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British Journal of Anaesthesia 86 (3): 366±71 (2001)

Post-operative recovery after inguinal herniotomy in


ex-premature infants: comparison between sevo¯urane and
spinal anaesthesia
J. M. Williams*, P. A. Stoddart, S. A. R. Williams and A. R. Wolf

Department of Anaesthesia, The Royal Hospital for Sick Children, Bristol BS2 8ET, UK
*Corresponding author: Sir Humphry Davy Department of Anaesthesia, Bristol Royal In®rmary, Marlborough Street,
Bristol BS2 8HW, UK

We prospectively studied the post-operative recovery pro®le of 28 ex-premature infants


undergoing inguinal herniotomy. All infants had a post-conceptual age of less than 46 weeks at
the time of surgery and were randomized to receive either sevo¯urane (group 1, 14 patients)
or spinal anaesthesia (group 2, 14 patients). All patients received supplemental caudal analgesia
before skin incision. Cardiorespiratory function was continuously recorded in all patients
before and after surgery. A blinded observer analysed each paired recording for prede®ned
episodes of apnoea, hypoxaemia or bradycardia and the reports were used to compare the
two groups. Spinal anaesthesia was attempted unsuccessfully in four patients in group 2. Five
patients in group 1 demonstrated an `excess' number of episodes (median 4, range 3±12) of
clinically silent post-operative cardiorespiratory complications. (`Excess' in our study was
de®ned as a 3-fold or greater increase in the number of post-operative episodes of bradycardia
or apnoea relative to pre-operative occurrence). Three of these patients had pre-existing
abnormal respiratory function and accounted for 80% of the episodes (26/32) of post-operative
bradycardia and all ®ve episodes of post-operative apnoea identi®ed. All episodes of bradycar-
dia and apnoea were temporally unrelated. None of the remaining patients in group 2 demon-
strated an unacceptable number of post-operative cardiorespiratory complications. Our
limited study suggests that general anaesthesia with an inhalational agent such as sevo¯urane
may induce or unmask abnormalities of cardiopulmonary function in predisposed infants. Spinal
anaesthesia may be preferable but it is potentially stressful for the infant and associated with a
clinically signi®cant failure rate.
Br J Anaesth 2001; 86: 366±71
Keywords: anaesthesia, paediatric; anaesthetics volatile, sevo¯urane; anaesthetic techniques,
subarachnoid
Accepted for publication: October 16, 2000

Inguinal hernias are common in former pre-term infants and advantages of this approach, awake spinal anaesthesia has
require early repair to avoid the risks of incarceration.1 2 not gained universal acceptance amongst paediatric anaes-
However, the risk of life-threatening apnoea after surgery thetists and many institutions have rejected it.2 3 10
is signi®cant in this group regardless of the anaesthetic The introduction into paediatric practice in the UK of
technique used.2±4 The reported incidence of post-operative sevo¯urane and des¯urane with their properties of enhanced
respiratory dysfunction ranges from 20 to 50% and re¯ects recovery characteristics may offer a more practical solution.
the variation in both anaesthetic technique and study In neonates undergoing pyloromyotomy, it has been
design.2 5±9 Spinal anaesthesia appears to reduce the risk observed that recovery after des¯urane is twice as fast as
of respiratory dysfunction but does not abolish it.2 8 iso¯urane with less post-operative ventilatory disturbance.11
Moreover, the technique requires considerable expertise, Sevo¯urane has similar recovery characteristics but unlike
is contraindicated in some infants, has a reported failure rate des¯urane provides excellent conditions for inhalation
of 10±20%, and can be of insuf®cient duration for surgery. induction.12 13
As a result, the technique may need to be abandoned or We therefore designed a prospective, randomized pilot
supplemented with sedatives or anaesthetic agents, negating study that would re¯ect both clinical practice at our
any potential bene®ts.2 7 Therefore, despite the perceived institution and explore the hypothesis that the `recovery

Ó The Board of Management and Trustees of the British Journal of Anaesthesia 2001
Comparison between sevo¯urane and spinal anaesthesia

pro®le' after sevo¯urane anaesthesia is comparable with Table 1 Patient characteristics and intra-operative data. A comparison of
post-conceptual age (PCA), gestational age (GA), weight (Wt), pre-operative
that after spinal anaesthesia. With neither group experien- haemoglobin (Hb) and anaesthetic time (induction±skin closure) for the two
cing an increase in the number of episodes of apnoea, groups (median [range]). There was no signi®cant difference between the
hypoxaemia or bradycardia relative to pre-operative levels. groups with regard to and variable. n=number of patients

Group 1 Group 2
(n=14) sevo¯urane (n=10) spinal

Patients and methods PCA (weeks) 38 [32±46] 40 [36±44]


GA (weeks) 30 [23±35] 8 [26±33]
After obtaining Ethical Committee approval and informed Wt (kg) 2.6 [1.2±3.5] 2.8 [1.7±3.6]
parental consent we studied 28 patients undergoing inguinal Hb (g dl±1) 10.2 [9.0±13.4] 10.9 [9.6±12.7]
Bilateral repairs (n) 7 5
herniotomy. All infants had been born at less than 36 weeks
Induction±incision (min) 23 [16±29] 19 [11±28]
gestation and had a post-conceptual age (PCA) of less than Incision±closure (min) 26 [10±45] 28 [12±48]
46 weeks at the time of surgery. Infants with pre-existing
cardiac, neuromuscular or metabolic diseases were ex-
cluded from participation in the study. Pre-operative
haemoglobin concentration and a history of `pre-existing
Table 2 Number of episodes of pre- and post-operative apnoea and
abnormal respiratory function', with or without an on-going bradycardia recorded in each subject. a, apnoea lasting 15 s or longer;
requirement for supplemental oxygen therapy, were noted b, bradycardia (less than 100 beat min±1) for at least 5 s. Y, yes; N, no.
(Tables 1 and 2). We de®ned `pre-existing abnormal *Subjects identi®ed as exhibiting an `excess' of post-operative
cardiorespiratory complications
respiratory function' as the persistence of clinical features
of respiratory distress in association with an abnormal chest Subject Group Abnormal respiratory Number of episodes
no. function/oxygen
radiograph beyond the ®rst 28 days of life, either occurring therapy
alone or in combination with a `current' history of apnoea Pre-op 12 h Post-op 12 h
(i.e. episodes witnessed within the 2 weeks before surgery).
Patients were allocated randomly, using random number a b a b
1* 1 Y/Y ± ± ± 10
tables, to receive either sevo¯urane anaesthesia with caudal 2 1 N ± ± ± ±
analgesia (group 1) or awake spinal anaesthesia with caudal 4 1 N ± ± ± ±
7 1 Y ± 5 ± ±
analgesia (group 2). No sedative pre-medication was
8 1 Y/Y ± ± ± ±
administered but all patients received paracetamol 15 mg 11 1 N ± 1 ± ±
kg±1 per rectum 1 h before surgical incision. 14* 1 Y/Y ± 3 4 12
16 1 N ± ± ± 1
In group 1, general anaesthesia was induced with a 2
17* 1 N ± 1 ± 3
MAC equivalent value for age of sevo¯urane in 100% 18* 1 N ± 1 ± 3
oxygen (1 MAC=3.2% in neonates).14 15 Atracurium 0.5 mg 22* 1 Y/Y ± ± 1 4
24 1 N ± ± ± ±
kg±1 was used to provide muscle relaxation for tracheal
26 1 N ± ± ± ±
intubation and the lungs were ventilated to normocapnia 28 1 N ± 1 ± 1
with an end-tidal sevo¯urane concentration of 0.5±1.0 MAC 6 2 N ± ± ± ±
10 2 Y/Y ± 1 ± 1
in an air±oxygen mixture until completion of skin closure.
12 2 N 1 2 ± 1
In group 2, spinal anaesthesia was established with 0.5% 13 2 Y ± 1 ± 1
bupivacaine 1 mg kg±1. Patients were placed in the left 15 2 N ± ± ± ±
20 2 N ± 1 1 2
lateral position and a 25-gauge short bevelled spinal needle
21 2 Y/Y ± 2 ± ±
inserted in the midline through either the fourth or ®fth 23 2 Y/Y ± 1 ± 1
lumbar interspace until free ¯owing cerebrospinal ¯uid was 25 2 N ± ± 1 2
27 2 N ± ± ± ±
obtained. To ensure that the groups were comparable to one
another in terms of the duration and intensity of analgesia
provided in the initial post-operative period, both patient
groups received before skin incision a single injection of
0.25% bupivacaine 2 mg kg±1 through a 22-gauge cannula All patients were monitored for a 12 h period pre- and
inserted into the caudal epidural space.16 17 `Induction to post-operatively using a portable three channel continuous
incision' (group 1, start of gaseous induction to surgical cardiorespiratory monitor (Nellcor Puritan-Bennett
incision; group 2, skin penetration with spinal needle to EdenTrace II Plus) with internal memory multi-channel
surgical incision) and `incision to closure' times were recorder interfaced with an EdenTec 3310 Assurance
recorded for both patient groups (Table 1). monitor. This integrated monitoring system provided con-
Upon completion of skin closure, sevo¯urane adminis- tinuous contemporaneous recordings of respiratory effort
tration in group 1 was discontinued and residual neuromus- and pattern (impedance pneumography/air¯ow thermistor),
cular block antagonized with neostigmine 50 mg kg±1 and heart rate (ECG) and haemoglobin oxygen saturation (pulse
glycopyrrolate 10 mg kg±1. oximeter) for each patient. In order to allow each patient to

367
Williams et al.

Table 3 Comparison of median [range of medians] pre- and post-operative cardiorespiratory changes within and between the groups. There was no
statistically signi®cant difference either within or between the groups (P>0.05). *Patient 22

Sevo¯urane group 1 (n=14) Spinal group 2 (n=10)

Pre-op Post-op Pre-op Post-op

SpO2 (%) 97 [88*±99] 97 [90*±100] 96 [93±99] 96 [92±99]


Heart rate 150 [128±179] 155 [137±176] 142 [134±150] 150 [138±168]
Per cent time SpO2 <90% 6 [1±63*] 6 [0±48*] 6 [0±17] 5 [2±28]
Number of episodes of SpO2 <90% h±1 9 [3±20] 10 [4±14] 6 [2±11] 7 [3±16]

act as their own control, those infants presenting for surgery


with an on-going oxygen requirement were prescribed a
constant ¯ow rate of supplemental nasal oxygen for the
duration of the perioperative period of cardiorespiratory
monitoring (Table 2).
Using the following analysis criteria, each computer-
generated printout was individually analysed for evidence
of either movement artefact or electrode dislodgement by an
investigator (J.M.W.) blinded to the anaesthetic technique
used. An event was de®ned as being a result of an artefact if
one or both of the following occurred: (1) one or more of the
above waveforms out of range or unrecognizable and (2) a
SpO2 less than 90% for more than 20 s with no associated
bradycardia or apnoea.
Clinical signi®cance was de®ned as a bradycardia of less
than 100 beat min±1 for at least 5 s, a haemoglobin oxygen
saturation (SpO2) of less than 90% for more than 10 s and
Fig 1 Group distribution of `excess' post-operative cardiorespiratory
apnoea as a sustained respiratory pause of 15 s or longer, or complications related to pre-operative respiratory function.
less than 15 s if accompanied by an SpO2 less than 90% or
bradycardia. These manually validated reports, in which
each subject acted as their own control, were then used to
Table 4 Total number of post-operative episodes of apnoea and bradycardia
draw comparisons between the two groups in terms of the recorded in relation to the pre-operative respiratory function of those patients
number of `excess' post-operative cardiorespiratory com- in group 1, subsequently identi®ed as exhibiting an `excess' of post-operative
plications recorded. `Excess' in our study was de®ned as a cardiorespiratory complications

3-fold or more increase in the number of post-operative Abnormal Normal


episodes of bradycardia or apnoea relative to pre-operative respiratory respiratory
function function
occurrence.
In accordance with departmental guidelines regarding the Number of patients 3 2
routine post-operative observation and care of infants Episodes of apnoea 5 0
potentially at risk of respiratory dysfunction, real-time Episodes of bradycardia 26 6

apnoea monitoring (Graseby MR10 respiration monitor) in


combination with nurse observation was undertaken for all
study patients in the post-operative period. Five patients (four receiving supplemental oxygen) in group
In view of the small sample size, data are reported as 1 and four patients (three receiving supplemental oxygen) in
median (range). Comparison of cardiorespiratory changes group 2 ful®lled the study de®nition of `pre-existing
within and between groups (Table 3) was performed using abnormal respiratory function' (Table 2). No patients had
the Mann-Whitney U test. A P<0.05 was considered a current history of apnoea or were receiving respiratory
statistically signi®cant. stimulants in the 2-week period before surgery.
Spinal anaesthesia was attempted unsuccessfully in four
patients in group 2 (28% failure rate). All had normal
Results respiratory function and went on to have their surgery
Twenty-eight patients were recruited into the study. Both successfully completed under general anaesthesia but were
groups were comparable in terms of PCA, gestational age excluded from further analysis.
(GA), weight (Wt), pre-operative haemoglobin level (Hb) Median pre- and post-operative values for heart rate,
and anaesthetic time (induction±skin closure) (Table 1). SpO2, relative duration of a decrease of SpO2 (per cent time

368
Comparison between sevo¯urane and spinal anaesthesia

SpO2 less than 90%) and number of episodes of desaturation (range 2.5±3.7 mg kg±1) used by Peutrell and Hughes in
(SpO2 less than 90% h±1) in group 1 were comparable to their study of a combined spinal±epidural technique.17
values recorded in group 2 (Table 3). Several studies to date have determined that the incidence
In group 1, three out of the ®ve patients with pre-existing of clinically signi®cant post-operative apnoea falls expo-
abnormal respiratory function and two out of the nine nentially with time from the completion of surgery.2 6 19
patients with normal respiratory function experienced an Proposed aetiological factors for this include the hang-over
excess of post-operative cardiorespiratory complications effect of residual anaesthetic agents combined with an
(Table 2). In contrast, none of the 10 patients in group 2 elevated plasma level of circulating endorphins. The
exhibited an excess of post-operative complications when contribution of the latter is in turn related to the intensity
compared with their respective pre-operative recordings and duration of the surgical insult.5 19 By attempting to
(Fig. 1). ensure that both groups were comparable in terms of the
Table 4 relates the total number of post-operative duration and intensity of analgesia provided, we hoped to be
episodes of apnoea and bradycardia recorded to the pre- able to detect in the initial post-operative period any excess
operative respiratory function of those patients in group 1 cardiorespiratory complications attributable to residual
identi®ed as exhibiting an excess of post-operative cardior- anaesthesia alone.
espiratory complications (Table 2). The three patients with The results of our pilot study suggest that despite the
abnormal respiratory function accounted for 80% of the enhanced recovery characteristics of sevo¯urane, the recov-
episodes (26/32) of post-operative bradycardia and all ®ve ery pro®le in this vulnerable age group may not be
episodes of post-operative apnoea identi®ed. All recorded comparable to that of `awake' spinal anaesthesia in all
episodes of apnoea (®ve in group 1 and two in group 2) were infants. However, balanced against this, was our inability to
temporally unrelated to the recorded episodes of bradycar- establish spinal anaesthesia in four subjects (28%), despite
dia and haemoglobin oxygen desaturation (SpO2 less than the technique being performed by experienced paediatric
90%) (Tables 2 and 3). anaesthetists. This highlights the considerable expertise and
One patient in group 1 (patient no. 22), presented for practice required and is one of the primary reasons why the
surgery with a median SpO2 less than 90%. This level of seemingly advantageous procedure of spinal anaesthesia has
hypoxaemia persisted throughout the post-operative period not gained universal acceptance in many paediatric institu-
and accounted for the wide range in the duration of tions.3 7 These ®ndings need to be interpreted within the
hypoxaemia (median per cent time SpO2 less than 90%; 63 context of the limited size of the study and, therefore,
versus 48%) recorded for each study period (Table 3). require further comment.
The concurrent use post-operatively, as per hospital Viewed as a whole, the recovery pro®le of both groups
policy, of real-time apnoea monitoring in combination with appeared comparable with neither group experiencing a
nurse observation failed to detect any of the above recorded signi®cant number of episodes of hypoxaemia (SpO2 less
episodes of cardiorespiratory disturbance. All resolved than 90% h±1) relative to pre-operative levels (Table 3). It
spontaneously without intervention. must, however, be appreciated that these results were based
on computer generated recordings and are therefore sus-
ceptible to artefact.20 The addition of real-time video
surveillance in a sleep study unit would have helped to limit
Discussion the impact of the unde®ned noise-to-signal ratio of the
We have endeavoured to design a study that re¯ects as recording system, but because of the unpredictable sched-
closely as possible clinical practice at The Royal Hospital uling of surgery this was not a feasible option. An observer
for Sick Children in Bristol. After the work conducted at our blinded to the anaesthetic technique used, therefore checked
institution by Peutrell and Hughes, a combined approach of the validity of each recording manually.
separate spinal and caudal epidural injections has been the Five out of the 14 patients (36%) in group 1 compared
preferred method of anaesthesia for those infants presenting with none of the 10 patients in group 2 exhibited an excess
for lower abdominal surgery who are thought to be at risk of of post-operative cardiorespiratory complications (Table 2).
post-operative cardiorespiratory complications.17 We have In patients with pre-existing abnormal respiratory function,
found this approach provides anaesthesia of a suf®cient three out of ®ve patients in group 1 demonstrated an excess
quality and duration to permit the completion of bilateral of post-operative cardiorespiratory complications compared
inguinal herniotomies without the need for additional with none of four in group 2 (Fig. 1). We propose a number
incremental boluses of local anaesthetic. The dosing regime of possible explanations to account for this difference
(bupivacaine 3 mg kg±1) in the awake-spinal±caudal group between the groups.
has been used without untoward sequelae at our institution First, with reference to a standard premature infant
for at least the last decade. It is less than the 3.8 mg kg±1 growth chart, we established that those patients in group 2
dose used by Gunter and colleagues18 to establish single with pre-existing abnormal respiratory function were born
injection caudal epidural anaesthesia and compares favour- `small-for-gestational-age' (less than 10th percentile) as
ably with the mean total dose of bupivacaine 2.8 mg kg±1 opposed to `appropriate-for-gestational-age' (10th±90th

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Williams et al.

percentile) when compared with the birth weights of appropriate potent inhalational agent with which to maintain
corresponding patients in group 1.21 Cote and colleagues general anaesthesia in high risk infants.
have determined that when controlled for age, haematocrit In conclusion, spinal anaesthesia may be preferable to
(greater than 30%) and institution, small-for-gestational-age general anaesthesia for ex-premature infants undergoing
infants seem to have a somewhat lower risk of post- lower abdominal surgery within the ®rst weeks of life. But
operative apnoea.19 until this has been demonstrated in large prospective,
Second, it is possible that the observed differences controlled studies in comparison with modern low solubility
between the two subgroups are purely a function of the potent inhalational agents, we will continue to have
level of monitoring. In our study, the concurrent use of reservations about routinely subjecting our patients to an
standard real-time post-operative apnoea monitoring in awake technique that is potentially stressful for the infant
combination with nurse observation, as per hospital policy, and associated with a clinically signi®cant failure rate.
failed to detect any of the subsequently computer identi®ed
adverse episodes (Tables 2 and 4). This raises the interesting
question whether cardiorespiratory complications only References
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