Mark S. Slaughter
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Mark S. Slaughter has a total of 408 co-authors. Here are the top co-authors by number of shared publications:
Jaimin R. Trivedi
23 shared publicationsMichael A. Sobieski
13 shared publicationsErin M. Schumer
Department of Cardiovascular and Thoracic Surgery, University of Louisville, Louisville, KY, USA
12 shared publicationsSteven C. Koenig
University of Louisville
12 shared publicationsAllen Cheng
Department of Cardiovascular and Thoracic Surgery, University of Louisville, Louisville, Kentucky
11 shared publications- Michele Gallo
Department of Cardiovascular and Thoracic Surgery, University of Louisville, Louisville, Kentucky
10 shared publications
Latest Publications
- 28 October 2026
- Published by Wolters Kluwer Health in ASAIO Journal
- Vol. 72 (11) , 881
From the Editor’s Desk: The Future Has Arrived!
Was not provided for this article.
- 28 October 2026
- Published by Wolters Kluwer Health in ASAIO Journal
- Vol. 72 (11) , 881
From the Editor’s Desk: The Future Has Arrived!
Was not provided for this article.
- 10 September 2026
- Published by Wolters Kluwer Health in ASAIO Journal
- Vol. 72 (11) , e385
Letter to the Editor: Side Port Resistance Limits Distal Perfusion Flow (Matsumoto et al.)
Was not provided for this article.
- 10 September 2026
- Published by Wolters Kluwer Health in ASAIO Journal
- Vol. 72 (11) , e385
Letter to the Editor: Side Port Resistance Limits Distal Perfusion Flow (Matsumoto et al.)
Was not provided for this article.
- Open Access
- 22 August 2026
- Published by Elsevier in JTCVS Open
- Vol. 33
Pilot safety and efficacy trial of amiodarone-infused biologic acellular biatrial patches to prevent new-onset postoperative atrial fibrillation
- 22 August 2026
- Published by Elsevier in JTCVS Open
- Vol. 33
Open AccessPilot safety and efficacy trial of amiodarone-infused biologic acellular biatrial patches to prevent new-onset postoperative atrial fibrillation
- Open Access
Integrative Clinical-Molecular Modeling Identifies LRRN4CL as a Determinant of Structural and Functional Myocardial Improvement
Background: Mechanical ventricular unloading and systemic circulatory support with left ventricular assist devices (LVADs) enable myocardial recovery in a subset of advanced heart failure (HF) patients, but predictors and mechanisms of recovery are not well understood. Integrating clinical and molecular data may improve identification of patients most likely to recover and uncover biologically relevant targets in HF. Methods: We collected and analyzed left ventricular apical myocardial tissue and clinical data from 208 patients undergoing LVAD implantation across five centers. Pre-implant transcriptomic profiles (22,373 mRNA transcripts) were integrated with 59 clinical variables using supervised machine learning with repeated cross-validation to identify and prioritize features associated with myocardial recovery, defined as a binary outcome based on improvement in left ventricular ejection fraction (LVEF ≥40%) and left ventricular end-diastolic diameter (LVEDD ≤5.9 cm). We also modeled functional (LVEF) and structural (LVEDD) improvement as a continuous outcome without any predefined LVEF and LVEDD pathological thresholds. Feature prioritization was followed by validation in human myocardial tissue and mechanistic interrogation in human induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs). Results: Integrative models achieved modest discrimination for myocardial recovery as a binary categorical outcome (maximum mean cross-validated area under the curve 0.73±0.15), identifying clinical features such as HF duration, LVEDD, HF pharmacologic therapy, and device configuration. Leucine-rich repeat neuronal 4C-like (LRRN4CL), measured in human myocardium, consistently emerged as a top transcriptomic predictor across both binary and continuous metric models (functional and structural). Higher pre-LVAD LRRN4CL expression was associated with reduced likelihood of myocardial recovery and localized primarily to cardiomyocytes. In iPSC-CMs, LRRN4CL overexpression localized to the sarcoplasmic reticulum, induced transcriptional remodeling characterized by suppression of contractile pathways and activation of stress programs, impaired calcium handling, impaired contraction?relaxation kinetics, and diminished mitochondrial respiratory reserve capacity. Conclusions: Integration of clinical and myocardial transcriptomic data identifies LRRN4CL as a novel marker associated with impaired myocardial recovery following LVAD-mediated ventricular unloading and systemic circulatory support. These findings move beyond predictive modeling, linking integrative computational discovery to cardiomyocyte dysfunction and providing a translational framework for biologically informed risk stratification and therapeutic targeting for myocardial recovery.
Open AccessIntegrative Clinical-Molecular Modeling Identifies LRRN4CL as a Determinant of Structural and Functional Myocardial Improvement
Background: Mechanical ventricular unloading and systemic circulatory support with left ventricular assist devices (LVADs) enable myocardial recovery in a subset of advanced heart failure (HF) patients, but predictors and mechanisms of recovery are not well understood. Integrating clinical and molecular data may improve identification of patients most likely to recover and uncover biologically relevant targets in HF. Methods: We collected and analyzed left ventricular apical myocardial tissue and clinical data from 208 patients undergoing LVAD implantation across five centers. Pre-implant transcriptomic profiles (22,373 mRNA transcripts) were integrated with 59 clinical variables using supervised machine learning with repeated cross-validation to identify and prioritize features associated with myocardial recovery, defined as a binary outcome based on improvement in left ventricular ejection fraction (LVEF ≥40%) and left ventricular end-diastolic diameter (LVEDD ≤5.9 cm). We also modeled functional (LVEF) and structural (LVEDD) improvement as a continuous outcome without any predefined LVEF and LVEDD pathological thresholds. Feature prioritization was followed by validation in human myocardial tissue and mechanistic interrogation in human induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs). Results: Integrative models achieved modest discrimination for myocardial recovery as a binary categorical outcome (maximum mean cross-validated area under the curve 0.73±0.15), identifying clinical features such as HF duration, LVEDD, HF pharmacologic therapy, and device configuration. Leucine-rich repeat neuronal 4C-like (LRRN4CL), measured in human myocardium, consistently emerged as a top transcriptomic predictor across both binary and continuous metric models (functional and structural). Higher pre-LVAD LRRN4CL expression was associated with reduced likelihood of myocardial recovery and localized primarily to cardiomyocytes. In iPSC-CMs, LRRN4CL overexpression localized to the sarcoplasmic reticulum, induced transcriptional remodeling characterized by suppression of contractile pathways and activation of stress programs, impaired calcium handling, impaired contraction?relaxation kinetics, and diminished mitochondrial respiratory reserve capacity. Conclusions: Integration of clinical and myocardial transcriptomic data identifies LRRN4CL as a novel marker associated with impaired myocardial recovery following LVAD-mediated ventricular unloading and systemic circulatory support. These findings move beyond predictive modeling, linking integrative computational discovery to cardiomyocyte dysfunction and providing a translational framework for biologically informed risk stratification and therapeutic targeting for myocardial recovery.
- Open Access
- 17 April 2026
- Published by Elsevier in The Journal of Heart and Lung Transplantation
- Vol. 45 (10) , 1537-1549
Determining the individualized probability of myocardial recovery: The multicenter RecoverHeart calculator
- 17 April 2026
- Published by Elsevier in The Journal of Heart and Lung Transplantation
- Vol. 45 (10) , 1537-1549
Open AccessDetermining the individualized probability of myocardial recovery: The multicenter RecoverHeart calculator
- 25 March 2026
- Published by Wiley in Clinical Transplantation
- Vol. 40 (3) , e70516
Increased Resource Utilization Post 2018 Heart Allocation Policy Change
The 2018 United Network of Organ Sharing (UNOS) heart allocation policy change has shifted the way patients are bridged to heart transplant. The true cost of the policy change has not been examined using a large national database. The Healthcare Cost and Utilization Project Database (HCUP) National Inpatient Sampling database (2015–2022) was used to identify adult heart transplant recipients before and after the policy change, examining resource utilization between the two policy periods. There was an increase in the use of temporary mechanical circulatory support devices in the current era, along with a longer mean length of stay and more discharges to non‐acute facilities. Despite similar inpatient mortality rates, the median total inpatient charge increased significantly (Old Policy: $685,263 vs. New Policy: $959,756; p < 0.001). The length of stay has also increased in the current policy period, and more patients are discharged to rehabilitation facility or places other than home. The increase in charge is also reflected in the total cost to the hospital (Old Policy: $172,935 ($122,611–$ 271,196) vs. New Policy: $241,277 ($167,353–$ 363,415), p <0.001). These findings further highlight increased resource utilization in current heart transplantation practice in the United States, warranting further discussion of healthcare utilization and outcomes.- 25 March 2026
- Published by Wiley in Clinical Transplantation
- Vol. 40 (3) , e70516
Increased Resource Utilization Post 2018 Heart Allocation Policy Change
The 2018 United Network of Organ Sharing (UNOS) heart allocation policy change has shifted the way patients are bridged to heart transplant. The true cost of the policy change has not been examined using a large national database. The Healthcare Cost and Utilization Project Database (HCUP) National Inpatient Sampling database (2015–2022) was used to identify adult heart transplant recipients before and after the policy change, examining resource utilization between the two policy periods. There was an increase in the use of temporary mechanical circulatory support devices in the current era, along with a longer mean length of stay and more discharges to non‐acute facilities. Despite similar inpatient mortality rates, the median total inpatient charge increased significantly (Old Policy: $685,263 vs. New Policy: $959,756; p < 0.001). The length of stay has also increased in the current policy period, and more patients are discharged to rehabilitation facility or places other than home. The increase in charge is also reflected in the total cost to the hospital (Old Policy: $172,935 ($122,611–$ 271,196) vs. New Policy: $241,277 ($167,353–$ 363,415), p <0.001). These findings further highlight increased resource utilization in current heart transplantation practice in the United States, warranting further discussion of healthcare utilization and outcomes.- Open Access
- 3 March 2026
- Published by Elsevier in JTCVS Open
- Vol. 30
Local amiodarone delivery via an extracellular collagen matrix patch to reduce new-onset postoperative atrial fibrillation
- 3 March 2026
- Published by Elsevier in JTCVS Open
- Vol. 30
Open AccessLocal amiodarone delivery via an extracellular collagen matrix patch to reduce new-onset postoperative atrial fibrillation
- 3 February 2026
- Published by Springer Nature in Cardiovascular Engineering and Technology
- Vol. 17 (3) , 317-326
Engineering Development of a Bi-directional Arterial Cannula with Peripheral Access for Cardiopulmonary Bypass
Purpose Cardiopulmonary bypass (CPB) is a well-established procedure that uses cannulae during cardiac surgery to drain and return blood. In challenging cases (e.g. aortic dissection, reoperation), peripheral cannulation in vessels such as the axillary artery are used. However, standard cannulae at these sites may inhibit blood flow to distal extremities or require grafts that increase surgical time. This study evaluates a novel, flexible-tip arterial cannula designed for bi-directional flow. Methods A 22Fr body cannula was developed to achieve a pressure loss (ΔP) < 100 mmHg and 80/20 bi-directional flow distribution between tip outlets. A full factorial design of experiments (2-levels, 4 factors: tip A-width, B-height, C-depth, D-outlet shape) was completed to evaluate sixteen cannula tip designs using benchtop hydraulic and bi-directional flow models. Prototypes were fabricated using 3D printing via stereolithography (Form 3 + , Formlabs, Somerville, MA) with a flexible (50A) cured resin. Results The most efficient cannula design (A − , B + , C + , D + ) achieved 4 L/min of total bi-directional flow at a ΔP of 74 mmHg. The average ΔP at 4 L/min for all candidate design was 87 ± 9 mmHg (range 72–100 mmHg). Primary outlet flow distribution averaged 81% ± 6% (range 70–95%) at 1-5 L/min flow rates. Tip width had the greatest influence on ΔP, followed by outlet shape, depth, and their interactions, respectively. Cylindrical and prolate spheroid shaped tips outperformed spherical designs. Conclusion The novel cannula demonstrated feasibility and proof-of-concept as evidenced by bi-directional flow with ΔP comparable to commercial cannulae. Future work will involve CFD modeling and pre-clinical validation (e.g. hemolysis, cadaver fit) to support development of a low-cost, clinical grade bi-directional flow cannula for peripheral CPB to reduce surgical complexity and lower risk of adverse events.
- 3 February 2026
- Published by Springer Nature in Cardiovascular Engineering and Technology
- Vol. 17 (3) , 317-326
Engineering Development of a Bi-directional Arterial Cannula with Peripheral Access for Cardiopulmonary Bypass
Purpose Cardiopulmonary bypass (CPB) is a well-established procedure that uses cannulae during cardiac surgery to drain and return blood. In challenging cases (e.g. aortic dissection, reoperation), peripheral cannulation in vessels such as the axillary artery are used. However, standard cannulae at these sites may inhibit blood flow to distal extremities or require grafts that increase surgical time. This study evaluates a novel, flexible-tip arterial cannula designed for bi-directional flow. Methods A 22Fr body cannula was developed to achieve a pressure loss (ΔP) < 100 mmHg and 80/20 bi-directional flow distribution between tip outlets. A full factorial design of experiments (2-levels, 4 factors: tip A-width, B-height, C-depth, D-outlet shape) was completed to evaluate sixteen cannula tip designs using benchtop hydraulic and bi-directional flow models. Prototypes were fabricated using 3D printing via stereolithography (Form 3 + , Formlabs, Somerville, MA) with a flexible (50A) cured resin. Results The most efficient cannula design (A − , B + , C + , D + ) achieved 4 L/min of total bi-directional flow at a ΔP of 74 mmHg. The average ΔP at 4 L/min for all candidate design was 87 ± 9 mmHg (range 72–100 mmHg). Primary outlet flow distribution averaged 81% ± 6% (range 70–95%) at 1-5 L/min flow rates. Tip width had the greatest influence on ΔP, followed by outlet shape, depth, and their interactions, respectively. Cylindrical and prolate spheroid shaped tips outperformed spherical designs. Conclusion The novel cannula demonstrated feasibility and proof-of-concept as evidenced by bi-directional flow with ΔP comparable to commercial cannulae. Future work will involve CFD modeling and pre-clinical validation (e.g. hemolysis, cadaver fit) to support development of a low-cost, clinical grade bi-directional flow cannula for peripheral CPB to reduce surgical complexity and lower risk of adverse events.
- 13 January 2026
- Published by Elsevier in The Journal of Heart and Lung Transplantation
- Vol. 45 (5) , 833-834
Transcutaneous energy transfer system for left ventricular assist device support: Current challenges and new technology
- 13 January 2026
- Published by Elsevier in The Journal of Heart and Lung Transplantation
- Vol. 45 (5) , 833-834
Transcutaneous energy transfer system for left ventricular assist device support: Current challenges and new technology