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Cardiopulmonary Bypass
Third Edition
P bli h d li b C b id i i P
P bli h d li b C b id i i P
Cardiopulmonary Bypass
Edited by
Florian Falter
Royal Papworth Hospital, Cambridge
Albert C Perrino
Yale University Medical Center, New Haven, CT
Robert A. Baker
Flinders Medical Centre and Flinders University, Adelaide
The editors are very grateful to Dr Ghosh, who started this project and led the first two editions
from idea to printed book
P bli h d li b C b id i i P
Shaftesbury Road, Cambridge CB2 8BS, United Kingdom
One Liberty Plaza, 20th Floor, New York, NY 10006, USA
477 Williamstown Road, Port Melbourne, VIC 3207, Australia
314–321, 3rd Floor, Plot 3, Splendor Forum, Jasola District Centre,
New Delhi – 110025, India
103 Penang Road, #05–06/07, Visioncrest Commercial, Singapore 238467
www.cambridge.org
Information on this title: www.cambridge.org/9781009009621
DOI: 10.1017/9781009008143
© Cambridge University Press & Assessment 2022
This publication is in copyright. Subject to statutory exception and to the provisions
of relevant collective licensing agreements, no reproduction of any part may take
place without the written permission of Cambridge University Press & Assessment.
First published 2009
Second edition 2015
Third edition 2022
Printed in the United Kingdom by TJ Books Limited, Padstow Cornwall
A catalogue record for this publication is available from the British Library.
Library of Congress Cataloging-in-Publication Data
Names: Falter, Florian, editor. | Perrino, Albert C., Jr. editor. | Baker, Robert A,
1960- editor.
Title: Cardiopulmonary bypass / edited by Florian Falter, Albert C. Perrino,
Robert A. Baker.
Other titles: Cardiopulmonary bypass (Ghosh)
Description: Third edition. | Cambridge, United Kingdom ; New York, NY :
Cambridge University Press, [2022] | Preceded by Cardiopulmonary
bypass / edited by Sunit Ghosh, Florian Falter, Albert C. Perrino, Jr.
Second edition. 2015 | Includes bibliographical references and index.
Identifiers: LCCN 2022010263 (print) | LCCN 2022010264 (ebook) |
ISBN 9781009009621 (paperback) | ISBN 9781009008143 (epub)
Subjects: MESH: Cardiopulmonary Bypass–methods | Cardiac Surgical
Procedures–methods
Classification: LCC RD598 (print) | LCC RD598 (ebook) | NLM WG 168.5 |
DDC 617.4/120592–dc23/eng/20220511
LC record available at https://lccn.loc.gov/2022010263
LC ebook record available at https://lccn.loc.gov/2022010264
ISBN 978-1-009-00962-1 Paperback
Cambridge University Press & Assessment has no responsibility for the
persistence or accuracy of URLs for external or third-party internet websites
referred to in this publication and does not guarantee that any content on
such websites is, or will remain, accurate or appropriate.
..................................................................
Every effort has been made in preparing this book to provide accurate and up-to-
date information that is in accord with accepted standards and practice at the time
of publication. Although case histories are drawn from actual cases, every effort has
been made to disguise the identities of the individuals involved. Nevertheless, the
authors, editors, and publishers can make no warranties that the information
contained herein is totally free from error, not least because clinical standards are
constantly changing through research and regulation. The authors, editors, and
publishers therefore disclaim all liability for direct or consequential damages
resulting from the use of material contained in this book. Readers are strongly
advised to pay careful attention to information provided by the manufacturer of
any drugs or equipment that they plan to use.
P bli h d li b C b id i i P
Contents
List of Contributors vi
Foreword ix
Alan Merry 11 Myocardial Preservation during
Cardiopulmonary Bypass 102
Gudrun Kunst, Luc Puis and Tom Gilbey
1 Human Factors and Teamwork in 12 Weaning from Cardiopulmonary Bypass 112
Cardiac Surgery 1 Joanne F Irons, Kenneth G Shann
Lindsay Wetzel, David Fitzgerald, Thoralf M and Michael Poullis
Sundt and James H Abernathy III
13 Intraoperative Mechanical Circulatory
2 Equipment for Cardiopulmonary Bypass 9 Support and Other Uses of
Simon Anderson and Amanda Crosby Cardiopulmonary Bypass 123
Mark Buckland and Jessica Underwood
3 Monitoring during
Cardiopulmonary Bypass 25 14 Mechanical Circulatory Support 138
Richard F Newland and Pascal Starinieri Jason M Ali, Ayyaz Ali and Yasir Abu-Omar
4 Cardiopulmonary Bypass Circuit Setup and 15 Cardiopulmonary Bypass for Pediatric
Safety Checks 34 Cardiac Surgery 150
Victoria Molyneux and Shahna Helmick Joseph J Sistino and Timothy J Jones
5 Priming Solutions for Cardiopulmonary 16 Coagulopathy and Hematological Disorders
Bypass Circuits 42 Associated with
Filip De Somer and Robert Young Cardiopulmonary Bypass 156
Bruce D Spiess and Erik Ortmann
6 Anticoagulation for
Cardiopulmonary Bypass 49 17 Inflammation and Organ Damage during
Martin Besser and Linda Shore-Lesserson Cardiopulmonary Bypass 166
R Clive Landis and Sherif Assaad
7 Conduct of Cardiopulmonary Bypass 57
Christiana Burt, Timothy A Dickinson, Narain 18 Neuromonitoring and Cerebral Morbidity
Moorjani and Caitlin Blau Associated with
Cardiopulmonary Bypass 175
8 Minimal Invasive Etienne J Couture, Stéphanie Jarry and André
Extracorporeal Circulation 71 Y Denault
Kyriakos Anastasiadis, Polychronis Antonitsis,
Helena Argiriadou and Apostolos 19 Renal Morbidity Associated with
Deliopoulos Cardiopulmonary Bypass 184
Juan Pablo Domecq and Robert C Albright
9 Considerations for Operations Involving Deep
Hypothermic Circulatory Arrest 80 20 Common and Uncommon Disasters during
Pingping Song and Joseph E Arrowsmith Cardiopulmonary Bypass 194
Gregory M Janelle, Jane Ottens and Michael Franklin
10 Metabolic Management during
Cardiopulmonary Bypass 92
Jonathan Brand and Edward M Darling
Index 205 v
P bli h d li b C b id i i P
Contributors
P bli h d li b C b id i i P
List of Contributors
vii
P bli h d li b C b id i i P
List of Contributors
viii
P bli h d li b C b id i i P
Foreword
Six years after the publication of the second edition of edition, the editors have achieved a consistency of
Cardiopulmonary Bypass, Florian Falter, Robert style and message with a minimum of repetition.
Baker and Albert C Perrino have produced a substan- Thus, the book feels coherent and has a logical flow
tial revision of this highly regarded text. Success in of ideas. As before, there is effective use of illustra-
cardiac surgery requires each member of the team to tions and tables and a good bibliography of selected
be expert in the theory and capable in the practice of references for each chapter. The book will continue to
their individual discipline, but it also requires them to provide an outstanding introduction to this field of
work together effectively as a team, often for long practice, both for surgeons and anesthetists, who pri-
hours under considerable stress. It is thus very pleas- marily need to understand and contribute to the
ing to see a strong new emphasis on teamwork, com- management of cardiopulmonary bypass or mechan-
munication and human factors added to this already ical circulatory support, and for perfusionists who
excellent book. This emphasis is reflected in the also have to set up and run the equipment. For those
renewed authorship of each chapter, which (in most already expert in this field, it will provide a technically
cases) now includes all three of the disciplines key to up-to-date source for revision of the relevant topics
the management of cardiopulmonary bypass – anes- from a highly contemporary perspective.
thesia, perfusion and surgery. The list of editors and The editors work in leading institutions in their
authors is a “Who’s Who” of this field and reflects not respective countries (England, Australia and the
only deep expertise in the relevant topics but also United States). Each is known for leadership and
established ability to disseminate knowledge through innovation within their discipline. The same can be
lecturing and writing. The result, as one might expect, said for the chapter authors. It is unsurprising that the
is a scientifically sound, clearly written and highly book carries a tone of authority that will leave readers
accessible text. It is a text that will (like the previous confident in the reliability of the information and the
edition) be an excellent source of practical hands-on soundness of the perspectives within it.
advice on how to apply the underpinning principles I offer the editors and the authors my hearty
to the everyday practice of cardiopulmonary bypass congratulations.
within the dynamic context of cardiac surgery.
The number of chapters has increased from 16 to Alan Merry FANZCA, FFPMANZCA, FRSNZ
20, but new material has been incorporated through- Professor of Anaesthesiology, University of
out. The themes of teamwork, communication, Auckland,
checklists and safety (both Safety-I and Safety-II) Specialist in Anaesthesia, Auckland City Hospital,
run through the entire book. As with the previous New Zealand.
ix
P bli h d li b C b id i i P
P bli h d li b C b id i i P
Chapter
Human Factors and Teamwork in
1 Cardiac Surgery
Lindsay Wetzel, David Fitzgerald, Thoralf M Sundt and James H Abernathy III
Safety 1 Safety 2
Definition of That as few things as possible go wrong. That as many things as possible go right.
Safety
Safety Reactive, respond when something happens or Proactive, continuously trying to anticipate
management is categorized as an unacceptable risk. developments and events.
principle
View of the Humans are predominantly seen as a liability or Humans are seen as a resource necessary for
human factor hazard. They are a problem to be fixed. system flexibility and resilience. They provide
in safety flexible solutions to many potential
management problems.
Accident Accidents are caused by failures and Things basically happen in the same way,
investigation malfunctions. The purpose of an investigation regardless of the outcome. The purpose of
is to identify the causes. an investigation is to understand how things
usually go right as a basis for explaining how
things occasionally go wrong.
Risk assessment Accidents are caused by failures and To understand the conditions where
malfunctions. The purpose of an investigation performance variability can become difficult
is to identify causes and contributory factors. or impossible to monitor and control.
Reprinted from, From Safety-I to Safety-II: A White Paper, Hollnagel E et al. Retrieved from www.england.nhs.uk/signuptosafety/wp-content/
uploads/sites/16/2015/10/safety-1-safety-2-whte-papr.pdf. Copyright 2015 by Erik Hollnagel, Robert L Wears, Jeffrey Braithwaite.
errors made by individuals at the service delivery end 2 embraces the variability in the healthcare delivery
(the operating room team); latent failures are organ- system and seeks to understand it. For example: Sally,
izational deficiencies (hospital wide, governmental, a perfusionist, is sought-after for complicated cases.
manufacturers, etc.) that are lurking in the back- She is talented clinically, communicates well, shares
ground contributing to active failures. Latent failures what she is thinking, makes good decisions and is
can be thought of as the holes in the Swiss cheese. steady under pressure. Sally’s resilience serves the
When errors occur, the majority of healthcare team well and, when Sally is there, it performs better.
organizations focus on the active failures, the most Rather than punishing people for making poor deci-
obvious of failures, through investigations like root sions (Safety 1), Safety 2 seeks to understand what
cause analyses or Morbidity & Mortality conferences. Sally does well and how this can be transferred to
Questions typically asked are: “who made mistakes?” other situations.
or “who didn’t follow the rules?.” This type of think- The two different perspectives are best summar-
ing with an emphasis on the negative has been coined ized in Table 1.1.
“Safety 1.” Safety 1 seeks to find the errors, the flaws,
the vulnerabilities. An alternative perspective, how-
ever, has emerged called “Safety 2.” In delivering The Human Factors Perspective
complex, complicated healthcare we do a lot of good Catchpole and McCulloch define human factors as:
and most times, we do it correctly. We manage to do “Enhancing clinical performance through an under-
this despite operating in increasingly complex standing of the effects of teamwork, tasks, equipment,
systems, with ever changing providers and more and workspace, culture and organization on human behav-
more demanding patients. The reason things go right ior and abilities and application of the knowledge in
is not that people behave as they are supposed to but clinical settings.” Or, stated more simply, “The science
because people adapt to the conditions they work in of improving human performance and well-being by
to make outcomes better. Understanding how people examining all the effectors of human performance.”
and the systems they work in adjust in order to Insights into the human factors perspective show
2
provide great care is how “Safety 2” is framed. Safety us that stress and fatigue, shortcomings in human
Figure 1.1 Systems Engineering Initiative for Patient Safety (SEIPS) 2.0: A model of work system and patient safety. (Reprinted from Holden RJ,
Carayon P, Gurses AP et al. SEIPS 2.0: A human factors framework for studying and improving the work of healthcare professionals and patients. Ergonomics.
2013;56(11):1669–1686.)
memory, interruptions and distractions, overesti- healthcare performance and outcomes. It celebrates
mation of ability and overreliance on multi-tasking measures which foster quality patient care and pin-
can make even the most seasoned healthcare pro- points interventions which can help healthcare organ-
viders commit medical errors. One of the first frame- izations achieve and maintain surgical excellence. It is
works by which we can understand these complex juxtaposed to individual-centered approaches which
interactions is the Systems Engineering Initiative for contend that human error is due to deficiencies on a
Patient Safety (SEIPS) (see Figure 1.1). personal level and remedies that are focused on discip-
The SEIPS model provides a framework through linary, punitive and litigious means.
which we can identify and addresses modifiable
factors in the interaction of people and their environ-
ments with regard to patient safety events. For Teamwork
instance, the perfusionist (person) operating the car- Salas and coworkers have described teamwork as “a
diopulmonary bypass machine (tool) requires correct distinguishable set of two or more people who inter-
ergonomics, visual and auditory feedback. The com- act dynamically, interdependently, and adaptively
plex machine the person operates should be situated towards a common and valued goal, who have each
in a location that provides short tubing length, is not been assigned specific roles or functions to perform
at risk of being hit by opening OR doors and provides and who have a limited life-span membership.”
the perfusionist with clear lines of sight to the Teams share a common mission and must adapt to
anesthesiologist, the surgeon and the monitor so that the dynamics and demands of various tasks in order
communication is unencumbered (environment). to achieve their end goal. Teams collaborate, they
Outcomes are not only affected by technical skill, synthesize and integrate information and coordinate
but by the intersection of healthcare environment, among members to share responsibilities in a way
team ethos, workload, team member morale, technol- that makes best use of the strengths of each individ-
ogy, effective communication and organizational vari- ual. Successful teamwork is characterized by mutual
ables. The SEIPS model contends that medical error trust, effective communication, realistic goal setting,
can be a natural consequence of system wide break- fair division of tasks, desire to achieve a common goal 3
downs in the vast array of factors which influence and a shared passion for excellence.
Figure 1.2 Mental workload in the cardiac surgery operating room varies across the cardiac surgery procedure for individual providers
depending on task complexity and responsibilities. CRNA indicates certified registered nurse anesthetist; CST, certified surgical technologist;
NASA, National Aeronautics and Space Administration; Postop, postoperative; Prep, surgical preparation; RN, registered nurse; and TLX, Task
Load Index. (Reprinted from The Journal of Thoracic and Cardiovascular Surgery, Volume 139, Issue 2, RK Wadhera et al., Is the “sterile cockpit” concept applicable
to cardiovascular surgery critical intervals or critical events? The impact of protocol-driven communication during cardiopulmonary bypass, Pages 312–319.
Copyright © 2010, with permission from Elsevier.)
The Joint Commission recognizes communication during takeoff and landing or in unusual or stressful
as one of the top three contributing factors to sentinel situations. This principle is equally applicable to pro-
events. Broadly speaking, communication is “the ceedings in the cardiac operating room – going on
exchange of information between a sender and a and coming off bypass, as an example, are treated
receiver.” Effective communication is characterized similar to starting and landing. Some healthcare
by clarity, comprehensiveness and confirming that organizations have implemented the rule that when
the message has been relayed effectively. It contrib- one member of the team spots trouble they call out
utes to a shared mental awareness, clarifies what team “10,000 feet” to get attention and change the mood
members are worried about, identifies any issues that and focus in the room to problem-solving mode.
have arisen previously during similar moments and Closed-loop communication or “call back,” whereby
establishes an understanding of how to successfully the speaker’s message is repeated or paraphrased by
navigate these scenarios. Fostering an environment the receiver, is an effective way to reduce communi-
which cultivates open, truthful, adaptable, succinct cation ambiguity, miscues, and non-verbalized critical
and constructive communication is critical to any actions.
successful team. We must recognize that at no point during a case
Clear communication is vital during times of is the mental workload the same for all providers
stress. Critical situations don’t need bystanders, they (Figure 1.2). While the patient is on bypass the per-
require the key team members to be in the room and fusionist is working hard while the anesthesiologist
rely on them adhering to their assigned roles. The might have less to concentrate on; during the induc-
“sterile cockpit” concept, widely in use in military and tion of anesthesia, the surgeon will usually be doing
commercial aviation, describes the banning of non- something unrelated; during the vitally important
essential communication during critical periods asso- instrument count the scrub and circulating nurses
4 ciated with high-risk and high mental workload. In are ensuring nothing will be left behind while the rest
aviation, chatting is not allowed below 10,000 feet of the room is congratulating themselves on a job well
done. Understanding when different members find hand, overcome challenges in such a way that both
themselves in a period of increased mental workload performance and cohesion are at least sustained, if
helps the entire team to identify the times where we not improved, eventually leading to improved out-
can help our colleagues. comes. The underpinnings of resilience are a shared
Transition of care is an especially high-risk period vision and mission, healthy relationships and invested
for communication breakdown. Handoff of a patient team members. Resilient teams
when OR staff change shift or from operating room to – support each other and encourage recovery after
ICU staff are particularly vulnerable times. In the difficult situations,
absence of standardized clinical practice guidelines, – don’t lay blame on individuals after such
handoffs between providers may be highly variable situations but engage in learning through effective
and unstructured, missing important content items communication and constructive criticism to
during transfer. Poor information transfers also lead facilitate a different outcome in the future.
to incomplete clinical tasks and disruptions in care.
A team which can band together during times of
Standardized handoffs, such as the recently published
duress and lean on one another for support will
AmSECT perfusion handoff tool or the Formula
invariably arise from challenging situations stronger
1 type OR to ICU handoff tool proposed by
and better equipped to deal with future problems.
Catchpole, greatly improve the accuracy of informa-
This is particularly true for the cardiac operating
tion transfer (see Figure 1.3).
room.
Leadership
Leadership style in the cardiac operating room can Practical Solutions
have a significant impact on the function of the entire Breakdown in teamwork is commonly attributed to a
team. Transactional leaders focus more on individual lack of role clarity among team members or ineffect-
tasks, responsibilities and blame. They rarely see the ive communication. Proposals to improve communi-
big picture and engage in unilateral communication cation and to reduce the possibility of error include,
which is not conducive to a team focused environ- but are not limited to, standardized intraoperative
ment. Transformational leaders foster an environ- communication, preoperative briefings, and post-
ment of enthusiasm, learning, cooperation and a operative debriefings.
collective mission. Studies have shown a higher level
of teamwork and information sharing with trans- Standardized Conversations
formational leadership styles. Within a culture of
Standardizing communication practices facilitates
excellence, there must also be a commitment to
stronger team communication and helps all
respect. Professionalism and courtesy are not negoti-
team members “speak the same language.”
able. Effective leaders aim to flatten the hierarchy,
Communicating in a closed-loop, or read-back, fash-
create familiarity and foster an environment where
ion ensures that the entire team is aware of what is
everyone feels safe to speak up and participate. If
occurring and helps in retaining the shared mental
there was an easy button for establishing a culture of
model. Operating rooms can be chaotic places
excellence and effective leadership, we might not have
where background noise makes hearing difficult.
a need for this chapter. Personal and institutional
Acknowledging comments and questions ensures that
willingness to embrace tools such as Just Culture are
communications have been heard and understood.
important to tilt behavior toward personal account-
Repeating back essential information confirms that
ability and adaptability.
the sender’s message has been received. It is import-
ant to foster an environment where closed-loop com-
Repair, Recovery and Resilience munication is encouraged and not looked at as
Resilience alludes to the capacity of individuals and of disengagement (i.e. the individual repeating the mes-
teams to withstand and recover from pressures, stres- sage was not paying attention and hence needs clari-
sors and challenges. Failure to recover from an unex- fication.) Knowing team members by name helps to
pected event is a characteristic of poor performing make communications more direct and removes 5
perioperative programs. Resilient teams, on the other ambiguity as to who is being addressed.
Figure 1.3 AmSECT perfusionist handoff checklist. (Reproduced with kind permission of the AmSECT Safety Committee.)
6
Teamwork
& Leadership
Cooperation
COMMUNICATION
Situation Decision
Awareness Making
• Frequent updates • Decisions clearly
• Announces changes of plan communicated
• Clarifying confusion • Responsibility clear
• Input encouraged • Regular reviews
Figure 1.4 A visual model with the basic but critical concepts enabling teams to work together effectively. (Reproduced with kind permission
from Atrainability, https://atrainability.co.uk)
Cardiopulmonary bypass (CPB) provides optimum The heart lung machine and circuitry used in
conditions for cardiothoracic surgery by combining procedures today has advanced significantly since
a pump to substitute for the function of the heart and the advent of extracorporeal circulation and the first
a gas exchange device, the “oxygenator,” to act as an attempts at its use. The basic principles, however,
artificial lung. CPB therefore allows the heart and remain the same to this day:
lungs to be temporarily suspended, to facilitate car- Venous blood is drained by gravity or assistance
diac, vascular or thoracic surgery in a safe, still, blood- into a reservoir via a cannula placed in a large
less and controlled environment. vein, most typically the right atrium or vena cava.
Blood is then pumped through the oxygenating
History device and an arterial filter. Transit through the
The first successful open procedures were performed oxygenator reduces the partial pressure of carbon
in 1954 by Dr. Clarence Walton Lillehei using a cross- dioxide in the blood and raises oxygen content.
circulation technique, acting as an extracorporeal cir- Current models have the oxygenator, heat
cuit. This approach worked by circulating the parent’s exchanger and filter incorporated in one
arterial blood into the recipient and controlling the component (Figure 2.1 a and b)
amount of venous blood being returned, giving the It is next returned into the patient’s arterial system
surgeon up to an hour to perform cardiac surgery. through a cannula in a large artery, most typically
The concept of the heart lung machine (HLM) and the aorta.
cardiopulmonary bypass circuit arose from this tech- Older technology and bypass circuits consisted of
nique of “cross-circulation.” large components that required manual cleaning,
The development of the heart lung machine in were reused after sterilization, and were primed with
1953 was preceded by a number of perfusion pumps. up to 14 units of blood. Due to the advances in
The design of the first such pump originated in technology and techniques, CPB circuits today are
1935 by Charles Lindbergh in collaboration with Dr. more reliable, have more safety devices and are
Alex Carrel. The pump was used to keep organs disposable.
functioning outside of the body with a solution
developed by Carrel to perfuse organs, only limited
by the eventual failure of the organ itself or the Tubing
breakdown of the constituents in the perfusate. In The cardiopulmonary bypass circuit is created with
1953 Dr. John Gibbon used the first total CPB system. tubing connected to the various components required
Gibbon operated on four patients with congenital to support the circulatory system and allow close
heart disease with only one survivor, and considered monitoring. Table 2.1 provides an overview of the
this series of work a failure, however his efforts were main components of a HLM. Different types of
an inspiration to researchers around the world. The tubing may be used throughout the circuit depending
emergence of the DeWall-Lillehei helix reservoir with on what function it serves, for example, tubing used
a bubble oxygenator in 1955 was the first disposable, to monitor pressure is different to tubing for the
efficient, and inexpensive bypass circuit, this innov- actual circulatory support. Tubing should be pos-
ation fueled the rapid expansion into open-heart sur- itioned in an orientation that avoids kinks and allows
gery after 1956. for smooth curves to limit areas of high velocity or 9
(a) Venous
Femoral Vent return
catheters Sucker catheter catheter
Venous
HCT/SAT Cardioplegia
Venous cannula
cardiotomy reservoir
Venous
BGM Arterial
Cardioplegia cannula
Arterial BGM Arterial Bubble
detector solution
• Bubble trap
• Temperature
• Pressure
To cardioplegia Centrifugal Blood from Heat exchange
pump (or Roller oxygenator
Oxygenator with
roller pump) pump
reservoir and
heat exchange
Dual
Arterial Suction Vent Cardioplegia cooler/heater
Temperature
control and Perfusion system (heart-lung machine)
monitoring
system
Figure 2.1 (a) Typical configuration of a basic cardiopulmonary bypass circuit. BGM = blood gas monitor; SAT = oxygen saturation. (b) Full HLM in use.
10
Table 2.1. Components of the CPB machine and the Table 2.2. Commonly used biocompatible tubing coatings
extracorporeal circuit
Manufacturer and Description of Coating
Equipment Function Coating Properties
Oxygenator system, Oxygenate, remove carbon Gore – Carmeda Covalent bonding of heparin
venous reservoir, dioxide and cool/ molecules
oxygenator, heat rewarm blood
exchanger Baxter - Duraflo II Heparin ionically joined with
ammonium and attached to
Gas line and FiO2 blender Delivers fresh gas to the surface
oxygenator in a
controlled mixture Terumo – Xcoating Biopassive polymer creates
hydrophobic and hydrophilic
Arterial pump Pumps blood at a set flow properties without heparin
rate to the patient
Maquet – Bioline Heparin and albumin attached
Cardiotomy suckers and Scavenges blood from the to polypeptides on tubing
vents operative field and vents surface
the heart
LivaNova – P.H.I.S.O. Phosphorylcholine
Arterial line filter Removes microaggregates Coating
and particulate matter
>40 μm Medtronic – Cortiva Endpoint-attached heparin
BioActive Surface coating
Cardioplegia systems Deliver high-dose
potassium solutions to
arrest the heart and
preserve the
myocardium PVC when the tubing is occluded but can release
more particles. Silicone rubber is sometimes utilized
Cannulae Connect the patient to the
extracorporeal circuit in the arterial pump roller head as an alternative to
commonly used PVC tubing.
Tubing used during CPB is subject to repeated
compression in pump roller heads. This intermittent
stagnation. Any junctions or connections between compression can degrade the integrity of the walls of
components have to be secured tightly to prevent the tubing and may cause plastic micro particles to be
leaks or air ingress. Clinicians must consider the released, this is called spallation.
intended use of the tubing when choosing materials Tubing can be made with a biocompatible coating
to create the circuit. (see Table 2.2), which may help reduce the inflamma-
Polyvinylchloride (PVC) is the predominant tory response to foreign material. Sequelae from the
tubing material used today in cardiopulmonary inflammatory response include platelet activation, ini-
bypass, but latex rubber and silicone rubber are other tiation of the coagulation cascade, decreased levels of
options. PVC is made up of polymer chains with circulating coagulation factors, activation of endothe-
polar carbon-chloride (C-Cl) bonds. These bonds lial cells and leukocytes, releasing mediators that may
result in considerable intermolecular attraction between contribute to capillary leakage and tissue edema. This
the polymer chains, making PVC a fairly strong material. is discussed in more detail in Chapter 17.
On its own, PVC is a rigid plastic, but plasticizers are There are a number of surface coatings available
added to the type of tubing used in a circuit, which make on the market today. One type of circuit coating uses
it malleable and easier to manipulate. both hydrophobic and hydrophilic properties to form
Silicone rubber is a semi organic synthetic. Its a new layer on top of the tubing that reduces protein
structure consists of a chain of silicon and oxygen denaturation and platelet adhesion. Since this coating
atoms rather than carbon and hydrogen atoms, as is is made from a non-heparin-based biopassive poly-
the case with other types of rubber. The molecular mer Poly(2-methoxyethylacrylate) (PMEA), this
structure of silicone rubber results in a very flexible tubing can be used on heparin sensitive or intolerant 11
but weak chain. Silicone produces less hemolysis than patients. Another type of biocompatible tubing is
Table 2.3. Tubing sizes commonly used in different parts of the extracorporeal circuit (adults only)
Tubing size Prime Max flow (l/min) Max flow (l/ Function
volume (To keep min)
(cc/ft/ml/ pressure (To keep
30cm) gradient <10 Reynolds
mmH*) number
<1000*)
3/16” (4.5 mm) 5.4 /4.7 0.2 1.8 Cardioplegia section of the blood
cardioplegia delivery system
1/4” (6.0 mm) 9.84/8.5 0.9 2.1 Suction tubing, blood section of the blood
cardioplegia delivery system
3/8” (9.0 mm) 21.6 /19.1 4.0 3.7 Arterial pump line for flow rates <6.7 l/
minute, majority of the arterial tubing in
the extracorporeal circuit
1/2” (12.0 mm) 42/33.9 7.0 5.0 Venous line, larger tubing is required to
gravity drain blood from the patient
*
Source: Hessel EA II, Hill AG in Gravlee GP et al.: Cardiopulmonary Bypass: Principles and Practice. Lippincott Williams & Wilkins, 2000,
Table 5.4
made from phosphorylcholine that mimics the nat- to crystalloid needed, and the type of delivery device.
ural endothelium to reduce platelet activation and cell When choosing tubing for scavenging blood from the
adhesion to the tubing surface. Some tubing contains surgical field and venting of the heart or aorta, the
heparin, which should be noted when providing care decision is usually based on institutional protocol, but
to a heparin intolerant patient. Some institutions will take into account the volume of the tubing length
maintain a small stock of non-coated circuits for these and the displacement per revolution of the pump
patients. Regardless of the type or manufacturer head.
selected, biocompatible tubing can improve platelet
preservation and reduce the inflammatory response
to foreign surfaces. Arterial Cannulae
Selecting the appropriate tubing size is based on The arterial cannula is used to deliver oxygenated,
the application. Larger bore tubing requires less pressurized blood from the HLM directly into the
pump head revolutions needed to displace the same patient’s arterial system. The size of the vessel that is
amount of volume as smaller tubing, meaning less being cannulated and the patient’s required blood
mechanical stress from repeated compression. The flow are considered in selecting the appropriately
internal diameter as well as the length should be sized cannula.
carefully considered as both will affect the priming The ascending aorta is most used as the site of
volume. While a larger internal diameter allows for arterial cannulation for routine cardiovascular sur-
greater flow at lower pressures, it has a higher prime gery allowing antegrade flow to the cerebral and body
volume, increased contact activation, less resistance, circulation. The asceding aorta is large caliber, has a
and a larger pressure gradient. There are many low associated incidence of aortic dissection
factors to consider when selecting the best fit for the (0.01–0.09%), and is easy access when using a median
application required (see Table 2.3). When deciding sternotomy approach. After sternotomy and expos-
upon the size of arterial and venous tubing, the ure, the surgeon can assess the size of the aorta before
patient’s body surface area (BSA) and calculated car- choosing the most appropriate caliber cannula (see
diac index can help guide the appropriate size of Figure 2.2).
tubing. Tubing for cardioplegia administration is Developments in cannula design allow the use of
12 based on the solution being used, the ratio of blood thin wall cannulae. By having a larger effective
18 Fr
160 160
Pressure Loss (mm Hg)
120 120 20 Fr
24 Fr
80 80
22 Fr
40 40
24 Fr
0 0
0 1 2 3 4 5 6 0 1 2 3 4 5 6
Flow Rate (L/min of water) Flow Rate (L/min of water)
Select Series® Straight Tip Arterial Cannulae Edwards Soft flow/EZ glide)
200
100
20 Fr 21 Fr. Straight
160
80
Pressure Loss (mm Hg)
140
60 22 Fr
21 Fr. Curved
80 24 Fr. Straight
40 24 Fr
24 Fr. Curved
20 40
0 0
0 1 2 3 4 5 6
0 1 2 3 4 5 6
Flow Rate (L/min of water) Flow Rate (L/min), H2O at Room Temperature
Figure 2.4 Femoral reinforced cannula. Biomedicus Life SupportTM 21Fr. (Reproduced with ©2020 Medtronic. All rights reserved. Used with the
permission of Medtronic.)
imaging or transesophageal echocardiography (TEE) a bloodless field for the surgeon. Figure 2.5 shows
is used to confirm correct cannula position. Axillary commonly used venous cannulae.
and subclavian cannulation is most commonly Femoral cannulation can be utilized for more
achieved by suturing a dacron graft end-to-side onto complex surgery. In this instance, a long cannula,
the vessel and a 3/8 3/8 inch connector to connect which is in essence an elongated single-stage cannula,
to the HLM arterial line. is typically passed over a guide wire up the femoral
vein into the IVC and RA to achieve venous drainage.
These cannulae are generally placed under TEE
Venous Cannulae guidance. As with arterial cannulation sites, the size
Venous cannulation provides the means to drain and length of the venous cannulae are patient specific
deoxygenated blood from the patient’s venous system and are determined by body surface area (BSA),
into the extracorporeal circuit. It is important to use required full flow and vessel size. In an average height
appropriately sized cannulae in order to obtain max- adult (170 cm, 80 kg), a 25 Fr/55 cm cannula provides
imum venous drainage from the patient so that full sufficient venous drainage from the IVC. However, in
flow can be achieved when CPB is commenced. The smaller patients, a 38cm length cannula may be a
type of venous cannulation used depends on the better option to ensure the cannula is short enough
operation being undertaken. For cardiac surgery not to be positioned in the IVC and not too long to
involving opening chambers of the right heart, for potentially perforate the right atrium or SVC during
example, coronary artery bypass grafts (CABG) or cannulation.
aortic valve replacement (AVR), a two-stage venous
cannula is often used. The tip of this type of cannula Perfusion Pumps
sits in the inferior vena cava (IVC) and drains blood
Perfusion pumps, in the arterial position, propel
from the IVC through holes around the tip; a second
blood forward through the circuit. There are two
series of holes a few centimeters above the tip is sited
main types: positive displacement roller pumps and
in the right atrium to drain venous blood from the
the impeller centrifugal pumps.
superior vena cava (SVC).
During procedures that require the right atrium
(RA) to be opened, bicaval cannulation, where a Roller Pumps
single-stage cannula sits in each of the inferior and A peristaltic pump or “roller pump” is a positive
superior vena cava, is necessary. The two single-stage displacement pump used for moving fluid. Initial
cannulae are connected to the venous line of the CPB HLM technology in the 1950s used a similar peristal-
circuit using a Y-connector. This approach avoids air tic pump, and the technology has not greatly changed
entry into the CPB circuit from the distal series of from its inception. The raceway or the pump header
holes of a two-stage cannula, as they would be sitting accepts a length of tubing, the rotor and roller com-
in the open RA. Air entry would impede venous bination inside the middle of the pump housing
14 drainage – or stop it completely in case of an “air rotate in a clockwise or counterclockwise direction.
lock” – leading to the patient’s calculated full flow Typically, there will be two or more rollers that com-
becoming unachievable in addition to not providing press the tubing and a clutch mechanism to set the
Figure 2.5 Commonly used venous cannulae (a) DLPTM single-stage cannula (b) Bi-caval cannulation technique (c) MC2TM two-stage cannula. 15
(Reproduced with ©2020 Medtronic. All rights reserved. Used with the permission of Medtronic.)
Omega, or
horseshoe raceway
degree of tubing occlusion, regulating the amount of pressure. As they operate independently of resistance
compression applied to the tubing. Under-occlusive, or pressure, pressures within the circuit must be
or too loose, tubing may result in retrograde flow or monitored. It is essential to limit the pump flow if
inaccurate flow calculations, while over-occlusion, or system pressure becomes excessive. Sudden occlusion
too tight, may increase hemolysis, spallation, and of the inlet of the roller head can create extreme
inaccurate flow calculations. The roller head occlu- negative pressure to the point where the tubing may
sion should be measured before each case to ensure it cavitate and create air bubbles in the circuit.
has the desired setting for the operation. The methods Very similar to the heart, output of a roller pump
to test occlusions are described in detail in Chapter 4. is determined by the internal diameter of the tubing
As the rollers compress and occlude the tubing, the (= stroke volume) and the number of revolutions of
fluid is moved in the corresponding direction(see the pump head (= beats per minute). The larger the
Figure 2.6). The tubing inside the raceway is held in a tubing in the raceway, the less rpms are needed to
fixed position by brackets or a locking mechanism and maintain the same output of smaller tubing. Note that
returns to its natural state once the roller passes over it. reading or recording blood flow directly from the
This intermittent occlusion creates positive and negative arterial roller head does not account for any shunts
pressures on either side of the occlusion point, which is that may be present downstream in the circuit, and
the driving force for the movement of fluid. Positive thus the actual flow reaching the patient may be less.
pressure created by the roller propels fluid and the recoil
of the tubing creates negative pressure refilling the tube.
Roller pumps can be used in any position. They Centrifugal Pumps
can be belt driven or have direct drive systems and are Centrifugal pumps are non-occlusive pumps and utilize
16
not affected by circuit resistance or hydrostatic a magnet and impeller combination to propel blood
(b)
Figure 2.7 Centrifugal pump head (a) Medtronic AffinityTM. (b) Schematic cut through of AffinityTM centrifugal pump. (Reproduced with ©2020
Medtronic. All rights reserved. Used with the permission of Medtronic.)
through the CPB circuit. The pump consists of a hard amount of forward flow will decrease, unless the rpms
outer shell which incorporates an impeller design are altered to counter this. For this reason, centrifugal
coupled magnetically with an electric motor and shaft pumps have the potential to allow retrograde flow,
or pin. When the console is turned on and the rpms are however most flow meters will alert the user if this
increased, the cones or fins spin rapidly, creating posi- occurs. Unlike roller pumps whose flow is calculated
tive pressure that propels fluid forward (see Figure 2.7). based on tubing diameter and rpm (stroke volume and
Centrifugal pumps, much like the heart, are after- beats per minute), centrifugal heads require ultrasonic 17
load sensitive. If the post-pump resistance increases, the or electromagnetic meters to accurately determine
blood flow. Unlike rollers, centrifugal pumps do not Table 2.4. Common centrifugal heads, adult sizes
need to be pressure regulated because they will not be Manufacturer Centrifugal Brief Description
able to generate forward flow if the tubing is kinked, Head
clamped, or suddenly occluded. When used for CPB, a
special centrifugal head motor that can be manually LivaNova Revolution Open impeller design,
with impregnated
operated must be available as backup.
nylon magnet and
The perceived benefits of the centrifugal pump are
seal-less low friction
its low prime volume and, because of its non- bearings – 57 ml
occlusive nature, less hemolysis. Despite extensive prime volume
research, there is little clinical evidence to show any
Terumo CAPIOX SP Polycarbonate housing,
benefit of CPB with centrifugal over CPB with roller
impeller design, lip
pumps. Centrifugal pumps may produce less hemoly-
seal – 45 ml prime
sis and platelet activation than roller pumps, but this volume
does not correlate with any difference in clinical out-
come. Centrifugal pumps are less likely to create air Medtronic Affinity CP Low profile fins,
ceramic pivot
embolism situations because as air is introduced to
bearings, no stasis
the cone, the pump will deprime and cease forward
zones – 40 ml prime
flow. Clinicians should remain vigilant, though, as volume
there have been reports of air ingress into circuits
using centrifugal pumps. Centrifugal pumpheads are Abbott - Centrimag Free-floating
Thoratec magnetically
expensive, adding a signficant additional cost to the
levitated rotor, has
CPB circuit. Clinicians favoring centrifugal systems
no bearings or seals
have argued that the ability to create smaller circuits creating minimal
due to remote drive capabilities, allows the circuit to stasis zones – 31 ml
be closer to the surgical field unlike the fixed console prime volume
based roller head position. The new generation roller
Gettinge - Rotaflow RF- Peg-top, one-point
pumps have largely overcome this issue and tubing
Maquet 32 sapphire bearing –
length has decreased significantly in recent years. The 32 ml prime volume
decision to use centrifugal pumps or roller pumps for
CPB is largely determined by institutional factors
rather than clinical indication. Table 2.4 summarizes
commonly used adult centrifugal pump heads. The reservoir acts as a chamber for the venous blood
Centrifugal head technology is not only used in to drain into before it is pumped through the oxygen-
cardiopulmonary bypass cases but also in extracor- ator and permits ready access for the addition of fluids
poreal membrane oxygenation (ECMO) and ven- and drugs. To reduce the risk of perfusion accidents, the
tricular assist devices (VADs). Certain models level of fluid is monitored for the duration of CPB to
possess fins or channels to help avoid areas of stagna- prevent the reservoir from emptying and air entering
tion, while others have magnetically levitated bearing- the circuit. Each manufacturer details the minimum
less motors to reduce heat generation. Each has a set safe fluid level necessary to achieve the rated flow of
rpm needed to generate forward flow, this minimum their device. Low level alarms (see also Chapter 3), often
number will be different with blood viscosity (hemo- coupled to automatic cessation of pump flow when
globin) and patients’ vascular resistance pressure. triggered, add additional safety. Gross air embolism
incidents can still occur if arterial flow exceeds venous
drainage, subsequently emptying the reservoir.
Reservoirs Vacuum-assisted venous drainage may be used to
Cardiotomy reservoirs may be hardshell or softshell optimize venous drainage during CPB. Using vacuum
(collapsible). Hardshell reservoirs usually comprise of assistance can reduce hemodilution and subsequent
a durable polycarbonate housing, a high-efficiency transfusion requirements because improved drainage
18 polyester depth filter and a polyurethane defoamer requires fewer “top-ups” with crystalloids or colloids.
(see Figure 2.8). With the top of the cardiotomy reservoir positioned
Oxygenators
The evolution of the oxygenator has been critical to
the success of cardiac surgery and advanced patient
care. Oxygenators are most often described as artifi-
cial lungs as they provide an alveolar capillary system
for gas transfer. The general design goals are efficient
gas exchange, low prime volume, minimized trauma
to blood and efficient cooling and heating capabilities.
Figure 2.8 Fusion reservoir. (Reproduced with ©2020 Medtronic. All
TM
There are two main types of oxygenators com-
rights reserved. Used with the permission of Medtronic.)
monly used in adult cases today, microporous poly-
propylene (PPL) and non-porous polymethylpentene
(PMP). Both are hollow fiber membrane oxygenators,
which are named for the membrane that separates the
at the level of the patient’s atrium, a negative pressure gas and blood phases. The main difference is their
of approximately 60 mmHg is applied when max- duration of use – the PMP type oxygenators typically
imal gravity drainage is reached. The negative pres- maintain gas exchange longer. While PPL oxygen-
sure can be increased by small amounts during CPB, ators are more common, extended use can cause
when the fluid in the reservoir decreases to the safety plasma leaks across the membrane from the blood
limit level. For weaning from bypass, the negative phase into the gas phase, resulting in decreased gas
pressure is gradually decreased to zero, the reservoir exchange efficiency. The non-porous fibers of the
is opened, and the venous line progressively closed. PMP oxygenator make them more durable than
Blood scavenged from the operative field via PPL, and they are typically used for longer term
suckers is also returned to the reservoir. Suction relies applications such as ECMO. The lack of pores does
on the “Venturi” effect, which is the change in pres- not allow exchange of volatile anesthetics, making
sure and fluid velocity through a narrowing in a tube. PMP oxygenators unsuitable for use with CPB.
Suctioning blood from the operative field causes Oxygenators are regulated by federal guidelines,
damage to blood cells and also results in concomitant allowing their use for periods of time usually up to six
entrainment of high volumes of air. The salvaged hours. While using them longer is designated as off
blood may contain tissue and other debris and is label, it is a widespread and acceptable application of
highly activated with inflammatory cells. It is vital the technology to facilitate bridging to recovery or
that this blood is filtered through the reservoir before transplantation when other advanced treatments
being pumped to the patient. Advances in technology have failed.
have seen a more widespread use of reservoirs con- Once entering the device, blood first passes over
taining separate chambers for venous blood and car- the integrated heat exchanger before moving into the
diotomy suction, allowing the suction blood only to oxygenator compartment, where gas exchange takes
be added into the circuit when required. Segregating place (see Figure 2.9). O2 concentration and flow of
suction blood that way has the advantage that it can the sweep gas, which drives gas exchange, are regu-
be passed through a specific filter that absorbs lipid lated with a gas blender and a flow meter integrated
cells, which have been shown to impair oxygenator into the HLM. The sweep is piped into the oxygenator
effectiveness. The reservoir is constantly vented to inlet port, its distribution throughout the membrane’s 19
prevent the entrained air causing a pressure buildup, capillary system varies with the oxygenator used and
the patient’s size. Typically the flow is 2–4 l/min for Cooling the blood, and thus cooling the patient,
adults, depending on blood flow and the desired CO2 results in a lower metabolic demand that helps ensure
removal rate. Volatile anesthetics can be added all tissues are being adequately perfused while on
depending on oxygenator type and HLM in use. bypass. Chapters 9 and 10 discuss temperature man-
Gas scavenging can be attached to the exhaust port. agement and rewarming strategies in more detail.
Gas sampling to determine O2 consumption and end- Intended duration of use, requirement for volatile
tidal CO2 can be attached at this point as well. anesthetics, prime volume, biocompatible coating, gas
Integrating the heat exchanger and arterial line exchange capacity, and the heat exchanger’s efficiency
filter into the oxygenator has decreased circuit size are the main determinants that inform the choice of
and reducted prime volume. The heat exchanger is oxygenator used for a case.
separated from the blood phase by a highly thermal
conductive material and is biologically inert. An Gas Supply System
external heater cooler is connected with thick water
The gas supply is connected to the blender, which
lines, usually made of antimicrobial-coated tubing.
mixes oxygen and air to provide the desired FiO2
Fine control of the water bath temperature allows
and to a flow meter to regulate sweep gas flow (see
precise regulation of the patient temperature.
Figure 2.10). CO2 may be added to the sweep when
pH-stat blood gas management is desired during
hypothermia or cases requiring deep hypothermic
circulatory arrest (DHCA, see Chapter 9). Blending
units and flow meters may be mechanical, but are
now mostly digitally controlled via the HLM.
Continuous inspired O2 analysis is mandatory to
prevent the inadvertent administration of a hypoxic
mixture.
20
Table 2.5. Filtration devices used within the cardiopulmonary Depth filters create a tortuous path between fibers
bypass circuit
and retain particles mechanically. Screen filters are
Filter type Application and specification the most common type and are typically made of a
woven polyester mesh. They are usually pleated to
Gas line Removes 99.999% of bacteria found in
allow for a larger surface area in a confined space
the gas stream minimizing cross-
contamination between the patient
and trap particulates or emboli that are larger than
and the equipment their particular pore size. Filters come in a size range
from 0.2 μm for gas line filters to 40μm for arterial
Pre-CPB 0.2 μm filter is used during the priming
line filters.
and recirculation phase. It is
0.2μm pre-bypass filters are meant to capture any
designed for the removal of
inadvertent particulate debris and particles left from the manufacturing process and are
microbial contaminants and their removed after priming and before initiating bypass.
associated endotoxins Separate arterial line filters are indicated for use in
all CPB procedures where the oxygenator does not
Arterial line Designed to remove microemboli
have an integrated filter. The main goal of an arterial
>20 μm in size from the perfusate
during extracorporeal circulation. filter, whether integrated into the oxygenator or not,
This includes gas emboli, fat emboli is to stop gaseous macro-emboli from entering the
and aggregates composed of circulation, although there is some debate about
platelets, red blood cells and other their effectiveness. Several arterial filters with varying
debris. Pore size depends on characteristics are commercially available (see
manufacturer Table 2.6).
Venous Designed to remove debris and gross The US Food and Drug Administration (FDA)
reservoir air, some models may contain a have outlined key areas of importance pertaining to
defoamer to reduce bubbles from arterial line filters (FDA, 2000). The following list sets
incoming suction or ports forth the risks to health associated with this device
Cardioplegia Blood cardioplegia: >40 μm filter. that were identified in the proposed classification
Crystalloid cardioplegia: >0.2 μm ruling (dated February 26, 1979), as well as additional
filter. Low priming volume filter for adverse event reporting since the classification ruling:
cell-free solutions. Removes Amount of damage to formed blood elements,
inadvertent particulate debris and clotting and hemolysis
microbial contaminants and their Degree of pressure drop resulting in inadequate
associated endotoxins
blood flow, damage to the device or structural
Leukodepletion Reduces the levels of leukocytes, integrity and damage to the arterial line
either from the arterial line or Structural integrity of the product
cardioplegia system, and excludes
Excessive pressure gradients, for example, blood
microemboli >40 μm
damage and inadequate blood flow
Blood Designed to reduce the levels of Filtration efficiency and gas emboli-handling
transfusion leukocytes and microaggregates capacities
from one unit of packed red blood
User error
cells or whole blood, used when
giving blood products to the Blood incompatibility and the requirements of
patient ISO 10993: Biological Evaluation of Medical
Devices
Cell salvage Designed for the filtration of salvaged
blood, to remove potentially
Compatibility of the product when exposed to
harmful microaggregates,
circulating blood and infections
leukocytes and lipid particles Shelf life
These stringent criteria aim to ensure the production
bubble traps can reduce this significantly. Table 2.5 of high-quality arterial line filters that will not
gives an overview of the filters most commonly used have any deleterious effects on the CPB circuit or 21
in CPB circuits. patient.
Table 2.6. Different commercially available arterial line filters, both external and integrated
Suckers and Vents (LV) apex can be associated with particularly serious
consequences including:
The suckers allow spilled blood from the operative
field to be returned to the circuit via the reservoir, but LV wall rupture if inadequately closed
they can also be used to help salvage emergency Damage to the LV wall due to excessive suction
situations. In case of life-threatening, excessive bleed- Embolization through air entrained into the LV
ing before venous cannulation has been established, through the vent site.
the suckers can be used to scavenge blood to the
venous reservoir and subsequently be transfused back Cardioplegia Delivery Systems
into the patient via the arterial line. This is commonly One of the major concerns during cardiac surgery is
known as “sucker bypass” and grants the surgeon protection of the myocardium during procedures.
time to attempt to fix the problem at least Cardioplegia solution is administered to maintain
temporarily. controlled and protected electrical arrest of the myo-
“Vent” suckers are used to drain blood from the cardium during the ischemic period. Chapter 11 is
left ventricular cavity, typically via these sites: dedicated to myocardial protection techniques.
Aortic root Regardless of the type of cardioplegia delivery
Right superior pulmonary vein device, monitoring of temperature, appropriate deliv-
Left atrium or pulmonary artery ery pressure, and time intervals between doses are
Left ventricle critical to the success of the operation.
Left ventricular apex Cardioplegia delivery systems typically include a
line for pressure monitoring, an over-pressure relief
The main reasons for venting the heart during CPB
valve, and a recirculation line for easy priming or de-
are to:
airing. Pressure monitoring is essential when deliver-
prevent distension of the heart ing cardioplegia into small vessels and the coronary
evacuate air from the cardiac chambers during the sinus to prevent damage. An air detection device is
de-airing phase of the procedure often added to the infusion line for additional protec-
improve surgical exposure tion against microemboli. Most cardioplegia delivery
reduce myocardial rewarming systems today have their own dedicated integrated
create a dry surgical field. heat exchanger. This heat exchanger and accompany-
There are complications associated with all sites used ing water lines are separate from the oxygenator since
for venting, most commonly relating to injury to cardioplegia is typically delivered at temperatures
22 much colder than the patient’s core temperature.
tissues at the site. Venting via the left ventricular
filtered and their level should be monitored when caused by CPB, mainly through minimizing circuit
using a hemoconcentrator. size, introducing biocompatible surfaces where
possible and reducing prime volume to as little
Miniaturized Extracorporeal as 500 ml. As promising as the concept sounds, it
has not yet found its way into mainstream
Circulation (MiECC) clinical practice. MiECC is discussed in detail in
There has been increasing interest in miniaturized Chapter 8.
bypass circuits. Their aim is to decrease the trauma
24
25
Table 3.1. Summary of Class I recommendations CPB Table 3.2. Recommended extracorporeal circuit parameters for
monitoring parameters from the 2019 EACTS/EACTA/ Standards of Monitoring and Safety during CPB by the Society of
EBCP guidelines Clinical Perfusion Scientists of Great Britain and Ireland and the
American Society of ExtraCorporeal Technology Standards and
It is recommended that pressure monitoring devices are Guidelines for Perfusion Practice.
used on the arterial line and cardioplegia delivery
systems during CPB. Oxygen saturation of the blood in the arterial line
A bubble detector is recommended during CPB Oxygen saturation of the blood in the venous return line
procedures on all inflow lines. The flow of the blood to the patient (best measured
It is recommended to use a level sensor during CPB after shunt lines with a separate flow meter)
procedures utilizing a (hard-shell) reservoir. Arterial line pressure (preferably before AND after the
Continuous arterial line pressure monitoring oxygenator)
(preoxygenator and postoxygenator) in the CPB Gas flow and oxygen fraction to the oxygenator
circuit is recommended.
Venous occlusion percentage
Continuous oxygenator arterial outlet temperature
Oxygen concentration in the gas to the oxygenator
monitoring is recommended.
Level sensor during CPB procedures utilizing (hard-shell)
It is recommended to continuously monitor SvO2 and
reservoir
HCT levels during CPB.
Cardioplegia dose, delivery method, line pressure
Monitoring of blood gas analyses through regular
(antegrade), coronary sinus pressure (retrograde), and
intervals or continuous observation is recommended
ischemic intervals
during CPB.
Blood temperature at the arterial outlet and venous inlet
It is recommended to objectively report, adequately
of the oxygenator
record and properly analyse all adverse events related
to CPB practice in an efficient and timely manner. Water temperature in the heater-cooler system
It is recommended that the perfusionist collect data Anticoagulation – Activated Clotting Time (ACT)
concerning the conduct of perfusion via a clinical
Arterial blood gases (regularly or continuously)
registry or database and use such data to actively
containing the following measurements:
participate in institutional and departmental quality
assurance and improvement programmes. pH
It is recommended that the venous line pressure be pCO2
monitored when using assisted venous drainage. pO2
SaO2
HCO3
supply and exchange, together with an oxygen analyzer Base excess
to display the O2 concentration delivered at any point in
Haemoglobin (Hb)
time, is mandatory. Volatile anesthetics may also be used
via the heart lung machine gas delivery system during Haematocrit (HCT)
CPB to maintain anesthesia and/or as an adjunct to Potassium
blood pressure control. A scavenging system for waste
Sodium
anesthetic gases is recommended as being mandatory in
many countries, as volatile anesthetic agent waste is a Glucose (or other point-of-care device)
risk to staff. The end-tidal anesthetic gas concentration Lactate
can be monitored at the oxygenator exhaust port.
rectum, pulmonary artery, jugular bulb, arterial Table 3.3. 2015 STS/SCA/AmSect Clinical Practice Guidelines on
temperature monitoring during CPB
inflow, and venous return. Nasopharyngeal, jugular
bulb and arterial inflow temperature give an estimate CLASS I RECOMMENDATIONS
of cerebral temperature. Due to its invasive nature
The oxygenator arterial outlet blood temperature is
and cumbersome placement, jugular bulb probes are recommended to be utilized as a surrogate for
rarely used and the oxygenator arterial outlet blood cerebral temperature measurement during CPB. (Class
temperature is recommended as the surrogate for I, Level C)
cerebral temperature. Oxygenator inlet and outlet
To monitor cerebral perfusate temperature during
temperatures are measured using thermistors.
warming, it should be assumed that the oxygenator
Monitoring the temperature of the arterial blood arterial outlet blood temperature under-estimates
delivered to the body and of venous return blood cerebral perfusate temperature. (Class I, Level C)
helps to protect sensitive organs such as the brain
and to confirm adequacy of cooling and rewarming. Surgical teams should limit arterial outlet blood
temperature to <37°C to avoid cerebral
A temperature gradient of less than 10°C between
hyperthermia. (Class 1, Level C)
arterial outlet and venous inlet is recommended
during cooling to avoid cerebral injury, generation Temperature gradients between the arterial outlet and
of gaseous emboli or outgassing when blood is venous inflow on the oxygenator during CPB cooling
returned to the patient. Maintaining a low gradient should not exceed 10°C to avoid generation of
gaseous emboli. (Class 1, Level C)
between inflow and outflow temperature is equally
important during rewarming from hypothermia as a CLASS IIa RECOMMENDATIONS
fast temperature rise is associated with poor neuro- Pulmonary artery or nasopharyngeal temperature recording
logical outcomes. The perfusate temperature to the is reasonable for weaning and immediate post-bypass
body should not exceed 37°C. temperature measurement. (Class IIa, Level C)
The measurement accuracy of the thermistors is Rewarming when arterial blood outlet temperature 30°C:
affected by their immersion depth. The recommenda- i. To achieve the desired temperature for separation from
tions with regard to temperature monitoring during bypass, it is reasonable to maintain a temperature
CPB published in the 2015 STS/SCA/AMSECT gradient between arterial outlet temperature and the
Clinical Practice Guidelines are summarized in venous inflow of 4°C. (Class IIa, Level B)
Table 3.3. ii. To achieve the desired temperature for separation from
bypass, it is reasonable to maintain a rewarming rate of
0.5°C/min. (Class IIa, Level B)
Pressure Rewarming when arterial blood outlet temperature
Adequate blood pressure is one of the factors neces- <30°C: To achieve the desired temperature for
sary for adequate perfusion of vital organs. It is gen- separation from bypass, it is reasonable to maintain a
erally agreed that in most cases a mean systemic maximal gradient of 10°C between arterial outlet
arterial pressure (MAP) of 50–80 mmHg provides temperature and venous inflow. (Class IIa, Level C)
sufficient end-organ perfusion while cerebral autore-
gulation is preserved.
Circuit pressures are monitored primarily for safety
reasons, in order to avoid over-pressurization and the vasculature, coronary ostia or coronary sinus,
potential for circuit disconnection, cannula dislodge- depending on the route of delivery. The most com-
ment or vascular and tissue injury. Monitoring of cir- monly used mode of giving cardioplegia is antegrade,
cuit line pressure can also provide an indication of directly into the aortic root proximal to the aortic cross-
adequate positioning of cannulae, in particular ensuring clamp or into the coronary ostia at a line pressure of
that the aortic cannula is correctly positioned to avoid 80–150 mmHg. Retrograde cardioplegia is adminis-
dissection. Both pre- and post-oxygenator monitoring tered via a catheter in the coronary sinus, using a flow
is recommended to detect changes in transmembrane of 200–400 ml/min to a coronary sinus pressure of
pressure, as rises may indicate platelet deposition/aggre- between 30 and 80 mmHg.
gation within the oxygenator. Cardioplegia line pres- Servo regulation of pump flow rate coupled to 27
sure monitoring may avoid injury to the coronary pressure limits is an important safety feature of the
HLM. The higher limit has to be set in a way that Low Level and Air Bubble Detection
stops the pump causing injury at the cannulation site,
Heart lung machines have alarm systems embedded
generally at <250 mmHg. Cardioplegia pressure is
within monitoring on the display panel of the HLM.
typically limited at lower pressures, depending on
Alarms either provide an audible and/or visual indi-
the route of delivery (<150 mmHg antegrade and
cation to the perfusionist or, more critically, can
<80 mmHg retrograde).
adjust or entirely stop pump flow if necessary when
The negative pressure inside the venous reservoir
servo-regulated. Checking alarm levels and function-
is monitored when either vacuum-assisted venous
ality is part of the pre CPB checklist; alarms must be
drainage (VAVD) or kinetic-assisted venous drainage
engaged prior to the initiation of CPB.
(KAVD) is used. The vacuum is typically adjusted in a
The low level alarm is a critical safety feature on
way that the negative pressure does not exceed
the HLM. A sensor on the venous reservoir is placed
30mmHg in order to reduce hemolysis and the risk
at a level below which there is the danger of emptying
of air entrainment into the venous line or across the
the reservoir and entraining air into the arterial cir-
membrane oxygenator. The latter can potentially lead
culation (see Figure 3.1a). If triggered, the servo regu-
to serious harm to the patient through gaseous arter-
lation will stop or significantly reduce the flow rate of
ial micro emboli or massive arterial embolization.
the arterial pump in addition to sounding an acoustic
Negative pressure in the venous line during kinetic-
alarm. The pump will only resume flow once the fluid
assisted venous drainage should not exceed ‒80
level is above the sensor again. Ultrasonic air bubble
mmHg to avoid cavitation and hemolysis. Other cir-
detectors on the arterial side of the HLM operate in
cuit pressures monitored may include antegrade or
the same way to protect against gross air embolism
retrograde cerebral perfusion with servo regulation
(see Figure 3.1b). Both alarm systems received a Class
limits around 150 mmHg for antegrade and
I recommendation in the 2019 EACTS/EACTA/
80 mmHg retrograde.
EBCP guidelines.
Circuit pressures are usually monitored using
Bubble detectors may also be used in the cardio-
reusable electronic transducers, where the fluid is
plegia line, and the venous line in minimized
28 isolated from the transducer by a dedicated disposable
CPB circuits. Although contemporary equipment,
circuit component.
Similar to the more advanced devices above, they lack improved neurocognitive function in patients under-
in accuracy but are valuable tools for observing and going NIRS based algorithms to improve oxygen
recording trends. supply/demand ratio, recent randomized trials and a
As a minimum, it is recommended to continu- recently published meta-analysis and systematic
ously monitor SvO2 and Hct and perform full blood review showed no clinical benefit. Cerebral saturation
gas analyses at regular intervals throughout the dur- monitoring is discussed in more detail in Chapter 18
ation of CPB (Class I recommendation, 2019 EACTS/ and its clinical application in Chapter 9.
EACTA/EBCP guidelines).
Oxygen Delivery and Carbon
Cerebral Oxygen Saturation Dioxide Extraction
Adverse cerebral outcomes after cardiac surgery are Oxygen delivery (DO2) is determined by hemoglobin,
associated with increased mortality, prolonged ICU
arterial blood flow, oxygen saturation and PaO2.
and hospital stay and the use of additional healthcare
Many current HLM monitors are able to continuously
resources. Continuous monitoring of cerebral oxygen
calculate and display DO2 during CPB. Alternatively
saturation may provide a tool to detect an imbalance
it can be calculated manually from reference charts.
between cerebral oxygen demand and supply and may
Evidence from a randomized trial and multicenter
decrease the likelihood of intraoperative cerebral injury.
registry data shows that a goal-directed perfusion
Near-infrared spectroscopy (NIRS) can be used to
strategy to maintain oxygen delivery index (DO2i)
monitor cerebral oxygen saturation during cardiac sur- during CPB > 280 mL/min/m2 reduces the incidence
gery. Self-adhesive sensors containing the infrared light of acute kidney injury following cardiac surgery.
source and detectors are placed on one or both sides of the
forehead. Cerebral desaturation is defined as a 20% reduc-
tion from baseline values or an absolute decrease below Anticoagulation Monitoring
50% taking the duration of desaturation into account. Systemic heparinization is required for CPB to avoid
The evidence regarding its clinical benefit is how- coagulation due to contact activation and stasis in the
30
ever contradictory. Although early studies showed reservoir or the operating field. Safe anticoagulation is
ascertained by measuring the activated clotting time need for temporary atrial or ventricular pacing.
(ACT), which is generally done in the operating Pulmonary artery catheter – although not used rou-
theater. The ACT is a highly unspecific whole blood tinely in many parts of the world, the PAC may be
coagulation assay and is influenced by factors such as used to provide assessments of cardiac output and
temperature, hematocrit, fibrinogen level and platelet pulmonary artery pressure, which may help guide
count or function. The majority of centers around the inotropic support during separation from CPB.
world target ACT values between 450 and 550 Transesophageal echocardiography – TEE is
seconds. The ACT is typically measured every 20–30 widely used in cardiac surgery. Recent guidelines by
minutes and recorded in the perfusion record. the American Society of Anesthesiologists and the
The 2018 STS/SCA/AMSECT Clinical Practice Society of Cardiovascular Anesthesiologists recom-
Guidelines recommend as Class 1 evidence that “a mend that, in the absence of contraindications,
functional whole blood test of anticoagulation, in the intraoperative TEE be performed in all cardiac valve
form of a clotting time, should be measured and should and thoracic aortic procedures (Class 1) and is rea-
demonstrate adequate anticoagulation before initi- sonable for CABG operations (Class IIa). The advan-
ation of, and at regular intervals during cardiopul- tages in the use of TEE prior to CPB include
monary bypass. (Level of Evidence C)”
confirming the preoperative diagnosis,
Furthermore, a Class IIa recommendation in the
same publication states “it is reasonable to maintain detecting undiagnosed pathologies,
activated clotting time above 480 seconds during CPB. confirming the success of surgical intervention,
However, this minimum threshold value is an approxi- particularly in valve repairs and replacements,
mation and may vary based upon the bias of the confirming appropriate de-airing after open
instrument being used. For instruments using ‘max- chamber surgery and
imal activation’ of whole blood or microcuvette tech- guiding inotrope management by continuous
nology, values above 400 seconds are frequently assessment of left and right ventricular function.
considered therapeutic. (Level of Evidence C)”
It is important to note that ACT devices from
different manufacturers must not be used inter- Documentation of Intraoperative
changeably. Anticoagulation during cardiopulmonary Monitoring Data: The Cardiopulmonary
bypass is discussed in detail in Chapter 6.
Bypass Record
The CPB or perfusion record is a legal record and
Hemodynamic Monitoring should therefore be accurate and legible. Historically,
Assessment of myocardial function is important both the perfusion record had been handwritten, with the
pre CPB and during separation from CPB. perfusionist documenting physiological parameters
Hemodynamic monitoring includes the electrocar- and heart lung machine values. Typically, this
diogram (ECG), pulmonary artery catheter (PAC) happened every 5–10 minutes, when changes
and transesophageal echocardiography (TEE). occurred or when events or interventions (e.g., drug
Electrocardiogram – ECG monitoring is one of administration) required documentation. A manual
the minimum monitoring requirements during anes- record will always be a snapshot of what occurs
thesia. Although native cardiac function is unneces- during bypass and may be incomplete or inaccurate,
sary during CPB, the ECG can provide important with errors able to be introduced in a number of ways.
clues to These inadequacies include missing data, biased
efficacy of initial cardioplegia delivery by recording, transcription error and subjectivity of
broadening QRS complexes and the appearance of observation. There are a number of systems that are
towering T waves, able to generate an electronic record with the aid of
adequacy of myocardial protection by showing data collection software. They provide automatic data
signs of electrical activity, acquisition and integrate data from the HLM and
early signs of ischemia (ST segment changes or other monitoring systems in the operating room,
ventricular tachyarrhythmias) after cross-clamp most importantly the anesthetic, hemodynamic
removal or before weaning off CPB and
31
monitoring (Figure 3.4). As the number of monitors
in the operating room increases, the operating team Scientists of Great Britain and Ireland for Standards
needs to observe, record, and respond to more and of Monitoring and Safety during CPB and is a Class
more data. Where this is recorded automatically, the IIa recommendation in the 2019 EACTS/EACTA/
perfusionist and the anesthesiologist are less dis- EBCP guidelines. Comprehensive records also pro-
tracted and more able to concentrate on the patient vide individual departments with the ability to define
rather than on documenting the procedure. The CPB quality metrics based on institutional guidelines.
integrity of the data from automatic data acquisition
removes the bias that is inherent in the manual
record. Application of Electronic Perfusion Data
Apart from creating a record of the patient and Generating an accurate perfusion record is only one
heart lung machine physiological parameters, these component of the value that can be gained from
products provide documentation of CPB equipment, automated electronic perfusion data collection
priming solutions, fluid balance, coagulation and systems. The data provide an enormous resource for
blood gas values, cardioplegia and drug administra- ongoing research activities and quality management.
tion. Electronic perfusion data collection, including The importance and benefits of quality assurance and
32 the ability to produce a printout, is a general recom- quality improvement in healthcare delivery are well
mendation of the Society of Clinical Perfusion recognized. The collected data can be used to monitor
and improve quality of care processes and to report glucose, arterial outlet temperature, and blood gas
practices at an individual or institutional level, or to management during CPB utilizing electronic data.
facilitate multicenter reporting through participation These benchmarks provide a baseline for the imple-
in a CPB registry. mentation of multicenter continuous quality
improvement processes for perfusion practice. By
Registry examining CPB data and related outcomes, registries
have been able to define risk factors associated with
Some examples of CPB registries include the
adverse outcomes.
Northern New England Cardiovascular Disease
One of the problems inherent in determining
Study Group, the Australian and New Zealand
relationships between CPB parameters and the clin-
Collaborative Perfusion Registry (ANZCPR) and the
ical measures of outcomes is the low rate of adverse
PERFORM registry (USA), which is an integral part
events, resulting in the requirement of large cohorts
of the Michigan Society of Thoracic and
to achieve adequate and statistically well powered
Cardiovascular Surgeon Quality Collaborative’s pro-
studies. Amalgamation of collected data provides a
gram. Electronic data collection meets the needs of
means to increase cohort size and therefore reduce
registry endeavors because it provides a method of
the confounding effects of variations in patient risk
transferring de-identified data from multiple sites,
factors and practice changes over time. Registry data
integration of this data into a central database, and a
also play an important role in confirming the gener-
means to generate calculated CPB parameters and
alizability of results of clinical studies and in recom-
perform complex data analysis. The ANZCPR has a
mending them for implementation into clinical
defined process of core metrics and uses these to
practice.
calculate benchmarks for the management of blood
33
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