Department of Pathology, Bharati Vidyapeeth Medical College & Research Centre, Pune, Maharashtra, India
 Short Communication   
								
																Delaying Blood Transfusion in Thalassemic Children with Supplementation of Omega 3 Fatty Acids and Protein: A Novel Strategy 
																Author(s): Amol Kumar*, Ansh Chaudhary and Bhupendra Chaudhary             
								
																
						 Background: Thalassemia is an inherited genetic hemoglobin disorder wherein, afflicted child is born when both parents are carriers for defective alpha or beta hemoglobin
  gene. The thalassemias are the most common genetic disorder on a worldwide basis. The requirement of frequent blood transfusions in these patients pose a substantial
  burden on the health care system.
Methods: A prospective observational study was conducted across 6 months (July 2018-December 2018) in a tertiary care hospital, Pune. The present study included 30
  registered patient and their past 6 months record of blood transfusion (esp frequency), previous hemoglobin levels, height and weight. All these parameters were compared
  6 months after supplementation with omega 3 fatty acids and proteins.
Results: 16 of 28 patient showed that the a.. Read More»
						  
																DOI:
								10.37421/2795-6172.2021.5.127															  
Journal of Clinical Research received 11 citations as per Google Scholar report