Preferred treatment approach | Alternative regimens | Comments | |
L. loa monoinfection | |||
L. loa microfilariae <2500/mL |
|
| DEC can provoke serious adverse effects, including shock and/or fatal encephalopathy, in patients with high microfilarial loads. Avoid DEC in pregnancy. |
L. loa microfilariae 2500 to 20,000/mL |
|
| Ivermectin can provoke serious adverse effects, including fatal encephalopathy, in patients with high microfilarial loads – but has a higher safety threshold than DEC. |
L. loa microfilariae >20,000/mL |
| WHO allows albendazole use in 2nd and 3rd trimester pregnancy[1]. | |
L. loa coinfection with onchocerciasis§ | |||
L. loa microfilariae <20,000/mL |
|
| DEC is contraindicated in onchocerciasis. The risk of ivermectin administration should be weighed against the severity of clinical manifestations in deciding whether to treat with ivermectin at presentation. L. loa microfilaremia should be reassessed at 6 and 12 months to determine the risk of subsequent administration of ivermectin. Use of doxycycline is a regimen of last resort; doxycycline does not take effect quickly and acts primarily against adult worms (which are not responsible for blindness or itching). |
L. loa microfilariae ≥20,000/mL |
| ||
L. loa coinfection with lymphatic filariasis | Same as for L. loa monoinfection | ||
L. loa coinfection with onchocerciasis and lymphatic filariasis | Same as for L. loa coinfection with onchocerciasis |
This table is intended for use in conjunction with UpToDate content on Loa loa infection. Treatment of loiasis is complex and best undertaken in consultation with an experienced clinician. All doses are for oral administration in patients with normal kidney and liver function. Dose reduction of DEC may be warranted in patients with reduced kidney function.
DEC doses are expressed as citrate salt. Some products express dosing according to DEC base (approximate conversion is 2:1); review product-specific information carefully. DEC is not commercially available in the United States; it is available from the CDC drug service at +1 (404) 639-2888 (email [email protected]).
CDC: Centers for Disease Control and Prevention; DEC: diethylcarbamazine; L. loa: Loa loa; WHO: World Health Organization.
* Albendazole for treatment of loiasis has only been demonstrated to be curative in loiasis that is refractory to diethylcarbamazine.
¶ Microfilarial counts should be checked 2 to 4 weeks after ivermectin to ensure that the microfilarial load is <2500/mL prior to diethylcarbamazine.
Δ Reduction of microfilaremia with albendazole can take up to 6 months. In children <6 years, a dose reduction of albendazole may be needed; however, specific recommendations are not available[1].
◊ If albendazole reduces microfilaremia to <20,000/mL but >2500/mL, ivermectin should be administered for further reduction of microfilaremia below 2500/mL prior to administration of diethylcarbamazine.
§ Treatment of patients with onchocerciasis-loiasis coinfection requires careful attention; refer to UpToDate text for further discussion of treatment approach.