Strongyloides stercoralis: Difference between revisions
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==Treatment== | ==Treatment== | ||
===Uncomplicated strongyloidiasis, normal immune system=== | ===Uncomplicated strongyloidiasis, normal immune system=== | ||
*Albendazole 400 mg BID x 7d | *[[Albendazole]] 400 mg BID x 7d | ||
:'''''OR''''' | :'''''OR''''' | ||
*Ivermectin 200 mcg/kg daily x 1-2d (drug of choice) | *[[Ivermectin]] 200 mcg/kg daily x 1-2d (drug of choice) | ||
*Can consider albendazole prophylaxis in immigrants from endemic regions with consistent clinical presentation | *Can consider albendazole prophylaxis in immigrants from endemic regions with consistent clinical presentation | ||
===Immunosuppressed=== | ===Immunosuppressed=== | ||
*Combo therapy: albendazole 400 mg BID x 7d AND ivermectin 200 mcg/kg daily x 1-2d | *Combo therapy: albendazole 400 mg BID x 7d AND ivermectin 200 mcg/kg daily x 1-2d | ||
Revision as of 13:58, 18 March 2015
Background
- Intestinal nematode; roundworm
- Endemic in tropical/subtropical areas such as Africa, Southeast Asia, Central/South America
Life Cycle
- Present in contaminated soil => larvae penetrate skin of hosts walking barefoot => enter venous circulation, migrate to lungs, then are expectorated to pharynx and swallowed => larvae develop into females that lay eggs asexually into GI tract, which hatch into larvae and are excreted into stool
- Larvae either become sexually reproducing males/females or filariform larvae that can reinfect host
- Autoinfection: Unique to Strongyloides; GI larvae can migrate from GI tract to venous system, then to lungs and proceed with life cycle
- Can lead to dramatic increase in worm burden and hyperinfection in immunocompromised
Risk factors
- Corticosteroid use, immunosuppression
- Transplantation
- Hematologic neoplasm
- Human T-lymphotropic virus-1 infection (HTLV-1)
- Malnutrition
- Diabetes
- Chronic renal failure
- Chronic alcohol use
Clinical significance
- Chronic infection in immunosuppressed can lead to fulminant dissemination with case fatality rate as high as 70%; strong index of suspicion is needed in such cases
Diagnosis
Clinical Presentation
- Asymptomatic in up to 60% of those infected
- Nonspecific GI complaints are most common presentation
- Weight loss, diarrhea, abdominal pain, vomiting
- Dermatologic
- Larva currens: rapidly progressive pruritic linear eruption due to migration of larvae
- Perianal pruritis
- Foot pruritus (“ground itch”)
- Respiratory
- Dry cough
- Wheezing
- Loeffler’s-like syndrome: fever, SOB, wheezing, pulmonary infiltrates
Immunocompromised patients
- Respiratory and systemic Sx such as fever will be more common
- Disseminated disease will invade multiple organ systems, including liver and brain
Differential Diagnosis
- Inflammatory bowel disease
- Schistosomiasis
- Filariasis
- Hookworm
- Toxocara canis
- Atopic dermatitis
- Asthma
- Allergic bronchopulmonary aspergillosis
- Coccidioidomycosis
- HIV
- Churg-Strauss syndrome
- Eosinophilic leukemia
Work-Up
- High index of suspicion, good travel history
Labs
- Notable eosinophilia in up to 70% of cases, though can be absent in immunosuppressed
- Gram negative bacteremia may be present in immunocompromised
- Uncomplicated strongyloidiasis: 3 serial stool samples screened for ova and parasites, as well as ELISA for Strongyloides
- Complicated strongyloidiasis: blood/sputum Cx, in addition to above
Treatment
Uncomplicated strongyloidiasis, normal immune system
- Albendazole 400 mg BID x 7d
- OR
- Ivermectin 200 mcg/kg daily x 1-2d (drug of choice)
- Can consider albendazole prophylaxis in immigrants from endemic regions with consistent clinical presentation
Immunosuppressed
- Combo therapy: albendazole 400 mg BID x 7d AND ivermectin 200 mcg/kg daily x 1-2d
- Abx may need to be continued until there is evidence that parasite is cleared
Disposition
- Often diagnosed in outpatient setting, can discharge uncomplicated cases in those who are not immunosuppressed
- Immunocompromised patients or those with systemic symptoms will require admission
Sources
- Buonfrate D, Requena-Mendez A, Angheben A, Munoz J, Gobi F, Van Den Ende J, Bisoffi Z. Severe strongyloidiasis: a systematic review of case reports. BMC Infectious Diseases 2013, 13: 78. doi:10.1186/1471-2334-13-78
- Feely NM, Waghorn DJ, Dexter T, Gallen I, Chiodini. Strongyloides stercoralis hyperinfection: difficulties in diagnosis and treatment. Anaesthesia 2010; 65: 298-301.
- Greaves D, Coggle S, Pollar C, Aliyu SH, Moore EM. Strongyloides stercoralis infection. BMJ 2013;347:f4610 doi: 10.1136/bmj.f4610 (Published 30 July 2013).
- Lim S, Katz K, Krajden S, Fuksa M, Keystone JS, Kain KC. Complicated and fatal Strongyloides infection in Canadians: risk factors, diagnosis and management. CMAJ 2004; 171 (5): 479-484.
- http://www.ncbi.nlm.nih.gov/pubmed/15635141
Authors
Kyle Brown, MD and Alex Koyfman, MD
