KONZA is working to improve to healthcare through both interoperability and transformative data analytics. This nationwide exchange allows connected physicians and hospitals to share patient information while employing powerful analytic reports designed to help improve clinical outcomes, reduce inefficiencies, and positively impact patient safety.
What is Health Information Exchange (HIE)?
HIE is the electronic exchange of clinical information among healthcare organizations. This exchange of patient clinical data allows physicians, nurses, and other healthcare providers to securely and efficiently access patients’ health records.
Why is health information exchange important?
HIE allows healthcare providers to quickly access their patients’ data across disparate health care systems, reducing treatment delays and enhancing clinical decision making. Additionally, HIE improves patient care coordination and transitions of care by allowing healthcare professionals to access their patients’ most recent test results, procedures, diagnosis, medications, allergies, and more.
What patient data comes into an HIE?
Patient data received by the HIE may include: a list of facilities where the patient was seen, admit and discharge dates, lab results, procedures and diagnoses, current and past medications, allergies, chief complaint, visit notes, operation notes, and the patients’ primary care providers.
Will KONZA connect with other HIEs?
KONZA connects with other HIEs across the nation. KONZA also connects with public health agencies, federal agencies such as the Veteran’s Administration, national lab companies, and prescription monitoring programs.
How will KONZA help the nation connect for better care?
Physicians and other clinicians can securely share critical patient information at the point of care, supporting improved care quality and better patient health outcomes. Patients can easily view their medical information from participating providers on one secure patient portal. Physicians and other clinicians can more easily meet quality reporting obligations under the emerging performance and value-based payment systems adopted by federal and commercial health plans.
How do we know KONZA will work?
The proven HIE technology is already successfully operating in Kansas, Connecticut, Georgia, Missouri, New Jersey, and South Carolina. This is a “turnkey” HIE.
Who is in charge of KONZA ?
KONZA began its initial startup in the spring of 2018 with a physician advisory committee. The advisory committee developed foundational policies and procedures to support the HIE infrastructure. The diverse advisory committee includes health care providers, health care facilities, government, consumers, payers, and other stakeholders. KONZA controls access to and use of all exchange data, all subject to federal law, including HIPAA.
Who will participate in KONZA ?
Patients receive care from many types of clinicians, so KONZA encourages physicians, nurses, psychologists, and other health professionals to participate. Patients receive care in many locations, so KONZA encourages physician offices, hospitals, skilled nursing facilities, behavioral health facilities, federally-qualified health centers (FQHC), and other sites to participate in the exchange.
Will patients have to participate in KONZA? Will they have to pay?
Patients can choose to opt out of including their personal health information in KONZA. There is no charge for patients to participate in KONZA.
How can I exchange health information?
To receive more information regarding the exchange of health information, please contact KONZA at 800.435.2104.
The KONZA data warehouse stores and aggregates clinical data from all KONZA member's EHR systems as well as any other connected HINs. This data is normalized and populated into a standard data architecture which is then delivered in the form of custom developed, web-based dashboard reports. Participants can also request specially created ad-hoc reports based upon desired criteria as long as the data appears in the data warehouse. Access to this information in such a manner will be necessary for successful clinical integration, care coordination, quality reporting and transition to performance-based payment models.
A Qualified Clinical Data Registry (QCDR) is a CMS-approved entity that collects clinical data on behalf of clinicians for data submission. By achieving registry status, the Doctors Quality Reporting Network (DQRN) marries the collection of patient data and the submission of data in one entity for physicians. The DQRN currently submits ONC and Drummond certified electronic clinical quality measures (eCQMs), Promoting Interoperability and Improvement Activities (IA) to CMS. These measures are standardized and intended to provide reliable indicators of high quality patient care. The metrics cover management of chronic diseases, preventive care screening, use of appropriate medications, use of electronic medical records, patient engagement and overall cost of care reductions.
Quality Measure Calculator
To utilize the DQRN, physicians and clinicians must be participating members in the Kansas Health Information Network.