Fast Track in Ambulatory Surgery-5!22!2010

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    Fast Tracking inAmbulatory Surgery

    T. J. Gan, M.D., F.R.C.A. FFARCS(I)

    Professor and Vice Chairman

    Director of Clinical Research

    Department of Anesthesiology

    Duke University Medical Center

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    Outline

    Anesthetic techniques

    Effective management of

    PONV

    Pain

    NMB

    Monitoring depth of anesthesia

    PACU fast track and discharge scoring systems

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    Freestanding ASCs in the United States

    0

    1000

    2000

    3000

    4000

    5000

    1980 1982 1984 1986 1988 1990 1992 1994 1996 1998 2000 2002 2004 2005

    The number offreestanding ASCs

    jumped to 5,068 during2005

    Source: Verispan and William Blair & Co., LLC Estimates

    RS Daniels, Outpatient Surgery;Jan 2006:108-111

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    Inhalational vs. Intravenous

    AnestheticRecovery Profile

    ** p

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    Inhalational vs. Intravenous

    AnestheticRecovery Profile

    *

    * p

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    Choice of Anesthetic Agents

    in Fast-Tracking

    51 women undergoing GYN laparoscopy

    Propofol for induction

    Randomized to

    Propofol, sevoflurane and desflurane

    BIS monitored to keep at 60 Triple antiemetic prophylaxis

    Local anesthetic infiltration

    Coloma et al. Anesth Analg 2001;93:112-5

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    Propofol vs. Sevo vs. Des

    Coloma et al. Anesth Analg 2001;93:112-5

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    TIVA (Prop/Remi) versus Desflurane

    in Children ENT Procedures

    Remifentanil

    Propofol

    Desflurane

    Nitrous

    SponVentilation

    11 4 min 7 3 min

    Eye Opening 11 4 min 14 7 min

    Aldrete Score

    9

    17 7 min 17 7 min

    Agitation 44% 80%

    Grundmann et al. Acta Anesth Scndinavica 1998;42:845-50

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  • 7/30/2019 Fast Track in Ambulatory Surgery-5!22!2010

    12/62Larsen B et al. Anesth Analg 2000;90:168-74

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    Compared propofol, Isoflurane, Sevoflurane

    and Desflurane

    Propofol vs. Isoflurane 18 studies Propofol vs. Desflurane 13 studies

    Propofol vs. Sevoflurane 11 studies

    Isoflurane vs. Sevoflurane 6 studies

    Isoflurane vs. Desflurrane 4 studies

    Sevoflurane vs. Desflurane 6 studies

    Gupta et al. Anesth Analg 2004;98:632-41

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    Systematic Analysis - Results

    Early recovery

    Faster with desflurane than propofol and isoflurane

    Faster with Sevoflurane than isoflurane

    Intermediate recovery (Home readiness)

    Sevoflurane faster than isoflurane (5 min)

    PONV, PDNV, rescue antiemetic and headache

    Propofol better than inhalational agents

    Gupta et al. Anesth Analg 2004;98:632-41

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    General Anesthesia

    vs.

    Regional Anesthesia

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    Outpatient hand surgery

    Randomized to

    GAPropofol/Isoflurane/Fentanyl

    IVRA0.5% lidocaine

    Axillary Blocklidocaine/chlorrprocaine

    Regional groups received sedation with

    propofol

    Chan et al. Anesth Analg 2001;93:1181-4

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    Chan et al. Anesth Analg 2001;93:1181-4

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    Spinal vs. GA - Outcomes

    Korhonen et al. anesth Analg 2004;99:1668-73

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    Spinal Anethesia vs.

    Desflurane GA

    Korhonen et al. anesth Analg 2004;99:1668-73

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    50 outpatients for open rotator cuff repair

    Randomized to

    Fast track GA with LA infiltration (bupivacaine0.25%)

    Interscalene block (ropivavaine 0.75%)

    Outcomes: Phase I and II recovery

    Daily activities up to 2 weeks.

    Patient satisfaction

    Hadzic A et al. Anesthesiology 2005;102:1001-7

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    Hadzic A et al. Anesthesiology 2005;102:1001-7

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    Management of PONV

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    Functional Interference

    Due to Nausea and/or Vomiting

    Emesis Nausea Functional Interference

    White et al. Anesth Analg 2008;107:452-8

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    PONV Occurring in the PACU* and/or

    Within 48 Hours After PACU Discharge

    * PACU=postanesthesia care unit.

    Carroll NV et al. Anesth Analg. 1995;80:903909.

    36%

    Nearly 65% of patients did not experience PONV symptoms until afterdischarge from the PACU.

    36%

    Initial PONV in the PACU and/orWithin 48 Hours After PACU Discharge

    (45/58)

    Initial PONV in the PACU

    (21/58)

    78%

    PatientsWhoExperiencedPONV,%

    0

    20

    40

    60

    80

    100

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    PONV Risk Scores

    Risk Factors Points

    Female 1

    History of

    PONV/motion

    sickness

    1

    Postop Opioid 1

    Non-Smoker 1

    %

    Apfel C, et al. Acta Anaesthesiol Scand1998;42:495-501.

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    Cumulative Incidence of PONV

    TDS + Ondansetron vs. Ondansetron

    P

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    Results: PONV risk reduction

    Ondansetron 26%

    Dexamethasone 26%

    Droperidol 26%

    Propofol 19%

    Nitrogen 12% (nitrous oxide exclusion)

    Remifentanil not significant

    High-Risk PONV Patients (N=4,123)

    Factorial Designed Trial:

    6 Interventions for PONV Prevention

    Apfel CC, et al. N Engl J Med. 2004;350:2441-2451.

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    *Ondansetron;

    dexamethasone;

    droperidol.Apfel CC, et al. N Engl J Med. 2004;350:2441-2451. Adapted with permission.

    Factorial Designed Trial: Ondansetron,

    Dexamethasone, and DroperidolAntiemetic Drug Combination Outcomes (N=5,161)

    Average value for eachnumber of antiemetics

    Incidence for eachantiemetic or combination

    In

    cidenceofPostoperative

    NauseaandVomiting(%)

    60

    50

    40

    30

    20

    10

    0

    No. of Antiemetics

    0 321

    *

    **

    Al ith f PONV P h l i

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    Algorithm for PONV Prophylaxis

    Evaluate risk of PONV in surgical patient and patients concerns

    Moderate High

    Consider regionalanesthesia

    Low

    No prophylaxis unless thereis medical risk of

    sequelae from vomiting Not Indicated

    If general anesthesia is used, reduce baselinerisk factors when clinically practical &

    consider using nonpharmacologic therapies

    Patients at moderate risk

    Consider antiemetic prophylaxiswith monotherapy (adults) or

    combination therapy (children & adults)

    Patients at high risk

    Initiate combination therapy with2 or 3 prophylactic agents

    from different classes

    Avoid opioids (IIIA)

    Avoid N2O (IIA)

    Avoid high dose reversal agent (IIA)

    Adequate hydration (IIIA)

    Propofol anesthetic (IA)

    Gan et al. Anesth Analg 2003;97:62-71Gan JAMA 2002;287:1233-6

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    Gan et al. A&A 2007;105:1615-28

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    Management of Pain

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    Postoperative Pain: All Patients

    (in Hospital up to 2 Weeks)

    83

    13

    47

    2118

    77

    19

    49

    23

    8

    0

    10

    20

    30

    40

    50

    60

    70

    80

    90

    100

    %

    ofpatie

    nts

    1999 1993

    Any pain Slightpain

    Moderatepain

    Severepain

    Extremepain

    1Apfelbaum, Gan et al. Anesth Analg. 2003;97:534-40; 2Warfield et al. Anesthesiology. 1993

    1

    2

    Patients worst pain

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    24% had pain score 7

    24% delayed PACU

    discharge by pain

    Maximum pain score

    predictive of total recovery

    Lower pain score (by 25%)

    if LA or NASID were used

    Pavlin et al. Anesth Analg 2002;95:627-34

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    Sustained

    currents

    Peripheral

    Nociceptive

    Fibers

    TransientActivation

    ACUTEPAIN

    Woolf. Ann Intern Med. 2004;140:441; Petersen-Felix. Swiss Med Weekly. 2002;132:273-278;

    Woolf. Nature.1983;306:686-688; Woolf et al. Nature. 1992;355:75-8.

    Surgeryor

    injury

    causesinflammation

    Long-Term Consequences of Acute Pain:

    Potential for Progression to Chronic Pain

    Sustained

    Activation

    Peripheral

    Nociceptive

    Fibers

    Sensitization

    CHRONICPAIN

    CNS

    Neuroplasticity

    Hyperactivity

    StructuralRemodeling

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    Acute Postoperative Pain Has Been Associated With

    Chronic Pain After Common Procedures

    Incidence of Chronic

    Post-Surgical Pain

    US Surgical Volumes

    (1000s)1

    Amputation 57-62%2 159

    Breast surgery 27-48%3,4 479

    Thoracotomy 52-61%5,6 Unknown

    Inguinal hernia repair 19-40%7,8 609

    Coronary artery bypass 23-39%9-11 598

    Caesarean section 12%12 220

    1. Kehlet et al. Lancet. 2006;367:1618-1625; 2. Hanley et al. J Pain. 2007;8:102-10; 3. Carpenter et al. Cancer Prac.1999;7:66-70; 4. Poleschuk et al. J Pain. 2006;7:626-634; 5. Katz et al. Clin J Pain. 1996;12:50-55; 6. Perttunen et al. Acta

    Anaesthesiol Scand. 1999;43:563-567; 7.Massaron et al. Hernia. 2007;11:517-525; 8. ODwyer et al. Br J Surg.

    2005;92:166-170; 9. Steegers et al. J Pain. 2007;8:667-673; 10. Taillefer et al. J Thorac Cardiovasc Surg. 2006;131:1274-1280; 11. Bruce et al. Pain. 2003;104:265-273; 12. Nikolajsen et al. Acta Anaesthesiol Scand. 2004;48:111-116.

    Factors correlated with thedevelopment of post-surgical chronic pain1:

    1. Nerve injury2. Inflammation

    3. Intense acute postoperative pain

    M lti d l b l d

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    Kehlet H, et al. Anesth Analg 1993;77:104856

    Playford RJ, et al. Digestion 1991;49:198203

    Multimodal or balanced

    analgesia

    doses of each analgesic

    Improved anti-

    nociception due tosynergistic/

    additive effects

    May severity of sideeffects of each drug

    Potentiation

    Opioid

    ConventionalNSAIDs/coxibs,

    paracetamol,

    nerve blocks

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    Adjunctive Analgesics

    NSAIDs and COX-2 selective inhibitors (coxibs)

    Acetaminophen

    Local anesthetics

    Ketamine

    Gabapentin / pregabalin

    Clonidine / dexmedetomidine

    Steroids

    Non pharmacological techniques

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    52 RPCTs (~5000 patients)

    Acetaminophen, NSAIDs or COX-2 inhibitors

    Average morphine consumption49 mg/24hrs

    15-55 % decrease in morphine consumption

    VAS pain decreased by 1 cm

    NSAIDs / COX-2 Specific inhibitors

    nausea from 28.8% to 22%

    Sedation 15.4% to 12.7%

    Renal failure 0% to 1.7%

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    Morphine Consumption 24 hours

    Elia et al. Anesthesiology 2005;103:1296-1304

    R i l A th i i

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    Regional Anesthesia in

    Ambulatory Surgery 1800 patients receiving upper or lower extremity block with

    0.5% ropivacaine

    Interscelene, supraclavicular, axillary, lumbar plexus, emoral and

    sciatic block

    Discharged on the day of surgery

    Conversion to GA 1-6%

    No opioid in PACU89% to 92%

    Require opioid up to 7 days21% to 27%

    Persistent parasthesia 0.25%, resolved within 3 months

    Klein et al. Anesth Analg 2002;94:65

    70

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    Hadzic et al. Anesthesiology 2004;101:127-32

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    Ambulatory Infusion Pump

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    Management ofNeuromuscular

    Blockade

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    Reversal of Rocuronium 0.45 mg/kg

    Bevan JC et al. Anesth Analg 1999;89:333

    339

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    Cisatracurium vs. Rocuronium

    Cisatracurium Rocuronium

    TOF 0.9 atEOS

    27% 7%

    TOF atreversal

    63 7% 40 19%

    EOS to

    TOF = 0.9

    10 9 min 18 13 min

    Cammu et al. Eu J Anaesth 2002;19:129-34

    R id l P l i

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    Residual Paralysis

    Debaene et al. Anesthesiology 2003;98:1042-8

    Time between the administration of a single dose of

    NMB and the arrival in the PACU.

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    Sugammadex

    Angewandte Chemie 2002:41:266 -270

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    First Human Exposure to

    ORG25969

    Gijsenbergh et al.

    29 healthy men

    Anesthesia: propofol target-controlled infusion andremifentanil

    Rocuronium 0.6mg/kg

    Placebo or sugammadex ranging from 0.1 to 8.0

    mg/kg

    Gijsenbergh, Francois Anesthesiology. 103(4):695-703, 2005.

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    Phase 1

    Gijsenbergh, Francois Anesthesiology. 103(4):695-703, 2005.

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    Depth of Anesthesia Monitoring

    CLINICAL UTILITY TRIAL

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    Emergence Times

    109

    66

    0

    3

    6

    9

    12

    OPEN EYES RESPOND TO

    COMMAND

    Standard

    PracticeBIS

    * p < 0.001

    CLINICAL UTILITY TRIAL:

    EMERGENCE TIMES

    Gan TJ, et al. Anesthesiology, Oct. 1997.

    CLINICAL UTILITY TRIAL

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    CLINICAL UTILITY TRIAL:

    PACU DISCHARGE TIME

    Eligible for Discharge from PACU

    37

    31

    20

    25

    30

    35

    40

    Minutes

    Standard Practic

    BIS

    BIS

    Patients16%Faster

    thanStandardPractice

    Gan TJ, et al. Anesthesiology, Oct. 1997.

    CLINICAL UTILITY TRIAL

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    Total Propofol Used Per Case

    1252

    964

    0

    250

    500

    750

    1000

    1250

    1500

    StandardPractice

    BIS

    23% Less Propofol Used

    CLINICAL UTILITY TRIAL:

    DRUG USAGE

    Gan TJ, et al. Anesthesiology, Oct. 1997.

    * p

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    2.1

    1.7

    1 2 3

    Average

    Score

    StandardPractice

    BIS

    ExcellentOriented on Arrival

    Good

    Fast Recovery

    Fair

    Slow Recovery

    * p < 0.001

    CLINICAL UTILITY TRIAL:

    BLINDED PACU ASSESSMENTS

    Gan TJ, et al. Anesthesiology, Oct. 1997.

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    PACU Discharge Criteria

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    PACU

    Discharge

    Max 10

    Score 9

    Aldrete JA. J Clin Anesth 1995;7:89-91

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    PADS

    Max 10

    Score 9

    Fit for

    discharge

    Chung et al. J Clin Anesth 1995;80:896-902

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    Eligible for fast-

    track

    Score of 12

    No score < 1 in

    any category

    White et al. Anesth Analg 1999;88:1069-72

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    Factors Delaying Discharge

    Preoperative

    Female

    Increasing ageCHF

    Intraoperative

    Long duration of surgeryGA

    Spinal anesthesia

    Postoperative

    Pain

    PONB

    Drowsiness

    No escort

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    Factors delaying discharge

    Mandatory oral fluid intake Mandatory voiding

    Risk factors for postop urinary retention

    Type of surgery (anorectal, hernia,vaginal/pelvic gynecological surgery)

    Old age

    Male sexSpinal/epidural

    Duration of surgery > 60 min

    Intraoperative fluid > 750 mL

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    Summary

    Use short acting drugs

    IV or inhalational anesthetic are recommended

    Regional anesthesia can have postdischarge

    advantages

    Optimal antiemetic prophylaxis

    Comprehensive perioperative analgesic regimen

    Beware of residual paralysis

    Aggressively adopt bypass and discharge criteria

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    Questions