This document summarizes a presentation on hemodynamic monitoring given in 2012. The presentation discusses various technologies for measuring cardiac output both invasively and non-invasively. It compares technologies such as pulse contour analysis, thermodilution, Doppler, and bioreactance. The presentation also summarizes a study evaluating the PulsioFlex device for guiding fluid management decisions.
Minimaly invasive hemodynamic monitoring for hepatic patients Dr.Mahmoud Abbas
Minimaly invasive Cardiovascular monitoring in hepatic patients in the icu lecture presented by Dr Khaled Yassen at the Egyptian African Critical care Summit
Many tools are nowadays available to monitor patients’ hemodynamics in the intensive care unit (ICU) and in the operating room (OR) settings. Some monitoring tools are invasive such as the pulmonary artery catheter (PAC), some others are less invasive such as transpulmonary thermodilution (TPD) systems, some others are called minimally invasive such as uncalibrated arterial pulse wave analysis (PWA) devices, and some others are non invasive such as volume-clamp method, applanation tonometry, esophageal Doppler, bioreactance, CO2 rebreathing, and pulse wave transit time. Recently, the European Society of Intensive Care Medicine has provided recommendations about the use of hemodynamic monitoring in patients with shock. To summarize, except the PAC and the TPD systems, the other hemodynamic monitoring tools are not recommended for the two following reasons: 1) they provide cardiac output but not other important hemodynamic variables, although some of them also provide stroke volume variation (SVV) or pulse pressure variation (PPV), and 2) their validity has been questioned in cases of shock requiring vasopressors. The uncalibrated PWA devices or esophageal Doppler seem to be more suitable in the OR setting when no vasopressor is used. The advantage of the PAC is to provide pulmonary artery pressure and pulmonary artery occlusion pressure. The advantage of TPD systems is to provide global end-diastolic volume (a measure of global cardiac preload), extravascular lung water (a measure of lung edema), pulmonary vascular permeability index (a measure of lung capillary leak), cardiac function index (a measure of systolic cardiac function), PPV and SVV (dynamic indices of fluid responsiveness). The PAC and TPD systems are indicated in cases of shock either when the patient also has a severe ARDS initially or when the shock state does sufficiently respond to the initial therapy administered on the basis of clinical examination, central venous oxygen saturation, carbon dioxide pressure gap, PPV and echocardiography.
Minimaly invasive hemodynamic monitoring for hepatic patients Dr.Mahmoud Abbas
Minimaly invasive Cardiovascular monitoring in hepatic patients in the icu lecture presented by Dr Khaled Yassen at the Egyptian African Critical care Summit
Many tools are nowadays available to monitor patients’ hemodynamics in the intensive care unit (ICU) and in the operating room (OR) settings. Some monitoring tools are invasive such as the pulmonary artery catheter (PAC), some others are less invasive such as transpulmonary thermodilution (TPD) systems, some others are called minimally invasive such as uncalibrated arterial pulse wave analysis (PWA) devices, and some others are non invasive such as volume-clamp method, applanation tonometry, esophageal Doppler, bioreactance, CO2 rebreathing, and pulse wave transit time. Recently, the European Society of Intensive Care Medicine has provided recommendations about the use of hemodynamic monitoring in patients with shock. To summarize, except the PAC and the TPD systems, the other hemodynamic monitoring tools are not recommended for the two following reasons: 1) they provide cardiac output but not other important hemodynamic variables, although some of them also provide stroke volume variation (SVV) or pulse pressure variation (PPV), and 2) their validity has been questioned in cases of shock requiring vasopressors. The uncalibrated PWA devices or esophageal Doppler seem to be more suitable in the OR setting when no vasopressor is used. The advantage of the PAC is to provide pulmonary artery pressure and pulmonary artery occlusion pressure. The advantage of TPD systems is to provide global end-diastolic volume (a measure of global cardiac preload), extravascular lung water (a measure of lung edema), pulmonary vascular permeability index (a measure of lung capillary leak), cardiac function index (a measure of systolic cardiac function), PPV and SVV (dynamic indices of fluid responsiveness). The PAC and TPD systems are indicated in cases of shock either when the patient also has a severe ARDS initially or when the shock state does sufficiently respond to the initial therapy administered on the basis of clinical examination, central venous oxygen saturation, carbon dioxide pressure gap, PPV and echocardiography.
Arterial Blood Gas (ABG)Procedure and Interpretation \Mohammad Al-me`ani. ,...almaani
Arterial Blood Gas (ABG)Procedure and Interpretation
Understand ABG and its terms.
Know some of the indication and contraindications for performing an arterial puncture.
Be able to demonstrate the technique for performing an arterial puncture.
Understand the interpretation of ABG.
Diagnostic guidelines for peripheral arterial diseasePerimed
The aim of this document is to summarize the recommendations and diagnostic guidelines provided by different societies and associations for the assessment of peripheral arterial disease, critical limb ischemia, diabetic foot ulcers and chronic wounds.
A neglected topic for way too long, the interest in fluid therapy seems to be quickly rising as the medical community is making a shift from looking at fluids as a mere method of stabilization towards the appreciation of its relevant side effects.
Many questions remain to be answered indeed:
Is the upgrade from saline 0.9% to balanced crystalloids worth the extra cost?
Does HES still have a place in the OR?
Do we have to fill the gap left by HES on ICU with crystalloids, other colloids or even albumin?
Is it really impossible to avoid fluid overload by using only crystalloids?
Is there still a definitive place for human albumin?
How do we treat and monitor specific patient populations, like patients with trauma, liver failure, brain edema and right heart failure among others?
How do we avoid a one-size-fits-all regimen in perioperative goal-directed therapy?
What with the fluids beyond resuscitation?
And what do the authors of the big fluid trials do in real life themselves?
The 9th International Fluid Academy Day will again be a 1 day concise meeting on all aspects of fluid managament and hemodynamic monitoring in the critically ill.
Date: October 26th 2019, 8:00 - 18:00
A neglected topic for way too long, the interest in fluid therapy seems to be quickly rising as the medical community is making a shift from looking at fluids as a mere method of stabilization towards the appreciation of its relevant side effects.
Many questions remain to be answered indeed:
Is the upgrade from saline 0.9% to balanced crystalloids worth the extra cost?
Does HES still have a place in the OR?
Do we have to fill the gap left by HES on ICU with crystalloids, other colloids or even albumin?
Is it really impossible to avoid fluid overload by using only crystalloids?
Is there still a definitive place for human albumin?
How do we treat and monitor specific patient populations, like patients with trauma, liver failure, brain edema and right heart failure among others?
How do we avoid a one-size-fits-all regimen in perioperative goal-directed therapy?
What with the fluids beyond resuscitation?
And what do the authors of the big fluid trials do in real life themselves?
The 9th International Fluid Academy Day will again be a 1 day concise meeting on all aspects of fluid managament and hemodynamic monitoring in the critically ill.
Date: October 26th 2019, 8:00 - 18:00
A neglected topic for way too long, the interest in fluid therapy seems to be quickly rising as the medical community is making a shift from looking at fluids as a mere method of stabilization towards the appreciation of its relevant side effects.
Many questions remain to be answered indeed:
Is the upgrade from saline 0.9% to balanced crystalloids worth the extra cost?
Does HES still have a place in the OR?
Do we have to fill the gap left by HES on ICU with crystalloids, other colloids or even albumin?
Is it really impossible to avoid fluid overload by using only crystalloids?
Is there still a definitive place for human albumin?
How do we treat and monitor specific patient populations, like patients with trauma, liver failure, brain edema and right heart failure among others?
How do we avoid a one-size-fits-all regimen in perioperative goal-directed therapy?
What with the fluids beyond resuscitation?
And what do the authors of the big fluid trials do in real life themselves?
The 9th International Fluid Academy Day will again be a 1 day concise meeting on all aspects of fluid managament and hemodynamic monitoring in the critically ill.
Date: October 26th 2019, 8:00 - 18:00
A neglected topic for way too long, the interest in fluid therapy seems to be quickly rising as the medical community is making a shift from looking at fluids as a mere method of stabilization towards the appreciation of its relevant side effects.
Many questions remain to be answered indeed:
Is the upgrade from saline 0.9% to balanced crystalloids worth the extra cost?
Does HES still have a place in the OR?
Do we have to fill the gap left by HES on ICU with crystalloids, other colloids or even albumin?
Is it really impossible to avoid fluid overload by using only crystalloids?
Is there still a definitive place for human albumin?
How do we treat and monitor specific patient populations, like patients with trauma, liver failure, brain edema and right heart failure among others?
How do we avoid a one-size-fits-all regimen in perioperative goal-directed therapy?
What with the fluids beyond resuscitation?
And what do the authors of the big fluid trials do in real life themselves?
The 9th International Fluid Academy Day will again be a 1 day concise meeting on all aspects of fluid managament and hemodynamic monitoring in the critically ill.
Date: October 26th 2019, 8:00 - 18:00
A neglected topic for way too long, the interest in fluid therapy seems to be quickly rising as the medical community is making a shift from looking at fluids as a mere method of stabilization towards the appreciation of its relevant side effects.
Many questions remain to be answered indeed:
Is the upgrade from saline 0.9% to balanced crystalloids worth the extra cost?
Does HES still have a place in the OR?
Do we have to fill the gap left by HES on ICU with crystalloids, other colloids or even albumin?
Is it really impossible to avoid fluid overload by using only crystalloids?
Is there still a definitive place for human albumin?
How do we treat and monitor specific patient populations, like patients with trauma, liver failure, brain edema and right heart failure among others?
How do we avoid a one-size-fits-all regimen in perioperative goal-directed therapy?
What with the fluids beyond resuscitation?
And what do the authors of the big fluid trials do in real life themselves?
The 9th International Fluid Academy Day will again be a 1 day concise meeting on all aspects of fluid managament and hemodynamic monitoring in the critically ill.
Date: October 26th 2019, 8:00 - 18:00
A neglected topic for way too long, the interest in fluid therapy seems to be quickly rising as the medical community is making a shift from looking at fluids as a mere method of stabilization towards the appreciation of its relevant side effects.
Many questions remain to be answered indeed:
Is the upgrade from saline 0.9% to balanced crystalloids worth the extra cost?
Does HES still have a place in the OR?
Do we have to fill the gap left by HES on ICU with crystalloids, other colloids or even albumin?
Is it really impossible to avoid fluid overload by using only crystalloids?
Is there still a definitive place for human albumin?
How do we treat and monitor specific patient populations, like patients with trauma, liver failure, brain edema and right heart failure among others?
How do we avoid a one-size-fits-all regimen in perioperative goal-directed therapy?
What with the fluids beyond resuscitation?
And what do the authors of the big fluid trials do in real life themselves?
The 9th International Fluid Academy Day will again be a 1 day concise meeting on all aspects of fluid managament and hemodynamic monitoring in the critically ill.
Date: October 26th 2019, 8:00 - 18:00
A neglected topic for way too long, the interest in fluid therapy seems to be quickly rising as the medical community is making a shift from looking at fluids as a mere method of stabilization towards the appreciation of its relevant side effects.
Many questions remain to be answered indeed:
Is the upgrade from saline 0.9% to balanced crystalloids worth the extra cost?
Does HES still have a place in the OR?
Do we have to fill the gap left by HES on ICU with crystalloids, other colloids or even albumin?
Is it really impossible to avoid fluid overload by using only crystalloids?
Is there still a definitive place for human albumin?
How do we treat and monitor specific patient populations, like patients with trauma, liver failure, brain edema and right heart failure among others?
How do we avoid a one-size-fits-all regimen in perioperative goal-directed therapy?
What with the fluids beyond resuscitation?
And what do the authors of the big fluid trials do in real life themselves?
The 9th International Fluid Academy Day will again be a 1 day concise meeting on all aspects of fluid managament and hemodynamic monitoring in the critically ill.
Date: October 26th 2019, 8:00 - 18:00
A neglected topic for way too long, the interest in fluid therapy seems to be quickly rising as the medical community is making a shift from looking at fluids as a mere method of stabilization towards the appreciation of its relevant side effects.
Many questions remain to be answered indeed:
Is the upgrade from saline 0.9% to balanced crystalloids worth the extra cost?
Does HES still have a place in the OR?
Do we have to fill the gap left by HES on ICU with crystalloids, other colloids or even albumin?
Is it really impossible to avoid fluid overload by using only crystalloids?
Is there still a definitive place for human albumin?
How do we treat and monitor specific patient populations, like patients with trauma, liver failure, brain edema and right heart failure among others?
How do we avoid a one-size-fits-all regimen in perioperative goal-directed therapy?
What with the fluids beyond resuscitation?
And what do the authors of the big fluid trials do in real life themselves?
The 9th International Fluid Academy Day will again be a 1 day concise meeting on all aspects of fluid managament and hemodynamic monitoring in the critically ill.
Date: October 26th 2019, 8:00 - 18:00
A neglected topic for way too long, the interest in fluid therapy seems to be quickly rising as the medical community is making a shift from looking at fluids as a mere method of stabilization towards the appreciation of its relevant side effects.
Many questions remain to be answered indeed:
Is the upgrade from saline 0.9% to balanced crystalloids worth the extra cost?
Does HES still have a place in the OR?
Do we have to fill the gap left by HES on ICU with crystalloids, other colloids or even albumin?
Is it really impossible to avoid fluid overload by using only crystalloids?
Is there still a definitive place for human albumin?
How do we treat and monitor specific patient populations, like patients with trauma, liver failure, brain edema and right heart failure among others?
How do we avoid a one-size-fits-all regimen in perioperative goal-directed therapy?
What with the fluids beyond resuscitation?
And what do the authors of the big fluid trials do in real life themselves?
The 9th International Fluid Academy Day will again be a 1 day concise meeting on all aspects of fluid managament and hemodynamic monitoring in the critically ill.
Date: October 26th 2019, 8:00 - 18:00
A neglected topic for way too long, the interest in fluid therapy seems to be quickly rising as the medical community is making a shift from looking at fluids as a mere method of stabilization towards the appreciation of its relevant side effects.
Many questions remain to be answered indeed:
Is the upgrade from saline 0.9% to balanced crystalloids worth the extra cost?
Does HES still have a place in the OR?
Do we have to fill the gap left by HES on ICU with crystalloids, other colloids or even albumin?
Is it really impossible to avoid fluid overload by using only crystalloids?
Is there still a definitive place for human albumin?
How do we treat and monitor specific patient populations, like patients with trauma, liver failure, brain edema and right heart failure among others?
How do we avoid a one-size-fits-all regimen in perioperative goal-directed therapy?
What with the fluids beyond resuscitation?
And what do the authors of the big fluid trials do in real life themselves?
The 9th International Fluid Academy Day will again be a 1 day concise meeting on all aspects of fluid managament and hemodynamic monitoring in the critically ill.
Date: October 26th 2019, 8:00 - 18:00
A neglected topic for way too long, the interest in fluid therapy seems to be quickly rising as the medical community is making a shift from looking at fluids as a mere method of stabilization towards the appreciation of its relevant side effects.
Many questions remain to be answered indeed:
Is the upgrade from saline 0.9% to balanced crystalloids worth the extra cost?
Does HES still have a place in the OR?
Do we have to fill the gap left by HES on ICU with crystalloids, other colloids or even albumin?
Is it really impossible to avoid fluid overload by using only crystalloids?
Is there still a definitive place for human albumin?
How do we treat and monitor specific patient populations, like patients with trauma, liver failure, brain edema and right heart failure among others?
How do we avoid a one-size-fits-all regimen in perioperative goal-directed therapy?
What with the fluids beyond resuscitation?
And what do the authors of the big fluid trials do in real life themselves?
The 9th International Fluid Academy Day will again be a 1 day concise meeting on all aspects of fluid managament and hemodynamic monitoring in the critically ill.
Date: October 26th 2019, 8:00 - 18:00
A neglected topic for way too long, the interest in fluid therapy seems to be quickly rising as the medical community is making a shift from looking at fluids as a mere method of stabilization towards the appreciation of its relevant side effects.
Many questions remain to be answered indeed:
Is the upgrade from saline 0.9% to balanced crystalloids worth the extra cost?
Does HES still have a place in the OR?
Do we have to fill the gap left by HES on ICU with crystalloids, other colloids or even albumin?
Is it really impossible to avoid fluid overload by using only crystalloids?
Is there still a definitive place for human albumin?
How do we treat and monitor specific patient populations, like patients with trauma, liver failure, brain edema and right heart failure among others?
How do we avoid a one-size-fits-all regimen in perioperative goal-directed therapy?
What with the fluids beyond resuscitation?
And what do the authors of the big fluid trials do in real life themselves?
The 9th International Fluid Academy Day will again be a 1 day concise meeting on all aspects of fluid managament and hemodynamic monitoring in the critically ill.
Date: October 26th 2019, 8:00 - 18:00
A neglected topic for way too long, the interest in fluid therapy seems to be quickly rising as the medical community is making a shift from looking at fluids as a mere method of stabilization towards the appreciation of its relevant side effects.
Many questions remain to be answered indeed:
Is the upgrade from saline 0.9% to balanced crystalloids worth the extra cost?
Does HES still have a place in the OR?
Do we have to fill the gap left by HES on ICU with crystalloids, other colloids or even albumin?
Is it really impossible to avoid fluid overload by using only crystalloids?
Is there still a definitive place for human albumin?
How do we treat and monitor specific patient populations, like patients with trauma, liver failure, brain edema and right heart failure among others?
How do we avoid a one-size-fits-all regimen in perioperative goal-directed therapy?
What with the fluids beyond resuscitation?
And what do the authors of the big fluid trials do in real life themselves?
The 9th International Fluid Academy Day will again be a 1 day concise meeting on all aspects of fluid managament and hemodynamic monitoring in the critically ill.
Date: October 26th 2019, 8:00 - 18:00
This symposium provides an overview of the (r)evolution in intensive care medicine. The programme is based on lectures of 20 minutes where each speaker presents in two 10 minute talks (in der Beschränkung zeigt sich erst der Meister) the good things that happened in the last 40 years in critical care vs our mistakes or what is missing with respect to that topic. At the end of the session the speakers participate in an interactive round table discussion with online voting to get the audience involved. Will be discussed: Theoretical concepts, basic physiology and pathophysiology, monitoring, and future directions.
This symposium provides an overview of the (r)evolution in intensive care medicine. The programme is based on lectures of 20 minutes where each speaker presents in two 10 minute talks (in der Beschränkung zeigt sich erst der Meister) the good things that happened in the last 40 years in critical care vs our mistakes or what is missing with respect to that topic. At the end of the session the speakers participate in an interactive round table discussion with online voting to get the audience involved. Will be discussed: Theoretical concepts, basic physiology and pathophysiology, monitoring, and future directions.
This symposium provides an overview of the (r)evolution in intensive care medicine. The programme is based on lectures of 20 minutes where each speaker presents in two 10 minute talks (in der Beschränkung zeigt sich erst der Meister) the good things that happened in the last 40 years in critical care vs our mistakes or what is missing with respect to that topic. At the end of the session the speakers participate in an interactive round table discussion with online voting to get the audience involved. Will be discussed: Theoretical concepts, basic physiology and pathophysiology, monitoring, and future directions.
This symposium provides an overview of the (r)evolution in intensive care medicine. The programme is based on lectures of 20 minutes where each speaker presents in two 10 minute talks (in der Beschränkung zeigt sich erst der Meister) the good things that happened in the last 40 years in critical care vs our mistakes or what is missing with respect to that topic. At the end of the session the speakers participate in an interactive round table discussion with online voting to get the audience involved. Will be discussed: Theoretical concepts, basic physiology and pathophysiology, monitoring, and future directions.
This symposium provides an overview of the (r)evolution in intensive care medicine. The programme is based on lectures of 20 minutes where each speaker presents in two 10 minute talks (in der Beschränkung zeigt sich erst der Meister) the good things that happened in the last 40 years in critical care vs our mistakes or what is missing with respect to that topic. At the end of the session the speakers participate in an interactive round table discussion with online voting to get the audience involved. Will be discussed: Theoretical concepts, basic physiology and pathophysiology, monitoring, and future directions.
This symposium provides an overview of the (r)evolution in intensive care medicine. The programme is based on lectures of 20 minutes where each speaker presents in two 10 minute talks (in der Beschränkung zeigt sich erst der Meister) the good things that happened in the last 40 years in critical care vs our mistakes or what is missing with respect to that topic. At the end of the session the speakers participate in an interactive round table discussion with online voting to get the audience involved. Will be discussed: Theoretical concepts, basic physiology and pathophysiology, monitoring, and future directions.
This symposium provides an overview of the (r)evolution in intensive care medicine. The programme is based on lectures of 20 minutes where each speaker presents in two 10 minute talks (in der Beschränkung zeigt sich erst der Meister) the good things that happened in the last 40 years in critical care vs our mistakes or what is missing with respect to that topic. At the end of the session the speakers participate in an interactive round table discussion with online voting to get the audience involved. Will be discussed: Theoretical concepts, basic physiology and pathophysiology, monitoring, and future directions.
Global launch of the Healthy Ageing and Prevention Index 2nd wave – alongside...ILC- UK
The Healthy Ageing and Prevention Index is an online tool created by ILC that ranks countries on six metrics including, life span, health span, work span, income, environmental performance, and happiness. The Index helps us understand how well countries have adapted to longevity and inform decision makers on what must be done to maximise the economic benefits that comes with living well for longer.
Alongside the 77th World Health Assembly in Geneva on 28 May 2024, we launched the second version of our Index, allowing us to track progress and give new insights into what needs to be done to keep populations healthier for longer.
The speakers included:
Professor Orazio Schillaci, Minister of Health, Italy
Dr Hans Groth, Chairman of the Board, World Demographic & Ageing Forum
Professor Ilona Kickbusch, Founder and Chair, Global Health Centre, Geneva Graduate Institute and co-chair, World Health Summit Council
Dr Natasha Azzopardi Muscat, Director, Country Health Policies and Systems Division, World Health Organisation EURO
Dr Marta Lomazzi, Executive Manager, World Federation of Public Health Associations
Dr Shyam Bishen, Head, Centre for Health and Healthcare and Member of the Executive Committee, World Economic Forum
Dr Karin Tegmark Wisell, Director General, Public Health Agency of Sweden
Navigating Challenges: Mental Health, Legislation, and the Prison System in B...Guillermo Rivera
This conference will delve into the intricate intersections between mental health, legal frameworks, and the prison system in Bolivia. It aims to provide a comprehensive overview of the current challenges faced by mental health professionals working within the legislative and correctional landscapes. Topics of discussion will include the prevalence and impact of mental health issues among the incarcerated population, the effectiveness of existing mental health policies and legislation, and potential reforms to enhance the mental health support system within prisons.
Navigating the Health Insurance Market_ Understanding Trends and Options.pdfEnterprise Wired
From navigating policy options to staying informed about industry trends, this comprehensive guide explores everything you need to know about the health insurance market.
Welcome to Secret Tantric, London’s finest VIP Massage agency. Since we first opened our doors, we have provided the ultimate erotic massage experience to innumerable clients, each one searching for the very best sensual massage in London. We come by this reputation honestly with a dynamic team of the city’s most beautiful masseuses.
Antibiotic Stewardship by Anushri Srivastava.pptxAnushriSrivastav
Stewardship is the act of taking good care of something.
Antimicrobial stewardship is a coordinated program that promotes the appropriate use of antimicrobials (including antibiotics), improves patient outcomes, reduces microbial resistance, and decreases the spread of infections caused by multidrug-resistant organisms.
WHO launched the Global Antimicrobial Resistance and Use Surveillance System (GLASS) in 2015 to fill knowledge gaps and inform strategies at all levels.
ACCORDING TO apic.org,
Antimicrobial stewardship is a coordinated program that promotes the appropriate use of antimicrobials (including antibiotics), improves patient outcomes, reduces microbial resistance, and decreases the spread of infections caused by multidrug-resistant organisms.
ACCORDING TO pewtrusts.org,
Antibiotic stewardship refers to efforts in doctors’ offices, hospitals, long term care facilities, and other health care settings to ensure that antibiotics are used only when necessary and appropriate
According to WHO,
Antimicrobial stewardship is a systematic approach to educate and support health care professionals to follow evidence-based guidelines for prescribing and administering antimicrobials
In 1996, John McGowan and Dale Gerding first applied the term antimicrobial stewardship, where they suggested a causal association between antimicrobial agent use and resistance. They also focused on the urgency of large-scale controlled trials of antimicrobial-use regulation employing sophisticated epidemiologic methods, molecular typing, and precise resistance mechanism analysis.
Antimicrobial Stewardship(AMS) refers to the optimal selection, dosing, and duration of antimicrobial treatment resulting in the best clinical outcome with minimal side effects to the patients and minimal impact on subsequent resistance.
According to the 2019 report, in the US, more than 2.8 million antibiotic-resistant infections occur each year, and more than 35000 people die. In addition to this, it also mentioned that 223,900 cases of Clostridoides difficile occurred in 2017, of which 12800 people died. The report did not include viruses or parasites
VISION
Being proactive
Supporting optimal animal and human health
Exploring ways to reduce overall use of antimicrobials
Using the drugs that prevent and treat disease by killing microscopic organisms in a responsible way
GOAL
to prevent the generation and spread of antimicrobial resistance (AMR). Doing so will preserve the effectiveness of these drugs in animals and humans for years to come.
being to preserve human and animal health and the effectiveness of antimicrobial medications.
to implement a multidisciplinary approach in assembling a stewardship team to include an infectious disease physician, a clinical pharmacist with infectious diseases training, infection preventionist, and a close collaboration with the staff in the clinical microbiology laboratory
to prevent antimicrobial overuse, misuse and abuse.
to minimize the developme
3. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 3
What I really need to know is…
When do I start giving fluids?
When do I stop giving fluids?
When do I start emptying?
When do I stop emptying?
SEE
MORE
THAN
OTHERS
benefit of fluid administration?
risk of fluid administration?
benefit of fluid removal?
risk of fluid removal?
4. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 4
Today’s Agenda
• Introduction
• From Invasive to Less invasive
• Results of PulsioFlex study
• Results of NexFin study
• Wrap it up
5. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 5
HD Monitoring
Anno 2012
Introduction
6. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 6
Disclosure
The speaker consults for the following companies:
BMEYE
Edwards
PULSION Medical Systems
manu.malbrain@skynet.be
7. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 7
Cardiac output (CO) is the main determinant of
oxygen delivery
Physical examination and vital signs alone often fail to
reflect significant derangements in CO
Many of our therapeutic efforts are aimed at
increasing the CO
The monitoring of CO is therefore very useful for
proper decision-making in critically ill and high-risk
surgical patients.
Some statements on CO measurement
Thanks to Azriel Perel
8. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 8
Bodies of two Air France
passengers found CNN.COM June
6, 2009
The airline had failed to replace a part that
monitors speed, as recommended by the
manufacturer, based on technological
developments and improvements.
The fact that this statement is not
supported by EBM tells us more about the
shortcomings of EBM than those of the
measurement of CO
9. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 9
The two main reasons to measure CO are:
Identification of patients who have low (or high)
CO values that are not evident clinically
Measurement of the response to diagnostic and
therapeutic interventions
It is time to consider
CARDIAC OUTPUT
as just another vital sign!
10. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 10
A Perel, M Maggiorini, M Malbrain, JL Teboul, J Belda, E
Fernández-Mondéjar, M Kirov, J Wendon
The PiCClin Study
206 critically ill patients were evaluated by 166
residents and 146 specialists.
EVLWiGEDViSVRCO
124
(40.8%)
154
(49%)
107
(34.3%)
110
(34.9%)
Within ±
20%
83
(27.3%)
97
(30.9%)
46
(14.7%)
170
(54%)
Under-
estimation
>20%
11. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 11
Because of the complexity of assessment of
clinical variables in septic patients, direct
measurement of CO by invasive hemodynamic
monitoring is advisable.
14. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 14
Funk DJ, Moretti EW, Gan TJ. Anesth Analg 2009;108:887–97
With the advancing age of the surgical population and the
increasing prevalence of ischemic heart disease, the need for
monitoring of organ flow is likely to increase.
Clinicians (both in the OR and the critical care setting) are
looking more toward the use of minimally or noninvasive
monitors of CO.
Of the available monitors, the ED and the arterial pulse
contour devices seem to have the greatest potential at
replacing the PAC for CO measurement.
15. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 15
What hemodynamic monitoring do you routinely
use for the management of high-risk surgery
patients?
16. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 16
HD Monitoring
Anno 2012
Less invasive
CO…
17. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 17
Real Time beat to beat CO
Real Time Preload + Afterload
Adequacy data
Minimally invasive
Widely applicable
Simple to Operate and Understand
Measured variables
Clear Data Display + Interpretation
Cardiac Output Monitoring
Nurse driven at the bedside
Neonates to adults
Ideal
System
18. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 18
• Fick
– Difficult, large room for
error, “Gold” standard
– NiCO2
• Bioimpedance
– Variable ICU accuracy
– Cardiodynamics
• Doppler
– Accurate, but user
dependent
– HemoSonic, Deltex, WAKI
• Pulse Contour Analysis
– PiCCO/EV 1000
– PulseCO
– Vigileo/ Pulsioflex
• Thermodilution
– Vigilance PAC, CEDVi
– (PiCCO)
• Indicator Dilution
– Invasive
– (LiDCO)
Available technologies for
continuous Cardiac Output
19. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 19
PA catheter
Advancedmonitoring Which device for monitoring cardiac output?
PiCCO EV 1000
cardiac output cardiac output cardiac output
PAP - PAOP GEDVi GEDVi
EVLWi - PVPI EVLWi - PVPI
GEF - dpmax GEF - dpmax
20. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 20
• Advantages
– ‘Simple’ catheter
– No added fluid
– No calibration
– “Operator independent”
– SVO2 / Volumetric measurements
• Disadvantages
– Invasive
– Non continuous (3-6 minutes)
– Slow response to change
– Poor signal to noise ratio
– Non verifiable data
Vigilance - CEDVI
Gold Standard
RV end-diastolic volume (RVEDV)
(pulmonary artery thermodilution)
21. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 21
1. Transpulmonary thermodilution
2. Arterial Pulse contour analysis
Algorithm after calibration
What is TPTD technology ?
Global end-diastolic volume (GEDV)
(transpulmonary thermodilution)
Intrathoracic blood volume (ITBV)
(thermo-dye transpulmonary dilution)
PiCCO
or
EV1000
22. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 22
Cardiac output measurement
by transpulmonary
thermodilution
RA LARV LVPBV
EVLW
Cardiac
output
23. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 23
1. Transpulmonary lithiumdilution
2. Pulse power analysis algorithm combined with
indicator dilution calibration
What is LiDCO/PulseCO
technology ?
24. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 24
•Indicator dilution technique
•Lithium chloride (0.15-0.3 mmol) marker
•Intravenous bolus (peripherally or centrally)
•Ion selective electrode attached to arterial line
•CO computed
26. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 26
1. CO estimation
2. Pulse Contour Analysis
What is Vigileo technology ?
CO = HR * SV
• Heart Rate
measurement
• Biometric and
dynamic
compensation for
the vasculature
• Pulse pressure
measurement
proportional to
Stroke Volume
27. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 27
Trending Stroke Volume
• Arterial pressure is sampled at 100 Hz
(i.e., 20sec x 100Hz = 2000 data points)
• An equivalent for pulse pressure is achieved by taking the
standard deviation (SD) of the 2000 sampled data points
• SD(Arterial pressure) - Pulse Pressure - Stroke Volume
• Changes in stroke volume will result in corresponding changes
in the pulse pressure
• SV estimates are updated over 20 seconds
20 sec.
28. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 28
SD is a measure of variation of the AP
↑ AP Variation ➔ ↑ SD(AP) ➔ ↑ SV
Therefore, with a constant vasculature …
↓ AP Variation ➔ ↓ SD(AP) ➔ ↓ SV
20 sec. 20 sec.20 sec.
41. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 41
1. Indirect Fick Principle
2. Respiratory Mechanics
What is NiCO2 technology ?
42. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 42
What is NiCO2 technology ?
43. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 43
What is NiCO2 technology ?
44. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 44
Arterial pressure
Esophageal Doppler
Flotrac/Vigileo
Pulsioflex
LidCOrapid
AP catheter
CVP
PiCCO
EV 1000
Basic monitoring Advanced monitoring
OR monitoring
45. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 45
Different panel of hemodynamic information
Arterial pressure
Esophageal Doppler
Vigileo/Pulsioflex
LidCOrapid
PAC
CVC / ScvO2
PiCCO/EV1000
vasomotor
tone
lung
water
cardiac
contractility
tissue
oxygenation
preloadCO/SV preload
dependance
Different monitoring devices
46. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 46
HD Monitoring
Anno 2012
How to compare
2 techniques?
47. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 47
1. Correlations…
Gold standard Gold standard
Inverse correlation
Not equivalent
Good correlation
Systematic
overestimation
Gold standard
Poor correlation
Systematic
underestimation
48. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 48
1. Correlations…
• Pearson correlation
(p<0.01)
• Line of identity
crosses “0”
• Linear relation
• R2>0.6
• R>0.75
49. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 49
COPA-COA
(COPA-COA)/2
Bias
Limits of Agreement = ± 2 SD
Normal HighLow
CO = 3 ± 1 l/min CO = 8 ± 1 l/min
± 12.5%
<35%
2. Bland and Altman…
51. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 51
PRECISE
ACCURAT
E
IMPRECISE
ACCURAT
E
PRECISE
INACCURATE
IMPRECISE
INACCURATE
52. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 52
Are uncalibrated CO monitors
accurate enough to guide therapy?
53. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 53
Anesthesia Analgesia 2009, 108:707
When evaluating the role of new CO devices in clinical care,
the fundamental question is whether the new device can
replace thermodilution CO measurement as a guide to clinical
decisions.
Despite the large number of studies evaluating new CO
devices, few, if any, answer this fundamental question.
54. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 54
HD Monitoring
Anno 2012
PulsioFlex Study
ZNA Stuivenberg
55. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 55
PulsioFlex Escalation Study
56. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 56
Reference:
NEXFIN !left !right
Finger
Edema !yes !no Date
Hospital
Patient ID (anonym) Height cm Weight kg
Age Y Gender female. ! male !
Medication
Obs 6 PiCCO2 Pulsioflex Nexfin/radial NIV/Monitor Other
Time +8hrs ADsys SaO2:
ADdia Blood T°:
MAP Periph T°:
SVV Nex Hgb: CVP:
PPV dobu:
dPmax Rythm: levo:
SVRI ulti:
SVI dorm:
HR dipri:
Auto CI 1.* CCI 2. 3. 4. other:
Obs 7 ADsys SaO2:
Time + 2 hrs ADdia Blood T°:
MAP Periph T°:
SVV CVP:
PPV dobu:
dPmax Rythm: levo:
SVRI ulti:
SVI dorm:
HR dipri:
CCI other:
Obs 8 ADsys SaO2:
Time + 4 hrs ADdia Blood T°:
MAP Periph T°:
SVV CVP:
PPV dobu:
dPmax Rythm: levo:
SVRI ulti:
SVI dorm:
HR dipri:
CCI other:
Obs 9 ADsys SaO2:
Time + 6 hrs ADdia Blood T°:
MAP Periph T°:
SVV CVP:
PPV dobu:
dPmax Rythm: levo:
SVRI ulti:
SVI dorm:
HR dipri:
CCI other:
Obs10+16hrs ADsys SaO2:
MV Mode ADdia Blood T°:
RR MAP Periph T°:
TV SVV Nex Hgb: CVP:
IPAP PPV dobu:
PEEP dPmax Rythm: levo:
FiO2 SVRI GEF: ulti:
pO2/pCO2 / SVI GEDVi: dorm:
pH/lact / HR EVLWi: dipri:
HCO3/BE / CCI 1. 2. 3. TPTD CI(5): other:
Auto CI 4.
!Brachial/Axillar !Radial !Femoral
PiCCO2 !De-escalation Arm
PiCCO placement !left !right
Observation: PULSIOFLEX vs. PiCCO2 8 - 16 hrs (PulsioFlex AUTOcalibration*)
PiCCO2 !escalation Arm
Fluid Balance/8hrs
!Brachial/Axillar !Radial !Femoral
Pulsioflex placement !left !right
Reference:
NEXFIN !left !right
Finger
Edema !yes !no Date
Hospital
Patient ID (anonym) Height cm Weight kg
Age Y Gender female. ! male !
Medication
Time 0 PiCCO2 Pulsioflex Nexfin/radial NIV/Monitor Other
MV Mode ADsys SaO2:
RR ADdia Blood T°:
TV MAP Periph T°:
IPAP SVV Nex Hgb: CVP:
PEEP PPV dobu:
FiO2 dPmax Rythm: levo:
pO2/pCO2 / SVRI GEF: ulti:
pH/lact / SVI GEDVi: dorm:
HCO3/BE / HR EVLWi: dipri:
Auto CI 5. CCI 2. 3. 4. TPTD CI*(1): other:
Obs 2 ADsys SaO2:
Time + 2 hrs ADdia Blood T°:
MAP Periph T°:
SVV CVP:
PPV dobu:
dPmax Rythm: levo:
SVRI ulti:
SVI dorm:
HR dipri:
CCI other:
Obs 3 ADsys SaO2:
Time + 4 hrs ADdia Blood T°:
MAP Periph T°:
SVV CVP:
PPV dobu:
dPmax Rythm: levo:
SVRI ulti:
SVI dorm:
HR dipri:
CCI other:
Obs 4 ADsys SaO2:
Time + 6 hrs ADdia Blood T°:
MAP Periph T°:
SVV CVP:
PPV dobu:
dPmax Rythm: levo:
SVRI ulti:
SVI dorm:
HR dipri:
CCI other:
Obs 5 + 8hrs
ADsys SaO2:
MV Mode ADdia Blood T°:
RR MAP Periph T°:
TV SVV Nex Hgb: CVP:
IPAP PPV dobu:
PEEP dPmax Rythm: levo:
FiO2 SVRI GEF: ulti:
pO2/pCO2 / SVI GEDVi: dorm:
pH/lact / HR EVLWi: dipri:
HCO3/BE / CCI 1. 2. 3. TPTD CI(5): other:
Auto CI 4.
Pulsioflex placement !left !right
!Brachial/Axillar !Radial !Femoral
PiCCO2 !De-escalation Arm
Fluid Balance/8hrs
Observation: PULSIOFLEX vs. PiCCO2 0 - 8 hrs (PulsioFlex calibration with TPTD*)
PiCCO2 !escalation Arm
PiCCO placement !left !right
!Brachial/Axillar !Radial !Femoral
57. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 57
Patients
• So far, 37 mechanically ventilated ICU patients
included
• All Escalation
Age Gender height weight BMI APACHE SAPS SOFA
mean 53,2 20,0 172,8 84,1 28,3 26,0 51,1 9,8
SD 15,5 Male 9,4 22,4 7,9 6,4 11,9 2,7
8h time periods 1 2 3 4
PICCO2 Femoral
Pulsioflex Radial Femoral
Calibration TDCI AutoCI TDCI AutoCI
58. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 58
Regression PiCCI vs PulseCI
59. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 59
Correlation with TPTDCI
Pulsioflex
Pulse contour
PiCCO2
Pulse contour
ProAQT
Auto Calibration
60. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 60
Bland and Altman
PICCI-PULSECI TDCI-PICCI TDCI-PULSECI TDCI-AUTOCI
n 440 182 182 182
mean 3,7 0,00 3,7 0,04 3,7 0,04 3,7 0,03
SD 1,1 0,58 1,1 0,40 1,0 0,58 0,9 0,61
min/LLA 1,7 -1,16 1,5 -0,76 1,8 -1,13 2,0 -1,20
max/ULA 7,0 1,17 6,9 0,84 6,7 1,20 6,6 1,25
COVA 30% 29% 26% 24%
PE 8,0 31,5% 7,9 21,6% 7,7 31,4% 7,6 32,9%
PE 31.5%
PE 21.6%
PE 31.4% PE 32.9%
61. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 61
Concordance: Changes in CI
62. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 62
Effect of therapeutic
intervention
• In total 40 interventions
• Passive leg raising (n=13)
• Fluid bolus 500ml/30 minutes (n=11)
• Increase or decrease of vasopressor (n=10)
• Increase or decrease of dobutamine (n=5)
• Increase in sedation (n=1)
66. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 66
The Nexfin applies 3 major steps in the
non-invasive measurement of CCO.
The Nexfin: Principles of measurement
67. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 67
An inflatable cuff* is wrapped around the middle
phalanx of the 2nd, 3rd or 4th finger.
* 3 sizes
1. Measurement of continuous beat-by-beat finger BP
68. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 68
The diameter of the finger
arteries is measured by a pair of
LED’s.
The cuff inflates and relaxes to
keep the diameter constant
throughout the cardiac cycle.
The pressure that is needed to
keep the diameter constant is
continuously recorded generating
a real-time pressure waveform.
Volume Clamp Technology
1. Measurement of continuous beat-by-beat finger BP
69. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 69
2. Transformation of finger BP to brachial BP by a
transfer function based on a vast clinical database
70. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 70
3. Calculation of the CCO from the brachial BP waveform
Nexfin CO-Trek
The Nexfin CO-Trek method is based on the
hemodynamic version of Ohm's law
ΔP/Q = Zin
Thus, when the arterial input impedance (Zin) is
known, a given pressure (P) allows for the
calculation of the related flow (Q).
79. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 79
PiCCI
NEXCI
art rad MAP
NEXMAP
PiCCOMAP
80. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 80
• 35 year old man, suicide attempt, Levo 0.45y
Case study
Agitation, pain midazolam
Small drift
PiCCI
NEXCI
81. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 81
Case study
Agitation, pain
midazolam
MAP
NEXMAP
• 35 year old man, suicide attempt, Levo 0.45y
85. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 85
Conclusions
• TRULY non-invasive
• Reasonable results in a really critically ill
patient sample (n=45)
• Performs even better than other more
invasive techniques
• Correlates excellent with invasive MAP
• LA for CI acceptable although % error too big
• Better patient selection needed
86. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 86
The Future for NEXFIN
Double Cuff for continuous CCI
Hygienic properties
Longer connectors
Physiocal optimisation
Quantification of SVV and PPV
Could be used in ER (pattern
recognition) and OR setting
87. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 87
HD Monitoring
Anno 2012
Conclusions
88. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 88
Evidence Based Medicine
Does my new monitoring device does as
well as the gold standard?
Does my new monitoring device give
new or additional information?
Does the interpretation of the data
change my treatment?
Does the new-variable-driven treatment
change patient outcome?
89. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 89
The Parachute Study
Gordon C S Smith, Jill P Pell BMJ 2003; 327:1459-60
WHAT DO WE KNOW WHAT THIS STUDY ADDS
• No RCCT on parachute
• Basis for parachute use
Purely observational
• Efficacy explained by
Healthy cohort
• He who believes in EBM
Comes down
to earth
with a bump…
• Widely used
• Gravitational challenge
Prevent death
Prevent injury
• Adverse effects
Failure
Iatrogenic
• Studies free fall
no 100% mortality
90. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 90
No monitoring device can improve
patient-centered outcomes unless it
is coupled to a treatment that
improves outcome.
91. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 94
• Non invasive technologies offer useful
additional information
• This can alter our treatment strategy
• There is a learning curve with any new
technology
• Each technology is different and needs to
be assessed on its own merits
• By knowing the pitfalls we can obtain new
and important information
• This can also alter our treatment…
Summary
manu.malbrain@skynet.be
92. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 95
HD Monitoring
Anno 2012
Wrap it Up
93. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 96
What I really need to know
When do I start giving fluids?
When do I stop giving fluids?
When do I start emptying?
When do I stop emptying?
SEE
MORE
THAN
OTHERS
benefit of fluid administration?
risk of fluid administration?
benefit of fluid removal?
risk of fluid removal?
GEF/GEDVi↓ PPV↑ PLR+
GEF/GEDVi↑ PPV↓ PLR-
EVLW↑/PVPI↑ IAP↑/APP↓ FB+
ICG-PDR↓ APP↓ ScvO2↓ FB--
94. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 101
WGAP Meeting at ESICM
ACS Workshop at ISICEM
95. 2nd iFAD 17/11/2012 Hemodynamic Moitoring Anno 2012 102
3rd
MARK THE DATE!
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