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Barriers to and Facilitators of Iron Therapy in Children with Iron Deficiency Anemia
Jacquelyn M Powers1, Margaret Nagel2, Jean L Raphael3
1Department of Pediatrics, Baylor College of Medicine, Houston, TX; Section of Hematology/Oncology, Baylor College of Medicine, Houston, TX; Texas Children's Hospital, Houston, TX.
Insights
Parents found challenges with iron therapy for children with iron deficiency anemia (IDA) due to side effects and taste. Interventions should focus on parental motivation and health benefits to improve adherence.
Area of Science:
- Pediatrics
- Hematology
- Nutritional Science
Background:
- Iron deficiency anemia (IDA) is a common nutritional deficiency in young children.
- Successful treatment of IDA requires consistent adherence to iron therapy.
Purpose of the Study:
- To explore parental perspectives on barriers and facilitators to effective iron therapy for children with IDA.
- To inform the development of interventions promoting adherence to iron treatment.
Main Methods:
- Prospective, mixed-methods study involving 20 children (9 months to 4 years) diagnosed with IDA and their parents.
- Semistructured interviews with primary caregivers to gather in-depth insights into their experiences with IDA and its treatment.
Main Results:
- Key barriers included difficulty administering oral iron due to side effects and poor taste.
- Facilitators included clear instructions, support from healthcare providers and family, and motivation driven by the child's health improvement.
- Parental stress and anxiety were linked to therapy adherence and follow-up.
Conclusions:
- Interventions should prioritize increasing parental motivation by highlighting the health benefits of iron therapy.
- Focusing on parental motivation may be more effective than solely providing knowledge about IDA.
- Strategies should aim to improve adherence to oral iron and avoid more invasive treatments.
Objective:
To characterize barriers to and facilitators of successful iron therapy in young children with iron deficiency anemia (IDA) from an in-depth parental perspective.
Study Design:
Prospective, mixed methods study of children age 9 months to 4 years with a diagnosis of nutritional IDA by clinical history and laboratory criteria and their parents. Clinical data were obtained from the electronic health record. Semistructured interviews focused on knowledge of IDA, clinical effects, experience with iron therapies, and motivation were conducted with the parent who identified as the child's primary caregiver.
Results:
Twenty patient-parent dyads completed the study; 80% (n = 16) identified as Hispanic/Latino (white). Patients' median age was 23 months (50% male); median initial hemoglobin concentration was 8.2 g/dL and duration of oral iron therapy was 3 months. Parents' median age was 29 years (85% female); 8 interviews (40%) were conducted in Spanish. Barriers included difficulty in administering oral iron owing to side effects and poor taste. Facilitators included provision of specific instructions; support from healthcare providers and additional caregivers at home; motivation to benefit child's health, which was strengthened by strong emotional reactions (ie, stress, anxiety) to therapy and follow-up; and an appreciation of child's improvement with successful completion of therapy.
Conclusions:
Our findings support the need for interventions designed to promote oral iron adherence in children with IDA. Rather than focusing on knowledge content related to IDA, interventions should aim to increase parental motivation by emphasizing the health benefits of adhering to iron therapy and avoiding more invasive interventions.
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