Literature DB >> 16614011

Positive effects of tertiary centres for amyotrophic lateral sclerosis on outcome and use of hospital facilities.

A Chiò1, E Bottacchi, C Buffa, R Mutani, G Mora.   

Abstract

OBJECTIVE: To evaluate the effects of tertiary centres for amyotrophic lateral sclerosis (ALS) on ALS outcome and the use of hospital facilities.
METHODS: The study was based on the data of an epidemiological, prospective, population-based register on ALS (Piemonte and Valle d'Aosta Register for amyotrophic lateral sclerosis, PARALS). The 221 patients recruited between 1995 and 1996 were prospectively followed up for outcome and use of hospital-based services.
RESULTS: In all, 97 patients were followed up by tertiary ALS centres and 124 by general neurological clinics. Patients followed up by tertiary ALS centres were found to be 4 years younger and underwent percutaneous endoscopic gastronomy and non-invasive positive-pressure ventilation more often. Patients followed up by tertiary ALS centres were found to have a considerably longer median survival time (1080 v 775 days), even when stratifying by age, site of onset and respiratory function at diagnosis. In Cox multivariate analysis, attending a tertiary ALS centre was observed to be an independent positive prognostic factor. Moreover, patients attending a tertiary ALS centre were admitted to hospital less often (1.2 v 3.3) and were more frequently admitted for planned interventions. Conversely, patients followed up by general neurological clinics were more frequently admitted for acute events. Also, the hospital stay was considerably shorter for patients attending tertiary ALS centres (5.8 v 12.4 days).
CONCLUSIONS: Improved survival was seen in patients with ALS attending tertiary ALS centres, independently from all other known prognostic factors, possibly through a better implementation of supportive treatments. Moreover, because of these centres, the hospitalisation rate was markedly reduced, thus offering a cost-effective service to patients with ALS and to the community as a whole.

Entities:  

Mesh:

Year:  2006        PMID: 16614011      PMCID: PMC2077622          DOI: 10.1136/jnnp.2005.083402

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  13 in total

1.  Practice parameter: the care of the patient with amyotrophic lateral sclerosis (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology: ALS Practice Parameters Task Force.

Authors:  R G Miller; J A Rosenberg; D F Gelinas; H Mitsumoto; D Newman; R Sufit; G D Borasio; W G Bradley; M B Bromberg; B R Brooks; E J Kasarskis; T L Munsat; E A Oppenheimer
Journal:  Neurology       Date:  1999-04-22       Impact factor: 9.910

2.  A multidisciplinary quality management system for the early treatment of severely injured patients: implementation and results in two trauma centers.

Authors:  Steffen Ruchholtz; Christian Waydhas; Ulrike Lewan; Karl Piepenbrink; Dietmar Stolke; Jörg Debatin; Leonhard Schweiberer; Dieter Nast-Kolb
Journal:  Intensive Care Med       Date:  2002-08-13       Impact factor: 17.440

3.  Validity of hospital morbidity records for amyotrophic lateral sclerosis. A population-based study.

Authors:  Adriano Chiò; Giovannino Ciccone; Andrea Calvo; Marco Vercellino; Nicoletta Di Vito; Paolo Ghiglione; Roberto Mutani
Journal:  J Clin Epidemiol       Date:  2002-07       Impact factor: 6.437

4.  Measuring interdisciplinary team performance in a long-term care setting.

Authors:  Helena Temkin-Greener; Diane Gross; Stephen J Kunitz; Dana Mukamel
Journal:  Med Care       Date:  2004-05       Impact factor: 2.983

5.  Effect of noninvasive positive-pressure ventilation on survival in amyotrophic lateral sclerosis.

Authors:  L S Aboussouan; S U Khan; D P Meeker; K Stelmach; H Mitsumoto
Journal:  Ann Intern Med       Date:  1997-09-15       Impact factor: 25.391

Review 6.  Motor neuron disease.

Authors:  P N Leigh; K Ray-Chaudhuri
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-08       Impact factor: 10.154

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

Authors:  B J Traynor; M Alexander; B Corr; E Frost; O Hardiman
Journal:  J Neurol Neurosurg Psychiatry       Date:  2003-09       Impact factor: 10.154

8.  Prognosis of amyotrophic lateral sclerosis and the effect of referral selection.

Authors:  J R Lee; J F Annegers; S H Appel
Journal:  J Neurol Sci       Date:  1995-10       Impact factor: 3.181

9.  Amyotrophic lateral sclerosis: predictors for prolongation of life by noninvasive respiratory aids.

Authors:  J R Bach
Journal:  Arch Phys Med Rehabil       Date:  1995-09       Impact factor: 3.966

10.  Home based management in multiple sclerosis: results of a randomised controlled trial.

Authors:  C Pozzilli; M Brunetti; A M V Amicosante; C Gasperini; G Ristori; L Palmisano; M Battaglia
Journal:  J Neurol Neurosurg Psychiatry       Date:  2002-09       Impact factor: 10.154

View more
  44 in total

1.  ALS multidisciplinary clinic and survival. Results from a population-based study in Southern Italy.

Authors:  Stefano Zoccolella; Ettore Beghi; Guerrino Palagano; Angela Fraddosio; Vito Guerra; Vito Lepore; Isabella Laura Simone; Paolo Lamberti; Luigi Serlenga; Giancarlo Logroscino
Journal:  J Neurol       Date:  2007-04-13       Impact factor: 4.849

2.  Predictors of emergent feeding tubes and tracheostomies in amyotrophic lateral sclerosis (ALS).

Authors:  Amy Y Tsou; Jason Karlawish; Leo McCluskey; Sharon X Xie; Judith A Long
Journal:  Amyotroph Lateral Scler       Date:  2012-05

3.  Amyotrophic lateral sclerosis: clinical management and research update.

Authors:  Jinsy Andrews
Journal:  Curr Neurol Neurosci Rep       Date:  2009-01       Impact factor: 5.081

4.  The evaluation of bulbar dysfunction in amyotrophic lateral sclerosis: survey of clinical practice patterns in the United States.

Authors:  Emily K Plowman; Lauren C Tabor; James Wymer; Gary Pattee
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2017-04-20       Impact factor: 4.092

5.  Discriminant ability of the Eating Assessment Tool-10 to detect aspiration in individuals with amyotrophic lateral sclerosis.

Authors:  E K Plowman; L C Tabor; R Robison; J Gaziano; C Dion; S A Watts; T Vu; C Gooch
Journal:  Neurogastroenterol Motil       Date:  2015-10-28       Impact factor: 3.598

Review 6.  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

Review 7.  Clinical diagnosis and management of amyotrophic lateral sclerosis.

Authors:  Orla Hardiman; Leonard H van den Berg; Matthew C Kiernan
Journal:  Nat Rev Neurol       Date:  2011-10-11       Impact factor: 42.937

Review 8.  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

Review 9.  Multidisciplinary care in Amyotrophic Lateral Sclerosis: a systematic review and meta-analysis.

Authors:  Filipe Emanuel Oliveira de Almeida; Anne Kelly do Carmo Santana; Fernanda Oliveira de Carvalho
Journal:  Neurol Sci       Date:  2021-01-14       Impact factor: 3.307

Review 10.  Prognostic factors in ALS: A critical review.

Authors:  Adriano Chiò; Giancarlo Logroscino; Orla Hardiman; Robert Swingler; Douglas Mitchell; Ettore Beghi; Bryan G Traynor
Journal:  Amyotroph Lateral Scler       Date:  2009 Oct-Dec
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.