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pdfPATIENT ID: ___ ___ ___ ___ ___ ___ ___ ___ ___
DATE REPORTED TO EIP SITE:
___ ___ - ___ ___ - ___ ___ ___ ___
2020 Extended-Spectrum Beta-Lactamase (ESBL)-Producing Enterobacteriaceae
Multi-site Gram-Negative Surveillance Initiative (MuGSI)
Form Approved
OMB No. 0920-0978
Healthcare-Associated Infections Community Interface (HAIC) Case Report
Patient’s Name:
Phone no. (
)
MRN:
Address:
City:
State
ZIP:
Hospital:
----Patient Identifier information is not transmitted to CDC---DEMOGRAPHICS
1. STATE:
2. COUNTY:
3. STATE ID:
____ ____
_____________
___ ___ ___ ___ ___ ___ ___ ___ ___
___ ___ - ___ ___ - ___ ___ ___ ___
6. AGE:
8a. ETHNIC ORIGIN:
7. SEX AT BIRTH:
5. DATE OF BIRTH:
____ ____ ____
□ Days □ Mos. □ Yrs.
4a. LABORATORY ID WHERE
INCIDENT SPECIMEN IDENTIFIED:
________________________
□ MALE □ FEMALE
□ Unknown
□ Check if transgender
□
□
□
4b. FACILITY ID WHERE PATIENT TREATED:
_______________________________
8b. RACE: (Check all that Apply)
□ American Indian or Alaska □ Native Hawaiian or
Hispanic or Latino
Not Hispanic or Latino
Unknown
Native
Other Pacific Islander
□ White
□ Asian
□ Black or African American □ Unknown
10. ORGANISM:
Extended-Spectrum Cephalosporin-resistant:
9. DATE OF INCIDENT SPECIMEN COLLECTION (DISC):
___ ___ - ___ ___ - ___ ___ ___ ___
□Escherichia coli
□Klebsiella pneumoniae
□Klebsiella oxytoca
11. INCIDENT SPECIMEN COLLECTION SITE:
□ Blood □ Bone □ CSF □ Internal body site (specify):___________ □ Joint/synovial fluid □ Muscle
□ Peritoneal fluid □ Pericardial fluid □ Pleural fluid □ Urine □ Other normally sterile site (specify): ______________
12. LOCATION OF SPECIMEN COLLECTION:
□ OUTPATIENT:
□ INPATIENT:
Facility
ID:____________
Emergency room
Facility
ID:____________
□
□ Clinic/Doctor's office
□ Dialysis center
□ Surgery
□ Observational/
□ ICU
□ OR
□ Radiology
□ Other inpatient
Clinical decision unit
□ LTCF
Facility
ID:____________
□ LTACH
Facility
ID:____________
□ Autopsy
□ Other (specify):
_______________
□ Unknown
□ Other outpatient
14. WAS THE PATIENT HOSPITALIZED ON THE DAY OF OR IN THE
29 CALENDAR DAYS AFTER THE DISC?
□ Yes □ No □ Unknown
IF YES, DATE OF ADMISSION:
16. PATIENT OUTCOME:
___ ___ - ___ ___ - ___ ___ ___ ___
□ Survived
DATE OF DISCHARGE: ___ ___ - ___ ___ - ___ ___ ___ ___ OR
□ Date unknown
IF SURVIVED, DISCHARGED TO:
□ Left against medical advice (AMA)
13. WHERE WAS THE PATIENT LOCATED ON THE 3RD CALENDAR DAY BEFORE THE
DISC?
□ Private residence
□ LTCF
Facility ID: _______________
□
Hospital inpatient
Facility ID: _______________
Was the patient transferred from
this hospital?
□ LTACH
Facility ID: ___________________
□ Homeless
□ Incarcerated
□ Other (specify):________________
□ Unknown
□ Yes □ No □ Unknown
15a. WAS THE PATIENT IN AN ICU IN THE 7 DAYS BEFORE THE DISC?
□ Yes □ No □ Unknown
IF YES, DATE OF ICU ADMISSION: ___ ___ - ___ ___ - ___ ___ ___ ___ OR
□ Date unknown
15b. WAS THE PATIENT IN AN ICU ON THE DAY OF INCIDENT SPECIMEN COLLECTION
OR IN THE 6 DAYS AFTER THE DISC?
□ Yes □ No □ Unknown
IF YES, DATE OF ICU ADMISSION: ___ ___ - ___ ___ - ___ ___ ___ ___ OR
□ Died
DATE OF DEATH:
□ Private residence □ LTCF Facility ID:______ □ LTACH Facility ID: ______
□ Other (specify): ________ □ Unknown
___ ___ - ___ ___ - ___ ___ ___ ___ OR
□ Date unknown
□ Unknown
□ Date unknown
ON THE DAY OF OR IN THE 6 CALENDAR DAYS BEFORE DEATH, WAS THE PATHOGEN
OF INTEREST ISOLATED FROM A SITE THAT MEETS THE CASE DEFINITION?
□
Yes
□ No □ Unknown
Public reporting burden of this collection of information is estimated to average 28 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 Information Collection Review Office, 1600 Clifton Road NE, MS
D-74, Atlanta, Georgia 30329; ATTN: PRA (0920-0978).
Version Date: 07/2020
PAGE 1 OF 4
Form Approved
OMB No. Form
0920-0978
Approved
OMB
No. 0920-0978
Exp. Date:
XX-XX-XXXX
□
17a. TYPES OF INFECTION ASSOCIATED WITH CULTURE(S): (Check all that apply)
None
□ Epidural Abscess
□ Cellulitis
□
□ Abscess, not skin
□ Chronic ulcer/wound (not decubitus) □ Meningitis
□
□ AV fistula/graft infection
□ Osteomyelitis
□ Decubitus/pressure ulcer
□
□ Bacteremia
□ Peritonitis
□ Empyema
□
□ Bursitis
□ Pneumonia
□
□ Catheter site infection (CVC) □ Endocarditis
18. UNDERLYING CONDITIONS: (Check all that apply)
□
□
□ AIDS/CD4 count < 200
Chronic pulmonary disease
□ Primary immunodeficiency
□ Transplant, hematopoietic stem cell
□ Transplant, solid organ
□ Diabetes mellitus
□ With chronic complications
LIVER DISEASE
□ Chronic liver disease
□ Ascites
□ Cirrhosis
□ Hepatic encephalopathy
□ Variceal bleeding
□ Hepatitis C
□ Treated, in SVR
□ Current, chronic
CARDIOVASCULAR DISEASE
CVA/Stroke/TIA
Congenital heart disease
Congestive heart failure
Myocardial infarction
Peripheral vascular disease (PVD)
GASTROINTESTINAL DISEASE
□
□
□
□
□
□
□
19. SUBSTANCE USE
(Check all that
apply) □ None
□
□
□
□
□
□
□
□
□
□
□
Malignancy, hematologic
Malignancy, solid organ (non-metastatic)
Malignancy, solid organ (metastatic)
ALCOHOL
ABUSE:
□ Unknown
□ Tobacco
□ E-nicotine delivery system
□ Marijuana
□ Yes
□ No
□ Unknown
□ None □ Unknown
PREVIOUS HOSPITALIZATION IN THE YEAR BEFORE DISC:
□
□
□
□
□
□
□
□
□
□ Yes □ No
□ Yes □ No □ Unknown
Facility ID: __________
Facility ID: __________
OVERNIGHT STAY IN LTACH IN THE YEAR BEFORE DISC:
□ Yes □ No □ Unknown
□ Yes □ No □ Unknown
Facility ID: __________
SURGERY IN THE YEAR BEFORE DISC:
□ Yes □ No □ Unknown
CURRENT CHRONIC DIALYSIS:
□ Yes □ No □ Unknown
IF YES, TYPE:
□ Hemodialysis □ Peritoneal □ Unknown
_____kg
□ Unknown
Version Date: 07/2020
21b. HEIGHT:
_________ft. _______ in. OR
_____cm
□ Skin popping
□ Skin popping
□ Skin popping
□ Skin popping
□ Skin popping
□ Skin popping
□ Skin popping
□ Skin popping
□ Non-IDU
□ Non-IDU
□ Non-IDU
□ Non-IDU
□ Non-IDU
□ Non-IDU
□ Non-IDU
□ Non-IDU
□ Unknown
□ Unknown
□ Unknown
□ Unknown
□ Unknown
□ Unknown
□ Unknown
□ Unknown
□ Yes □ No □ N/A (patient not hospitalized or did not have DUD)
DAYS BEFORE DISC:
□ Yes □ No □ Unknown
□ Unknown
□
URINARY CATHETER IN PLACE ON THE DISC (UP TO
THE TIME OF COLLECTION), OR AT ANY TIME IN THE 2
□ Yes □ No □ Unknown
IF YES, CHECK ALL THAT APPLY:
□ Indwelling Urethral Catheter □ Suprapubic Catheter
CALENDAR DAYS BEFORE DISC:
□ Condom Catheter
□ Other (specify):__________
ANY OTHER INDWELLING DEVICE IN PLACE ON THE DISC (UP
TO THE TIME OF COLLECTION), OR AT ANY TIME IN THE 2
CALENDAR DAYS BEFORE DISC: □ Yes □ No □ Unknown
IF YES, CHECK ALL THAT APPLY:
□ ET/NT Tube □ Gastrostomy Tube
□ Tracheostomy □ Nephrostomy Tube
PATIENT TRAVELED INTERNATIONALLY
IN THE YEAR BEFORE DISC:
□ AV fistula/graft □ Hemodialysis central line □ Unknown
_________lbs. ______ oz. OR
□ IDU
□ IDU
□ IDU
□ IDU
□ IDU
□ IDU
□ IDU
□ IDU
□ NG Tube
□ Other (specify):
_____________
IF HEMODIALYSIS, TYPE OF VASCULAR ACCESS:
21a. WEIGHT:
MODE OF DELIVERY: (Check all that apply)
Check here if central line in place for > 2 calendar days:
□
OVERNIGHT STAY IN LTCF IN THE YEAR BEFORE DISC:
DUD or abuse
DUD or abuse
DUD or abuse
DUD or abuse
DUD or abuse
DUD or abuse
DUD or abuse
DUD or abuse
□
□
Urinary tract problems/
abnormalities
Premature birth
Spina bifida
CENTRAL LINE IN PLACE ON THE DISC (UP TO THE TIME OF
COLLECTION), OR AT ANY TIME IN THE 2 CALENDAR
IF YES, DATE OF DISCHARGE CLOSEST TO DISC :___ ___ - ___ ___ - ___ ___ ___ ___
DATE UNKNOWN
Connective tissue disease
Obesity or morbid obesity
Pregnant
MuGSI CONDITIONS
Chronic kidney disease
Lowest serum creatinine: ________mg/DL
□ Unknown or not done
Marijuana, cannabinoid (other than smoking)
Opioid, DEA schedule I (e.g., heroin)
Opioid, DEA schedule II-IV (e.g., methadone, oxycodone)
Opioid, NOS
Cocaine
Methamphetamine
Other (specify): _____________
Unknown substance
WAS INCIDENT SPECIMEN COLLECTED 3 OR MORE CALENDAR
DAYS AFTER HOSPITAL ADMISSION?
OR,
□
□
□
Hemiplegia
Paraplegia
Quadriplegia
DURING THE CURRENT HOSPITALIZATION, DID THE PATIENT RECEIVE
MEDICATION ASSISTED TREATMENT (MAT) FOR OPIOID USE DISORDER?
20. RISK FACTORS: (Check all that apply)
□
Burn
Decubitus/pressure ulcer
Surgical wound
Other chronic ulcer or chronic
wound
Other (specify):___________
OTHER
□ Unknown
DOCUMENTED USE DISORDER (DUD)/ABUSE:
□
□
□
□
□
□
□
□
□
□
□
□
RENAL DISEASE
□
□ Yes
□ No
□ Unknown
SKIN CONDITION
Cerebral palsy
Chronic cognitive deficit
Dementia
Epilepsy/seizure/seizure disorder
Multiple sclerosis
Neuropathy
Parkinson’s disease
Other (specify): ________________
OTHER SUBSTANCES: (Check all that apply) □ None
SMOKING:
17E. 5(&855(1787,
Surgical incision infection
Surgical site infection (internal)
Traumatic wound
Urinary tract infection
Other (specify): ____________
PLEGIAS/PARALYSIS
MALIGNANCY
Diverticular disease
Inflammatory bowel disease
Peptic ulcer disease
Short gut syndrome
□
□
□
□
□
NEUROLOGIC CONDITION
□ HIV infection
Cystic fibrosis
CHRONIC METABOLIC DISEASE
□
□
□
□
□
□ None □ Unknown
IMMUNOCOMPROMISED CONDITION
CHRONIC LUNG DISEASE
□ Unknown □ Colonized
Pyelonephritis
Septic arthritis
Septic emboli
Septic shock
Skin abscess
21c. BMI:
_________
□ Unknown
□ Yes □ No □ Unknown
COUNTRY: ____________, ____________, ____________
PATIENT HOSPITALIZED WHILE VISITING
COUNTRY(IES) ABOVE:
□ Yes □ No □ Unknown
PAGE 2 OF 4
Form Approved
Form
Approved
OMB No.
0920-0978
OMBXX-XX-XXXX
No. 0920-0978
Exp. Date:
URINE CULTURES ONLY:
23. SIGNS AND SYMPTOMS ASSOCIATED WITH URINE CULTURE.
URINE CULTURES
ONLY: 22. RECORD THE
COLONY COUNT:
________________
Please indicate if any of the following symptoms were reported during the 5 day time period including the
2 calendar days before through the 2 calendar days after the DISC.
Symptoms for patients
≤ 1 year of age only:
□ Unknown
□ None
□ Costovertebral angle pain or tenderness
□ Dysuria
□ Fever [temperature ≥ 100.4 °F (38 °C)]
24a. DID THE PATIENT HAVE A
POSITIVE TEST(S) FOR SARS-CoV-2
(MOLECULAR ASSAY, SEROLOGY OR
OTHER CONFIRMATORY TEST) ON OR
BEFORE THE DISC?
Yes
No
Unknown
□ Frequency
□ Suprapubic tenderness
□ Urgency
□ Apnea
□ Bradycardia
□ Lethargy
□ Vomiting
24b. IF YES, COMPLETE TABLE BELOW:
Specimen collection date
FIRST positive test for SARS-CoV-2
on or before the DISC:
Test type
Molecular assay
/
/
Serology
Unknown
Unknown
MOST RECENT positive test for
SARS-CoV-2 on or before the DISC:
Other (specify):
/
Molecular assay
/
Serology
Unknown
Unknown
24c. COVID-NET CASE ID:
24d. NNDSS IDs (PLEASE
PROVIDE AT LEAST ONE OF THE
FOLLOWING WHEN APPLICABLE):
Other (specify):
Local Case ID:
Local Record ID:
State case identifier:
Legacy case identifier:
25a. WAS THE
INCIDENT
SPECIMEN
POLYMICROBIAL?
□ Yes
Yes
□ No
□ Unknown
Unknown
25b. WHAT SCREENING/ CONFIRMATORY
METHOD WAS USED FOR ESBL
IDENTIFICATION?
(Check all that apply):
None
Unknown
□
□
□ Broth Microdilution (ATI detection)
□ ESBL well
□ Expert rule (ATI flag)
□ Unknown
□ Broth Microdilution (Manual)
□ Disk Diffusion
□ E-test
□ Molecular test (specify):_____________
□ Other non-molecular test (specify):_______
25c. IF SCREENING/ CONFIRMATORY
METHOD WAS USED, WHAT WAS THE
RESULT?
□ Positive
Positive
□ Positive
Positive
□ Positive
Positive
□ Positive
Positive
□ Positive
Positive
□ Positive
Positive
□ Positive
Positive
Positive
□ Positive
26a. IS ANTIMICROBIAL USE (IV OR ORAL) IN THE 30 DAYS BEFORE THE DISC DOCUMENTED?
26b. IF YES, CHECK ALL ANTIMICROBIALS USED IN THE 30 DAYS BEFORE THE DISC: (Check all that apply)
□ Amikacin
□ Amoxicillin
□ Amoxicillin/clavulanic acid
□ Ampicillin
□ Ampicillin/sulbactam
□ Azithromycin
□ Aztreonam
□ Cefazolin
□ Cefdinir
□ Cefepime
□ Cefixime
□ Cefotaxime
□ Cefoxitin
□ Cefpodoxime
□ Ceftaroline
□ Ceftazidime
□ Ceftazidime/avibactam
□ Ceftizoxime
□ Ceftolozane/tazobactam
□ Ceftriaxone
□ Cefuroxime
□ Cephalexin
□ Ciprofloxacin
□ Clarithromycin
□ Clindamycin
□ Dalbavancin
□ Daptomycin
□ Delafloxacin
□ Doripenem
□ Doxycycline
□ Ertapenem
□ Fidaxomicin
□ Fosfomycin
□ Gentamicin
□ Imipenem/cilastatin
□ Levofloxacin
□ Linezolid
□ Meropenem
□ Meropenem/vaborbactam
□ Metronidazole
□ Moxifloxacin
□ Nitrofurantoin
□ Oritavancin
□ Penicillin
□ Piperacillin/tazobactam
□ Negative
Negative
□ Negative
Negative
□ Negative
Negative
□ Negative
Negative
□ Negative
Negative
□ Negative
Negative
□ Negative
Negative
□ Negative
Negative
□ Indeterminate
Indeterminate
□ Indeterminate
Indeterminate
□ Indeterminate
Indeterminate
□ Indeterminate
Indeterminate
□ Indeterminate
Indeterminate
□ Indeterminate
Indeterminate
□ Indeterminate
Indeterminate
Indeterminate
□ Indeterminate
□ Unknown
Unknown
□ Unknown
Unknown
□ Unknown
Unknown
□ Unknown
Unknown
□ Unknown
Unknown
□ Unknown
Unknown
□ Unknown
Unknown
□ Unknown
□ Yes □ No □ Unknown
□ Unknown
□ Polymyxin B
□ Polymyxin E (colistin)
□ Rifaximin
□ Tedizolid
□ Telavancin
□ Tigecycline
□ Tobramycin
□ Trimethoprim
□ Trimethoprim/sulfamethoxazole
□ Vancomycin
□ IV
□ PO
□ Other (specify): _____________________
□ Other (specify): _____________________
REMINDER: Any prior antimicrobial use that is not noted above should be documented in the other (specify) field.
Version Date: 07/2020
PAGE 3 OF 4
Form Approved
OMB No.
0920-0978
Form
Approved
OMB No. 0920-0978
Exp. Date: XX-XX-XXXX
27. SUSCEPTIBILITY RESULTS:
Please complete the table below based on the information found in the indicated data source. Shaded antibiotics are required to have the MIC entered into
the MuGSI-CM system, if available.
Data Source
Data Source
Antibiotic
Antibiotic
Medical Record
Medical Record
MIC
MIC
Interp
Interp
Microscan
Microscan
MIC
MIC
Interp
Interp
Vitek
Vitek
MIC
MIC
Interp
Interp
Phoenix
Phoenix
MIC
MIC
Interp
Interp
Amikacin
Amikacin
Amoxicillin/Clavulanate
Amoxicillin/Clavulanate
Ampicillin
Ampicillin
Ampicillin/Sulbactam
Ampicillin/Sulbactam
Aztreonam
Aztreonam
Cefazolin
Cefazolin
CEFEPIME
CEFEPIME
CEFOTAXIME
CEFOTAXIME
CEFTAZIDIME
CEFTAZIDIME
Ceftazidime/Avibactam
CEFTRIAXONE
Ceftolozane/Tazobactam
Cephalothin
CEFTRIAXONE
Ciprofloxacin
Cephalothin
COLISTIN
Ciprofloxacin
Kirby-Bauer
Kirby-Bauer
Zone
Interp
Zone
Diam
Interp
Diam
E-test
E-test
MIC
MIC
Interp
Interp
DORIPENEM
COLISTIN
ERTAPENEM
DORIPENEM
Gentamicin
Doxycycline
IMIPENEM
ERTAPENEM
Levofloxacin
Fosfomycin
MEROPENEM
Gentamicin
Moxifloxacin
IMIPENEM
Nitrofurantoin
Imipenem-relebactam
Piperacillin/Tazobactam
Levofloxacin
POLYMYXIN B
MEROPENEM
TIGECYCLINE
Meropenem-vaborbactam
Tobramycin
Minocycline
Trimethoprim-sulfamethoxazole
Moxifloxacin
Meropenem-vaborbactam
Nitrofurantoin
Minocycline
Piperacillin/Tazobactam
Doxycycline
Plazomicin
Plazomicin
POLYMYXIN B
Tetracycline
Rifampin
Rifampin
Tetracycline
Ceftazidime/Avibactam
TIGECYCLINE
Ceftolozane/Tazobactam
Tobramycin
Fosfomycin
Imipenem-relebactam
Trimethoprim-sulfamethoxazole
27a.
WAS CASE FIRST IDENTIFIED THROUGH AUDIT?
27b. CRF STATUS:
28a. WAS
CASE FIRST IDENTIFIED THROUGH AUDIT? 28b. CRF STATUS:
□ Yes
Yes
□ No
No
27d. COMMENTS:
28c. SO INITIALS:
Complete□ Complete
□ Pending
Pending
□ Chart unavailable after 3 requests
27c. SO INITIALS:
28d. DATE OF ABSTRACTION:
___ ___ - ___ ___ - ___ ___ ___ ___
Chart unavailable after 3 requests
28e. COMMENTS:
CS295460-B
PAGE 4 OF 4
File Type | application/pdf |
File Modified | 2020-07-23 |
File Created | 2018-09-13 |