Dr Vishram Buche Dept Of Pediatric Intensive Care Central India’s Child Hospital And Research Institute Nagpur.

Slides:



Advertisements
Similar presentations
DM SEMINAR FEBRUARY 27, 2004 OXYGEN - CARBON DIOXIDE TRANSPORT NAVNEET SINGH DEPARTMENT OF PULMONARY AND CRITICAL CARE MEDICINE PGIMER CHANDIGARH.
Advertisements

Formulas related to O2 transport Fiona Campbell BS, RRT-NPS Spring 2008.
Oxygen Therapy By Dr. Yasser Moustafa Assist. Prof.Pulmonology Ain Shams University.
The golden hour(s) for severe sepsis and septic shock treatment
Improving Oxygenation
Introduction to StO 2 Monitoring. Assess Tissue Perfusion Rapidly & Noninvasively.
Dr Archna Ghildiyal Associate Professor Department of Physiology KGMU Respiratory System.
Hatem O.Qutub MD,FCCP,FCCM.  Definition & Facts  Goals  Pathophysiology  Visibility of Permissive hypoxemia  How to monitor Permissive hypoxemia.
Oxygen Content Equation and Oxygen Transport 1. The Key to Blood Gas Interpretation: Four Equations, Three Physiologic Processes Equation Physiologic.
Dr. Abdul-Monim Batiha Monitoring in Critical Care Dr. Abdul-Monim Batiha.
Bengt Gerdin Oxygenation in patients with exceptionally high oxygen demand - and the role of hemotherapy.
Faisal Malmstrom, Critical Care Department SKMC
Oxygen Debt Critical Care Medicine Boston Medical Center Boston University School of Medicine Bradley J. Phillips, M.D. TRAUMA-ICU NURSING EDUCATIONAL.
Leanna R. Miller, RN, MN, CCRN,-CMC, PCCN-CSC CEN, CNRN, CMSRN, NP Education Specialist LRM Consulting Nashville, TN.
Integration of Cardiovascular and Respiratory Function  Oxygen consumption is the amount of O 2 taken up and consumed by the body for metabolic processes.
Matthew Boland MD, FCCP Pulmonary/CCM. A definition of SHOCK Global tissue hypoxia “global” implying systemically while “tissue hypoxia” implies inadequate.
Sepsis.
OXYGEN EQUILIBRIUM AND TRANSPORT
Blood Gases: Pathophysiology and Interpretation
Oxygen: Consumption and Delivery PICU Resident Talk Stanford School of Medicine Pediatric Critical Care Medicine June 2010.
Haemodynamic Monitoring Theory and Practice. 2 Haemodynamic Monitoring A.Physiological Background B.Monitoring C.Optimising the Cardiac Output D.Measuring.
Author(s): Louis D’Alecy, 2009 License: Unless otherwise noted, this material is made available under the terms of the Creative Commons Attribution–Non-commercial–Share.
Chapter 6 The Respiratory System and Its Regulation.
OXYGEN THERAPY Dora M Alvarez MD Oxygen Delivery Systems A-a Gradient Oxygen Transport Oxygen Deliver to Tissues.
Objectives Discuss the principles of monitoring the respiratory system
OXYGENATION AND ACID-BASE EVALUATION
Respiratory System Physiology
Pathophysiology of Respiratory Failure Fern White & Annabel Fothergill.
Respiratory Regulation During Exercise
Emergency Oxygen Professor Thida Win 10/03/2015SCN Emergency Oxygen Event.
Analysis and Monitoring of Gas Exchange
Protective Lung Strategy Mazen Kherallah, MD, FCCP
Haemodynamic Monitoring Theory and Practice. 2 Haemodynamic Monitoring A.Physiological Background B.Monitoring C.Optimizing the Cardiac Output D.Measuring.
Patient Monitoring Stuart Nurre, MS, R.R.T.. Oxygenation Goal of respiratory therapy is return the patient to a normal oxygenation status, while minimizing.
HYPOXIA RESPIRATORY FAILURE
Shock and Anaphylaxis Chapter 37 Written by: Melissa Dearing – LSC-Kingwood.
Pediatric Septic Shock
ARTERIAL BLOOD GAS ANALYSIS Arnel Gerald Q. Jiao, MD, FPPS, FPAPP Pediatric Pulmonologist Philippine Children’s Medical Center.
 How much oxygen do you need? ◦ “natural experiments” ◦ “critical care research”  Is oxygen toxic?
Learning objectives Understand the Effect of low oxygen pressure on the body. Understand the Effect of high partial pressure of individual gases on the.
RESPIRATORY 221 WEEK 4 CH.8. Oxygen transport Mixed venous blood – pulmonary capillary - PvO2 40mmHg - PAO2 100mmHg – diffuses through pressure gradient.
Assistant Prof: Nermine Mounir Riad Ain Shams University, Chest Department.
Respiratory Respiratory Failure and ARDS. Normal Respirations.
1 Mosby items and derived items © 2011, 2006 by Mosby, Inc., an affiliate of Elsevier Inc. Chapter 5 Oxygenation Assessments Oxygenation Assessments.
Pierre SQUARA, MD Clinique Ambroise Paré, Neuilly Should we (can we) measure and optimize VO 2 in shock.
Control of Breathing. Objectives 1.Distinguish between the automatic and conscious/voluntary control of breathing. Identify the key structures involved.
Oxygen Transport: A Clinical Review Bradley J. Phillips, M.D.
Ventilation Strategies in ARDS MICU-ER Joint Conference Dr. Rachmale, Dr. Prasankumar 12/3/08.
© 2007 McGraw-Hill Higher Education. All rights reserved. Chapter 11 Oxygen Transport.
RESPIRATORY FAILURE DR. Mohamed Seyam PhD. PT. Assistant Professor of Physical Therapy.
Dr Vishram Buche Central India’s CHILD hospital & Research Institute, NAGPUR.
By: Richard Smith FM-20 FPC/Critical Care
Invasive Mechanical Ventilation
PSK4U Respiratory Dynamics.
The transport of oxygen
pH PC02 Condition Decreased Increased Respiratory acidosis
1.9 Copyright UKCS #
HYPOXIA RESPIRATORY FAILURE
Flow Monitoring Approaches
Ventilation Perfusion Relationships
The Respiratory System and Its Regulation
Chapter 22 – The Respiratory System
Acute Respiratory Failure
CLINICAL INTERPRETATION OF ABG
Competency Title : Observations and The Deteriorating Patient for HCAs Competency Lead : Vikki Crickmore, Sister, Critical Care Outreach Team September.
Nathir Obeidat University of Jordan
Arterial Blood Gas Analysis
Arterial blood gas By Maha Subih.
RESPIRATORY REGULATION DURING EXERCISE
Presentation transcript:

Dr Vishram Buche Dept Of Pediatric Intensive Care Central India’s Child Hospital And Research Institute Nagpur

PERMISSIVE H YPOXEMIA Lung protective strategy Lung protective strategy Oxy/Baro. trauma

PERMISSIVE HYPOXEMIA….. (PH) PEEP Prone ventilation Lung recruitment manoeuvres (LRM) Pressure controlled inverse ratio ventilation (PC-IRV) Low TV and permissive hypercapnia L UNG P ROTECTIVE S TRATEGIES………..

Definition & Facts…….Goals…….Pathophysiology……Visibility of Permissive hypoxemia….Monitoring Permissive hypoxemia..? O BJECTIVES 6 Take home massage / conclusion….

D EFINITION ………

A rapid ↓ in CaO 2 developing < 6 hrs Acute hypoxemia ↓ CaO 2 occurring in 6 hrs to 7 days (e.g., pneumonia) ↓ CaO 2 occurring in 6 hrs to 7 days (e.g., pneumonia) Subacute hypoxemia ↓ CaO 2 for 7–90 days (e.g., prolonged ARDS, high altitude) ↓ CaO 2 for 7–90 days (e.g., prolonged ARDS, high altitude) Sustained hypoxemia Prolonged ↓ of CaO 2 for over 90 days (e.g., COPD) Prolonged ↓ of CaO 2 for over 90 days (e.g., COPD) Chronic hypoxemia Cross-generational ↓ CaO 2 (e.g., Tibetan highland residents) Cross-generational ↓ CaO 2 (e.g., Tibetan highland residents) Generational hypoxemia Crit Care Med 2013; 41:0–0 FACTS : C LINICAL CLASSIFICATION OF HYPOXIA

…….. F ACTS …… Wilson DF, Erecinska M: The oxygen dependence of cellular energy metabolism. Adv Exp Med Biol 1986; 194:229–239

How much ↓SaO 2 is tolerated in the critically ill is difficult to determine and still remains unclear Targeting normoxemia…….. in acute situations, NOT achievable/ beneficial in critically ill patients with subacute or sustained hypoxemia VO 2 is governed by metabolic activity rather than oxygen supply, but this relationship can be modified during the inadequate oxygen supply Wilson DF, Erecinska M: The oxygen dependence of cellular energy metabolism. Adv Exp Med Biol 1986; 194:229–239 …….. F ACTS ……..

Prolonged hypoxia….VO 2 ↓es 40 to 60% (down-regulation of "non-essential" cellular processes) ↓ in VO 2 not only attenuates the deficient DO 2, but also make cells less susceptible to hypoxic injury even if DO 2 falls to critical level This phenomenon is reversible on re-exposure to normoxia and is not associated with demonstrable long- term cellular harm. This is "oxygen conformance" Wilson DF, Erecinska M: The oxygen dependence of cellular energy metabolism. Adv Exp Med Biol 1986; 194:229–239 …….. F ACTS ……..

F ACTS …….. C LINICAL "A CCLIMATIZATION " TO H YPOXEMIA AND C ELLULAR H YPOXIA Exposure to subacute and sustained hypoxemia permits a coordinated process of adaptation, referred to as acclimatization. It is unlikely that critically ill patients mount such effective cardiorespiratory countermeasures to increase oxygen delivery as a result of their underlying pathology Levett DZ, Radford EJ, Menassa DA, et al; Acclimatization of skeletal muscle mitochondria to high-altitude hypoxia during an ascent of Everest. FASEB J 2012; 26: 1431– Levy RJ, Deutschman CS: Deficient mitochondrial biogenesis in critical illness: Cause, effect, or epiphenomenon? Crit Care 2007; 11:158 3.Ruggieri AJ, Levy RJ, Deutschman CS: Mitochondrial dysfunction and resuscitation in sepsis. Crit Care Clin 2010; 26:567–575, x

1.Levett DZ, Radford EJ, Menassa DA, et al; Acclimatization of skeletal muscle mitochondria to high-altitude hypoxia during an ascent of Everest. FASEB J 2012; 26: 1431– Levy RJ, Deutschman CS: Deficient mitochondrial biogenesis in critical illness: Cause, effect, or epiphenomenon? Crit Care 2007; 11:158 3.Ruggieri AJ, Levy RJ, Deutschman CS: Mitochondrial dysfunction and resuscitation in sepsis. Crit Care Clin 2010; 26:567–575, x F ACTS …….. C LINICAL "A CCLIMATIZATION " TO H YPOXEMIA AND C ELLULAR H YPOXIA Skeletal muscle biopsies of healthy volunteers exposed to sustained hypoxia at high altitude…… 1 Deactivation of mitochondrial biogenesis 2 Down-regulation of mitochondrial uncoupling, …………….resulting in improved efficiency of ATP production. Comparable changes in mitochondrial biogenesis also occur in critically ill patients and may reflect similar adaptive responses

G OAL OF P ERMISSIVE H YPOXEMIA

…relatively low SaO 2, while maintaining adequate DO 2 …....the detrimental effects of high ventilatory support on pulmonary and other systems as well ….morbidity and mortality in selected hypoxemic patients who have had sufficient time to adapt this low PO 2 M INIMIZE … A CCEPT … R EDUCE …

DO 2 x (SaO 2 -SvO 2 ) = Oxygen Balance Oxygen Balance Oxygen Delivery DO 2 Oxygen Delivery DO 2 VO 2 /DO 2 is normally 25% Rising VO 2 /DO 2 ratio is a sign of inadequate tissue oxygenation Oxygen Consumption VO 2 Oxygen Consumption VO 2 DO 2 x (SaO 2 -SvO 2 ) = = CO x CaO 2 O 2 demand

PaO 2 SaO 2 OXY (Sat) 98% HAEMOGLOBIN 2 % Dissolved Oxygen O. D. C. PAO 2 A.C.I. CaO 2 Content of oxygen Ml/100 of blood Delivery Of Oxygen DO 2 Cardiac output D ETERMINANTS OF O 2 D ELIVERY …………… VO 2

O 2 unloaded from Hb during normal metabolism O 2 unloaded from Hb during normal metabolism O 2 reserves that can be unloaded from Hb to tissues with increased demands O 2 reserves that can be unloaded from Hb to tissues with increased demands Vol % CaO 2

DO 2 Oxygen delivery ml/min VO 2 Oxygen consumption ml/min Delivery dependant consumption Delivery Independant consumption Lactic acid Oxygen extraction O 2 ER VO 2 -DO 2 relationship…. 250 C-DO 2 60% O 2 ER……………………….25% 300

Oxygen delivery DO 2 Oxygen consumption VO 2 Delivery dependant consumption Delivery Independant consumption Lactic acid Oxygen extraction O 2 ER Critic DO VO 2 -DO 2 relationship….

Vol % CaO Hb Saturation (%) PO 2 (mmHg) 40

Oxygen Therapy in Critical Illness D S Martin; M Patrick William Grocott, Crit Care Med. 2013;41(2):423­432 1.Precise control of arterial oxygenation 2.Permissive hypoxemia

Individualised therapeutic target of O 2 Age Clinical setting Underlying disease Chronicity Comorbidities Arterial oxygenation Hypoxia Hyperoxemia P RECISE CONTROL OF ARTERIAL OXYGENATION ………….C ONCEPTOGRAM Where do we stand ?

Permissive hypoxemia target zone Hypoxia Hyperoxemia P ERMISSIVE HYPOXEMIA …….. CONCEPTOGRAM acclimatization Arterial oxygenation Individualised therapeutic target of O 2 hypoxemia It Can Be done…..!!

V ISIBILITY OF P ERMISSIVE HYPOXEMIA ……..!!!!

Why do I have to allow patient to low O 2..? T HERAPY INTERVENTION M ECHANICAL VENTILATION Prone positioning HFOV Inhaled NO ECMO Prone positioning HFOV Inhaled NO ECMO High FiO 2 High Positive pressure High FiO 2 High Positive pressure

O BSERVATIONS ……….. 1) Improved oxygenation but unchanged outcome 2) Deterioration in oxygenation but unchanged outcome 3) Improved outcome despite unchanged oxygenation

S TRATEGY OF PERMISSIVE HYPOXEMIA Aims for an SaO 2 ….. “82% -- 88%”, PaO 2 … Not to direct a specific SaO 2 goal but, rather, a careful balance between the target SaO 2 and the ventilatory support required to achieve a higher SaO 2 The actual goal SaO 2 will probably differ between patients and vary in an individual patient over time

H OW TO MONITOR P ERMISSIVE HYPOXEMIA H OW TO MONITOR P ERMISSIVE HYPOXEMIA ………… ?

Cellular O 2 markers Clinical Abnormal skin perfusion, ↓ed urine output, Hypotension. Lactate……… Lacti-time?, pH Mixed venous oxygen saturation (SvO 2 ) < 50% Mixed veno-arterial CO 2 gradient ….VO 2 < 180 ml/min or < 2.4 ml/kg/min ….(SaO 2 - SvO 2 ) > 50%, O 2 ER < 60% B IOMARKERS OF HYPOXIA ……………….. OR E ND POINTS OF LOW PO 2 ………………..

Gastric Intra mucosal pH Real-time in vivo speckle laser Near infrared spectroscopy (NIRS) Fluorescence quenching Micro dialysis A DVANCE T ISSUE O XYGENATION M ONITORING

What are the potential risks of p ermissive hypoxemia ? Is p ermissive hypoxemia equally tolerated by different organ systems?

The SELECTION of optimum SaO 2 goals is essential if cellular hypoxia and hyperoxia as well (and ventilation) are to be avoided. There are NO generally acceptable THRESHOLDS for the lower limit of oxygenation that can be tolerated and individual evaluation is crucial when determining prescribed targets.

 NEW TECHNOLOGIES and biomarkers ….. patient selection, and provide an umbrella of safety with regards to tissue oxygenation.  At present, any immediate change in clinical practice toward permissive hypoxemia is NOT JUSTIFIED in the absence of experimental data in critically ill patients.  Permissive Hypoxemia in critically ill patients should be a high RESEARCH PRIORITY

T AKE HOME MASSAGE  The body can survive hypoxia by mean of " ACCLIMATIZATION “  Permissive hypoxemia has a target end point  Bed side monitoring by pH, Lactate, SvO 2, O 2 ER…accepted indictors for adequacy of tissue oxygenation

Abdelsalam M. Permissive hypoxemia: Is it time to change our approach? Chest 2006;129(1): Guyton AC, Hall JE. Textbook of medical physiology: transport of oxygen and carbon dioxide in the blood and tissue fluids. Philadelphia: Mosby Elsevier Saunders; 2006: Mohamed Abdelsalam MD and Ira M Cheifetz MD FAARC Goal directed therapy with ARDS : permissive hypoxemia RESPIRATORY CARE Nov 2010 Vol 55 NO. 11 D S Martin : Oxygen therapy in critical illness : Crit Care Med 2013;41(2):

T HANKS