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DOI 10.1161/jaha.116.005426

Медицинская библиотека · Journal of the American Heart Association · 2017

Cardioprotective Effects of Intracoronary Morphine in ST-Segment Elevation Myocardial Infarction Patients Undergoing Primary Percutaneous Coronary Intervention: A Prospective, Randomized Trial.

Gwag Hye Bin, Kim Eun Kyoung, Park Taek Kyu, Lee Joo Myung, Yang Jeong Hoon, Song Young Bin, Choi Jin-Ho, Choi Seung-Hyuk, Lee Sang Hoon, Chang Sung-A, Park Sung-Ji, Lee Sang-Chol, Park Seung Woo, Jang Woo Jin, Lee Mirae, Chun Woo Jung, Oh Ju Hyeon, Park Yong Hwan, Choe Yeon Hyeon, Gwon Hyeon-Cheol, Hahn Joo-Yong

СтатьяМногоцентровое исследованиеРандомизированное исследованиеПеревод в очереди

Аннотация

BACKGROUND

A cardioprotective role of morphine acting via opioid receptors has been demonstrated, and previous preclinical studies have reported that morphine could reduce reperfusion injury and myocardial infarct size in a way similar to that of ischemic periconditioning. This study aimed to evaluate the effect of intracoronary morphine on myocardial infarct size in patients with ST-elevation myocardial infarction undergoing primary percutaneous coronary intervention.

METHODS AND

RESULTS

This study was designed as a 2-center, prospective, randomized, open-label, blinded end point trial. A total of 91 ST-elevation myocardial infarction patients with thrombolysis in myocardial infarction flow grade of 0 to 1 undergoing primary percutaneous coronary intervention were randomly assigned to a morphine or control group at a 1:1 ratio. The morphine group received 3 mg of morphine sulfate diluted with 3 mL of normal saline, and the control group received 3 mL of normal saline into a coronary artery immediately after restoration of coronary flow. The primary end point was myocardial infarct size assessed by cardiac magnetic resonance imaging The cardiac magnetic resonance images were evaluated for 42 and 38 patients in the morphine and control groups, respectively. Myocardial infarct size was not different between the 2 groups (25.6±11.2% versus 24.6±10.5%, P=0.77), nor was the extent of microvascular obstruction or myocardial salvage index (6.0±6.3% versus 5.1±4.6%, P=0.91; 31.1±15.2% versus 30.3±10.9%, P=0.75, respectively). There was no difference in peak creatine kinase-MB level, final thrombolysis in myocardial infarction flow, myocardial brush grade, or complete resolution of ST-segment.

CONCLUSIONS

Intracoronary morphine administration could not reduce myocardial infarct size in ST-elevation myocardial infarction patients undergoing primary percutaneous coronary intervention.

CLINICAL TRIAL REGISTRATION: URL: http://www.clinicaltrials.gov. Unique identifier: NCT01738100.

Для цитирования: Gwag Hye Bin, Kim Eun Kyoung, Park Taek Kyu, Lee Joo Myung, Yang Jeong Hoon, Song Young Bin, Choi Jin-Ho, Choi Seung-Hyuk, Lee Sang Hoon, Chang Sung-A, Park Sung-Ji, Lee Sang-Chol, Park Seung Woo, Jang Woo Jin, Lee Mirae, Chun Woo Jung, Oh Ju Hyeon, Park Yong Hwan, Choe Yeon Hyeon, Gwon Hyeon-Cheol, Hahn Joo-Yong. Cardioprotective Effects of Intracoronary Morphine in ST-Segment Elevation Myocardial Infarction Patients Undergoing Primary Percutaneous Coronary Intervention: A Prospective, Randomized Trial.. Journal of the American Heart Association. 2017. DOI: 10.1161/jaha.116.005426.

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