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Published on: September 22, 2020
Association between stress hormones and perioperative risk in patients with critical limb ischemia undergoing
Yoshimitsu Soga1, Mitsuyoshi Takahara2, Osamu Iida3
1Department of Cardiology, Kokura Memorial Hospital, Kitakyushu, Japan.
Insights
High levels of stress hormones like epinephrine and cortisol are linked to increased risk of major adverse cardiovascular events (pMACE) in critical limb ischemia (CLI) patients after revascularization. These hormones also correlate with higher 30-day mortality.
Area of Science:
- Cardiovascular Medicine
- Endocrinology
- Vascular Surgery
Background:
- Critical limb ischemia (CLI) is associated with poor clinical outcomes.
- The impact of stress hormones on CLI patient outcomes after revascularization is not well understood.
- Perioperative major adverse cardiovascular events (pMACE) are a significant concern in CLI patients.
Purpose of the Study:
- To investigate the association between stress hormone levels and the risk of pMACE in CLI patients undergoing revascularization.
- To determine if specific stress hormones predict adverse cardiovascular events in this population.
- To explore the relationship between stress hormones and short-term mortality following revascularization.
Main Methods:
- Analysis of 467 CLI patients with pre-revascularization stress hormone levels (epinephrine, norepinephrine, dopamine, cortisol).
- Primary endpoint: pMACE (all-cause mortality, myocardial infarction, stroke) within 30 days.
- Propensity score matching employed to mitigate confounding factors.
Main Results:
- pMACE occurred in 4.5% of patients.
- Elevated epinephrine, dopamine, and cortisol levels were observed in patients with pMACE.
- Post-matching analysis revealed significantly higher epinephrine and cortisol levels in the pMACE group.
- Multivariate analysis confirmed independent associations of epinephrine and cortisol with pMACE risk.
Conclusions:
- Stress hormones, specifically epinephrine and cortisol, are significantly associated with pMACE risk in CLI patients undergoing revascularization.
- Both epinephrine and cortisol levels predict 30-day mortality after revascularization in CLI patients.
- These findings highlight the potential role of stress hormone monitoring in risk stratification for CLI patients.
Background:
It is well known that the clinical outcome of patients with critical limb ischemia (CLI) is poor. However, the relationship between stress-related hormone levels and CLI outcome remains unclear. The aim of this study was to reveal the association of stress hormones with the risk of a perioperative major adverse cardiovascular event (pMACE) in CLI patients undergoing surgical and endovascular revascularization.
Methods:
The study analyzed 467 CLI patients who had levels of stress-related hormones (epinephrine, norepinephrine, dopamine, and cortisol) measured before undergoing revascularization. The primary end point was pMACE, including all-cause mortality, myocardial infarction, and stroke within 30 days after revascularization. Propensity score matching was used to try to control for potential confounding.
Results:
Of the 467 patients analyzed, pMACE was observed in 21 patients (4.5%). The crude comparison of stress-related hormone levels between those with and those without pMACE showed that those with pMACE had a higher level of epinephrine, dopamine, and cortisol compared with those without pMACE. After propensity matching (20 patients with pMACE and 192 patients without pMACE), epinephrine and cortisol levels were significantly higher in those with pMACE. Multivariate analysis confirmed that both epinephrine and cortisol levels were related to the risk of pMACE independently of each other. The Cox proportional hazards regression model demonstrated that both hormones were associated with 30-day mortality but not with longer term mortality.
Conclusions:
Stress-related hormone (epinephrine and cortisol) levels were significantly associated with the risk of pMACE in CLI patients undergoing revascularization. Both hormones were related to 30-day mortality.
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