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OMB Control No.:0920-1305
Expiration date: xx/xx/xxxx
QID:________
Chronic Q Fever – Enhanced Surveillance
ENROLLMENT/FIRST FORM
1.
2.
3.
4.
5.
6.
When was this patient first diagnosed with chronic Q fever? ____________ (mm/yyyy)
Patient’s date of birth ______________ (mm/dd/yyyy)
Sex of patient: Male Female Transgender Non-binary Something Else Not specified
State of residence ________
Race: White Black American Indian/Alaska Native Asian Pacific Islander Not specified
Hispanic ethnicity: Yes No Unknown
Acute Q Fever History:
7. Was this patient previously diagnosed with acute Q fever? Yes No Unknown
(If ‘no’ or ‘unknown’, skip to question 8)
a. Date of acute Q fever diagnosis: _____________ (mm/dd/yyyy) or Date Unknown
b. How was initial diagnosis made?
PCR Paired Serology Single serology Other __________________ Unknown
c. Was the patient treated for acute Q fever? Yes No Unknown
i. If yes, what medication(s) were/was used and for what
duration__________________________________________
d. Was treatment completed? Yes No Unknown
8. For female patients: was this patient pregnant at the time of acute Q fever diagnosis?
Yes No Unknown NA
(If ‘no’ or ‘unknown’, skip to question 9)
a. In which trimester did the symptoms begin (if unknown use diagnosis): 1st (weeks 1-12)
2nd (weeks 13-28) 3rd (weeks 29-42) Unknown
b. Was the patient treated during pregnancy? Yes No Unknown (If ‘no’ or ‘unknown’, skip
to question 8f)
c. At what week gestation did treatment begin? _____ weeks
d. When was treatment discontinued? _______ weeks or Still receiving treatment
e. Was treatment completed? Yes No Unknown
f. What antibiotics were used? Trimethoprim/sulfamethoxazole Other __________
Unknown
g. What was the duration of treatment? ______ weeks
h. Did this patient develop placentitis? Yes No Unknown
i. Did the patient develop any of the following complications of pregnancy (select all that apply):
intrauterine growth restriction (IUGR) stillbirth miscarriage
premature delivery Other→Please specify other complications:
__________________________________
Public reporting burden of this collection of information is estimated to 20 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 H21-8,
Atlanta, Georgia 30333; ATTN: PRA 0920-1305
QID:________
j.
Where any of the following newborn complications present?
malformations (specify type:__________) hyperbilirubinemia
kernicterus
Other→Please specify other complications: _______
k. What was the gestational age at birth? _____________ weeks Unknown
l. What was the weight at birth? ________ lbs. _________ozs. Unknown
Risk Factors:
9. Did this patient have a history of any of the following cardiovascular conditions? (check all that apply):
Rheumatic heart disease
Aortic valve stenosis
Aortic valve prolapse
Aortic valve regurgitation
Mitral valve stenosis
Mitral valve prolapse
Mitral valve regurgitation
Pulmonic valve stenosis
Pulmonic valve prolapse
Pulmonic valve regurgitation
Tricuspid valve stenosis
Tricuspid valve prolapse
Tricuspid valve regurgitation
Prosthetic valve
→Which valve was replaced? (check all that apply)
Aortic
Mitral
Pulmonic
Tricuspid
→Date of most recent replacement: _______________ (mm/dd/yyyy)
→What type of valve replacement did the patient receive?
Manufactured mechanical valve
Human Donor valve Bioprostheticbovine Bioprosthetic- porcine
→History of >1 valve replacement Yes No Unknown
Aneurysm
Vascular graft/stent
Atrial septal defect
Patent ductus arteriosus
Ventricular septal defect
Tetralogy of Fallot
Other congenital heart defect →Please specify:_______________________________
Other heart valve problem →Please specify:______________________________
Clinical Findings:
10. What clinical signs and symptoms has the patient exhibited during the course of their illness? Select all
that apply.
relapsing fever chills weight loss night sweats fatigue Shortness of breath
hepatosplenomegaly Other __________
QID:________
11. Did this patient have culture negative endocarditis? Yes No Unknown
(If ‘no’ or ‘unknown’, skip to question 12)
a. Please specify affected valve(s) (Check all that apply):
Aortic valve
Mitral valve
Pulmonary valve
Tricuspid valve
Unknown or None
b. What imaging technologies were used to diagnose endocarditis (check all that apply)?
Transthoracic echocardiogram
Transesophageal echocardiogram
PET Scan CT Scan MRI
Other __________
c. Was infected valve removed? Yes No Unknown
(If ‘no’ or ‘unknown’, skip to question 12)
d. If yes, specify date of removal: ___________________ (mm/dd/yyyy)
e. If removed, was the valve tested for presence of Coxiella burnetii? Yes
No
Unknown
(If ‘no’ or ‘unknown’, skip to question 12)
f. Testing method: PCR
IHC
Culture
Next-generation sequencing
Unknown
g. Results: Positive
Negative
Results not available
12. Did this patient have a vascular infection (i.e. infection of vascular graft, stent, or aneurysm) caused by
Coxiella burnetii?
Yes No Unknown
(If ‘no’ or ‘unknown’, skip to question 13)
a. If yes, please specify which type of vascular infection
vascular graft
stent
aneurysm
other ____
b. Please specify location of infection: abdominal aorta thoracic aorta
other ____
c. Specify date of graft/stent placement: ___________________ (mm/dd/yyyy)
NA
d. Was infected graft/stent removed or aneurysm repaired? Yes
No
Unknown
(If ‘no’ or ‘unknown’, skip to question 12f)
e. If yes, specify date of removal or repair: ___________________ (mm/dd/yyyy)
f. Was the vascular infection tested for presence of Coxiella burnetii? Yes
No
Unknown
(If ‘no’ or ‘unknown’, skip to question 13)
g. Testing method: PCR
IHC
Culture
Next-generation sequencing
Unknown
a. PCR Results: Positive Negative
Results not available
b. IHC Results: Positive Negative
Results not available
c. Culture Results: Positive
Negative
Results not available
d. NGS Results: Positive
Negative
Results not available
13. Did this patient have an osteoarticular infection (e.g. osteomyelitis or spondylodiscitis) caused by
Coxiella burnetii? Yes No Unknown
(If ‘no’ or ‘unknown’, skip to question 14)
a. Please specify location of osteoarticular infection :_________________________________
b. Was this a native joint? Yes No Unknown
c. Was surgical debridement of the diseased tissue and bone performed? Yes No
Unknown
(If ‘no’ or ‘unknown’, skip to question 14)
QID:________
d. If yes, specify date of most recent debridement: ___________________ (mm/yyyy)
e. During the debridement, was any tissue tested for presence of Coxiella burnetii? Yes No
Unknown
(If ‘no’ or ‘unknown’, skip to question 14)
f. Testing method: PCR
IHC
Culture
Next-generation sequencing
Unknown
a. PCR Results: Positive Negative
Results not available
b. IHC Results: Positive Negative
Results not available
c. Culture Results: Positive
Negative
Results not available
d. NGS Results: Positive
Negative
Results not available
14. Did this patient have evidence of granulomatous hepatitis? Yes No Unknown
(If ‘no’ or ‘unknown’, skip to question 15)
a. Which of the following liver enzymes was elevated? (check all that apply)
Alk Phos
ALT
AST LDH
Bilirubin
b. Was a liver biopsy performed? Yes No Unknown
(If ‘no’ or ‘unknown’, skip to question 15)
c. Was the biopsy tested for presence of Coxiella burnetii? Yes No Unknown
(If ‘no’ or ‘unknown’, skip to question 15)
d. Testing method: PCR IHC Culture
Next-generation sequencing Unknown
a. PCR Results: Positive Negative
Results not available
b. IHC Results: Positive Negative
Results not available
c. Culture Results: Positive
Negative
Results not available
d. NGS Results: Positive
Negative
Results not available
15. Did this patient develop lymphadenopathy? Yes No Unknown
(If ‘no’ or ‘unknown’, skip to question 16)
a. Please specify location of lymphadenopathy(s): (check all that apply)
Cervical
Supraclavicular
Axillary
Perihilar
Mediastinal
Mesenteric Inguinal
Popliteal
Other:___________________________________________________
b. Was a lymph node biopsy performed? Yes No Unknown
(If ‘no’ or ‘unknown’, skip to question 16)
c. Was the biopsy tested for presence of Coxiella burnetii? Yes No Unknown
(If ‘no’ or ‘unknown’, skip to question 16)
d. Testing method: PCR
IHC
Culture
Next-generation sequencing
Unknown
a. PCR Results: Positive Negative
Results not available
b. IHC Results: Positive Negative
Results not available
c. Culture Results: Positive
Negative
Results not available
d. NGS Results: Positive
Negative
Results not available
16. Did this patient develop either of the following complications? (check all that apply)
Psoas abscess
Cardiac abscess
Empyema or other pulmonary abscess
Other abscess → please specify location(s):_________________________________________
Ruptured aneurism
None of the above
(If none of the above selected, skip to question 17.)
a. Was medical intervention performed? Yes No Unknown
(If ‘no’ or ‘unknown’, skip to question 17)
QID:________
b. What interventions were performed? incision and drainage marsupialization
indwelling drain
Other, specify __________________________________
c. Was any material from the abscess or rupture tested for Coxiella burnetii? Yes No
Unknown
(If ‘no’ or ‘unknown’ skip to question 17.)
d. What was the method used to test material from the abscess?
PCR IHC Culture
Unknown
e. What was the result of testing? Positive
Negative
Results not available
17. Did this patient develop an embolic stroke or infarct? Yes No Unknown
(If ‘no’ or ‘unknown’, skip to question 18.)
a. Please specify location: ___________________________________________________________
b. Date of stroke or infarct occurrence:_____________ (mm/dd/yyyy)
18. Was this patient admitted to the hospital for this illness? Yes No Unknown
(If ‘no’ or ‘unknown’, skip to question 19.)
a. First date of admission: __/__/____ and date of discharge: __/__/____
b. Please provide the number of times the patient was hospitalized at least overnight for
complications of chronic Q fever since the initial chronic Q diagnosis. _____________
19. Which antibiotics did the patient receive? Doxycycline Hydroxychloroquine None Other
________ (please write name of medication)
a. How long has/was the patient on antibiotic therapy? ______(months)
b. Has the patient completed antibiotic therapy? Yes No Unknown
c. Was the patient taken off any antibiotic during treatment due to side effects? Yes No
Unknown ((If ‘no’ or ‘unknown’, skip to question 19e.)
d. If yes which medication (s) were stopped? Doxycycline Hydroxychloroquine Other
________
e. And what were the side effects? nausea vomiting fatigue photosensitivity
Other:______ Unknown
f. Did the patient develop any of the following side effects or complications from antibiotic
therapy (select all that apply)?
Nausea/other GI upset
Retinal damage
QT prolongation
Photosensitivity
irreversible skin pigmentation
Other _______________
None
20. On average, how frequently were Q fever serologies collected from the patient? Every _____ months
(on average)
a. What was the highest Phase 1 IgG titer value recorded
date _______
b. What was the highest Phase 2 IgG titer value recorded
date _______
c. What was the lowest Phase 1 IgG titer value recorded
date _______
d. What was the lowest Phase 2 IgG titer value recorded
date _______
21. Did the patient die from complications of this illness? Yes No Unknown
(If ‘no’ or ‘unknown’, skip to end of survey.)
a. Date of death: __/__/____
b. Cause of death per death certificate: _____________________________________________
File Type | application/pdf |
Author | Straily, Anne Marie (CDC/OPHSS/CSELS) (CTR) |
File Modified | 2023-09-01 |
File Created | 2023-09-01 |