Oral health in systemic sclerosis: A scoping review

Author:

Gagarine Maria12ORCID,Cañedo-Ayala Mara1,Cook Vanessa1,Discepola Marie-Nicole1ORCID,Guillot Genevieve3,Leader David M45,Lim Mathew AWT6,Yap Tami6,Furst Daniel E7,Gietzen Amy8,Lapointe McKenzie Jo-Ann9,Van Pelt Shelley10,Vidiricaire Louise3,Carrier Marie-Eve1,Krishnan Ankur1,Tao Lydia1,Kwakkenbos Linda111213,Thombs Brett D12141516ORCID

Affiliation:

1. Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC, Canada

2. Department of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, QC, Canada

3. Sclérodermie Québec, Longueuil, QC, Canada

4. Department of Comprehensive Care, School of Dental Medicine, Tufts University, Boston, MA, USA

5. Department of Public Health and Community Medicine, School of Medicine, Tufts University, Boston, MA, USA

6. Melbourne Dental School, University of Melbourne, Carlton, VIC, Australia

7. University of California at Los Angeles, Los Angeles, CA, USA

8. Tristate Chapter, National Scleroderma Foundation, Danvers, MA, USA

9. Scleroderma Manitoba, Oak Bluff, MB, Canada

10. Washington Evergreen Chapter, National Scleroderma Foundation, Danvers, MA, USA

11. Department of Clinical Psychology, Behavioural Science Institute, Radboud University, Nijmegen, The Netherlands

12. Department of IQ Health, Radboud University Medical Center, Nijmegen, The Netherlands

13. Department of Psychiatry, Radboud University Medical Center, Nijmegen, The Netherlands

14. Department of Psychiatry, McGill University, Montreal, QC, Canada

15. Department of Medicine, McGill University, Montreal, QC, Canada

16. Department of Psychology, McGill University, Montreal, QC, Canada

Abstract

Background: Limited research on oral health in systematic sclerosis poses a significant challenge for people with systematic sclerosis and health care professionals. We conducted a scoping review to map existing research on oral health–related quality of life in systematic sclerosis across domains including (1) oral manifestations or symptoms, (2) functional consequences, (3) psychosocial aspects, (4) associated patient factors and (5) self-care and management considerations. Methods: We searched MEDLINE, EMBASE, SCOPUS and CINAHL databases to 10 March 2023 for studies on oral health in people with systematic sclerosis. Study data were mapped into pre-specified domains of oral health–related quality of life, subtopics and types of research and reported in tabular form. Results: Of 1460 unique studies reviewed, 91 were eligible and included in the scoping review; of these, 69 (76%) were published as full-text versions, 72 (79%) were from Europe or North America, and 63 (69%) included ⩽50 participants. Only 1 study had >200 participants (N = 382). By domains, 85 (93%) studies reported aspects of oral manifestations or symptoms, with the most common subtopics being oral opening and mandibular function, sicca, periodontitis and soft tissue changes and pathology; 36 (40%) studies provided information on associated patient factors, 23 (25%) on self-care and management, 19 (21%) on psychosocial aspects and 6 (7%) on functional consequences. No studies related to interventions included >50 participants. Conclusion: Most studies on oral health in systematic sclerosis report on manifestations or symptoms, and there are relatively few studies on other important domains. Most studies have been conducted with small samples. Updated systematic reviews should evaluate the quality of existing evidence in domains where enough studies have been done. Large, well-conducted primary studies are needed to address knowledge gaps across domains, including studies that test approaches for supporting oral self-care, improving routine professional care and addressing major disability-causing manifestations.

Funder

scleroderma society of ontario

Publisher

SAGE Publications

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