Professional Documents
Culture Documents
Office-based anesthesia
Authors: Fred E Shapiro, DO, FASA, Brian M Osman, MD
Section Editor: Girish P Joshi, MB, BS, MD, FFARCSI
Deputy Editor: Nancy A Nussmeier, MD, FAHA
All topics are updated as new evidence becomes available and our peer review process is complete.
Literature review current through: Dec 2022. | This topic last updated: Apr 09, 2021.
INTRODUCTION
This topic will review potential advantages and concerns, patient and procedure selection,
and anesthetic and postoperative management of patients undergoing procedures in office-
based settings.
While only urgent and emergency surgical and other interventional procedures were
performed initially during the novel coronavirus disease 2019 (COVID-19) pandemic, elective
procedures, including office-based procedures, have been resumed in many institutions.
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Strategies to minimize infection risks during anesthesia and surgery vary according to local
resources and institutional protocols. Details regarding preoperative planning and
intraoperative management during the COVID-19 pandemic are available in a separate topic
[2-4]. (See "COVID-19: Perioperative risk assessment and anesthetic considerations, including
airway management and infection control".)
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SAFETY CONCERNS
Safety concerns have centered around the adequacy of individual facility resources and
governmental regulations for office-based facilities.
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Since the types of procedures and patient populations eligible for an office-based setting are
increasing in number and complexity, additional regulations have been implemented by
accreditation and state regulatory agencies, although uniformity and evidence-based
standards of care are lacking [10]. For example, the New York Department of Health has
mandated that office-based surgery practices must provide continuous monitoring of end-
tidal carbon dioxide using capnography during moderate or deep sedation, as well as during
general anesthesia, consistent with the 2018 American Society of Anesthesiologists (ASA)
practice guidelines for moderate procedural sedation and analgesia [13,14]. However, not all
states have this mandate.
Other differences in state regulations exist. For example, although patients may develop MH
after exposure to a triggering anesthetic agent (see "Malignant hyperthermia: Diagnosis and
management of acute crisis"), guidelines presented in 2017 by the Society for Ambulatory
Anesthesia (SAMBA) recognize that this is unlikely in office-based facilities that perform
procedures exclusively with oral or intravenous sedatives/analgesics ("class B" facility) [15].
Such facilities typically do not stock dantrolene, the antidote for MH, because no known
triggers (eg, volatile inhalation anesthetic agents) are used in the facility. Since SCh is
considered a trigger for MH, many such facilities do not stock SCh. However, SAMBA's
position statement notes that the risk of losing a patient's airway and needing appropriate
drugs such as SCh to manage this emergency exceeds the risk of an MH event [15]. Thus,
some accreditation and state regulatory agencies now allow facilities to stock SCh to manage
emergency airway rescue without requiring they also stock dantrolene to manage MH.
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Similar professional society guidelines emphasizing core patient safety principles for office-
based surgical procedures have been endorsed by the American College of Surgeons (ACS)
[18], the World Federation of Societies of Anaesthesiologists (WFSA) [19], and some state
medical societies [20].
Use of checklists
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their implementation (eg, no incentive to use a checklist, no mandate from a local or federal
regulatory agency, too time-consuming, lack of training).
Details regarding management of specific crisis situations can be found in separate topics:
PATIENT SELECTION
Use of a detailed screening questionnaire completed by the patient may help to ensure a
thorough risk assessment [30]. Subsequently, review of the patient's medical records
includes evaluation for medical conditions that may confer unacceptable risk in an office-
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based setting [10,31]. Since nearly all office-based procedures are elective, the
anesthesiologist has time to consider whether medical management of certain conditions is
optimal (eg, asthma, anemia) before surgery. All appropriate testing should be completed
and available before or on the day of the scheduled procedure. (See "Preoperative evaluation
for anesthesia for noncardiac surgery" and "Preoperative medical evaluation of the healthy
adult patient".)
The demand for office-based procedures for patients with challenging comorbidities may
exceed the qualifications of some office-based surgical teams, particularly if there would be
limited availability of additional personnel for management of an emergency. Thus, higher-
risk patients or procedures should ideally be performed in facilities that are formally
accredited (eg, by the American Association for Accreditation of Ambulatory Surgical Facilities
or the Accreditation Association For Ambulatory Health Care), and should be performed by
board-certified surgeons who are credentialed for the same procedures at a local hospital
[1,32-36]. (See 'Government regulations' above.)
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and detailed discussions for each abnormality or disease can be found in various UpToDate
topics.
Other reasons for rescheduling procedures — Other factors that may prompt rescheduling
of an otherwise suitable patient on the day of surgery include active infection, acute
exacerbation of a comorbid condition, failure to abstain from ingestion of food or clear
liquids for an appropriate amount of time ( table 5) (see "Preoperative fasting in adults"),
suspicion of acute substance intoxication, or absence of a planned escort for transport after
discharge.
PROCEDURE SELECTION
The planned procedure is a factor in determining whether a patient can safely undergo
surgery in an office-based setting [1,10,11,40]. Examples of procedures that are often
performed in this setting include selected liposuction procedures; aesthetic facial and breast
surgery; ophthalmologic procedures; oral, maxillofacial, otolaryngology, and complex dental
procedures; gastrointestinal endoscopy; gynecologic procedures; orthopedic and podiatry
procedures; and endovascular or other vascular procedures [1,11]. (See 'Anesthetic
considerations and outcomes for selected procedures' below.)
The surgeon/proceduralist and the anesthesiologist are jointly responsible for determining
whether the following conditions are met [1]:
● The procedure is within the surgeon's scope of practice and the facility's capabilities.
● The duration and degree of complexity of the procedure allow for recovery and
discharge from the facility on the same day [16]. For example, the American Society of
Plastic Surgery has recommended that office-based procedures be limited to six hours,
and be completed by 3:00 PM, as long as the office remains fully staffed until a later
hour to meet patient recovery needs [41]. As newer surgical and anesthetic techniques
have been developed, longer and more complicated procedures have been performed
in office-based settings. However, duration has been correlated with a higher incidence
of unplanned hospital admission as well as increased incidence of postoperative nausea
and vomiting (PONV), pain, and bleeding [42,43]. In a retrospective study of more than
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1.4 million ambulatory surgery patients in Massachusetts and New York states,
procedural categories with a higher likelihood of unplanned hospital admission
included vascular, mediastinal, pulmonary, urinary, nervous system, gastrointestinal,
endocrine, lymphatic, and musculoskeletal surgery [37].
Surgical procedures that are not appropriate for the office setting include those associated
with major fluid shifts or blood loss that may require transfusion, and those expected to
result in moderate to severe postoperative pain, particularly if postoperative opioid
administration may be necessary. (See 'Recovery and discharge' below and 'Local or regional
anesthetic techniques' below.)
ANESTHETIC MANAGEMENT
As with any ambulatory setting, the anesthetic goals for a patient having office-based
surgery are safety and rapid recovery from the effects of anesthetic agents, minimal side
effects, and rapid discharge from the office facility [10].
Although minimal, moderate, or deep sedation (with or without local anesthesia) are
common techniques, general anesthesia occurs along a continuum ( table 7) [10]. Thus,
the anesthesiologist must be able to "rescue" the patient from an anesthetic level that
becomes deeper than originally intended to avoid hypoxia or aspiration [48,49]. (See
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Although not specific for office-based anesthesia, a closed claims analysis of monitored
anesthesia care (MAC) claims is relevant for many office-based procedures [50]. Compared
with claims for general anesthetic cases, MAC claims involved older and sicker patients in
that analysis. Severe respiratory depression was identified as the most common cause of
injury [50]. Similar to general anesthesia, 40 percent of the claims were related to permanent
brain damage or death and were deemed preventable in 46 percent (eg, by improved
vigilance of the practitioner, better monitoring, and/or more reliable anesthesia alarms).
Short duration — To facilitate rapid discharge after the procedure (ideally, one hour or
less), only short-acting agents are used to produce either sedation (eg, propofol, ketamine,
midazolam, dexmedetomidine) or general anesthesia (eg, propofol, ketamine,
dexmedetomidine, and/or inhalation agents such as nitrous oxide, sevoflurane or
desflurane) [10]. Short-acting opioids may be used to provide analgesia (eg, fentanyl or
remifentanil).
Many anesthesiologists use nitrous oxide in combination with intravenous agents or with a
volatile anesthetic agent. Nitrous oxide reduces the doses of other agents and may reduce
costs and expedite emergence from anesthesia because of its rapid offset [51,52]. (See
"Maintenance of general anesthesia: Overview", section on 'Nitrous oxide gas' and
"Inhalation anesthetic agents: Clinical effects and uses", section on 'Nitrous oxide'.)
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Anesthetic techniques to minimize PONV include use of total intravenous anesthesia, usually
with propofol alone or in combination with an opioid [53]. Also, dexmedetomidine may be
used as an adjunct anesthetic agent because this alpha-2 agonist provides some analgesia
and sedation. Other techniques include use of neuraxial anesthesia (spinal or epidural) or
peripheral nerve blocks with or without catheters. Furthermore, opioid-sparing analgesics
are used when feasible (eg, acetaminophen and/or nonsteroidal antiinflammatory drugs
[NSAIDs]). (See "Postoperative nausea and vomiting", section on 'Anesthetic factors' and
"Postoperative nausea and vomiting", section on 'Reduction of baseline risk'.)
In the postoperative period, rescue treatment for patients who develop PONV should include
a drug from a different class than any that have already been administered, unless the effect
of the first drug has worn off or a potentially inadequate dose has been administered.
Serotonin receptor antagonists such as ondansetron are particularly useful as rescue agents,
especially for same-day surgery patients, because they are nonsedating. In rare cases, it may
be necessary to admit a patient with persistent severe PONV to an inpatient facility. (See
"Postoperative nausea and vomiting", section on 'Rescue therapy'.)
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Maximum allowable doses of local anesthetic agents that appear in various publications are
rough guidelines that are not evidence-based, and don't take into account the site or
technique of administration, or patient factors that increase toxicity risk ( table 8) [6,58].
Furthermore, calculated doses should be based on lean, rather than actual body weight
(calculator 1 and calculator 2). Addition of epinephrine to local anesthetic solutions can slow
the rate of absorption and reduce peak plasma levels, but do not prevent systemic toxicity in
all patients.
Optimal pain management often involves a multimodal approach that includes combinations
of drugs and techniques [59]. Although opioid medications have been a mainstay in
perioperative pain management and are effective in the acute setting, unwanted side effects
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that are particularly undesirable in the outpatient setting include nausea and vomiting,
itching, constipation, respiratory depression, and altered mental status, as well as possible
dependence and tolerance issues. Thus, we use parenteral and/or enteral nonopioid
analgesics to reduce opioid requirements. These include acetaminophen and nonsteroidal
antiinflammatory drugs (NSAIDs) such as ketorolac, ibuprofen, or celecoxib ( table 10).
When appropriate, we also use regional techniques and long-acting local anesthetics (eg,
bupivacaine or ropivacaine with peripheral nerve blocks or liposomal bupivacaine for wound
infiltration). Other techniques include high-volume local infiltration analgesia [60] and
delivery of local anesthetics through wound catheters [61]. (See "Management of acute
perioperative pain in adults", section on 'Strategy for perioperative pain control' and
"Management of acute perioperative pain in adults", section on 'Therapeutic options'.)
Safe recovery and discharge depend on the office-based staff's ability to deliver appropriate
intensity and duration of postoperative monitoring. Complications such as respiratory events
(the most common mechanism of injury), delayed emergence from anesthesia, pain,
nausea/vomiting, urinary retention, and hypothermia must be recognized and treated. (See
"Overview of post-anesthetic care for adult patients".)
Discharge criteria are designed to determine a patient's readiness to safely leave the office
recovery area after surgery ( table 11). Fully trained nurses should be available to care for
all postoperative patients until discharge. Ideally, an anesthesiologist should assess each
patient prior to release to home. (See "Overview of post-anesthetic care for adult patients",
section on 'Discharge from the post-anesthesia care unit'.)
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Most literature reviews of adverse outcomes and mortality after various types of office-based
surgical procedures have concluded that surgery in this setting is safe and cost-effective
[1,8,10,21,28,40,59,63]. Improvements in patient outcomes are likely due to implementation
of more stringent credentialing and accreditation regulations, as well as use of routine safety
checklists and emergency manuals, as discussed above [1,4]. (See 'Safety concerns' above.)
Since the large injectate volumes that are employed may result in hypervolemia, close
attention to fluid and electrolyte balance is particularly important in the intraoperative and
postoperative periods [10,38]. Patients are also at risk for hypothermia because the injectate
fluids are not typically warmed. Active warming devices (eg, forced air warmers) are used in
many plastic surgery offices to avoid and treat hypothermia [10]. We agree with the
guidelines of the American Society of Plastic Surgeons stating that the total volume of
aspirant, including supernatant fat and fluid, should be limited to 5000 mL if the liposuction
procedure is performed in isolation, or 2000 mL if performed with a concurrent aesthetic
surgical procedure [10,40,41]. Body mass index is taken into account; the volume of aspirate
removed should be proportional to the patient's overall size [64]. Generally, aspirate volumes
>5000 mL are performed in an acute-care hospital or licensed/accredited facility due to
increased risk of complications [64].
The dose of epinephrine in the infiltrate solution used for the tumescent technique should
not exceed 0.07 mg/kg (eg, <5 mg in a 70 kg patient) in order to minimize risk for
cardiovascular effects [10]. Although epinephrine is rapidly metabolized with a half-life of
approximately two minutes, sustained peak levels have been demonstrated during and after
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Also, the dose of lidocaine in the infiltrate solution used for the tumescent technique is
typically 35 to 55 mg/kg, which is considerably higher than the 4.5 mg/kg maximum
recommended dose for regional anesthetic techniques [67-69]. These high doses are usually
well-tolerated because the tumescent technique results in single compartment clearance,
similar to that of a sustained-release medication [67,70]. However, absorption of local
anesthetic from the subcutaneous tissue is variable; thus, timing for onset of symptoms of
lidocaine toxicity is unpredictable [69,71]. Although blood lidocaine levels typically peak 12 to
16 hours after initial injection of infiltrate solution, peaks may occur within two hours of
injection, particularly if tumescent lidocaine without epinephrine is used (eg, for endovenous
laser therapy). Thus, close postoperative monitoring in the office-based recovery area is
necessary, and lipid emulsion should be immediately available for prompt treatment
( table 9) [69,70]. (See "Local anesthetic systemic toxicity", section on 'Lipid rescue'.)
The patient may not show signs of systemic local anesthetic toxicity (eg, dizziness, peripheral
numbness, metallic taste, tinnitus, confusion/anxiety, seizures) until after discharge home.
This is clinically relevant because signs of local anesthetic toxicity must be rapidly recognized,
and appropriate emergency procedures initiated [72,73]. All patients and their caregivers
should receive instructions regarding the need to seek emergency department care
immediately if signs or symptoms of local anesthetic toxicity become apparent after
discharge. (See "Local anesthetic systemic toxicity", section on 'Clinical presentation of
toxicity'.)
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In a prospective cohort review evaluating the safety of cosmetic surgery performed between
2008 and 2013 on the body, breast, face, or combination of regions in more than 129,000
patients (having a total of nearly 184,000 procedures), 15.9 percent were performed in an
accredited office-based setting by board-certified plastic surgeons, rather than in an
ambulatory surgery center (ASC) setting (57.4 percent) or hospital (26.7 percent) [8].
Complication rates, including hematomas, infections, and postoperative pulmonary
dysfunction, were lowest in the office-based setting (1.3 percent), compared with the ASC
setting (1.9 percent), or the hospital setting (2.4 percent). In a 2018 retrospective review of
174 patients undergoing primary facelift under local anesthesia with oral sedation in an
office-based setting, no mortality was reported, and complications were minor (primarily
hematoma formation [13 percent], with only two patients requiring operative evacuation)
[78]. Older retrospective studies of cosmetic surgery performed in an office-based setting
have noted similar low risks of significant complications [34,36,46,47,79-81]. Taken together,
these studies suggest that accredited office-based surgery suites are generally a safe
alternative to ASCs or hospitals for cosmetic surgical procedures. However, careful patient
selection is necessary, as noted above. (See 'Patient selection' above.)
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2000 and 2003, there were 13 procedure-related deaths, with seven involving elective
cosmetic procedures, five of which were performed under general anesthesia [32,33]. A
subsequent study noted mandatory reports of 31 deaths in Florida during office-based
plastic surgery over the seven-year period from 2000 to 2007 [74].
In particular, fire and facial burns are a particular risk for any facial procedure that requires
use of a laser, or even routine electrocautery, due to the presence of supplemental oxygen
(or nitrous oxide) in combination with combustible substances such as paper drapes and
alcohol prep [38]. Thus, nitrous oxide should not be used, and, when possible, avoidance of
supplemental oxygen is ideal (see "Fire safety in the operating room"). In a study MAC
conducted by the American Society of Anesthesiologists (ASA) using a closed claims
database, many of the patients were undergoing facial surgery [50]. Severe respiratory
depression was identified as the most common cause of injury in all MAC cases (21 percent),
followed by facial burn injuries in the presence of supplemental oxygen during facial surgery
(17 percent) [50]. Thus, these cases are among the highest-risk procedures performed in the
office setting [10].
Also, patients undergoing abdominoplasty may be at greater risk for later postoperative
complications such as venous thromboembolism and emergency department or hospital
admission, particularly if the procedure is performed concurrently with other cosmetic
surgery (eg, liposuction, breast procedures) [77,82].
Oral and maxillofacial procedures — Oral, maxillofacial, and other head and neck surgical
procedures that are not complex (eg, tonsillectomy, nasal or intranasal procedures) may be
performed in an office-based setting [6].
In one large prospective cohort study of more than 34,000 patients undergoing oral or
maxillofacial surgery in this setting, 72 percent received deep sedation or general anesthesia,
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15.5 percent received conscious sedation, and 12.5 percent received local anesthesia [45].
There were no deaths in this large study, and only two patients in this study had
complications requiring hospitalization, while 94 percent reported satisfaction with the
anesthetic.
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● The number of elective surgical procedures performed in the office-based setting has
expanded rapidly. Compared with hospital settings, the major advantages of office-
based anesthesia for surgical procedures are patient and surgeon convenience, cost
containment, and possibly lower nosocomial infection rates. (See 'Potential advantages
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● Safety concerns have centered around the adequacy of individual facility resources and
governmental regulations for office-based facilities. We use guidelines for office-based
anesthesia adopted by the American Society of Anesthesiologists (ASA), including
standard monitoring ( table 6). We also use routine and crisis checklists to further
ensure patient safety. (See 'Safety concerns' above and 'Standard monitors' above.)
● Patients at higher risk for complications during anesthesia and surgery are identified
preoperatively. Examples include potentially difficult airway, obstructive sleep apnea,
morbid obesity, severe or exacerbated chronic obstructive pulmonary disease, recent
myocardial infarction within the past six months or recent stroke within the past three
months, end-stage kidney or liver disease, severe anemia, sickle-cell disease, abnormal
bleeding or clotting tendency, extremes of age, acute or chronic substance abuse,
inability to cooperate due to severe anxiety or poorly controlled psychiatric problems,
history of anaphylaxis, or family history of malignant hyperthermia (MH). In some
cases, ensuring optimal medical treatment may reduce risk, but in other cases, the
patient should be referred to a facility that can handle complications that may occur.
(See 'Patient selection' above.)
• The procedure is within the surgeon's scope of practice and the facility's capabilities
• The duration and degree of complexity of the procedure will allow recovery and
discharge for the facility on the same day
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● To facilitate a rapid discharge after the procedure, only short-acting agents are used to
produce either sedation or general anesthesia. Similarly, short-acting opioid agents are
used to control pain. (See 'Selection of anesthetic agents' above.)
● Safe recovery and discharge depend on the office-based staff's ability to deliver
appropriate intensity and duration of postoperative monitoring. Complications such as
respiratory events, delayed emergence from anesthesia, pain, PONV, urinary retention,
and hypothermia must be recognized and treated. Standard discharge criteria are used
to supplement the assessment of the responsible anesthesiologist for release home.
(See 'Recovery and discharge' above.)
● Anesthetic considerations and outcomes for selected procedures are discussed above
and in separate topics (see 'Anesthetic considerations and outcomes for selected
procedures' above):
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GRAPHICS
Monitors
Heart rate/ECG
Pulse oximeter
Temperature
Capnography
Airway supplies
Nasal cannulae
Oral airways
Facemasks
Laryngoscopes with blades in multiple sizes and styles (eg, Macintosh and Miller)
Stylettes
Cardiac defibrillator
Emergency drugs
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Anesthetic drugs
Safe delivery of office-based anesthesia requires the availability of the listed equipment.
ECG: electrocardiogram; LMA: laryngeal mask airway; ACLS: advanced cardiac life support.
Modified with permission from: Hausman LM, Rosenblatt MA. Office-Based Anesthesia. In: Clinical Anesthesia, 7th ed,
Barash PG, Cullen BF, Stoelting RK, et al (Eds), Lippincott Williams & Wilkins, Philadelphia 2013. Copyright © 2013
Lippincott Williams & Wilkins. www.lww.com.
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4. Surgeon qualification
a. Training
5. Office administration
6. Anesthesiologist requirements
9. Ancillary care
10. Equipment
13. Temperature
BLS: basic life support; ACLS: advanced cardiac life support; PALS: pediatric advanced life support.
Reproduced with permission from: Hausman LM, Rosenblatt MA. Office-Based Anesthesia. In: Clinical Anesthesia, 7th ed,
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Barash PG, Cullen BF, Stoelting RK, et al (Eds), Lippincott Williams & Wilkins, Philadelphia 2013. Copyright © 2013
Lippincott Williams & Wilkins. www.lww.com.
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__ No __ Yes
__ Not applicable
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This checklist is not intended to be comprehensive. Additions and modifications to fit local
practice are encouraged.
Reproduced with permission from: Weiser T, Haynes A, Dziekan G, et al. Effect of a 19-item surgical safety checklist
during urgent operations in a global patient population. Ann Surg 2010; 251:976. Copyright © 2010 Lippincott Williams
& Wilkins.
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The Institute for Safety in Office-Based Surgery constructed a 28-step perioperative checklist to identify and co
different phases of an invasive office procedure. This checklist is not intended to be comprehensive. Additions
practice are encouraged.
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DVT: deep vein thrombosis; NPO: nil per os (nothing by mouth); AED: automated external defibrillator; MH: ma
emergency medical services; N/A: not applicable; EBL: estimated blood loss.
Credit: Richard Urman, Fred Shapiro, Copyright the Institute for Safety in Office-Based Surgery.
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ASA II A patient with mild systemic disease Mild diseases only without
substantive functional limitations.
Current smoker, social alcohol
drinker, pregnancy, obesity
(30<BMI<40), well-controlled
DM/HTN, mild lung disease.
ASA IV A patient with severe systemic Recent (<3 months) MI, CVA, TIA, or
disease that is a constant threat to CAD/stents, ongoing cardiac ischemia
life or severe valve dysfunction, severe
reduction of ejection fraction, sepsis,
DIC, ARDS, or ESKD not undergoing
regularly scheduled dialysis.
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The addition of "E" to the numerical status (eg, IE, IIE, etc) denotes Emergency surgery (an
emergency is defined as existing when delay in treatment of the patient would lead to a
significant increase in the threat to life or body part).
BMI: body mass index; DM: diabetes mellitus; HTN: hypertension; COPD: chronic obstructive
pulmonary disease; ESKD: end-stage kidney disease; PCA: post conceptual age; MI: myocardial
infarction; CVA: cerebrovascular accident; TIA: transient ischemic attack; CAD: coronary artery
disease; DIC: disseminated intravascular coagulation; ARDS: acute respiratory distress syndrome.
ASA Physical Status Classification System (Copyright © 2014) is reprinted with permission of the American Society of
Anesthesiologists, 1061 American Lane, Schaumburg, Illinois 60173-4973.
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Fasting requirements at
Country, year Comments
time of induction
Australian and New Zealand 1 hour clear fluid (≤3 Up to 400 mL of clear liquid
College of Anaesthetists [4] mL/kg/hour) for infants and up to 2 hours prior to
children induction for adults is likely
2 hours clear liquids adults safe
3 hours breast milk for
infants <6 months
4 hours formula for infants
<6 months
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Pediatric societies
Joint statement from 1 hour clear liquids for Encourage intake of clear
Association of Paediatric children up to 16 years of liquids
Anaesthetists of Great age
Britain and Ireland,
European Society for
Paediatric Anaesthesiology,
L'Association Des
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Anesthésistes-
Réanimateurs Pédiatriques
d'Expression Française [9]
The Society for Paediatric 1 hour clear liquids for Encourage intake of clear
Anaesthesia of New children liquids
Zealand and Australia [11]
References:
1. Practice Guidelines for Preoperative Fasting and the Use of Pharmacologic Agents to Reduce the Risk of
Pulmonary Aspiration: Application to Healthy Patients Undergoing Elective Procedures: An Updated Report by the
American Society of Anesthesiologists Task Force on Preoperative Fasting and the Use of Pharmacologic Agents to
Reduce the Risk of Pulmonary Aspiration. Anesthesiology 2017; 126:376.
2. Smith I, Kranke P, Murat I, et al. Perioperative fasting in adults and children: guidelines from the European Society
of Anaesthesiology. Eur J Anaesthesiol 2011; 28:556.
3. Frykholm P, Disma N, Andersson H, et al. Pre-operative fasting in children: A guideline from the European Society
of Anaesthesiology and Intensive Care. Eur J Anaesthesiol 2022; 39:4.
4. Australian and New Zealand College of Anaesthetists. Guideline on pre-anaesthesia consultation and patient
preparation. Available at: https://www.anzca.edu.au/getattachment/d2c8053c-7e76-410e-93ce-
3f9a56ffd881/PS07-Guideline-on-pre-anaesthesia-consultation-and-patient-preparation (Accessed on September
8, 2021).
5. Association of Anaesthetists of Great Britain and Ireland. Pre-operative Assessment and Patient Preparation - The
Role of the Anaesthetist. Available at: https://anaesthetists.org/Home/Resources-publications/Guidelines/Pre-
operative-assessment-and-patient-preparation-the-role-of-the-anaesthetist-2 (Accessed on October 8, 2021).
6. Dobson G, Chow L, Filteau L, et al. Guidelines to the Practice of Anesthesia - Revised Edition 2020. Can J Anaesth
2020; 67:64.
7. Søreide E, Eriksson LI, Hirlekar G, et al. Pre-operative fasting guidelines: an update. Acta Anaesthesiol Scand 2005;
49:1041.
8. Verbandsmitteilung DGAI. Praeoperatives Nuechternheitsgebot bei elektiven Eingriffen. Anaesthesiol Intensivmed
2004; 12:722.
9. Thomas M, Morrison C, Newton R, Schindler E. Consensus statement on clear fluids fasting for elective pediatric
general anesthesia. Paediatr Anaesth 2018; 28:411.
10. Rosen D, Gamble J, Matava C, Canadian Pediatric Anesthesia Society Fasting Guidelines Working Group. Canadian
Pediatric Anesthesia Society statement on clear fluid fasting for elective pediatric anesthesia. Can J Anaesth 2019;
66:991.
11. Society for Paediatric Anaesthesia in New Zealand and Australia. Available at:
https://www.anzca.edu.au/getattachment/d2c8053c-7e76-410e-93ce-3f9a56ffd881/PS07-Guideline-on-pre-
anaesthesia-consultation-and-patient-preparation (Accessed on October 22, 2021).
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Primary physiologic
Monitoring Derived Additiona
process/parameter Principle
equipment information function
targeted
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Circulation Cardiac ECG The ECG monitor Heart rate and ST segment
activity detects, amplifies, rhythm depression/elev
displays, and and trend over
records the ECG with an audible
signal. alarm warning
significant
arrhythmias or
asystole
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automatically
inflate and deflate
the cuff, and have
electronic
pressure sensors
that record the
pressure
oscillations of the
arteries. The
pressure at which
maximal
oscillations occur
as the cuff is
deflated
corresponds with
MAP. Proprietary
algorithms are
used to calculate
systolic and
diastolic BP.
Temperature monitoring is conditional and can be waived according to the ASA document.
O 2 : oxygen; CO 2 : carbon dioxide; ETCO 2 : end-tidal carbon dioxide; ECG: electrocardiogram; BP:
blood pressure; MAP: mean arterial pressure.
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a. Drug-induced sedation
a. Drug-induced sedation
b. Patient responds purposefully to verbal commands either alone or with light tactile
stimulation
3. Deep sedation/analgesia
a. Drug-induced sedation
b. Patient cannot be easily aroused but can respond purposefully to repeated or painful
stimulation
4. General anesthesia
c. Ventilatory function is often impaired; patient may require assistance in maintaining a patent
airway
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Reproduced with permission from: Hausman LM, Rosenblatt MA. Office-Based Anesthesia. In: Clinical Anesthesia, 7th ed,
Barash PG, Cullen BF, Stoelting RK, et al (Eds), Lippincott Williams & Wilkins, Philadelphia 2013. Copyright © 2013
Lippincott Williams & Wilkins. www.lww.com.
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Maximum
Duration of Duration of dose* ¶
Onset
Anesthetic anesthesia* analgesia* (mg/kg)
(minutes)
(hours) (hours) without/with
epi
2% lidocaine 10 to 20 2 to 5 3 to 8 4.5/7
1.5% 10 to 20 2 to 5 3 to 10 5/7
mepivacaine
Adapted from: Gadsen J. Local Anesthetics: Clinical Pharmacology and Rational Selection. The New York School of
Regional Anesthesia website, October 2013.
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Etiology
Risk factors
Signs and symptoms* LAST can occur >15 minutes after injection of LA
CNS: ¶
Tinnitus
Circumoral numbness
Metallic taste
Agitation
Dysarthria
Seizures
Loss of consciousness
Respiratory arrest
Cardiovascular: ¶
Hypotension
Bradycardia
Ventricular arrhythmias
Cardiovascular collapse
Treatment*
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For further information, refer to UpToDate content on local anesthetic systemic toxicity.
LA: local anesthetic; LAST: local anesthetic systemic toxicity; CNS: central nervous system; TPN:
total parenteral nutrition; ACLS: advanced cardiac life support; IBW: ideal body weight; IV:
intravenous.
* Not all signs and symptoms occur in every patient.
¶ Cardiovascular collapse may occur without CNS signs or symptoms, especially with rapid
intravascular injection.
Reference:
1. Neal JM, Barrington MJ, Fettiplace MR, et al. The Third American Society of Regional Anesthesia and Pain Medicine
Practice Advisory on Local Anesthetic Systemic Toxicity: Executive Summary 2017. Reg Anesth Pain Med 2018;
43:113.
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Usual
Maximum
analgesic Selected characteristics and role
Drug dose per
dose in therapy
day (mg)
(intravenous)
Para-aminophenol derivative
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Nonselective NSAIDs*
Ketorolac Age <65 years Age <65 years A frequently used option for short-
and weight ≥50 and weight term treatment of acute pain when
kg: 15 to 30 mg ≥50 kg: 120 oral NSAID administration is not
IV every 6 hours mg IV per day available, and as part of a
for up to five multimodal analgesic regimen for
Age ≥65 years
days the treatment of moderate to severe
or weight <50
pain when rapid onset is required
kg: 15 mg IV Age ≥65 years
(eg, postoperatively).
every 6 hours or weight <50
kg: 60 mg per Onset ~30 minutes.
day IV for up Duration of platelet dysfunction ~24
to five days hours.
Administered as IV bolus over 15
seconds in minimal fluid volume.
Risk of gastropathy and renal failure
is related to dose and duration of
use.
Patients should be well hydrated
and without significant kidney
disease (CrCl >60 mL/minute).
Avoid use in patients with a history
of ischemic heart disease, stroke, or
heart failure.
According to the US label, NSAID use
is contraindicated for the treatment
of perioperative pain in the setting
of coronary artery bypass graft
(CABG) surgery.
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NSAID: nonsteroidal antiinflammatory drug; IV: intravenous; CABG: coronary artery bypass graft;
COX-2: cyclooxygenase isoform 2; CrCl: creatinine clearance.
* Nonselective NSAIDs inhibit platelet functioning and are contraindicated as preemptive
analgesics before major surgery and intraoperatively prior to establishment of hemostasis. Use
of parenteral NSAIDs should not exceed five days. In some countries, a maximum duration of use
of ≤2 days or a single dose is recommended. Safety concerns are addressed in the UpToDate
topic review of nonselective NSAIDs overview of adverse effects.
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Vital signs
Activity
1 = Requires assistance
0 = Unable to ambulate
Pain
2 = Yes
1 = No
Surgical bleeding
Modified with permission from: Fowler MA, Spiess BD. Postanesthesia recovery. In: Clinical Anesthesia, 7th ed, Barash PG,
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Cullen BF, Stoelting RK, et al (Eds), Lippincott Williams & Wilkins, Philadelphia 2013. Copyright © 2013 Lippincott
Williams & Wilkins. www.lww.com.
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