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dc.contributor.advisorLoesnihari, Ricke
dc.contributor.advisorSungkar, Taufik
dc.contributor.authorSasmita, Afrianda Wira
dc.date.accessioned2023-09-21T07:40:17Z
dc.date.available2023-09-21T07:40:17Z
dc.date.issued2023
dc.identifier.urihttps://repositori.usu.ac.id/handle/123456789/87687
dc.description.abstractBackground: Hepatitis B virus (VHB) is the world's leading infectious disease that is still a public health problem and can develop into cirrhosis of the liver. The inflammatory response is one of the mechanisms that play a role in pathogenesis of chronic hepatitis B and liver cirrhosis. Many studies have used elevated levels of Pentraxin 3 as a predictor of the severity in Chronic Hepatitis B patients with or without liver cirrhosis. Method: The design of this study is cross-sectional consecutive sampling. The study population is chronic hepatitis patients with and without liver cirrhosis admitted to Gastroenterohepathology department of RSUP H. Adam Malik Medan. Result: The demographic characteristic of the study is dominated by male in the two study groups. This study found a significant difference between the mean value of Pentraxin 3 in Hepatitis B chronic patient with liver cirrhosis group compared to the group without liver cirrhosis (p<0,001). Conclusion: There is a significant difference between the level of Pentraxin 3 in Hepatitis B Chronic patient with liver cirrhosis compared to Hepatitis B Chronic patient without liver cirrhosis group (p<0,001) in which the level of Pentraxin 3 in Hepatitis B Chronic with liver cirrhosis group is higher compared to group without liver cirrhosis. Therefore the level of Pentraxin 3 can be used as an alternative marker to assess the progression of liver cirrhosis in Hepatitis B Chronic patients.en_US
dc.language.isoiden_US
dc.publisherUniversitas Sumatera Utaraen_US
dc.subjectPentraxin 3en_US
dc.subjectHepatitis B Chronicen_US
dc.subjectLiver cirrhosisen_US
dc.subjectSDGsen_US
dc.titlePerbedaan Kadar Pentraxin 3 pada Pasien Hepatitis B Kronik dengan Sirosis dan Tanpa Sirosisen_US
dc.typeThesisen_US
dc.identifier.nimNIM197111001
dc.identifier.nidnNIDN0025086107
dc.identifier.nidnNIDN0017107901
dc.identifier.kodeprodiKODEPRODI11719#Ilmu Patologi Klinik
dc.description.pages104 Halamanen_US
dc.description.typeTesis Magisteren_US


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