SAFE EX-VIVO CORONARY ANGIOGRAPHY WITH ISOSMOTIC CONTRAST AGENT

Citation
Db. Schmit et al., SAFE EX-VIVO CORONARY ANGIOGRAPHY WITH ISOSMOTIC CONTRAST AGENT, Journal of thoracic and cardiovascular surgery, 112(2), 1996, pp. 306-309
Citations number
8
Categorie Soggetti
Respiratory System","Cardiac & Cardiovascular System",Surgery
ISSN journal
00225223
Volume
112
Issue
2
Year of publication
1996
Pages
306 - 309
Database
ISI
SICI code
0022-5223(1996)112:2<306:SECAWI>2.0.ZU;2-#
Abstract
Plain-film coronary angiography of the cardiac explant on the operatin g table should be considered when conventional cardiac catheterization is desired but unavailable. We compared the effects of three contrast solutions on cold-preserved, isolated guinea pig hearts. Hearts were excised, perfused for 30 minutes, and arrested with Plegisol solution at 7 degrees C. Twenty minutes after arrest, experimental hearts were perfused with one of three solutions: hyperosmolar Hexabrix solution ( n = 6), hyperosmolar Renografin-76 solution (n = 6), or diluted, isosm otic Omnipaque solution (n = 8). The hearts were flushed with cold Ple gisol solution 5 minutes later. Control hearts received no contrast du ring arrest (n = 9). The hearts were reperfused after 1 hour of arrest , and coronary blood Bow (in millimeters per minute), left ventricular developed pressure (in millimeters of mercury), and rate of developed pressure (in millimeters of mercury per second) were measured, Endoth elium-dependent smooth muscle relaxation to bradykinin administration and endothelium-independent relaxation to sodium nitroprusside adminis tration were also assessed, No significant difference in myocardial or endothelial function was noted between control hearts and hearts perf used with Omnipaque solution. Hearts perfused with Renografin solution or Hexabrix solution, however, were found to have significantly impai red endothelial and myocardial function. We conclude that an isosmotic contrast solution should be used for ex vivo coronary angiography in cold-preserved hearts to avoid impairment of endothelial and myocardia l function.