eMedicine Specialties > Pediatrics: General Medicine > Parasitology

Fascioliasis: Treatment & Medication

Author: Robert W Tolan Jr, MD, Chief, Division of Allergy, Immunology and Infectious Diseases, The Children's Hospital at Saint Peter's University Hospital; Clinical Associate Professor of Pediatrics, Drexel University College of Medicine
Contributor Information and Disclosures

Updated: Jan 22, 2009

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

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

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

Contributor Information and Disclosures

Author

Robert W Tolan Jr, MD, Chief, Division of Allergy, Immunology and Infectious Diseases, The Children's Hospital at Saint Peter's University Hospital; Clinical Associate Professor of Pediatrics, Drexel University College of Medicine
Robert W Tolan Jr, MD is a member of the following medical societies: American Academy of Pediatrics, American Medical Association, American Society for Microbiology, American Society of Tropical Medicine and Hygiene, Infectious Diseases Society of America, Pediatric Infectious Diseases Society, Phi Beta Kappa, and Physicians for Social Responsibility
Disclosure: GlaxoSmithKline Honoraria Speaking and teaching; MedImmune Honoraria Consulting; MedImmune Honoraria Speaking and teaching; Merck Honoraria Speaking and teaching; Novartis Honoraria Speaking and teaching; sanofi pasteur Grant/research funds Unrestricted research grant; sanofi pasteur  Consulting; sanofi pasteur Honoraria Speaking and teaching; Tap Honoraria Speaking and teaching; Baxter Healthcare Honoraria Speaking and teaching

Medical Editor

Glenn J Fennelly, MD, MPH, Director, Division of Pediatric Infectious Diseases, Jacobi Medical Center; Associate Professor, Department of Pediatrics, Albert Einstein College of Medicine
Glenn J Fennelly, MD, MPH is a member of the following medical societies: Pediatric Infectious Diseases Society
Disclosure: Nothing to disclose.

Pharmacy Editor

Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine
Disclosure: Pfizer Inc Stock Investment from financial planner; Avanir Pharma Stock Investment from financial planner ; WebMD Salary and stock Employment and investment from financial planner

Managing Editor

Martin Weisse, MD, Program Director, Associate Professor, Department of Pediatrics, West Virginia University
Martin Weisse, MD is a member of the following medical societies: Ambulatory Pediatric Association, American Academy of Pediatrics, and Pediatric Infectious Diseases Society
Disclosure: Nothing to disclose.

CME Editor

Daniel Rauch, MD, FAAP, Director, Pediatric Hospitalist Program, Associate Professor, Department of Pediatrics, New York University School of Medicine
Daniel Rauch, MD, FAAP is a member of the following medical societies: Ambulatory Pediatric Association, American Academy of Pediatrics, and Society of Hospital Medicine
Disclosure: Baxter Honoraria Consulting; Pfizer Honoraria Consulting

Chief Editor

Russell W Steele, MD, Head, Division of Pediatric Infectious Diseases, Ochsner Children's Health Center; Clinical Professor, Department of Pediatrics, Tulane University School of Medicine
Russell W Steele, MD is a member of the following medical societies: American Academy of Pediatrics, American Association of Immunologists, American Pediatric Society, American Society for Microbiology, Infectious Diseases Society of America, Louisiana State Medical Society, Pediatric Infectious Diseases Society, Society for Pediatric Research, and Southern Medical Association
Disclosure: None None None

 
 
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