Form 0920-0879 PEDIATRIC HEPATITIS OF UNKNOWN ETIOLOGY MEDICAL RECORD A

[NCSTLTPHIW] Information Collections to Advance State, Tribal, Local and Territorial (STLT) Governmental Agency System Performance, Capacity, and Program Delivery

Attachment A_Pediatric Hepatitis of Unknown Etiology Medical Record Abstraction Form Controls_17Jan2024

[PHIC/NCIRD] Pediatric Hepatitis-Adenovirus Case Control Evaluation, United States 2022-2026 (24CN)

OMB: 0920-0879

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Attachment A: PEDIATRIC HEPATITIS OF UNKNOWN ETIOLOGY MEDICAL RECORD ABSTRACTION FORM: CONTROLS

Control ID: _________________________________

MATCHED CASE ID:__________________________


Form Approved: OMB No. # 0920-0879

Exp. Date 08/31/2026

Version 19 Aug 2022

General Instructions:

  • Please complete the form for all children who are enrolled as controls in the case-control evaluation to examine the potential causes of pediatric hepatitis of unknown etiology.

  • Yellow fields do not need to be submitted to CDC.

  • Greyed out fields do not require information.

  • ControlID: Please assign using the caseID followed by a dash and two numbers (ie. ‘-01-04’). For example, if the caseID = ‘GA0001’ the control ID would be GA0001-01 for the first enrolled control and so on for each additional control enrolled (up to a maximum of 4 controls per case).

  • Some sections may be best completed by a clinician (e.g. Clinical Info)

  • Vaccination information should be captured from the state Immunization Information System as the primary source.

  • Any relevant information that does not fit in a designated section can be noted in the “Notes” section.

  • All dates should be in the format MM/DD/YYYY.

Reminder about adenovirus testing:

  • CDC is requesting residual/available respiratory, stool, and blood (including whole blood, plasma or serum) specimens be sent to CDC for testing and (if adenovirus positive) typing.

  • Please refer to the specimen protocol for additional instructions on testing/shipping of specimens.


Submission Instructions:

CDC requests submission of completed forms on a rolling basis. Please upload completed forms to the ShareFile folder via one of the following:

  1. Scanned/electronic copy of the completed form

  2. CSV export from REDCap database (if using CDC REDCap data structure in state/local REDCap instance)



For questions related to form completion or submission instructions, email [email protected]


Date form completed: ____/____/_______

DEMOGRAPHICS

Yellow fields do not need to be submitted to CDC

Patient’s name (Last, First, M.I.) ______________________________________

DOB: ____/____/_______

Age: Days Months Years

Sex assigned at birth: Male Female Refused Don’t know

Street Address:

City: County: State: Zip: _____________

Phone (Cell/Home): _________________________

Phone (Cell/Home): _________________________

Ethnicity: □ Hispanic or Latino

Not Hispanic or Latino

Unknown

Race □ American Indian/Alaska Native □ Native Hawaiian/Pacific Islander

(check all that apply) □ Asian □ White

Black/African American □ Other (________________)


SIGNS/SYMPTOM HISTORY

Did the patient have any of the following signs/symptoms in the past 2 weeks?

Category of signs/symptoms

Check all that apply:

First Respiratory sign/symptom Onset: ____/_____/____

Unknown

Cough □ Congestion □ Rhinorrhea

Sore throat □ Wheezing □ Shortness of breath

Conjunctivitis (pink eye)

First GI sign/symptom Onset: _____/_____/______

Unknown

Diarrhea □ Nausea

Vomiting □ Abdominal Pain

Date of systemic sign/symptom Onset: _____/_____/______

Unknown

Fatigue □ Fever (Max) ________ °F

Decreased appetite □ Other, specify:


CLINICAL INFORMATION

Yellow fields do not need to be submitted to CDC.

For date of initial evaluations, please note the date that the child first sought medical care for this illness.

Patient Height: __________ □ ft/in □ cm □ Unknown

Patient Weight: ___________ Ibs □ Kg □ Unknown

Reason patient was receiving medical care:


Tonsillectomy

Ear tubes (Tympanostomy)

Illness of infectious etiology, specify

_____________________

Other surgical procedure, specify ____________________

Chronic illness, specify ____________________

Injury, specify___________________________

Other, specify ___________________________

Date of evaluation: _____/_____/______ □ Unknown

Where was the patient first identified?

Primary care provider

Urgent care

Emergency department

Hospital

Unknown

Other, specify ______________

Name of facility:

________________________

Was the patient hospitalized for this illness? Yes No Unknown

If patient was hospitalized: Hospital: __________________________ Medical Record #: _________

Admission Date (Initial Hospital):____/____/_______ Unknown admission date

Was the patient transferred from another hospital? Yes No Unknown

If yes, which hospital? _________________________ Transfer Date: ___/___/______ Unknown

Final patient outcome: Survived, discharge home

Survived, discharged other location

Died If yes, was an autopsy performed? □ Yes □ No □ Unknown

Unknown

Date of discharge / death: _____/_____/_______ □ Unknown date of discharge/death




If patient was hospitalized: ICD-10 discharge codes:

Primary code: Other codes (list up to 10):

















Were there additional codes beyond those listed above: □ Yes □ No □ Unknown


UNDERLYING HEALTH CONDITIONS

Did the patient have any of the following underlying health conditions? Yes No Unknown

If yes, check all that apply:

Asthma (or Reactive Airway Disease)

Congenital Heart Disease

Diabetes Mellitus (Type 1 or 2)

Leukemia/Lymphoma

Sickle cell anemia

Seizure/Seizure disorder


Other cancer, specify___________________________________

Developmental disorder, specify__________________________

Premature Birth (Gestational age at birth: ___________ weeks)

History of any transplant, specify _________________________

Other condition, specify ________________________________


ADENOVIRUS TESTING

Provide information on any repeat testing or multiple sample types in the ‘Other sample, specify’ fields and write-in the specimen type.

Diagnostic Test

Tested/Result

Specimen Collection Date (mm/dd/yyyy)

Is specimen available for shipping to CDC?

Stool

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

If tested, specify type: □ Multipanel PCR □ Other PCR □ Antigen


Yes No Unkn

Respiratory or throat


Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

If tested, specify type: □ Multipanel PCR □ Other PCR □ Antigen


Yes No Unkn

Whole blood

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn


Yes No Unkn

Plasma

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn


Yes No Unkn

Serum

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn


Yes No Unkn

Other sample, specify ___________________

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn


Yes No Unkn

Other sample, specify ___________________

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn


Yes No Unkn

Other sample, specify ___________________

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn


Yes No Unkn

Diagnostic test

Value and units

Specimen Collection Date (mm/dd/yyyy)

Specimen type

Blood qPCR

_________ □ copies/mL □ IU/mL


Whole blood □ Plasma □ Serum

_________ □ copies/mL □ IU/mL


Whole blood □ Plasma □ Serum

_________ □ copies/mL □ IU/mL


Whole blood □ Plasma □ Serum

_________ □ copies/mL □ IU/mL


Whole blood □ Plasma □ Serum

_________ □ copies/mL □ IU/mL


Whole blood □ Plasma □ Serum

Adenovirus typing results

Not Sent (not typed) Type 41 Could not be typed Other type, specify_________ Pending










GASTROINTESTINAL TESTING

Greyed out fields do not require information. If multiple stool samples were collected/tested, mark pathogens detected on any specimen and provide details in the “Summary of Clinical Assessment” section.

Was a stool specimen collected for testing?

Yes No, skip to next section Unknown

Date of first specimen collection

_____/_____/______

Gastrointestinal panel testing

Test Performed

Test Type

Pathogens Detected (check all that apply)

Yes

No

Unknown

Luminex xTAG

Biofire / FilmArray

Other: ________________

Unknown

No pathogens detected

Campylobacter

Clostridium difficile

Plesiomonas shigelloides

Salmonella

Yersinia enterocolitica

Vibrio

Vibrio cholerae

Enteroaggregative E. coli (EAEC)

Enteropathogenic E. coli (EPEC)

Enterotoxigenic E. coli (ETEC) lt/st

Shiga-like toxin-producing E. coli (STEC)

E. coli O157

Shigella/Enteroinvasive E. coli (EIEC)

Cryptosporidium

Cyclospora cayetanensis

Entamoeba histolytica

Giardia lamblia

Astrovirus

Norovirus GI/GII

Rotavirus A

Sapovirus (I, II, IV and V)

Non-panel tests

Pathogen

Tested/Result

Test Type

Details

Bacterial culture

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn


If positive, pathogen:


Norovirus

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

PCR □ Other:

GI □GII □ Not specified

Sapovirus

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

PCR □ Other:

I □ II □ III □ IV

Not specified

Astrovirus

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

PCR □ Other:

Type:

Not specified

Rotavirus

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

PCR □ EIA

Other: _________

Genotype:

Not specified

Ova & Parasite

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn


If positive, pathogen isolated: _____________

C. difficile

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

Name of test: _____________



RESPIRATORY TESTING

Greyed out fields do not require information

Was a respiratory specimen collected for testing?

Yes □ No Unknown

If yes, specify specimen type ___________________

Date of specimen collection _____/_____/______

Respiratory panel testing

Test Performed

Test Type

Pathogens Detected (check all that apply)

Yes

No

Unknown

Luminex NxTAG RPP

Luminex NxTAG RPP + SARS-CoV-2

Luminex VERIGENE RP Flex

Biofire / FilmArray RPP

Biofire / FilmArray PN

Other: ___________________

Unknown

No pathogens detected


Coronavirus HKU1

Coronavirus NL63

Coronavirus 229E

Coronavirus OC43

SARS-CoV-2

Human Metapneumovirus

Human Rhinovirus/Enterovirus

Influenza A

Influenza A/H1

Influenza A/H3

Influenza A/H1-2009

Influenza B

Respiratory Syncytial Virus


Parainfluenza Virus 1

Parainfluenza Virus 2

Parainfluenza Virus 3

Parainfluenza Virus 4

Bordetella parapertussis

Bordetella pertussis

Chlamydia pneumoniae

Mycoplasma pneumoniae

Other :

Other respiratory specimen tests conducted

Pathogen

Tested/Result

Details

Date (mm/dd/yyyy)

SARS-CoV-2 PCR

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn



SARS-CoV-2 Antigen

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn



SARS-CoV-2, Serology (anti-nucleocapsid)

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn



SARS-CoV-2, Serology (anti-spike)

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn



SARS-CoV-2, Other specify______________

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn



Other test (specify): ____________________

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

If positive, pathogen isolated:


Other test (specify): ____________________

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

If positive, pathogen isolated:



OTHER VIRAL TESTING

Pathogen / Test Type

Tested/Result

Test/Specimen Type

Date (mm/dd/yyyy)

Cytomegalovirus- PCR

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

Whole blood PCR

Plasma PCR


Epstein-Barr virus (EBV)- PCR

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

Whole blood PCR

Plasma PCR


EBV- Viral Capsid Antigen IgG

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn




EBV- Viral Capsid Antigen IgM

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn



EBV- Nuclear Antigen (EBNA) IgG

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn



EBV- Early antigen (EA) IgG

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn



Human herpesvirus 6

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

PCR □ Other:


Human herpesvirus 7

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

PCR □ Other:


Varicella-zoster virus

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

PCR □ Other:


Enterovirus

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

PCR □ Other:


Human immunodeficiency virus

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

PCR □ Other:


Parvovirus B19

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

PCR □ Other:


Herpes simplex virus-1

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

PCR □ Other:


Herpes simplex virus-2

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

PCR □ Other:


Measles

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

PCR □ Other:


Leptospirosis

Not tested □ Pos □ Neg □ Indeterm □ Pending □ Unkn

PCR □ Other:




PATIENT HISTORY OF COVID-19

List the most recent positive test. Any additional positive tests can be noted in the “Summary of clinical assessment” section.


Has this patient previously tested positive for SARS-CoV-2? (before current illness)

Positive test

Test Type

Date (most recent, mm/dd/yyyy)

Yes □ No Unknown

PCR Antigen Serology Unknown

Date Unknown


LABORATORY MARKERS

Greyed out fields do not require information

Test Name

Initial Value

Date (mm/dd/yyyy)

Highest Value

Date (mm/dd/yyyy)

Alanine aminotransferase (ALT, U/L)





Aspartate aminotransferase (AST, U/L)





Total bilirubin (mg/dL)





Conjugated bilirubin (mg/dL)





Unconjugated bilirubin (mg/dL)





INR (International Normalized Ratio)





Alkaline phosphatase (ALP, U/L)





Ammonia (µg/dL)





Prothrombin time (PT)





White blood cell (WBC) count (Cells x 109/L)





Total Lymphocyte Count (Cells x 103/µL)





Absolute Neutrophil Count (Cells x 103/µL)





Hemoglobin (HGB, g/dL)





Platelets (Plt, Cells x 109/L)





Sodium (Na, mEq/L)





Chloride (Cl, mmol/L)





Potassium (K, mEq/L)





Carbon dioxide (C02, mmol/L)





Blood urea nitrogen (BUN, mg/dL)





Creatinine (mg/dL)





Glucose (mg/dL)





Calcium (mg/dL)





Albumin (g/dL)





Uric acid (UA, mg/dL)





Fibrinogen





C-reactive protein (CRP, mg/dL)





Erythrocyte Sedimentation Rate (ESR, mm/hr)





Antinuclear antibody (ANA)





Smooth muscle antibody (ASMA)





Liver kidney microsomal antibody (LKM)





Immunoglobulin (IgG)







VACCINATION INFORMATION

Information on vaccinations received should be captured from the state Immunization Information System as the primary source.

For SARS-CoV-2 vaccination, please indicate the vaccine manufacturer for each dose.

Greyed out fields do not require information.


Vaccination

Date Dose 1 (mm/dd/yyyy)

Date Dose 2 (mm/dd/yyyy)

Date Dose 3 (mm/dd/yyyy)

Date Dose 4 (mm/dd/yyyy)

Date Dose 5 (mm/dd/yyyy)

Hepatitis B







Rotavirus






DTaP/Tdap






Hib






PCV13






IPV






MMR






Varicella






Hepatitis A






SARS-CoV-2

(add vaccine manufacturer below date)

Manufacturer:

Manufacturer:

Manufacturer:



Influenza*






Additional vaccines / doses

(list vaccine & date)






*past year only





NOTES

Use this section to document any other relevant info or notes
















1

CDC estimates the average public reporting burden for this collection of information as 45 minutes per response, including the time for reviewing instructions, searching existing data/information sources, gathering and maintaining the data/information needed, and completing and reviewing the collection of information. An agency may not conduct or sponsor, and a person is not required to respond to a collection of information unless it displays a currently valid OMB control number. Send comments regarding this burden estimate or any other aspect of this collection of information, including suggestions for reducing burden to CDC/ATSDR Information Collection Review Office, 1600 Clifton Road NE, MS D-74, Atlanta, Georgia 30333; ATTN: PRA (0920-0879).


File Typeapplication/vnd.openxmlformats-officedocument.wordprocessingml.document
AuthorAlmendares, Olivia M. (CDC/DDID/NCIRD/DVD)
File Modified0000-00-00
File Created2024-07-19

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