Form Approved
OMB No. 0920-1011
Exp. Date 01/31/2023
VIM-Carbapenem Resistant Pseudomonas aeruginosa (VIM-CRPA)
Outbreak Investigation
Abstraction Form
Patient Name: |
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Medical Record Number: |
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Outbreak ID Number: |
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Jurisdiction: |
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ARLN ID: |
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DO NOT SEND THIS FIRST PAGE TO CDC
PLEASE KEEP FOR YOUR RECORDS
Please complete the tables below, either on paper or directly into REDCap. If information is unknown, please write “NA.” Thank you!
Today’s Date (mm-dd-yyyy): |
Abstractor’s Initials: |
Patient Demographics |
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Patient sex: □ Female □Male |
Patient Age (yrs): |
Patient ethnicity (please select only one):
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Patient race (please select all that apply):
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Isolate information |
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Date of collection of first positive VIM-CRPA culture or screening test (mm-dd-yyyy): |
Specimen source: |
Type of facility where specimen collected:
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Facility name: |
Facility State (2-letter abbreviation): |
Inpatient Admission Information |
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Is the patient currently admitted or has been admitted to a facility in the 3 months prior to date of first VIM-CRPA(+)? □ Yes □ No |
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If yes, please list all inpatient admissions in the 3 months prior to date of first VIM-CRPA(+) |
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Name of facility |
Type of facility (LTACH, ACH, Nursing home, Inpatient rehab, other) |
Facility state (2-letter abbrev) |
Admit date |
Admit diagnosis |
Admitted from (Home, LTACH, Nursing Home, Rehab, Other) |
Discharge Date |
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Status of admission: |
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□ Still Inpatient □ Discharged Home □ Deceased: Date______________ Cause of Death______________ |
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All discharge diagnoses: |
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Outpatient Information: |
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Has the patient visited an outpatient clinic in the 3 months prior to date of first VIM-CRPA(+)? □ Yes □ No |
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If yes, please list all outpatient healthcare visits in the 3 months prior to first VIM-CRPA(+) |
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Date |
Clinic Name |
Type of clinic/specialty (e.g., ophthalmology) |
Reason for visit |
Care received (incl. procedures) |
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Past Medical History (check all that apply):
□ Myocardial infarction
□ Congestive heart failure (EF_____)
□ Peripheral vascular disease
□ Cerebrovascular disease
□ Dementia
□ Chronic lung disease
□ Connective tissue disease
□ Ulcer disease
□ Diabetes Mellitus
□ Hemiplegia
□ Paraplegia
□ Moderate or severe renal disease
□ Solid tumor (non-metastatic)
□ Lymphoma, Multiple Myeloma
□ Mild liver disease
□ Moderate or severe liver disease
□ Dialysis Dependent
□ HIV (CD4____)
□ AIDS
□ Major Trauma (30d prior to admission)
□ Previous Surgery (30d prior to admission)
□ Obesity
□ Metastatic solid tumor
□ Other Malignancy (type_____________)
□ Hypertension
□ Other: ____________________________
□ Other Immunosuppression
(please specify ____________________)
□ Leukemia
□ Ocular disease
□ Glaucoma
□ Cataracts
□ Diabetic retinopathy
□ Macular degeneration
□ Other___________
Clinical History: |
History of Present Illness (Give a brief summary of patient’s illness, MDRO screening):
________________________________________________________________________________________________________________________________________________________________________________________________________________________
____________________________________________________________________________________________________________
____________________________________________________________________________________________________________
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Healthcare outside of state of VIM-CRPA(+) |
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Has the patient received any healthcare outside of the state (but within the United States) where the VIM-CRPA(+) culture was identified (inpatient or outpatient), anytime during the year prior to their first VIM-CRPA(+)? □ Yes □No |
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If yes, please list all patient healthcare that has not already been listed above. |
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Date |
Facility name |
Facility type |
State |
Reason for visit |
Inpatient/Outpatient |
Procedures performed |
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Did the patient receive any medical care outside of the US anytime during the year prior to their first VIM-CRPA(+)? □ Yes □No |
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If yes, please list medical care outside of the US |
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Dates of care |
Country |
Facility type |
Facility name |
Inpatient/Outpatient |
Type of care received (including any procedures) |
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Microbiology: Did patient have any other cultures (screening or clinical) collected in the 6 months prior to first VIM-CRPA culture? □ Yes □ No If yes, please list below -- Please be sure to include any CRPA negative cultures. |
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Date |
Specimen Source (e.g., blood, urine) |
Positive for P. aeruginosa? (Yes/No) |
Carbapenem resistant? (Yes/No/ Unknown) |
Carbapenemase mechanism testing performed (Yes/No; if Yes indicate results (e.g., VIM, IMP, KPC, etc) |
ARLN ID (if pos) |
Indication (Screening or clinical) |
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Microbiology: Did patient have any other screening swabs collected (non-culture-based) in the 6 months prior to first VIM-CRPA (+)? □ Yes □ No If yes, please list below -- Please be sure to include any negative results. |
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Date |
Type (admit, PPS, discharge)
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Specimen Source (e.g., rectal swab) |
VIM + (Yes/No/ unknown) |
Organism genus, species (if unknown, put NA) |
ARLN ID (if VIM+) |
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Medications Received |
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Was the patient on medication or antibiotics at any time 3 months prior to first VIM-CRPA (+) culture? □ Yes □ No |
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If yes, please list all medications the patient has taken 3 months prior to their first VIM-CRPA(+) culture |
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Name (generic) |
Route (IV, PO, etc.) |
Dates |
Manufacturer |
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Non-invasive radiology (e.g., X rays, CTs, Ultrasound, Swallow study, etc.): Did patient have any non-invasive radiologic studies, inpatient or outpatient, 3 months prior to first VIM-CRPA(+) culture? □ Yes □ No If yes, please list below. |
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Date |
Type of Study |
Inpatient or Outpatient |
Location (e.g., bedside, radiology) |
Facility name |
Notes (e.g., brand of U/S gel) |
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Invasive Procedures: Please list all procedures, inpatient or outpatient, 3 months prior to the positive culture (e.g., scopes, OR procedures, interventional radiology) |
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Date |
Procedure |
Inpatient or Outpatient
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Location (e.g., bedside,
OR) |
Facility name |
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Devices: Please list 3 months prior to the identification of first VIM-CRPA(+) |
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Device |
Site |
Date Inserted |
Date Removed (if still present, please write NA) |
□ Central Venous Catheter (e.g., CVC, PICC) |
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□ Non-invasive urinary catheter (e.g., Condom Catheter) |
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□ Invasive urinary catheter (e.g., Foley) |
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□ Suprapubic urinary catheter |
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Feeding Tube: □Nasogastric/Nasoduodenal □ PEG/PEJ (stomach) |
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□ Endotracheal tube |
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□ Tracheostomy tube |
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□ Noninvasive ventilation |
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□ Mechanical ventilation |
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□ Surgical drain |
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□ Other: describe__________ |
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□ Other: describe__________ |
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□ Other: describe__________ |
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Respiratory Therapy |
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Did the patient receive mechanical ventilation anytime in the 3 months prior to their first VIM-CRPA(+): □ Yes □No If yes: |
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Dates of ventilation:
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Ventilator brand: |
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Did the patient receive a tracheostomy?
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CPAP/BIPAP |
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Does the patient currently use a CPAP or BIPAP, or has used one anytime 3 months prior to first VIM-CRPA(+)?
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Nebulizers and Humidifiers |
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Did the patient receive any nebulizer treatments in the 3 months prior to first VIM-CRPA (+)?
If yes please fill in the below |
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Diluent for Nebulizer |
Dates diluent used |
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Did the patient use a humidifier in the 3 months prior to first VIM-CRPA (+)?
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Eye care |
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Did the patient use contact lenses or bandage lenses within the 3 months prior to first VIM-CRPA(+)?
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Does the patient receive routine eye care?
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If yes, type of eye care?
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Please list all products used for patient eye care within the 3 months prior to first VIM-CRPA(+), including contact lens solution, not including medications listed above |
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Product name |
Date(s) |
Brand |
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Oral care |
What type of oral care does the patient receive in the 3 months prior to the first VIM-CRPA (+) culture? Please select all types of care the patient has received:
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Skin & wound care |
How is the patient bathed in the 3 months prior to first VIM-CRPA(+)?
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Does the patient receive any wound care currently or in the 3 months prior to first VIM-CRPA(+)?
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If yes, please select all that apply:
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Please list all topical products (lotions, ointments, antiseptics, etc) used on the patient in the 3 months prior to the first VIM-CRPA(+) unless it’s listed in the medication section. |
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Product |
Manufacturer |
Lot #s (if available) |
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Diet (List all 3 months prior to the first positive culture, including NPO): |
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Diet ordered |
Route |
Dates |
If enteral or parenteral feeding, brand name |
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Consult Services (List all 3 months prior to first positive culture): □ Yes □ No If yes, please list below. |
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Service |
Start Date |
End Date |
□ Occupational Therapy |
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□ Physical Therapy |
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□ Respiratory Therapy |
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□ Wound Care Team |
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□ Dialysis |
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□ Other: Specify___________ |
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Other Notes:
Public reporting burden of this collection of information is estimated to average 60 minutes per response, including the time for reviewing instructions, searching existing data sources, gathering and maintaining the data 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 Reports Clearance Officer; 1600 Clifton Road NE, MS D-74 Atlanta, Georgia 30333; ATTN: PRA (0920-1011)
File Type | application/vnd.openxmlformats-officedocument.wordprocessingml.document |
Author | Amanda |
File Modified | 0000-00-00 |
File Created | 2023-08-18 |