Page 105 - Abstract Book KONIKA 18
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Allergy Immunology

                                               P-AI-005
              Clinical Characteristic of Juvenile Idiopathic Arthritis in Dr. Soetomo Hospital
                                              Surabaya

                         Diah Budiarti, Azaria Amelia Adam, Ratih Kumala Sari, Zahrah Hikmah,
                                 Azwin Mengindera Putera Lubis, Anang Endryanto
              Department of Child Health. Faculty of Medicine Universitas Airlangga/Dr. Soetomo General Academic Hospital,
                                         Surabaya, East Java, Indonesia

                                               Abstract
            Background Juvenile idiopathic arthritis (JIA) is a common chronic rheumatic disease that limits the daily
            activities and productivity of the patient. By definition, disease onset prior to the age of 16 years and arthritis
            persisting for longer than 6 weeks are required criteria for diagnosis of JIA. Objective To determine the
            clinical characteristics of children with JIA at a tertiary health care center in Surabaya, Indonesia Methods A
            retrospective study was conducted in the pediatric Allergy and Immunology outpatient clinic of Dr. Soetomo
            General Hospital, Surabaya to identify patients with a diagnosis of JIA according to ILAR criteria, between
            year 2014 and 2019. Results A total of 27 children with JIA were included in this study. JIA was found 52%
            in girl and 48% in boy. The median age of disease onset was 8 years. Polyarticular was the most predominant
            subtype in 14 (51%) patients, followed by oligoarticular type in 11 (40%) patients. Nine (33.3%) patients
            were rheumatoid factor positive.  The common chief complaints were arthralgia, swollen and stiffness of
            joint, and fever. Six (22.2%) children came with joint contracture. Only 1 patient presenting with uveitis
            and subluxated lens. Oral NSAID such as ibuprofen was the most common therapeutic choice, followed by
            oral steroids, and methotrexate. Conclusion This study provides a clinical characteristics data of JIA with a
            higher frequency of oligoarthritis that can improve the understanding and therapeutic approach.
                             Keywords: juvenile idiopathic arthritis; children; rheumatic disease



                                                P-AI-006
                  Clinical Characteristic of Children with Henoch Scholein Purpura in
                                    Dr. Soetomo Hospital Surabaya

              Diah Budiarti, Azaria Amelia Adam, Ratih Kumala Sari, Zahrah Hikmah, Azwin Mengindera Putera Lubis
              Department of Child Health. Faculty of Medicine Universitas Airlangga/Dr. Soetomo General Academic Hospital,
                                         Surabaya, East Java, Indonesia
                                               Abstract
            Background Henoch Schonlein Purpura (HSP) is a systemic vasculitis disease that is common in children
            whose major manifestations include non-thrombocytopenic purpura, arthritis or arthralgia, abdominal pain,
            and renal involvement. Objective To describe demographic, clinical profile, and management of HSP in
            children. Method All patients were diagnosed as HSP at pediatric Allergy and Immunology outpatient clinic
            of Dr. Soetomo General Academic Hospital, Surabaya between years 2014 and 2019 were enrolled in this
            study. Clinical characteristics, laboratory findings, and therapy of all children were evaluated descriptively
            retrospectively. Microsoft Excel was used for data analysis. Results A total 40 children had enrolled in this
            study. Male to female ratio was 1.2:1. The median age was 9 years. Twenty-eight (70%) patients were referral
            from other hospitals. The first symptom was non-thrombocytopenia skin purpura, mainly concentrated at
            the lower extremities and buttocks, following with gastrointestinal symptoms, and arthritis knee and ankle
            joint, both in 31 (77.5%) patients. Dominant gastrointestinal symptoms were abdominal pain, vomiting, and
            bloody diarrhea. Microscopic hematuria and proteinuria were in 7 (17.5%) patients. An increased ESR was
            reported in 22 patients (55%). ASO titer was higher in 5 children (12.5%). Seventy percent of patients were
            given NSAID, followed by oral steroid in 17 (42.5%) patients. An allergic diet was given to 11 patients.
            Conclusion HSP in children had equal gender distribution. Non-thrombocytopenia skin purpura at lower
            extremities and buttocks was most common symptom. Management of HSP included NSAID, oral steroids,
            and an allergic diet.
                              Keywords: children; Henoch Schonlein Purpura; abdominal pain



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