Literature DB >> 11180749

Lambert-Eaton Myasthenic Syndrome.

John Newsom-Davis1.   

Abstract

Weakness and autonomic dysfunction in Lambert-Eaton myasthenic syndrome (LEMS) can be partially or fully controlled by 3,4-Diaminopyridine. Intravenous immunoglobulin or plasma exchange (PE) plasmapheresis) provides short-term improvement in severely affected patients. In those at risk from paraneoplastic LEMS (cigarette smokers), an intensive search for lung cancer should be undertaken, and specific tumor therapy instituted that likely will improve the neurologic deficit. Prednisolone (1.5 mg per kg of body weight administered on alternate days, maximum dosage is 100 mg) is indicated in those with paraneoplastic or nonparaneoplastic LEMS who fail to respond sufficiently to symptomatic treatment. The addition of azathioprine or cyclosporine is indicated as corticosteroid sparing medications in nonparaneoplastic LEMS. When remission or optimal improvement is judged to be present, prednisolone should be tapered to the minimum dose that effectively controls symptoms. If full withdrawal is achieved, azathioprine dose reduction is similarly initiated. In nonparaneoplastic LEMS patients failing to respond to azathioprine after 1 to 2 years of therapy, physicians should consider substituting cyclosporine.

Entities:  

Year:  2001        PMID: 11180749     DOI: 10.1007/s11940-001-0047-0

Source DB:  PubMed          Journal:  Curr Treat Options Neurol        ISSN: 1092-8480            Impact factor:   3.598


  23 in total

1.  Favourable prognosis in Lambert-Eaton myasthenic syndrome and small-cell lung carcinoma.

Authors:  P Maddison; J Newsom-Davis; K R Mills; R L Souhami
Journal:  Lancet       Date:  1999-01-09       Impact factor: 79.321

2.  A treatment algorithm for Lambert-Eaton myasthenic syndrome.

Authors:  J Newsom-Davis
Journal:  Ann N Y Acad Sci       Date:  1998-05-13       Impact factor: 5.691

3.  Wide spectrum of symptomatic treatment in Lambert-Eaton myasthenic syndrome.

Authors:  S J Oh; D S Kim; K H Kwon; A Tseng; H Mussell; G C Claussen
Journal:  Ann N Y Acad Sci       Date:  1998-05-13       Impact factor: 5.691

4.  A randomized trial of 3,4-diaminopyridine in Lambert-Eaton myasthenic syndrome.

Authors:  D B Sanders; J M Massey; L L Sanders; L J Edwards
Journal:  Neurology       Date:  2000-02-08       Impact factor: 9.910

5.  Long-term follow-up of Lambert-Eaton syndrome treated with intravenous immunoglobulin.

Authors:  S Muchnik; A S Losavio; A Vidal; L Cura; C Mazia
Journal:  Muscle Nerve       Date:  1997-06       Impact factor: 3.217

6.  Cardiac arrest following an iatrogenic 3,4-diaminopyridine intoxication in a patient with Lambert-Eaton myasthenic syndrome.

Authors:  C E Boerma; J H Rommes; R B van Leeuwen; J Bakker
Journal:  J Toxicol Clin Toxicol       Date:  1995

7.  Plasma exchange and immunosuppressive drug treatment in the Lambert-Eaton myasthenic syndrome.

Authors:  J Newsom-Davis; N M Murray
Journal:  Neurology       Date:  1984-04       Impact factor: 9.910

8.  Distribution of electrophysiological abnormality in Lambert-Eaton myasthenic syndrome.

Authors:  P Maddison; J Newsom-Davis; K R Mills
Journal:  J Neurol Neurosurg Psychiatry       Date:  1998-08       Impact factor: 10.154

9.  The Lambert-Eaton myasthenic syndrome. A review of 50 cases.

Authors:  J H O'Neill; N M Murray; J Newsom-Davis
Journal:  Brain       Date:  1988-06       Impact factor: 13.501

10.  Effects of intravenous immunoglobulin on muscle weakness and calcium-channel autoantibodies in the Lambert-Eaton myasthenic syndrome.

Authors:  P G Bain; M Motomura; J Newsom-Davis; S A Misbah; H M Chapel; M L Lee; A Vincent; B Lang
Journal:  Neurology       Date:  1996-09       Impact factor: 9.910

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