左心室功能,堵塞和empagliflozin对心肌梗塞后心力衰竭风险的影响
Jacob A Udell1, Mark C Petrie2, W Schuyler Jones3
1Women's College Hospital, University of Toronto, Toronto, Ontario, Canada; Peter Munk Cardiac Centre, Toronto General Hospital, University of Toronto, Toronto, Ontario, Canada.
Journal of the American College of Cardiology
|April 8, 2024
概括
恩帕格利弗洛辛显著减少了急性心肌梗塞 (AMI) 后的心力衰竭住院的病例,无论左心室喷射率 (LVEF) 或拥堵. 这一发现为治疗AMI后患者使用empagliflozin提供了新的见解.
科学领域:
- 心脏病学 心脏病学
- 药理学 药理学是指药理学的学科.
- 临床试验 临床试验
背景情况:
- 已知empagliflozin在急性心肌梗塞 (AMI) 后使用可以减少心力衰竭 (HF) 住院.
- 然而,在这种情况下,其对所有原因死亡率的影响仍然不清楚.
- 左心室喷射分数 (LVEF) 和拥堵对结果和empagliflozin疗效的影响需要进一步评估.
研究的目的:
- 评估LVEF严重程度,拥堵或两者之间的关联,以及AMI后患者的结果.
- 确定empagliflozin在这些患者中减轻HF风险的有效性.
- 分析Empagliflozin在不同LVEF和拥堵子组中的影响.
主要方法:
- 在EMPACT-MI试验中,在14天内随机选择了6,522名AMI患者,他们减少了LVEF (<45%) 或对empagliflozin或安慰剂的拥堵.
- 患者的随访时间中位数为17.9个月,以评估HF住院和死亡率.
- 根据基线LVEF,拥堵的存在和治疗臂,分析了结果.
主要成果:
- 较低的LVEF和拥堵的存在独立地与所有原因死亡,首次HF住院和总HF住院的风险显著增加有关.
- 恩帕格利弗洛辛在首次HF住院患者 (HR:0.77) 和总HF住院患者 (RR:0.67) 中显著减少.
- 无论基线LVEF或拥堵状况如何,在所有子组中均可观察到这些好处,且安全性概况相似.
结论:
- 在AMI后的患者中,受损的LVEF和拥堵是不良结果的显著预测因素.
- 恩帕格利弗洛辛有效地减少了AMI患者的HF住院,包括那些减少LVEF和/或拥堵的患者.
- 药物的安全性概况在这个人群中不同LVEF和拥堵水平上保持一致.
更多相关视频
相关概念视频
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
422
The activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) contributes to cardiac remodeling, and inhibiting the RAAS is a pharmacological target in heart failure management. As a result, neurohumoral modulation is a crucial treatment principle for managing heart failure. This approach involves using medications like ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), β-blockers, mineralocorticoid receptor antagonists (MRAs), and neutral...
422
Heart Failure Drugs: β-Blockers
337
β-adrenergic antagonists, commonly known as β-blockers, block the effects of sympathetic neurotransmitters such as noradrenaline (NA) and adrenaline (ADR). They have several beneficial effects in heart failure treatment. They reduce heart rate, the force of contraction, and cardiac muscle relaxation. They also slow the atrial-ventricular conduction rate and raise the threshold for arrhythmias. The concentration of β-blockers determines their effects on bronchodilation,...
337
Pathophysiology of Heart Failure
1.6K
Heart failure (HF) is a progressive syndrome involving ventricles that leads to inadequate cardiac output. It can be classified based on location and output or ejection fraction. Ejection fraction (EF) is an essential measurement in the diagnosis and surveillance of HF. Reduced EF corresponds to systolic heart failure (HFrEF). However, HF with preserved ejection fraction (HFpEF) is becoming increasingly prevalent. Also known as diastolic HF, this form of HF is related to aging. The...
1.6K
Heart Failure Drugs: Diuretics
370
Heart failure and kidney perfusion are interconnected in a complex way. Reduced renal perfusion and venous congestion are two significant factors that contribute to renal dysfunction in heart failure. The kidneys, primarily responsible for fluid balance in the body, are adversely affected due to compromised cardiac output and increased venous pressure. In response to reduced renal perfusion, the kidneys activate neurohumoral mechanisms to restore balance. However, these mechanisms can be...
370
Imbalances in Cardiac Output
1.4K
The heart's primary function is to pump blood throughout the body, maintaining a balance between blood sent out (cardiac output) and blood returning (venous return). If this balance is disrupted, it can result in congestive heart failure (CHF), a severe condition where the heart becomes an inefficient pump, leading to inadequate blood circulation.
CHF can occur due to the failure of either side of the heart. Left-side failure leads to pulmonary congestion—the right side continues to send...
CHF can occur due to the failure of either side of the heart. Left-side failure leads to pulmonary congestion—the right side continues to send...
1.4K
Dipeptidyl Peptidase 4 Inhibitors
182
Dipeptidyl peptidase 4 (DPP-4) is a serine protease widely distributed in the body. It's involved in the inactivation of GLP-1 and GIP hormones, which are crucial for insulin regulation. DPP-4 inhibitors, such as sitagliptin (Januvia), saxagliptin (Onglyza), linagliptin (Tradjenta), alogliptin (Nesina), and vildagliptin (Galvus), help increase the proportion of active GLP-1, enhancing insulin secretion. These inhibitors work by competitively binding to DPP-4. This binding causes a...
182


