Ventilation-Induced Modulation of Pulse Oximeter Waveforms: A Method for the Assessment of Early Changes in Intravascular Volume During Spinal Fusion Surgery in Pediatric Patients.

BACKGROUND: Scoliosis surgery is often associated with substantial blood loss, requiring fluid resuscitation and blood transfusions. In adults, dynamic preload indices have been shown to be more reliable for guiding fluid resuscitation, but these indices have not been useful in children undergoing surgery. The aim of this study was to introduce frequency-analyzed photoplethysmogram (PPG) and arterial pressure waveform variables and to study the ability of these parameters to detect early bleeding in children during surgery. METHODS: We studied 20 children undergoing spinal fusion. Electrocardiogram, arterial pressure, finger pulse oximetry (finger PPG), and airway pressure waveforms were analyzed using time domain and frequency domain methods of analysis. Frequency domain analysis consisted of calculating the amplitude density of PPG and arterial pressure waveforms at the respiratory and cardiac frequencies using Fourier analysis. This generated 2 measurements: The first is related to slow mean arterial pressure modulation induced by ventilation (also known as DC modulation when referring to the PPG), and the second corresponds to pulse pressure modulation (AC modulation or changes in the amplitude of pulse oximeter plethysmograph when referring to the PPG). Both PPG and arterial pressure measurements were divided by their respective cardiac pulse amplitude to generate DC% and AC% (normalized values). Standard hemodynamic data were also recorded. Data at baseline and after bleeding (estimated blood loss about 9% of blood volume) were presented as median and interquartile range and compared using Wilcoxon signed-rank tests; a Bonferroni-corrected P value <0.05 was considered statistically significant. RESULTS: There were significant increases in PPG DC% (median [interquartile range] = 359% [210 to 541], P = 0.002), PPG AC% (160% [87 to 251], P = 0.003), and arterial DC% (44% [19 to 84], P = 0.012) modulations, respectively, whereas arterial AC% modulations showed nonsignificant increase (41% [1 to 85], P = 0.12). The change in PPG DC% was significantly higher than that in PPG AC%, arterial DC%, arterial AC%, and systolic blood pressure with P values of 0.008, 0.002, 0.003, and 0.002, respectively. Only systolic blood pressure showed significant changes (11% [4 to 21], P = 0.003) between bleeding phase and baseline. CONCLUSIONS: Finger PPG and arterial waveform parameters (using frequency analysis) can track changes in blood volume during the bleeding phase, suggesting the potential for a noninvasive monitor for tracking changes in blood volume in pediatric patients. PPG waveform baseline modulation (PPG DC%) was more sensitive to changes in venous blood volume when compared with respiration-induced modulation seen in the arterial pressure waveform.

Photoplethysmography.

The photoplethysmographic (PPG) waveform, also known as the pulse oximeter waveform, is one of the most commonly displayed clinical waveforms. First described in the 1930s, the technology behind the waveform is simple. The waveform, as displayed on the modern pulse oximeter, is an amplified and highly filtered measurement of light absorption by the local tissue over time. It is optimized by medical device manufacturers to accentuate its pulsatile components. Physiologically, it is the result of a complex, and not well understood, interaction between the cardiovascular, respiratory, and autonomic systems. All modern pulse oximeters extract and display the heart rate and oxygen saturation derived from the PPG measurements at multiple wavelengths. "As is," the PPG is an excellent monitor for cardiac arrhythmia, particularly when used in conjunction with the electrocardiogram (ECG). With slight modifications in the display of the PPG (either to a strip chart recorder or slowed down on the monitor screen), the PPG can be used to measure the ventilator-induced modulations which have been associated with hypovolemia. Research efforts are under way to analyze the PPG using improved digital signal processing methods to develop new physiologic parameters. It is hoped that when these new physiologic parameters are combined with a more modern understanding of cardiovascular physiology (functional hemodynamics) the potential utility of the PPG will be expanded. The clinical researcher's objective is the use of the PPG to guide early goal-directed therapeutic interventions (fluid, vasopressors, and inotropes), in effect to extract from the simple PPG the information and therapeutic guidance that was previously only obtainable from an arterial pressure line and the pulmonary artery catheter.

Impact of lower body negative pressure induced hypovolemia on peripheral venous pressure waveform parameters in healthy volunteers.

Lower body negative pressure (LBNP) creates a reversible hypovolemia by sequestrating blood volume in the lower extremities. This study sought to examine the impact of central hypovolemia on peripheral venous pressure (PVP) waveforms in spontaneously breathing subjects. With IRB approval, 11 healthy subjects underwent progressive LBNP (baseline, -30, -75, and -90 mmHg or until the subject became symptomatic). Each was monitored for heart rate (HR), finger arterial blood pressure (BP), a chest respiratory band and PVP waveforms which are generated from a transduced upper extremity intravenous site. The first subject was excluded from PVP analysis because of technical errors in collecting the venous pressure waveform. PVP waveforms were analyzed to determine venous pulse pressure, mean venous pressure, pulse width, maximum and minimum slope (time domain analysis) together with cardiac and respiratory modulations (frequency domain analysis). No changes of significance were found in the arterial BP values at -30 mmHg LBNP, while there were significant reductions in the PVP waveforms time domain parameters (except for 50% width of the respiration induced modulations) together with modulation of the PVP waveform at the cardiac frequency but not at the respiratory frequency. As the LBNP progressed, arterial systolic BP, mean BP and pulse pressure, PVP parameters and PVP cardiac modulation decreased significantly, while diastolic BP and HR increased significantly. Changes in hemodynamic and PVP waveform parameters reached a maximum during the symptomatic phase. During the recovery phase, there was a significant reduction in HR together with a significant increase in HR variability, mean PVP and PVP cardiac modulation. Thus, in response to mild hypovolemia induced by LBNP, changes in cardiac modulation and other PVP waveform parameters identified hypovolemia before detectable hemodynamic changes.

Perioperative dilemma: challenges of the management of a patient on mega doses of morphine and methadone.

High doses of opioids are often needed in the management of cancer-related pain. A discussion of a patient's perioperative opioid management and mechanisms contributing to opioid-induced hyperalgesia (OIH) are presented. In the present case report, a patient on high doses of opioids, including morphine and methadone, with severe worsening back pain and a history of increasing opioid requirements for the last 2 months due to metastatic leiomyosarcoma to the femur, spine, and neck is described. Use of high dose opioids is associated with numerous challenges, including tolerance. The successful management of this patient was multimodal and included the use of potent analgesics, N-methyl-D-aspartatereceptor antagonists, and the α-2 agonist clonidine.

Analysis of plethysmographic waveform changes induced by beach chair positioning under general anesthesia.

During shoulder surgery, patients typically are placed in the beach chair position. In rare cases, this positioning has resulted in devastating outcomes of postoperative cerebral ischemia (Cullen and Kirby in APSF Newsl 22(2):25-27, 2007; Munis in APSF Newsl 22(4):82-83, 2008). This study presents a method to noninvasively and continuously hemodynamically monitor patients during beach chair positioning by using the photoplethysmograph signal recorded from a commercial pulse oximeter. Twenty-nine adults undergoing shoulder surgery were monitored before and after beach chair positioning with electrocardiogram, intermittent blood pressure, end tidal carbon dioxide, and photoplethysmograph via Nellcor finger pulse oximeter. Fast Fourier transform (FFT) was used to perform frequency-domain analysis on the photoplethysmograph (PPG) signal for data segments taken 80-120 s before and after beach chair positioning. The amplitude density of respiration-associated PPG oscillations was quantified measuring the height of the FFT peak at respiratory frequency. Results were reported as (median, interquartile range) and statistical analysis was performed using Wilcoxon sign rank test. Data were also collected when vasoactive drugs phenylephrine and ephedrine were used to maintain acceptable mean arterial pressure during a case. With beach chair positioning, all subjects who did not receive vasoactive drugs showed an increase in the FFT amplitude density of respiration-associated PPG oscillations (p < 0.0001) without change in pulse-associated PPG oscillations. The PPG was more accurate at monitoring the change to beach chair position than blood pressure or heart rate. With vasoactive drugs, pulse-associated PPG oscillations decreased only with phenylephrine while respiration-associated oscillations did not change. Frequency domain analysis of the PPG signal may be a better tool than traditional noninvasive hemodynamic parameters at monitoring patients during beach chair position surgery.

Laryngeal physiology and voice acoustics are maintained after minimally invasive parathyroidectomy.

OBJECTIVES: This prospective single-arm study investigated both laryngeal physiology and voice acoustic measures in patients undergoing minimally invasive parathyroidectomy (MIP) due to primary hyperparathyroidism (primary HPTH). BACKGROUND: Avoidance of recurrent or superior laryngeal nerve injury and maintenance of normal laryngeal physiology and vocal function are key goals in the treatment of primary HPTH. No data are available comparing pre- and postoperative MIP laryngeal physiology and voice acoustics. METHODS: Patients served as their own controls and underwent identical pre- and postoperative assessment. True vocal fold mobility was assessed and recorded using transnasal fiber-optic laryngoscopy. Vocal capacity was recorded with maximum phonation time and vocal stability by frequency-based voice measures, that is, mean fundamental frequency (F0), standard deviation of the fundamental frequency (F0SD), and jitter and shimmer as measured by relative average perturbation and mean shimmer in decibels, respectively. RESULTS: A total of 104 patients were enrolled [26 men, mean age = 53 years, range 29-79 years; 78 women, mean age = 56 years, range 16-83 years). All completed the protocol and were analyzed according to intent to treat. MIP was accomplished in 95 patients, and 9 were converted to general anesthesia. The cure rate was 100%, as evidenced by normalization of serum calcium levels. Both real-time agreement and blinded inter- and intrarater reliability testing for laryngeal physiology ratings were 100%. One patient (<1%) exhibited a recurrent laryngeal nerve injury. No significant differences (P > 0.05) were found for any voice acoustic parameter between pre- and postoperative MIP (ie, maximum phonation time, F0, F0SD, relative average perturbation, or shimmer in decibels). CONCLUSIONS: MIP can be performed with exquisite disease control and without significant effects on laryngeal physiology or voice acoustic measures. For the first time, both physiologic and acoustic data support the use of MIP.

Respiratory physiology and the impact of different modes of ventilation on the photoplethysmographic waveform.

The photoplethysmographic waveform sits at the core of the most used, and arguably the most important, clinical monitor, the pulse oximeter. Interestingly, the pulse oximeter was discovered while examining an artifact during the development of a noninvasive cardiac output monitor. This article will explore the response of the pulse oximeter waveform to various modes of ventilation. Modern digital signal processing is allowing for a re-examination of this ubiquitous signal. The effect of ventilation on the photoplethysmographic waveform has long been thought of as a source of artifact. The primary goal of this article is to improve the understanding of the underlying physiology responsible for the observed phenomena, thereby encouraging the utilization of this understanding to develop new methods of patient monitoring. The reader will be presented with a review of respiratory physiology followed by numerous examples of the impact of ventilation on the photoplethysmographic waveform.

Impact of central hypovolemia on photoplethysmographic waveform parameters in healthy volunteers. Part 1: time domain analysis.

INTRODUCTION: Our study sought to explore changes in photoplethysmographic (PPG) waveform param- eters, during lower body negative pressure (LBNP) which simulated hypovolemia, in spontaneously breathing volunteers. We hypothesize that during progressive LBNP; there will be a preservation of ear PPG parameters and a decrease in finger PPG parameters. METHODS: With IRB approval, 11 volunteers underwent a LBNP protocol at baseline, 30, 75, and 90 mm Hg (or until the subject became symptomatic). Subjects were monitored with finger and ear pulse oximeter probes, an ECG, and a finger arterial blood pressure monitor. The square root of the mean of the squared differences between adjacent NN intervals (RMSSD) which is the time domain analysis of the heart rate variability (HRV) was measured. PPG waveforms were analyzed for height, area, width 50, maximum and minimum slope. Data are presented as median and inter-quartile range. Friedman ANOVA and Wilcoxon tests were used to identify changes in hemo- dynamic and PPG parameters, P < 0.017 was considered statistically significant. RESULTS: There were no significant changes in the blood pressure variables at LBNP(30), but at and beyond LBNP(75), the decreases in systolic, mean and pulse pressure were significant as was the increase in diastolic pressure. Heart rate increased significantly at LBNP(30), reaching a maximum of 75.4% above baseline at the symptomatic phase while RMSSD showed significant reduction at LBNP(75). Finger PPG height, area, width 50, and maximum slope decreased significantly at LBNP(30) and during symptomatic phase they showed a reduction of 59.4, 76.9, 27.4 and 51.6%, respectively. Ear PPG height, area, width 50 and maximum slope did not change significantly until the LBNP(75), reached. During symptomatic phase, the respective declines reached 39.3, 61.0, 21.4 and 34.9%. CONCLUSION: PPG waveform parameters may prove to be sensitive and specific as early indicators of blood loss. These PPG changes were observed before profound decreases in arterial blood pressure. The relative sparing of central cutaneous blood flow is consistent with the increased parasympathetic innervation of central structures.

Impact of central hypovolemia on photoplethysmographic waveform parameters in healthy volunteers part 2: frequency domain analysis.

OBJECTIVE: The photoplethysmographic (PPG) waveforms are modulated by the respiratory, cardiac and autonomic nervous system. Lower body negative pressure (LBNP) has been used as an experimental tool to simulate loss of central blood volume in humans. The aim of our research is to understanding PPG waveform changes during progressive hypovolemia. METHODS: With IRB approval, 11 volunteers underwent a LBNP protocol at baseline, 30, 75, and 90 mmHg (or until the subject became symptomatic). Subjects were monitored with finger and ear pulse oximeter probes, ECG, and finger arterial blood pressure monitor (FABP). Heart rate variability (HRV) was analyzed to high frequency (HRV-HF) (0.12-0.4 Hz) and low frequency (HRV-LF) (0.04-0.12 Hz). Frequency analysis of PPG waveforms were computed to low (0.04-0.11 Hz) frequency (PPG-LF), intermediate (0.12-0.18 Hz) frequency (PPG-IF), respiratory (0.19-0.3 Hz) frequency (PPG-Resp.) and cardiac (0.75-2.5 Hz) frequency (PPG-Cardiac)during different phases of LBNP protocol RESULTS: Heart rate increased significantly while systolic, mean and pulse pressure of the FABP declined slowly together with significant reductions in HRV-HF (0.12-0.4 Hz) and HRV-LF (0.04-0.12 Hz) power at LBNP(75). There was significant reduction in finger PPG-Cardiac modulation which is consistent with the reduction in the pulse pressure of the FABP. As the LBNP progress there was shift in the amplitude density of the ear PPG-Cardiac to PPG-Resp. Oscillation as an evidence of progressive hypovolemia with reduction in pulse pressure and increase in the respiratory induced variations. At LBNP(75), there were significant increased (>140% increase from the baseline) in ear PPG-IF (0.12-0.18 Hz) in the meantime HRV-HF showed significant reduction (>89%) from the baseline. At the symptomatic phase; there was a shift in ear PPG-IF to PPG-Resp. With an increase in the ear PPG-Resp. Modulation to ≥175% from the baseline CONCLUSION: The pulse oximeter waveform contains a complex mixture of the effect of cardiac, venous, autonomic, and respiratory systems on the central and peripheral circulation. The occurrence of autonomic modulation needs to be taken into account when studying signals that have their origins from central sites (e.g. ear and forehead).

The best fit function for the tee short axis left ventricular ejection fraction and radionuclear "gold standard" relationship is curvilinear.

OBJECTIVE: The objective of this study was to determine the function that best expressed the true shape of the regression line between transgastric short axis (TGSA) transesophageal echocardiographic (TEE)) views of the left ventricle (LV) and radionuclear LVEF. METHODS: The literature was searched for relevant articles published between 1979 and 2007. Articles that directly compared TGSA LVEF with radionuclear LVEF were reviewed. Inclusion criteria included the provision that TGSA estimations be acquired by manual tracing of the endocardial border. Digital tabular data sets were created from electronically scanned graphic data (Photoshop, Adobe Systems, Inc., San Jose, CA). Software consisted of SPSS (SPSS, Inc., Chicago, IL). Analysis was by regression curve fitting with standard parametric and LOWESS (locally weighted scatterplot smoothing) data-driven models. RESULTS: Three articles met our study design criteria. The studies generated a total of 32 patients with 99 data points. These data were pooled and analyzed. The LOWESS regression surface demonstrated non-linearity. The best "goodness of fit" template function was determined by selecting the function with the highest R-squared value. The best fit (R(2) = 0.807) consisted of a polynomial function with a power trajectory. CONCLUSION: Linear regression analysis provides a linear regression function. Thus, analyses are forced to conform to a straight-line relationship, irrespective of the disposition of the data points. By contrast, parametric and nonparametric regression models allow a choice of functions. This feature permits construction of a more appropriate "goodness of fit" curve. In this study, our purpose was to determine the function that best expressed the true shape of the regression line. Results indicated that the relationship between TEE TGSA and radionuclear LVEF was curvilinear.