# Volatile Anesthesia in Contemporary Cardiac Surgery: Clinical Implications, Organ Protection and Perspectives for Personalized Perioperative Care

**Authors:** Debora Emanuela Torre, Carmelo Pirri

PMC · DOI: 10.3390/jpm16030138 · 2026-03-01

## TL;DR

This paper reviews how volatile anesthetics like sevoflurane and desflurane may protect organs during heart surgery, but their clinical benefits remain inconsistent.

## Contribution

The paper systematically evaluates the biological mechanisms and clinical outcomes of volatile anesthetics in cardiac surgery, highlighting the need for personalized approaches.

## Key findings

- Volatile anesthetics trigger mitochondrial protective pathways like K-ATP channel activation and ROS signaling.
- Clinical studies suggest benefits in myocardial protection and reduced systemic inflammation, but results are inconsistent.
- Patient-specific factors and surgical variability influence outcomes, calling for refined perioperative strategies.

## Abstract

Background: Interest in inhalational anesthesia in cardiac surgery has resurged as volatile anesthetics exert biological effects extending beyond hypnosis. Sevoflurane and desflurane activate mitochondrial cytoprotective signaling pathways, modulate inflammatory and endothelial responses and may attenuate ischemia–reperfusion injury during cardiopulmonary bypass, potentially influencing postoperative organ function and recovery. Methods: This narrative review critically examines experimental and clinical evidence on the use of volatile anesthetics in cardiac anesthesia. The current literature was analyzed to elucidate mechanistic foundations of myocardial and extracardiac organ protection, hemodynamic and metabolic effects, and the influence of patient-specific vulnerability profiles on perioperative outcomes. Results: Preclinical studies consistently demonstrate that volatile anesthetics trigger mitochondrial protective pathways, including K-ATP channel activation, controlled reactive oxygen species signaling and inhibition of the mitochondrial permeability transition pore. Clinical studies suggest potential benefits in myocardial protection and modulation of systemic inflammatory and microcirculatory responses. However, translation into consistent clinical outcome improvement remains heterogeneous, influenced by variability in surgical procedures, anesthetic protocols and patient risk stratification. Conclusions: Volatile anesthetics exhibit mechanistic properties supporting a potential role in organ protection during cardiac surgery. Nevertheless, clinical evidence remains inconclusive, underscoring the need for refined patient stratification and precision-based perioperative strategies. Identifying knowledge gaps and research priorities may facilitate rational, individualized integration of inhalational anesthesia into contemporary cardiac surgical practice.

## Linked entities

- **Chemicals:** sevoflurane (PubChem CID 5206), desflurane (PubChem CID 42113)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TNNI3 (troponin I3, cardiac type) [NCBI Gene 7137] {aka CMD1FF, CMD2A, CMH7, RCM1, TNNC1, cTnI}, TNNT2 (troponin T2, cardiac type) [NCBI Gene 7139] {aka CMD1D, CMH2, CMPD2, LVNC6, RCM3, TnTC}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** myocardial depressant (MESH:D003866), infarct (MESH:D007238), calcium overload (MESH:D019190), acute lung injury (MESH:D055371), contractile dysfunction (MESH:D006331), delirium (MESH:D003693), impaired ventricular function (MESH:D018754), bleeding (MESH:D006470), multiorgan impairment (MESH:D060825), coagulation disturbances (MESH:D001778), insulin resistance (MESH:D007333), injury to (MESH:D014947), myocardial infarction (MESH:D009203), organ dysfunction (MESH:D009102), ischemic (MESH:D002545), acute kidney injury (MESH:D058186), neurological complications (MESH:D002493), coronary artery disease (MESH:D003324), inflammatory (MESH:D007249), low cardiac output syndrome (MESH:D002303), Myocardial ischemia (MESH:D017202), myocardial injury (MESH:D009202), Ischemia (MESH:D007511), edema (MESH:D004487), pulmonary dysfunction (MESH:D011660), Reperfusion Injury (MESH:D015427), Myocardial Protection (MESH:C536411), cognitive dysfunction (MESH:D003072), necrotic (MESH:D009336), endothelial (MESH:D005642), lung injury (MESH:D055370), myocardial stunning (MESH:D017682), hypothermia (MESH:D007035), hypoxic (MESH:D002534)
- **Chemicals:** oxygen (MESH:D010100), carbon (MESH:D002244), lactate (MESH:D019344), nitric oxide (MESH:D009569), phosphate (MESH:D010710), isoflurane (MESH:D007530), Gas (MESH:D005708), ROS (MESH:D017382), K-ATP (-), desflurane (MESH:D000077335), calcium (MESH:D002118), glucose (MESH:D005947), CO2 (MESH:D002245), NO (MESH:D009614), ATP (MESH:D000255), Sevoflurane (MESH:D000077149)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC13027520/full.md

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Source: https://tomesphere.com/paper/PMC13027520