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Peer-reviewed veterinary case report

Kidney function changes during heartworm treatment in dogs

By Vetter, C Autumn M et al.·Published in Parasites & vectors·2023·Department of Small Animal Medicine and Surgery, United States·View original on PubMed

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Original publication title: Evaluation of renal values during treatment for heartworm disease in 27 client-owned dogs.

Species:
dog

Plain-English summary

A group of 27 dogs being treated for heartworm disease had their kidney function monitored during treatment. The dogs received a combination of medications, including doxycycline and melarsomine, which is the standard treatment for heartworm. Researchers measured kidney health markers before treatment, during, and after the treatment period. They found that while there were no major changes in kidney function overall, one specific marker (SDMA) showed improvement after the second dose of melarsomine. This suggests that the treatment protocol is safe for the kidneys of dogs with heartworm disease.

People also search for: dog heartworm treatment · heartworm disease kidney problems · melarsomine side effects in dogs

Abstract

BACKGROUND: Canine heartworm disease (CHD) caused by Dirofilaria immitis remains a common preventable disease with increasing incidence in some parts of the USA. The treatment guidelines of the American Heartworm Society (AHS) currently recommend monthly macrocyclic lactone administration, 28 days of doxycycline given orally every 12 h and three injections of melarsomine dihydrochloride (1 injection on day 2 of treatment followed 30 days later by 2 injections 24 h apart). Minocycline has also been utilized when doxycycline is unavailable. The systemic effects of CHD, which particularly impact cardiac and renal function, have been described, with infected dogs often experiencing renal damage characterized by an increase in serum concentrations of renal biomarkers. Although the AHS treatment protocol for CHD has been shown to be safe and effective in most cases, the potential for complications remains. No study as of yet has evaluated changes in symmetric dimethylarginine (SDMA), a sensitive marker of renal function, during treatment for CHD. The purpose of the present study was to evaluate renal function in dogs by measuring serum creatinine and SDMA concentrations during the adulticide treatment period. METHODS: Serum creatinine and SDMA concentrations were measured in 27 client-owned dogs affected by CHD at the following time points: prior to starting doxycycline or minocycline therapy (baseline), during doxycycline or minocycline therapy (interim), at the time of the first dose of melarsomine (first dose), at the time of the second dose of melarsomine (second dose) and at the dog's follow-up visit after treatment, occurring between 1 and 6 months after completion of therapy (post-treatment). Concentrations of creatinine and SDMA were compared between time points using a mixed effects linear model. RESULTS: Mean SDMA concentrations following the second dose of melarsomine were significantly lower (-1.80 ug/dL, t-test, df = 99.067, t = -2.694, P-Value = 0.00829) than baseline concentrations. There were no other statistically significant differences in the concentration of either biomarker between the baseline and the other time points in CHD dogs undergoing treatment. CONCLUSIONS: The results suggest that the current AHS protocol may not have a substantial impact on renal function.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/37291617/