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SNAPSHOTS
OF
HEMODYNAMICS
BASIC SCIENCE FOR THE CARDIOLOGIST
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B. Swynghedauw (ed.): Molecular Cardiology for the Cardiologist. SecondEdition. 1998 ISBN 0-7923-8323-0B. Levy, A. Tedgui (eds.): Biology of the Arterial Wall. 1999
ISBN 0-7923-8458-XM.R. Sanders, J.B. Kostis (eds.): Molecular Cardiology in ClinicalPractice. 1999 ISBN 0-7923-8602-7B.Ostadal, F. Kolar (eds.): Cardiac Ischemia: From Injury to Protection. 1999
ISBN 0-7923-8642-6H. Schunkert, G.A.J. Riegger (eds.): Apoptosis in Cardiac Biology. 1999
ISBN 0-7923-8648-5A. Malliani, (ed.): Principles of Cardiovascular Neural Regulation in Healthand Disease. 2000 ISBN 0-7923-7775-3P. Benlian: Genetics of Dyslipidemia. 2001 ISBN 0-7923-7362-6D. Young: Role of Potassium in Preventive Cardiovascular Medicine. 2001
ISBN 0-7923-7376-6E. Carmeliet, J. Vereecke: Cardiac Cellular Electrophysiology. 2002
ISBN 0-7923-7544-0C. Holubarsch: Mechanics and Energetics of the Myocardium. 2002
ISBN 0-7923-7570-XJ.S. Ingwall: ATP and the Heart. 2002 ISBN 1-4020-7093-4W.C. De Mello, M.J. Janse: Heart Cell Coupling and Impuse Propagation inHealth and Disease. 2002 ISBN 1-4020-7182-5P.P.-Dimitrow: Coronary Flow Reserve – Measurement and Application: Focuson transthoracic Doppler echocardiography. 2002 ISBN 1-4020-7213-9G.A. Danieli: Genetics and Genomics for the Cardiologist. 2002
ISBN 1-4020-7309-7F.A. Schneider, I.R. Siska, J.A. Avram: Clinical Physiology of the Venous System.2003. ISBN 1-4020-7411-5Can Ince: Physiological Genomics of the Critically Ill Mouse. 2004
ISBN 1-4020-7641-XWolfgang Schaper, Jutta Schaper: Arteriogenesis. 2004
ISBN 1-4020-8125-1eISBN 1-4020-8126-X
Nico Westerhof, Nikos Stergiopulos, Mark I.M. Noble: Snapshots of Hemodynamics:An aid for clinical research and graduate education. 2005
ISBN 0-387-23345-8eISBN 0-387-23346-6
KLUWER ACADEMIC PUBLISHERS – DORDRECHT/BOSTON/LONDON
Snapshots of Hemodynamics
An aid for clinical research andgraduate education
Nico WesterhofLaboratory for Physiology,
VU University medical centerAmsterdam, the Netherlands
Nikos StergiopulosLaboratory of Hemodynamics and Cardiovascular Technology,
Swiss Federal Institute of TechnologyLausanne, Switzerland
Mark I.M. NobleCardiovascular Medicine,
Aberdeen UniversityAberdeen, Scotland
Springer
eBook ISBN: 0-387-23346-6Print ISBN: 0-387-23345-8
Print ©2005 Springer Science + Business Media, Inc.
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No part of this eBook may be reproduced or transmitted in any form or by any means, electronic,mechanical, recording, or otherwise, without written consent from the Publisher
Created in the United States of America
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©2005 Springer Science + Business Media, Inc.
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CONTENTS
PREFACEACKNOWLEDGEMENT
PART A BASICS OF HEMODYNAMICSCHAPTER 1CHAPTER 2CHAPTER 3CHAPTER 4CHAPTER 5CHAPTER 6CHAPTER 7CHAPTER 8CHAPTER 9CHAPTER 10CHAPTER 11
VISCOSITYLAW OF POISEUILLEBERNOULLI’S EQUATIONTURBULENCE
ARTERIAL STENOSISRESISTANCEINERTANCEOSCILLATORY FLOW THEORYLAW OF LAPLACEELASTICITYCOMPLIANCE
PART B CARDIAC HEMODYNAMICSCHAPTER 12CHAPTER 13CHAPTER 14CHAPTER 15CHAPTER 16CHAPTER 17CHAPTER 18CHAPTER 19
CARDIAC MUSCLE MECHANICSPRESSURE-VOLUME RELATION
PUMP FUNCTION GRAPHWORK, ENERGY AND POWEROXYGEN CONSUMPTION & HEMODYNAMICSPOWER AND EFFICIENCYCORONARY CIRCULATIONASSESSING VENTRICULAR FUNCTION
PART C ARTERIAL HEMODYNAMICSCHAPTER 20CHAPTER 21CHAPTER 22CHAPTER 23CHAPTER 24CHAPTER 25CHAPTER 26CHAPTER 27CHAPTER 28
WAVE TRAVEL AND VELOCITYWAVE TRAVEL AND REFLECTION
WAVEFORM ANALYSISARTERIAL INPUT IMPEDANCEARTERIAL WINDKESSELDISTRIBUTED MODELSTRANSFER OF PRESSUREVASCULAR REMODELINGBLOOD FLOW AND ARTERIAL DISEASE
PART D INTEGRATIONCHAPTER 29CHAPTER 30
DETERMINANTS OF PRESSURE & FLOWCOMPARATIVE PHYSIOLOGY
PART E APPENDICESAPPENDIX 1APPENDIX 2APPENDIX 3APPENDIX 4APPENDIX 5APPENDIX 6APPENDIX 7
TIMES & SINES: FOURIER ANALYSISBASIC HEMODYNAMIC ELEMENTSVESSEL SEGMENTBASIC ASPECTSBOOKS FOR REFERENCESYMBOLSUNITS AND CONVERSION FACTORS
INDEX
viixi
137
111517212529313541
495157636971758191
9799
105109113121127131137143
147149155
161163167169173177179181
183
PREFACE
This book is written to help clinical and basic researchers, as well as graduatestudents, in the understanding of hemodynamics. Recent developments ingenetics and molecular biology on the one hand, and new non-invasivemeasurement techniques on the other hand, make it possible to measure andunderstand the hemodynamics of heart and vessels better than ever before.Hemodynamics makes it possible to characterize, in a quantitative way, thefunction of the heart and the arterial system, thereby producing informationabout what genetic and molecular processes are of importance forcardiovascular function.
We have made the layout of the book such that it gives a short overviewof individual topics, in short chapters only giving the essentials, so that it iseasy to use it as a quick reference guide. It is not necessary to read the bookfrom cover to cover. Each chapter is written in such a way that one is able tograsp the basic and applied principles of the hemodynamic topic. If moredetails or broader perspectives are desired one can go to the other, related,chapters to which the text refers, or the textbooks listed in the ‘Referencebooks’ section (Appendix 5).
To bring the essentials even more directly across, every chapter starts witha ‘box’ containing a figure and caption, which give the basic aspects of thesubject. It is often sufficient to study the contents of this box alone to obtainthis basic information. Chapters end with a section ‘Physiological andClinical relevance’ to place the information into perspective. The part inbetween, called ‘Description’, can be used to get more detailed informationand find some references to more detailed work.
More comprehensive information on the subjects discussed can be foundin textbooks on physiology and cardiology, as well as special books onhemodynamics. A number of these books are listed in the section ‘Referencebooks’ (Appendix 5). More literature also can easily be found on the internet.In the chapters the number of references therefore is limited to a few only.
NW, NS, and MIMN
How to use the
Snapshots of Hemodynamics
Chapter 2 Law of Poiseuille Chapter and title
DescriptionWith laminar flow through a uniform tube of radiusthe velocity profile over the cross-section is aparabola.
Physiological and clinical relevanceThe more general form of Poiseuille’s law given
above, i.e., allows us to derive resistance,
R, from mean pressure and mean flow measurement.
The box contains a figure witha short text that illustrates themain message of the chapter.
The ‘Description” sectiongives the essential backgroundand discusses the differentaspects of the subject.
The ‘Physiological andclinical relevance’ sectionplaces the subject in a broaderphysiological context andshows clinical applications.
A limited number of refe-rences is given. Major refe-rence books are given inAppendix 5.
References1.
2.
The Murgo JP, Westerhof N, Giolma JP,Altobelli SA. Aortic input impedance in normalman: relationship to pressure wave forms.Circulation 1980;62:101-116.Murgo JP, Westerhof N, Giolma JP, Altobelli
ACKNOWLEDGEMENT
The authors wish to thankDr. Ben Delemarre, Prof. Dr. Walter Paulus and Prof. Dr. P Segers forreading the manuscript and giving many excellent suggestions.We thank Jan Paul Barends for all his help in aspects of layout andpresentation.
xi
Part ABasics of Hemodynamics
Chapter 1 VISCOSITY
Description
Consider the experiment shown in the figure in the box. The top plate ismoved with constant velocity, v, by theaction of a shear force F, while the bottomplate is kept in place (velocity is zero). Theresult is that the different layers of bloodmove with different velocities. The differencein velocity in the different blood layerscauses a shearing action between them.
The rate of shear, is the relativedisplacement of one fluid layer with respectto the next. In general, the shear rate is theslope of the velocity profile, as shown in thefigure on the right. In our particular example the velocity profile is linear,going from zero at the bottom to v at the top plate. Therefore, the slope of thevelocity profile, and thus the rate of shear, is equal to v/h, h being thedistance between the plates. The units of shear rate are 1/s. The force neededto obtain a certain velocity, is proportional to the contact area, A, betweenfluid and plates. It is therefore convenient, instead of force, to use the termshear stress, defined as the force per area with units Pa or
We may think of the following experiment: we pull the top plate atdifferent velocities v and we measure the shear force F. Then we plot theshear stress, against the shear rate, The resulting relation is given in thefigure in the box and the slope is the viscosity:
The units of viscosity are or Poise with1 Pa·s =10 Poise. Fluids with a straight relationship between shear stress andshear rate are called Newtonian fluids, i.e., viscosity does not depend onshear stress or shear rate. Viscosity is sometimes called dynamic viscosity in
VELOCITY and shear rate for ageneral profile.
contrast to the kinematic viscosity, which is defined as viscosity divided bydensity thus
Viscosity of blood
Blood consists of plasma and particles, with99% of the particle volume taken by the redblood cells, RBC’s, or erythrocytes. Thus thered blood cells mainly determine thedifference between plasma and bloodviscosity. The viscosity of blood thereforedepends on the viscosity of the plasma, incombination with the hematocrit (volume %of red blood cells, Ht) and red celldeformability. Higher hematocrit and lessdeformable cells imply higher viscosity. The relation between hematocrit andviscosity is complex and many formulas exist. One of the simplest is the oneby Einstein:
Einstein’s relation for the viscosity offluids containing particles applies onlyto very low particle concentrations.Nevertheless, it gives some indication.The viscosity of plasma is about 0.015Poise (1.5 centipoise, cP) and theviscosity of whole blood at aphysiological hematocrit of 40 - 45% isabout 3.2 cP, or Pa·s.
Blood viscosity depends not only onplasma viscosity and hematocrit, but
also on the size, shape and flexibility of the red blood cells. For instance, thehematocrit of camel blood is about half of that of human blood, but thecamel’s red blood cells are more rigid, and the overall effect is a similar bloodviscosity.
Anomalous viscosity or non-Newtonian behavior of blood
The viscosity of blood depends on itsvelocity. More exactly formulated, whenshear rate increases viscosity decreases.At high shear rates the doughnut-shapedRBC’s orient themselves in the directionof flow and viscosity is lower. Forextremely low shear rates formation ofRBC aggregates may occur, therebyincreasing viscosity to very high values. Ithas even been suggested that a certainminimum shear stress is required beforethe blood will start to flow, the so-calledyield stress. In large and medium sizearteries shear rates are higher than so viscosity is practically constant.
4 Basics of Hemodynamics
VISCOSITY of plasma and blood.
VISCOSITY as function of shear rate forhematocrit of 48.
VISCOSITY as function of hematocrit.
Viscosity 5The physiological range of wall shear stress is 10 to 20 or 1 to 2Pa, with 1Pa = 0.0075 mmHg. Several equations exist that relate shear stressand shear rate of blood, e.g., Casson fluid, and Herschel-Bulkley fluid [1,2].
Viscosity also depends on the size ofblood vessel. In small blood vessels and athigh velocities, blood viscosity apparentlydecreases with decreasing vessel size. Thisis known as the Fahraeus-Lindqvist effect,and it begins to play a role in vesselssmaller than 1 mm in diameter. Red bloodcells show axial accumulation, while theconcentration of platelets appears highest atthe wall. The non-Newtonian character ofblood only plays a role in the microcircula-tion.
Viscosity depends on temperature. Adecrease of 1°C in temperature yields a 2% increase in viscosity. Thus in acold foot blood viscosity is much higher than in the brain.
How to measure viscosity
Blood viscosity is measured using viscometers. Viscometers consistessentially of two rotating surfaces, as a model of the two plates shown in thebox figure. Blood is usually prevented from air contact and temperature iscontrolled. When comparing data on viscosity one should always keep inmind the measurement technique, as results are often device dependent.
Physiological and clinical relevance
The anomalous character of blood viscosity results from the red blood cells,and the effects are mainly found in the microcirculation at low shear andsmall diameters. The effects are of little importance for the hemodynamics oflarge arteries. Thus, in hemodynamics, it may be assumed that viscosity isindependent of vessel size and shear rate.
Determination of blood viscosity in vivo is almost impossible. Inprinciple, the pressure drop over a blood vessel and the flow through it,together with vessel size, can be used to derive viscosity on the basis ofPoiseuille’s law. However, the vessel diameter in Poiseuille’s law (Chapter 2)appears as the fourth power, so that a small error in the vessel diameter leadsto a considerable error in the calculated viscosity. Also, the mean pressuredrop over a segment of artery is typically a fraction of 1 mmHg. Moreover,hematocrit is not the same in all vessels due to plasma skimming effects. Andfinally, Poiseuille’s law may only be applied when there are no effects of inletlength (see Chapter 2).
The main purpose of the circulation is to supply tissues with oxygen.Oxygen supply is the product of flow and oxygen content. The hematocritdetermines the (maximum) oxygen carrying capacity of blood and itsviscosity, and therefore the resistance to blood flow. These counteractingeffects on oxygen transport result in an optimal hematocrit of about 45 in thehuman at sea level, with a small difference between males and females. Itappears that in mammals, blood viscosity is similar, but the hematocrit is not
VISCOSITY as function of vesselsize.
6 Basics of Hemodynamicsbecause of the different size, shape and flexibility of the red blood cells asmentioned above.
Low hematocrit, as in anemia, decreases oxygen content and viscosity ofblood. The former lowers oxygen supply and the latter increases blood flowthus increasing supply. Inversely, polycythemia increases oxygen content butlowers blood flow. At high altitude, where oxygen tension is lower and thusoxygen saturation in the blood is lower, a larger hematocrit is advantageous.In endurance sports higher hematocrit is more efficacious during increasedoxygen demand. This is the reason EPO is sometimes used by the athletes.
References
1.2.
Merrill EW. Rheology of blood. Physiol Rev 1969;49:863-888.Scott Blair GW, Spanner DC. An introduction to biorheology. 1974,Amsterdam, Elsevier Sc Publ.