JNNP

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS REGISTER
[Advanced]

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this link to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Add article to my folders
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Traynor, B J
Right arrow Articles by Hardiman, O
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Traynor, B J
Right arrow Articles by Hardiman, O
Journal of Neurology Neurosurgery and Psychiatry 2003;74:1258-1261
© 2003 BMJ Publishing Group


PAPER

Effect of a multidisciplinary amyotrophic lateral sclerosis (ALS) clinic on ALS survival: a population based study, 1996–2000

B J Traynor1,*, M Alexander1, B Corr1, E Frost2, O Hardiman1

1 Department of Neurology, Beaumont Hospital, Dublin, Ireland
2 The Irish MND Association, Coleraine House, Dublin, Ireland

Correspondence to:
Correspondence to:
Dr Traynor, Massachusetts General Hospital East, Cecil B. Day Lab, Building 114, Room 3125, 16th Street, Charlestown, MA 02129, USA;
btraynor{at}partners.org

Background: In recent years, there has been a paradigm shift in the method of healthcare delivery to amyotrophic lateral sclerosis (ALS) patients with the emergence of multidisciplinary ALS clinics that cater exclusively for patients with this condition. The impact of multidisciplinary management has not been previously evaluated.

Methods: Using data from the Irish ALS Register, we conducted a prospective, population based study of all ALS cases diagnosed in Ireland over a five year period to evaluate the effectiveness of a multidisciplinary clinic on ALS survival.

Results: Eighty two (24%) patients attended the multidisciplinary ALS clinic, with the remaining 262 (76%) cases followed in a general neurology clinic. The ALS clinic cohort was an average of five years younger (60.1 v 65.6 years) and were more likely to receive riluzole than the general neurology cohort (99% v 61%). The median survival of the ALS clinic cohort was 7.5 months longer than for patients in the general neurology cohort (logrank = 15.4, p < 0.0001). Overall, one year mortality was decreased by 29.7%. Prognosis of bulbar onset patients was extended by 9.6 months if they attended the ALS clinic. Using multivariate analysis, attendance at the ALS clinic was an independent covariate of survival (HR = 1.47, p = 0.02).

Conclusions: ALS patients who received their care at a multidisciplinary clinic had a better prognosis than patients attending a general neurology clinic. The data suggest that active and aggressive management enhances survival, particularly among ALS patients with bulbar dysfunction. The effect of clinic type must be considered in future clinical trials design.


Keywords: amyotrophic lateral sclerosis; Ireland; multidisciplinary clinic; survival; population based

Abbreviations: ALS, amyotrophic lateral sclerosis; IMNDA, Irish Motor Neurone Disease Association; NIPPV, non-invasive positive pressure ventilation




This article has been cited by other articles:


Home page
BMJHome page
C. J McDermott and P. J Shaw
Diagnosis and management of motor neurone disease
BMJ, March 22, 2008; 336(7645): 658 - 662.
[Full Text] [PDF]


Home page
J. Neurol. Neurosurg. PsychiatryHome page
G Logroscino, B J Traynor, O Hardiman, A Chio', P Couratier, J D Mitchell, R J Swingler, E Beghi, and for EURALS
Descriptive epidemiology of amyotrophic lateral sclerosis: new evidence and unsolved issues
J. Neurol. Neurosurg. Psychiatry, January 1, 2008; 79(1): 6 - 11.
[Abstract] [Full Text] [PDF]


Home page
JAMAHome page
H. Mitsumoto and J. G. Rabkin
Palliative Care for Patients With Amyotrophic Lateral Sclerosis: "Prepare for the Worst and Hope for the Best"
JAMA, July 11, 2007; 298(2): 207 - 216.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
E. J. Sorenson, J. Mandrekar, B. Crum, and J. C. Stevens
Effect of referral bias on assessing survival in ALS
Neurology, February 20, 2007; 68(8): 600 - 602.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
S. Cronin, M. J. Greenway, S. Ennis, D. Kieran, A. Green, J.H.M. Prehn, and O. Hardiman
Elevated serum angiogenin levels in ALS
Neurology, November 28, 2006; 67(10): 1833 - 1836.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
R. Dubinsky, J. Chen, and S.-M. Lai
Trends in hospital utilization and outcome for patients with ALS: analysis of a large U.S. cohort.
Neurology, September 12, 2006; 67(5): 777 - 780.
[Abstract] [Full Text] [PDF]


Home page
J. Neurol. Neurosurg. PsychiatryHome page
A Chio, E Bottacchi, C Buffa, R Mutani, G Mora, and the PARALS
Positive effects of tertiary centres for amyotrophic lateral sclerosis on outcome and use of hospital facilities
J. Neurol. Neurosurg. Psychiatry, August 1, 2006; 77(8): 948 - 950.
[Abstract] [Full Text] [PDF]


Home page
Arch NeurolHome page
A. Czaplinski, A. A. Yen, E. P. Simpson, and S. H. Appel
Slower Disease Progression and Prolonged Survival in Contemporary Patients With Amyotrophic Lateral Sclerosis: Is the Natural History of Amyotrophic Lateral Sclerosis Changing?
Arch Neurol, August 1, 2006; 63(8): 1139 - 1143.
[Abstract] [Full Text] [PDF]


Home page
Stem CellsHome page
L. Chi, Y. Ke, C. Luo, B. Li, D. Gozal, B. Kalyanaraman, and R. Liu
Motor Neuron Degeneration Promotes Neural Progenitor Cell Proliferation, Migration, and Neurogenesis in the Spinal Cords of Amyotrophic Lateral Sclerosis Mice
Stem Cells, January 1, 2006; 24(1): 34 - 43.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
J. P. Van den Berg, S. Kalmijn, E. Lindeman, J. H. Veldink, M. de Visser, M. M. Van der Graaff, J.H.J. Wokke, and L. H. Van den Berg
Multidisciplinary ALS care improves quality of life in patients with ALS
Neurology, October 25, 2005; 65(8): 1264 - 1267.
[Abstract] [Full Text] [PDF]


Home page
J Oncol PractHome page
T. Mulvey

J. Oncol. Pract, September 1, 2005; 1(3): 82 - 83.
[Full Text] [PDF]


Home page
J. Neurol. Neurosurg. PsychiatryHome page
R B Forbes, S Colville, G W Cran, and R J Swingler
Unexpected decline in survival from amyotrophic lateral sclerosis/motor neurone disease
J. Neurol. Neurosurg. Psychiatry, December 1, 2004; 75(12): 1753 - 1755.
[Abstract] [Full Text] [PDF]


Home page
J. Neurol. Neurosurg. PsychiatryHome page
M Hutchinson, R Galvin, B Sweeney, T Lynch, R Murphy, J Redmond, B J Traynor, and O Hardiman
Effect of a multidisciplinary clinic on survival in amyotrophic lateral sclerosis * Author's reply
J. Neurol. Neurosurg. Psychiatry, August 1, 2004; 75(8): 1208 - 1209.
[Full Text] [PDF]


Home page
J. Neurol. Neurosurg. PsychiatryHome page
P N Leigh, S Abrahams, A Al-Chalabi, M-A Ampong, L H Goldstein, J Johnson, R Lyall, J Moxham, N Mustfa, A Rio, et al.
The management of motor neurone disease
J. Neurol. Neurosurg. Psychiatry, December 1, 2003; 74(90004): iv32 - 47.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS REGISTER
Terms and conditions relating to subscriptions purchased online  ¦  Website terms and conditions  ¦  Privacy policy
Copyright © 2003 by the BMJ Publishing Group Ltd.