REVIEW article

Front. Cardiovasc. Med., 17 February 2026

Sec. Heart Failure and Transplantation

Volume 13 - 2026 | https://doi.org/10.3389/fcvm.2026.1726345

Clinical management of aortic valve regurgitation after left ventricular assist device implantation: prediction, assessment, and treatment strategies

    SL

    Sen Li

    YX

    Yingjian Xu

    SZ

    Shiqi Zhang

    ZH

    Zhifu Han *

    XL

    Xiangyu Liu *

  • Department of Clinical Research, Aerospace Taixin Technology Co., Ltd., TianJin, China

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Abstract

Left ventricular assist devices (LVADs) have become a core treatment modality for end-stage heart failure. However, aortic regurgitation (AR) remains a common postoperative complication that significantly threatens patient outcomes. This narrative review examines the pathophysiological mechanisms, predictive factors, assessment methods, and intervention strategies for AR following LVAD implantation, aiming to provide guidance for clinical practice. Studies have shown that preoperative age ≥60 years, female gender, lower body surface area, mild AR, proximal ascending aorta diameter/body surface area > 15.5 mm/m2, and higher cumulative dose of beta-blockers increase the risk of AR. Postoperative aortic valve opening restriction and prolonged LVAD support time are strong predictors of significant AR. Among device types, axial flow pumps have a higher incidence of AR than fully magnetic levitation centrifugal pumps; Traditional assessment methods have limited applicability and should be combined with hemodynamic characteristics (such as central venous pressure, pulmonary capillary wedge pressure, and pulmonary artery pulsatility index) and multimodal imaging techniques such as transthoracic echocardiography (AR width/LVOT width ratio), transesophageal echocardiography, and cardiac magnetic resonance imaging; Preoperative repair or replacement of moderate or severe AR can reduce postoperative risks, and transcatheter aortic valve replacement (TAVR) is the preferred treatment for significant AR postoperatively. Future efforts should focus on optimizing the assessment system and improving device design to enhance long-term patient outcomes.

Introduction

Heart failure is a highly prevalent chronic cardiovascular disease worldwide, and its incidence in China has been steadily rising with the acceleration of population aging (1, 2). Currently, non-pharmacological treatment options for heart failure include heart transplantation and left ventricular assist device (LVAD) support (3). Among these, heart transplantation was once considered the “gold standard” treatment for end-stage heart failure, significantly improving patient outcomes and quality of life. However, the scarcity of donor organs and surgical resource limitations have resulted in extremely low coverage rates, far from meeting clinical needs (4). Additionally, LVAD, as the core technology for mechanical circulatory support, has seen a steady increase in the application of destination therapy (DT), reaching 81.1% in 2021, as shown in Figure 1, making it an important alternative treatment option for end-stage heart failure patients (5).

Figure 1

Stacked bar chart showing device strategy for primary CF LVAD between 2012 and 2021. Categories include Bridge to Transplant, Bridge to Candidacy, and Destination Therapy, with percentages for each year, illustrating the trends over time.

The proportion of DT treatment has increased year by year.

However, as LVAD support time increases, the clinical risks associated with aortic regurgitation (AR) become increasingly evident. Following LVAD implantation, reduced left ventricular pressure leads to an increase in transvalvular pressure gradient across the aortic valve. Combined with the high shear stress generated by retrograde blood flow, this can trigger aortic valve remodeling and functional deterioration (6). This pathological change creates a “vicious cycle”—blood pumped into the aorta via the LVAD then flows back into the left ventricle through the incompetent aortic valve, significantly reducing effective cardiac output and leading to recurrent heart failure symptoms in patients. In severe cases, emergency heart transplantation may even be required (7). Studies show that the incidence of significant AR within one year post-LVAD implantation reaches 25%–30%, and is closely associated with increased patient mortality (810). Therefore, AR has a significant impact on patient prognosis, and its mechanisms and intervention strategies require further investigation.

The pathogenesis of aortic regurgitation (AR) is complex and involves multiple factors. Following LVAD implantation, pathological processes such as increased transvalvular pressure gradient, retrograde blood flow formation, local high shear stress, and aortic root tissue remodeling interact synergistically to promote the development of AR (7, 11). Additionally, the reduced pulse pressure gradient and weakened aortic pulsatility caused by the LVAD further accelerate the deterioration of aortic valve function (12). Studies have shown that aortic valve dysfunction is a serious long-term complication faced by LVAD patients, but there remains controversy regarding its pathophysiological mechanisms and treatment strategies.

Although the clinical significance of AR is well-established, there remains debate regarding its predictive models, assessment criteria, and optimal timing for intervention. This comprehensive review focuses on the predictive factors, assessment methods, and treatment strategies for AR following LVAD implantation, aiming to provide evidence-based guidance for optimizing clinical management to improve patient long-term survival rates and quality of life.

Predictors of AR following LVAD implantation

The occurrence of AR following LVAD implantation is not a random event; its risk can be predicted through a combination of preoperative baseline characteristics and postoperative key factors. Identifying these predictors in detail can help clinicians develop early intervention strategies to reduce the risk of AR occurrence (Table 1).

Table 1

Category Risk factors
Preoperative factors Age ≥60 years; Female gender; BSA <2.0 m2; Mild AR at baseline; Aortic root diameter/BSA >15.5 mm/m2
Postoperative/Device factors Aortic valve opening restriction; Prolonged LVAD support duration; Axial flow pumps (vs. Centrifugal)
Surgical factors Anastomosis inclination angle ≥90°

Predictors and risk factors for aortic regurgitation after LVAD implantation.

Preoperative baseline characteristics

Multiple studies have confirmed that preoperative clinical indicators can effectively predict the risk of postoperative AR. When analyzing clinical data from a large number of LVAD implant patients, some studies have examined the association between various preoperative clinical characteristics and the occurrence of postoperative AR. For example, multiple studies have shown that patients aged ≥60 years have a significantly higher risk of developing AR after LVAD implantation compared to younger patients, suggesting that age is an important influencing factor for postoperative AR (8, 13). From a physiological mechanism perspective, as age increases, the tissue structure of the aortic valve undergoes progressive degenerative changes, leading to reduced elasticity and compliance of the valve leaflets. Consequently, following LVAD implantation, the aortic valve is more prone to functional impairment in response to hemodynamic changes, thereby triggering AR (14).

Gender factors are also associated with the risk of postoperative AR. A retrospective study by Lauren K et al. based on the INTERMACS database showed that female gender is an independent risk factor for moderate-to-severe postoperative AR (13). Some studies speculate that this may be related to the cardiovascular anatomical structure and physiological characteristics of women, such as the relatively smaller size of the aortic root in women, which may make them more sensitive to hemodynamic changes under LVAD support, thereby increasing the risk of AR. This provides a potential anatomical basis for why women are more prone to AR after LVAD implantation (15). Additionally, a cross-sectional study of 438 patients with hypertension and left ventricular hypertrophy (including 266 women and 172 men) found significant correlations between aortic root dilation in women and cardiac output, mild aortic regurgitation (16).

Body surface area is also a key predictive indicator, with studies showing that a lower body surface area is a known risk factor for AR occurrence under LVAD support (8, 13). This may be because patients with smaller body surface areas have relatively smaller hearts and aortas, and after LVAD implantation, the hemodynamic balance within the heart is more easily disrupted, affecting the coordination of aortic valve opening and closing, ultimately leading to AR occurrence.

The preoperative status of the aortic valve plays a crucial predictive role in the occurrence of postoperative AR. A clinical study involving 316 patients who underwent LVAD implantation showed that at 1 year postoperatively, the proportion of patients without significant new-onset AR was 94.5% among those without preoperative AR, while the proportion was 64.6% among those with mild preoperative AR (17). Related studies have also indicated that even mild AR prior to surgery significantly increases the likelihood of AR worsening postoperatively (13).

Anatomical parameters of the aortic root play a significant role in predicting the risk of postoperative aortic regurgitation (AR). Studies have shown that when the proximal ascending aorta diameter/body surface area exceeds 15.5 mm/m2, the risk of postoperative AR significantly increases (18). Following LVAD implantation, the pulse pressure difference decreases, leading to changes in the mechanical stress on the aortic wall. This results in reduced elastin content and smooth muscle cell apoptosis in the aortic wall, causing an increase in the diameter of the aortic root within six months postoperatively. This root dilation disrupts the normal valve leaflet closure mechanism of the aortic valve, preventing complete closure of the leaflets and thereby triggering AR (19).

Additionally, preoperative medication use is also considered to be associated with the risk of postoperative AR. Imamura et al. (20) found that a higher cumulative dose of beta-blockers prior to surgery is also a predictive factor for significant AR postoperatively. Furthermore, studies have found that patients who have used beta-blockers long-term (defined as chronic use exceeding 60 days) have a higher absolute incidence of adverse cardiac events before adjustment compared to non-users, but their risk is reduced after adjustment, suggesting that long-term use is related to the condition of specific surgical patients and may reflect the association between cumulative dose and etiology and disease progression (21).

Postoperative key factors

Postoperative factors are equally important in predicting the risk of aortic regurgitation (AR). The open state of the aortic valve is considered one of the strongest predictors of postoperative AR. In a study on exercise-induced aortic valve opening, researchers divided LVAD postoperative patients into an exercise group and a control group, with the exercise group receiving regular aerobic exercise training in the early postoperative period. The results showed that the frequency of aortic valve opening in the exercise group was significantly higher than that in the control group (22). Additionally, in patients receiving long-term LVAD support, aortic valve function gradually deteriorates over time, significantly increasing the risk of developing significant AR (23). Therefore, promoting aortic valve opening has become one of the clinical treatment strategies.

LVAD device-related factors significantly influence the occurrence of postoperative AR. Studies have shown that support duration is positively correlated with the risk of AR, meaning that as LVAD support duration increases, the incidence of AR also increases (8). Device type is also an important factor influencing the incidence of AR. Compared with fully magnetic levitation centrifugal pumps (such as HeartMate 3), axial flow pumps (such as HeartMate II) have a higher incidence of AR, and patient readmission rates also increase (24, 25). This may be related to the constant high-speed operation mode of axial flow pumps, which causes the valve to endure high mechanical loads over the long term, accelerating valve wear and functional deterioration.

Among surgical technical factors, the angle of artificial vessel anastomosis significantly influences the risk of postoperative AR. In vitro simulation studies have shown that a lower anastomosis position, an inclination angle of less than 90°, and an azimuth angle of 60° or 120° help reduce blood flow stagnation at the aortic root and create normal wall shear stress and moderate pressure conditions in that region (26). Therefore, selecting a smaller anastomosis angle and a 60° azimuth angle to establish an optimal blood flow pattern is an important strategy for effectively reducing the risk of postoperative AR in LVAD surgery (Figure 2).

Figure 2

Diagram showing aortic flow dynamics. The left, labeled \"Optimal Configuration,\" has an azimuth angle of sixty degrees with smooth flow through the ascending aorta. The right, labeled \"Suboptimal Configuration,\" shows a one hundred twenty degree azimuth angle, with flow stagnation and wall shear stress near the graft and LVAD outflow.

Schematic diagram illustrating the optimal anastomosis inclination angle (<90°) and azimuth angle for the LVAD outflow graft to minimize hemodynamic stress on the aortic root.

Methods for assessing AR after LVAD surgery

After LVAD implantation, patients experience significant changes in their hemodynamic patterns, limiting the applicability of traditional AR assessment systems. Therefore, it is necessary to combine hemodynamic characteristics with imaging techniques to develop targeted assessment strategies for accurately determining the severity of AR and its impact on the circulatory system.

Changes in hemodynamic characteristics

Following LVAD implantation, patients experience a fundamental shift in their hemodynamic patterns, presenting numerous new challenges and characteristics for the development and assessment of AR. Traditionally, aortic regurgitation primarily occurs during cardiac diastole, when blood flows back from the aorta into the left ventricle. However, under LVAD support, due to its continuous blood flow pattern, left ventricular pressure remains relatively stable and consistently below aortic pressure throughout the cardiac cycle. This unique hemodynamic state prevents the aortic valve from opening normally during systole, resulting in continuous regurgitation throughout the cardiac cycle (6). In an in vitro study based on CT imaging, Kassi et al. (27) developed a simulation model incorporating a HeartMate II axial flow pump. Their findings demonstrated that as pump speed increased, both net pump flow and retrograde regurgitant volume increased significantly. Unlike traditional diastolic regurgitation, LVAD patients may experience full-cycle regurgitation—increased pump speed causes left ventricular pressure to remain consistently below aortic pressure, resulting in the aortic valve remaining closed during systole (6).

Hemodynamic monitoring parameters are crucial in assessing the condition of AR patients post-LVAD surgery. Hemodynamic monitoring revealed that AR patients had higher central venous pressure (CVP) (11 ± 5 vs. 8 ± 5 mmHg, P = 0.03), higher pulmonary capillary wedge pressure (PCWP) (16 ± 6 vs. 12 ± 6 mmHg, P = 0.02), and lower pulmonary artery pulsatility index (PAPI) (2.3 ± 1.3 vs. 3.6 ± 2.4, P = 0.01) (28). These changes in indicators reflect the impact of AR on the circulatory system from multiple dimensions: increased CVP suggests increased right ventricular load, which may be related to left ventricular volume overload affecting right ventricular function through interventricular septal interaction (29, 30); Elevated PCWP directly reflects increased left atrial pressure, which is a direct consequence of AR-induced increased left ventricular preload (31); and decreased PAPI reflects reduced right ventricular drive capacity in the pulmonary circulation, associated with mismatched right ventricular afterload increase and improved left ventricular function post-LVAD implantation, serving as an early marker of deteriorating cardiopulmonary function (32).

Imaging assessment techniques

Imaging techniques are key tools for assessing AR after LVAD implantation, with different methods offering distinct advantages, often used in combination in clinical practice (Table 2).

Table 2

Modality Parameters Significance
TTE Parameters AR jet width/LVOT width ratio; Pressure half-life (PHT); Vena contracta (VC) TTE provides semi-quantitative assessment
TEE Parameters LVAD inflow/outflow conduit position; Valve structure visualization TEE is superior for structural analysis and excluding conduit artifacts

Recommended echocardiographic parameters for assessment of AR in LVAD patients.

Transthoracic echocardiography (TTE) is the preferred imaging modality for assessing AR due to its non-invasive nature, convenience, and widespread application. Color Doppler imaging can be used to observe the characteristics of the regurgitant jet, and the severity of AR can be semi-quantitatively assessed using the ratio of regurgitant jet width to left ventricular outflow tract (LVOT) width (AR width/LVOT width) (33, 34). Additionally, measuring the left ventricular end-diastolic diameter (LVEDD) and end-systolic diameter (LVESD) can assess left ventricular volume load and functional status (35). For patients with continuous-flow LVAD (cf-LVAD), guidelines for assessing AR severity recommend a multi-parameter approach based on traditional TTE parameters, including pressure half-life (PHT), vena cava diameter (VC), the ratio of jet width to LVOT width, and confirmation of hemodynamic outcomes (27).

Transesophageal echocardiography (TEE) Compared to TTE, TEE is not affected by chest wall interference, providing clearer images and is suitable for patients with poor image quality or requiring high-precision assessment (36). Following LVAD implantation, TEE can be used to ensure adequate cardiac exhaustion and successful LVAD activation, while assessing the position and blood flow distribution of the LVAD inflow and outflow conduits. This information is critical for determining AR status, as abnormal conduit positioning may affect hemodynamics and thereby influence AR status (37). Additionally, 3D-TEE multi-plane reconstruction has been successfully applied in transcatheter mitral and tricuspid valve interventions, aiding in the formulation of treatment plans for related cardiac conditions (38).

Cardiac magnetic resonance imaging (CMR) is a well-established diagnostic technique for evaluating valvular heart disease and has become increasingly widespread in clinical practice in recent years. Its advantages include the provision of high-quality images without the use of ionizing radiation and, in some cases, without the need for contrast agents. CMR enables a comprehensive assessment of the heart, including biventricular function, left ventricular remodeling, myocardial fibrosis, and associated valvular lesions (39). CMR can accurately quantify AR and provide precise assessment of regurgitation through the acquisition of relevant data, offering reliable evidence for subsequent analysis and clinical decision-making (40). Additionally, CMR can assess left ventricular remodeling and function, detect myocardial fibrosis, and aid in prognosis determination; it can also display aortic root lesions, assisting in the development of personalized treatment plans (39, 41).

Computed tomography angiography (CTA) can automatically identify key anatomical landmarks of the aortic root and generate precise quantitative data such as aortic root diameter, aiding physicians in more accurately assessing aortic root conditions and providing data support for evaluating AR risk (42, 43). In summary, in clinical practice, multiple imaging techniques are often combined to achieve precise assessment of AR post-LVAD implantation, thereby optimizing treatment decisions.

Treatment strategies for AR associated with LVAD implantation

Preoperative intervention

AR significantly impacts the efficacy of LVAD treatment; therefore, assessing the severity of AR and implementing appropriate interventions prior to LVAD implantation is critical. For patients with mild or lower-grade AR, aortic valve intervention is typically not required; however, for patients with moderate or higher-grade AR, correction during LVAD implantation is recommended to optimize treatment outcomes and reduce postoperative complications.

Although concomitant aortic valve surgery may increase surgical risk, the benefits of aortic valve intervention typically outweigh the risks associated with LVAD failure (e.g., reduced pump performance) caused by significant AR postoperatively (44).

Based on the patient's specific condition, aortic valve treatment strategies can be divided into the following three types:

  • (1)

    Aortic valve closure: In certain specific cases, complete closure of the aortic valve may be considered to prevent its opening and thereby avoid the development of progressive AR postoperatively. Common surgical procedures include the use of pericardial patches or surgical suturing (45). For example, a new method involves using a polytetrafluoroethylene (PTFE) patch to close a mechanical aortic valve by filling the gap between the annulus and the leaflets and securing the valve in the closed position. The specific procedure involves cutting a low-porosity PTFE felt patch into four circles to create a double-layered gap-filling patch, which is then sutured and fixed to the mechanical valve to achieve valve closure (46). This method avoids circulatory circuit issues caused by aortic regurgitation (AR), such as cardiogenic shock, inadequate perfusion, and multi-organ failure, thereby improving the patient's hemodynamic status and quality of life (47). However, if the mechanical aortic valve is closed during LVAD implantation, there is a risk of sudden death if the LVAD ceases to function (48). Studies have shown that in acute myocardial infarction patients undergoing LVAD implantation, those with aortic valve closure have significantly lower survival rates compared to those with aortic valve repair or replacement (49). Therefore, aortic valve closure is not recommended as the primary surgical procedure.

  • (2)

    Aortic valve replacement: For patients requiring long-term LVAD therapy, aortic valve replacement is a common strategy. Bioprosthetic valve replacement is recommended, and mechanical aortic valves are not advised. Currently, bioprosthetic valve replacement is widely used in LVAD patients (50, 51). From a mechanistic perspective, patients under LVAD support have low-frequency or even prolonged non-opening of the aortic valve. If a mechanical aortic valve is selected, the lack of sufficient blood flow to wash the valve leaflets can significantly increase the risk of thrombosis (52, 53). If patients have previously received a mechanical aortic valve before surgery, it should be replaced with a bioprosthetic valve during LVAD implantation (48). Compared to mechanical valves, bioprosthetic valves have the advantage of not requiring long-term anticoagulation, which can further reduce the bleeding risk associated with anticoagulant therapy, especially for LVAD patients with additional high-risk factors for bleeding (54). It should be noted that bioprosthetic valves are prone to long-term degeneration, and over time, leaflet deterioration or fusion may occur, which might require additional interventions (55). Additionally, transcatheter aortic valve replacement (TAVR), as a minimally invasive treatment modality, is increasingly being applied in LVAD-related AR patients (56, 57).

  • (3)

    Aortic valve repair: When the aortic valve structure is largely intact, with only partial lesions such as leaflet prolapse or perforation, aortic valve repair is a suitable option. By repairing the diseased leaflets to restore the normal structure and function of the aortic valve, regurgitation can be effectively reduced (58). In AR patients, aortic valve repair and replacement have comparable perioperative outcomes, but the long-term reintervention rate is higher for repair (59). In a study of AR patients prior to LVAD implantation, patients who underwent aortic valve repair combined with LVAD implantation showed a significant reduction in AR severity during postoperative follow-up (60). Aortic valve repair methods include leaflet repair techniques (such as leaflet folding and leaflet perforation repair) and annulus reconstruction techniques (61, 62). Repair using an aortic valve annulus ring can reduce the incidence of AR by counteracting further expansion of the aortic root, and the procedure is relatively simple with favorable outcomes (63) (Figure 3).

Figure 3

Illustration showing four heart valve repair techniques. Panel A depicts the Central Closure Technique with Park's stitch. Panel B shows the Patch Closure Technique. Panel C illustrates Aortic Valve Repair with directional arrows. Panel D displays Bioprosthetic Valve Replacement.

Illustrations of surgical techniques for aortic regurgitation (AR). (A) Central coaptation is restored using a central closure technique like the Park's stitch. (B) A patch is used to close a defect or perforation and reinforce the closure. (C) Repair of a prolapsing aortic valve cusp. (D) Replacement of the native valve with a stented bioprosthesis.

Postoperative management

Following LVAD implantation, effective management of AR is critical for patient outcomes. Treatment strategies are categorized into non-surgical and surgical approaches.

Non-surgical treatment

Optimizing anti-heart failure drug therapy aims to improve cardiac function, reduce cardiac workload, and alleviate the adverse hemodynamic effects caused by AR (64, 65). Angiotensin-converting enzyme inhibitors (ACEIs) or angiotensin II receptor blockers (ARBs) inhibit the renin-angiotensin-aldosterone system (RAAS), reducing peripheral vascular resistance, alleviating afterload on the heart, and decreasing left ventricular pressure, thereby helping to relieve AR-induced volume and pressure overload on the left ventricle (66). RAS inhibitors and statins As part of the secondary prevention treatment regimen for aortic valve regurgitation patients following aortic valve replacement surgery, RAS inhibitor therapy is associated with better long-term outcomes (64). Over 50% of heart failure patients require diuretic therapy after LVAD implantation. Furosemide has been used for over 50 years to relieve congestion in patients with fluid overload and is the most commonly used loop diuretic for hospitalized patients with decompensated heart failure (67, 68). However, it is important to note that excessive diuresis may lead to hypovolemia, impairing the normal pumping function of the LVAD. Higher diuretic doses prior to surgery are associated with an increased risk of early right heart failure following LVAD implantation (69).

Secondly, adjusting the pump speed and flow settings of the LVAD can optimize the patient's hemodynamic characteristics (70). Appropriate adjustment of pump speed can increase effective cardiac output and ensure adequate organ perfusion (70, 71). Flow regulation is equally important; adjusting the LVAD's flow settings can alter left ventricular filling and emptying states, affecting aortic valve opening and closing. Studies indicate that increasing LVAD flow can moderately elevate aortic pressure, aiding in reducing regurgitation, but may also lead to increased regurgitant flow (72). Beyond acute pump speed adjustment, preventative strategies focusing on intermittent pump speed modulation have gained increasing attention. The Lavare cycle, available in HeartMate 3 devices, periodically reduces pump speed to create transient pulsatility, facilitating aortic valve opening and promoting blood flow wash-out at the aortic root (73). This intermittent speed reduction helps prevent valve leaflet fusion and reduces thrombus formation on the aortic valve cusps, potentially mitigating the progression of AR in long-term LVAD support (74). Similarly, artificial pulse algorithms that periodically alter pump speed have been shown to increase the frequency of aortic valve opening events, which may preserve valve function and delay the onset of significant AR (75).

Surgical treatment

For patients who develop significant AR postoperatively or who fail to respond to medical therapy, surgical intervention should be initiated as early as possible. Surgical approaches are broadly categorized into two types: invasive surgery (aortic valve closure, repair, and surgical aortic valve replacement) and transcatheter aortic valve replacement (TAVR) (76). While invasive surgical techniques are well-established and effective, they carry a higher risk of re-thoracotomy for LVAD patients.

TAVR offers advantages such as minimal trauma and fewer postoperative complications compared to invasive surgery, making it more suitable for surgical treatment of significant AR in LVAD patients (57). It is important to note that TAVR was initially primarily used for patients with aortic valve stenosis, who typically have concomitant aortic valve thickening and calcification. Therefore, compared to patients with aortic valve stenosis, patients with AR may lack sufficient calcification to stabilize the valve, thereby increasing the risk of valve displacement (77, 78). The absence of annular calcification in LVAD patients with pure AR presents unique challenges for TAVR, as traditional valve anchoring mechanisms rely heavily on calcific deposits to secure the prosthesis (79). Self-expanding valves may offer advantages over balloon-expandable valves in this population due to their continuous radial force and ability to conform to non-calcified annular geometry, though careful sizing remains critical to prevent migration (80). Additionally, the enlarged aortic root in LVAD patients can lead to a larger annulus size, which may affect valve anchoring and increase the risk of paravalvular leakage (81, 82). Recent case series have demonstrated successful TAVR in LVAD patients using both self-expanding and balloon-expandable platforms, with careful pre-procedural CT planning essential for optimal valve sizing and positioning (83).

Discussion

As a core alternative treatment for end-stage heart failure, the continuous increase in the proportion of “purposeful treatment” with LVAD confirms its clinical value (5). However, AR, as one of the most prominent complications after LVAD surgery, not only affects treatment outcomes but also directly threatens patient survival. Its clinical management complexity and specificity require further in-depth discussion (8). This paper discusses the clinical management challenges, mechanism associations, and optimization strategies for AR following LVAD implantation based on existing research evidence, providing guidance for clinical practice.

The pathophysiological mechanisms of AR following LVAD implantation exhibit a complex interplay of multiple factors. The reduced left ventricular pressure under LVAD support leads to increased transvalvular pressure gradients, combined with shear forces generated by retrograde blood flow, triggering valve remodeling, reduced elasticity, and functional deterioration. This “reflux-volume overload-deterioration of cardiac function” vicious cycle may reduce effective cardiac output, exacerbate heart failure symptoms, and even necessitate emergency heart transplantation (7, 84).

Accurate identification of high-risk populations is a prerequisite for optimizing AR clinical management. Existing studies have identified multidimensional predictive factors, encompassing preoperative baseline characteristics and postoperative key factors. At the preoperative level, independent risk factors include age ≥60 years, female gender, body surface area <2.0 m2, mild AR at baseline, proximal ascending aorta diameter/body surface area >15.5 mm/m2, and high cumulative dose of beta-blockers. Postoperative core factors include aortic valve opening restriction, prolonged LVAD support time, and device type (axial flow pumps carry higher risk). Additionally, surgical technical factors such as artificial vessel anastomosis with an inclination angle <90° and azimuth angle of 60° can reduce risk. However, current predictive models have limitations: existing studies are primarily based on single-center data and lack a unified risk scoring system; some factors (such as the mechanism of action of beta-blockers) remain poorly understood and may be confounded by patients' underlying conditions. Future studies should utilize multicenter cohort research to integrate clinical, imaging, and device parameters, develop dynamic predictive models, and achieve individualized risk stratification.

Changes in hemodynamic patterns post-LVAD implantation (such as full-cycle reflux) limit the applicability of traditional AR assessment methods, necessitating the establishment of a targeted assessment system. Hemodynamic monitoring shows that AR patients have significantly elevated central venous pressure (CVP) and pulmonary capillary wedge pressure (PCWP), while the pulmonary artery pulsatility index (PAPI) is reduced. These indicators can reflect the extent of circulatory system involvement at an early stage and assist in assessing the impact of AR on cardiac function. The combined application of imaging techniques is central to precise assessment. Transthoracic echocardiography (TTE) is the preferred method, using the AR width/LVOT width ratio for semi-quantitative assessment of regurgitation severity, though its accuracy is influenced by image quality; transesophageal echocardiography (TEE) clearly displays valve structure and catheter position, making it suitable for high-precision assessment; Cardiac magnetic resonance imaging (CMR) quantifies regurgitation, assesses myocardial fibrosis, and evaluates aortic root lesions, providing comprehensive information for prognostic assessment. In clinical practice, hemodynamic indicators and multimodal imaging should be combined to achieve a comprehensive assessment of “anatomy-function-prognosis”.

AR interventions should follow the principles of “individualization and staged treatment”, combining preoperative prevention with postoperative stepwise therapy. For patients with moderate or severe AR, valve repair or replacement is performed preoperatively: repair is suitable for lesions with intact structure; bioprosthetic valves are recommended for replacement, while mechanical valves are not advised. Aortic valve closure is only used as a life-saving measure due to the risk of sudden death. Mild AR can be improved by optimizing medications (e.g., ACEI/ARB to reduce afterload, diuretics to control volume) and adjusting LVAD pump speed. Significant AR is primarily treated with transcatheter aortic valve replacement (TAVR), but CTA assessment of the annulus size is required to reduce the risk of displacement and paravalvular leakage. The timing of intervention remains controversial and should be decided based on symptoms, hemodynamics, and imaging progression. Currently, the timing of intervention remains controversial: some studies advocate “early intervention” to prevent worsening heart function, while others believe that “symptom-driven” intervention is more cost-effective. Future randomized controlled trials are needed to clarify the intervention threshold and develop decision-making criteria based on patient symptoms, hemodynamics, and imaging progression.

The clinical management of AR after LVAD implantation still faces numerous challenges, and future efforts should focus on the following directions: developing LVADs with adaptive flow patterns to promote aortic valve opening through dynamic adjustment of pump speed and reduce valve load; exploring new technologies such as contrast echocardiography and myocardial strain imaging to improve the sensitivity of early AR diagnosis; developing specialized TAVR valves for LVAD patients and optimizing anchorage design; Establishing a long-term monitoring network encompassing AR progression, cardiac function evolution, and quality of life to provide evidence for optimizing treatment strategies. Innovations in pump design, including devices with physiological pulsatility algorithms that more closely mimic native cardiac function, hold promise for reducing the hemodynamic stress on the aortic valve and potentially decreasing AR incidence (85). Furthermore, the development of specialized TAVR valves designed specifically for non-calcified annuluses, incorporating novel anchoring mechanisms such as commissural alignment or atrial cuff designs, may expand treatment options for LVAD patients with significant AR who are not candidates for surgical intervention (86) (Figure 4).

Figure 4

Flowchart of AR assessment in LVAD patients. It categorizes AR into mild, moderate, and severe. Mild AR suggests medical optimization with ACEI/ARB therapy, diuretics, pump speed adjustment, and Lavare cycle. Moderate AR involves close monitoring and medical therapy, with reassessment for progression. Severe AR requires surgical intervention, with options being TAVR (preferred) or SAVR/Repair.

Proposed management algorithm for aortic regurgitation in LVAD patients, ranging from pharmacological optimization for mild AR to surgical intervention (TAVR/SAVR) for severe symptomatic AR.

Conclusion

In summary, the management of AR following LVAD implantation requires comprehensive optimization across the entire chain of prediction, assessment, and intervention, achieved through multidisciplinary collaboration to enable personalized treatment. Preoperative risk stratification utilizing established predictors such as age, gender, body surface area, baseline valve status, and aortic root dimensions allows for targeted prophylactic interventions. Postoperative surveillance combining hemodynamic monitoring with multimodal imaging ensures timely detection of AR progression, while a stepwise treatment approach from medical optimization to transcatheter or surgical intervention provides a framework for individualized patient management. With ongoing technological innovation and accumulation of evidence, there is potential to significantly reduce the incidence of AR and improve long-term outcomes for patients with end-stage heart failure.

Statements

Author contributions

SL: Methodology, Writing – review & editing, Data curation. YX: Data curation, Writing – original draft. SZ: Writing – original draft. ZH: Data curation, Writing – original draft. XL: Writing – original draft.

Funding

The author(s) declared that financial support was not received for this work and/or its publication.

Conflict of interest

The author(s) were employed by Aerospace Taixin Technology Co., Ltd.

Generative AI statement

The author(s) declared that generative AI was not used in the creation of this manuscript.

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Summary

Keywords

aortic regurgitation, heart failure, left ventricular assist device, predictive factors, transcatheter aortic valve replacement

Citation

Li S, Xu Y, Zhang S, Han Z and Liu X (2026) Clinical management of aortic valve regurgitation after left ventricular assist device implantation: prediction, assessment, and treatment strategies. Front. Cardiovasc. Med. 13:1726345. doi: 10.3389/fcvm.2026.1726345

Received

16 October 2025

Revised

19 January 2026

Accepted

26 January 2026

Published

17 February 2026

Volume

13 - 2026

Edited by

Giuseppe Santoro, Gabriele Monasterio Tuscany Foundation (CNR), Italy

Reviewed by

Tahir Yagdi, EGE University, Türkiye

Emad Alamouti-Fard, Independent Researcher, Toronto, Canada

Updates

Copyright

* Correspondence: Zhifu Han Xiangyu Liu

†These authors share first authorship

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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