Literature DB >> 24372800

Development of a model to guide decision making in amyotrophic lateral sclerosis multidisciplinary care.

Anne Hogden1, David Greenfield1, Peter Nugus1,2, Matthew C Kiernan3.   

Abstract

BACKGROUND: Patients with amyotrophic lateral sclerosis (ALS) face numerous decisions for symptom management and quality of life. Models of decision making in chronic disease and cancer care are insufficient for the complex and changing needs of patients with ALS .
OBJECTIVE: The aim was to examine the question: how can decision making that is both effective and patient-centred be enacted in ALS multidisciplinary care? SETTING AND PARTICIPANTS: Fifty-four respondents (32 health professionals, 14 patients and eight carers) from two specialized ALS multidisciplinary clinics participated in semi-structured interviews. Interviews were transcribed, coded and analysed thematically.
RESULTS: Comparison of stakeholder perspectives revealed six key themes of ALS decision making. These were the decision-making process; patient-centred focus; timing and planning; information sources; engagement with specialized ALS services; and access to non-specialized services. A model, embedded in the specialized ALS multidisciplinary clinic, was derived to guide patient decision making. The model is cyclic, with four stages: 'Participant Engagement'; 'Option Information'; 'Option Deliberation'; and 'Decision Implementation'. DISCUSSION: Effective and patient-centred decision making is enhanced by the structure of the specialized ALS clinic, which promotes patients' symptom management and quality of life goals. However, patient and carer engagement in ALS decision making is tested by the dynamic nature of ALS, and patient and family distress. Our model optimizes patient-centred decision making, by incorporating patients' cyclic decision-making patterns and facilitating carer inclusion in decision processes.
CONCLUSIONS: The model captures the complexities of patient-centred decision making in ALS. The framework can assist patients and carers, health professionals, researchers and policymakers in this challenging disease environment.
© 2013 John Wiley & Sons Ltd.

Entities:  

Keywords:  caregivers; motor neurone disease; patient-centred care; stakeholder perspectives

Mesh:

Year:  2013        PMID: 24372800      PMCID: PMC5060893          DOI: 10.1111/hex.12169

Source DB:  PubMed          Journal:  Health Expect        ISSN: 1369-6513            Impact factor:   3.377


  46 in total

1.  Establishment of an Australian motor neurone disease registry.

Authors:  Matthew C Kiernan; Paul Talman; Robert D Henderson; Rodney Harris
Journal:  Med J Aust       Date:  2006-04-03       Impact factor: 7.738

2.  Effectiveness of strategies for informing, educating, and involving patients.

Authors:  Angela Coulter; Jo Ellins
Journal:  BMJ       Date:  2007-07-07

3.  Prospective study of palliative care in ALS: choice, timing, outcomes.

Authors:  S M Albert; P L Murphy; M L Del Bene; L P Rowland
Journal:  J Neurol Sci       Date:  1999-10-31       Impact factor: 3.181

4.  EFNS guidelines on the clinical management of amyotrophic lateral sclerosis (MALS)--revised report of an EFNS task force.

Authors:  Peter M Andersen; Sharon Abrahams; Gian D Borasio; Mamede de Carvalho; Adriano Chio; Philip Van Damme; Orla Hardiman; Katja Kollewe; Karen E Morrison; Susanne Petri; Pierre-Francois Pradat; Vincenzo Silani; Barbara Tomik; Maria Wasner; Markus Weber
Journal:  Eur J Neurol       Date:  2011-09-14       Impact factor: 6.089

5.  When and how to initiate discussion about prognosis and end-of-life issues with terminally ill patients.

Authors:  Josephine M Clayton; Phyllis N Butow; Martin H N Tattersall
Journal:  J Pain Symptom Manage       Date:  2005-08       Impact factor: 3.612

Review 6.  Some difficult decisions in ALS/MND.

Authors:  David J Oliver; Martin R Turner
Journal:  Amyotroph Lateral Scler       Date:  2010-08

Review 7.  Multidisciplinary care for adults with amyotrophic lateral sclerosis or motor neuron disease.

Authors:  Louisa Ng; Fary Khan; Susan Mathers
Journal:  Cochrane Database Syst Rev       Date:  2009-10-07

8.  Clinical phenotypes and natural progression for motor neuron disease: analysis from an Australian database.

Authors:  Paul Talman; Andrew Forbes; Susan Mathers
Journal:  Amyotroph Lateral Scler       Date:  2009-04

9.  Is language impairment more common than executive dysfunction in amyotrophic lateral sclerosis?

Authors:  Lorna J Taylor; Richard G Brown; Stella Tsermentseli; Ammar Al-Chalabi; Christopher E Shaw; Catherine M Ellis; P Nigel Leigh; Laura H Goldstein
Journal:  J Neurol Neurosurg Psychiatry       Date:  2012-10-02       Impact factor: 10.154

10.  Caregiver burden in amyotrophic lateral sclerosis is more dependent on patients' behavioral changes than physical disability: a comparative study.

Authors:  Patricia Lillo; Eneida Mioshi; John R Hodges
Journal:  BMC Neurol       Date:  2012-12-07       Impact factor: 2.474

View more
  7 in total

Review 1.  Prognostic factors for the course of functional status of patients with ALS: a systematic review.

Authors:  Huub Creemers; Hepke Grupstra; Frans Nollet; Leonard H van den Berg; Anita Beelen
Journal:  J Neurol       Date:  2014-11-11       Impact factor: 4.849

2.  Therapeutic decisions in ALS patients: cross-cultural differences and clinical implications.

Authors:  Peter M Andersen; Magdalena Kuzma-Kozakiewicz; Jürgen Keller; Helena E A Aho-Oezhan; Katarzyna Ciecwierska; Natalia Szejko; Cynthia Vázquez; Sarah Böhm; Gisela Badura-Lotter; Thomas Meyer; Susanne Petri; Katharina Linse; Andreas Hermann; Olof Semb; Erica Stenberg; Simona Nackberg; Johannes Dorst; Ingo Uttner; Ann-Cristin Häggström; Albert C Ludolph; Dorothée Lulé
Journal:  J Neurol       Date:  2018-05-04       Impact factor: 4.849

3.  Development of patient decision support tools for motor neuron disease using stakeholder consultation: a study protocol.

Authors:  Anne Hogden; David Greenfield; Jashelle Caga; Xiongcai Cai
Journal:  BMJ Open       Date:  2016-04-06       Impact factor: 2.692

4.  Discrete choice experiment for eliciting preference for health services for patients with ALS and their informal caregivers.

Authors:  Katy Tobin; Sinead Maguire; Orla Hardiman; Miriam Galvin; Bernie Corr; Charles Normand
Journal:  BMC Health Serv Res       Date:  2021-03-09       Impact factor: 2.655

Review 5.  Talking about the end of life: communication patterns in amyotrophic lateral sclerosis - a scoping review.

Authors:  Anke Erdmann; Celia Spoden; Irene Hirschberg; Gerald Neitzke
Journal:  Palliat Care Soc Pract       Date:  2022-03-15

6.  Engaging Specialist Palliative Care in the Management of Amyotrophic Lateral Sclerosis: A Patient-, Family-, and Provider-Based Approach.

Authors:  Karla T Washington; Klaudia Kukulka; Raghav Govindarjan; David R Mehr
Journal:  J Palliat Care       Date:  2020-02-17       Impact factor: 1.980

Review 7.  Amyotrophic lateral sclerosis: improving care with a multidisciplinary approach.

Authors:  Anne Hogden; Geraldine Foley; Robert D Henderson; Natalie James; Samar M Aoun
Journal:  J Multidiscip Healthc       Date:  2017-05-19
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.