Literature DB >> 23097303

Need for online information and support of patients with systemic sclerosis.

Rosalie van der Vaart1, Han Repping-Wuts, Constance H C Drossaert, Erik Taal, Hanneke K A Knaapen-Hans, Mart A F J van de Laar.   

Abstract

OBJECTIVE: Interactive health communication applications (IHCAs) offer interesting possibilities to support systemic sclerosis (SSc) patients, since SSc is an uncommon, severe disease that needs a multidisciplinary treatment. This study aimed to investigate patients' needs for a hospital-based IHCA.
METHODS: A survey study was conducted among a large sample (n = 429) of SSc patients of the University Medical Centre St. Radboud in Nijmegen, The Netherlands. Patients were asked about their current disease-related internet use, their perceived importance of diverse information topics, and their usefulness of 8 widely used online health services. To examine how disease specific their needs were, the results of SSc patients were compared with the results of a sample of rheumatoid arthritis (RA) patients (n = 1,284).
RESULTS: In total, 746 patients (44% of the approached patients) returned a completed questionnaire and fulfilled all of the inclusion criteria. Of them, 569 (76%) had internet access. SSc patients used the internet especially for information (85%), and they expressed a need for information on physical, psychological, and social consequences of the disease. Concerning a hospital-based IHCA, e-consults, information about disease and treatment, and home access to their electronic medical records were perceived as most useful. SSc patients were more positive about the usefulness of the online applications than were RA patients, especially for e-consults and peer support forums.
CONCLUSION: It would be valuable to offer SSc patients a hospital-based IHCA, including the online information and support they desire. When taking the needs of patients into account, an IHCA could become a valuable addition to their regular treatment.
Copyright © 2013 by the American College of Rheumatology.

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Year:  2013        PMID: 23097303     DOI: 10.1002/acr.21875

Source DB:  PubMed          Journal:  Arthritis Care Res (Hoboken)        ISSN: 2151-464X            Impact factor:   4.794


  9 in total

Review 1.  A comprehensive framework for navigating patient care in systemic sclerosis: A global response to the need for improving the practice of diagnostic and preventive strategies in SSc.

Authors:  Lesley Ann Saketkoo; Tracy Frech; Cecília Varjú; Robyn Domsic; Jessica Farrell; Jessica K Gordon; Carina Mihai; Nora Sandorfi; Lee Shapiro; Janet Poole; Elizabeth R Volkmann; Monika Lammi; Kendra McAnally; Helene Alexanderson; Henrik Pettersson; Faye Hant; Masataka Kuwana; Ami A Shah; Vanessa Smith; Vivien Hsu; Otylia Kowal-Bielecka; Shervin Assassi; Maurizio Cutolo; Cristiane Kayser; Victoria K Shanmugam; Madelon C Vonk; Kim Fligelstone; Nancy Baldwin; Kerri Connolly; Anneliese Ronnow; Beata Toth; Maureen Suave; Sue Farrington; Elana J Bernstein; Leslie J Crofford; László Czirják; Kelly Jensen; Monique Hinchclif; Marie Hudson; Matthew R Lammi; Jennifer Mansour; Nadia D Morgan; Fabian Mendoza; Mandana Nikpour; John Pauling; Gabriela Riemekasten; Anne-Marie Russell; Mary Beth Scholand; Elise Seigart; Tatiana Sofia Rodriguez-Reyna; Laura Hummers; Ulrich Walker; Virginia Steen
Journal:  Best Pract Res Clin Rheumatol       Date:  2021-09-15       Impact factor: 4.991

2.  Patient and healthcare professional eHealth literacy and needs for systemic sclerosis support: a mixed methods study.

Authors:  Agnes Kocher; Michael Simon; Andrew A Dwyer; Catherine Blatter; Jasmina Bogdanovic; Patrizia Künzler-Heule; Peter M Villiger; Diana Dan; Oliver Distler; Ulrich A Walker; Dunja Nicca
Journal:  RMD Open       Date:  2021-09

3.  Health-care utilization in Dutch systemic sclerosis patients.

Authors:  Jessica Meijs; Elisabeth J M Zirkzee; Anne A Schouffoer; Stella M Henquet; Monique A A Caljouw; Theo Stijnen; Tom W J Huizinga; Annemie J M Schuerwegh; Theodora P M Vliet Vlieland
Journal:  Clin Rheumatol       Date:  2013-08-28       Impact factor: 2.980

4.  Randomized Controlled Trial to Evaluate an Internet-Based Self-Management Program in Systemic Sclerosis.

Authors:  Dinesh Khanna; Jennifer Serrano; Veronica J Berrocal; Richard M Silver; Pedro Cuencas; Sharon L Newbill; Josephine Battyany; Cynthia Maxwell; Mary Alore; Laura Dyas; Robert Riggs; Kerri Connolly; Saville Kellner; Jody J Fisher; Erica Bush; Anjali Sachdeva; Luke Evnin; Dennis W Raisch; Janet L Poole
Journal:  Arthritis Care Res (Hoboken)       Date:  2019-02-05       Impact factor: 4.794

5.  How do patients with systemic sclerosis experience currently provided healthcare and how should we measure its quality?

Authors:  Julia Spierings; Cornelia H M van den Ende; Rita M Schriemer; Hein J Bernelot Moens; Egon A van der Bijl; Femke Bonte-Mineur; Marieke P D de Buck; Meeke A E de Kanter; Hanneke K A Knaapen-Hans; Jacob M van Laar; Udo D J Mulder; Judith Potjewijd; Lian A J de Pundert; Thea H M Schoonbrood; Anne A Schouffoer; Alja J Stel; Ward Vercoutere; Alexandre E Voskuyl; Jeska K de Vries-Bouwstra; Madelon C Vonk
Journal:  Rheumatology (Oxford)       Date:  2020-06-01       Impact factor: 7.580

6.  Digital crowdsourcing: unleashing its power in rheumatology.

Authors:  Martin Krusche; Gerd R Burmester; Johannes Knitza
Journal:  Ann Rheum Dis       Date:  2020-06-11       Impact factor: 19.103

7.  The Scleroderma Patient-centered Intervention Network (SPIN) Cohort: protocol for a cohort multiple randomised controlled trial (cmRCT) design to support trials of psychosocial and rehabilitation interventions in a rare disease context.

Authors:  Linda Kwakkenbos; Lisa R Jewett; Murray Baron; Susan J Bartlett; Dan Furst; Karen Gottesman; Dinesh Khanna; Vanessa L Malcarne; Maureen D Mayes; Luc Mouthon; Serge Poiraudeau; Maureen Sauve; Warren R Nielson; Janet L Poole; Shervin Assassi; Isabelle Boutron; Carolyn Ells; Cornelia Hm van den Ende; Marie Hudson; Ann Impens; Annett Körner; Catarina Leite; Angela Costa Maia; Cindy Mendelson; Janet Pope; Russell J Steele; Maria E Suarez-Almazor; Sara Ahmed; Stephanie Coronado-Montoya; Vanessa C Delisle; Shadi Gholizadeh; Yeona Jang; Brooke Levis; Katherine Milette; Sarah D Mills; Ilya Razykov; Rina S Fox; Brett D Thombs
Journal:  BMJ Open       Date:  2013-08-07       Impact factor: 2.692

8.  The educational needs of people with systemic sclerosis: a cross-sectional study using the Dutch version of the Educational Needs Assessment Tool (D-ENAT).

Authors:  Anne Schouffoer; Mwidimi E Ndosi; Thea P M Vliet Vlieland; Jorit J L Meesters
Journal:  Rheumatol Int       Date:  2015-08-31       Impact factor: 2.631

9.  Identifying unmet needs in SSc-ILD by semi-qualitative in-depth interviews.

Authors:  Anna-Maria Hoffmann-Vold; Elisabeth Bendstrup; Theodoros Dimitroulas; Roger Hesselstrand; Antonio Morais; Ritva Peltomaa; Vanessa Smith; Joep Welling; Madelon C Vonk; Wim A Wuyts
Journal:  Rheumatology (Oxford)       Date:  2021-12-01       Impact factor: 7.580

  9 in total

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