# Cardioplegia Strategies in Minimally Invasive Aortic Valve Replacement: An Inverse Probability of Treatment Weighting Analysis

**Authors:** Lukman Amanov, Sadeq Ali-Hasan-Al-Saegh, Arian Arjomandi Rad, Antonia Annegret Jauken, Prokopis-Andreas Zotos, Jawad Salman, Thanos Athanasiou, Ezin Deniz, Stefan Ruemke, Bastian Schmack, Arjang Ruhparwar, Alina Zubarevich, Alexander Weymann

PMC · DOI: 10.3390/medicina62020373 · 2026-02-13

## TL;DR

This study compares different heart protection methods during aortic valve surgery and finds that Calafiore and Custodiol strategies reduce complications like atrial fibrillation and heart injury.

## Contribution

The novel use of inverse probability weighting to balance baseline differences reveals superior outcomes with Calafiore and Custodiol cardioplegia strategies.

## Key findings

- Calafiore and Custodiol strategies significantly reduced new-onset atrial fibrillation compared to Buckberg and St Thomas’.
- These strategies also showed lower myocardial injury biomarker release and fewer respiratory complications.
- Mortality and resource use remained similar across all strategies after balancing baseline factors.

## Abstract

Background and Objectives: Optimal myocardial protection during minimally invasive aortic valve replacement (MIAVR) is debated. We compared four cardioplegia strategies. Materials and Methods: Consecutive MIAVR patients (January 2010–April 2025) at a single centre were analysed retrospectively. Cardioplegia regimens were Buckberg (n = 131), Calafiore (n = 153), Custodiol HTK (n = 146) and St Thomas’ (n = 113). Because substantial baseline imbalances were present in the unadjusted cohort, inverse probability of treatment weighting (IPTW) based on a multinomial propensity score was applied to achieve covariate balance between groups. IPTW was performed using a comprehensive propensity model that incorporated (1) baseline demographic and clinical characteristics, (2) anatomical factors, including bicuspid valve morphology. Procedural time variables were assessed in secondary sensitivity analyses. After IPTW application, all variables, including procedural times, achieved balance (ASMD < 0.1). Postoperative outcomes were then compared in this fully balanced pseudo-population. The Scheffé post hoc test was performed. Results: Groups were demographically comparable except for more bicuspid valves in Buckberg. New-onset paroxysmal atrial fibrillation occurred in 31.2% (Buckberg) and 26.5% (St Thomas’) versus 7.1% (Calafiore) and 2.0% (Custodiol) (p < 0.01). Respiratory insufficiency followed a similar pattern (p = 0.02). Intensive-care and hospital stay, major complications, left-ventricular ejection fraction, and 30-day mortality (0.6–3.0%) were equivalent. Bicuspid anatomy independently prolonged operative metrics but did not influence biomarkers. Conclusions: After comprehensive inverse probability weighting that balanced groups on all baseline characteristics and anatomical factors, Calafiore and Custodiol cardioplegia strategies maintained significantly lower rates of new-onset atrial fibrillation (9.3% and 3.8% vs. 28.5% for Buckberg, p < 0.01), reduced myocardial injury biomarker release (peak CK 520 and 510 vs. 920 U/L, p < 0.01), and decreased respiratory complications (7.8% and 8.1% vs. 16.2%, p = 0.01), while mortality, stroke, and resource utilisation measures remained comparable across strategies.

## Linked entities

- **Diseases:** atrial fibrillation (MONDO:0004981)

## Full-text entities

- **Genes:** CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}
- **Diseases:** NIDDM (MESH:D003924), valve failure (MESH:D006333), endocarditis (MESH:D004696), thromboembolic (MESH:D013923), AR (MESH:D001022), IDDM (MESH:D003922), coronary artery disease (MESH:D003324), Ovale (MESH:D054092), sepsis (MESH:D018805), DVT (OMIM:612862), bicuspid valve (MESH:D000082882), left atrial appendage (MESH:D059446), atrial fibrillation or flutter (MESH:D001282), reperfusion injury (MESH:D015427), death (MESH:D003643), intracranial bleeding (MESH:D013345), myocardial infarction (MESH:D009203), infective (MESH:D007239), AF (MESH:D001281), ischemic stroke (MESH:D002544), deep vein thrombosis (MESH:D020246), vascular injury (MESH:D057772), paravalvular leak (MESH:D019559), osteoporosis (MESH:D010024), AV (MESH:D054537), Respiratory insufficiency (MESH:D012131), Arrhythmias (MESH:D001145), MIAVR (MESH:D001024), bleeding (MESH:D006470), Myocardial Injury (MESH:D009202), COPD (MESH:D029424), Conduction block (MESH:D006327), delirium (MESH:D003693), stroke (MESH:D020521), acute kidney injury (MESH:D058186), stenosis (MESH:D003251), ischemia (MESH:D007511), seizures (MESH:D012640), arrhythmic sequelae (OMIM:212500), Myocardial Protection (MESH:C536411), regurgitation (MESH:D008944), aortic valve disease (MESH:D000082862), injury to (MESH:D014947), conduction disease (MESH:D004194), pain (MESH:D010146), respiratory complications (MESH:D012140), wound dehiscence (MESH:D013529), renal failure (MESH:D051437), calcified valve (MESH:D006349), pulmonary complication (MESH:D008171), ischemic (MESH:D002545), diabetes (MESH:D003920), LBBB (MESH:D002037), calcification (MESH:D002114), Cardiac arrest (MESH:D006323)
- **Chemicals:** tryptophan (MESH:D014364), heparin (MESH:D006493), magnesium (MESH:D008274), ACC (-), potassium (MESH:D011188), bicarbonate (MESH:D001639), oxygen (MESH:D010100), histidine (MESH:D006639)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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Source: https://tomesphere.com/paper/PMC12942088