Catheter Precision Announces Accepted Publication in Leading European Medical Journal
Rhea-AI Summary
Catheter Precision (NYSE American: VTAK) announced that a VIVO study has been accepted for publication in EP Europace on April 13, 2026. The 31‑patient study mapped 48 VTs and found ECGi mapping with VIVO accurately predicted arrhythmogenic substrate for scar‑dependent VT and may improve procedural efficiency.
The study reported VIVO localization in NICM patients showed 100% specificity and 66.7% sensitivity for epicardial VTs versus a four‑step ECG algorithm (sensitivity 50%, specificity 0%). The company plans a larger multi‑center study later in 2026.
AI-generated analysis. Not financial advice.
Positive
- Study accepted in EP Europace, a leading electrophysiology journal
- VIVO mapped 48 ventricular tachycardias across 31 patients
- NICM specificity 100% and sensitivity 66.7% for epicardial VT localization
- Company plans a larger multi‑center study later in 2026
Negative
- Small sample size: only 31 patients, limiting statistical power
- Sensitivity below 70% (66.7%) may miss some epicardial VT localizations
News Market Reaction – VTAK
On the day this news was published, VTAK gained 2.52%, reflecting a moderate positive market reaction. Argus tracked a peak move of +12.0% during that session. Our momentum scanner triggered 3 alerts that day, indicating moderate trading interest and price volatility. This price movement added approximately $84K to the company's valuation, bringing the market cap to $3.42M at that time.
Data tracked by StockTitan Argus on the day of publication.
Key Figures
Market Reality Check
Peers on Argus
VTAK was down 1.65% while peers were mixed: BBLG appeared in momentum scanners moving down 3.97% and TIVC moved up 9.58%. With no clear directional clustering and no peer news, the setup looks stock-specific rather than a sector-wide move.
Historical Context
| Date | Event | Sentiment | Move | Catalyst |
|---|---|---|---|---|
| Mar 25 | Aviation platform update | Positive | -4.2% | Expanded Flyte Hops Vision Jet regional platform and fleet growth plans. |
| Mar 31 | Earnings and strategy | Positive | -3.8% | Reported 2025 results with strong revenue growth and outlined strategic expansion. |
| Apr 02 | Asset sale process | Positive | -1.1% | Hired advisor to market cardiac electrophysiology assets and focus on Flyte. |
| Apr 06 | LockeT clinical data | Positive | +2.1% | Peer‑reviewed LockeT study in 139 patients showing strong safety and efficacy profile. |
| Apr 08 | Conference attendance | Positive | -1.7% | Planned presence at EHRA conference to showcase data and support LockeT adoption. |
Across recent announcements—conference plans, clinical data, strategic shifts, and results—VTAK often traded down following ostensibly positive news, with only one clear positive reaction to favorable LockeT data.
Over the last few weeks, VTAK has reported multiple developments, including Flyte Hops expansion on Mar 25, 2025 results and strategic expansion on Mar 31, engaging a strategic advisor to market its cardiac electrophysiology business on Apr 2, LockeT clinical data acceptance on Apr 6, and EHRA conference attendance plans on Apr 8. Despite generally constructive news, four of these five events were followed by negative price reactions, showing a tendency for softness around updates.
Market Pulse Summary
This announcement highlights peer‑reviewed clinical evidence supporting VIVO’s accuracy in scar‑dependent ventricular tachycardia, including 100% specificity and 66.7% sensitivity versus weaker performance from a traditional ECG algorithm. It adds to recent clinical and strategic updates across VTAK’s portfolio. Investors may watch for the planned larger multi‑center study, ongoing efforts to monetize cardiac assets, and how these data points influence adoption and potential transaction value for the VIVO platform.
Key Terms
ventricular tachycardia medical
electrocardiographic imaging medical
electrophysiology medical
electroanatomical mapping medical
epicardial medical
non-ischemic cardiomyopathy medical
specificity medical
AI-generated analysis. Not financial advice.
Clinical Evidence Further Demonstrates Efficacy and Accuracy of VIVO for Ventricular Procedures
FORT MILL, S.C., April 13, 2026 (GLOBE NEWSWIRE) -- Catheter Precision, Inc. (NYSE American: VTAK) (“VTAK” or the “Company”) today announced that the results of a recently concluded VIVO study have been accepted in EP Europace, the leading European electrophysiology journal.
The EP Europace journal provides an avenue of communication for top-quality European and international original, scientific work and reviews in the fields of arrhythmias, pacing and cellular electrophysiology. The journal offers readers a collection of contemporary, original, peer-reviewed papers, invited papers and editorial comments, together with book reviews and correspondence.
The accepted manuscript titled “Accuracy of a non-invasive electrocardiographic imaging system in scar-dependent ventricular tachycardia: Relationship to arrhythmogenic substrate and imaging defined scar” highlights the feasibility of VIVO for scar-related ventricular tachycardia (VT) was led by Professor Tarv Dhanjal, MBChB(hons) PhD FRCP FESC FEHRA, Professor of Cardiology (University of Warwick). This study included 31 patients and mapped 48 VTs with VIVO and standard of care electroanatomical mapping systems to determine accuracy. The study concluded that ECGi mapping with VIVO can accurately predict the arrhythmogenic substrate for scar-dependent VT and incorporation of ECGi mapping to conventional VT ablation workflows may improve procedural efficiency.
Of additional importance, this study compares VIVO’s predictability of epicardial VTs to a four step ECG based algorithm. In patients with Non-ischemic cardiomyopathy (NICM), the VIVO localization had a
About VIVO™
Catheter Precision’s VIVO (View Into Ventricular Onset), is a non-invasive 3D imaging system that enables physicians to identify the origin of ventricular arrhythmias pre-procedure, thereby streamlining workflow and reducing procedure time. VIVO has received marketing clearance from the U.S. FDA and has the CE Mark.
About Catheter Precision
Catheter Precision is an innovative U.S.-based medical device company bringing new solutions to market to improve the treatment of cardiac arrhythmias. It is focused on developing groundbreaking technology for electrophysiology procedures by collaborating with physicians and continuously advancing its products.
Cautionary Note Regarding Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as “believe,” “expect,” “anticipate,” “potential,” “will,” “may,” and similar expressions are intended to identify forward-looking statements. These statements include, but are not limited to, expectations regarding potential strategic transactions, valuation outcomes, market opportunities, and the Company’s growth strategy. These statements involve risks and uncertainties that could cause actual results to differ materially. For a discussion of these risks, please refer to the Company’s filings with the SEC, including its most recent Forms 10-K and 10-Q. The Company undertakes no obligation to update any forward-looking statements.
CONTACTS:
Investor Relations
973-691-2000
IR@catheterprecision.com
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