different Diagnostic Criteria and Efficacy of Plasma Exchange
title_full Survival Analysis of Transplant-Associated Thrombotic Microangiopathy Under Different Diagnostic Criteria and Efficacy of Plasma Exchange
title_fullStr Survival Analysis of Transplant-Associated Thrombotic Microangiopathy Under Different Diagnostic Criteria and Efficacy of Plasma Exchange
title_full_unstemmed Survival Analysis of Transplant-Associated Thrombotic Microangiopathy Under Different Diagnostic Criteria and Efficacy of Plasma Exchange
title_short Survival Analysis of Transplant-Associated Thrombotic Microangiopathy Under Different Diagnostic Criteria and Efficacy of Plasma Exchange
title_sort survival analysis of transplant-associated thrombotic microangiopathy under different diagnostic criteria and efficacy of plasma exchange
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290434/
https://www.ncbi.nlm.nih.gov/pubmed/37337423
http://dx.doi.org/10.12659/AOT.939890
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