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.
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.
Intra-operative determinants of postoperative AKIscanFOAM
A presentation by Peter Noordzij at the 2017 meeting of the Scandinavian Society of Anaestesiology and Intensive Care Medicine.
All available content from SSAI2017: https://scanfoam.org/ssai2017/
Delivered in collaboration between scanFOAM, SSAI & SFAI.
This session focuses on considerations and challenges in meeting the health care needs of a growing global population. Attention will be placed on task shifting – the delegation of health interventions to less specialized health workers.
Advancing dialysis multinational guidelines for increased time and frequency ...AdvancingDialysis.org
Clinical practice guidelines and appropriate indications from 5 medical societies in North America, Europe and Asia for increased hemodialysis frequency and time.
A presentation by Max Bell at the 2017 meeting of the Scandinavian Society of Anaestesiology and Intensive Care Medicine.
All available content from SSAI2017: https://scanfoam.org/ssai2017/
Delivered in collaboration between scanFOAM, SSAI & SFAI.
Relative Hyperoxia in cyanotic congenital heart disease on veno-arterial ECMO...Texas Children's Hospital
Extracorporeal membrane oxygenation (ECMO) is an
established intervention for respiratory or cardiorespiratory
support in children with congenital heart disease (CHD)
when all other interventions have failed. Hyperoxia
following successful resuscitation has been associated with
increased mortality in pediatric and adult studies,
including, specifically, hyperoxia during ECMO
management. We hypothesized that this effect may be
pronounced in patients with lower arterial oxygen
saturation at baseline, such as those with cyanotic CHD. We
aimed to determine if relative hyperoxia in children with
cyanotic single ventricle circulation on Veno-Arterial (VA)-
ECMO is a risk factor for mortality in a large multicenter
registry analysis.
Intra-operative determinants of postoperative AKIscanFOAM
A presentation by Peter Noordzij at the 2017 meeting of the Scandinavian Society of Anaestesiology and Intensive Care Medicine.
All available content from SSAI2017: https://scanfoam.org/ssai2017/
Delivered in collaboration between scanFOAM, SSAI & SFAI.
This session focuses on considerations and challenges in meeting the health care needs of a growing global population. Attention will be placed on task shifting – the delegation of health interventions to less specialized health workers.
Advancing dialysis multinational guidelines for increased time and frequency ...AdvancingDialysis.org
Clinical practice guidelines and appropriate indications from 5 medical societies in North America, Europe and Asia for increased hemodialysis frequency and time.
A presentation by Max Bell at the 2017 meeting of the Scandinavian Society of Anaestesiology and Intensive Care Medicine.
All available content from SSAI2017: https://scanfoam.org/ssai2017/
Delivered in collaboration between scanFOAM, SSAI & SFAI.
Relative Hyperoxia in cyanotic congenital heart disease on veno-arterial ECMO...Texas Children's Hospital
Extracorporeal membrane oxygenation (ECMO) is an
established intervention for respiratory or cardiorespiratory
support in children with congenital heart disease (CHD)
when all other interventions have failed. Hyperoxia
following successful resuscitation has been associated with
increased mortality in pediatric and adult studies,
including, specifically, hyperoxia during ECMO
management. We hypothesized that this effect may be
pronounced in patients with lower arterial oxygen
saturation at baseline, such as those with cyanotic CHD. We
aimed to determine if relative hyperoxia in children with
cyanotic single ventricle circulation on Veno-Arterial (VA)-
ECMO is a risk factor for mortality in a large multicenter
registry analysis.
Enhanced Recovery After Surgery (ERAS®) is the Enhanced Recovery After Surgery (ERAS®) is the implementation of patient-focused, standardized, evidencefocused, standardized, evidencefocused, standardized, evidencefocused, standardized, evidencefocused, standardized, evidencefocused, standardized, evidence-based, interdisciplinary perioperative guidelines.
Learn more about Enhanced Recovery Canada:
http://ow.ly/hR3j30jsnjR
Major surgery is a considerable physiologic insult that can be
associated with significant morbidity and mortality. The prevention of perioperative morbidity is a determining factor in providing high-quality in health care, since the occurrence of postoperative complications adversely affects postoperative survival and increase healthcare costs
Introduction of the NZ Health IT Plan enables better gout management - Reflections of an early adopter. Presented by Peter Gow, Counties Manukau DHB, at HINZ 2014, 12 November 2014, 11.37am, Plenary Room
Background: The transition from resident physician to independent practitioner is an important period for young physicians.Optimally, they would feel well prepared to independently care for all patients presenting to them for anesthesia, however, this is unlikely Methods: A survey was emailed to all accredited anesthesiology residency program coordinators in April 2018 for further distribution to their CA3 residents. The survey collected data on the resident’s perception of his or her preparedness to manage a variety of anesthesia cases, patients with comorbid conditions, and ethical issues as well as perform various procedures.
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.
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 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.
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.
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.
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.
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.
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.
share - Lions, tigers, AI and health misinformation, oh my!.pptxTina Purnat
• Pitfalls and pivots needed to use AI effectively in public health
• Evidence-based strategies to address health misinformation effectively
• Building trust with communities online and offline
• Equipping health professionals to address questions, concerns and health misinformation
• Assessing risk and mitigating harm from adverse health narratives in communities, health workforce and health system
Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachAyurveda ForAll
Explore the benefits of combining Ayurveda with conventional Parkinson's treatments. Learn how a holistic approach can manage symptoms, enhance well-being, and balance body energies. Discover the steps to safely integrate Ayurvedic practices into your Parkinson’s care plan, including expert guidance on diet, herbal remedies, and lifestyle modifications.
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
263778731218 Abortion Clinic /Pills In Harare ,sisternakatoto
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- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
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Antimicrobial stewardship to prevent antimicrobial resistanceGovindRankawat1
India is among the nations with the highest burden of bacterial infections.
India is one of the largest consumers of antibiotics worldwide.
India carries one of the largest burdens of drug‑resistant pathogens worldwide.
Highest burden of multidrug‑resistant tuberculosis,
Alarmingly high resistance among Gram‑negative and Gram‑positive bacteria even to newer antimicrobials such as carbapenems.
NDM‑1 ( New Delhi Metallo Beta lactamase 1, an enzyme which inactivates majority of Beta lactam antibiotics including carbapenems) was reported in 2008
These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists
16. #ifad219 report of fluid day spain (colomina)
1. Maria J. Colomina
Data September 30th 2019
Anesthesia & Critical Care Department
Bellvitge University Hospital – Barcelona - Spain
Haemostasis, Transfusion Medicine and Fluid Therapy Section -
Spanish Society of Anesthesiology, Resuscitation and Pain Therapy
2. M. Basora – C. Cassinello – R. Ferrandis – P. Guilabert – J.L. Jover – J.V. Llau – J. Ripollés
Data September 30th 2019 Fluid Day Study_MJ. Colomina et al._ 2019
4. A more modern approach is to ask which fluid regimen is associated with the best outcome.
Surprisingly, only a few such studies were published before this millennium.
Fluid Day Study_MJ. Colomina et al._ 2019
What happened in the meantime?
Robert G. Hahn
5. Intra & postoperative period?
Fluid Day Study_MJ. Colomina et al._ 2019
What’s the context?
6. It is unclear what type of fluids are the most used
It is unclear what volume of fluids are administered during
routine surgical procedures
It is unclear if the fluid management is
is used by specific control (monitoring)
And whether significant variability exits
What’s the context?
Fluid Day Study_MJ. Colomina et al._ 2019
7. Maintenance fluid therapy in a tertiary hospital: A prevalence study.
Uña Orejón R, Gisbert de la Cuadra L, Garríguez Pérez D, Díez Sebastián J, Ureta Tolsada MP.
Rev Esp Anestesiol Reanim. 2017 Jun - Jul;64(6):306-312. doi: 10.1016/j.redar.2016.12.006. Epub 2017 Feb 14.
[Pilot study of intravenous fluid therapy management in adult patients at a tertiary care hospital].
Cordero Cruz AM, Moreno Villares JM, Gomis Muñoz P, Valero Zanuy MÁ, Calleja Hernández MÁ.
Nutr Hosp. 2012 May-Jun;27(3):943-7. doi: 10.3305/nh.2012.27.3.5744.
What are our research questions?
Fluid Day Study_MJ. Colomina et al._ 2019
• The purpose of intravenous fluid therapy (IFT) is to maintain or restore internal equilibrium by administering fluids and/or different
electrolyte components. Its correct use and the prevention of complications arising from their misuse depend on the knowledge of
the medical team on this subject. We analyzed this issue in different clinical areas of a tertiary hospital.
• The professionals who prescribe IFT perceive the need to design IFT training programs, together with the production of
guides and consensus protocols.
• To assess the types of maintenance fluids used in our hospital, comparing their volume and composition to the standards
recommended by the guidelines.
• Normal Saline Solution is the most frequently used solution. In contrast to excess doses of sodium and chlorine, there is a great
deficit of other ions, buffering agents and caloric intake in the fluid therapy regimens that are usually prescribed.
8. What are our research questions?
Fluid Day Study_MJ. Colomina et al._ 2019
Variability in practice and factors predictive of total crystalloid administration during abdominal surgery:
retrospective two-centre analysis.
Lilot M, Ehrenfeld JM, Lee C, Harrington B, Cannesson M, Rinehart J.
Br J Anaesth. 2015 May;114(5):767-76. doi: 10.1093/bja/aeu452. Epub 2015 Jan 13.
• Variation in clinical practice in the perioperative environment and intensive care unit is a major challenge facing modern medicine.
The objective of the present study was to analyse intraoperative crystalloid administration practices at two academic medical centres
in the USA.
• The average corrected crystalloid infusion rate across all providers at both institutions was 7.1 (sd 4.9) ml kg(-1) h(-1), an overall cCOV
of 70%. Individual providers ranged from 2.3 (sd 3.7) to 14 (sd 10) ml kg(-1) h(-1). The final regression model strongly favoured
personnel as predictors over other patient predictors.
Perioperative Fluid Utilization Variability and Association With Outcomes: Considerations for Enhanced Recovery
Efforts in Sample US Surgical Populations.
Thacker JK, Mountford WK, Ernst FR, Krukas MR, Mythen MM.
Ann Surg. 2016 Mar;263(3):502-10. doi: 10.1097/SLA.0000000000001402.
• To study current perioperative fluid administration and associated outcomes in common surgical cohorts in the United States.
• The study showed significant associations between high fluid volume given on the day of surgery with both increased LOS (odds
ratio 1.10-1.40) and increased total costs (odds ratio 1.10-1.50). High fluid utilization was associated with increased presence of
postoperative ileus for both rectal and colon surgery patients. Low fluid utilization was also associated with worse outcomes.
9. A correct Fluid optimization
would probably lead to
decreased variability and
improved outcomes
10. What are our research questions?
What are the types of fluids we use in our daily
practice?
What is the total amount administered during
the intraoperative and postoperative period?
Does the amount and type of fluids change with
the type of patient or type of surgery?
Do we use specific monitoring for fluid therapy?
Fluid Day Study_MJ. Colomina et al._ 2019
11. Hypothesis:
Fluid therapy in the surgical environment is administered in a
protocolized manner and in accordance with the recommendations
of the different clinical practice guidelines.
Objectives:
To analyze the management of perioperative fluid therapy
in our daily practice for any type of surgery
To know the type and quantity of fluids that are
administered for any type of surgical setting
To determine the existence of factors that may influence the
variability of the management of perioperative fluid therapy
12. Methods
• Fluid Day was a prospective, national, multicentre observational study
• Designed by Haemostasis, Transfusion Medicine and Fluid Therapy Section
• Funded & Sponsored by Spanish Society of Anaesthesiology
• National code: HTF-FLU-2018-01 / AEMPS: SED-HEA-2018-01
• Clinical Trials Network (awarded IJ/BCCB 2018)
• Distributed recruitment centralised data collection (HUB)
• >130 hospitals, each with a regional co-ordinator (RC)
• Each RC aims to get as many centres as possible
• Aiming for 3000- 3,500 patients
• 2 days observational period (18 and 20 February 2019)
Fluid Day Study_MJ. Colomina et al._ 2019
13. Methods
Inclusion Criteria:
• Patients over 18 years of age surgically treated during the 24 hours
of the two-day study of both programmed and emergency surgery
Exclusion Criteria:
• Interventions performed outside the surgical area: complementary
examination cabinets.
• Interventions that do not require the presence of an
anesthesiologist.
• Ophthalmologic surgery
• Surgery performed with local anesthesia.
Fluid Day Study_MJ. Colomina et al._ 2019
14. Fluid Day Study_MJ. Colomina et al. _ 2019
Methods
Demographic
Sex, age, weight and height,
ASA
Commorbidities
Cardiac, pulmonary, Kidney
function, … until 23 in total
Elixhauser score
Surgical procedure
Type and duration of
intervention.
Postoperative follow-up
time and destination
Crystalloids
• SF 0.9%
• RL
• Isofundin ®
• Plasmalyte®
• SGA 5%- 10%
• SGS ........ ml
Colloids
• HEA 130 / 0.4
• Gelatins
• Albumin
Monitoring
Use of goal-
guided Fluid
Therapy protocols
Other …
15. Methods
•Aortic surgery
•Cardiac surgery
•Intra-thoracic procedures
with lung resection
•Major transplant surgery
(heart, lung, liver)
•Intracranial and spine surgery
•Gynecologic and urologic
surgery
•Intra-abdominal surgery
without bowel resection
•Intra-thoracic surgery without
lung resection
•Cardiac catheterization
procedures including
electrophysiology studies,
ablations, AICD, pacemaker
•Colorectal surgery with bowel
resection
•Kidney transplant
•Major joint replacement
(shoulder, knee, and hip)
•Open radical prostatectomy,
cystectomy
•Major oncologic general
surgery or gynecologic surgery
•Major oncologic head and neck
surgery
•Hernia repair
•ENT procedures without
planned flap or neck dissection
•Diagnostic cardiac
catheterization
•Interventional radiology
•GI endoscopy with stent
placement
•Cystoscopy
Low Risk
Procedures
associated with
minimal
physiologic
effect
High Risk
Procedures with
possible
significant effect
on
hemodynamics,
blood loss
Very High Risk
Procedures with
major impact on
hemodynamics,
fluid shifts, possible
major blood loss
Intermediate
Risk
Procedures
associated with
moderate
changes in
hemodynamics,
risk of blood loss
Surgery Risk Stratification
https://www.uclahealth.org/anes/risk-stratification
Fluid Day Study_MJ. Colomina et al._ 2019
16. Methods Patient Medical Risk Stratification
https://www.uclahealth.org/anes/risk-stratification
Low Risk
•Hypertension
•Hyperlipidemia
•Asthma
•Other chronic, stable medical condition without significant functional impairment
•Age 70 or older
•Non-insulin dependent diabetes
•History of treated, stable CAD
•Morbid obesity (BMI > 30)
•Mild renal insufficiency
High Risk
•Recent coronary stent
•Chronic CHF
•Insulin-dependent diabetes mellitus
•Renal insufficiency: creatinine > 2
•Moderate COPD: FEV1 50% to 70%
•Obstructive sleep apnea
•History of stroke or TIA
•Known diagnosis of dementia
•Chronic pain syndrome
ASA I – II
ASA III – IV
Fluid Day Study_MJ. Colomina et al._ 2019
20. Study population
[All]
n=6314
N
Sex, N(%) Men 3091 (49.0%) 6314
Women 3223 (51.0%)
Years, average (SD) 57.8 (17.1) 6314
Years, Median
[C1;C3]
60.0 [45.0;71.0] 6314
BMI, average (SD) 27.6 (5.56) 6199
IMC, Media
[C1;C3]
26.8 [23.9;30.3] 6199
Old pyramid
Fluid Day Study_MJ. Colomina et al._ 2019
21. HTA 2411 (39.2%)
Obesity 1010 (16.4%)
Diabetes 913 (14.8)+
COPD 655 (10.6%)
Depresion 492 (8%)
Hypothyroidism 468 (8%)
HTA, with complications 468 (7.6%)
Cardiac arrhythmia 425 (7%)
Neurological diseases 387 (7%)
Tumor witouth metastasis 364 (6%)
0 10 20 30
Comorbidities*
%
71% patients with any comorbidities
*10 most prevalents comorbidities
Fluid Day Study_MJ. Colomina et al. _ 2019
25. Post-surgical care
78%
17%
3% 1% 1%
PARU
DS
Critical Care Anesthesia ICU Intermediate care Warm
%surgeries
PARU
Postanesthesia
recovery room
Unit
DS
Day surgery
ICU
Intensive Care Unit
Fluid Day Study_MJ. Colomina et al._ 2019
26. All
Surgery Low-
Intermediate &
Patient Low Risk
Surgery Low-
Intermediate &
Patient High Risk
Surgery High-Very high &
Patient Low Risk
Surgery High-Very high &
Patient High Risk
N
N=6314 N=3830 N=943 N=987 N=554
Crystalloids
Crystalloids, N (%) 6203 (98.2%) 3758 (98.1%) 924 (98.0%) 975 (98.8%) 546 (98.6%) 6314
Crystalloids number+,
Median [Q1;Q3]
2.00
[1.00;2.00]
2.00
[1.00;2.00]
2.00 [1.00;2.00]
2.00
[1.00;2.00]
2.00
[1.00;2.00]
6203
Balanced, N (%) 4912 (79.2%) 2973 (79.1%) 699 (75.6%) 802 (82.3%) 438 (80.2%) 6203
Normal Saline ,N (%) 2883 (46.5%) 1651 (43.9%) 462 (50.0%) 475 (48.7%) 295 (54.0%) 6203
Medical dilution, N (%) 1749 (28.2%) 1019 (27.1%) 269 (29.1%) 297 (30.5%) 164 (30.0%) 6203
Other: Dextrose
component, N (%)
396 (6.38%) 195 (5.19%) 87 (9.42%) 57 (5.85%) 57 (10.4%) 6203
Fluid Day Study_MJ. Colomina et al. _ 2019
Type of Fluids Intraoperative period
27. All
Surgery Low-
Intermediate &
Patient Low Risk
Surgery Low-
Intermediate &
Patient High Risk
Surgery High-Very high
& Patient Low Risk
Surgery High-Very high &
Patient High Risk
N
N=6314 N=3830 N=943 N=987 N=554
Colloids
Colloids, N (%) 466 (7.51%) 153 (4.06%) 104 (11.3%) 120 (12.3%) 89 (16.4%) 6207
Total ml, Median
[Q1;Q3]
500 [300;500] 500 [350;500] 500 [250;500] 500 [500;500] 500 [300;500] 465
Total ml/Kg, Median
[Q1;Q3]
6.25 [4.31;7.69] 6.25 [4.58;7.69] 6.02 [3.79;8.33] 6.10 [4.93;7.14] 6.37 [4.49;8.48] 460
HEA*, N (%) 274 (58.8%) 93 (60.8%) 60 (57.7%) 79 (65.8%) 42 (47.2%) 466
Gelatin*, N (%) 163 (35.0%) 52 (34.0%) 36 (34.6%) 37 (30.8%) 38 (42.7%) 466
Albumin*, N (%) 37 (7.94%) 9 (5.88%) 12 (11.5%) 5 (4.17%) 11 (12.4%) 466
Type of Fluids Intraoperative period
Fluid Day Study_MJ. Colomina et al. _ 2019
28. Fluid Day Study_MJ. Colomina et al._ 2019
Type of Fluids Intraoperative period
Surgery High Risk & Patient High Risk with intraoperative colloids
All
N=89
Types of Surgery, N (%):
Cardiac Trasplant 1 (1.12%)
Cardiac Surgery 23 (25.8%)
Vascular Surgery 6 (6.74%)
Neurosurgery 6 (6.74%)
Thoracic surgery 3 (3.37%)
General 13 (14.6%)
Orthopedic & Trauma 23 (25.8%)
Plastic & Reconstructive 1 (1.12%)
O.R.L. 2 (2.25%)
Urology 9 (10.1%)
Liver transplant 1 (1.12%)
Other 1 (1.12%)
29. Fluid Day Study_MJ. Colomina et al._ 2019
Dose & Total amount Intraoperative period
All
Surgery Low-
Intermediate
& Patient Low Risk
Surgery Low-
Intermediate
& Patient High Risk
Surgery High-Very high
& Patient Low Risk
Surgery High-Very high
& Patient High Risk
N
N=6314 N=3830 N=943 N=987 N=554
Crystalloid administrated = crystalloid + medical dilution
Total ml/Kg ,
Median [Q1;Q3]
8.33 [5.43;13.3] 7.69 [5.00;11.8] 8.33 [5.26;13.3] 11.1 [6.91;17.2] 12.5 [6.86;20.6] 6142
Total ml/Kg / h surgery ,
Median [Q1;Q3]
6.35 [4.17;9.52] 6.67 [4.23;10.0] 6.00 [4.04;9.08] 6.41 [4.36;9.33] 5.46 [3.83;8.17] 6039
Total ml/Kg with medical
dilution,
Median [Q1;Q3]
9.04 [6.00;14.3] 8.29 [5.56;12.3] 9.17 [5.81;14.1] 12.0 [7.78;18.3] 13.2 [7.62;21.8] 6158
Corrected crystalloid administrated = crystalloid + medical dilution - estimated blood loss - urine output
Total ml/Kg,
Median [Q1;Q3]
6.71 [3.97;10.7] 6.49 [4.08;10.0] 6.67 [3.73;10.5] 7.72 [4.29;12.5] 7.44 [3.11;13.0] 6126
Total ml/Kg / h surgery,
Median [Q1;Q3]
5.15 [3.00;8.21] 5.64 [3.35;8.82] 4.99 [2.91;7.65] 4.62 [2.61;7.29] 3.66 [1.67;6.14] 6023
Total ml/Kg with medical
dilution,
Median [Q1;Q3]
7.44 [4.61;11.5] 7.14 [4.67;10.6] 7.40 [4.23;11.3] 8.74 [5.20;13.5] 8.33 [3.70;14.0] 6142
30. Fluid Day Study_MJ. Colomina et al._ 2019
Dose & Total amount Postoperative period
All
Surgery Low-
Intermediate
& Patient Low Risk
Surgery Low-
Intermediate
& Patient High Risk
Surgery High-Very high
& Patient Low Risk
Surgery High-Very high
& Patient High Risk
N
N=6314 N=3830 N=943 N=987 N=554
Crystalloid administrated = crystalloid + medical dilution
Total ml/Kg ,
Median [Q1;Q3]
5.26 [2.86;9.24] 4.62 [2.67;7.65] 5.56 [2.94;10.0] 6.90 [3.85;12.8] 8.73 [4.15;18.3] 5511
Total ml/Kg / h,
Median [Q1;Q3]
3.92 [2.15;7.32] 3.90 [2.12;7.19] 3.96 [2.14;7.88] 4.01 [2.35;7.10] 3.88 [2.00;7.50] 5420
Total ml/Kg with medical
dilution,
Median [Q1;Q3]
5.56 [3.06;9.80] 5.00 [2.78;8.20] 5.92 [3.11;10.6] 7.40 [4.16;13.9] 9.21 [4.44;20.8] 5607
Corrected crystalloid administrated = crystalloid + medical dilution - estimated blood loss - urine output
Total ml/Kg,
Median [Q1;Q3]
3.53 [1.44;6.94] 3.37 [1.49;6.35] 3.64 [1.54;7.14] 3.79 [1.43;8.51] 4.05 [0.67;10.5] 5455
Total ml/Kg / h,
Median [Q1;Q3]
2.80 [1.05;6.03] 3.06 [1.23;6.37] 2.71 [1.06;6.13] 2.47 [0.76;5.21] 1.97 [0.28;4.83] 5364
Total ml/Kg with medical
dilution,
Median [Q1;Q3]
3.87 [1.67;7.35] 3.68 [1.67;6.72] 4.05 [1.80;7.69] 4.24 [1.79;9.32] 4.61 [1.07;12.2] 5550
31. Fluid Day Study_MJ. Colomina et al._ 2019
Fluid Therapy management
All
Surgery Low-
Intermediate
& Patient Low Risk
Surgery Low-
Intermediate
& Patient High Risk
Surgery High-Very
high
& Patient Low Risk
Surgery High-Very high
& Patient High Risk
N
N=6246 N=3791 N=928 N=980 N=547
Basic Monitoring
(NIBP,EGC, SpO2,
Et.Co2), N (%)
6187 (99.1%) 3757 (99.1%) 917 (98.8%) 968 (98.8%) 545 (99.6%) 6246
Invasive BP, N (%) 630 (10.1%) 133 (3.52%) 122 (13.2%) 169 (17.3%) 206 (38.0%) 6215
VCP, N (%) 243 (3.91%) 40 (1.06%) 41 (4.43%) 61 (6.27%) 101 (18.6%) 6207
Urinary output, N (%) 1915 (30.9%) 830 (22.0%) 357 (38.6%) 415 (42.7%) 313 (57.4%) 6207
Avanced Hemodynamic
Monitoring, N (%)
206 (3.32%) 32 (0.85%) 36 (3.90%) 53 (5.42%) 85 (15.6%) 6213
32. Fluid Day Study_MJ. Colomina et al._ 2019
Fluid Therapy management
Surgery High-Very high Risk & Patient High Risk
All N
N=547
Basic Monitoring (PANI,EGC, SpO2), N (%) 545 (99.6%) 547
Avanced Hemodynamic Monitoring, N (%) 85 (15.6%) 546
Pulmonary Artery Catheter (PAC), N (%) 11 (12.9%) 85
Transpulmonary Thermodilution (TPT), N (%) 2 (2.35%) 85
Transesophageal Echocardiography (TEE), N (%) 51 (60.0%) 85
Transthoracic Echocardiography (TTE), N (%) 3 (3.53%) 85
Pulse wave contour analysis (PWC) invasive, N (%) 39 (45.9%) 85
Pulse wave contour analysis (PWC) non invasive, N (%) 4 (4.71%) 85
Esophageal Doppler, N (%) 2 (2.35%) 85
Other, N (%) 2 (2.35%) 85
Fluid challenge (1), N (%) 80 (14.7%) 543
Fluid challenge (2), N (%) 24 (30.0%) 80
Fluid challenge (3), N (%) 6 (26.1%) 23
33. Fluid Day Study_MJ. Colomina et al._ 2019
Fluid Therapy management
All
Surgery Low-
Intermediate
& Patient Low Risk
Surgery Low-
Intermediate
& Patient High Risk
Surgery High-Very
high
& Patient Low Risk
Surgery High-Very high
& Patient High Risk
N
N=6246 N=3791 N=928 N=980 N=547
Intraoperative
Hemocomponents, N (%) 172 (2.79%) 18 (0.48%) 50 (5.44%) 24 (2.48%) 80 (14.8%) 6166
Fluid challenge (1), N (%) 396 (6.41%) 151 (4.03%) 88 (9.61%) 77 (7.93%) 80 (14.7%) 6174
Fluid challenge (2), N (%) 87 (22.2%) 21 (14.0%) 22 (25.3%) 20 (26.7%) 24 (30.0%) 392
Fluid challenge (3), N (%) 18 (21.4%) 3 (14.3%) 6 (30.0%) 3 (15.0%) 6 (26.1%) 84
Postoperative
Hemocomponents, N (%) 80 (1.36%) 16 (0.44%) 24 (2.76%) 20 (2.20%) 20 (4.29%) 5868
Fluid challenge (1), N (%) 136 (2.32%) 42 (1.16%) 23 (2.66%) 28 (3.07%) 43 (9.21%) 5865
Fluid challenge (2), N (%) 36 (26.5%) 7 (16.7%) 8 (34.8%) 6 (21.4%) 15 (34.9%) 136
Fluid challenge (3), N (%) 6 (16.7%) 1 (14.3%) 1 (12.5%) 1 (16.7%) 3 (20.0%) 36
35. The type of fluids:
Crystalloids were used in 98.2% of surgeries.
79% of cases used balanced solutions, colloids in 8% of patients.
Volume of fluids administered:
Total ml/Kg / h: 5.15 [3.00;8.21]
Total ml/Kg with medical dilution 7.44 [4.61;11.5]
Fluid management:
Surgery High-Very high & Patient High N=547 / 85 (15.6%)
Surgery High-Very high & Patient Low N=980 / 53 (5.42%)
Discusion
Fluid Day Study_MJ. Colomina et al._ 2019
36. n(%)
Exponentiated coefficients
[IC95%]
% change P-value ICC AIC N
Surgery risk
Intermediate vs Low 3768 (62.39%) 0.936 [0.915;0.958] -6.36 <0.001 0.055 35529 6039
High vs Low 962 (15.93%) 0.861 [0.837;0.885] -13.92 <0.001
Very high vs Low 520 (8.61%) 0.854 [0.826;0.882] -14.64 <0.001
Patient factors
Age (yrs)
scale(age) 0.985 [0.977;0.993] <0.001 0.056 35653 6039
scale(age)^2 1.009 [1.003;1.016] 0.006
ASA
II vs I 3440 (56.96%) 0.934 [0.916;0.952] -6.59 <0.001 0.056 35541 6039
III vs I 1285 (21.28%) 0.888 [0.867;0.909] -11.24 <0.001
IV-V vs I 138 (2.29%) 0.786 [0.746;0.828] -21.4 <0.001
Commorbidity
Y vs N 4256 (70.85%) 0.923 [0.908;0.939] -7.65 <0.001 0.057 35424 6007
Number of commorbidities 0.971 [0.967;0.976] -2.89 <0.001 0.058 34914 5930
Commorbidities > 3 vs <3 or
not
718 (12.11%) 0.901 [0.881;0.922] -9.89 <0.001 0.057 34982 5930
Gender, Female vs Male 3087 (51.12%) 1.047 [1.031;1.062] +4.66 <0.001 0.056 35644 6039
Scale(Hb), preoperative 1.002 [0.992;1.013] +0.22 0.677 0.056 34418 5818
Factors associated with the variability of crystalloid use: % Univariate factors associated with crystalloids
Fluid Day Study_MJ. Colomina et al._ 2019
37. Miller TE1, Myles PS. Perioperative Fluid Therapy for Major Surgery.
Anesthesiology. 2019 May;130(5):825-832. doi: 10.1097/ALN.0000000000002603.
Fluid Day Study_MJ. Colomina et al._ 2019
Dose: 7.14 mL[4.67;10.6] Dose: 7.40 mL [4.23;11.3]
Dose: 8.74 mL [5.20;13.5] Dose: 8.33 mL [3.70;14.0]
Avanced M: 32 (0.85%)
FC: 151 (4.03%)
Avanced M: 36 (3.90%)
FC: 88 (9.61%)
Avanced M: 53 (5.42%)
FC: 77 (7.93%)
Avanced M: 85 (15.6%)
FC: 80 (14.7%)
38. Take messages at home:
• There is a clear tendency to fluid
overload patients in any type of surgery.
• Balanced crystalloids are the most used
in our daily practice, with minimum use of
colloids.
• The management of fluid therapy with
monitoring should improve especially in
patients and surgeries with high risk.
Fluid Day Study_MJ. Colomina et al. _ 2019
39. We believe
FLUID DAY STUDY
is an example of
collaborative
research between
different centers
with the objective
to answer a clinical
question that could
in the future be
applied into clinical
practice
Fluid Day Study_MJ. Colomina et al._ 2019
Editor's Notes
Good afternoon,
Thanks to the scientific committee of this meeting for having invited me to participate
and present the preliminary results of our study on the management of fluid therapy in the immediate intra and postoperative period.
The Spanish Fluid day study has been designed by a magnificent team of anesthesiologists
who are members of the hemostasis, transfusion medicine and fluid therapy section of the SEDAR.
And thank you very much for their effort to carry out this study
This study was supported by SEDAR.
First, this is my conflict of interest
The fluid therapy management during the perioperative period,
as the editorial points out, may be more complex than we think.
We have few good quality scientific studies and, most of them were dedicated especially to critical patients.
But in the perioperative period there is increasing evidence that intraoperative fluid administration has a definitive effect on surgical patient outcomes
there is a lower contribution of studies and the majority have focused on some specific type of surgery, for example abdominal surgery.
Our question is
How is fluid therapy managed in the usual surgical environment:
Intraoperative and postoperative period until the first 24 hours
Probably, The variability in the administration of perioperative fluid therapy has shown that
it can have important repercussions in the immediate postoperative evolution,
especially in certain types of complex patients and in highly complex surgeries.
At least in moderate to high risk patients
I am goin to comment two spanish studies
At the same time, two studies published related at the variability in diffefrent scenarios
Who included intraoperative period
For that,
We think that
And our main questions focused on the following
Methods: A multicenter prospective observational cross-sectional study - 24-hour Prevalence Cut off is proposed to evaluate the fluid therapy administered by anesthesiologists in surgical patients.
The study will be carried out simultaneously in all hospitals that decide to participate throughout the Spanish territory and the follow-up period will be a maximum of 24 hours. T
Two different weekly days will be chosen to include the maximum number of episodes and types of surgeries.
Relevance: The clinical practice guidelines with their recommendations or suggestions offer a safety tool for patients based on current scientific evidence, hence the importance of its correct implementation. Sometimes problems of dissemination of information or limitations in the application of the same can cause that these objectives are not met.
The variables that collect the clinical characteristics of the patients, the characteristics of the surgical process and the fluids used will be analyzed according to the type of variable.
We recorded these data in both periods:
Intra and postoperative periods.
In order to classified the differents types of surgery,
Risk factors that increase the likelihood of perioperative morbidity and mortality may include the patient’s underlying health problems as well as factors associated with each specific type of surgery. By combining risk scores for patient co-morbidity and the complexity of surgery, we can stratify overall risk and determine which patients should undergo more extensive preoperative evaluation.
Risk factors that increase the likelihood of perioperative morbidity and mortality may include the patient’s
underlying health problems as well as factors associated with each specific type of surgery.
By combining risk scores for patient co-morbidity and the complexity of surgery,
we can stratify overall risk and determine which patients should undergo more extensive preoperative evaluation.
These were the preliminary results
The majority of people included were men and women from forty to seventy years of age
And moderate over weight
Related to the type of surgery, lthe most prevalent
Chedul
Profile surgeries
Crystalloids were used in 6203 (98.2%) interventions. In 25% of the interventions a single crystalloid was used,
between 50% and 75% 2 crystalloids were used and in 25% of the interventions 2 crystalloids or more were used.
The most commonly used crystalloid were the balanced ones.
The same data was found for the postoperative period
Colloids were used in 466 (7.51%) interventions.
A single colloid was used in 75% of the interventions, and 1 or more colloids were used in 25% of the interventions.
The maximum number of colloids used was 2 in the same intervention.
The colloids most used were the HEA.
8.7% of patients very high risk 1% from total haigh risk recieved colloids
Colloids were used in 466 (7.51%) interventions.
A single colloid was used in 75% of the interventions, and 1 or more colloids were used in 25% of the interventions.
The maximum number of colloids used was 2 in the same intervention.
The colloids most used were the HEA.
Probably, The variability in the administration of perioperative fluid therapy has shown that
it can have important repercussions in the immediate postoperative evolution,
especially in certain types of complex patients and in highly complex surgeries.
At least in moderate to high risk patients
P-value column: Factors statistically explained the volume of crystalloids administered.
% Change column: In the categorical variables the% reduction or increase in the respect factor one of reference. In the non-standardized numerical variables the% reduction or increase of the factor for each unit of the factor. In standardized numerical variables the% reduction or increase of the factor for each standard deviation of the factor.
ICC column: The% of the variability of crystalloids administration explained by the hospital where the intervention was performed
For example: The complexity of the surgery explained the volume of crystalloids administered statistically significantly. The more complex the intervention, the less administration of crystalloids compared to low-risk surgeries. We see that in intermediate surgeries it was reduced by -6.36% with respect to low risk surgeries, in those of high risk it was reduced by -13.92% and in those of very high risk by -14.64%. Using the risk of surgery as the only explanatory variable, only 5.5% of the variability in colloid volume was explained by the hospital where the intervention was performed (CHF = 0.055)
We have shown that there is variability in clinical practice,
We have shown that there is variability in clinical practice and it's knowledge will help us to improve.
Fortunately, conducting these high quality studies will help guide our practice in fluid therapy.
The knowledge of these, and the reflexive inclusion of the key findings in contemporary practice, should improve the care of patients undergoing major surgery.