Literature DB >> 12847177

ALS patients on TPPV: totally locked-in state, neurologic findings and ethical implications.

Hideaki Hayashi1, Edward Anthony Oppenheimer.   

Abstract

Seventy patients with ALS using tracheostomy positive pressure ventilation (TPPV) were evaluated for impaired communication. Severely impaired communication is divided into the totally locked-in state (TLS) and the minimal communication state (MCS). TLS occurred in 8 of 70 (11.4%). In the 33 patients on TPPV for more than 5 years, TLS developed in 6 (18.2%) and MCS in 11 (33.1%). Respiratory management for ALS allows long-term survival if mechanical ventilation is used.

Entities:  

Keywords:  Empirical Approach; Health Care and Public Health

Mesh：

Year:  2003        PMID： 12847177     DOI： 10.1212/01.wnl.0000069925.02052.1f

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


  21 in total

Review 1.  The full spectrum of ethical issues in the care of patients with ALS: a systematic qualitative review.

Authors:  F Seitzer; H Kahrass; G Neitzke; D Strech
Journal:  J Neurol       Date:  2015-07-30       Impact factor: 4.849

2.  Advance care planning for patients with amyotrophic lateral sclerosis.

Authors:  Benjamin H Levi; Zachary Simmons; Courtney Hanna; Allyson Brothers; Erik Lehman; Elana Farace; Megan Bain; Renee Stewart; Michael J Green
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2017-03-05       Impact factor: 4.092

3.  Brain-computer interface: current and emerging rehabilitation applications.

Authors:  Janis J Daly; Jane E Huggins
Journal:  Arch Phys Med Rehabil       Date:  2015-03       Impact factor: 3.966

4.  Towards a user-friendly brain-computer interface: initial tests in ALS and PLS patients.

Authors:  Ou Bai; Peter Lin; Dandan Huang; Ding-Yu Fei; Mary Kay Floeter
Journal:  Clin Neurophysiol       Date:  2010-03-29       Impact factor: 3.708

Review 5.  Symptom Management and End-of-Life Care in Amyotrophic Lateral Sclerosis.

Authors:  Carlayne E Jackson; April L McVey; Stacy Rudnicki; Mazen M Dimachkie; Richard J Barohn
Journal:  Neurol Clin       Date:  2015-11       Impact factor: 3.806

6.  Respiratory Muscle Strength as a Predictive Biomarker for Survival in Amyotrophic Lateral Sclerosis.

Authors:  Michael I Polkey; Rebecca A Lyall; Ke Yang; Erin Johnson; P Nigel Leigh; John Moxham
Journal:  Am J Respir Crit Care Med       Date:  2017-01-01       Impact factor: 21.405

Review 7.  Supportive and symptomatic management of amyotrophic lateral sclerosis.

Authors:  Esther V Hobson; Christopher J McDermott
Journal:  Nat Rev Neurol       Date:  2016-08-12       Impact factor: 42.937

8.  Respiratory and nutritional support in amyotrophic lateral sclerosis.

Authors:  Namita A Goyal; Tahseen Mozaffar
Journal:  Curr Treat Options Neurol       Date:  2014-02       Impact factor: 3.598

9.  P300-based brain-computer interface (BCI) event-related potentials (ERPs): People with amyotrophic lateral sclerosis (ALS) vs. age-matched controls.

Authors:  Lynn M McCane; Susan M Heckman; Dennis J McFarland; George Townsend; Joseph N Mak; Eric W Sellers; Debra Zeitlin; Laura M Tenteromano; Jonathan R Wolpaw; Theresa M Vaughan
Journal:  Clin Neurophysiol       Date:  2015-02-07       Impact factor: 3.708

10.  Brain-computer interface (BCI) evaluation in people with amyotrophic lateral sclerosis.

Authors:  Lynn M McCane; Eric W Sellers; Dennis J McFarland; Joseph N Mak; C Steve Carmack; Debra Zeitlin; Jonathan R Wolpaw; Theresa M Vaughan
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2014-02-20       Impact factor: 4.092
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