Form Approved
OMB No. 0920-1385
Exp. Date: 3/31/26
	
Triazole-resistant Aspergillus fumigatus case report form
Unique patient ID (DCIPHER): ________________
ARLN specimen ID: ________________ | ARLN isolate ID:________________ | ARLN patient ID:________________
| Form completion data | ||
| Name of person completing this form: _______________________ Institution: _______________________ Email: ____________________ Telephone: ___________________ Date form completed: _________________ 
 Date of incident specimen collection (DISC)*: ______-______-___________ (mm-dd-yyyy) *This is the earliest date that a patient had a positive test for triazole-resistant A. fumigatus | ||
| 
				 | ||
| 
 | A. Patient demographics | |
| 
				 | 1. Age at DISC: (use months or days if patient was aged <2 years) | 
				 ________ □ Years □ Months □ Days □ Unknown | 
| 
				 | 2.Assigned sex at birth | □ Male □ Female □ Unknown | 
| 3. Gender identity | □ Male □ Female □ Transgender, non-binary, or another gender □ Prefer not to answer/Decline □ Unknown | |
| 
				 | 4. Ethnic origin | □ Hispanic or Latino □ Not Hispanic or Latino □ Unknown | 
| 
				 | 5. Race (select all that apply) | □ American Indian/Alaska Native □ Asian □ Black/African American □ Native Hawaiian/Pacific Islander □ White □ Unknown | 
| 
				 | 6. Patient's county of residence (Please do not write the word “County”; for example, write “Cook” instead of “Cook County”): 
 | 
				 _______________________ □ Unknown | 
| 
				 | 7. Patient’s state, jurisdiction, or territory of residence | 
 _______________________ □ Unknown | 
| 
				 | 8. Patient’s country of residence (e.g., USA) | 
				 _______________________ □ Unknown | 
| 
				 | 9. Healthcare facility name 
 (Note: ‘healthcare facility’ refers to the facility where the patient’s incident specimen was collected) | 
				 
 _______________________ □ Unknown | 
| 
				 | 10. Healthcare facility CMS ID # | 
				 _______________________ □ Unknown | 
| A. Patient Demographics (continued) | |
| 11. Healthcare facility ZIP code 
 | 
			 _______________________ □ Unknown | 
| 12. Healthcare facility state, jurisdiction, or territory | 
			 _______________________ □ Unknown | 
| 13. Healthcare facility type | □ Acute care hospital (ACH) □ Long-term acute care hospital (LTACH) □ Skilled nursing facility with ventilated residents (vSNF) □ Skilled nursing facility without ventilated residents (SNF) □ Outpatient □ Unknown □ Other ________________________ | 
| B. Patient underlying risk factors & medical conditions present during the 2 years before DISC (unless other timeframe specified) | |
| 1. Cancer □ Yes □ No □ Unknown □ Hematologic malignancy specify type: _____________ □ Solid organ malignancy specify type:____________ □ Chemotherapy If yes, specify: ________________ 
 | 3. Chronic pulmonary diagnosis □ Yes □ No □ Unknown □ Chronic obstructive pulmonary disease (COPD) or emphysema □ Bronchiectasis □ Cystic fibrosis □ Allergic bronchopulmonary aspergillosis (ABPA) □ Pulmonary fibrosis □ Asthma □ Interstitial Lung Disease □ Other chronic pulmonary diagnosis (specify):____________ 
 | 
| 2. HIV infection □ Yes □ No □ Unknown If yes, choose one of the below Ever had CD4 < 200 cells/mm3 within past 6 months □ Yes □ No □ Unknown 
 | |
| 4. Positive respiratory viral test in 120 days before or after DISC □ Yes □ No □ Unknown 
 If yes, (select all that apply): □ SARS-CoV-2 (PCR or antigen test) □ antigen □ PCR □ unknown test type □ Influenza □ Other respiratory virus (specify) ________________ | 5. Transplant received within 2 years before DISC □ Yes □ No □ Unknown 
 □ Solid organ transplant: □ Lung □ Heart □ Kidney □ Pancreas □ Liver □ Skin graft □Other:___________________________ 
 □ Hematopoietic stem cell transplant (HSCT) | 
| 6. Other selected conditions: □ Yes □ No □ Unknown □ Cardiovascular disease (specify): _________________ □ Diabetes mellitus □ End stage renal disease/dialysis □ Autoimmune disease(s) or inherited immunodeficiency(-ies) (specify): _________________________ □ Medications/therapies that weaken the immune system □ TNF-alpha inhibitors (e.g., infliximab, adalimumab, etanercept) □ Other (specify): ____________________________________________ □ Cirrhosis □ Liver disease without cirrhosis □ Systemic lupus erythematosus □ Active tuberculosis □ Pregnant □ Pregnant on DISC Gestational age (weeks):_______ Unknown □ Post-partum (gave birth within 6 weeks before DISC) | 7. Other potentially relevant clinical information? □ Yes (specify below) □ No □ Unknown ________________________________ ________________________________ ________________________________ ________________________________ ________________________________ 
 | 
| C. Patient diagnosis and outcomes | |
| 1. According to treating clinicians, which clinical syndrome(s) related to Aspergillus did the patient have? | □ Invasive pulmonary aspergillosis (IPA) 
 □ Other disease/syndrome(s) related to A. fumigatus: ___________________ 
 □ Aspergillus was not believed to be causing clinical illness or is not mentioned in medical records 
 □ Unknown 
 | 
| 2. Was the patient hospitalized at an acute care hospital in the 30 days before to 30 days after DISC? | □ Yes □ No □ Unknown If yes, dates of admission of hospitalization most proximal to DISC, 
 Admission date: ______-______-___________ (mm-dd-yyyy) 
 Discharge date: ______-______-___________ (mm-dd-yyyy) □ Still hospitalized 
 If yes, 
 Received ICU-level care in the 14 days before DISC?: □ Yes □ No □ Unknown 
 Received ICU-level care in the 14 days after DISC?: □ Yes □ No □ Unknown 
 Discharge ICD-10 diagnosis code(s): _________________________________ | 
| 3. Died within 30 days after DISC? 
 | □ No 
 □ Yes, date of death _______ - _______- ______________ (mm-dd-yyyy) Cause(s) of death _________________ 
 
 □ Unknown | 
| 
 | D. Antifungal treatment: Did the patient receive antifungal drugs during the 60 days before to 30 days after the DISC? □ Yes □ No □ Unknown (If yes, please complete the table below for each drug received). | |||
| Select one of the following to complete each row of the table | ||||
| Amphotericin B lipid complex (ABLC) Liposomal Amphotericin B (L-AmB) Amphotericin B colloidal dispersion (ABCD) Anidulafungin (ANF) | Caspofungin (CAS) Fluconazole (Not mold-active) (FLC) Flucytosine (5FC) Ibrexafungerp (IBR) | Isavuconazole (ISA) Itraconazole (ITC) Micafungin (MFG) Posaconazole (PSC) Voriconazole (VRC) | Other drug (specify): ________________________ Unknown drug (UNK) 
 | |
| Drug Abbrev | b. First date given (mm-dd-yyyy) | c. Last date given (mm-dd-yyyy) | d. Indication 
 | e. Therapeutic drug monitoring (TDM) | 
| 
			 | ___ ___ - ___ ___ - ___ ___ ___ ___ 
			 □ Start date unknown □ Start date was >60 days before DISC | ___ ___ - ___ ___ - ___ ___ ___ ___ 
 □ Still on treatment at time CRF completed □ Stop date unknown 
 | □ Prophylaxis □ Treatment for Aspergillus □ Treatment for non-Aspergillus infection 
 | □ Yes Date of earliest TDM: TDM level: 
 Date of second TDM: TDM level: 
 □ No | 
| 
			 | ___ ___ - ___ ___ - ___ ___ ___ ___ 
 □ Start date unknown □ Start date was >60 days before DISC | ___ ___ - ___ ___ - ___ ___ ___ ___ 
 □ Still on treatment at time CRF completed □ Stop date unknown 
 | □ Prophylaxis □ Treatment for Aspergillus □ Treatment for non-Aspergillus infection 
 | □ Yes Date of earliest TDM: TDM level: 
 Date of second TDM: TDM level: 
 □ No | 
| 
			 | ___ ___ - ___ ___ - ___ ___ ___ ___ 
 □ Start date unknown □ Start date was >60 days before DISC | ___ ___ - ___ ___ - ___ ___ ___ ___ 
 □ Still on treatment at time CRF completed □ Stop date unknown 
 
 | □ Prophylaxis □ Treatment for Aspergillus □ Treatment for non-Aspergillus infection 
 | □ Yes Date of earliest TDM: TDM level: 
 Date of second TDM: TDM level: 
 □ No | 
| 
			 | ___ ___ - ___ ___ - ___ ___ ___ ___ 
 □ Start date unknown □ Start date was >60 days before DISC | ___ ___ - ___ ___ - ___ ___ ___ ___ 
 □ Still on treatment at time CRF completed □ Stop date unknown 
 | □ Prophylaxis □ Treatment for Aspergillus □ Treatment for non-Aspergillus infection 
 | □ Yes Date of earliest TDM: TDM level: 
 Date of second TDM: TDM level: 
 □ No | 
| 
			 | ___ ___ - ___ ___ - ___ ___ ___ ___ 
 □ Start date unknown □ Start date was >60 days before DISC | ___ ___ - ___ ___ - ___ ___ ___ ___ 
 □ Still on treatment at time CRF completed □ Stop date unknown 
 | □ Prophylaxis □ Treatment for Aspergillus □ Treatment for non-Aspergillus infection 
 | □ Yes Date of earliest TDM: TDM level: 
 Date of second TDM: TDM level: 
 □ No | 
| Supplemental patient interview form: Note that “you” in these questions refers to the patient. | |||||||||||||||||
| 1. Person interviewed | □ Patient □ Someone other than the patient, (specify relationship to patient): _______________ | ||||||||||||||||
| 2. What was your job or occupation before [DISC]? | 
			 ___________________________ □ Unemployed □ Student □ Retired □ N/A □ Refused to answer □ Unknown | ||||||||||||||||
| 3. What was your industry before [DISC]? | ___________________________ □ Unemployed □ Student □ Retired □ N/A □ Refused to answer □ Unknown | ||||||||||||||||
| 3. Did you travel outside of [healthcare facility state] within 3 months before [DISC]? (note: if healthcare facility is in a different state from patient’s residence, then please count time spent in the patient’s home state as “travel”) 
 List state(s), territory(-ies), jurisdiction(s), country(-ies) | 
			 □ Yes □ No □ Unknown 
 
 
 
 
 
 __________________________________________________________________ 
 __________________________________________________________________ 
 
 | ||||||||||||||||
| 4. Did you perform any of the following activities during the 90 days before [DISC] | 
 
 | ||||||||||||||||
Additional comments: _____________________________________________________________________________________________
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CDC estimates the average public reporting burden for this collection of information as 30 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 this burden to CDC/ATSDR CDC/ATSDR Information Collection Review Office, 1600 Clifton Road NE, MS H21-8, Atlanta, Georgia 30333; ATTN: PRA (0920-1385).
	
| File Type | application/vnd.openxmlformats-officedocument.wordprocessingml.document | 
| Author | Williams, Samantha (CDC/NCEZID/DFWED/MDB) | 
| File Modified | 0000-00-00 | 
| File Created | 2024-07-20 |