Elsevier

Journal of Hepatology

Volume 57, Issue 6, December 2012, Pages 1207-1213
Journal of Hepatology

Research Article
Delayed endoscopy increases re-bleeding and mortality in patients with hematemesis and active esophageal variceal bleeding: A cohort study

https://doi.org/10.1016/j.jhep.2012.07.038Get rights and content

Background & Aims

Active bleeding is a poor prognostic indicator in patients with acute esophageal variceal bleeding. This study aimed at determining indicators of 6-week re-bleeding and mortality in patients with “active” esophageal variceal bleeding, particularly emphasizing the presenting symptoms and timing of endoscopy to define the treatment strategy.

Methods

From July 2005 to December 2009, cirrhotic patients with endoscopy-proven active esophageal variceal bleeding were evaluated. Cox proportional hazards regression analysis was used to determine the indicators of 6-week re-bleeding and mortality. Outcome comparisons were performed by Kaplan–Meier method and log rank test.

Results

In 101 patients, the overall 6-week and 3-month re-bleeding rates were 25.7% (n = 26) and 29.7% (n = 30), respectively. The overall 6-week and 3-month mortality was 31.7% (n = 32) and 38.6% (n = 39), respectively. Door-to-endoscopy time (hr), MELD score, and portal vein thrombosis were indicators of 6-week re-bleeding, while hematemesis upon arrival, MELD score, and hepatocellular carcinoma were indicators of 6-week mortality. Overall mortality was poorer in hematemesis than in non-hematemesis patients (39.7% vs. 10.7%, p = 0.007). In hematemesis patients, 6-week re-bleeding rate (18.9% vs. 38.9%, p = 0.028) and mortality (27% vs. 52.8%, p = 0.031) were lower in those with early (⩽12 h) than delayed (>12 h) endoscopy. In non-hematemesis patients, early and delayed endoscopy had no difference on 6-week re-bleeding rate (17.6% vs. 18.2%, p = 0.944) and mortality (11.8% vs. 9.1%, p = 0.861).

Conclusions

It is likely that early endoscopy (⩽12 h) is associated with a better outcome in hematemesis patients, but a randomized trial with larger case numbers is required before making a firm conclusion.

Introduction

Esophageal variceal bleeding (EVB) is one of the most life-threatening complications of liver cirrhosis [1], [2]. Despite advances in management and therapy, mortality with each episode of EVB is still about 20–25% [3], [4]. Several prognostic indicators, including the Child-Turcotte-Pugh (CTP) score, the model for end-stage liver disease (MELD) score, active bleeding at endoscopy, hypovolemic shock, hepatic venous pressure gradient, hepatocellular carcinoma (HCC), portal vein thrombosis, serum bilirubin, and creatinine and albumin levels, have been identified to predict mortality after EVB [5], [6], [7], [8]. However, most risk factors are derived from studies without fulfilling the recent standard therapeutic protocol of prophylactic antibiotics and combination vasoactive agents, endoscopic ligation and subsequent non-selective beta-blocker for secondary prevention.

Active bleeding, either spurting or oozing from esophageal varices at endoscopy, occurs in 10–68% of EVB patients [9], [10], [11], [12], [13], and is persistently identified as an important predictor of failure to control bleeding, early re-bleeding, and mortality [4], [5], [14], [15], [16]. However, further assessment of the prognostic indicators in such high-risk patients is not determined.

The optimal timing of endoscopic treatment for EVB patients is empirical. Current guidelines of major professional societies recommend that endoscopy should be performed as soon as possible (within 12 h of admission) in cirrhotic patients with EVB, but the suggestion is based on expert opinion and requires corroborating evidence [2].

The aim of this study is to determine the prognostic indicators of 6-week re-bleeding and mortality in patients with “active” EVB on current standard treatment, with particular emphasis on presenting symptoms and timing of endoscopy.

Section snippets

Patients

From July 2005 to December 2009, cirrhotic patients who presented at our hospital with suspected EVB were referred to the portal hypertension team of our hospital. If active EVB was proven by endoscopy, the patient was invited to enter the cohort. The exclusion criteria were (1) age <18 years; (2) terminal illness of a major organ (e.g., severe heart failure, chronic obstructive pulmonary disease, and malignancy except HCC); and (3) treatment of acute variceal bleeding (i.e., vasoactive agents

Patient characteristics

There were 528 patients admitted due to EVB who were screened for eligibility but only 121 (23%) presented with active EVB at endoscopy. Among them, 20 were excluded for the following reasons: loss to follow-up within three months after EVB (n = 9), without regular EVL (n = 5), and with terminal systemic disease or non-hepatic malignancy (n = 6). The remaining 101 cirrhotic patients with active EVB were included. Their mean age was 57 years and their most common etiology for cirrhosis was viral

Discussion

Variceal bleeding is the most severe complication of liver cirrhosis. Several prognostic indicators have been identified to predict re-bleeding and mortality after EVB [5], [6], [7], [8]. Active spurting or oozing during endoscopy is an indicator of failure to control bleeding, early re-bleeding, and mortality [4], [5], [14], [15], [16]. However, not all patients with active variceal bleeding will have re-bleeding or early mortality. Thus, it is very important to identify the risk factors in

Financial support

This work was supported in part by a grant (NSC 99–2314-B-010–049-MY3) from National Science Council, Republic of China.

Conflict of interest

The authors who have taken part in this study declared that they do not have anything to disclose regarding funding or conflict of interest with respect to this manuscript.

Acknowledgements

We wish to thank Ms. Pui-Ching Lee and Yi-Chian Chiang for preparing the manuscript.

References (24)

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    Citation Excerpt :

    Six-week mortality has been reported to be around 10% to 30% [24–26] and our overall 6-week mortality was 20%. Although our study was not designed to compare the outcomes of patients according to the compliance with the recommendations, results of controlled trials have shown that the compliance with these recommendations improves the outcome, namely rebleeding and 6-week mortality [6,25,27–30]. In our population, no significant differences were obtained between the two studied populations concerning rebleeding rates.

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These authors contributed equally to this work.

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