Trypanosoma cruzi: Difference between revisions
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Trypanosoma cruzi
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Revision as of 12:53, 16 August 2019
- Causes Chagas disease (South American trypanosomiasis)
Microbiology
- Protozoan parasite
Life Cycle
Epidemiology
- Endemic throughout the Americas from the southern half of the United States to Argentina
- Particularly in rural, impoverished areas
- A small number of autochthonous cases of Chagas disease in the US
- Reservoirs include armadillos, opossums, raccoons, woodrats, some other rodents, and domestic dogs
- Triatomine vector species for trypanosomiasis belong to the genera Triatoma, Rhodnius, and Panstrongylus
- Bugs live in substandard dwellings (especially wood, mud, or stone houses)
- Vector is present from southern US to southern Argentina
- Transmission is via feces, either in direct contact with mucous membranes (especially conjunctivae), breaks in the skin, or contaminating the bite of the insect
- Can also be transmitted via blood transfusion or vertically from mother to child or via ingestion of contaminated food and drink
Pathophysiology
- Infective metacyclic trypomastigotes from feces enter the skin or mucosa
- Multiply in host cells as amastigotes, developing into trypomastigotes intracellularly and rupturing the cell, releasing more trypomastigotes
- Chagoma develops at site of inoculation
- Intracellular amastigotes visible as characteristic pseudocysts on histopathology
- Hematogenous spread to distant sites, especially muscles, with the cycle repeating
- Especially tropic for myocardium, where it causes biventricular enlargement, thinning of ventricular walls, apical aneurysms, and mural thrombi
- Parasitemia maintained for years
Clinical Presentation
Acute disease
- Often asymptomatic
- Incubation period of about 1 week
- Usually mild febrile illness, sometimes with hepatosplenomegaly, rash, edema, local inflammation
- Incurs in 20% of infections
- More common in children
- Nodular lesions ("chagomas") may develop at site of inoculation
- Romaña sign if periorbital, often with ipsilateral lymphadenopathy
- Often 1-2 weeks after exposure
- Acute myocarditis, pericardial effusion, and meningoencephalitis in 1-5%
Indeterminate phase
- Following acute infection, may enter a latent phase
Chronic disease
- Following acute infection can remain asymptomatic (indeterminate form)
- Cardiac complications in 25-30% (1.5-5% per year)
- Non-ischemic dilated biventricular (right more than left) cardiomyopathy with heart failure
- Apical aneurysms and mural thrombi
- Conduction defects, with heart blocks, bundle branch blocks, sinus node dysfunction, bradycardia, and ventricular arrhythmias
- Can cause sudden cardiac death
- GI involvement in 10-15%
- Megaesophagus, with dysphagia, odynophagia, chest pain, cough, and regurgitation
- May result in aspiration and recurrent pneumonias
- Megacolon, with constipation and abdominal pain
- Megaesophagus, with dysphagia, odynophagia, chest pain, cough, and regurgitation
- Meningoencephalitis
- Other: polyneuropathy, stroke syndrome
Immunocompromised patients
- May have reactivation following immune suppression or HIV
- Severe acute infection; may have skin lesions and cerebral masses/abscesses
- Meningoencephalitis
Diagnosis
Acute disease
- Direct microscopy blood film or tissue biopsy (e.g. lymph node, bone marrow, pericardial fluid, CSF)
- In immunocompromised, these other samples are even more important
- Hemoculture is only 50% sensitive and takes several weeks
- Serology for IgM is useless
- PCR is sensitive and specific
- Xenodiagnosis
Indeterminate and chronic disease
- No gold standard
- Serology for IgG is most useful
- Detectable after 6 to 9 months following infection
- Many assays (ELISA, indirect hemagglutination, chemiluminescence, and IFA)
- PCR (of blood) less sensitive
Management
Acute
- Treatment is most useful in acute disease, congenital Chagas, and children with chronic infection up to 18 years
- It can decrease illness severity and mortality
- Start ASAP before infection can become established
- However, treatment may not result in parasitologic cure
- Treatment options
- Nifurtimox: 90-120 day treatment course; AEs include anorexia, weightloss, neurologic symptoms
- Benznidazole: 60 day treatment course; AEs include hypersensitivity, GI upset, rare polyneuropathy and agranulocytosis
- Adverse events are common during treatment
Chronic
- Less clear benefit to antiparasitic treatment
- Cardiac disease
- May benefit from pacemaker in patients with conduction disease
- Monitor with ECG q6mo
- May need heart transplantation, though this can become complicated by ongoing chronic infection or recrudescence
- May benefit from pacemaker in patients with conduction disease
- Megaesophagus: balloon dilatation or surgical management
- Megacolon may need surgical management
Prevention
- Screening immigrants and then following up with regular cardiac screening, if positive
- Avoid sleeping in dilapidated dwellings in endemic countries, use insect repellent and bed nets
- Improve housing in endemic areas
Canadian Blood Services
- Samples are only tested for antibodies when increased risk is present, determined by the donor screening questions
- No reported cases since screening began in 2010