STUDI PENGGUNAAN PROTON PUMP INHIBITOR PADA PASIEN SIROSIS HEPATIK DENGAN HEMATEMESIS MELENA (Penelitian dilakukan di Instalasi Rawat Inap Rumah Sakit Universitas Airlangga Surabaya)
Cirrhosis is a diffuse process characterized by fibrosis and changes in the normal liver structure and leads to improper liver function, thus triggering an increase in hepatic vascular resistance that leads to hematemesis melena. Proton Pump Inhibitor (PPI) is an anti-acid secretory agent to pre...
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Format: | Theses and Dissertations NonPeerReviewed |
Language: | Indonesian Indonesian |
Published: |
2017
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Subjects: | |
Online Access: | http://repository.unair.ac.id/65436/1/FF%20FK%2044-17%20Zak%20s%20Abstrak.pdf http://repository.unair.ac.id/65436/2/FF%20FK%2044-17%20Zak%20s%20Sec.pdf http://repository.unair.ac.id/65436/ http://lib.unair.ac.id |
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Institution: | Universitas Airlangga |
Language: | Indonesian Indonesian |
Summary: | Cirrhosis is a diffuse process characterized by fibrosis and
changes in the normal liver structure and leads to improper liver function,
thus triggering an increase in hepatic vascular resistance that leads to
hematemesis melena. Proton Pump Inhibitor (PPI) is an anti-acid
secretory agent to prevent re-bleeding and may be given as adjunctive
therapy in hepatic cirrhosis patients with hematemesis melena. This
study aimed to examine the characteristics of samples, the profile of PPI
use during inpatient care, and to identify the possibility of Drug Related
Problem (DRP) in hepatic cirrhosis patients with hematemesis melena.
The study had been conducted from January 1, 2014 to December 31,
2016. This study was observational retrospective study which was
analyzed descriptively from April to June 2017 by time limited sampling
method and had been through etic review. Based on the inclusion criteria,
104 hepatic cirrhosis patients were found and there were 39 with
hematemesis melena who was given PPI as therapy. The most widely use
of PPI were intravenous route omeprazole with dose of 1x40mg and
2x40mg (61,54%), oral route of omeprazole with dose of 2x20 mg
(7,69%), intravenous route of pantoprazole with dose of 1x40mg and
2x40mg (5,13%), and intravenous route of lansoprazole with dose of
1x30mg and 2x30mg (48,72%). The DRP was found in 10,26% (n=23)
of patients and it was allegedly occurred because of the interaction
between omeprazole and furosemide. Finally, it was recommended to
perform collaboration between physician and pharmacist to optimize
therapy by preventing drug interaction and monitoring adverse effect in
PPI use. |
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