Literature DB >> 22989611

Tracheostomy mechanical ventilation in patients with amyotrophic lateral sclerosis: clinical features and survival analysis.

Rossella Spataro1, Valeria Bono, Santino Marchese, Vincenzo La Bella.   

Abstract

BACKGROUND: Tracheostomy mechanical ventilation (TMV) is performed in amyotrophic lateral sclerosis (ALS) patients with a respiratory failure or when the non-invasive ventilation (NIV) is no longer effective. We evaluated the clinical characteristics and survival of a cohort of tracheostomized ALS patients, followed in a single ALS Clinical Center.
METHODS: Between 2001 and 2010, 87 out of 279 ALS patients were submitted to TMV. Onset was spinal in 62 and bulbar in 25. After tracheostomy, most patients were followed up through telephone interviews to caregivers. A complete survival analysis could be performed in fifty-two TMV patients.
RESULTS: 31.3% ALS patients underwent tracheostomy, with a male prevalence (M/F=1.69) and a median age of 61 years (interquartile range=47-66). After tracheostomy, nearly all patients were under home care. TMV ALS patients were more likely than non-tracheostomized (NT) patients to be implanted with a PEG device, although the bulbar-/spinal-onset ratio did not differ between the two groups. Kaplan-Meyer analysis showed that tracheostomy increases median survival (TMV, 47 months vs NT, 31 months, p=0.008), with the greatest effect in patients younger than 60 at onset (TMV ≤ 60 years, 57.5 months vs NT ≤ 60 years, 38.5 months, p=0.002).
CONCLUSIONS: TMV is increasingly performed in ALS patients. Nearly all TMV patients live at home and most of them are fed through a PEG device. Survival after tracheostomy is generally increased, with the stronger effect in patients younger than 60. This survival advantage is apparently lost when TMV is performed in patients older than 60. The results of this study might be useful for the decision-making process of patients and their families about this advanced palliative care.
Copyright © 2012. Published by Elsevier B.V.

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Year:  2012        PMID: 22989611     DOI: 10.1016/j.jns.2012.08.011

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


  14 in total

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2.  Robot-assisted total gastrectomy for gastric cancer in a patient with amyotrophic lateral sclerosis receiving long-term tracheostomy invasive ventilation.

Authors:  Masaaki Nishi; Ryosuke Miyamoto; Kasane Shima; Hirokazu Miki; Hideo Terasawa; Chie Takasu; Kozo Yoshikawa; Takuro Oyama; Katsuya Tanaka; Yuishin Izumi; Mitsuo Shimada
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3.  The capacity to consent to treatment in amyotrophic lateral sclerosis: a preliminary report.

Authors:  Rossella Spataro; Vincenzo La Bella
Journal:  J Neurol       Date:  2020-08-06       Impact factor: 4.849

4.  Amyotrophic Lateral Sclerosis: Integrated care provides the best quality of life.

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5.  Hospitalizations due to respiratory failure in patients with Amyotrophic Lateral Sclerosis and their impact on survival: a population-based cohort study.

Authors:  Federica Edith Pisa; Giancarlo Logroscino; Paolo Giacomelli Battiston; Fabio Barbone
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6.  Transition from in-hospital ventilation to home ventilation: process description and quality indicators.

Authors:  Marc Kastrup; Benjamin Tittmann; Tanja Sawatzki; Martin Gersch; Charlotte Vogt; Max Rosenthal; Simone Rosseau; Claudia Spies
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Review 7.  Maximizing the Survival of Amyotrophic Lateral Sclerosis Patients: Current Perspectives.

Authors:  Osama A Khairoalsindi; Ahmad R Abuzinadah
Journal:  Neurol Res Int       Date:  2018-08-12

8.  Patient characteristics and outcomes of a home mechanical ventilation program in a developing country.

Authors:  Narongkorn Saiphoklang; Apichart Kanitsap; Pitchayapa Ruchiwit; Pattarin Pirompanich; Thiti Sricharoenchai; Christopher B Cooper
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Review 9.  Disease-modifying and symptomatic treatment of amyotrophic lateral sclerosis.

Authors:  Johannes Dorst; Albert C Ludolph; Annemarie Huebers
Journal:  Ther Adv Neurol Disord       Date:  2017-10-09       Impact factor: 6.570

Review 10.  Communication Matters-Pitfalls and Promise of Hightech Communication Devices in Palliative Care of Severely Physically Disabled Patients With Amyotrophic Lateral Sclerosis.

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Journal:  Front Neurol       Date:  2018-07-27       Impact factor: 4.003

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