Demographics, complete when MIS is first suspected
Sex at birth
integer
Please provide the patient’s date of birth. If this is not known, please provide their age in years OR months.
date
Please provide the patient’s date of birth. If this is not known, please provide their age in years OR months.
integer
Please provide the patient’s date of birth. If this is not known, please provide their age in years OR months.
integer
Please document the ethnicity reported by the family. Document all that applies.
text
Onset of current illness and vital signs, complete when MIS is first suspected
Please provide the date of patient/carer reported onset of the first symptom that you clinically believe was related to this episode of MIS.
date
Please provide the date of patient/carer reported onset of fever (self-reported or measured)
date
Please enter the peripheral body temperature in degrees Celsius (°C) (rectal if < 3 months) in the space provided.
text
Enter the heart rate measured in beats per minute. This may be measured manually or by electronic monitoring.
integer
Enter the respiratory rate in breaths per minute. Manual rather than electronic measurement is preferred where possible. Record the highest respiratory rate documented at first suspicion of MIS.
integer
Please enter the systolic blood pressure measured in millimetres of mercury (mmHg), in the relevant sections. Use any recognised method for measuring blood pressure.
integer
Please enter the diastolic blood pressure measured in millimetres of mercury (mmHg), in the relevant sections. Use any recognised method for measuring blood pressure.
integer
Dehydration
text
Capillary refill time is measured by pressing on the sternum for five seconds with a finger or thumb until the underlying skin turns white and then noting the time in seconds needed for the colour to return once the pressure is released.
text
For all patients, irrespective of ventilation or supplemental oxygen requirement, please enter the percentage oxygen saturation at the time of admission. Measured by pulse oximetry or by arterial blood gas analysis.
text
For all patients, irrespective of ventilation or supplemental oxygen requirement, please enter the percentage oxygen saturation at the time of admission. Measured by pulse oximetry or by arterial blood gas analysis.
text
State the least responsive condition of the patient during the calendar day (not counting normal sleep).
text
Measured as the circumference of the left upper arm at the mid-point between the tip of the shoulder and the tip of elbow.
integer
Length / Height
integer
Weight
integer
Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected
Please provide details of the clinical features present when MIS is clinically first suspected, clinically assessed according to local standard/ranges, or follow the WHO standardised age-ranges for children in the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/ Add the number of days the patient has had fever (self-reported or measured) prior to assessment.
text
Please provide details of the clinical features present when MIS is clinically first suspected, clinically assessed according to local standard/ranges, or follow the WHO standardised age-ranges for children in the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/ Add the number of days the patient has had fever (self-reported or measured) prior to assessment.
integer
Please provide details of the clinical features present when MIS is clinically first suspected, clinically assessed according to local standard/ranges, or follow the WHO standardised age-ranges for children in the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
text
Please provide details of the clinical features present when MIS is clinically first suspected, clinically assessed according to local standard/ranges, or follow the WHO standardised age-ranges for children in the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
text
Please provide details of the clinical features present when MIS is clinically first suspected, clinically assessed according to local standard/ranges, or follow the WHO standardised age-ranges for children in the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/
text
Please provide details of the clinical features present when MIS is clinically first suspected, clinically assessed according to local standard/ranges, or follow the WHO standardised age-ranges for children in the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/ Examples include redness, swelling, or dryness of the lips; redness of the throat; strawberry tongue.
text
Please provide details of the clinical features present when MIS is clinically first suspected, clinically assessed according to local standard/ranges, or follow the WHO standardised age-ranges for children in the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/ Examples include pain, swelling, or redness of the fingers, toes, hands, or feet.
text
Please provide details of the clinical features present when MIS is clinically first suspected, clinically assessed according to local standard/ranges, or follow the WHO standardised age-ranges for children in the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/ Please follow the normal standard ranges for blood pressure appropriate to the age, size, and sex of the child.
text
Please provide details of the clinical features present when MIS is clinically first suspected, clinically assessed according to local standard/ranges, or follow the WHO standardised age-ranges for children in the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/ Please follow the normal standard ranges for heart rate appropriate to the age, size, and sex of the child.
text
Please provide details of the clinical features present when MIS is clinically first suspected, clinically assessed according to local standard/ranges, or follow the WHO standardised age-ranges for children in the WHO pocket guide: www.who.int/maternal_child_adolescent/documents/9241546700/en/ A normal capillary refill time should be 2 seconds or less.
text
Pale/motted skin
text
Cold hands/feet
text
Urinary output in mL/kg/hr
text
Chest pain
text
Please follow the normal standard ranges for respiratory rate appropriate to the age, size, and sex of the child.
text
Any signs of difficulties breathing or achieving adequate oxygenation.
text
Abdominal pain
text
Diarrhoea
text
Vomiting
text
Other signs and symptoms
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
integer
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
integer
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
integer
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
integer
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
integer
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
integer
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
integer
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
integer
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
integer
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
text
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
integer
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
integer
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
integer
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
integer
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
integer
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
integer
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
integer
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
integer
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
integer
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
integer
Please provide details of any other signs and symptoms present at the time when MIS is first suspected. This is in addition to the clinical features listed in section "Possible signs and symptoms of multisystem inflammatory syndrome, complete when MIS is first suspected".
integer
Haemorrhage Site specification
text
Other symptom(s) specification
text
Recent history
Recent admission to hospital
integer
If patient has been admitted to hospital more than once (prior to this episode) within the last 3 months, record the most recent discharge date.
date
Similar problems refer to the MIS illness episode and symptoms or previous COVID-19 admission
integer
Recent history of COVID-19 infection
text
Recent history of respiratory infection
integer
Any person who lives in the same household as the patient, or other close contact with laboratory-confirmed COVID-19 infection diagnosed in the last 4 weeks prior to date of onset of this illness episode.
integer
A previous clinical diagnosis of Kawasaki disease, prior to the current illness episode.
integer
Any genetically linked family member with a previous clinical diagnosis of Kawasaki disease.
integer
Co-morbidities, past history (complete when MIS is first suspected)
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. This is defined as an inflammatory and degenerative diseases of connective tissue structures. It includes chronic arthropathies and arthritis, connective tissue disorders and vasculitides. Please specify in the space provided.
integer
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. This is defined as an inflammatory and degenerative diseases of connective tissue structures. It includes chronic arthropathies and arthritis, connective tissue disorders and vasculitides. Please specify in the space provided.
text
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. Elevated arterial blood pressure diagnosed clinically.
integer
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. Please include any of coronary artery disease, heart failure, congenital heart disease, cardiomyopathy, rheumatic heart disease. Please specify in the space provided.
integer
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. Please include any of coronary artery disease, heart failure, congenital heart disease, cardiomyopathy, rheumatic heart disease. Please specify in the space provided.
text
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. Clinician-diagnosed asthma
integer
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. Patients currently receiving treatment for active tuberculosis (any site). Do not include latent tuberculosis.
integer
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. Please include any of chronic obstructive pulmonary disease (chronic bronchitis, chronic obstructive pulmonary disease (COPD), emphysema), cystic fibrosis, bronchiectasis, interstitial lung disease, pre-existing requirement for long term oxygen therapy. Do not include asthma. Please specify in the space provided.
integer
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. Please include any of chronic obstructive pulmonary disease (chronic bronchitis, chronic obstructive pulmonary disease (COPD), emphysema), cystic fibrosis, bronchiectasis, interstitial lung disease, pre-existing requirement for long term oxygen therapy. Do not include asthma. Please specify in the space provided.
text
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. Type 2 diabetes mellitus requiring oral or subcutaneous treatment or insulin dependent Type 1.
integer
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. Current solid organ or haematological malignancy. Please do not include malignancies that have been declared ‘cured’ ≥5 years ago with no evidence of ongoing disease. Do not include non-melanoma skin cancers. Do not include benign growths or dysplasia.
integer
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. Please include any of splenectomy, non-functional spleen, and congenital asplenia.
integer
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. Any congenital or acquired immunodeficiency syndrome. Do not include HIV, which should be entered under HIV. Please specify in the space provided.
integer
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. Any congenital or acquired immunodeficiency syndrome. Do not include HIV, which should be entered under HIV. Please specify in the space provided.
text
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. Please include any of clinician-diagnosed chronic kidney disease or history of kidney transplantation.
integer
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. Any chronic liver disease, including cirrhosis or a history of variceal bleeding, or hepatitis.
integer
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. Include any e.g. cerebral palsy, multiple sclerosis, motor neurone disease, muscular dystrophy, myasthenia gravis, severe learning difficulty.
integer
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. Any long-term disorder of the red or white blood cells, platelets or coagulation system requiring regular or intermittent treatment. Do not include leukaemia, lymphoma or myeloma, instead include these under malignancy.
integer
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. History of laboratory-confirmed HIV infection.
integer
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. List any significant risk factors or comorbidities that existed prior to admission and are ongoing, that are not already listed.
integer
Please record if any of these comorbidities existed prior to admission. In general, do not include past comorbidities that are no longer ongoing. List any significant risk factors or comorbidities that existed prior to admission and are ongoing, that are not already listed.
text
Pre-admission and chronic medication: Were any of the following taken within 14days of admission (complete when MIS is first suspected)?
Taken within 14 days of admission. Examples include aspirin, ibuprofen, naproxen, celecoxib, diclofenac, diflunisal, etodolac, indomethacin, ketoprofen, ketorolac, nabumetone, oxaprozin, piroxicam, salsalate, sulindac, tolmetin. Specify generic names and route.
integer
Taken within 14 days of admission. Examples include aspirin, ibuprofen, naproxen, celecoxib, diclofenac, diflunisal, etodolac, indomethacin, ketoprofen, ketorolac, nabumetone, oxaprozin, piroxicam, salsalate, sulindac, tolmetin. Specify generic names and route.
text
Taken within 14 days of admission. Examples include aspirin, ibuprofen, naproxen, celecoxib, diclofenac, diflunisal, etodolac, indomethacin, ketoprofen, ketorolac, nabumetone, oxaprozin, piroxicam, salsalate, sulindac, tolmetin. Specify generic names and route.
integer
Taken within 14 days of admission. Examples include prednisolone, betamethasone, dexamethasone, hydrocortisone, methylprednisolone, deflazacort and fludrocortisone.. Specify generic names and route.
integer
Taken within 14 days of admission. Examples include prednisolone, betamethasone, dexamethasone, hydrocortisone, methylprednisolone, deflazacort and fludrocortisone.. Specify generic names and route.
text
Taken within 14 days of admission. Examples include prednisolone, betamethasone, dexamethasone, hydrocortisone, methylprednisolone, deflazacort and fludrocortisone.. Specify generic names and route.
integer
Taken within 14 days of admission.
integer
Taken within 14 days of admission.
text
Taken within 14 days of admission.
integer
Any other medications taken in the 14 days prior to admission.
integer
Any other medications taken in the 14 days prior to admission.
text
Any other medications taken in the 14 days prior to admission.
integer
Any other medications taken in the 14 days prior to admission.
text
Any other medications taken in the 14 days prior to admission.
integer
Any other medications taken in the 14 days prior to admission.
text
Any other medications taken in the 14 days prior to admission.
integer
Laboratory results (complete with results of tests ordered at the time MIS is first suspected) (* record units if different from those listed) Record the worst value between 00:00 to 24:00 on day of assessment (if Not Available write ‘N/A’):
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know. Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know. Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Total WBC count is the total white blood cell count in blood.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Total WBC count is the total white blood cell count in blood.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. (Ht or HCT), also known as packed cell volume (PCV) or erythrocyte volume fraction (EVF), is the volume percentage (%) of red blood cells in blood.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. (Ht or HCT), also known as packed cell volume (PCV) or erythrocyte volume fraction (EVF), is the volume percentage (%) of red blood cells in blood.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. APTT is the activated partial thromboplastin time. Record the highest value. APTR is the activated partial thromboplastin ratio. Record the highest value.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. APTT is the activated partial thromboplastin time. Record the highest value. APTR is the activated partial thromboplastin ratio. Record the highest value.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. PT is the prothrombin time. Record the highest value.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. PT is the prothrombin time. Record the highest value.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. INR is the international normalised ratio. Record the highest value.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. INR is the international normalised ratio. Record the highest value.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Procalcitonin or PCT refers to blood procalcitonin. Record the highest value.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Procalcitonin or PCT refers to blood procalcitonin. Record the highest value.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. CRP is C-reactive protein and refers to the blood (serum or plasma) CRP level. Record the highest value.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. CRP is C-reactive protein and refers to the blood (serum or plasma) CRP level. Record the highest value.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Creatinine refers to serum creatinine. Record the highest value.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Creatinine refers to serum creatinine. Record the highest value.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Blood urea nitrogen is also known as ‘urea’, measured in a blood sample. Record the highest value.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Blood urea nitrogen is also known as ‘urea’, measured in a blood sample. Record the highest value.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Pro-BNP (also called NT-proBNP) is pro B-type natriuretic peptide. Record the highest value.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Pro-BNP (also called NT-proBNP) is pro B-type natriuretic peptide. Record the highest value.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Troponin Record type of Troponin and the highest value.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Troponin Record type of Troponin and the highest value.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Creatine kinase (CK, or creatine phosphokinase, CPK) refers to total creatine kinase measured in the blood. Record the highest value.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Creatine kinase (CK, or creatine phosphokinase, CPK) refers to total creatine kinase measured in the blood. Record the highest value.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. LDH is lactate dehydrogenase. Record the highest value.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. LDH is lactate dehydrogenase. Record the highest value.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Triglycerides refers to the total triglycerides measured in the blood.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Triglycerides refers to the total triglycerides measured in the blood.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. ALT/SGPT: ALT is alanine transaminase (also called serum glutamic pyruvate transaminase, SGPT). Record the highest value.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. ALT/SGPT: ALT is alanine transaminase (also called serum glutamic pyruvate transaminase, SGPT). Record the highest value.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. ESR is the erythrocyte sedimentation rate. Record the highest value.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. ESR is the erythrocyte sedimentation rate. Record the highest value.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. D-dimer Record the highest value.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. D-dimer Record the highest value.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. IL-6 is Interleukin 6. Record the highest value.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. IL-6 is Interleukin 6. Record the highest value.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. IL-10 is Interleukin 10. Record the highest value.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. IL-10 is Interleukin 10. Record the highest value.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. AST/SGOT is aspartate transaminase (also called serum glutamic oxaloacetic transaminase, SGOT). Record the highest value.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. AST/SGOT is aspartate transaminase (also called serum glutamic oxaloacetic transaminase, SGOT). Record the highest value.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Lactate refers to blood lactate. Record the highest value.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Lactate refers to blood lactate. Record the highest value.
boolean
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Ferritin Record the highest value.
float
Please record all laboratory results available from tests conducted on the day MIS is first suspected. If the unit of measurement is different from those listed, please record the unit. Additional units will be available in the eCRF. If you cannot find the unit used in the eCRF, please use a unit converter such as: http://unitslab.com/ or equivalent or email us to let us know Please give the ‘worst value’, which refers to values furthest from the normal physiological range or laboratory normal range. Results that were rejected by the clinical team (e.g. haemolysed blood samples) should not be reported. Ferritin Record the highest value.
boolean
Imaging and pathogen testing (complete when results of tests ordered at the time MIS is first suspected are available)
Please complete this section with the results of any tests that were ordered as the time MIS is first suspected. Record if a test was performed even if findings were normal. If abnormal findings were detected, specify these in the free text field. Record if X-ray and/or CT were performed, if infiltrates and any other significant findings.
integer
Please complete this section with the results of any tests that were ordered as the time MIS is first suspected. Record if a test was performed even if findings were normal. If abnormal findings were detected, specify these in the free text field. Record if X-ray and/or CT were performed, if infiltrates and any other significant findings.
text
Please complete this section with the results of any tests that were ordered as the time MIS is first suspected. Record if a test was performed even if findings were normal. If abnormal findings were detected, specify these in the free text field. Record if an electrocardiogram (ECG) was performed, even if the result was normal. Indicate any significant findings.
integer
Please complete this section with the results of any tests that were ordered as the time MIS is first suspected. Record if a test was performed even if findings were normal. If abnormal findings were detected, specify these in the free text field. Record if an electrocardiogram (ECG) was performed, even if the result was normal. Indicate any significant findings.
text
Please complete this section with the results of any tests that were ordered as the time MIS is first suspected. Record if a test was performed even if findings were normal. If abnormal findings were detected, specify these in the free text field. Record if echocardiography was performed, even if the result was normal. Indicate any significant findings.
integer
Please complete this section with the results of any tests that were ordered as the time MIS is first suspected. Record if a test was performed even if findings were normal. If abnormal findings were detected, specify these in the free text field. Record if echocardiography was performed, even if the result was normal. Indicate any significant findings.
integer
Please complete this section with the results of any tests that were ordered as the time MIS is first suspected. Record if a test was performed even if findings were normal. If abnormal findings were detected, specify these in the free text field. Record if echocardiography was performed, even if the result was normal. Indicate any significant findings.
integer
Please complete this section with the results of any tests that were ordered as the time MIS is first suspected. Record if a test was performed even if findings were normal. If abnormal findings were detected, specify these in the free text field. Record if echocardiography was performed, even if the result was normal. Indicate any significant findings.
integer
Please complete this section with the results of any tests that were ordered as the time MIS is first suspected. Record if a test was performed even if findings were normal. If abnormal findings were detected, specify these in the free text field. Record if echocardiography was performed, even if the result was normal. Indicate any significant findings.
integer
Please complete this section with the results of any tests that were ordered as the time MIS is first suspected. Record if a test was performed even if findings were normal. If abnormal findings were detected, specify these in the free text field. Record any other cardiac imaging performed, e.g. cardiac MRI. Please specify the type of imaging and the results in the space provided.
integer
Please complete this section with the results of any tests that were ordered as the time MIS is first suspected. Record if a test was performed even if findings were normal. If abnormal findings were detected, specify these in the free text field. Record any other cardiac imaging performed, e.g. cardiac MRI. Please specify the type of imaging and the results in the space provided.
text
Please complete this section with the results of any tests that were ordered as the time MIS is first suspected. Record if a test was performed even if findings were normal. If abnormal findings were detected, specify these in the free text field. Record any other cardiac imaging performed, e.g. cardiac MRI. Please specify the type of imaging and the results in the space provided.
text