Cardioplegia cannula

Claim 1

An aortic root cannula for introduction into the heart organ during open heart surgery to selectively administer cardioplegic liquid, permit venting of the heart chamber, and monitor pressure in the heart vessel which comprises: (a) a first body element as a base unit having a top and bottom side and a primary cannula extension on the bottom side, a flanged transverse body portion extending to each side of said cannula to form an insertion stop for said cannula, and a main passage entering the top of said first body extending through said body portion and said primary cannula, (b) a secondary passage formed in the top of said transverse body portion parallel to and spaced from said main passage and an open sided recess on the bottom of said body portion surrounding said cannula and in communication with said secondary passage, (c) a secondary body element secured to the bottom of said first body element received within said open-sided recess to close said recess and having a top surface lying within said recess shaped to permit flow from said secondary passage around said primary cannula, said secondary body having a secondary outer cannula projection fitted over said primary cannula, (d) an axially extending passage in one of the surfaces of one of said cannula extending from said recess to the distal end of said cannulae to connect said secondary passage and the area at the end of said cannulae whereby said secondary passage may be connected to a pressure monitoring device, (e) a tubular extension affixed to said first body aligned with said main passage for housing a needle penetrator and to be connected to a source of cardioplegic liquid and medication, and an auxiliary connection to said tubular extension also communicating with said main passage to be connected to a subatmospheric source for venting the heart vessel through said cannulae, (f) said cannulae also having transverse registering ports open to the exterior of said cannulae.