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Investigation of a combination of amiodarone and itraconazole for treatment of american trypanosomiasis (chagas disease) in dogs

  • Roy Madigan(corresponding author)
    ,
  • Sean Majoy
    ,
  • Kristine Ritter
    ,
  • Juan Luis Concepción
    ,
  • María Elizabeth Márquez
    ,
  • Sasha Caribay Silva
*Corresponding author for this work
  • From Animal Hospital of Smithson Valley
    ,
  • LTC Daniel E. Holland Military Working Dog Hospital
    ,
  • Universidad de los Andes
    ,
  • VRL Laboratories
    ,
  • Venezuelan Science Incubator and the Zoonosis and Emerging Pathogens Regional Collaborative Network
    ,
  • Universidad Tecnológica de Pereira
Research Output:
Contribution to journal
Article
Peer-review

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 317-329 (13 pages)

Journal (Volume, Issue Number)

Journal of the American Veterinary Medical Association (Volume 255, Issue 3)

Publication milestones

  • Published - 08/2019

Publication status

Published - 08/2019

ISSN

0003-1488

Publication IDs

  • Scopus: 85069778630
  • PubMed: 31298647

Abstract

OBJECTIVE To evaluate clinical, serologic, parasitological, and histologic outcomes of dogs with naturally occurring Trypanosoma cruzi infection treated for 12 months with amiodarone and itraconazole. ANIMALS 121 dogs from southern Texas and southern Louisiana. PROCEDURES Treatment group dogs (n = 105) received a combination of amiodarone hydrochloride (approx 7.5 mg/kg [3.4 mg/lb], PO, q 24 h, with or without a loading dosage protocol) and itraconazole (approx 10 mg/kg [4.5 mg/lb], PO, q 24 h, adjusted to maintain a plasma concentration of 1 to 2 µg/mL) for 12 months. Control group dogs (n = 16) received no antitrypanosomal medications. Serologic assays for anti-T cruzi antibodies, PCR assays for T cruzi DNA in blood, and physical evaluations were performed 1, 6, 9, 12, and 24 months after study initiation. Adverse events were recorded. Outcomes of interest were recorded and compared between groups. RESULTS 86 of 105 treatment group dogs and 8 of 16 control group dogs survived and completed the study (5/19 and 6/7 deaths of treatment and control group dogs, respectively, were attributed to T cruzi infection). Mean survival time until death attributed to T cruzi was longer (23.19 vs 15.64 months) for the treatment group. Results of PCR assays were negative for all (n = 92) tested treatment group dogs (except for 1 dog at 1 time point) from 6 to 24 months after study initiation. Clinical improvement in = 1 clinical sign was observed in 53 of 54 and 0 of 10 treatment and control group dogs, respectively; adverse drug events were minor and reversible. CONCLUSIONS AND CLINICAL RELEVANCE Results suggested efficacy of this trypanocidal drug combination for the treatment of T cruzi infection in dogs. (J Am Vet Med Assoc 2019;255:317-329).

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