Rapid

by RapidAI (formerly iSchemaView)  · Based in United States →Clinical AI Platform Enhancing Assessment & Transforming Care
Emergency Medicine Neurology Radiology

Contact for pricing
Regulatory Status Disclosed

Overview

RapidAI, formerly iSchemaView, offers an AI-enabled software platform designed to assist clinicians in assessing medical images. The platform is utilized across various specialties, including neurovascular, cardiac and vascular, and radiology, and is applicable in acute care settings, such as stroke centers, as well as for longer-term patient management.

  • What it does: RapidAI’s platform processes and analyzes CT and MR images to provide insights that support clinical decision-making. It goes beyond basic detection to offer quantitative and contextualized information for various conditions.
  • Who it is for: The tool is intended for physicians, radiologists, and care teams involved in diagnosing and managing conditions across neurovascular (e.g., ischemic stroke, ICH, aneurysms), cardiac and vascular (e.g., aortic assessment, pulmonary embolism), and general radiology. It aims to support workflows in hospitals and healthcare systems.
  • How it fits a clinical or practice workflow: RapidAI integrates with existing hospital systems, including PACS, EHR, and worklist providers, to streamline radiology workflows and facilitate communication among care teams. It can automatically send images for processing and deliver results to PACS, email, and mobile apps. The platform is designed to provide real-time collaboration and alerts for urgent cases.
  • Notable capabilities: Key features include deep clinical AI for detailed insights, workflow integration for seamless execution, enterprise infrastructure for scalability and security, and data analytics for performance visibility. Specific modules address neurocritical assessment, ischemic stroke, aneurysm detection and tracking, aortic assessment, and pulmonary embolism detection. The platform also offers Navigator Pro for radiology case prioritization and AI interpretation assistance.

Reviewed by Pouyan Golshani, MD — Interventional Radiologist

Key Features

  • AI-enabled medical imaging analysis platform
  • Automated processing of CT and MRI images
  • Detection of large vessel occlusion (LVO) and intracranial hemorrhage (ICH)
  • CT perfusion (CTP) and MR perfusion maps
  • CT angiography (CTA) maps and 3D reconstruction
  • ASPECTS scoring from CT scans
  • Mobile app for real-time notifications and image viewing
  • Integration with PACS, email, text, and third-party systems
  • Customizable notifications for hospitals and physicians
  • Aneurysm and aortic analysis capabilities

Use Cases

  • Acute stroke assessment and diagnosis
  • Patient triage and clinical decision making in cerebrovascular emergencies
  • Selection of patients for mechanical thrombectomy
  • Monitoring of cerebral aneurysms
  • Detection and monitoring of aortic aneurysms and dissections
  • Facilitating communication and collaboration among stroke care teams

What Physicians Need to Know

Evidence Base
Clinical Decision Support (CDS) tools, including those leveraging AI, are built upon a robust evidence base comprising established clinical guidelines, extensive medical literature, and patient-specific data. They integrate both traditional evidence-based protocols and, in some cases, predictive AI models to generate recommendations.
Clinical Validation Studies
Validation studies for CDS systems, particularly for medication review, commonly use real-life patient data to assess the quality and accuracy of the system's output. These studies report on the frequency of generated alerts and aim to ensure the tool's recommendations are clinically useful and of high quality.
Alert Fatigue Management
Managing alert fatigue is critical, as excessive or irrelevant alerts can lead to clinicians ignoring important warnings. Effective strategies include designing alerts to align with decision-making moments, reducing interruptions, implementing alert tiering to prioritize critical information, and establishing strong governance for alert quality and lifecycle. Replacing interruptive alerts with passive decision support can significantly reduce alert burden.
Override Rate Data
High override rates, sometimes exceeding 85% for drug interaction alerts, are a direct indicator of alert fatigue. Monitoring EHR audit logs for alert types, triggers, and provider responses helps evaluate the relationship between alert burden and override rates, with efforts focused on reducing burden to improve the impact of remaining alerts.
Drug Interaction Checking
A core feature of many CDS tools is comprehensive drug interaction checking, which identifies and prevents significant interactions between prescription drugs, over-the-counter medications, alternative therapies, and even nutrients. These modules often utilize extensive commercial databases and offer configurability to fine-tune alerts based on severity and specific categories.
Differential Diagnosis Support
CDS tools provide support for differential diagnosis by analyzing patient data, including symptoms, lab results, and medical history, to generate potential diagnoses. They help clinicians interpret complex medical data and identify patterns or anomalies to enhance diagnostic accuracy and efficiency.
Guideline Update Frequency
CDS systems are designed to continuously integrate the latest research and evidence-based guidelines into clinical workflows. Advanced approaches, such as NLP-enabled systems, aim to support rapid updates to clinical guidelines by integrating diverse sources of primary and synthesized evidence.
Clinical Workflow Integration
Seamless integration with existing Electronic Health Record (EHR) systems and clinical workflows is paramount for the adoption and effectiveness of CDS tools. This involves organizing, filtering, and presenting relevant information at the appropriate point in time within the clinician's workflow, without causing disruption.
Decision Audit Trail
EHR systems are mandated to implement audit logs that track user activities, including how clinicians interact with and respond to CDS alerts. These audit trails provide a secure, time-stamped electronic record, allowing for the reconstruction of events and monitoring the real-world impact and usage of CDS interventions.
Physician Tip

To maximize the benefits of 'Rapid' (or any similar CDS tool), actively engage with its evidence-based recommendations while always applying your clinical judgment. Provide feedback on alert relevance and timing to help refine the system and reduce alert fatigue. Utilize the differential diagnosis support to broaden your diagnostic considerations and ensure comprehensive patient evaluation. Understand how the tool integrates into your EHR to leverage its full potential within your daily workflow. For specialized areas, be aware that tools like 'RapidAI' exist for specific fields such as vascular medicine, offering deep contextual data and AI-powered insights for faster, life-changing decisions in those domains.

Effective CDS tools are engineered for seamless integration with major Electronic Health Record (EHR) systems (e.g., Epic, Cerner, MEDITECH) to deliver real-time, patient-specific recommendations directly at the point of care. This integration typically involves leveraging existing patient data from the EHR for context-aware insights and feeding back clinician actions and feedback to continuously improve protocols. Advanced systems may consolidate suggestions and alerts from multiple AI and evidence-based CDS tools into a unified dashboard. Crucially, interoperability and high data quality are essential for reliable outcomes and effective communication across care teams.

Details

Category Neurology AI, Radiology & Imaging AI
Pricing Contact for pricing Standard Package: $65,520/year; Perfusion for Existing Site: $14,000; Activation Fee: $7,500
DeploymentOn-premise server or cloud-based virtual system
Compliance
BAA AvailableUnknown AI-estimated
HIPAA Compliant Yes AI-estimated
FDA Status 1 AI-estimated

RapidAI has received multiple FDA clearances for its various modules, including Rapid CTA, Rapid ICH, Rapid LVO, Rapid ASPECTS, and Rapid SDH, which assist in the assessment of cerebrovascular diseases like stroke by analyzing CT and MRI images. The company's K232156 for Rapid ASPECTS (v3) was cleared on January 19, 2024.

Integrations
EHR Not specified
Specialties Emergency Medicine, Neurology, Radiology

What the Web Says

RapidAI is an AI-powered platform primarily designed for stroke and vascular imaging, aiding physicians in the rapid diagnosis and treatment of conditions like stroke, subdural hematomas, and aneurysms. It analyzes brain scans (CT and MRI) and provides results within minutes, integrating with hospital systems via PACS and mobile apps. While it has the potential to improve acute stroke care by creating efficiencies in the diagnostic process, its impact on many important clinical outcomes, such as patient harms, mortality, and quality of life, remains uncertain due to limitations in available evidence.

Overall: Mixed

Strengths

  • Expedites treatment decisions by providing rapid analysis of brain scans (CT and MRI).
  • Accurate in detecting intracranial hemorrhages (ICH) and large vessel occlusions (LVO) when combined with clinician interpretation.
  • Helps focus radiologists' interpretation to specific regions of anatomy.
  • Facilitates transfer of patients requiring more intervention.
  • Integrates with existing radiology workflows and systems like PACS.
  • Offers mobile alerts for time-sensitive findings and in-app messaging for team coordination.

Limitations

  • Impact on patient harms, mortality, quality of life, and length of hospital stay is uncertain due to limited evidence.
  • Cost-effectiveness for stroke detection is currently unknown.
  • Can be susceptible to motion artifacts and performs poorly with LVO detection in cases of poor contrast boluses.
  • May produce false positives, for example, in ICH detection at the falx or dural calcifications.
  • Requires radiologist confirmation on every study, as it is not intended for autonomous interpretation.
  • Some employee reviews mention a toxic sales culture and horrible executive team.

Based on reviews from: Elion, Indeed.com, Reddit, RapidAI Publications, NCBI Bookshelf, Canada's Drug Agency, SoftFinders, Slashdot

Last updated: 2026-07-21

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Press & Coverage

RapidAI Press Releases
RapidAI Highlights Research Depth and Industry Leadership at ISC 2026 With 28 Clinical Abstracts
RapidAI announced 28 scientific abstracts accepted at the International Stroke Conference (ISC) 2026, showcasing new clinical research on AI-driven gains in aneurysm detection, stroke interpretation, and enterprise imaging efficiency. The findings reflect the impact of their deep clinical AI delivered through the Rapid Enterpriseu2122 platform.
2026-02
RapidAI Press Releases
RapidAI and AWS Strengthen Relationship: Accelerate Global Deployment of Deep Clinical AI
RapidAI and Amazon Web Services (AWS) announced a strengthened working relationship to accelerate the global adoption and scalability of deep clinical AI in healthcare, focusing on co-development and go-to-market alignment. This collaboration aims to bring together AWS's AI infrastructure with RapidAI's clinical expertise and multimodal healthcare data.
2025-12
RapidAI Press Releases
RapidAI Extends the Reach of Deep Clinical AI with Five New FDA Clearances
RapidAI announced U.S. Food and Drug Administration (FDA) clearance for five new imaging modules: Rapid DeltaFuseu2122, Rapid LMVO, Rapid MLS, Rapid OH, and Rapid Aortic for measurement. These clearances significantly expand the Rapid Enterpriseu2122 Platform, reinforcing RapidAI's commitment to deep clinical intelligence and seamless workflow integration.
2025-11
NeuroNews
RapidAI gains US FDA clearances for five new imaging modules
RapidAI received US FDA clearance for five new imaging modules, including Rapid DeltaFuse, Rapid LMVO, Rapid MLS, Rapid OH, and Rapid Aortic for measurement. These additions expand the Rapid Enterprise platform, aiming to reduce cognitive burden for radiologists and improve clinical decision-making.
2025-11
Vascular News
RapidAI earns US FDA clearance for AI-driven aortic measurement and surveillance product
RapidAI announced US FDA clearance for Aortic Management, part of Rapid Aortic, a comprehensive deep clinical AI solution for acute assessment and longitudinal management of aortic disease. This product provides AI-powered insights to identify and track aortic aneurysms, dissections, and other anomalies.
2025-11
AuntMinnie
RapidAI gets 5 new FDA clearances
RapidAI has received U.S. Food and Drug Administration (FDA) clearance for five imaging modules: Rapid DeltaFuse, Rapid LMVO, Rapid MLS, Rapid OH, and Rapid Aortic for measurement. These clearances significantly expand the company's Rapid Enterprise platform for neurology and vascular care.
2025-11
Canadian Journal of Health Technologies (Published by Canada's Drug Agency)
RapidAI for Stroke Detection and AI Implementation Review
This implementation review for AI-enabled medical devices, specifically focusing on RapidAI for stroke detection, serves as a foundational report to be tailored for each AI topic and updated with the latest developments in regulation and management of AI in Canada.
2024-11
Stroke: Vascular and Interventional Neurology - American Heart Association Journals
RapidAI Compared With Human Readers of Acute Stroke Imaging for Detection of Intracranial Vessel Occlusion
This article discusses a study comparing RapidAI with human readers for detecting intracranial vessel occlusion in acute stroke imaging, highlighting the use of LR graphs to assess the superiority of RapidAI in ruling in and out the presence of intracranial occlusion.
2024-01

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Suggest an Edit → | Last Verified: 2026-04-20 | First Added: 2026-04-20
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