TY - JOUR
T1 - Reproducibility of dynamic cerebral autoregulation parameters
T2 - A multi-centre, multi-method study
AU - Sanders, Marit L.
AU - Claassen, Jurgen A.H.R.
AU - Aries, Marcel
AU - Bor-Seng-Shu, Edson
AU - Caicedo, Alexander
AU - Chacon, Max
AU - Gommer, Erik D.
AU - Van Huffel, Sabine
AU - Jara, José L.
AU - Kostoglou, Kyriaki
AU - Mahdi, Adam
AU - Marmarelis, Vasilis Z.
AU - Mitsis, Georgios D.
AU - Müller, Martin
AU - Nikolic, Dragana
AU - Nogueira, Ricardo C.
AU - Payne, Stephen J.
AU - Puppo, Corina
AU - Shin, Dae C.
AU - Simpson, David M.
AU - Tarumi, Takashi
AU - Yelicich, Bernardo
AU - Zhang, Rong
AU - Panerai, Ronney B.
AU - Elting, Jan Willem J.
N1 - Publisher Copyright:
© 2018 Institute of Physics and Engineering in Medicine.
Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 2018/12/7
Y1 - 2018/12/7
N2 - Objective: Different methods to calculate dynamic cerebral autoregulation (dCA) parameters are available. However, most of these methods demonstrate poor reproducibility that limit their reliability for clinical use. Inter-centre differences in study protocols, modelling approaches and default parameter settings have all led to a lack of standardisation and comparability between studies. We evaluated reproducibility of dCA parameters by assessing systematic errors in surrogate data resulting from different modelling techniques. Approach: Fourteen centres analysed 22 datasets consisting of two repeated physiological blood pressure measurements with surrogate cerebral blood flow velocity signals, generated using Tiecks curves (autoregulation index, ARI 0-9) and added noise. For reproducibility, dCA methods were grouped in three broad categories: 1. Transfer function analysis (TFA)-like output; 2. ARI-like output; 3. Correlation coefficient-like output. For all methods, reproducibility was determined by one-way intraclass correlation coefficient analysis (ICC). Main results: For TFA-like methods the mean (SD; [range]) ICC gain was 0.71 (0.10; [0.49-0.86]) and 0.80 (0.17; [0.36-0.94]) for VLF and LF (p = 0.003) respectively. For phase, ICC values were 0.53 (0.21; [0.09-0.80]) for VLF, and 0.92 (0.13; [0.44-1.00]) for LF (p < 0.001). Finally, ICC for ARI-like methods was equal to 0.84 (0.19; [0.41-0.94]), and for correlation-like methods, ICC was 0.21 (0.21; [0.056-0.35]). Significance: When applied to realistic surrogate data, free from the additional exogenous influences of physiological variability on cerebral blood flow, most methods of dCA modelling showed ICC values considerably higher than what has been reported for physiological data. This finding suggests that the poor reproducibility reported by previous studies may be mainly due to the inherent physiological variability of cerebral blood flow regulatory mechanisms rather than related to (stationary) random noise and the signal analysis methods.
AB - Objective: Different methods to calculate dynamic cerebral autoregulation (dCA) parameters are available. However, most of these methods demonstrate poor reproducibility that limit their reliability for clinical use. Inter-centre differences in study protocols, modelling approaches and default parameter settings have all led to a lack of standardisation and comparability between studies. We evaluated reproducibility of dCA parameters by assessing systematic errors in surrogate data resulting from different modelling techniques. Approach: Fourteen centres analysed 22 datasets consisting of two repeated physiological blood pressure measurements with surrogate cerebral blood flow velocity signals, generated using Tiecks curves (autoregulation index, ARI 0-9) and added noise. For reproducibility, dCA methods were grouped in three broad categories: 1. Transfer function analysis (TFA)-like output; 2. ARI-like output; 3. Correlation coefficient-like output. For all methods, reproducibility was determined by one-way intraclass correlation coefficient analysis (ICC). Main results: For TFA-like methods the mean (SD; [range]) ICC gain was 0.71 (0.10; [0.49-0.86]) and 0.80 (0.17; [0.36-0.94]) for VLF and LF (p = 0.003) respectively. For phase, ICC values were 0.53 (0.21; [0.09-0.80]) for VLF, and 0.92 (0.13; [0.44-1.00]) for LF (p < 0.001). Finally, ICC for ARI-like methods was equal to 0.84 (0.19; [0.41-0.94]), and for correlation-like methods, ICC was 0.21 (0.21; [0.056-0.35]). Significance: When applied to realistic surrogate data, free from the additional exogenous influences of physiological variability on cerebral blood flow, most methods of dCA modelling showed ICC values considerably higher than what has been reported for physiological data. This finding suggests that the poor reproducibility reported by previous studies may be mainly due to the inherent physiological variability of cerebral blood flow regulatory mechanisms rather than related to (stationary) random noise and the signal analysis methods.
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U2 - 10.1088/1361-6579/aae9fd
DO - 10.1088/1361-6579/aae9fd
M3 - Research Article
C2 - 30523976
AN - SCOPUS:85058910412
SN - 0967-3334
VL - 39
JO - Physiological Measurement
JF - Physiological Measurement
IS - 12
M1 - 125002
ER -