Literature DB >> 6388775

The doctor as patient: an encounter with Guillain-Bárré syndrome.

D Bowes.   

Abstract

The author describes the course and treatment of a severe acute illness that began with cranial nerve palsies and ataxia and progressed rapidly to generalized weakness with respiratory embarrassment. There was no sensory loss or elevation of the protein level in the cerebrospinal fluid. The Miller Fisher variant of Guillain-Barré syndrome was diagnosed. At the height of the illness, a period lasting about 2 weeks, the author was almost completely paralysed, retaining only a little motion in some fingers and one foot; she was able to breathe on her own but required suctioning through a tracheostomy, and her eyes had to be taped shut because of her facial paralysis. She remained mentally alert throughout. Proper care of such a helpless patient demands not only excellent technical performance of many nursing procedures but a sensitivity to the patient as a person. The author describes the many shortcomings of the care she received and the value of physiotherapy in her rehabilitation and makes a number of specific recommendations for the care of critically ill conscious patients.

Entities:  

Mesh:

Year:  1984        PMID: 6388775      PMCID: PMC1483651     

Source DB:  PubMed          Journal:  Can Med Assoc J        ISSN: 0008-4409            Impact factor:   8.262


  7 in total

1.  RELATION OF MULTIPLE CRANIAL NERVE DYSFUNCTION TO THE GUILLAIN-BARR'E SYNDROME.

Authors:  T L MUNSAT; J E BARNES
Journal:  J Neurol Neurosurg Psychiatry       Date:  1965-04       Impact factor: 10.154

2.  A Guillain-Barré variant: ophthalmoplegia, ataxia and areflexia.

Authors:  M J Davis
Journal:  Mt Sinai J Med       Date:  1975 Mar-Apr

3.  The ataxic form of polyradiculoneuritis (Landry-Guillain-Barre syndrome). Clinical and pathologic observations.

Authors:  R B RICHTER
Journal:  J Neuropathol Exp Neurol       Date:  1962-04       Impact factor: 3.685

4.  The Landry-Guillain-barré syndrome. Complications, prognosis and natural history in 123 cases.

Authors:  N B Löffel; L N Rossi; M Mumenthaler; J Lütschg; H P Ludin
Journal:  J Neurol Sci       Date:  1977-08       Impact factor: 3.181

5.  The CNS in Guillain-Barré syndrome.

Authors:  A H Ropper
Journal:  Arch Neurol       Date:  1983-07

6.  Brainstem encephalitis and the syndrome of Miller Fisher: a clinical study.

Authors:  A N Al-Din; M Anderson; E R Bickerstaff; I Harvey
Journal:  Brain       Date:  1982-09       Impact factor: 13.501

7.  Criteria for the diagnosis of the Guillain-Barré syndrome. A critique of the NINCDS guidelines.

Authors:  C M Poser
Journal:  J Neurol Sci       Date:  1981 Nov-Dec       Impact factor: 3.181

  7 in total
  5 in total

1.  Impaired joint mobility in Guillain-Barré syndrome: a primary or a secondary phenomenon?

Authors:  I Soryal; E Sinclair; J Hornby; B Pentland
Journal:  J Neurol Neurosurg Psychiatry       Date:  1992-11       Impact factor: 10.154

2.  A physician's experience of a "minor" illness.

Authors:  S M McNair
Journal:  Can Fam Physician       Date:  1996-12       Impact factor: 3.275

3.  Residual health status after Guillain-Barré syndrome.

Authors:  R A Bernsen; H M Jacobs; A E de Jager; F G van der Meché
Journal:  J Neurol Neurosurg Psychiatry       Date:  1997-06       Impact factor: 10.154

4.  The physician-patient relationship: a patient-physician's view.

Authors:  Jeffrey H Ennis
Journal:  Can Fam Physician       Date:  1990-12       Impact factor: 3.275

5.  The landry-guillain-barré strohl syndrome 1859 to 1992 a historical perspective.

Authors:  A K Afifi
Journal:  J Family Community Med       Date:  1994-01
  5 in total

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