Modelling the cardiovascular system for assessing the blood pressure curve
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Abstract
A four compartment model of the cardiovascular system is developed. To allow for easy interpretation and to minimise the number of parameters, an effort was made to keep the model as simple as possible. Using a standard method (Matlab function fminsearch) to calculate the parameter values led to unacceptable run times or nonconvergence. Consequently we developed an algorithm which first finds the most important model parameters and uses these as a basis for a four stage process which accurately determines all parameter values. This process is then applied to data from three ICU patients. Good agreement between the model and measured arterial pressure is demonstrated in all cases.
Keywords
Blood pressure Compartment model Parameter estimationIntroduction
The human cardiovascular system conveys nutrients and oxygen to tissues and maintains the gas and fluid exchange with tissue that is necessary for homeostasis. The health of this system is important, and diagnosing cardiovascular problems in a timely and noninvasive manner is a matter of significant medical interest. A key indicator of cardiovascular health is the blood pressure and the way that it varies with time.
 1.
Detection of cardiac arrhythmia (irregular heartbeat);
 2.
Estimating cardiac output;
 3.
Estimating hypovolemia (a decreased volume of circulating blood in the body);
 4.
Monitoring respiratory variation (which in turn may be related to fluid responsiveness in ventilated patients with circulatory failure);
 5.
Detecting attenuation of the peripheral pulse waveform — depending on different base pathologies such as sepsis or severe respiratory distress, such attenuation/damping may be considered an important measure for the assessment of microcirculation and tissue perfusion.
More comprehensive lists of examples of clinical uses for a detailed blood pressure curve may be found in [5, 18, 22, 23].
Currently there exist two principal methods for measuring blood pressure: the sphygmomanometer and the catheter. However, there is much interest in developing a reliable noninvasive, continuous monitoring technique for blood pressure. The work in this paper is motivated by a recent development which allows the blood pressure to be related to the output of a pulse oximeter (the photoplethysmograph or pleth) [19]. To maximise the information gained from this signal requires an understanding of the blood pressure curve. The specific goal of this paper is then to produce a mathematical model capable of accurately reproducing the dominant features of the blood pressure curve and in particular the dicrotic notch (a small dip in the blood pressure curve associated with aortic valve closure), and the variation due to respiratory sinus arrhythmia (RSA). Abnormalities with the dicrotic notch may indicate problems with the valve or poor vascular resistance caused, for example, by severe septic shock. To allow for easy interpretation and to minimise the number of parameters, an effort was made to keep the model as simple as possible. In the following section we will describe the compartment approach that was used to model the human cardiovascular system. Subsequent sections deal with model refinements and parameter estimation. Finally we compare our model results with data taken from a radial artery catheter. All catheters were zeroed, calibrated and a flush test performed before taking any measurement [20].
Methods
Mathematical models
We model the cardiovascular system using a compartment model. The main components of the system are the heart, arteries and veins. The system includes the pulmonary circulation, a closed loop through the lungs where blood is oxygenated, and the systemic circulation. Oxygenated blood enters the systemic system at the left heart and is then pumped into the aorta. The aorta branches into smaller arteries, arterioles and capillaries, where oxygen exchange takes place, and enters the systemic veins through which it flows in vessels of progressively increasing size toward the right heart. The right heart pumps CO_{2} rich blood into the lungs, closing the loop.
Compartment models are a particular type of lumped parameters model. They consist of splitting the system into sections, named compartments. The main assumption is that each compartment is homogeneous in some way. The first description of the cardiovascular system as a compartment model was published in 1733 and termed the windkessel model. This was later translated into a mathematical model in 1899, see [21]. Since the development of the windkessel model, many adaptations and different approaches have been proposed to describe the cardiovascular system. In the following we will use a differential equation approach. Differential equation models of the cardiovascular system vary from a pair of first order ordinary differential equations [15] to systems of more than 40 coupled differentialdelay equations [6, 9, 25, 26]. Ottesen’s approach [15] is to split the system into arterial and venous compartments, with nonpulsatile flow, and a source term that models the effect of the left ventricle. At the other end of the spectrum, Ursino et al. and Grodins [9, 25, 26] describe the pulsatile flow of blood through multiple compartments including the lungs, compliant arteries and veins and driven by a heart that is regulated by a sophisticated nervous feedback control system that responds to blood pressure and chemistry in a variety of ways. Despite this level of complexity, in general, compartment models are conceptually quite simple. They involve dividing the cardiovascular system into a number of compliant zones or compartments and as the blood passes through each zone it must be conserved. The change in volume in each zone is simply the difference between the flux entering from upstream and that leaving downstream. The heart drives this flux and the flow is resisted by the vessels through the shear stress at vessel walls.
In the present study we have tried to take the simplest approach possible, along the lines of Ottesen’s model, whilst still being able to capture important features of the blood pressure signal. Initially we employed a three compartment model, involving the arteries, veins and left ventricle. However, one of our main goals was to have our model exhibit a dicrotic notch in arterial pressure. The dicrotic notch is the name given to the pressure fluctuation seen when the aortic valve closes. This closure is caused by the pressure drop across the valve becoming negative. The size and location in time of the notch provides important information about the health of the valve and the aorta. For example, in aortic insufficiency, the aortic valve does not completely close so that after each heart beat, the blood that has left the aorta comes back immediately to the left ventricle. This behaviour results in a complete absence of dicrotic notch in the pressure signal [10].
In the threecompartment model the arterial pressure is an average across the whole arterial system, so that using this as a measure of when the valve closes leads to late closure in the model, and a temporarily reversed blood flow throughout the arterial system.
where V represents the volume and Q the flux of blood. The subscripts e,a,v,L V represent exit, arterial, venous and left ventricle and dots indicate the derivative with respect to time. The first equation indicates that the rate of change of volume in the exit region depends on the difference between the rates at which fluid flows in from the left ventricle and fluid flows out of the aortic arch. In the arteries the volume increases due to fluid flowing in from the arch and decreases as it flows out of the arteries into the veins, leading to the second equation. The third equation expresses a similar material balance for the venous system, and the fourth equation for the left ventricle. Hence these equations express conservation of blood volume. Note, we assume the blood to be incompressible, see [17], changes in pressure are associated with the compliance of blood vessels rather than the relatively small compressibility of blood itself, and conservation of blood volume is equivalent to the more fundamental principle of conservation of blood mass.
In a compliant elastic vessel we may relate the pressure to the volume via V=V _{0}+C p, where C is a constant, termed the compliance, and V _{0} is a constant giving the volume at pressure p=0 (the value of the compliance is discussed in detail later) [12]. This equation serves to define the compliance. Note, this definition admits the possibility of zero volume, this would indicate a collapse of the vessel. Physically this is possible, however, we do not work in this regime and so assume V>0.
Note, we assume that the compliance of the blood vessels is a constant whereas the elastance, representing the contraction of the heart muscle, is a controlled variable that varies in a prescribed manner with time [24].
We may relate the fluxes to the pressure by considering standard, unidirectional pressuredriven laminar flow (Poiseuille flow) in a pipe which leads to a relation of the form Q∝Δ p. This may be expressed as Q=Δ p/R where R can be thought of as the effective resistance to flow [12]. Obviously the cardiovascular system does not consist of a single straight pipe and blood flow is often turbulent so this definition of Q is rather approximate and the resistance R must represent the many intricacies of the system, rather than simply the viscous resistance from the classical Poiseuille flow model.
Model refinements
The above system, Eqs. (3–6), constitutes our basic set of equations but still requires certain refinement: the driving mechanism for the flow is not defined, neither is there a mechanism to describe the dicrotic notch or the aortic valve.
The driving mechanism for the flow comes through the definition of the elastance, which serves as a simple model of the pumping action of the heart muscle. Modelling of the elastance is discussed in a number of papers. Whilst there is some difference in the fine detail, the general form is of a sequence of roughly Gaussian curves when contraction occurs, separated by flat regions denoting the relaxation [7, 14, 16]. In [6] the elastance has an approximately square wave form. However Suga [24] points out that a more gradual rise in elastance is essential if it is to be consistent with the Fenn effect in cardiac muscle, where the shortening of muscle produces heat.
where the diastolic elastance E _{ d } is constant and a(t)= sin2(ω t).
The constants in the above definitions c _{1},c _{2},c _{3} represent half the variation of elastance height, the number of heart beats per respiration (typically around 5) and half the variation of ω respectively. The constant ω _{0} is an angular frequency ω _{0}=(2π/60)×H R where H R is an average heart rate in beats/minute.
where R _{ e0} is the constant value when the valve is fully open. The factor ε _{1}≪1 ensures that the exponential term remains small whenever p _{ LV }−p _{ e }>0 but it increases rapidly when p _{ LV }−p _{ e }<0. The constant A _{1} is chosen such that the product A _{1}(p _{ LV }−p _{ e }) rises sufficiently rapidly as the valve closes. In practice we set \(\epsilon _{1}=10^{5}, A_{1}=\frac {1}{2}\): these values are simply chosen to provide the correct properties. Since the exit region is significantly shorter than the arterial region we also assume R _{ e0}≪R _{ a }. Another option would be to simply set a switch via a Heaviside function. However, our subsequent numerical calculations showed that this led to a poor representation of the pressure around the dicrotic notch. Ellwein et al. [8] employ a similar, but cutoff, exponential representation for all heart valves. They do not include the factor ε _{1}≪1 but choose A _{1}=2 which is greater than our value, and this has a similar effect.
However, since this region is of lesser interest to avoid more parameter estimation we use a Heaviside function for R _{ v } (tests confirm this makes no noticeable difference to the results).
The constants c _{4},c _{5},c _{6} indicate the height of the pulse, the sharpness and the position of the centre. The times t _{ n },n=1,2,…, are when p _{ e }=p _{ LV } and so indicate when the valve should begin closing. The maximum value of f occurs when t=t _{ n }+Δ t hence Δ t denotes the delay in closure after the pressure drop becomes negative. It therefore controls the position of the dicrotic notch and is an important indicator of the health of the valve. In general its maximum value is much lower than the other terms in the equation and so it represents only a small contribution to the pressure. In the numerical solution we use Δ t from the previous cycle, with the first value chosen as some typical value.
Parameter value estimation
Key to the success of the mathematical model is the choice of parameter values. Obviously this is not a simple task given that there are twentyone parameter values as well as four initial conditions. Hence we will now describe in detail our procedure for calculating parameter values.
Parameter  Value  Units  Parameter  Value  Units 

C _{ e }  1.5  ml/mmHg  C _{ a }  1.5  ml/mmHg 
C _{ v }  50  ml/mmHg  R _{ e0}  0.016  s ·mmHg/ml 
R _{ a }  0.06  s ·mmHg/ml  R _{ LV }  1.2  s ·mmHg/ml 
R _{ v }  0.016  s ·mmHg/ml  T _{ sys }  T/3  s 
T _{ dia }  2T/3  s  T  0.9  s 
E _{ d }  0.06  mmHg/ml  E _{ s0}  3.0  mmHg/ml 
ε  10^{−5}  A _{1}  0.5  
R _{ eM }  10  s ·mmHg/ml  c _{1}  0.1  mmHg/ml 
c _{2}  6  beats/breath  c _{3}  0.01  s ^{−1} 
c _{4}  500  c _{5}  4 log100  
c _{6}  7.5  ω _{0}  7.54 
We then set C _{ e }=C _{ a } and C _{ v }=20C _{ a }. Note that the value of 20 assumed here for the ratio of venous to arterial compliance is consistent with a number of other studies, including [10] who cite a ratio of 8, [12] who cite a ratio of 24, [25] who uses 33, and a range of 10–20 in [13]. Similarly, the systemic resistance may be estimated from the arterial pressure signal, see [1]. Typical values for other parameter values are given the literature, see [6, 7, 15] for example.
Sensitivity analysis
The sensitivity analysis consisted in perturbing each parameter of the model and integrating the system of equations to see how the resulting arterial pressure changes with such perturbations. This approach is based on the procedure described in [4].
L _{2} distance between arterial pressure signals for each parameter and perturbation
q=0.05  q=0.1  q=0.2  

E _{ d }  22.66  E _{ d }  32.26  E _{ d }  39.52 
p _{ a0}  20.27  p _{ a0}  28.73  p _{ a0}  34.90 
ϕ  19.75  ϕ  20.35  E _{ s0}  28.41 
ω _{0}  10.10  E _{ s0}  20.01  A  20.23 
E _{ s0}  14.17  ω _{0}  17.75  ω _{0}  20.10 
R _{ LV }  9.92  R _{ LV }  14.04  R _{ LV }  20.04 
A  9.69  A  13.81  ϕ  19.66 
R _{ e0}  7.09  R _{ e0}  9.93  R _{ e0}  14.11 
c _{2}  6.19  p _{ v0}  7.23  p _{ v0}  10.20 
p _{ v0}  5.15  c _{6}  6.51  R _{ a }  9.16 
c _{6}  4.78  R _{ a }  6.49  c _{6}  8.60 
R _{ a }  4.62  c _{4}  5.88  c _{4}  8.35 
c _{4}  4.16  c _{2}  5.37  c _{2}  6.81 
c _{3}  3.18  c _{5}  4.16  c _{5}  5.94 
ε  3.17  ε  4.13  ε  5.76 
c _{5}  2.94  c _{3}  3.64  R _{ eM }  4.70 
R _{ eM }  2.23  R _{ eM }  3.51  c _{3}  4.32 
c _{1}  1.28  c _{1}  1.81  c _{1}  2.56 
Δ t _{0}  0  Δ t _{0}  0  Δ t _{0}  0 
From Table 2 and the results described in [21] we deduce the 6 most important parameters to be: 1. E _{ d } (and C _{ v }); 2. E _{ s0} (and C _{ a },C _{ e }); 3. p _{ a }(0) (and p _{ e }(0),p _{ LV }(0)); 4. A; 5. R _{ LV }; 6. ω _{0}. The final parameter ω _{0} is not estimated, since it may be calculated directly from the pressure signal (and similarly for ϕ). Consequently in the following section we begin by estimating the remaining top five parameters and subsequently make adjustments to the remaining parameter values.
Parameter estimation
The four stage method used to determine parameter values is described in detail in [21] so we only provide a brief outline below.
In Table 1 we present the set of parameter values used at the beginning of each calculation. The majority of these values are taken from [6, 7, 15] although some, such as ε are simply educated guesses. A number of parameter values are read from the data, such as p _{ a0},p _{ v0},ϕ,Δ t _{0},ω _{0} and so these are not included in the table.
Stage 1: Approximate Gradient Descent method for the five significant parameters

Set Θ=Θ _{0} and compute ω _{0} and c _{2} from the patient’s signal.
 Compute δ _{ μ } and δ _{ σ } and then:

If \(\frac {\delta _{\mu }}{\mu (\hat {p}_{a})}>\frac {\delta _{\sigma }}{\sigma (\hat {p}_{a})}, \Theta _{n+1}=\Theta _{n}\alpha \nabla \mu \)

else Θ _{ n+1}=Θ _{ n }−α∇σ.


Repeat until the desired tolerance is repeated.
Stage 2: NelderMead method applied to the five significant parameters
As with the previous two objective functions, this was evaluated over a time period of three respiratory cycles. The initial vector of parameter values were those obtained in the previous stage. The dependent parameters were also recalculated at each step.
Stage 3: NelderMead method applied to all parameters
The method adopted in the previous section was then applied to all parameter values. If stages 1 and 2 are neglected then this approach does not converge. Now that the signals are relatively close, convergence is almost always achieved (this will be discussed later). From now on we neglect the interdependence of some parameters. For example, from the governing equations, Eqs. (3–6), it is clear that E _{ d } can be interpreted as an inverse compliance. Hence until now we used E _{ d }=1/C _{ v } to model venous return. We will discuss the validity of this relation in “Comparison with experimental data” section.
At the end of this stage the correspondence between p _{ a } and \(\hat {p}_{a}\) is in general very good with the exception of the dicrotic notch, which in the simulation occurs well below the true position. This is most likely due to minimising the L _{2} distance: since the notch takes up only a very small part of the signal the L _{2} distance will necessarily be small and so we cannot expect the same level of accuracy to be achieved in modelling the notch as in other parts of the signal.
Stage 4: Manual refinement
Given that the model output at this stage is so close to the signal it was decided not to build a new set of objective functions to focus solely on the minor parameters. To be specific the parameters adjusted at this stage were c _{4},c _{5},c _{6} (which describe the notch) and c _{1} (which describes the change in elastance height due to respiration). Consequently, for this final refinement we adjusted one parameter at a time up and down by about 1%.
Results and discussion
Comparison with experimental data

Patient 1 This patient shows normal values of blood pressure (120/70 mmHg) and heart rate (79 bpm) but a very small dicrotic notch with no real peak. Respiratory variations are small. The patient’s pathology was tagged under the category “transplantation”.

Patient 2 This patient’s pathology was tagged under the category “haemorrhagic”. The loss of blood led to low values of blood pressure (85/45 mmHg). Due to this fact they were administered norepinephrine (a vasoconstrictor drug). The heart rate was high (100 bpm), as a natural reaction to the low blood pressure. The dicrotic notch is absent and there is little respiratory variation in systolic pressure.

Patient 3 This patient shows normal values of blood pressure (135/60 mmHg) and normal heart rate (80 bpm) with a large dicrotic notch. Respiratory variations are in the order of 5 mmHg in systolic pressure. The patient’s pathology was tagged under the category “neurologic” (related to the nervous system). There was also a small dose of vasoconstrictor drugs.
Parameter values for Patient 1
Parameter  Value  Parameter  Value  Parameter  Value 

R _{ e0}  0.0055222  p _{ a0}  55.0000  E _{ s0}  0.57000 
R _{ a }  0.020797  p _{ v0}  16.628  ϕ  0.33334 
R _{ LV }  0.41279  p _{ L V0}  49.714  R _{ eM }  10.009 
R _{ v }  0.0055259  ω _{0}  8.3706  ε  0.00001 
C _{ e }  1.6946  c _{3}  0.00049874  A  0.40341 
C _{ a }  2.0000  c _{2}  4.0153  Δ t _{0}  0.75786 
C _{ v }  15.0000  c _{1}  0.01000  c _{4}  150.00 
p _{ e0}  49.896  E _{ d }  0.065511  c _{5}  18.445 
c _{6}  1.0000 
Parameter values for Patient 2
Parameter  Value  Parameter  Value  Parameter  Value 

R _{ e0}  0.0038808  p _{ a0}  17.355  E _{ s0}  0.34 
R _{ a }  0.0154  p _{ v0}  5.7844  ϕ  0.33273 
R _{ LV }  0.29025  p _{ L V0}  17.355  R _{ eM }  10.116 
R _{ v }  0.0038895  ω _{0}  10.578  ε  0.000010049 
C _{ e }  2.9196  c _{3}  0.00010007  A  0.4515 
C _{ a }  2.9193  c _{2}  7.003  Δ t _{0}  0.59617 
C _{ v }  55.456  c _{1}  0.006  c _{4}  0.0000077731 
p _{ e0}  17.355  E _{ d }  0.0181  c _{5}  18.436 
c _{6}  4.5053 
Parameter values for Patient 3
Parameter  Value  Parameter  Value  Parameter  Value 

R _{ e0}  0.0049252  p _{ a0}  21.781  E _{ s0}  0.64627 
R _{ a }  0.018469  p _{ v0}  7.2597  ϕ  0.33338 
R _{ LV }  0.39929  p _{ L V0}  21.761  R _{ eM }  10.004 
R _{ v }  0.0049253  ω _{0}  8.3339  ε  0.000010007 
C _{ e }  1.54  c _{3}  0.0001251  A  0.43995 
C _{ a }  1.0459  c _{2}  4.0001  Δ t _{0}  0.75182 
C _{ v }  50.000  c _{1}  0.015  c _{4}  400 
p _{ e0}  21.783  E _{ d }  0.029022  c _{5}  1.000 
c _{6}  3.5000 
Conclusions
In this paper we put forward a simple model of the blood pressure curve. The model takes into account the dicrotic notch or incissura that results from the closure of the aortic valve. This is important because it allows our model to account for aortic insufficiency [10] and pressure changes in the vascular tree that result from changes in vascular compliance and vascular resistance. Another contribution of the work is the simple refinement to model respiratory sinus arrythmia in the blood pressure curves.
One important limitation of this model is that it cannot account for differences in blood volume. For example, in the event of haemorraghic shock blood volume becomes variable and the variations observed in pulse pressure can no longer be attributed to respiratory sinus arrythmia. However, the simplicity of the model allows for further refinements in order to model different conditions including blood loss and haemorragic shock.
Beyond the simplicity of the model and the parameters obtained for different patients, it is also worth mentioning that further studies are needed to assess the physiological and clinical relevance of the parameters that we obtain. The parameters obtained in this paper are physiologically relevant but it is also necessary to assess their value for different conditions and a much larger number of patients.
The results presented in the previous sections clearly indicate that our fourcompartment model can accurately reproduce a blood pressure signal, with the correct choice of parameter values. The model is capable of reproducing a wide variety of pressure signals. In fact, if the goal is simply a rough characterisation of the blood pressure signal, then the initial stages of the analysis proved sufficient. This showed that the 5 most important parameters in our model are E _{ d },E _{ s0},p _{ a }(0),A,R _{ LV }. Provided these are determined accurately, in our case this was achieved through the gradient descent method, then the model will provide a satisfactory description of the signal.
The fourstage parameter estimation method was vital to the success of the analysis. We have made little effort to optimise this process, since our main goal was to develop and verify the compartment model. However, this provides one direction for future work. For example the final stage involved manual refinement since the L _{2} error for the dicrotic notch parameters was small due to the small width of the region. The technique of previous stages could instead be applied to a reduced region around the notch. Employing the Conjugate Gradient method rather than simple Gradient Descent should reduce the number of iterations required.
Based on the output of our model in the future we hope to be able to interpret the parameter values in some way in order to make some recommendation concerning the health of the patient. This will comprise the next stage of this investigation. In order to achieve this we note that the vascular tree can be modelled as a NonLinear TimeVariant Channel and there are tools that can either linearize this system or we can simply live with these nonlinearities and make predictions (Kalman Filters). On the positive side we have a large amount of data from arterial catheters on which to validate the method.
Notes
Acknowledgments
The initial work for this paper was carried out at the Centre de Recerca Matemàtica during December 2010 at the Workshop on Mathematical modeling of blood flow and the baroreflex system. We acknowledge the assistance of other participants at that workshop, including Michelle De Decker, Francesc Font, Jonathan Low (all from the CRM) and Dr. Andrew Fowler, Stokes Professor at the University of Limerick, Ireland.
Financial support was provided through a Ministerio de Ciencia e Innovación grant MTM201456218 and the Mathematics Applications Consortium for Science and Industry (www.macsi.ul.ie) based at the University of Limerick, funded by Science Foundation Ireland grant 12/IA/1683.
ASdT would like to thank Dr Ataee of the University of British Columbia for helping sort out the intricacies of the sensitivity analysis.
Authors’ contributions
TM and VRR supervised the project. TM carried out the majority of the writing of the paper, VRR proposed the original problem and provided all background medical knowledge and data. ASdT developed the algorithms for parameter estimation and carried out the comparisons with data. All members were involved in model development and writing. All authors read and approved the final manuscript.
Competing interests
The authors declare that that they have no competing interests.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
 1.Augusto JF, Teboul JL, Radermacher P, Asfar P (2011) Interpretation of blood pressure signal: physiological bases, clinical relevance and objectives during shock states. Intensive Care Med 37: 411–419.CrossRefGoogle Scholar
 2.Bernardi L, Keller F, Sanders M, Reddy PS, Griffith B, Meno F, Pinsky MR (1989) Respiratory sinus arrhythmia in the denervated human heart. J Appl Physiol 67: 1447–1455.Google Scholar
 3.Berntson GG, Cacioppo JT, Quigley KS (1993) Respiratory sinus arrhythmia: Autonomic origins, physiological mechanisms, and psychophysiological implications. Psychophysiology 30: 183–196.CrossRefGoogle Scholar
 4.Brouse C, Dumont GA, Boyce WT, Ataee P, Hahn JO (2010) Identification of cardiovascular baroreflex for probing homeostatic stability. Comput Cardiol 37: 141–144.Google Scholar
 5.Cannesson M, Besnard C, Durand PG, Bohe J, Jacques D (2005) Relation between respiratory variations in pulse oximetry plethysmographic waveform amplitude and arterial pulse pressure in ventilated patients. Crit Care 9: R562–R568.CrossRefGoogle Scholar
 6.Chapman SJ, Fowler AC, Hinch R (2010) An introduction to mathematical physiology. Mathematical Institute, Oxford University (preprint). http://www3.ul.ie/fowlera/courses/bio/physiolbook.pdf.
 7.Dat M (2010) Modeling cardiovascular autoregulation of the preterm infant. Thesis Eindhoven University of Technology.Google Scholar
 8.Ellwein LM, Tran HT, Zapata C, Novak V, Olufsen MS (2008) Sensitivity analysis and model assessment: mathematical models for arterial blood flow and blood pressure. Cardiovasc Eng 8: 94–108. doi:10.1007/s1055800790473.CrossRefGoogle Scholar
 9.Grodins F (1959) Integrative cardiovascular physiology: a mathematical synthesis of cardiac and blood vessel hemodynamics. Quart Rev Biol 34(2): 93–116.CrossRefGoogle Scholar
 10.Guyton AC, Hall JE (2000) Textbook of medical physiology. Saunders Elsevier, Philadelphia.Google Scholar
 11.Hose DR, Narracotta AJ, Penrose JMT, Baguley D, Jones IP, Lawford PV (2006) Fundamental mechanics of aortic heart valve closure. J Biomechs 39: 958–967. doi:10.1016/j.jbiomech.2005.01.029.CrossRefGoogle Scholar
 12.Keener J, Sneyd J (1998) Mathematical physiology. SpringerVerlag, New York.zbMATHGoogle Scholar
 13.Klabunde RECardiovascular Physiology. http://www.cvphysiology.com/Blood%20Pressure/BP004; a website maintained by R.E. Klabunde, Ph.D., Professor of Physiology, Marian University College of Osteopathic Medicine, Indianapolis, Indiana.
 14.Oommen B, Karamanoglu M, Kovacs SJ (2003) Modelling time varying elastance: The meaning of load independence. Cardiovasc Engng 3(4): 123–130.CrossRefGoogle Scholar
 15.Ottesen JT (1997) Modelling of the baroreflexfeedback mechanism with timedelay. J Math Biol 36: 41–63.MathSciNetCrossRefzbMATHGoogle Scholar
 16.Palladino JL, Mulier JP, Noordergraaf A (1998) Defining ventricular elastance In: Proceedings of the 20th Annual International Conference of the IEEE Engineering in Medicine and Biology Society, Vol. 20, No 1,1998. doi:10.1109/IEMBS.1998.745923.
 17.Pedley TJ (2003) Mathematical modelling of arterial fluid dynamics. J Engng Math 47: 419–444.MathSciNetCrossRefzbMATHGoogle Scholar
 18.Reisner MD, Reisner A, Shaltis PA, McCombie D, Asada HH (2008) Utility of the Photoplethysmogram in Circulatory Monitoring. Anesthesiology 108(5): 950–958.CrossRefGoogle Scholar
 19.Ribas VJPatent: System and apparatus for the noninvasive measurement of blood pressure. WO2010043728 (A1) ; ES2336997 (A1). Ribas Ripoll V.J.; Sabirmedical S.L. https://www.google.com/patents/US20110196244.
 20.RuizRodríguez JC, RuizSanmartín A, Ribas V, Caballero J, GarcíaRoche A, Riera J, Nuvials X, de Nadal M, de SolaMorales O, Serra J, Rello J (2013) Innovative continuous noninvasive cuffless blood pressure monitoring based on photoplethysmography technology. Intensive Care Med 39(9): 1618–1625.CrossRefGoogle Scholar
 21.Saez de Tejada Cuenca A (2012) Mathematical modelling of the blood pressure signal. MSc in Mathematics Engng, U. Politecnica Catalunya.Google Scholar
 22.Shelley K, Shelley S (2001) Pulse Oximeter Waveform: Photoelectric Plethysmography. In: Lake CL, Hines RL, Blitt CD (eds)Clinical monitoring: practical applications for anesthesia and critical care.. WB Saunders, Philadelphia. pp. 420–428.Google Scholar
 23.Shelley KH (2007) Photoplethysmography: beyond the calculation of arterial oxygen saturation and heart rate. Anesth Analg 105: S31–S36.CrossRefGoogle Scholar
 24.Suga H (2003) Cardiac energetics: from emax to pressurevolume area. Clin Exp Pharmacol Physiol 30: 580–585.CrossRefGoogle Scholar
 25.Ursino M (1998) Interaction between carotid baroregulation and the pulsating heart: a mathematical model. Am J Physiol 275. (Heart Circ. Physiol. 44):H1733–H1747.Google Scholar
 26.Ursino M, Fiorenzi A, Belardinelli E (1996) The role of pressure pulsatility in the carotid baroreflex control: a computer simulation study. Comput Biol Med 26: 297–314.CrossRefGoogle Scholar
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