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. Author manuscript; available in PMC: 2021 Jan 13.
Published in final edited form as: Physiol Meas. 2020 Oct 6;41(9):095002. doi: 10.1088/1361-6579/abad49

Table 2.

The categorised groups and variability of signals in each quality group.

Groups (n) CV% of MABP CV% of MFv
RMCA LMCA
Un-A (raw data; n=166) 4.72 (3.98 – 5.46) 7.53 (6.11 – 8.94) 7.78 (6.96 – 8.60)
Group A (n=167) 4.05 (3.79 – 4.31)x 6.33 (5.34 – 7.32) 5.62 (5.27 – 5.98)***
Group B (n=65) 4.14 (3.73 – 4.55) 6.80 (5.37 – 8.23) 11.7 (-0.07 – 23.4)
Group C (n=25) 7.05 (5.56 – 8.53) 5.12 (3.92 – 6.33) 5.02 (3.86 – 6.17)
Group D (n=42) 5.53 (4.51 – 6.55) 5.86 (5.14 – 6.57) 6.30 (5.35 – 7.25)
Group E (n=154) 4.95 (4.50 – 5.40) No Data Side Signal Side
61.8 (48.5 – 75.2) 12.5 (7.9 – 17.1)

Un-A: Median-filtered but no manual cleaning; Group A: All optimal in both ABP and CBFV; Group B: Either side or both sides of CBFV are adequate; Group C: ABP is adequate or unusable and CBFV is optimal; Group D: ABP is adequate or unusable and CBFV is optimal or adequate; and Group E: ABP is optimal, adequate, or unusable, one side of CBFV is optimal or adequate but the other side of CBFV is unusable (i.e. quality = 1: severe artefact) or no data (i.e. quality = 0; the measured signal is noise, with no usable information of CBFV being measured).

Data are presented as mean (95% Confidence Interval). MABP, mean arterial blood pressure; MFv, mean cerebral blood flow velocity; CV%, percentage of coefficient of variation;

x

p = 0.069;

***

p <0.0001 (for Un-A vs. Group A, by paired sample t-test).

p-trend <0.05;

p-trend <0.0001 for Group A–E.

Two patients with only left-sided window are in Groups A and B respectively.