Clinical Course and Prognosis of Hemolytic Jaundice in Neonates in North East of Iran
Journal Title: Macedonian Journal of Medical Sciences (MJMS) - Year 2011, Vol 4, Issue 4
Abstract
Background: Hemolytic jaundice is the most serious cause of hyperbilirubinemia among neonates. It may develop to kernicterus due to misdiagnosis or inappropriate treatment. The aim of this study is to determine the prevalence rate of hemolytic jaundice, predisposing factors and assessment of treatment and complications in hemolytic jaundice. Methods: This prospective descriptive study has been performed on 1568 newborns with jaundice as their chief complaint, in a seven-year period at Ghaem hospital in Mashhad, Iran. 795 neonates were included in our study (237 infants with hemolytic jaundice and 558 infants with idiopathic jaundice). Complete physical examinations and laboratory tests were performed and data were recorded. Statistical analysis was carried out, using SPSS 11.5 statistical package. Results: In the present study, significant differences were determined between two groups of hemolytic and idiopathic jaundice for total serum bilirubin, hematocrit, time of jaundice appearance, age of admission, hospitalization period and incidence of kernicterus (p<0.001). Newborns with ABO incompatibility (17%), Rh disease (7%), G6PD deficiency (6%) and minor blood group immunization (2%) were developed to hyperbilirubinemia, respectively. Among the newborns affected with kernicterus, 12 cases were placed in group with ABO hemolytic disease (9%), 3 cases were in Rh isoimmunization group (5.5%), 4 cases were in G6PD deficiency group (8.9%) and 9 cases were idiopathic (1.6%). Conclusion: Jaundice due to hemolysis is associated with a higher serum bilirubin and more complications like kernicterus. ABO incompatibility was the most common reason of hemolytic jaundice among neonates in north east of Iran. Special attention to ABO incompatibility and G6PD enzyme screening may decrease complications and improve the prognosis.
Authors and Affiliations
Hassan Boskabadi| Neonatal Research Center, Department of Pediatrics, Ghaem Hospital, Mashhad University of Medical Sciences (MUMS), Mashhad, Iran, Gholamali Maamouri| Neonatal Research Center, Department of Pediatrics, Ghaem Hospital, Mashhad University of Medical Sciences (MUMS), Mashhad, Iran, Shahin Mafinejad| Department of pediatric, Fellowship of Neonatology, MUMS, Mashhad, Iran, Farzaneh Rezagholizadeh| Department of pediatric, Ghaem Hospital, MUMS, Mashhad, Iran
Neck Circumference as a Simple Screening Measure for Identifying Egyptian Overweight and Obese Adults
Background: Neck circumference (NC) is a simple screening measure for identifying overweight and obesity. Aims: To determine whether a single measure of NC might be used to identify overweight and obesity, and to defi...
A Randomized Double Blind Clinical Study on the Efficacy of Low Level Laser Therapy in Reducing Pain After Simple Third Molar Extraction
Aim. The aim of this clinical study was to test the efficacy of Low level laser therapy (LLLT) in controlling post-operative pain after simple third molar extraction in a double blind, randomized placebo control study....
Epithelioid Angiosarcoma of the Adrenal Gland. Report of a Case and Review of the Literature
Background: Primary mesenchymal neoplasms of the adrenal gland are rare, and a malignant one is an extraordinary finding. Angiosarcomas are uncommon neoplasms and account for less than 1% of sarcomas. Due to their rari...
The Impact of Social Assistance Programs on Reducing Inequities in Health Care Among Vulnerable Groups in the Republic of Macedonia (A Small Scale Descriptive Study)
Aim. The aim of this research was to look at the impact of social assistance programs on reducing social inequities in health care among the vulnerable groups in Macedonia. Materials and methods. A small scale descrip...
Genetic Variants in the Methylenetetrahydrofolate Reductase Gene in Egyptian Children with Conotruncal Heart Defects and their Mothers
Aim: This study aimed at evaluation of MTHFR 677C/T and 1298A/C polymorphisms in MTHFR gene as maternal risk factors in conotruncal heart defects (CTDs). Material and Methods: Thirty cases with CTDs and their mothers a...