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BJA Advance Access originally published online on March 15, 2007
British Journal of Anaesthesia 2007 98(5):677-681; doi:10.1093/bja/aem055
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© The Board of Management and Trustees of the British Journal of Anaesthesia 2007. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org

Postoperative analgesia with intravenous fentanyl PCA vs epidural block after thoracoscopic pectus excavatum repair in children

D. Butkovic1,*, S. Kralik1, M. Matolic1, M. Kralik2, S. Toljan1 and L. Radesic1

1 Children's Hospital Zagreb, Department of Anaesthesiology, Reanimatology and Intensive Care, Zagreb, Croatia
2 Clinical Hospital Centre Rebro, Clinical Institute of Diagnostic and Interventional Radiology, Zagreb, Croatia

* Corresponding author: Children's Hospital Zagreb, Department of Anaesthesiology, Reanimatology and Intensive Care, Klaiceva 16, 10000 Zagreb, Croatia. E-mail: diana.butkovic1{at}zg.htnet.hr

Accepted for publication January 25, 2007.


    Abstract
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
Background: The aim of this prospective, randomized trial was to compare analgesia, sedation, and cardiorespiratory function in children after thoracoscopic surgery for pectus excavatum repair, using two types of analgesia—epidural block with bupivacaine plus fentanyl vs patient-controlled analgesia (PCA) with fentanyl.

Methods: Twenty-eight patients scheduled for thoracoscopic pectus excavatum surgery were randomly assigned to receive either thoracic epidural block or i.v. PCA for postoperative analgesia. Pain was assessed using a visual-analogue scale (VAS). The Ramsay sedation score, arterial pressure, ventilatory frequency, and heart rate were also measured, and blood gas analysis was performed regularly during the first 48 h after surgery.

Results: A significant decrease in the VAS pain score, Ramsay sedation score, heart rate ventilatory frequency, systolic and diastolic blood pressure, and PaCO2, and a significant increase in PaO2 and oxygen saturation were found over time. Patients in the PCA group had significantly higher PaCO2 values. In addition, a significantly slower decline of systolic blood pressure and heart rate, and faster recovery of PaCO2 were found in PCA patients than in patients with epidural block.

Conclusions: I.V. fentanyl PCA is as effective as thoracic epidural for postoperative analgesia in children after thoracoscopic pectus excavatum repair. Bearing in mind the possible complications of epidural catheterization in children, the use of fentanyl PCA is recommended.

Keywords: analgesia, patient controlled; analgesic techniques, epidural; analgesics opioid, fentanyl; children; procedure, Nuss


    Introduction
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
Post-thoracotomy pain is one of the most intense forms of postoperative pain, and analgesia after thoracic surgery is important for the patients' respiratory function after the surgery.1 2 An endoscopic modification of the Nuss procedure for pectus excavatum repair in children is gaining acceptance and is believed to be associated with fewer complications. In this procedure, a curved steel bar is individually shaped for each patient and placed through an endoscopically created retrosternal tunnel. Once positioned, the steel bar is turned over, thereby correcting the deformity.37 The procedure is associated with severe postoperative pain, although this is less than that after thoracotomy.

Systemic opioids, non-steroid anti-inflammatory drugs (NSAIDs), and regional analgesia, such as intercostal, intrapleural, paravertebral, and epidural block, are most commonly used for management of post-thoracotomy pain, and after the endoscopic Nuss procedure.1 2

Epidural analgesia is frequently used after major thoracic and abdominal procedures in children. The efficacy of epidural block with bupivacaine plus fentanyl has been reported in adults and children.818 Epidural opioids have been combined synergistically with local anaesthetics to block spinal nociceptive pathways and reduce the dose-related adverse effects of both classes of drug.1 8 16 Small doses of opioids, in combination with local anaesthetics, can improve analgesia three-fold compared with local anaesthetics alone.13

Fentanyl being a lypophilic opioid differs from morphine in epidural analgesia because of the limited rostral spread and is associated with less sedation and respiratory depression.12 13 Fentanyl is usually given as a continuous infusion because of its relatively short half-life. Fentanyl administered as a continuous infusion acts predominantly on supraspinal nociceptive pathways, producing non-segmental analgesia. Bolus administration of epidural fentanyl causes segmental analgesia, acting on the spinal level.12 13

Epidural analgesia is, however, associated with spinal cord and nerve root lesions, high spinal blockade, significant systemic toxicity, epidural haematoma, and infections. Fortunately, such complications are rare.18

Patient-controlled analgesia (PCA with or without a background infusion) is a well-established method of relieving postoperative pain in children as young as 5 yr old.1921 PCA does, however, have major and minor adverse effects, such as nausea, vomiting, sedation, or respiratory depression. Hence, monitoring of respiratory function and level of sedation is mandatory.20

The aim of this prospective, randomized study was to compare two types of postoperative analgesia, namely epidural block with bupivacaine plus fentanyl and PCA with fentanyl in terms of postoperative pain, sedation, arterial pressure, heart rate, ventilatory frequency, blood gases, and adverse effects in children undergoing the Nuss procedure for thoracoscopic pectus excavatum repair.


    Methods
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
After obtaining the Hospital Ethics Committee's approval and informed consent from the parents, 28 children (mean age 14.54 yr, range 8–19 yr) scheduled for thoracoscopic repair of pectus excavatum were randomly assigned to receive either epidural or PCA analgesia.

The exclusion criteria were NSAIDs use, coagulation disorders, allergy to local anaesthetics, American Society of Anaesthesiologists (ASA) grade more than III, inability to understand how to use the PCA device, and patients' or parents' objection to an epidural catheter.

All children were premedicated with midazolam 0.3 mg kg–1 orally. Before the induction of general anaesthesia, a thoracic epidural catheter was placed, an i.v. line was introduced, and bolus of 500 ml of isotonic saline given to each child in the epidural group. In most patients in the epidural group, a 20-gauge epidural catheter was inserted through an 18-gauge needle at the Th 7-8 or Th 8-9 intervertebral space using loss of resistance in the lateral position with non-invasive monitoring of arterial pressure, ECG, and pulse oxymetry. However, in small children, a catheter of 24-gauge was introduced through a 20-gauge needle. The catheter tip was advanced 2–3 cm into the epidural space.

A test dose of 0.1 ml kg–1 of 0.25% bupivacaine with 1:200.000 epinephrine was given. A cold sensitivity test was used to determine the extent of the block.

Patients in the PCA group were given i.v. line for postoperative PCA. The use of the PCA system was explained to the patients on two occasions, before and after the operation.

Anaesthesia was induced by midazolam 0.2 mg kg–1, fentanyl 2 µg kg–1, and rocuronium 0.8 mg kg–1. After the trachea was intubated, anaesthesia was maintained with isoflurane (end-tidal concentration 0.8%) in oxygen–nitrous oxide (FIO2 = 0.5). Additional fentanyl and rocuronium were administered at the discretion of the anaesthesiologist. Isotonic saline was used for intraoperative fluid maintenance.

A bolus of 0.125% bupivacaine and fentanyl was administered epidurally to patients in the epidural group before bar reversion, whereas children in the PCA group received i.v. additional bolus of fentanyl.

Postoperatively, patients were transferred to intensive care unit. In the epidural group, analgesia was maintained with bupivacaine 0.125% and fentanyl 2 µg ml–1 epidurally, with infusion rate of 0.15 ml kg–1 h–1. In the PCA group, patients received basal infusion rate of 0.05 ml kg–1 h–1, boluses of 0.1 ml kg–1, and a lockout interval of 10 min. For the PCA, 1 mg of fentanyl was diluted in 500 ml of isotonic saline.

The intensity of pain was assessed at intervals during the first two postoperative days using a 10 point visual analogue scale (VAS) at 2, 4, 6, 12, 18, 24, 36, and 48 h postoperatively. The level of sedation was determined using the Ramsay sedation score (range from 1 to 6) at 2, 6, 12, and 24 h postoperatively. Ventilatory frequency, heart rate, systolic and diastolic blood pressure, arterial blood oxygen saturation, and partial pressure of oxygen (PaO2) and carbon dioxide (PaCO2) were all measured at 2, 4, 6, 12, 18, and 24 h. Side-effects, such as pruritus, nausea, vomiting, and respiratory depression, were noted.

Statistical analysis was performed using SPSS software package for Windows, version 13.0. Normality of the distributions was tested by Kolmogorow–Smirnov test and homogeneity of variance was tested by Levene's test. The Mann–Whitney test was used to determine the significance of difference between the groups. Any difference between frequencies was analysed by {chi}2 test. Fisher's exact test was used when there was an expected frequency of less than 5. Main effects and interaction between factors were analysed by one-way within-subjects analysis of variance (ANOVA) and by two-way mixed ANOVA in repeated measures model. Sphericity assumption was tested by Mauchly's test. Greenhouse–Geisser correction to the degrees of freedom and P-value was applied if no or mild violation of sphericity was present. If the violation was stronger, the more conservative Huynh–Feldt correction was used. The significance level used was 0.05.


    Results
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
No significant differences in age, sex, body weight, ASA grade, and duration of surgery were found between two groups (P > 0.05). The principal patients' data are shown in Table 1. Preoperative pulmonary function tests, measured by spirometry, were normal in all patients, as were cardiological findings (ultrasonography and ECG).


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Table 1 Patient data. Gender, ASA, and side-effects are given as frequencies (percentages), body weight and duration of surgery as mean (SD) (95% CI), and age as mean (range)

 
A decrease in VAS score was seen at every time-point relative to the previous measurement. The same was true for Ramsay sedation score, PaCO2, systolic and diastolic blood pressure, heart rate, and ventilatory frequency. The opposite was found for PaO2 and oxygen saturation where there was increase in every successive measurement.

The one-way within-subjects ANOVA, done for all patients (data not shown) and separately for patients with different type of analgesia (Fig. 1), showed that there was significant effect of time elapsed after the surgery on all parameters (P < 0.001).

Contrast analysis showed that the effects were linear for PaCO2 and PaO2, but more complex than linear, with significant quadratic components, for Ramsay sedation score, systolic and diastolic blood pressure, heart rate, ventilatory frequency, and oxygen saturation. Furthermore, there were significant cubic and order four components for VAS score.

Two-way mixed model ANOVA analysis showed that there was a significant main effect of type of analgesia on PaCO2 (P = 0.007), with PCA patients exhibiting on average 0.607 kPa higher values (Fig. 1H). No effect of type of analgesia was found on other parameters (VAS score, Ramsay sedation score, systolic and diastolic arterial blood pressure, heart rate, ventilatory frequency, PaO2, and oxygen saturation, P = 0.658, 0.602, 0.555, 0.647, 0.161, 0.755, 0.228, and 0.929, respectively).


Figure 1
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Fig 1 Plots of the means of the VAS (A), Ramsay sedation score (B), heart rate (C), systolic (D) and diastolic (E) blood pressure, ventilatory frequency (F), PaO2 (G), PaCO2 (H), and oxygen saturation (I) vs time elapsed after surgery, separately for patients in epidural (solid line, n = 14) and PCA group (dotted line, n = 14). Please note the different slopes of the curves in C, D, and H, and separated curves in H.

 
However, there was a significant interaction between time of measurement and type of analgesia for systolic arterial blood pressure and PaCO2 (P = 0.006 and 0.017, respectively) and moderate interaction for heart rate (P = 0.036). This is due to the fact that PCA patients exhibited slower decline of elevated systolic blood pressure (Fig. 1D) and heart rate (Fig. 1C) and faster recovery of significantly higher PaCO2 (Fig. 1H) when compared with the patients with epidural analgesia.


    Discussion
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
The present study suggests that the efficacy of postoperative analgesia after the thoracoscopic pectus excavatum repair in children does not differ between PCA with fentanyl and epidural infusion of fentanyl plus bupivacaine. Neither an overall effect of type of analgesia on the VAS score nor an interaction between time of VAS score assessment and type of analgesia was seen. Likewise, there was no significant effect of type of analgesia on the Ramsay sedation score, implying that both analgesic regimes produced the same level of sedation.

Rawal22 reported that the risk of life-threatening respiratory depression in patients with i.v. PCA is approximately 0.9%. In our study, respiratory depression was evaluated by the ventilatory frequency and sedation scores as recommended by the European Society of Regional Anaesthesia.23 In the PCA group, postoperative PaCO2 values were found to be on average significantly higher compared with the epidural group. Nevertheless, the increased PaCO2 in the PCA group showed faster recovery towards initial values. These higher PaCO2 values could be attributed to: (i) the effect of opioids on respiration with an increase in baseline PaCO2 and blunting of PaCO2 response, which is supported by the finding of the same increase in ventilatory frequency in both groups and (ii) beneficial effects of thoracic epidural analgesia compared with the PCA on respiration, such as improved diaphragmatic function with earlier mobilization, as described in a study by Licker and collaegues.24

Cardiovascular depression and hypotension due to local anaesthetic-induced negative inotropic effects in thoracic epidural analgesia25 were not seen in our study and the two groups did not differ in terms of systolic and diastolic blood pressure, or heart rate. However, patients in the epidural group showed faster decline in systolic blood pressure and heart rate than children in the PCA group.

A previous study reported an incidence of nausea and vomiting after epidural opioids of approximately 30%, compared with 87% during PCA.14 In our study, 29% (4/14) of the patients in the PCA group developed nausea, whereas 36% (5/14) of the children in the epidural group had nausea or pruritus. No significant difference in side-effects rate was found.

Kavanagh and colleagues1 have made a meta-analysis of current techniques for pain control after thoracic surgery. They compared the use of opioids, NSAIDs, ketamine, and regional analgesia. Their conclusion was that the combination of thoracic epidural local anaesthetics and opioids can essentially abolish post-thoracotomy pain, but possible complications and cost–benefit issues have to be considered. McBride and colleagues12 investigated whether continuous epidural analgesia after pectus excavatum repair is as safe an alternative as high-dose narcotics in children. They found that the epidural analgesia eliminates the potential disadvantages of sedation and respiratory depression, both of which were associated with the use of high-dose narcotics. Cassady and colleagues13 compared continuous thoracic epidural analgesia with bupivacaine–fentanyl combination and PCA with morphine in adolescents undergoing posterior spinal fusion, and found them comparable in terms of effectiveness and safety.

Bozkurt14 compared neuroendocrine response and analgesic efficacy of morphine-epidural and morphine-PCA in children after major genitourinary or lower abdominal surgery and found that both techniques provided sufficient pain relief and attenuation of the hormonal response. Lejus and colleagues15 evaluated epidural analgesia with bupivacaine and fentanyl in 348 children, and found excellent pain control in 86% of patients, with only mild complications (nausea, vomiting, pruritus, and urinary retention) in a minority of patients. Bloch and colleagues16 compared an i.v. infusion tramadol with epidural morphine for post-thoracotomy pain in adults, and concluded that thoracic epidural analgesia may result in earlier recovery of respiratory function, but the procedure was not without risk. Their study suggests that postoperative infusion of tramadol, on the basis of pain scores, analgesic requirements, and respiratory variables, is at least as effective as thoracic epidural morphine.

In conclusion, PCA with fentanyl is as effective as epidural block with bupivacaine and fentanyl in postoperative pain control and recovery of children after thoracoscopic surgery for pectus excavatum repair. Bearing in mind the possible complications of thoracic epidural catheter placement in children, the results of the present study support the usage of fentanyl PCA over epidural block.


    Acknowledgements
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
The authors are grateful to Jane Surtees and especially to Nigel McTurner for their valuable suggestions and comments on the manuscript.


    References
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
1 Kavanagh BP, Katz J, Sandler AN. Pain control after thoracic surgery: a review of current techniques. Anesthesiology (1994) 81:737–59.[ISI][Medline]

2 Hammer GB. Pediatric thoracic anesthesia. Anesth Clin North Am (2002) 20(1):153–80.[CrossRef][Medline]

3 Jacobs JP, Quintessenza JA, Morell VO, Botero LM, van Gelder HM, Tchervenkov CI. Minimally invasive endoscopic repair of pectus excavatum. Eur J Cardiothoracic Surg (2002) 21(5):869–73.[Abstract/Free Full Text]

4 Nuss D, Croiton DP, Kelly RE, Goretsky MJ, Nuss RJ, Gustin TS. Review and discussion of the complications of minimally invasive pectus excavatum repair. Eur J Ped Surg (2002) 12(4):230–4.[CrossRef]

5 Engum S, Rescorla F, West K, Rouse T, Scherer LR, Grosfeld J. Is the grass greener? Early results of the Nuss procedure. J Pediatr Surg (2000) 35(2):246–51.[CrossRef][ISI][Medline]

6 Inge TH, Owings E, Blewett CJ, et al. Reduced hospitalization cost for patients with pectus excavatum treated using minimally invasive surgery. Surg Endosc (2003) 17(10):1609–13.[CrossRef][ISI][Medline]

7 Ong CC, Choo K, Morreau P, Auldist A. The learning curve in learning curve: a review of Nuss procedure in teenagers. ANZ J Surg (2005) 75:421–4.[CrossRef][ISI][Medline]

8 Hergert M, Rosolski T, LestinHG, Stranz G. Postoperative epidural analgesia—current status, indications and management. Anaesthesiol Reanimat (2002) 27(6):152–9.[Medline]

9 Williams DG, Howard RF. Epidural analgesia in children. A survey of current opinions and practices amongst UK pediatric anaesthetists. Pediatr Anaesth (2003) 13(9):769–76.[CrossRef][ISI][Medline]

10 Ginosar Y, Riley ET, Angst MS. The site of action of epidural fentanyl in humans: the difference between infusion and bolus administration. Anesth Analg (2003) 97:1428–38.[Abstract/Free Full Text]

11 Ginosar Y, Columb MO, Cohen SE, et al. The site of action of epidural infusions in the presence of local anesthetics: a minimum local analgesic concentration infusion study in nulliparous labor. Anesth Analg (2003) 97:1439–45.[Abstract/Free Full Text]

12 McBride WJ, Dicker R, Abajian JC, Vane DW. Continuous thoracic epidural infusions for postoperative analgesia after pectus deformity repair. J Pediatr Surg (1996) 3181:105–7.

13 Cassady JF jr, Lederhaas G, Cancel DD, Cummings RJ, Loveless EA. A randomized comparison of the effects of continuous thoracic epidural analgesia and intravenous patient-controlled analgesia after posterior spinal fusion in adolescents. Reg Anesth Pain Med (2000) 25(3):246–53.[CrossRef][ISI][Medline]

14 Bozkurt P. The analgesic efficacy and neuroendocrine response in paediatric patients treated with two analgesic techniques: using morphine-epidural and patient-controlled analgesia. Paediatric Anaesthesia (2002) 12:248–54.[CrossRef][ISI][Medline]

15 Lejus C, Surbled M, Schwoerer D, et al. Postoperative epidural analgesia with bupivacaine and fentanyl: hourly pain assessment in 348 pediatric cases. Paediatr Anaesth (2001) 11:327–32.[CrossRef][ISI][Medline]

16 Bloch MB, Dyer RA, Heijke SA, James MF. Tramadol infusion for postthoracotomy pain relief: a placebo-controlled comparison with epidural morphine. Anesth Analg (2002) 94:523–8.[Abstract/Free Full Text]

17 Kasai T, Yaegeshi K, Hirose M, Tanaka Y. Spinal cord injury in a child caused by an accidental dural puncture with a single-shot thoracic epidural needle. Anesth Analg (2003) 96(1):65–7.[Abstract/Free Full Text]

18 Straford MA, Wilder RT, Berde CB. The risk of infection from epidural analgesia in children: a review of 1620 cases. Anesth Analg (1995) 80(21):234–8.[Abstract]

19 Peters JW, Bandell Hoekstra IE, Abu-Saad H, Bouwmeester J, Meursing AE, Tibboel D. Patient controlled analgesia in children and adolescents: A randomized controlled trial. Paediatr Anaesth (1999) 9:235–41.[CrossRef][ISI][Medline]

20 McDonald AJ, Cooper MG. Patient-controlled analgesia: an appropriate method of pain control in children. Paediatr Drugs (2001) 3:273–84.[CrossRef][Medline]

21 Yildiz K, Tercan E, Dogru K, Ozkan U, Boyaci A. Comparison of patient-controlled analgesia with and without a background infusion after appendicectomy in children. Paediatr anaesth (2003) 13:427–31.[CrossRef][ISI][Medline]

22 Rawal N. Epidural and spinal agents for postoperative analgesia. Surg Clin North Am (1999) 79:313–344.[CrossRef][ISI][Medline]

23 Aguilar JL, Benhamou D, Bonnet F, et al. ESRA guidelines for the use of epidural opioids. Int Monit Reg Anesth (1997) 9:3–8.

24 Licker M, Spiliopoulos A, Tschopp JM. Influence of thoracic epidural analgesia on cardiovascular autonomic control after thoracic surgery. Br J Anaesth (2003) 91:525–31.[Abstract/Free Full Text]

25 Veering BT, Cousins MJ. Cardiovascular and pulmonary effects of epidural anaesthesia. Anaesth Intens Care (2000) 28:620–35.[ISI][Medline]


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Is fentanyl PCA really a better choice than thoracic epidural in children?
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British Journal of Anaesthesia, 3 Apr 2007 [Full text]

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