Evidence map›Paper›PMID 41213824›Full record

SynthesisOpen heart2025

Intravascular haemolysis following pulsed field ablation pulmonary vein isolation for atrial fibrillation: a systematic review.

Thomas Wan Yu Koh, Christian Tang, Joshua Kovoor, Ammar Zaka, Aashray Gupta, Brandon Stretton, Stephen Bacchi, Pramesh Kovoor

Abstract readSystematic Review
In one paragraph

Synthesis in Open heart, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pulsed field ablation for the interventional treatment of atrial fibrillation: a scientific statement of the European Heart Rhythm Association of the European Society of Cardiology, the Heart Rhythm Society, the Asia Pacific Heart Rhythm Society, the Latin American Heart Rhythm Society, and the Canadian Heart Rhythm Society.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2026
    Guideline
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Thomas Wan Yu KohCardiology, Gold Coast University Hospital, Southport, Queensland, Australia thomas.koh@health.qld.gov.au.ORCID http://orcid.org/0009-0006-5279-0122
Christian TangGold Coast University Hospital, Southport, Queensland, Australia.
Joshua KovoorFaculty of Health and Medical Sciences, The University of Adelaide, Adelaide, South Australia, Australia.
Ammar ZakaGold Coast University Hospital, Southport, Queensland, Australia.ORCID http://orcid.org/0009-0004-4513-9601
Aashray GuptaThe University of Adelaide, Adelaide, South Australia, Australia.
Brandon StrettonThe University of Adelaide, Adelaide, South Australia, Australia.
Stephen BacchiThe University of Adelaide, Adelaide, South Australia, Australia.
Pramesh KovoorWestmead Hospital, The University of Sydney Faculty of Medicine and Health, Sydney, New South Wales, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPulsed field ablation (PFA) has emerged as a promising non-thermal alternative to conventional atrial fibrillation (AF) ablation techniques. However, intravascular haemolysis has been increasingly recognised as a potential complication, with variable incidence and clinical significance.

objectiveTo systematically review the available clinical evidence on PFA-related haemolysis, focusing on biochemical markers, clinical manifestations and device-specific differences.

methodsPubMed, Embase and Cochrane databases were searched until 20 May 2025 for clinical studies evaluating primarily PFA-pulmonary vein isolation for AF that reported haemolysis, acute kidney injury (AKI) or relevant biomarker changes. The primary outcome was evaluation of incidence and biochemical evidence of PFA-related haemolysis. Secondary outcomes included incidence of AKI and its clinical consequences.

results12 studies (≈20 000 patients) were included. Biomarker evidence of haemolysis was consistent, with postablation lactate dehydrogenase elevations of 250-438 U/L and bilirubin 15-48 µmol/L, often accompanied by reduced haptoglobin and elevated free haemoglobin. Incidence of haemolysis varied widely (0-94.3%), reflecting heterogeneity in definitions and reporting. Clinical sequelae were uncommon: haemoglobinuria was observed in five studies, and AKI occurred in 83 patients (0.4%), 12 requiring transient dialysis. All returned to baseline renal function except one patient with severe chronic kidney disease. Procedural factors and catheter design may influence haemolysis burden. Observations of lower haemolytic biomarker changes with devices such as PulseSelect, Affera and Volt are preliminary and require confirmation, given the predominance of Farawave data.

conclusionsHaemolysis is a reproducible biochemical outcome of PFA, but clinically significant events such as AKI are rare and usually reversible. Catheter design, energy delivery and patient baseline renal function are likely to modulate haemolysis risk. Standardised haemolysis definitions and prospective head-to-head comparisons across PFA platforms are needed to clarify clinical relevance and optimise safety. PROSPERO REGISTRATION NUMBER: CRD420251069612.

Indexed as

Atrial FibrillationCatheter AblationHemolysisIrreversible Electroporation TherapyPostoperative ComplicationsAcute Kidney InjuryBilirubinHaptoglobinsHemoglobinuriaHumansIncidenceLactate DehydrogenasesPulmonary VeinsRisk FactorsTreatment OutcomeBilirubinHaptoglobinsLactate DehydrogenasesAblation TechniquesAtrial FibrillationCatheter AblationSystematic Reviews as Topic

Identifiers

PMID41213824
PMCPMC12603721

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.