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HYPOTHERMIC NEUROPROTECTION  IN THE NEWBORN: A COOL IDEA Steven M. Donn, M.D. Professor of Pediatrics Chief, Division of Neonatal-Perinatal Medicine C.S. Mott Children’s Hospital University of Michigan Health System
DISCLOSURE ,[object Object]
HYPOXIC-ISCHEMIC ENCEPHALOPATHY (HIE) ,[object Object],[object Object],[object Object],[object Object]
NEONATAL PREDICTORS OF LTND:  Patient Selection Criteria ,[object Object],[object Object],[object Object],[object Object]
HIE PATHOPHYSIOLOGY ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
HUMAN NEONATAL TRIALS ,[object Object],[object Object]
BACKGROUND ,[object Object],[object Object],[object Object],[object Object]
Post-HI Hypothermia in P7 Rats ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
Prolonged Post-HI Hypothermia I ,[object Object],[object Object],[object Object],[object Object],[object Object]
Prolonged Post-HI Hypothermia II ,[object Object],[object Object],[object Object],[object Object],[object Object]
EEG – dramatically improved Time (hours) EEG (µV) Seizures not suppressed Slide c/o Alistair Gunn
SUMMARY of ANIMAL DATA ,[object Object],[object Object],[object Object],[object Object]
The Cool Cap Study By parental permission, Dr Durand, Oakland
PRIMARY HYPOTHESIS ,[object Object]
Anticipated Issues in Trial Design  ,[object Object],[object Object],[object Object],[object Object],[object Object]
aEEG CRITERIA ,[object Object],[object Object],[object Object],[object Object],[object Object]
 
Anticipated Issues in Trial Design   ,[object Object],[object Object]
SOLUTION ,[object Object],By parental permission, Dr Durand, Oakland
The Cool Cap Trial ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
MODERATE to SEVERE HIE ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
PRIMARY OUTCOME ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
TRIAL STATISTICS ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
BASELINE DATA Cooled Control Number 116 118 Initial pH (mean, SD) 6.9 (0.2) 6.9 (0.2) Five min Apgar 0 – 3 77%   68% Pre-randomization aEEG:  Moderately Abnormal 54% 64% Severely Abnormal 36% 27% Seizures present 59% 64% Age at Randomization (h) 4.8 (2.6-6) 4.7 (2.1-6.1)
Primary Outcome # Enrolled 235 Final Count 234 Cancelled 1 Lost to Follow-up 16 18-Month Primary Outcome 218 Cooled 108 Control 110 Favorable 49 (45%) Unfavorable 59 (55%) Favorable 37 (34%) Unfavorable 73 (66%)
EFFICACY RESULTS ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Stratification by Baseline aEEG To allow for multiple comparisons, p<0.025 required for significance Excluding most severe abnormalities in aEEG < 6 hours A priori – anticipated to respond 172/218 In controls (n=88) 66% unfavourable outcome (39% mortality ) Most abnormal aEEG < 6 hours A priori – unlikely to respond 46/218 In controls (n=22) 68% unfavourable outcome (36% mortality)
Fisher’s exact p=0.02; logistic regression,  OR: 0.42 (0.22, 0.80), p=0.009 A priori defined group excluding  infants with severely abnormal aEEG with seizure n=172 Cooled 84 Control 88 Favorable 44 (52%) Unfavorable 40 (48%) Favorable 30 (34%) Unfavorable 58 (66%)
Cooling Improved Intact Survival  Excluding the Most Abnormal Baseline aEEG ,[object Object],[object Object],[object Object],[object Object],[object Object]
NUMBER NEEDED to TREAT (Per Survivor with Improved Outcome) ,[object Object],[object Object],[object Object],[object Object]
Infants with the Most Abnormal Baseline aEEG  ( Severe suppression of background  plus  seizures,  46/218 ) ,[object Object],[object Object],[object Object],[object Object]
ADVERSE EFFECTS ,[object Object],[object Object],[object Object],[object Object]
PERINATAL COMPLICATIONS Cooled    Non-Cooled   P   Sinus Bradycardia/tachy 10 9%   1 1%  0.004 * Hypotension (<40mmHg) 62 55%   64 52%  0.60 Coagulopathy  21 19%   17 14%  0.38 Prolonged coagulation  56 50%   50 42%  0.29 Abnormal renal function  73 65%   83 70%  0.48 Hyponatremia 49 44%   46 39%  0.50 Hypokalemia  71 63%   73 62%  0.89 Bone marrow depr.  36 32%   26 22%  0.10 Elevated liver enzymes 42 38%   62 53%  0.02
PERINATAL COMPLICATIONS Cooled    Non-Cooled   P  Metabolic acidosis 22 20%   27 23%   0.63 Respiratory distress  94 84%   92 78%   0.31 Hypoglycemia  14 13%   20 17%   0.36 Infection 1 1%   2 2%   1.00 Acute Mortality 27 23%   26 22%   0.88 (Deaths in the first week of life are not defined an adverse event)
CONCLUSIONS ,[object Object],[object Object]
CONCLUSIONS (II) ,[object Object],[object Object],[object Object]
Other Neonatal Hypothermia Trials:  “South Carolina Body Cooling Trial” (I) ,[object Object],[object Object],[object Object],[object Object],Eicher  et al , Pediatr Neurol 32:11 & 32:18, 2005
“ South Carolina Body Cooling Trial”  (II) 5 8 Lost/incomplete followup 4/17 (24%) (p=0.4) 5/12 (42%) Severe cognitive abnormality 4/17 (24%) (p=0.053) 7/11 (64%) Severe motor disability 10 (31%) (p=0.35) 14 (42%) Death 52% (p=0.019) 84% Death or severe disability Hypothermic (n=32) Normothermic (n=33) Outcome
“ South Carolina Body Cooling Trial” (III) ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Other Neonatal Hypothermia Trials:  NICHD NRN Body Cooling Trial (I) ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Shankaran  et al . NEJM 353:1574-84, 2005
Copyright ©2002 American Academy of Pediatrics Shankaran,  et al. Pediatrics 2002;110:377-385 The infant lies supine on the infant-size blanket
NICHD NRN Body Cooling Trial (II) Shankaran  et al . NEJM 353:1574 52% 40% MDI >85 NS 23% 21% MDI 70-84 25% 39% MDI < 70 .85 (.64-1.13) .69 (.44-1.07) .68 (.44-1.05) .68 (.38-1.22) .72 (.54-.95) OR (CI) 72% 85% Death/dis after Sev HIE 32% 48% Death/dis after Mod HIE 24% 37% Death by 18 mo. 19% 30% Disabling CP 44% 62% Death or mod/sev dis. HT NT Outcome
NICHD  vs . Cool Cap trials ,[object Object],[object Object],[object Object],[object Object]
Summary of Three Large Trials ,[object Object],[object Object],[object Object],[object Object]
Limitations of All Three Trials ,[object Object],[object Object],[object Object],[object Object],[object Object]
The Future of Neonatal Cooling ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Remember: =
PRACTICALITIES of BRAIN COOLING
 
Practical Issues for  Referring Hospitals (I) ,[object Object],[object Object],[object Object],[object Object],[object Object]
Practical Issues for Referring Hospitals (II) ,[object Object],[object Object],[object Object],[object Object],[object Object]
 
Rectal Temperature
Implications ,[object Object],[object Object],[object Object],[object Object],[object Object]
Issues Ahead ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
The Cool Cap Study Group ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Thank you!

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Hypothermic Neuroprotection In The Newborn

  • 1. HYPOTHERMIC NEUROPROTECTION IN THE NEWBORN: A COOL IDEA Steven M. Donn, M.D. Professor of Pediatrics Chief, Division of Neonatal-Perinatal Medicine C.S. Mott Children’s Hospital University of Michigan Health System
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  • 12. EEG – dramatically improved Time (hours) EEG (µV) Seizures not suppressed Slide c/o Alistair Gunn
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  • 14. The Cool Cap Study By parental permission, Dr Durand, Oakland
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  • 25. BASELINE DATA Cooled Control Number 116 118 Initial pH (mean, SD) 6.9 (0.2) 6.9 (0.2) Five min Apgar 0 – 3 77% 68% Pre-randomization aEEG: Moderately Abnormal 54% 64% Severely Abnormal 36% 27% Seizures present 59% 64% Age at Randomization (h) 4.8 (2.6-6) 4.7 (2.1-6.1)
  • 26. Primary Outcome # Enrolled 235 Final Count 234 Cancelled 1 Lost to Follow-up 16 18-Month Primary Outcome 218 Cooled 108 Control 110 Favorable 49 (45%) Unfavorable 59 (55%) Favorable 37 (34%) Unfavorable 73 (66%)
  • 27.
  • 28. Stratification by Baseline aEEG To allow for multiple comparisons, p<0.025 required for significance Excluding most severe abnormalities in aEEG < 6 hours A priori – anticipated to respond 172/218 In controls (n=88) 66% unfavourable outcome (39% mortality ) Most abnormal aEEG < 6 hours A priori – unlikely to respond 46/218 In controls (n=22) 68% unfavourable outcome (36% mortality)
  • 29. Fisher’s exact p=0.02; logistic regression, OR: 0.42 (0.22, 0.80), p=0.009 A priori defined group excluding infants with severely abnormal aEEG with seizure n=172 Cooled 84 Control 88 Favorable 44 (52%) Unfavorable 40 (48%) Favorable 30 (34%) Unfavorable 58 (66%)
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  • 34. PERINATAL COMPLICATIONS Cooled Non-Cooled P Sinus Bradycardia/tachy 10 9% 1 1% 0.004 * Hypotension (<40mmHg) 62 55% 64 52% 0.60 Coagulopathy 21 19% 17 14% 0.38 Prolonged coagulation 56 50% 50 42% 0.29 Abnormal renal function 73 65% 83 70% 0.48 Hyponatremia 49 44% 46 39% 0.50 Hypokalemia 71 63% 73 62% 0.89 Bone marrow depr. 36 32% 26 22% 0.10 Elevated liver enzymes 42 38% 62 53% 0.02
  • 35. PERINATAL COMPLICATIONS Cooled Non-Cooled P Metabolic acidosis 22 20% 27 23% 0.63 Respiratory distress 94 84% 92 78% 0.31 Hypoglycemia 14 13% 20 17% 0.36 Infection 1 1% 2 2% 1.00 Acute Mortality 27 23% 26 22% 0.88 (Deaths in the first week of life are not defined an adverse event)
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  • 39. “ South Carolina Body Cooling Trial” (II) 5 8 Lost/incomplete followup 4/17 (24%) (p=0.4) 5/12 (42%) Severe cognitive abnormality 4/17 (24%) (p=0.053) 7/11 (64%) Severe motor disability 10 (31%) (p=0.35) 14 (42%) Death 52% (p=0.019) 84% Death or severe disability Hypothermic (n=32) Normothermic (n=33) Outcome
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  • 42. Copyright ©2002 American Academy of Pediatrics Shankaran, et al. Pediatrics 2002;110:377-385 The infant lies supine on the infant-size blanket
  • 43. NICHD NRN Body Cooling Trial (II) Shankaran et al . NEJM 353:1574 52% 40% MDI >85 NS 23% 21% MDI 70-84 25% 39% MDI < 70 .85 (.64-1.13) .69 (.44-1.07) .68 (.44-1.05) .68 (.38-1.22) .72 (.54-.95) OR (CI) 72% 85% Death/dis after Sev HIE 32% 48% Death/dis after Mod HIE 24% 37% Death by 18 mo. 19% 30% Disabling CP 44% 62% Death or mod/sev dis. HT NT Outcome
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