Your data on MRCVSonline
The nature of the services provided by Vision Media means that we might obtain certain information about you.
Please read our Data Protection and Privacy Policy for details.

In addition, (with your consent) some parts of our website may store a 'cookie' in your browser for the purposes of
functionality or performance monitoring.
Click here to manage your settings.
If you would like to forward this story on to a friend, simply fill in the form below and click send.

Your friend's email:
Your email:
Your name:
 
 
Send Cancel

Review does not support use of ACEIs in dogs with preclinical MMVD
The study found that administration of ACEIs to dogs with preclinical MMVD and cardiomegaly results in little or no difference in the risk of developing congestive heart failure

Researchers review adverse events of angiotensin-converting enzyme inhibitor use.

The use of angiotensin-converting enzyme inhibitors (ACEIs) for managing preclinical myxomatous mitral valve disease (MMVD) in dogs results in little or no difference in the risk of developing conegestive heart failure, according to new research.

The study, published in the Journal of Small Animal Practice, is the first comprehensive systematic review and meta-analysis on the efficacy and adverse events of ACEIs for the condition, often seen in cavalier King Charles spaniels and dachshunds.

It found that administration of ACEIs to dogs with preclinical MMVD and cardiomegaly results in little or no difference in the risk of developing congestive heart failure and may result in little or no difference in cardiovascular-related and all-cause mortality. 

The study was conducted by researchers in Argentina, Italy, Austria and Chile, who set out to evaluate the efficacy of and adverse events from the administration of ACEIs, via a systematic review of published evidence conducted according to the Cochrane Handbook for Systematic Reviews of Interventions.

Certainty of evidence was assessed using the GRADE approach, and the main finding in relation to dogs with preclinical MMVD and cardiomegaly backed by a high certainty of evidence. The certainty of evidence relating to the efficacy of ACEI administration in dogs without cardiomegaly was low.

Dr Pablo Donati, corresponding author for the paper, commented: “In recent times, multiple clinical trials have provided fundamental information to veterinary cardiology. In the era of evidence-based medicine, systematic reviews and meta-analyses have emerged as a fundamental tool for clinical decision-making by gathering, appraising and summarizing the best available evidence. 

"It is the hope of the authors that this systematic review and meta-analysis helps in the decision-making process for the treatment of preclinical myxomatous mitral disease with angiotensin-converting enzyme inhibitors in dogs.” 

Nicola Di Girolamo, Editor of JSAP, added: “In line with other leading journals, the JSAP is prioritizing the publication of methodologically sound systematic reviews such as this one. However, our readers should be aware that the findings of systematic reviews should always be considered in light of their internal validity, i.e. the quality of the included studies, and their external validity, i.e. the generalizability of the included studied to the individual patient.”

Image (C) Dr Pablo Donati.

 

Become a member or log in to add this story to your CPD history

Defra shares new Sanitary and Phytosanitary guidance

News Story 1
 Defra has published guidance for the vet sector ahead of a proposed UK-EU Sanitary and Phytosanitary agreement.

The agreement, which will change the movement and trade of animals and related products, could see reductions in checks, paperwork and certification. As well as describing regulatory developments, the advice highlights the importance of animal ID, registration and traceability in disease control and other compliance arrangements.

The guidance can be found here. More detail is expected as negotiations progress. 

Click here for more...
News Shorts
Lords Committee opens Pet Parasite Medication inquiry

The House of Lords Environment and Climate Change Committee will launch its inquiry into Pet Parasite Medication (PPM) on Wednesday (3 June).

Focusing on treatments containing fipronil and imidacloprid, the inquiry will seek to understand distribution pathways and the impacts of PPM use and non-use on biodiversity and human health. It will also cover current regulation, monitoring, and the potential implications for pets and their owners.

The committee will hear evidence from environmental non-governmental organisations and research institutes. The public can follow the proceedings live on Parliament TV or in person in the Palace of Westminster.