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6.16.2025

Coming Soon: System-Wide Expansion of Electronic Consents

As part of UVA Health’s ongoing efforts to streamline workflows and enhance patient care, we’re expanding the use of electronic consents (e-consents) across our system. 

Currently, around 40% of perioperative cases use e-consents. Broader adoption has been limited since not all consent forms have been available electronically — until July 1. A new, system-wide initiative will complete our transition to e-consents and eliminate paper forms across key areas. 

Continue reading to learn what’s changing and when — and how you can prepare. 

What Is an E-Consent? 

An e-consent is a digital version of a patient consent form, completed directly within Epic. Instead of filling out paper forms, providers use dropdown menus and required fields to capture all essential information. Details like the procedure name, treatment team, and date are automatically populated—reducing errors and saving time. 

Required fields help ensure every e-consent meets UVA Health’s documentation standards for accuracy, completeness, and compliance. 

What’s Changing? 

What’s Not Changing? 

Signature Collection:

There are several options available to collect patient signatures on e-consents: 

Team members should use the signature collection options available in their department, as access may vary. 

E-Consents Timeline:  

The transition has already begun with an early adopter phase that launched in April. Roll out will continue with two more phases in the coming months: 

Phase 1 – April 8, 2025: Complete   

Phase 2 –  

June 17, 2025 

July 1, 2025 

Phase 3 – Fall 2025 

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How to Prepare for E-Consents: 

This transition to e-consents marks a significant step forward in improving the accuracy, efficiency, and consistency of our consent process — ultimately enhancing the patient experience. Thank you for supporting our journey toward safer, more efficient patient care.  

For answers to frequently asked questions, continue reading below.  

E-Consents Frequently Asked Questions: 

How long is the Procedural Consent with Blood Panel 1 good? 

The consent is good for the duration of the patient’s inpatient stay or 6 months, whichever is shorter, per Informed Decision-making Medical Center Policy v.2 (see Attachment A, item #3). 

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Can we do serial consents?  

Serial consents may be completed using the new Procedural Consent with Blood Panel 1 e-consent form. See screenshot at right.  

Will e-consents affect capacity forms for situations where in-patients lose ability/gain ability to provide informed consents? 

The e-consent project will not impact the capacity form process, which will continue to be on paper. However, if a patient lacks capacity and Procedural Consent with Blood Panel 1 is needed, the legal guardian will sign the e-consent. 

What are the specific changes to the Panels 1-5 and Surgical Procedure e-consents? 

What e-consent forms may be used for non-case-based procedures, or procedures with no case request?  

All non-case-based e-consent forms are found under Miscellaneous Consents. This includes the Surgical Procedure Consent (previously listed under Procedural Consents), which should be used for cases without a case request (e.g., in-clinic procedures, bedside procedures, etc.).  

What training is available to help me prepare the new e-consents? 

There is a seven-minute Workday learning module and an Epic Learning Library tip sheet that cover the new blood consents. 

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