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Cardiovascular disease is a leading cause of mortality among TTP survivors in clinical remission
Immune-mediated thrombotic thrombocytopenic purpura (iTTP) survivors experience high rates of adverse health sequelae and increased mortality over long-term follow-up. We conducted this multicenter cohort study to evaluate long-term mortality and causes of death in iTTP survivors. Between 2003 and 2...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Society of Hematology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8864652/ https://www.ncbi.nlm.nih.gov/pubmed/34461629 http://dx.doi.org/10.1182/bloodadvances.2020004169 |
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author | Sukumar, Senthil Brodsky, Max Hussain, Sarah Yanek, Lisa Moliterno, Alison Brodsky, Robert Cataland, Spero R. Chaturvedi, Shruti |
author_facet | Sukumar, Senthil Brodsky, Max Hussain, Sarah Yanek, Lisa Moliterno, Alison Brodsky, Robert Cataland, Spero R. Chaturvedi, Shruti |
author_sort | Sukumar, Senthil |
collection | PubMed |
description | Immune-mediated thrombotic thrombocytopenic purpura (iTTP) survivors experience high rates of adverse health sequelae and increased mortality over long-term follow-up. We conducted this multicenter cohort study to evaluate long-term mortality and causes of death in iTTP survivors. Between 2003 and 2020, 222 patients were enrolled in the Ohio State University and Johns Hopkins TTP registries and followed for a median of 4.5 (interquartile range [IQR], 75 0.4-11.5) years. Nine patients died during their first iTTP episode, and 29 patients died during follow-up. Mortality rate was 1.8 times higher than expected from an age-, sex-, and race-adjusted reference population. Cardiovascular disease was a leading primary cause of death (27.6%) tied with relapsed iTTP (27.6%), followed by malignancy (20.7%), infection (13.8%), and other causes (10.3%). Male sex (hazard ratio [HR], 3.74; 95% confidence interval [CI], 1.65-8.48), increasing age (HR, 1.04; 95% CI, 1.01-1.07), and number of iTTP episodes (HR, 1.10; 95% CI, 1.01-1.20) were associated with mortality in a model adjusted for African American race (HR, 0.70; 95% CI, 0.30-1.65), hypertension (HR, 0.47; 95% CI, 0.20-1.08), chronic kidney disease (HR 1.46; 95% CI, 0.65-3.30), and site (HR, 1.46; 95% CI, 0.64–3.30). There was a trend toward shorter survival in patients with lower ADAMTS13 activity during remission (P = .078). Our study highlights the need for survivorship care and investigation focused on cardiovascular disease and early mortality in TTP survivors. |
format | Online Article Text |
id | pubmed-8864652 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society of Hematology |
record_format | MEDLINE/PubMed |
spelling | pubmed-88646522022-02-23 Cardiovascular disease is a leading cause of mortality among TTP survivors in clinical remission Sukumar, Senthil Brodsky, Max Hussain, Sarah Yanek, Lisa Moliterno, Alison Brodsky, Robert Cataland, Spero R. Chaturvedi, Shruti Blood Adv Clinical Trials and Observations Immune-mediated thrombotic thrombocytopenic purpura (iTTP) survivors experience high rates of adverse health sequelae and increased mortality over long-term follow-up. We conducted this multicenter cohort study to evaluate long-term mortality and causes of death in iTTP survivors. Between 2003 and 2020, 222 patients were enrolled in the Ohio State University and Johns Hopkins TTP registries and followed for a median of 4.5 (interquartile range [IQR], 75 0.4-11.5) years. Nine patients died during their first iTTP episode, and 29 patients died during follow-up. Mortality rate was 1.8 times higher than expected from an age-, sex-, and race-adjusted reference population. Cardiovascular disease was a leading primary cause of death (27.6%) tied with relapsed iTTP (27.6%), followed by malignancy (20.7%), infection (13.8%), and other causes (10.3%). Male sex (hazard ratio [HR], 3.74; 95% confidence interval [CI], 1.65-8.48), increasing age (HR, 1.04; 95% CI, 1.01-1.07), and number of iTTP episodes (HR, 1.10; 95% CI, 1.01-1.20) were associated with mortality in a model adjusted for African American race (HR, 0.70; 95% CI, 0.30-1.65), hypertension (HR, 0.47; 95% CI, 0.20-1.08), chronic kidney disease (HR 1.46; 95% CI, 0.65-3.30), and site (HR, 1.46; 95% CI, 0.64–3.30). There was a trend toward shorter survival in patients with lower ADAMTS13 activity during remission (P = .078). Our study highlights the need for survivorship care and investigation focused on cardiovascular disease and early mortality in TTP survivors. American Society of Hematology 2022-02-16 /pmc/articles/PMC8864652/ /pubmed/34461629 http://dx.doi.org/10.1182/bloodadvances.2020004169 Text en © 2022 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved. |
spellingShingle | Clinical Trials and Observations Sukumar, Senthil Brodsky, Max Hussain, Sarah Yanek, Lisa Moliterno, Alison Brodsky, Robert Cataland, Spero R. Chaturvedi, Shruti Cardiovascular disease is a leading cause of mortality among TTP survivors in clinical remission |
title | Cardiovascular disease is a leading cause of mortality among TTP survivors in clinical remission |
title_full | Cardiovascular disease is a leading cause of mortality among TTP survivors in clinical remission |
title_fullStr | Cardiovascular disease is a leading cause of mortality among TTP survivors in clinical remission |
title_full_unstemmed | Cardiovascular disease is a leading cause of mortality among TTP survivors in clinical remission |
title_short | Cardiovascular disease is a leading cause of mortality among TTP survivors in clinical remission |
title_sort | cardiovascular disease is a leading cause of mortality among ttp survivors in clinical remission |
topic | Clinical Trials and Observations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8864652/ https://www.ncbi.nlm.nih.gov/pubmed/34461629 http://dx.doi.org/10.1182/bloodadvances.2020004169 |
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