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Prognosis of late elderly patients with chronic hepatitis C after achieving a sustained viral response by direct‐acting antivirals

BACKGROUND AND AIM: We investigated the prognosis of late elderly patients (≥75 years old) after the achievement of a sustained viral response (SVR) by direct‐acting antivirals (DAAs). METHODS: One hundred and four late elderly patients and 251 young patients (≤74 years old) who had achieved an SVR...

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Autores principales: Takakusagi, Satoshi, Takagi, Hitoshi, Kosone, Takashi, Sato, Ken, Kakizaki, Satoru, Uraoka, Toshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7812467/
https://www.ncbi.nlm.nih.gov/pubmed/33490621
http://dx.doi.org/10.1002/jgh3.12459
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author Takakusagi, Satoshi
Takagi, Hitoshi
Kosone, Takashi
Sato, Ken
Kakizaki, Satoru
Uraoka, Toshio
author_facet Takakusagi, Satoshi
Takagi, Hitoshi
Kosone, Takashi
Sato, Ken
Kakizaki, Satoru
Uraoka, Toshio
author_sort Takakusagi, Satoshi
collection PubMed
description BACKGROUND AND AIM: We investigated the prognosis of late elderly patients (≥75 years old) after the achievement of a sustained viral response (SVR) by direct‐acting antivirals (DAAs). METHODS: One hundred and four late elderly patients and 251 young patients (≤74 years old) who had achieved an SVR were included. We compared the cumulative hepatocellular carcinoma (HCC) incidence rates and survival rates after DAA administration. Furthermore, the factors associated with HCC incidence and the causes of death after DAA administration were also investigated. RESULTS: The cumulative HCC incidence rates for 1 and 3 years were 2.9% and 11.7% in the late elderly patients and 2.4% and 5.4% in the young patients, respectively. The cumulative survival rates for 1 and 3 years were 100% and 95.6% in the late elderly patients and 100% and 96.4% in the young patients, respectively, with no significant differences in those rates noted (P = 0.133, P = 0.322, respectively). In the late elderly patients, only a history of HCC was a significant factor associated with HCC incidence after DAA administration. Five late elderly patients died after achieving an SVR, and malignant liver tumor was the cause of death in three of those patients. CONCLUSIONS: The prognosis did not differ markedly between late elderly patients and young patients. The factor most strongly influencing the prognosis of late elderly patients was likely liver disease, including HCC. DAAs should be introduced even in late elderly patients who can be expected to have a relative long‐term survival.
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spelling pubmed-78124672021-01-22 Prognosis of late elderly patients with chronic hepatitis C after achieving a sustained viral response by direct‐acting antivirals Takakusagi, Satoshi Takagi, Hitoshi Kosone, Takashi Sato, Ken Kakizaki, Satoru Uraoka, Toshio JGH Open Original Articles BACKGROUND AND AIM: We investigated the prognosis of late elderly patients (≥75 years old) after the achievement of a sustained viral response (SVR) by direct‐acting antivirals (DAAs). METHODS: One hundred and four late elderly patients and 251 young patients (≤74 years old) who had achieved an SVR were included. We compared the cumulative hepatocellular carcinoma (HCC) incidence rates and survival rates after DAA administration. Furthermore, the factors associated with HCC incidence and the causes of death after DAA administration were also investigated. RESULTS: The cumulative HCC incidence rates for 1 and 3 years were 2.9% and 11.7% in the late elderly patients and 2.4% and 5.4% in the young patients, respectively. The cumulative survival rates for 1 and 3 years were 100% and 95.6% in the late elderly patients and 100% and 96.4% in the young patients, respectively, with no significant differences in those rates noted (P = 0.133, P = 0.322, respectively). In the late elderly patients, only a history of HCC was a significant factor associated with HCC incidence after DAA administration. Five late elderly patients died after achieving an SVR, and malignant liver tumor was the cause of death in three of those patients. CONCLUSIONS: The prognosis did not differ markedly between late elderly patients and young patients. The factor most strongly influencing the prognosis of late elderly patients was likely liver disease, including HCC. DAAs should be introduced even in late elderly patients who can be expected to have a relative long‐term survival. Wiley Publishing Asia Pty Ltd 2020-11-23 /pmc/articles/PMC7812467/ /pubmed/33490621 http://dx.doi.org/10.1002/jgh3.12459 Text en © 2020 The Authors. JGH Open published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Takakusagi, Satoshi
Takagi, Hitoshi
Kosone, Takashi
Sato, Ken
Kakizaki, Satoru
Uraoka, Toshio
Prognosis of late elderly patients with chronic hepatitis C after achieving a sustained viral response by direct‐acting antivirals
title Prognosis of late elderly patients with chronic hepatitis C after achieving a sustained viral response by direct‐acting antivirals
title_full Prognosis of late elderly patients with chronic hepatitis C after achieving a sustained viral response by direct‐acting antivirals
title_fullStr Prognosis of late elderly patients with chronic hepatitis C after achieving a sustained viral response by direct‐acting antivirals
title_full_unstemmed Prognosis of late elderly patients with chronic hepatitis C after achieving a sustained viral response by direct‐acting antivirals
title_short Prognosis of late elderly patients with chronic hepatitis C after achieving a sustained viral response by direct‐acting antivirals
title_sort prognosis of late elderly patients with chronic hepatitis c after achieving a sustained viral response by direct‐acting antivirals
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7812467/
https://www.ncbi.nlm.nih.gov/pubmed/33490621
http://dx.doi.org/10.1002/jgh3.12459
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