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Timing of Endoscopy for Acute Variceal Bleeding in Patients With Cirrhosis

Timing of Endoscopy for Acute Variceal Bleeding in Patients With Cirrhosis (CHESS1905): a Nationwide Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04957875
Enrollment
3300
Registered
2021-07-12
Start date
2019-12-16
Completion date
2020-06-02
Last updated
2023-04-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cirrhosis, Liver, Portal Hypertension, Varice Bleed

Brief summary

Cirrhotic patients with AVB across 34 university medical centers in 30 cities in China from February 2013 to May 2020 who underwent endoscopy within 24 hours were included in this study. Patients were divided into an urgent endoscopy group (endoscopy \<6h after admission) and an early endoscopy group (endoscopy 6-24h after admission). Outcomes included the incidence of 5-day rebleeding, in-hospital mortality, need for intensive care unit (ICU) and the length of hospital stay after the endoscopy management. Multivariable analysis was performed to identify risk factors for rebleeding. A propensity score matching (PSM) analysis was performed to achieve a balance at baseline between the urgent and early groups.

Interventions

DEVICEemergency endoscopic therapy

When cirrhotic patients presented with AVB to the emergency department, emergency physicians consulted gastroenterologists on duty to assess the patient for suitability for endoscopy, usually after initial stabilization. Performance of endoscopy and its timing was at the discretion of the gastroenterologist on call. Therapeutic endoscopy for AVB was performed within 24 hours after consultation by an experienced attending endoscopist, using standard forward-viewing upper gastrointestinal video endoscopes at individual centers. Written informed consent for endoscopy was obtained before each procedure. The standard of care at all hospitals was to administer a vasoactive agent and antibiotics upon the patient's presentation. Packed red blood cells were transfused at the discretion of the attending gastroenterologist.

Sponsors

LanZhou University
CollaboratorOTHER
Beijing Shijitan Hospital, Capital Medical University
CollaboratorOTHER
Beijing 302 Hospital
CollaboratorOTHER
Tianjin Third Central Hospital
CollaboratorOTHER
The Sixth People's Hospital of Shenyang
CollaboratorOTHER
Shanxi Bethune Hospital
CollaboratorOTHER
Linyi People's Hospital
CollaboratorOTHER
Sir Run Run Shaw Hospital
CollaboratorOTHER
Hepatopancreatobiliary Surgery Institute of Gansu Province
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* established diagnosis of cirrhosis (based on liver biopsy or the combination of clinical, biochemical, and imaging findings) * witnessed or reported evidence of gastrointestinal haemorrhage (hematemesis, melenemesis, or hematochezia) * esophageal or gastric varices confirmed endoscopically as the source of bleeding

Exclusion criteria

* severe dysfunction of a major extrahepatic organ (e.g., heart failure, pulmonary disease, and terminal malignancy except hepatocellular carcinoma) * history of endoscopic therapy for varices (ligation or sclerotherapy) within three months * incomplete or missing data

Design outcomes

Primary

MeasureTime frame
the incidence of 5-day rebleeding after emergency endoscopy6 months

Secondary

MeasureTime frame
the in-hospital mortality6 months
need for ICU6 months
the length of hospital stay6 months

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026