Exam 2 Flashcards

1
Q

Nasal intubation passes tube through which meatus

A

inferior turbinate/ meatus

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2
Q

What is the pharynx responsible for, location

A

Airway patency
obstruction

musclar tube from the back of skull to the border of the cricoid cart

join nasal and oral cavities down to the esophagus

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3
Q

Primary cause of airway obstruction in anesthesia

A

loss of phayngeal muscle tone

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4
Q

Nasopharynx

A

nose to soft pallet

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5
Q

oropharynx

A

soft pallet to epiglottis

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6
Q

Hypopharynx

A

Epiglottis to cricoid cart

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7
Q

Larynx

A

Epiglottis to lower end of cricoid cartilage (6th cervical vertebrae)

Responsible for; Inlet to trachea
Phonation
Airway protection

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8
Q

Unpaired Laryngeal cartilages

A

Thyroid- largest (support soft tissue)
Cricoid
Epiglottis

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9
Q

Paired Laryngeal cartilages

A

Arytenoid
Corniculate
Cuneiform

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10
Q

Where does the vocal ligament attach

A

artenoid cartilage and the thyroid cart at the thyroid notch

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11
Q

Trachea extends, length, shape, closed by, bound to?

A

Extends from inferior cricoid membrane to carina

10 to 15 cm - adult

C-shaped cartilage

Closed posteriorly by longitudinal trachealis muscle

Anteriorly bounded by tracheal rings

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12
Q

Reasons for receiving difficult airway notice

A

difficult mask ventilation
difficult laryngoscopy
difficult intubation or failed intubation

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13
Q

Inter-incisor distance

A

Mouth opening
Prefer > 6 cm (3 finger breadths)

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14
Q

Large tongue name

A

Macroglossia

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15
Q

Edentulousness meaning

A

lack of teeth – lack of teeth = hard to ventilate

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16
Q

Sniffing position

A

Cervical flexion and atlanto-occipital extension
Aligns oral, pharyngeal, and laryngeal axis

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17
Q

sternomental distance

A

Distance between sternal notch and chin

Head in full extension
Mouth closed
>12.5 cm preferred

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18
Q

Thyromental distance

A

Submandibular compliance
Prefer > 6.5 cm (3 finger breadths)
Tip of chin to thyroid notch

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19
Q

Prognathic ability

A

Extension of lower incisors beyond upper incisors
Upper lip bite test

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20
Q

Mallampati Test

A

The patient is seated upright with head neutral
Mouth open
Tongue protruded
No phonation

Visibility of oropharyngeal structures
Class I - IV

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21
Q

Mallampati class I

A

Fauces (arch), pillars (tonsils), entire uvula, and soft palate

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22
Q

Mallampati class ii

A

Fauces, portion of the uvula, and soft palate

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23
Q

Mallampati class iii

A

Base of the uvula and soft palate

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24
Q

Mallampati class iv

A

Only hard palate

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25
BURP
External manipulation and backward, upward, rightward pressure
26
Optimal external laryngeal manipulation (OELM)
Move the larynx to align up glottis
27
Cormack-lehane classification
Classification of laryngeal view/ view of the glottis Grade I-IV
28
CL- Grade 1
Entire full glottis
29
CL- Grade 2
Only the posterior portion of the glottis
30
CL- Grade 3
No part of the glottis and only epiglottis
31
CL- Grade 4
Epiglottis cannot be seen
32
Criteria associated with difficult mask ventilation (OBESE)
Obesity, BMI > 30kg/m2 Beard Edentulous Snorer, OSA Elderly, male Age > 55 Mallampati 3 or 4
33
Reasons to do an awake intubation
Suspected difficult laryngoscopy Suspected difficult ventilation with face mask/supraglottic airway Significant increased risk of aspiration Increased risk of rapid desaturation Suspected difficult emergency invasive airway
34
Achalasia
Esophageal outflow obstruction d/t inadequate relaxation of the LES Dilated hypomotile esophagusLES hypertension and reduced peristalsis
35
LES normal resting tone
29 mmHg > 29 hypertensive
36
s/s of Achalasia and risk
dysphagia (solids/liquids), regurgitation, heartburn, chest pain RISK; Aspiration (sleep sitting up) Esophageal CA
37
TX for achalasia
relieves obstruction… not peristalsis. Nitrates, CCB, - low dose Botox, - relax LES pneumatic dilation, - balloon inflates in the distal esophagus to dilate and inflate. Heller myotomy, - cutting smm at LES (distal to esoph and fundus of stomach) per oral endoscopic myotomy (POEM) 
38
Anesthesia Concerns for Achalasia and npo
aspiration ➔ RSI or awake intubation  POEM – NPO up to 48 hours (decreased peristalsis) Heller still should be NPO for 24-48 hr
39
Distal Esophageal Spasm, dx and tx
Spastic distal esophagus Mimics anginal pain DX; Esophagram-Cork screw or rosary bead appearance TX: Nitroglycerin, trazodone, and imipramine (antidepressants), and sildenafil (PDI)
40
Esophageal diverticula tx
Esophageal wall outpouching tx; removal
41
Esophageal diverticula Locations/ names
Pharyngoesophageal (Zenker’s diverticulum) Mid-esophageal Epiphrenic (supradiaphragmatic diverticulum)
42
Esophageal diverticula s/s
Bad breath Dysphagia
43
Esophageal diverticula anesthesia
Aspiration risk No cricoid pressure Intubate w/ head elevated Avoid NGT or OGT- risk perforating
44
Odynophagia
pain w/ swallowing. Hx of esophagitis. Or esophageal ulcers
45
Globus sensation
lump in throat. “psych problem”.
46
Hiatal hernia
Part of the stomach enters the thoracic cavity through esophageal hiatus (diaphragm) Not generally repaired
47
Sliding hiatal hernia
GE junction and fundus slide upward 
48
Paraesophageal hernia 
GE junction doesn’t move Pouch of stomach herniates next to the GE junction through esophageal hiatus
49
Esophageal Tumors location and type
Progressive dysphagia and weight loss Squamous cell- mid esophagus adenocarcinomas- distal (most common)
50
Esophageal Tumors s/s
Pancytopenia Dehydration Lung injury (post-chemo and radiation) Malnourishment 
51
Esophageal Tumors tx
Esophagectomy, chemotherapy, or radiation 
52
GERD
Reflux causing esophageal mucosal injury or at extraesophageal sites (and upward) <29 mmhg usually 13 mmhg
53
Anti-reflux mechanisms
LES, crural diaphragm- sit where LES is GE junction location- lower than crural LES pressure- (gerd = hypotesive)
54
GE junction/LES incompetence 
Transient LES relaxation LES hypotension Anatomic distortion of GE junction (hernia)
55
GERD s/s
Heartburn Regurgitation Dysphagia Chest pain chronic cough
56
GERD complications
Esophagitis Laryngopharyngeal reflux variant (chronic cough) Recurrent pulmonary aspiration
57
GERD tx
Lifestyle modification- avoid high fat/ acidic food, avoid drinking, peppermint. PPIs > H2 antagonists Nissen fundoplication- wrap fundus and illeus to make stronger.
58
GERD Anesthesia concerns and meds to give pre op
Aspiration risk Cimetidine and ranitidine (works better) Famotidine (longer duration of action)> cimetidine PPIs- day or or day before sx. Sodium citrate + metoclopramide - DM, MO, and pregnant pts  RSI + cricoid pressure
59
PH of stomach acid
2.5
60
Peptic Ulcer Disease where and s/s
Ulcers in the mucosal lining of stomach or duodenum  Burning epigastric pain- usually w/ worsening ulcers/ with fasting
61
Primary cause of peptic ulcer disease
Helicobacter pylori  - protinflammatory cytokines = effect parietal cells = reduce duodenal muscousa bicarb
62
Gastric ulcer and causes
usually in body of the stomach Form of PUD NSAIDs – common cause H. pylori + NSAIDs use
63
Peptic Ulcer Disease risk factors for death
Bleeding Peritonitis- from perforation Dehydration Perforation Sepsis
64
Peptic Ulcer disease population it effects
etoh elderly
65
Peptic Ulcer disease Complications
Bleeding -Mortality 10% to 20% Perforation- Untreated duodenal ulceration - 10% risk, Sudden and severe epigastric pain Gastric outlet obstruction
66
Gastric outlet obstruction s/s and anesthesia concerns
Acute or slow development  S/S: vomiting, dehydration, and hypochloremic alkalosis Anesthesia Consideration Full stomach (RSI), NGT, hydration, IV antisecretory drugs (ex: PPIs)
67
PEPTIC ULCER DISEASE Treatment
Antacids, H2 Receptor Antagonists PPIs Prostaglandin Analogues Cytoprotective agents
68
H2 Receptor Antagonists
Inhibits basal and stimulated HCL secretion Cimetidine, ranitidine, famotidine, and nizatidine --more potenta and longer duration of action- tx for 4-6 weeks
69
PPIs
Inhibits all phases of gastric acid secretion Omeprazole, pantoprazole
70
Prostaglandin Analogues
Maintains mucosal integrity Misoprostol 
71
Cytoprotective agents
Creates physicochemical barrier Sucralfate peptobismol
72
Antacids
OTC for symptomatic relief of dyspepsia Aluminum/magnesium hydroxide  Calcium carbonate
73
Peptic Ulcer Disease Treatment for H pylori
Triple combination therapy – 14 days PPI (2 x strength) + 2 ABXs - Clarithromycin and amoxicillin or metronidazole, tetracycline
74
Peptic Ulcer Disease surgical Treatment
Correcting immediate problem Hemorrhage, perforation, and obstruction remove source and fix anatomy, prevent long term complications/ SE.
75
Peptic Ulcer Disease surgical Treatment
Correcting immediate problem Hemorrhage, perforation, and obstruction remove source and fix anatomy, prevent long term complications/ SE.
76
Peptic Ulcer Disease surgical Treatment
Correcting immediate problem Hemorrhage, perforation, and obstruction remove source and fix anatomy, prevent long term complications/ SE.
77
Dumping Syndrome
Emptying hyperosmolar gastric contents into proximal small bowel Release of vasoactive GI hormones (histamin, ang 2, NO, bradykinin)
78
Dumping Syndrome
Emptying hyperosmolar gastric contents into proximal small bowel Release of vasoactive GI hormones (histamin, ang 2, NO, bradykinin)
79
Dumping Syndrome tx
Dietary modifications- more glucose or carbs with meal Octreotide therapy
80
Dumping sydrome late and early s/s
Early – 15-30 mins post-prandial Nausea, epigastric discomfort, diaphoresis, crampy abd pain, diarrhea, tachycardia, palpitations, dizziness or syncope Late – 1-3 hours post-prandial Vasomotor symptoms secondary to hypoglycemia d/t excessive insulin release 
81
Ulcerative colitis s/s
Diarrhea, rectal bleeding, tenesmus, passage of mucous, crampy abdominal pain, anorexia, N/V, fever, and weight loss
82
tenesmus
constant urge to go to the bathroom
83
Inflammatory bowel disease Ulcerative colitis
Mucosal disease…. All or most of the colon to rectum severe- hemm
84
Ulcerative colitis Complications
Massive hemorrhage Toxic megacolon- dilated transverse colon, loss of segments. Obstruction Perforation 
85
Ulcerative colitis tx
Total proctocolectomy- curative removing colon and rectum.
86
crohn's diesease 
Acute or chronic bowel inflammation at terminal ileum/cecal valve- connection of small bowel and large bowel
87
Crohns disease s/s
Weight loss, inflammatory mass, bowel spasm, postprandial pain Malnutrition, steatorrhea, stricture formation- narrowing -> obstruction
88
crohn's disease complications
Stricture, obstruction, abscess, or fistula
89
crohn's disease tx/ sx
Small bowel resection d/t fistula or obstruction Total protocolectomy w/ end ileostomy- not curative
90
Inflammatory bowel disease Medical treatment
5-Acetylsalicylic acid (5-ASA)- Anti-inflammatory  Glucocorticoids- UC and Crohn's ABX – Ciprofloxacin or metronidazole Azathioprine and 6-mercaptopurine- Purine analogues Methotrexate and cyclosporine Immunosuppressive 
91
Carcinoid tumors og,secretes
Originate from the GI tract <25% in lung tissue  Secrete GI peptides and/or vasoactive substances Insulin, histamine, serotonin
92
foregut
Thymus, esophagus lung stomach duodenum pancreas
93
Midgut
appendix ileum ascending colon
94
Midgut
appendix ileum ascending colon
95
hindgut
distal large bowel rectum
96
Seretonin secreted location
high in midgut low in forgut and rare in hindgut
97
Carcinoid sydrome location
atypical in foregut typical in midgut rare in hindgut
98
CARCINOID TUMORS WITHOUT CARCINOID Syndrome 
found with appendecomy- may or may not remove.
99
CARCINOID TUMORS W/ SYSTEMIC SYMPTOMS D/T SECRETED PRODUCTS
GI peptides and /or vasoactive substances- found in midgut over the foregut Midgut carcinoids (produce more mediators) > foregut carcinoids Non-producing tumors- present as mass or bowel obstruction.
100
Small intestine carcinoid presentation w/ %
abd pain (51%), intestinal obstruction (31%), tumor (17%), GI bleed (11%)
101
Rectrum carcinoid presentation
Bleeding (39%), constipation (17%), Diarrhea (17%)
102
Bronchus Carcinoid presentation
Asymtomatic (31%)
103
Carcinoid tumors carcinoid syndrome s/s
Serotonin and vasoactive substances released in systemic circulation  Serotonin - diarrhea Histamine - responsible for puriting flushing Both for bronchoconstriction Signs and symptoms Flushing, diarrhea, hypotension, HTN, bronchoconstriction, wheezing
104
Carcinoid tumors Carcinoid crisis
Intense flushing, diarrhea, abdominal pain, tachycardia, HTN or hypotension Fatal w/o treatment Spontaneous or provoked by stress, chemotherapy, or biopsy
105
Drugs that may provoke mediator release
sux, mivacurium, atracurium, tubocurarine, epi, ne , dop , isoprterenol, thiopental
106
Carcinoid tumors treatment
Serotonin blockers Histamine blockers Somatostatin analogues (>80% patients) Octreotide, histamine blockers, and ipratropium 
107
Serotonin blockers
5HT1/2 - diarrhea 5HT3 (ondansetron) – diarrhea and nausea; occasionally relieve flushing 
108
Histamine blockers
prevent Flushing 
109
Somatostatin analogues
(>80% patients) Prevents crisis development Lanreotide (most common, SUBq x 4wks) Octreotide (24-28 before sx)
110
Octreotide, histamine blockers, and ipratropium prevent…..
prevent Bronchoconstriction
111
Autodigestion prevented by protective mechanisms for pancrease
Packaging of proteases in precursor form Synthesis of protease inhibitors  Low intra-pancreatic concentration of calcium 
112
Causes of pancreatitis
Gallstones and ETOH abuse - 60% to 80% AIDS, hyperparathyroidism, and trauma
113
Acute Pancreatitis signs and symptoms
Mid-epigastric pain, N/V, abd distention (ileus) Dyspnea, low-grade fever, tachycardia, hypotension Shock d/t hypovolemia Increased serum amylase and lipase 
114
Acute pancreatitis  ranson criteria
> 55 years WBC count > 16,000 cells/mm3 BUN >16 mmol/L Aspartate transaminase > 250 units/L Arterial PaO2 < 60 mmHg Fluid deficit > 6 L Blood glucose > 200 mg/dL w/o a history of DM Lactate dehydrogenase > 350 IU/L Corrected calcium concentration < 8 mg/dL  Fall in Hct >10% Metabolic acidosis with a base deficit > 4 mmol/L Mortality r/t number of criteria present 0-2 criteria <5% mortality  3-4 criteria 20% mortality 5-6 criteria 40% mortality 7-8 criteria 100% mortality
115
Acute pancreatitis complications
DIC ARDS SHOCK Renal Failure Hypotension Arterial hypoxemia infection of the necrotic panc material or abscess formation 25% of pts experience complications
116
Acute pancreatitis  Treatment
Aggressive IVF administration Colloid replacement NPO Enteral/TPN  NGT suction  Pain management  Removal of gallstones
117
Chronic pancreatitis how and causes
Persistent inflammation w/ irreversible damage Loss of exocrine and endocrine function  Chronic ETOH abuse, CF, and hyperparathyroidism
118
Signs and symptoms of Chronic pancreatitis
Post-prandial, epigastric pain Thin, emaciated, steatorrhea DM
119
Treatment of Chronic pancreatitis
Management of pain, DM, and malabsorption 
120
Gi bleeding Upper acute s/s
Hypotension and tachycardia w/ blood loss >25% of total blood volume Hct - normal Anemia Orthostatic hypotension – Hct <30% BUN >40 mg/dL
121
Causes of Gi bleeding Upper acute
Esophageal variceal bleeding, malignancy
122
Gi bleeding Upper tx
Upper endoscopy Active bleeding ------Endoscopic coagulation (burn, clips)
123
Gi bleeding Upper Anesthetic Considerations
Aspiration risk – ETT… RSI
124
GI bleeding Lower and causes
Abrupt passage of bright red blood and clots via the rectum Diverticulosis, tumors, ischemic colitis, infectious colitis
125
GI bleeding Lower tx
Sigmoidoscopy/colonoscopy Angiography and embolic therapy Surgery
126
Part of properly assessing Mallampati includes:
* NO phonation
127
2. What is the LEAST LIKELY cause of dental injury during anesthesia?
* Aggressive mask ventilation
128
3. Prognathic ability is a measurement of:
* The extension of the lower incisors beyond the upper incisors. * The ability of the lower incisors to bite the upper lip.
129
4. What information regarding the patient’s anesthetic history would indicate a potential airway concern?
* Report of cut lips and broken teeth. * Report of excessive sore throat.
130
5. Which airway assessment finding is more predictive of difficult intubation than a high BMI>
* Cervical traction.
131
1. A 34-year-old patient diagnosed with acute pancreatitis is scheduled for surgery in the morning. The patient has the following laboratory values: WBC: 18,000 Platelets: 150,000 AST: 376 BUN: 22 What is the patient’s risk for mortality?
* 40%
132
2. An adenocarcinoma esophageal tumor is located at:
* At the mid-esophagus
133
3. Which medication will induce remission in patient with Ulcerative Colitis and Crohn’s disease?
* 5-Acetylsalicylic acid
134
4. For patients with a history of esophageal diverticula, what are the anesthetic concerns?
* Increased risk of aspiration * Apply cortical pressure during induction.
135
. In a patent with carcinoid tumors, how early should octreotide be administered to prevent crisis during surgery:
* 24 hours!
136
1.Which statement BEST describes acromegaly?
* Decreased amount of neuromuscular blockers is recommended.
137
2.Which anesthetic plan is ideal for a patient with systemic lupus erythematosus?
* Order pre-operative CBC and ECG.
138
3.Preoperative findings of Duchenne muscular dystrophy include:
* Kyphoscoliosis
139
4.Signs and symptoms of scleroderma include:
Small bowel hypomotility. * Decreased pulmonary compliance.
140
5.Anesthetic considerations for syndrome of inappropriate anti-diuretic hormone (SIADH) include:
* Measurement of urine osmolality. * Titrating intravenous fluid.
141
6.A diagnosis of Grave’s disease is consistent with:
* Weight loss.
142
7.In patients with carcinoid tumors, how early should octreotide be administered to prevent crisis during surgery:
* 24 hours.
143
8.All of the anesthetic considerations are indicated in a patient with hyperparathyroidism EXCEPT:
* Administration of 40 mg of rocuronium. o Pre-operative ECG. o Avoiding the use of midazolam pre-operatively. o IV fluid administration.
144
9.Which statement BEST characterizes myasthenia gravis?
* Fatiguability of skeletal muscle with repetitive use.
145
10.What are treatments indicated for a patient with rheumatoid arthritis?
* Corticosteroids and DMARDS.
146
Scleroderma
Inflammation and autoimmunity Vascular injury with vascular obliteration Tissue fibrosis and organ sclerosis
147
Xerostomia
dry mouth
148
CREST syndrome s/s of scleroderma
calcinosis Raynauds Esophageal dysfunction sclerodactyly- thick and tight skin Telangiectasis- cap dilation Skin: Taut skin MS: Limited mobility/contractures, skeletal muscle myopathy Nervous System: Nerve compression CV: Systemic and pulmonary HTN, dysrhythmias, vasospasm in small arteries of fingers, CHF Pulmonary: Diffuse interstitial pulmonary fibrosis, decreased pulmonary compliance Renal: Decreased renal blood flow and systemic HTN GI: Xerostomia, poor dentition, fibrosis of GI tract, reflux
149
Scleroderma Treatment
Alleviating symptoms… ACE-I
150
Scleroderma Anesthesia Management
Airway: Mandibular motion, small mouth opening, neck ROM, oral bleeding  hard stick Decreased pulmonary compliance and reserve, avoid increasing PVR GI: Aspiration Eyes: corneal abrasions Regional anesthesia Keep warm VTE prophylaxis Positioning Pulse ox difficulties
151
Pseudohypertrophy Muscular Dystrophy Duchenne Muscular Dystrophy (DMD) what and who
Mutation in the dystrophin gene Fatty infiltration = pseudohypertrophic  2-5 y/o boys
152
Duchenne Muscular Dystrophy (DMD) initial s/s
waddling gait, frequent falling, difficulty climbing stairs
153
Pseudohypertrophy Muscular Dystrophy S/S
CNS: Intellectual disability  MS: Kyphoscoliosis, skeletal muscle atrophy, serum CK 20-100x normal CV: Sinus tachycardia, cardiomyopathy, EKG abnormalities Pulmonary: weakened respiratory muscles and cough, OSA GI: Hypomotility, gastroparesis
154
Pseudohypertrophy Muscular Dystrophy Anesthesia Management
Airway: weak laryngeal reflexes and cough Pulmonary: weakened muscles CV: Pre-op EKG and/or echo based on the severity GI: Delayed gastric emptying Avoid succinylcholine Pharyngeal and respiratory muscle weakness Rhabdomyolysis MH – increased incidence; Dantrolene Regional > GA 
155
Myasthenia Gravis
Chronic autoimmune disorder NMJ - Decreased functional post-synaptic ACh receptors Muscle weakness w/ rapid exhaustion of voluntary muscles  Partial recovery with rest ACh receptor-binding antibodies and thymus abnormalities
156
Myasthenia Gravis S/S
Ptosis, diplopia, and dysphagia Dysarthria and difficulty handling saliva Isolated respiratory failure Arm, leg, or trunk muscle weakness Myocarditis Autoimmune diseases associated -RA, SLE, pernicious anemia, hyperthyroidism 
157
Myasthenic crisis w/ s&s
Drug resistance or insufficient drug therapy  S/S: severe muscle weakness and respiratory failure 
158
Cholinergic crisis w/ s&s
Excessive anticholinesterase treatment S/S: muscarinic side effects – profound muscle weakness, salivation, miosis, bradycardia, diarrhea, abdominal pain 
159
Edrophonium/Tensilon Test
1-2 mg IVP  Improves myasthenic crisis, makes cholinergic crisis worse
160
Myasthenia Gravis Treatment
Anticholinesterases -First line of treatment -Pyridostigmine > neostigmine Thymectomy -Induces remission -Reduced use of immunosuppressives -Reduces ACh receptor antibody levels -Full benefit delayed Immunosuppression -Corticosteroids, azathioprine, cyclosporine, mycophenolate Immunotherapy -Plasmapheresis --Removes antibodies from circulation  -Immunoglobulin --Temporary effect
161
Myasthenia Gravis Anesthesia Management
Aspiration risk Weakened pulmonary effort Marked sensitivity to nondepolarizing muscle relaxants Resistance to succinylcholine Intermediate-acting muscle relaxant Intubate without NMBD
162
Osteoarthritis complications and OG
Degenerative process affecting articular cartilage Minimal inflammation Joint trauma Pain present with motion, relieved by rest Weight-bearing and distal interphalangeal joints Heberden nodes Degenerative disease – vertebral bodies and intervertebral disks  Protrusion of the nucleus pulposus Compression of nerve roots  Middle to lower c-spine and l-spine
163
Osteoarthritis Treatment 
PT and exercise Maintaining muscle function Pain relief Joint replacement surgery
164
Osteoarthritis Anesthesia Management 
Airway  Limited ROM
165
Rheumatoid Arthritis
Autoimmune-mediated, systemic inflammatory disease Proximal interphalangeal and metacarpophalangeal joints Rheumatoid nodules at pressure points Rheumatoid factor Single or multiple joints Painful synovial inflammation, swelling, and increased fluid Morning stiffness Symmetrical distribution of several joints Fusiform swelling Synovitis of temporomandibular joint Affects nearly all joints Except t-spine and lumbosacral spine 
166
Rheumatoid Arthritis  S/S Atlantoaxial subluxation
Atlantoaxial subluxation Odontoid process protrudes into the foramen magnum Pressure on the spinal cord or impairs vertebral artery blood flow
167
Rheumatoid Arthritis  S/S Cricoarytenoid arthritis 
Acute – hoarseness, dyspnea, and stridor w/ tenderness over the larynx; swelling and redness of arytenoids Chronic – asymptomatic or variable degrees of hoarseness, dyspnea, and upper airway obstruction 
168
Rheumatoid Arthritis  S/S
Atlantoaxial subluxation Cricoarytenoid arthritis  Osteoporosis NM: Weakened skeletal muscles -Peripheral neuropathies CV: Pericarditis, accelerated coronary atherosclerosis Pulmonary: Restrictive lung changes  Hematology: anemia, neutropenia, elevated platelets Keratoconjunctivitis sicca and xerostomia
169
Rheumatoid Arthritis Treatment
NSAIDS Decrease joint swelling, relieve stiffness, provide analgesia  COX-1 inhibitors, COX-2 inhibitors Corticosteroids Decrease joint swelling, pain, and morning stiffness  DMARDs (Disease-modifying antirheumatic drugs)- methotrexate Tumor necrosis factor (TNF-alpha) inhibitors and interleukin (IL-1) inhibitors  Surgery
170
Rheumatoid Arthritis Anesthesia Management 
Airway  -Atlantoaxial subluxation -TMJ limitation -Cricoarytenoid joints Severe rheumatoid lung disease Protect eyes Stress dose
171
Systemic Lupus Erythematosus
Multisystem chronic inflammatory Antinuclear antibody production 
172
Systemic Lupus Erythematosus Typical manifestations:
Antinuclear antibodies Characteristic malar rash Thrombocytopenia Serositis Nephritis
173
Systemic Lupus Erythematosus S/S
Polyarthritis and dermatitis Symmetrical arthritis -No spinal involvement -Avascular necrosis of femoral head or condyle CNS: Cognitive dysfunction, psychological changes CV: Pericarditis, coronary atherosclerosis, Raynaud’s Pulmonary: Lupus pneumonia, restrictive lung disease, vanishing lung syndrome Renal: Glomerulonephritis, decreased GFR  GI/Liver: ABD pain, pancreatitis, elevated liver enzymes NM: Skeletal muscle weakness Hematology: Thromboembolism, thrombocytopenia, hemolytic anemia, Skin: Butterfly-shaped malar rash, discoid lesions, alopecia
174
Systemic Lupus Erythematosus Treatment
NSAIDs or ASA Anti-malarial; Hydroxychloroquine and quinacrine Corticosteroids Immunosuppressants; Methotrexate, azathioprine
175
Systemic Lupus Erythematosus Anesthesia Management
Based upon manifestations and organ dysfunction Airway: recurrent laryngeal nerve palsy, cricoarytenoid arthritis  Stress dose of corticosteroids
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Malignant Hyperthermia
Hypermetabolic syndrome Genetic mutation -Ryanodine receptor - RYR1 gene -Dihydropyridine receptor Exposure to inhaled VA and succinylcholine 50% mortality Family history Uncontrolled elevation of sarcoplasmic calcium Sustained activation of muscle contraction Rhabdomyolysis
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Malignant Hyperthermia S/S Early
hypercarbia tachypnea (if respiration is spontaneous sinus tachycardia masseter muscle spasm generalized muscle rigidity Peaked T waves metabolic and respiratory acidosis
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Malignant Hyperthermia S/S Late
Hyperthermia cola-colored urine/ rhabdo elevated CPK cardiac dysrhythmia acute renal failure cardiovascular collapse DIC.
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Malignant Hyperthermia Treatment
D/C all triggering gas/drugs Hyperventilate with 100% O2 at 10 L/min Change breathing circuit and soda lime Dantrolene; 20 mg + 3 G mannitol, Mix with 60 mL sterile water -Initial dose 2.5 mg/kg -Max upper limit 10 mg/kg Treat arrythmias Monitor urine output
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Malignant Hyperthermia Post-Op
Transfer to ICU 24-48 hours Report to MH registry MH testing for pt and family members -Muscle biopsy contracture testing --Halothane plus caffeine contracture test