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J Thorac Cardiovasc Surg 2000;119:856-857
© 2000 The American Association for Thoracic Surgery
LETTERS TO THE EDITOR |
Department of Anesthesiology and Reanimatology, Gunma University, School of Medicine, 3-39-22, Showa-machi, Maebashi, Gunma 371-8511, Japan
Reply to the Editor:
We appreciate the comments of Miyamoto and Miyamoto. As we described previously, it is not clear which type of pulsatile waveform has positive effects on cerebral circulation and improves outcome of patients.
1
The internal jugular venous oxygen saturation (SjvO 2) value expressed in Fig 1 was the value measured in a blood sample drawn from a jugular venous catheter. At the same time, we continuously measured the SjvO 2 value and regional cerebral oxygenation using an analysis system (Explorer system, Baxter Healthcare Corp, Irvine, Calif) and found that there were no changes in the SjvO 2 and regional cerebral oxygenation values throughout the study. In our previous study,
2 we reported a close correlation between the oxygen saturation value measured by the optical catheter and the oxygen saturation value in sampled blood by the blood gas analyzer. Therefore we do not think that the change in Sjvo2 would be observed if the value had been measured more frequently during cardiopulmonary bypass (CPB). It remains controversial whether cerebral autoregulation is intact during CPB.
3,4 Newman and associates
3 reported that an increase in cerebral blood flow was observed by an increase in mean arterial pressure. In contrast, Sadahiro and the associates
4 reported that cerebral blood flow was constant when mean arterial pressure was higher than 50 mm Hg. At present, there is no solid agreement concerning the acceptable level of mean arterial pressure during CPB.
As we described previously, however, our pulse pressure was a physiologic pulse waveform. A higher pulse pressure (>40 mm Hg) might have had a positive effect of high-pressure intra-aortic balloon pumping (IABP) on cerebral circulation.
1
We did not measure the plasma catecholamine levels in the two groups; therefore it was not known whether plasma levels could have some effects on cerebral microcirculation in our study. Cerebral microcirculation might be affected by plasma catecholamine level, as they described. However, other factors, such as renin-angiotensin and thromboxane A2, might have effects on cerebral microcirculation.
5
12/8/104876 doi:10.1067/mtc.2000.104876
References
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