Mode
Text Size
Log in / Sign up

ECG parameter P0PV1 identifies CRT-D benefit and harm in non-LBBB heart failure patients

ECG parameter P0PV1 identifies CRT-D benefit and harm in non-LBBB heart failure patients
Photo by Samuel Ramos / Unsplash
Key Takeaway
Consider P0PV1 as a potential, unvalidated marker for CRT-D response in non-LBBB HF patients.

This was a post-hoc analysis of the MADIT-CRT randomized controlled trial, involving 535 patients with non-left bundle branch block (non-LBBB), wide QRS, and low left ventricular ejection fraction. The study assessed whether a novel ECG variable, P0PV1, could identify differential risk and response to cardiac resynchronization therapy with defibrillator (CRT-D) compared to implantable cardioverter-defibrillator (ICD) alone.

In patients receiving only an ICD, those with P0PV1 in the longest quintile (quintile 5) had a more than threefold increased risk of heart failure or death (30% of patients, p<0.001). When treated with CRT-D, this high-risk subgroup experienced a 66% lower risk of HF/death compared to ICD (95% CI: 0.22-0.68, p=0.001). Conversely, patients with a shorter P0PV1 (<201 ms) had a 64% increased risk of HF/death with CRT-D versus ICD (95% CI: 1.12-2.55, p=0.012), suggesting potential harm.

Safety and tolerability data were not reported. The primary limitation is that this is a post-hoc analysis; the authors note prospective studies are warranted to confirm the findings. The results propose a potential ECG marker for personalizing CRT-D therapy in non-LBBB patients but should not be used to guide clinical decisions until validated in prospective trials.

Study Details

Study typeRct
EvidenceLevel 2
PublishedApr 2026
View Original Abstract ↓
BACKGROUND: PR-interval reflects atrioventricular timing but does not well characterize adverse hemodynamics. Novel ECG parameters of conduction may identify benefit from non-dyssynchronous ventricular pacing to correct long atrioventricular conduction delays. OBJECTIVE: Evaluating novel ECG parameters to identify risk of heart failure (HF)/death and benefit vs harm by CRT-D in MADIT-CRT non-LBBB patients. METHODS: We analyzed intervals from ECGs in 535 non-LBBB patients enrolled in MADIT-CRT, using ImageJ. Onset of atrial activation, P wave zero crossing in V1, latest P offset, earliest QRS onset, and time to the first R peak in V1 and V6 were determined. Endpoints included HF or death. Associations between novel conduction measures and clinical outcomes in ICD patients (n = 209), and CRT-D (n = 326) vs. ICD benefit, were assessed using Kaplan-Meier and multivariable Cox regression analyses. RESULTS: We identified the delay from P zero crossing to the first R peak in V1 (P0PV1) at quintile 5 as the strongest risk predictor in ICD patients (n = 159, 30%), over PR-interval, for all endpoints (p < 0.001), with a more than threefold risk increase. In this group, CRT-D was associated with a 66% lower risk of HF/Death (95% CI: 0.22-0.68, p = 0.001) vs. an ICD. However, in patients with a P0PV1 < 201 ms, CRT-D vs. an ICD was associated with a 64% increased risk of HF/death (95% CI: 1.12-2.55, p = 0.012), with significant bidirectional interaction (p-value < 0.001). CONCLUSIONS: We propose a novel variable, P0PV1, to identify risk and benefit vs. harm from CRT-D in HF patients with non-LBBB. Prospective studies are warranted to confirm our findings.
Free Newsletter

Clinical research that matters. Delivered to your inbox.

Join thousands of clinicians and researchers. No spam, unsubscribe anytime.