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Outcomes in 1096 patients with severe thrombotic thrombocytopenic purpura before the Caplacizumab era

INTRODUCTION: Thrombotic thrombocytopenic purpura (TTP) is a diagnostic and therapeutic emergency. Therapeutic plasma exchange (TPE) combined with immunosuppression has been the cornerstone of the initial management. To produce optimal benefits, emerging treatments must be used against a background...

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Autores principales: Van de Louw, Andry, Mariotte, Eric, Darmon, Michael, Cohrs, Austin, Leslie, Douglas, Azoulay, Elie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8360509/
https://www.ncbi.nlm.nih.gov/pubmed/34383822
http://dx.doi.org/10.1371/journal.pone.0256024
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author Van de Louw, Andry
Mariotte, Eric
Darmon, Michael
Cohrs, Austin
Leslie, Douglas
Azoulay, Elie
author_facet Van de Louw, Andry
Mariotte, Eric
Darmon, Michael
Cohrs, Austin
Leslie, Douglas
Azoulay, Elie
author_sort Van de Louw, Andry
collection PubMed
description INTRODUCTION: Thrombotic thrombocytopenic purpura (TTP) is a diagnostic and therapeutic emergency. Therapeutic plasma exchange (TPE) combined with immunosuppression has been the cornerstone of the initial management. To produce optimal benefits, emerging treatments must be used against a background of best standard of care. Clarifying current uncertainties is therefore crucial. METHODS: The objective of this study was to analyze a large high-quality database (Marketscan) of TTP patients managed between 2005 and 2014, in the pre-caplacizumab era, in order to assess the impact of time to first TPE and use of first-line rituximab on mortality, and whether mortality declines over time. RESULTS: Among the 1096 included patients (median age 46 [IQR 35–55], 70% female), 28.8% received TPE before day 2 in the ICU. Hospital mortality was 7.6% (83 deaths). Mortality was independently associated with older age (hazard ratio [HR], 1.024/year; 95% confidence interval [95%CI], [1.009–1.040]), diagnosis of sepsis (HR, 2.360; 95%CI [1.552–3.588]), and the need for mechanical ventilation (HR, 4.103; 95%CI, [2.749–6.126]). Factors independently associated with lower mortality were TPE at ICU admission (HR, 0.284; 95%CI, [0.112–0.717]), TPE within one day after ICU admission (HR, 0.449; 95%CI, [0.275–0.907]), and early rituximab therapy (HR, 0.229; 95% CI, [0.111–0.471]). Delayed TPE was associated with significantly higher costs. CONCLUSIONS: Immediate TPE and early rituximab are associated with improved survival in TTP patients. Improved treatments have led to a decline in mortality over time, and alternate outcome variables such as the use of hospital resources or longer term outcomes therefore need to be considered.
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spelling pubmed-83605092021-08-13 Outcomes in 1096 patients with severe thrombotic thrombocytopenic purpura before the Caplacizumab era Van de Louw, Andry Mariotte, Eric Darmon, Michael Cohrs, Austin Leslie, Douglas Azoulay, Elie PLoS One Research Article INTRODUCTION: Thrombotic thrombocytopenic purpura (TTP) is a diagnostic and therapeutic emergency. Therapeutic plasma exchange (TPE) combined with immunosuppression has been the cornerstone of the initial management. To produce optimal benefits, emerging treatments must be used against a background of best standard of care. Clarifying current uncertainties is therefore crucial. METHODS: The objective of this study was to analyze a large high-quality database (Marketscan) of TTP patients managed between 2005 and 2014, in the pre-caplacizumab era, in order to assess the impact of time to first TPE and use of first-line rituximab on mortality, and whether mortality declines over time. RESULTS: Among the 1096 included patients (median age 46 [IQR 35–55], 70% female), 28.8% received TPE before day 2 in the ICU. Hospital mortality was 7.6% (83 deaths). Mortality was independently associated with older age (hazard ratio [HR], 1.024/year; 95% confidence interval [95%CI], [1.009–1.040]), diagnosis of sepsis (HR, 2.360; 95%CI [1.552–3.588]), and the need for mechanical ventilation (HR, 4.103; 95%CI, [2.749–6.126]). Factors independently associated with lower mortality were TPE at ICU admission (HR, 0.284; 95%CI, [0.112–0.717]), TPE within one day after ICU admission (HR, 0.449; 95%CI, [0.275–0.907]), and early rituximab therapy (HR, 0.229; 95% CI, [0.111–0.471]). Delayed TPE was associated with significantly higher costs. CONCLUSIONS: Immediate TPE and early rituximab are associated with improved survival in TTP patients. Improved treatments have led to a decline in mortality over time, and alternate outcome variables such as the use of hospital resources or longer term outcomes therefore need to be considered. Public Library of Science 2021-08-12 /pmc/articles/PMC8360509/ /pubmed/34383822 http://dx.doi.org/10.1371/journal.pone.0256024 Text en © 2021 Van de Louw et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Van de Louw, Andry
Mariotte, Eric
Darmon, Michael
Cohrs, Austin
Leslie, Douglas
Azoulay, Elie
Outcomes in 1096 patients with severe thrombotic thrombocytopenic purpura before the Caplacizumab era
title Outcomes in 1096 patients with severe thrombotic thrombocytopenic purpura before the Caplacizumab era
title_full Outcomes in 1096 patients with severe thrombotic thrombocytopenic purpura before the Caplacizumab era
title_fullStr Outcomes in 1096 patients with severe thrombotic thrombocytopenic purpura before the Caplacizumab era
title_full_unstemmed Outcomes in 1096 patients with severe thrombotic thrombocytopenic purpura before the Caplacizumab era
title_short Outcomes in 1096 patients with severe thrombotic thrombocytopenic purpura before the Caplacizumab era
title_sort outcomes in 1096 patients with severe thrombotic thrombocytopenic purpura before the caplacizumab era
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8360509/
https://www.ncbi.nlm.nih.gov/pubmed/34383822
http://dx.doi.org/10.1371/journal.pone.0256024
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