SynthesisFrontiers in medicine2026
Caregivers' experiences of caring for children with developmental dysplasia of the hip: a qualitative descriptive review.
Synthesis in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
0 citing papers in PubMed.
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Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Developmental dysplasia of the hip (DDH) is a common pediatric orthopedic condition. Caregivers of children with DDH often face significant challenges that may affect their quality of life. This review aimed to systematically identify, appraise, summarize the available qualitative evidence on caregivers' experiences of caring for children with DDH. Methods: We systematically searched eight databases (Embase, Cochrane Library, Web of Science, PubMed, CINAHL, PsycINFO, ERIC, and ProQuest) from inception to May 2025. Two researchers independent screened studies, extracted data, and assessed methodological quality using the Joanna Briggs Institute critical appraisal checklist for qualitative research. A meta-aggregative approach was used to categorize and summarize themes reported in the primary studies. Confidence in each summary finding was assessed using GRADE-CERQual. Results: Eight studies met the inclusion criteria. These included four interview-based studies (total 66 participants) and four survey-based studies with open-ended questions (total 1,522 participants). Four main themes were identified: (1) a challenging and often delayed diagnostic process; (2) treatment devices complicate daily parenting tasks; (3) inadequate or ill-timed informational and practical support; and (4) gradual adaptation and skill development over time. Conclusion: Caregivers of children with DDH face substantial challenges during diagnosis, treatment, and daily care. The findings highlight the potential value of timely, practical, and empathetic support that addresses informational needs and acknowledges the adaptive work families undertake. Future research should employ more in-depth qualitative designs to capture the nuanced processes of caregiver adaptation.
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