1. The document describes a case of a 28-year-old female with cyanotic congenital heart disease who underwent an arterial switch operation with integrated ECMO support.
2. ECMO is a form of extracorporeal life support used for both cardiac and respiratory failure in adults. It involves pumping blood out of the body to an artificial lung for gas exchange before returning it to circulation.
3. The key components of an ECMO circuit include a blood pump, membrane oxygenator, tubing, heat exchanger, and monitoring equipment. Proper anticoagulation and flow rates are important for safety and effectiveness.
Utilizacion del ECMO en el distress respiratorio. Presentacion de sesiones cientificas del departamento de cirugia cardiaca de la clinica universidad de navarra
Utilizacion del ECMO en el distress respiratorio. Presentacion de sesiones cientificas del departamento de cirugia cardiaca de la clinica universidad de navarra
PowerPoint presentation on ECMO (Extracorporeal Membrane Oxygenation). Part 2 focuses on Monitoring ECMO patients
Ventilatory strategies, Sedation and pain control, Weaning, Complications and recent advances in ECMO. For better understanding please have a look at ECMO part 1 before going through part 2.
A brief yet comprehensive coverage of ICU role in ECMO cases. Presentation has been prepared in order to help ICU fellows and registrars to understand the importance of their role and to know necessary actions they have to take in case of need.
This workshop will outline the basic principles of extracorporeal life support made easy by key-experts in the field. During the course delegates will gain a good understanding of ECMO in the following areas: Theoretical concepts, basic physiology and pathophysiology, cardiac and respiratory support and monitoring, alarm settings and monitoring, role of cardiac ultrasound during ECMO, newest technologies, circuits and devices, practical hands-on sessions and simulations.
ECMO, DEFINITION, ETIOLOGY, INDICATION, CONTRAINDICATION, TYPES OF ECMO, VENOVENOUS ECMO, VENO ARTERIAL ECMO, NURSING CARE OF PATIENT ON ECMO, WEANING FROM ECMO,
PowerPoint presentation on ECMO (Extracorporeal Membrane Oxygenation). Part 2 focuses on Monitoring ECMO patients
Ventilatory strategies, Sedation and pain control, Weaning, Complications and recent advances in ECMO. For better understanding please have a look at ECMO part 1 before going through part 2.
A brief yet comprehensive coverage of ICU role in ECMO cases. Presentation has been prepared in order to help ICU fellows and registrars to understand the importance of their role and to know necessary actions they have to take in case of need.
This workshop will outline the basic principles of extracorporeal life support made easy by key-experts in the field. During the course delegates will gain a good understanding of ECMO in the following areas: Theoretical concepts, basic physiology and pathophysiology, cardiac and respiratory support and monitoring, alarm settings and monitoring, role of cardiac ultrasound during ECMO, newest technologies, circuits and devices, practical hands-on sessions and simulations.
ECMO, DEFINITION, ETIOLOGY, INDICATION, CONTRAINDICATION, TYPES OF ECMO, VENOVENOUS ECMO, VENO ARTERIAL ECMO, NURSING CARE OF PATIENT ON ECMO, WEANING FROM ECMO,
Shay McGuinness talks about what ECMO is, the history of its use in New Zealand and how their ECMO retrieval system works there. This was recorded live at the inaugural ICN NZ meeting, with support from ANZICS NZ.
Veno-Arterial Ecmo (VA-ECMO) & Their basicGunalan M.M
VA ECMO stands for Venoarterial Extracorporeal Membrane Oxygenation. It's a life-saving medical procedure used in critical situations where the heart and lungs are unable to function adequately. VA ECMO involves diverting blood from the body, oxygenating it outside the body, and then returning it to the arterial system, effectively bypassing the heart and lungs. This allows time for the organs to rest and heal, supporting patients with severe cardiac or respiratory failure.
New Drug Discovery and Development .....NEHA GUPTA
The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
263778731218 Abortion Clinic /Pills In Harare ,sisternakatoto
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Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
2. CASE:
• 28 YR OLD FEMALE WITH
• PREOPERATIVE PROFILE: H/O CYANOSIS SINCE BIRTH WITH RECURRENT LRTI,CLUBBING+,SPO2 ON
ROOM AIR-58%,BSA=1.4 SQ MTR
• DIAGNOSIS OF CCHD,INC Qp, d-TGA,LARGE OS-ASD(BIDIRECTIONAL SHUNTING),NO VSD,SEV PAH,
BVFNL,NO CLOT/VEG/PE,NSR, 2D ECHO-TRIVIAL TR/PR, RVSP=RAP+80, Ao/Laes=28/30,
Lves/Lved=25/40, Lves/PW(LV)ed=8/8,EF=65%, NO AS/COA/PDA, B/L CONFLUENT PA,D SHAPED LV, LV
MASS=57 GM,LV MASS INDEX=42 GM/SQ CM,
• LV ANGIO:LVSP= 57 mmHg LESS THAN 2/3 OF RVSP=101 mmHg
• CECT: CORONARIES ARISING FROM SEPARATE FACING PA’s,MULTIPLE APC’s, LEFT AORTIC ARCH WITH
BOVINE BRANCHING PATTERN, AP COMPRESSION OF LEFT PROXIMAL BRONCHUS BY DILATED LPA.
• ASO WITH INTEGRATED ECMO, AoClX=70 MINS.
17. HISTORY OF ECMO
• ECLS / development of the heart-lung machine BY Dr. John H. Gibbon Jr.
• ECMO was introduced for the treatment of severe acute respiratory
distress syndrome (ARDS) in the 1970s.
• Dr. Theodore Kolobow - flow patterns in the membrane lung, method of
layering silicone and the design of vascular access catheters
• There was revival of interest only after Dr. Robert H. Bartlett in 1976
reported the first neonatal ECMO survivor, baby Esperanza.
• an ECMO registry was established in 1980 at the University of Michigan.
• Dr. John Toomasain in 1984 created the Neonatal ECMO Registry.
• In 1989, charter for Extracoporeal Life Support Organization (ELSO) was
formed with the purpose of stimulating multi-institutional research in the
field of acute lung injury and its therapy.
18. Uses of extracorporeal membrane oxygenation
In adults
• Cardiac failure
• Respiratory failure
19. Use and Strategy
Cardiopulmonary Extracorporeal Life Support (ECLS) is indicated in
severe, refractory circulatory failure with reversibility and/or timely,
reasonable therapeutic options.
• 1. There are four primary strategies for ECLS use, depending on the
• therapeutic objective for the patient.
• a) Bridge to recovery (reversible disease),
• b) Bridge to bridge (goal to transition to VAD or oxygenator),
• c) Bridge to organ transplantation
• d) Bridge to decision (providing time for recovery, diagnosis, or
• determination of candidacy for alternative support /transplantation).
20. Use of extracorporeal life support for cardiac failure should be
considered for patients with evidence of inadequate end organ perfusion
and oxygen delivery resulting from inadequate systemic cardiac output.
a) Hypotension despite maximum doses of two inotropic or vasopressor
medications.
b) Low cardiac output with evidence of end organ malperfusion despite
medical support
c) Low cardiac output with mixed venous, or superior caval central venous
(for single ventricle patients) oxygen saturation <50% despite maximal
medical support.
d) Low cardiac output with persistent lactate >4.0 and persistent upward
trend despite optimization of volume status and maximal medical
management.
21. ACUTE CARDIAC FAILURE: INDICATIONS
I. Patient condition
A. Indication for ECMO in adult cardiac failure is cardiogenic shock:
1. Inadequate tissue perfusion manifested as hypotension and low cardiac
output despite adequate intravascular volume.
2. Shock persists despite volume administration, inotropes and
vasoconstrictors, and intraaortic balloon counterpulsation if appropriate.
3. Typical causes: Acute myocardial infarction, Myocarditis, Peripartum
Cardiomyopathy, Decompensated chronic heart failure, Post cardiotomy
shock.
4. Septic Shock is an indication in some centers
22. ….INDICATIONS (CONTD….)
• Options for temporary circulatory support
Surgical temporary VAD: Abiomed, Levitronix
Percutaneous VAD:TandemHeart, Impella
• ECMO: Advantages: Biventricular support, bedside immediate application,
oxygenation,Biventricular failure, Refractory malignant arrythmias, Heart
failure with severe pulmonary failure
• ECMO is a bridge to…
Recovery: Acute MI after revascularization, Myocarditis, Postcardiotomy
Transplant: Unrevascularizable acute MI, Chronic heart failure
Implantable circulatory support: Ventricular assist devices….
Surgical temporary VAD: Abiomed, Levitronix
Percutaneous VAD: TandemHeart, Impella
23. Contraindications to ECMO
1. Absolute:
• Unrecoverable heart and not a candidate for transplant or VAD,
• Advanced age,
• Chronic organ dysfunction (emphysema, cirrhosis, renal failure),
• Compliance (financial, cognitive, psychiatric, or social limitations),
• Prolonged CPR without adequate tissue perfusion.
2. Relative:
• Contraindication for anticoagulation,
• Advanced age,
• Obesity.
24. Vascular Access
• A. Postcardiotomy
• Intrathoracic cannulae: ensure site hemostasis, Patch chest open for
frequent exploration.
• B. Non-postcardiotomy
• Percutaneous femoral artery and vein, Typically most rapid access, 15-21 Fr
arterial, 21-28 Fr venous (advance to right atrium if possible).
• Percutaneous jugular vein, 21-28 Fr to right atrium,
• Common carotid via surgical exploration……10-15% watershed cerebral
infarction with carotid ligation, 8-10 mm end to side polyester graft
• Femoral arterial cannulation associated with ipsilateral leg ischemia,
• Percutaneous distal cannulation of superficial femoral artery (may require
ultrasound or fluoroscopic guidance),
• Surgical exploration of superficial femoral artery,
• Surgical exploration of posterior tibial artery 8Fr retrograde cannula.
25. Extracorporeal membrane oxygenation
indication indices for >80% predicted mortality
Likely to die (predicted 80% mortality)
• Oxygenation Index (OI) > 40 or > 35 for 4 hours {{OI = (MAP × FiO2 ×
100) / PaO2}}
• Ventilation Index (VI) > 90 for 4 hours {{VI = RR × PIP – PEEP/1000}}
• Alveolar–arterial oxygen difference [(A − a)DO2] >600 − 624 mmHg (at
sea level) despite 4–12 hours of medical management
(A − a)DO2 = [atmospheric pressure – 47] – (PaCO2 + PaO2)/FiO2
• PaO2 < 50 mmHg for 2–12 hours (FiO2 of 100%)
• Acute deterioration PaO2: < 30–40 mmHg (FiO2 of 100%)
• pH < 7.25 for 2 hours
• Intractable hypotension
27. The circuit is planned to be capable of total support for the patient
involved. Access is always venoarterial. The circuit components are
selected to support blood flow 3 L/m2/min.
• a) Neonates 100 cc/kg/min
• b) Infants and children 80 cc/kg/min
• c) Adults 60 cc/kg/min
2. The best measure of adequate systemic perfusion is a circuit mixed
venous saturation greater than 70%
28. CIRCUIT COMPONENTS
The basic circuit includes a
• blood pump,
• a membrane lung,
• conduit tubing.
• heat exchanger,
• monitors,
• alarms.
29. BLOOD PUMP
modified roller with inlet pressure control/ centrifugal / axial rotary pump with
inlet pressure control/ peristaltic pump).
• a) Inlet (suction) pressure. With the inlet line occluded, the suction pressure should not
exceed -300 mmHg. The inlet pressure can be very low (-300 mmHg) when the venous
drainage is occluded (chattering) which causes hemolysis. Inlet pressure in excess of -300
mmHg can be avoided by inherent pump design or through a servocontrolled pressure
sensor on the pump inlet side.
• b) Outlet pressure. With the outlet line occluded, the outlet pressure should not exceed
400 mm/Hg (inherent in the pump design or by a servocontrolled system).
• c) Power failure. The pump should have a battery capable of at least one-hour operation,
and a system to hand crank the pump in the event of power failure. The pump and circuit
should have a mechanism to alarm for or prevent reverse flow (arterial to venous in the
VA mode) if the power fails.
• d) Hemolysis. The plasma hemoglobin should be less than 10 mg/dl under most
conditions.
30. Membrane lung (Oxygenator)
• A)silicone rubber,/a microporous hollow-fibre (e.g. polypropylene), /
a solid hollow-fibre membrane (e.g. polymethylpentene
• b) Membrane surface area and mixing in the blood path determine
the maximum oxygenation, described as “rated flow” or “maximal
oxygen delivery”.
• c) Rated flow is the blood flow rate at which venous blood (saturation
75%, Hb 12 g/dl) will be fully saturated (95%) at the outlet of the
membrane lung. Maximal O2 delivery is the amount of oxygen
delivered per minute when running at rated flow.
• d) This is calculated as outlet minus inlet O2 content (typically 4-5
cc/dL, same as the normal lung) times blood flow.
31. Sweep gas
a) The sweep gas can be 100% oxygen, carbogen (5% CO2, 95% O2)
or a mixture of oxygen and compressed room delivered via an oxygen-
air blender.
b) The initial sweep gas flow rate is usually equal to the blood flow rate
(1:1).
c) Increasing the sweep flow will increase CO2 clearance but will not
affect oxygenation.
d) Water vapor can condense in the membrane lung resulting in poor
CO2 clearance, and may be cleared by intermittently increasing sweep
gas flow to a higher flow.
32. Priming the circuit
a) Isotonic electrolyte solution resembling normal extracellular fluid
including 4-5 mEq/L potassium. The prime is circulated through a
reservoir bag until all bubbles are removed.
b) Before attaching the circuit to the patient, the water bath is turned
on to warm the fluid.
33. HEAT EXCHANGER
• Heat exchangers require an external water bath, which circulates
heated (or cooled) water through the heat exchange device.
a) In general, the temperature of the water bath is maintained <40º
Celsius, and usually at 37º.
b) Contact between the circulating water and the circulating blood is very
rare, but should be considered if small amounts of blood or protein are
present in the circulating water, or if unexplained hemolysis occurs.
c) The water in the water bath is not sterile and may become
contaminated. The water bath should be cleaned and treated with a
liquid antiseptic from time to time.
34. MONITORS
a) Monitoring of blood flow is by direct measurement using an ultrasonic detector, or calculated
based on pump capacity and revolutions per minute for a roller pump using standardized tubing.
b) Pre- and post- membrane lung blood pressure measurements can include maximum pressure servo
regulation control to avoid over pressuring.
c) Pre- pump venous drainage line pressure (to avoid excessive negative suction pressure by the pump)
can be used as a servo regulation system to prevent excessive suction.
d) Pre- and post- membrane lung oxyhemoglobin saturation measurements: The venous oxyhemoglobin
saturation is a valuable parameter for managing and monitoring both circuit and patient factors related
to oxygen delivery and consumption. The post membrane lung saturation monitor will determine if the
membrane lung is working at rated flow, and if function is deteriorating. Blood gases are measured from
pre-oxygenator and post-oxygenator sites either by continuous on line monitoring or batch sampling. The
primary purpose of measuring blood gases (as opposed to online saturation) is to determine the inlet
and outlet PCO2 to evaluate membrane lung function, and blood pH to determine metabolic status.
e) Circuit access for monitors, blood sampling, and infusions. Luer connectors and stopcocks provide
access to the blood in the circuit.
35. ALARMS
a) Pre- and post- membrane lung pressure alarms. These
measurements will determine the transmembrane lung pressure
gradient. Clotting in the oxygenator is represented by increasing
membrane lung pressure gradient.
b) Many centers use a bubble detector on the blood return line.
Pressure and bubble detector alarms can be used to clamp lines and
turn the pump on or off to automate these safety factors.
36. TUBING AND BRIDGE
• Internal diameter in inches is:
(1) 3/16: 1.2 L/min;
(2) ¼: 2.5 L/min;
(3) 3/8: 5 L/min;
(4) ½: 10 L/min
c) A “bridge” between the arterial and venous lines close to the patient
is a useful circuit component, particularly for periods off bypass during
VA access, during weaning, or during an emergency. However, when
clamped the bridge is a stagnant area that can contribute to
thrombosis and possibly infection. In general, if a bridge is used, it
should be maintained closed during most of the ECLS run, with a
system for purging the bridge of stagnant blood when it is not in use.
37. Anticoagulation on ECMO
• Heparin is required after arterial and venous cannulation, 100 IU/kg
bolus followed by infusion of 125 IU/kg/hour to maintain an ACT at
180–200 s.
42. Targets on veno-venous extracorporeal
membrane oxygenation
• SaO2 - 85–95%
• PaO2 - 45–55 mmHg
• Hematocrit >5% of normal baseline
43. Factors increasing oxygenation on venovenous
extracorporeal membrane oxygenation
• Increasing ECMO flow (no change in systemic flow)
• Decreasing % of recirculated flow
• Increased hemoglobin
• Increased mixed venous oxygen (decreased oxygen consumption)
• Increased cardiac output
44. Advantages of veno-venous extracorporeal
membrane oxygenation
• Avoids ligation of carotid artery
• Thromboembolism to systemic artery avoided
• Decreased risk of neuronal injury
• Decreased potential for ischemic lung injury
• Preserves normal physiological pulsations
45. Variants of veno-venous extracorporeal
membrane oxygenation
• Single site cannulation
• Two site cannulation
• Extracorporeal CO2 removal (ECO2R)
• Tidal flow VV ECMO
46. Indications for conversion from veno-venous
to veno-arterial-venous or veno-arterial
extracorporeal membrane oxygenation
• Inability to maintain systemic perfusion
• Maximal ionotropic support with inadequate systemic pressures
• Poor cardiac function on echocardiogram
• High serum lactate > 8 mmol/l and persistent metabolic acidosis
• Ongoing base excess ≥ -6
• Deterioration of cardiac function
47. O2 exchange (blood flow variables)
Dependent on:
• O2 concentration (driving gradient)
• Blood flow rate
• Blood path thickness
• Membrane surface area
• Membrane diffusion characteristics
• Independent of sweep gas flow