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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

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