Objective:
This study aims to asses the patients' compliance with essential hypertension in respect to antihypertensive
medications, follow-up, dietary pattern and health habits, to identify the associated long-term complications, and
to find out the relationship between patient's compliance, and demographic characteristics such as age, gender,
level of education, and duration of disease.
Methodology:
A descriptive study was carried out in Nasiriyah Teaching Hospital to achieve presented objectives .
Results:
The results of the study revealed that there were a significant association between educational level and total
patient's compliance, a significant association was found between the duration of disease and complications, the
majority (63%) of the sample was non-complaint, most of them was males with low level of education and
(70%) of them had complications. A greater number (21%) suffering from (Cerebrovascular accident).
Recommendation:
The research recommends that establishing well-equipped specialized hypertension clinics, educational program
should be designed, antihypertensive drugs should be supported by government, antihypertensive medications
must be obtained from the out patient clinic to avoid buying them from private pharmacies to maintain patients
compliance, and further study can be conducted in Iraq to determine the impact of non-compliance of patients
with essential hypertension.
Abstract
β-thalassemia major is a genetic disease that causes sever defect in normal hemoglobin synthesis. The patients with β-thalassemia major need periodic blood transfusions that can result in accumulation of body iron, so treatment with iron chelating agent is required. Complications of this iron overload affecting many vital organs, including the liver. The aim of this work was to evaluate liver enzymes in β -thalassemia major patients with deferasirox versus without it. Two groups of β-thalassemia major patients were involved in this study named group A; 40 β-thalassemia patients of blood transfusion dependent without deferasirox, group B; 40 β-thalassemia patients of blood transfusion dependent on de
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