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Early experience of intravascular lithotripsy in unprotected calcified left main coronary artery disease
Kerrick Hesse1, Farhan Shahid2, Raheel Ahmed1
1The Freeman Hospital, Newcastle Upon Tyne, United Kingdom.
Insights
Intravascular lithotripsy (IVL) is a feasible treatment for severely calcified unprotected left main coronary artery (LMCA) disease, showing comparable safety and efficacy to rotational atherectomy (RA). Further trials are needed to confirm these findings.
Area of Science:
- Interventional Cardiology
- Cardiovascular Disease
- Medical Device Technology
Background:
- Treatment of unprotected severely calcified left main coronary artery (LMCA) disease presents significant interventional challenges.
- Intravascular lithotripsy (IVL) and rotational atherectomy (RA) are established treatments for coronary calcification outside the LMCA.
- This study evaluates the feasibility of IVL compared to RA in unprotected LMCA disease.
Purpose of the Study:
- To assess the feasibility and outcomes of intravascular lithotripsy (IVL) versus rotational atherectomy (RA) for treating unprotected severely calcified left main coronary artery (LMCA) disease.
- To compare procedural success, angiographic success, and major adverse cardiac events (MACE) at one year between IVL and RA in LMCA disease.
Main Methods:
- Retrospective analysis of IVL and RA procedures for unprotected LMCA disease performed between January 2019 and April 2022.
- Evaluation of procedural and angiographic success (stent delivery with <50% residual stenosis, no complications).
- Assessment of one-year composite of major adverse cardiac events (MACE).
Main Results:
- Procedural and angiographic success rates were high (≥84%) across IVL and RA groups for LMCA and non-LMCA treatments.
- One-year MACE rates were comparable: 22.7% for LMCA IVL, 19.8% for LMCA RA, and 21.4% for non-LMCA IVL.
- IVL was predominantly used as a second-line or bailout technique in LMCA and non-LMCA calcified lesions.
Conclusions:
- Intravascular lithotripsy (IVL) is a feasible adjuvant calcium modification technique for unprotected calcified LMCA disease, often used as a second or third-line treatment.
- The safety and efficacy of IVL in this setting appear comparable to rotational atherectomy (RA).
- Larger randomized controlled trials are warranted to formalize the use of IVL in unprotected calcified LMCA disease.
Background:
Treatment of unprotected severely calcified left main coronary artery (LMCA) disease is a complex interventional procedure. Intravascular lithotripsy (IVL) and rotational atherectomy (RA) are safe and effective methods of treating coronary calcification in the non-LMCA setting. This retrospective analysis assessed the feasibility of IVL versus RA in unprotected LMCA disease.
Methods:
We analyzed IVL and RA procedures performed at a large tertiary hospital in the Northeast of England from January 1, 2019 to April 31, 2022. Major safety and efficacy endpoints were procedural and angiographic success, defined by stent delivery with <50 % residual stenosis and without clinical or angiographic complications, respectively. Another important clinical endpoint was the composite of major adverse cardiac events (MACE) at 1 year.
Results:
From 242 patients, 44 had LMCA IVL, 81 had LMCA RA and 117 had non-LMCA IVL. Patients with LMCA disease were older and more likely to have aortic stenosis. IVL was a second-line or bailout technique in 86.4 % LMCA and 92.2 % non-LMCA cases. Procedural and angiographic success rates were ≥ 84 % across all groups (p > 0.05). In 3 LMCA IVL and 3 LMCA RA cases arrhythmias and cardiac tamponade complicated the procedures respectively. At 1 year, MACE occurred in 10/44 (22.7 %) LMCA IVL, 16/81 (19.8 %) LMCA RA and 25/117 (21.4 %) cases (p > 0.05).
Conclusion:
In our single center retrospective analysis, IVL is feasible in unprotected calcified LMCA as a second-line and third-line adjuvant calcium modification technique. Its use in unprotected calcified LMCA disease should be formalized with the undertaking of large randomized controlled trials.
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