Literature DB >> 27931023

Increased Need for Gastrointestinal Surgery and Increased Risk of Surgery-Related Complications in Patients with Ehlers-Danlos Syndrome: A Systematic Review.

Marie-Louise Kulas Søborg1, Julie Leganger, Jacob Rosenberg, Jakob Burcharth.   

Abstract

BACKGROUND/AIMS: Ehlers-Danlos syndromes (EDSs) constitute a rare group of inherited connective tissue diseases, characterized by multisystemic manifestations and general tissue fragility. Most severe complications include vascular and gastrointestinal (GI) emergencies requiring acute surgery. The purpose of this systematic review was to assess the causes of GI-related surgery and related mortality and morbidity in patients with EDSs.
METHODS: A systematic search was conducted in PubMed, Embase, and Scopus to identify relevant studies. Preferred Reporting Items for Systematic Reviews and Meta-Analysis guidelines for systematic reviews were followed. According to eligibility criteria, data were extracted and systematically screened by 2 authors.
RESULTS: Screening process identified 11 studies with a total of 1,567 patients. Findings indicated that patients with EDSs had a higher occurrence of surgery demanding GI manifestations, including perforation, hemorrhage, rupture of intra-abdominal organs, and rectal prolapse. Most affected was the vascular subtype, of which up to 33% underwent GI surgery and suffered from a lowered average life expectancy of 48 years (range 6-78). Secondary complications of surgery were common in all patients with EDSs.
CONCLUSION: Studies suggested that patients with EDSs present an increased need for GI surgery, but also an increased risk of surgery-related complications, most predominantly seen in the vascular subtype.
© 2016 S. Karger AG, Basel.

Entities:  

Mesh:

Year:  2016        PMID: 27931023     DOI: 10.1159/000449106

Source DB:  PubMed          Journal:  Dig Surg        ISSN: 0253-4886            Impact factor:   2.588


  6 in total

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Authors:  Stephen Kucera; Stephen N Sullivan
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2.  Ehlers-Danlos syndromes: state of the art on clinical practice guidelines.

Authors:  Alberto Sulli; Rosaria Talarico; Carlo Alberto Scirè; Tadej Avcin; Marco Castori; Alessandro Ferraris; Charissa Frank; Jürgen Grunert; Sabrina Paolino; Stefano Bombardieri; Matthias Schneider; Vanessa Smith; Maurizio Cutolo; Marta Mosca; Fransiska Malfait
Journal:  RMD Open       Date:  2018-10-18

3.  Diagnosed prevalence of Ehlers-Danlos syndrome and hypermobility spectrum disorder in Wales, UK: a national electronic cohort study and case-control comparison.

Authors:  Joanne C Demmler; Mark D Atkinson; Emma J Reinhold; Ernest Choy; Ronan A Lyons; Sinead T Brophy
Journal:  BMJ Open       Date:  2019-11-04       Impact factor: 2.692

Review 4.  Ehlers-Danlos Syndrome: Immunologic contrasts and connective tissue comparisons.

Authors:  Mareesa Islam; Christopher Chang; M Eric Gershwin
Journal:  J Transl Autoimmun       Date:  2020-12-20

5.  Laparoscopic sacral hysteropexy for pelvic organ prolapse in a patient affected by marfan syndrome: a case report.

Authors:  G Campagna; L Vacca; D Caramazza; G Panico; S Mastrovito; G Scambia; A Ercoli
Journal:  Facts Views Vis Obgyn       Date:  2021-12

6.  Enteroatmospheric fistula repair in Ehlers-Danlos syndrome type IV: a novel management technique using ABRA device.

Authors:  Omar Zubair; Kellee Slater
Journal:  BMJ Case Rep       Date:  2020-09-23
  6 in total

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