Literature DB >> 32915347

Things left unsaid: important topics that are not discussed between patients with systemic sclerosis, their carers and their healthcare professionals-a discourse analysis.

Christopher P Denton1, Bee Laird2, Lizette Moros3, Jose Luis Luna Flores3.   

Abstract

INTRODUCTION: Systemic sclerosis (SSc) is a rare condition that can be complicated by interstitial lung fibrosis (SSc-ILD)-a major cause of mortality. This study explored information and communication needs of patients with SSc-ILD and their carers to understand what they are and whether they are met.
METHODS: Qualitative research was performed, including in-depth individual interviews and observed conversations between pairs of patients, physicians and nurses, and between patients and physicians discussing experiences of SSc-ILD. The study was performed in Germany, Italy, Spain, the UK and the USA. Participants included 42 SSc-treating physicians, 21 patients with diagnosed SSc-ILD, 16 specialist nurses and five carers.
RESULTS: Prognosis and mortality were the main unspoken topics acknowledged by patients, carers and healthcare professionals. Patients and carers felt afraid to ask physicians about mortality, and most physicians reported avoiding the question because their duty was to give patients hope and avoid causing additional distress. Patients often felt unable to ask physicians about relationships, family and work because of time constraints or because they felt these were not topics physicians would be concerned about. Often, specialist nurses felt that they had insufficient knowledge to provide adequate support.
CONCLUSION: Key topics, including mortality and prognosis, are rarely openly discussed, leaving patients uncertain and anxious about the future. By communicating about difficult but important topics, physicians and nurses could help patients and carers manage and plan their lives. This study shows that a multi-professional team-based communication approach is likely to better address patient needs and priorities. KEY POINTS: • Key topics in SSc or SSc-ILD, such as mortality and prognosis, are rarely openly discussed in clinical consultations. • By communicating difficult but important topics, physicians and nurses could help patients manage their disease and plan their lives. • A multi-professional team-based communication approach is likely to better address patient needs and priorities and could be easily implemented without the need for significant additional resources.

Entities:  

Keywords:  Interstitial lung disease; Interstitial lung fibrosis; Patient–physician communication; Specialist nurse; Systemic sclerosis

Mesh:

Year:  2020        PMID: 32915347      PMCID: PMC7943486          DOI: 10.1007/s10067-020-05371-2

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN: 0770-3198            Impact factor:   2.980


  12 in total

1.  Standards for reporting qualitative research: a synthesis of recommendations.

Authors:  Bridget C O'Brien; Ilene B Harris; Thomas J Beckman; Darcy A Reed; David A Cook
Journal:  Acad Med       Date:  2014-09       Impact factor: 6.893

2.  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

3.  Mortality in systemic sclerosis: an international meta-analysis of individual patient data.

Authors:  John P A Ioannidis; Panayiotis G Vlachoyiannopoulos; Anna-Bettina Haidich; Thomas A Medsger; Mary Lucas; Clement J Michet; Masataka Kuwana; Hidekata Yasuoka; Frank van den Hoogen; Liane Te Boome; Jacob M van Laar; Nicolette L Verbeet; Marco Matucci-Cerinic; Athanasios Georgountzos; Haralampos M Moutsopoulos
Journal:  Am J Med       Date:  2005-01       Impact factor: 4.965

4.  Appearance self-esteem in systemic sclerosis--subjective experience of skin deformity and its relationship with physician-assessed skin involvement, disease status and psychological variables.

Authors:  W G J M van Lankveld; M C Vonk; H Teunissen; F H J van den Hoogen
Journal:  Rheumatology (Oxford)       Date:  2007-02-17       Impact factor: 7.580

5.  Causes and risk factors for death in systemic sclerosis: a study from the EULAR Scleroderma Trials and Research (EUSTAR) database.

Authors:  Anthony J Tyndall; Bettina Bannert; Madelon Vonk; Paolo Airò; Franco Cozzi; Patricia E Carreira; Dominique Farge Bancel; Yannick Allanore; Ulf Müller-Ladner; Oliver Distler; Florenzo Iannone; Raffaele Pellerito; Margarita Pileckyte; Irene Miniati; Lidia Ananieva; Alexandra Balbir Gurman; Nemanja Damjanov; Adelheid Mueller; Gabriele Valentini; Gabriela Riemekasten; Mohammed Tikly; Laura Hummers; Maria J S Henriques; Paola Caramaschi; Agneta Scheja; Blaz Rozman; Evelien Ton; Gábor Kumánovics; Bernard Coleiro; Eva Feierl; Gabriella Szucs; Carlos Alberto Von Mühlen; Valeria Riccieri; Srdan Novak; Carlo Chizzolini; Anna Kotulska; Christopher Denton; Paulo C Coelho; Ina Kötter; Ismail Simsek; Paloma García de la Pena Lefebvre; Eric Hachulla; James R Seibold; Simona Rednic; Jirí Stork; Jadranka Morovic-Vergles; Ulrich A Walker
Journal:  Ann Rheum Dis       Date:  2010-06-15       Impact factor: 19.103

6.  Prevalence, incidence, survival, and disease characteristics of systemic sclerosis in a large US population.

Authors:  Maureen D Mayes; James V Lacey; Jennifer Beebe-Dimmer; Brenda W Gillespie; Brenda Cooper; Timothy J Laing; David Schottenfeld
Journal:  Arthritis Rheum       Date:  2003-08

7.  Needs and preferences regarding health care delivery as perceived by patients with systemic sclerosis.

Authors:  Anne A Schouffoer; Elisabeth J M Zirkzee; Stella M Henquet; Monique A A Caljouw; Gerda M Steup-Beekman; Jacob M van Laar; Theodora P M Vliet Vlieland
Journal:  Clin Rheumatol       Date:  2011-01-18       Impact factor: 2.980

8.  Illness representations of systemic lupus erythematosus and systemic sclerosis: a comparison of patients, their rheumatologists and their general practitioners.

Authors:  Seher Arat; Jan L Lenaerts; Ellen De Langhe; Patrick Verschueren; Philip Moons; Joris Vandenberghe; Veerle Taelman; Rene Westhovens
Journal:  Lupus Sci Med       Date:  2017-11-14

9.  Patients' views and needs about systemic sclerosis and its management: a qualitative interview study.

Authors:  Luc Mouthon; Sophie Alami; Anne-Sophie Boisard; Benjamin Chaigne; Eric Hachulla; Serge Poiraudeau
Journal:  BMC Musculoskelet Disord       Date:  2017-05-30       Impact factor: 2.362

Review 10.  Unmet Needs in Systemic Sclerosis Understanding and Treatment: the Knowledge Gaps from a Scientist's, Clinician's, and Patient's Perspective.

Authors:  Marta Cossu; Lorenzo Beretta; Petra Mosterman; Maria J H de Hair; Timothy R D J Radstake
Journal:  Clin Rev Allergy Immunol       Date:  2018-12       Impact factor: 8.667

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  2 in total

Review 1.  The Role of the Multidisciplinary Health Care Team in the Management of Patients with Systemic Sclerosis.

Authors:  Nicola Farina; Giovanni Benanti; Giacomo De Luca; Anna Palmisano; Giovanni Peretto; Sara Tomassetti; Veronica Giorgione; Ornella Forma; Antonio Esposito; Silvio Danese; Lorenzo Dagna; Marco Matucci-Cerinic; Corrado Campochiaro
Journal:  J Multidiscip Healthc       Date:  2022-04-20

2.  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

  2 in total

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