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Minimal Access Aortic Valve Surgery

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10 May 2023

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11 May 2023

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Abstract
Minimally invasive approaches to the aortic valve have been described since 1993, with great hopes that they would become universal and facilitate day-case cardiac surgery. The literature has shown that these procedures can be undertaken with equivalent mortality, similar operative time, comparative cost and some benefits in hospital length of stay. The competing efforts of the transcatheter aortic valve implantation for these same outcomes have provided an excellent range of treatment options for patients from the Heart Team. We describe the current state of the art, including technical considerations, caveats and complications of minimal access aortic surgery and predict future directions in this space.
Keywords: 
Subject: Medicine and Pharmacology  -   Cardiac and Cardiovascular Systems

1. Introduction

Aortic valve disease is common, affecting 1 in 100 adults in the United States and some 6 million or so individuals worldwide [1,2,3]. A heterogenous spectrum of conditions with different aetiologies and pathophysiology can lead to valve stenosis, regurgitation and endocarditis. The natural history of these conditions is progressive, with symptom progression from angina, breathless or syncope eventually culminating in heart failure and death. In the western world, senile degenerative stenosis predominates, whilst elsewhere rheumatic disease is more prevalent. The onset of symptoms is thought to mark an inflection point where compensatory mechanisms are exhausted and prognosis worsens quickly. Most patients with severe aortic stenosis will develop symptoms within 5 years and event-free survival may be as low as 21% at two years [4,5]. Even with moderate aortic stenosis, progression leads to poor prognostic disease in 38% of patients within five years [6]. No medical treatments influence the natural history of aortic stenosis [7].
Treatment for aortic valve conditions, therefore, is invariably replacement of the diseased valve in 99% of cases [8]. While repair procedures have gained traction in some cases, replacement of the valve has remained the principle strategy since its inception in 1958. Outcomes have been excellent, with mortality from isolated, uncomplicated and conventional aortic valve replacement consistently less than 1% [9].
Despite excellent outcomes for surgery, a 33% rate of surgical turn-down for patients over the age of 75y in the Euro Heart Survey prompted a search for less invasive means of treatment of aortic valve disease [10]. The first percutaneous transcatheter aortic valve implantation (TAVI) in man was performed in 2002 [11]. Over the last two decades, the technology has matured and increased in efficacy and scope, leading to increasingly liberal recommendations for its use in the guidelines [12]. Conversely, the 2017 European Society of Cardiology / European Association of Cardio-Thoracic Surgery guidelines did not reference minimal access approaches for valve surgery at all, and when refreshed in 2021, these were still not discussed [13]. Transcatheter techniques, with a compellingly short recovery time even in highly comorbid patients, have been a driver to reduce the invasiveness of conventional surgical approaches. Complications associated with TAVI such as cerebrovascular embolic events, vascular complications, conduction disorders and prosthetic valve dysfunction are gradually being addressed, but provide good rationale to consider the known excellent pedigree of surgical valve replacement as a first line treatment for the majority of patients requiring intervention.
Having both approaches available in the armamentarium of the Heart Team serves the needs of patients well. Nevertheless, there remains an appetite to marry the reduced invasiveness of TAVI with the meticulous decalcification and directly visualized seating of uncrimped valves. At the turn of the millennium, Chitwood predicted that 21st Century cardiac surgery procedures would be performed minimally invasive as day-cases, with patients returning to normal activity within one or two weeks [14]. Nearly 25 years later, this is true of percutaneous interventions, but remains an elusive goal in surgery.
In this state-of-the-art review, we describe advances in surgical technique that have improved quality and outcomes in minimal access aortic valve surgery and present a vision for future direction.

2. Minimal Access Options

While the terms minimally invasive and minimal access are often used interchangeably, these overlapping philosophies can be disparate. In particular, the relative technical challenges of performing surgery through reduced access incisions can increase cardiopulmonary bypass and ischaemic surgical time, paradoxically increasing the invasiveness of the procedure. The invasiveness of cardiac surgery, some posit, is as much contributed to by the deleterious effects of cardiopulmonary bypass, as it is the trauma of sternotomy, which is generally well tolerated [15,16]. Efforts to mitigate for both, in order to make incremental gains, include a plethora of techniques and approaches, each with various advantages, disadvantages and prerequisites. The most common are summarized here and it is worth noting that there is a paucity of evidence to support preferring one approach over others [17].

2.1. Approach

2.1.1. Hemi-sternotomy

The hemi-sternotomy (also known as partial sternotomy or limited sternotomy) approach that is now the most common approach to minimally invasive aortic valve surgery was developed after initial work using mini-thoracotomy [18,19]. The rationale for this was to avoid the subcostal neurovascular bundles that can cause post-thoracotomy pain if retracted and also to improve access to the great vessels for central cannulation.
The skin incision (Figure 1) is made over the upper midline in order to access the aorta, with J-shaped, L-shaped, or chevron sternotomy into the right, left or bilateral intercostal spaces (Figure 2). The length of the sternotomy can vary and may be into third or fourth intercostal space. Accordingly, the length of the incision can also vary, with 5cm being a typical lower limit. This modifiable access can be utilized to undertake not only aortic valve replacement but also surgery of the aortic root, ascending aorta and hemi-arch [20].
The upper hemi-sternotomy approach can provide sufficient access to perform complete central cannulation with conventional instruments and cannulae, if desired, although modifications and training to facilitate surgery are well described [21,22]. A 2017 Cochrane review of randomised controlled trials comparing full sternotomy to hemi-sternotomy found that across 10 included studies the evidence was of low certainty due to biases and small sample sizes [23]. For most major outcomes, including peri-operative mortality, pain or quality of life, there was no significant difference. Blood loss was slightly lower with hemi-sternotomy compared to full sternotomy (mean difference 153ml lower compared to 400ml), and index admission costs were also higher (a mean difference of £1190 (~$1470) more for hemi-sternotomy). Following the publication of the Cochrane review, the publication of two well designed trials performed in the UK, MAVRIC and Mini-Stern prompted a revised review of the literature.

The MAVRIC Trial

The Manubrium-limited Mini-sternotomy versus Conventional Sternotomy for Aortic Valve Replacement (MAVRIC) trial was a single centre, randomised controlled trial comparing patients undergoing AVR via manubrium-limited mini-sternotomy group and AVR via conventional sternotomy group [24,25].
Patients in the intervention arm received a manubrium-limited mini-sternotomy, performed using a 5-7cm midline skin incision dividing the manubrium from the sternal notch to 1cm below the manubrium-sternal junction. Cardiopulmonary bypass (CPB) was established with an ascending aortic cannula and percutaneous femoral venous cannulation. Those in the usual care arm received conventional median sternotomy.
The primary outcome was the proportion of patients who received a red cell transfusion post-operatively and within 7 days of AVR surgery.
The trial reported that mini-sternotomy was not found to be superior to conventional sternotomy with respect to red cell transfusion requirements within 7 days of surgery. The proportion of patients receiving red cell transfusion transfusions was 23 of 135 in both groups, Odds ratio 1.0 (95% CI: 0.5, 2.0) and risk difference of 0.0 (95% CI: -0.1, 0.1). However, secondary endpoints showed that there was a statistically significant difference with respect to transfusion volumes of non-red cell blood components. Mini-sternotomy also resulted in a relative reduction in chest drain losses, however, higher blood loss in the conventional group did not translate into red cell transfusions. Patients in the mini-sternotomy group had significantly longer bypass and cross clamp times and worse lung function at 4 days post-surgery. Lung function at twelve weeks, and adverse event rates were otherwise not different between groups.

Mini-Stern Trial

Mini-Stern was a multi-centre, open-label, pragmatic randomized controlled trial with a primary end-point of postoperative length of hospital stay and time to fitness for discharge. In total, 222 patients were randomised, finding that mini-sternotomy patients had no difference in length of stay (median 7 (interquartile range [IQR] 6 – 10) vs 7 (IQR 6 – 10), p=0.692) and no difference in time to fitness for discharge (median 5 (IQR 5 – 10) vs median 6 (IQR 5 – 9), p=0.560). Mini-sternotomy was £1719 more expensive per patient compared to full sternotomy in the first year following surgery. There was no significant difference in EQ-5D based quality adjusted life years (QALYs) and therefore at a willingness to pay threshold of £20,000 per QALY, there was only a 3.7% chance that mini-sternomy was cost-effective.

Current Meta-Analysis

As of August 2021, there were fourteen published randomised controlled trials of 1395 participants comparing hemisternotomy with full median sternotomy, due to be published shortly as an update of the previous Cochrane review. Countries of origin included Austria, Czech Republic, Spain, Italy, Germany, France, Egypt, Russia, Sweden, Serbia and the United Kingdom [26,27,28,29,30,31,32,33,34,35,36,37,38,39]. All but one were single-centre studies of elective, isolated aortic valve replacements, typically excluding patients with poor left ventricular function. The European studies were predominantly focused on patients with degenerative heart valve disease, and therefore an older population, whereas the study from Egypt included younger patients, presumably with rheumatic heart disease. Surgical strategy was broadly similar between studies, with aortic arterial cannulation and either central or femoral venous cannulation. Venting strategies – often considered a source of concern in minimally invasive aortic valve replacement due to potential compromises in bloodless field, de-airing or left ventricular decompression – were variable.
The risk ratio for peri-operative mortality was 0.93 (95% confidence interval [CI] 0.45 – 1.94, in 10 studies, but with low certainty). The mean difference in cardiopulmonary bypass time was 10.7 minutes longer with ministernotomy (95% CI 3.3 – 18.0 in 10 studies, but with very low certainty). The mean difference in aortic cross-clamp time was 6.1 minutes longer with ministernotomy (95% CI 0.8 – 11.3 across 12 studies, but also with very low certainty). Even in the context of the uncertainty, these mean differences in extra-corporeal circulation and ischaemic times are likely to have very little clinical impact. Exclusion of one trial [31] where rapid deployment valves were used to facilitate expedient surgery in the minimally invasive arm only, and not in the full sternotomy arm, did not impact the findings of the small increase in bypass and cross-clamp times.
There was a modest reduction in length of stay in patients undergoing mini-sternotomy (mean difference 1.1 days less (95% CI -1.9 to -0.3 days across 11 studies with very low certainty). It is important to note that for most of these studies, trial protocols were not published a priori or at all. Outcome measures such as hospital length of stay, which might be contingent on different criteria between studies and which were considered at high risk of bias from blinding, were not directly comparable. Similar issues arose with intensive care length of stay which, in studies at low risk of bias, was marginally lower with minimally invasive surgery (-0.45 days, 95% CI -0.84 to -0.06).
In-hospital pain assessments were also no different between minimally invasive or full sternotomy (standardized mean difference -0.19 for minimally invasive, 95% CI -0.43 to 0.04 with low certainty). Equally, there was no difference in quality of life measures after discharge from hospital (mean difference 0.03, 95% CI 0.00 to 0.06 across 4 studies with low certainty). Finally, pulmonary function tests – considered a surrogate marker for comfort and capability following disruption of the thoracic skeleton – were also minimally different between the two approaches (mean difference 2.1% higher with mini-sternotomy, 95% CI 0.74 to 3.41).
This new meta-analysis would appear to demonstrate that ministernotomy aortic valve replacement is as safe as full-sternotomy surgery, but with few of the anticipated advantages to pain, quality of life or breathing that are cited as reasons to have minimally invasive surgery. Length of stay in hospital and on the intensive care unit were modestly better with minimally invasive surgery, but at an increased cost over standard of care.

2.1.2. Right Anterior Mini-thoracotomy

The Right Anterior mini-Thoracotomy (RAT) approach, using central cannulation, was first described by Rao and Kumar in 1993 [40]. Cosgrove and Sabik first applied the term “minimally invasive” to a 10cm thoracotomy with excision of two costal cartilages, utilising femoral bypass [41]. The main advantage of this approach is the absolute preservation of sternal integrity and the absence of lateral traction, similar to the parasternal approach described by Cohn [42]. The corollary to these benefits is the need for femoral cannulation because of the limited access, necessitating a second incision in the groin and retrograde perfusion, which may offset the cosmetic advantage, quality of life and satisfaction with minimally invasive surgery [43]. A rate of 1% non-union of the transected ribs may also cause intractable post-thoracotomy pain.
Figure 3. Schematic of right anterior minithoracotomy through second intercostal space.
Figure 3. Schematic of right anterior minithoracotomy through second intercostal space.
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Initially, meta-analyses found RAT to have shorter hospital stays compared to hemi-sternotomy [44,45], despite higher rates of bleeding, transfusion and conversion to full sternotomy. A more recent comprehensive network meta-analysis of propensity matched and randomised studies compared full sternotomy, hemi sternotomy and right anterior mini-thoracotomy [46]. This found no difference in surgical time, hospital length of stay or ventilation time between the two minimally invasive approaches. As with previous meta-analyses, return to theatre for bleeding was more common with right anterior mini-thoracotomy compared to hemi-sternotomy (RR 1.65, 95% CI 1.18 – 2.30, p=0.003).
The network meta-analysis included 42 studies, including 29 propensity matched studies and 13 randomised controlled trials. The majority compared median sternotomy to hemisternotomy, with 9 comparing RAT to full sternotomy and 2 comparing RAT to hemisternotomy. Of note, only one randomized study evaluated RAT, so much of the evidence was observational, albeit adjusted with propensity matched techniques. Again, the majority of the included studies were European in origin, and methodological quality was fraught with uncertainty. The fact that this study identified a significant peri-operative mortality advantage of hemi-sternotomy over median sternotomy (relative risk (RR) 0.60, 95% CI 0.41 – 0.90) or RAT (RR 0.50, 95% CI 0.27 – 0.97) should be interpreted with caution. A meta-analaysis of randomised trials with didactic scrutiny of methodology and quality found no difference in mortality between hemi-sternotomy and full-sternotomy [23]. There exists, too, little rationale to explain why hemi-sternotomy should reduce mortality; indeed, all plausible mechanisms for a mortality difference between minimally invasive aortic valve replacement might suggest that minimal access approaches are at higher risk than conventional surgery for peri-operative mortality. It is our interpretation, therefore, that while the network meta-analysis favours hemi-sternotomy as the access of choice for aortic valve surgery (over both full sternotomy and right anterior mini-thoracotomy), the evidence to support this is scant.
The authors of a recent consensus statement [47] acknowledged the increased technical challenge of a right anterior mini-thoracotomy approach. Additional equipment such as thoracosopes, long-handled instruments and soft tissue retractors require specific training. Cost comparisons vary across publications. In some, the need for additional equipment and consumables increases the costs of RAT up to US$4209 higher than full sternotomy, compared to US$290 more for hemisternotomy [48,49]. In others, the costs of RAT is between US$1891 to US$3887 lower when propensity matched across real-world registry data [50,51].
The right anterolateral mini-thoracotomy (in the third intercostal space) can be used to perform multiple valve replacements, including the aortic, mitral and tricuspid valves [52,53,54].
Table 1. Advantages and disadvantages of aortic valve surgery approaches.
Table 1. Advantages and disadvantages of aortic valve surgery approaches.
Full sternotomy Hemi-sternotomy Right anterior minithoracotomy
Access Unfettered view to whole mediastinum and whole heart Good access to aortic root, limited to whole heart Most challenging view
Sternal disruption Whole sternum To 2nd – 4th intercostal space unilaterally or bilaterally None, although costal cartilages sometimes divided (may include right mammary artery ligation)
Cannulation Full central Variable – from full central to aortic arterial only Typically requires peripheral cannulation
Instruments Standard cardiac Variable – can be standard or long-handled Typically requires long-handled
Technical difficulty Baseline Learning curve easily traversed, including for trainee surgeons Accepted to be technically challenging
Adjuncts Required None Variable – possible with standard equipment. Facilitated by rapid deployment valves, suture placement devices and knot tying devices Facilitated by rapid deployment valves, suture placement devices and knot tying devices.
Light source advantageous.
Single lung ventilation.
Benefits (from most recent meta-analyses) * Reduced intensive care and hospital length of stay;
Reduced ventilation time
Reduced hospital length of stay;
Reduced ventilation time;
Lower stroke rate;
Lower pacemaker rate
Risks * Increased operative time;
Increased costs
Increased operative time;
Increased costs (including vs ministernotomy)
* compared to median sternotomy unless stated otherwise.

2.1.4. Hybrid approach (Sternotomy + Transcatheter Aortic Valve Implantation)

While strictly not minimal access, and ostensibly not minimally invasive, patients not fit for conventional aortic valve replacement who also require coronary artery revascularization may benefit from lower invasiveness using a hybrid approach. Sternotomy may be performed in order to undertake off-pump coronary artery bypass grafting, with concomitant trans-aortic or trans-femoral TAVI. The avoids the sequelae of cardiopulmonary bypass in patients who may not tolerate it, while still allowing complete revascularization and management of aortic stenosis [55,56,57].

2.2. Cannulation and Cardiopulmonary Bypass

2.2.1. Central

Hemi-sternotomy to the third or fourth space usually provides sufficient access to the aorta and right atrium to cannulate for arterial inflow and venous drainage centrally. The right superior pulmonary vein may or may not be accessible with this approach. Standard cannulae may be used, although to aid retraction of the pipes out of the field of view, some surgeons prefer angled venous pipes or a flat/low-profile cannula. Vacuum-assist can also help to improve the venous drainage.

2.2.2. Peripheral

Where the incision limits the access to the aorta, there may only be space in the surgical field for the cross clamp, cardioplegia site and aortotomy. In this case, peripheral cannulation, typically at the femorals, is utilized. Percutaneous methods are possible, but direct surgical access is the more commonly performed approach. Complications arising from groin cannulation may occur in 10.8% of cases, with seromas in up to 5% [48].

2.2.3. Hypothermia and systemic hyperkalaemia

In the context of re-operative minimal access surgery, systemic hypothermia to 20oC along with systemic hyperkalaemia at 7mmol/L can support myocardial protection in the presence of patent left internal mammary bypass grafts [58]. This requires ultrafiltration on cardiopulmonary bypass following cardiac reperfusion. Retrograde flooding of the field from the left coronary ostium in the presence of an unclamped left internal mammary graft can be mitigated for by use of intermittent circulatory arrest to facilitate suture placement, or with peri-operative percutaneous balloon occlusion of the left internal mammary by cardiology.

2.2.4. Venting (and imaging)

Reduced access to the left ventricle for inspection or manual decompression mandates the use of a trans-oesophageal echo during minimally invasive aortic valve surgery. Where this may be omitted in special circumstances in conventional sternotomy, such as oesophagectomy or oesophageal stricture, the risks are much greater in minimal access surgery where the left ventricle cannot be directly assessed.
Dependent on the level of access, left ventricular venting can be achieved in different ways including:
  • Right superior pulmonary vein
  • Pulmonary artery
  • Trans-aortic
Access to the pulmonary veins is typically not possible except in larger partial sternotomy approaches (i.e. fourth intercostal space). The pulmonary artery is usually easily accessible, although the visualization reduces considerably once the cross-clamp is removed. Access further deteriorates off cardiopulmonary bypass and therefore it is imperative to achieve haemostasis of the vent site early. The trans-aortic vent approach is usually sufficient to provide a bloodless field for surgery, but is limited should venting be required during reperfusion as the left ventricle cannot be reached manually.

2.3. Adjuncts

2.3.1. Rapid deployment valves

Sutureless and rapid deployment valves have been described as obvious companions for minimal access aortic valve replacement, to mitigate for the increased cardiopulmonary bypass and cross-clamp times that are otherwise seen [31,59].

2.3.2. Automatic suture / knotting devices

Automatic suture placement or knotting devices reduce invasiveness in minimal access valve surgery by expediting valve implanatation and therefore reducing cross-clamp and cardiopulmonary bypass time [60]. The use of the Cor-Knot ® device (LSI Solutions, Victor, NY) for valve surgery was noted to also lead to more reproducible valve implanation with lower rates of paravalular leak [61]. The same manufacturer has also released an automated annular suturing device to expedite this stage of valve implantation, but there are no published series to show that this is effective yet.

2.3.3. Transvenous pacing, cannulation and venting

A variety of options exist for percutaneous support of cardiopulmonary bypass from the right jugular. These include:
  • Transvenous pacing can be floated using an inflatable balloon tip into the right ventricle for endocardial pacing if the anterior right ventricle is not accessible
  • Coronary sinus cannulation via the right internal jugular was previously possible using the Proplege device (Edwards LifeSciences, Irvin, CA) but as the strategies for antegrade cardioplegia alone showed good efficacy, this is no longer available
  • Pulmonary artery venting through a percutaneously floated catheter has again lost favour as trans-aortic and direct pulmonary artery or pulmonary vein venting have been shown to be efficacious and safe

2.3.4. Thoracoscopes

Direct visualization of the aorta (sufficient to apply a cross-clamp), aortic valve and aortic annulus is possible through both hemi-sternotomy and right anterior mini-thoracotomy approaches. Thoracoscopes can also be utilized to improve light and view for areas that might be more difficult to see due to overhanging thoracic cage. Use of scopes for lighting and/or transmitted video images may, however, limit access for instruments in some cases. This can in part be mitigated for by use of other adjuncts such as automatic suture placement or knotting devices [47].

2.3.5. Robot assistance

Robotic aortic valve replacement has been attempted since 2004 [62], with a renewed interest in recent years [63]. In place of either hemi-sternotomy or right anterior mini-thoractomy, a right lateral mini-thoracotomy is utilized as the working port, along with 4 arms, which spares division of the costal cartilage or sacrifice of the right internal mammary artery. This has the advantage of an intact thoracic skeleton, superior visualization and virtually unrestricted range of movement in the working space, but with a steep learning curve, high capital investment costs and ongoing consumable expenditure.

2.4. Special circumstances

2.4.1. Concomitant procedures

As minimal access incisions have gained favour, indications for the procedures amenable to this approach have expanded. The hemi-sternotomy approach has been successfully utilized for aortovascular procedures including valve sparing root replacement [64]

2.4.2. Re-do procedures

Previous sternotomy, even in the presence of patent coronary artery bypass grafts, is not a contraindication to a minimally invasive approach. These can be performed with low-conversion rates of 2.6% [58]. Minimisation of the dissection and mobilization of the heart mean that bleeding complications are low. Technical challeges from the presence of patent grafts may require alternative strategies for cardioplegic arrest (including systemic hyperkalaemia, deeper hypothermia and brief periods of circulatory arrest).

2. Minimal Access Pre-operative planning / setup

Additional assessment and preparation is required for minimal access aortic valve surgery. These requirements vary depending on the approach adopted and not all practitioners employ all these steps.
  • CT scan pre-operatively can allow assessment of the position of the aorta relative to the incision planned. If peripheral cannulation is intended, this can also determine if the femoral vessels are adequate calibre and the descending aorta free of mobile atheroma that may preclude retrograde perfusion.
  • Short acting anaesthetic drugs should be considered to facilitate early extubation and enhanced recovery.
  • A sheath in the right internal jugular vein can be introduced at the time of induction of anaesthesia if the usual access limits epicardial pacing wires.
  • A bag of saline behind the shoulder blades can elevate and expand the chest, providing an improved approach to the mediastinum.
  • External defibrillator pads are required to cardiovert ventricular fibrillation as internal paddles cannot be applied to the heart
  • Trans-oesophageal echocardiography is mandated for minimally invasive aortic valve surgery as the direct visualization of the right and left ventricular function is impaired
  • Double lumen tube or bronchial blocker for selective ventilation of the right lung can facilitate the early learning curve [65].
  • Carbon dioxide field flooding can aid de-airing at the end of the case where cardiac massage is not possible and venting is limited. Passive and limited active de-airing can therefore be supplemented with displacement of air in the cardiac chambers with highly soluble CO2.

3. Outcomes

It is unlikely that minimally invasive methods of aortic valve surgery would have been permitted to develop if peri-operative mortality was not equivalent to conventional full sternotomy. While the excellent current outcomes for isolated aortic valve replacement mean that most series do not have sufficient power to demonstrate a difference, it is apparent that there is no excess mortality.
Some credence has been placed on minimal access surgery to therefore also improve outcomes in other areas in order to justify the technical challenege and increased costs.

3.1. Pain

For studies that examined post-operative pain scores between minimal-access and full-sternotomy surgery, there was considerable bias in the reporting [23]. Protocolised analgesic pathways were seldom cited and blinding was only utilised in one trial. The timing of pain score assessments also varied considerably between studies. The overall assessment following review was that minimal access aortic valve surgery did not reduce pain compared to sternotomy.

3.2. Respiratory Mechanics

The impact of full median sternotomy on respiratory function following surgery is often cited as a reason to favour minimal access approaches. While there might be small differences in peri-operative lung function parameters between non-sternotomy and full-sternotomy approaches, the main advantage to respiratory mechanics came in time to return-to-baseline. For partial sternotomy, this was one month, whereas for full sternotomy this was up to three months [66].

3.3. Quality of Life

Five randomised controlled trials studied quality of life following surgery. Between 6-12 weeks following operation, there was no difference in the quality of life scores between hemi-sternotomy and full-sternotomy [23].

4. Discussion

Chitwood’s prediction (or aspiration) that cardiac surgery would culminate in routine minimally invasive approaches that would emulate general surgery’s day-case model still seem very distant a quarter of century on. The benefits of minimal access surgery have not been realized as predicted and in the intervening decades, transcatheter techniques have improved and expanded their remit to low-risk patients [67]. Cost-effectiveness of percutaneous methods has also improved, such that TAVI procedures are now competitive against surgical valves [68].
In the absence of demonstrable superiority, there is therefore more incentive than ever to propagate minimal access approaches to aortic valve replacement. Where these procedures can be done with minimal or no additional equipment, at similar cost and with no increase in complications, the new standard should surely be the procedure with the same outcomes, same costs… and a smaller incision?
The current state of the art in minimal access aortic valve surgery is advanced. Even in groups such as octogenarians, re-do operations and root/ascending aorta replacement, the results for minimal access aortic surgery can be excellent [69]. The procedure is reproducible and can be undertaken by surgeons in training without compromise to patient safety [70]. Peri-operative and one-year mortality are no different in a real-world setting and length of stay is typically reduced using a minimal-access approach [71].
As transcatheter aortic valve implantation also gathers momentum, gaining approval for increasingly lower-risk patient groups, there is a need to ensure that patients are provided with procedures of good pedigree. Surgeons looking to mitigate for the increased operative times of minimally invasive aortic valve replacement may turn to sutureless aortic valves, which draw parallels with transcatheter valves. Where TAVI valves have higher rates of paravalvular leak, pacemaker implantation and vascular complications [72], however, sutureless valves can offer the advantage of full decalcification and placement under direct vision. Whether these benefits offset the need for thoracic cage disruption and cardiopulmonary bypass and cross-clamping remains to be seen, particularly in the small or calcified root.
Further research is also still required to elucidate the differences between hemi-sternotomy and right anterior minithoracotomy. The former remains the more accessible minimally invasive approach, with familiar setup, angles and equipment to those trained in conventional full sternotomy. Proponents of the right anterior mini-thoractomy, however, will argue that if a partial-sternotomy is superior to a full-sternotomy, it stands to reasons that no sternotomy should be better still. However, it remains to be compellingly proven that the additional challenges of RAT do not neutralize the benefits provided of maintaining the sternum fully intact. Current syntheses of the existing literature are disparate in their conclusions.
Future directions for this procedure involve ensuring that it is, indeed, developed as the new standard of care for aortic valve procedures. Once this is accepted universally, the process of reducing invasiveness as well as access can be developed. Enhanced Recovery After Surgery (ERAS) have been slow to be adopted in cardiac surgery in general and much less in minimal access cardiac surgery. Protocols are needed for patients with reduced incisions that differ to those used for conventional surgery, and might meaningfully engage and utilize the operative advantages to expedite the patient journey more effectively [73].

5. Conclusions

Minimal access aortic valve surgery is at a watershed moment where it could plausibly become the new standard of care for aortic valve disease, as laparoscopic procedures have become for general surgery. Economic viability will need to be demonstrated in order for this to happen, but moreover, a surgical appetite must grow for non-inferior procedures where benefits are still being developed and demonstrated.

Author Contributions

All authors contributed to the writing and editing and have read and agreed to the published version of the manuscript.

Funding

The Article Processing Charge for this review was waived by Journal of Cardiovascular Development and Disease

Informed Consent Statement

Not applicable for this review.

Data Availability Statement

No new research data was generated for this review.

Conflicts of Interest

Declare conflicts of interest or state “The authors declare no conflict of interest.” Authors must identify and declare any personal circumstances or interest that may be perceived as inappropriately influencing the representation or interpretation of reported research results. Any role of the funders in the design of the study; in the collection, analyses or interpretation of data; in the writing of the manuscript; or in the decision to publish the results must be declared in this section. If there is no role, please state “The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results”.

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Figure 1. Hemisternotomy incision.
Figure 1. Hemisternotomy incision.
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Figure 2. Schematic of chevron shaped hemi-sternotomy into bilateral second intercostal spaces.
Figure 2. Schematic of chevron shaped hemi-sternotomy into bilateral second intercostal spaces.
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