Literature DB >> 14993141

Coronary hyperemic dose responses of intracoronary sodium nitroprusside.

Walter A Parham1, Andre Bouhasin, Jeffrey P Ciaramita, Souheil Khoukaz, Steven C Herrmann, Morton J Kern.   

Abstract

BACKGROUND: Sodium nitroprusside is one of several agents considered effective for treating the no-reflow phenomenon during acute coronary interventions. However, the coronary hyperemic dose responses and systemic hemodynamic effects of intracoronary nitroprusside have yet to be determined in humans. The purpose of this study was to compare the hyperemic and hemodynamic responses of intracoronary nitroprusside to intracoronary adenosine in patients during cardiac catheterization with angiographically normal anterior descending arteries. METHODS AND
RESULTS: In 21 patients, coronary blood flow velocity (0.014-inch Doppler flow wire), heart rate, and blood pressure were measured in unobstructed left anterior descending coronary arteries at rest, after intracoronary adenosine (30- to 50-microg boluses), and after 3 serial doses (0.3-, 0.6-, and 0.9-microg/kg boluses) of intracoronary nitroprusside. Coronary reserve was calculated as hyperemia/basal coronary flow velocity. In an additional 9 patients with intermediate stenoses (53+/-7%), 14 fractional flow reserve (FFR) measurements (using 0.014-inch pressure wire) were performed with both intracoronary adenosine and nitroprusside (0.6 microg/kg). Intracoronary nitroprusside produced equivalent coronary hyperemia with a longer duration ( approximately 25%) compared with intracoronary adenosine. Intracoronary nitroprusside (0.9 microg/kg) decreased systolic blood pressure by <20%, with minimal change in heart rate, whereas intracoronary adenosine had no effect on these parameters. FFR measurements with intracoronary nitroprusside were identical to those obtained with intracoronary adenosine (r=0.97).
CONCLUSIONS: Compared with adenosine, intracoronary nitroprusside produces an equivalent but more prolonged coronary hyperemic response in normal coronary arteries. Intracoronary nitroprusside, in doses commonly used for the treatment of the no-reflow phenomenon, can produce sustained coronary hyperemia without detrimental systemic hemodynamics. On the basis of FFR measurements compared with adenosine, sodium nitroprusside also appears to be a suitable hyperemic stimulus for coronary physiological measurements.

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Year:  2004        PMID: 14993141     DOI: 10.1161/01.CIR.0000118470.52908.D9

Source DB:  PubMed          Journal:  Circulation        ISSN: 0009-7322            Impact factor:   29.690


  11 in total

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Journal:  J Thromb Thrombolysis       Date:  2008-09-26       Impact factor: 2.300

2.  Advances in Coronary No-Reflow Phenomenon-a Contemporary Review.

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3.  Pathophysiology, Diagnosis, and Management of Coronary No-Reflow Phenomenon.

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4.  Feasibility and safety of intracoronary nicorandil infusion as a novel hyperemic agent for fractional flow reserve measurements.

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Review 5.  Coronary pressure-derived fractional flow reserve in the assessment of coronary artery stenoses.

Authors:  Nikolaos Kakouros; Frank J Rybicki; Dimitrios Mitsouras; Julie M Miller
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Review 6.  Pathophysiology, Diagnosis, and Management of Coronary No-Reflow Phenomenon.

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Review 7.  Spontaneous and procedural plaque embolisation in native coronary arteries: pathophysiology, diagnosis, and prevention.

Authors:  Giovanni Luigi De Maria; Niket Patel; George Kassimis; Adrian P Banning
Journal:  Scientifica (Cairo)       Date:  2013-12-19

Review 8.  Fractional flow reserve in acute coronary syndromes: A review.

Authors:  Nikunj R Shah; Rasha Al-Lamee; Justin Davies
Journal:  Int J Cardiol Heart Vasc       Date:  2014-11-11

Review 9.  Research progress on the molecular mechanism of coronary microvascular endothelial cell dysfunction.

Authors:  Jianying Deng
Journal:  Int J Cardiol Heart Vasc       Date:  2021-04-10

10.  Intracoronary fixed dose of nitroprusside via thrombus aspiration catheter for the prevention of the no-reflow phenomenon following primary percutaneous coronary intervention in acute myocardial infarction.

Authors:  Yu-Jun Zhao; Xiang-Hua Fu; Xiao-Xiao Ma; Dong-Ying Wang; Qiu-Li Dong; Yan-Bo Wang; Wei Li; Kun Xing; Xin-Shun Gu; Yun-Fa Jiang
Journal:  Exp Ther Med       Date:  2013-06-04       Impact factor: 2.447

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