Deep Hypothermic Circulatory Arrest in Pediatric Cardiac Surgery 2009

1. Deep Hypothermic Circulatory Arrest in Pediatric Cardiac Surgery2009 Nabila Fahmy, MD Professor of Anesthesiology Ain Shams University Zukass2001@yahoo.com

2. Cessation of the blood circulation for some time during surgery of the arch and repair of congenital heart defects is normally required to allow a bloodless operation field.. • Hypothermia is the most important mechanism for end-organ protection, particularly the brain, during such operations. • Cardiopulmonary bypass is used for core cooling before deep hypothermic circulatory arrest (DHCA) is initiated .

3. WHAT IS DHCA?

4. DEEP HYPOTHERMIC CIRCULATORY ARREST (DHCA) • Mild hypothermia – 30 C to 34 C Moderate hypothermia – 25 C to 30 C Deep hypothermia – 15 C to 22 C • Circulatory arrest – no flow in the blood vessels • DHCA – no blood flow during deep hypothermia

5. HOW DO WE DO DHCA?

6. TECHNIQUE OF DHCA • Usually planned • Most protocols involving DHCA involve the following : • Administration of barbiturates, usually thiopental for the reduction of cerebral metabolism. • Mannitol to help reduce potential increased intracranial pressure and to reduce free radicals. • Steroids to promote cell membrane integrity and reduce brain swelling. • Cooling is started before CPB by simply cooling the operating room and with ice packing to the head After systemic heparinization and cannulation are performed, CPB is started and cooling is begins for at least 20-30 minutes. The patient's body temperature is monitored by means of esophageal, tympanic, and rectal routes. After adequate cooling is achieved, the circulation is arrested to allow the surgeon to perform the critical part of the reconstruction. The duration of DHCA is limited to the shortest time possible. After circulation is restarted, the rest of the repair is performed during the rewarming phase. • The anesthetic and surgical plan involves mutual goals of tissue and organ protection by decreasing cellular metabolism and substrate delivery during the absence of perfusion.

7. WHY DHCA?

8. ADVANTAGES OF DHCA • Bloodless operating field with improved exposure • Decreased exposure to cardiopulmonary bypass with its sequelae (such as activation of white cells and endothelium, activation of cascades, consumption of coagulation factors and platelets, hemolysis, etc.) • Diminished risk of embolism (solids and gases) • No cannulas in the operating field • Less distortion of heart - cannulas are not in place • DHCA offers brain protection for a period of about 30-60 minutes. • Reduced CMRO2 to be approximately 10%-15% of its normothermic base line. • Lower plasma activated complement (C3a), interleukin 8, interleukin 6 (when compared with low-flow CPB) Bellinger DC, et al. N Engl J med. 1995;332:549-555

9. The duration of DHCA is limited to the shortest time possible as (landmark boston circulatory arrest study, march 2007) • 3-5 mins of cerebral ischemia can be tolerated at 37 c. • 15 mins 27 c. • 41 mins 17 c.

11. CEREBRAL PHYSIOLOGY DURING CARDIAC SURGERY • CLINICAL STUDIES (Greeley, Kern, Ungerdeider) • HAVE BEEN UNDERTAKEN IN THE LATE 1980s • TRHOUGH MID 1990s TO UNDERSTAND • NEUROPHYSIOLOGY IN INFANTS AND CHILDREN • DURING CARDIAC SURGERY INVOLVING CPB • AND DHCA • CNS HAS A HIGH METABOLIC NOTE & LIMITED ENERGY STORES • CNS IS THE MOST SENSITIVE ORGAN TO ISCHEMIA • ATTENTION HAS BEEN CENTERED ON NEUROLOGIC OUTCOME WHEN PERFUSION IS REDUCED, LEADING TO NEUROLOGIC COMPLICATIONS IN THE POSTOPERATIVE PERIOD.

12. THE REPORTED INCIDENCE OF NEUROLOGICAL COMPLICATIONS AFTER PEDIATRIC CARDIAC SURGERY RANGES FROM 2% TO 25% Austin EH III,Edmonds HI,Auden SM et al. Benefit of neurophysiological monitoring for pediatric Cardiac surgery.J Thorac Cardiovasc Surg 1997;114 :707-15 Menache CC,du Plessis AJ,Wessel DL et al. Current incidence of acute neurologic complications After open heart operation in children Ann Thorac Surg 2002; 73:1752.8

13. Neurologic morbidity include • seizures • stroke • changed tone and mental status • motor disorders - • time to recovery of EEG activity . • Abnormal cognitive function • Post Pump choreoatherosis paraplegia • Areas most vulnerable to ischemic Injury : • Neocortex • Hippocompus • Striatum

14. mechanism of brain injury involves binding of glutamate to NMDA receptor , increasing the intracellular ca++ and subsequently activates proteases phospholipases and deoxyribonucleases , promotes the generation of free radicals cell injury , cell death . Hypothermia the release of glutamate During DHCA , microemboli can be detected .

15. THE ETIOLOGY OF NEUROLOGICAL DYSFUNCTION IN CHILDREN IS FOR THE MOST PART ISCHEMIA PATHOPHYSIOLOGIC MECHANISMS ACCOUNTING FOR NEUROLOGIC INJURY INCLUDE: rate and extent of cooling and rewarming management of CPB prolonged DHCA anemia low cardiac output

18. UNDER DEEP HYPOTHERMIC CPB • CBF IS REDUCED BUT THERE IS AN • EXPONENTIALLY GREATER REDUCTION • IN CMRO2. • A STATE OF LUXURY PERFUSION EXISTS • WITH AN EXCESS OF FLOW RELATIVE • TO OXYGEN CONSUMPTION; 1:75 (conferring cerebral protection) • IN PATIENTS UNDERGOING DHCA CBF AND • CMRO2 REMAIN DECREASED AFTER • REWARMING AND WEANING FROM CPB Sara Lozano, MD , Emad Mossad, MD – Journal of Cardiothoracic and Vascular Anesthesia. Volume 18, Issue 5, Pages 645-656 (October 2004)

20. IMPROVING NEUROLOGIC OUTCOMES

21. Acid -- Base Management BLOOD GAS MANAGEMENT (a-stat vs pH-stat) DURING CPB SIGNIFICANTLY AFFECTS CEREBRAL PHYSIOLOGY AN MAY HAVE AN IMPACT ON NEUROLOGICAL OUTCOME

22. Changes in cellular pH during hypothermia are mediated through pco2 homeostasis. When blood is cooled during cardiopulmonary bypass, pH becomes more alkaline. pH-stat strategy – adding carbon dioxide - compensates for this shift. This situation causes pH to increase as temperature decreases and electrochemical neutrality to be maintained. Carbon dioxide is a potent cerebral vasodilator. α-stat strategy – electrochemical neutrality is maintained by keeping pH normal in temperature-uncorrected gases.

23. i.e, α-stat strategy – arterial blood measured at 37 C with pH of 7.40 and arterial pCO2 of 40 mm Hg (the hypothermic blood is alkalemic and hypocapneic) pH-stat strategy – hypothermic arterial blood at pH of 7.40 and arterial pCO2 of 40 mm Hg (blood at 37 C is acidemic and hypercapneic)

24. StatpH stat pH 7.4 pH 7.26 PaCO2 40 mmHg PaCO2 56 mmHg lab 37oC 28 oC pH 7.56 pH 7.56+CO2 pH 7.4 PaCO2 26 mmHg PaCO2 26 mmHg PaCO2 40 mmHg

25. ADVANTAGES/DISADVANTAGES α-stat strategy: preserves autoregulation, optimizes cellular enzyme activity, but less metabolic suppression pH-stat strategy: improves cerebral blood flow, cerebral oxygenation, and brain cooling efficiency during CPB, but greater risk of microembolism and free radical-mediated damage

26. Higher Hematocrit Improves Cerebral Outcome After Deep Hypothermic Circulatory Arrest Shin’oka T, Shum-Tim D, Jonas RA, Lidov HGW, Laussen PC, Miura T and du Plessis A Children’s Hospital Boston/Harvard Medical School J Thorac Cardiovasc Surg 1996;112:1610-21 Extreme hemodilution (hematocrit < 10%) causes inadequate oxygen delivery during early cooling and higher hematocrit (30%) achieved with blood prime results in improved cerebral recovery after circulatory arrest.

27. Temperature Management No difference between surface and core cooling. Provide adequate duration of cooling (> 20 min) before institution of DHCA. Avoid rapid cooling, avoid rapid rewarming and hyperthermia in postoperative period. Sharma R, et al. Neurological evaluation and intelligence testing in the child with operated congenital heart disease. Ann Thorac Surg 2000; 70: 575–581 Cottrell SM et al. Early postoperative body temperature and developmental outcome after open heart surgery in infants. Ann Thorac Surg 2004; 77: 66–71

28. Neuroprotective drugs

31. CPB: cardiopulmonary bypass; EEG: electroencephalograph; NAC: N-acetyl cysteine; NMDA: N-methyl D-aspartate Langley SM, et al. Eur J Cardiothorac Surg 2000. Clancy RR, et al. Pediatrics 2001. Miller SP, et al. Ann thorac Surg 2004. Bickler PE, Fahlman CS. Anesth Analg 2006, 103.

33. EEG • it is a rough guide to anesthetic depth • it is affected by temperature,CPB,anesthetics • not easy to use • BIS (BISPECTRAL INDEX) • it is currently used to guide the depth of anesthesia • easy to use - less reliable during hypothermia • SjVO2 (JUGULAR VENOUS BULB OXYMETRY) • it is considered the gold standard of global cerebral • oxygenation • it is invasive • Unilateral SjVO2 may not reflect contralateral events

34. TCD (TRANSCRANIAL DOPPLER ULTRASOUND) • it is a sensitive real-time monitor of CBF, can detect microemboli • it monitor the middle cerebral artery • Absent signal during DHCA. • S- 100B (Biochemical marker) • Detects preexisting neurologic deficit • Multiple sampling periods required • NIRS (NEAR-INFRARED SPECTROSCOPY) • it is a non-invasive optical technique • most devices utilize 2-4 wavelengths of infrared light • at 700-1000 nm, where oxygenated and deoxygenated • hemoglobin have distinct absorption spectra • two depth of light penetration are used to subtract • out data from the skin and skull resulting in brain • oxygenation value • Changes in cerebral vascular composition will affect rSO2 reading • Useful during DHCA.

37. Conclusion • Survival after neonatal and infant cardiac surgery has improved dramatically, but quality of life, including neurodevelopmental outcomes, still needs study and improvement. It is important to protect the brain using established strategies,and test new strategies with carefully designed follow-up studies. Potential exists for significant improvement in this area.

38. Thank you