Efficacy, safety and tolerance of imidocarb dipropionate versus atovaquone or buparvaquone plus azithromycin used to treat sick dogs naturally infected with the Babesia microti-like piroplasm

Parasit Vectors. 2017 Mar 13;10(1):145. doi: 10.1186/s13071-017-2049-0.

Abstract

Background: Piroplasmosis caused by the Babesia microti-like piroplasm (Bml) is increasingly being detected in dogs in Europe. Sick dogs show acute disease with severe anaemia associated with thrombocytopenia with a poor response to current available drugs. This study assesses the safety and tolerance of three treatments and compares their efficacy over a full year of follow up in dogs naturally infected with Bml.

Methods: Fifty-nine dogs naturally infected with Bml were randomly assigned to a treatment group: imidocarb dipropionate (5 mg/kg SC, 2 doses 14 d apart) (IMI); atovaquone (13.3 mg/kg PO q 8 h, 10 d)/azithromycin (10 mg/kg PO q 24 h, 10 d) (ATO); or buparvaquone (5 mg/kg IM, 2 d apart)/azithromycin (same dosage) (BUP). Before and after treatment (days 15, 45, 90 and 360), all dogs underwent a physical exam, blood tests and parasite detection (blood cytology and PCR). Clinical efficacy was assessed by grading 24 clinical and 8 clinicopathological signs from low to high severity.

Results: Before treatment, most dogs had severe regenerative anaemia (88.13%) and thrombocytopenia (71.4%). On treatment Day 45, clinical signs were mostly reduced in all dogs, and by Day 90, practically all dogs under the ATO or BUP regimen were clinically healthy (76.4 and 88%, respectively). Highest percentage reductions in laboratory abnormalities (82.04%) were detected in animals treated with ATO. Over the year, clinical relapse of Bml was observed in 8 dogs (8/17) treated with IMI. However, on Day 360, these animals had recovered clinically, though clinicopathological abnormalities were still present in some of them. Parasitaemia was PCR-confirmed on Days 90 and 360 in 47.05 and 50% of dogs treated with ATO, 68 and 60.08% with BUP, and 94.1 and 73.3% with IMI, respectively. Even after 360 days, 13.3% of the dogs treated with IMI returned a positive blood cytology result.

Conclusions: IMI showed the worse clinical and parasitological, efficacy such that its use to treat Bml infection in dogs is not recommended. The treatments ATO and BUP showed better efficacy, though they were still incapable to completely eliminate PCR-proven infection at the recommended dose. All three treatments showed good tolerance and safety with scarce adverse events observed.

Keywords: Atovaquone; Azithromycin; Babesia microti-like piroplasm; Buparvaquone; Canine piroplasmosis; Imidocarb dipropionate; Therapeutic efficacy.

MeSH terms

  • Animals
  • Antiprotozoal Agents / adverse effects
  • Antiprotozoal Agents / therapeutic use*
  • Atovaquone / administration & dosage
  • Atovaquone / adverse effects
  • Atovaquone / therapeutic use*
  • Azithromycin / administration & dosage
  • Azithromycin / adverse effects
  • Azithromycin / therapeutic use*
  • Babesia microti / drug effects
  • Babesia microti / isolation & purification
  • Babesia microti / physiology
  • Babesiosis / drug therapy*
  • Babesiosis / epidemiology
  • Babesiosis / parasitology
  • Dog Diseases / drug therapy*
  • Dog Diseases / epidemiology
  • Dog Diseases / parasitology
  • Dogs
  • Drug Therapy, Combination
  • Europe / epidemiology
  • Female
  • Imidocarb / administration & dosage
  • Imidocarb / adverse effects
  • Imidocarb / analogs & derivatives*
  • Imidocarb / therapeutic use
  • Male
  • Naphthoquinones / administration & dosage
  • Naphthoquinones / adverse effects
  • Naphthoquinones / therapeutic use*
  • Parasitemia / drug therapy
  • Parasitemia / epidemiology
  • Parasitemia / veterinary
  • Polymerase Chain Reaction

Substances

  • Antiprotozoal Agents
  • Naphthoquinones
  • buparvaquone
  • Azithromycin
  • Imidocarb
  • Atovaquone
  • imidocarb dipropionate