TY - JOUR
T1 - Assessment of cerebrovascular and cardiovascular responses to lower body negative pressure as a test of cerebral autoregulation
AU - Brown, Clive M.
AU - Dütsch, Matthias
AU - Hecht, Martin J.
AU - Neundörfer, Bernhard
AU - Hilz, Max J.
N1 - Funding Information:
First author (AB) is thankful to the Abu Dhabi National Oil Company (ADNOC) Oil Subcommittee (OSC) Research and Development team for sponsoring the fund for his postdoctoral study in ?Characterization and Modeling in Capillary Transition Zones in Carbonate Reservoirs? project. Abu Dhabi Company for Onshore Oil Operations (ADCO), Abu Dhabi Marine Operating Company (ADMA-OPCO) and the Petroleum Institute, Abu Dhabi are gratefully acknowledged for supporting the work.
PY - 2003/4/15
Y1 - 2003/4/15
N2 - The aim of this study was to determine whether lower body negative pressure (LBNP), combined with noninvasive methods of assessing changes in systemic and cerebral vascular resistance, is suitable as a method for assessing cerebral autoregulation. In 13 subjects we continuously assessed heart rate, blood pressure, cerebral blood flow velocity (CBFV) and cardiac output during graded levels of LBNP from 0 to -50 mm Hg. With increasing levels of LBNP, cardiac output declined significantly (to 55.8±4.5% of baseline value) but there was no overall change in mean arterial pressure. CBFV also fell at higher levels of LBNP (to 81.4±3.2% of baseline) but the percentage CBFV change was significantly less than that in cardiac output (P<0.01). The maximum increase in cerebrovascular resistance (pulsatility ratio) was significantly less than that in total peripheral resistance (17±6% vs. 105±16%, P<0.01). Spectral analysis showed that the power of low-frequency oscillations in mean arterial pressure, but not CBFV, increased significantly at the -50 mm Hg level of LBNP. These results show that, even during high levels of orthostatic stress, cerebral autoregulation is preserved and continues to protect the cerebral circulation from changes in the systemic circulation. Furthermore, assessment of cardiovascular and cerebrovascular parameters during LBNP may provide a useful clinical test of cerebral autoregulation.
AB - The aim of this study was to determine whether lower body negative pressure (LBNP), combined with noninvasive methods of assessing changes in systemic and cerebral vascular resistance, is suitable as a method for assessing cerebral autoregulation. In 13 subjects we continuously assessed heart rate, blood pressure, cerebral blood flow velocity (CBFV) and cardiac output during graded levels of LBNP from 0 to -50 mm Hg. With increasing levels of LBNP, cardiac output declined significantly (to 55.8±4.5% of baseline value) but there was no overall change in mean arterial pressure. CBFV also fell at higher levels of LBNP (to 81.4±3.2% of baseline) but the percentage CBFV change was significantly less than that in cardiac output (P<0.01). The maximum increase in cerebrovascular resistance (pulsatility ratio) was significantly less than that in total peripheral resistance (17±6% vs. 105±16%, P<0.01). Spectral analysis showed that the power of low-frequency oscillations in mean arterial pressure, but not CBFV, increased significantly at the -50 mm Hg level of LBNP. These results show that, even during high levels of orthostatic stress, cerebral autoregulation is preserved and continues to protect the cerebral circulation from changes in the systemic circulation. Furthermore, assessment of cardiovascular and cerebrovascular parameters during LBNP may provide a useful clinical test of cerebral autoregulation.
KW - Cerebral autoregulation
KW - Cerebral blood flow
KW - Doppler
KW - Impedance cardiography
KW - Middle cerebral artery
KW - Orthostatic hypotension
KW - Spectral analysis
UR - http://www.scopus.com/inward/record.url?scp=0037445603&partnerID=8YFLogxK
U2 - 10.1016/S0022-510X(02)00438-0
DO - 10.1016/S0022-510X(02)00438-0
M3 - Article
C2 - 12639728
AN - SCOPUS:0037445603
SN - 0022-510X
VL - 208
SP - 71
EP - 78
JO - Journal of the Neurological Sciences
JF - Journal of the Neurological Sciences
IS - 1-2
ER -