CNAP HD: Noninvasive Hemodynamic Monitoring in Research

Cardiac Output (CNCO® ) and further essential hemodynamic parameters calculated from the continuous non-invasive arterial pressure curve (CNAP®) by means of the Pulse Contour Analysis shows high accuracy and high trending ability (precision) compared to invasive clinical standards (e.g. thermodilution and PiCCO) with valuable benefit for scientific and clinical research.

By Dr. Jürgen Fortin, CEO, CNSystems

Pulse Contour Analysis (PCA) for deriving complete Hemodynamics from continuous blood pressure wave (CNAP)

Pulse Contour Analysis (PCA)[1] derives important physiological information on preload, contractility, afterload and compliance of the heart from the well validated CNAP® Continuous Noninvasive Arterial Pressure Curve[2],[3]. By adding biometric patient data Stroke Volume (SV) and therefrom Continuous Noninvasive Cardiac Output (CNCO®), both essential hemodynamic markers, are calculated. Further hemodynamic parameters such as Systemic Vascular Resistance (SVR) as well as all indexed values SI, CI or SVRI are derived completing the hemodynamic picture.

Validation: CNCO® is clinically validated against invasive methods

Non-invasive continuous CNCO® is the non-invasive continuous cardiac output calculated from CNAP® Arterial Pressure as described above.

Accuracy of CNCO® compared to clinical standards such as invasive thermodilution (TD) or PiCCO is expressed as percentage error. In 1999, Critchley and Critchley suggested a percentage error of 30% or less[4]. In clinical practice, however, percentage errors of 40-45% are more realistic for the interchangeability between two CO-measurement methods (meta-analysis by Peyton and Chong[5]).

Trending ability is the precise tracking of changes in CO. According to Critchley, Lee and Ho, reliable trending ability[6] is indicated by concordance rates of > 90%. Vincent and colleagues state that following hemodynamic trends may be more important than absolute values[7].

CNCO® shows both high accuracy as well as high trending ability (precision) compared to the invasive clinical standards thermodilution and PiCCO fulfilling all Critchley criteria:

Bland-Altman plots show

  • Small bias and narrow limits of agreement
  • Percentage errors ≤ 30% (according to strict Critchley standard [8],[9])
  • Concordance rates ≥ 90% (according to standard [10])

Read more on CNAP accuracy here and here.

Benefit of continuous BP, CO & SVR in research (examples)

Blood pressure, cardiac output and vascular resistance are used to differentiate between challenge and threat states (positive and negative stress)[11],[12] and to quantify emotional response[13] in psychophysiological studies. A challenging situation causes a far bigger rise in cardiac output than a threating state. Total peripheral resistance rises in threat state but shows strong decrease in the challenging situation.

CNCO® is available with the CNAP® HD feature, currently only available in Europe.

For more information on CNAP, to include references to studies and research and plots, click here.

[1] https://en.wikipedia.org/wiki/Cardiac_output#Pulse_Pressure_methods
[2] Jeleazcov C et. al. Precision and accuracy of a new device (CNAP®) for continuous noninvasive arterial blood pressure monitoring: assessment during general anaesthesia. BJA. 2010; 105(3):264-272
[3] Biais, M. et. al. Continuous non-invasive arterial pressure measurement: Evaluation of CNAPTM device during vascular surgery Ann Fr Anesthesia
[4] Critchley, L. A., & Critchley, J. A. (1999). A meta-analysis of studies using bias and precision statistics to compare cardiac output measurement techniques. Journal of clinical monitoring and computing, 15(2), 85–91
[5] Peyton PJ, Chong SW: Minimally invasive measurement of cardiac output during surgery and critical care. Anesthesiology 2010; 113:1220-35

[6] Critchley LA, Lee A, Ho AMH: A critical review of the ability of continuous cardiac output monitors to measure trends in cardiac output. Anesth Analg 2010; 111:1180-92.

[7] Vincent JL et al.: Clinical review: Update on hemodynamic monitoring – a consensus of 16. Critical Care 2011, 15:229.

[8] Critchley, L. A., & Critchley, J. A. (1999). A meta-analysis of studies using bias and precision statistics to compare cardiac output measurement techniques. Journal of clinical monitoring and computing, 15(2), 85–91

[9] Peyton PJ, Chong SW: Minimally invasive measurement of cardiac output during surgery and critical care. Anesthesiology 2010; 113:1220-35.

[10] Critchley LA, Lee A, Ho AMH: A critical review of the ability of continuous cardiac output monitors to measure trends in cardiac output. Anesth Analg 2010; 111:1180-92.

[11] Kirby, L. D., & Wright, R. A. (2003). Cardiovascular correlates of challenge and threat appraisals: A critical examination of the Biopsychosocial Analysis. Personality and Social Psychology Bulletin, 7, 216-233.

[12] Tomaka, J., Blascovich, J., Kelsey, R. M., & Leitten, C. L. (1993). Subjective, physiological, and behavioral effects of threat and challenge appraisal. Journal of Personality and Social Psychology, 65, 248-260.

[13] Lackner, H. K., Weiss, E. M., Schulter, G., Hinghofer-Szalkay, H., Samson, A. C., & Papousek, I. (2013). I got it! Transient Cardiovascular Response to the Perception of Humor. Biological Psychology, 93, 33–40.

For more information on BIOPAC’s Noninvasive Blood Pressure monitoring and measurement systems and advanced functionality in the area of cardiovascular hemodynamics, to include CNAP noninvasive blood pressure systems, visit BIOPAC’s NIBP page or view BIOPAC’s NIBP amplifiers (MRI and small animal applications are also supported) and related equipment for a wide variety of research applications.

BIOPAC Systems, Inc. provides life science researchers and educators with data acquisition and analysis systems that inspire people and enable greater discovery about life.  Visit us at www.biopac.com.

Electrodermal Activity (EDA)

Typically, EDA is measured as skin conductance and a small direct constant voltage (0.5 vdc) is used as excitation source across the skin electrodes.

By Alan Macy, BIOPAC Systems, Inc.

Electrodermal activity measurement is subject to electrically-related characteristics of the skin. There are two phenomena associated with this type of skin activity. One is skin potential, which is a self-generated potential intrinsic to the skin. This potential is a consequence associated with dissimilar skin layers placed in proximity coupled with the presence and movement of interstitial fluids. An evoked skin potential response is called the sympathetic skin response. This change in skin potential can be evoked by electrical, auditory or magnetic stimulation. The other phenomenon associated with skin electrical activity can be measured when a stimulation (excitation) current is injected through, or a voltage is applied across, attached skin electrodes. The current or voltage stimulation is typically at constant (DC) level, or at low frequency, because the skin impedance is high. The application of excitation current or voltage produces a corresponding voltage or current, respectively, that changes over time subject to physiological state. In these cases, the skin’s resistance, impedance, conductance or admittance is being measured, corresponding to the type of electrical stimulation used.

EDA Measurements – subject to electrical excitation type:

Skin Resistance – Direct Constant Current (not commonly used)

Skin Conductance – Direct Constant Voltage (most commonly used)

Skin Impedance – Alternating Constant Current (not commonly used)

Skin Admittance – Alternating Constant Voltage (sometimes used)

Typically, EDA is measured as skin conductance and a small direct constant voltage (0.5 vdc) is used as excitation source across the skin electrodes. The skin admittance method (alternating constant voltage excitation) may provide some advantages in measurement in that this method does not polarize the skin electrodes during EDA recording. Skin conductance is usually measured in units of “Siemens” although sometimes “mho” is used. The unit “mho” comes from the reverse spelling of “ohm”, the unit of resistance. One mho equals one Siemen.  The conductivity of the skin is small, so values are given in microsiemens (uS) or micromhos (umho).

Changes in the electrically-related characteristics of the skin is correlated to eccrine sweat gland activity. Eccrine glands are in nearly all skin locations and are found, in highest concentrations, on the palms of hands, fingertips and soles of the feet. EDA, measured as skin conductance, is a physiological signal that indicates increased sympathetic nervous system (SNS) activity. This aspect of EDA is representative of changes in the electrical conductance of the skin due to eccrine (sweat) gland activity. SNS activity increases sweat gland secretions. Eccrine glands only receive activation signals from the SNS, so increased EDA is an indicator of increased arousal.

There are two aspects to skin conductance measurements, namely phasic and tonic. Tonic value is the average skin conductance level (SCL), that is relatively consistent over time, and is related to arousal. The phasic component  of skin conductance is the change of the skin conductance, over a short time period, in reaction to a stimulus. For a skin conductance response (SCR), the skin conductance rises in a short time period and then returns to tonic levels. SCRs are characterized by four different parameters: the response peak amplitude, latency of response, rise time to the response peak, and recovery time after peak.

For more information on BIOPAC’s EDA research solutions, including real-time live raw EDA data as well as real-time filtering or calculation channels including High-pass filtered/AC Coupled EDA, visit BIOPAC’s EDA Analysis page or view BIOPAC’s full line of electrodes, amplifiers, and wearable, wireless transmitters and loggers.

Additionally, a link to a recently updated EDA SCR Analysis Guide for Psychological Experiments came be found here.

BIOPAC Systems, Inc. provides life science researchers and educators with data acquisition and analysis systems that inspire people and enable greater discovery about life.  Visit us at www.biopac.com.

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