Prehospital pulse-dose glucocorticoid on index of microvascular resistance in patients with ST-segment elevation myocardial infarction: a sub-study of the PULSE-MI trial.

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Tác giả: Ole Ahlehoff, Lars Bredevang Andersen, Lia Evi Bang, Rasmus Paulin Beske, Helle Collatz Christensen, Thomas Engstrøm, Fredrik Folke, Christian Hassager, Lene Holmvang, Reza Jabbari, Jacob Lønborg, Jasmine Melissa Marquard, Mikko Minkkinen, Lars Nepper-Christensen, Laust Emil Roelsgaard Obling, Frants Pedersen, Rikke Sørensen, Hans-Henrik Tilsted, Niels Vejlstrup, Yan Zhou

Ngôn ngữ: eng

Ký hiệu phân loại: 297.1248 Sources of Islam

Thông tin xuất bản: England : Journal of inflammation (London, England) , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 723790

 BACKGROUND: Microvascular injury in patients with ST-segment elevation myocardial infarction (STEMI) occurs in up to 50%, yet no therapeutic target exists. Inflammation contributes directly to myocardial damage in STEMI and may also cause deleteriously effects on the microcirculation. The aim of this prespecified sub-study was to determine the effect of prehospital pulse-dose glucocorticoid on the microcirculation determined by index of microvascular resistance (IMR) and its relation to inflammation. The PULSE-MI trial was a 1:1 randomized, blinded, placebo-controlled clinical trial in patients with STEMI transferred for primary percutaneous coronary intervention (PCI) investigating the cardioprotective effects of prehospital pulse-dose glucocorticoid (methylprednisolone 250 mg) compared with placebo. In this prespecified sub-study, we investigated microvascular function as IMR by thermodilution after primary PCI and inflammation defined by C-reactive protein (CRP) at 24 hours after onset of STEMI. RESULTS: Of 530 patients included in the PULSE-MI trial, 295 (56%) were assessed with coronary physiology of whom 142 (48%) were treated with glucocorticoid and 153 (52%) with placebo. Baseline characteristics were overall well-balanced in both groups. The median IMR in the glucocorticoid group was 23 (interquartile range (IQR), 11-38) and 18 (IQR, 11-42) in the placebo group (p=0.49). CRP upon arrival did not differ between treatment groups (p=0.81), but CRP at 24 hours was significantly lower in the glucocorticoid group compared to placebo (p<
 0.001). CONCLUSIONS: Prehospital glucocorticoid did not impact IMR assessed immediately after primary PCI, albeit this compound, demonstrated significant anti-inflammatory effects as determined by CRP levels at 24 hours. TRIAL REGISTRATION: http://www. CLINICALTRIALS: gov
  Unique Identifier: NCT05462730.
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