Orthopedic Surgery Flashcards

1
Q

Anesthesia Mngt issues associated with orthopedic procedures?

A
Airway
Positioning 
Blood/Fluid Loss 
Temperature Conservation 
*Post-op pain
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2
Q

How is Congenital dislocation of the hip caused?

A

Prolonged displacement of the fetal femoral head in from the acetabulum resulting in posterior dislocation during hip flexion

-Severity ranges fro joint laxity to irreducible displacement

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3
Q

What is the treatment for congenital dislocation of the hip ? (CHD)

A
  • Pavlick Harness

- Fluoroscopy guided closed reduction and spica casting

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4
Q

T/F: the procedure for CHD is long and painful?

A

FALSE

Short and not painful

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5
Q

What is the greatest concern during CHD repair?

A

LOSS OF AIRWAY

  • IH via mask, LMA, ETT
  • Pt lifted from OR table to the spica casting frae then back to OR table
  • Disconnect circuit during position changes, ( remember to DC N2) prior to circuit disconnect )
  • Monitor breath sounds continuously
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6
Q

What is another big concern during CHD surgery?

A

Laryngospasm

A lot of movement, pt must be in STAGE III to prevent this, strict attention to securing the device so it does not becomes dislodged during position changes

  • Easiest is to use ETT
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7
Q

Congenital Clubfoot, a structural deformity- shortened medial tendons of the lower leg, Achilles tendon- what was does the foot point?

A

Downward and inward

Plantar and inversion

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8
Q

What is the treatment for Congenital club foot?

A
  • Manipulation and casting

- Surgical Correction and casting at 3-6 months

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9
Q

What are our options for anes. mngt during congenital clubfoot?

A

General and Regional

  • IH and then caudual injection with bupivacaine 0.25% 1ml/kg
  • Analgesia for 4-6 hours, decreases IHA requirement
  • IV opioids instead of caudal
  • -Fentanyl 2-5 mcg/kg
  • -MSO4 0.1 mg/kg
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10
Q

Do we want to use an ETT or maintain SV during congenital club foot repair?

A

ETT- cnt monitor breath sounds

  • Tourniquets are utilized
  • Position and padding up upper extremities
  • Intraop glucose monitoring and USE of glucose containing solution
  • Temperature conservation

*Usually have sx 3-6 months of age

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11
Q

What is osteogenesis Imperfects?

A

Defect of collagen production resulting in abnormal bones, ligaments, teeth, sclera

**Pts suffer fractures after innocuous contact or trauma

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12
Q

What are clinical presentations of Osteogenesis Imperfecta?

A
  • Bowing of long bones and kyphoscoliosis
  • Ostosclerosis and deafness ( bones in inner ear don’t vibrate )
  • Hypermetabolic-NOT MH
  • Platelet abnormalities and decreased Factor VIII levels in 30%
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13
Q

Anesthetic Management of OI?

A
  • *VITAL gentle manipulation of the C-spine and airway
  • -Atlantooccipital instability
  • -Cervical and mandibular fxs occur easily
  • -Airway cartilages and teeth are easily damaged
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14
Q

How do you management a normal vs difficult airway in its with OI?

A

Normal-routine IH or IV induction and intubation

Difficult: Awake fiberoptic

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15
Q

When do you give muscle relaxants in pts with OI?

A

Only AFTER adequate mask ventilation is established

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16
Q

What medications can we give for analgesia in OI?

A

Fentanyl 2-5 mcg/kg

MSO4 0.1 mg/kg

17
Q

Special considerations on anes. mango with pts who have OI?

A
  • Meticulous attention to positioning and padding of extremities
  • Avoid aggressive heat conservation measures and anti-muscarinics - signs like MH
  • Tourniquets are utilized
  • Succinylcholine induced fasciculations can cause fractures
18
Q

T/F: Cerebral Palsy ( CP) is evolving encephalopathy or any progressive central motor deficit r/t hypoxic or anoxic cerebral damage in the perinatal period?

A

FALSE

STATIC encephalopathy
NONprogressive

19
Q

What is the etiology of CP?

A
Prematurity 
Birth Trauma
Hypoglycemia 
Intrauterine and neonatal infections 
Congenital vascular malformations
20
Q

What other diseases is CP associated with?

A

Mental Retardation
Seizures Disorders
Abnormalities of Vision, Speech, hearing, behavior and cognition

21
Q

What is the clinical presentation on CP?

A

Skeletal muscle spasticity and contractures

  • Impairment of laryngeal and pharyngeal reflexes- GERD, aspiration
  • Poor dental hygiene
22
Q

How do we management CP patients peri-operatively ?

A
  • Mod-sev airway ETT r/t predisposition to aspiration
  • Pre - medicate individualized
  • -Intra Nassal Midazolam 0.2-0.3 mg/kg
  • -Intra muscular ketamine 5-10 mg/kg
  • -SCh does NOT produce exaggerated K release
  • Response to NDNMB normal
  • Opioids are okay but caution with impaired alertness or airway reflexes
  • Caudal decrease IHA requirement and provides post op analgesia
23
Q

What are disorders and drug interactions we need to be aware of with patients and CP?

A

Seizure Disorder:

  • Phenobarbital, phenytoin, carbamazepine - TAKE day of procedure
  • Phenobarbital- hepatic enzyme INDUCER

Spasticity:

  • Dantrolene
  • Baclofen
24
Q

Why are fractures common in this population?

A

Trauma

-Evaluate for injury to c-spine and other organ systems

25
What are our considerations in surgical repairs of fxs?
Urgent/Emergent: vascular compromise, large hematoma, hypotension Delayed stabilize and admit
26
Anes. mngt for fxs?
- RSI and ETT for ED/Urgent/Elective repair - Analgesia - IV opioids/caudal - Have blood product available - Temperature Conservation
27
What is Myelodysplasia?
Congenital failure of the middle or caudal end of the neural tube to close
28
What does Myelodysplasia result in?
Spina Bifida Meningocele Myelomeningocele Review Slide 25
29
What is the clinical presentation in meningocele ?
- Neural function intact - Spinal cord is tethered by sacral nerve roots - In not repaired, results in orthopedic and or urologic symptoms
30
What are myelomeningocele signs and symptoms?
- Varying degrees of sensory and motor deficits - Dilation of upper urinary tract - Spasticity - Scoliosis
31
When do we repair myelodisplasia?
Surgical repair on first day of life | -Lack of skin covering defect, prone to infection and sepsis
32
How to we manage myelodysplasia peri operatively ?
- Routine induction/standard agents - ETT with LATERAL decubitus position or SUPINE supported on towels or a donut to avoid putting pressure on the sac - Use of neurometric monitoring ( avoid NDNMBs initially) - Careful pre-op assessment of intravascular volume- potential for hypovolemia due to seepage of fluid from sac - Blood loss is not extensive - Temperature conservation measures
33
Scolliosis
An entire brainscape on one of the other ones we have :)