Toxoplasma gondii: Difference between revisions
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Toxoplasma gondii
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=== HIV === |
=== HIV === |
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* Pyrimethamine 200 mg PO once, followed by dose based on body weight: |
* [[Pyrimethamine]] 200 mg PO once, followed by dose based on body weight: |
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** Body weight β€60 kg: pyrimethamine 50 mg PO daily + sulfadiazine 1000 mg PO q6h + leucovorin 10β25 mg PO daily (can increase to 50 mg daily or BID) |
** Body weight β€60 kg: [[pyrimethamine]] 50 mg PO daily + [[sulfadiazine]] 1000 mg PO q6h + leucovorin 10β25 mg PO daily (can increase to 50 mg daily or BID) |
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** Body weight >60 kg: pyrimethamine 75 mg PO daily + sulfadiazine 1500 mg PO q6h + leucovorin 10β25 mg PO daily (can increase to 50 mg daily or BID) |
** Body weight >60 kg: [[pyrimethamine]] 75 mg PO daily + [[sulfadiazine]] 1500 mg PO q6h + leucovorin 10β25 mg PO daily (can increase to 50 mg daily or BID) |
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* Alternatives |
* Alternatives |
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** Pyrimethamine (leucovorin) |
** [[Pyrimethamine]] (with leucovorin) plus [[clindamycin]] 600 mg IV or PO q6h |
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** TMP-SMX (TMP 5 mg/kg and SMX 25 mg/kg) (IV or PO) BID |
** [[TMP-SMX]] (TMP 5 mg/kg and SMX 25 mg/kg) (IV or PO) BID |
||
** Atovaquone 1500 mg PO BID + pyrimethamine (leucovorin) |
** [[Atovaquone]] 1500 mg PO BID + pyrimethamine (leucovorin) |
||
** Atovaquone 1500 mg PO BID + sulfadiazine |
** [[Atovaquone]] 1500 mg PO BID + sulfadiazine |
||
** Atovaquone 1500 mg PO BID |
** [[Atovaquone]] 1500 mg PO BID |
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=== Pregnancy === |
=== Pregnancy === |
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* Pyrimethamine is relatively contraindicated in pregnancy as it is toxic to the young fetus |
* [[Pyrimethamine]] is relatively contraindicated in pregnancy as it is toxic to the young fetus |
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* If life-threatening, should likely need treatment and consider abortion (if early in pregnancy) |
* If life-threatening, should likely need treatment and consider abortion (if early in pregnancy) |
||
* Spiromycin is safe, and decreases transmission to fetus, but is not enough to treat CNS disease |
* [[Spiromycin]] is safe, and decreases transmission to fetus, but is not enough to treat CNS disease |
||
== Prevention == |
== Prevention == |
Revision as of 13:45, 19 September 2019
- Protozoan parasite associated with cats and raw beef mostly known for causing opportunistic infections and congenital infections
Microbiology
- Protozoan parasite
- Organized into twelve haplotypes
Epidemiology
- Zoonotic disease with worldwide distribution
- Modes of transmission
- Ingesting tissue cysts in meat, or oocytes in food or water
- Solid-organ transplantation, especially heart
- Vertical or transplacental transmission
- Case reports of lab-acquired needlestick transmission
- Theoretical risk with blood transfusion
- Seroprevalence around 10-18% in Canada 12
- As high as 60% in Nunavut, however 3
- There are large parts of South and Central America, as well as Pacific Islands, that have very high seroprevalence 4
Life Cycle
- The only definitive hosts are in the Felidae family, essentially housecats and their relatives
- Intermediate hosts are many, and include birds and rodents
- An infected cat sheds oocytes into the environment (for 1 to 3 weeks), where they spend 1 to 5 days sporulating
- Each sporulated oocyst contains two sporocysts, and each sporocyst contains four sporozoites
- Intermediate hosts ingest the sporozoites, where they mature into tachyzoites
- Tachyzoites migrate to brain and muscle, where they encyst and become bradyzoites
- Bradyzoites are ingested by a cat, completing the life cycle
Pathophysiology
- Following ingestion, bradyzoites and sporozoites invade the small intestinal mucosa and develop into tachyzoites within the gut epithelium
- There, they insert themselves into monocytes and other nucleated cells
- Infected cells travel throughout the body, carrying the tachyzoite with them
- Infection triggers a Th-1 response
Clinical Presentation
Immunocompetent
- Asymptomatic in 80% of primary infections
- Symptoms, when they occur, can involve fever, cervical lymphadenopathy (painless and rubbery), myalgias, and weakness/fatigue
- May mimic infectious mononucleosis
- Can also cause chorioretinitis
- Severity of illness depends in part on genotype, with strain II in North America and Europe being less severe
- Rarely, unusual strains may cause pneumonitis, myocarditis, meningoencephalitis, or polymyositis, and can lead to death
Immunocompromised
- May be from primary infection or, more commonly, reactivation
- Unlike in immunocompetent people, it is always a serious infection in the immunocompromised
- Major risk factor is cellular immunodeficiency, as in HIV and some immunosuppressive medications
- In HIV, beware with CD4 < 100
- Typically presents with CNS involvement as encephalitis
- Symptoms include fever, headache, lethargy, incoordination, ataxia, hemiparesis, loss of memory, dementia, or seizures
- Can also present with pneumonitis (especially with bone marrow transplant), chorioretinitis, or myocarditis, and rarely involves essentially any other organ
Pregnancy
- As with other immunocompetent people, it is largely asymptomatic
- Only half of women can identify a significant risk factor 5
- Risk of transmission to fetus is with parasitemia associated with primary infection, so women who are seropositive are not at risk of having a child with congenital infection
Congenital
- Can be acquired during maternal parasitemia associated with primary infection
- Risk of transplacental infection of fetus is lowest in first trimester and highest in third
- 85% of infected babies are asymptomatic at birth; 15% symptomatic
- Symptom severity increases is highest in first trimester and lowest in third
- Classic triad of chorioretinitis (most common), intraparenchymal cerebral calcifications, and hydrocephalus
- Others: thrombocytopenia, hepatitis, hepatosplenomegaly, cataracts, strabismus, microphthalmia
Diagnosis
- Immunocompetent or pregnant women with primary infection: IgG/IgM serology, possibly with avidity testing for pregnant women
- Fetus, to rule out congenital infection following maternal primary infection: PCR of amniotic fluid
- Newborn, to rule out congenital infection: PCR of placenta or cord, or serology
- Immunocompromised patient, to diagnose cerebral or disseminated disease: PCR of blood, CSF, BAL, or tissue
- Patient with chorioretinitis: Parallel serologies from aqueous humour and serum, or PCR of aqueous humour
Serology
- ELISA IgG for prior exposure; ELISA IgM for acute infection
- IgM titres plateau within 1 month, and IgG within 2-3 months
- IgM is still detectable for months or years after infection
- IgM avidity testing can help to assess how recently the infection was acquired
- Provides a measure of how tightly the antibodies bind, which is highest in early infection
- A high avidity ratio (weak binding) suggests that the infection was acquired at least 4 months prior
PCR
- Not routinely done
- May be helpful from CSF or vitreous humour
- Not helpful on brain biopsy tissue
Management
- In general, in the setting of known HIV and one or more suspicious lesions, treat empirically for CNS toxoplasmosis and reassess with repeat imaging at around 10 days, at which time there should be some response
- First-line is a combination of pyrimethamine and sulfadiazine
- Pyrimethamine (with folinic acid) is the backbone
- The second agent is typically sulfadiazine, which can be replaced with clindamycin if needed
- Encephalitis: pyrimethamine 200 mg load followed by 50-75 mg/day
- Infection during pregnancy: pyrimethamine 100 mg daily for 2 days followed by 25 to 50 mg/day
- Alternatives
HIV
- Pyrimethamine 200 mg PO once, followed by dose based on body weight:
- Body weight β€60 kg: pyrimethamine 50 mg PO daily + sulfadiazine 1000 mg PO q6h + leucovorin 10β25 mg PO daily (can increase to 50 mg daily or BID)
- Body weight >60 kg: pyrimethamine 75 mg PO daily + sulfadiazine 1500 mg PO q6h + leucovorin 10β25 mg PO daily (can increase to 50 mg daily or BID)
- Alternatives
- Pyrimethamine (with leucovorin) plus clindamycin 600 mg IV or PO q6h
- TMP-SMX (TMP 5 mg/kg and SMX 25 mg/kg) (IV or PO) BID
- Atovaquone 1500 mg PO BID + pyrimethamine (leucovorin)
- Atovaquone 1500 mg PO BID + sulfadiazine
- Atovaquone 1500 mg PO BID
Pregnancy
- Pyrimethamine is relatively contraindicated in pregnancy as it is toxic to the young fetus
- If life-threatening, should likely need treatment and consider abortion (if early in pregnancy)
- Spiromycin is safe, and decreases transmission to fetus, but is not enough to treat CNS disease
Prevention
- Cats: hand hygiene after handling cat, use gloves and wash hands when handling litter, wash litter tray with hot >60ΒΊC water, keep litter out of kitchen
- Soil: use gloves for gardening, wash hands after soil contact
- Water: avoid tap water in highly endemic countries, avoid ingestion of lake and river water
- Food: avoid raw oysters/clams/mussels, wash all vegetables/fruits/herbs, cook meat well down
Further Reading
- Epidemiology of and Diagnostic Strategies for Toxoplasmosis. Clin Microbiol Rev. 2012;25(2):264. doi: [10.1128/CMR.05013-11]
References
- ^ Samar Shuhaiber, Gideon Koren, Rada Boskovic, Thomas R Einarson, Offie Porat Soldin, Adrienne Einarson. Seroprevalence of Toxoplasma gondiiinfection among veterinary staff in Ontario, Canada (2002): Implications for teratogenic risk. BMC Infectious Diseases. 2003;3(1). doi:10.1186/1471-2334-3-8.
- ^ EL Ford-Jones, I Kitai, M Corey, R Notenboom, N Hollander, E Kelly, H Akoury, G Ryan, I Kyle, R Gold. Seroprevalence of Toxoplasma Antibody in a Toronto Population. Canadian Journal of Infectious Diseases. 1996;7(5):326-328. doi:10.1155/1996/172651.
- ^ V. Messier, B. LΓ©vesque, J.-F. Proulx, L. Rochette, M. D. Libman, B. J. Ward, B. Serhir, M. Couillard, N. H. Ogden, Γ. Dewailly, B. Hubert, S. DΓ©ry, C. Barthe, D. Murphy, B. Dixon. Seroprevalence of Toxoplasma gondii Among Nunavik Inuit (Canada). Zoonoses and Public Health. 2009;56(4):188-197. doi:10.1111/j.1863-2378.2008.01177.x.
- ^ Georgios Pappas, Nikos Roussos, Matthew E. Falagas. Toxoplasmosis snapshots: Global status of Toxoplasma gondii seroprevalence and implications for pregnancy and congenital toxoplasmosis. International Journal for Parasitology. 2009;39(12):1385-1394. doi:10.1016/j.ijpara.2009.04.003.
- ^ K. Boyer, D. Hill, E. Mui, K. Wroblewski, T. Karrison, J. P. Dubey, M. Sautter, A. G. Noble, S. Withers, C. Swisher, P. Heydemann, T. Hosten, J. Babiarz, D. Lee, P. Meier, R. McLeod. Unrecognized Ingestion of Toxoplasma gondii Oocysts Leads to Congenital Toxoplasmosis and Causes Epidemics in North America. Clinical Infectious Diseases. 2011;53(11):1081-1089. doi:10.1093/cid/cir667.