Ova and Parasites Endemic to Tropical Areas: Diagnostic and Treatment Approach
Initial Diagnostic Strategy for Returning Travelers and Migrants
All patients with tropical exposure should undergo concentrated stool microscopy and Strongyloides serology regardless of geographic location, as these are the foundational screening tests. 1
Risk-Stratified Testing Based on Geographic Exposure
For patients with travel history to endemic tropical regions:
- Concentrated stool microscopy is the primary diagnostic modality, though sensitivity for Strongyloides is significantly lower than for other parasites 2
- Strongyloides serology (sensitivity >80%) should be performed on all patients regardless of symptoms or eosinophilia, as the parasite can persist indefinitely through autoinfection 2
- Single stool examination is insufficient - at least 2-3 independently collected specimens are required for adequate sensitivity, particularly in high-prevalence settings where two specimens achieve 92% sensitivity 3
- Giardia-specific testing (antigen detection or PCR with sensitivity/specificity >95%) is recommended for patients with watery diarrhea 1
Geographic-Specific Parasites Requiring Targeted Investigation
East and Southern Africa (Lakes Malawi, Victoria, Okavango delta):
- Schistosoma haematobium: Serology plus nitrocellulose-filtered terminal urine microscopy (midday collection increases sensitivity); urine dipstick alone has inadequate sensitivity 1
- Treatment: Praziquantel 40 mg/kg for light infections 1
Southeast Asia, Central/South America:
- Strongyloides stercoralis: Serology is essential as stool microscopy has poor sensitivity; repeated stool examinations (≥3 samples) often needed 2
- Treatment: Ivermectin 200 μg/kg PO for 2 consecutive days 4, 1
Worldwide distribution (geohelminths):
- Ascaris lumbricoides, Trichuris trichiura, Hookworm: Concentrated stool microscopy 1
- Treatment: Albendazole 400 mg single dose 1
Critical Pre-Treatment Screening to Prevent Life-Threatening Complications
Before administering diethylcarbamazine (DEC) or ivermectin, absolutely exclude:
- Onchocerciasis: Skin snips, slit lamp examination, or test dose DEC 50 mg 5, 1
- Loiasis: Daytime blood microscopy (10 AM-2 PM) if travel to Central/West Africa 5, 1
- DEC is contraindicated with onchocerciasis or high-load loiasis (>1000 microfilariae/ml) due to risk of blindness and fatal encephalopathy 5
Management of Immunocompromised Patients
Patients requiring immunosuppressive therapy (especially corticosteroids) from endemic regions must be screened and empirically treated for Strongyloides before initiating immunosuppression to prevent fatal hyperinfection syndrome. 2
High-Risk Immunosuppression Scenarios:
- Corticosteroid therapy (highest risk) 2
- Anti-TNF therapy, calcineurin inhibitors 2
- HTLV-1 infection, hematologic malignancies, chemotherapy 2
Treatment for Immunocompromised:
- Extended ivermectin regimen: 200 μg/kg PO on days 1,2,15, and 16 1
- Multiple treatment courses may be required; cure may not be achievable in severely immunocompromised patients 4
- Never initiate corticosteroids without Strongyloides assessment - this can precipitate fatal hyperinfection syndrome 2
Specific Clinical Syndromes and Their Management
Tropical Pulmonary Eosinophilia (TPE)
Diagnostic criteria:
- Eosinophil count typically >3 × 10⁹/L 6
- Strongly positive filarial serology with negative blood microfilariae 6
- Chest X-ray showing interstitial shadowing in 80% of cases 6
Treatment:
- DEC 6 mg/kg/day divided into 3 doses for 14-21 days (21 days may reduce relapse rates) 5
- Add doxycycline 200 mg daily for 6 weeks to target Wolbachia bacteria 5
- Prednisolone 20 mg/day for 5 days for ongoing alveolitis or severe disease 6
- 20% of patients relapse and require re-treatment 6
Acute Schistosomiasis (Katayama Syndrome)
- Presents 5-12 weeks post-exposure with fever, urticaria, eosinophilia 1
- Treatment: Praziquantel 40 mg/kg; prednisolone 30 mg daily for 5 days may reduce symptom duration 1
Loeffler's Syndrome
- Larval migration through lungs (Ascaris, hookworm, Strongyloides) 1
- Presents 1-2 weeks post-infection with fever, urticaria, wheeze, dry cough 1
- Treatment directed at underlying helminth 1
When NOT to Test for Ova and Parasites
Routine O&P testing is NOT indicated for:
- Nosocomial diarrhea - yield is essentially zero; test only for C. difficile 7
- Patients without travel history to endemic areas - extremely low yield unless specific risk factors present (HIV, institutionalization, prior parasitic disease, smoking) 1, 8
- Hospital admission <3 days with diarrhea <7 days without risk factors - selective testing reduces unnecessary testing by 51% 8
Empiric Treatment Considerations
In the absence of specific diagnosis, empiric treatment with albendazole may be considered for patients with persistent eosinophilia and appropriate geographic exposure 1
Common Pitfalls to Avoid:
- Do not rely on eosinophilia for Strongyloides diagnosis - it may be absent during hyperinfection syndrome 2
- Serology may remain positive for years after successful schistosomiasis treatment - do not use to assess treatment success 1
- Timing matters: Eosinophilia may be transient during tissue migration phase; stool microscopy becomes positive only when organisms reach gut lumen 1
- Cross-reactivity: Filarial serology may be positive in strongyloidiasis; expert interpretation recommended 1