Hematemesis On Hepatic Cirrhosis Patients in Area With Limited Facilities
Hematemesis On Hepatic Cirrhosis Patients in Area With Limited Facilities
Hematemesis On Hepatic Cirrhosis Patients in Area With Limited Facilities
CASE REPORT
Article history:
Received 2 May 2018 Esophageal variceal haemorrhage is one of the more dangerous complications of hepatic
Received in revised form 25 May cirrhosis. Initial treatment can determine patient mortality and morbidity. But not all
2018 hospitals have adequate facilities and medicines to handle it. The 53-year-old woman came
with a diagnosis of ascites and hematemesis. At the initial examination found hypotension.
Accepted 29 May 2018
Laboratory results show anemia, thrombocytopenia, and leukocytosis. The next morning
the patient's condition worsened and was transferred to ICU. During the ICU patients
receive 10 lpm oxygen support, cefobactam, pantoprazole, PRC transfusion, and dopamine.
Keywords: Patients begin conscious on the 5th day of treatment. Then the patient started getting
Hematemesis diuretics on day 6 and propranolol on day 9. On day 13 the patient's condition improved
Esophageal varices and the patient was discharged for outpatient treatment. Limitations of the endoscopic tool
Hepatic Cirrhosis cause not every hospital in Indonesia can perform emergency endoscopy for therapy.
However, with rapid and appropriate pharmacological therapy, patients can be helped not
to fall into mortality and prevent recurrent bleeding.
.
Introduction risk of esophageal variceal haemorrhage than patients
with milder liver disease (Child-Pugh A and B)(4).
Esophageal variceal haemorrhage is one of the Approximately 30% or 1/3 of patients with
more dangerous complications of hepatic cirrhosis. In esophageal varices will experience bleeding within 1
hepatic cirrhosis, hepatic architecture changes due to year after diagnosis (5). Mortality within six weeks of
liver cell necrosis become regenerative nodules (1). This bleeding is about 15-20%, ranging from 0% in patients
change causes increased blood flow and resistance in the with grade A children to about 30% of patients with
portal vein. Portal hypertension leads to dilatation of grade C (2). If not in therapy, esophageal varices
blood vessels especially those from the azygos vein, mortality is 20-60%, but if therapy was done then the
which then causes varicose veins in the gastrointestinal mortality decreased to 20% (4).
tract (2). The initial treatment of bleeding in the
Esophageal varices are closely related to the gastrointestinal tract can determine the patient's mortality
severity of hepatic cirrhosis. Approximately 30% of and morbidity, so it should be handled rapidly and
newly diagnosed patients with hepatitis cirrhosis already appropriately. Not all hospitals have adequate facilities
have varicose veins and increase to 90% after 10 years and medicines to deal with, therefore we want to share
(3). Severe liver disease (Child-Pugh C) has a greater case reports of severe hematemesis handling in limited
facilities.
the esophagus or gastric, the choice of therapy may be by endoscopic examination which is the standard standard
ligation or sclerotherapy (7) (figure 2). In this case, the for diagnosis, assessing possible varicose veins and
hospital actually has an endoscope but only as a management based on the underlying disease.
diagnostic tool, so that the patient is considered The limitations of expensive endoscopic devices and
endoscopic after a stable vital condition. rare operator personnel make not every hospital in
Indonesia can perform emergency endoscopes. However,
Table 2. Comparison of mortality risk and re-bleeding with rapid and appropriate pharmacological therapy, it
with combination therapy (9) can help patients not to fall into mortality and prevent
recurrent bleeding.
Management Rebleeding report Mortality report
No 55-67% 23-64% Conflict of Interest
management
Inhibitor ß 37-57% 13-39% The author stated there is no conflict of interest
EIS 34-53% 18-36%
EIS + inhibitor 19-49% 7-26%
ß References
EBL 20-43% 19-34%
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obliteration after 2-4 sessions, then the first surveillance
done 1-3 months after obliteration then every 6-12
months. ISMN is given at an initial dose of 10 mg per
oral per night, increased to a maximum dose of 2 x 20mg
daily or blood pressure> 95mmHg (10)
Summary