Literature DB >> 26143527

Factors influencing the survival period in Japanese patients with sporadic Creutzfeldt-Jakob disease.

Yasushi Iwasaki1, Akio Akagi2, Maya Mimuro3, Tetsuyuki Kitamoto4, Mari Yoshida5.   

Abstract

Although Japanese cases of sporadic Creutzfeldt-Jakob disease (sCJD) generally involve longer survival periods compared to those from other countries, details regarding the factors influencing survival are unclear. To determine the influence of certain factors on survival, we retrospectively assessed 51 Japanese MM1-type sCJD patients with respect to background, clinical course, and disease management. No significant differences were found between men and women, tracheotomy and nontracheotomy patients, or patients treated in public and other types of hospitals. Although the survival period of tube-fed patients was significantly longer than that of patients who were not tube fed, survival of patients fed via a nasal tube did not differ significantly from that of gastrostomy-fed patients. The proportion of tube-fed patients was 68.6% (35/51). Disease duration was not significantly associated with age or year of onset. However, it was associated with time from onset to first recognition of myoclonus, first recognition of periodic sharp-wave complexes on electroencephalogram, and progression to the akinetic mutism state. Mechanical ventilation was not performed for any patient. Because the total disease duration increased in cases with a slowly progressive clinical course as a natural outcome, we concluded that the most crucial factor contributing to the prolonged survival of Japanese sCJD patients was tube feeding once the akinetic mutism state had been reached.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Akinetic mutism state; Creutzfeldt–Jakob disease; Gastrostomy; Total disease duration; Tracheotomy; Tube feeding

Mesh:

Year:  2015        PMID: 26143527     DOI: 10.1016/j.jns.2015.06.065

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  10 in total

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Authors:  Yasushi Iwasaki; Keiko Mori; Masumi Ito; Yoshinari Kawai; Ken-Ichiro Hoshino; Yuko Kawabata; Maya Mimuro; Mari Yoshida
Journal:  Prion       Date:  2017-05-16       Impact factor: 3.931

2.  Incidence of and Mortality Due to Human Prion Diseases in Taiwan: A Prospective 20-Year Nationwide Surveillance Study from 1998 to 2017.

Authors:  Chih-Ching Liu; Ling-Yun Fan; Yu Sun; Chung-Te Huang; Ta-Fu Chen; Chien-Jung Lu; Wan-Yuo Guo; Yang-Chyuan Chang; Ming-Jang Chiu
Journal:  Clin Epidemiol       Date:  2020-10-14       Impact factor: 4.790

3.  Three sporadic cases of Creutzfeldt-Jakob disease in China and their clinical analysis.

Authors:  Xingbang Wang; Na Li; Aifen Liu; Lin Ma; Peiyan Shan; Wenjing Jiang; Qun Zhang
Journal:  Exp Ther Med       Date:  2017-07-25       Impact factor: 2.447

4.  Survival Patterns of Human Prion Diseases in Spain, 1998-2018: Clinical Phenotypes and Etiological Clues.

Authors:  Laura Tejedor-Romero; Teresa López-Cuadrado; Javier Almazán-Isla; Miguel Calero; Fernando J García López; Jesús de Pedro-Cuesta
Journal:  Front Neurosci       Date:  2022-01-20       Impact factor: 4.677

5.  Rapidly Progressive Probable Sporadic Creutzfeldt-Jakob Disease.

Authors:  Moustafa M Elziny; Shaimaa S Elsaid
Journal:  Cureus       Date:  2022-03-17

6.  Long-term preservation of pharyngeal swallowing function in MM2-cortical-type sporadic Creutzfeldt-Jakob disease.

Authors:  Yuichi Hayashi; Kenjiro Kunieda; Takuya Kudo; Akio Kimura; Ichiro Fujishima; Takayoshi Shimohata
Journal:  Prion       Date:  2021-12       Impact factor: 3.931

7.  Predictive Factors for Early Initiation of Artificial Feeding in Patients With Sporadic Creutzfeldt-Jakob Disease.

Authors:  Pei-Chen Hsieh; Han-Tao Li; Chun-Wei Chang; Yih-Ru Wu; Hung-Chou Kuo
Journal:  Front Neurol       Date:  2018-07-03       Impact factor: 4.003

8.  Clinicopathological findings of a long-term survivor of V180I genetic Creutzfeldt-Jakob disease.

Authors:  Yuichi Hayashi; Yasushi Iwasaki; Masahiro Waza; Shinei Kato; Akio Akagi; Akio Kimura; Takashi Inuzuka; Katsuya Satoh; Tetsuyuki Kitamoto; Mari Yoshida; Takayoshi Shimohata
Journal:  Prion       Date:  2020-12       Impact factor: 3.931

9.  Enteral feeding is associated with longer survival in the advanced stages of prion disease.

Authors:  Kirsty McNiven; Akin Nihat; Tze How Mok; Selam Tesfamichael; Veronica O'Donnell; Peter Rudge; John Collinge; Simon Mead
Journal:  Brain Commun       Date:  2019-09-10

10.  System degeneration in an MM1-type sporadic Creutzfeldt-Jakob disease case with an unusually prolonged akinetic mutism state.

Authors:  Yasushi Iwasaki; Keiko Mori; Masumi Ito; Yoshinari Kawai; Akio Akagi; Yuichi Riku; Hiroaki Miyahara; Atsushi Kobayashi; Tetsuyuki Kitamoto; Mari Yoshida
Journal:  Prion       Date:  2021-12       Impact factor: 3.931

  10 in total

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