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Babesiosis

Babesiosis: Excerpt from The 5-Minute Pediatric Consult

Oluwakemi B. Badaki, MDFrances M. Nadel, MD, MSCE

Babesiosis - BASICS

Babesiosis - description

  • Human babesiosis is a tick-borne malarialike illness characterized by fever, malaise, and hemolytic anemia.
  • Most infected individuals are asymptomatic.

Babesiosis - general prevention

  • Prevention begins with avoidance of tick bites.
  • Simple measures include wearing long-sleeved shirts and long pants, with pants tucked into the socks in tick-infested areas.
  • Avoid endemic regions during the peak months of May to September.
  • Light clothing will make ticks easier to see.
  • Spraying the bottoms of one’s pants with a tick repellent may also be helpful.
  • Children and dogs should be inspected for ticks after being outside.
  • High-risk individuals may want to avoid endemic areas from May to September.
  • Currently, there is no universal laboratory screening of blood products.
  • Prophylaxis is not recommended after a tick bite.
  • Currently, there is no vaccine available.

Babesiosis - epidemiology

  • The 1st human case in the US was reported from California in 1966.
  • Transmission usually occurs in the summer and early fall.
  • In the US, most cases have been reported from the Northeast, Midwest, and Pacific Coast.
    • Endemic areas include Rhode Island, Massachusetts, and New York.
    • Cases have been reported in New Jersey, Maryland, Virginia, Georgia, Wisconsin, and Minnesota.

Babesiosis - incidence

There were >450 confirmed cases of human babesiosis diagnosed in the US between 1968 and 1993.

Babesiosis - prevalence

Difficult to ascertain because asymptomatic infection appears to be common in endemic areas.

  • It has been reported, for instance, that seroprevalence is as high as 9% in some endemic areas of Rhode Island.

Babesiosis - risk factors

  • Asplenia (functional or anatomic)
  • Malignancy
  • HIV/AIDS
  • Immunosuppressive medications
  • Primary immunodeficiency syndrome
  • Extremes of age, especially age >50 years

Babesiosis - genetics

There is no known genetic predisposition.

Babesiosis - pathophysiology

  • A bite from an infected tick transmits the protozoa.
  • Incubation period:
    • Usually 1–4 weeks
    • Can be as long as 9 weeks
  • Infection of the erythrocyte causes membrane damage and lysis, which promotes adherence to the endothelium and microvascular stasis.
  • The spleen plays an important role in decreasing the protozoal load, through antibody production and filtering abnormally shaped infected red blood cells.

Babesiosis - etiology

  • Human babesiosis is caused by the intraerythrocytic parasite of the Babesia genus.
  • In the northeast US, Babesia microti is the most commonly isolated agent.
  • Babesia divergens is the responsible agent in Europe.
  • WA-1 and MO-1 cause babesiosis in western US and Missouri, respectively.
  • Ixodes dammini (Ixodes scapularis), the same tick responsible for Lyme disease, is the invertebrate vector for B. divergens.
  • Rarely, the disease has been acquired through transplacental/perinatal transmission or through transfusion of contaminated blood products.
    • Babesiosis is the most common tick-borne disease transmitted by contaminated blood transfusions

Babesiosis - associated conditions

It is estimated that 11–23% of patients have concurrent Lyme disease.

Babesiosis - DIAGNOSIS

Babesiosis - signs & symptoms

Babesiosis - history

  • Few patients recall a tick bite.
  • Patients live in or have recently traveled to an endemic region.
  • Initial symptoms begin 1–4 weeks after the tick bite and are vague. They may include progressive fatigue, malaise, headaches, and anorexia, accompanied by intermittent fevers as high as 40°C.
  • Chills, myalgias, and arthralgias may follow these symptoms.
  • Less common complaints include cough, sore throat, abdominal pain, and emotional lability.

Babesiosis - physical exam

  • Fever is often the only finding.
  • Mild conjunctival injection and pharyngeal erythema
  • Some may have mild hepatomegaly and/or splenomegaly.
  • Jaundice or hematuria may also be seen.
  • Petechiae and ecchymosis occur in rare cases, most often in the presence of severe illness with associated shock and/or DIC.

Babesiosis - tests

Babesiosis - lab

  • Giemsa- or Wright-stained thick and thin blood smears may demonstrate the intraerythrocytic ring form:
    • This is often confused with the ring form of Plasmodium falciparum, the etiologic agent of malaria.
    • Rarely, the pathognomonic “Maltese Cross” forms of the Babesia parasite may also be seen on the blood smear
    • Multiple smears should be performed as initial smears may be falsely negative.
  • Indirect immunofluorescent assay:
    • Antigen-specific for B. microti
    • In endemic areas, the test has a sensitivity of 91% and a specificity of 99%.
    • Can be used when blood smears are negative
    • In general, a titer = 1:64 indicates exposure.
    • Titer = 1:256 suggests acute infection.
    • There is little correlation between titer levels and severity of disease.
    • Immunoglobulin levels decline rapidly within months of recovery.
  • Polymerase chain reaction is highly sensitive and specific.
  • Isolation of the parasite can be done by intraperitoneal injection of a patient’s blood into a golden hamster, but results take weeks.
  • Other tests: Most of the abnormal routine test results are the result of hemolysis.
  • Urinalysis:
    • Proteinuria
    • Hemoglobinuria
  • CBC:
    • Normal leukocyte count/leukopenia
    • Normocytic/normochromic anemia
    • Thrombocytopenia
    • Atypical lymphocytosis
    • Reticulocytosis
  • Possible positive Coombs test
  • Elevated ESR
  • Liver function tests: Elevated bilirubin, lactate dehydrogenase, and liver transaminases
  • In asymptomatic patients, these tests are often normal.

False negatives:

  • The blood smears may not demonstrate the protozoan at low levels of parasitemia.
  • Serologic false positives for B. microti include cross-reactivity with other Babesia sp. or malarial organisms.
  • Theoretical serologic false positives for WA1:
    • Rheumatoid factor
    • Antinuclear antibody
    • Antibody to Toxoplasma gondii

Babesiosis - differencial diagnosis

  • Nonspecific viral syndrome
  • Malaria
  • Influenza
  • Lyme disease
  • Ehrlichiosis

Babesiosis - TREATMENT

Babesiosis - general measures

Those with mild clinical disease usually recover without treatment.

Babesiosis - special therapy

  • For life-threatening infections, exchange transfusion has been successful.
  • Progressive respiratory distress may require mechanical ventilation.

Babesiosis - medication

Babesiosis - first line

Asplenic, immunodeficient, or symptomatic patients should be treated with clindamycin and quinine.

  • The pediatric dose of clindamycin is 20–40 mg/kg/d divided into 3 doses for 7–10 days.
  • The adult dose is 600 mg PO t.i.d. or 1,200 mg IV b.i.d. for 7–10 days.
  • Quinine is dosed 10–25 mg/kg/d divided into 3 doses for 7–10 days.
  • Adult dose is 650 mg PO t.i.d. for 7–10 days.

Babesiosis - second line

  • Combination of atovaquone and azithromycin:
    • Has similar treatment effectiveness with fewer side effects (such as vertigo, tinnitus and GI upset) than clindamycin and quinine in adults
    • Use of atovaquone and azithromycin has not been studied in the pediatric population; clindamycin and quinine are the recommended treatment choice for symptomatic children.
  • In areas endemic for Lyme disease and Ehrlichiosis, consider adding doxycycline until lab confirmation of absence of either disease in the patient with Babesiosis.

Babesiosis - FOLLOW UP

When to expect improvement:

  • Some improvement of symptoms should be noted within 24–48 hours of onset of therapy.
  • Those who are only mildly affected usually have resolution of their symptoms over a few weeks.
  • For severely affected and immunodeficient patients, the convalescent period may be as long as 18 months.
  • In untreated asymptomatic individuals, parasitemia may persist for months to years.
  • Long-term complications are rare.
  • Recrudescence has been reported.

  • Signs to watch for:
    • Respiratory distress, especially after treatment has begun
    • Pancytopenia and lymphadenopathy: May indicate the development of hemophagocytic syndrome
  • Pitfalls:
    • Children who are from endemic areas and have an acute febrile illness may be misdiagnosed with a nonspecific viral illness
    • One should be suspicious for a coinfection with Lyme disease or Ehrlichiosis (Human anaplasmosis) in those who are not responding to standard therapy.
    • Delayed recognition of this uncommon disease may be life threatening in the immunocompromised patient.
    • In endemic areas, babesiosis should be considered in a posttransfusion febrile illness in at-risk populations.

Babesiosis - complications

  • Rarely fatal in the US
  • Pancytopenia and overwhelming secondary bacterial sepsis may occur.
  • Serious and fulminant complications have been described:
    • Pulmonary edema and adult respiratory distress syndrome, often happening after treatment has begun
    • CHF
    • Renal failure
    • Hemophagocytic syndrome/disseminated intravascular coagulation
    • Seizures/coma
  • Those coinfected with Lyme disease are susceptible to more severe disease and complications.

Babesiosis - bibliography

  1. Aguero-Rosenfeld ME. Laboratory aspects of tick-borne diseases: Lyme, human granulocytic ehrlichiosis and babesiosis. Mount Sinai J. Med. 2003;70:197–206.
  2. Buckingham SC. Tick-borne infections in children: Epidemiology, clinical manifestations, and optimal management strategies. Paediatr Drugs. 2005;7(3):163–176.
  3. Filbin MR, Mylonakis EE, Callegari L, et al. J Emerg Med. 2001;20(1):21–24.
  4. Homer MJ, Aguilar-Delfin I, Telford SR 3rd, et al. Babesiosis. Clin Microbiol Rev. 2000;13(3):451–469.
  5. Krause PJ. Babesiosis. Med Clin North Am. 2002;86(2):361–373.
  6. Krause PJ. Babesiosis diagnosis and treatment. Vector Borne Zoonotic Dis. 2003;3(1):45–51.
  7. Krause PJ. Babesiosis. Med Clin North Am. 2002;86:361–373.
  8. McGinley-Smith DE, Tsao SS. Dermatoses from ticks. J Amer Acad Dermatol. 2003;49:363–392; quiz 393–396.
  9. Pantanowitz L, Telford SR 3rd,, Cannon ME. The impact of babesiosis on transfusion medicine. Transfus Med Rev. 2002;16(2):131–143.
  10. Wormser GP, Dattwyler RJ, Shapiro ED, et al. The clinical assessment, treatment, and prevention of Lyme disease, human granulocytic anaplasmosis, and babesiosis: Clinical practice guidelines by the Infectious Diseases Society of America. Clin Infect Dis. 2006;43(9):1089–1134.

Babesiosis - CODES

Babesiosis - icd9

088.82 Babesiosis

Babesiosis - FAQ

  • Q: How long does a tick have to be attached for infection to occur?
  • A: In general, successful transmission requires at least 24 hours of attachment.
  • Q: How should a tick be removed?
  • A: The tick should be grasped with forceps as close to its head as possible and pulled straight up. If possible, it should be saved for identification.
  • Q: Does infection confer lifetime immunity?
  • A: Reinfection is possible.

Book Source Details

  • Book Title: The 5-Minute Pediatric Consult
  • Author(s): M. William Schwartz MD; et al.
  • Year of Publication: 2008
  • Copyright Details: The 5-Minute Pediatric Consult, Copyright © 2008 Lippincott Williams & Wilkins.

More About Babesiosis

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Copyright notice for book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.




More About This Book:
Title: The 5-Minute Pediatric Consult
Authors: M. William Schwartz MD; et al.
Publisher: Lippincott Williams & Wilkins
Copyright: 2008
ISBN: 0-7817-7577-9

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