Full-Time
EHR-integrated platform for patient-reported analytics
No salary listed
Remote in USA + 1 more
More locations: Chicago, IL, USA
Remote
Bachelor's
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PatientIQ provides a healthcare technology platform that improves patient care through engagement and analytics. It connects with electronic health records (EHRs) to collect patient-reported outcomes (PROs) and analyzes this data to generate actionable insights for clinicians. The product combines data science with engineering to deliver dashboards and analytics that hospitals and clinics can use to monitor and improve patient outcomes. The company differentiates itself by its emphasis on EHR integration, PRO data collection, and applied analytics, supported by subscription access and services such as data analytics and research support. Its goal is to move medicine forward by turning patient data into practical improvements in care and outcomes.
Company Size
51-200
Company Stage
Series B
Total Funding
$20M
Headquarters
Chicago, Illinois
Founded
2016
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EHR Integration isn't a feature - It's the foundation: how PatientIQ embeds into existing workflows. Kara Linde: Jun 18, 2026 12:35:39 PM Outcomes programs fail quietly. Not because the clinical teams didn't want the data. Not because the technology was broken. They fail because they added one more system, one more login, one more thing a coordinator had to remember to do at the end of a busy clinic day. The assumption baked into many outcomes platforms is that clinical staff will adapt to the tool. PatientIQ is built on the opposite premise: the tool adapts to how care already happens. The Workflow Problem No One Wants to Admit Most health systems pursuing patient-reported outcomes end up with a collection process that lives entirely outside the EHR. A patient gets a survey link from a separate system. A staff member manually reconciles the response. Someone exports a report that doesn't quite match how the EMR structures data. The burden compounds. This isn't a failure of effort - it's a failure of architecture. When an outcomes platform is bolted onto a clinical workflow rather than built into it, the friction accumulates at every step. Collection rates suffer. Staff burn out on manual follow-up. And the data that does come in can't be acted on where clinical decisions are actually made: inside the EHR, at the point of care. The result is a familiar pattern: an outcomes program that works well in a pilot, then quietly degrades as the clinical team's attention turns elsewhere. What Native EHR Integration Actually Means PatientIQ integrates natively with 50+ EHR systems, including Epic, Cerner, Oracle Health, and Athenahealth. That word - natively - is doing a lot of work, so it is worth unpacking. Native integration means the connection is bidirectional and event-driven. When a visit is scheduled and a patient chart is updated in the EHR, PatientIQ detects that event automatically. The patient is enrolled in the appropriate care pathway. PRO surveys are assigned based on the procedure or condition. The patient receives a text or email and completes their survey on a phone - no app download, no portal login, no staff intervention required. When the response comes back, it appears directly in the clinician's EHR workflow. The care team does not toggle between systems. They do not need to know what PatientIQ looks like. The outcomes data is just there, where the work happens. This is different from an integration that syncs data overnight or pushes results to a separate dashboard. It is different from a middleware layer that requires an IT project to configure and another one to maintain. The architecture is designed so that outcomes measurement becomes a property of the existing clinical workflow - not a parallel process that competes with it. Why This Changes What Outcomes Data Is Worth The practical consequence of deep EHR integration is not just operational convenience. It changes the quality and completeness of the data itself. PatientIQ achieves an 80%+ blended collection rate across all survey timepoints - not by adding headcount, but by removing the friction that causes non-response through automation and engineering. Patients engage with their care in the same way they are already being communicated with. Staff don't have to chase down missing surveys. Data arrives consistently, across the patient population, without anyone having to manage it. For health systems trying to meet CMS reporting requirements, build a quality improvement program, or contribute to a registry, consistent collection rates are not a nice-to-have. They are what separates usable data from a dataset full of gaps. A collection rate in the 30-50% range - common in manual or standalone-system environments - does not support the kind of analysis that clinical leaders need to act on. Data that comes from 80%+ of your patients across every survey timepoint, captured without adding staff burden, is a different asset entirely. The IT Perspective: What "No Additional Steps" Actually Costs From a health system IT team's vantage point, every new clinical tool carries an integration cost. Deployment timelines, custom builds, ongoing maintenance, and the organizational lift of training staff on a new system all factor in. PatientIQ is designed to minimize this surface area. The platform integrates with existing EHR infrastructure without requiring custom development on the provider side. Implementation is designed to fit within existing IT project structures rather than create new ones. And because the data flows through existing clinical workflows, staff training requirements are minimal - clinical teams continue using the systems they already know. This matters particularly for health systems managing multiple sites, service lines, or EHR instances. PatientIQ supports enterprise deployment at scale while maintaining the flexibility to configure care pathways, survey instruments, and reporting by specialty, location, or provider group. Outcomes Data Where Clinical Decisions Get Made The most important thing about EHR integration is not the technical architecture. It is what becomes possible when outcomes data exists in the same place as the clinical record. When a surgeon can see a patient's PRO trend directly in the EHR before a visit, that data informs the conversation - not a post-visit report that arrives days later. When a quality leader can pull outcomes alongside EHR-documented clinical variables, the analysis has the context to be meaningful. When a registry submission draws from automated, EHR-integrated collection rather than manual extraction, the data is complete enough to matter. This is the gap that integration is actually closing: not between two software systems, but between measurement and the clinical decisions that measurement is supposed to support. PatientIQ's approach to EHR integration is not a feature listed on a spec sheet. It is the structural choice that determines whether an outcomes program produces data or produces insight. See how PatientIQ integrates with your EHR environment.
How PatientIQ helped MASH rethink Long-Term Outcomes in Hip Arthroscopy. For years, one-year outcomes have served as a convenient benchmark in orthopedic research. They are familiar, widely reported, and often treated as a proxy for long-term success. But for patients undergoing hip arthroscopy, particularly young and active individuals, that timeline does not always reflect the full recovery journey. The Multicenter Arthroscopy Study of the Hip (MASH) Research Group set out to better understand what happens after that first year. By partnering with PatientIQ, the group uncovered insights that challenge how success is defined and when it should be measured in hip arthroscopy. Why Long-Term Outcomes Matter in Hip Arthroscopy Hip arthroscopy for femoroacetabular impingement syndrome (FAI) is commonly performed in athletic and pre-arthritic patients with high expectations for function, sport, and quality of life. While many patients show improvement within the first year, recovery does not always follow a linear path. To evaluate outcomes in this population, the MASH Research Group used the International Hip Outcome Tool - 12 (iHOT-12), a validated patient-reported outcome measure designed to assess hip-related quality of life in young, active patients. The instrument captures symptoms, function, sports participation, and social impact, making it well suited for longer-term follow-up. The challenge was not choosing the right outcome measure. It was collecting consistent, high-quality data over time. Traditional PRO collection methods often struggle beyond early postoperative milestones. Manual outreach, inconsistent follow-up, and fragmented systems can result in incomplete datasets, especially at one- and two-year intervals. Without reliable longitudinal PRO data, clinicians risk misinterpreting recovery trajectories or prematurely labeling procedures as unsuccessful. A Multicenter Research Question Needed a Better Approach The MASH Research Group wanted to understand whether patient-reported outcomes (PROs) meaningfully change between one and two years following hip arthroscopy, and which patients are most likely to improve over time. Answering that question required more than periodic surveys. It required infrastructure that could support: * Automated PRO collection at predefined milestones * Sustained patient engagement over multiple years * Centralized data aggregation across institutions * Reduced administrative burden for research teams To support this work, MASH partnered with PatientIQ to modernize how PROs were collected, managed, and analyzed across participating sites Automating Follow-Up Without Losing the Patient Voice PatientIQ enabled the MASH Research Group to automate PRO distribution and reminders at key postoperative intervals, including one- and two-year follow-ups. Patient-friendly engagement workflows helped maintain high compliance, even years after surgery. For research teams, automation reduced the time and effort required to track down responses. For patients, it created a simpler and more consistent way to report how they were feeling over time. Centralized data aggregation allowed outcomes from multiple sites to be analyzed together within a single platform. This made it possible to study large, multi-center cohorts without the complexity of manual data consolidation As one MASH investigator noted: "Using PatientIQ to track and analyze long-term patient-reported outcomes has been a game-changer for our clinical research. The platform's automation and analytics capabilities have enhanced the quality of our data, leading to meaningful insights that directly inform our practice and improve patient care." - Dr. Shane Nho, Midwest Orthopaedics at Rush, MASH Research Group member What Long-Term Data Revealed With consistent longitudinal PRO data in place, the MASH Research Group was able to analyze changes in functional status between one and two years postoperatively. The results challenged conventional assumptions. More than one in five patients demonstrated improvement in functional status between year one and year two, while the majority of patients maintained their outcomes over time. Notably, patients who appeared to have abnormal function at the one-year mark were often the most likely to show meaningful improvement by year two. Without long-term PRO data, these patients might have been incorrectly classified as poor responders or considered for additional intervention too early. These findings suggest that evaluating outcomes at one year may underestimate the true benefit of hip arthroscopy for some patients. Why Timing Matters in Clinical Decision-Making The implications of these findings extend beyond research. When outcomes are assessed too early, clinicians may make decisions based on incomplete information. Long-term PRO data provides a clearer picture of recovery, supporting more informed conversations about expectations, follow-up care, and the need for further intervention. With PatientIQ-powered analytics, MASH researchers were also able to examine how patient-specific factors such as age, BMI, and hip morphology influenced recovery over time. These insights help refine how success is defined and measured, moving beyond a single time-based benchmark. Advancing Research Without Adding Burden One of the most important lessons from the MASH case study is that better research does not require more manual work. It requires better systems. By automating patient engagement and PRO collection, PatientIQ helped the MASH Research Group focus on analysis rather than administration. The result was a more complete dataset capable of supporting nuanced, clinically meaningful insights. Explore the Full Case Study This blog only scratches the surface of the MASH Research Group's findings. The full case study dives deeper into how long-term PROs changed the interpretation of hip arthroscopy success and revealed recovery patterns that one-year data alone can miss. Inside, you'll see how PatientIQ supported multi-center research at scale and enabled more confident, data-driven decisions without adding operational complexity. Download the full case study to see how MASH advanced hip arthroscopy research with PatientIQ. Read it here
Newswise - CHICAGO, IL - PatientIQ, a leading health care technology company specializing in patient outcomes data, has expanded its support for national clinical registries with the launch of electronic health record (EHR)-integrated data submission for the American Spine Registry (ASR) - a collaborative effort between the American Association of Neurological Surgeons (AANS) and the American Association of Orthopaedic Surgeons (AAOS).
Innovation was front and center for PatientIQ at the AAOS 2025 Annual Meeting.
"DataPRO leverages the unmatched depth and breadth of the PatientIQ dataset to bring performance benchmarking to the forefront of healthcare, and redefines how the industry utilizes real-world patient outcomes to drive better decisions and better care." - Matt Gitelis, CEO and Founder of PatientIQ