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Page 2 of 22Sickle Cell Disease in Ontario: An Epidemiologic Profile Based on Health Systems Administrative Data Jacob Pederast,1,2 Lane Tunja Ajay,3 Elaine Kim,4 Michael A. Campbell,4 Erin Graves4 1Departmentof
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01
Obtain a medical history form to record any relevant information about the patient's health.
02
Perform a physical examination to check for any symptoms or signs of sickle cell disease.
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Request a blood test to confirm the presence of sickle cell disease and determine the type and severity.
04
Consult with a hematologist for further evaluation and management of the disease.
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Begin treatment as recommended by the hematologist to manage symptoms and prevent complications.

Who needs sickle cell disease in?

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Individuals with a family history of sickle cell disease
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People from certain ethnic backgrounds, such as African, Mediterranean, Middle Eastern, and Indian descent
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Anyone experiencing symptoms of sickle cell disease, such as chronic pain, fatigue, and frequent infections
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Sickle cell disease is a genetic blood disorder characterized by the production of abnormal hemoglobin, leading to distorted, sickle-shaped red blood cells.
Individuals diagnosed with sickle cell disease may be required to file for certain medical benefits or treatment plans, particularly for insurance or government assistance.
Filling out information related to sickle cell disease typically involves providing personal health information, medical history, and details about the treatment received on appropriate medical forms or applications.
The purpose of sickle cell disease documentation is to enable proper diagnosis, treatment plans, eligibility for healthcare services, and to facilitate research and funding for the disease.
Information reported may include patient demographics, diagnosis details, treatment history, and any complications arising from the disease.
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