BJA Advance Access originally published online on September 3, 2004
British Journal of Anaesthesia 2004 93(5):634-638; doi:10.1093/bja/aeh252
© The Board of Management and Trustees of the British Journal of Anaesthesia 2004
Effects of milrinone on jugular bulb oxygen saturation and cerebrovascular carbon dioxide reactivity in patients undergoing coronary artery bypass graft surgery
1 Department of Anesthesiology and Pain Medicine and Anesthesia and Pain Research Institute, and 4 Yonsei Cardiovascular Research Institute, Yonsei University School of Medicine, Seoul, Korea. 2 Department of Anesthesiology and Pain Medicine, Yonsei University School of Medicine, Seoul, Korea. 3 Department of Anesthesiology and Pain Medicine, Inha University School of Medicine, Inchon, Korea
* Corresponding author. E-mail: yjoh{at}yumc.yonsei.ac.kr
Background. Jugular bulb oxygen saturation (
) is a surrogate marker for global cerebral oxygenation. The effect of milrinone on
and the cerebrovascular carbon dioxide reactivity (CCO2R) was investigated.
Methods. Thirty patients scheduled for coronary artery bypass graft surgery (CABG) were studied prospectively. After sternotomy, normoventilation (at T1;
=4.75.0 kPa) and hyperventilation (at T2;
=3.33.7 kPa) were induced and the changes in
(
) and
(
), and
(CCO2R) were measured. After normoventilation was re-established (at T3), milrinone 50 µg kg1 was given (at T4), followed by hyperventilation (at T5), and
,
and CCO2R were measured.
Results. After milrinone administration at normoventilation (T3 and T4), cardiac index and mixed venous oxygen saturation increased, while mean arterial pressure and systemic vascular resistance index decreased, without a significant change in
. Before milrinone administration (T1 and T2), hyperventilation decreased
and
, and
showed positive linear correlation with
. After milrinone administration (T4 and T5), hyperventilation decreased
and
, and
showed positive linear correlation with
. There was no significant difference in CCO2R before and after milrinone administration (13.3 (5.7)% kPa1 and 12.3 (3.9)% kPa1, respectively).
Conclusions. Although milrinone induced significant haemodynamic changes,
and CCO2R were unchanged during its administration.