Javascript must be enabled to continue!
Significance of New Index Matos and Carvalho Index in differentiation of iron deficiency anemia and beta thalassemia trait.
View through CrossRef
Objective: To assess the value of the Matos and Carvalho index (MCI) in detecting beta thalassemia traits in patients with microcytic hypochromic anemia. Study Design: Retrospective study. Setting: Department of Hematology, CHK Central Laboratory Dr Ruth KM Pfau Civil Hospital Karachi, Pakistan. Period: 1st July to 31st December 2022. Methods: All newly diagnosed cases of iron deficiency and Beta Thalassemia trait were included. 297 patients with an age range of 1–60 years were evaluated. We calculated 4 discrimination indices in all patients with hemoglobin (Hb) values of <10 g/dL. The patient groups were evaluated according to red blood count; the Mentzer index (MI); the Srivastava index (SI) and Matos and Carvalho index (MCI). In this study complete blood counts for red cell indices were processed on a Hematology analyzer (XN-1000), HPLC was done on Arkray HA-8108T and serum ferritin was done on a chemistry analyzer (COBAS 501). Results: 297 patients were included in the present study with hypochromic, microcytic anemia for beta thalassemia trait (BTT) and iron deficiency anemia (IDA). HPLC detected 141 patients with BTT, while 156 were diagnosed with IDA. The average age of Patients with BTT was 14.5 years, whereas the average age of IDA patients was 20.6 years. The Mentzer index correctly identified patients at 64.6%, followed by MCI and SI at 63.2%, 62.2%, and 55.2%, respectively. Conclusion: The Matos & Carvalho Index offers an easy and accessible way to enhance thalassemia detection and iron deficiency anemia by the simple test of CBC at the frontline. In this study Srivastava index (SI) demonstrated the most robust reliability levels when distinguishing between beta thalassemia trait and Iron deficiency anemia. However, the absence of red cell indices and methods that possess 100% specificity, efficacy, and sensitivity hinders the differentiation of BTT from other hypochromic microcytic anemia.
Independent Medical Trust
Title: Significance of New Index Matos and Carvalho Index in differentiation of iron deficiency anemia and beta thalassemia trait.
Description:
Objective: To assess the value of the Matos and Carvalho index (MCI) in detecting beta thalassemia traits in patients with microcytic hypochromic anemia.
Study Design: Retrospective study.
Setting: Department of Hematology, CHK Central Laboratory Dr Ruth KM Pfau Civil Hospital Karachi, Pakistan.
Period: 1st July to 31st December 2022.
Methods: All newly diagnosed cases of iron deficiency and Beta Thalassemia trait were included.
297 patients with an age range of 1–60 years were evaluated.
We calculated 4 discrimination indices in all patients with hemoglobin (Hb) values of <10 g/dL.
The patient groups were evaluated according to red blood count; the Mentzer index (MI); the Srivastava index (SI) and Matos and Carvalho index (MCI).
In this study complete blood counts for red cell indices were processed on a Hematology analyzer (XN-1000), HPLC was done on Arkray HA-8108T and serum ferritin was done on a chemistry analyzer (COBAS 501).
Results: 297 patients were included in the present study with hypochromic, microcytic anemia for beta thalassemia trait (BTT) and iron deficiency anemia (IDA).
HPLC detected 141 patients with BTT, while 156 were diagnosed with IDA.
The average age of Patients with BTT was 14.
5 years, whereas the average age of IDA patients was 20.
6 years.
The Mentzer index correctly identified patients at 64.
6%, followed by MCI and SI at 63.
2%, 62.
2%, and 55.
2%, respectively.
Conclusion: The Matos & Carvalho Index offers an easy and accessible way to enhance thalassemia detection and iron deficiency anemia by the simple test of CBC at the frontline.
In this study Srivastava index (SI) demonstrated the most robust reliability levels when distinguishing between beta thalassemia trait and Iron deficiency anemia.
However, the absence of red cell indices and methods that possess 100% specificity, efficacy, and sensitivity hinders the differentiation of BTT from other hypochromic microcytic anemia.
Related Results
Tracing Hematological Shifts in Pregnancy: How Anemia and Thrombocytopenia Evolve Across Trimesters
Tracing Hematological Shifts in Pregnancy: How Anemia and Thrombocytopenia Evolve Across Trimesters
Abstract
Introduction
Given pregnancy's significant impact on hematological parameters, monitoring these changes across trimesters is crucial. This study aims to evaluate hematolog...
Comprehensive analysis of a-and b-thalassemia genotypes and hematologic phenotypes
Comprehensive analysis of a-and b-thalassemia genotypes and hematologic phenotypes
Background: Guizhou Province is an area with high incidence of thalassemia. However, there are few large-sample studies on the correlation between genotypes and phenotypes in Guizh...
De Novo Anemia and Relationship with Vitamin C Deficiency and Zinc Deficiency in a Southern Delaware Population, a Retrospective Analysis
De Novo Anemia and Relationship with Vitamin C Deficiency and Zinc Deficiency in a Southern Delaware Population, a Retrospective Analysis
Abstract
Background:
Vitamin C is an essential dietary nutrient. It is a water soluble vitamin that exists in the body primarily in the reduced form A...
Thalassemia Phenotypes and Associated Mortality among Yemeni Patients: A Single-Center Retrospective Analysis
Thalassemia Phenotypes and Associated Mortality among Yemeni Patients: A Single-Center Retrospective Analysis
Objective: To retrospectively analyze thalassemia phenotypes and associated mortality among Yemeni patients seeking healthcare in Sana’a city, Yemen.
Methods: This retrospect...
Thalassemia Phenotypes and Associated Mortality among Yemeni Patients: A Single-Center Retrospective Analysis
Thalassemia Phenotypes and Associated Mortality among Yemeni Patients: A Single-Center Retrospective Analysis
Objective: To retrospectively analyze thalassemia phenotypes and associated mortality among Yemeni patients seeking healthcare in Sana’a city, Yemen.
Methods: This retrospect...
DIAGNOSTIC VALUE OF MENTZER INDEX FOR THALASSEMIA PREDICTION IN SUSPECTED PATIENTS OF PUNJAB
DIAGNOSTIC VALUE OF MENTZER INDEX FOR THALASSEMIA PREDICTION IN SUSPECTED PATIENTS OF PUNJAB
Thalassemia is a genetic disease and became a worldwide problem. Worldwide, about 3-8% of population are suffered from beta thalassemia. The aim of this study was to use Mentzer in...
Iron deficiency unveiled: Exploring its intersection with beta thalassemia trait
Iron deficiency unveiled: Exploring its intersection with beta thalassemia trait
Objective: To identify the coexistence of iron deficiency anaemia in patients of beta thalassemia trait in Rawalpindi, Punjab, Pakistan.
Material and Methods: A cross-sectional stu...
Effect of Iron replacement therapy in Pregnant Beta Thalassemia Carrier Patients with Coexisting Iron Deficiency Anemia.
Effect of Iron replacement therapy in Pregnant Beta Thalassemia Carrier Patients with Coexisting Iron Deficiency Anemia.
Iron deficiency anemia (IDA) and β -Thalassemia trait are two prevalent etiologies of microcytic hypochromic anemia. Pregnant women with IDA face significant risk of short-term and...

