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Editor
Courtney A. Hardy, MD
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Mark Twite, MD, BCh
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Stuart R. Hall, MD
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President's Message
Letter from the Editor
Call for CCAS Directors Nominations
Preview of the CCAS
Program at Pediatric Anesthesiology 2010
CCAS/STS Database Update
Fellowship Training Update
An Interesting Case
The Anesthetic and Cardiopulmonary Bypass Management of an 800g Premature Neonate for the Arterial Switch Operation
PRO vs. CON
Should NIRS Monitoring Be Considered Standard of Care on Every Case Involving CPB?
Literature Reviews
1. Perioperative stroke in infants undergoing open heart operations for congenital heart disease.
2.
Brain maturation is delayed in infants with complex congenital heart defects.
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 The Anesthetic and Cardiopulmonary Bypass Management of an 800g Premature Neonate for the Arterial Switch Operation
By Erin A. Gottlieb MD and Dean B. Andropoulos MD
Division of Pediatric Cardiovascular Anesthesiology
Baylor College of Medicine
Texas Children’s Hospital
Houston, TX
This patient was a female triplet delivered at 28 1/7 weeks
of gestation. APGARS were 7 & 8. She was desaturated to the 60s with no
increase in saturation with supplemental oxygen. Transthoracic echocardiogram
revealed d-transposition of the great arteries with intact ventricular septum
(d-TGA/IVS), PFO and PDA. Prostaglandin E1 was started to maintain
ductal patency, and plans were made for surgical intervention.
On the day of surgery, the patient was 20 days old and was
transported to the operating by a neonatal transport team. She was intubated
with a 2.5 uncuffed oral endotracheal tube. Vascular access included a 1 Fr
neo-PICC and a 24g peripheral IV.
After the placement of routine monitors, the patient was
induced with fentanyl 10 mcg and pancuronium 0.15mg. A right radial 24g
arterial line and a right femoral 2.5 Fr 5 cm central venous line were placed
percutaneously. The 2.5 uncuffed endotracheal tube was
exchanged for a 3.0 uncuffed tube uneventfully due to leak. The patient’s
temperature was maintained at 35-36°C. Infusions were PGE1 and D10Plasmalyte
(2 cc/hr), and blood glucose was monitored closely. The maintenance anesthetic
consisted of fentanyl, midazolam and low concentration isoflurane. The Dräger
Apollo machine ventilator was used (North American Dräger,
Telford
,
PA
).
A oxygen saturation in the low 90s was maintained on
an FiO2 of 0.3, and PaCO2 was kept in the 40-50s without
difficulty. Cerebral saturation (rSO2) ranged from 50-69 in the
prebypass period. Hypotension was treated with calcium chloride 10 mg given
twice and phenylephrine 1 mcg given once. Systemic anticoagulation was achieved
with heparin 400 units.
The cardiopulmonary bypass prime consisted of 175 cc of
reconstituted, washed whole blood (packed RBC and FFP). The goal mean arterial
pressure was 30 mmHg, and flows was 150cc/kg or
120-130 cc/min. A 6 Fr Maquet was used for the arterial cannula, and a 14 Fr
Polystan was used for the venous cannula. Standard crystalloid cardioplegia and
zero balance ultrafiltration were used. The initiation and weaning of
cardiopulmonary bypass was controlled by a custom venous occluder. After
initiation of cardiopulmonary bypass, the patient was cooled to 22° C over more
than 30 minutes. Phentolamine 0.25 mg was given at the beginning of bypass to
vasodilate and promote even cooling. The bypass time was 267 minutes, the
aortic cross clamp time was 139 minutes, and the period of deep hypothermic
circulatory arrest was 5 minutes. The rSO2 ranged from 62-93 on CPB.
Separation from CPB was uneventful on milrinone 0.375
mcg/kg/min (no loading dose), nitroglycerin 1 mcg/kg/min, CaCl2 10
mg/kg/hr, epinephrine 0.03 mcg/kg/hr and inhaled
nitric oxide (iNO) at 10 ppm. Protamine 5.2 mg was administered,
and 5 cc of platelets were given empirically after protamine. The rSO2 ranged
from 64-71 in the post-bypass period. There was a short period of instability
associated with sternal closure with desaturation, ST changes and hypotension
which was treated with a CaCl2 bolus, epinephrine bolus (2 mcg), 5%
albumin (5 cc), an increase in iNO to 20 ppm and an increase in ventilation.
The sternum remained closed.
The patient was transported to the Cardiovascular Intensive
Care Unit (CVICU) on a Giraffe Omnibed (Ohmeda Medical, Laurel, MD). Vasoactive
drugs on arrival to CVICU were nitroglycerin 1 mcg/kg/min, CaCl2 10
mg/kg/hr, epinephrine 0.07 mcg/kg/min and iNO at 20
ppm. Total fentanyl dose was 175 mcg (206 mcg/kg), and total midazolam dose was
0.7 mg (0.8 mg/kg).
The patient recovered in the CVICU for a number of days and
was subsequently transferred to the NICU until she was ready for discharge
home. At her last clinic visit, she was doing well with no evidence of
neurological injury.
The careful preparation that went into this case was
critical to its successful completion. A multidisciplinary team with members
from Neonatology, Cardiovascular Anesthesiology, Cardiovascular Surgery,
Cardiovascular Intensive Care, Nursing and Perfusion made a plan for the
preoperative, operative and postoperative care of this patient. In the
operating room, the patient was attended to by two attending surgeons, two
attending anesthesiologists, two perfusionists, two scrub nurses and two
circulating nurses. Preoperatively, the patient was cared for in the NICU with
cardiology input. Postoperatively, the patient was cared for in the CVICU by both NICU and CVICU attending physicians and nurses,
practitioners familiar with both very low birth weight, premature and
postoperative cardiac surgery patients.
Lung immaturity was carefully considered. Oxygen saturation
in the 80s with a PaCO2 in the 40s was considered adequate. The
patient was ventilated with the Dräger Apollo machine ventilator in pressure
control mode with careful monitoring of exhaled tidal volumes to detect changes
in compliance. Surfactant was available, though not used, for administration
prior to separation from cardiopulmonary bypass.
In order to decrease the risk of retinopathy of prematurity,
the patient’s eyes were kept covered as much as possible, and exposure to
bright light was avoided. The lowest FiO2 possible was used to
maintain the SpO2 in the 80s pre-bypass and 88-93 post-bypass. In
addition, wide fluctuations in PaO2 were avoided.1
The immaturity of the brain was also an important
consideration. It is known that cerebral autoregulation is not preserved during
hypothermic CPB and that flow is pressure passive at moderate and profound
hypothermia in infants.2 In addition, there are concerns about the
possibility of anesthesia-induced neuronal cell loss in the developing brain.3-5
The timing of operation for d-TGA/IVS is controversial. The
arguments for early operation include minimizing deconditioning of the left
ventricle, minimizing infection and hospital acquired illness and avoiding
prolonged PGE1 infusion. The arguments for postponing surgery
include the possibility of stabilizing comorbidities such as NEC or IVH,
allowing the patient to grow and allowing further brain maturity which may
decrease the risk of white matter injury. However, the risk factors for
morbidity and mortality from the arterial switch operation are age > 30
days, gestational age and birth weight.6-9
References
1 Spaeth JP, O’Hara IB, and Kurth CD. Anesthesia for the Micropremie.
Semin Perinat 1998;22:390-401.
2Ramamoorthy C and Andropoulos DB. Neurological monitoring and
Outcome. In: Andropouls DB, Stayer SA and Russell IA, editors. Anesthesia
for Congenital Heart Disease, 2nd ed. Oxford, UK:
Wiley-Blackwell; 2010, in press.
3Loepke AW.
Developmental neurotoxicity of sedatives and anesthetics: A concern for
neonatal and pediatric critical care medicine. Pediatr Crit Care Med 2009;11:000-000.
4Jevtovic-Todorovic V and Olney JW. PRO: Anesthesia-Induced Developmental Neuroapoptosis:
Status of the Evidence. Anesth Analg 2008;106:1659-1663.
5Loepke AW, McGowan Jr FX and Soriano SG. CON: The Toxic Effects of Anesthetics in the
Developing Brain: The Clinical Perspective. Anesth Analg 2008;106:1664-1669.
6Qamar ZA, Goldberg CS, Devaney EJ, et al. Current Risk
Factors and Outcomes for the Arterial Switch Operation. Ann Thorac Surg 2007;84:871-9.
7Duncan BW, Poirier NC, Mee RBB, et al. Selective
Timing for the Arterial Switch Operation. Ann Thorac Surg 2004;77:1691-7.
8Roussin
R, Belli E, Bruniaux J, et al. Surgery
for Transposition of the Great Arteries in Neonates Weighing Less than 2,000
Grams: A Consecutive Series of 25 Patients. Ann Thorac Surg 2007;83:173-8.
9Dibardino DJ, Allison AE, Vaughn WK, et al. Current
Expectations for Newborns Undergoing the Arterial Switch Operation. Ann Surg 2004;239:588-598.

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