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Lombardy diagnostic and therapeutic network of thrombotic microangiopathy

BACKGROUND: Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening thrombotic microangiopathy (TMA) requiring urgent treatment. Standardization of its diagnosis and optimal management is challenging. This study aimed to evaluate the role of centralized, rapid testing of ADAMTS13 in pa...

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Autores principales: Mancini, I., Agosti, P., Boscarino, M., Ferrari, B., Artoni, A., Palla, R., Spreafico, M., Crovetti, G., Volpato, E., Rossini, S., Novelli, C., Gattillo, S., Barcella, L., Salmoiraghi, M., Falanga, A., Peyvandi, F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9229100/
https://www.ncbi.nlm.nih.gov/pubmed/35739601
http://dx.doi.org/10.1186/s13023-022-02400-y
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author Mancini, I.
Agosti, P.
Boscarino, M.
Ferrari, B.
Artoni, A.
Palla, R.
Spreafico, M.
Crovetti, G.
Volpato, E.
Rossini, S.
Novelli, C.
Gattillo, S.
Barcella, L.
Salmoiraghi, M.
Falanga, A.
Peyvandi, F.
author_facet Mancini, I.
Agosti, P.
Boscarino, M.
Ferrari, B.
Artoni, A.
Palla, R.
Spreafico, M.
Crovetti, G.
Volpato, E.
Rossini, S.
Novelli, C.
Gattillo, S.
Barcella, L.
Salmoiraghi, M.
Falanga, A.
Peyvandi, F.
author_sort Mancini, I.
collection PubMed
description BACKGROUND: Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening thrombotic microangiopathy (TMA) requiring urgent treatment. Standardization of its diagnosis and optimal management is challenging. This study aimed to evaluate the role of centralized, rapid testing of ADAMTS13 in patients experiencing acute TMAs requiring plasma-exchange (PEX) and to estimate the incidence of TTP in a large Italian Region. METHODS: We perfomed a cohort study in the frame of the project “Set-up of a Lombardy network for the study and treatment of patients undergoing apheresis”, including 11 transfusion centers in the Region. Consecutive patients referred from 2014 to 2016 with acute TMAs requiring PEX were enrolled. Centralized ADAMTS13 activity testing was performed at the Milan Hemophilia and Thrombosis Center within 24 h. RESULTS: Forty-three TMA patients (44 events) were enrolled, of whom 35 (81%) had severe ADAMTS13 deficiency. Patients with severe ADAMTS13 deficiency were younger, mainly women, with a higher prevalence of autoimmune disorders and a lower prevalence of cancer. Clinical and laboratory characteristics of patients with and without severe ADAMTS13 deficiency largely overlapped, with a lower platelet count being the only baseline marker that significantly differed between the two patient groups (ADAMTS13 activity < 10% vs ≥ 10%: median difference of -27 × 10(9)/l, 95% CI − 37 to − 3). PEX treatment was initiated in all patients, but soon discontinued in cases without severe ADAMTS13 deficiency. In this group, the mortality rate was higher and no episode exacerbations or relapses within 6 months occured. The estimated average annual incidence of acute acquired TTP events was 1.17 [0.78–1.55] per million people. CONCLUSIONS: Severe ADAMTS13 deficiency distinguished two groups of patients with largely overlapping clinical features but different treatment and disease course. This study provides a feasible model implemented in a large Italian region for the practical clinical approach to TMAs and underlines the importance of urgent ADAMTS13 activity testing for an accurate differential diagnosis and therapeutic approach. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-022-02400-y.
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spelling pubmed-92291002022-06-25 Lombardy diagnostic and therapeutic network of thrombotic microangiopathy Mancini, I. Agosti, P. Boscarino, M. Ferrari, B. Artoni, A. Palla, R. Spreafico, M. Crovetti, G. Volpato, E. Rossini, S. Novelli, C. Gattillo, S. Barcella, L. Salmoiraghi, M. Falanga, A. Peyvandi, F. Orphanet J Rare Dis Research BACKGROUND: Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening thrombotic microangiopathy (TMA) requiring urgent treatment. Standardization of its diagnosis and optimal management is challenging. This study aimed to evaluate the role of centralized, rapid testing of ADAMTS13 in patients experiencing acute TMAs requiring plasma-exchange (PEX) and to estimate the incidence of TTP in a large Italian Region. METHODS: We perfomed a cohort study in the frame of the project “Set-up of a Lombardy network for the study and treatment of patients undergoing apheresis”, including 11 transfusion centers in the Region. Consecutive patients referred from 2014 to 2016 with acute TMAs requiring PEX were enrolled. Centralized ADAMTS13 activity testing was performed at the Milan Hemophilia and Thrombosis Center within 24 h. RESULTS: Forty-three TMA patients (44 events) were enrolled, of whom 35 (81%) had severe ADAMTS13 deficiency. Patients with severe ADAMTS13 deficiency were younger, mainly women, with a higher prevalence of autoimmune disorders and a lower prevalence of cancer. Clinical and laboratory characteristics of patients with and without severe ADAMTS13 deficiency largely overlapped, with a lower platelet count being the only baseline marker that significantly differed between the two patient groups (ADAMTS13 activity < 10% vs ≥ 10%: median difference of -27 × 10(9)/l, 95% CI − 37 to − 3). PEX treatment was initiated in all patients, but soon discontinued in cases without severe ADAMTS13 deficiency. In this group, the mortality rate was higher and no episode exacerbations or relapses within 6 months occured. The estimated average annual incidence of acute acquired TTP events was 1.17 [0.78–1.55] per million people. CONCLUSIONS: Severe ADAMTS13 deficiency distinguished two groups of patients with largely overlapping clinical features but different treatment and disease course. This study provides a feasible model implemented in a large Italian region for the practical clinical approach to TMAs and underlines the importance of urgent ADAMTS13 activity testing for an accurate differential diagnosis and therapeutic approach. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-022-02400-y. BioMed Central 2022-06-23 /pmc/articles/PMC9229100/ /pubmed/35739601 http://dx.doi.org/10.1186/s13023-022-02400-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits 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/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Mancini, I.
Agosti, P.
Boscarino, M.
Ferrari, B.
Artoni, A.
Palla, R.
Spreafico, M.
Crovetti, G.
Volpato, E.
Rossini, S.
Novelli, C.
Gattillo, S.
Barcella, L.
Salmoiraghi, M.
Falanga, A.
Peyvandi, F.
Lombardy diagnostic and therapeutic network of thrombotic microangiopathy
title Lombardy diagnostic and therapeutic network of thrombotic microangiopathy
title_full Lombardy diagnostic and therapeutic network of thrombotic microangiopathy
title_fullStr Lombardy diagnostic and therapeutic network of thrombotic microangiopathy
title_full_unstemmed Lombardy diagnostic and therapeutic network of thrombotic microangiopathy
title_short Lombardy diagnostic and therapeutic network of thrombotic microangiopathy
title_sort lombardy diagnostic and therapeutic network of thrombotic microangiopathy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9229100/
https://www.ncbi.nlm.nih.gov/pubmed/35739601
http://dx.doi.org/10.1186/s13023-022-02400-y
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