Use case 1 · Cardiology — predictive deterioration
ML predicts cardiac deterioration 48 hours earlier from RPM streams plus vitals. 22% readmission reduction in cardiac cohorts. Tiered escalation to clinical team.
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AI features built for specialty workflows — cardiology, oncology, behavioral health, orthopedics, dermatology, ophthalmology, gastroenterology. Specialty EHR integration. Disease-specific AI. Fixed-price productized tiers.
$45K Discovery · $95K Production-Ready · $145K Pilot-Ready
Specialty Clinics AI is the engineering of AI features purpose-built for specialty practice workflows — cardiology, oncology, behavioral health, orthopedics, dermatology, ophthalmology, gastroenterology, endocrinology, and other clinical specialties. Modern 2026 specialty AI deployments require disease-specific data models, specialty EHR integration (athenaPractice, eClinicalWorks, OncoEMR, NextGen, ModMed, Epic Beaker), specialty-appropriate AI features (cardiac RPM, oncology decision support, behavioral health screening, lesion classification), and BAA-eligible inference paths. Productized fixed-price tiers: $45K (4-week Discovery), $95K (8-week Production-Ready), $145K (12-week Pilot-Ready).
Cardiac RPM with predictive event detection, AI ECG interpretation assist, post-MI care pathway automation, heart failure exacerbation prediction, AFib detection from wearable data.
Treatment guideline matching (NCCN, ASCO), trial eligibility identification per patient, tumor-board prep automation, oral oncolytic adherence AI, symptom management AI during chemotherapy.
PHQ-9/GAD-7 augmented with conversational AI screening, risk stratification and care routing, AI session note drafting (clinician-reviewed), medication adherence AI for psychiatric medications.
Pre-surgical risk stratification, post-op rehab adherence tracking, AI-paced rehab protocols, outcomes write-back to surgeon, AI imaging triage for fracture and joint imaging.
Lesion triage and dermoscopy-image classification, tele-dermatology workflows, in-clinic AI imaging triage, AI patient intake for tele-derm. Requires FDA SaMD pathway for diagnostic features.
Diabetic retinopathy and glaucoma screening from retinal images, AI-augmented OCT interpretation, primary-care-deployable screening workflows. Requires FDA SaMD pathway.
AI colonoscopy quality metrics, polyp detection assist, IBD flare prediction, GI symptom triage chatbot, hepatology decision support.
CGM-stream plus insulin AI assist, diabetic management AI, thyroid management AI, obesity medication management workflows.
Disease-specific patient education, symptom tracking, AI symptom triage tuned to specialty, post-visit AI check-ins, multilingual chat.
ML predicts cardiac deterioration 48 hours earlier from RPM streams plus vitals. 22% readmission reduction in cardiac cohorts. Tiered escalation to clinical team.
AI drafts tumor-board briefing materials from patient chart, recent imaging, recent labs, and current NCCN/ASCO guidelines. Cuts prep time 60–70%.
PHQ-9/GAD-7 augmented with conversational AI screening. Risk stratification and care routing. Reduces wait time to appropriate level of care.
AI lesion classification at patient intake. Triages urgency, routes to appropriate clinician, captures dermoscopy images and patient history. FDA SaMD pathway required for diagnostic features.
Diabetic retinopathy and glaucoma screening deployable in primary-care settings, expanding the addressable patient population. FDA SaMD pathway required.
Free 30-min architecture call. We’ll scope your AI use case, specialty EHR integration path, and the right tier for your practice size.
Epic (including Epic Beaker for lab and Epic Radiant for radiology), Cerner-Oracle (including PowerChart specialty modules), Athena (athenaPractice, athenaClinicals), Allscripts, eClinicalWorks, NextGen, ModMed (ophthalmology, dermatology, gastroenterology, orthopedics, OB-GYN), OncoEMR (oncology), Greenway Intergy, AdvancedMD, Practice Fusion, and Meditech. Integration via FHIR R4, HL7 v2 via Mirth Connect, or SMART on FHIR launch where supported.
Some features do, most don’t. AI features that diagnose, screen, or directly influence treatment decisions for an individual patient typically require FDA SaMD pathway — lesion classification, diabetic retinopathy screening, polyp detection, autonomous diagnosis. Ambient documentation, patient engagement, decision support with reviewer-in-the-loop, and operations AI usually don’t. We scope FDA pathway on every engagement.
Yes. We integrate with PACS systems (GE Centricity, Philips IntelliSpace, Sectra, Carestream, Merge) via DICOM, and with RIS systems via HL7 ORM/ORU messages. Specialty imaging AI typically integrates at the PACS/RIS layer rather than the EHR layer.
The Discovery Sprint is sized for small practices ($45K, 4 weeks). Single-clinician specialty practices can deploy patient engagement AI, AI scheduling, and ambient documentation profitably. Larger AI features (oncology decision support, cardiac RPM AI) require larger patient volume to produce documented ROI — typically 5+ clinicians or 1,000+ active patients.
Yes. Pre-signed BAA templates with OpenAI, Anthropic, AWS Bedrock, and Google. Zero-data-retention configuration verified in writing. Audit logging on every model output. Override-and-audit UX on every clinical AI feature. Zero HIPAA findings on shipped software across 785+ healthcare implementations.
State-specific regulations for behavioral health (42 CFR Part 2 for substance use disorder, state-level telehealth restrictions, prescribing rules for controlled substances) are handled in every behavioral health engagement. We scope state-specific compliance per engagement.
4-week Discovery, 8-week Production-Ready, 12-week Pilot-Ready. Full production with specialty EHR integration adds 16–32 weeks. FDA SaMD pathway (for diagnostic AI features) adds 6–18 months depending on device class and clinical evidence requirements.
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