Evidence map›Paper›PMID 34028078›Full record

ArticleJournal of veterinary internal medicine2021

Clinical efficacy of a benazepril and spironolactone combination in dogs with congestive heart failure due to myxomatous mitral valve disease: The BEnazepril Spironolactone STudy (BESST).

Melissa Coffman, Emilie Guillot, Thomas Blondel, Catherine Garelli-Paar, Shuo Feng, Susanne Heartsill, Clarke E Atkins

Open access · goldAbstract readMulticenter StudyRandomized Controlled Trial, Veterinary
In one paragraph

Article in Journal of veterinary internal medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
5.0field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 42 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 3 countries.

Melissa CoffmanPharmaceutical Innovation & Development, Ceva Animal Health, Lenexa, Kansas, USA.ORCID https://orcid.org/0000-0002-6156-6484
Emilie GuillotCompanion Animal Franchise, Ceva Santé Animale, Libourne, France.ORCID https://orcid.org/0000-0002-6892-4176
Thomas BlondelInnovation & Development, Ceva Santé Animale, Libourne, France.ORCID https://orcid.org/0000-0001-6316-967X
Catherine Garelli-PaarCompanion Animal Franchise, Ceva Santé Animale, Libourne, France.
Shuo FengInnovation & Development, Ceva Biomune, Lenexa, Kansas, USA.
Susanne HeartsillVeterinary Services, Ceva Animal Health, Lenexa, Kansas, USA.ORCID https://orcid.org/0000-0002-7315-3927
Clarke E AtkinsDepartment of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina, USA.ORCID https://orcid.org/0000-0002-4463-4625
Département Santé Animale · FRCeva Animal Health (United Kingdom) · GBAmerican College of Healthcare Architects · USNorth Carolina State University · US

Funding

Ceva Santé Animale
6 · The paper itself

Abstract

backgroundThe renin-angiotensin-aldosterone system (RAAS), when chronically activated, is harmful and RAAS-suppressive drugs are beneficial in the treatment of congestive heart failure (CHF). Mineralocorticoid receptor antagonists are widely used in the treatment of CHF in people. HYPOTHESIS/

objectivesTo determine if a mineralocorticoid receptor antagonist (spironolactone) is beneficial and safe in CHF due to myxomatous mitral valve disease (MMVD) of varying severity, we hypothesized that, when combined with furosemide, a combination product (S+BNZ) containing the ACE inhibitor (ACE-I), benazepril, and spironolactone, would be superior to benazepril alone. ANIMALS: Five hundred and sixty-nine client-owned dogs, with MMVD and CHF (ACVIM Stage C) of ≤10-days' duration.

methodsAfter initial stabilization, dogs were randomized into a positive-controlled, double-blind, multicenter trial, to receive furosemide plus S+BNZ or furosemide plus benazepril. The primary outcome variable was the percentage of dogs reaching cardiac endpoint before Day 360. Cardiac endpoint was defined as cardiac death or euthanasia, recurrence of pulmonary edema, necessity for nonauthorized cardiac drug(s) or a furosemide dosage >8 mg/kg/d.

resultsA significantly lower percentage of dogs treated with S+BNZ reached the primary outcome variable by Day 360 (OR = 0.56; 95% CI, 0.32-0.98; P = .04) and risk of dying or worsening from cardiac causes, was significantly reduced (HR = 0.73; 95% CI = 0.59-0.89, P = .002) vs benazepril alone. Adverse events, potentially associated with treatment, were rare and equal between groups. CONCLUSION AND CLINICAL IMPORTANCE: The combination of S+BNZ is effective, safe, and superior to benazepril alone, when used with furosemide for the management of mild, moderate or severe CHF caused by MMVD in dogs.

Indexed as

Dog DiseasesHeart FailureAnimalsBenzazepinesDogsMitral ValveSpironolactoneTreatment OutcomebenazeprilBenzazepinesSpironolactoneACE inhibitoraldosterone breakthroughmitral regurgitationMRARAAS

Identifiers

PMID34028078
PMCPMC8295662
OpenAlexW3165206479

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.