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7/30/2019 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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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