Spectrum of hemoglobinopathies in a tertiary care centre

Background: Thalassemia and other structural hemoglobinopathies are the most common single gene disorders throughout the world with the highest frequency in the tropics, subtropics, Mediterranean basin and Southeast Asia. This study aims to provide a better assessment on the spectrum of hemoglobinop...

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Main Authors: Nisha Sharma, Anil Dev Pant, Usha Manandhar
Format: Article
Language:English
Published: Association of Clinical Pathologists of Nepal 2020-05-01
Series:Journal of Pathology of Nepal
Subjects:
Online Access:https://www.nepjol.info/index.php/JPN/article/view/27369
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spelling doaj-912262f50cb24c47b98ad2cfdf43f49a2020-11-25T04:02:06ZengAssociation of Clinical Pathologists of NepalJournal of Pathology of Nepal2091-07972091-09082020-05-011011645164910.3126/jpn.v10i1.2736927369Spectrum of hemoglobinopathies in a tertiary care centreNisha Sharma0Anil Dev Pant1Usha Manandhar2Institute of Medicine, Tribhuvan University Teaching Hospital, Maharajgunj, Kathmandu, NepalInstitute of Medicine, Tribhuvan University Teaching Hospital, Maharajgunj, Kathmandu, NepalInstitute of Medicine, Tribhuvan University Teaching Hospital, Maharajgunj, Kathmandu, NepalBackground: Thalassemia and other structural hemoglobinopathies are the most common single gene disorders throughout the world with the highest frequency in the tropics, subtropics, Mediterranean basin and Southeast Asia. This study aims to provide a better assessment on the spectrum of hemoglobinopathies in our context. Materials and Methods: This descriptive study was done at our tertiary care center, from November 2014 to October 2015. Hematological indices were derived from coulter counter, haemoglobin electrophoresis was carried out by cellulose acetate medium at alkaline PH. Sickling test, Hb H inclusions demonstration and Hb F estimation were performed. Parental screening was done wherever feasible. Results: Out of 350 cases referred from various out-patient departments of TUTH and different peripheral hospitals for suspected hemoglobinopathies, 97 cases (27.71%) had hemoglobinopathies. The most predominant hemoglobinopathy was thalassemia (57.73%) followed by sickle cell disorders (28.87%) and Hb D/Hb E hemoglobinopathies (13.40%). Most disorders were observed in the age group 21-30 years with many of the cases seen clustered in the families and a slight male preponderance. Terai region (71.13%) had a very high number. A significant high frequency of thalassemia (33.93%) and sickle cell disorders (75%) were seen in Tharu community. Conclusion: Hemoglobinopathies were seen widespread in Nepal. An extensive screening of the population is important to assess the prevalence of hemoglobinopathies, which will help in identification of carriers and take adequate therapeutic and preventive measures.https://www.nepjol.info/index.php/JPN/article/view/27369hbd/hbe hemoglobinopathieshemoglobin electrophoresishemoglobinopathiessickle cell disordersthalassemia
collection DOAJ
language English
format Article
sources DOAJ
author Nisha Sharma
Anil Dev Pant
Usha Manandhar
spellingShingle Nisha Sharma
Anil Dev Pant
Usha Manandhar
Spectrum of hemoglobinopathies in a tertiary care centre
Journal of Pathology of Nepal
hbd/hbe hemoglobinopathies
hemoglobin electrophoresis
hemoglobinopathies
sickle cell disorders
thalassemia
author_facet Nisha Sharma
Anil Dev Pant
Usha Manandhar
author_sort Nisha Sharma
title Spectrum of hemoglobinopathies in a tertiary care centre
title_short Spectrum of hemoglobinopathies in a tertiary care centre
title_full Spectrum of hemoglobinopathies in a tertiary care centre
title_fullStr Spectrum of hemoglobinopathies in a tertiary care centre
title_full_unstemmed Spectrum of hemoglobinopathies in a tertiary care centre
title_sort spectrum of hemoglobinopathies in a tertiary care centre
publisher Association of Clinical Pathologists of Nepal
series Journal of Pathology of Nepal
issn 2091-0797
2091-0908
publishDate 2020-05-01
description Background: Thalassemia and other structural hemoglobinopathies are the most common single gene disorders throughout the world with the highest frequency in the tropics, subtropics, Mediterranean basin and Southeast Asia. This study aims to provide a better assessment on the spectrum of hemoglobinopathies in our context. Materials and Methods: This descriptive study was done at our tertiary care center, from November 2014 to October 2015. Hematological indices were derived from coulter counter, haemoglobin electrophoresis was carried out by cellulose acetate medium at alkaline PH. Sickling test, Hb H inclusions demonstration and Hb F estimation were performed. Parental screening was done wherever feasible. Results: Out of 350 cases referred from various out-patient departments of TUTH and different peripheral hospitals for suspected hemoglobinopathies, 97 cases (27.71%) had hemoglobinopathies. The most predominant hemoglobinopathy was thalassemia (57.73%) followed by sickle cell disorders (28.87%) and Hb D/Hb E hemoglobinopathies (13.40%). Most disorders were observed in the age group 21-30 years with many of the cases seen clustered in the families and a slight male preponderance. Terai region (71.13%) had a very high number. A significant high frequency of thalassemia (33.93%) and sickle cell disorders (75%) were seen in Tharu community. Conclusion: Hemoglobinopathies were seen widespread in Nepal. An extensive screening of the population is important to assess the prevalence of hemoglobinopathies, which will help in identification of carriers and take adequate therapeutic and preventive measures.
topic hbd/hbe hemoglobinopathies
hemoglobin electrophoresis
hemoglobinopathies
sickle cell disorders
thalassemia
url https://www.nepjol.info/index.php/JPN/article/view/27369
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