What Is Left Atrial Appendage Occlusion (LAAO)?

Left Atrial Appendage Occlusion (LAAO) is a specialized, minimally invasive cardiac procedure designed to reduce the risk of stroke in patients with non-valvular Atrial Fibrillation (Afib). It serves as an alternative to long-term oral anticoagulation, the standard therapy for stroke prevention in Afib. The procedure permanently seals off the Left Atrial Appendage (LAA), a small heart pouch where most stroke-causing blood clots originate. By occluding this structure, LAAO prevents clots from forming and traveling to the brain, offering a mechanical solution for stroke risk reduction.

Understanding the Left Atrial Appendage and Stroke Risk

The Left Atrial Appendage (LAA) is a small, muscular, ear-shaped pouch attached to the upper left chamber of the heart, known as the left atrium. While its exact function is not fully understood, its complex, trabeculated interior creates an environment where blood can easily become stagnant.

In non-valvular Atrial Fibrillation, the upper chambers of the heart beat rapidly and irregularly, causing inefficient pumping. This chaotic rhythm causes blood to pool, particularly within the LAA’s convoluted structure, rather than flowing smoothly. This blood stasis promotes the formation of blood clots, or thrombi.

These blood clots can break free from the LAA, travel out of the heart, and enter the bloodstream, a process called embolism. If a clot travels to the brain and blocks a blood vessel, it results in an ischemic stroke. More than 90% of the stroke-causing clots that originate in the heart in non-valvular Afib patients are formed specifically within the LAA. Closing off this structure directly addresses the source of the stroke risk.

The LAA Occlusion Procedure: How It Works

LAAO is a percutaneous procedure, performed using catheters inserted through a small incision, typically while the patient is under general anesthesia. The process begins with inserting a catheter into the femoral vein in the upper leg. This catheter is then guided up to the right side of the heart using continuous imaging, such as fluoroscopy or transesophageal echocardiography (TEE).

To reach the left atrium, which contains the LAA, the physician must perform a transseptal puncture. This involves using a specialized needle to cross the interatrial septum, the thin wall separating the right and left atria. Once the catheter is in the left atrium, it is maneuvered toward the opening of the LAA.

A self-expanding occlusion device is delivered through the catheter and carefully deployed to completely seal the LAA opening. The device conforms to the LAA orifice, permanently closing it off from the rest of the left atrium. Confirmation of the device’s correct position and stability, along with the absence of significant blood flow around the device (peri-device leak), is verified immediately using TEE.

Patient Eligibility and Post-Procedure Management

LAAO is a treatment option reserved for patients with non-valvular Afib who have a high calculated stroke risk (CHA2DS2-VASc score of 2 or greater) but also face a high risk of major bleeding complications from long-term oral anticoagulation therapy. This high bleeding risk may stem from a history of intracranial hemorrhage, recurrent gastrointestinal bleeding, or other serious adverse events related to blood thinners.

The procedure is designed to offer stroke prevention without long-term dependency on daily oral anticoagulants. Following the successful placement of the device, patients are placed on a short-term regimen of blood-thinning medications to allow the heart tissue to fully integrate the device. This post-procedure period typically involves dual antiplatelet therapy for a period that often lasts 45 days.

After this initial phase, the regimen is usually adjusted, and the long-term goal is to discontinue oral anticoagulation entirely. The device is considered fully integrated through a process called endothelialization, where natural tissue grows over the exposed metal surface, which typically takes about six months. Confirmation is achieved through a follow-up imaging scan, such as a TEE, allowing the patient to transition to antiplatelet therapy or, in some cases, no blood thinners.