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Evaluation of microcirculatory protection in percutaneous revascularisation: A stent implantation technique and
Muhammad Aetesam-Ur-Rahman1, Tian X Zhao1, Kitty Paques1
1Department of Interventional Cardiology, Royal Papworth Hospital, Cambridge, UK.
Insights
A slow drug-eluting stent (DES) implantation technique significantly reduces coronary microvascular dysfunction (CMD) after percutaneous coronary intervention (PCI). This improved microvascular function may help alleviate angina symptoms in patients with stable coronary artery disease.
Area of Science:
- Cardiovascular Medicine
- Interventional Cardiology
- Biomedical Engineering
Background:
- Coronary microvascular dysfunction (CMD) following percutaneous coronary intervention (PCI) is a significant concern, potentially leading to persistent angina.
- The method of stent implantation, including balloon inflation technique and material properties, may influence the development of post-PCI CMD.
Purpose of the Study:
- To investigate the impact of a slow versus standard drug-eluting stent (DES) implantation technique on coronary microvascular function after elective PCI.
- To evaluate secondary endpoints including myocardial injury and angina symptoms.
Main Methods:
- Thirty-six patients with stable angina undergoing elective PCI were randomized to a slow DES implantation technique or a standard technique.
- Coronary microvascular resistance (IMR) and coronary flow reserve (CFR) were assessed using PressureWire X thermodilution, alongside optical coherence tomography (OCT) pre- and post-PCI.
- Secondary outcomes included changes in cardiac troponin I (cTnI) and Seattle Angina Questionnaire (SAQ) scores.
Main Results:
- The slow DES implantation technique resulted in a significant improvement in the index of microvascular resistance (IMR), indicating less CMD (median difference -4.14, p=0.04).
- Coronary flow reserve (CFR) showed a numerical increase in the slow DES group, though not statistically significant (p=0.46).
- No significant differences were observed in changes in cardiac troponin I or SAQ scores at 3 months between the groups.
Conclusions:
- A slow stent implantation technique is associated with reduced coronary microvascular dysfunction after elective PCI in patients with stable angina.
- This finding suggests that optimizing stent deployment strategy can mitigate microvascular impairment.
Background:
Coronary microvascular dysfunction (CMD) after percutaneous coronary intervention (PCI) is prognostically important and may also be a cause of persistent angina. The stent balloon inflation technique or material properties may influence the degree of CMD post-PCI.
Methods:
Thirty-six patients with stable angina attending for elective PCI were randomized to either slow drug eluting stent (DES) implantation technique (DES slow group): +2 atm. every 5 s., maintained for a further 30 s or a standard stent implantation technique (DES std group): rapid inflation and deflation. PressureWire X with thermodilution at rest and hyperemia and optical coherence tomography (OCT) were performed pre- and post-PCI. Combined primary endpoints were changes in index of microvascular resistance (delta IMR) and coronary flow reserve (delta CFR) following PCI. The secondary endpoints included differences in cardiac troponin I (delta cTnI) at 6 h post-PCI, Seattle angina questionnaire (SAQ) at 1, 3, 6, and 12 months and OCT measures of stent results immediately post-PCI and at 3 months.
Results:
Both groups were well matched, with similar baseline characteristics and OCT-defined plaque characteristics. Delta IMR was significantly better in the DES slow PCI arm with a median difference of -4.14 (95% CI -10.49, -0.39, p = 0.04). Delta CFR was also numerically higher with a median difference of 0.47 (95% CI -0.52, 1.31, p = 0.46). This did not translate to improved delta median cTnI (1.5 (34.8) vs. 0 (27.5) ng/L, p = 0.75) or median SAQ score at 3 months, (85 (20) vs. 95 (17.5), p = 0.47).
Conclusion:
Slow stent implantation is associated with less CMD after elective PCI in patients with stable angina.
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