Literature DB >> 26420568

Work participation in adults with Marfan syndrome: Demographic characteristics, MFS related health symptoms, chronic pain, and fatigue.

Gry Velvin1,2, Trine Bathen1, Svend Rand-Hendriksen1,3, Amy Østertun Geirdal2.   

Abstract

Marfan syndrome (MFS) is a severe autosomal dominant connective tissue disorder that might influence peoples work ability. This cross sectional study aims to investigate work participation in adults with verified MFS diagnosis and to explore how the health related consequences of MFS and other factors might influence work participation. The prevalence of health problems in young adults compared to older adults with MFS was examined in association to work participation. A postal questionnaire including questions about work participation, demographic characteristics, MFS related health problems, chronic pain, and fatigue was sent to 117 adults with verified MFS (Ghent 1), and 62% answered. Fifty-nine percent were employed or students, significantly lower work participation than the General Norwegian Population (GNP), but higher than the Norwegian population of people with disability. Most young adults worked full-time despite extensive health problems, but the average age for leaving work was low. Few had received any work adaptations prior to retiring from work. In multiple logistic regression analysis, only age, lower educational level and severe fatigue were significantly associated with low work participation; not MFS related health problems or chronic pain. Fatigue appears to be the most challenging health problem to deal with in work, but the covariance is complex. Focus on vocational guidance early in life, more appropriate work adaptations, and psychosocial support might improve the possibility for sustaining in work for adults with MFS. More research about work challenges in adults with MFS is needed.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  Marfan related health problems; c; demographic characteristics; fatigue; hronic pain; work participation

Mesh:

Year:  2015        PMID: 26420568     DOI: 10.1002/ajmg.a.37370

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  11 in total

1.  Genetic diagnostics of inherited aortic diseases : Medical strategy analysis.

Authors:  Y von Kodolitsch; K Kutsche
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2.  Satisfaction with life in adults with Marfan syndrome (MFS): associations with health-related consequences of MFS, pain, fatigue, and demographic factors.

Authors:  Gry Velvin; Trine Bathen; Svend Rand-Hendriksen; Amy Østertun Geirdal
Journal:  Qual Life Res       Date:  2016-01-04       Impact factor: 4.147

Review 3.  A Review of Psychosocial Factors of Marfan Syndrome: Adolescents, Adults, Families, and Providers.

Authors:  Cory Nielsen; Ileana Ratiu; Mitra Esfandiarei; Angela Chen; Elif Seda Selamet Tierney
Journal:  J Pediatr Genet       Date:  2019-07-25

4.  Characterization of pain, disability, and psychological burden in Marfan syndrome.

Authors:  Traci J Speed; Vani A Mathur; Matthew Hand; Bryt Christensen; Paul D Sponseller; Kayode A Williams; Claudia M Campbell
Journal:  Am J Med Genet A       Date:  2016-11-14       Impact factor: 2.802

5.  Health-Related Quality of Life in Children and Young Adults with Marfan Syndrome.

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Journal:  J Pediatr       Date:  2018-09-27       Impact factor: 4.406

6.  Chronic pain and fatigue in adults with congenital unilateral upper limb deficiency in Norway. A cross-sectional study.

Authors:  Heidi Johansen; Trine Bathen; Liv Øinæs Andersen; Svend Rand-Hendriksen; Kristin Østlie
Journal:  PLoS One       Date:  2018-01-03       Impact factor: 3.240

7.  Education and work participation among adults with congenital unilateral upper limb deficiency in Norway: A cross-sectional study.

Authors:  Heidi Johansen; Trine Bathen; Liv Øinæs Andersen; Svend Rand-Hendriksen; Kristin Østlie
Journal:  PLoS One       Date:  2018-12-12       Impact factor: 3.240

8.  Marfan syndrome in childhood: parents' perspectives of the impact on daily functioning of children, parents and family; a qualitative study.

Authors:  Jessica Warnink-Kavelaars; Anita Beelen; Sarah Dekker; Frans Nollet; Leonie A Menke; Raoul H H Engelbert
Journal:  BMC Pediatr       Date:  2019-07-29       Impact factor: 2.125

9.  Parenting a child with Marfan syndrome: Distress and everyday problems.

Authors:  Jessica Warnink-Kavelaars; Hedy A van Oers; Lotte Haverman; Annemieke I Buizer; Mattijs W Alsem; Raoul H H Engelbert; Leonie A Menke
Journal:  Am J Med Genet A       Date:  2020-10-09       Impact factor: 2.802

10.  Marfan syndrome in adolescence: adolescents' perspectives on (physical) functioning, disability, contextual factors and support needs.

Authors:  Jessica Warnink-Kavelaars; Anita Beelen; Tine M H J Goedhart; Lisanne E de Koning; Frans Nollet; Mattijs W Alsem; Leonie A Menke; Raoul H H Engelbert
Journal:  Eur J Pediatr       Date:  2019-10-16       Impact factor: 3.183

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