TY - JOUR
T1 - General anesthesia suppresses normal heart rate variability in humans
AU - Matchett, Gerald
AU - Wood, Philip
N1 - Funding Information:
This study was approved by the University of Texas-Southwestern Medical Center Institutional Review Board (IRB), Study No. #STU 102011-021, on December 28, 2011. (IRB Chairperson George Buchanan, University of Texas Southwestern Medical Center Institutional Review Board, 5323 Harry Hines Blvd, Dallas TX 75390-8843, USA. Tel.: 214-648-3060. Fax: 214-648-2171). Financial support and sponsorship by the Department of Anesthesiology & Pain Management at the University of Texas-Southwestern Medical Center, and the Department of Mathematics at the University of Wisconsin-Madison. No conflicts of interest are reported by the authors. Gerald Matchett is the local principal investigator for a research trial funded by WEX Pharmaceuticals, Inc. and Premier Research, Inc. which is unrelated to this study. No Prior Presentation or Prior Publication. Philip Wood was partly supported by an National Science Foundation (NSF) Postdoctoral Research Fellowship.
Publisher Copyright:
© 2014 AIP Publishing LLC.
PY - 2014/6/1
Y1 - 2014/6/1
N2 - The human heart normally exhibits robust beat-to-beat heart rate variability (HRV). The loss of this variability is associated with pathology, including disease states such as congestive heart failure (CHF). The effect of general anesthesia on intrinsic HRV is unknown. In this prospective, observational study we enrolled 100 human subjects having elective major surgical procedures under general anesthesia. We recorded continuous heart rate data via continuous electrocardiogram before, during, and after anesthesia, and we assessed HRV of the R-R intervals. We assessed HRV using several common metrics including Detrended Fluctuation Analysis (DFA), Multifractal Analysis, and Multiscale Entropy Analysis. Each of these analyses was done in each of the four clinical phases for each study subject over the course of 24 h: Before anesthesia, during anesthesia, early recovery, and late recovery. On average, we observed a loss of variability on the aforementioned metrics that appeared to correspond to the state of general anesthesia. Following the conclusion of anesthesia, most study subjects appeared to regain their normal HRV, although this did not occur immediately. The resumption of normal HRV was especially delayed on DFA. Qualitatively, the reduction in HRV under anesthesia appears similar to the reduction in HRV observed in CHF. These observations will need to be validated in future studies, and the broader clinical implications of these observations, if any, are unknown.
AB - The human heart normally exhibits robust beat-to-beat heart rate variability (HRV). The loss of this variability is associated with pathology, including disease states such as congestive heart failure (CHF). The effect of general anesthesia on intrinsic HRV is unknown. In this prospective, observational study we enrolled 100 human subjects having elective major surgical procedures under general anesthesia. We recorded continuous heart rate data via continuous electrocardiogram before, during, and after anesthesia, and we assessed HRV of the R-R intervals. We assessed HRV using several common metrics including Detrended Fluctuation Analysis (DFA), Multifractal Analysis, and Multiscale Entropy Analysis. Each of these analyses was done in each of the four clinical phases for each study subject over the course of 24 h: Before anesthesia, during anesthesia, early recovery, and late recovery. On average, we observed a loss of variability on the aforementioned metrics that appeared to correspond to the state of general anesthesia. Following the conclusion of anesthesia, most study subjects appeared to regain their normal HRV, although this did not occur immediately. The resumption of normal HRV was especially delayed on DFA. Qualitatively, the reduction in HRV under anesthesia appears similar to the reduction in HRV observed in CHF. These observations will need to be validated in future studies, and the broader clinical implications of these observations, if any, are unknown.
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U2 - 10.1063/1.4882395
DO - 10.1063/1.4882395
M3 - Article
C2 - 24985443
AN - SCOPUS:84922472802
SN - 1054-1500
VL - 24
JO - Chaos
JF - Chaos
IS - 2
M1 - 023129
ER -