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Published on: April 8, 2019
Quality of Life (QoL) and the Factors Affecting it in Transfusion-dependent Thalassemic Children
Kapil Chordiya1, Vikash Katewa2, Pramod Sharma1
1Department of Pediatrics, Dr. S. N. Medical College, Jodhpur, Rajasthan, India.
Insights
Higher age, frequent transfusions, and injectable chelation negatively impact quality of life (QoL) in children with transfusion-dependent thalassemia. Interventions should target these factors to improve QoL.
Area of Science:
- Pediatrics
- Hematology
- Quality of Life Research
Background:
- Thalassemia is a significant genetic blood disorder requiring lifelong treatment.
- Transfusion-dependent thalassemia (TDT) necessitates regular blood transfusions and chelation therapy.
- Understanding factors influencing Quality of Life (QoL) is crucial for comprehensive patient care.
Purpose of the Study:
- To evaluate the Quality of Life (QoL) in transfusion-dependent thalassemic children.
- To identify specific factors affecting QoL in this pediatric population.
Main Methods:
- A study involving 93 transfusion-dependent thalassemic children aged 8-18 years.
- Quality of Life assessed using the Pediatric Quality of Life (PedsQL) measurement model.
- Data collected on age, transfusion frequency, chelation therapy, and other relevant factors.
Main Results:
- School functioning had the lowest mean PedsQL score (57.4).
- Younger children (8-12 years) reported higher PedsQL scores than older children (13-18 years).
- Children with less frequent transfusions and those on combined chelation therapy showed better QoL.
Conclusions:
- Higher age, increased transfusion frequency, and injectable chelation are associated with lower QoL in thalassemic children.
- Targeted programs and interventions focusing on these domains are recommended to enhance QoL.
- QoL was not significantly affected by gender, education, family history, ferritin levels, splenectomy, or consanguinity.
Objectives:
To evaluate the Quality of life (QoL) and the factors affecting it in transfusion-dependent thalassemic children.
Methods:
Current study was conducted at Department of Pediatrics, Dr. SNMC, Jodhpur. Ninety-three transfusion-dependent thalassemic children aged between 8 and 18 y were enrolled. Quality of life was assessed using Pediatric Quality of Life (PedsQL) measurement model in thalassemic children.
Results:
Mean age of children was 11.8 ± 3.2 y. Lowest mean score was observed in School functioning (57.4) while in Physical functioning, Emotional functioning and Social functioning it was 73.9, 82.2 and 83.49 respectively. Mean PedsQL score was higher in 8-12 y age group as compared to 13-18 y (p = 0.024). PedsQL score was higher in children who required transfusion once in a month (p = 0.028) and children on combined chelation therapy as compared to children who were on injectable chelator (p = 0.039). Health Related QoL was not affected with gender, education status, family history of thalassemia, ferritin level, splenectomy or consanguinity.
Conclusions:
Factors related with low QoL in current study were higher age, increased transfusion frequency and injectable mode of chelation. In order to improve the QoL in thalassemic children appropriate programmes and interventions should be started targeting above domains.
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