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Background:
Sickle Cell Disease (SCD) is a group of inherited red blood cell disorders
characterized by presence of abnormal hemoglobin resulting in formation of hard
and sticky C-shaped red cells and look like a C-shaped farm tool called a
“sickle.” People with SCD can live full lives and enjoy most of the activities
that other people do provided the they adhere to the standard of treatment.
Hence the need to the study Factors Affecting the Adherence to Standard
Treatment Guidelines of Sickle Cell Disease in The Upper East Region.
Results: The
mean age of respondents (HCP) was 39.55, most were in the age brackets of
31-40. There was a significant association between those who were employed and
the unemployed with a P< 0.001. Frequency of sick falls, having active NHIS,
and income level were statistically significant in influencing adherence to
treatment guidelines among respondents.
71% of regional hospital healthcare providers were conducting regular
SCD screenings, 51% screening in the remaining health facilities, 67% of the
staff of the regional hospital had specialized SCD clinics, 35% in the other facilities having designated
days for SCD clients’ services and only 8(11%) from CHPS compounds. While 32%
had support from HCP, 116(42%) rated the support as poor. Hydroxyurea prescription
was limited to only the regional hospital.
57% of respondents were diagnosed of the condition during their sick
period and only 18% and 4% were through routine screening and mass screening
respectively. 117(64%) had support systems for SCD treatment. 41% had knowledge
on their condition and management, 32% were knowledgeable, and 76(27%) were not
knowledgeable. 195(71%) did not allow misconception and stigma to affect their
adherence. (31%) placed financial
restrictions first.
Conclusion:
The
findings of this study has uncovered the factors
affecting adherence to standard SCD Treatment Guidelines of SCD Patients
in the Upper East Region and Ghana at large.
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