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Updated: May 29, 2025

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Impact of Dedicated Thalassemia Day Care Services: Pediatric Hematologist's Perspective
Ritika Khurana1, Purva Kanvinde1, Parth Ganatra1
1Department of Pediatric Hematology-Oncology, Bai Jerbai Wadia Hospital for Children, Mumbai, India.
Insights
Dedicated thalassemia day care services significantly improved patient hemoglobin levels and iron overload management. These centers offer a supportive environment, enhancing the quality of life for children with thalassemia and their families.
Area of Science:
- Hematology
- Pediatrics
- Public Health
Background:
- Thalassemia poses chronic psychosocial challenges for children and caregivers.
- Effective management requires specialized day care centers led by hematologists or pediatricians.
- This study evaluates the impact of dedicated thalassemia day care services.
Purpose of the Study:
- To assess the impact of a dedicated thalassemia day care center on patient outcomes.
- To evaluate improvements in hemoglobin levels and iron overload management.
- To determine the effectiveness of integrated care including psychosocial support and prevention strategies.
Main Methods:
- Retrospective analysis of data from a pediatric hospital's thalassemia day care center (established March 2020).
- Inclusion of 88 children with thalassemia, with a multidisciplinary team (hematologist, counselor, nurses, social worker, etc.).
- Implementation of transfusion guidelines, provision of quality blood products, regular monitoring of iron overload, and engagement with NGOs.
Main Results:
- Increased patient registrations from 88 to 157 within three years.
- Improved mean pre-transfusion hemoglobin from 8.2 g/dL to 9.5 g/dL.
- No blood-transmitted viral infections acquired; identification of 14 sibling matches for bone marrow transplant, with 9 successful transplants.
- Screening identified 8 carrier mothers and 15 couples for antenatal screening, alongside positive psychosocial feedback from families.
Conclusions:
- Dedicated thalassemia day care centers improve healthcare delivery, leading to better hemoglobin and iron overload status.
- These centers provide a more comfortable and supportive environment for transfusions.
- Integrated care, including prevention and psychosocial support, enhances patient well-being and outcomes.
Background:
Thalassemia is a chronic condition which has psychosocial impact on children and their caregivers. To ensure appropriate medical management and social support, it is important that these children are enrolled in a proper day care centre led by a haematologist or trained paediatrician. This study assesses the impact of dedicated thalassemia day care services in lives of patients with thalassemia.
Material And Methods:
Retrospective analysis of qualitative and quantitative data of children in Thalassemia Day care centre (established in March 2020) of a Pediatric hospital in Mumbai, India was done. A team comprising of hematologist, counselor, staff nurses, social worker, porters and blood bank technician was appointed. A total of 88 children with Thalassemia who were initially taking treatment in general wards were enrolled. Transfusion guidelines to maintain pre-transfusion hemoglobin between 9 and 10.5 g/dl were prepared. Better hematocrit of blood, fresh blood and leucodepletion filters were provided to all. Iron overload status was checked by serum ferritin and T2* MRI periodically and chelation optimized. Steps to strengthen primary and secondary prevention of thalassemia were taken. NGOs were engaged to assist patients socially and financially.
Results:
Thalassemia day care centre (TDC) started in March 2020 with 88 registrations and as of March 2023, we are supporting 157 patients. Baseline pre-transfusion Hb was available for only 64/88 (72%) and ferritin levels in 62/88 (70%) patients prior to TDC as rest were not following up with hematologist. Amongst 66 patients, pre transfusion hemoglobin improved from mean of 8.2 g/dl (6.5-10.6 g/dl) (pre TDC) to 9.5 g/dl (8-10.6 g/dl) (post TDC). No patient has acquired a blood transmitted viral infection in these 3 years. Mean serum ferritin levels were 3285 ng/ml amongst 63 patients pre TDC and 3870 ng/ml amongst 88 patients post 3 years of TDC. HLA typing camps helped us in identifying 14 sibling matches, out of which 9 underwent successful Bone marrow transplant. As primary prevention strategy, 201 anemic pregnant females were screened and 8 carrier mothers were identified. For secondary prevention, 15 couples underwent antenatal screening to prevent birth of a child with thalassemia. Team also ensured psychosocial well-being of families, which is reflected in the positive feedback given by patients post 3 years of day care. Seven CMEs or awareness programs have been conducted by the team to spread awareness.
Conclusion:
With a dedicated centre, we are now able to provide appropriate healthcare to patients which has helped in improving their hemoglobin as well as iron overload status. Children and families now have a more friendly and comfortable environment for taking transfusions.
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