Pre-hospital pulse glucocorticoid therapy in patients with ST-segment elevation myocardial infarction transferred for primary percutaneous coronary intervention: a randomized controlled trial (PULSE-MI)

被引:4
|
作者
Madsen, Jasmine Melissa [1 ]
Obling, Laust Emil Roelsgaard [1 ]
Rytoft, Laura [1 ]
Folke, Fredrik [2 ,3 ]
Hassager, Christian [1 ]
Andersen, Lars Bredevang [4 ]
Vejlstrup, Niels [1 ]
Bang, Lia Evi [1 ]
Engstrom, Thomas [1 ]
Lonborg, Jacob Thomsen [1 ]
机构
[1] Copenhagen Univ Hosp, Rigshosp, Heart Ctr, Dept Cardiol, Copenhagen, Denmark
[2] Copenhagen Univ Hosp, Copenhagen Emergency Med Serv, Copenhagen, Denmark
[3] Copenhagen Univ Hosp Herlev, Dept Cardiol, Copenhagen, Denmark
[4] Reg Zealand Emergency Med Serv, Naestved, Denmark
关键词
ST-segment elevation myocardial infarction; Pre-hospital intervention; Randomized controlled trials; Inflammation; Reperfusion Injury; Steroid; Cardioprotection; Cardiac magnetic resonance; MAGNETIC-RESONANCE; MICROVASCULAR OBSTRUCTION; STENT IMPLANTATION; SIZE; STEMI; METHYLPREDNISOLONE; ANGIOPLASTY; HEMORRHAGE; DAMAGE;
D O I
10.1186/s13063-023-07830-y
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background Inflammation in ST-segment elevation myocardial infarction (STEMI) is an important contributor to both acute myocardial ischemia and reperfusion injury after primary percutaneous coronary intervention (PCI). Methylprednisolone is a glucocorticoid with potent anti-inflammatory properties with an acute effect and is used as an effective and safe treatment of a wide range of acute diseases. The trial aims to investigate the cardioprotective effects of pulse-dose methylprednisolone administered in the pre-hospital setting in patients with STEMI transferred for primary PCI.Methods This trial is a randomized, blinded, placebo-controlled prospective clinical phase II trial. Inclusion will continue until 378 patients with STEMI have been evaluated for the primary endpoint. Patients will be randomized 1:1 to a bolus of 250 mg methylprednisolone intravenous or matching placebo over a period of 5 min in the pre-hospital setting. All patients with STEMI transferred for primary PCI at Rigshospitalet, Copenhagen University Hospital, Denmark, will be screened for eligibility. The main eligibility criteria are age >= 18 years, acute onset of chest pain with < 12 h duration, STEMI on electrocardiogram, no known allergy to glucocorticoids or no previous coronary artery bypass grafting, previous acute myocardial infarction in assumed culprit, or a history with previous maniac/psychotic episodes. Primary outcome is final infarct size measured by late gadolinium enhancement on cardiac magnetic resonance (CMR) 3 months after STEMI. Secondary outcomes comprise key CMR efficacy parameters, clinical endpoints at 3 months, the peak of cardiac biomarkers, and safety.Discussion We hypothesize that pulse-dose methylprednisolone administrated in the pre-hospital setting decreases inflammation and thus reduces final infarct size in patients with STEMI treated with primary PCI.
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页数:14
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