dc.contributor.advisor |
Van Rensburg, Gisela Hildegard
|
|
dc.contributor.author |
Marais, Nadia
|
|
dc.date.accessioned |
2022-08-13T07:26:19Z |
|
dc.date.available |
2022-08-13T07:26:19Z |
|
dc.date.issued |
2021-11 |
|
dc.date.submitted |
2022-08 |
|
dc.identifier.uri |
https://hdl.handle.net/10500/29243 |
|
dc.description.abstract |
Clubfoot is one of the most common musculoskeletal congenital disorders and annually
affects around 174 000 babies worldwide. Untreated clubfoot leads to significant
permanent impairment and problems with ambulation, thus presenting a potential public
health dilemma. Clubfoot can however be corrected with a non-surgical method referred
to as the Ponseti method. This gives a child normal, pain free mobility and the potential
to grow up as a productive member of society. Treatment for clubfoot needs to be
implemented as soon as possible after birth of the child to produce the best results and
avoid possible relapse of the clubfoot. Diagnosis and treatment of clubfoot starting at, or
later than three months of age, is regarded as late detection and treatment. The purpose
of this study was to determine the healthcare-seeking behaviour of guardians of children
with clubfoot at or after the age of three months to promote early detection and treatment.
A qualitative study was conducted to explore the reasons for seeking healthcare at
Ponseti clinics for children that were three months or older; and to describe the challenges
that the guardians experienced in seeking healthcare for their children. Data collection
was done through semi-structured interviews at two public sector hospitals in KwaZulu Natal Province.
Two major themes emerged from the study, namely discovering the clubfoot deformity,
and the challenges guardians experienced in seeking healthcare for their children with
clubfoot. There is a lack of knowledge about clubfoot resulting in late detection and
initiation of treatment; and that clubfoot is a treatable condition which can result in the
child leading a normal life if treated with the Ponseti method. Participants attending
antenatal care were not informed by health practitioners of clubfoot being a potential birth defect. In some cases, guardians approached health practitioners early, but were referred
late to a Ponseti clinic. Guardians in the study experienced several challenges when
seeking healthcare for their children, including financial, transport and family responsibility
challenges. They described having a child with clubfoot as an emotionally taxing journey.
Recommendations are made for education, practice, policy, and research. An information
brochure was designed to promote early detection and treatment of clubfoot. |
en |
dc.format.extent |
1 online resource (xiv, 148 leaves) : illustrations (chiefly color), graphs (chiefly color), color map |
|
dc.language.iso |
en |
en |
dc.subject |
Clubfoot |
en |
dc.subject |
Early detection |
en |
dc.subject |
Healthcare-seeking behaviour |
en |
dc.subject |
Ponseti |
en |
dc.subject |
Treatment of clubfoot |
en |
dc.subject.ddc |
617.58506 |
|
dc.subject.lcsh |
Clubfoot -- Treatment -- South Africa |
en |
dc.subject.lcsh |
Clubfoot -- Early detection -- South Africa |
en |
dc.title |
Early detection and treatment of clubfoot in a rural setting in South Africa |
en |
dc.type |
Dissertation |
en |
dc.description.department |
Health Studies |
en |
dc.description.degree |
M.P.H. |
|