Heart failure & cardiomyopathies

Percutaneous intramyocardial septal radiofrequency ablation: a novel treatment for drug-refractory non-obstructive hypertrophic cardiomyopathy with severe septal hypertrophy

HeartPublished single-arm, open-label, prospective study

Authors' conclusion

PIMSRA was associated with a reduction of myocardial septal thickness and improvement in functional status in patients with NOHCM. The absence of major adverse events is also encouraging, but larger studies with a control arm are needed to confirm long-term safety.

Study context

Population
Adult patients with drug-refractory non-obstructive hypertrophic cardiomyopathy (NOHCM) and severe septal hypertrophy (≥28 mm)enrolled between June 2017 and June 2023, median follow-up 15 months
Participants
20 patients
Exposure
Before vs after percutaneous intramyocardial septal radiofrequency ablation (PIMSRA)
  • PIMSRAn = 20
Outcome
Major adverse clinical events
Follow-up
Within 30 days after the procedure

Main finding

As reported in the abstract

  • No major adverse clinical events occurred

Observational data: associations, not effects.

Further findings

OutcomeMean difference (mm) (95% CI)
Maximum interventricular septal thicknessAfter PIMSRAvs before PIMSRADecreased from 31.3 mm to 17.4 mm−13.9 (−15.92 to −11.88)
OutcomeMean difference (95% CI)
KCCQ-12 scoreAfter PIMSRAvs before PIMSRAImproved from 65.6 to 84.418.78 (11.62–25.93)

Left atrial volume index and left ventricular mass index

Decreased significantly

Global longitudinal strain and global radial strain

Improvements observed, indicating possibly enhanced myocardial performance

Arrhythmias (atrial fibrillation, high-grade conduction block, non-sustained ventricular tachycardia) · during the follow-up

No increased risk found

Original publication

Percutaneous intramyocardial septal radiofrequency ablation: a novel treatment for drug-refractory non-obstructive hypertrophic cardiomyopathy with severe septal hypertrophy. Heart. Published 7 March 2025. doi:10.1136/heartjnl-2024-325334

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