Treatment of Strongyloides Infection
For patients with suspected or confirmed Strongyloides infection, treat with ivermectin 200 μg/kg orally for 2 consecutive days, which provides cure rates of 77-100% with excellent tolerability. 1, 2, 3
Standard Treatment Regimen
- Ivermectin 200 μg/kg orally for 2 consecutive days is the first-line treatment for uncomplicated strongyloidiasis in immunocompetent patients 1, 2, 3
- Take on an empty stomach with water to optimize absorption 3
- Albendazole 400 mg daily for 3 days is an alternative but significantly less effective option, with cure rates of only 38-63% compared to ivermectin's 77-100% 2
Immunocompromised Patients: Critical Modification Required
For immunocompromised patients, use an extended regimen: ivermectin 200 μg/kg on days 1,2,15, and 16. 1, 2
- This includes patients on corticosteroids, anti-TNF therapy, calcineurin inhibitors, chemotherapy, or those with HTLV-1 infection or hematologic malignancies 4
- Multiple treatment courses at 2-week intervals may be required, and cure may not be achievable in severely immunocompromised hosts 3
- Suppressive therapy (once monthly) may be necessary for control of extra-intestinal strongyloidiasis 3
Pre-Treatment Screening: Mandatory in High-Risk Scenarios
Before initiating any immunosuppressive therapy (especially corticosteroids), screen patients from endemic tropical/subtropical regions for Strongyloides and treat empirically if testing is unavailable. 2, 4
- Endemic regions include most of Africa, Central and South America, Southeast Asia, Middle East, former Soviet Union states, and rural Appalachian regions of the southern United States 4
- Long-term travelers (>1 month) to endemic areas warrant screening even years after exposure due to the parasite's ability to persist indefinitely through autoinfection 4, 5
- Critical pitfall to avoid: Never initiate corticosteroids without Strongyloides assessment, as this can precipitate potentially fatal hyperinfection syndrome 2, 4
Loa loa Co-Infection: Essential Pre-Treatment Assessment
In patients with significant exposure to West or Central Africa, exclude Loa loa infection BEFORE treating with ivermectin. 1, 3
- Co-infection with Loa loa can cause serious or fatal encephalopathy following ivermectin treatment 3
- Symptoms include confusion, lethargy, stupor, seizures, coma, neck/back pain, conjunctival hemorrhage, and urinary/fecal incontinence 3
- Implement careful post-treatment follow-up in these patients 3
Diagnostic Approach for Suspected Cases
- Serology (ELISA with recombinant antigens) is the primary diagnostic method, with sensitivity exceeding 80% 4, 5
- Stool microscopy has poor sensitivity for Strongyloides; at least 3 concentrated stool samples are needed, though sensitivity remains limited 4, 5
- Many experts recommend treating seropositive patients despite negative stool examinations 4
- Eosinophilia may be absent during hyperinfection syndrome, so do not rely on it for diagnosis 4
Post-Treatment Monitoring
- Repeat stool examinations are necessary to document clearance of infection 3
- Serology and eosinophil count should be monitored, with significant reductions expected at approximately 96 days and 270 days respectively after successful treatment 6
- For empirical treatment of asymptomatic eosinophilia, repeat treatment at 8 weeks to treat any residual worms once they have developed into adults 1
Clinical Presentations Requiring Immediate Treatment
- Larva currens: itchy, linear, urticarial rash moving several millimeters per second around trunk, upper legs, and buttocks 2
- Löffler's syndrome: fever, urticaria, wheeze, dry cough occurring 1-2 weeks after infection due to larval lung migration 1, 5
- Hyperinfection syndrome: gastrointestinal bleeding, pneumonia, sepsis, meningitis, or unexplained gram-negative bacteremia in immunosuppressed patients 2, 4
Special Populations
- Pregnancy: Ivermectin is Category C and should not be used during pregnancy; safety has not been established 3
- Lactation: Ivermectin is excreted in breast milk; treatment should only be undertaken when risk of delayed treatment outweighs possible risk to newborn 3
- Pediatric: Safety not established in children weighing less than 15 kg 3