The present study aimed to assess awareness of sickle cell anemia patients regarding pharmacologic and non-pharmacologic approached to control pain crisis, and to identify the effective approaches used to control pain crisis at Al Qatif governorate. Data was collected at al Qatif Hospital using questionnaire sheet and health assessment sheet. The questionnaire sheet was composed of several areas, including socio-demographic data, SCA patients knowledge questionnaire sheet. And the health assessment sheet was included health history, visual Analog Scale and management approaches of pain crisis. SCA Saudi patients' age ranged between 15-40 years old. The researcher collected data by distribution of questionnaires over the study participants.S...
Samuel N Uwaezuoke,1 Adaeze C Ayuk,1 Ikenna K Ndu,2 Chizoma I Eneh,2 Ngozi R Mbanefo,1 Osita U Ezenw...
used health care utilization as a proxy for pain and underlying vaso-occlusion. However, utilization...
Pain is the clinical hallmark for sickle cell disease (SCD). The objective of this study was to surv...
Sickle cell disease has a variety of signs and symptoms, the most common being painful vaso-occlusiv...
Objective. To examine the factors associated with the use of complementary and alternative medicine ...
Background: Sickle cell pain crisis is a common medical emergency in Nigeria. The treatment approa...
OBJECTIVE: The aim of this exploratory, cross-sectional study was to evaluate pain in sickle cell di...
Objective: To investigate the health care provider attitude during the management of sickle cell dis...
Sickle cell disease (SCD) is a hereditary illness characterized by hemolytic anemia, end-organ damag...
Sickle-cell disease (SCD) is a wide-spread inherited hemolytic anemia that is due to a point mutatio...
Sickle Cell Anemia is a debilitating genetic condition effecting nearly a million people in the Unit...
Sickle cell disease (SCD) is a long-term condition that would benefit from a long-term conditions ap...
Sickle cell disease can lead to serious complications, such as stroke, acute chest syndrome, pulmona...
Sickle cell disease (SCD) is associated with significant morbidity, mortality and impaired quality o...
OBJECTIVES: Pain is the most common reason for admission to the Emergency Department (ED) in patient...
Samuel N Uwaezuoke,1 Adaeze C Ayuk,1 Ikenna K Ndu,2 Chizoma I Eneh,2 Ngozi R Mbanefo,1 Osita U Ezenw...
used health care utilization as a proxy for pain and underlying vaso-occlusion. However, utilization...
Pain is the clinical hallmark for sickle cell disease (SCD). The objective of this study was to surv...
Sickle cell disease has a variety of signs and symptoms, the most common being painful vaso-occlusiv...
Objective. To examine the factors associated with the use of complementary and alternative medicine ...
Background: Sickle cell pain crisis is a common medical emergency in Nigeria. The treatment approa...
OBJECTIVE: The aim of this exploratory, cross-sectional study was to evaluate pain in sickle cell di...
Objective: To investigate the health care provider attitude during the management of sickle cell dis...
Sickle cell disease (SCD) is a hereditary illness characterized by hemolytic anemia, end-organ damag...
Sickle-cell disease (SCD) is a wide-spread inherited hemolytic anemia that is due to a point mutatio...
Sickle Cell Anemia is a debilitating genetic condition effecting nearly a million people in the Unit...
Sickle cell disease (SCD) is a long-term condition that would benefit from a long-term conditions ap...
Sickle cell disease can lead to serious complications, such as stroke, acute chest syndrome, pulmona...
Sickle cell disease (SCD) is associated with significant morbidity, mortality and impaired quality o...
OBJECTIVES: Pain is the most common reason for admission to the Emergency Department (ED) in patient...
Samuel N Uwaezuoke,1 Adaeze C Ayuk,1 Ikenna K Ndu,2 Chizoma I Eneh,2 Ngozi R Mbanefo,1 Osita U Ezenw...
used health care utilization as a proxy for pain and underlying vaso-occlusion. However, utilization...
Pain is the clinical hallmark for sickle cell disease (SCD). The objective of this study was to surv...