Evidence gaps in veterinary medicine
How good is the evidence for what we actually do?
Some of small-animal practice is backed by well-conducted trials. Some of it rests on one small study, on a result borrowed from human medicine, or on nothing but convention. Very little of it is labelled, so a clinician has no easy way to tell which kind of recommendation they are following.
This site works through small-animal practice one clinical question at a time and records the answer. Each question gets two marks: how far the evidence can be relied on, and which way it points. Where no study exists, that is written down as well, because an untested practice and a disproven one are not the same thing.
The map runs specialty by specialty across small-animal practice, and every specialty on it is being built out and expanded. Further ones are added as the work goes on.
The specialties
Open the gap map →The gap map covers each of these, worked through the same way and to the same standard. All of them are being expanded as the literature is covered, and further specialties are added as the work goes on.
Small-animal cardiology
Mitral valve disease, the cardiomyopathies, the management of heart failure and the common arrhythmias. Every question is graded against the strongest evidence that exists for it, with the reasons for the grade listed underneath.
Anaesthesia and analgesia
Protocol selection, multimodal analgesia and the monitoring thresholds in routine use, across species and procedure types.
Antimicrobials
Empirical drug selection, duration of therapy, and the evidence behind the first-line recommendations made in common presentations.
Nutrition and supplements
Therapeutic diets, joint supplements and nutraceuticals, a field in which marketing claims and trial evidence diverge more often than in most others.
Dermatology
Atopic disease, otitis, and the long-term management protocols that rest largely on convention.
Oncology
Protocol comparisons, adjuvant therapy, and the outcome measures that are used to judge both.
If you work in one of these areas and would be willing to draft entries or check them, that speeds the work up considerably. Write to contact@evidencegap.vet.
What the two marks mean
The first mark says how far the evidence behind a question can be relied on. It follows GRADE, the system used for the same purpose in human medicine.
The second mark says which way that evidence points. The two are kept apart because a question can rest on weak evidence and still point clearly, and because nobody looked and somebody looked and found nothing are different answers that are routinely treated as the same one.
Study design sets the starting point of an assessment and not its conclusion. A trial that was funded by the manufacturer, measured a surrogate outcome and has never been replicated does not outrank a well-conducted observational study by virtue of being a trial. The specific reasons certainty was not rated higher are recorded against every question, so that each judgement can be examined rather than accepted. The full method is on the map page.
Find a clinical question or practice
24 entries indexedShowing all 24 entries. Type to narrow the list.
Myxomatous mitral valve disease (dogs)
- Pimobendan in preclinical stage B2 diseaseModerate
- Does preclinical pimobendan shorten survival once heart failure develops?Low
- Pimobendan in congestive heart failureModerate
- ACE inhibitors before heart failureModerate
- Spironolactone added to standard heart-failure therapyLow
- Spironolactone with benazepril to delay the onset of heart failureModerate
- Furosemide dose and dosing frequency in stage C diseaseNo evidence
Dilated cardiomyopathy (dogs)
Feline cardiomyopathy
- Clopidogrel to prevent recurrent arterial thromboembolismModerate
- Atenolol in preclinical hypertrophic cardiomyopathyLow
- Pimobendan in feline congestive heart failureVery low
- Rapamycin (sirolimus) in subclinical hypertrophic cardiomyopathyVery low
- Any therapy that delays the onset of heart failure in hypertrophic cardiomyopathyNo evidence
- Do glucocorticoids precipitate congestive heart failure?Low
Congestive heart failure: management
Arrhythmias
Nothing matches that term. Try a drug name, a test, or a condition.
Latest commentaries
All commentaries →-
Commentary · Canine cardiology · August 2026
Pimobendan in preclinical stage B2 mitral valve disease
The trial was reconstructed from its published survival curves. Reclassifying nine dogs removes the significance of the primary result, the event proportions alone are not significant, and the subsequent full approval rests on a single-arm study that was measured against a benchmark it was never required to beat.
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Commentary · Feline cardiology · August 2026
Steroids and heart failure in cats: science, or an old wives' tale?
The belief that corticosteroids precipitate heart failure in cats rests on two papers published in 2004 and 2006. Neither paper demonstrates the effect, the controlled studies that followed found no cardiac change, and the largest cohort reported no excess of heart failure in treated cats.
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Editorial appraisal · Feline cardiology · August 2026
Rapamycin (sirolimus) for subclinical hypertrophic cardiomyopathy in cats
The published report and the FDA record disagree with each other about whether the endpoint of the single supporting trial was specified before the data were examined. The regulatory summary states that it was not.
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Editorial appraisal · Canine cardiology · June 2026
Torasemide as an alternative to furosemide in canine congestive heart failure
Non-inferiority demonstrated on a composite endpoint is a weaker claim than this result is generally taken to support. This appraisal is in preparation.
Three ways the evidence falls short
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Absence of direct evidence
Some interventions in routine use have never been tested against a control in the species they are given to. Dietary sodium restriction in canine congestive heart failure is one such practice, and although it is close to universal, the trial that would justify it has not been performed.
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Borrowed evidence
Other recommendations are carried across from human medicine, or from one species to another, without data establishing that the finding transfers. Dose, pharmacokinetics and disease phenotype rarely translate cleanly between species, and the assumption that they do is seldom stated explicitly.
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Consensus in place of data
A third group consists of screening intervals, treatment thresholds and monitoring conventions that originated in expert judgement and were subsequently cited as though they had been established by study. Such conventions may well turn out to be correct, but they should be identified as consensus rather than as evidence.
The same drugs, in people
Read the comparison →Much of small-animal cardiology is extrapolated from human cardiology, and the extrapolation is seldom stated. The diseases differ enough that a human trial rarely settles a veterinary question. Drug classes, though, travel further than diseases do, and several of these have been tested in people at a scale veterinary medicine will never reach.
Oral inotropes increased mortality against placebo. Suppressing asymptomatic ventricular ectopy after myocardial infarction more than doubled it, with no warning on any intermediate measure. Beta blockade in non-obstructive hypertrophic cardiomyopathy reduced exercise capacity. Glucocorticoids are given in human heart failure on purpose, to improve diuresis, rather than withheld.
A companion page takes each intervention class in turn: what was tested, what it showed, and how close the analogy actually is.
Scope
Every specialty on the map is being expanded, and more are added as the work goes on. Cardiology currently holds 24 entries across 5 disease areas. No specialty is covered exhaustively, because each takes the questions and practices that come up often enough to be worth appraising.
Method
Entries are written from the primary reports, not from abstracts or from what other papers say about them. A citation that cannot be checked against the record is not used. Gradings are revised when new work appears, and the reasons behind each are listed under the entry.
Corrections and additions
Proposed entries, disputed gradings and citations that should be here are all welcome. Contributions are credited.
contact@evidencegap.vetEditorial appraisals of published literature. Not peer reviewed, and not clinical advice.