A review of respiratory manifestations and their management in Ehlers-Danlos syndromes and hypermobility spectrum disorders

Author:

Chohan Karan1,Mittal Nimish12345,McGillis Laura2,Lopez-Hernandez Laura2,Camacho Encarna26,Rachinsky Maxim2,Mina Daniel Santa245,Reid W Darlene378ORCID,Ryan Clodagh Mai136,Champagne Kateri Agnes9,Orchanian-Cheff Ani10ORCID,Clarke Hance125,Rozenberg Dmitry126ORCID

Affiliation:

1. Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada

2. GoodHope Ehlers Danlos Syndrome Clinic, Toronto General Hospital, Toronto, Ontario, Canada

3. KITE—Toronto Rehab-University Health Network, Toronto, Ontario, Canada

4. Faculty of Kinesiology and Physical Education, University of Toronto, Toronto, Ontario, Canada

5. Department of Anaesthesia and Pain Management, University of Toronto, Toronto, Ontario, Canada

6. Division of Respirology, University Health Network, Toronto, Ontario, Canada

7. Physical Therapy, University of Toronto, Toronto, Ontario, Canada

8. Interdepartmental Division of Critical Care Medicine, University of Toronto, Toronto, Ontario, Canada

9. Sleep Medicine Institute, Town of Mount-Royal, Quebec, Canada

10. Library and Information Services, University Health Network, Toronto, Ontario, Canada

Abstract

Background: Ehlers-Danlos Syndromes (EDS) and Hypermobility Spectrum Disorders (HSD) are a heterogeneous group of heritable genetic connective tissue disorders with multiple characteristics including joint hypermobility, tissue fragility, and multiple organ dysfunction. Respiratory manifestations have been described in EDS patients, but have not been systematically characterized. A narrative review was undertaken to describe the respiratory presentations and management strategies of individuals with EDS and HSD. Methods: A broad literature search of Medline, Embase, Cochrane Database of Systematic Reviews, and Cochrane CENTRAL was undertaken from inception to November 2020 of all study types, evaluating EDS/ HSD and pulmonary conditions. This narrative review was limited to adult patients and publications in English. Results: Respiratory manifestations have generally been described in hypermobile EDS (hEDS), classical and vascular EDS subtypes. Depending on EDS subtype, they may include but are not limited to dyspnea, dysphonia, asthma, sleep apnea, and reduced respiratory muscle function, with hemothorax and pneumothorax often observed with vascular EDS. Respiratory manifestations in HSD have been less frequently characterized in the literature, but exertional dyspnea is the more common symptom described. Respiratory symptoms in EDS can have an adverse impact on quality of life. The respiratory management of EDS patients has followed standard approaches with thoracotomy tubes and pleurodesis for pleural manifestations, vocal cord strengthening exercises, continuous positive pressure support for sleep apnea, and exercise training. Reduced respiratory muscle function in hEDS patients responds to inspiratory muscle training. Conclusion: Respiratory symptoms and manifestations are described in EDS and HSD, and have generally been managed using conservative non-surgical strategies. Research into the prevalence, incidence and specific respiratory management strategies in EDS and HSD is needed to mitigate some of the associated morbidity.

Funder

GoodHope Ehlers-Danlos Syndrome Foundation Grant

Publisher

SAGE Publications

Subject

Pulmonary and Respiratory Medicine

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