Minimally invasive reoperative aortic valve replacement: a systematic review and meta-analysis
Systematic Review

Minimally invasive reoperative aortic valve replacement: a systematic review and meta-analysis

Kevin Phan1,2, Jessie J. Zhou1, Nithya Niranjan1, Marco Di Eusanio1,3, Tristan D. Yan1,4

1The Collaborative Research (CORE) Group, Macquarie University, Sydney, Australia; 2Westmead Hospital, Sydney Medical School, University of Sydney, Sydney, Australia; 3Cardiovascular Surgery Department, Sant’Orsola-Malpighi Hospital, Bologna University, Bologna, Italy; 4Department of Cardiothoracic Surgery, Royal Prince Alfred Hospital, University of Sydney, Sydney, Australia

Correspondence to: Tristan D. Yan. Professor of Cardiovascular and Thoracic Surgery, The Collaborative Research (CORE) Group, Macquarie University, Sydney, Australia. Email:

Background: With prolonged life expectancy and more frequent use of biological prostheses, an increasingly higher proportion of patients are undergoing aortic valve replacement (AVR) after previous sternotomy. We critically appraised the quantity and quality of evidence to demonstrate the efficacy and safety of the minimally invasive (MIrAVR) versus conventional (CrAVR) approaches for reoperative AVR.

Methods: Electronic searches were performed using six databases from their inception to April 2014. Relevant studies utilizing a MIrAVR were identified. Data were extracted and analyzed according to predefined clinical endpoints.

Results: Four single-arm and seven comparative observational studies including a total of 441 MIrAVR patients were included for quality assessment, data extraction and analysis. In-hospital mortality ranged from 0-9.5%, and was similar between the MIrAVR and CrAVR groups (RR, 0.77; 95% CI, 0.39-1.54; P=0.46). Stroke rates ranged from 2.6-8% and were also similar between the two cohorts. The rates of pacemaker implantation, renal failure and reoperation for bleeding were not significantly different between the two groups. There were no reports of myocardial infarctions in the included studies. No significant difference in hospital stay was observed for the MIrAVR versus CrAVR group.

Conclusions: The current literature suggests that MIrAVR has similar efficacy and mortality outcomes compared to CrAVR without compromise to myocardial protection or hospitalization duration. It appears to be a valid alternative option for patients requiring reoperative AVR.

Keywords: Minimally invasive; aortic valve replacement (AVR); reoperative; systematic review

Submitted Jul 13, 2014. Accepted for publication Jul 20, 2013.

doi: 10.3978/j.issn.2225-319X.2014.08.02


Given extended life expectancies and improved survival rates of modern procedures, there is an increasing number of patients undergoing reoperative cardiac surgery (1). Conventional reoperative aortic valve replacement (CrAVR) is particularly challenging, often due to severe calcified aortic stenosis following previous sternotomy for coronary artery bypass grafting (CABG) (2) or degeneration of aortic bioprostheses (3). These complicated cases are often associated with prolonged cross-clamp and cardiopulmonary bypass durations, increased blood loss and poorer survival rates (4,5).

Minimally invasive rAVR (MIrAVR) is an alternative approach to conventional sternotomy with comparable mortality rates but reduced hospitalization, intensive care stay and improved cosmesis (6). While minimally invasive valvular surgery is becoming increasingly accepted for primary operations, MIrAVR has not been well defined. MIrAVR may be advantageous in avoiding large, open dissections, minimizing trauma and reducing injury to cardiac structures such as previous patent grafts (7,8), while still having the benefits of reduced intensive care and hospital stay. On the other hand, MIrAVR procedures are technically more demanding for the operating surgeon and myocardial protection may be a concern (9), especially in patients with patent coronary artery bypass grafts. A systematic review and meta-analysis was carried out to assess the current evidence on the efficacy and safety of MIrAVR versus CrAVR.


Literature search strategy

Electronic searches were performed using Ovid Medline, PubMed, Cochrane Central Register of Controlled Trials (CCTR), Cochrane Database of Systematic Reviews (CDSR), ACP Journal Club, and Database of Abstracts of Review of Effectiveness (DARE) from their date of inception to April 2014. To achieve the maximum sensitivity of the search strategy, we combined the terms: “minimally invasive OR ministernotomy OR hemisternotomy OR partial upper sternotomy OR minithoracotomy” AND “aortic valve replacement OR AVR” AND “reoperative OR redo OR resternotomy” as either key words or MeSH terms. The reference lists of all retrieved articles were reviewed for further identification of potentially relevant studies, assessed using the inclusion and exclusion criteria. Expert academic cardiothoracic surgeons (M.D.E, T.D.Y) were consulted as to whether they knew of any unpublished data.

Selection criteria

Eligible studies for the present systematic review and meta-analysis were those in which patient cohorts underwent MIrAVR after a previous sternotomy and operation. Studies that did not include mortality or complications as endpoints were excluded. When institutions published duplicate studies with accumulating numbers of patients or increased lengths of follow-up, only the most complete reports were included for quantitative assessment at each time interval. All publications were limited to those involving human subjects and in the English language. Abstracts, case reports, conference presentations, editorials, reviews and expert opinions were excluded.

Data extraction and critical appraisal

All data were extracted from article texts, tables and figures. Two investigators independently reviewed each retrieved article (K.P, J.J.Z). Discrepancies between the two reviewers were resolved by discussion and consensus (K.P, J.J.Z, N.N). If the study provided medians and interquartile ranges instead of means and standard deviations (SDs), we imputed the means and SDs as described by Hozo et al. (10). As quality scoring is controversial in meta-analyses of observational studies, two reviewers (K.P, J.J.Z) independently appraised each article using the criteria for case series quality assessment recommended by the National Health Service Center for Reviews and Dissemination (11) (University of York, Heslington, United Kingdom). The final results were reviewed by senior investigators (M.D.E, T.D.Y).

Statistical analysis

The relative risk (RR) was used as a summary statistic. In the present study, both fixed- and random-effect models were tested. In the fixed-effects model, it was assumed that the treatment effect in each study was the same, whereas in the random-effects model, it was assumed that there were variations between studies. χ2 tests were used to study heterogeneity between trials. The I2 statistic was used to estimate the percentage of total variation across studies, owing to heterogeneity rather than chance, with values greater than 50% considered as substantial heterogeneity. If there was substantial heterogeneity, the possible clinical and methodological reasons for this were explored qualitatively. In the present meta-analysis, the results using the random-effects model were reported to take into account the possible clinical diversity and methodological variation between studies. Specific analyses considering confounding factors were not possible because raw data were not available. Data are presented as means ± SD. Weighted means (WM) were calculated by determining the total number of events divided by total sample size. Pearson’s statistic was used to calculate correlation for meta-regression meta-analysis. All P values were 2-sided. All statistical analysis was conducted with Review Manager Version 5.2.1 (Cochrane Collaboration, Software Update, Oxford, United Kingdom) and the metafor package for R version 3.01.


Literature search

A total of 685 references were identified through the six electronic database searches (Figure 1). After exclusion of duplicate or irrelevant references, 566 potentially relevant articles were retrieved. After detailed evaluation of these articles, 27 studies remained for assessment. After applying the selection criteria, 11 articles (7,8,12-20) were selected for qualitative analysis. Of these, 7 observational studies (7,8,14,15,17,19,20) were included for quantitative analysis. The study characteristics are summarized in Table 1. Of the 11 included articles, 441 patients underwent rAVR via a MIrAVR, and 1,145 patients via the conventional sternotomy approach. Baseline patient characteristics and myocardial protection strategies are summarized in Tables 2 and 3, respectively.

Figure 1 PRISMA search strategy for the present systematic review and meta-analysis.
Table 1
Table 1 Summary characteristics of included studies in the present systematic review and meta-analysis
Full table
Table 2
Table 2 Baseline characteristics of patients undergoing reoperative aortic valve replacement via a minimally invasive approach
Full table
Table 3
Table 3 Myocardial protection strategies for included studies
Full table

Quality appraisal

All included studies except one (15) were retrospective, observational studies, seven of which had comparative control groups. There were four studies which included greater than 50 patients undergoing rAVR by a MIrAVR (7,14,15,17), while seven studies assessed fewer than 50 patients (8,12,13,16,18-20). A partial upper sternotomy or ministernotomy approach for resternotomy was used in eight studies (7,8,13,14,16-18,20) (n=302, while a minithoracotomy approach was employed by three studies (12,15,19) (n=139). Only five studies reported mean or median follow-up, which were all greater than or equal to 24 months (7,14,16,18,19).

The cardioplegia strategy was reported in all included studies, with three studies using retrograde approach (7,11,18), two studies using antegrade approach (16,19), five studies using the combined approach (6,12,14,15,17), and one study using either approach (13). Temperatures used during cardiopulmonary bypass (CPB) were reported in all included studies except for two (12,17). CPB duration was reported in all but three studies (12,13,15), while cross-clamp duration was not reported in three studies (13,15,17). In-hospital mortality was reported in all included studies. Stroke outcomes were reported in seven studies (7,13,14,16,18-20), reoperations for bleeding in six studies (7,14,16,18-20) and myocardial infarctions in four studies (13,14,18,20). The percentage of patients with previous coronary bypass grafting (CABG) operations was reported in seven studies (7,8,14,16,18-20).

Assessment of mortality and morbidity

In-hospital mortality outcomes are outlined in Table 4, with a WM of 4.1% (range: 0-9.5%) for the 11 included studies. Seven comparative observational studies investigating rAVR via MIrAVR versus CrAVR were available for meta-analysis. The risk of in-hospital mortality was not significantly different between MIrAVR and CrAVR groups (3.8% vs. 5.4%; RR, 0.77; 95% CI, 0.39-1.54; P=0.46; I2=17%; Figure 2). There was also a significant negative correlation between midpoint of study period and in-hospital mortality (r2=0.6884; P=0.021; Figure 3).

Table 4
Table 4 Assessment of morbidity and mortality in reoperative aortic valve replacement via a minimally invasive approach
Full table
Figure 2 Forest plot of the relative risk of in-hospital mortality after minimally invasive reoperative aortic valve replacement (MIrAVR) versus conventional reoperative aortic valve replacement (CrAVR).
Figure 3 Bubble chart showing correlation between the midpoint of the study period and in-hospital mortality rate. Studies with n ≤20 and with mixed concomitant valve and arch surgery were excluded. The solid line indicates the correlation trend line, while dotted lines indicate the 95% confidence interval.

The rates of stroke ranged from 2.6-8%, with a WM of 5.7%. Meta-analysis also showed similar rates of stroke between MIrAVR and CrAVR cohorts (5.9% vs. 3.2%; RR, 1.88; 95% CI, 0.75-4.68; P=0.18; I2=0%; Figure 4). No myocardial infarctions were reported by the included studies. The WM incidence of renal failure was 2.3% (range: 0-5.3%), and this was not significantly different between MIrAVR versus CrAVR (1.3% vs. 5.7%; RR, 0.33, 95% CI, 0.10-1.04; P=0.06; I2=0%). Reoperation for bleeding ranged from 0-21%, but was not significantly different between MIrAVR and CrAVR cohorts (3.0% vs. 4.4%; RR, 0.72; 95% CI, 0.25-2.06; P=0.55; I2=21%). Blood transfusion requirements were reported in three studies, with a WM of 56.2% (range: 0-72%). Pacemaker implantation requirements ranged from 0-10.5%, while wound infection occurred in a WM of 1.5% of cases (range: 0-5.3%). Hospital stay duration was reported by eight studies, and ranged from 6.9-12.9 days (WM: 8.5 days). Intensive care unit (ICU) stay duration was reported by seven studies, and ranged from 1.1-3 days (WM: 2.1 days). No difference in ICU stay was observed between MIrAVR versus CrAVR cohorts. Hospital stay was also similar for the MIrAVR versus CrAVR group (WMD, −0.62 days; 95% CI, −2.20-0.96; P=0.44; I2=91%; Figure 5).

Figure 4 Forest plot of the relative risk of perioperative stroke after minimally invasive reoperative aortic valve replacement (MIrAVR) versus conventional reoperative aortic valve replacement (CrAVR).
Figure 5 Forest plot for the mean difference in length of hospital stay after minimally invasive reoperative aortic valve replacement (MIrAVR) versus conventional reoperative aortic valve replacement (CrAVR).

Assessment of operative outcomes

Cross-clamp duration ranged from 51-93 minutes, with a WM of 78.4 minutes. CPB duration ranged from 67-156 minutes, with a WM of 133.6 minutes. No significant difference between MIrAVR and CrAVR was observed for cross-clamp duration (P=0.67; Figure 6) or CPB duration (P=0.40; Figure 7). The rate of conversion was low, with a WM of 0.9%, ranging from 0-2.8%. The proportion of patients using aortic, femoral arterial, femoral venous and right atrial cannulation is reported in Table 5.

Figure 6 Forest plot for the mean difference in cross-clamp duration with minimally invasive reoperative aortic valve replacement (MIrAVR) versus conventional reoperative aortic valve replacement (CrAVR).
Figure 7 Forest plot for the mean difference in cardiopulmonary bypass duration with minimally invasive reoperative aortic valve replacement (MIrAVR) versus conventional reoperative aortic valve replacement (CrAVR).
Table 5
Table 5 Operative outcomes of patients undergoing reoperative aortic valve replacement via a minimally invasive approach
Full table


Reoperative aortic valve surgery represents a surgical challenge associated with increased mortality rates and complications (21). This is particularly pertinent for patients with previous sternotomy for CABG operations, where injury to patent grafts represents a serious concern (8). In this setting, the MIrAVR may avoid hazardous tissue dissections and reduce surgical trauma but is more technically demanding and potentially associated with sub-optimal myocardial protection strategies (7,9). The safety and efficacy of MIrAVR were investigated in the present meta-analysis and systematic review.

While comparable mortality rates and complications have been reported for MIrAVR and CrAVR, the outcomes for rAVR are not well established. From the results of the present meta-analysis, in-hospital mortality was not found to be significantly different between MIrAVR and CrAVR groups. Mortality rates ranged from 0-9.5% for the MIrAVR. The in-hospital mortality rates also negatively correlated with the midpoint of the study period, suggesting improvement in survival outcomes over time (Figure 3), a trend that may continue in the future. This may be partially explained by the learning curve associated with minimally invasive techniques, with lower mortality rates reported in recent years (0-3.9%). The incidences of stroke were also comparable between the MIrAVR and CrAVR cohorts (5.9% vs. 3.2%; P=0.18 and were similar to values reported by previous meta-analyses on primary AVR cases. While it is expected that the reduced invasiveness of MIrAVR would reduce reoperations required for bleeding and transfusions, there were no significant differences found between the cohorts, a result possibly attributable to the low statistical power and small sample size of the included studies. No significant reduction in hospital stay was noted in the MIrAVR group. Overall, MIrAVR appears to have comparable complication rates and length of stay compared with CrAVR, lending support to its role as a safe alternative to median sternotomy for reoperative AVR.

The procedural duration of AVR is of great clinical interest, as prolonged cross-clamp and CPB durations have been shown to be associated with inflammation and poorer surgical outcomes (22,23). In the present study, the cross-clamp and CPB durations were similar between minimally invasive and conventional sternotomy cohorts for rAVR. Considering limitations in both surgical vision and maneuverability in a limited working space, this outcome is unexpected. However, by minimizing the surgical isolation of the heart often completed on CPB during CrAVR, MIrAVR may reduce the overall CPB time. In addition, disparities in operational duration may also be mitigated with the evolution of technical skill and experience in minimally invasive surgery, traversing the initial learning curve phase. The introduction of sutureless AVR technologies will further obviate and alleviate the technical challenges involved in traditional AVR (24,25). Given that annular sutures do not need to be securely tied down to hold the valve in place, the sutureless approach facilitates smaller incisions and shorter cross-clamp, CPB and procedural durations, ideal for reoperations (26). However, it remains to be seen if these newer sutureless valve technologies are suitable for reoperative aortic valve operations.

The major concern in minimally invasive reoperations is the optimal myocardial protection strategy (8,9,20). Typically, the standard approach involves isolation and occlusion of patent CABG grafts, antegrade or retrograde cardioplegia infusion, and moderate or mild hypothermia. These conditions are easily met during conventional reoperative aortic valve surgery. However, during minimally invasive reoperative surgery, given the reduced surgical field of ministernotomy and minithoracotomy incisions, it is difficult to isolate and control internal thoracic artery (ITA) grafts during clamping (9). In these cases, an alternative approach is to leave patent grafts unoccluded, resulting in constant perfusion of the myocardium with oxygenated blood. Cardioplegia is well delivered and deeper levels of systemic hypothermia are used to compensate for the sub-optimal conductance of myocardial protection. As a result, perfect arrest is not always achieved, and with the heart still fibrillating, the risk of postoperative myocardial infarction becomes a serious concern. Notably, the present study showed the incidence of myocardial infarction to be nil in all studies. As such, the current evidence seems to suggest that, in carefully selected patients, such ‘no-touch’ (9) hypothermic cardioplegia provides acceptable myocardial protection. Furthermore, proponents of MIrAVR have also suggested that by avoiding dissection and occlusion of grafts, there is reduced risk of ITA injury and embolism due to manipulation of atherosclerotic vein grafts (8,13,19,27).


The current meta-analysis is limited by small, retrospective studies with inadequate statistical power, which may have underestimated complication rates. Resource-related outcomes such as economic costs, pain scores and quality of life outcomes were not reported by the included studies. The heterogeneity of cross-clamp and CPB outcomes, as well as hospitalization time, may be accounted for by considering the inherent variation in the patient populations, which comprise patients with a wide variety of previous cardiac operations. This ranged from prior CABG and patent grafts to prior sternotomy for AVR or mitral valve surgery with concurrent surgical ablation, with the latter known to have different postoperative outcomes (28,29).

Given the technical challenges involved in minimally invasive reoperative surgery, it is likely that the current evidence is based on outcomes from highly experienced expert surgeons at high-volume academic centers. As such, the current results may only be representative of carefully selected patient and surgeon populations, and may not be reproducible for surgeons with lesser experience. Variation in procedural outcome may also be due to inherent differences between the ministernotomy and minithoracotomy approaches employed. Furthermore, long-term outcomes were not available, making it difficult to comprehensively evaluate the comparative risks and benefits of MIrAVR and CrAVR. Given the promising data to date, future registry or prospectively randomized trials should be carried out to more definitively assess the MIrAVR.


Minimally invasive approaches to rAVR represent a potential alternative to median sternotomy, with similar mortality and morbidity outcomes, and adequate myocardial protection. MIrAVR appears to have acceptable outcomes in carefully selected patients, and these are likely to further improve with the learning curve of the procedure and emergence of sutureless valve technology. However, there remains a lack of robust clinical evidence and adequately powered, randomized studies are warranted to comprehensively evaluate the efficacy and safety of MIrAVR.


Disclosure: The authors declare no conflict of interest.


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Cite this article as: Phan K, Zhou JJ, Niranjan N, Di Eusanio M, Yan TD. Minimally invasive reoperative aortic valve replacement: a systematic review and meta-analysis. Ann Cardiothorac Surg 2015;4(1):15-25. doi: 10.3978/j.issn.2225-319X.2014.08.02

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