Manual of Equine Anesthesia and Analgesia

Manual of Equine Anesthesia and Analgesia
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A fully updated new edition of this practical guide to managing anesthesia in horses and other equids, providing updated and expanded information in a concise, easy-to-read format  Manual of Equine Anesthesia and Analgesia  provides practitioners and veterinary students with concise, highly practical guidance to anesthetizing horses, donkeys, and mules. Using a bulleted quick-reference format, this popular resource covers the basic physiological and pharmacological principles of anesthesia, patient preparation and monitoring, and the management of sedation and anesthesia. Chapters written by leading veterinary anesthesiologists contain numerous clinical images and illustrations, case examples, tables, diagrams, and boxed summaries of important points.  Now in full color, the second edition features extensively revised and updated information throughout. New sections cover chronic pain, management of horses undergoing MRI, ventilators, nerve blocks for reproductive surgery, muscle relaxants, various new drugs, paravertebral anesthesia, treatment of pain using acupuncture and physical rehabilitation techniques, and more. Up-to-date appendices contain drug lists and dosages as well as equations related to equine cardiovascular and respiratory systems. This concise, easy-to-follow guide:  Provides practical, clinically oriented information on anesthetizing equids Uses a bulleted format designed for fast access of key information Offers step-by-step instructions and diagrams of nerve blocks of the limbs, head, and ophthalmic structures Includes new coverage of topics including regulation of extracellular fluid and blood pressure, acid-base disorders, and hemodynamic effects of autonomic drugs  Manual of Equine Anesthesia and Analgesia, Second Edition,  remains a must-have resource for all equine practitioners and veterinary students involved with anesthetizing horses.

Оглавление

Группа авторов. Manual of Equine Anesthesia and Analgesia

Table of Contents

List of Tables

List of Illustrations

Guide

Pages

Manual of Equine Anesthesia and Analgesia

List of Contributors

Preface

Acknowledgments

1 Preoperative Evaluation and Patient Preparation. The Risk of Equine Anesthesia

I Risk of equine anesthesia

II Classification of physical status (see Box 1.1)

Box 1.1 ASA Classification System

III Risk factors. A Age and physical status

B Type of surgery and recovery

C Time of day

D Body position

E Drug choice

F Duration and management of anesthesia

Suggested Reading

Patient Preparation

I Preparation of the horse. A Evaluation

B Laboratory tests

C Physical examination

D History

E Fasting

F Medications

G Jugular catheter

H Flushing the oral cavity

I Removal of shoes

Suggested Reading

2 Serum Chemistry and Hematology

I Complete blood count (CBC) A Erythrocytes

B Leukocytes

Neutrophils

Eosinophils

Lymphocytes

Monocytes and Basophils

C Platelets

Thrombocytosis (platelet count >400 000/μl)

Thrombocytopenia (platelet count <75 000/μl)

II Blood chemistry interpretation

A Creatine kinase (CK)

B Aspartate aminotransferase (AST)

C Gamma glutamyl transferase (GGT)

Urinary GGT

D Alkaline phosphatase(ALP)

E Sorbitol (Iditol) dehydrogenase (SDH)

F Total bilirubin(TBIL)

G Serum bile acids(SBA)

H Blood urea nitrogen(BUN) andcreatinine(Cr)

Pre‐renal azotemia

Renal azotemia

Post‐renal azotemia

III Plasma proteins

A Albumin

Hypoalbuminemia can result from:

B Globulins

Hyperglobulinemia

Hypoglobulinemia

C Fibrinogen

IV Lactate

Suggested Reading

3. The Cardiovascular System: Physiology of the Cardiovascular System

I Anatomy. A Chambers

Atria

Ventricles

Atrio‐ventricular valves

Semilunar valves

B Structural or “skeletal” components of the heart

C Neural input to the heart

II Cardiac contractions. A Initiation

B Components of the specialized electrical conducting system

III Unique features of the equine heart

IV Circulatory systems

A Components of the systemic circulation

B Components of the pulmonary circulation

C Blood

V Cardiovascular physiology

A Events occurring during late diastole

B Events occurring during systole

C Events occurring at the end of the ejection period (late systole/early diastole)

D Events occurring during early diastole

VI Cardiovascular function and clinical applications

A Cardiac output

Factors affecting cardiac output:

B Heart rate

Factors influencing HR:

C Stroke volume (SV)

Preload

Afterload

Contractility (inotropy)

Relaxation (lusitropy)

D Blood Pressure (see Table 3.2)

E Physics of flow

Ohm's law

Poiseuille's law (Hagan‐Poiseuille)

Laplace's law

Starling's law (Frank‐Starling mechanism, see Table 3.1)

F Tissue oxygen delivery

Box 3.1 Effects of Decreases in [Hb] and SaO2 on CaO2

VII Anesthesia. A Effects of anesthetic drugs (see Table 3.3)

B Effects of cardiovascular disease

VIII Cardiovascular disease in horses presented for anesthesia. A Diseases of the conducting system

Atrial fibrillation

B Congenital disease

C Primary myocardial disease

D Secondary cardiovascular compromise

IX Anesthetic plan for horses with cardiovascular disease. A Patient preparation

B Sedation and induction

C Maintenance

D Recovery

Evaluation of the Cardiovascular System

I Cardiovascular evaluation. A Body condition

B Edema

C Mucous membranes

Color:

Moistness:

Exposure:

Capillary refill time(CRT):

D Peripheral arteries (pulses)

Sites for palpation:

Assessment of the pulse:

E Peripheral veins

Jugular vein waveforms

Occluding the jugular vein

F Heart. Cardiac silhouette

Heart rate

Heart rhythm

Auscultation

Left side heart sounds:

Right side heart sounds:

Normal heart sounds (see Figure 3.1)

ECG (see Section III below)

II Heart murmurs

A Location

B Timing in cardiac cycle

C Intensity

Sounds

D Physiologic (non‐pathologic) murmurs

E Pathologic murmurs

III Electrocardiogram. The elements of the ECG (see Figure 3.3)

B Evaluation of the ECG

Is each QRS complex preceded by a P wave?

Is each P wave followed by a QRS complex?

IV Arrhythmias

A Bradycardia

B Tachycardia

C Second‐degree AV blockade (see Figure 3.4)

D Atrial fibrillation (see Figure 3.5)

Treatment of atrial fibrillation

E Atrial flutter

F Premature atrial contractions(PACs)

Treatment

G Premature ventricular complexes(PVCs) (see Figures 3.6 and 3.7)

Treatment of single PVCs

Treatment of multiple PVCs

H Ventricular tachycardia(VT) (see Figure 3.8)

Treatment

Suggested Reading

4 The Respiratory System: Anatomy of the Equine Respiratory System

I Organization of respiratory system

A Conducting components

B Gas exchange components

II Tubular organs

A Tunica mucosa

B Tunica submucosa

C Tunica muscularis

D Tunica adventitia

III Nasal cavity

IV Paranasal sinuses

V Pharynx

Guttural pouch

VI Larynx (see Figure 4.1)

A Cartilages

B Innervation of the larynx

VII Trachea

VIII Lungs and pulmonary circulation

A Blood supply

B Nerve supply

IX Bronchi and bronchioles

X Respiratory epithelium

XI Alveolar region

A Alveoli

B Type I pneumocytes

C Type II pneumocytes

XII Blood–air barrier

XIII Muscles of respiration

Suggested Reading

Physiology of the Respiratory System

I Alveolar ventilation (VA)

A Mechanics of ventilation

B Work of breathing

C Lung and airway resistance

II Lung volumes (see Figure 4.2) A Minute ventilation (VE)

B Tidal volume (VT)

C Dead space

D Measurement of dead space – Bohr equation

Factors that increase dead space include

E Functional residual capacity(FRC)

III Pulmonary compliance

A Distribution of alveolar ventilation

B Factors decreasing pulmonary compliance

IV Alveolar perfusion. A Lung blood flow

B Distribution of blood flow in lung

C Hypoxic pulmonary vasoconstriction

D Ventilation/perfusion (V/Q) ratio (see Figure 4.4)

V Alveolar gas exchange. A Composition of gases

B Movement of gases

C Factors influencing diffusion

D Carbon dioxide

E Oxygen

F Alveolar‐arterial oxygen gradient [P(A-a)O2]

G Arterial/alveolar ratio

H Oxygen carriage

I Oxygen binding to Hb

J Shunting and oxygenation

VI Effects of sedation and anesthesia on respiratory function. A Sedation

B General anesthesia

C Mechanisms for decreased oxygenation

Suggested Reading

Evaluation of the Respiratory System

A Patient history

B Physical examination

Auscultation

Airway Management

I Larynx. A Function

B Innervation

C Recurrent laryngeal nerve neuropathy

D Iatrogenic laryngeal neuropathy

E Hyperkalemic periodic paralysis(HYPP)

II Assessment of airway. A History

B Physical examination

C Situations in which difficulty is to be expected

III Airway equipment

A Mouth gag

B Laryngoscope

C Endotracheal tubes

D Inflatable cuffs

IV Complications of airway intubation. A Tissue damage

B Edema

C Over inflation of the cuff

D Lubrication

V Intubation of trachea. A Difficulty

B Position

C Technique

D Confirmation of tracheal tube placement

E Intubation of the difficult airway

VI Extubation of the trachea

VII Airway obstruction

A Signs of airway obstruction include:

B Laryngospasm

C Obstruction of the upper airway. At induction

Management

Intraoperative obstruction

At extubation

Management

D Obstruction of the nasal passages due to edema

E Obstruction of the nasal passages due to nasal bleeding

Suggested Reading

Tracheostomy

I Terminology

Temporary tracheostomy

Permanent tracheostomy (see Figure 4.11)

II Indications

III Surgical anatomy

IV Tracheostomy tubes (see Figure 4.12)

V Technique

VI Post‐operative care

VII Complications

Suggested Reading

5 The Renal System

I Role of the kidney

II Normal anatomy and physiology

A The nephron

The glomerulus

Proximal convoluted tubule

Loop of Henle

Distal convoluted tubule(DCT)

Collecting duct

Equine urine

B Renal blood flow and GFR. Renal blood flow(RBF)

Renal plasma flow(RPF)

Filtration fraction(FF)

Glomerular filtration rate(GFR)

Autoregulation

Tubuloglomerular feedback(TGF)

C Urine formation

D Urine volume in the horse

Comments:

III Renin‐Angiotensin‐Aldosterone‐System(RAAS) (see Figure 5.2)

Renin

Angiotensin I to Angiotensin II

Effects of Angiotensin II

Angiotensin III and IV

Aldosterone

Angiotensin‐converting enzyme (ACE) inhibitors (e.g. enalapril)

IV Effects of anesthetics on renal function

A Changes in RBF with anesthetics

B Inhalational anesthetics

Methoxyflurane

Sevoflurane

Compound A

C α2 adrenergic agonists

D Other injectable sedatives and anesthetics. Phenothiazines

Benzodiazepines

Opioids

NMDA antagonists

Propofol

E Intermittent positive pressure ventilation

F Stress

V Diuretics

A Osmotic diuretics (e.g. mannitol)

B Carbonic anhydrase inhibitors (e.g. acetazolamide)

Use in potential HYPP episodes: (see HYPP Chapter 38)

C Loop diuretics (e.g. furosemide)

D Thiazide diuretics (e.g. hydrochlorothiazide)

E Potassium sparing diuretics

Aldosterone inhibitors (e.g. spironolactone)

Sodium channel blockers (e.g. amiloride)

VI Nonsteroidal anti‐inflammatory drugs

Suggested Reading

6 Neurophysiology and Neuroanesthesia

I Neurophysiology. Membrane potentials

B Synaptic transmission

C Brain metabolism

D Cerebral blood flow

E Cerebral perfusion pressure(CPP)

F Cerebrospinal fluid(CSF)

II Central nervous system pathophysiology. A Seizures

B Intracranial pressure (ICP) increase

III Neuroanesthesia

A Cerebral metabolic rate

B Cerebral blood flow and perfusion pressure. Anesthetic drugs

Increased PaCO2

Positive pressure ventilation of lungs

Venous return

Head position

C Autoregulation

IV Neuroanesthesia for specific procedures

A CSF withdrawal

B Increased intracranial pressure. Includes head trauma, abscess, and tumor removal

Preparation

Sedation, premedication, and induction

Induction of anesthesia in foals

Sedation of adult horses

Maintenance of anesthesia

C Cerebral edema

Drug‐induced decompression

Ventilation

D Seizures

Anesthesia of horses prone to seizures

Suggested Reading

7 The Autonomic Nervous System

I General organization of the ANS (functional anatomy)

A Central autonomic nervous system

B Peripheral autonomic nervous system

C Afferent input

D Efferent output

II Physiology of the autonomic nervous system. A Neurotransmitters

B Synthesis, duration of action, and degradation of ACh

C Synthesis, duration of action, and removal of NE

D Receptors on the effector organs. Cholinergic receptors are subdivided into muscarinic and nicotinic

Adrenergic receptors are subdivided into alpha (α1 and α2), beta (β1 and β2), and dopaminergic (DA)

Dopaminergic receptors

III Function of the adrenal medulla. A SNS innervation of the adrenals

B Effect of NE release from adrenals

C Effect of EPI release from adrenals

IV Autonomic effects on the cardiovascular system. A The heart

B Systemic blood vessels

C Effects of SNS and PNS stimulation on arterial pressure

D Cardiovascular autonomic reflexes

V Autonomic effects on the pulmonary system

VI Pharmacology of the ANS. A Drugs that act on adrenergic effector organs (sympathomimetic drugs)

B Drugs that cause release of NE from nerve endings

C Drugs that have a PNS potentiating effect (anticholinesterase drugs)

D Drugs that block cholinergic activity at effector organs (antimuscarinic drugs) (see Table 7.5)

VII Clinical use of autonomic drugs

A Hypotension (see Chapter 38)

B Cardiac arrest

C Bradycardia

D Circulatory shock

E Bronchodilation

F Priapism (see Chapter 38)

G Reversal of neuromuscular block (see Chapter 15)

H Spasmolytic effect

Suggested Reading

8 Electrolyte and Fluid Therapy: Electrolytes

I Sodium

A Hyponatremia (<125 mEq/l)

B Hypernatremia (>155 mEq/l)

II Potassium

A Hypokalemia (<3.1 mEq/l)

B Hyperkalemia (>6.0 mEq/l)

III Chloride

A Hypochloremia (<90 mEq/l)

B Hyperchloremia (>110 mEq/l)

IV Calcium

A Hypocalcemia (<5.4 mEq/l)

B Hypercalcemia (>6.7 mEq/l)

Suggested Reading

Fluid Therapy

I Introduction

II Total body water

III Solute distribution

Effective osmoles

Effective osmolality

Osmolality

Osmolarity

Colloid oncotic pressure (COP)

ICF versus ECF

IV Fluid dynamics

Capillary hydrostatic pressure (Pc)

Capillary oncotic pressure (πC)

Interstitial hydrostatic pressure (Pi)

Interstitial oncotic pressure(πi)

A Starling's equation

B Revised Starling equation

V Administration of exogenous fluids

A Crystalloids

B Colloids

Synthetic colloids

Clinical use of colloids:

Adverse effects of colloids:

Suggested Reading

9 Acid‐Base Physiology: Traditional Approach

Acidemia

Acidosis

Alkalemia

Alkalosis

I Traditional approach to acid‐base interpretation. A Henderson‐Hasselbalch equation

Lewis Acid

Values for the Henderson‐Hasselbalch equation

B pH and hydrogen ions (see Box 9.1)

C Buffers

The carbonic acid‐bicarbonate buffer system

Non‐bicarbonate buffer systems

Role of the renal system in buffering

D Base excess

E Total CO2 (TCO2)

F Anion gap

G Primary disturbances in acid‐base (see Table 9.1)

Sodium bicarbonate dose is generally calculated as follows:

Anion gap

Winter's formula for use in metabolic acidosis

Winter's formula for use in metabolic alkalosis

Physicochemical Approach

I Brief review of physicochemistry and definitions

A Strong electrolytes

B Weak electrolytes

C Law of electroneutrality

D Strong ion difference(SID) variables

PaCO2

Strong ion difference

Total weak acid concentration (Atot)

E Strong ion gap and unmeasured anions

II Acid‐base disorders: definitions

III Examples of metabolic abnormalities causing acid‐base derangements

A SID acidosis. Hyperchloremia

B Lactic acidosis

C SID alkalosis. Hypochloremic alkalosis

D Atot acidosis

E Atot alkalosis

IV Examples of the physicochemical approach. Example 1:

Example 2:

Suggested Reading

10 Hemostasis and Hemotherapy: Hemostasis

I Normal physiology

II Primary hemostasis. A Adhesion

B Activation

C Aggregation

D Thrombin

E Platelet plug formation

III Secondary hemostasis. A Enzymatic reactions

B Cascade or waterfall model of coagulation

C The cell‐based model of coagulation

Initiation stage

Amplification

Propagation

D Anticoagulants

IV Fibrinolysis

V Coagulation testing

A Primary hemostasis

B Secondary hemostasis

C Fibrinolysis

D Coagulation profiles

E Viscoelastic coagulation tests

VI Coagulopathy

A Defects in primary hemostasis

B Defects in secondary hemostasis

C Hereditary and acquired causes of hypocoagulation

D Treatment for bleeding patients

E Thrombosis

Therapy

F DIC

Clinical signs

Treatment

Hemotherapy

I Indications for hemotherapy

A Oxygen delivery (DO2)

B Preload

Colloid osmotic pressure (COP)

C Diseases resulting in low [RBC]/[Hb] include

D Transfusion triggers

Acute blood loss

Clinical signs of hypovolemic shock

Chronic anemia

Immunoglobulins

II Types of blood products

Whole blood

Autotransfusion

Plasma products

Fresh plasma

Fresh frozen plasma

Frozen plasma

Platelets

Packed red blood cells (pRBC)

III Collecting blood products

A Donors

B Blood typing of donors

C Recipient

D Crossmatching

E Emergency transfusions

Blood collection

IV Administering blood products

Non‐hemolytic reactions

Hemolytic reactions

Replacement of TP/albumin

Box 10.2 Plasma Volume for Transfusion in Hypoproteinemia

Suggested Reading

11 Thermoregulation

I Introduction

II Physics principles applied to thermoregulation

III Mechanisms of heat transfer

A Conduction

Clinical example

B Convection

Clinical examples

C Evaporation

Clinical example

D Radiation

Clinical example

IV Homeostasis of body temperature

V Control of body temperature

A Afferent mechanism

B Central mechanism

Autonomic control

Behavioral control

C Effector mechanism

Autonomic responses

Behavioral responses

VI General considerations regarding thermoregulation during anesthesia

A Effects of individual drugs on thermoregulation

VII Physiologic consequences of hypothermia. A Central nervous system

B Cardiovascular system

C Respiratory

D Miscellaneous

VIII Classification of hypothermia. A Etiology‐based

B Temperature‐based

IX Hypothermia in the foal

X Hypothermia in the adult horse

XI Prevention and treatment of hypothermia

A Proactive heat management

Methods of preventing hypothermia include:

B Warming Devices. Passive

Active

Other considerations

XII Hyperthermia

A Clinical signs of hyperthermia include

B Treatment of horses with hyperthermia

Suggested Reading

12 Pharmacology of Drugs Used in Equine Anesthesia: Phenothiazines

I Mechanism of action of acepromazine

II Physiologic effects

III Clinical use of acepromazine. A Standing sedation

B Premedication prior to general anesthesia

C Contraindications

Suggested Reading

Butyrophenones

I Mechanism of action

II Physiologic effects

III Clinical use of azaperone

IV Contraindications

Suggested Reading

α2‐Adrenergic Agonists

I α2‐receptor subtypes

A α2A subtype

B α2B‐subtype

C α2C‐subtype

II Mechanism of action

III Physiological effects

IV Clinical use of α2 agonists. A Standing sedation

B Premedication prior to general anesthesia

C Maintenance of anesthesia

D Epidural analgesia

E Individual drugs

V Contraindications

VI Adrenergic antagonists

A Mechanism of action

B Physiologic effects

C Clinical use

D Adverse reactions

E Vatinoxan (MK‐467)

Suggested Reading

Opioids

I Opioid receptor types

A Mu (μ) opioid receptor (MOP, OP3)

B Kappa (κ) opioid receptor(KOP, OP2)

C Delta (δ) opioid receptors(DOP, OP1)

II Mechanism of action

A Full agonists

B Partial agonists

C Mixed agonist/antagonists

D Antagonists

III Physiologic effects of opioids. A Central nervous system

B Cardiovascular system

C Respiratory system

D Gastrointestinal system

E Urinary system

F Miscellaneous

IV Clinical use of opioids. A Standing sedation

B Premedication prior to general anesthesia

C Epidural analgesia

D Opioids and ileus

V Individual drugs

Tramadol

I Mechanism of action

II Physiologic effects

III Clinical use

Suggested Reading

Trazadone

I Mechanism of action

II Physiologic effects

III Clinical use

Suggested Reading

Benzodiazepines

I Mechanism of action

II Physiologic effects

III Clinical use

A Chemical restraint

B Induction of anesthesia

C Maintenance of anesthesia

D Individual benzodiazepine drugs

IV Benzodiazepine antagonists. A Flumazenil

B Mechanism of action

C Physiologic effects

D Clinical use

Suggested Reading

Guaifenesin

I Mechanism of action

II Physiologic effects

III Clinical use

A To improve induction quality

B To maintain anesthesia

IV Contraindications

Suggested Reading

Ketamine

I Mechanism of action

II Physiologic effects

III Clinical use. A Induction of anesthesia

B Maintenance of anesthesia

C MAC reduction

D Epidural analgesia

E Analgesia in the awake horse

F Potentiation of α2‐induced sedation in standing horse

Suggested Reading

Tiletamine and Zolazepam (TZ)

I Mechanism of action

II Physiologic effects

III Clinical use

A Induction of anesthesia

Suggested Reading

Alfaxalone

I Mechanism of action

II Physiologic effects

III Clinical use

A Induction of anesthesia

B Maintenance of anesthesia

Suggested Reading

Propofol

I Mechanism of action

II Physiologic effects

III Clinical use

A Induction of anesthesia

B Propofol as a co‐induction drug with ketamine

C Maintenance of anesthesia

Suggested Reading

Barbiturates

I Receptor activity of barbiturates

A Use for euthanasia

Intravenous lidocaine

I Mode of action

II Clinical use of intravenous lidocaine. A As an adjunct to general anesthetics

B To provide analgesia in the awake horse

III Metabolism

VI Adverse effects

A CNS effects

B Cardiovascular effects

C Methemoglobinemia

Suggested Reading

Horse‐related drug Regulations in Europe

I Regulations

II Anesthesia‐related drugs that are not allowed in food producing animals

13 Inhalational Anesthetics

I Introduction

II Mechanism of action

Immobility

Unconsciousness

III Minimum alveolar concentration (MAC)

A MAC Derivatives

B Factors that decrease MAC

C Factors that increase MAC

IV Pharmacokinetics

A Absorption

The rate of delivery of anesthetic to the alveoli is determined by the following factors. The inspired partial pressure of inhalant (Pi)

Vaporizer setting

Oxygen flow rate

Volume of anesthetic circuit

C Alveolar ventilation and alveolar partial pressure (PA)

D The rate at which the anesthetic is removed from the alveolus

Solubility of the anesthetic in blood (see Table 13.1)

Cardiac output of the patient

Alveolar‐to‐venous partial pressure difference

E Distribution

F Metabolism

Elimination

V Pharmacodynamics. A Cardiovascular effects

B Respiratory effects

C Central nervous system effects

D Renal effects

E Hepatic effects

F Analgesia

VI Nitrous oxide

A Mechanism of action

B Pharmacokinetics

C Pharmacodynamics

D Clinical use of N2O

Suggested Reading

14 Local Anesthetics

I Mechanism of action

II Physicochemical properties. A Chemical structure

B Structure–activity relationships. Molecular weight(MW)

pKa

Lipid solubility

Protein binding

Stereoisomerism

III Pharmacokinetics. A Absorption

Dose

Injection site

Lipid solubility

Vasoconstrictors

B Distribution

Effect of pulmonary uptake

Effect of hypercapnia

C Metabolism and excretion

Aminoesters

Aminoamides

IV Local anesthetic adjuvants and combinations. A Epinephrine

B α2 agonists. Effects on peripheral nerve blocks

Effects on epidural anesthesia

C Bicarbonate

D Hyaluronidase

E Carbon dioxide

F Combinations of local anesthetics

V Local anesthetic toxicity

A Systemic toxicity. CNS

Cardiovascular system(CVS)

Blood

B Local tissue toxicity. Neurotoxicity

Chondrotoxicity

C Allergic reactions

VI Local anesthetic agents. A Lidocaine (see Table 14.3)

B Mepivacaine

C Bupivacaine

D Ropivacaine

E Proparacaine and Tetracaine

F Procaine

VII Clinical use. A Local and regional techniques

B Intravenous lidocaine

Suggested Reading

15 Neuromuscular Blocking Agents in Horses

I Introduction

II Physiology of the neuromuscular junction

III Neuromuscular blocking agents

A Pharmacology

B Physiology

III Individual NMBAs. A Benzylisoquinolones

Atracurium

Cisatracurium

B Neurosteroids

Vecuronium

Rocuronium

C Residual NMB

IV Pharmacologic reversal of NMB. A Acetylcholinesterase inhibitors

Clinical implications:

B Reversal drugs

C Selective relaxant binding agents

Suggested Reading

16 Non‐steroidal Anti‐Inflammatory Drugs and Corticosteroids. Non‐steroidal Anti‐Inflammatory Drugs

I Arachidonic acid cascade

A Isoenzymes of COX

B Synthesis of prostaglandins

C Role of prostaglandins

II Mechanism of action of NSAIDs

III Clinical uses of NSAIDs. A Musculoskeletal analgesia

B Use in gastrointestinal (GI) disease

C Anti‐endotoxin effects

D Perioperative analgesia

IV Specific NSAIDs used in equine practice. A Flunixin meglumine

B Phenylbutazone

C Diclofenac

D Firocoxib

E Meloxicam

F Grapiprant

V Adverse effects of NSAIDs. A Gastrointestinal tract

Stomach and Duodenum

NSAID‐induced enteropathy

B Renal effects

C Hematologic

D Risk factors for NSAID related adverse effects

Corticosteroids

I Mechanism of action of glucocorticoids

II Clinical uses of glucocorticoids. A Musculoskeletal injuries

B Noninfectious inflammatory airway disease

C Immunosuppression

D Topical administration

E Mating‐induced endometritis

III Specific glucocorticoids used in equine practice. A Dexamethasone

B Prednisone

C Prednisolone

D Betamethasone

E Triamcinolone

F Isoflupredone

IV Inhaled corticosteroids

A Fluticasone

B Beclomethasone

V Adverse effects of glucocorticoids. A Musculoskeletal system

B Gastrointestinal Tract

C Metabolic effects

D Coagulation

E Hepatic

F Suppression of HPAA

G Immunosuppression

H Wound healing

Suggested Reading

17 Anesthetic Machines and Equipment

I Introduction

II High‐pressure system

A Cylinder storage of oxygen

Box 17.1 Oxygen Cylinder Conversion Factors

B Pressure regulators

C Liquid oxygen storage

D Oxygen concentrators

III Intermediate‐pressure system

IV Low‐pressure system

A Flowmeter

B The anesthetic vaporizer

C The common gas outlet

D Breathing circuits

E Components of the circle system. One‐way valves

Breathing circuit

Carbon dioxide (CO2) absorbent

Reaction of CO2 with soda lime

Reservoir bag

Adjustable pressure limiting (APL) valve (“pop‐off valve”)

V Time constant for anesthesia circuit (τ)

VI Scavenging system

Collection mechanism

Connection to interface

Interface

Connection to elimination system

Elimination system

VII Ventilators

A Mallard Large Animal Anesthesia Ventilator System

B Drager/Anesco

C Tafonius

D Bird mark respirator

VIII Endotracheal tubes

A Cleaning endotracheal tubes

IX Demand valves

Suggested Reading

18 Positioning the Anesthetized Horse

I Introduction

II Problems associated with recumbency

III Preventing complications in lateral recumbency. A Padding

B Positioning

IV Preventing complications in dorsal recumbency. A Padding

B Positioning (see Figures 18.2–18.6)

V Dorsal recumbency with head‐down position (Trendelenburg)

A Circulatory changes

B Ventilatory changes

Suggested Reading

19 Monitoring the Anesthetized Horse. Monitoring the Central Nervous System

I Awareness during anesthesia

II Monitoring the depth of anesthesia

III Methods of monitoring the depth of anesthesia. A Evaluation of the eye. Position

Nystagmus

Lacrimation

Palpebral reflex

Corneal reflex

Effects of Ketamine or Tiletamine

B Movement

C Anal tone

D Physiologic parameters

E Concentrations of inhalational anesthetic in expired gases

F Quantitative EEG (See Section IV below) IV EEG

A EEG findings in the horse

EEG recording in the horse

B Auditory evoked potentials (AEP)

C Bispectral index (BIS)

BIS in the Horse

Suggested Reading

Cardiovascular Monitoring

I Direct palpation of arterial pulse

II ECG

III Blood pressure monitoring

A Non‐invasive (indirect) arterial blood pressure measurement

Oscillometric technique

B Invasive (direct) arterial blood pressure measurement

Inaccuracies in measurement

Complications of arterial catheterization

IV Cardiac output monitoring

Indicator‐based methods

A Thermodilution

B Lithium dilution

Technique

Disadvantages:

C Fick method

Disadvantages:

D Imaging methods

Pulse contour analysis

Echocardiography

Transthoracic bioimpedance

Suggested Reading

Respiratory Monitoring

I Monitoring respiratory rate and tidal volume. A Spontaneous ventilation

B Controlled ventilation

Pressure‐volume and flow‐volume loops

II Monitoring carbon dioxide

A Minute ventilation (VE)

B Alveolar ventilation (VA)

III Types of capnographs and capnometers. A Time capnography

B Volume capnography

IV Types of gas CO2analyzers. A Sidestream capnometers

Advantages:

Disadvantages:

B Mainstream capnometers

Advantages:

Disadvantages:

V Normal time capnogram (see Figure 19.10)

A Phase I

B Phase II

C Phase III

D Phase 0

VI Abnormal PECO2 values and waveforms. A Absence of PECO2 waveform

B Cardiogenic oscillations

C Widened α angle

D Widened β angle

E Elevated baseline

F Hypoventilation

G Hyperventilation

H Resisting the ventilator

I Cardiac arrest

VII Monitoring the inspired oxygen concentration

Technology

VIII Pulse oximetry

A Types of pulse oximeters

Transmission probe (see Figure 19.18a)

Reflectance probes (see Figure 19.18b)

Co‐oximetry

B Technology

Transmission pulse oximetry

Reflection pulse oximetry

C Factors that may affect accuracy

D Advantages of pulse oximetry

E Disadvantages

IX Arterial blood gas analysis

A Arterial oxygen partial pressure (PaO2)

B Arterial carbon dioxide partial pressure (PaCO2)

Suggested Reading

Anesthetic Agent Monitoring

I Technology

A Factors that may affect accuracy

Monitoring Temperature

I Thermal compartments. Core compartment

Peripheral compartment

II Monitoring sites. A Core temperature. Pulmonary artery

Aorta

B Near‐Core

Rectum

Esophagus

Nasopharynx

Urinary bladder

C Peripheral. Skin

III Technologies

Thermistor (see Figure 19.19)

Thermocouple

Infra‐Red

IV Hazards of temperature monitoring. Thermal burn

Probe contamination

Incorrect temperature readings

Faulty probe

Suggested Reading

Monitoring Neuromuscular Function

I Peripheral nerve stimulation

A Current

B Duration of stimuli

C Pattern of stimulation

II Repetitive stimulation and fade. A TOF

Advantages of TOF

III Methods to measure the evoked response. A Mechanomyography

B Alternative methods

Visual or tactile:

Acceleromyography (AMG):

Electromyography

IV Peripheral motor nerves used for monitoring neuromuscular blockade

Peroneal:

Radial:

Facial:

Suggested Reading

20 Standing Sedation

I Indications for standing sedation

II Advantages of standing sedation over general anesthesia

III Disadvantages of standing sedation

IV Patient evaluation and preparation

V Drug administration

A Premedication with IM administered drugs

Examples of IM Premedication Protocols

B Bolus injections

Examples of IV Bolus Doses of alpha2 Agonists ± an Opioid

C Continuous rate infusions (CRI)

Examples of α2‐agonist CRIs

D Opioids as part of the CRI. Examples of Opioid Doses (IV) When used in Conjunction with an α2 Agonist

E Ketamine use in standing sedation

F Intravenous lidocaine use in standing sedation

G Reversal of sedation

21 General Anesthesia Techniques

I Sedation

A Reasons to sedate prior to anesthesia induction

B Drugs used for sedation prior to induction

II Induction of anesthesia

A Drugs used for induction of anesthesia (see Table 21.2)

III Maintenance of anesthesia

Inhalational Anesthesia

I Clinical use of inhalational anesthetics

II Potential advantages of inhalational anesthesia

III Potential disadvantages of inhalational anesthetics

IV Recovery quality

Total Intravenous Anesthesia (TIVA) I Potential advantages of TIVA over inhalational anesthesia

II Potential disadvantages of TIVA

III Methods of drug delivery

A Intermittent injection of drugs

B Drip technique

C Infusion pump

D Syringe pump

E Computerized syringe pump

IV Choice of injectable drugs

V Drug combinations used for TIVA

A α2 agonists + Ketamine

B α2 agonist + Ketamine + Guaifenesin

C Propofol

D Alfaxalone

Partial Intravenous Anesthesia (PIVA)

I Potential advantages of PIVA

II Potential disadvantages of PIVA

III Choice of IV drugs for PIVA

IV Drugs and drug regimens used in PIVA

A Lidocaine

B α2 agonists

Medetomidine/Dexmedetomidine/Xylazine

Dexmedetomidine

Xylazine

Detomidine/Romifidine

C Ketamine

D Ketamine and α2 agonists

E Lidocaine + Ketamine

Suggested Reading

22. Anesthesia of the Head and Neck. Anesthesia of the Head

A Infraorbital nerve block

Location

Technique (within the infraorbital canal)

B Maxillary nerve block

Location

Technique

C Mandibular alveolar (or inferior alveolar) nerve block

Location

Extra‐oral approach

Intra‐oral approach

D Mental nerve block

Location

Technique (within the mandibular canal)

E Ethmoidal nerve block

Location

Technique

Suggested Reading

Maxillary Nerve Block in Donkeys

I Indications

II General principles. A Local anesthetic drug selection and doses

B Ultrasound‐guided maxillary blockade allows for:

C Equipment

III Patient preparation. A Physical restraint

B Chemical restraint

C Preparation of injection site

IV General technique

Needle insertion. Blind technique

Ultrasound guided approach

V Checking for desensitization

VI Complications

VII Specific techniques for maxillary block. A Blind maxillary nerve block

Angled approach (see Figure 22.6)

Perpendicular approach (see Figure 22.7)

B Ultrasound‐guided maxillary nerve block (see Figure 22.8)

Cervical Plexus Block

I Introduction

II Indications for the block

III Contraindications

IV Clinical anatomy (see Figure 22.10)

V Expected distribution of anesthesia

A Local anesthetic

B Patient preparation and positioning

VI Step‐by‐step performance of the block. A Surface anatomy and landmarks (see Figure 22.12)

B Ultrasound anatomy (see Figure 22.13)

C Needle insertion technique (see Figure 22.14)

VII Complications

Suggested Reading

23 Anesthesia of the Eye

I Restraint. A Intravenous sedation

II Topical local anesthesia. A Topical anesthesia

B Proparacaine and tetracaine

C Adverse effects of topical anesthetics

III Subconjunctival anesthetic injection. A Technique

B Indication

IV Subcutaneous injectable local anesthesia. A Technique

B Local anesthetic drugs

C Adjunctive agents

Hyaluronidase

Epinephrine

Bicarbonate

α2agonists

D Methods of using injectable local anesthetics

V Motor nerve blocks. A Auriculopalpebral nerve (see Figure 23.1 and 23.2)

Location

VI Sensory nerve blocks (see Figures 23.1–23.3) A Supraorbital nerve

Location

Technique

B Lacrimal nerve

C Infratrochlear nerve

D Zygomatic nerve

VII Deep orbital nerve blocks. A Nerves blocked

Oculomotor nerve

Trochlear nerve

Trigeminal nerve

Abducens nerve

B Techniques. Four‐point block

Peterson‐type block

Supraorbital fossa block (see Figure 23.5)

C Potential complications of deep orbital blocks

VIII Field block anesthesia of the eye. A Line blocks

B Infiltration anesthesia of the eye

Suggested Reading

24 Anesthesia of the Limbs

I Indications

II General principles. A Selection of the local anesthetic drug and dose

B Deposition of local anesthetic

C Equipment

III Patient preparation. A Physical restraint

B Chemical restraint

C Preparation of the injection site

IV General technique

A Needle insertion

B Localization of lameness

V Checking for desensitization

VI Complications

VII Forelimb: distal aspect. A Palmar digital nerve block at the level of the cartilages of the foot

B Midpastern semi‐ring block

C PDN block at the level of the base of the proximal sesamoid bones (abaxial sesamoid, or basisesamoid, nerve block)

D Low four‐point nerve block (i.e. Low palmar nerve block)

E High four‐point block (i.e. High palmar nerve block)

F Lateral palmar nerve block

Site 1

Site 2

VIII Forelimb: proximal aspect

A Median nerve

B Ulnar nerve

C Medial cutaneous antebrachial nerve

IX Hind limb. A Plantar digital nerve block at the level of the cartilages of the foot

B Mid‐pastern ring block

C Plantar digital nerve block at the level of the base of the proximal sesamoid bones (abaxial sesamoid or basisesamoid nerve block)

D Low six‐point nerve block (i.e. low plantar nerve block)

E High six‐point nerve block (i.e. high plantar nerve block)

F Tibial and peroneal (Fibular) nerve blocks. Tibial Nerve

G Deep and superficial peroneal nerves

Suggested Reading

25. Anesthesia of the Perineum and Testicle. Pudendal Nerve Block – Electrostimulation Technique

I Target nerves and region anesthetized

II Location (see Figure 25.3)

III Technique. Desensitizing superficial planes

Desensitizing the pudendal plexus

IV Choice and volume of anesthetic

V Caution

Pudendal Nerve Block – Blind Approach

A Location

B Technique

C Choice of anesthetic

Local Anesthesia for Castration

I Introduction

II Nerve supply

III Uptake and distribution of IT administered drugs

IV Volume of IT local anesthetic

Suggested Reading

26 Anesthesia of the Abdominal Wall. Thoracolumbar Paravertebral Block (TPVB) – Electrostimulation Technique

A Location

B Technique

Desensitizing superficial planes

Desensitizing the thoracolumbar nerves

Paravertebral Nerve Block – Blind Technique

I Indications

A Equipment

II Patient preparation. A Physical restraint

B Chemical restraint

C Preparation of injection site

III General technique

A Needle insertion

Transversus Abdominis Plane Block

I Indications

II Anatomy

III TAP block

A Flank approach

Technique

Results

B Intercostal ventral approach (see – Küls et al., Suggested reading)

Technique

Results

C Subcostal approach (see Suggested reading – Freitag et al.)

Technique

Results

Caudal Intercostal Block for Abdominal Surgery (CIBAS)

I Anatomy

Technique

Drugs administered

II Disadvantages of the CIBAS technique

Suggested Reading

27 Epidural Analgesia and Anesthesia

I Anatomy and technique for caudal epidural. A Location

B Technique

C Verification of needle or catheter placement

II Indications for epidural drug administration

III Contraindications

IV Effects. A Analgesia

B Anesthesia

C Other spinal effects

D Systemic effects

V Complications

VI Drugs. A Local anesthetics

Lidocaine (2%) or mepivacaine (2%)

Ropivacaine (0.5%)

B Opioids

Morphine (0.1–0.2 mg/kg)

Methadone (0.1 mg/kg)

C α2 agonists

Xylazine (0.17–0.22 mg/kg)

Detomidine (0.01–0.06 mg/kg)

D Ketamine

E Combinations. Opioids and α2agonists

Suggested Reading

28 Pathophysiology of Pain

I Introduction. A Acute vs. chronic pain

B Five general steps in the pain pathway

Transmission

Transduction

Modulation

Projection

Perception

II Ascending nociceptive pathways

III Types of nociceptors

Transient receptor potentialion channels (TRPs)

Neuronal sodium channels (NaV)

Acid‐sensing ion channels (ASICs)

Glutamate receptors

Neurokinin 1 receptors (NK‐1)

Lamellated corpuscles

IV Descending modulatory pathways

V Development of chronic pain states. A Peripheral sensitization

B Central sensitization

NMDA receptor

C Neuropathic pain

VI Physiologic consequences of pain

Suggested Reading

29 Pain Recognition in Horses

I Introduction

II Steps necessary to implement pain scoring in the hospital routine

A Select a practical and applicable pain scale

B Select a key person responsible for the procedures of clinical pain‐scoring

Develop local routines for pain scoring

D Assessment

E Conduct training sessions for all caregiving personnel

III How pain scoring is performed – key points

A Use a structured score sheet (e.g. Table 29.2)

B View the horse, as discretely as possibly, during a quiet time in the stall

C Timing

D Recommended intervals for assessing pain

Recommendations

IV Video assistance. Key points

V Factors that influence pain scoring. Key points

A Baseline measures or input from owner should be considered

B Fear and stress

C Medication

D Owner contact and other social intervention

VI Interpretation of pain scores. Key points

VII Guide on how to use the Equine Pain Scale (EPS) (see Table 29.2) Key points

A Detailed description of the EPS

B Pain Face, present or not

C Gross pain behavior

D Activity

Location in the stall

F Posture/weightbearing

G Head position

H Attention toward the painful area

I Interactive behavior

J Response to food

VIII Interpretation and actions due to EPS Pain Scores

A Key points – Action for score “4”

Suggested Reading

30 Management of Pain:The Pharmacologic Approach to Pain Management

I Drug classes commonly utilized for management of pain in horses. A Non‐steroidal anti‐inflammatory drugs(NSAIDs)

B Opioids

Mu opioid receptors

C α2‐adrenergic agonists

D N‐methyl‐D‐aspartate receptor antagonists

E Local anesthetics

F Gabapentin

II Pain management

III Examples of case management using balanced analgesia

Premedication:

Induction:

Premedication:

Induction

Local anesthesia:

Suggested Reading

Rehabilitation Modalities for Acute and Chronic Pain in Horses

I Introduction

II Pain assessment

A Lameness assessment

B Articular pain

C Pressure algometry

III Rehabilitation modalities used to treat acute and chronic musculoskeletal pain. A Therapeutic laser (Light amplification by stimulated emission of radiation.) (see Figure 30.3)

Analgesic effects of laser therapy

B Acupuncture

C Cryotherapy

D Thermotherapy

E Electrical stimulation (Transcutaneous electrical nerve stimulation [TENS]) (see Figure 30.4)

F Extracorporeal shockwave therapy (see Figure 30.5)

Suggested Reading

Equine Acupuncture

I Introduction

II Mechanism of acupuncture‐induced analgesia

III Patient evaluation and treatment

A Acupuncture techniques

Acupressure

Dry needle

Hemoacupuncture

Aquapuncture

Electroacupuncture (EA)

Moxibustion

Lasers and infrared light sources

Implanted materials

B Choice of technique

C Number of treatments required

IV Evaluation of the musculoskeletal system

V Environment

VI Patient tolerance

VII Needle placement

VIII Treatment of musculoskeletal pain

A Foot pain. Non‐laminitic foot pain

Laminitic foot pain

B Joint pain

C Tendon and ligament injuries

D Cervical pain

Case report:

E Thoracolumbar pain

F Pelvic region pain (see Figure 30.10)

G Gastrointestinal pain

Summary

Suggested Reading

31 Anesthesia of Foals

I Transition to adult life. A Transition to adult circulation

B Reopening of shunts

II Respiratory system of the neonatal foal

A Breathing pattern

B Control of breathing

C Arterial blood gas values in neonatal foals

III Cardiovascular system of the foal (see Table 31.1)

IV Thermoregulation

A Heat production

B Heat loss is exacerbated by:

C Neutral thermal environment

D Effects of anesthesia on heat balance

E Effects of hypothermia on anesthesia

V Drug metabolism and excretion

A Injectable drugs. Neonatal foals

Older foals

B Inhalational anesthetics

VI Sedation and general anesthesia. A Preoperative evaluation

B Fasting

C Sedation. Neonates

Older foals

Benzodiazepines

Opioids

α2agonists

α2antagonists

D Induction of anesthesia with intravenous drug(s)

Ketamine (2–3 mg/kg, IV)

Propofol (2–4 mg/kg, IV) or alfaxalone (1–3 mg/kg, IV)

Example induction protocols for neonatal foal

Propofol (1–3 mg/kg, IV) administered slowly to effect

Induction protocol for older, healthy foal. Example 1

Induction protocol for older foal. Example 2 (Combining drugs)

E Induction of anesthesia with an inhalational anesthetic

Reasons for rapid uptake of volatile anesthetics in neonate

F Maintenance of anesthesia

Volatile anesthetics

Partial intravenous anesthesia (PIVA)

Neonatal foal – Example PIVA protocol

Older foal ‐ Example of PIVA protocol

Total intravenous anesthesia (TIVA)

VII Monitoring and patient care. A Positioning and padding

B Monitoring (see Chapter 19)

Depth of anesthesia

Cardiovascular system

Respiratory system

Body temperature

Blood glucose

VIII Recoveries

IX Managing the mare at induction and recovery

Examples of sedation regimens for the mare

Induction phase

Recovery phase

X Analgesia for the neonatal foal

Examples of balanced anesthesia

NSAIDs

Flunixin meglumine

Phenylbutazone

Meloxicam

Opioids

XI Anesthesia for foals with uroabdomen

A Clinical presentation

Clinical signs

B Metabolic changes

Hyponatremia([Na+] < 125 mEq/l)

Hyperkalemia([K+] > 5.5 mEq/l)

C Preoperative treatment

Plasma volume expansion

Reduce plasma [K+]

Reverse membrane effects of hyperkalemia

D Anesthesia (see sections E and F)

Sedation

Induction

Maintenance

E Monitoring

F Analgesia

Suggested Reading

32 Anesthesia of Horses with Intestinal Emergencies (Colic)

I Preoperative evaluation

II Preparation for anesthesia

A Fluid therapy

Isotonic fluids (e.g. lactated Ringer's)

Hypertonic saline

Synthetic colloids

Acid‐base correction

B Sedation and analgesia

α2 agonists

Non‐steroidal anti‐inflammatory drugs (NSAIDs)

Opioids

Phenothiazines

C Anti‐endotoxin therapy

Polymyxin B

NSAIDs

D Antimicrobial therapy

III Sedation and induction

IV Intubation and oxygenation

V Maintenance of anesthesia

VI Intraoperative support. A Fluid therapy. Isotonic fluids

Colloids

B Cardiovascular support (see Chapter 38)

Preload

Inotropic support

Calcium infusions

C Respiratory support (see Chapter 38)

VII Recovery

VIII Intraoperative use of phenylephrine

Suggested Reading

33 Anesthesia of the Geriatric Horse

I Definition of geriatric

II Mechanisms of aging

III The impact of aging on body systems

IV Pharmacologic considerations in geriatric horses

V Anesthetic considerations in geriatric horses

Suggested Reading

34 Anesthesia and Pregnancy

I Physiology of pregnancy (see Table 34.1)

A Cardiovascular

B Respiratory

C Renal

D Uterus

II Factors affecting drug disposition during pregnancy. A Maternal

B Placental

C Fetal

III Anesthesia concerns in the pregnant mare. A Compression of the vena cava

B Hypoventilation, hypoxemia, and impaired gas exchange

C Myopathy

D Recovery

IV Anesthetic management in pregnancy

A Sedation and premedication. Acepromazine

α2 agonists

Opioids

Flunixin meglumine

B Induction. Ketamine

Diazepam

Midazolam

Guaifenesin

C Maintenance

D Specific monitoring. Direct blood pressure

Arterial blood gas analysis

Electrocardiography

FHR

E Cardiovascular supportive measures

F Recovery

G Pain management

V Managing anesthesia in the pregnant mare

A Non‐obstetric procedures. Abdominal surgery for intestinal emergency

Trauma

B Obstetric procedures. Uterine torsion

Dystocia/Cesarean section (see Table 34.2)

Live foal at presentation (see Figures 34.1 and 34.2)

Dead foal at presentation

Suggested Reading

35 Anesthesia for Equine Imaging

Magnetic resonance imaging. I Introduction

A Specific challenges

II MRI safety

III MRI scanning room equipment

A MRI‐safe equipment

B MRI‐compatible equipment

C Use of non‐ferrous anesthetic equipment

D Use of ferromagnetic equipment

IV Patient preparation

V Patient positioning

Box 35.1 Avoid Excessive Traction on Limbs

VI Anesthesia and monitoring. A Anesthesia (see Chapter 21)

B Monitoring

Blood pressure

Urine collection

Assessing anesthetic depth

ECG

Pulse oximetry

Temperature

VII MRI contrast media

Low‐field standing MRI. I Introduction

A Advantages of low‐field MRI

B Disadvantages of low‐field MRI

II MRI safety

III Patient preparation

Patient limitations

IV Standing sedation for image acquisition

A Concerns in standing sedation

V Monitoring

Computed tomography

I Introduction

II Radiation safety

III Equipment and facilities. A Conventional recumbent CT under general anesthesia

B Standing CT

Performing a head CT in a modified, adapted standard CT scanner:

IV Patient preparation for CT

A Conventional recumbent CT

B Standing head CT in a modified scanner

V Anesthesia, sedation, and image acquisition. A Conventional recumbent CT under general anesthesia

B Standing CT of the head

VI Monitoring

VII CT contrast media

A Adverse effects

Radiographic myelography

I Introduction

II Radiation safety

III Patient and procedure preparation

IV Anesthesia, monitoring, and procedure. A Anesthesia

B Monitoring

C Procedure

V Myelographic contrast media

VI Recovery

Suggested Reading

36 Anesthesia of Donkeys and Mules:Anatomic, Physiologic, and Behavioral Differences

I Anatomical differences

A Upper airway

B Endotracheal intubation (see Airway management Chapter 4)

C Nasogastric intubation

D Jugular catheterization

E Epidural anesthesia

F Miscellaneous anatomic differences. Distal colon

Nasolacrimal duct

Dentition

Vertebral formula

II Physiologic differences

A Evolution in a desert environment

III General behavioral characteristics

IV Preoperative evaluation

A Blood and chemistry differences

Suggested Reading

Sedation and Anesthesia of Donkeys and Mules

I Differences in drug dosages compared to horses

II Sedation of donkeys and mules

III Induction of anesthesia

Ketamine (2.5–3 mg/kg)

Ketamine (2.5–3 mg/kg) + benzodiazepine (e.g. diazepam/midazolam 0.05–0.1 mg/kg)

Ketamine (2.5 mg/kg) + Propofol (0.5–1.0 mg/kg)

Propofol (2.0 mg/kg)

Alfaxalone (2.0 mg/kg)

Thiopental (5–8 mg/kg)

Tiletamine + zolazepam (1–2 mg/kg)

IV Maintenance of anesthesia. A Inhalational anesthetics

B Total intravenous anesthesia (TIVA)

Example of TIVA: donkey (150–200 kg)

C Partial intravenous anesthetic (PIVA)

V Recovery from anesthesia

VI Analgesia

A Non‐steroidal anti‐inflammatory drugs (NSAIDS)

Phenylbutazone

Flunixin meglumine

Meloxicam

Carprofen

B Opioids

Butorphanol

Morphine

Hydromorphone

Buprenorphine

Suggested Reading

Donkey Pain Assessment Scales

I Natural pain responses in donkeys

II Pain assessment scales for acute pain in equids. A Current types of pain assessment scales

Composite Pain Scales(CPS) consisting of:

Facial expression‐based Pain Scales (FAP) consisting of:

B Basic set‐up of pain assessment scales

C Primary use and advantages of using pain scales

III Donkey pain assessment scales for acute pain

A Donkey composite pain scale (Donkey CPS)

B Donkey facial expression‐based pain scale

C Which scale to use

D How to carry out a COMPASS and/or FAP for acute pain manually. Preparation (See Table 36.1)

E How to carry out a COMPASS and/or FAP for acute pain by means of EPWA(the Equine Pain and Welfare App)

IV Donkey pain assessment scales for chronic pain. A The Donkey Chronic pain scale (See Table 36.4)

B THE DCP CPS for chronic pain assessment to perform manually. Preparation

V Donkey grimace scale (DGS)

VI Pain assessment in mules and hinnies

Suggested Reading

37 Remote Capture of Equids

I General considerations. A The decision to use remote delivery

B Trauma reduction

C Environment

II Equipment. A Choice of delivery equipment. Distance

Trauma

Familiarity

B Equipment options. Pole syringe

Blow pipe

Pistol

Rifles (see Figure 37.1)

III Pharmacology. A Choice of drugs

B α2 agonists and antagonists

Xylazine

Detomidine

Romifidine

Medetomidine

Yohimbine (0.1–0.2 mg/kg, IM) or tolazoline (2–4 mg/kg, IM)

Atipamezole

C Phenothiazines and butyrophenones

D Opioids and opiates. Morphine

Butorphanol

Thiafentanil

Etorphine

E Dissociative anesthetics. Ketamine

Telazol (Zoletil®)

IV Monitoring and supportive care. A Field anesthesia

B Monitoring

C Oxygenation

D Position and padding

V Sedation of fractious horses. A The decision to use IM sedation

B Sedative protocol

VI Sedation and anesthesia of captive feral horses. A Technique

VII Remote capture of free‐ranging feral horses. A Techniques

B Telazol - α2 mixtures

VIII Wild equids. A Techniques

B Zebra

Adult Grevy's zebra

Common zebra

C Przewalski's horse

Suggested Reading

38 Complications:Intraoperative Hypotension

I Common causes of hypotension. A Inhalational anesthetics

B Hypovolemia

Static measures of preload

Dynamic measures of preload

PPV

C Bradycardia

Treatment

II Treatment of hypotension

A Positive inotropic agents

Dobutamine

Ephedrine

Dopamine

Epinephrine

Calcium salts

B Vasopressors. Norepinephrine(NE)

Phenylephrine

Vasopressin

Suggested Reading

Intraoperative Hypertension

I Characterization

II Causes of hypertension in anesthetized horses. A Inadequate plane of anesthesia

B Medications. α2 agonists

Sympathomimetic drugs

C Nociception

Somatic

Visceral

Sympathetic

D Miscellaneous causes

Suggested Reading

Hypoxia and Hypoxemia

I Introduction

II Hypoxia

A Causes of hypoxia

III Hypoxemia

A Causes of hypoxemia

Ventilation‐Perfusion (V/Q) mismatch

Shunt (Low V/Q mismatch)

Hypoventilation

Diffusion impairment

Low‐inspired oxygen

B Other factors likely to exacerbate hypoxemia

C Clinical signs of hypoxemia

IV Problems with oxygen delivery

A Central supply

B Anesthetic machine

C Anesthesia circuit

D Endotracheal tube

E Ventilator

V Improving arterial oxygen partial pressure (PaO2 ) A Correct mechanical failures

B Institute intermittent positive pressure ventilation

C Optimize the inspiratory: expiratory ratio

D Increase the FIO2

E Positive end‐expiratory pressure (PEEP)

F Alveolar recruitment maneuvers ( ARM s)

G Aerosolized albuterol

VI Postoperative hypoxemia. A Causes

Pulmonary shunting may result from:

Airway obstruction

B Supplemental oxygen

Suggested Reading

Hypercarbia

I Causes of hypercarbia. A Decreased CO2 elimination

Inadequate ventilation

Decreased lung compliance

B Increased CO2 production

C Increased CO2 delivery to lungs

II Effects of hypercarbia on the cardiovascular system

A Mild increase in PaCO2 (55–65 mmHg) was associated with:

B Moderate increase in PaCO2 (75–85 mmHg) was associated with:

C Severe increase in PaCO2 (>90 mmHg) was associated with:

III Other effects of hypercarbia

IV Management of hypercarbia

Suggested Reading

Pulmonary Edema as a Consequence of Airway Obstruction

I Clinical signs

II Proposed pathogenesis

III Treatment

Suggested Reading

Endotoxemia

I Treatment of endotoxemic horses

II Drugs used in the treatment of endotoxemic horses. A Non‐steroidal anti‐inflammatory drugs (NSAIDs)

B Polymyxin B (PB)

C Lidocaine

D Dimethyl sulfoxide (DMSO)

Suggested Reading

Postanesthetic Myopathy

I Localized myopathy

A Contributing factors

B Pathogenesis. Decreased perfusion

Ischemic injury

Reperfusion of ischemic muscle

C Clinical signs

Laboratory data

Non‐dependent limb myopathy

II Generalized myopathy

A Clinical signs

B Pathogenesis

III Reducing the incidence of postanesthetic myopathy

Dantrolene

IV Sequelae

V Treatment

Suggested Reading

Neuropathy

I Factors contributing to peripheral nerve damage

II Radial nerve injury. A Clinical signs

B Sequelae

C Outcome

III Femoral nerve injury

A Clinical signs

B Sequelae

IV Peroneal nerve injury

A Clinical signs

B Sequelae

V Facial nerve injury (see Figure 38.4)

A Clinical signs

B Sequelae

VI Spinal cord myelomalacia

A Clinical signs

B Sequelae

VII Myelogram associated neuropathy

VIII Cerebral cortical necrosis

A Clinical signs

B Sequelae

IX Treatment of peripheral neuropathies

Suggested Reading

Hyperkalemic Periodic Paralysis (HYPP)

I Introduction

A Triggers for HYPP

II Pathogenesis

III Clinical signs. A Awake horses

B Anesthetized horses

IV Laboratory findings

Diagnosis

V Perioperative preparation and anesthesia. A Owner education

B Diuretic therapy prior to anesthesia

C Patient evaluation

D Pre‐anesthetic sedation

E Anesthesia

VI Intraoperative monitoring

VII Managing an episode of HYPP during anesthesia

A Hyperkalemia (for a more complete description see Chapter 31)

Calcium borogluconate

Dextrose

Insulin

Dobutamine

Hypertonic saline

β2agonists

Sodium bicarbonate

B Hyperthermia

C Decrease PaCO2

VIII Recovery

Suggested Reading

Malignant Hyperthermia

I Introduction

II Clinical signs and immediate diagnostic findings

III Diagnosis

IV Treatment

V Prevention

Suggested Reading

Delayed Awakening and Recovery

I Delayed awakening

A Patient factors. Age

Hypothermia

Genetic factors

Body condition score

Comorbidities

B Drugs

C Anesthesia‐associated pathological changes

II Surgically‐induced pathological changes

III Management of delayed awakening

Suggested Reading

Paraphimosis and Priaprism

I Definitions. A Paraphimosis

B Priapism

II Causes of Paraphimosis and Priapism

III Signs of paraphimosis

IV Signs of priapism

V Treatment for paraphimosis

VI Treatment for priapism

A Sequelae to priapism

Suggested Reading

Anaphylactic and Anaphylactoid Reactions

Anaphylactic reactions

Incidence

Causes

II Anaphylactoid reactions

Incidence

Causes:

III Clinical manifestations

IV Diagnosis

V Treatment

Intra‐carotid and Perivascular Injections

I Factors contributing to intracarotid injection

II Verification of jugular puncture

III Sequelae of failed jugular injection. A Hematoma formation

B Recurrent laryngeal nerve damage

C Horner's syndrome

D Esophageal injury

E Tissue slough or abscess

IV Signs and sequelae of intracarotid injection

A Responses to intracarotid injection

B Treatment

C Prognosis

Equine Cardiopulmonary Resuscitation

I Introduction

II Causes of cardiopulmonary arrest in horses

Foals

III Components of CPR

A Preparedness and prevention. Personnel training:

Equipment:

Foals:

B Basic life support

Chest compressions:

D Post‐arrest care and monitoring

IV Conclusion

Suggested Reading

39 Recovery from Anesthesia

I Risk of morbidity and mortality during recovery

II Predisposing risk factors

III Unassisted vs. assisted recovery

IV Recovery stalls. A Structural features designed to optimize conditions for recovery

B Useful design features for various methods of assisted recovery

V Pre‐recovery preparation

VI Recovery phase. A Positioning and padding

B Sedation and analgesia

C Ensure a patent airway and administer oxygen (see “Airway Management” Chapter 3)

D Other

VII Methods of recovery

A Unassisted recovery

B Personnel within recovery stall assisting horse manually

Technique

C Head and tail rope recovery (see Figure 39.4)

Requirements

Technique

D Deflating air pillow (see Figure 39.2)

Technique

E Large animal vertical lift (LAL) or alternatively the Becker Sling (see Figure 39.7)

F Sling recovery

Technique

Available sling systems

G Pool Recovery

Available pool systems

Suggested Reading

40 Euthanasia

I Important considerations. A Location

B Insurance

C Permission

D Secondary veterinary opinion

E Welfare issues

F Written consent

G Verbal consent

H Written records

I Postmortem examination

J Disposal of the body

K Grief and owner considerations

II The ideal euthanasia solution

III Techniques

A Hypoxia‐inducing agents

B Central nervous system (CNS) depressant drugs

C Adjunctive injectable methods of euthanasia

Potassium chloride (KCl)

Box 40.1 Potassium Chloride (Preparation for Euthanasia)

Magnesium sulfate (MgSO4)

Box 40.2 Magnesium Sulfate (Preparation for Euthanasia)

Intrathecal lidocaine hydrochloride

D Physical method of euthanasia that result in brain damage. Free Bullet

Captive bolt (see Figure 40.3)

IV Confirmation of death

Suggested Reading

Index. a

b

c

d

e

f

g

h

i

j

k

l

m

n

o

p

q

r

s

t

u

v

w

x

y

z

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Second Edition

.....

Dr. Ron Jones, MVSc, FRCVS, DVA, DrMedVet, DECVAA, DACVAA (Hon) Oxton, Prenton Merseyside CH43 5UF England

Dr. Daniel G. Kenney, VMD, DACVIM Health Sciences Centre Ontario Veterinary College The University of Guelph Ontario, Canada

.....

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