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BJA Advance Access originally published online on July 1, 2006
British Journal of Anaesthesia 2006 97(3):414-418; doi:10.1093/bja/ael172
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© The Board of Management and Trustees of the British Journal of Anaesthesia 2006. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org

The effect of epidural sufentanil in ropivacaine on urinary retention in patients undergoing gastrectomy

J. Y. Kim1, S. J. Lee2,3, B. N. Koo2,3,*, S. H. Noh4, H. K. Kil2,3, H. S. Kim1 and S. Y. Ban2

1 Department of Anaesthesiology and Pain Medicine, Gachon Medical School Gil Medical Center Incheon, South Korea
2 Department of Anaesthesiology and Pain Medicine, Yonsei University College of Medicine Seoul, Korea
3 Anaesthesia and Pain Research Institute, Yonsei University College of Medicine Seoul, Korea
4 Department of Surgery, Yonsei University College of Medicine Seoul, Korea

*Corresponding author: Department of Anaesthesiology and Pain Medicine, Yonsei University College of Medicine, 134 Shinchon-Dong, Seodaemun-Gu, CPO Box 8044, Seoul 120-752, Korea. E-mail: koobn{at}yumc.yonsei.ac.kr

Accepted for publication May 30, 2006.


    Abstract
 Top
 Abstract
 Introduction
 Materials and methods
 Results
 Discussion
 REFERENCES
 
Background. Although epidural opioids have excellent analgesic property, their side-effects limit its use in patient-controlled epidural analgesia (PCEA). This study was designed to compare side-effects of epidural sufentanil in ropivacaine with that of morphine in ropivacaine focusing on lower urinary tract function after major abdominal surgery.

Methods. In total 60 patients undergoing gastrectomy were randomly allocated to receive either sufentanil in ropivacaine (Group S, n=30) or morphine in ropivacaine (Group M, n=30) for their PCEA. Epidural catheter was inserted between the 7th and 8th thoracic spine. Visual analogue pain score and side-effects such as nausea, vomiting, pruritus, hypotension and urinary retention were evaluated during postoperative days (PODs) 1 and 2 in the postanaesthetic care unit.

Results. The incidence of serious to major micturition problem in Group S was lower than that in Group M (P<0.001). The incidence of pruritus, nausea and vomiting was also lower in Group S than in Group M on POD 1.

Conclusions. The lower incidence of major/serious micturition problem in patients receiving sufentanil in ropivacaine thoracic epidural analgesia suggests that continuation of urinary drainage may not be necessary from POD 1 onwards.

Keywords: analgesics opioid, morphine; analgesic opioid, sufentanil; kidney, urine; surgery, gastrointestinal


    Introduction
 Top
 Abstract
 Introduction
 Materials and methods
 Results
 Discussion
 REFERENCES
 
Epidural administration of opioids mixed with a local anaesthetic has become popular in perioperative analgesia. However, the side-effects of opioids such as respiratory depression, itching, nausea, vomiting and urinary retention can be major problems. In particular, their effects on lower urinary tract function lead to routine bladder catheterization, which increases the risk of urinary tract infection.13

Recently, in healthy male volunteers, intrathecal opioids were reported to decrease bladder function by suppression of detrusor contractility, and the recovery of normal lower urinary tract function was significantly faster after intrathecal sufentanil than after morphine.4 However, pathogenesis of postoperative urinary retention is multifactorial, and includes the use of drugs that affect urinary detrusor function, intraoperative damage to the pelvic autonomic nerve and stress-induced activation of inhibitory sympathetic reflexes.57 In addition, local anaesthetic drugs are used for postoperative epidural analgesia to provide improved analgesia after major abdominal operations.

This study was designed to compare the side-effects of epidural sufentanil in ropivacaine with that of morphine in ropivacaine after a major abdominal surgery. We focused on lower urinary tract function, thereby, assessing the optimal duration of routine bladder catheterization in patients undergoing gastrectomy.


    Materials and methods
 Top
 Abstract
 Introduction
 Materials and methods
 Results
 Discussion
 REFERENCES
 
After obtaining approval of the institutional Ethics Committee and written informed consent, 60 ASA I–II patients undergoing gastrectomy were recruited. Using sealed envelope system, the patients were randomly allocated to one of the two groups to receive either sufentanil in ropivacaine (Group S, n=30) or morphine in ropivacaine (Group M, n=30) for the postoperative epidural analgesia. Before surgery, patients were instructed on the use of the patient-controlled epidural analgesia (PCEA) device and visual analogue scale (VAS) pain score. Patients and anaesthetists were blinded to the treatment group and an independent researcher prepared the study solution consisting of 275 ml mixture of ropivacaine 0.2%, and sufentanil 250 µg (0.9 µg ml–1) in Group S or morphine 10 mg (36 µg ml–1) in Group M.

Patients with known urological disease, spinal disease, coagulopathy and on any medication that might have influenced the sympathetic nervous system were excluded from this study. Patients who had refused neuraxial anaesthesia were also excluded. Patients who were to undergo surgery in the afternoon were excluded because the indwelling urinary catheter was to be removed in the morning of the first postoperative day (POD 1).

All the patients were premedicated with i.m. midazolam 2 mg and glycopyrrolate 0.2 mg. Before the induction of general anaesthesia, an epidural catheter was inserted between the 7th and 8th thoracic spine (T7–8) and the catheter was advanced 3 cm upwards. After a test dose of lidocaine 2%, 3 ml with epinephrine (1:200 000), lidocaine 2%, 5 ml was given via epidural route. General anaesthesia was induced with i.v. thiopental sodium (4 mg kg–1), fentanyl (1.5 µg kg–1), and rocuronium (0.8 mg kg–1). No additional i.v. opioid agent was given after this. After induction of anaesthesia, indwelling urinary catheter was inserted. Anaesthesia was maintained with oxygen/air (50:50) and sevoflurane, and vecuronium was given for continued muscle relaxation. The end-tidal concentration of sevoflurane was adjusted to maintain arterial blood pressure within 20% of baseline values. Arterial blood pressure below 20% of baseline was treated with boluses of ephedrine. After induction of general anaesthesia, epidural analgesia was started using a silicone balloon infuser (Accufuser®, Woo Young Medical Co. Ltd, Korea) containing the study solution. The balloon pump infuser lasted for 2 days; it was set to 5 ml h–1 for continuous infusion and 0.5 ml for bolus dose with a 15 min lockout period. The tracheal tube was removed in the operating theatre at the end of surgery. In the postanaesthetic care unit (PACU), in addition to VAS pain score, patients were evaluated for the side-effects of epidural opioids such as nausea, vomiting, pruritus and the incidence of hypotension by an investigator blinded to group allocation of the patients. Motor block was evaluated using a previously described scale (1=no motor block, 2=knee blocked and mobility of ankle preserved, 3=mobility of ankle difficult, and 4=knee and ankle blocked) and the sensory block level was evaluated by response to a cold stimulus to the skin. Patients with VAS pain score higher than 5 were given i.m. meperidine 25 mg as rescue analgesia. In the morning of POD 1, indwelling urinary catheter was removed. A nurse who was blinded to the patient group recorded the incidence whenever a patient complained of nausea, vomiting, pruritus or micturition problem until POD 2. Motor block, sensory block and VAS pain scores at rest and during coughing were recorded in the morning of POD 1 and 2. Blood pressures were measured every 6 h until POD 2. To assess micturition problem, patients were to report the need to void, and their urine volume whether it was <200 or >700 ml. They were also to report lack of urge or feeling of incomplete micturition. If the patients were unable to void 6 h after the removal of the urinary catheter, the bladder was drained with in-and-out catheterization and urine volume was checked. Micturition problems were classified according to a previously used classification by Vercauteren and colleagues8 (Table 1) and the bladder was drained with in-and-out or indwelling catheterization in patients with serious or major problem, respectively. Epidural catheter was removed after the silicone balloon infuser was empty.


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Table 1 Classification of micturition problems

 
In a previous study, Vercauteren and colleagues8 have shown that low dose bupivacaine–sufentanil group reduced the grade of micturition problem to 1.0 (SD 1.0) compared with 1.9 (1.2) in the high dose bupivacaine–sufentanil group on POD 1. A sample size was calculated based on this effect, with {alpha}=0.05 and ß=0.2. In total, 27 patients were required in each group in order to detect a statistically significant difference between the groups. A total of 30 patients were recruited in each group to compensate for loss of data during follow-up. As there was no withdrawal, the result of 30 patients were included in this study. Retrospective power calculation showed the power of this study to be 91%.

Statistical analyses were performed using the statistical package for social sciences statistical software (SPSS 10.0, SPSS Inc., Chicago, IL). Chi-square test, t-test, Mann–Whitney U-test and Fisher’s exact test were used to compare variables between the groups where appropriate. Results are expressed as mean (SD) or number of patients. P-value <0.05 was considered statistically significant.


    Results
 Top
 Abstract
 Introduction
 Materials and methods
 Results
 Discussion
 REFERENCES
 
Patient characteristics and data from the perioperative periods are listed in Table 2. The duration of surgery, blood loss, urine output and amount of fluids infused between the two groups were comparable (Table 2). The level of the sensory block to cold stimulus ranged from T3–T6 to T10–L2. The ranges of the level of sensory block (upper and lower segments) were similar between the two groups. None of the patients had motor block (all were scale 1). The extension of sensory blockade was not checked because patients were unable to distinguish the level of cold sense during continuous infusion of study mixture. There were no significant differences in VAS pain scores at rest and during coughing between two groups throughout the study period (Table 3). The dose of study mixture infused was the same for all patients because the balloon infuser was removed when the container became empty, with an average time of 44.4 (5.4) h in Group M and 43.3 (6.6) h in Group S.


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Table 2 Patient characteristics and data from the perioperative period. Data are mean (range), mean (SD) or number of patients

 

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Table 3 Postoperative visual analogue scale (VAS) pain score and side-effects in the postanaesthetic care unit (PACU), and on postoperative days (PODs) 1 and 2. Values are mean (SD) or the number of patients. The incidence of pruritus was significantly higher in Group M than in Group S on POD 1 (P=0.012). The incidence of nausea and vomiting (PONV) was also significantly higher in Group M group than in Group S on POD 1 (P=0.021)

 
Side-effects of epidural opioids except micturition problems are listed in Table 3. Two patients in Group M and one in Group S were hypotensive in PACU. They were treated with ephedrine and discharged from PACU when the blood pressure was maintained near normal for over an hour. The blood pressure was stable in all patients in the ward. The incidence of pruritus was significantly higher in Group M than that in Group S on POD 1 (P<0.05). The incidence of nausea and vomiting was also significantly higher in Group M than in Group S on POD 1 (P<0.05). None of the patients had respiratory depression.

The number of patients with micturition problems is listed in Table 4. The number of patients with serious to major micturition problem in Group S was significantly less than that in Group M on POD 1 and POD 2 (all P<0.001). Throughout the study period, no patient in Group S had any serious or major micturition problem. On the other hand, 12 (40%) patients in Group M complained of serious micturition problem and one patient needed indwelling bladder catheterization because the patient produced <200 ml urine twice, complained of incomplete voiding sense and could not void for more than 6 h after previous micturition. No patient had urinary problems at 30 days follow-up.


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Table 4 Number of patients with micturition problems. The number of patients with serious to major micturition problems in Group S group was significantly less than that in Group M group on POD 1 and POD 2

 

    Discussion
 Top
 Abstract
 Introduction
 Materials and methods
 Results
 Discussion
 REFERENCES
 
The results of this prospective, randomized, double-blind study indicate that, during postoperative epidural analgesia, compared with epidural morphine, epidural sufentanil has a lower incidence of opioid-induced side-effects including micturition problems that may necessitate the bladder catheterization.

Studies on the effect of neuraxial morphine on lower urinary tract function have shown that intrathecal morphine suppresses bladder contraction.4 9 10 However, the exact mechanism has not been elucidated. In 1983, Rawal and colleagues10 reported that 2, 4 and 10 mg of epidural morphine decreased detrusor contractility with increased maximal bladder capacity, and that these effects were reversed with naloxone. Intravenous or intramuscular morphine had little effect on detrusor muscle. The authors suggested the spinal action of morphine was because of the rapid onset of detrusor relaxation after epidural morphine administration. Regardless of the mechanism, urinary retention is one of the side-effects of epidural opioids.

The pharmacokinetics of an epidurally administered drug has been a subject of much discussion. The site of action of epidurally administered lipophilic opioids is under debate. Some studies report that epidurally administered lipophilic opioids such as alfentanil, sufentanil and fentanyl produce their effects mostly via systemic mechanism and little via spinal mechanism.1115 Bernards and colleagues11 measured drug concentration in each compartment after epidural administration of different opioids and reported that in the epidural space, lipophilic drugs had negligible access to the spinal cord; thus had less bioavailability because of possible sequestration, and/or rapid vascular uptake from the epidural space. However, this does not indicate that the action of lipophilic opioids on the spinal cord is not the predominant one. Other studies on epidural fentanyl or sufentanil after thoracotomy report that thoracic epidural administration of lipophilic opioids show superior analgesic effect when compared with that in lumbar epidural space.1618 Hansdottir and colleagues16 17 19 published a series of studies on epidural sufentanil infusion after thoracotomy. They demonstrated that concentrations of epidural sufentanil were higher in CSF than in plasma and that sufentanil was highly localized in CSF to the level of administration both after single bolus and infusion.16 19 They also proved in a clinical study that after thoracotomy, epidural sufentanil analgesia was optimal when tailored to the site of nociceptive input and combined with bupivacaine.17 These data support dermatomal restriction of lipophilic opioids, which allows reduction in the drug amount to be administered. In this study, epidural catheters were inserted at the T7–8 interspace, which corresponds to the surgical incision site but not associated with detrusor activity. Therefore, probably both systemic absorption and dermatomal restriction of epidural sufentanil caused the reduction in micturition problem during epidurally administered sufentanil.

The concentration of sufentanil used in this study (0.9 µg ml–1) was based on other studies, in which the dose ranged from 0.5 to 1 µg ml–1 for major abdominal surgical pain.2022 The equianalgesic concentration of epidural opioids used in this study was based on the recommended 50 µg ml–1 for epidural morphine and 1–2 µg ml–1 for epidural sufentanil to be continuously infused at a rate of 4–8 ml h–1.23

In this study, the opioid was mixed with a local anaesthetic, ropivacaine, to reduce the incidence of opioid-related side-effects and to improve analgesia.2426 The effects of neuraxial local anaesthetics on bladder function are different from those of opioids. A complete absence of urge and detrusor contractility with spinal anaesthesia was reported up to recovery of sensation of pinprick in the S2–S3 dermatome, which contains most of the fibres concerned with the control of the bladder and urethral sphincters.27 As the epidural block was administered at the thoracic level using segmental technique and the concentration of the ropivacaine was the same (0.2%) for both groups, this would not have influenced the result of this study.

Unlike epidural morphine, none of the patients who received epidural sufentanil had serious and/or major micturition problems on POD 1 in this study. This result suggests that urinary catheter inserted in the operating theatre could be removed in the morning of POD 1. This may have important clinical implications because routine catheterization beyond 24 h may increase the risk of subsequent urinary infection and voiding problems.1 2 18 Furthermore, if recently introduced portable ultrasound scan is available, indwelling urinary catheter may be removed at the end of the surgery because the ultrasound is reported to measure bladder volume accurately.2830

In conclusion, the low incidence of micturition problems in patients receiving sufentanil in continuous thoracic epidural analgesia suggests that routine bladder catheterization from POD 1 onwards may not be necessary.


    REFERENCES
 Top
 Abstract
 Introduction
 Materials and methods
 Results
 Discussion
 REFERENCES
 
1 Givens CD and Wenzel RP. Catheter-associated urinary tract infections in surgical patients: a controlled study on the excess morbidity and costs. J Urol 1980; 124:646–8[Web of Science][Medline]

2 Platt R, Polk BF, Murdock B, Rosner B. Mortality associated with nosocomial urinary-tract infection. N Engl J Med 1982; 307:637–42[Abstract]

3 Benoist S, Panis Y, Denet C, Mauvais F, Mariani P, Valleur P. Optimal duration of urinary drainage after rectal resection: a randomized controlled trial. Surgery 1999; 125:135–41[Web of Science][Medline]

4 Kuipers PW, Kamphuis ET, van Venrooij GE, et al. Intrathecal opioids and lower urinary tract function: a urodynamic evaluation. Anesthesiology 2004; 100:1497–503[CrossRef][Web of Science][Medline]

5 Petros JG, Rimm EB, Robillard RJ, Argy O. Factors influencing postoperative urinary retention in patients undergoing elective inguinal herniorrhaphy. Am J Surg 1991; 161:431–3[CrossRef][Web of Science][Medline]

6 Gonullu NN, Gonullu M, Utkan NZ, Dulger M, Gokgoz S, Karsli B. Postoperative retention of urine in general surgical patients. Eur J Surg 1993; 159:145–7[Web of Science][Medline]

7 Tammela T. Postoperative urinary retention—why the patient cannot void. Scand J Urol Nephrol Suppl 1995; 175:75–7[Medline]

8 Vercauteren MP, Van Den Bergh L, Kartawiadi SL, Van Boxem K, Hoffmann VL. Addition of bupivacaine to sufentanil in patient-controlled epidural analgesia after lower limb surgery in young adults: effect on analgesia and micturition. Reg Anesth Pain Med 1998; 23:182–8[Web of Science][Medline]

9 Dray A and Metsch R. Inhibition of urinary bladder contractions by a spinal action of morphine and other opioids. J Pharmacol Exp Ther 1984; 231:254–60[Abstract/Free Full Text]

10 Rawal N, Mollefors K, Axelsson K, Lingardh G, Widman B. An experimental study of urodynamic effects of epidural morphine and of naloxone reversal. Anesth Analg 1983; 62:641–7[Abstract/Free Full Text]

11 Bernards CM, Shen DD, Sterling ES, et al. Epidural, cerebrospinal fluid, and plasma pharmacokinetics of epidural opioids (part 1): differences among opioids. Anesthesiology 2003; 99:455–65[CrossRef][Web of Science][Medline]

12 Coda BA, Brown MC, Schaffer RL, Donaldson G, Shen DD. A pharmacokinetic approach to resolving spinal and systemic contributions to epidural alfentanil analgesia and side-effects. Pain 1995; 62:329–37[CrossRef][Web of Science][Medline]

13 Coda BA, Brown MC, Risler L, Syrjala K, Shen DD. Equivalent analgesia and side effects during epidural and pharmacokinetically tailored intravenous infusion with matching plasma alfentanil concentration. Anesthesiology 1999; 90:98–108[CrossRef][Web of Science][Medline]

14 Glass PS, Estok P, Ginsberg B, Goldberg JS, Sladen RN. Use of patient-controlled analgesia to compare the efficacy of epidural to intravenous fentanyl administration. Anesth Analg 1992; 74:345–51[Abstract/Free Full Text]

15 Miguel R, Barlow I, Morrell M, Scharf J, Sanusi D, Fu E. A prospective, randomized, double-blind comparison of epidural and intravenous sufentanil infusions. Anesthesiology 1994; 81:346–52[Web of Science][Medline]

16 Hansdottir V, Woestenborghs R, Nordberg G. The pharmacokinetics of continuous epidural sufentanil and bupivacaine infusion after thoracotomy. Anesth Analg 1996; 83:401–6[Abstract]

17 Hansdottir V, Bake B, Nordberg G. The analgesic efficacy and adverse effects of continuous epidural sufentanil and bupivacaine infusion after thoracotomy. Anesth Analg 1996; 83:394–400[Abstract]

18 Guinard JP, Mavrocordatos P, Chiolero R, Carpenter RL. A randomized comparison of intravenous versus lumbar and thoracic epidural fentanyl for analgesia after thoracotomy. Anesthesiology 1992; 77:1108–15[Web of Science][Medline]

19 Hansdottir V, Woestenborghs R, Nordberg G. The cerebrospinal fluid and plasma pharmacokinetics of sufentanil after thoracic or lumbar epidural administration. Anesth Analg 1995; 80:724–9[Abstract]

20 Suttner S, Lang K, Piper SN, Schultz H, Rohm KD, Boldt J. Continuous intra- and postoperative thoracic epidural analgesia attenuates brain natriuretic peptide release after major abdominal surgery. Anesth Analg 2005; 101:896–903[Abstract/Free Full Text]

21 Joris JL, Jacob EA, Sessler DI, Deleuse JF, Kaba A, Lamy ML. Spinal mechanisms contribute to analgesia produced by epidural sufentanil combined with bupivacaine for postoperative analgesia. Anesth Analg 2003; 97:1446–51[Abstract/Free Full Text]

22 Brodner G, Mertes N, Van Aken H, et al. What concentration of sufentanil should be combined with ropivacaine 0.2% wt/vol for postoperative patient-controlled epidural analgesia? Anesth Analg 2000; 90:649–57[Abstract/Free Full Text]

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25 de Leon-Casasola OA and Lema MJ. Postoperative epidural opioid analgesia: what are the choices? Anesth Analg 1996; 83:867–75[Abstract]

26 Tejwani GA, Rattan AK, McDonald JS. Role of spinal opioid receptors in the antinociceptive interactions between intrathecal morphine and bupivacaine. Anesth Analg 1992; 74:726–34[Abstract/Free Full Text]

27 Kamphuis ET, Ionescu TI, Kuipers PW, de Gier J, van Venrooij GE, Boon TA. Recovery of storage and emptying functions of the urinary bladder after spinal anesthesia with lidocaine and with bupivacaine in men. Anesthesiology 1998; 88:310–6[CrossRef][Web of Science][Medline]

28 Rosseland LA, Stubhaug A, Breivik H. Detecting postoperative urinary retention with an ultrasound scanner. Acta Anaesthesiol Scand 2002; 46:279–82[CrossRef][Web of Science][Medline]

29 Lamonerie L, Marret E, Deleuze A, Lembert N, Dupont M, Bonnet F. Prevalence of postoperative bladder distension and urinary retention detected by ultrasound measurement. Br J Anaesth 2004; 92:544–6[Abstract/Free Full Text]

30 Keita H, Diouf E, Tubach F, et al. Predictive factors of early postoperative urinary retention in the postanesthesia care unit. Anesth Analg 2005; 101:592–6[Abstract/Free Full Text]


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This Article
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