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Infection & Tropical Diseases

                                               O-ITD-005
                         Free Radical (Malondialdehyde) as A Shock Biomarker
                                    in Dengue Hemorrhagic Fever

                                     Ira Megasari, Husein Albar, Dasril Daud
              Department of Child Health, Faculty of Medicine, Universitas Hasanuddin, Makassar, South Sulawesi, Indonesia

                                               Abstract
            Background Although there have been many advances in management of DHF, the morbidity and
            mortality rates are still high. Until now, there is no biomarker that can predict the occurance of DHF/DSS.
            Objective To compare the levels of malondialdehyde in DHF and DSS and assess MDA levels that can be
            used as biomarkers of shock. Methods This cross-sectional study was conducted in Makassar, from April
            2019 to February 2020. Serum malondialdehyde was collected in 73 patients with clinical diagnosis of DHF
            and DSS (age range: 1 month to 18 years) who met the inclusion and exclusion criteria. Data was analyzed
            using SPSS. Results 73 patients were enrolled, consisting of 56 DHF and 17 DSS. There were no significant
            differences based on gender, nutritional status, and age between the  groups. The average MDA levels in
            both groups were increased whether the higher level of MDA was found in DSS group with P=0.003. The
            cutt-off point of MDA level < 2.18 nmol / ml has a diagnostic value to show that shock not yet occur with
            negative predictive value 86.4%, OR 0.258 95%CI 0.08 to 08.  Conclusion In this study, MDA values
            < 2.18 nmol/mL may be used as biomarker that shock has not occured in DHF.
                           Keywords: malondialdehyd;, dengue hemorrhagic fever; biomarker; shock


                                               O-ITD-006
                      The Prevalence of Viral Hepatitis after Multiple Transfusions
               in Children with Thalassemia at Dr. Mohammad Hoesin Hospital Palembang

                                  Enggrajati Silitonga, Yulia Iriani, Ariesti Kamila
               Department of Child Health, Faculty of Medicine, Universitas Sriwijaya/Mohammad Hoesin General Hospital,
                                      Palembang, South Sumatera, Indonesia
                                               Abstract
            Background Transfusion-dependent conditions such as thalassemia are at risk of viral hepatitis B (VHB)
            and C (VHC) infection. The prevalence of post-transfusion viral hepatitis was influenced by vaccination
            coverage and health facilities.  Objective To determine the prevalence and risk factors of VHC and VHB in
            thalassemia patients at Dr Mohammad Hoesin Hospital (RSMH). Methods It was a cross-sectional study.
            Data were obtained from pediatric inpatient and outpatient medical records at RSMH from June 2018 to
            June 2021. Hepatitis C virus (HCV) infection was screened by anti-HCV test and confirmed by PCR RNA
            HCV. Risk factors were analyzed with X2 test. Results There were 184 thalassemia patients; 57.8% were
            boys, and the median age was 8 (range 1-17) years old. The HCV seroprevalence was 36/184 (19.5%),
            80.5% with positive HCV RNA. The interval between diagnosis of VHC and thalassemia was 77.67 (range
            5-134) months. 30/36 (83,5%) seropositive subjects were asymptomatic. Viral hepatitis B occurred in 8/184
            (4.9%). The interval between diagnosis of VHB and thalassemia was 77.12 (range 56-96) months. Eight
            VHB patients also HCV seropositive. Patients suffered from post-transfusion viral hepatitis showed a higher
            number of multiple transfusions (OR 3.427; 95%CI 0.77 to 15.19; P=0.087). Conclusion The total prevalence
            of viral hepatitis with multiple blood transfusions is 19.5 %. There is a significant association between viral
            hepatitis with multiple transfusions.
                               Keywords: viral hepatitis; multiple transfusion; thalassemia










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