Getting SCD is God’s will
SCD patients do not survive
Is a disease of poor people
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Parent’s myth and misconceptions regarding SCD |
Individual barriers |
Patients doubt on HU that it causes cancer and infertility
Patients read and know the side effects of HU
Patients are not aware of HU uses that affect adherence
The cost of HU affect compliance
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Medical doctors worries and fears to prescribe HU |
Shortage of lab machine for reticulocyte count
Absence of paediatric formulation
Lab tests are only available in a tertiary hospital
Some facilities are not allowed to have HU
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Lack of infrastructural support |
Health facility barriers |
A special permit is needed to access HU
Few pharmacies sell HU
Not available in most health facilities
Few pills are provided per visit
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Limited availability of HU in health facilities |
Permit delay initiation of HU to patient
HU is covered by insurance after 1 year of use
Some insurance scheme does not cover HU
Insurance bureaucracy at initiation
Insurance agencies are profit-oriented
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Limitations of HU insurance coverage |
Health system barriers |
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High cost of HU |
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Restrictive policy on the use of HU |
The disease is not contagious
SS is an inherited disease
HU raise blood amount
HU use reduces the frequency of hospital visits
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Parent’s awareness of the disease and the use of HU |
Having adequate knowledge of the SCD |
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Medical doctors’ knowledge about SCD and the use of HU in its management |
Insurance help on HU accessibility
Insurance reduces the cost of HU
Insurance coverage raise HU adherence
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Readiness of Health Insurance to cover or to offer special permit for HU |
Opportunities for HU access to patients with SCD |
Being available in HF without restrictions
HU is available in community outlets
Availability in private health facilities
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Availability of HU in health facilities |