Long-term ventilatory support in spinal muscular atrophy
Before ethical issues regarding prolonging life in patients with degenerative disease can be considered, the quality of life with medical intervention must be delineated. We have followed 15 patients with spinal muscular atrophy who have been treated with mechanical ventilation. They have received a...
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Veröffentlicht in: | The Journal of pediatrics 1989-12, Vol.115 (6), p.904-909 |
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creator | Gilgoff, Irene S. Kahlstrom, Emily MacLaughlin, Eithne Keens, Thomas G. |
description | Before ethical issues regarding prolonging life in patients with degenerative disease can be considered, the quality of life with medical intervention must be delineated. We have followed 15 patients with spinal muscular atrophy who have been treated with mechanical ventilation. They have received assisted ventilation for an average of 8 years 10 months (range 5 months to 23 years 10 months). Three of the patients required full-time ventilator assistance at the time of initiation of ventilation; the remaining 12 used nighttime ventilation for an average of 8 years 7 months. Nine patients continue to receive nighttime ventilation only. Two patients died after 5 years and 14 years of assisted ventilation, respectively. Of the 10 patients more than 18 years of age, three graduated from college, two are in college, three graduated from high school, and two completed eleventh grade. One patient is a mother of a healthy child. Two patients are employed, and two others have found fulfilling volunteer work. Ventilator support has not significantly interfered with these patients' plans and expectations. |
doi_str_mv | 10.1016/S0022-3476(89)80740-1 |
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We have followed 15 patients with spinal muscular atrophy who have been treated with mechanical ventilation. They have received assisted ventilation for an average of 8 years 10 months (range 5 months to 23 years 10 months). Three of the patients required full-time ventilator assistance at the time of initiation of ventilation; the remaining 12 used nighttime ventilation for an average of 8 years 7 months. Nine patients continue to receive nighttime ventilation only. Two patients died after 5 years and 14 years of assisted ventilation, respectively. Of the 10 patients more than 18 years of age, three graduated from college, two are in college, three graduated from high school, and two completed eleventh grade. One patient is a mother of a healthy child. Two patients are employed, and two others have found fulfilling volunteer work. 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We have followed 15 patients with spinal muscular atrophy who have been treated with mechanical ventilation. They have received assisted ventilation for an average of 8 years 10 months (range 5 months to 23 years 10 months). Three of the patients required full-time ventilator assistance at the time of initiation of ventilation; the remaining 12 used nighttime ventilation for an average of 8 years 7 months. Nine patients continue to receive nighttime ventilation only. Two patients died after 5 years and 14 years of assisted ventilation, respectively. Of the 10 patients more than 18 years of age, three graduated from college, two are in college, three graduated from high school, and two completed eleventh grade. One patient is a mother of a healthy child. Two patients are employed, and two others have found fulfilling volunteer work. Ventilator support has not significantly interfered with these patients' plans and expectations.</description><subject>Adolescent</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Emergency and intensive respiratory care</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Infant</subject><subject>Intensive care medicine</subject><subject>Medical sciences</subject><subject>Muscular Atrophy, Spinal - therapy</subject><subject>Prognosis</subject><subject>Quality of Life</subject><subject>Respiration, Artificial</subject><subject>Retrospective Studies</subject><subject>Tracheostomy</subject><subject>Vital Capacity</subject><issn>0022-3476</issn><issn>1097-6833</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtP3TAQRi0EglvgJyBlU9QuQsfxe1UhBLTSlVhQ1tbEdlqjvGonSPffN_chumQ1iznfN6NDyBWFGwpUfnsGqKqScSW_aPNVg-JQ0iOyomBUKTVjx2T1jpyRTzm_AoDhAKfktBJaVJVcEb0e-t_lFFJXvIV-ii1OQ9oUeR7HIU1F7Is8xh7bopuzm1tMBU5pGP9sLshJg20Ol4d5Tl4e7n_d_SjXT48_727XpWMGphI507L2jNecAxqmkAovKdfKo6tr551UANILbJREr4VqaidqIYWqGqGRnZPrfe-Yhr9zyJPtYnahbbEPw5ytMoxXwsACij3o0pBzCo0dU-wwbSwFuzVmd8bsVofVxu6MWbrkrg4H5roL_j11ULTsPx_2mB22TcLexfy_3IhKMFAL933PhcXGWwzJZhdD74KPKbjJ-iF-8Mk_LlWH4w</recordid><startdate>19891201</startdate><enddate>19891201</enddate><creator>Gilgoff, Irene S.</creator><creator>Kahlstrom, Emily</creator><creator>MacLaughlin, Eithne</creator><creator>Keens, Thomas G.</creator><general>Mosby, Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19891201</creationdate><title>Long-term ventilatory support in spinal muscular atrophy</title><author>Gilgoff, Irene S. ; Kahlstrom, Emily ; MacLaughlin, Eithne ; Keens, Thomas G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-a4386bd34b440a937a15d61487dacbbcdc67006d5af76ad857fbc5b56572f58a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Adolescent</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Emergency and intensive respiratory care</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Infant</topic><topic>Intensive care medicine</topic><topic>Medical sciences</topic><topic>Muscular Atrophy, Spinal - therapy</topic><topic>Prognosis</topic><topic>Quality of Life</topic><topic>Respiration, Artificial</topic><topic>Retrospective Studies</topic><topic>Tracheostomy</topic><topic>Vital Capacity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gilgoff, Irene S.</creatorcontrib><creatorcontrib>Kahlstrom, Emily</creatorcontrib><creatorcontrib>MacLaughlin, Eithne</creatorcontrib><creatorcontrib>Keens, Thomas G.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of pediatrics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gilgoff, Irene S.</au><au>Kahlstrom, Emily</au><au>MacLaughlin, Eithne</au><au>Keens, Thomas G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-term ventilatory support in spinal muscular atrophy</atitle><jtitle>The Journal of pediatrics</jtitle><addtitle>J Pediatr</addtitle><date>1989-12-01</date><risdate>1989</risdate><volume>115</volume><issue>6</issue><spage>904</spage><epage>909</epage><pages>904-909</pages><issn>0022-3476</issn><eissn>1097-6833</eissn><coden>JOPDAB</coden><abstract>Before ethical issues regarding prolonging life in patients with degenerative disease can be considered, the quality of life with medical intervention must be delineated. We have followed 15 patients with spinal muscular atrophy who have been treated with mechanical ventilation. They have received assisted ventilation for an average of 8 years 10 months (range 5 months to 23 years 10 months). Three of the patients required full-time ventilator assistance at the time of initiation of ventilation; the remaining 12 used nighttime ventilation for an average of 8 years 7 months. Nine patients continue to receive nighttime ventilation only. Two patients died after 5 years and 14 years of assisted ventilation, respectively. Of the 10 patients more than 18 years of age, three graduated from college, two are in college, three graduated from high school, and two completed eleventh grade. One patient is a mother of a healthy child. Two patients are employed, and two others have found fulfilling volunteer work. Ventilator support has not significantly interfered with these patients' plans and expectations.</abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>2585226</pmid><doi>10.1016/S0022-3476(89)80740-1</doi><tpages>6</tpages></addata></record> |
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subjects | Adolescent Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Biological and medical sciences Child Child, Preschool Emergency and intensive respiratory care Follow-Up Studies Humans Infant Intensive care medicine Medical sciences Muscular Atrophy, Spinal - therapy Prognosis Quality of Life Respiration, Artificial Retrospective Studies Tracheostomy Vital Capacity |
title | Long-term ventilatory support in spinal muscular atrophy |
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