# Cardiopulmonary Protection of Modified Remote Ischemic Preconditioning in Mitral Valve Replacement Surgery: A Randomized Controlled Trial

**Authors:** Lianqin Zhang, Kang Zhou, Tianchu Gu, Jingjing Xu, Mengzhu Shi, Jiang Zhu, Jindong Liu

PMC · DOI: 10.1155/2024/9889995 · Cardiovascular Therapeutics · 2024-06-24

## TL;DR

A modified version of a blood flow restriction technique reduced heart and lung damage during heart valve surgery, according to a clinical trial.

## Contribution

This study demonstrates that repeated modified remote ischemic preconditioning reduces cardiopulmonary injury in mitral valve replacement surgery.

## Key findings

- Modified RIPC significantly reduced cardiac biomarkers like cTnI, CK-MB, and LDH after surgery.
- The modified RIPC group had lower rates of acute lung injury and improved oxygen levels.
- Inflammatory markers like IL-6 and TNF-α were reduced in the modified RIPC group.

## Abstract

Background: Remote ischemic preconditioning (RIPC) is reported to have early-phase and delayed-phase organ-protective effects. Previous studies have focused on the organ protection of a single RIPC protocol, and the clinical outcomes remain uncertain. Whether the modified RIPC (mRIPC) protocol performed repeatedly provides cardiopulmonary protection is still uncertain.

Methods: In this single-center, randomized, controlled trial, 86 patients undergoing elective mitral valve replacement (MVR) surgery were randomized 1:1 to receive either mRIPC or no ischemic preconditioning (control). Three cycles of 5 min ischemia and 5 min reperfusion induced by a blood pressure cuff served as the RIPC stimulus. mRIPC was induced at the following three time points: 24 h, 12 h, and 1 h before surgery. Blood samples were withdrawn at 10 min after intubation (T0), at 1 h after aortic declamping (T1), and at 6 h (T2), 12 h (T3), and 24 h (T4) after surgery to measure the serum concentrations of myocardial enzymes and other biomarkers, including cardiac troponin I (cTnI), which was the primary endpoint of this study. Creatine kinase isoenzyme (CK-MB), lactate dehydrogenase (LDH), inotropic score (IS), and inflammatory mediators were also measured. Blood gas analysis was conducted to calculate the PaO2/FiO2 ratio and A-aDO2, and the incidence of acute lung injury (ALI) was also recorded.

Results: mRIPC significantly decreased the serum concentrations of cTnI, CK-MB, and LDH at T2, T3, and T4 (p < 0.01), and the IS decreased compared with that in the control group (12.0 ± 1.0 vs. 14.2 ± 1.1, p < 0.01). In addition, the incidence of ALI in the mRIPC group was decreased (32.6% vs. 51.2%, p = 0.039), and the PaO2/FiO2 was higher at T4 (p < 0.05). Compared with those in the control group, the levels of interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) were decreased at T1, T2, T3, and T4 (p < 0.05) in the mRIPC group, and the level of IL-10 increased at the same time.

Conclusions: mRIPC decreased the incidence of myocardial and lung injury in MVR surgery, providing new evidence for the clinical application of RIPC in valve surgery.

Trial Registration: ClinicalTrials.gov (NCT01406678).

## Linked entities

- **Proteins:** IL6 (interleukin 6), IL10 (interleukin 10)
- **Diseases:** acute lung injury (MONDO:0006502)

## Full-text entities

- **Genes:** IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, TNNI3 (troponin I3, cardiac type) [NCBI Gene 7137] {aka CMD1FF, CMD2A, CMH7, RCM1, TNNC1, cTnI}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** Remote Ischemic (MESH:D002545), inflammatory (MESH:D007249), reperfusion (MESH:D015427), ischemia (MESH:D007511), myocardial and lung injury (MESH:D055370), ALI (MESH:D055371)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11221996/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC11221996/full.md

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Source: https://tomesphere.com/paper/PMC11221996