Prognostic value of left ventricular global longitudinal strain for predicting postoperative myocardial infarction in patients with major non-cardiac surgery
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 871
研究概览
简要总结
Background: The usefulness of preoperative measurement of left ventricular global longitudinal strain (LVGLS) for predicting prognosis in patients undergoing non-cardiac surgery has not been evaluated. We analyzed the prognostic value of LVGLS in predicting postoperative 30-day cardiovascular events and myocardial injury after non-cardiac surgery (MINS). Methods: This prospective cohort study was conducted in two referral hospitals and included 871 patients who underwent non-cardiac surgery <1 month after preoperative echocardiography. Those with ejection fraction <40%, valvular heart disease, and regional wall motion abnormality were excluded. The co-primary endpoints were the (1) composite incidence of all-cause death, acute coronary syndrome (ACS), and MINS and (2) composite incidence of all-cause death and ACS. Results: Among the 871 participants enrolled (mean age: 72.9 years; female: 60.8%), there were 43 cases of the primary endpoint (4.9%): 10 deaths, 3 ACS, and 37 MINS. Participants with impaired LVGLS (=16.6%) had a higher incidence of the co-primary endpoints (log-rank P < 0.001 and 0.015) than those without. The result was similar after adjustment with clinical variables and preoperative troponin T levels (hazard ratio = 1.30, 95% confidence interval [CI] = 1.03-1.65; P = 0.027). In sequential Cox analysis and net reclassification index, LVGLS had an incremental value for predicting the co-primary endpoints after non-cardiac surgery. Among the 538 (61.8%) participants who underwent serial troponin assay, LVGLS predicted MINS independently from the traditional risk factors (odds ratio = 3.54, 95% CI = 1.70-7.36; P = 0.001). Conclusions: Preoperative LVGLS has an independent and incremental prognostic value in predicting early postoperative cardiovascular events and MINS.
研究设计
- 研究类型
- Observational Study
入排标准
- 年龄范围
- 45(Year) 至 0No Limit(—)
- 性别
- All
入选标准
- •1. The patient who has at least one cardiovascular risk factor among patients undergoing non-cardiac major surgery
- •(1) Non-cardiac major surgery
- •? Major orthopedic surgery
- •? Major General Surgery
- •? Major urology or gynecology surgery
- •? Major neurosurgery
- •? Major vascular surgery
- •? Major thoracic surgery
- •(2) Cardiovascular risk factors
- •? Age (over 65 years old)
- •? Coronary artery disease
- •? Peripheral artery disease
- •? History of stroke or transient ischemic accident
- •? Diabetes Mellitus
- •? Chronic kidney disease
- •? Heart failure
- •? Uncontrolled hypertension (Systolic blood pressure over 140 mmHg despite hypertension)
- •? Q wave, T inversion, or ST depression in electrocardiogram
- •2. Over 45-year old
- •3. Informed consent
排除标准
- •(1) A person who is unable to understand the purpose and method of this clinical trial due to more than moderate degree of dementia, mental illness or neurological disease
- •(2) Low risk minor surgery
- •: ear/nose/throat surgery, ophthalmology, thyroid, parathyroid, breast, local anorectal procedure, breast, salpingectomy, endometrial ablation, peripheral nerve surgery, cosmetic surgery, hand surgery, arterio-venous access surgery for dialysis
- •(3) left ventricular ejection fraction below 40% on transthoracic echocardiography
- •(4) Regional wall motion abnormality on transthoracic echocardiography
- •(5) More than moderate degree of valvular heart disease on transthoracic echocardiography
- •(6) Left bundle branch block on electrocardiogram
- •(7) Atrial fibrillation on electrocardiogram
