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Microbiology !!navigator!!

Babesiosis is caused by intraerythrocytic protozoa of the genus Babesia. B. microti, the cause of most cases, is the etiologic agent in the northeastern and upper midwestern United States, and B. duncani is responsible for disease on the West Coast. B. divergens causes disease in Europe. The deer tick (Ixodes scapularis) transmits B. microti.

Epidemiology !!navigator!!

In the United States, infections occur most frequently in the Northeast and upper Midwest. In 2011, >1100 cases were reported in the United States, with ~75% of cases presenting in July and August; this number is probably an underestimate, given that most pts experience a mild and self-limiting disease and may not seek medical attention.

Clinical Manifestations !!navigator!!

Most pts develop a mild illness, but immunosuppressed pts may have more severe disease.

  • After an incubation period of 1-4 weeks, pts gradually develop fevers, fatigue, and weakness. Other symptoms may include chills, sweats, myalgias, arthralgias, headache, and—less often—photophobia, shortness of breath, and abdominal pain.
  • Severe babesiosis is associated with parasitemia levels of >4%.
    • - Risk factors include an age of >50 years, male gender, asplenia, HIV infection/AIDS, malignancy, hemoglobinopathy, and immunosuppression.
    • - Complications include ARDS, DIC, CHF, renal failure, and splenic infarcts and rupture.
    • - The fatality rate is 5-9% among all hospitalized pts and 20% among immunocompromised pts.

Diagnosis !!navigator!!

Giemsa-stained thin smears identify intraerythrocytic Babesia parasites, which appear round, pear-shaped, or ameboid.

  • Ring forms resembling P. falciparum but without pigment are most common.
  • Tetrads (“Maltese crosses”)—formed by four budding merozoites—are pathognomonic for B. microti and other small Babesia species.
  • PCR and serology can also be used for diagnostic purposes.

Treatment: Babesiosis

  • Mild to moderate illness should be treated with atovaquone (750 mg PO q12h) plus azithromycin (500 mg PO on day 1 followed by 250 mg/d PO) for 7-10 days.
    • - Clindamycin plus quinine is equally effective but not as well tolerated.
  • Severe disease should be treated with clindamycin (300-600 mg q6h IV or 600 mg q8h PO) plus quinine (650 mg q6-8h PO) for 7-10 days.
    • - High-dose azithromycin (600-1000 mg/d) plus atovaquone is an alternative.
    • - Consider exchange transfusion in pts with high-level parasitemia (>10%); hemoglobin levels of 10 g/dL; or pulmonary, hepatic, or renal compromise.
    • - Immunocompromised pts generally need longer courses of treatment (e.g., 6 weeks), with at least 2 weeks of therapy after parasites are no longer detected on blood smear.
  • B. duncani and B. divergens infections can be treated with IV clindamycin and quinine for 7-10 days.


Outline

Outline

Section 7. Infectious Diseases