Cardiothoracic Surgery Research Laboratory

Cardiac surgery

The Cardiothoracic Surgery Research Laboratory is focused on developing surgical treatments for cardiothoracic conditions, including atrial fibrillation, and translating them into clinical practice.

Established over 40 years ago, our lab conducts innovative research backed by multiple sources of funding, including an R01 grant from the NIH. The lab has two main areas of research focus:

  • Surgical treatment of cardiac arrhythmias and rhythm management
  • Ablation technology

The Cardiothoracic Surgery Research Laboratory is led by Christian Zemlin, PhD, MSc, whose work focuses on the mechanisms and treatment of arrhythmias. His research has been funded by the American Heart Association, the NIH, intramural funding and industry.

Zemlin earned his master’s degree in physics from the Technical University of Berlin and his doctorate in theoretical physics from Humboldt University in Berlin in 2002. He completed his postdoctoral research in cardiac electrophysiology at SUNY Upstate Medical University in Syracuse.

His research uses voltage-sensitive fluorescent probes to experimentally study cardiac activity, and computer modeling to understand how arrhythmias are initiated and maintained. Zemlin developed a new ablation modality for cardiac tissue based on ultrashort electric pulses that cause irreversible electroporation.

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Principal investigator

Christian W. Zemlin, PhD, MSc

Christian W. Zemlin, PhD, MSc

Associate Professor of Surgery and Biomedical Engineering
Director, Cardiac Surgical Research Laboratory
Section of Cardiac Surgery
Division of Cardiothoracic Surgery

Contact

Christian Zemlin, PhD, MSc
Clinical Sciences Research Building
Email: zemlinc@wustl.edu
Phone: 314-362-8300

Opportunities

Apply for a training position in our lab

Areas of research focus

Surgical treatment of cardiac arrhythmias and rhythm management

For the past four decades, our laboratory has conducted studies to develop surgical treatments for cardiac arrhythmias and translated them into clinical practice.

Our earliest efforts were directed at arrhythmias associated with ischemic heart disease, Wolff-Parkinson-White syndrome, and atrioventricular node reentry, and resulted in clinical interventions routinely used today.

For each arrhythmia, we initially defined the fundamental substrates and mechanisms in animal experiments.

The surgical approach was worked out first in the laboratory and then perfected in clinical studies to account for the differences between animal and human arrhythmia mechanisms.

The validity of this innovative approach has been borne out by the long-term success and adoption of these interventional approaches both by surgeons and electrophysiologists.

Schematic drawing of the Cox-Maze procedure: atria, nonconductive lesions (heavy lines), and propagating electrical impulses (arrows). By placing the lesions in the pattern of a maze, they can be placed close enough to prevent the development of macro-reentry anywhere in either atrium and still allow the sinus impulse to activate all of the atrial myocardium except the encircled pulmonary veins and excised atrial appendages.

Our work has led to the development of the most successful single treatment for atrial fibrillation (AF), the Cox-Maze procedure. In the Cox-Maze procedure, lines of scar are created on the atria to disrupt potential reentrant pathways.

Our laboratory also spearheaded the effort to simplify the Cox-Maze procedure by replacing the surgical incisions with lesions created using thermal ablation technology, which made the procedure easier to perform with less morbidity while preserving its high efficiency.

The Cox-Maze procedure has become the gold standard for the treatment of AF, and it is the only surgical procedure to have received FDA approval.”

In a propensity-matched study of patients with AF undergoing heart surgery, a concomitant Cox-Maze procedure resulted in a 10-year survival rate of 62%, compared to 42% for patients who did not receive a Cox-Maze procedure.

Ablation technology

In the original Cox-Maze procedure, lesions were created by cutting and sewing tissue. To simplify the procedure, cryoablation and radiofrequency ablation were introduced. Both methods are thermal: Cryoablation cools the tissue to kill it while radiofrequency ablation heats the tissue until it dies.

Our laboratory has tested every major cryoablation and radiofrequency ablation device that has been used clinically, as well as alternative technologies such as focused ultrasound and microwave ablation that were never widely adopted clinically.

Currently, a new ablation approach called pulsed field ablation (PFA) is in clinical testing. PFA uses strong electric fields to electroporate the membranes of cells. The figure on the right illustrates PFA ablation of an atrial appendage. The ablation clamp closely resembles those used in radiofrequency ablation.

Pulsed field ablation (PFA) clamp used to ablate tissue via electroporation.

Current research

Chronic severe mitral regurgitation and atrial fibrillation

Mitral regurgitation (MR) is the most common valvular disease in humans. Many MR patients later develop atrial fibrillation. To understand the underlying mechanisms, we developed an animal model of MR, based on avulsing some of the chordae that hold the mitral valve in place.

After chordae have been avulsed, MR can be demonstrated in a transthoracic echocardiogram (see Panel A), and the valve shows coaptation defect (Panel B). After MR creation, left atrial volume increased dramatically, by about 200% over 9.5 months.

We are now using this model of MR to understand the molecular mechanisms of atrial and ventricular remodeling with the goal of developing interventions to prevent atrial fibrillation and other secondary diseases.

We are also studying the effects of mitral regurgitation in patients referred for surgery with without atrial fibrillation. We are using novel, noninvasive imaging technology, in attempt to define the underlying substrate in atrial fibrillation. We hope to use this information in the future to guide surgical ablation.

Animal model of atrial fibrillation. A: Transthoracic echocardiogram (apical 4-chamber view) of mitral valve shows an eccentric regurgitant jet. B: 3D reconstruction of the mitral valve illustrates coaptation defect. C: Left atrial volume increases over 9 months after the creation of MR. (n=6).

Bipolar radiofrequency ablation

An important treatment option for patients with atrial fibrillation is the ablation of cardiac tissue to create nonconducting lesions that disrupt the pathways of reentrant arrhythmias. In current clinical practice, cardiac ablation is performed thermally, either by heating tissue with radiofrequency currents or by freezing it with a cryogen. We are regularly testing new thermal ablation devices for their ability to create transmural lesions.

View image
A single ablation with AtriCure’s Encompass clamp created a “Figure of 8” box lesion, (green arrow), on the endocardial surface of the left atrial posterior wall. There was no evidence of clot, charring, or pulmonary vein damage. RA = right atrium, LA = left atrium, PVs = Pulmonary veins.

Nanosecond pulsed field ablation of cardiac tissue

Nanosecond pulsed field ablation (PFA) is an alternative to the thermal ablation methods described above. PFA is nonthermal and relies on strong electric fields to disrupt cell membranes in order to ablate tissue. PFA can significantly reduce ablation times while providing excellent ablation depth. It also avoids thermal effects such as char buildup on the ablation clamp that can lead to incomplete lesions for radiofrequency ablation.

View image
Nanosecond pulsed field ablation (nsPFA) of cardiac tissue. A: Section of atrial wall tissue showing a lesion (white) created with nsPFA. B: The lesion from (A) as a Gomori trichrome stain. C: Abrupt transition from surviving tissue (left) to ablated tissue (right). D: High-resolution GMT stain of nsPFA-ablated tissue.

Optogenetics and sonogenetics in the heart

The beating of the cardiomyocytes that make up the heart is synchronized by electrical signals that are generated by the sinus node and propagate over the heart. If the heart is genetically modified to include light-sensitive ion channels, activation can be achieved with a light (optogenetics). Similarly, adding ultrasound-sensitive ion channels allows stimulation with ultrasound (sonogenetics).

In collaboration with Drs. Chao Zhou, Jianmin Cui, and Hong Chen from the Department of Biomedical Engineering, we are developing murine models of optogenetics and sonogenetics in the heart, enhancing the options for non-invasive stimulation of the heart.

View image
Experimental setup for ultrasound stimulation of Langendorff-perfused hearts. A: Photograph of a naïve heart in our ultrasound testing setup. B: Activation map that shows propagating cardiac activity following successful activation. Activation was initiated with an electrical stimulus, delivered via an electrode at the position marked “X” (ultrasound did not initiate electrical activity in naïve hearts).

Our team

Ralph J. Damiano Jr., MD

Ralph J. Damiano Jr., MD

Evarts A. Graham Professor of Surgery
Section of Cardiac Surgery
Division of Cardiothoracic Surgery

Matthew R. Schill, MD

Matthew R. Schill, MD

Assistant Professor of Surgery
Section of Cardiac Surgery
Division of Cardiothoracic Surgery

Christian W. Zemlin, PhD, MSc

Christian W. Zemlin, PhD, MSc

Associate Professor of Surgery and Biomedical Engineering
Director, Cardiac Surgical Research Laboratory
Section of Cardiac Surgery
Division of Cardiothoracic Surgery

Fellows

  • Jack Yi, MD
  • Ruth Obiarinze, MD

Staff

  • Lab supervisor: Samantha Procasky, MS
  • Veterinary technician III: Kristen Barth

Emeritus investigator

News and updates

In the news
Lab updates 2025

Abstract accepted for STS annual meeting 2025

Dr. Jack Yi’s abstract “Impact of Tricuspid Regurgitation on Outcomes after Cox-Maze IV Procedure” was accepted for a poster presentation at the STS Annual Meeting from January 24-26th in Los Angeles, California.

Lab updates 2024

Annual pool party and Dr. Yu send off

Dr. Jakraphan Yu completed his one-year research fellowship with our lab in June 2024. We sent him off with our annual pool party and he received a framed certificate from Drs. Damiano and Zemlin. We wish him the best for his work at Vajira Hospital in Bangkok, Thailand.

Drs. Schill and Zemlin receive pilot grant from the Department of Surgery

Drs. Schill and Zemlin received a pilot research award from the Department of Surgery. They are principal investigators on the proposal “Endovascular Catheter-Based Application of Electroporation”, which was submitted jointly with Dr. Zayed from Vascular Surgery and Genin from Mechanical Engineering. The award is $50k over one year, with the goal of developing the project to the point at which it can secure federal funding.

Yu receives 2024 Kouchoukos Award

Dr. Jakraphan Yu (center) from our lab receives the Kouchoukos award from Drs. Kouchoukos (left) and Kreisel (right)

Lab alumni

  • Meghan Kelly, MD
  • Ali Khiabani, MD
  • Joshua Manghelli, MD
  • Martha McGilvray, MD
  • Robert McGregor, MD
  • Tariana Yates, MD
  • Jakrakphan Yu, MD