Literature DB >> 30705970

Patient-reported outcome instruments for assessing Raynaud's phenomenon in systemic sclerosis: A SCTC Vascular Working Group Report.

John D Pauling1,2, Tracy M Frech3, Michael Hughes4, Jessica K Gordon5, Robyn T Domsic6, Marina E Anderson7, Francesca Ingegnoli8, Neil J McHugh1,2, Sindhu R Johnson9, Marie Hudson10, Francesco Boin11, Voon H Ong12, Marco Matucci-Cerinic13, Nezam Altorok14, Marina Scolnik15, Mandana Nikpour16, Ankoor Shah17, Janet E Pope18, Dinesh Khanna19, Ariane L Herrick4,20.   

Abstract

The episodic nature of Raynaud's phenomenon (RP) in systemic sclerosis (SSc) has led to a reliance on patient-reported outcome (PRO) instruments such as the Raynaud's Condition Score (RCS) diary. Little is known about the utilisation in routine clinical practice and health professional attitudes towards existing PRO instruments for assessing SSc-RP. Members of the Scleroderma Clinical Trials Consortium Vascular Working Group (SCTC-VWG, n=28) were invited to participate in a survey gauging attitudes towards the RCS diary and the perceived need for novel PRO instruments for assessing SSc-RP. Nineteen SCTC-VWG members (68% response rate) from academic units based in North America (n=9), Europe (n=8), South America (n=1) and Australasia (n=1) took part in the survey. There was broad consensus that RCS diary returns could be influenced by factors including seasonal variation in weather, efforts made by patients to avoid or ameliorate attacks of RP, habituation to RP symptoms, evolution of RP symptom characteristics with progressive obliterative microangiopathy, patient coping strategies, respondent burden and placebo effect. There was consensus that limitations of the RCS diary might be a barrier to drug development (79% of respondents agree/strongly agree) and that a novel PRO instrument for assessing SSc-RP should be developed with the input of both clinicians and patients (84% agree/strongly agree). Perceived potential limitations of the RCS diary have been identified along with concerns that such factors might impede drug development programs for SSc-RP. There is support within the systemic sclerosis community for the development of a novel PRO instrument for assessing SSc-RP.

Entities:  

Keywords:  Patient Reported Outcomes; Raynaud’s Phenomenon; Scleroderma; Survey; Systemic Sclerosis

Year:  2018        PMID: 30705970      PMCID: PMC6350902          DOI: 10.1177/2397198318774307

Source DB:  PubMed          Journal:  J Scleroderma Relat Disord        ISSN: 2397-1983


  10 in total

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Authors:  Janet Pope; Sarah Harding; Sarit Khimdas; Ashley Bonner; Murray Baron
Journal:  J Rheumatol       Date:  2012-01-15       Impact factor: 4.666

6.  Frequency and impact of symptoms experienced by patients with systemic sclerosis: results from a Canadian National Survey.

Authors:  Marielle Bassel; Marie Hudson; Suzanne S Taillefer; Orit Schieir; Murray Baron; Brett D Thombs
Journal:  Rheumatology (Oxford)       Date:  2010-12-11       Impact factor: 7.580

Review 7.  Evidence that the strategy is more important than the agent to treat rheumatoid arthritis. Data from clinical trials of combinations of non-biologic DMARDs, with protocol-driven intensification of therapy for tight control or treat-to-target.

Authors:  Theodore Pincus; Isabel Castrejón
Journal:  Bull Hosp Jt Dis (2013)       Date:  2013

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Journal:  Br J Rheumatol       Date:  1998-09

10.  Vasoactive Therapy in Systemic Sclerosis: Real-life Therapeutic Practice in More Than 3000 Patients.

Authors:  Pia Moinzadeh; Gabriela Riemekasten; Elise Siegert; Gerhard Fierlbeck; Joerg Henes; Norbert Blank; Inga Melchers; Ulf Mueller-Ladner; Marc Frerix; Alexander Kreuter; Christian Tigges; Nina Lahner; Laura Susok; Claudia Guenther; Gabriele Zeidler; Christiane Pfeiffer; Margitta Worm; Sigrid Karrer; Elisabeth Aberer; Agnes Bretterklieber; Ekkehard Genth; Jan C Simon; Joerg H W Distler; Ruediger Hein; Matthias Schneider; Cornelia S Seitz; Claudia Herink; Kerstin Steinbrink; Miklos Sárdy; Rita Varga; Hartwig Mensing; Christian Mensing; Percy Lehmann; Gunther Neeck; Christoph Fiehn; Manfred Weber; Matthias Goebeler; Harald Burkhardt; Michael Buslau; Keihan Ahmadi-Simab; Andrea Himsel; Aaron Juche; Ina Koetter; Annegret Kuhn; Michael Sticherling; Martin Hellmich; Kathrin Kuhr; Thomas Krieg; Jan Ehrchen; Cord Sunderkoetter; Nicolas Hunzelmann
Journal:  J Rheumatol       Date:  2015-11-15       Impact factor: 4.666

  10 in total
  7 in total

Review 1.  Raynaud's phenomenon.

Authors:  Ariane L Herrick
Journal:  J Scleroderma Relat Disord       Date:  2019-02-13

Review 2.  Patient-reported outcome instruments in clinical trials of systemic sclerosis.

Authors:  John D Pauling; Joana Caetano; Corrado Campochiaro; Giacomo De Luca; Ana Maria Gheorghiu; Maria Grazia Lazzaroni; Dinesh Khanna
Journal:  J Scleroderma Relat Disord       Date:  2019-11-25

3.  Raynaud's phenomenon.

Authors:  Ashraful Haque; Michael Hughes
Journal:  Clin Med (Lond)       Date:  2020-11       Impact factor: 2.659

Review 4.  The Relationship between Pulmonary Damage and Peripheral Vascular Manifestations in Systemic Sclerosis Patients.

Authors:  Barbara Ruaro; Marco Confalonieri; Francesco Salton; Barbara Wade; Elisa Baratella; Pietro Geri; Paola Confalonieri; Metka Kodric; Marco Biolo; Cosimo Bruni
Journal:  Pharmaceuticals (Basel)       Date:  2021-04-23

5.  Considerations for a combined index for limited cutaneous systemic sclerosis to support drug development and improve outcomes.

Authors:  Alain Lescoat; Susan L Murphy; David Roofeh; John D Pauling; Michael Hughes; Robert Sandler; François Zimmermann; Rachel Wessel; Whitney Townsend; Lorinda Chung; Christopher P Denton; Peter A Merkel; Virginia Steen; Yannick Allanore; Francesco Del Galdo; Dominique Godard; David Cella; Sue Farrington; Maya H Buch; Dinesh Khanna
Journal:  J Scleroderma Relat Disord       Date:  2020-10-05

6.  Study Protocol: A Randomized Controlled Prospective Single-Center Feasibility Study of Rheopheresis for Raynaud's Syndrome and Digital Ulcers in Systemic Sclerosis (RHEACT Study).

Authors:  Jan-Gerd Rademacher; Björn Tampe; Angela Borisch; Rosa Marie Buschfort; Andrea von Figura; Thomas Asendorf; Peter Korsten
Journal:  Front Med (Lausanne)       Date:  2022-04-14

7.  What narrative devices do people with systemic sclerosis use to describe the experience of pain from digital ulcers: a multicentre focus group study at UK scleroderma centres.

Authors:  Jennifer Jones; Michael Hughes; John Pauling; Rachael Gooberman-Hill; Andrew J Moore
Journal:  BMJ Open       Date:  2020-06-11       Impact factor: 2.692

  7 in total

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