To systematically identify, appraise, and summarize qualitative evidence on caregivers’ experiences of caring for children with developmental dysplasia of the hip (DDH), emphasizing the significance of these experiences.
Key Findings:
Caregivers experience a challenging and often delayed diagnostic process, as reported in multiple studies.
There is inadequate or ill-timed informational and practical support, as highlighted by several participants.
Caregivers gradually adapt and develop skills over time, demonstrating resilience.
Interpretation:
The findings underscore the significant challenges faced by caregivers of children with DDH, highlighting the need for timely and empathetic support that addresses their informational needs and may influence future caregiver training and resources.
Limitations:
The review is limited to qualitative studies, which may not capture all aspects of caregiver experiences, potentially leading to incomplete insights.
Variability in methodological rigor among included studies may affect the reliability of findings, necessitating cautious interpretation.
Conclusion:
Caregivers of children with DDH face substantial challenges, indicating a need for improved support systems that recognize their experiences. Future research should focus on in-depth qualitative designs to better understand caregiver adaptation processes.
