Free On-line Access

SPCI - Sociedade Portuguesa de Cuidados Intensivos

Revista Brasileira de Terapia Intensiva

AMIB - Associação de Medicina Intensiva Brasileira


ISSN: 0103-507X
Online ISSN: 1982-4335

Ícone Fechar

How to Cite


Bento L, Fonseca-Pinto R, Póvoa P. Monitorização do sistema nervoso autônomo em ambiente de cuidados intensivos como ferramenta de prognóstico. Revisão sistemática. Rev Bras Ter Intensiva. 2017;29(4):481-489





Autonomic nervous system monitoring in intensive care as a prognostic tool. Systematic review

Monitorização do sistema nervoso autônomo em ambiente de cuidados intensivos como ferramenta de prognóstico. Revisão sistemática

Luis Bento1, Rui Fonseca-Pinto2,3, Pedro Póvoa4,5

1 Medical Emergency Unit, Centro Hospitalar de Lisboa Central, EPE - Lisbon, Portugal.
2 Instituto Politécnico de Leiria - Leiria, Portugal.
3 Instituto de Telecomunicações, MSP - Leiria, Portugal.
4 Multipurpose Intensive Care Unit, São Francisco Xavier Hospital - West Lisbon Hospital Center - Lisbon, Portugal.
5 NOVA Medical School, CEDOC, Universidade Nova de Lisboa - Lisbon, Portugal.

Conflicts of interest: None.

Submitted on April 15, 2016
Accepted on April 18, 2017

Corresponding author: Luis Bento, Centro Hospitalar de Lisboa Central, Rua José António Serrano, Lisbon 1150-199, Portugal



OBJECTIVE: To present a systematic review of the use of autonomic nervous system monitoring as a prognostic tool in intensive care units by assessing heart rate variability.
METHODS: Literature review of studies published until July 2016 listed in PubMed/Medline and conducted in intensive care units, on autonomic nervous system monitoring, via analysis of heart rate variability as a prognostic tool (mortality study). The following English terms were entered in the search field: ("autonomic nervous system" OR "heart rate variability") AND ("intensive care" OR "critical care" OR "emergency care" OR "ICU") AND ("prognosis" OR "prognoses" OR "mortality").
RESULTS: There was an increased likelihood of death in patients who had a decrease in heart rate variability as analyzed via heart rate variance, cardiac uncoupling, heart rate volatility, integer heart rate variability, standard deviation of NN intervals, root mean square of successive differences, total power, low frequency, very low frequency, low frequency/high frequency ratio, ratio of short-term to long-term fractal exponents, Shannon entropy, multiscale entropy and approximate entropy.
CONCLUSION: In patients admitted to intensive care units, regardless of the pathology, heart rate variability varies inversely with clinical severity and prognosis.

Keywords: Autonomic nervous system; Heart rate variability; Intensive care; Prognosis.



Since the 1970s, with the introduction of the Swan-Ganz catheter,(1) there has been significant progress in the capacity of invasive and non-invasive hemodynamic monitoring in intensive care units (ICU) and an improved understanding of the pathophysiological phenomena responsible for the hemodynamic instability of critical patients.

Despite these remarkable advances, there is no unanimity as to what therapeutic objectives should be achieved in patients with hemodynamic instability admitted to the ICU,(2) for the time being maintaining an individual therapeutic attitude guided not by hemodynamic monitoring data but by the integration of the different variables that can be obtained using multiple monitoring methods.

This situation results from an overvaluation of our view of the cardiovascular system according to physics principles rather than a look at the capacity and adjustment of the real-time responses of critical patients to the pathophysiological changes induced by the disease and imposed by our therapeutic attitudes, either pharmacological or not. More important than the "normalization" of a given parameter is its temporal adjustment.

Recent studies(3-5) have described several hemodynamic monitoring methods, from the most invasive, such as the Swan-Ganz catheter, to the less invasive, such as bioimpedance and bioreactance methods. However, although the autonomic nervous system (ANS) is responsible for the homeostasis of the cardiocirculatory system through the balance between the activity of the sympathetic and parasympathetic ANS, no reference is made to the monitoring of its activity and/or its balance in ICU patients.

Heart rate variability (HRV) translates the oscillations in the duration of intervals between consecutive heart beats (NN intervals) (Figure 1) and is related to the influences of the ANS on the sinus node, translating the heart''s capacity to respond to multiple physiological and environmental stimuli, such as breathing, physical exercise, hemodynamic and metabolic changes, orthostatism and responses to stress induced by diseases. Moreover, the study of HRV of the ANS is only possible in the presence of sinus rhythm.

Figure 1 - Ten-second cardiotocogram showing heart rate variability.

The objective of this article is to present a systematic review of studies involving autonomic nervous system monitoring of adult patients admitted to the intensive care units by analyzing the association of multiple heart rate variability assessment measures with the hospitalization outcome. Prospective and retrospective randomized controlled or cohort studies were included.


In this systematic review, we used the checklist Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA)(6) as a guide to reach the standards accepted in systematic reviews.

The literature review of studies conducted in ICUs on ANS monitoring was conducted by searching all of the measures described for HRV analysis methods (Tables 1 and 2) as a prognostic tool (mortality study), published in or before July 2016 (inclusive) using the PubMed/MEDLINE database. The following English terms were entered in the search field, yielding 421 articles: ("autonomic nervous system" OR "heart rate variability") AND ("intensive care" OR "critical care" OR "emergency care" OR "ICU") AND ("prognosis" OR "prognoses" OR "mortality").

Table 1 - Methods for the study of heart rate variability(7,8,9)
1. Linear methods - time domain
    a. Statistical measures
        i. SDNN - Standard deviation of all normal NN intervals
        ii. SDANN - Standard deviation of the average normal NN interval calculated over 5-minute intervals
        iii. SDNNi - Mean of the standard deviations of all normal NN calculated over 5-minute intervals
        iv. rMSSD - Square root of the mean squared differences of successive normal NN intervals
        v. SDSD - Standard deviation of differences between adjacent normal NN intervals
        vi. NN50 - Number of pairs of adjacent normal NN intervals differing by more than 50 milliseconds
        vii. pNN50 - Percentage of normal NN intervals differing by more than 50 milliseconds from the adjacent interval
    b. Geometric measures
        i. Triangular index
        ii. TINN - Triangular interpolation of normal NN intervals histogram
        iii. Differential index
        iv. Logarithmic index
2. Linear methods - frequency domain
    a. Long-term analysis (5 minutes)
        i. Total power
        ii. VLF - Very low frequency
        iii. LF - Low frequency
        iv. LFn - Low frequency in normalized units
        v. HF - High frequency
        vi. HFn - High frequency in normalized units
        vii. LF/HF - Low frequency/high frequency ratio
    b. Long-term analysis (24 hours)
        i. Total power
        ii. ULF - Ultra low frequency
        iii. VLF - Very low frequency
        iv. LF - Low frequency
        v. HF - High frequency
        vi. α - Slope of the linear interpolation of the spectrum in a logarithmic scale
3. Time-frequency analysis methods
    a. Time-varying parametric models
        i. Autoregression models
    b. Non-parametric methods
        i. Short-time Fourier transform (STFT)
        ii. Wavelet transform (WT)
        iii. Hilbert-Huang transform
        iv. Wigner-Ville transform
4. Non-linear methods
    a. Detrended fluctuation analysis (total DTA, α1, α2 and α1/α2)
    b. Correlation function
    c. Hurst exponent
    d. Fractal dimension
    e. Lyapunov exponent
    f. Sample entropy
    g. Multiscale entropy
    h. Approximate entropy (ApEn)
    i. Shannon entropy
Table 1 - Methods for the study of heart rate variability(7,8,9)
Table 2 - Definition of measures for the study of heart rate variability in the time domain(7)

Unit Definition
SDNN ms Standard deviation of all normal NN intervals
SDNNi ms Standard deviation of NN calculated over 5-minute intervals
SDANN ms Standard deviation of the average NN interval
rMSSD ms Root mean square of the successive NN interval difference
pNN50 % Normal-to-normal NN intervals whose difference exceeds 50 milliseconds
Table 2 - Definition of measures for the study of heart rate variability in the time domain(7)

After applying the filters to limit the studies to those involving humans aged over 19 years, without language restriction, 193 articles were excluded.

After reading the abstracts of the 228 selected studies, 180 articles were excluded: 11 reported the monitoring of pediatric patients, 16 were conducted outside the intensive care setting, 119 were not related to ANS monitoring, four did not analyze HRV, 28 did not focus on prognosis and two were review studies.

The 48 articles selected were grouped and cataloged in EndNote® and were read in full. Afterwards, 32 articles were excluded: 21 because they were not studies of ICU patients (11 were performed in the Emergency Department, five in the prehospital setting, two in the Cardiothoracic Surgery Service and two in the Cardiology Service, and one study was conducted during the anesthetic period) and 11 because they did not report mortality data.

The references of the 16 selected articles were reviewed, and whenever there was reference to a new study, that study was evaluated; at the end of the review process, 18 articles were selected (Figure 2).

Figure 2 - Article selection protocol.(6)
HRV - heart rate variability; ICU - intensive care unit.

The quality of evidence for each selected study was assessed using the Methodological Index for Non-Randomized Studies (MINORS) tool.(10)

The article review (data extraction and quality of evidence) was conducted by one author, with the information later independently verified by two others.

Table 3 shows the characteristics of the selected studies.

Table 3 - Characteristics of the selected studies

Characteristics Evaluated outcomes Results MINORS (score/total)
Pfeifer et al.(11) Prospective cohort study
Patients admitted to the ICU after cardiac arrest, subjected to therapeutic hypothermia
N = 18
28-day mortality There was a more pronounced reduction in HRV immediately after the rewarming phase in patients who died compared with survivors (SDNN 10.9 versus 40.2, Shannon entropy 2.2 versus 3.7) 15/24
Riordan et al.(12) Retrospective cohort study
Multiple trauma patients admitted to the ICU
N = 2,178
Risk of death in the subgroups based on trauma location and mechanism and on probability of survival Decreased MSE was significantly associated with increased mortality, being an independent factor of probability of survival in the multivariate analysis, with OR 0.87 - 0.94; the difference in median HR of MSE between survivors and non-survivors was highest (15.9 versus 5.9) when the primary trauma mechanism was penetrating 10/24
Kahraman et al.(13) Prospective cohort study
Patients admitted to the ICU with head trauma with Glasgow coma scale score < 9 and need for ICP monitoring
N = 25
Capacity to predict intracranial hypertension, cerebral hypoperfusion, in-hospital mortality or functional outcome HRVi* can predict in-hospital mortality, with a sensitivity of 67% and a specificity of 91-100% 15/24
Mowery et al.(14) Retrospective cohort study
Patients with head trauma and ICP monitoring
N = 145
Intracranial hypertension and mortality There is a relationship between percentage of ICP rise and cardiac decoupling with mortality. Each percentage increase had an increased risk of death of 1.04 and 1.03, respectively 15/24
Norris et al.(15) Retrospective cohort study
Trauma patients admitted to the ICU
N = 285
In-hospital mortality There was a decrease in HRV (increase in HRVi*), OR 1.04 ± 0.01 and MSE OR 0.88 ± 0.03, in deceased patients 12/24
Papaioannou et al.(16) Prospective cohort study
Head trauma
N = 20
Neurological dysfunction
ICU mortality
It was associated with increased mortality, reduced heart rate variability, reduced baroreflex sensitivity and sustained LF/HF ratio reduction 17/24
Norris et al.(17) Retrospective cohort study
Trauma patients admitted to the ICU
N = 2,088
Mortality Cardiac decoupling was associated with increased mortality OR 1.035 - 1.052 13/24
Grogan et al.(18) Retrospective cohort study
Trauma patients admitted to the ICU
N = 923
ICU mortality Patients with loss of heart rate volatility during the first 24 hours of hospitalization have a higher probability of death 10/24
Rapenne et al.(19) Prospective cohort study
Severe head trauma
N = 20
Brain death
Neurological recovery (Glasgow coma scale)
On the first post-trauma day, an increase in the parasympathetic tone (rMSSD and TP) may be associated with imminent brain death 17/24
Winchell et al.(20) Retrospective cohort study
Patients with severe head trauma
N = 80
Primary: in-hospital mortality and probability of discharge to the home
Secondary: CPP and ICP
Low HRV was associated with increased mortality; patients with a predominance of sympathetic activity and with a low HF/LF ratio had improved survival 16/24
Brown et al.(21) Prospective cohort study
Patients admitted to the ICU with severe sepsis or septic shock
N = 48
Primary outcome: suspension of vasoactive amines within the first 24 hours of ICU admission
Secondary outcome: 28-day mortality
The ratio between short- and long-term fractal exponents was associated with 28-day mortality; all patients who died had ratios < 0.75 18/24
Schmidt et al.(22) Prospective cohort study
Patients with multiple organ dysfunction syndrome
N = 90
Analysis of survival at 180 and 365 days lnVLF† with a cutoff point of 3.9 was a strong predictor of 28-day and 2-month mortality in patients with multiple organ dysfunction syndrome 18/24
Schmidt et al.(23) Prospective cohort study
Patients with multiple dysfunction syndrome
N = 90
28-day mortality lnVLF† with a cut-off point of 3.9 was a strong predictor of 28-day mortality 20/24
Gujjar et al.(24) Prospective cohort study
Acute stroke
N = 25
ICU mortality LFn was an independent predictor of survival, with a regression coefficient of -6.73 and an OR of 0.002 19/24
Haji-Michael et al.(25) Prospective cohort study
Neurosurgical patients with Glasgow coma scale score < 13
N = 29
3-month outcome Patients who died had decreased HRV, LF/HF ratio and baroreflex sensitivity 18/24
Papaioannou et al.(26) Prospective cohort study
General ICU population
N = 53
ICU mortality The minimum ApEn value correlated with mortality (r = 0.41; p = 0.01) 16/24
Yien et al.(27) Prospective cohort study
General population admitted for noncardiac causes
N = 52
Mortality Deceased patients had decreased VLF and LF band power 16/24
Winchell et al.(28) Prospective cohort study
General ICU population
N = 742
Mortality The relative risk of death in patients with low HRV was 7.4, with an increased HF/LF ratio of 4.55 19/24

MINORS - Methodological Index for Non-Randomized Studies; ICU - intensive care unit; HRV - heart rate variability; MSE - multiscale entropy; OR - odds ratio; HR - hazard ratio; HRVi - integer heart rate variability; ICP - intracranial pressure; LF/HF - ratio between the low frequency component and the high frequency component; CPP - cerebral perfusion pressure; TP - total power.

* Calculation of the standard deviation of the electrocardiogram signal collected every 1-4 seconds during a 5-minute interval;

natural logarithm of VLF.

Table 3 - Characteristics of the selected studies


The 18 selected studies are presented in table 3. The type of study, study population, number of patients included, HRV variables studied in the ANS monitoring, most relevant conclusions and quality of evidence were also analyzed.

All studies reviewed were cohort, prospective or retrospective studies. The sample size was very heterogeneous, ranging from 18(11) to 2,178(12) patients; the sample size was not previously calculated in any study. The most studied pathology was trauma, mainly of the head, with a total of nine studies,(12-20) and with the same number of studies on patients with severe sepsis and septic shock,(21) multiple dysfunction syndrome,(22,23) patients undergoing therapeutic hypothermia after cardiac arrest,(11) with stroke(24) and neurosurgical patients;(25) three studies focused on the general population admitted to the ICU, without discriminating the reason for admission. The conclusions of all of the studies were obtained by comparing the groups according to the outcome evaluated, namely, mortality.

The results presented included increases in mortality associated with reduction in HRV (entropy 0.65 ± 0.24 versus 0.84 ± 0.26; p < 0.05), reduction in the baroreflex (transfer function 0.43 ± 29 versus 1.11 ± 0.74; p < 0.05) and a sustained reduction of the low frequency/high frequency ratio (LF/HF ratio 0.22 ± 0.29 versus 0.62 ± 28; p < 0.01);(16) reductions in HRV, with odds ratios (ORs) of 1.03(14) and of 1.035 - 1.052;(17) loss of heart rate volatility during the first 24 hours of hospitalization, translated as a coefficient of 0.05 in the logistic regression model (95% confidence interval [95% CI] 1.033 - 1.071);(18) integer heart rate variability (HRVi) with a sensitivity of 67% and a specificity of 91 - 100% to predict the mortality rate(13) or OR of 1.04;(15) and reduction in HRV in patients admitted to the ICU after cardiac arrest and undergoing therapeutic hypothermia, with a standard deviation of all normal NN intervals of 10.9 ± 4.1 versus 40.2 ± 19.5 (p = 0.01) and a Shannon entropy of 2.2 ± 0.4 versus 3.7 ± 0.6 (p = 0.008) for deceased versus surviving patients in the rewarming period. Concordant results were observed in the pre-hypothermia period.(11) There was also an increase in the parasympathetic tone as measured by the square root of the mean squared differences of successive intervals (rMSSD) (34.07 ± 6.54 versus 15.51 ± 3.90; p = 0.01) in patients with severe head injury;(19) decreased power in the low frequency band (low frequency in standard units in patients with severe stroke 18.90 ± 1.36 versus 49.66 ± 2.10; p = 0.02; in the general population p < 0.05 with Scheffé analysis);(24,27) decreased natural logarithm of the very low frequency band (lnVLF £ 3.9 with OR 2.9; in the general population p < 0.05 with Scheffé analysis);(22,23,27,28) and decreased ratio of short- to long-term fractal exponents; all patients admitted to the ICU with severe sepsis or septic shock who died had a ratio of < 0.75 (p = 0.04).(21) The following were also found: decreased multiscale entropy in trauma patients (8.9 versus 16.6; p < 0.0001; 7.5 versus 11.2; p < 0.001 in patients with survival probabilities < 0.25; 7.7 versus 12.8; p < 0.01 for patients with survival probabilities of 0.25 to 0.50; 9.4 versus 15.0; p < 0.001 for patients with survival probabilities of 0.50 to 0.75; 9.9 versus 16.1; and p < 0.001 among those with survival probabilities ³ 0.75).(12,15) Decreased approximate entropy (mean ApEn 0.53 ± 0.25 versus 0.62 ± 0.28; p = 0.04; minimum ApEn 0.24 ± 0.23 versus 0.48 ± 0.23; p = 0.01) with a Pearson coefficient of 0.41 (p = 0.01) was also found.(26)

Thus, these studies showed that, in patients admitted to the ICU, regardless of the pathology that led to hospitalization, HRV varied inversely with clinical severity and prognosis.(29)


The control of the cardiovascular system is ensured by the balance between the activity of the sympathetic ANS, which enervates the entire myocardium, and the parasympathetic ANS, which enervates the sinus node, the atrial myocardium and the atrioventricular node.(30) The influence of the ANS on the heart depends on the information it receives from the baroreceptors, chemoreceptors, atrial receptors, ventricular receptors, changes in the respiratory system, vasomotor system, renin-angiotensin-aldosterone system and thermoregulatory system.(31) All of these influences condition the HRV, and the standards for its measurement, physiological interpretation and applicability were published in 1996.(7)

The HRV can be analyzed using different methods, with linear methods being the most used in clinical practice.

The time domain is analyzed using various measures and reflects the variation in the duration of NN intervals resulting from the depolarization of the sinus node.

Analysis of the frequency domain decomposes the HRV into the high frequency band, ranging between 0.15 and 0.4 Hz, which corresponds to the respiratory modulation, translating the parasympathetic activity; the low frequency band, ranging between 0.04 and 0.15 Hz, which corresponds to sympathetic and parasympathetic activity; the very low frequency band, ranging between 0.003 and 0.04 Hz, which reflects the thermoregulation cycles; and ultra low frequency components, with variations below 0.003 Hz, modulated by the circadian rhythm and neuroendocrine axes.

The inverse relationship enters the very low frequency band, and the prognosis was first described in the 1960s,(32) when it was observed that NN interval reduction preceded fetal distress.

The first study conducted in the ICU was published in 1996 and concluded that HRV reduction was related to increased mortality.(28) Since then, all studies conducted in the ICU have almost exclusively focused on the evaluation of HRV, which varies inversely with clinical severity and prognosis.(29)

Examples of clinical conditions in which HRV is predictive of patient survival include diabetes,(33) cancer,(34) heart failure,(35) acute myocardial infarction,(36) stroke,(37) epilepsy,(38) Parkinson''s disease(39) and kidney failure,(40) among others.

In patients admitted to the ICU, in addition to being used as a prognostic tool, HRV has also been described as a screening tool for multiple trauma patients,(41) as a tool for individual monitoring of organ dysfunction,(42) as a non-invasive tool for pain monitoring(43) and as an independent predictor factor for the prolongation of hospital stay in patients undergoing heart surgery(44) and has been used as a tool for successful extubation decision-making.(45,46)

Some limitations were identified in the studies reviewed. There is no uniformity in the variables studied for HRV assessment, although the studies are concordant in the conclusions presented; furthermore, the quality of the evidence is low, due mainly to the sampled studies being cohort studies.


Heart rate variability occurs inversely to clinical severity and prognosis. The difficulty of introducing autonomic nervous system monitoring in the daily practice of intensive care units is due to the limitation of its use as a prognostic tool and, above all, to the difficulties involved in continuous and dynamic monitoring and in the interpretation and applicability of its results.

Successful implementation depends on heart rate variability monitoring going from a prognostic tool to a real-time monitoring instrument in order to be useful in therapeutic guidance; for example, as a guide for fluid therapy through analysis of the high frequency component and for treatment with vasoactive amines through analysis of the low frequency/high frequency ratio.


Swan HJ, Ganz W. Hemodynamic monitoring: a personal and historical perspective. Can Med Assoc J. 1979;121(7):868-71. Link PubMed
Joosten A, Alexander B, Cannesson M. Defining goals of resuscitation in the critically ill patient. Crit Care Clin. 2015;31(1):113-32. Link DOILink PubMed
Vincent JL, Rhodes A, Perel A, Martin GS, Della Rocca G, Vallet B, et al. Clinical review: Update on hemodynamic monitoring--a consensus of 16. Crit Care. 2011;15(4):229. Link DOILink PubMed
Ramsingh D, Alexander B, Cannesson M. Clinical review: Does it matter which hemodynamic monitoring system is used? Crit Care. 2013;17(2):208. Link DOILink PubMed
Kenaan M, Gajera M, Goonewardena SN. Hemodynamic assessment in the contemporary intensive care unit: a review of circulatory monitoring devices. Crit Care Clin. 2014;30(3):413-45. Link DOILink PubMed
Liberati A, Altman DG, Tetzlaff J, Mulrow C, Gotzsche PC, Ioannidis JP, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate healthcare interventions: explanation and elaboration. BMJ. 2009;339:b2700. Link DOILink PubMed
Heart rate variability. Standards of measurement, physiological interpretation, and clinical use. Task Force of The European Society of Cardiology and The North American Society of Pacing and Electrophysiology. Eur Heart J. 1996;17(3):354-81. Link DOILink PubMed
Rajendra Acharya U, Paul Joseph K, Kannathal N, Lim CM, Suri JS. Heart rate variability: a review. Med Biol Eng Comput. 2006;44(12):1031-51. Link DOILink PubMed
Bailon R, Laguna P, Mainardi L, Sornmo L. Analysis of heart rate variability using time-varying frequency bands based on respiratory frequency. Conf Proc IEEE Eng Med Biol Soc. 2007;2007:6675-8. Link PubMed
Slim K, Nini E, Forestier D, Kwiatkowski F, Panis Y, Chipponi J. Methodological index for non-randomized studies (minors): development and validation of a new instrument. ANZ J Surg. 2003;73(9):712-6. Link DOILink PubMed
Pfeifer R, Hopfe J, Ehrhardt C, Goernig M, Figulla HR, Voss A. Autonomic regulation during mild therapeutic hypothermia in cardiopulmonary resuscitated patients. Clin Res Cardiol. 2011;100(9):797-805. Link DOILink PubMed
Riordan WP Jr., Norris PR, Jenkins JM, Morris JA Jr. Early loss of heart rate complexity predicts mortality regardless of mechanism, anatomic location, or severity of injury in 2178 trauma patients. J Surg Res. 2009;156(2):283-9. Link DOILink PubMed
Kahraman S, Dutton RP, Hu P, Stansbury L, Xiao Y, Stein DM, et al. Heart rate and pulse pressure variability are associated with intractable intracranial hypertension after severe traumatic brain injury. J Neurosurg Anesthesiol. 2010;22(4):296-302. Link DOILink PubMed
Mowery NT, Norris PR, Riordan W, Jenkins JM, Williams AE, Morris JA Jr. Cardiac uncoupling and heart rate variability are associated with intracranial hypertension and mortality: a study of 145 trauma patients with continuous monitoring. J Trauma. 2008;65(3):621-7. Link DOILink PubMed
Norris PR, Stein PK, Morris JA Jr. Reduced heart rate multiscale entropy predicts death in critical illness: a study of physiologic complexity in 285 trauma patients. J Crit Care. 2008;23(3):399-405. Link DOILink PubMed
Papaioannou V, Giannakou M, Maglaveras N, Sofianos E, Giala M. Investigation of heart rate and blood pressure variability, baroreflex sensitivity, and approximate entropy in acute brain injury patients. J Crit Care. 2008;23(3):380-6. Link DOILink PubMed
Norris PR, Ozdas A, Cao H, Williams AE, Harrell FE, Jenkins JM, et al. Cardiac uncoupling and heart rate variability stratify ICU patients by mortality: a study of 2088 trauma patients. Ann Surg. 2006;243(6):804-12; discussion 812-4. Link DOILink PubMed
Grogan EL, Morris JA Jr., Norris PR, France DJ, Ozdas A, Stiles RA, et al. Reduced heart rate volatility: an early predictor of death in trauma patients. Ann Surg. 2004;240(3):547-54; discussion 554-6. Link DOILink PubMed
Rapenne T, Moreau D, Lenfant F, Vernet M, Boggio V, Cottin Y, et al. Could heart rate variability predict outcome in patients with severe head injury? A pilot study. J Neurosurg Anesthesiol. 2001;13(3):260-8. Link DOILink PubMed
Winchell RJ, Hoyt DB. Analysis of heart-rate variability: a noninvasive predictor of death and poor outcome in patients with severe head injury. J Trauma. 1997;43(6):927-33. Link DOILink PubMed
Brown SM, Tate Q, Jones JP, Knox DB, Kuttler KG, Lanspa M, et al. Initial fractal exponent of heart rate variability is associated with success of early resuscitation in patients with severe sepsis or septic shock: a prospective cohort study. J Crit Care. 2013;28(6):959-63. Link DOILink PubMed
Schmidt H, Hoyer D, Hennen R, Heinroth K, Rauchhaus M, Prondzinsky R, et al. Autonomic dysfunction predicts both 1- and 2-month mortality in middle-aged patients with multiple organ dysfunction syndrome. Crit Care Med. 2008;36(3):967-70. Link DOILink PubMed
Schmidt H, Müller-Werdan U, Hoffmann T, Francis DP, Piepoli MF, Rauchhaus M, et al. Autonomic dysfunction predicts mortality in patients with multiple organ dysfunction syndrome of different age groups. Crit Care Med. 2005;33(9):1994-2002. Link DOILink PubMed
Gujjar AR, Sathyaprabha TN, Nagaraja D, Thennarasu K, Pradhan N. Heart rate variability and outcome in acute severe stroke: role of power spectral analysis. Neurocrit Care. 2004;1(3):347-53. Link DOILink PubMed
Haji-Michael PG, Vincent JL, Degaute JP, van de Borne P. Power spectral analysis of cardiovascular variability in critically ill neurosurgical patients. Crit Care Med. 2000;28(7):2578-83. Link DOILink PubMed
Papaioannou VE, Maglaveras N, Houvarda I, Antoniadou E, Vretzakis G. Investigation of altered heart rate variability, nonlinear properties of heart rate signals, and organ dysfunction longitudinally over time in intensive care unit patients. J Crit Care. 2006;21(1):95-103; discussion 103-4. Link DOILink PubMed
Yien HW, Hseu SS, Lee LC, Kuo TB, Lee TY, Chan SH. Spectral analysis of systemic arterial pressure and heart rate signals as a prognostic tool for the prediction of patient outcome in the intensive care unit. Crit Care Med. 1997;25(2):258-66. Link DOILink PubMed
Winchell RJ, Hoyt DB. Spectral analysis of heart rate variability in the ICU: a measure of autonomic function. J Surg Res. 1996;63(1):11-6. Link DOILink PubMed
Gang Y, Malik M. Heart rate variability in critical care medicine. Curr Opin Crit Care. 2002;8(5):371-5. Link DOILink PubMed
Brodde OE, Bruck H, Leineweber K, Seyfarth T. Presence, distribution and physiological function of adrenergic and muscarinic receptor subtypes in the human heart. Basic Res Cardiol. 2001;96(6):528-38. Link DOILink PubMed
Berntson GG, Bigger JT Jr., Eckberg DL, Grossman P, Kaufmann PG, Malik M, et al. Heart rate variability: origins, methods, and interpretive caveats. Psychophysiology. 1997;34(6):623-48. Link DOILink PubMed
Hon EH, Lee ST. Electronic evaluation of the fetal heart rate. VIII. Patterns preceding fetal death, further observations. Am J Obstet Gynecol. 1963;87:814-26. Link PubMed
França da Silva AK, Penachini da Costa de Rezende Barbosa M, Marques Vanderlei F, Destro Christofaro DG, Marques Vanderlei LC. Application of heart rate variability in diagnosis and prognosis of individuals with diabetes mellitus: systematic review. Ann Noninvasive Electrocardiol. 2016;21(3):223-35. Link DOILink PubMed
Zhou X, Ma Z, Zhang L, Zhou S, Wang J, Wang B, et al. Heart rate variability in the prediction of survival in patients with cancer: A systematic review and meta-analysis. J Psychosom Res. 2016;89:20-5. Link DOILink PubMed
Wu L, Jiang Z, Li C, Shu M. Prediction of heart rate variability on cardiac sudden death in heart failure patients: a systematic review. Int J Cardiol. 2014;174(3):857-60. Link DOILink PubMed
Huikuri HV, Stein PK. Heart rate variability in risk stratification of cardiac patients. Prog Cardiovasc Dis. 2013;56(2):153-9. Link DOILink PubMed
Yperzeele L, van Hooff RJ, Nagels G, De Smedt A, De Keyser J, Brouns R. Heart rate variability and baroreceptor sensitivity in acute stroke: a systematic review. Int J Stroke. 2015;10(6):796-800. Link DOILink PubMed
Lotufo PA, Valiengo L, Benseñor IM, Brunoni AR. A systematic review and meta-analysis of heart rate variability in epilepsy and antiepileptic drugs. Epilepsia. 2012;53(2):272-82. Link DOILink PubMed
Maetzler W, Liepelt I, Berg D. Progression of Parkinson''s disease in the clinical phase: potential markers. Lancet Neurol. 2009;8(12):1158-71. Link DOILink PubMed
Zhang J, Wang N. Prognostic significance and therapeutic option of heart rate variability in chronic kidney disease. Int Urol Nephrol. 2014;46(1):19-25. Link DOILink PubMed
Ryan ML, Thorson CM, Otero CA, Vu T, Proctor KG. Clinical applications of heart rate variability in the triage and assessment of traumatically injured patients. Anesthesiol Res Pract. 2011;2011:416590. Link PubMed
Green GC, Bradley B, Bravi A, Seely AJ. Continuous multiorgan variability analysis to track severity of organ failure in critically ill patients. J Crit Care. 2013;28(5):879.e1-11. Link DOI
Boselli E, Daniela-Ionescu M, Bégou G, Bouvet L, Dabouz R, Magnin C, et al. Prospective observational study of the non-invasive assessment of immediate postoperative pain using the analgesia/nociception index (ANI). Br J Anaesth. 2013;111(3):453-9. Link DOILink PubMed
Stein PK, Schmieg RE Jr., El-Fouly A, Domitrovich PP, Buchman TG. Association between heart rate variability recorded on postoperative day 1 and length of stay in abdominal aortic surgery patients. Crit Care Med. 2001;29(9):1738-43. Link DOILink PubMed
Arcentales A, Caminal P, Diaz I, Benito S, Giraldo BF. Classification of patients undergoing weaning from mechanical ventilation using the coherence between heart rate variability and respiratory flow signal. Physiol Meas. 2015;36(7):1439-52. Link DOILink PubMed
Huang CT, Tsai YJ, Lin JW, Ruan SY, Wu HD, Yu CJ. Application of heart-rate variability in patients undergoing weaning from mechanical ventilation. Crit Care. 2014;18(1):R21. Link DOILink PubMed

Responsible editor: Jorge Ibrain Figueira Salluh

Submission On-line

Indexed in




Associação de Medicina Intensiva Brasileira - AMIB

Rua Arminda nº 93 - 7º andar - Vila Olímpia - São Paulo, SP, Brasil - Tel./Fax: (55 11) 5089-2642 | e-mail: [email protected]

Cookie Policy

GN1 - Systems and Publications