Condition reference
GastrointestinalChronic enteropathy / inflammatory bowel disease
Explore the linked guideline and related drug references. A matching drug entry does not establish a treatment recommendation.
WSAVA guideline
Endoscopic, Biopsy and Histopathologic Guidelines for the Evaluation of Gastrointestinal Inflammation in Companion Animals
WSAVA defines IBD as idiopathic chronic GI disorders with mucosal inflammation within the chronic-enteropathy (CE) spectrum, set apart from food- and antibiotic-responsive disease by response to immunosuppressives but not to diet or antibiotics alone (§Scope of the Problem). IBD is never a histology-only diagnosis: all 5 criteria are required, including chronicity > 3 weeks and failed diet/antibacterial/anthelmintic trials. Biopsy standards are quantitative (cat ~6; dog ~6–7 adequate or 10–15 marginal) and lesions graded 0–3 at 40×; lacteal dilation is the one lesion linked to hypoalbuminemia. The lymphoma boundary is settled by CD3/CD79a IHC plus TCRG clonality PCR (IHC first). No drug doses are printed.
WSAVA GI Standardization Group; Washabau et al., JVIM 2010;24:10–26 + report forms
Key findings
- 5 criteria (all required): (1) chronic GI signs > 3 weeks; (2) histopathologic mucosal inflammation; (3) other causes excluded; (4) inadequate response to dietary, antibacterial, anthelmintic trials; (5) clinical response to anti-inflammatory/immunosuppressive agents (§Definition of IBD). Breeds: Siamese, GSD, Basenji, Wheaten, Shar Pei.
- CE spectrum: IBD responds to immunosuppressives but NOT to dietary or antibiotic therapy alone.
- Biopsy numbers: cat ~6 marginal-or-adequate stomach/duodenum samples diagnose villus atrophy + mild-to-moderate infiltration; dog ~6–7 adequate or 10–15 marginal gastric/duodenal; canine duodenal crypt lesions ~13 adequate or 28 marginal; skilled endoscopists need fewer (§Endoscopic Biopsy).
- Adequate sample = at least 3 villi with full mucosal depth (mucosa–muscularis mucosae border); inadequate = villus tips only (Figs 1–3).
- Duodenal lesions (Table 3): villus stunting, epithelial injury, crypt distension, lacteal dilation, mucosal fibrosis + IEL, LP lymphocytes/plasma cells, LP eosinophils, LP neutrophils — each 0–3 at 40×. Dog anchors: villus 722±170 μm, crypt 1,279±203 μm, V:C 0.7±0.3; cryptal-LP leukocytes 156.3±24.9 vs tip 100.7±43.9; cryptal eosinophils 9.8±7.5 per 10,000 μm².
- Lymphoma vs IBD: 2 feline variants — small-cell lymphocytic villus T-cell (older cats) and large-cell lymphoblastic (any age, aggressive). HE often insufficient → IHC CD3/CD79a (32-cat study: 5 "lymphomas" were IBD); TCRG clonality: polyclonal 9/9 IBD vs clonal 22/28 T-cell lymphoma cats; IHC retains precedence; both on paraffin tissue from one biopsy set.
- Histology ↔ clinic: lacteal dilation ↔ hypoalbuminemia; severity at diagnosis did not predict 3-year outcome (70 dogs); prednisone+metronidazole or cyclosporine improved signs without histologic change — biopsy documents inflammation but cannot alone diagnose or prognose.
- Helicobacter: IBD- vs Helicobacter-gastritis often indistinguishable on HE; dual inflammation + mucosal invasion (Warthin-Starry/PCR/FISH) differentiates.
Drugs named in WSAVA’s own guideline text
As printed in WSAVA’s document, not this app’s own extracted data — see “Related drugs in this reference” below for that.
Prednisone (🐕) — [dose not printed in source]
With metronidazole — improved signs, no significant histologic change
Metronidazole (🐕) — [dose not printed in source]
Partner to prednisone in same study
Cyclosporine (🐕) — [dose not printed in source]
Clinically successful; duodenal lymphocytes unchanged
Anti-inflammatory / immunosuppressive agents (🐕🐈) — [dose not printed in source]
Criterion 5 — response defines IBD within the CE spectrum
Antibacterial / anthelmintic / probiotic trials (🐕🐈) — [dose not printed in source]
Pre-diagnosis therapeutic trials (criterion 4)
NSAIDs (🐕🐈) — [dose not printed in source]
Named as gastritis cause, not IBD therapy
Recommendations
Diagnose IBD only with all 5 criteria; run diet/antibacterial/anthelmintic trials BEFORE the label
Consensus — Conclusion (b)
Endoscopic biopsy preferred; EARLY with severe weight loss, poor BCS, anorexia, hypoalbuminemia, US infiltrates
Consensus — Conclusion (a)
Biopsy the ileum whenever gastroduodenoscopy/colonoscopy is performed
Consensus — Conclusion (a)
Sample counts: cat ~6; dog 6–7 adequate or 10–15 marginal; crypt lesions 13/28
Evidence-based (Class II/III)
Insist path reports state sample number + quality (adequate/marginal/inadequate); use WSAVA grading (40×, 0–3)
Consensus — Conclusions (d), (e)
If HE cannot separate small-cell lymphoma: IHC CD3/CD79a ± TCRG clonality; IHC retains precedence
Group endorsement of cited evidence
Do not separate IBD- vs Helicobacter-gastritis on HE alone; histology alone cannot diagnose or prognose
Group conclusion
Related drugs in this reference (6)
The quoted line under each drug is its own already-extracted indication text that matched this condition — the reason it’s listed, not a paraphrase. Open a drug for its full species/route breakdown, calculator, and complete adverse-effect list.
Showing 6 of 6 linked drug records. Open a record for species, route and source details.
AZATHIOPRINE
“IMHA, pemphigus, IBD, other immune-mediated diseases (steroid-sparing)”
Source dose preview: 2 mg/kg initial, q24h, PO (Dog)
Adverse-effect notes: **Bone marrow suppression (leukopenia, anemia, thrombocytopenia)** — **Principal adverse effect** · GI upset, poor hair growth, pancreatitis, hepatotoxicity — Reported
CHLORAMBUCIL
“**Chronic low-grade intestinal lymphoma (with prednisolone); refractory/severe IBD; pemphigus foliaceus; eosinophilic granuloma complex** — preferred over cyclo…”
Source dose preview: 0.1–0.2 mg/kg, q24–48h, PO (Dog)
Adverse-effect notes: Myelosuppression (mild, gradual) — Lower than cyclophosphamide — the point of choosing it · GI toxicity, anorexia — Occasional
CLONIDINE
“Refractory IBD adjunct (4th-line per Washabau)”
Source dose preview: 0.01–0.05 mg/kg, q12h, PO (Dog)
Adverse-effect notes: Sedation — Common · **Hypotension, collapse, bradycardia** — Cardiovascular core effects
CYCLOSPORINE
“Atopic dermatitis (well-established, similar efficacy to prednisolone), perianal fistulas, IMHA (refractory), IBD”
Source dose preview: 5 mg/kg (range 2.5–7 mg/kg), q24h x 30 days, then taper to EOD/2x-week, PO, ≥1h before or 2h after meal (Dog)
Adverse-effect notes: Vomiting, anorexia, diarrhea — Most common, especially early in therapy · Gingival hyperplasia, hypertrichosis, papillomatosis — With chronic use
METRONIDAZOLE
“Giardia, other enteric protozoa, anaerobic infections, adjunct for IBD/colitis”
Source dose preview: 15–25 mg/kg, q12–24h x 5–7 days, PO (Dog)
Adverse-effect notes: **Neurotoxicity (ataxia, nystagmus, head tilt, seizures)** — **Dose-related, typically >60 mg/kg/day or chronic "recommended" dosing** · Hepatotoxicity, vomiting, anorexia — Reported
TYLOSIN
“Chronic enteropathy / antibiotic-responsive diarrhea (ARD); tylosin-responsive diarrhea; tear staining (epiphora, extra-label cosmetic)”
Source dose preview: 20–40 mg/kg (or 25 mg/kg fixed), q12h (or q24h), PO (Dog)
Adverse-effect notes: GI upset (anorexia, diarrhea) — Main oral effect · Pain/local reaction at IM injection sites — Injectable use (rare parenteral use in small animals)
From pack #11 summary + `text/gi_EN_washabau2010_full_web.txt`; numbers as printed. No doses in source — every row flagged. Ileal/colonic biopsy minimums not quantified [verify].