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SEVERE COMBINED IMMUNODEFICIENCY (SCID) CANADIAN Pediatric SURVEILLANCE PROGRAM 2305 St. Laurent Blvd. Ottawa ON K1G 4J8 Tel: (613 5269397, ext. 239 Fax: (613 5263332 Email: PSP cps.ca Website: www.cps.ca
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How to fill out severe combined immunodeficiency (SCID):

01
Complete the patient's personal information: Provide the patient's full name, date of birth, gender, and contact details. This information is crucial for identifying the individual and ensuring accurate record-keeping.
02
Gather medical history: Include details about the patient's past and present medical conditions, allergies, surgeries, and medications. It is important to focus on any history or symptoms related to immunodeficiency.
03
Document family history: Investigate if there are any known cases of severe combined immunodeficiency or other immunodeficiency disorders in the patient's family. This can help identify potential genetic factors contributing to SCID.
04
Record immunization details: Note the patient's immunization history, including administered vaccines, dates, and any adverse reactions. Vaccination records are essential for assessing the patient's immune system's response to previous immunizations.
05
Perform a physical examination: Document the findings from a thorough physical examination, paying special attention to signs of immunodeficiency such as recurrent infections, poor growth, and abnormal lymph nodes.
06
Conduct laboratory tests: Request relevant laboratory investigations, such as complete blood counts, immunoglobulin levels, and lymphocyte subsets. These tests aid in confirming the diagnosis of SCID and assessing the patient's immune status.
07
Consult with a specialist: Consider referring the patient to an immunologist or an expert in immunodeficiency disorders. They can provide further guidance on managing SCID and offer recommendations for treatment options such as hematopoietic stem cell transplantation or gene therapy.

Who needs severe combined immunodeficiency (SCID)?

01
Infants with recurrent, severe, or life-threatening infections: SCID is usually identified in infants who experience frequent bacterial, viral, or fungal infections that do not respond well to treatment. These infections can be severe and pose a significant risk to the child's health.
02
Individuals with a family history of SCID: Genetic mutations are a common cause of SCID. If there are known cases of SCID or other immunodeficiency disorders within the family, it is important to evaluate the patient for potential SCID.
03
Patients with symptoms indicative of immunodeficiency: Individuals displaying symptoms such as persistent thrush or yeast infections, chronic diarrhea, failure to thrive, poor growth, or a history of opportunistic infections should be evaluated for SCID. These symptoms may suggest underlying immunodeficiency disorders, including SCID.
It is crucial to promptly diagnose and manage severe combined immunodeficiency (SCID) to prevent life-threatening complications and improve the patient's quality of life. Seeking medical attention, particularly from immunology specialists, is essential for accurate diagnosis and appropriate treatment strategies.
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Severe combined immunodeficiency (SCID) is a rare genetic disorder that affects the immune system, leaving individuals vulnerable to infections.
Healthcare providers and laboratories are required to report cases of SCID to public health authorities.
Healthcare providers need to report cases of SCID to the appropriate health department using the designated reporting forms or online reporting systems.
The purpose of reporting SCID is to track and monitor cases of the disorder, implement appropriate interventions, and prevent transmission of infectious diseases.
Information such as patient demographics, clinical symptoms, laboratory test results, and treatment history must be reported on SCID forms.
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