Literature DB >> 17352943

Comprehensive care in Huntington's disease: a physician's perspective.

Martha A Nance1.   

Abstract

Huntington's disease is a slowly progressive neurodegenerative disorder with wide-ranging effects on affected individuals and their families. Until a cure is found for the disease, patients and their families will continue to need care over years, even generations. The ideal care for HD is provided by a team, led by a physician, with input from rehabilitation therapists, nurses, psychologists, genetic counselors, social workers, and other health care providers. The goals of care are to maximize the quality of life at all points through the course of the disease, in part by anticipating problems that are likely to arise at the next stage of the illness. We describe below an approach to comprehensive care, and introduce the concept of the "Huntington disease molecule", in which the patient, in the center, is surrounded by a shell of immediate and extended family members, with bonds extended in multiple directions to provider who can give appropriate medical care, education, crisis management, research opportunities, address family issues, maximize function, and prepare for the future.

Entities:  

Mesh:

Year:  2006        PMID: 17352943     DOI: 10.1016/j.brainresbull.2006.10.027

Source DB:  PubMed          Journal:  Brain Res Bull        ISSN: 0361-9230            Impact factor:   4.077


  17 in total

1.  Identification of health-related quality of life (HRQOL) issues relevant to individuals with Huntington disease.

Authors:  Noelle E Carlozzi; David S Tulsky
Journal:  J Health Psychol       Date:  2012-03-16

2.  Health-related quality of life in caregivers of individuals with traumatic brain injury: development of a conceptual model.

Authors:  Noelle E Carlozzi; Anna L Kratz; Angelle M Sander; Nancy D Chiaravalloti; Tracey A Brickell; Rael T Lange; Elizabeth A Hahn; Amy Austin; Jennifer A Miner; David S Tulsky
Journal:  Arch Phys Med Rehabil       Date:  2014-09-17       Impact factor: 3.966

3.  Coordinated multidisciplinary care for ambulatory Huntington's disease patients. Evaluation of 18 months of implementation.

Authors:  Ruth B Veenhuizen; Branda Kootstra; Wilma Vink; Janneke Posthumus; Pleuntje van Bekkum; Margriet Zijlstra; Jelleke Dokter
Journal:  Orphanet J Rare Dis       Date:  2011-11-18       Impact factor: 4.123

4.  Hospital Admissions of Huntington's Disease Patients in a Huntington's Disease Centre Between 2011 and 2016: A Retrospective Analysis.

Authors:  Marina Peball; Beatrice Heim; Philipp Ellmerer; Florian Frank; Nadia Busin; Matyas Galffy; Atbin Djamshidian; Klaus Seppi
Journal:  Mov Disord Clin Pract       Date:  2022-05-05

5.  HDQLIFE: development and assessment of health-related quality of life in Huntington disease (HD).

Authors:  N E Carlozzi; S G Schilling; J-S Lai; J S Paulsen; E A Hahn; J S Perlmutter; C A Ross; N R Downing; A L Kratz; M K McCormack; M A Nance; K A Quaid; J C Stout; R C Gershon; R E Ready; J A Miner; S K Barton; S L Perlman; S M Rao; S Frank; I Shoulson; H Marin; M D Geschwind; P Dayalu; S M Goodnight; D Cella
Journal:  Qual Life Res       Date:  2016-08-13       Impact factor: 4.147

Review 6.  Need for palliative care for neurological diseases.

Authors:  Leandro Provinciali; Giulia Carlini; Daniela Tarquini; Carlo Alberto Defanti; Simone Veronese; Eugenio Pucci
Journal:  Neurol Sci       Date:  2016-06-14       Impact factor: 3.307

7.  Reliability and Validity of the HD-PRO-TriadTM, a Health-Related Quality of Life Measure Designed to Assess the Symptom Triad of Huntington's Disease.

Authors:  Nicholas R Boileau; Julie C Stout; Janes S Paulsen; David Cella; Michael K McCormack; Martha A Nance; Samuel Frank; Jin-Shei Lai; Noelle E Carlozzi
Journal:  J Huntingtons Dis       Date:  2017

8.  Utilisation of Healthcare and Associated Services in Huntington's disease: a data mining study.

Authors:  Monica Busse; Dr Hasan Al-Madfai; Joyce Kenkre; G Bernhard Landwehrmeyer; Annarita Bentivoglio; Anne Rosser
Journal:  PLoS Curr       Date:  2011-01-21

9.  The many facets of unawareness in huntington disease.

Authors:  Elizabeth McCusker; Clement T Loy
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2014-11-12

10.  Unmet needs for healthcare and social support services in patients with Huntington's disease: a cross-sectional population-based study.

Authors:  Marleen R van Walsem; Emilie I Howe; Kristin Iversen; Jan C Frich; Nada Andelic
Journal:  Orphanet J Rare Dis       Date:  2015-09-28       Impact factor: 4.123

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.