Choosing patient-tailored hemodynamic monitoring
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This article is one of ten reviews selected from the Yearbook of Intensive Care and Emergency Medicine 2010 (Springer Verlag) and co-published as a series in Critical Care. Other articles in the series can be found online at http://ccforum.com/series/yearbook. Further information about the Yearbook of Intensive Care and Emergency Medicine is available from http://www.springer.com/series/2855.
KeywordsMean Arterial Pressure Pulmonary Artery Catheter Fluid Responsiveness Hemodynamic Monitoring Extravascular Lung Water
central venous pressure
intensive care unit
mean arterial pressure
pulmonary artery catheter
pulmonary artery occlusion pressure
central venous oxygen saturation.
Currently, the number and (worldwide) availability of techniques for hemodynamic monitoring in the critically ill patient is overwhelming, as nicely summarized elsewhere [1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11]. Techniques vary from completely invasive to non-invasive, from intermittent to continuous, and differ in basic principles, methods, parameters, and costs, among others. The older a device, the more literature is available, but the latter may not always help in choosing hemodynamic monitoring tools for departments or for individual patients, i.e. patient-tailored monitoring.
This chapter is not intended to compare one technique to another, which has been done abundantly in the literature, but to provide a conceptual framework to guide therapy of individual patients in various hospital settings by defining the elements that may help to choose among the available techniques, in the absence of a clear evidence-based survival benefit of any hemodynamic monitoring tool [12, 13, 14, 15, 16]. First, a brief discussion of what is available and of underlying basic principles seems warranted, since knowledge of possibilities, limitations and pitfalls is required before responsible choices can be made. We will not address tools to monitor the microcirculation.
What do we have and what can they do?
What do we have and what can they do?
Central venous catheter (many companies)
Pulmonary artery catheter and modifications (some companies)
Modelflow pulse contour analysis (BMI-TNO)
Flotrac/Vigileo (Edwards Life Sciences)
Pulse-dye densitometry PDD (Nihon Kohden)
Bioimpedance cardiography (Aesculon, Osypka Medical)
CardioQ (Deltex Medical)
Ultrasonic cardiac output monitors (Uscom)
Echocardiographs (some companies)
Cardiac pressures and volumes
Cardiac output, flow, velocity/time
Cardiac anatomy and regional function
Carbon dioxide-related variables
There is a large amount of literature concerning the comparability of techniques and derived parameters, such as (absolute values and changes in) cardiac output and preload indicators [4, 5, 6, 7, 18, 19]. However, the manner in which the comparability (or clinically important absence thereof) is judged varies greatly among studies. Uniformly accepted criteria to assess the clinical relevance of comparability of monitoring techniques and parameters are lacking. For instance, comparability of techniques for tracking changes and trends in cardiac output may be more relevant in clinical practice than the degree of agreement of absolute values, provided that 'low' and 'high' values can be separated . Moreover, literature on the practical utility of many of these devices and parameters is scarce, so that negativism regarding their practical value may predominate [16, 20]. There is, however, some literature to suggest that insertion of a pulmonary artery catheter (PAC) and measuring hemodynamic variables may influence the clinical appraisal of hemodynamics at the bedside and may help or prompt the treating physician to change treatment.
Since its introduction in the 1970s, the PAC has indeed become the reference standard for hemodynamic monitoring and measurement of cardiac output [13, 14, 15]. A substantial knowledge database has been built up since then, in a variety of institutions, patient populations, and circumstances . However, in the absence of any rigidly proven survival benefit, the catheter has become discredited in critical care medicine [12, 13, 14, 15, 16]. The lack of apparent benefit may relate, in part, to adverse effects of insertion, improper use, poor interpretation of hemodynamic data, and inadequate treatment decisions based on the collected variables, or combinations of these factors . Conversely, the value of pulmonary artery pressures, pulmonary artery occlusion pressure (PAOP), mixed venous oxygen saturation (SvO2), and right heart volumes, some of the variables that can be uniquely assessed at the bedside of the critically ill patient with help of the PAC and right-sided thermodilution, remains hotly debated [13, 14, 15, 20]. The patient population or circumstance that is most likely to benefit from pulmonary artery catheterization is, therefore, still being actively looked for [13, 14, 15, 21, 22].
A second generation hemodynamic monitoring principle includes the less invasive transpulmonary (dye) thermodilution technique, e.g. PiCCO. This technique offers the unique possibility of estimating cardiac preload volumes, measurements of which are not confounded by mechanical ventilation in contrast to pressure and dynamic indices of preload and fluid responsiveness, and of extravascular lung water as a direct measure of pulmonary edema and permeability. Dilutional methods to measure cardiac output include the transpulmonary lithium and indocyanine green (pulse dye) techniques, allowing peripheral injections and peripheral and, for pulse dye, non-invasive detection.
Pulse-contour or pulse-power methods, needing relatively frequent recalibration for optimal performance in tracking changes in cardiac output, are often incorporated in dilutional cardiac output measurement devices needing arterial access [5, 18]. Some of these methods are truly non-invasive, however. The algorithms used differ from one method to the other, some perform better than others, and the need for recalibration upon changes in time or in vascular tone upon treatment continue to limit their independent applicability [5, 18]. Calibration can also be performed by ultrasonically obtained aortic diameter for the otherwise well performing Model flow method . The algorithm used in the latter method computes the aortic flow waveform from pulsating arterial blood pressure by simulating a nonlinear, self-adaptive (three-element Windkessel) model of the aortic input impedance. Characteristic impedance and compliance of the aorta non-linearly depend on arterial pressure, and peripheral resistance adapts to changes in blood flow. The degree of non-linearity depends on the subject's sex, age, height, and weight.
An arterial waveform analysis without external calibration, the FloTrac/Vigileo system, is supposed to be relatively independent of vascular tone . Each arterial waveform detected via an arterial catheter is analyzed with a frequency of 100 Hz. The arterial waveform is analyzed for 8 different characteristics, including the upstroke and downslope of the curve. Each curve is analyzed separately and additional curves are analyzed and compared with former and subsequent curves. From this analysis, which takes 20 seconds, the average curve is given, by means of the standard deviation of the given characteristics of the curves. From the given stroke volume and heart rate, the cardiac output is determined, which is updated every 20 seconds. A filter is embedded in the computer to adjust for excesses in systolic blood pressures and heart rates. The accuracy of this method has increased with consecutive software versions.
Doppler ultrasound methods estimate cardiac output by measuring aortic blood flow velocity [10, 11, 24, 25] and multiplying it by the cross-sectional area of the aorta at the insonation point. The probe is introduced orally or nasally and placed at the level of the descending aorta. Some systems measure the descending aortic diameter; others use a monogram to estimate it. Limitations of the technique include operator-dependency in finding the optimal angle of insonation, turbulent flow, and changes in relative perfusion of upper and lower body parts via the aorta. Obviously, echocardiography yields clinically useful information on cardiac anatomy and (regional) function that is hard to obtain otherwise, in addition to non-unique parameters, such as cardiac filling and output [26, 27]. The technique is highly dependent on available expertise and commitment.
Factors affecting choices
Theoretical considerations for choosing among hemodynamic monitoring tools
• Safety and side effects
• Versatility, number, relevance and utility of parameters
• Can be utilized by nurses and physicians: Ease of use, user-friendliness, education, learning curve
• Possibilities for assessing fluid responsiveness, goal-directed therapy and other resuscitation strategies of proven outcome benefit even if not decreasing mortality
• Demonstrated treatment alterations
• Acceptable cost-effectiveness
Hardware considerations for choosing among hemodynamic monitoring tools
• Expertise: Personal, colleagues, and in the literature
• Ease of use and interpretation; operator-dependency
• Level of integration in monitors
• Uniformity of applicability
• Continuous vs intermittent
• Invasive vs non-invasive
• Accuracy/reproducibility of parameters
• Response time to interventions and accurate trending
Patient-bound considerations for tailoring hemodynamic monitoring
• Cardiac rhythm, function, and valvular disease
• Mechanical ventilation: Tidal volume, frequency, positive end-expiratory pressure
• Type, severity and stage of (anticipated) disease warranting hemodynamic monitoring, such as shock and acute lung injury
• Type of circulatory support and change contemplated therein: Fluids, drugs, devices for circulatory support
• Vascular access and other anatomic factors (contraindications)
Some hemodynamic optimization strategies, such as fluid management guided by prediction of fluid responses, early goal-directed therapy, and perioperative hemodynamic optimization or fluid restriction, may help to improve patient outcomes, in terms of reducing complications, lengths of stay, and prevention of overhydration, for example, even irrespective of vital status [1, 16, 25, 28, 29, 30, 31, 32, 33]. Devices and parameters to assess fluid responsiveness include transpulmonary dilution-derived cardiac volumes, esophageal Doppler flow and echocardiographic indices, and dynamic indices provided by pulse-contour methods [10, 11, 24, 25, 33, 34]. In contrast, central venous pressure (CVP) monitoring may suffice in successful fluid restriction policies . The well-known outcome (survival) benefit of early goal-directed therapy in septic shock, with treatment guided by CVP, central venous oxygen saturation (ScvO2) and MAP, has been confirmed by others, since the landmark paper by Rivers et al.  and this approach is included in current guidelines on the management of septic shock [1, 31], even though CVP may poorly predict fluid responses . Hence, monitoring tools could be judged on their ability to provide parameters that help physicians to implement the strategies mentioned, even if these are slightly different from those originally used in demonstrating benefit but apply similar physiologic and clinical concepts [1, 15, 30, 37, 38, 39]. For example, the benefit of perioperative hemodynamic optimization with help of the PAC , transpulmonary/lithium dilution [29, 30], esophageal Doppler [10, 11, 24, 25], or dynamic indices  could translate into a benefit of optimization of central/mixed venous oxygen saturation since all are intended to optimize tissue oxygenation . Nevertheless, not all devices and parameters have been successfully evaluated yet in hemodynamic optimization strategies and these issues continue to be subject to ongoing research and debate [1, 15, 37, 39, 40]. Thus, we may need to formulate and test hemodynamic monitoring strategies, rather than to evaluate performance and efficacy of single devices and parameters. The rationale of these strategies may be enforced if led by physiological and clinical considerations as well as by epidemiological and economic issues. Finally, effectiveness could be defined in terms of the clinical utility of devices and parameters that may go beyond their formally reported efficacy.
Hardware considerations (Table 3) include the environment where the hemodynamic monitoring is used. Different departments may have different facilities, patient populations and staffing, and pressures on time by emergencies may drive choices for less invasive techniques that can be applied immediately by most of the available staff. Non-invasive hemodynamic monitoring devices may also be of help in departments without facilities for invasive techniques, such as step-down units, long-term facilities, and stroke units. By virtue of definition, any device that is able to accurately detect rapid changes in cardiac output upon fluid challenge would suffice in evaluating fluid responsiveness and some methods may be too slow to fulfill this criterion.
General considerations regarding patient-bound factors (Table 4) include the notion that the sicker the patient the greater the need for accurate hemodynamic parameters to be collected to supplement clinical judgment and the greater likelihood that invasive, rather than less invasive, techniques will meet these needs. In the patient with severe septic shock admitted to the intensive care unit (ICU) for instance, non-invasive arterial waveform analysis-derived cardiac output measurements are less useful as they are affected by vascular tone and require repeated recalibration, at least in the initial resuscitation phase. In patients with or at great risk of pulmonary edema, hemodynamic monitoring by transpulmonary dilution and measurements of extravascular lung water could be chosen to help to prevent harmful overhydration and prolonged mechanical ventilation, unless the patient will anyway need to be intubated and mechanically ventilated. Catheters in the femoral artery are relatively contraindicated during/after aortic-bifemoral reconstruction, and transesophagal echocardiography is not feasible during/after esophageal resection. Esophageal disease may be a contraindication for the use of esophageal Doppler probes, which are also poorly tolerated in awake, non-intubated patients [10, 20, 25]. The presence of cardiac disease and mechanical ventilation may also affect choices. It is likely that a PAC and measurement of PAOP is more helpful in guiding (fluid) management in the presence of systolic/diastolic cardiac dysfunction than during hypovolemic shock, for example [21, 34]. In severe left-sided valvular disease, right-sided measurements of cardiac output are probably preferable to transpulmonary ones, even though the debate on the confounding effect of even minimal tricuspid regurgitation on these measurements has not yet ended. In the presence of endocarditis, intracardiac catheters may be relatively contraindicated. In contrast, a suspected ventricular septal defect may require monitoring with help of a PAC, echocardiography, or both. In mechanically ventilated patients, filling pressures that are confounded by airway pressures may be less useful in predicting and guiding fluid responses than volumetric preload measurements [34, 36], whereas the currently proposed superiority of dynamic indices  can be questioned, as they are affected by ventilatory frequency and tidal volume. Finally, pulse-contour methods are sensitive to arrhythmias, aortic valve regurgitation, intra-aortic balloon pumping and peripheral vascular disease.
Conclusions and perspective
This chapter attempts to provide a conceptual framework for choosing patient-tailored hemodynamic monitoring from available techniques, in an era dominated by lack of proven survival benefits for any hemodynamic monitoring device. Decisions for implementing different hemodynamic monitoring devices may improve when systematically considering the relevant issues, according to a predefined checklist, for example. This approach may help to end debates on the use of hemodynamic monitoring equipment from single perspectives only, but obviously choices may differ from one hospital, unit, patient and physician to another, given the variability in facilities, clinical presentations, and expertise. One tool may supplement another, so that it is advisable to gain expertise in more than one method, particularly in training environments. Health technology assessment institutions and agencies can be of help in advising on these complex issues and emergency and intensive care medicine organizations could benefit from their expertise [1, 12, 13, 25, 41]. The underlying idea, of course, is that helping physicians to direct therapy using numbers rather than signs and symptoms, and helping the medical community by providing clear clinical guidelines on hemodynamic monitoring strategies will effectively result in health care improvements. Perhaps, we also need a new research agenda on these issues.
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