Surgical Treatment of Postinfarction Ventricular Septal Rupture
Daniele Ronco, Matteo Matteucci, Mariusz Kowalewski, Michele De Bonis, Francesco Formica, Federica Jiritano, Dario Fina, Thierry Folliguet, Nikolaos Bonaros, Claudio Francesco Russo, Sandro Sponga, Igor Vendramin, Carlo De Vincentiis, Marco Ranucci, Piotr Suwalski

TL;DR
Surgery for a heart condition called ventricular septal rupture after a heart attack has a high early death rate, and this hasn't improved in 20 years.
Contribution
A large international multicenter study reveals persistent high mortality and identifies risk factors for early death after surgical treatment of postinfarction ventricular septal rupture.
Findings
Early mortality rate after surgery for postinfarction ventricular septal rupture was 40.4% and did not improve over 20 years.
Older age, preoperative cardiac arrest, and postoperative need for mechanical support were independently associated with higher mortality.
Delayed surgery was linked to better survival, suggesting potential benefits of tailored preoperative and perioperative management.
Abstract
What are the early outcomes of surgical treatment of postinfarction ventricular septal rupture? In this cohort study of 475 patients from 26 different centers worldwide, the early mortality rate for surgically treated ventricular septal rupture was 40.4%, mostly due to low cardiac output, and it did not improve in the last 2 decades. The findings of this study suggest that patient-tailored preoperative and perioperative management of postinfarction ventricular septal rupture should be addressed to improve the current suboptimal survival rates. This cohort study assesses the clinical characteristics and early outcomes for patients who received surgery for postinfarction ventricular septal rupture and identifies factors independently associated with mortality. Ventricular septal rupture (VSR) is a rare but life-threatening mechanical complication of acute myocardial infarction…
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
Click any figure to enlarge with its caption.
Figure 1
Figure 2| Variable | Patients, No. (%) | |||
|---|---|---|---|---|
| All (N = 475) | Survived (n = 283) | Died (n = 192) | ||
| Age, mean (SD), y | 68.5 (10.1) | 66.8 (10.1) | 71 (9.7) | <.001 |
| Men | 290 (61.1) | 180 (63.6) | 110 (57.3) | .17 |
| Women | 185 (48.9) | 103 (36.4) | 82 (42.7) | |
| BMI, mean (SD) | 26.1 (4.1) | 25.9 (4.1) | 26.3 (4.1) | .26 |
| Hypertension | 278 (58.5) | 171 (60.4) | 107 (55.7) | .31 |
| Dyslipidemia | 152 (32) | 98 (34.6) | 54 (28.1) | .14 |
| Diabetes | 107 (22.5) | 60 (21.2) | 47 (24.5) | .40 |
| Stroke or TIA | 26 (5.5) | 13 (4.6) | 13 (6.8) | .31 |
| Smoking habit | 177 (37.3) | 115 (40.6) | 62 (32.3) | .07 |
| COPD | 42 (8.8) | 22 (7.8) | 20 (10.4) | .32 |
| Chronic kidney disease | 61 (12.8) | 28 (9.9) | 33 (17.2) | .02 |
| Peripheral vascular disease | 42 (8.8) | 29 (10.2) | 13 (6.8) | .19 |
| LVEF <45% | 205 (43.2) | 117 (41.3) | 88 (45.8) | .33 |
| Hemodynamic presentation | ||||
| Cardiogenic shock | 213 (44.8) | 95 (33.6) | 118 (61.5) | <.001 |
| Cardiac arrest | 46 (9.7) | 14 (4.9) | 32 (16.7) | <.001 |
| Cardiac tamponade | 21 (4.4) | 11 (3.9) | 10 (5.2) | .49 |
| Preoperative IABP | 273 (57.5) | 149 (52.7) | 124 (64.6) | .01 |
| Preoperative ECMO | 32 (6.7) | 13 (4.6) | 19 (9.9) | .02 |
| Preoperative revascularization | 158 (33.3) | 79 (27.9) | 79 (41.1) | .003 |
| Time to surgery ≥7 d | 152 (47.9) | 105 (57.4) | 47 (35.1) | <.001 |
| Surgical status | ||||
| Elective | 77 (16.2) | 55 (19.4) | 22 (11.5) | <.001 |
| Urgent | 186 (39.2) | 124 (43.8) | 62 (32.3) | |
| Emergent or salvage | 212 (44.6) | 104 (36.8) | 108 (56.2) | |
| Variable | Patients, No. (%) | |||
|---|---|---|---|---|
| All (N = 475) | Survived (n = 283) | Died (n = 192) | ||
| VSR site | ||||
| Anterior and apical | 235 (53.9) | 149 (58.7) | 86 (47.3) | .02 |
| Posterior | 201 (46.1) | 105 (41.3) | 96 (52.7) | |
| Concomitant postinfarction mechanical complications | 25 (5.3) | 13 (4.6) | 12 (6.3) | .43 |
| Repair technique | ||||
| Infarct exclusion | 78 (17.4) | 50 (19.1) | 28 (15 | .26 |
| Other techniques | 371 (82.6) | 212 (80.9) | 159 (85) | |
| CPB time, median (IQR), min | 137.0 (104.0-181.0) | 128.0 (98.0-169.5) | 152.5 (118.8-192.5) | .001 |
| ACC time, median (IQR), min | 90.0 (69.0-115.0) | 85.0 (67.3-112.8) | 95.5 (73.3-121.8) | .01 |
| Concomitant CABG | 235 (49.5) | 144 (50.9) | 91 (47.4) | .46 |
| Other concomitant procedures | ||||
| FWR or PMR repair | 21 (4.4) | 12 (4.2) | 9 (4.7) | .82 |
| Other procedures | 76 (16.0) | 48 (17.0) | 28 (14.6) | .49 |
| Postoperative inotropes | 364 (76.6) | 213 (75.3) | 151 (78.6) | .39 |
| Postoperative IABP | 303 (63.8) | 163 (57.6) | 140 (72.9) | .001 |
| Postoperative ECMO | 65 (13.7) | 23 (8.1) | 42 (21.9) | <.001 |
| Rethoracotomy for bleeding | 51 (11.1) | 20 (7.1) | 31 (17.6) | <.001 |
| Recurrent or residual VSR | 59 (12.9) | 33 (11.7) | 26 (14.8) | .33 |
| Requiring reoperation | 25 (5.4) | 15 (5.3) | 10 (5.7) | .86 |
| Not requiring reoperation | 34 (7.4) | 18 (6.4) | 16 (9.1) | .28 |
| Variable | Patients, No. (%) (N = 475) |
|---|---|
| Intraoperative mortality | 16 (3.4) |
| Ventilation time, mean (SD), d | 5.2 (8.3) |
| ICU stay, mean (SD), d | 11 (23) |
| Hospital stay, mean (SD), d | 23.4 (27.4) |
| In-hospital mortality | 192 (40.4) |
| Causes of death | |
| Intraoperative | 16 (8.3) |
| No CPB weaning | 11 (5.7) |
| Incontrollable bleeding | 5 (2.9) |
| Low cardiac output syndrome | 70 (36.5) |
| Multiorgan failure | 53 (27.6) |
| Recurrent or residual VSR | 8 (4.2) |
| Sepsis | 7 (3.6) |
| Arrhythmia | 6 (3.1) |
| Cerebrovascular accident | 6 (3.1) |
| Acute kidney injury | 6 (3.1) |
| Bowel infarction | 6 (3.1) |
| Free-wall rupture | 4 (2.1) |
| Acute myocardial infarction | 3 (1.6) |
| Pneumonia | 3 (1.6) |
| Unknown | 4 (2.1) |
| Postoperative complications | |
| Cardiac | |
| Low cardiac output syndrome | 115 (25.1) |
| Right ventricular failure | 29 (6.3) |
| Free-wall rupture | 5 (1.1) |
| Cardiac tamponade | 16 (3.5) |
| Atrial fibrillation | 48 (10.5) |
| Pacemaker implant | 13 (2.8) |
| Cardiac arrest | 16 (3.5) |
| Acute myocardial infarction | 9 (2) |
| Infectious | |
| Sepsis | 49 (10.7) |
| Mediastinitis | 6 (1.3) |
| Pulmonary | |
| Pneumonia | 46 (10) |
| Respiratory distress syndrome | 23 (5) |
| Tracheostomy | 9 (2) |
| Kidney | |
| Acute kidney injury | 93 (20.3) |
| Kidney replacement therapy | 41 (8.9) |
| Neurological | |
| Cerebrovascular accident | 25 (5.4) |
| Delirium | 22 (4.8) |
| Other | |
| Gastrointestinal complications | 13 (2.8) |
| Limb ischemia | 10 (2.2) |
| Coagulopathy | 7 (1.5) |
Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
Taxonomy
TopicsCardiac Structural Anomalies and Repair · Mechanical Circulatory Support Devices · Cardiac Valve Diseases and Treatments
Introduction
Ventricular septal rupture (VSR) is a rare but life-threatening mechanical complication of acute myocardial infarction (AMI).^1,2^ Due to the introduction and continuous improvement of early percutaneous revascularization strategies, its incidence has decreased to approximately 0.25% of AMI cases.^3,4,5,6^ However, if left untreated, it is almost inevitably fatal.^2^ Nevertheless, even when prompt surgery can be offered, in-hospital mortality remains very high. The rate of in-hospital mortality has not changed over the years, making VSR the most lethal cardiac surgical condition.^1,3,6^
Percutaneous closure devices and mechanical circulatory supports (MCS) may offer alternative or synergistic strategies to treat these patients, both preioperatively and postoperatively.^7,8^ However, surgery remains the standard treatment for postinfarction VSR. Early repair is generally recommended and is often required because of the presence of hemodynamic instability, but clear indications on ideal management and timing of intervention have not yet been well established.^3,6,9,10^ Moreover, given the low incidence of this condition, most reports consist of single-center studies with limited patient cohorts or studies of national registries.^1,11,12,13,14,15,16^
We conducted an international, multicenter, retrospective study on mechanical complications of AMI, the Mechanical Complications of Acute Myocardial Infarction: an International Multicenter Cohort (CAUTION) Study. The investigation was designed to evaluate early outcomes and to identify possible prognostic factors associated with early mortality among patients who underwent surgical repair of postinfarction VSR.
Methods
Patient Population and Study Design
The patients were recruited from the database of the CAUTION study (NCT03848429), a retrospective multicenter trial aimed at evaluating the postoperative outcomes of patients undergoing surgery for post-AMI mechanical complications. The study described in this article included all adult patients (aged >18 years) who underwent surgical repair of postinfarction VSR between January 2001 and December 2019 in 26 different centers worldwide, identified through surgical records. The study protocol was authorized by the local ethical committees of each center and conducted in accordance with the guidelines of the Declaration of Helsinki^17^ for patient data use and evaluation. The requirement for informed consent was waived considering the retrospective nature of the study. A unified patient data set was used to collect pertinent information, including clinical history, diagnostic workup, and operative and postoperative data from medical records. This report follows the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) reporting guideline.
Definitions and End Points
Cardiogenic shock was defined as persistent hypotension (systolic blood pressure <90 mm Hg) with reduction in cardiac index (<1.8 L/min/m^2^) despite maximal treatment. Urgent surgery was defined as surgery required during the same hospitalization for patients who were not admitted in an elective regimen. Emergent surgery was defined as surgery that occurred within 24 hours, while salvage surgery was defined as procedures for patients who required cardiopulmonary resuscitation while going to the operating room. Among surgical techniques, infarct exclusion was described as postinfarction VSR repair accomplished according to the technique described by David et al^11^ or any of its subsequent modifications,^14^ while other techniques included infarct excision and any other technique adopted, comprising sandwich technique and direct closure, with or without the use of a patch.
The primary end point of this study was early mortality, defined as death from any cause within 30 days after surgery or during the same hospitalization related to the operation. Intraoperative mortality was defined as death occurring during the operation. The secondary end point was the identification of prognostic factors associated with early mortality.
Statistical Analysis
Continuous variables were tested for distribution normality with the Shapiro-Wilk test and reported as mean and SD (for variables not violating the normality assumption) or median and IQR (for variables violating the normality assumption). Categorical variables were reported as frequency and percentage. For patients who survived vs those who died, continuous variables were compared individually with the t test or Mann-Whitney U test, while categorical variables were compared with the χ^2^ or Fisher exact test, as appropriate. Subsequently, variables of clinical interest that achieved a P < .10 at the univariate analysis and had less than 20% missing data were tested for multicollinearity and then entered into a multivariate logistic regression analysis, tested with the Hosmer-Lemeshow goodness-of-fit test, to identify independent variables associated with in-hospital mortality. Data analyses were performed using the software package SPSS Statistics version 26.0 for Windows (IBM). A 2-tailed P < .05 was considered statistically significant.
Results
Clinical Characteristics
A total of 475 patients were included in this study. Baseline and preoperative patients’ characteristics are presented in Table 1. The mean (SD) age was 68.5 (10.1) years, and 290 (61.1%) were men. The most frequent comorbidity was hypertension, followed by dyslipidemia and diabetes. VSR occurred after ST-elevation myocardial infarction in nearly 90% of patients (366 of 416 [88.0%]) and during the first ischemic episode in three-quarters of patients (348 of 475 [73.3%]), while only 67 (14.1%) had undergone previous revascularization procedures. Preoperative coronary angiography was performed in 397 patients (83.6%), showing multivessel coronary artery disease (CAD) in 226 cases (56.9%). Nearly half of patients developed cardiogenic shock before the operation (213 patients [44.8%]), and approximately 1 in 10 patients (46 [9.7%]) had cardiac arrest. The median (IQR) time from AMI to VSR diagnosis was 2.0 (0.3-5.6) days, while the median (IQR) time from VSR to surgery was 2.0 (0.5-7.0) days. Preoperative intra-aortic balloon pump (IABP) or extracorporeal membrane oxygenation (ECMO) were required in 273 patients (57.5%) and 32 patients (6.7%), respectively. Emergent or salvage operation was performed in nearly half of the patients (212 [44.6%]).
Surgical Repair
Operative and perioperative data are reported in Table 2. Anterior/apical VSR was slightly more common. Another concomitant post-AMI mechanical complication (ie, left ventricular free-wall rupture or papillary muscle rupture) was present in 25 patients (5.3%). Concomitant coronary artery bypass graft (CABG) was performed in half of patients, while other concomitant procedures were required in 76 cases (16.0%), mostly including valve procedures or surgical ventricular reconstruction. Moreover, only 72 patients who underwent concomitant CABG (15.2%) also received a preoperative percutaneous revascularization. Nearly two-thirds of patients required postoperative IABP (303 [63.8%]), while ECMO was necessary in approximately 15% of cases (65 [13.7%]). Other MCS adopted included implantation of an Impella device in 5 patients (1.1%) and right or left ventricular assist devices in 2 patients (0.4%) each. Rethoracotomy for bleeding was required in approximately 10% of cases (51 [11.1%]). Residual/recurrent VSR was reported in 59 patients (12.9%), demanding reoperation in 25 (42.4%) of them; in 2 cases (3.4%), residual VSR was closed percutaneously.
Postoperative Outcomes
Early postoperative outcomes are reported in Table 3. The most common complications identified among surgical survivors were low cardiac output syndrome (LCOS) and acute kidney injury, followed by sepsis, atrial fibrillation, and pneumonia.
Early mortality occurred in 192 patients (40.4%), with 16 (3.4%) intraoperative deaths, either due to ventricular failure, precluding cardiopulmonary bypass (CPB) weaning, or incontrollable bleeding. LCOS and multiorgan failure were by far the most common causes of early mortality (LCOS, 70 [36.5%]; multiorgan failure, 53 [27.6%]); other cardiac causes accounted for approximately one-tenth of deaths (Table 3). Overall, 8 patients (1.9%) died because of VSR recurrence. A difference in early mortality was observed among different centers (median [IQR] mortality, 41.1% [25.8%-49.5%]). In the nearly 20 years considered for the study, the mortality rate did not change substantially, with a median (IQR) yearly mortality of 41.7% (32.6%-50.0%) (eFigure in the Supplement). Most patients were hospitalized for nearly 1 month after surgical correction, with a few reaching nearly 3 months of hospitalization.
At univariate analysis, older age, smoking, chronic kidney disease, preoperative cardiogenic shock or cardiac arrest, percutaneous revascularization, preoperative need of IABP or ECMO, time from AMI to surgery of less than 7 days, and urgent and emergent/salvage surgery were associated with early mortality (Table 1). For example, cardiogenic shock (survived: 95 [33.6%]; died, 118 [61.5%]; P < .001) and early surgery (time to surgery ≥7 days, survived: 105 [57.4%]; died, 47 [35.1%]; P < .001) were associated with lower survival. Similarly, a significantly higher mortality rate was observed in patients with posterior VSR, longer CPB and cross-clamp times, and in those who required rethoracotomy for bleeding or postoperative support with IABP or ECMO. As presented in Figure 1, patients who died had significantly shorter time from AMI to VSR occurrence compared with those who survived (mean [SD] time, 3.2 [4.1] days vs 8.9 [29.8] days; P = .04) and shorter interval from VSR occurrence to surgery (mean [SD] time, 3.3 [6.1] days vs 7.8 [16.1] days; P < .001). However, since data from these last 2 variables as well as for the timing of AMI surgery timing were complete in less than 80% of patients, they were not included in the multivariate model.
Mean Timing of Ventricular Septal Rupture (VSR) Occurrence and RepairAMI indicates acute myocardial infarction. Dots represent individual cases, and the whiskers mark the SD.
Multivariate analysis showed that older age (odds ratio [OR], 1.05; 95% CI, 1.02-1.08; P = .001), preoperative cardiac arrest (OR, 2.71; 95% CI, 1.18-6.27; P = .02), preoperative percutaneous revascularization (OR, 1.63; 95% CI, 1.003-2.65; P = .048), and postoperative need of IABP (OR, 2.98; 95% CI, 1.46-6.09; P = .003) or ECMO (OR, 3.19; 95% CI, 1.30-7.38; P = .01) support were independently associated with early mortality. ORs with 95% CIs are presented in Figure 2.
Association of Patient and Clinical Characteristics With Early MortalityECMO indicates extracorporeal membrane oxygenation; IABP, intra-aortic balloon pump; VSR, ventricular septal rupture.
Discussion
VSR is a rare but life-threatening mechanical complication of AMI. Thanks to the continuous improvement of early reperfusion strategies, including thrombolysis and percutaneous coronary intervention (PCI), its incidence has decreased from 2% to approximately 0.2% of AMI.^3,4,5,6,18^ If treated conservatively, this condition is almost inevitably fatal.^2^ However, despite prompt intervention, in-hospital mortality still ranges from 19% to 65%.^1,11,12^ Using data from 26 centers around the world, we analyzed the early outcomes of patients undergoing surgical repair of postinfarction VSR during the last 20 years.
The major findings of this study include the following: (1) the early mortality rate was 40.4%; (2) older age, preoperative cardiac arrest and percutaneous revascularization, and postoperative need for IABP or ECMO support were independently associated with early mortality; (3) longer durations from AMI to VSR and from VSR to surgery were associated with lower mortality; and (4) recurrent VSR was not associated with higher mortality. To our knowledge, the current analysis represents the largest multicenter observational study to date evaluating early outcomes among patients undergoing surgical repair of postinfarction VSR.
In our population, older age was independently associated with mortality, in accordance with previous studies.^2,3,16,19^ Although female sex has been historically associated with VSR occurrence and mortality, our sample mostly consisted of men (61.1%); however, we found no association between sex and early mortality.^2,20^ Chronic kidney disease was associated with early mortality, as reported by other studies.^1,14,16,21^
Interestingly, preoperative percutaneous revascularization, including both thrombolysis and PCI, were independently associated with mortality. Although requiring further investigation, this may be related to the higher hemorrhagic risk following percutaneous procedures. Indeed, as previously observed by Becker et al,^20^ thrombolysis may cause myocardial hemorrhage during the lytic state of infarct evolution, thus possibly accelerating VSR occurrence up to the first 24 hours from AMI.^2^ On the other hand, while PCI improves morbidity and mortality in patients with AMI, it has also been shown to reduce the risk of cardiac rupture when compared with thrombolysis.^22^ However even among patients undergoing PCI, myocardial rupture tends to occur earlier than in the prethrombolytic era.^5^ In our study, a shorter time from AMI to VSR occurrence was associated to early mortality (Figure 1A), possibly because of the myocardial hemorrhagic weakening induced by percutaneous revascularization that might also increase the surgical repair difficulty, thereby partially justifying a worse outcome.
However, it should be noted that only one-third of patients underwent preoperative revascularization, given that nearly 20% of patients could not undergo preoperative coronarography, thereby precluding any chance of revascularization, and half of patients received CABG, with limited overlap between percutaneous and surgical revascularization (15.2% of patients). Nevertheless, concomitant CABG was not associated with early mortality, in accordance with some reports.^12,23,24^ The role of concomitant CABG in this setting is still debated because advantages of revascularization are often contrasted by a higher surgical risk and longer CPB and cross-clamp times. Considering that VSR is a post-AMI complication, treatment of the underlying CAD is advocated to provide ischemic border perfusion and protect from the additive long-term ischemic risk of CAD.^25^ Moreover, while most surgeons do not revascularize the infarct-related artery because of technical issues related to the procedure, CABG may be particularly important in multivessel CAD, which has also been associated with higher mortality.^25^
The unfavorable prognosis associated with VSR is strongly influenced by clinical status at time of surgery.^1,6,26^ Indeed, most patients present in labile hemodynamic conditions, ranging from acute pulmonary edema to cardiac arrest.^1,3,16,23^ The negative effect of hemodynamic instability on patients’ survival may also result from other concomitant negative prognostic factors, such as VSR and infarct size, and biventricular impairment.^1,2,24,27,28^ However, in our study, preoperative left ventricular function was not associated with early mortality. On the other hand, nearly half of patients developed cardiogenic shock before surgery, and approximately 10% had cardiac arrest. These conditions were significantly associated with early mortality, in accordance with previous reports.^1,12,14,16,23,26^
The high prevalence of cardiogenic shock often requires aggressive treatment with temporary MCS devices, including IABP.^1,6,29,30^ However, while IABP in this setting is recommended by the current guidelines (Class IIa), ECMO and other MCS devices have not yet been considered.^9^ In our study, both preoperative IABP and ECMO supports were associated with early mortality, in accordance with previous reports, probably due to worse hemodynamic conditions of patients requiring MCS.^1,24^ Nevertheless, considering the number of patients presenting with cardiogenic shock, we observed a low adoption rate of preoperative ECMO, with recent reports ranging from 4% to 22%.^14,16,29^ The use of preoperative MCS devices in VSR represents a relatively recent approach, proposed for patients with more critical illness to improve hemodynamics and delay repair until the patient is in better condition.^6,7,26,29,31,32,33^ Indeed, preoperative MCS adoption is sometimes discouraged by the potential interactions of MCS- and VSR-related pathophysiology, which can be anticipated and carefully managed with a patient-tailored, preimplantation analysis.^7,34,35^
The low adoption of preoperative MCS may also be related to the high proportion of patients undergoing an emergent or salvage procedure (44.6%), probably preferred over attempting to delay the repair until after patient stabilization. However, emergent surgery was associated with a higher mortality, in accordance with most studies.^1,15,16^ Timing of surgery in VSR is still a matter of debate. Indeed, while US guidelines recommend immediate surgery for all patients with VSR, European ones suggest delayed repair in patients who respond well to aggressive therapy.^1,9,10,15,16,28^ Such uncertainty expressed by the guidelines on this topic may itself explain the high rate of early surgery as a general indication for VSR patients in some centers, rather than a forced choice due to unstable hemodynamics. Similar to other reports, we found that the time from VSR occurrence to surgery was significantly shorter for patients who died, reinforcing the association between early intervention and higher mortality and potentially highlighting the need for a paradigm shift in the management of patients with VSR (Figure 1B).^6,15,26,29,30,31,35^ Timing from AMI to VSR and from VSR to surgery were not included in the multivariate analysis because approximately 30% of patients were missing these data; therefore, we could not perform further between-group comparisons. However, it is reasonable to suppose that the evidence provided by such a difference is strong enough to represent a significant result. Despite possible selection biases, usually based on the idea that patients in more stable condition are more likely to survive until a delayed surgery, the improved survival for delayed VSR repair is commonly attributed to the myocardial recovery from ischemia and to the evolution of necrotic, friable tissue into a fibrotic, resistant scar, which is more suitable for repair.^1,6,29,36^
Posterior VSR was associated with higher mortality, in accordance with a meta-analysis published by our group in 2021.^24^ This association may be due to more frequent right ventricular involvement and the more challenging surgical implications of posterior/basal VSR repair.^24,28,37^ Conversely, the presence of other post-AMI mechanical complications or concomitant procedures during surgery was not associated with mortality.
In-hospital mortality was remarkably high (40.4%), although comparable with other reports, confirming that postinfarction VSR is the most lethal cardiac surgical condition, reaching rates as high as 60% of patients.^1,12,16,24^ Moreover, it is noteworthy that 8.3% of deaths were intraoperative, indicating that improvements are needed in the management protocols of these patients.^35^ Indeed, as presented in the eFigure in the Supplement, the temporal trend of early mortality for surgically treated VSR remained high and unchanged over the last 2 decades, despite surgical and technological advancements.^3,24^ Most of the patients died due to LCOS or multiorgan failure, highlighting the severe effects of this condition on biventricular function, despite proper repair.^12^
While the need of rethoracotomy for bleeding was higher among patients who died, residual or recurrent VSR was not associated with higher mortality, even when it required a reintervention, in accordance with other studies.^12,13,37^ However, the VSR recurrence rate remained high (12.9%), and in 8 patients, it also represented the cause of death.
Although compatible with the severity of VSR, the high incidence of LCOS and its systemic effects as either a postoperative complication or cause of death might identify a subgroup with greater clinical severity and/or suboptimal management, especially in the first days following surgery. This may also be reflected by the low adoption rate of more aggressive postoperative MCS devices (13.7% for ECMO and 1.9% for other MCS) besides IABP; these devices may act as a protective measure in the early postoperative period, possibly contributing to improved morbidity and mortality.^7,27,35,36^ In accordance with other reports, our study showed that the postoperative need for IABP or ECMO supports was independently associated with mortality, probably because they were reserved only as last-resort for patients with VSR and more severe clinical conditions.^1,16^ However, broader prophylactic MCS adoption for patients with impaired ventricular function might improve outcomes, as described in various reports, with encouraging results.^7,26,29,35,36^ Nevertheless, further studies are required to examine the potential effects of MCS in both preoperative and postoperative periods on outcomes as well as their impact on overall postinfarct VSR management, including the timing of surgery.
Limitations
This study has limitations. First, due to its retrospective nature, both selection bias and unmeasured confounders cannot be excluded. Second, the multicenter design required a data collection form with a limited number of variables to avoid missing data; thus, the possibility that nonreported variables could have influenced the results of the analysis cannot be completely ruled out. Moreover, we could not include the timing from AMI to VSR and from VSR to surgery in the multivariate analysis, due to a proportion of missing data approximating 30%. Furthermore, this study was limited to operative outcomes and did not providing information on the durability of surgical repair of post-AMI VSR as well as late outcome. Such outcomes may be also influenced by the small number of patients for each center, which could affect surgical approach uniformity and surgeons’ experience. Additionally, data concerning other VSR patients managed conservatively or who died without surgery in all participating centers are lacking, making a comprehensive analysis of the actual prevalence of VSR not feasible.
Conclusions
Postinfarction VSR remains a severe condition with a challenging management in all its phases, from preoperative to perioperative periods. Despite many advancements in the management of AMI and in the surgical techniques of VSR repair, early mortality in this study was confirmed to be very high (40.4%), with no signs of improvements over the last 2 decades. Delayed surgery may be associated with better survival. Old age, preoperative cardiac arrest and percutaneous revascularization, and postoperative need for IABP or ECMO were independently associated with early mortality, which was mainly related to LCOS. Further prospective studies addressing enhanced preoperative and perioperative patient management are warranted to hopefully improve the currently suboptimal rate of early mortality.
The reference list from the paper itself. Each links out to its DOI / PubMed record.
- 1Arnaoutakis GJ, Zhao Y, George TJ, Sciortino CM, Mc Carthy PM, Conte JV. Surgical repair of ventricular septal defect after myocardial infarction: outcomes from the Society of Thoracic Surgeons National Database. Ann Thorac Surg. 2012;94(2):436-443. doi:10.1016/j.athoracsur.2012.04.02022626761 PMC 3608099 · doi ↗ · pubmed ↗
- 2Crenshaw BS, Granger CB, Birnbaum Y, ; GUSTO-I (Global Utilization of Streptokinase and TPA for Occluded Coronary Arteries) Trial Investigators. Risk factors, angiographic patterns, and outcomes in patients with ventricular septal defect complicating acute myocardial infarction. Circulation. 2000;101(1):27-32. doi:10.1161/01.CIR.101.1.2710618300 · doi ↗ · pubmed ↗
- 3Elbadawi A, Elgendy IY, Mahmoud K, . Temporal trends and outcomes of mechanical complications in patients with acute myocardial infarction. JACC Cardiovasc Interv. 2019;12(18):1825-1836. doi:10.1016/j.jcin.2019.04.03931537282 · doi ↗ · pubmed ↗
- 4Figueras J, Alcalde O, Barrabés JA, . Changes in hospital mortality rates in 425 patients with acute ST-elevation myocardial infarction and cardiac rupture over a 30-year period. Circulation. 2008;118(25):2783-2789. doi:10.1161/CIRCULATIONAHA.108.77669019064683 · doi ↗ · pubmed ↗
- 5French JK, Hellkamp AS, Armstrong PW, . Mechanical complications after percutaneous coronary intervention in ST-elevation myocardial infarction (from APEX-AMI). Am J Cardiol. 2010;105(1):59-63. doi:10.1016/j.amjcard.2009.08.65320102891 · doi ↗ · pubmed ↗
- 6Jones BM, Kapadia SR, Smedira NG, . Ventricular septal rupture complicating acute myocardial infarction: a contemporary review. Eur Heart J. 2014;35(31):2060-2068. doi:10.1093/eurheartj/ehu 24824970335 · doi ↗ · pubmed ↗
- 7Gambaro A, Rosenberg A, Galiatsou E, Stock UA. Pros and cons of different types of mechanical circulatory support device in case of postinfarction ventricular septal defect. ASAIO J. 2021;67(6):e 110-e 113. doi:10.1097/MAT.000000000000129033060409 · doi ↗ · pubmed ↗
- 8Giblett JP, Jenkins DP, Calvert PA. Transcatheter treatment of postinfarct ventricular septal defects. Heart. 2020;106(12):878-884. doi:10.1136/heartjnl-2019-31575132111641 · doi ↗ · pubmed ↗
