eMedicine Specialties > Pediatrics: General Medicine > Parasitology
Fascioliasis: Treatment & Medication
Updated: Jan 22, 2009
- Overview
- Differential Diagnoses & Workup
- Treatment & Medication
- Follow-up
- Multimedia
Treatment
Medical Care
- Bithionol continues to be the drug of choice (DOC) in fascioliasis,4 although it is available in the United States only under an investigational protocol from the Centers for Disease Control and Prevention (CDC).
- A new fasciolicide, triclabendazole, cured 31 of 40 infected Egyptian children with 1 day of therapy.5 A second day of treatment cured the remaining 9 children. Further studies of the safety and efficacy of triclabendazole are pending. This agent is not currently available in the United States.
- Praziquantel is safe, although it may not be effective against Fasciola hepatica (Fh). Praziquantel administration is recommended only if bithionol or triclabendazole is unavailable.
- Medications previously used but no longer recommended because of toxicity or unproven efficacy include emetine, dehydroemetine, chloroquine, albendazole, and mebendazole.
- Fascioliasis complicated by ascending cholangitis requires treatment with appropriate antibacterial antibiotics.
Surgical Care
- Patients with ascending cholangitis may require surgery.
- Although one study promoted endoscopic flushing of the gallbladder with povidone-iodine for patients in whom oral fasciolicides proved ineffective,6 this technique has had no further validation.
Consultations
- An infectious diseases specialist and gastroenterologist should be consulted in patients with suspected fascioliasis.
- A surgeon may be consulted.
- Patients with an ectopic infection or a visceral larva migrans–like illness may require additional consultations for specific manifestations of the condition.
- Consult the CDC Drug Service (404-639-3670) to obtain bithionol.
Medication
New fasciolicides are being used in small numbers of children with encouraging results and minimal toxicities. The best studied agent, bithionol, is available from the CDC Drug Service (see CDC Drug Service: Bithionol). Despite limited data on their use and safety in US children, these new fasciolicides are the DOC because of the poorer efficacy and greater toxicities of older, more familiar agents. The Medical Letter (2000 Edition) and many experts recommend triclabendazole, a veterinary drug not approved for human use in the United States, as the DOC.7
Anthelmintics
Parasite biochemical pathways are different from the human host; thus, toxicity is directed to the parasite, egg, or larvae. The mechanism of action varies within the drug class. Antiparasitic actions may include the following:
- Inhibition of microtubules causes irreversible block of glucose uptake
- Tubulin polymerization inhibition
- Depolarizing neuromuscular blockade
- Cholinesterase inhibition
- Increased cell membrane permeability, resulting in intracellular calcium loss
- Vacuolization of the schistosome tegument
- Increased cell membrane permeability to chloride ions via chloride channels alteration
Bithionol (Lorothidol, Bitin)
Inhibits oxidative phosphorylation in the parasite, leading to blockade of ATP synthesis. DOC because of its safety and effectiveness for Fh and Fg. Most supporting data are from developing countries. It is a phenolic compound structurally related to hexachlorophene. Available from the CDC.
Adult
30-50 mg/kg on alternate days PO divided tid for 5-15 treatment days; some patients may require repeat treatment courses
Pediatric
Administer as in adults
None reported
Documented hypersensitivity
Pregnancy
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Precautions
May cause anorexia, nausea, vomiting, diarrhea, abdominal pain, hypotension, dizziness, headache, photosensitivity, or pruritus
Triclabendazole (Fasinex)
Recent reports suggest this veterinary drug is safe, well tolerated, and effective in adults and children. It remains the second DOC until further data accumulate, supporting its preferential use. Binds selectively to fluke tubulin, disrupting microtubule formation and function. As of 2009, is unavailable in the United States.
Adult
10-20 mg/kg/d PO pc divided q12-24h for 1 dose
Pediatric
Administer as in adults
None reported
Documented hypersensitivity
Pregnancy
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Precautions
May cause transient dizziness and headache
Praziquantel (Biltricide)
Although generally safe and effective for other trematode infections, praziquantel appears much less efficacious against Fh and Fg. Because it is readily available and more familiar than triclabendazole (Fasinex), it is the third DOC. Reserve use for situations in which the first and second DOC are unobtainable. Praziquantel increases permeability of the trematode tegument to calcium, causing contraction of the parasite muscle.
Adult
25 mg/kg/dose PO q8h for 1 d
Pediatric
Administer as in adults
Hydantoins may reduce serum praziquantel concentrations, possibly leading to treatment failures
Documented hypersensitivity; ocular cysticercosis
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Precautions
Destruction of parasite within eyes can cause irreparable lesions (ocular cysticercosis should not be treated with praziquantel); caution while driving or performing other tasks requiring alertness on day of and day following treatment; minimal increases in liver enzyme levels reported; when fluke infection associated with cerebral cysticercosis, hospitalize patient for duration of treatment
Corticosteroids
Corticosteroids may ameliorate the treatment course in children with severe acute phase infection.
Prednisolone (Pediapred, Delta-Cortef, Econopred)
A short course that is given for 2 d preceding fasciolicidal therapy in children with severe acute phase infection is reported anecdotally to ameliorate the course of the illness and to decrease fever, pain, pruritus, and toxicity.
Adult
2 mg/kg/d PO divided q12-24h; not to exceed 60 mg/d
Pediatric
Administer as in adults
Decreases effects of salicylates and toxoids (for immunizations); phenytoin, carbamazepine, barbiturates, and rifampin decrease effects
Documented hypersensitivity; viral, fungal or tubercular skin lesions
Pregnancy
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Precautions
Caution in hyperthyroidism, osteoporosis, cirrhosis, nonspecific ulcerative colitis, peptic ulcer, diabetes, and myasthenia gravis; mood changes, seizures, hyperglycemia, diarrhea, nausea, abdominal distension, and GI bleeding are unusual with short courses of therapy
More on Fascioliasis |
| Overview: Fascioliasis |
| Differential Diagnoses & Workup: Fascioliasis |
Treatment & Medication: Fascioliasis |
| Follow-up: Fascioliasis |
| Multimedia: Fascioliasis |
| References |
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Further Reading
Keywords
fascioliasis, abdominal pain, airway obstruction, ascending cholangitis, biliary colic, cattle, dysphagia, Fasciola gigantica, F gigantica, Fg, Fasciola hepatica, F hepatica, Fh, foreign body sensation, halzoun (Lebanese), hepatomegaly, jaundice, liver fluke, marrerra (Sudanese), pancreatitis, parasitic infection, pharyngitis, sashimi, severe anemia, sheep liver fluke, sheep liver fluke disease, subcutaneous nodules
Treatment & Medication: Fascioliasis