The mortality rates from Acute Variceal Haemorrhage remain significant and first line therapy may fail in 15-25% of patients. The self-expandable metal stent has been described in case series as having a very high efficacy at control of haemorrhage from oesophageal varices when used as rescue therapy. This randomised controlled trial aims to assess for any potential superiority of the stent over 'standard' endoscopic techniques as primary or rescue therapy for bleeding oesophageal varices.
Despite improvements in recent years, mortality from variceal bleeding remains significant. The routine use of banding ligation, vasoactive drugs, and antibiotics has had an impact on survival rates such that survival rates of patients with Childs-Pugh A and B class cirrhosis may be as high as 90% at 30 days. However, the successful outcome of variceal bleeding is compromised in some patients because of initial failure to control bleeding or early re-bleeding, both of which have a significant impact on mortality. The SX-Ella Danis stent (Ella-CS, Hradec Kralove, Czech Republic) is a removable, covered, self-expanding mesh-metal stent (SEMS) that can be deployed in the lower oesophagus over an endoscopically placed guidewire without radiological screening. The stent controls bleeding by tamponade of varices in the lower oesophagus. The series reported to date suggest that the self-expandable covered stents can provide 100% haemostasis rates when applied for refractory oesophageal variceal bleeding. Given the potentially lower risks of re-bleeding and safe, easy insertion techniques the self-expandable covered stents may offer a superior alternative to standard endoscopic therapy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
14
A removable stent designed for the treatment of bleeding oesophageal varices.
Standard Medical and Endoscopic Therapy
United Bristol Hospitals NHS Foundation Trust
Bristol, United Kingdom
Barts Health NHS Trust
London, United Kingdom
Royal Free London NHS Foundation Trust
London, United Kingdom
Failure to Control Bleeding
Failure to control Bleeding (as defined by the Baveno V Criteria) or re-bleeding within 7 days.
Time frame: 7 days
Absence of Bleeding at 14 and 42 days
Time frame: 14 and 42 days
Participant Survival
Time frame: 7, 14, 42 days and 6 months
Absence of Stent Migration
for the duration of stent migration
Time frame: 7 days
Requirement for Blood products
Time frame: 7 days
Requirement for Analgesia and Sedation whilst Stent in in situ
Time frame: 7 days
Presence of Thoracic Pain or Dysphagia
Time frame: 7 days
Length of Intensive Care Unit and Total Hospital Stay
Time frame: Total Length of Intensive Care Unit and Hospital Stay (an average of 3 and 10 days respectively)
Requirement for additional endoscopic therapy or salvage therapy (such as TIPS)
Time frame: 7 days
Repeated presentation with variceal bleeding within 6 months
Time frame: 6 months
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