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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.

 

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FIVP launches CMA remedies survey

News Story 1
 FIVP has shared a survey, inviting those working in independent practice to share their views on the CMA's proposed remedies.

The Impact Assessment will help inform the group's response to the CMA, as it prepares to submit further evidence to the Inquiry Group. FIVP will also be attending a hearing in November.

Data will be anonymised and used solely for FIVP's response to the CMA. The survey will close on Friday, 31 October 2025. 

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News Shorts
CMA to host webinar exploring provisional decisions

The Competition and Markets Authority (CMA) is to host a webinar for veterinary professionals to explain the details of its provisional decisions, released on 15 October 2025.

The webinar will take place on Wednesday, 29 October 2025 from 1.00pm to 2.00pm.

Officials will discuss the changes which those in practice may need to make if the provisional remedies go ahead. They will also share what happens next with the investigation.

The CMA will be answering questions from the main parties of the investigation, as well as other questions submitted ahead of the webinar.

Attendees can register here before Wednesday, 29 October at 11am. Questions must be submitted before 10am on 27 October.

A recording of the webinar will be accessible after the event.