PIIS1467298725000716
PIIS1467298725000716
Please cite this article as: Bailey K, Briley J, Duffee L, Duke-Novakovski T, Grubb T, Love L, Kruse-
Elliott K, Martin-Flores M, McKune C, Oda A, Pang D, Posner L, Reed R, Sager J, Sakai D, Schultz A,
Shih ST, The American College of Veterinary Anesthesia and Analgesia Small Animal Anesthesia and
Sedation Monitoring Guidelines 2025, Veterinary Anaesthesia and Analgesia, https://doi.org/10.1016/
j.vaa.2025.03.015.
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© 2025 Published by Elsevier Ltd on behalf of Association of Veterinary Anaesthetists and American
College of Veterinary Anesthesia and Analgesia.
MONITORING RECOMMENDATIONS
The American College of Veterinary Anesthesia and Analgesia Small Animal Anesthesia
Authors:
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M Martin-Floresf, C McKuneg, A Odah, DSJ Pangi, LP Posnera, R Reedj, J Sagerk, DM Sakail,
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AW Schultzm, S Tenenbaum Shihn
1
Corresponding author
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re
Lydia Love
lP
Raleigh, NC 27606
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2
Co-first authors
a
Department of Molecular Biomedical Sciences
Raleigh, NC USA
b
Massachusetts Veterinary Referral Hospital
d
Veterinary Anesthesia & Analgesia Consulting & Education (VetAACE)
e
Sage Veterinary Centers and Ethos Veterinary Health
Reno, NV USA
of
ro
f
Department of Clinical Sciences
g
Mythos Veterinary LLC
h
CONSCIOUS
Tokyo, Japan
i
Faculty of Veterinary Medicine
University of Calgary
&
Faculty of Veterinary Medicine
Université de Montréal
j
Department of Large Animal Medicine
University of Georgia
k
Veterinary Emergency Group
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White Plains, NY, USA
ro
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l
Department of Small Animal Medicine and Surgery
re
University of Georgia
lP
m
Midmark Animal Health
n
Veterinary Referral Associates
The following authors are employees of or consultants for a company that manufactures
1 Abstract
2 The American College of Veterinary Anesthesia and Analgesia (ACVAA) in collaboration with the
3 North American Veterinary Anesthesia Society and the Academy of Veterinary Technicians in
4 Anesthesia and Analgesia have revised and expanded the 2009 guidelines (ACVA 2009). The 2025
5 guidelines include updated recommendations for monitoring circulation, oxygenation, ventilation, body
6 temperature, neuromuscular blockade, and anesthetic depth in feline and canine patients. Monitoring
7 during sedation (sedation specific guidelines are in the Monitoring During Sedation Section),
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8 recommendations for personnel managing the patient, and the use of cognitive aids have been
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9 incorporated. This document is meant to establish guidelines for monitoring small animals during
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sedation and in the perianesthetic time period. Further information concerning techniques, reference
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11 values, differential diagnoses, and details of various interventions can be found in the reference literature
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13 These guidelines use objective, evidence-based criteria whenever possible; however, some of the
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14 recommendations are a consensus of expert opinion and clinical experience. This document is intended
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15 to guide monitoring of small animal patients during sedation and anesthesia; it is not to be construed as a
16 standard of care as the choice of monitoring techniques and methods can vary depending on the type of
17 practice and spectrum of care considerations. Alternative methods are suggested if a minimally
20 neuromuscular blockade.
21
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22
23 Audience: Anyone providing anesthesia or sedation in small animal practice including but not limited to
26 Definitions:
27 Minimum Recommendations: Applicable to all anesthetized small animals (Table 1). If a minimum
28 monitoring modality cannot be used, the reason should be documented in the medical record.
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29 Alternatives: To be used only when minimum recommended options are not available. Their use should
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30 be documented in the medical record. re
31 Advanced Recommendations: Options to consider for veterinary patients with co-existing disease and/or
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34 Objective: To achieve an adequate anesthetic depth to prevent patient awareness and movement while
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36 Minimum Recommendations:
37 1. A dedicated anesthetist (see Personnel section) should repeatedly observe the animal to assess eye
38 position, muscle tone, including jaw muscle tone, and reflexes, including the palpebral reflex or
39 peripheral reflexes such as withdrawal of a limb. Special considerations for monitoring anesthetic
40 depth in the face of neuromuscular blockade use are outlined in that section below.
41 During anesthesia with volatile agents, the eyes will generally rotate ventromedially, body and
42 jaw muscle tone will be relaxed, and the palpebral reflex will be sluggish or absent (Bleijenberg et
43 al. 2011). Patients anesthetized with injectable protocols, especially with dissociative-based
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44 approaches, may not display the traditional progressive signs of reflex depression and muscle
45 relaxation.
46 2. A dedicated anesthetist should anticipate and monitor for indication of sympathetic responses,
47 including increases in heart rate, respiratory rate, and arterial blood pressure, in response to noxious
48 stimuli.
49 Advanced Recommendations:
50 1. Monitoring of inspired and expired inhalant concentrations is indicated whenever such technology is
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51 available to ensure adequate but not excessive inhalant delivery to the patient.
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52 2. Mathematical transformations of the electroencephalogram, e.g., Bispectral Index (BIS) or Patient
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53 State Index, may be useful in some clinical or laboratory settings (March & Muir 2003; Sakai et al.
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54 2023).
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55 Circulation Monitoring
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56 Objective: To confirm adequate tissue perfusion, ensuring delivery of oxygen and nutrients and removal
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58 Minimum Recommendations:
59 1. A dedicated anesthetist (see Personnel section) should continuously observe the patient, using
61 including manual palpation of the pulse, auscultation of the heart using an external or esophageal
62 stethoscope and/or continuous pulse rate detection via Doppler flow probe, and assessment of
64 2. Oscillometric blood pressure monitoring should be utilized with measurements taken at least every 5
65 minutes.
66 A mean arterial pressure < 60-65 mmHg should prompt assessment of the patient and
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67 intervention, which may include decreasing anesthetic depth, managing bradycardia and
69 Algorithms of oscillometric blood pressure monitors vary by manufacturer and have an impact
70 on the performance of the monitor. Clinicians are encouraged to check monitoring brands against
71 validation studies that compare performance against the American College of Veterinary Internal
72 Medicine Hypertension Consensus Panel and Veterinary Blood Pressure Society Recommendations
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74 3. Continuous electrocardiogram (ECG) monitoring to detect any changes in heart rate, rhythm, or
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75 conduction abnormalities.
76
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4. Time-based capnography is reflective of pulmonary perfusion when ventilation is constant and
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77 should be monitored continuously.
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78 Alternative Recommendations:
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79 When an oscillometric blood pressure device is unavailable or unreliable, a Doppler flow probe and
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80 sphygmomanometer with a cuff can be substituted. Doppler blood pressure (BP) readings generally
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81 display poor agreement with invasively measured pressures (da Cunha et al. 2014; Kennedy & Barletta
82 2015; Skelding & Valverde 2020b). Doppler BP readings of 90 mmHg or below should prompt
83 assessment of the patient and intervention as described for oscillometry. Doppler flow probes also
84 provide an audible signal of peripheral blood flow and pulse rhythm. The plethysmograph and audible
85 signal from a pulse oximeter can also be used to confirm the rate and rhythm of peripheral pulses.
86 Advanced Recommendations:
88 1. Invasive blood pressure measurement via arterial catheterization should be considered for critically
90 cardiovascular disease.
95 from a pulse oximeter waveform, Systolic Pressure Variation (SPV) or Pulse Pressure Variation
96 (PPV) from the invasive arterial pressure waveform during positive pressure ventilation can provide
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97 information on fluid responsiveness.
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99 3.
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Other forms of fluid responsiveness monitoring may be considered when available, including
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100 transthoracic or transesophageal echocardiography and ultrasound evaluation of caudal vena cava
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101 distensibility.
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102
103 4. Venous blood gas and lactate analysis can be useful in evaluating global perfusion parameters.
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107 1. The anesthetist should perform a routine anesthetic equipment check using a standardized checklist
108 prior to use of the machine and regularly assess the function of the oxygen source, flowmeter, and
110 2. A dedicated anesthetist (see Personnel section) should regularly assess mucous membrane color
111 (pink, cyanotic, or pale) and ventilatory efforts (chest excursion, auscultation, and reservoir bag
112 movement).
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113 Assessment of mucous membrane color requires access to the patient and appropriate lighting
114 (Comroe & Botelho 1947). In addition, the anesthetist should inflate the endotracheal tube cuff until
115 there is no audible leak at a breathing circuit manometer pressure of 20 cmH2O (or use a cuff
116 manometer) and perform bilateral auscultation of the chest following intubation to help ensure that
117 the endotracheal tube is placed in the trachea, rather than into one bronchus.
118 3. Pulse oximetry is recommended in all heavily sedated or anesthetized small animal patients.
119 The use of pulse oximetry has been associated with a decreased risk of mortality in veterinary
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120 anesthesia (Brodbelt et al. 2007; Itami et al. 2017; Matthews et al. 2017). A transmission probe on
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121 the tongue, ear, toe, or fold of skin can be utilized or a reflectance probe can be placed on a shaved
122
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or hairless area such as the underside of the base of the tail or metatarsus (Nixdorff et al. 2021). The
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123 variable pitch pulse tone and low saturation alarm should be easily audible. Pulse oximetry is a late
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124 indicator of an oxygenation problem when oxygen is being supplemented and therefore any value <
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125 95% should be investigated to ascertain patient status and rule out technical issues. Patient
126 (respiratory or cardiovascular) and equipment issues are potential causes of hypoxemia during
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129 1. Arterial Blood Gas (ABG) analysis and measurement of the partial pressure of oxygen in arterial
130 blood (PaO2) are useful for assessing pulmonary gas exchange.
131 Determination of PaO2 should be considered in patients with persistently low pulse oximetry
132 readings, pre-existing pulmonary disease, those undergoing thoracic or pulmonary procedures, or
133 situations in which ventilation-perfusion mismatch or shunt may occur (Farrell et al. 2019).
134 2. Measurement of the inspired oxygen concentration (FIO2) confirms that adequate oxygen is being
136 This monitoring modality is recommended whenever possible to confirm functional oxygen
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137 supply and to ascertain the percentage of oxygen delivered to the patient. In addition, FIO2
138 monitoring should be employed if the use of medical air mixtures is planned.
139 3. Co-oximetry (with an arterial blood sample) is more reliable than standard pulse oximetry when
140 dysfunctional hemoglobins are present (e.g., carboxyhemoglobin, methemoglobin) and will provide
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144 Minimum Recommendations:
145
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1. A dedicated anesthetist should consistently monitor the patient by observation of thoracic wall
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146 and/or reservoir bag/ventilator bellows movements during inhalation and exhalation, auscultation
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147 using a stethoscope (esophageal or external) for respiratory sounds to supplement other objective
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148 monitoring as necessary and utilize a manometer to assess peak airway pressures during positive
150 2. Time-based capnography (inspired and expired carbon dioxide CO2 analysis with a waveform)
151 should be utilized as it provides information on the partial pressure of carbon dioxide in respiratory
152 gases, can be used to evaluate the integrity of the endotracheal tube (or laryngeal mask airway) and
153 breathing circuit, pulmonary perfusion (including during cardiopulmonary resuscitation), and
154 ventilation status, and is useful in the differential diagnosis of hypoxemia (Hogen et al. 2018,
156 Inspiratory CO2 concentrations should be, or approach, 0 mmHg with normally functioning
157 anesthetic delivery equipment and minimal mechanical dead space. Mild increases in end-tidal CO2
158 concentrations may be tolerated in healthy patients but values > 60 mmHg should be addressed,
159 including decreasing anesthetic depth if possible and instituting positive pressure ventilation.
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162 Capnometry displays the partial pressure of inhaled and exhaled carbon dioxide and the
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165 2. An apnea monitor is designed to create audible noise during exhalation, or alarm during prolonged
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167 If capnography and capnometry are not available, an apnea monitor may be used though it will
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168 not evaluate adequacy of ventilation and may add dead space to the breathing circuit.
169
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3. During positive pressure ventilation, if an airway pressure manometer is not available, the anesthetist
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170 should visually evaluate the patient for adequate, but not excessive, thoracic excursions.
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172 1. Arterial (or venous) blood gas sampling enables measurement of partial pressure of carbon dioxide
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173 (PCO2).
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174 Measurement of arterial carbon dioxide (and oxygen) should be considered when ventilation is
175 abnormal prior to the procedure (patients with forebrain or brainstem disease, significant pulmonary
177 2. Spirometry can be used to provide information on lung/chest wall compliance and tidal volume.
178 Tidal volume measurement should be considered when changes in tidal volume are possible,
179 such as during thoracotomy and with asthmatic patients. Displayed spirometry loops can be analyzed
180 for abnormalities such as those produced by endotracheal tube cuff leaks, spontaneous breathing
181 during ventilator use, changes in pulmonary compliance, and the presence of airway secretions.
182
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184 Objective: To identify, prevent, and manage moderate to severe deviations from normal temperature
185 ranges.
187 1. The use of a digital thermometer to measure rectal body temperature at least every 15 minutes is
188 recommended in all moderately to heavily sedated, or anesthetized, small animal patients.
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189 2. Continuous measurement of body temperature via a thermistor inserted into the esophagus or rectum
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190 is desirable.
191
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3. Body temperature can be measured at different sites.
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192 Core body temperature refers to the temperature of internal organs and is measured invasively in
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193 the pulmonary artery using special intravenous catheters with thermistors. Esophageal and rectal
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194 temperature measurements are clinically reasonable substitutes in veterinary patients (Southward et
195 al. 2006; Hymczak et al. 2021). When a site other than rectal or esophageal placement is used for
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196 temperature measurement (e.g., axillary, nasal, tympanic, pharyngeal), any deviations from
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197 normothermia should be confirmed using a standard measurement site when possible (Ward et al.
198 2023).
199 4. Monitoring of body temperature at least every 30 minutes should continue into the recovery period
201 5. If body temperature decreases below 37.8˚C/100˚F, safe active external warming should be
202 instituted.
203 Passive insulation with towels, blankets, or drapes and protection from tables should always be
204 utilized. Safe active external warming methods include forced warm air, conductive blankets with a
205 functioning sensor, and warm water blankets. Electric heating pads, microwaved objects (e.g., rice
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206 socks, heated disks), and warmed saline bags may cause burns. Recommended devices must be
208
211 neuromuscular blocking agents (NMBA). This allows for identification of the onset of action of the
212 NMBA and quantification of the depth of neuromuscular blockade (i.e., deep, moderate, shallow, and
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213 minimal) (Table 2). Neuromuscular blockade monitoring guides the re-dosing or titration of infusion
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214 rates of NMBAs, assesses conditions for administration of reversal agents, and ensures adequate
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restoration of neuromuscular function before emergence from anesthesia.
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217 1. A peripheral nerve stimulator (PNS) should be used to provide subjective (visual or tactile)
219 Assessment includes the detection of twitches via Train of Four (TOF) count, 0 – 4, or Double
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220 Burst Suppression (DBS) count, 0–2 and identifying a fade within the TOF or DBS during shallow
221 or minimal NMB. NMBAs should not be administered without a peripheral nerve stimulator.
222 Capnometry or capnography, spirometry, and other ventilation monitors are not adequate surrogates
223 to monitor neuromuscular function (Martin-Flores et al. 2014). This recommendation differs from
225 2. As normal function cannot be determined by subjective means (Martin-Flores et al. 2019), it is
226 recommended to always administer pharmacological reversal when subjective PNS is used.
227 3. It is mandatory to only administer NMBAs during general anesthesia (injectable or inhalant).
228 Neuromuscular blockade will cease all skeletal neuromuscular function without inducing
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229 unconsciousness. Some clinical signs of the depth of anesthesia commonly used, such as muscle
230 (jaw) tone, palpebral reflex, or eye position, will be abolished (Cullen & Jones 1980). The loss of
231 ability to monitor muscle tone and peripheral reflexes may require greater emphasis on close
232 monitoring of autonomic responses, and the analysis of inhaled anesthetic agent concentrations
234 4. Heart rate monitoring should be in place when reversal agents are administered as they are
235 associated with an increase in vagal tone and could lead to life threatening bradyarrhythmia.
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236 Pre-treatment with anticholinergic drugs may be warranted but does not negate the need for pulse
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237 rate and ECG monitoring.
241 Baseline values often are > 1. Quantitative assessment allows the detection of residual NMB.
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242 Indirect reversal agents such as neostigmine should not be administered during deep neuromuscular
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243 blockade (i.e., TOF count = 0) as they will be ineffective. Reversal is more effective and predictable
245
247 Objective: To ascertain normal progression from the anesthetized state to independent maintenance of
248 homeostasis. The first three hours following the cessation of anesthesia in companion animals carries the
249 highest risk of morbidity and mortality (Brodbelt et al. 2008; Redondo et al. 2023).
250 At minimum, each physiological variable described below should be assessed at frequent regular time
251 intervals throughout the immediate postanesthetic period until the patient is deemed physiologically
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252 stable (warm, oriented, ambulatory, pain- and nausea-free) by the attending clinician and
253 cardiorespiratory variables have returned to normal. Patients that require ongoing physiological
254 monitoring and supportive care should remain under continuous observance and may require transfer to
255 an appropriate care unit (e.g., an intensive care unit) for continued management.
257 1. The recovery period encompasses the time from discontinuation of the delivery of anesthetic agents,
258 through extubation, until the patient can maintain their own physiological stability (see #9 below)
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259 and is therefore ready for discharge. Patients should be under continuous visual observation until this
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260 time.
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2. The anesthetist or designated recovery personnel should ensure patient safety through continued
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262 monitoring of physiological variables and communication of patient status with the team during the
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263 recovery period. At least one more person should be immediately available to help with patient care
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265 3. Oxygenation should be regularly assessed by examination of mucous membrane color, ventilatory
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266 efforts (patency of upper airway, chest excursions, and auscultation) and the use of a pulse oximeter
267 when possible. Monitoring of minimum requirements as previously described continues during the
269 4. Circulation should be regularly assessed by assessment of heart rate, rhythm, and in patients that
270 have been or are unstable, continued blood pressure measurements. Monitoring of minimum
271 requirements as previously described continues during the immediate postanesthetic period.
272 5. Ventilation should be regularly assessed by evaluating chest excursion and thoracic auscultation.
273 Monitoring of minimum requirements as previously described continues during the immediate
275 6. Temperature: Monitoring of minimum requirements as previously described continues during the
277 7. Pain assessment should be performed utilizing a pain scoring instrument for acute postoperative pain
278 (e.g., the Feline Grimace scale, Glasgow Composite Measures Pain Scale-Short Form, UNESP-
279 Botucatu Multidimensional Composite pain scale). These scales have been validated to various
280 degrees in certain clinical situations (Reid et al. 2007; Evangelista et al. 2019; Belli et al. 2021).
281 Clinicians must evaluate which scale is most appropriate for their clinical setting.
282 8. Documentation must be provided using a written or electronic record of the postanesthetic recovery
283 anesthesia event, including drugs administered, monitoring values, and interventional notes (see
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284 Record Keeping section below).
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285 9. Patient discharge should only occur once the patient is normothermic, mentally oriented, and
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286 ambulatory (unless the disease or surgical intervention precludes this), nausea- and pain-free.
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287 Advanced Recommendations:
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289 regular time intervals until the patient's vital parameters have returned to normal and are deemed stable.
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291 Objective: To ensure adequate oxygenation and hemodynamic stability in sedated patients to prevent,
293 Sedation is a dynamic continuum of central nervous system (CNS) depression and drowsiness
294 during which the patient displays less awareness of their surroundings while continuing to be responsive
295 to noxious stimuli. When deep enough, sedation may overlap with general anesthesia (ASA 2024). For
296 any moderate to profound sedation procedure, monitoring of cardiopulmonary status is required, an
297 intravenous catheter should be placed, and endotracheal intubation equipment and supplemental oxygen
298 should be readily available. Emergency medications and reversal agents should be calculated with a
299 digital or printed drug calculation sheet and be immediately available. Discharge criteria for when a
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300 patient has recovered from sedation and is ready to be released to the client and home are similar to
302 Sedation can be classified as mild, moderate, or deep/profound. Depth of sedation is dynamic and should
304 1. Mild sedation: Patient will readily respond to stimuli but is less likely to exhibit anxiety, excitement,
305 or other behaviors that interfere with ability to complete minimally painful procedures, such as a
306 basic physical examination, simple blood draw, or minor grooming procedures. The patient may not
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307 become or remain recumbent. While respiratory or cardiovascular problems are rare, continual
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308 observation during mild sedation is recommended and objective monitoring equipment should be
314 2. Moderate sedation: Patient remains responsive to auditory stimuli, light tactile stimulation, can
315 reposition if assisted or stimulated but is otherwise content to lie recumbent. Patients can usually
316 maintain a patent airway, ventilate and oxygenate adequately, and maintain stable cardiovascular
317 function. However, they should be observed continuously and monitored for any change in
319 a. Supplemental oxygen (by face mask or nasal prongs) (Ambros et al. 2018).
323 e. Other monitoring equipment, including BP and ECG, when indicated by patient status
324 3. Deep or profound sedation: Patient is not easily aroused but may still respond to repeated or painful
325 stimuli. In this state they cannot readily maintain sternal recumbency or reposition from lateral
326 recumbency. Deeply sedated patients often require assistance to maintain a patent airway,
327 oxygenation, or ventilation, but cardiovascular function is typically maintained. Deeply sedated
328 patients must be monitored for respiratory and cardiovascular abnormalities. The following is
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329 recommended:
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330 a. Supplemental oxygen (e.g., via face mask, nasal prongs, oxygen collars, nasal cannula,
331 etc.) -p
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333 c. Consider monitoring ECG, noninvasive blood pressure, and capnography via nasal prong
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334 or catheter
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335 d. Intubation should be performed if the patient is not maintaining their airway or is not
338 Objective: To ensure patient safety and maintain a record of drug administration, physiological
340 The presence of vigilant, trained personnel during the perianesthetic period is a key determinant
343 1. The anesthesia care team may consist of a combination of veterinary anesthesiologists, non-
345 anesthesia and analgesia, credentialed veterinary technicians, and veterinary professionals in
346 training. In some jurisdictions, veterinary assistants and veterinary paraprofessionals may also be
348
349 2. A licensed veterinarian credentialed veterinary technician, veterinary student under the direct
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350 supervision of a licensed veterinarian, hereby known as the anesthetist, should be responsible and
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351 always remain with the anesthetized patient, whether using sedation, partial or total intravenous
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352 anesthesia, or inhalational anesthesia. In some jurisdictions, a veterinary assistant under the
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353 supervision of a licensed veterinarian or a veterinary paraprofessional may fill this role. This
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354 individual is responsible for the perianesthetic preparation of the patient, including perianesthetic
355 physical examination, equipment selection, including functional testing for accuracy, anesthetic drug
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357
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358 3. Equipment Checklist: The anesthetist should utilize a standardized anesthesia checklist, including an
360
361 4. Emergency drugs and reversal agents: Doses should be calculated prior to sedation or anesthesia and
362 immediately available to the anesthetist. A digital (printed or immediately available on a hand-held
364
365 5. Patient Evaluation: The anesthetist should perform patient history evaluation, review current
366 medication, and perform a patient physical examination prior to the administration of anesthetic
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367 drugs.
368
369 6. Anesthetic Protocol: An individual anesthetic protocol should be created for each patient; a licensed
371
372 7. Record Keeping: Documentation of the anesthetic procedure is a key component of anesthetic safety
373 during the event, for retrospective study, in case reviews, and is a part of the medical record.
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374 a. The anesthetist should create and maintain a written or electronic record of the perianesthetic
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375 anesthesia event, including recovery, documenting drugs administered, monitored
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376 physiologic values, and interventional notes.
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377 b. While vigilant monitoring of the patient is continuous, heart rate, arterial blood pressure,
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378 arterial oxygen saturation, and end-tidal carbon dioxide should generally be recorded every 5
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379 minutes, and all other physiological variables at least every 15 minutes. In unstable
380 hemodynamic conditions, more frequent recording may be desirable (Gravenstein 1989,
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382 8. Patient Monitoring: The anesthetist should use patient monitoring recommendations as described
383 above for circulation, ventilation, oxygenation, and temperature regulation through use of hands-on
384 patient evaluation and electronic or multiparameter devices. The anesthetist should monitor vital
386 9. Communication: Direct and frequent communication of patient status should occur between the
388 a. A surgical safety checklist, tailored to the environment, should be utilized by the anesthesia
389 and surgical team to ensure quality standards and assess perianesthetic communication.
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390 b. If complications arise during the anesthetic period, intervention is administered by the
392 c. If a patient is transferred to another team member, including during the immediate recovery
393 period, patient care communication must be directed from the anesthetist to the team
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397 Advanced Recommendations:
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398 1. A board-certified veterinary anesthesiologist should lead the anesthesia care team whenever
399 possible.
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400
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401 References
403 12/28/2024
404 Ambros B, Carrozzo MV, Jones T (2018) Desaturation times between dogs preoxygenated via face
405 mask or flow-by technique before induction of anesthesia. Vet Anaesth Analg 45(4), 452-458. doi:
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408 parameters/standards-for-basic-anesthetic-monitoring accessed 02/04/2025
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413 Belli M, de Oliveira AR, de Lima MT, et al. (2021) Clinical validation of the short and long UNESP-
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414 Botucatu scales for feline pain assessment. PeerJ 9:e11225. doi: 10.7717/peerj.11225.
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415 Bleijenberg EH, van Oostrom H, Akkerdaas LC, et al. (2011) Bispectral index and the clinically
416 evaluated anaesthetic depth in dogs. Vet Anaesth Analg 38(6), 536-543. doi: 10.1111/j.1467-
417 2995.2011.00651.x.
418 Brodbelt DC, Pfeiffer DU, Young LE, et al. (2007) Risk factors for anaesthetic-related death in cats:
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424 Chrimes N, Higgs A, Hagberg CA, et al. (2022) Preventing unrecognised oesophageal intubation: a
425 consensus guideline from the Project for Universal Management of Airways and international airway
427 Comroe JH & Botelho S. (1947) The unreliability of cyanosis in the recognition of arterial anoxemia.
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432 by directly measured blood pressure and ultrasonic Doppler flow detector in cats. J Vet Emerg Crit Care
434 Evangelista MC, Watanabe R, Leung VSY, et al. (2019) Facial expressions of pain in cats: the
435 development and validation of a Feline Grimace Scale. Sci Rep 9(1):19128. doi: 10.1038/s41598-019-
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437 Farrell KS, Hopper K, Cagle LA, et al. (2019) Evaluation of pulse oximetry as a surrogate for PaO2 in
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438 awake dogs breathing room air and anesthetized dogs on mechanical ventilation. J Vet Emerg Crit Care
440 Gravenstein JS, de Vries A, Beneken JE (1989) Sampling intervals for clinical monitoring of variables
442 Hogen T, Cole SG, & Drobatz KJ (2018) Evaluation of end-tidal carbon dioxide as a predictor of return
443 of spontaneous circulation in dogs and cats undergoing cardiopulmonary resuscitation. J Vet Emerg Crit
445 Hymczak H, Gołąb A, Mendrala K, et al. (2021) Core Temperature Measurement-Principles of Correct
446 Measurement, Problems, and Complications. Int J Environ Res Public Health 18(20):10606. doi:
447 10.3390/ijerph182010606.
448 Itami T, Aida H, Asakawa M, et al. (2017) Association between preoperative characteristics and risk of
449 anaesthesia-related death in dogs in small-animal referral hospitals in Japan. Vet Anaesth Analg 44(3),
451 Kennedy MJ & Barletta M. (2015) Agreement Between Doppler and Invasive Blood Pressure
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455 development and use in veterinary anesthesia. Vet Anaesth Analg 32, 241-255.
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Table 1. Summary of minimum and advanced monitoring recommendations for monitoring
physiological variables during anesthesia in dogs and cats. CNS = central nervous system;
variability index; PPV = pulse pressure variation; SPV = systolic pressure variation.
f
● ●
oo
including muscle tone, eye position, &
r
reflexes
CNS
-p ●
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Inspired/expired inhalant concentrations
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EEG-based monitors ●
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Continuous ECG ● ●
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Pulse oximetry ● ●
Co-oximetry ●
VENTILATION Capnography ● ●
Blood gas analysis ●
Spirometry ●
●: recommended
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oo
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Table 2. Characteristics of neuromuscular blockade (NMB) are assessed subjectively and
objectively. Note that normal function and minimal neuromuscular blockade cannot be
f
Moderate NMB TOF count 1–3 TOF count 1–3
oo
Deep NMB TOF count 0 TOF count 0
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-p
* via acceleromyography. TOF = train-of-four. The threshold for normal function has been
Deep or Profound
Moderate Sedation
Sedation
Mild Sedation Patient remains
Patient is not easily
Patient will responsive to auditory
aroused but may still
readily respond to stimuli, light tactile
Sedation respond to repeated or
stimuli. May or stimulation, can
Guidelines painful stimuli. The
may not assume reposition if assisted or
f
patient cannot readily
oo
lateral stimulated but is
maintain sternal
r
recumbency. otherwise content to lie
-p
recumbent.
recumbency or reposition
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from lateral recumbency.
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Dedicated
● ● ●
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anesthetist
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Pulse oximetry ● ●
Jo
Temperature ● ●
Oscillometric
capnography
☐ The authors declare that they have no known competing financial interests or personal relationships
that could have appeared to influence the work reported in this paper.
☒ The authors declare the following financial interests/personal relationships which may be considered
as potential competing interests:
AW Schultz reports a relationship with Midmark Corp that includes: employment. J Sager reports a
relationship with Midmark Corp that includes: consulting or advisory. VAA Editor in Chief DSJ Pang If
there are other authors, they declare that they have no known competing financial interests or
personal relationships that could have appeared to influence the work reported in this paper.
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