Key result
LithiX contact intravascular lithotripsy yields a ~98% procedural success rate without in-hospital MACE.
Why the study?
To evaluate the LithiX lithotripsy device, which uses the Hertz contact mechanism to fragment calcium without requiring an external energy source, for calcified coronary lesions prior to stent implantation.
Does the LithiX Hertz contact intravascular lithotripsy device safely and effectively treat moderately to severely calcified de novo coronary lesions?
Does the LithiX Hertz contact intravascular lithotripsy device safely and effectively treat moderately to severely calcified de novo coronary lesions?
The novel Hertz contact intravascular lithotripsy device is feasible, safe, and effective for treating calcified coronary lesions, achieving optimal stent expansion with a low 30-day MACE rate.
HC-IVL achieves high procedural success and calcium fracture in calcified lesions; leaves open randomized comparisons to established IVL.
BACKGROUND: Calcified coronary lesions impede stent expansion and are associated with poor outcomes after percutaneous coronary interventions. Intravascular lithotripsy (IVL) has emerged as a safe and effective pretreatment to optimise stent implantation. AIMS: This study assesses the LithiX lithotripsy device, which uses the Hertz contact (HC) mechanism to fragment calcium while minimising injury to surrounding soft tissue, without requiring an external energy source. METHODS: The multicentre, prospective PINNACLE-I clinical trial enrolled patients with up to two moderately to severely calcified de novo lesions. The primary endpoints were <50% residual stenosis without in-hospital major adverse cardiovascular events (MACE) and the 30-day MACE rate. Clinical events were assessed up to 6 months. RESULTS: Sixty patients with 63 lesions were treated with successful delivery and use of the HC-IVL catheter and a median procedure time of 59.5 min (interquartile range: 40.5-76.0). The primary endpoint was achieved in 98.3%. All patients had residual stenosis <30% after stent placement. The 30-day MACE rate was 1.7%, due to 1 periprocedural target vessel non-Q-wave myocardial infarction. There were no cardiovascular deaths, no definite or probable stent thromboses, nor any device-related events up to 6 months of follow-up. The optical coherence tomography substudy in 32 subjects identified a wide range of calcium morphologies, including calcium arcs of 96-360° and calcified nodules. Following HC-IVL, calcium fractures were achieved in 90.6% of lesions, and the mean fracture depth was 0.81±0.33 mm. Stent expansion at the minimum stent area site was 96.7±25.5%. CONCLUSIONS: PINNACLE-I demonstrated the feasibility, safety, and efficacy of the novel HC-IVL to fracture calcified lesions and achieve optimal stent expansion in a broad range of calcium morphologies.
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Verheye et al. (2026) studied Calcified coronary artery disease (n=60). LithiX lithotripsy device (Hertz contact intravascular lithotripsy) was evaluated on <50% residual stenosis without in-hospital major adverse cardiovascular events (MACE). Hertz contact intravascular lithotripsy using the LithiX device achieved <50% residual stenosis without in-hospital MACE in 98.3% of patients, with a 30-day MACE rate of 1.7%.
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