Chapter 86
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1454 PART 5 ■ Anesthetic, Surgical, and Interventional Procedures: Considerations<br />
sevoflurane, and is also associated with a decrease in heart rate.<br />
With isoflurane and sevoflurane, a reduction of peripheral<br />
vascular resistance is the main cause of the reduced blood pressure<br />
and the heart rate will be maintained or even slightly increased. 149<br />
Most often, the degree of hypotension caused by the inhalational<br />
agents can be tolerated. However, if treatment is deemed necessary,<br />
a bolus administration of 5 to 10 mL/kg of crystalloid in the case<br />
of sevoflurane and isoflurane, 119,148 or administration of atropine if<br />
halothane is used, often suffices to correct the situation. 150 The<br />
concomitant administration of N 2<br />
O has different effects on<br />
the MAC requirements for the three volatile anesthetics<br />
mentioned above. The addition of 60% N 2<br />
O decreases the MAC<br />
values by 60%, 40%, and 25% for halothane, 151 isoflurane, 152 and<br />
sevoflurane, 119 respectively. To use N 2<br />
O together with halothane<br />
in an attempt to minimize the negative cardiovascular effects of<br />
halothane appears reasonable. However, whether supplemental<br />
use of N 2<br />
O is of significant value when isoflurane or sevoflurane<br />
is used can be debated.<br />
The preconditioning effect of sevoflurane is currently an area<br />
of great interest, and recent data has shown a myocardial pre -<br />
conditioning effect of sevoflurane in a neonatal rodent model. The<br />
mechanism behind this preconditioning effect of sevoflurane<br />
appeared to be a blockage of mitochondrial K ATP<br />
channels. 153<br />
The effect of inhalational agents on cerebral autoregulation is<br />
also an important topic in the context of neonatal anesthesia.<br />
Recent data suggest that cerebral autoregulation is preserved up<br />
to 1.5 MAC sevoflurane as assessed by the transient hyperemic<br />
response measured by transcranial Doppler. 154<br />
Opioids<br />
The use of moderate to high doses of opioids for maintenance of<br />
anesthesia is associated with a high degree of hemodynamic<br />
stability. This is especially useful in unstable patients or in the case<br />
of major surgery in the neonate. The use of fentanyl (10–50 g/kg)<br />
or sufentanil (35 g/kg) has been found capable of attenuating the<br />
neuroendocrine stress response and reducing morbidity; a reduc -<br />
tion in mortality has even been suggested in neonates undergoing<br />
corrective surgery for congenital heart defects. 15,24 Synthetic<br />
opioids are high clearance drugs and the metabolism is not so<br />
dependent on the maturation of the hepatic biotransformation<br />
system 155 (see <strong>Chapter</strong> 15). The terminal half-lives of fentanyl and<br />
sufentanil in the neonate are approximately 5 and 13 hours,<br />
respectively. 156 Because these drugs have a high clearance, their<br />
elimination is substantially prolonged in situations of compro -<br />
mised liver blood flow, for example, high abdominal pressure<br />
following closure of an omphalocele or gastroschisis. In this<br />
situation the terminal half-life of fentanyl has been reported to<br />
increase to 1.5 to 3 times the normal average value. 155<br />
When a regional anesthesia has not been performed for<br />
intraoperative analgesia, the repeat injection of small boluses of<br />
fentanyl (1–2 g/kg) can be used together with a volatile agent as a<br />
balanced anesthesia technique. 157 Some caution is recommended<br />
regarding the intraoperative doses of opioids in patients having<br />
received a regional anesthetic block. If there is intraoperative need<br />
to increase the depth of anesthesia, this should preferentially be<br />
accomplished by temporarily increasing the dose of volatile agent.<br />
Otherwise the patient will be exposed to the risk of a prolonged<br />
emergence with respiratory depression, possibly necessitating<br />
postoperative ventilation, since at the time of emergence the patient<br />
will have good analgesia from the regional block and, thus, will have<br />
no stimulatory effects of any pain. Such a situation can be overcome<br />
by the administration of naloxone, but the staff in the recovery<br />
room or NICU should be aware of the risks of renarcotization if a<br />
prolonged infusion of naloxone has not been started.<br />
5.6. Use of Regional Anesthesia<br />
Techniques<br />
The modern concept of a combination of a light general volatile<br />
anesthetic and a central or peripheral nerve block has proved to be<br />
of great benefit in neonatal surgery. 157,158 Apart from offering<br />
excellent intra- and postoperative analgesia, frequently making<br />
the perioperative administration of opioids unnecessary, regional<br />
anesthetic techniques provide muscle relaxation, making unnecessary<br />
the use of muscle relaxants except to facilitate tracheal<br />
intubation. A regional block also attenuates the magnitude of the<br />
surgically induced stress response 159 which is highly likely to be<br />
beneficial to the recovery of the patient. Retrospective data also<br />
indicate that a thoracic epidural block reduces the need for posto -<br />
perative ventilation compared to children receiving more tradi -<br />
tional postoperative analgesia with opioids. 157 A further advantage<br />
may also be earlier return of peristalsis following abdominal<br />
surgery in premature babies and neonates. 160 The use of epidural<br />
blocks has been found adequately safe in children, as shown in a<br />
large prospective audit (10,000 children), including more than<br />
500 epidurals performed in neonates. 161<br />
Although regional blocks offer considerable benefits in neo -<br />
nates compared to more traditional techniques, care must be taken<br />
regarding the dosing of local anesthetics in order to avoid toxi -<br />
city. 162 Generally accepted guidelines restrict a maximum bolus<br />
injection of bupivacaine to 1.5 (up to 2.0) mg/kg and a subsequent<br />
continuous infusion to maximum 0.2 mg/kg/h 163 and these dosage<br />
recommendation have recently been found to result in safe plasma<br />
levels in neonates, at least up to 48 hours postoperatively. 158<br />
Bupivacaine plasma levels of 2 to 4 g/L are generally believed to<br />
represent the threshold for CNS toxicity in children, but signi -<br />
ficantly lower plasma levels are associated with pretoxic symptoms<br />
in awake ex-premature infants receiving a caudal block. 164 Since<br />
the metabolism of lidocaine is relatively mature in neonates this<br />
local anesthetic might be an even better option than bupivacaine<br />
in neonates if a continuous infusion technique is con sidered.<br />
Determinations of plasma levels of lidocaine are usually readily<br />
available at most laboratories, making monitoring of the treatment<br />
possible and steady state conditions following conti nuous infusion<br />
will be reached within approximately 12 hours. 165 This provides a<br />
sharp contrast to bupivacaine infusion, where plasma concentra -<br />
tions of bupivacaine are still increasing in a significant portion of<br />
neonates following 48 hours of infusion. 158 Neonates receiving<br />
continuous regional blockades postoperatively should be cared for<br />
in the NICU or in a high dependence environ ment with appro -<br />
priate monitoring, for example, ECG, pulse oxi metry, respiratory<br />
rate, pain scoring, and general behavior of the neonate.<br />
Prevention of Heat Loss/Maintenance<br />
of Normal Body Temperature<br />
Every possible effort must be made to prevent perioperative<br />
hypothermia in the neonate (see <strong>Chapter</strong> 10). This can be<br />
accomplished by combining a number of different measures (Table<br />
<strong>86</strong>–10). If hypothermia still occurs despite precautions, attempts