Bombay Hospital Journal ContentsHomeArchivesSearchBooksFeedback

REVIEWS ARTICLES

CENTRAL-NEUROAXIAL BLOCKS IN PAEDIATRICS

Sunita Goel

 
INTRODUCTION
Advances in the neonatal care have resulted in the survival of a greater number of preterm infants.These infants are also often of a young post conceptual age. Anaesthesia for elective and emergency procedure in these infants presents a challenge with an increased risk of life threatening apnoeas after surgery.

Children are different : They have an inherent fear of needles like most adults. Central or peripheral blocks are done under GA or sedation to ensure an immobile patient and safe execution of the block. Many published series reveal low complication rates. However, assessment of these blocks and detection of signs of toxicity is difficult under sedation or GA
 
ANATOMY1
Line joining superior iliac crest
- Crosses the L3/4 interspace in adults
- Crosses the L5/S1 interspace in neonates
- Crosses the L5 vertebra in children
 
Dural sac
- Level S4 at birth
- Reaches S2 at the end of the first year
 
Spinal cord
- Terminates at L3 at birth
- Reaches L1 at the end of the first year
 
Sacrum
- In infancy, incomplete fusion of the sacrum makes it easy to enter via the posterior approach at all levels (S1 - S4) and the sacral hiatus is relatively larger and higher in neonates.
- After age 7, the dimensions are reduced and caudals become less easy to perform
 
Curvature
- At birth the vertebral column presents only an anterior concave curvature and the relationship between spinous processes to each other is similar and hence spinal and epidural techniques can be performed with the same orientation at any level.
- The cervical lordosis appears in the first 3 months of life with the ability to hold the head upright.
- From 6-9 months, the lumbar lordosis appears as the child learns to walk. This curvature makes spinal/epidural technique similar to adults.
Distance from skin to epidural space2 - increases with age (Fig. 1).



 
Positioning of patient
In preterm infants, it is recommended that in the lateral position, there should be partial neck extension or if done in the sitting position, the head should be supported, to reduce hypoventilation.
Gleason4 and colleagues measured transcutaneous pO2 and pCO2 in three positions.

1 Lateral position with neck flexion
2 Lateral position with partial neck extension
3 Sitting position with head support
 
Results
Mean transcutaneous pO2 decreased in all three with the largest drop in the flexed position and transcutaneous pCO2 increased only in the flexed position and remained elevated for 5 minutes after discontinuing the position.are awake, cooperative usually over the age of - over 7 years old. - increases the ease of epidural puncture. - But increases the risk of dural puncture because the spinal cord moves. Dorsally in this position and the pressure on the CSF is increased.

Lateral position - common position under GA. - If the size of pillow is correct, the line of spinous process is parallel to the operating table. - The pelvis does not play as important a role in children and adolescents as in adults

Prone position - Rarely used except for specific reasons e.g. Patients with large plaster cast or with spinal deformities. - May accentuate the lumbar lordosis thus making epidural access difficult (Use towels on each iliac spine or using a frame such as one used for scoliosis surgery)
 
Volume of injection5
Epidurals - Schulte - Stenberg formula6 ® volume required to block one spinal segment = 1/10 age in years (up to puberty).
In practice 0.5 - 1.0 ml/kg up to a maximum of 20 mls is used.

Caudal : One milliliter per kilogram of bupivacaine 0.125% with epinephrine 1:200,000 reliably produces 4 to 6 hours of analgesia. Higher concentrations have been used, but motor blockade is significantly increased without improving the quality or duration of pain control. The addition of opioids may increase the potency of the neuraxial block. Fentanyl 1 to 2 µg/kg may also prolong the block, but pruritus and nausea or vomiting are increased. Morphine (30 µg/kg) has also been used by this route, but side effects (nausea or vomiting and pruritus) often occur and the increased risk of respiratory depression precludes its use in out patients.

Epidural : In children older than 10 years of age, a simple formula calculates the volume (V) necessary to block one spinal segment:

V (in mL) = 1/10 x (age in years)

In younger children, the weight of the patient should be considered; 0.04 mL/kg/segment provides an initial bolus-dose estimate.
 
Assessment of blocks
Adults - loss of cold discrimination, loss of pain sensation, loss of light touch commonly used methods may not be applicable to neonates, infants and small children.

Differential sensory perception is also age dependent and limited by the cognitive and linguistic capability of the child.

1.5-2 year olds begin to use words to describe pain. 2-3 year olds begin to attribute pain to an external cause. 4-5 year old child only starts to discriminate between all or none and probably able to quantify the degree of pain.

The term paraesthesia is difficult to explain to a child and may not be comprehensible in children under 6 years old.

Assessment is mostly based on a physiological response (pulse rate, BP, respiratory rate or withdrawal reflex) to a noxious stimuli.

Other methods include loss of sensation to skin pinch, to finger nails and pin prick, the sensory level of blockade being regarded as the point at which a withdrawal response, facial grimace or cry occurs. (It has been suggested that a skin pinch is a more intense stimulus and may give a different estimate of sensory loss).
 
The test dose7,8
How reliable is it?

A test dose should be 0.1 mL/kg of a local anaesthetic solution with 5 µg/mL of epinephrine to a maximum volume of 3 mL. An increase in heart rate of 10 beats per minute above baseline occurring within 1 minute of injection is a reasonable predictor of intravascular injection for children anaesthetized with sevoflurane.9,10 This sign is less reliable in children anaesthetized with halothane.11 Pretreatment with atropine may improve the accuracy of heart rate changes in detecting intravascular injection for both inhalation agents.

Calculate max.dose, administer slowly or in small boluses and be vigilant
.
 
Contraindications
Contraindications are few and similar to those in adults. These include coagulopathy, infection at the insertion site, true local anaesthetic allergy, and abnormal superficial landmarks or lumbo-sacral myelomeningocoele because of the risk of malposition of the cord or dural sac. Progressive neurologic disease is a relative contraindication primarily because of medico-legal concerns.
 
COMPLICATIONS12
1. Complications of puncture
Subcutaneous and intramuscular injection - a feeling of a give similar to a loss of resistance can be felt especially in neonates because of the high degree of hydration and low density tissue.

Injection into paravertebral space - the loss of resistance felt is similar to that of the epidural space. The increase in the resistance of the ligamentum flavum is probably not felt. This may result in unilateral single spinal nerve block or a patchy block because the epidural space communicates freely with the paravertebral space.

Injury to discs, ligaments, blood vessels.

Dural puncture - incidence is about 2.5% or less in adults, 2% or less in children. Consequences of dural puncture in children are negligible. Postural puncture headache is exceptional before the age of 10 years and unusual before puberty.

Damage to spinal cord and nerve roots : Direct trauma to nerve roots, conus medullaris can occur. Sensory deficits may persists while the motor deficits may resolve over a few days. Usually other factors are involved e.g. vascular injury, hypotension or compression by an epidural haematoma of the spinal artery entering into the spinal cord or nerve root. Intraneural injection of LA can cause permanent damage to nerve fibres. In an awake patient this is manifested by paraesthesia when the needle penetrates the neural sheath and intense pain when the injection is made where a high resistance to injection is usually felt. Risks increases with the patient under GA
 
2. Complications of epidural catheter13

Puncturing the dura giving rise to spinal anaesthesia and postdural puncture headache..

Subdural placement causing an extensive block
Migration into vessel causing systemic symptoms
Migration into vessel causing systemic symptoms

Fracture
- can occur if pulled out through the needle, if the catheter has been left in for a long time resulting in adhesions, due to formation of loops or knots when a longer length of catheter is introduced or when multiple catheters are used at different levels.

Bacterial contamination, adhesion formation and nflammatory reactions increase with the amount of time left in the space.
 
Complication relating to the injected solution
Wrong solution - label, place in different tray

Intravascular injection14 : Damage to vascular plexus by needle or catheter. - Aspiration of blood is usually but not always seen. - Detection of toxicity may be difficult under GA. - Convulsions are unlikely to be seen under GA. Most episodes of convulsants are reported postoperatively during top ups or when continuous infusion is used. - Arrhythmias usually seen before CNS toxicity becomes manifest.

Subarachnoid injection15 : May lead to a total spinal which is rapid in onset. - Cardiorespiratory support if occurs but in children < 8 years old, hypotension is usually not seen. - Keep patient asleep.

Subdural injection16 : May present as a high sensory block. - Delay onset about 20 minutes after a presumed epidural injection. - Motor and sympathetic block usually minimal but may require support in some cases.

Complications due to opioids17 : Increases the quality and duration of analgesia but associated with side effects in 50% of cases. - Commonly pruritus nausea, vomiting, urinary retention. - Respiratory depression; the first signs usually appear after 3-24 hrs after injection and severe depression appears 2-3 hours after the initial signs. - Signs of respiratory depression usually but not always preceded by severe generalised pruritus and increasing somnolence. Treatment is supportive (ABC), stopping the opioid and consider giving naloxone 10 mcg/kg followed by an infusion of 10 mcg/kg/hr for 24 hours with close monitoring.

Cardiovascular effects18
: Cardiovascular changes related to spinal anaesthesia are less frequent in children. Minimal changes in heart rate and blood pressure have been noted following high thoracic spinal anaesthesia in neonates and infants. Above 5 years - Bradycardia and hypotension is seen more frequently.

Respiratory changes : Respiratory effects of spinal anaesthesia have generally occurred with high sensory and motor level above T1. Many of these problems were not due to excessive dosing but to factors such as leg lifting after spinal injection.

Post Dural Puncture headache19,20 : PDPH occurs in older children.

Partial or complete failure of block : Repeat procedure, repeat dose of LA or use alternative analgesia
Other complications : Infection and chemical meningitis

Dermoid cyst - due to the introduction of epidermal cells in the spinal canal and can cause spinal cord compression.
Poor psychological tolerance in children of a motor block

Flaring up of latent infections e.g. herpes

Allergy to LA : Shivering - thought to be due to the temperature of the injected solution < 37°C stimulating the temperature receptors in the epidural canal.
 
CONCLUSION
Paediatric regional anaesthesia is considered a safe and reliable technique providing a painfree state but even in skilled hands is not free of complications and requires strict attention to technical detail and precise, gentle manipulations.

The use of regional anaesthesia alone or in combination with other therapies is cost effective and also improve postoperative outcome.
 
ACKNOWLEDGEMENT
I would like to thank the Rameshwardas Birla Smarak Kosh Scholarship which enabled me to go for my fellowship to the KK Women’s and Childrens Hospital for Paediatric Anaesthesia and learn speciality work there.
 
REFERENCES
1.
Busoni P, Messeri A. Spinal anaesthesia in children. Surface Anatomy Anesth Analg 1989; 68 : 418-19.
2.
Bosenberg AT, Gouws E. Skin-epidural distance in children. Anaesthesia 1995; 50 : 895-97.
3.
Hasan MA, Howard RF, Lloyd-Thomas AR. Depth of epidural space in children. Anaesthesia 1994; 49 : 1085-87.
4.
Gleason CA, Martin RJ, Anderson JV, Carls WA, Sannitti KJ, Fanaroff AA. Optimal position for a spinal tap in preterm infants. Pediatrics 1983; 71 : 31-5.
5.
Sukhani R, Wahood A, Black PR. Calculating local anesthetic dose for infant spinal, body weight versus spinal length. Anesthe Analg 1993; 76 : 917-18.
6.
Schulte-Steinberg O. Regional anaesthesia for children. Ann Chir Gynaecol 1984; 73 : 158-65.
7.
Desparmet JF, Mateo J, Ecoffey C, Mazoit X. Efficacy of an epidural test dose in children anesthetized with halothane. Anesthesiology 1990; 72 (2) : 249-51.
8.
Desparmet JF. Epidural anesthesia in infants. Can J Anaesth 1999; 46 (12) : 1105-9.
9.
Tanaka M, Nishikawa T. Simulation of an epidural test dose with intravenous epinephrine in sevoflurane-anesthetized children. Anesth Analg 1998; 86 : 952-57.
10.
Tanaka M, Nishikawa T. The efficacy of a simulated intravascular test dose in sevoflurane-anesthetized children : a dose-response study. Anesth Analg 1999; 89 : 632-37.
11.
Kozek-Langenecker SA, Marhofer P, Jonas K, et al. Cardiovascular criteria for epidural test dosing in sevofluvane and halathane anesthetized in children. Anesth Analg 2000; 90 : 579-83.
12.
Goldman LJ. Complications in regional Anaesthesia. Paediatric Anaesthesia 1995; 5 : 41-6.
13.
Blety-Flandin C, Barrie G. Accidents following extradural analgesia in children. The results of a retrospective study. Pediatric Anaesthesia 1995; 5 : 41-6.
14.
Fisher QA, Shaffner DH, Yaster M. Detection of intravascular injection of regional anaesthetics in children. Can J Anaesth 1997; 44 : 592-98.
15.
Desparmet JF. Total Spinal anesthesia after caudal anesthesia in an infant. Anesth Analg 1990; 70 (6) : 665-7.
16.
Oliver A. Dural punctures in children : What should we do? Pediatric Anaesthesia 2002; 12 (6) : 473-7.
17.

Eck JB, Ross AK. Pediatric regional anaesthesia - What makes a difference? Best Prac Res Clin Anaesthesiol 2002; 16 (2) : 159-74.

18.
Tobias AJ. Spinal Anaesthesia in infants and children. Pediatric Anaesthesia 2000; 10 : 15-16.
19.
Kokki H, Hendolin H, Vainio J, Partanen J. A comparison of spinal anaesthesia and general anaesthesia. Anaesthetist 1992; 41 (2) : 765-8.
20.
Tobias JD, Lowe S, O’Dell N, Pietsch JB, Neblet III WW. Continuous regional anaesthesia in infants. Can J Anaesth 1993; 40 : 1065-68.
 
MONTELUKAST PLUS FLUTICASONE IS EQUIVALENT TO SALMETEROL AND FLUTICASONE

Adding montelukast to the treatment regimen of asthma patients whose symptoms remain uncontrolled by fluticasone provides equivalent control to adding salmeterol. In a double blind randomised controlled trial, Bjermer and colleagues randomised 1500 patients with uncontrolled asthma symptoms taking fluticasone to receive either montelukast or salmeterol as well. At one year, 20% of patients in each group had had an exacerbation of asthma. The authors say that the b agonist salmeterol and the anti-leukotriene montelukast are known to reduce the risk of exacerbation when combined with a corticosteroid, but the two had not been compared directly in a long term study with exacerbation of asthma as the primary end point.


BMJ 2003; 327 : 891
 

To Section TOC
Sponsor-Dr.Reddy's Lab