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What’s New In Pediatric ARDS Nancy G. Hoover, MD Medical Director, PICU Walter Reed AMC
New and Improved Acute  Respiratory Distress Syndrome Ashbaugh,  Lancet , 1967 Adult  Respiratory Distress Syndrome To distinguish from neonatal HMD/RDS Acute  Respiratory Distress Syndrome American-European Consensus conference, 1994
ARDS:  New Definition ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],1994  American-European Consensus  Conference
Clinical Disorders Associated with ARDS ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
The Problem: Lung Injury Other 4% Hemorrhage 5% Trauma 5% Noninfectious Pneumonia 14% Cardiac Arrest 12% Septic Syndrome 32% Infectious Pneumonia 28% Davis et al., J Peds 1993;123:35
ARDS - Pathogenesis ,[object Object],[object Object],[object Object],[object Object]
ARDS Pathogenesis ,[object Object],[object Object],[object Object],[object Object],[object Object]
ARDS - Pathophysiology ,[object Object],[object Object],[object Object],[object Object]
 
 
Phases of ARDS ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Phases of ARDS
ARDS - Outcomes ,[object Object],[object Object],[object Object],[object Object],[object Object]
ARDS - Principles of Therapy ,[object Object],[object Object]
It would seem ironic that the very existence of humans is fully dependent on a gas that, in excess quantities, is toxic and lethal Lynn D. Martin
Therapies for ARDS Innovations: iNO PLV Proning Surfactant Anti-Inflammatory Mechanical Ventilation Gentle ventilation: Permissive hypercapnia Low tidal volume Open-lung HFOV ARDS Extrapulmonary Gas Exchange
The Dangers of Overdistention ,[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],The Dangers of Atelectasis
Lung Injury Zones Atelectasis “ Sweet Spot” Overdistention
“Mechanical” Therapies in ARDS ,[object Object],[object Object],[object Object],[object Object]
Lower Tidal Volumes for ARDS ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],ARDS Network, NEJM, 342: 2000
Lower Tidal Volumes for ARDS * * * p < .001 ARDS Network, NEJM, 342: 2000 22% decrease
Ventilator Goals ,[object Object],[object Object],[object Object],[object Object]
Permissive Hypercapnia ,[object Object],Hickling,  Int Care Med , 1990
Physiologic Effects of Hypercapnia ,[object Object],[object Object],[object Object]
Physiologic Effects of Hypercapnia ,[object Object],[object Object],[object Object],[object Object],[object Object]
Physiologic Effects of Hypercapnia ,[object Object],[object Object],[object Object],[object Object],[object Object]
Permissive Hypercapnia Is it worth it? ,[object Object],[object Object],[object Object],[object Object],Hickling,  CCM , 1994 Nathens,  J Trauma,  2005 Sheridan,  J Trauma , 1995 Paulson,  J Pediatr , 1996
High Frequency Oscillation: A Whole Lotta Shakin’ Goin’ On
It’s not absolute pressure, but  volume  or  pressure  swings that promote lung injury or atelectasis. Reese Clark
[object Object],[object Object],[object Object],[object Object],High Frequency Ventilation
Differences Between CMV and HFOV
HFOV vs. CMV in Pediatric  Respiratory Failure: Results ,[object Object],[object Object],[object Object],Arnold et al, CCM, 1994
HFOV vs. CMV in Pediatric Respiratory Failure - Arnold et al,  CCM , 1994 *
[object Object],[object Object],[object Object],HFOV: Outcomes of Randomized Controlled Trials
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Indications for HFOV
Is turning the ARDS patient “prone” helpful?
Prone Positioning in ARDS ,[object Object],[object Object],[object Object],[object Object]
 
 
Prone Positioning in Adult ARDS ,[object Object],[object Object],[object Object],[object Object],[object Object],Gattinoni et al., NEJM, 2001
Conflicting Evidence for Proning? ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Pharmacological Therapies in ARDS ,[object Object],[object Object],[object Object],[object Object]
Surfactant in ARDS ,[object Object],[object Object],[object Object],[object Object]
Calf’s Lung Surfactant Extract in Acute Pediatric Respiratory Failure ,[object Object],[object Object],[object Object],[object Object],Wilson et al,  CCM , 24:1996 Wilson et al,  JAMA , 2005
Steroids in ARDS ,[object Object],[object Object],[object Object],[object Object],[object Object]
Effects of Prolonged Steroids in Unresolving ARDS ,[object Object],[object Object],[object Object],[object Object],[object Object],Meduri et al,  JAMA , 1998
Steroids in Unresolving ARDS ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Meduri et al,  JAMA , 1998
Steroids in Unresolving ARDS * * p<.01 *
What about after first 28 days? ,[object Object],[object Object],[object Object],[object Object],[object Object]
Inhaled Nitric Oxide in Respiratory Failure ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
ECMO and NO in Neonates ,[object Object],[object Object],Clark et al, NEJM, 2000
Effects of Inhaled Nitric Oxide In Children with AHRF ,[object Object],[object Object],[object Object],[object Object],Dobyns, et al., J. Peds, 1999
 
Inhaled NO and HFOV In Pediatric ARDS Dobyns et al.,  J Peds , 2000
Partial Liquid Ventilation ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Liquid Ventilation ,[object Object],[object Object],[object Object],[object Object],[object Object]
ARDS- “Mechanical” Therapies Low tidal volumes  Outcome benefit in      large study  Prone positioning Unproven outcome benefit  Open-lung strategy Outcome benefit in      small study HFOV Outcome benefit in      small study ECMO Proven in neonates      unproven in children
Pharmacologic Approaches to ARDS: Randomized Trials Steroids - acute no benefit - fibrosing alveolitis lowered mortality,    small study Surfactant possible benefit in    children Inhaled NO no benefit PLV  no benefit
“…We must discard the old approach and continue to search for ways to improve mechanical ventilation.  In the meantime, there is no substitute for the clinician standing by the ventilator…” Martin J. Tobin, MD
If you think about ECMO,  it is worth a call to consider ECMO
 
Pediatric ECMO ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Impact of ECMO on Survival in Pediatric Respiratory Failure ,[object Object],[object Object],[object Object],[object Object],[object Object],-Green et al, CCM, 24:1996
Impact of ECMO on Survival in Pediatric Respiratory Failure % Mortality p<0.05 Green et al,  CCM , 1996 mortality risk quartile

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New Therapies for Pediatric ARDS

  • 1. What’s New In Pediatric ARDS Nancy G. Hoover, MD Medical Director, PICU Walter Reed AMC
  • 2. New and Improved Acute Respiratory Distress Syndrome Ashbaugh, Lancet , 1967 Adult Respiratory Distress Syndrome To distinguish from neonatal HMD/RDS Acute Respiratory Distress Syndrome American-European Consensus conference, 1994
  • 3.
  • 4.
  • 5. The Problem: Lung Injury Other 4% Hemorrhage 5% Trauma 5% Noninfectious Pneumonia 14% Cardiac Arrest 12% Septic Syndrome 32% Infectious Pneumonia 28% Davis et al., J Peds 1993;123:35
  • 6.
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  • 10.  
  • 11.
  • 13.
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  • 15. It would seem ironic that the very existence of humans is fully dependent on a gas that, in excess quantities, is toxic and lethal Lynn D. Martin
  • 16. Therapies for ARDS Innovations: iNO PLV Proning Surfactant Anti-Inflammatory Mechanical Ventilation Gentle ventilation: Permissive hypercapnia Low tidal volume Open-lung HFOV ARDS Extrapulmonary Gas Exchange
  • 17.
  • 18.
  • 19. Lung Injury Zones Atelectasis “ Sweet Spot” Overdistention
  • 20.
  • 21.
  • 22. Lower Tidal Volumes for ARDS * * * p < .001 ARDS Network, NEJM, 342: 2000 22% decrease
  • 23.
  • 24.
  • 25.
  • 26.
  • 27.
  • 28.
  • 29. High Frequency Oscillation: A Whole Lotta Shakin’ Goin’ On
  • 30. It’s not absolute pressure, but volume or pressure swings that promote lung injury or atelectasis. Reese Clark
  • 31.
  • 33.
  • 34. HFOV vs. CMV in Pediatric Respiratory Failure - Arnold et al, CCM , 1994 *
  • 35.
  • 36.
  • 37. Is turning the ARDS patient “prone” helpful?
  • 38.
  • 39.  
  • 40.  
  • 41.
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  • 46.
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  • 48.
  • 49. Steroids in Unresolving ARDS * * p<.01 *
  • 50.
  • 51.
  • 52.
  • 53.
  • 54.  
  • 55. Inhaled NO and HFOV In Pediatric ARDS Dobyns et al., J Peds , 2000
  • 56.
  • 57.
  • 58. ARDS- “Mechanical” Therapies Low tidal volumes Outcome benefit in large study Prone positioning Unproven outcome benefit Open-lung strategy Outcome benefit in small study HFOV Outcome benefit in small study ECMO Proven in neonates unproven in children
  • 59. Pharmacologic Approaches to ARDS: Randomized Trials Steroids - acute no benefit - fibrosing alveolitis lowered mortality, small study Surfactant possible benefit in children Inhaled NO no benefit PLV no benefit
  • 60. “…We must discard the old approach and continue to search for ways to improve mechanical ventilation. In the meantime, there is no substitute for the clinician standing by the ventilator…” Martin J. Tobin, MD
  • 61. If you think about ECMO, it is worth a call to consider ECMO
  • 62.  
  • 63.
  • 64.
  • 65. Impact of ECMO on Survival in Pediatric Respiratory Failure % Mortality p<0.05 Green et al, CCM , 1996 mortality risk quartile

Hinweis der Redaktion

  1. Ashbaugh first described the syndrome of severe respiratory failure similar to infant hyline membrane disease
  2. PCWP higher than 18 mmHg are generally considered to be c/w left-heart failure and may be the cause of cargiogenic pulmonary edema.
  3. Gattinoni “Concept of Baby Lung”, Intensive Care Medicine, 2005: The &amp;quot; baby lung &amp;quot; concept originated as an offspring of computed tomography examinations which showed in most patients with acute lung injury/acute respiratory distress syndrome that the normally aerated tissue has the dimensions of the lung of a 5- to 6-year-old child (300-500 g aerated tissue). DISCUSSION: The respiratory system compliance is linearly related to the &amp;quot; baby lung &amp;quot; dimensions, suggesting that the acute respiratory distress syndrome lung is not &amp;quot;stiff&amp;quot; but instead small, with nearly normal intrinsic elasticity. Initially we taught that the &amp;quot; baby lung &amp;quot; is a distinct anatomical structure, in the nondependent lung regions. However, the density redistribution in prone position shows that the &amp;quot; baby lung &amp;quot; is a functional and not an anatomical concept. This provides a rational for &amp;quot;gentle lung treatment&amp;quot; and a background to explain concepts such as baro- and volutrauma. CONCLUSIONS: From a physiological perspective the &amp;quot; baby lung &amp;quot; helps to understand ventilator-induced lung injury. In this context, what appears dangerous is not the V(T)/kg ratio but instead the V(T)/&amp;quot; baby lung &amp;quot; ratio. The practical message is straightforward: the smaller the &amp;quot; baby lung ,&amp;quot; the greater is the potential for unsafe mechanical ventilation.
  4. Axial CT of an experimental model of ARDS showing the heterogeneous distribution of lung disease. The gravitationally nondependent lung region (ventral) is relatively spared, whereas the dependent lung region (dorsal) exhibits greater involvement
  5. Extrapulmonary techniques ECMO IVOX IV gas exchange Total Implantable Artificial Lung
  6. 40% vs. 31% mortality Vent-free days in the first 28 days was significantly higher in the low tidal volume group (12 +/- 11 vs. 10 +/-11;p=0.007
  7. In Stewart’s study, If peak pressure is &lt;30 and tidal volume is &lt;8 mL/kg, then there was no difference in mortality.
  8. Hickling, Intensive Care Med 1990
  9. When hypercapnia is produced through the limitation of tidal volumes and inspiratory airway pressures without adequate PEEP, the Qs/Qt ratio increases secondary to progressive derecruitment of alveolar units. Under such conditions, oxygenation will be further impaired by the hypercapnia-induced increase in cardiac output. This increase in cardiac output induces a worsening Qs/Qt ratio as blood flow increases preferentially to the gravitationally dependent, poorly ventilated lung regions and results in additional intrapulmonary shunting The increase in Qs/Qt can frequently be counteracted through the optimization of lung volume by means of recruitment maneuvers and application of suitable levels of PEEP. Hypercapnic acidosis enhances hypoxic pulmonary vasoconstriction, thus improving ventilation-perfusion matching, decreasing Qs/Qt, and increasing the PaO2. Hypercapnic acidosis positively affects oxygen availability to tissues by promoting a right shift in the oxygen–hemoglobin dissociation curve. Net effect is improvement in oxygenation
  10. Hypercapnic acidosis has been shown to cause marked sympathetic stimulation with predictable increases in cardiac output due to the augmentation of heart rate and stroke volume secondary to decreased systemic vascular resistance
  11. Within hours of the onset of sustained hypercapnic acidemia, the kidneys initiate compensatory net reabsorption of sodium bicarbonate, generally returning blood pH to physiologic levels within 2 days.
  12. Effect of prone position on ventilation distribution. In the supine position, the distribution of ventilation is preferentially distributed to the ventral regions. When the patient is prone, the stiffness of the dorsal chest wall favors the distribution of ventilation to the dorsal regions, facilitating reinflation in this area.
  13. Post-hoc analysis showed an improvement in 10-day mortality in the prone group but overall ventilator-free days, ICU discharge and length of hospitalization was unchanged
  14. In the study by Curely et al, you probably won’t see a benefit because with all of the other therapies, the mortality was so low, it would take a huge number of patients to show a mortality difference.