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Peptic ulcer bleeding in patients with or without cirrhosis: different diseases but the same prognosis?
M Rudler1, G Rousseau, H Benosman
1Department of Hepatogastroenterology, La Pitié-Salpêtrière Hospital, Assistance Publique-Hôpitaux de Paris, Pierre et Marie Curie University, France. marika.rudler@psl.aphp.fr
Insights
Peptic ulcer bleeding (PUB) in cirrhotic patients differs in cause, often linked to alcohol and portal hypertension, but shows similar outcomes to non-cirrhotic patients. This study highlights distinct PUB physiopathology in cirrhosis.
Area of Science:
- Gastroenterology
- Hepatology
- Internal Medicine
Background:
- Peptic ulcer bleeding (PUB) is a significant clinical concern.
- The specific physiopathology and prognosis of PUB in patients with cirrhosis remain underexplored.
- Understanding these differences is crucial for patient management.
Purpose of the Study:
- To investigate the risk factors associated with peptic ulcer bleeding (PUB) in patients with and without cirrhosis.
- To compare the clinical outcomes of PUB between cirrhotic and non-cirrhotic patient groups.
- To elucidate the unique characteristics of PUB in the context of liver cirrhosis.
Main Methods:
- Prospective cohort study of 203 patients with PUB admitted to an ICU of Hepatology and Gastroenterology.
- Patients were categorized into two groups: those with cirrhosis (Cirr+) and those without (Cirr-).
- Comparison of aetiologies, clinical characteristics, and outcomes, including re-bleeding, interventions, and mortality.
Main Results:
- Twenty-nine patients had cirrhosis (Cirr+), predominantly due to alcohol (97%).
- Aetiologies of PUB differed significantly: Helicobacter pylori and NSAIDs were less common in Cirr+ patients, while idiopathic PUB was more frequent.
- Outcomes such as re-bleeding, need for embolisation or surgery, and mortality were comparable between Cirr+ and Cirr- groups.
Conclusions:
- Peptic ulcer bleeding in cirrhotic patients appears to have a different physiopathology, often associated with portal hypertension and alcohol consumption.
- Despite differing aetiologies, the prognosis for PUB in cirrhotic patients in this series was similar to that in the general population.
- Further research into the role of portal hypertension and alcohol in cirrhotic PUB is warranted.
Background:
Physiopathology and prognosis of peptic ulcer bleeding (PUB) have never been described in cirrhotic patients.
Aim:
To assess risk factors and outcome of PUB in two groups of patients with PUB with or without cirrhosis.
Methods:
We included prospectively all patients with PUB referred to our ICU of Hepatology and Gastroenterology between January 2008 and March 2011. All patients were treated according to international recommendations. Diagnosis of cirrhosis was based on clinical, biological and morphological exams. Aetiologies, characteristics and outcomes of PUB were compared in cirrhotic vs. noncirrhotic patients.
Results:
A total of 203 patients with PUB were included prospectively. Twenty-nine patients had cirrhosis (group Cirr+), and 174 patients had no cirrhosis (group Cirr-). Demographic data were similar between the two groups except for age and alcohol consumption. Aetiology of cirrhosis was alcohol in 97% of cirrhotic patients. Characteristics of PUB were not different between the two groups. Ninety-three per cent of patients with cirrhosis had endoscopic portal hypertension. Aetiology of PUB was different between the group Cirr+ and Cirr- (Helicobacter pylori = 10.3% vs. 48.8%, P < 0.0001; NSAID's = 17.2% vs. 54.0%, P < 0.0001; idiopathic PUB = 79.3% vs. 23.8%, P < 0.0001). Outcome was comparable concerning re-bleeding (7.0% vs. 6.9%, P = 0.31), need for arterial embolisation (10.3 vs. 8.6%, P = 0.76), need for salvage surgery (0 vs. 1.7%, P = 0.31) and mortality (3.0% vs. 1.1%, P = 0.87).
Conclusions:
Physiopathology of PUB seems to be different in patients with cirrhosis. In cirrhotic patients, PUB occurs almost only in alcoholics. In our series, prognosis was similar to general population. PUB in cirrhosis might be related to portal hypertension and/or alcohol.
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