Literature DB >> 9808239

Discontinuation of mechanical ventilation in patients with amyotrophic lateral sclerosis.

G D Borasio1, R Voltz.   

Abstract

Mechanical ventilation, both invasive and non-invasive, may be an effective means of improving the quality of life and prolonging the survival of patients suffering from amyotrophic lateral sclerosis (ALS). However, the attitude towards this palliative measure varies greatly between different centres and countries. One of the arguments cited against this procedure is the fear that a patient might request the physician to discontinue life support. We believe that the question of withdrawal of mechanical ventilation can only be meaningfully addressed in the general context of palliative care. Here, we review possible modes of action in response to a patient's request for life support withdrawal and their medical, legal and ethical implications. We propose that the following goals should be pursued: (1) prevention of unwanted ventilation by early, open discussion with patient and relatives, (2) delivery of optimal palliative care by the caring team, (3) recognition of the patient's right to withdraw his/her consent to an invasive medical procedure. If these goals have been met, it may be medically, legally and ethically justified for the physician to take all necessary steps to ensure a peaceful death after discontinuation of life support.

Entities:  

Keywords:  Death and Euthanasia

Mesh:

Year:  1998        PMID: 9808239     DOI: 10.1007/s004150050273

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  11 in total

Review 1.  Management of motor neurone disease.

Authors:  R S Howard; R W Orrell
Journal:  Postgrad Med J       Date:  2002-12       Impact factor: 2.401

Review 2.  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

Review 3.  [Progressive muscle atrophy. A rarely diagnosed variant of amyotrophic lateral sclerosis].

Authors:  T Meyer; C Münch; F K H van Landeghem; N Borisow; J Dullinger; P Linke
Journal:  Nervenarzt       Date:  2007-12       Impact factor: 1.214

4.  Requests for euthanasia: origin of suffering in ALS, heart failure, and cancer patients.

Authors:  Maud Maessen; Jan H Veldink; Leonard H van den Berg; Henrike J Schouten; Gerrit van der Wal; Bregje D Onwuteaka-Philipsen
Journal:  J Neurol       Date:  2010-02-11       Impact factor: 4.849

Review 5.  Management of respiratory symptoms in ALS.

Authors:  Orla Hardiman
Journal:  J Neurol       Date:  2010-11-17       Impact factor: 4.849

6.  [BIPAP-mask-ventilation in terminal amyotrophic lateral sclerosis (ALS)].

Authors:  Theresa Sellner-Pogány; Heinz Lahrmann
Journal:  Wien Med Wochenschr       Date:  2009-12

7.  Depression and quality of life in patients with amyotrophic lateral sclerosis.

Authors:  Dorothée Lulé; Sonja Häcker; Albert Ludolph; Niels Birbaumer; Andrea Kübler
Journal:  Dtsch Arztebl Int       Date:  2008-06-06       Impact factor: 5.594

Review 8.  [End-of-life decisions, powers of attorney, and advance directives].

Authors:  R J Jox; H-J Hessler; G D Borasio
Journal:  Nervenarzt       Date:  2008-06       Impact factor: 1.214

9.  [Elective termination of respiratory therapy in amyotrophic lateral sclerosis].

Authors:  T Meyer; J S Dullinger; C Münch; J-P Keil; E Hempel; S Rosseau; N Borisow; P Linke
Journal:  Nervenarzt       Date:  2008-06       Impact factor: 1.214

10.  Ethical challenges in home mechanical ventilation: a secondary analysis.

Authors:  Knut Dybwik; Erik Waage Nielsen; Berit Støre Brinchmann
Journal:  Nurs Ethics       Date:  2011-12-19       Impact factor: 2.874

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