Literature DB >> 22591813

Patients' perspectives on quality of mental health care for people with MS.

D J Rintell1, D Frankel, S L Minden, B I Glanz.   

Abstract

OBJECTIVE: The objective was to obtain multiple sclerosis (MS) patients' report on their experience receiving mental health care.
METHODS: We convened focus groups at four MS clinical care centers to identify the aspects of mental health care that were important to people with MS. All patients (n=54) had received mental health care in the past year. Data were analyzed by coding comments under specific themes.
RESULTS: Patients wanted prompt intervention after diagnosis and ongoing screening for mental health problems; they prefer providers with knowledge about MS and experience working with people with MS; they appreciated being able to access mental health services that were on-site at their MS center and noted the benefit of inclusion of family members in treatment.
CONCLUSIONS: Mental health care should be provided promptly after diagnosis, with regular screening and interventions that include family members as indicated thereafter. Mental health providers should be familiar with MS, collaborate with neurologic care providers and provide services on-site at MS centers.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22591813     DOI: 10.1016/j.genhosppsych.2012.04.001

Source DB:  PubMed          Journal:  Gen Hosp Psychiatry        ISSN: 0163-8343            Impact factor:   3.238


  8 in total

1.  "Her illness is a project we can work on together": developing a collaborative family-centered intervention model for newly diagnosed multiple sclerosis.

Authors:  David Rintell; Richard Melito
Journal:  Int J MS Care       Date:  2013

2.  A Framework of Care in Multiple Sclerosis, Part 2: Symptomatic Care and Beyond.

Authors:  Scott D Newsome; Philip J Aliotta; Jacquelyn Bainbridge; Susan E Bennett; Gary Cutter; Kaylan Fenton; Fred Lublin; Dorothy Northrop; David Rintell; Bryan D Walker; Megan Weigel; Kathleen Zackowski; David E Jones
Journal:  Int J MS Care       Date:  2017 Jan-Feb

3.  "Putting one foot in front of the other": a qualitative study of emotional experiences and help-seeking in women with multiple sclerosis.

Authors:  Joanna Blundell Jones; Sue Walsh; Claire Isaac
Journal:  J Clin Psychol Med Settings       Date:  2014-12

4.  Identifying Barriers to and Facilitators of Health Service Access Encountered by Individuals with Multiple Sclerosis.

Authors:  Chantel D Mayo; Negar Farzam-Kia; Setareh Ghahari
Journal:  Int J MS Care       Date:  2021-02-23

5.  Qualitative study identifies life shifts and stress coping strategies in people with multiple sclerosis.

Authors:  Heidemarie Lex; Pollie Price; Lauren Clark
Journal:  Sci Rep       Date:  2022-04-20       Impact factor: 4.996

6.  PICO, PICOS and SPIDER: a comparison study of specificity and sensitivity in three search tools for qualitative systematic reviews.

Authors:  Abigail M Methley; Stephen Campbell; Carolyn Chew-Graham; Rosalind McNally; Sudeh Cheraghi-Sohi
Journal:  BMC Health Serv Res       Date:  2014-11-21       Impact factor: 2.655

Review 7.  'It struck at the heart of who I thought I was': A meta-synthesis of the qualitative literature examining the experiences of people with multiple sclerosis.

Authors:  Jane Desborough; Crystal Brunoro; Anne Parkinson; Katrina Chisholm; Mark Elisha; Janet Drew; Vanessa Fanning; Christian Lueck; Anne Bruestle; Matthew Cook; Hanna Suominen; Antonio Tricoli; Adam Henschke; Christine Phillips
Journal:  Health Expect       Date:  2020-06-24       Impact factor: 3.377

Review 8.  Patient and Provider Insights into the Impact of Multiple Sclerosis on Mental Health: A Narrative Review.

Authors:  Bryan E Davis; Lynsey Lakin; Cherie C Binns; Keisha M Currie; Mary R Rensel
Journal:  Neurol Ther       Date:  2021-04-20
  8 in total

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