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Survival analysis of spinal muscular atrophy type I
PURPOSE: The life expectancy of patients with spinal muscular atrophy (SMA) type I is generally considered to be less than 2 years. Recently, with the introduction of proactive treatments, a longer survival and an improved survival rate have been reported. In this study, we analyzed the natural cour...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Korean Pediatric Society
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3012277/ https://www.ncbi.nlm.nih.gov/pubmed/21218019 http://dx.doi.org/10.3345/kjp.2010.53.11.965 |
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author | Park, Hyun Bin Lee, Soon Min Lee, Jin Sung Park, Min Soo Park, Kook In Namgung, Ran Lee, Chul |
author_facet | Park, Hyun Bin Lee, Soon Min Lee, Jin Sung Park, Min Soo Park, Kook In Namgung, Ran Lee, Chul |
author_sort | Park, Hyun Bin |
collection | PubMed |
description | PURPOSE: The life expectancy of patients with spinal muscular atrophy (SMA) type I is generally considered to be less than 2 years. Recently, with the introduction of proactive treatments, a longer survival and an improved survival rate have been reported. In this study, we analyzed the natural courses and survival statistics of SMA type I patients and compared the clinical characteristics of the patients based on their survival periods. METHODS: We reviewed the medical records of 14 pediatric patients diagnosed with SMA type I during a 9-year period. We examined the demographic and clinical characteristics of these patients, calculated their survival probabilities, and plotted survival curves as on the censoring date, January 1, 2010. We also compared the characteristics of the patients who died before the age of 24 months (early-death, ED group) and those who survived for 24 months or longer (long-survival, LS group). RESULTS: The mean survival time was 22.8±2.0 months. The survival probabilities at 6 months, 12 months, 18 months, 24 months, and 30 months were 92.9%, 92.9%, 76.0%, 76.0%, and 65.1%, respectively. Birth weight was the only factor that showed a statistically significant difference between the ED and LS groups (P=0.048). CONCLUSION: In this study, the survival probabilities at 2 years were far greater than expected. Because of the limited number of patients and information in this study, the contribution of improved supportive care on longer survival could not be clarified; this may be elucidated in larger cohort studies. |
format | Text |
id | pubmed-3012277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | The Korean Pediatric Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-30122772011-01-07 Survival analysis of spinal muscular atrophy type I Park, Hyun Bin Lee, Soon Min Lee, Jin Sung Park, Min Soo Park, Kook In Namgung, Ran Lee, Chul Korean J Pediatr Original Article PURPOSE: The life expectancy of patients with spinal muscular atrophy (SMA) type I is generally considered to be less than 2 years. Recently, with the introduction of proactive treatments, a longer survival and an improved survival rate have been reported. In this study, we analyzed the natural courses and survival statistics of SMA type I patients and compared the clinical characteristics of the patients based on their survival periods. METHODS: We reviewed the medical records of 14 pediatric patients diagnosed with SMA type I during a 9-year period. We examined the demographic and clinical characteristics of these patients, calculated their survival probabilities, and plotted survival curves as on the censoring date, January 1, 2010. We also compared the characteristics of the patients who died before the age of 24 months (early-death, ED group) and those who survived for 24 months or longer (long-survival, LS group). RESULTS: The mean survival time was 22.8±2.0 months. The survival probabilities at 6 months, 12 months, 18 months, 24 months, and 30 months were 92.9%, 92.9%, 76.0%, 76.0%, and 65.1%, respectively. Birth weight was the only factor that showed a statistically significant difference between the ED and LS groups (P=0.048). CONCLUSION: In this study, the survival probabilities at 2 years were far greater than expected. Because of the limited number of patients and information in this study, the contribution of improved supportive care on longer survival could not be clarified; this may be elucidated in larger cohort studies. The Korean Pediatric Society 2010-11 2010-11-30 /pmc/articles/PMC3012277/ /pubmed/21218019 http://dx.doi.org/10.3345/kjp.2010.53.11.965 Text en Copyright © 2010 by The Korean Pediatric Society http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Park, Hyun Bin Lee, Soon Min Lee, Jin Sung Park, Min Soo Park, Kook In Namgung, Ran Lee, Chul Survival analysis of spinal muscular atrophy type I |
title | Survival analysis of spinal muscular atrophy type I |
title_full | Survival analysis of spinal muscular atrophy type I |
title_fullStr | Survival analysis of spinal muscular atrophy type I |
title_full_unstemmed | Survival analysis of spinal muscular atrophy type I |
title_short | Survival analysis of spinal muscular atrophy type I |
title_sort | survival analysis of spinal muscular atrophy type i |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3012277/ https://www.ncbi.nlm.nih.gov/pubmed/21218019 http://dx.doi.org/10.3345/kjp.2010.53.11.965 |
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