Caregiver Accessing Sickle Cell Care And The Use Of Telemedicine
To increase understanding of barriers to care and perceptions of telemedicine by caregivers of pediatric SCD patients in a medically under-resourced area3.
TreeBREAD Review
Research article overview in layman's terms.
Results from this study provide insight into how telemedicine may help address barriers to access to healthcare for pediatric SCD patients in geographically disparate areas.
This study shows that telemedicine can help pediatric patients with sickle cell disease get the health care they need, even when they live in areas where access to care is difficult. The researchers conducted interviews with the caregivers of the patients and found that they were open to the idea of telemedicine. This could be an important way to make sure that pediatric patients with SCD in the Midwest have access to the care they need and that their caregivers are able to manage their stress levels.
Caregiver experiences with accessing sickle cell care and the use of telemedicine
Abstract
Use Of Telemedicine
Sickle cell disease (SCD) is associated with a wide range of complications. However, a multitude of barriers prevent SCD patients from receiving adequate healthcare, including difficulties with transportation and lack of provider knowledge about disease sequelae. Importantly, studies have demonstrated the benefits of telemedicine in addressing barriers to healthcare. While previous studies have identified barriers to care through quantitative methods, few studies have explored barriers which affect the pediatric SCD patient population in the Midwest, wherein the geographical landscape can prohibit healthcare access. Furthermore, few studies have established acceptability of telemedicine among caregivers and patients with SCD.
Methods
This study aims to increase understanding of barriers to care and perceptions of telemedicine by caregivers of pediatric SCD patients in a medically under-resourced area in the Midwest. Researchers conducted semi-structured interviews with caregivers of children with SCD. The interviews were audio-recorded and transcribed. Thematic analyses were performed.
Results
Researchers interviewed 16 caregivers of 15 children with SCD. Thematic analyses of the interview transcripts revealed four broad themes regarding caregiver burden/stress, both facilitators and barriers to SCD healthcare, and general thoughts on the acceptability/usefulness of telemedicine.
Conclusion
This qualitative study describes common burdens faced by caregivers of SCD, barriers to and facilitators of SCD care in the Midwest, and caregiver perceptions of the usefulness and efficacy of telemedicine for SCD care.
Authors
Journal
Published Date
Keywords
DOI:
What's Your View on this Research Article?
Sharing is Loving
Is this website helping you in any way? We love to hear your feedback. Write to us and spread the words : )
0 Comments