eMedicine Specialties > Infectious Diseases > Bacterial Infections
Q Fever: Follow-up
Updated: Nov 18, 2008
Follow-up
Further Outpatient Care
- Acute Q fever
- Baseline transthoracic echocardiography should be performed to assess for vegetations.3
- Follow-up serology should be performed at least twice over 6 months. If phase I IgG antibodies are found in titers of 1:800 or more, transesophageal echocardiography should be performed along with serum PCR measurements, when possible.3
- Chronic Q fever
- Monthly follow-up serology and clinical assessment are recommended during antimicrobial therapy and for the first 6 months following withdrawal, then every 6 months for 2 years, and possibly yearly thereafter.
- Phase I IgG titers of 1:200 or less are the best predictor of cure.
- Perform echocardiography every 3 months during antimicrobial therapy and every 6 months for the first 2 years following drug withdrawal.
- High-risk populations should be screened for glucose-6-phosphate dehydrogenase deficiency before receiving hydroxychloroquine.
- If hydroxychloroquine is used, a yearly ophthalmologic evaluation is required to rule out retinal toxicity.
- Patients should be reminded of photosensitivity risk while on doxycycline therapy.
Deterrence/Prevention
- Vaccine prophylaxis9,1,5
- Vaccine is primarily used in at-risk people, such as veterinarians, abattoir workers, farmers, or others in occupations that require close contact with animals.
- A whole-cell killed vaccine (Q-Vax) has been licensed in Australia since 1989. Prevaccination screening is essential and includes history, skin testing, and serology, usually by indirect immunofluorescence. All 3 components must be negative before vaccine administration. Occasionally, large local reactions are reported.
- Acellular vaccines include a trichloroacetic extracted vaccine (Chemovaccine) from the former Czechoslovakia and a chloroform-methanol residue vaccine (CMR) from the United States. They have been promoted to be as effective as Q-Vax, but with fewer side effects. Phase I human trials using CMR proved that vaccination was safe. Although its efficacy has been demonstrated in rodents, sheep, and nonhuman primates, human data are lacking.
- No vaccine is available for children.
- Avoid ingestion of raw milk and exposure to animal birth products (eg, placenta), especially in the setting of immunosuppression, pregnancy, or known valvular heart disease.
- C burnetii must be cultured in biosafety level 3 laboratories.
Complications
- Chronic fatigue syndrome has been reported as a complication of acute Q fever.
- Chronic Q fever endocarditis can lead to severe heart failure.
- Reactivation of Q fever has been reported during pregnancy.
Prognosis
- Acute Q fever is a self-limited disease.
- Chronic Q fever carries mortality rates that can exceed 60%. Frequent relapses (50%) are observed despite adequate therapy.
Miscellaneous
Medicolegal Pitfalls
- Failure to obtain a specific serology in patients presenting with culture-negative endocarditis
- Failure to recognize specific host risk factors in patients with classic Q fever clinical presentations
More on Q Fever |
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Further Reading
Keywords
Q fever, query fever, Coxiella burnetii, C burnetii, Rickettsia burnetii, R burnetii, Rickettsia diaporica, R diaporica, zoonosis, zoonotic transmission, farm animals, livestock, bacterial infection, farm infection, chronic Q fever, chronic fatigue syndrome
Follow-up: Q Fever