Evidence Snapshot
Evidence Snapshot v24
Version
v@Model.VersionNumber
v@Model.VersionNumber
Generated
06/06/2026 00:55:39
06/06/2026 00:55:39
Reasoning Status
Not run
Not run
DAMNIT-V Evidence Prioritisation
Intent: All DAMNIT-V domains remain visible, but each is interpreted from the evidence actually collected. Low-evidence domains are retained for completeness without being over-prioritised.
Case Summary
Case Title: Vomiting Primary Complaint: Vomiting for 2 days Status: Open Date Opened: 30/05/2026 CLINICAL NARRATIVE Vomiting for 2 days , blood - was eating a bone INITIAL DIFFERENTIAL NOTES Suspect FB vs Garbage vs Bacterial infection LOCAL / REGIONAL CLINICAL CONTEXT No matching active local/regional clinical context entries found for the recorded species and presenting signs.
Evidence Status
Clinical intake documents: 1 Nutrition assessments: 71 RAC / Audiomixer documents: 0 Pathology / laboratory reports: 0 Imaging reports: 0 HTMA reports: 0 Microbiome reports: 0 Supplement reviews: 0 EVIDENCE PENDING / NOT YET ADDED - Food entries, treat entries, supplement entries - RAC / Audiomixer DOCX reports - Pathology / laboratory reports - Imaging reports - HTMA report if requested
RAC / Audiomixer Evidence Summary
Not recorded.
Domain-Source Weighted Priorities
Derived from current source scores: Clinical Intake, Nutrition, RAC, Pathology/Lab, Imaging, HTMA and Microbiome.
No domain priorities generated from current evidence.
DAMNIT-V Evidence-Conditioned Possibility Map
D - Degenerative / Structural
Evidence Found
- No direct supporting evidence currently collected.
Evidence Source
- No case-specific source identified
Current Interpretation
- None currently supported beyond DAMNIT-V completeness.
Missing Confirmation
- No missing evidence listed.
RAC Correlation Targets
- No RAC targets generated.
Physical Confirmation Targets
- No physical confirmation options generated.
A - Allergic / Reactive
Evidence Found
- No direct supporting evidence currently collected.
Evidence Source
- No case-specific source identified
Current Interpretation
- None currently supported beyond DAMNIT-V completeness.
Missing Confirmation
- No missing evidence listed.
RAC Correlation Targets
- No RAC targets generated.
Physical Confirmation Targets
- No physical confirmation options generated.
M - Metabolic / Nutritional
Evidence Found
- No direct supporting evidence currently collected.
Evidence Source
- No case-specific source identified
Current Interpretation
- None currently supported beyond DAMNIT-V completeness.
Missing Confirmation
- No missing evidence listed.
RAC Correlation Targets
- No RAC targets generated.
Physical Confirmation Targets
- No physical confirmation options generated.
N - Neoplastic / Nutrition
Evidence Found
- No direct supporting evidence currently collected.
Evidence Source
- No case-specific source identified
Current Interpretation
- None currently supported beyond DAMNIT-V completeness.
Missing Confirmation
- No missing evidence listed.
RAC Correlation Targets
- No RAC targets generated.
Physical Confirmation Targets
- No physical confirmation options generated.
I - Infectious / Inflammatory / Immune
Evidence Found
- No direct supporting evidence currently collected.
Evidence Source
- No case-specific source identified
Current Interpretation
- None currently supported beyond DAMNIT-V completeness.
Missing Confirmation
- No missing evidence listed.
RAC Correlation Targets
- No RAC targets generated.
Physical Confirmation Targets
- No physical confirmation options generated.
T - Toxic / Traumatic
Evidence Found
- No direct supporting evidence currently collected.
Evidence Source
- No case-specific source identified
Current Interpretation
- None currently supported beyond DAMNIT-V completeness.
Missing Confirmation
- No missing evidence listed.
RAC Correlation Targets
- No RAC targets generated.
Physical Confirmation Targets
- No physical confirmation options generated.
V - Vascular / Neurological
Evidence Found
- No direct supporting evidence currently collected.
Evidence Source
- No case-specific source identified
Current Interpretation
- None currently supported beyond DAMNIT-V completeness.
Missing Confirmation
- No missing evidence listed.
RAC Correlation Targets
- No RAC targets generated.
Physical Confirmation Targets
- No physical confirmation options generated.
Show original detailed snapshot
DAMNIT-V COMBINED EVIDENCE SNAPSHOT v24 ================================================== PATIENT ------- Name: Eddy Owner: Bright Species: Canine Breed: Border Collie Sex: Male Desexed Status: Life Stage: Activity Level: Current Weight kg: 23.00 Ideal Weight kg: BCS: 7.00 CASE ---- Case Title: Vomiting Primary Complaint: Vomiting for 2 days Status: Open Date Opened: 30/05/2026 CLINICAL NARRATIVE ------------------ Vomiting for 2 days , blood - was eating a bone INITIAL DIFFERENTIAL NOTES -------------------------- Suspect FB vs Garbage vs Bacterial infection LOCAL / REGIONAL CLINICAL CONTEXT --------------------------------- No matching active local/regional clinical context entries found for the recorded species and presenting signs. CLINICAL INTAKE DOCUMENTS ------------------------- DOCUMENT: History Type: Clinical History Source: Manual Uploaded: 30/05/2026 05:44 O called early today - dog is Vomiting NUTRITION ASSESSMENTS --------------------- Total nutrition assessments for this case: 71 LATEST NUTRITION ASSESSMENT --------------------------- Assessment ID: 70 Title: Nutrition Assessment Date: 05/06/2026 Feeding Goal: Maintenance Current Diet Type: Commercial complete Body Weight kg: 23.00 Ideal Weight kg: BCS: 7.00 Muscle Condition: Normal Appetite: Normal Owner Goals: Diet Concerns: Skin / Coat Notes: Digestive Notes: Stool Quality: Owner-Reactive Foods: O: Chicken, beef, lamb, roo, pork, cheese, eggs, yoghurt, kibble, wheat, peanut butter, Owner-Tolerated Foods: : Goat, venison, wild boar, [meat must have no fillers added - that's why Canine Country is best as raw food without fillers] blueberries, strawberries, raspberries, apples, bananas, mango, cucumber/gukes, broccoli/broccolini, cauliflower, pumpkin, peas, zucchini, beans, watermelon (all vegetables are cooked), he doesn’t like carrot or celery NUTRITION EVIDENCE SNAPSHOT --------------------------- Latest Assessment ID: 70 Assessment Date: 05/06/2026 Energy Intake: 420.7 kcal/day Estimated Requirement: 997.74 kcal/day Energy Percent: 42.2% Energy Status: Low / below estimated requirement Protein: 45.71 g/day Fat: 18.24 g/day Carbohydrate: 30.6 g/day Matched Diet Items: 7 / 19 Unmatched Diet Items: 12 Micronutrient Confidence: Partial / incomplete Nutrition Confidence: Moderate / partial evidence Owner-Reactive / Avoid Foods: O: Chicken, beef, lamb, roo, pork, cheese, eggs, yoghurt, kibble, wheat, peanut butter, Owner-Tolerated Foods: : Goat, venison, wild boar, [meat must have no fillers added - that's why Canine Country is best as raw food without fillers] blueberries, strawberries, raspberries, apples, bananas, mango, cucumber/gukes, broccoli/broccolini, cauliflower, pumpkin, peas, zucchini, beans, watermelon (all vegetables are cooked), he doesn’t like carrot or celery Ingredient-Derived Reactive Groups: cruciferous, fibre, fodmap, iodine_source, lectin, oxalate_possible, purine, salicylate_possible, sulphur RAC-Reactive Foods: Not yet connected. Future build will compare RAC-reactive foods against current diet, owner-reactive foods and tolerated foods. EVIDENCE INCLUDED ----------------- Clinical intake documents: 1 Nutrition assessments: 71 RAC / Audiomixer documents: 0 Pathology / laboratory reports: 0 Imaging reports: 0 HTMA reports: 0 Microbiome reports: 0 Supplement reviews: 0 EVIDENCE PENDING / NOT YET ADDED -------------------------------- - Food entries, treat entries, supplement entries - RAC / Audiomixer DOCX reports - Pathology / laboratory reports - Imaging reports - HTMA report if requested - Microbiome report if requested - Supplement review EVIDENCE STATUS --------------- Evidence Used In This Snapshot: - Clinical Intake: Used - Nutrition: Used Additional Evidence Available If Clinically Indicated: - RAC / Audiomixer screening: may help prioritise which physical tests or evidence domains should be pursued next. - Pathology / laboratory testing: available if clinical signs, risk assessment, or response to treatment justify testing. - Imaging: available if obstruction, foreign body, mass, trauma or structural disease remains a concern. - HTMA: available if mineral/toxic element patterning is clinically relevant. - Microbiome: available if chronic gastrointestinal, immune, dermatological or inflammatory patterns require deeper investigation. Clinical Context: A veterinary assessment is commonly made using the evidence that is clinically justified and practically available. This section records what was used and what could be added later, without implying that every possible test is required for every patient. EVIDENCE WEIGHTING ENGINE v1 ---------------------------- Domain weights used in this snapshot: - Imaging: 5 - Pathology / Laboratory: 5 - Clinical Examination: 4 - Clinical History / Intake: 4 - Nutrition: 3 - HTMA: 2 - Microbiome: 2 - RAC / Audiomixer: 1 - Supplement Review: 1 Current snapshot contains Clinical Intake and Nutrition evidence only. Imaging, pathology, HTMA, microbiome and RAC are pending. DIFFERENTIAL PRIORITIES v2 - WEIGHTED ------------------------------------- 1. Gastrointestinal foreign body / obstructive bone fragment Weighted Evidence Score: 12 Weighted Confidence: High Evidence: - [Clinical History +4] Vomiting reported. - [Clinical History +4] Bone ingestion/exposure reported. - [Clinical History +4] Blood reported with vomiting or gastrointestinal signs. 2. Acute gastritis / gastroenteritis Weighted Evidence Score: 8 Weighted Confidence: Moderate Evidence: - [Clinical History +4] Vomiting reported. - [Clinical History +4] Blood may indicate mucosal irritation, ulceration or injury. 3. Dietary indiscretion / garbage gut Weighted Evidence Score: 8 Weighted Confidence: Moderate Evidence: - [Clinical History +4] Vomiting reported. - [Clinical History +4] Dietary exposure history should be reviewed. 4. Food reactivity / intolerance contribution Weighted Evidence Score: 6 Weighted Confidence: Low-Moderate Evidence: - [Nutrition +3] Owner-reported reactive foods present. - [Nutrition +3] Nutrition snapshot shows ingredient-derived reactive burden evidence. AI DAMNIT-V EXPANSION v4.2.1 CATEGORY: D - Degenerative / Structural POTENTIAL PROCESSES - Delayed gastric emptying or gastroparesis causing chronic vomiting - Structural abnormalities such as gastric dilatation, pyloric stenosis, or intestinal strictures - Foreign body causing mechanical obstruction or mucosal injury (e.g., ingested bone fragment) - Structural damage to gastrointestinal mucosa leading to ulceration or bleeding - Age-related degeneration of smooth muscle or neural control of GI tract Physical confirmation methods: abdominal palpation, abdominal radiographs, ultrasound imaging, endoscopy CATEGORY: A - Allergic / Reactive POTENTIAL PROCESSES - Food hypersensitivity reactions causing gastrointestinal inflammation and vomiting - Hypersensitivity to specific dietary proteins or fillers - Environmental allergens inducing reactive GI symptoms - Immune-mediated mucosal hypersensitivity causing vascular permeability or edema - Trigger screening by dietary history review and elimination trials Physical confirmation methods: dietary trials, allergen-specific serology testing, histamine release or endoscopic biopsy CATEGORY: M - Metabolic / Nutritional POTENTIAL PROCESSES - Nutritional deficiencies or imbalances affecting GI mucosal integrity - Metabolic disturbances (e.g., hepatic insufficiency, renal failure) causing secondary vomiting - Electrolyte imbalances impacting GI motility or function - Hypercalcemia inducing vomiting reflex - Hypoadrenocorticism with GI signs Physical confirmation methods: serum biochemistry including electrolytes, hepatic and renal panels, endocrine testing (ACTH stimulation), dietary intake assessment CATEGORY: N - Neoplastic POTENTIAL PROCESSES - Gastric or intestinal tumors causing obstruction or mucosal ulceration - Lymphoma or other GI tract neoplasia producing vomiting and hematemesis - Metastatic disease impacting digestive organs - Mass effect causing secondary inflammation or bleeding in GI tract Physical confirmation methods: abdominal imaging (radiographs, ultrasound, CT), endoscopic visualization, biopsy and histopathology CATEGORY: I - Infectious / Inflammatory / Immune POTENTIAL PROCESSES - Infectious gastroenteritis (bacterial, viral, parasitic) causing vomiting and mucosal injury - Immune-mediated gastritis or enteritis - Inflammatory bowel disease presenting with vomiting and hemorrhage - Infectious agents such as Helicobacter spp. inducing gastric mucosal inflammation - Secondary mucosal damage due to inflammatory cell infiltration Physical confirmation methods: fecal examinations, bloodwork including CBC and inflammatory markers, endoscopic biopsy, culture and sensitivity testing CATEGORY: T - Toxic / Traumatic POTENTIAL PROCESSES - Ingestion of toxic substances causing vomiting and GI irritation - Physical trauma to the abdominal area or GI tract (e.g., bone puncture or laceration) - Chemical irritants or foreign body-induced mucosal damage - Gastric or esophageal burns induced by caustic agents or sharp foreign bodies Physical confirmation methods: history of toxin exposure, physical examination for trauma, imaging for foreign body detection, clinical pathology to assess organ damage CATEGORY: V - Vascular / Neurological POTENTIAL PROCESSES - Vascular compromise to GI tract causing ischemic injury and vomiting - Neurological disorders affecting vomiting center or GI motility (e.g., vestibular disease, encephalopathy) - Autonomic nervous system dysfunction altering motility or secretions - Central nervous system lesions inducing vomiting reflex Physical confirmation methods: neurological exam, cranial nerve assessment, abdominal Doppler ultrasound, advanced imaging (MRI, CT) of CNS if indicated CLINICAL USE NOTE ----------------- - DAMNIT-V keeps all domains visible. - RAC screening may help guide efficient physical confirmation testing. - Diagnosis remains with the clinician. DIFFERENTIAL POSSIBILITY MAP v1 -------------------------------- Purpose: broaden the clinical thinking before final prioritisation. This is not a diagnosis list; it is a structured map of plausible branches that may be explored using RAC screening and, where justified, physical confirmation testing. Gastrointestinal / Obstructive / Traumatic ------------------------------------------ Possible branches to consider: - Foreign body - Bone fragment irritation or obstruction - Gastritis - Enteritis - Gastrointestinal mucosal trauma - Intestinal pain / spasm - Pancreatic irritation - Peritonitis risk if deterioration occurs Suggested RAC screening targets: - GIT obstruction signal - Stomach trauma / irritation - Small intestinal trauma / irritation - Abdominal pain - Pancreas stress - Inflammation - Peritoneal irritation Possible physical confirmation if RAC/clinical evidence supports: - Abdominal radiographs - Abdominal ultrasound - CBC / biochemistry - Electrolytes / hydration assessment - Serial abdominal palpation and pain scoring - Surgical referral if obstruction/perforation concern increases Dietary / Food Reactivity / Toxicity ------------------------------------ Possible branches to consider: - Dietary indiscretion - Food intolerance flare - Reactive food exposure - High fat exposure / pancreatitis risk - Toxin or irritant ingestion - Microbiome disruption Suggested RAC screening targets: - Reactive foods currently in diet - Owner-reported reactive foods - Histamine / sulphur / lectin / oxalate / purine burden - Pancreas stress - Liver detoxification burden - Gut dysbiosis pattern Possible physical confirmation if RAC/clinical evidence supports: - Diet history review - Elimination / bland diet trial if stable - CBC / biochemistry if persistent or systemic signs - cPL / pancreatitis testing if indicated - Microbiome testing if chronic or recurrent Systemic / Metabolic / Infectious --------------------------------- Possible branches to consider: - Systemic infection / inflammatory disease - Renal or hepatic contribution - Endocrine/metabolic stress - Electrolyte disturbance - Pain-driven nausea Suggested RAC screening targets: - Kidney stress - Liver stress - Systemic inflammation - Electrolyte disturbance - Pain focus - Fever / infection pattern Possible physical confirmation if RAC/clinical evidence supports: - Temperature and physical exam - CBC / biochemistry - Urinalysis - Electrolytes - Further infectious disease testing if clinically indicated DAMNIT-V Integrative Screening Branches --------------------------------------- Possible branches to consider: - Degenerative / structural - Allergic / autoimmune / reactive - Metabolic / nutritional - Neoplastic - Infectious / inflammatory - Toxic / traumatic - Vascular / neurological Suggested RAC screening targets: - Run RAC screening across DAMNIT-V categories - Identify strongest organ/system signals - Identify strongest pathology-type signals - Compare RAC positives with clinical history and nutrition evidence Possible physical confirmation if RAC/clinical evidence supports: - Select physical confirmation based on strongest RAC-supported branch - Use pathology, imaging, HTMA, microbiome, or referral testing only where clinically justified RAC-GUIDED NEXT EVIDENCE v1 --------------------------- RAC is treated here as a screening and prioritisation layer. A positive RAC signal does not replace physical diagnosis, but it can increase the justification for targeted physical testing when cost, risk, or uncertainty make broad testing difficult. Suggested workflow: 1. Generate broad differential possibility map. 2. Run RAC screening against the most plausible branches. 3. Compare RAC positives with clinical history, nutrition, examination and owner observations. 4. Increase priority for physical confirmation where RAC and clinical evidence converge. 5. Record later confirmation and outcome so RAC predictions can be validated longitudinally. INTERPRETIVE CAUTION -------------------- This evidence snapshot is not a final diagnosis. It represents the evidence currently available at the time of generation. Later laboratory, imaging, HTMA, microbiome, RAC, nutrition, or supplement evidence may change the interpretation.
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