Evidence for altered epicardial coronary artery autoregulation as a cause of distal coronary vasoconstriction after successful percutaneous transluminal coronary angioplasty

Tim A. Fischell, Kurt N. Bausback, Thomas V. McDonald

Research output: Contribution to journalArticle

55 Scopus citations

Abstract

To determine whether vasoconstriction distal to the site of successful percutaneous transluminal coronary angioplasty (PTCA) is a result of altered autoregulation in a hypoperfused coronary artery, we examined the association of this distal vasoconstriction with lesion severity in 20 patients. Lesion severity was classified as moderate, severe or critical (> 1.0, 0.5-1.0, and < 0.5 mm, respectively). Quantitative coronary measurements were made at 3, 15, and 30 min after PTCA, and then after intracoronary (IC) nitroglycerin, in coronary segments distal to the dilated lesion (distal) and in a nonmanipulated vessel (control). Coronary vasoconstriction in the Distal segment after PTCA correlated with lesion severity, with 14±4%, 28±2%, and 41±5% vasoconstriction (vs. IC nitroglycerin, 30 min after PTCA) in the moderate, severe and critical lesion severity subgroups, respectively (P < 0.01 for critical or severe vs. moderate). This vasoconstriction was significantly greater than that observed in the corresponding control segment for patients with severe (P < 0.01), and critical (P < 0.001) lesions. These findings suggest that hypoperfused human epicardial coronary arteries "reset" their autoregulatory responsiveness and that distal vasoconstriction after PTCA is the result of this altered autoregulation. These findings have clinical implications concerning the etiology, prophylaxis and treatment of coronary spasm after PTCA and coronary bypass surgery.

Original languageEnglish (US)
Pages (from-to)575-584
Number of pages10
JournalJournal of Clinical Investigation
Volume86
Issue number2
DOIs
StatePublished - Aug 1990

Keywords

  • Angioplasty
  • Autoregulation
  • Coronary artery
  • Epicardial
  • Vasoconstriction

ASJC Scopus subject areas

  • Medicine(all)

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