Total artificial heart in patients with post-infarction ventricular septal defect

Ventricular septal defect (VSD) following acute myocardial infarction (AMI) is associated with very high mortality regardless of the treatment approach. Depending on the extent of infarction and size of the septal rupture, left-to-right shunting increases pulmonary blood flow, systemic blood flow is decreased, and cardiac function is severely compromised. Conservative medical therapy has dismal results, with a mortality rate nearing 90%, while the overall rate for patients undergoing surgical repair is 43%, with these patients having the worst outcomes of all cardiac surgical procedures (1,2). Experience with percutaneous transcatheter closure of post-AMI VSD is limited to small case series, with reports of mortality as high as 65% (3,4). In cases of small VSD with stable hemodynamics, percutaneous closure is a suitable treatment option.

An absence of large clinical trials or registry data means the optimal approach and timing of treatment remains controversial. In hemodynamically stable patients, there is equipoise for delayed surgical repair or percutaneous device placement to allow for collagen replacement of necrotic myocytes and strengthening of friable tissue that is needed for device anchoring or suture line strength. Stable patients without organ failure may be carefully monitored and safely undergo delayed closure. In the overall population undergoing surgical VSD repair, there is a significant survival advantage in delaying surgery for at least seven days (1). However, during the waiting period, the risk is high for developing cardiogenic shock or expansion of the VSD to the point of being inoperable (5).

Early development of cardiogenic shock following AMI/VSD is common and the mortality rate approaches 90% (6). Early coronary reperfusion and mechanical circulatory support (MCS) may stabilize hemodynamics, minimize shunting, help preserve organ function, and limit VSD expansion. A staged approach in treating patients with post-AMI VSD who also present with cardiogenic shock and pulmonary edema may improve outcomes in select patients (5) MCS with a percutaneous device that directly unloads the left ventricle is necessary to decrease left-to-right shunting and myocardial wall stress. If coronary revascularization is required, percutaneous coronary stent placement should be performed after MCS is initiated. Stabilized patients may be extubated, and inotropic medications are reduced while the infarcted area stabilizes. After approximately one week, transthoracic or transesophageal echocardiography is used to reassess the size and location of the VSD. If the VSD diameter is ≤2.5 cm, adequate septal margin exists for device anchoring with adequately thick myocardial free wall, the position of the VSD is central rather than apical, and there is no proximity to the aortic valve, percutaneous closure is the preferred choice of treatment. If percutaneous coronary revascularization or VSD repair is not feasible, surgical repair and coronary artery bypass should be performed.

Patients with severe refractory cardiogenic shock and biventricular failure may require durable MCS or heart transplantation (7). Although the implantable left ventricular assist device (LVAD) has been successfully used as a bridge to transplant in patients with post-AMI VSD (8), placement of the LVAD inflow conduit may be very difficult if the apical myocardium is extensively necrotic. Inflow placement through friable apical myocardium may result in catastrophic bleeding complications. In cases of severe valvular insufficiency, LVAD function may be compromised and device support may be inadequate. The total artificial heart (TAH) may be a suitable treatment option for select patients following AMI/VSD with refractory cardiogenic shock. These TAH candidates have a very low probability of success with surgical repair and percutaneous closure, yet they are suitable for heart transplantation. TAH implantation may be indicated for patients who are not responding to percutaneous mechanical support and are not candidates for surgical repair or percutaneous closure due to size and location of the VSD or who have other structural complications.

Post-AMI VSD with severe refractory cardiogenic shock is uncommon yet is a very challenging clinical scenario. Reports are scarce on the clinical use of the biventricular assist device or TAH, but have been demonstrated to have a positive outcome (7,9,10). Early TAH implantation can obviate the structural heart complications that lead to severe refractory cardiogenic shock and death. In patients with preserved neurologic and end-organ function, the TAH, as a bridge to heart transplant, offers the possibility of long-term survival following this devastating problem.

Acknowledgments

None.

Footnote

Conflicts of Interest: The author has no conflicts of interest to declare.

References

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