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pdf1. PATIENT ID:
2. STATE ID:
3. SPECIMEN ID:
4. DATE OF INCIDENT C. diff+ STOOL COLLECTION:
Form Approved
OMB No. 092-0978
/
CLOSTRIDIOIDES DIFFICILE INFECTION (CDI) SURVEILLANCE
EMERGING INFECTIONS PROGRAM CASE REPORT
Patient’s Name:
Phone No.: (
(Last, First, M.I.)
Address:
(State)
5. STATE:
6. COUNTY:
(Residence of Patient)
(Residence of Patient)
7. LABORATORY ID WHERE
INCIDENT SPECIMEN
IDENTIFIED
)
-
Chart Number:
(Number, Street, Apt. No.)
(City)
Hospital:
(Zip Code)
9. POSITIVE DIAGNOSTIC ASSAY FOR C. diff+
8. FACILITY ID WHERE
PATIENT TREATED
9a. EIA
Positive
Negative
Not tested
9b. GDH
Positive
Negative
Not tested
9c. Cytotoxin
Positive
Negative
Not tested
9d. NAAT (C. diff only)
Positive
Negative
Not tested
9e. NAAT (GI panel)
Positive
Negative
Not tested
9.e.1 If positive, was result suppressed?
9f. Other (specify):
10. DATE OF BIRTH:
/
/
12. SEX AT BIRTH:
Male
Female
/
13. ETHNIC ORIGIN:
Hispanic or Latino
11. AGE: (years):
No
Unknown
Positive
Negative
Not tested
14. RACE: (Check all that apply)
Unknown
Transgender
Unknown
Yes
Not Hispanic or Latino
Unknown
American Indian or
Alaska Native
Native Hawaiian or
Other Pacific Islander
Asian
White
Black or African American
Unknown
15. Was the patient hospitalized on the day of or in the 6 calendar days after the date of incident C. diff+ stool collection?
Yes
No
Unknown
/
/
Unknown
15a. If YES, Date of Admission:
16. Where was the patient located on the 3rd calendar day before the date of incident C. diff+ stool collection?
Private Residence
LTCF
Facility ID:
Hospital Inpatient
Facility ID:
Homeless
Incarcerated
16a. Was the patient transferred from this hospital?
LTACH
Yes
No
Unknown
Other (specify):
Unknown
Facility ID:
18. HCFO classification questions:
17. Location of incident C. diff+ stool collection
Outpatient
Facility ID:
Hospital Inpatient
Facility ID:
LTCF
Facility ID:
18a. Was incident C. diff+ stool collected at least 3 calendar
days after the date of hospital admission?
Yes (HCFO - go to 18d)
No
18b. Was incident C. diff+ stool collected in an outpatient
setting for a LTCF resident, or in a LTCF or LTACH?
Yes (HCFO - go to 18d)
No
Emergency room
ICU
LTACH
Clinic/doctor’s office
OR
Facility ID:
Dialysis center
Radiology
Surgery
Other inpatient
Observation/
Autopsy
Other (specify):
Clinical decision unit
Other outpatient
19. Patient Outcome
18c. Was the patient admitted from a LTCF or a LTACH?
Yes (HCFO - go to 18d)
No (CO - complete CRF)
Facility ID:
18d. If HCFO, was this case sampled for full CRF?
Yes (Complete CRF)
No (STOP data abstraction here!)
1
2
3
4
5
6
7
8
9
Unknown
10
Unknown
Survived
Died
19a. Date of discharge:
/
/
Unknown
19c. Date of death:
/
/
Unknown
Left against medical advice (AMA)
19b. If survived, discharged to:
Private residence
LTCF
Facility ID:
LTACH
Facility ID:
Other (specify):
Unknown
Public reporting burden of this collection of information is estimated to average 38 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 30329; ATTN: PRA (0920-0978).
CDC Rev. 08-2019
CS308111
Page 1 of 4
20. Exposures to healthcare in the 12 weeks before the date of incident C. diff+ stool collection
20a. Previous hospitalization
20a.1 If yes, date of discharge closest to date of incident C. diff+ stool collection:
/
/
Unknown
20b. Overnight stay in LTACH
20c. Overnight stay in LTCF
20d. Chronic dialysis
Hemodialysis
Peritoneal
Unknown
20d.1 Type
20e. Surgery
20f. ER visit
20g. Observation/CDU stay
21. UNDERLYING CONDITIONS: (Check all that apply)
Chronic lung disease
None
No
Unknown
Facility ID:
Yes
Yes
Yes
No
No
No
Unknown
Unknown
Unknown
Facility ID:
Facility ID:
Yes
Yes
Yes
No
No
No
Unknown
Unknown
Unknown
Unknown
Liver disease
Cystic fibrosis
Chronic pulmonary disease
Plegias/Paralysis
Chronic liver disease
Ascites
Cirrhosis
Hepatic encephalopathy
Variceal bleeding
Hepatitis C
Treated, in SVR
Current, chronic
Chronic metabolic disease
Diabetes mellitus
With chronic complications
Cardiovascular disease
CVA/Stroke/TIA
Congenital heart disease
Congestive heart failure
Myocardial infarction
Peripheral vascular disease (PVD)
Hemiplegia
Paraplegia
Quadriplegia
Renal disease
Chronic kidney disease
Lowest serum creatinine:
Unknown or not done
Burn
Decubitus/pressure ulcer
Surgical wound
Other chronic ulcer or chronic wound
Other (specify):
Malignancy, hematologic
Malignancy, solid organ (non-metastatic)
Malignancy, solid organ (metastatic)
Neurologic condition
Diverticular disease
Inflammatory bowel disease
Peptic ulcer disease
Short gut syndrome
Cerebral palsy
Chronic cognitive deficit
Dementia
Epilepsy/seizure/seizure disorder
Multiple sclerosis
Neuropathy
Parkinson’s disease
Other (specify):
Immunocompromised condition
HIV
AIDS/CD4 count < 200
Primary immunodeficiency
Transplant, hematopoietic stem cell
Transplant, solid organ
22a. Weight
Other
Connective tissue disease
Obesity or morbid obesity
Pregnancy
22b. Height
oz OR
kg
Unknown
mg/DL
Skin condition
Malignancy
Gastrointestinal disease
lbs
Yes
22c. BMI
ft
in OR
cm
Unknown
Unknown
23. Substance Use
23a. Smoking:
23b. Alcohol abuse:
None
Unknown
Tobacco
E-Nicotine Delivery System
23c. Other substances: (Check all that apply)
None
Marijuana
Unknown
Documented Use Disorder (DUD)/Abuse?
Marijuana/cannabinoid (other than smoking)
DUD or Abuse
Opioid, DEA schedule I (e.g., heroin)
DUD or Abuse
Opioid, DEA schedule II-IV (e.g., methadone, oxycodone)
DUD or Abuse
Opioid, NOS
DUD or Abuse
Cocaine
DUD or Abuse
Methamphetamine
DUD or Abuse
Other (specify):
DUD or Abuse
Unknown substance
DUD or Abuse
During the current hospitalization, did the patient receive medication assisted treatment
(MAT) for opioid use disorder?
24. Was CDI a primary or contributing reason
for patient’s admission?
Yes
No
Not Admitted
Unknown
Mode of delivery: (Check all that apply)
IDU
Skin popping
non-IDU
Unknown
IDU
Skin popping
non-IDU
Unknown
IDU
Skin popping
non-IDU
Unknown
IDU
Skin popping
non-IDU
Unknown
IDU
Skin popping
non-IDU
Unknown
IDU
Skin popping
non-IDU
Unknown
IDU
Skin popping
non-IDU
Unknown
IDU
Skin popping
non-IDU
Unknown
Yes
No
N/A (patient not hospitalized or did not have DUD)
25. Was ICD-9 008.45 or ICD-10 A04.7 listed on 26. Was the patient in an ICU on the day of or in
the discharge form?
the 6 days after the date of incident C. diff+
stool collection?
Yes
No
Not Admitted
Unknown
25a. If YES, what was the POA code
assigned to it?
Y, Yes
N, No
U, Unknown
CDC Rev. 08-2019
Yes
No
Unknown
W, Clinically Undetermined
Missing
Not Applicable
CS308111
Yes
No
Unknown
26a. If YES, date of ICU admission:
/
/
Unknown
Page 2 of 4
27. Symptoms (in the 6 calendar days before, the day of, or 1 calendar
day after the date of incident C. diff+ stool collection) (Check all that apply)
28. Toxic megacolon and ileus (in the 6 calendar days before, the day of, or
the 6 calendar days after the date of incident C. diff+ stool collection)
“Asymptomatic” documented in medical record
28a. Radiographic findings
28b. Clinical findings
Diarrhea by definition (unformed or watery stool, ≥ 3/day for ≥ 1 day)
Toxic megacolon
Toxic megacolon
Diarrhea documented, but unable to determine if it is by definition
Ileus
Ileus
Nausea
Both toxic megacolon and ileus
Both toxic megacolon and ileus
Vomiting
Neither toxic megacolon nor ileus
Neither toxic megacolon nor ileus
No diarrhea, nausea, or vomiting documented
Radiology not performed
Information not available
Information not available
Information not available
29. Was pseudomembranous colitis listed in the surgical pathology,
endoscopy, or autopsy report in the 6 calendar days before,
the day of, or the 6 calendar days after the date of incident
C. diff+ stool collection?
Yes
No
Not Done
Information not available
31. Were other enteric pathogens isolated from stool collected on the
date of incident C. diff+ stool collection?
Campylobacter
Norovirus
Rotavirus
Salmonella
Shiga Toxin-Producing E.coli
Shigella
Other (specify):
None
No other pathogens tested
Unknown
30. Colectomy
(related to CDI):
Yes
No
Unknown
30a. If YES, Date of Procedure:
/
/
Unknown
32. LABORATORY FINDINGS (in the 6 calendar days before, the
day of, or the 6 calendar days after the date of incident
C. diff+ stool collection):
32a. Albumin ≤2.5g/dl:
Yes
No
Not Done
Information not available
32b. White blood cell count ≤ 1,000/µl:
Yes
No
Not Done
Information not available
32c. White blood cell count ≥ 15,000/µl:
Yes
No
Not Done
Information not available
33. MEDICATIONS TAKEN in the 12 weeks before the date of incident C. diff+ stool collection:
33a. Proton pump inhibitor
(e.g. Omeprazole, Lansoprazole,
Pantoprazole, Rabeprazole)
33b. H2 Blockers
(e.g. Famotidine, Ranitidine, Cimetidine)
Yes
No
Unknown
Steroids
Chemotherapy
Other agents (specify):
None
Unknown
Yes
No
Unknown
33d. Antimicrobial therapy (Check all that apply)
Amikacin
Amoxicillin
Amoxicillin/clavulanic acid
Ampicillin
Ampicillin/sulbactam
Azithromycin
Aztreonam
Cefazolin
Cefdinir
Cefepime
Cefixime
Cefotaxime
None
Cefoxitin
Cefpodoxime
Ceftaroline
Ceftazidime
Ceftazidime/avibactam
Ceftizoxime
Ceftolozane/tazobactam
Ceftriaxone
Cefuroxime
Cephalexin
Ciprofloxacin
Clarithromycin
33c. Immunosuppressive therapy
(Check all that apply)
Unknown
Clindamycin
Dalbavancin
Daptomycin
Delafloxacin
Doripenem
Doxycycline
Ertapenem
Fosfomycin
Gentamicin
Imipenem/cilastatin
Levofloxacin
Linezolid
Meropenem
Meropenem/vaborbactam
Metronidazole
Moxifloxacin
Nitrofurantoin
Oritavancin
Penicillin
Piperacillin/tazobactam
Polymyxin B
Polymyxin E (colistin)
Rifaximin
Tedizolid
Telavancin
Tigecycline
Tobramycin
Trimethoprim
Trimethoprim/sulfamethoxazole
Vancomycin (IV)
Other (specify):
33e. Was patient treated for previous suspected or confirmed CDI in the 12 weeks before the date of incident C. diff+ stool collection?
Yes
No
Unknown
33e.1 If YES, which medication was taken (Check all that apply):
Metronidazole
CDC Rev. 08-2019
Vancomycin
Fidaxomicin
Other, (specify)
CS308111
Unknown
Page 3 of 4
34. Treatment for incident CDI
No treatment
Unknown treatment
34a.1 Course 1
Start Date:
/
/
Vancomycin (PO)
Vancomycin (Rectal)
Vancomycin (Unknown route)
Vancomycin taper (any route)
Unknown Stop Date:
/
/
Metronidazole (PO)
Metronidazole (IV)
Metronidazole (Unknown route)
Fidaxomicin
Unknown OR Duration (days)
Rifaximin
Nitazoxanide
Other (specify):
Unknown
Unknown Stop Date:
/
/
Metronidazole (PO)
Metronidazole (IV)
Metronidazole (Unknown route)
Fidaxomicin
Unknown OR Duration (days)
Rifaximin
Nitazoxanide
Other (specify):
Unknown
Unknown Stop Date:
/
/
Metronidazole (PO)
Metronidazole (IV)
Metronidazole (Unknown route)
Fidaxomicin
Unknown OR Duration (days)
Rifaximin
Nitazoxanide
Other (specify):
Unknown
Unknown Stop Date:
/
/
Metronidazole (PO)
Metronidazole (IV)
Metronidazole (Unknown route)
Fidaxomicin
Unknown OR Duration (days)
Rifaximin
Nitazoxanide
Other (specify):
Unknown
34a.2 Course 2
Start Date:
/
/
Vancomycin (PO)
Vancomycin (Rectal)
Vancomycin (Unknown route)
Vancomycin taper (any route)
34a.3 Course 3
Start Date:
/
/
Vancomycin (PO)
Vancomycin (Rectal)
Vancomycin (Unknown route)
Vancomycin taper (any route)
34a.4 Course 4
Start Date:
/
/
Vancomycin (PO)
Vancomycin (Rectal)
Vancomycin (Unknown route)
Vancomycin taper (any route)
34b.
Probiotics (specify):
34c.
Stool transplant Date:
/
/
Unknown
35. Previous unique CDI episode
36. Any recurrent C. diff+
(>8 weeks before the date of
episodes following this
incident C. diff+ stool collection):
incident C. diff+ episode?
Yes
No
Yes
No
35a. If YES, previous STATEID:
36a. If YES, Date of first
recurrent specimen:
/
40. Did the patient have a
POSITIVE test(s) for SARSCoV-2 (molecular assay,
serology or other confirmatory
test) on or before the DISC?
Yes
No
Unknown
41a. COVID-NET Case ID
37. CRF status:
Complete
Incomplete
Chart unavailable
after 3 requests
38. Initials of
S.O:
39. Date of abstraction:
/
/
/
40a. If YES, complete table below:
Specimen collection date
FIRST positive test for
SARS-CoV-2 on or before the
DISC:
/
Unknown
MOST RECENT positive test
for SARS-CoV-2 on or before
the DISC:
41b. NNDSS IDs (please
provide at least one of the
following when applicable):
/
/
/
Unknown
Test type
Molecular assay
Serology
Unknown
Other (specify):
Molecular assay
Serology
Unknown
Other (specify):
Local Case ID:
Local Record ID:
State case identifier:
Legacy case identifier:
Comments:
CDC Rev. 08-2019
CS308111
Page 4 of 4
File Type | application/pdf |
File Modified | 2020-07-28 |
File Created | 2019-08-06 |