Choice of Anesthesia for Outpatient Knee Arthroscopy

 

William F. Urmey, M.D.
Assistant Professor of Clinical Anesthesiology
Hospital for Special Surgery
Weil Medical College of Cornell University
New York, NY, USA 

 

 

Introduction 

          Regional anesthesia offers many advantages over general anesthesia for the outpatient, as listed in Table 1.

 

Table 1:        Advantages of Regional Anesthesia Compared to General Anesthesia
     

          Early discharge for outpatients

          Smooth transition to pain control

          Increased blood flow to extremity (ies)

          Theoretical decrease in reflex sympathetic dystrophy

          Decreased nausea/vomiting

          Decreased drowsiness

          Decreased urinary retention

          Avoids endotracheal intubation

          Lower admission rates
                                                                  

Regional anesthetics promote a smooth transition to postoperative analgesia by regional, parenteral, or oral administration of analgesics.  Some regional anesthetic techniques, e.g. femoral nerve blocks, can provide long lasting postoperative analgesia while allowing the patient to return home with adequate function.

Although many of the advantages of regional anesthesia for outpatient knee arthroscopy are obvious, there has been an inadequate number of prospective, controlled studies published to date.  This is in part due to the fact that the outpatient is a relatively new concept.  With the rapid expansion of outpatient surgery and ambulatory centers, we are just beginning to generate the necessary clinical and academic experience to begin defining the relevant issues for study.

          The goals of outpatient anesthesia for knee arthroscopy are listed below (Table 2).

 

Table 2:        Goals of Outpatient Anesthesia                                            

          Excellent surgical anesthesia

          Smooth transition to PACU/pain control

          Minimal side effects (sedation, nausea, vomiting, urinary retention, delirium, airway problem)

          Very low admission rate

          Very low complication rate

          Quick onset and offset of anesthesia                                                        

 

          Regional anesthesia has been shown to be extremely safe in several recent large-scale outcome studies.1-4  The  etiologies of most of the small number of complications that occurred in these studies are now understood.  Therefore regional anesthesia is the safest alternative for knee arthroscopy.  Auroy, et al.2 studied 103,730 regional anesthetics.  Only 34 serious neurological deficits occurred in this extremely large study group.  However, if examined more closely, 21/34 (62%) of the complications were associated with pain or paresthesia upon injection.  Of the remaining 13 complications, 12 were from spinal anesthetics.  Of these 12, 9 were associated with 5% intrathecal lidocaine.  In closed claim study by Aromaa, et al.1 only 7 claims for long-lasting neurological deficits resulted from 550,000 spinal and 170,000 epidural anesthetics.

          The choice of anesthetic for the outpatient is very important.  This was accented in a recent prospective, multivariate outcome study by Pavlin, et al.5  These investigators found that "the anesthetic technique was the most important determinant of discharge time (p = 0.001)".  The major reasons for prolongation of recovery times are listed in Table 3.  Pain was the most common reason for prolonged recovery in this study.

 

Table 3.  Reasons for Duration of Recovery ³50 Minutes in Phase 1 and ³70 Minutes in Phase 2 (From Pavlin et al.  Anesth Analg 1998;87:816-26.)

          Phase 1 Recovery     Phase 2 Recovery

          (Post anesthesia care unit)  (Dedicated outpatient recovery unit)

Reasons

Primary
reasons

Contributing
reasons

Primary
reasons

Contributing reasons

Pain

          16

23

          14

          19

Drowsy

          14

23

          10

          15

Nausea/vomiting

          4

11

          10

          15

Block unresolved

          6

6

          7

          9

Inadequate ventilation

          5

7

          1

          2

Cardiovascular problems

          4

2

          2

          4

Shivering

          2

4

          0

          0

Other

          1

2

          7

          11

Unable to void

          N/A

N/A

          8

          12

System factors

          9

12

          24

          41

Surgical factors

          0.3

0.3

          2

          36

Unspecified

          41

41

          10

          10

 

 

 

 

 

NA = not applicable

aFrequency of primary reasons is expressed as a percentage of all causes cited as the primary reason for discharge delay.  The total is 100%.  Of the patients, 408 went to Phase 1 and 293 (72%) were delayed in Phase 1 (excluding patients who bypassed Phase 1); 617 patients went to Phase 2, and 388 (63%) were delayed in Phase 2.

bFrequency of contributing reasons is expressed as the percentage of all delayed patients in whom a given reason was cited as one of the causes contributing to delay.  The total is >100% becasue the causes are not mutally exclusive, i.e. there may be more than one cause for delay.  Patients who were not delayed ³50 min in Phase 1 or ³70 min in Phase 2 were not included in the denominator for this analysis.

Phase 1 is the postanesthesia care unit.

Phase 2 is the dedicated outpatient recovery unit.

 

          Pain in the ambulatory knee arthroscopy patient poses a challenge to the anesthesiologist, especially with more complex arthroscopic procedures (e.g. anterior cruciate ligament reconstruction).  Effective methods must be used to control pain in these patients.  However, this must be done without untoward side effects which may lead to unplanned admissions.

          Pain in the day surgery patient increased nausea and vomiting, delayed discharge, increased contact with the medical facility, and increased unanticipated admissions according to a study by Tong and Chung.6  Orthopedic patients had the highest incidence of severe pain of all outpatients in a study by Chung et al.7

          Multimodal analgesia including non-steroidal anti-inflammatory agents, cryotherapy, local anesthetic infusions, intraarticular analgesia, and femoral nerve block can be very effective in eliminating or all but eliminating pain following arthroscopic knee surgery.

          Various methods of achieving anesthesia and analgesia for knee arthroscopic surgery will be presented and discussed below.  Central neuraxial techniques, femoral/sciatic nerve blocks, intraarticular/incisional injections, as well as combinations of these techniques will be presented with attention to postoperative analgesia as well as to intraoperative anesthesia.

         

Central Neuraxial Anesthesia

 

Spinal Anesthesia

          Spinal anesthesia is an excellent alternative for knee arthroscopic procedures of a predictable duration.  A single shot spinal anesthetic with a 27 gauge pencil-point needle is relatively atraumatic.  Spinal anesthesia is characterized by rapid onset, reliable duration and offset, both desirable for the outpatient.  Newer needle designs have eliminated any real concerns with regard to post dural puncture headache (PDPH), which has limited the use of spinal anesthesia in the past.  A 25-gauge Whitacre needle is associated with a PDPH rate of about 1%8  in young patients.  A 27 pencil-point needle is presumably associated with an even lower PDPH incidence.  Distribution of intrathecal plain local anesthetic in the subarachnoid space is ideal for knee arthroscopy as well as most lower extremity orthopedic procedures.  Isobaric local anesthetics diminish the hemodynamic changes associated with spinal anesthesia9 when compared to hyperbaric preparations.  The use of plain (isobaric) local anesthetics virtually eliminates high spinal anesthesia.

 

Choice of Local Anesthetic for Outpatient Spinal Anesthesia

          Lidocaine has the longest track record of safe use for outpatient spinal anesthesia.  Lidocaine has rapid onset of action, intermediate duration , and low toxicity in clinically recommended doses.  In a dose-response study, Urmey, et al.10 found that 40 to 60 mg lidocaine resulted in duration of motor block of 1 1/2 to 2 hours, making it an excellent choice for knee arthroscopy.

          In recent years, intrathecal lidocaine has been the focus of some controversy.  For the most part, hyperbaric (especially 5% concentration) preparations have been associated with possible neurotoxicity.  Concerns regarding intrathecal lidocaine neurotoxicity surfaced following its use during microcatheter continuous spinal anesthesia in the  late 1980's.  Many reports linked lidocaine and microcatheter use to cauda equina syndrome.11-13  This resulted in the withdrawal of microcatheters by the United States FDA in 1992.  Factors associated with cauda equina syndrome 12,13 included 1) hyperbaric solutions of lidocaine 2) microcatheter use 3) re-dosing through the microcatheter 4) poor onset, deficient blocks, and 5) high total lidocaine dosage (up to 300 mg!).

          Most recently, reports of transient radicular irritation (TRI) following intrathecal or epidural lidocaine use were published.14,15  In response to these reports, editorials were published whose authors questioned the continued use of intrathecal lidocaine16,17.  However, more recently, intrathecal mepivacaine in hyperbaric18 and isobaric19 preparations was found to be associated with similar (up to 30%) incidences of TRI.  Pollock, et al.20and Hampl, et al.21 have found similar incidences of TRI with 2% lidocaine as with 5% lidocaine.  Nevertheless, the author advocates the use of the lower effective concentrations of lidocaine.  Studies have shown that 1.5% or 2% hyperbaric lidocaine resulted in no difference or faster recovery postoperatively19-21. when compared to 5% hyperbaric drug.

          Recent data from Hampl, et al.22 showed that 2% prilocaine was associated with a 4% incidence of TRI compared to the 29% associated with 2% lidocaine.

          Whereas, it is important to look for improved alternative drugs and solutions, we must keep in mind the unique large clinical experience and unparalleled safety record of lidocaine.  All local anesthetics have rare associated neurotoxicity.  For example, bupivacaine was recently associated with cauda equina syndrome in an isolated case report.23

          Bupivacaine has been associated with much smaller rates of TRI than lidocaine in several studies20-22,24.  With this chemical structure in mind, there has been renewed interest in mepivacaine as an alternative to intrathecal lidocaine18,19,24-26.  Mepivacaine is an amide local anesthetic of intermediate duration with a chemical structure similar to that of bupivacaine.

          Mepivacaine has been safely used for spinal anesthesia for close to 40 years, since the first report on its intrathecal use in 196127.  The first publication of mepivacaine's use in a large scale study, reported good outcomes with no neurological complications following 20,000 mepivacaine spinal anesthetics28.

          In 1966, Lipton et al.29 compared hyperbaric mepivacaine 4% to tetracaine 1% in a double-blind study of vaginal deliveries.  They concluded that "the evidence...points to the superiority of mepivacaine as a more rapidly acting as well as a more profound spinal anesthetic agent."

          Henschel, et al.30 reported on a dose-response study of intrathecal plain mepivacaine in 159 patients with and without added epinephrine.  They found that "anesthetic duration increased with dosage and varied from 1 to over 3 hours, averaging over 3 hours with the addition of  epinephrine".

          Based on this study, Urmey began using plain mepivacaine 1.5% or 2% five years ago and reported on its use for intermediate-duration orthopedic procedures in 199725.  Use of isobaric mepivacaine was supported by a 1994 publication that demonstrated its favorable intrathecal distribution in a spine model31.

          Spinal mepivacaine has been more popular in Europe, where it has been marketed for years as a 4% hyperbaric preparation.

 

Association of Mepivacaine with TRI

          Intrathecal mepivacaine has been associated with TRI by case report 32 and prospective studies.18,19,24  In a study of 4% hyperbaric mepivacaine, Hiller and Rosenberg found a 30% incidence of TRI compared to 3% for bupivacaine.  The mepivacaine-associated TRI lasted up to 60 hours after anesthesia.

          Salmela and Aromaa found a similar incidence of TRI, 36.7%, with 4% mepivacaine in a study comparing it to lidocaine and bupivacaine.  Mepivacaine was found to have the highest incidence of TRI  (36.7%) compared to 23.3% for lidocaine and 0% for bupivacaine.  This was reported at the September, 1997 ESRA Annual Meeting.

          At this same meeting, Salazar, et al. reported on the incidence of TRI associated with isobaric 2% mepivacaine compared to 2% isobaric lidocaine in 80 patients.  These investigators also found the highest incidence of TRI, 7.5%,  with mepivacaine compared to 2.5% with lidocaine.  They concluded that the "election of 2% isobaric mepivacaine as an alternative to 2% isobaric lidocaine for short term surgery should be questioned.  In our study, the incidence of TRI was greater in patients receiving 2% isobaric mepivacaine".  They also found that duration of sensory and motor blockade was significantly longer with mepivacaine.  Following this, Liguori, et al.26 reported on a comparison of 60 mg 2% lidocaine to 45 mg 1.5% mepivacaine in 60 patients.  In this study, the incidence of TRI was 22% with lidocaine, but TRI was not reported with mepivacaine.

          Although mepivacaine has a place in spinal anesthesia for intermediate duration procedures, it is apparently not the answer to eliminating TRI.  It has been associated with higher incidences of TRI than lidocaine in 2 prospective studies and a lower incidence in one study.  With similar dosage and technique, mepivacaine's duration can be expected to be approximately 30-50% longer than that of lidocaine, but significantly shorter than equipotent doses of bupivacaine.  The discrepancy in incidences of TRI in various investigations may have to do with the qualitative nature of the phenomenon of TRI, patient positioning,  or possibly the milligram dosage used.  For example a recent report of 1,045 patients who received 3% hyperbaric lidocaine 30-45 mg showed a TRI incidence of only 0.4%.33

 

Lumbar Epidural Anesthesia

          Lumbar epidural anesthesia has been found to have favorable properties for day surgery.  In an excellent study of outpatient epidural anesthesia, Kopacz and Mulroy found that epidural anesthesia with chloroprocaine or lidocaine was associated with very favorable discharge times34.  In a study of epidural anesthesia for outpatient knee arthroscopy, Parness, et al35 found significant reductions in time to discharge, incidence of nausea and vomiting, and postoperative pain requiring treatment  compared to general anesthesia.

          Improvements in spinal needles and the development of matched needle sets for CSE anesthesia have changed how we perform outpatient regional anesthesia.  The result has been that spinal and CSE techniques are supplanting epidural anesthesia for outpatient orthopedic procedures.  There are a few reasons for this trend.  First, rapid onset of anesthesia is important in the day surgical patient.  Compared to epidural anesthesia, intrathecal local anesthetic injection has been found to have a significantly quicker onset of sensory and motor anesthesia both with spinal36 and CSE37,38 techniques for orthopedic surgery.  Second, the shortest duration local anesthetic for epidural use, chloroprocaine, has been associated with a syndrome of severe back pain.  Third, injection of a large dose of epidural local anesthetic is necessary to perform knee surgery (up to 30 mL of 2% lidocaine).  Urmey, et al. have recently found that 5 of 15 patients felt the incision after 20 mL epidural 2% lidocaine injected through the needle at L3-4 compared to 0 of 20 patients who received CSE anesthesia with an initial dose of 40 mg 2% lidocaine.  Finally, most practitioners use local anesthetics with added epinephrine for epidural anesthesia 34,39.  Whereas the author favors this practice, this results in much longer block offset times compared to intrathecal plain local anesthetics, making epidural anesthesia less than ideal for the outpatient.

 

 

Combined Spinal Epidural Anesthesia

          Single injection spinal anesthesia lacks the flexibility of a continuous technique.  To compensate for this shortcoming, anesthesiologists commonly overdose the patient to ensure adequate duration of surgical anesthesia.  In a study of dose response characteristics of lidocaine CSE anesthesia, Urmey et al.10 clearly demonstrated a dose-dependent increase in duration.  The CSE technique allowed this study to be completed ethically, by providing the "safety net" of an epidural catheter.  This allowed prolongation of surgical anesthesia in the small percentage of cases in which the surgery outlasted the duration of the initial intrathecal dose of lidocaine.  By reducing the initial intrathecal lidocaine dose to 40 mg, all measured ambulatory discharge milestones were considerably shortened.

          In a study that compared epidural anesthesia with 20 mL plain lidocaine to CSE with a 40 mg initial intrathecal dose, CSE was associated with a faster onset and a better  quality block.38  However, discharge characteristics were similar for both patient groups.

 

Combined Spinal Epidural as an Alternative to Chloroprocaine Epidural Anesthesia

          2-Chloroprocaine is a short-acting ester local anesthetic.  Chloroprocaine is characterized by properties that make it a useful drug for epidural anesthesia in the outpatient.  These properties include 1) rapid onset 2) short duration 3) low toxicity, and 4) rapid hydrolysis by plasma pseudocholinesterase.  Chloroprocaine has been a popular choice for outpatient epidural anesthesia based on these properties.

          However, the clinical use of chloroprocaine for regional anesthesia has not been devoid of complications or serious side effects.  Problems associated with the drug have included neurological deficits resulting from accidental or unrecognized intrathecal injection of 2-chloroprocaine.40-43  This was first reported in 1980.

          More recently, a syndrome of severe back pain has been associated with the use of epidural chloroprocaine.  This was first reported by Fibuch and Opper in 1988.44  Subsequent studies have shown that chloroprocaine associated back pain was due to the additive, ethylenediamine-tetracetic acid (EDTA), which was used as a preservative to prolong the drug's shelf life.

          The commercial preparation has undergone a rapid evolution.  Presently, plain chloroprocaine is marketed.  Hopefully, use of the plain drug will eliminate these clinical complications.

          Kopacz and Mulroy compared the use of epidural chloroprocaine with lidocaine and mepivacaine for ambulatory surgery.34  These authors found that epidural chloroprocaine was characterized by a significantly shorter duration than lidocaine or mepivacaine.  Subsequently, in a dose response study of CSE using lidocaine 2% plain, Urmey et al. evaluated three initial intrathecal doses of lidocaine, 40 mg, 60 mg, and 80 mg.10  In this study of 90 patients having ambulatory knee arthroscopy, the lowest dose of 40 mg lidocaine was found to have much shorter duration of sensory and motor blockade.  This duration was very similar to that reported by Kopacz and Mulroy for epidural chloroprocaine.  CSE with smaller dose lidocaine is an excellent alternative continuous regional anesthetic technique.  Onset and offset of anesthesia compares very favorably to epidural chloroprocaine.

          Compared to epidural anesthesia with 20 mL 2% lidocaine plain, Urmey et al.38 found that CSE with a 40 mg initial intrathecal dose was quicker to perform (97 vs 156 sec), had a more rapid onset (6 vs 14 min) and similar duration.  In addition, the plain lidocaine epidural group, close to 40% of patients could feel the surgical incision, necessitating epidural reinforcement or delay of surgery.  By contrast, none of the CSE patients were aware of the surgical incision.

 

Femoral Nerve Block

         

          This technically easy and highly effective regional anesthetic technique can be used for surgical anesthesia for anterior lower extremity procedures or in combination with sciatic nerve block or intraarticular local anesthesia.  Local anesthetic blockade of the femoral nerve is an excellent technique for anesthesia of the knee.45-49  However, in a recent study, Casati and Fanelli found that femoral-sciatic nerve block offered no advantage in terms of time to discharge when compared to hyperbaric bupivacaine spinal anesthesia for knee arthroscopy in the outpatient.50

          Continuous techniques for blocking the femoral nerve are increasingly popular.51 An extra or intracatheter may be used to provide analgesia over a 2-3 day period.  Similarly, Singelyn, et al. have reported a technique for continuous three-in-one blockade of the femoral, obturator, and lateral femoral cutaneous nerves by use of a modified Seldinger technique.52  Use of these techniques have been largely limited to inpatients thus far.

          The femoral nerve or 3-in-1 block can be used for surgical anesthesia with agents such as 2% lidocaine or 1.5%-2% mepivacaine in volumes of 25-30 mL.  However, most surgical procedures about the knee require that it be combined with sciatic nerve block  or intraarticular anesthesia to ensure anesthesia of the posterior lower extremity.  However, knee or quadriceps analgesia may be effectively achieved when femoral nerve block is combined with small amounts of parenteral analgesics.  25-30 mL 0.25% bupivacaine or ropivacaine with added epinephrine results in effective analgesia following knee surgery which may last greater than 24 hours.  A recent study showed that ropivacaine 0.5% had faster onset and better anesthesia characteristics than 0.25% bupivacaine (private communication with V. Tagariello).

          Edkin, et al. studied long acting femoral nerve block and found that 92% of patients who underwent ACL reconstruction required no additional analgesia.53  They found that bupivacaine 0.5% with epinephrine resulted in a mean duration of analgesia of 29 hours.  Femoral nerve block reduced parental analgesic use by 80% in recovery room and 40% overall54 in another study.  Similar findings have been reported by Tierney, et al.55

          Femoral nerve block is simple and a safe, effective means for providing postoperative analgesia and surgical anesthesia for selected procedures.  It is overlooked and is greatly underutilized.  It can be a major component of a balanced regimen for knee arthroscopic surgery when combined with anti-inflammatory, opioid, axial, intraarticular and cryotherapeutic techniques.

 

Postoperative Analgesia in the Knee Arthroscopy Patient

 

          Long-acting femoral nerve block provides excellent analgesia after knee surgery.  It is impractical, however, for the patient having routine less complex arthroscopic knee surgery (e.g. meniscectomy, debridement), due to the prolonged quadriceps paralysis and need for a brace.  Other analgesic modalities, used in conjunction with one another results in synergism and can be very effective in treating pain and allow for rapid, comfortable discharge.

          Whitelaw, et al.56 reported on the use of cryotherapy in the knee arthroscopy patient.  Barber, et al.57 found that cryotherapy lowered VAS scores, reduced oral analgesic use, and improved physical therapy milestones in the patient following arthroscopic surgery.

          Intraarticular analgesia with opiates and local anesthetics have also been studied extensively in the knee arthroscopy patient.  In a randomized, prospective, double-blinded study of patients following arthroscopic knee surgery, Heard et al.58 concluded that "Our results indicate that intraarticular injection of bupivacaine after arthroscopic knee surgery provides prolonged analgesia but that there is no significant prolonged analgesia provided by intraarticular morphine".  Similarly, Laurent et al. 59 and Wrench et al.60 have found that intraarticular opiates were ineffective.  Reuben et al.61 reported that "Patients receiving a multimodal analgesic regimen of perioperative nonsteroidal anti-inflammatory drugs, intraarticular bupivacaine, and external cooling did not receive any additional analgesia from intraarticular morphine".

          In a study of knee arthroscopic surgery patients, Tetzlaff, et al.62 compared four groups with different intraarticular injections:

          Group 1: 0.25% bupivacaine/epinephrine

          Group 2: 1 mg morphine/saline/epinephrine

          Group 3: 025% bupivacaine/2 mg MSO4/epinephrine

          Group 4: 0.25% bupivacaine/3 mg MSO4/epinephrine

They concluded that, "bupivacaine/morphine/epinephrine provided pain control and decreased opioid use int the PACU.  Increasing morphine dose did not improve clinical results."

          Finally intrathecal clonidine has been found to improve analgesia and decrease analgesic use.63,64

          It appears that cryotherapy, nonsteroidal anti-inflammatory drugs, and intraarticular local anesthetics possibly with clonidine, but not intraarticular opioids all have a place in the postoperative analgesic care of the patient following knee arthroscopic surgery.

 

Conclusion

 

          Regional anesthesia can work well for outpatient surgical procedures.  In a previous study published in 199365, Urmey, et al. showed that regional anesthesia could be used in 97.3% of patients (n = 907) with excellent outcome.  Recovery times and complications were comparable to previous reports of ambulatory anesthesia.  Extremely low rates of vomiting and urinary retention were found.  However, regional anesthesia is a technical specialty and careful, exact technique must be practiced in treating the outpatient.

 

 

References

 

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25.     Urmey WF:  Mepivacaine spinal anesthesia for lower extremity orthopedic surgery: an alternative to lidocaine or bupivacaine (abstract).  Reg Anesth 1997; 22:69

 

26.     Liguori GL, Zayas VM, Chisolm MF:  Transient Neurologic Symptoms after Spinal Anesthesia with Mepivacaine and Lidocaine.  Anesthesiology 1998; 88:619-23

 

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28.     El-Shirbing AM, Rasheed MH, Elmaghraby A, Motahew M:  Experiences with carbocaine in spinal anaesthesia.  Report of 20,000 cases.  Acta Anaesthesiol Scand 1966; 10:442-8

 

29.     Lipton E, Sennott FW, Batt B:  Mepivacaine for spinal anesthesia in vaginal delivery.  An objective comparison with tetracaine.  American Journal of Obstetrics and Gynecology 1966; 96:333-6

 

30.     Henschel EO, Remus CJ, Mustafa K, Jacoby JJ:  Isobaric mepivacaine in spinal anesthesia.  Anesth Analg 1967; 46:475-479

 

31.     Lambert DH, Lambert LA:  For spinal anesthesia, does specific gravity tell us anything about baricity (abstract).  Anesth Analg 1994; 78:S233

 

32.     Lynch J, zur Nieden M, Kasper S, Radbruch L:  Transient radicular irritation after spinal anesthesia with hyperbaric 4% mepivacaine.  Anesth Analg 1997; 85:872-3

 

33.     Morisaki H, Masuda J, Kaneko S, Ochiai R, Takeda J:  Transient neurologic sequelae in 1,045 patients undergoing spinal anesthesia with 3% hyperbaric lidocaine (abstract).  Anesthesiology 1997; 87:A781

 

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35.     Parnass SM, McCarthy RJ, Bach BR Jr, Corey ER, Hasson S, Werling MA, Ivankovich AD:  Beneficial impact of epidural anesthesia on recovery after outpatient arthroscopy.  Arthroscopy 1993; 9:91-5

 

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59.     Laurent SC, Nolan JP, Pozo JL, Jones CJ:  Addition of morphine to intra-articular bupivacaine doen not improve analgesia after day-case arthroscopy.  Br J Anaesth 1994; 72:170-3

 

60.     Wrench IJ, Taylor P, Hobbs GJ:  Lack of efficacy of intra-articular opioids for analgesia after day-case arthroscopy.  Anaesthesia 1996; 51:920-2

 

61.     Reuben SS, Steinberg RB, Cohen MA, Kilaru PA, Gibson CS:  Intraarticular morphine in the multimodal analgesic management of postoperative pain after amulatory anterior cruciate ligament repair.  Anesth Analg 1998; 86:374-8

 

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