Tiangsa Sembiring
Universitas Sumatera Utara

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The Effect of Glucocorticoids on Bone Profile in Pediatric Acute Lymphoblastic Leukemia Pramulya Prajogo; Bidasari Lubis; Siska Mayasari Lubis; Isti Ilmiati Fujiati; Tiangsa Sembiring; Hafaz Zakky Abdillah
Indonesian Journal of Global Health Research Vol. 8 No. 1 (2026): Indonesian Journal of Global Health Research
Publisher : GLOBAL HEALTH SCIENCE GROUP

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.37287/ijghr.v8i1.229

Abstract

Glucocorticoids are essential in treating acute lymphoblastic leukemia (ALL) but may disrupt bone metabolism, affecting calcium, magnesium, phosphate, and alkaline phosphatase levels. This cross-sectional study enrolled 30 children ≤18 years with ALL at Adam Malik Hospital, Medan, during April–May 2025 using consecutive sampling. All had received at least one week of glucocorticoid therapy and had complete bone profile data. Data were obtained from medical records and laboratory tests. Associations were analyzed using Spearman’s correlation, Mann-Whitney test, and multiple linear regression. Most patients were male (53.3%) and classified as high-risk (60%), with 60% receiving dexamethasone for a median of 7 weeks. Calcium, phosphate, and alkaline phosphatase levels were generally within the normal range, but 50% of patients developed hypermagnesemia. Magnesium levels were significantly associated with the type of glucocorticoid (p=0.010), treatment duration (p=0.014), and age at diagnosis (p=0.006). No significant associations were found between glucocorticoid duration and calcium, phosphate, or alkaline phosphatase levels. Magnesium levels are influenced by glucocorticoid type, treatment duration, and age at diagnosis. Further studies with larger samples and additional biomarkers are needed to comprehensively understand the effects of glucocorticoids on the bone profile of children.
Comparison of Clinical Characteristics and Cardiac Parameters in Children with Heart Failure Due to Congenital and Acquired Heart Disease Kadir Gani; Tina Christina Lumban Tobing; Sri Sofyani; Juliandi Harahap; Tiangsa Sembiring; Cynthea Prima Destarian
Indonesian Journal of Global Health Research Vol. 8 No. 6 (2026): Indonesian Journal of Global Health Research: December 2026
Publisher : GLOBAL HEALTH SCIENCE GROUP

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.37287/ijghr.v8i6.2549

Abstract

Heart failure in children is a serious clinical syndrome caused by congenital heart disease (CHD) and acquired heart disease (AHD). Differences in clinical profiles and cardiac parameters between these two etiologies are important for accurate diagnosis and appropriate management. The primary objective of this study was to compare the clinical characteristics and cardiac parameters in children with heart failure due to congenital heart disease (CHD) and acquired heart disease (AHD). An analytic observational retrospective cross-sectional study was conducted using medical records of 26 children with heart failure (13 CHD and 13 AHD) at H. Adam Malik General Hospital, Medan, from January to May 2026. Variables included age, sex, nutritional status, Ross classification, dominant symptoms, as well as left ventricular ejection fraction (LVEF), fractional shortening (FS), tricuspid annular plane systolic excursion (TAPSE), troponin, valvular involvement, left atrial enlargement, QRS duration, and QTc interval. Descriptive and bivariate analyses were performed according to data distribution. There were no significant differences in age, sex, and nutritional status between groups, with most patients being undernourished. The predominant symptom was dyspnea/tachypnea, and Ross classification did not differ significantly, although AHD more often presented in higher Ross classes. Median LVEF (63.1 vs 59, p=0.005) and FS (35 vs 30, p=0.007) were significantly higher in the CHD group, whereas QTc interval prolongation was more common in AHD. TAPSE, troponin, QRS duration, valvular involvement, and left atrial enlargement did not differ significantly between groups. Clinical manifestations of pediatric heart failure due to CHD and AHD are similar and insufficient to distinguish etiology, but AHD tends to be associated with more severe left ventricular systolic dysfunction.