Literature DB >> 20858692

An information aid for newly diagnosed multiple sclerosis patients improves disease knowledge and satisfaction with care.

A Solari1, V Martinelli, M Trojano, A Lugaresi, F Granella, A Giordano, M Messmer Uccelli, R D'Alessandro, E Pucci, P Confalonieri, C Borreani.   

Abstract

BACKGROUND: Patients report information deficits in the period surrounding diagnosis of multiple sclerosis (MS). We assessed the effectiveness of an add-on information aid for newly diagnosed MS patients.
METHODS: We randomly assigned 120 newly diagnosed MS patients from five Italian centres to diagnosis disclosure (current practice at the centre) or current practice plus information aid (ISRCTN81072971). The information aid consisted of a personal interview with a physician using a navigable compact disc and a take-home booklet. The primary composite endpoint was score in the highest tertile of MS knowledge and satisfaction with care questionnaires. Other endpoints were safety; treatment adherence; extra contacts/consultations; switching of care centre; and changes in Hospital Anxiety and Depression Scale and Control Preference Scale scores.
RESULTS: At 1 month, 30/60 intervention and 8/60 control patients achieved the primary endpoint (odds ratio [OR] 6.5, 95% CI 2.6-16.0; p < 0.001; number needed to treat [NNT] 3). Figures at 6 months were 26/60 intervention and 11/60 control patients (OR 3.4, 95% CI 1.5-7.8; p = 0.04; NNT 4). There were no adverse events. No significant treatment effects were seen on secondary outcomes.
CONCLUSION: The information aid was safe and significantly associated with attainment of the primary outcome at 1 and 6 months.

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Mesh:

Year:  2010        PMID: 20858692     DOI: 10.1177/1352458510380417

Source DB:  PubMed          Journal:  Mult Scler        ISSN: 1352-4585            Impact factor:   6.312


  23 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.  Experience of an information aid for newly diagnosed multiple sclerosis patients: a qualitative study on the SIMS-Trial.

Authors:  Claudia Borreani; Andrea Giordano; Monica Falautano; Alessandra Lugaresi; Vittorio Martinelli; Franco Granella; Carla Tortorella; Imma Plasmati; Marta Radaelli; Deborah Farina; Eleonora Dalla Bella; Elisabetta Bianchi; Nicola Acquarone; Guido Miccinesi; Alessandra Solari
Journal:  Health Expect       Date:  2011-11-01       Impact factor: 3.377

3.  Factors influencing patient satisfaction with the first diagnostic consultation in multiple sclerosis: a Swiss Multiple Sclerosis Registry (SMSR) study.

Authors:  Christian Philipp Kamm; L Barin; C Gobbi; C Pot; P Calabrese; A Salmen; L Achtnichts; J Kesselring; M A Puhan; V von Wyl
Journal:  J Neurol       Date:  2019-10-08       Impact factor: 4.849

4.  Development of a scale for the evaluation of the quality of the shared decision process in multiple sclerosis patients.

Authors:  Elena Álvarez-Rodríguez; César Manuel Sánchez-Franco; María José Pérez-Haro; Laura Bello-Otero; Marta Aguado-Valcarcel; Inés González-Suárez
Journal:  PLoS One       Date:  2022-05-13       Impact factor: 3.752

5.  "I Will Respect the Autonomy of My Patient": A Scoping Review of Shared Decision Making in Multiple Sclerosis.

Authors:  Anne Christin Rahn; Alessandra Solari; Heleen Beckerman; Richard Nicholas; David Wilkie; Christoph Heesen; Andrea Giordano
Journal:  Int J MS Care       Date:  2020-12-28

6.  Future MS care: a consensus statement of the MS in the 21st Century Steering Group.

Authors:  Peter Rieckmann; Alexey Boyko; Diego Centonze; Alasdair Coles; Irina Elovaara; Eva Havrdová; Otto Hommes; Jacques Lelorier; Sarah A Morrow; Celia Oreja-Guevara; Nick Rijke; Sven Schippling
Journal:  J Neurol       Date:  2012-08-31       Impact factor: 4.849

7.  Risk-benefit considerations in the treatment of relapsing-remitting multiple sclerosis.

Authors:  Alessandra Lugaresi; Maria di Ioia; Daniela Travaglini; Erika Pietrolongo; Eugenio Pucci; Marco Onofrj
Journal:  Neuropsychiatr Dis Treat       Date:  2013-06-24       Impact factor: 2.570

8.  Improving patient-physician dialog: commentary on the results of the MS Choices survey.

Authors:  Alessandra Lugaresi; Tjalf Ziemssen; Celia Oreja-Guevara; Delyth Thomas; Elisabetta Verdun
Journal:  Patient Prefer Adherence       Date:  2012-02-17       Impact factor: 2.711

9.  Presenting evidence-based health information for people with multiple sclerosis: the IN-DEEP project protocol.

Authors:  Sophie Hill; Graziella Filippini; Anneliese Synnot; Michael Summers; Deirdre Beecher; Cinzia Colombo; Paola Mosconi; Mario A Battaglia; Sue Shapland; Richard H Osborne; Melanie Hawkins
Journal:  BMC Med Inform Decis Mak       Date:  2012-03-16       Impact factor: 2.796

10.  Information provision for people with multiple sclerosis.

Authors:  Sascha Köpke; Alessandra Solari; Anne Rahn; Fary Khan; Christoph Heesen; Andrea Giordano
Journal:  Cochrane Database Syst Rev       Date:  2018-10-14
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