17 - IV Sedation Flashcards

1
Q

Spinal anesthesia

A
  • You are introducing anesthesia into the subarachnoid space
  • There is a 1-5% failure rate – unpredictable and unreliable
  • You will see a lot of this in your career because it is commonly used in foot surgery
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2
Q

Goals for spinal anesthesia

A
  • Prevention of pain
  • Adequate dermatomal level of anesthesia
  • Adequate duration of anesthesia
  • Skeletal muscle relaxation
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3
Q

Indications of spinal anesthesia

A
  • Lower extremity procedures
  • Hip and knee surgery
  • Perineal surgery
  • Lower abdominal surgery (C-section)
  • Posterior lower trunk surgery (hemorrhoids)
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4
Q

Contraindications of spinal anesthesia

A
  • Sepsis (hemodynamic instability)
  • Bacteremia (with caveats – on antibiotics and have been for a long time because you can get bleedings problems)
  • Skin infection at injection site (tattoos?) – issue in pregnant women (infectious area)
  • Severe hypovolemia
  • Coagulopathies and anticoagulants (can get hematoma)
  • Increased ICP (intracranial pressure)
  • Patient refusal, lack of cooperation
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5
Q

Technique for spinal anesthesia

A
  • Lateral, sitting, or prone position – having them sit up is the easiest way - Hard to determine midline, sagging back skin – iliac crest is L4 (landmark)
  • Cord ends at L1 – place needle between L2-3 and L5-S1
  • A larger gauge introducer can be placed through the skin into the interspace and the spinal needle is introduced through it
  • Approach can be midline or lateral (paramedian – alternate approach when midline doesn’t work due to calcification or other pathology)
    o This takes experience, need to practice to know what angle that will be
    o Trying to bypass area of surgery (from previous back surgery)
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6
Q

Epidural for labor

A

**Subarachnoid needle placement **

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7
Q

Spinal needles – different lengths, different shape of tips

A
  • Gertie marx – can shoot drug up or down depending on position
  • Sprotte
  • Whitacre
  • Quincke – can lead to spinal headache
  • **The smaller gauge needle you use, the less change of spinal headache **
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8
Q

Ultrasound guided spinal anesthesia

A
  • Can identify landmarks that are not easily identified by the skin alone
  • Used in obese individuals or anyone else
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9
Q

Height of spinal block

A

Dose of drug given - primary factor in what HEIGHT of spinal block you use
o Dose of drug give = volume x concentration
o “Weight of the agent” – heavier or lighter than CSF

  • Weight (baricity) of injected local anesthetic solution
  • Patient position – Sitting or lying (if they are lying are they head up or head down)
  • CSF volume (the “X” factor)
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10
Q

Height of block – Lesser determinants

A
  • Added vasoconstrictors
  • Coughing or bearing down (Valsalva)
  • Barbotage
  • Rate of injection ( hypobaric solution may be the exception )
  • Needle bevel direction ( except directional bevels )
  • Gender
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11
Q

Risks of spinal anesthesia

A
  • Nerve Damage
  • Bleeding
  • Infection
  • Headache
  • Failed block – can mean no block, low block, high block, unilateral block or total spinal block (total spinal anesthesia – some go unconscious when it reaches brain step, need to intubate because they cannot breathe)
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12
Q

Spinal local anesthetics

A

Bupivacaine is used mostly now for spinals

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13
Q

Isobaric bupivacaine spinal

A
  • Has a concentration of 0.5% and a baricity ( or specific gravity) approaching that of CSF
    o Used A LOT FOR CHARCOT – you will see this A LOT in your career
    o There will be a longer period of block so you can take longer to do this tricky procedure
  • Is given in a larger volume in the sitting or lateral position
  • Does not spread cephelad and settles in the lordotic area of the spinal cord
  • Has a longer duration of action - and very safe
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14
Q

Spinal additive drugs

A
  • You can add narcotics to blocks

- Fentanyl, morphine

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15
Q

Physiological effects of spinal anesthesia

A
  • Effects depend on the height and density of the block
  • The more thoracic segments blocked, the greater the effects (T5 and above)
  • Visceral blockade affects cardiovascular, pulmonary, GI, hepatic, renal, and endocrine systems
  • Unopposed parasympathetic nervous system activity leads to nausea and vomiting
  • Cardiovascular effects are a decrease SVR with pooling of blood in the vascular system below the level of the block (decreased venous return)
  • Decreased adrenal output (decreased catecholamine release)
  • Decreased activity of cardioaccelerator nerves(T3-5)
  • Decreased cardiac contractility
  • NOTE ALL of this leads to bradycardia and hypotension which has led to DEATH
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16
Q

Treatment for this physiological effect of spinal anesthesia

A
  • IV fluids
  • Vasopressors – ephedrine or phenylephrine
  • Trendelenberg position or raising of legs
  • Anticholinergic agent – atropine or glypyrrolate
  • Epinephrine if all else fails
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17
Q

Goals of conscious sedation

A
  • Understand need for a conscious sedation policy
  • Understand the concept of conscious sedation (sedation-analgesia)
  • Understand pharmacology of drugs used for conscious sedation
  • Understand pharmacology of reversal drugs
  • Understand monitoring requirements necessary for the safe conduct of conscious sedation
  • Understand what the JCAHO requires of the hospital (or facility) where conscious sedation is administered
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18
Q

Contraindications of conscious sedation

A
  • History of adverse reaction to sedative medication
  • Unstable cardiorespiratory status
  • Nonfasting state – relative contraindication since a lot of sedation is done in ER’s on patients with full stomachs – need to be careful
  • First trimester of pregnancy (elective cases you would never do)
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19
Q

Definitions

A
  • Minimal sedation
  • Moderate sedation/analgesia = Conscious Sedation - What we are talking about today
  • Deep sedation/analgesia
  • General anesthesia
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20
Q

Minimal sedation

A
  • Responds normally to verbal commands
  • Ventilatory & Cardiovascular function unaffected
  • Cognitive function & coordination may be impaired
  • Used commonly to treat anxiety
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21
Q

Moderate sedation/analgesia (conscious sedation)

A
  • Drug induced depression of consciousness
  • Pt’s respond purposely to verbal commands
  • Airway remains patent
  • Spontaneous ventilation and cardiovascular function usually maintained
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22
Q

Deep sedation/analgesia

A
  • Drug-induced L.O.C. from which pt’s are not easily aroused
  • May respond to repeated or painful stimuli
  • Ventilation may be impaired
  • Cardiovascular function usually maintained
23
Q

General anesthesia (skipped)

A
  • Drug induced L.O.C.
  • Pt’s do not respond to painful stimuli
  • Ventilation function often impaired
    o Airway assistance & positive pressure ventilation may be required
  • Cardiovascular function may be impaired
24
Q

MAC vs general anesthesia – Closed claim study

A
  • 35% of claims were for death
  • 13% were for brain damage
  • “In particular, inadequate oxygenation and/or ventilation – were the primary damaging event in a high percentage of MAC claims”
25
REMEMBER
EVERYONE RESPONDS DIFFERENTLY TO ANESTHESIA – hard to predict - Can’t know in every case - What are some predictors of drug requirements – Risk Factors
26
Predictors of how you will respond to anesthesia
- Age - Single or multiple organ system disease - History of drug or alcohol use - Anatomic problems o Airway anomalies o Sleep apnea - Delayed mental development - Uncooperative - Emergencies - Morbid obesity
27
Positioning for conscious sedation
- You need to place you position so that they can breathe on their own during sedation while you give your drug - Small amounts of midazolam or morphine can lead to compromised airway (lack of swallowing to get rid of oral secretions) Best position - Don’t lay flat, have them elevated at a 15 degree angle (or so) - Risk of dying when lying flat – want to maintain the “ear to sternal notch”
28
Lung volume chart
- You want their heads up because it is a mechanical issue - Residual volume cannot be eliminated (dead space in lungs) - When you are pregnant or obese, there is pressure on the diaphragm, leading to a decreased residual volume, compromising the oxygen reserve in the body - If you sit them up, there is greater diaphragmatic excursion and there is more space in the lungs - If there is a problem with the airway, you will “buy more time” if there is compromise of airway
29
Pre-procedural assessment by the physician
- History and physical with focus on cardiac, respiratory systems and airway - Labs based on findings related to procedure - Appropriate consultation - If you have a healthy patient, there is no way to do lab work to make it safer o Waste of time, waste of money, can get false positives o Lab ordering frequency was based on geographical location (unnecessary) o Generates money for the hospital, but there is no medical justification for this testing - This is what you do to EVERY patient, regardless of health status – nursing does this o Vital signs o Level of consciousness o Last intake of fluids or food - Previous heart intervention guidelines (not a lecture topic, but I’m talking about it anyway)
30
***When working on heart patients***
- If they are on long-term aspirin because of a previous procedure, you can LEAVE THEM ON ASPIRIN WHEN DOING SURGERY - IT WILL NOT INCREASE BLEEDING SIGNIFICANTLY = TEST QUESTION***
31
Fasting guidelines
``` Ingested Material o Clear Liquid = 2 Hours o Full Liquid = 4 Hours o Light Meal = 6 Hours o Heavy meal with fried or fatty foods will delay gastric emptying = 8 hours or longer ```
32
Candidate for conscious sedation
After all of this is done, it MUST be determined whether this patient is a CANDIDATE for conscious sedation (sedation/analgesia)
33
Provider qualificaiton
- Determined by the facility– KNOW THE GUIDELINES - Understanding of pharmacology of drugs used - Only drugs with reversal agents should be used for conscious sedation - ACLS preferable for provider OR - Have a qualified individual immediately available - An individual should be available to summon help - Provider should be able to rescue from one level beyond the anticipated level of sedation and be able to support oxygenation, hemodynamics and ventilation
34
5 classes of anesthetic agents
- GABAergic agents ( benzodiazepenes ) - Opiate receptor agonists ( fentanyl ) - NMDA receptor antagonists ( ketamine ) - Alpha-2 agonists ( clonidine ) - Dopaminergic agonists ( ie: PCP –used as an anesthetic in the 1950’s )
35
Medications used for conscious sedation
- Sedation: Benzodiazepines - Analgesia: Opiates - Why these agents?...because they their effects can be reversed
36
Benzodiazepine effects
NO EFFECT ON PAIN*** - Sedation - Hypnosis - Anxiolysis - Muscle relaxation - Anticonvulsant - Anterograde amnesia
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Benzodiazepine characteristics
``` Drugs o Diazepam (Valium) o Midazolam (Versed) ``` Half life o Half-life o 43 +/- 13 hours o 1.9 +/- 0.6 hours (Range – 1 to 4 Hrs) Metabolism o Hepatic metabolism with active metabolite alpha-1-hydroxymidazolam o (10 % as potent as parent drug) o Renal or liver disease can impair it’s elimination
38
Opiates effects
``` o Analgesia o Drowsiness o Mood changes o Mental clouding o Respiratory depression o Delay gastric emptying o Can produce nausea and sometimes vomiting o Interferes with urinary voiding reflex o Pruritis and sometimes urticaria ALL OF THESE HAVE Mu EFFECTS = these are the receptors they act on ```
39
Opiate drugs
o Morphine = 1, half-life = 2 hours, onset = 15-30 min o Meperidine = 0.1, half-life = 3 hours, onset = 2-5 min o Fentanyl = 100, half-life = 3-4 hours, onset = 2-5 min o Sufentanil = 1000, half-life = 3-4 hours, onset = 2-5 min
40
Opiate metabolism and dosing
- Hepatic metabolism with renal excretion of active metabolites - Lipid soluble compounds act more quickly due to ease in crossing blood-brain barrier MUST REMEMBER THAT WHEN GIVEN TOGETHER, THE DOSAGES OF BOTH THE OPIATE AND BENZODIAZEPINE MUST BE REDUCED! Rules for dosing o GO SLOW…GO LOW o Remember…once you give it, you can’t get it back
41
Monitoring
Oxygenation o Pulse oximetry with appropriate alarms that must be audible and preferably variable pitch o Supplemental oxygen recommended Ventilation o Direct observation o Auscultation o End tidal CO2 – A recent JCAHO requirement Circulation o Non-invasive – B.P. o Plethesmography o Continuous EKG (+/-) – recommend to always use if patient has cardiac history Level of consciousness o Continuous verbal communication o Note response to commands, tactile stimulation sometimes necessary
42
Record keeping
- Pre-procedural - Every 5 minutes during procedure - Appropriate intervals – post procedure up to discharge - Determined by your hospital
43
Reversal agents
- Flumazinil (Romazicon) - Naloxone (Narcan) - Should not be used routinely
44
Benzodiazepine reversal
- Flumazinil – 0.1 mg/ml - Give 0.1 to 0.2 mg over 15 seconds - May repeat up to a dose of 1.0 mg. - Response is usually 1-2 minutes - Competes with benzodiazepenes at the GABA receptor - Do not give to patients on chronic benzodiazepine therapy due to risk of seizures
45
Opiate reversal
- Competes with opiate at the mu receptor to reverse respiratory depression - Naloxone - 0.1 to 0.2 mg IV - Response in 1 minute - May repeat - Do not give too much or too fast due to risk of precipitating agitation, hypertension, tachycardia and diaphoresis
46
Reversal simultaneously
- Encourage deep breathing - Give supplemental oxygen - Positive pressure ventilation if spontaneous breathing is inadequate
47
Rescue
- If reversal agents are used, keep patient a minimum of two hours to ensure that sedation and cardio-respiratory depression do not recur. - Keep them in the hospital and continue monitoring them – do not send them home
48
Recovery care
- Should be in accordance with standard recovery and discharge criteria established at your institution.
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DO NOT USE THESE DRUGS for sedation
- Thiopental, Propofol, Etomidate, Ketamine should not be used unless credentialed to do so by hospital. - Person giving these drugs must be able to rescue from deep sedation or general anesthesia - Remember…anesthesia planes can change quickly and it is possible to reach deep sedation and beyond using only the drugs commonly used for conscious sedation
50
Meperidine
- 10 % as potent as Morphine - Has both anticholinergic and local anesthetic effects - Has short time of onset and is more euphoric making it a favorite narcotic for diversion - Hepatically metabolized to normeperidine which has a t1/2 5x greater than the parent drug o It is renally excreted o Toxic and hallucinogenic causing serotonin syndrome, seizures, delerium, dysphoria and tremor not reversed by Narcan - Do not use in pts with renal or hepatic failure - Not to be used in PCA analgesia
51
REVIEW
- Based on relative potencies | - 50 mcg Fentanyl = 5 mg Morphine = 50 mg Meperidine
52
If you don't trust these conversions
- Titrate the drug to effect and go slowly – especially with Morphine due to its slower onset
53
Recommendation
- If Fentanyl is unavailable or in short supply, most practitioners will opt for Meperidine - It is a safe drug in a one-time dose of up to 100 mg - In patients with hepatic or renal compromise, it should not be used at all
54
Automated infusion system
- Controlled feedback mechanism with a machine controlling your sedation, called McSleepy