Maelstrom Research Staging | SIC_No_underlying_medical_conditions

SIC_No_underlying_medical_conditions_Postrevaccination

Networks -

Variables -

Population

SIC – No underlying medical conditions

The population is composed of patients with no underlying medical conditions who received at least one dose of a COVID-19 vaccine and experienced rare and medically significant adverse events following immunization (AEFIs) without an alternate cause for their symptoms.

Selection Criteria

Newborns

Twins

Countries

Canada

Territory

Halifax, Quebec City, Montreal, Sherbrooke, Ottawa, Toronto, Hamilton, Saskatoon, Edmonton, Calgary, Vancouver

Ethnic Origin

Health Status

Participants are included if they experienced any of the following adverse effects after receiving a COVID-19 vaccine: anaphylaxis (onset <24 hours after immunization), immediate hypersensitivity (onset <4 hours after immunization), type III or IV hypersensitivity reactions, severe cutaneous or systemic reactions (e.g., Stevens-Johnson Syndrome, Toxic Epidermal Necrolysis), seizure or significant worsening of seizures in those with an underlying seizure disorder, Guillain-Barré Syndrome, acute disseminated encephalomyelitis, transverse myelitis or other suspected demyelinating condition, aseptic meningitis, encephalitis, thrombocytopenia, deep vein thrombosis, pulmonary embolism, stroke, heart failure and cardiogenic shock, cardiomyopathy, arrhythmia, myocarditis, pericarditis, acute kidney injury, acute liver injury, acute respiratory distress syndrome, other severe local or systemic symptoms causing work/school absenteeism or significant decline in function, mobility or cognition and requiring immediate medical attention, or severe COVID-19 requiring hospitalization with onset >2 weeks post-immunization.

Other Criteria

Patients with vaccine hesitancy or concerns will be excluded from the study.

Recruitment

Sources of recruitment

Specific population

Specific Population

Clinic patients

Supplementary Information

Participants are referred to the study by a healthcare provider (physician, nurse practitioner, public health physician).

Number of Participants

Number of Participants
Number of Participants with Biological Samples

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Data Collection Event

SIC - No underlying medical conditions - Post-revaccination

Information was or will be collected about the diagnosis, relative severity or seriousness, and outcome of the adverse event following immunization.

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Collected Dataset / SIC_No_underlying_medical_conditions_Postrevaccination

SIC_No_underlying_medical_conditions_Postrevaccination

Population

SIC – No underlying medical conditions

Data Collection Event

SIC - No underlying medical conditions - Post-revaccination

Files

Variables Classifications