Exam 1: Pediatric Anesthesia pt 2 (pg 18-40) Flashcards

(66 cards)

1
Q

What Transesophageal Fistula (TEF) are A, C, and E?

A
  • A: esophageal atresia (5-8%)
  • C: proximal pouch and distal fistula (most common type)
  • E: H type- very rare and occasionally detected later in life with recurrent pneumonias

pg 18

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2
Q

TEF occurs in 1/3,000 births, 80-85% of these infants have esophagetal atresia with?

A

with a distal esophageal pouch and a proximal TEF (Type C)

pg 19

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3
Q

TEF is usually located where in relation to the carina?

A

1-2 rings above the carina

pg 19

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4
Q

true or false: TEF occurs more in males.

A

FALSE: TEF is equal in males/females and all races

pg 19

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5
Q

When does TEF occur gestationally?

A
  • Weeks 4-5
  • d/t error is seperation of trachea from floor of foregut

pg 19

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6
Q

TEF is often associated with VACTERL. What does this acronym stand for?

A
  • Vertebral anomalies
  • Anus imperforate
  • Congenital heart disease
  • TracheoEsophageal fistula
  • Renal abnormalities
  • Limb abnormalities

pg 19

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7
Q

How is TEF diagnosed prenatally?

A
  • Polyhydramnios
  • Absent/small gastric bubble
  • blind ending upper pouch in fetal neck

pg 20

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8
Q

What signs/symptoms cause concern for TEF postnatally?

A
  • excessive salivation,
  • choking
  • coughing
  • regurgitation at the first feeding leading to cyanosis,
  • respiratory distress causing a distended abdomen from the stomach filling with air when the baby cries

pg 20

The 3 C’s

  • Choking
  • Coughing
  • Cyanosis
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9
Q

How is TEF confirmed post-birth?

A
  • Inability to pass NG tube into stomach more than 7cm.
  • o Dilated proximal esophagus with air in conjunction with air in the distal stomach on Xray, CT, or direct visualization via bronchoscopy/endoscopy

pg 20/21

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10
Q

The following image is likely for what?

A

TEF
* TEF with esophageal atresia
* Feeding tube coiled in esophageal pouch (yellow)
* Large volume of gas in abdomen (orange)

pg 21

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11
Q

why should the proximal pouch tube be secured and placed to continous suction before surgery?

A

suction lessens risk of aspiration

pg 22

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12
Q

What anesthetic airway maneuvers should be avoided prior to surgery for TEF?

A
  • Mask ventilation
  • Tracheal intubation

Likely to exacerbate distention.

pg 22

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13
Q

how would you stabilize infant prior to TEF surgery?

A
  • get IV access
  • correct e-lyte imbalances
  • type and cross for blood
  • evaluate other possible anomalies such as VACTERL

pg 22

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14
Q

How is TEF surgically repaired?

A
  • open via toractomy
  • frequently done now via thorascopic approach

pg 22

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15
Q

What positioning is common for TEF and why?

A

Left Lateral Decubitus

Right thoracotomy approach that helps avoid the aortic arch.

pg 22

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16
Q

is single lung ventilation required for TEF procedure?

A
  • no
  • low flow/ low pressure CO2 can be used to collapse the right lung for exposure

pg 22

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17
Q

What can help the surgeon identify the proximal pouch?

A

naso-esophageal tube

pg 22

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18
Q

Steps for surgical repair for TEF

A
  • Fistula is ligated 1st to prevent further air entrapment in the stomach
  • Primary “end to end” anastomosis of the esophagus follows the ligation

pg 23

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19
Q

Why do you want to keep the infant spontaneously breathing during TEF procedure?

A

to avoid PPV and achieve awake intubation (can be traumatic and difficult to achieve without a crying infant further adding more air to the stomach)

pg 23

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20
Q

What type of induction should be perfromed for pts undergoing TEF procedure?

A
  • IV induction is quicker, more stable, and the use of muscle relaxants can optimize intubating conditions

pg 23

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21
Q

Where should the ETT tip be placed in TEF patients?

A

Inbetween the fistual and carina

pg 23

o Purposeful R stem intubation and then slowly withdraw ETT while auscultating the L chest until BBS are heard.
o Verify with fiberoptic scope and guide ETT into correct placement if needed

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22
Q

Gentle mask ventilation with high peak pressures should be used on induced TEF patients. T/F?

A

False. Ensure peak pressures are low

pg 23

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23
Q

TEF Anesthetic considerations

A
  • Frequent ETT suctioning may be required
  • After surgical correction ventilation with increased I:E time to re-expand alveoli
  • Early extubation can help alleviated pressure on suture lines. However, many surgeons request post-op intubation for days to help prevent pneumonia, atelectasis, or emergent reintubation, & perforation of suture lines
  • An in aitu ETT allows suctioning and lung expansion
  • Maintain head in neutral position, preventing pulling on surgical esophageal anastomosis
  • An epidural catheter from the caudal space or an intrapleural catheter can be left in place for post-op analgesia

pg 24

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24
Q

What newborn condition is often diagnosed between 2 - 8 weeks of age with non-bilious projectile vomiting?

A

Pyloric stenosis

pg 25

  • occurs in 1/500 live births
  • more frequent in 1st born males (4:1)
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25
What is pyloric stenosis?
Hypertrophy/Hyperplasia of muscular layer of pylorus resulting in gastric outlet obstruction. | pg 25
26
What acid-base imbalance is typical for pyloric stenosis?
Metabolic alkalosis with hypokalemia & hypochloremia *(however chronic vomitting and severe cases can lead to metabolic acidosis)* | pg 26
27
Why does metabolic alkalosis occur with pyloric stenosis?
* Kidney excretion of HCO₃⁻ in attempt to maintain a normal blood pH * kidneys excrete H+ and then K⁺ to maintain euvolemia and retain sodium. | pg 26 ## Footnote * Renal response: conserve water and retain Na ions through upregulation of aldosterone. And which H and K ions (which are already in short supply from vomiting) are excreted in urine in exchange for Na. * Can lead to paroxysmal aciduria despite presence of metabolic alkalosis
28
hypertrophied pylorus muscle is described as?
an olived shaped mass in the RUQ | pg 25 lecture
29
how does pyloric stenosis present clinically?
* Projectile, non-bilious vomiting * Immediate postprandial vomiting * Infant is hungry between feedings (hungry vomiter) * On US: Target or donut sign | pg 25 lecture
30
Is pyloric stenosis a medical emergency typically?
No. 24-48 hours are typically taken to correct electrolyte imbalances | pg 26
31
what IVF are infants with pyloric stenosis started on for maintenance and electrolyte balance?
D5NS with 20mEq/L of K (10-20mL/kg/hr) | pg 26
32
When are infants with pyloric stenosis ready for surgey?
* Good skin turgor * Adequate UOP (1-2mL/kg/hr) * Na > 130mEq/L * K> 3.0 mEq/L * Cl> 85 mEq/L * Assess adequate hydration through fontanel assessment | pg 26
33
how is pyloric stenosis diagnosed?
Commonly via US and rarely with barium swallow and XRAY | pg 27
34
infants today are diagnosed quickly with pyloric stenosis, what is effect of this?
less likely to see severe fluid and e-lyte imbalances as in the past | pg 27
35
The "donut" sign is typical for what condition?
Pyloric stenosis | pg 27
36
what is a pyloromyotomy and how is it done?
* pyloric stenosis repai * Most commonly done open or laparoscopic | pg 28
37
how is open pyloromyotomy done?
open is done via periumbilical incision | pg 28/29
38
what are the benefits of laparoscopic pyloromyotomy?
reduced hospital stay, quicker return to oral feeding, preferred cosmetically | pg 28/30
39
How should an infant with pyloric stenosis be induced?
* preoxygenate with 100% O2 * RSI s/t gastric outlet obstruction * Then suction right, center, then left | pg 31
40
What supplies should you have for pyloric stenosis induction?
* towels * large red rubber catheter | pg 31
41
Set up for pyloric stenosis repair
* Styletted ETT * Mil 1 * small handle * Oral airway * mask * red rubber catheter * prop * TB syringe of succs * TB syringe lidocaine * atropine * Tylenol suppository | pg 31
42
What narcotics are typically used for pyloric stenosis?
Trick question. **No Narcotics**! | pg 32
43
What is the pediatric dose of lidocaine for induction?
Lidocaine 1-2 mg/kg | pg 32
44
What is the pediatric dose of atropine for induction?
Atropine 0.2 mg/kg | pg 32 ## Footnote reduces vagal bradycardia that occurs during induction with suctioning and induced vomiting with red rubber catheter
45
What is the pediatric dose of propofol for induction?
2-4 mg/kg | pg 32
46
What is the pediatric dose of succinylcholine for induction?
2mg/kg | pg 32
47
What is the pediatric dose for rectal tylenol?
30-40 mg/kg | pg 32
48
Why would you want to avoid using opioids intraop for pyloric stenosis repairs?
* Quick surgery (< 30min) * Minimal post-op pain and local is given in field at surgical sites | pg 32
49
What type of fluids are used for hydrating infants post-operative for pyloromyomectomy (until adequate oral intake occurs)?
Dextrose containing fluids (for calories & glucose). | pg 32
50
Preop alkalosis of pyloric stenosis pt's leads to post-op apnea, why?
The body’s response to alkalosis is hypoventilation and increased PCO2 so you will see some respiratory acidosis | pg 32 lecture
51
Pyloric stenosis repair necessitates an ____ extubation.
awake b/c considered full stomach and post op respiratory depression is common (apnea monitor for the 1st 24hrs post op) | pg 33
52
What do you want to monitor post op pyloric stenosis repair?
hypoglycemia | pg 33
53
What can be used in small doses after pyloric stenosis repair?
morphine 0.02-0.03 mg/kg | pg 33
54
What condition occurs in 1/2000 births which is a reult of occlusion of the omphalomesenteric artery during gestation and not associated with other congenital anomalies?
Gastroschisis | pg 33/34
55
Where are the herniated viscera typically located in gastroschisis patients?
Typically to the **right** of the umbilicus. | pg 34
56
Why are babies with gastroschisis a high risk for infection and fluid loss?
Functionally abnormal dilated and foreshortened bowel because they are exposed to amniotic fluid in utero and air after delivery which results in inflammation and edema | pg 34
57
What condition occurs in 1/5000 births, where there is failure of the gut to migrate from the yolk sac into the abdomen during gestation
Omphalocele | pg 33/35
58
omphalocele is associated with what abnormalaties?
* genetic * cardiac * urologic * metabolic abnormalities | pg 35
59
where does the omphalocele emerge from?
Emerges from umbilicus and covered in membranous sac | pg 35
60
Between gastroschisis and omphalocele, which one is the bowl morpholgically and usually functions normally?
omphalocele | pg 35
61
Gastroschisis vs Omphalocele: * cause: * location of defect: * associated with:
| pg 36
62
An easy way to remeber ompalocele vs gastroschisis
| pg 36
63
How do we manage both ompalocele and gastroschisis?
* Aimed at maintaining perfusion to the viscera and reducing fluid loss * Cover mucosal surfaces with sterile saline soaked dressings * A plastic wrap is placed over the herniated viscera to decrease evaporative loss and prevent heat loss and hypothermia (much more pronounced with gastroschisis) * Complete surgical reduction or staged reduction with a silastic pouch * The pouch size is reduced slowly allowing gradual accommodation of the abdominal contents into the abdominal cavity without compromising ventilation or organ perfusion. * Usually reduced over a weeks time | pg 38
64
Managment of Gastroschisis & Omphalocele: * Continued volume resuscitation: ____ * Measures to prevent ____ * Intragastric tube can measure pressure that exceeds ____mmHg after primary closure which can cause abdominal ischemia and can result in a surgical emergency * Bowel can become edematous and renal congestion can result in? * ____ and ____ discrepancies from upper and lower extremities * Decreased ____, ____, and ____
Managment of Gastroschisis & Omphalocele: * Continued volume resuscitation: **dextrose IVF** * Measures to prevent **hypothermia** * Intragastric tube can measure pressure that exceeds **20**mmHg after primary closure which can cause abdominal ischemia and can result in a surgical emergency * Bowel can become edematous and renal congestion can result in **decreased urine output, lower extremity congestion, and cyanosis from impeded venous return** * **BP and pulse ox** discrepancies from upper and lower extremities * Decreased **diaphragm function, bilateral lower lobe atelectasis, and respiratory failure** | pg 39 ## Footnote sry, im tired and cant be bothered trying to figure out how to seperate these into smaller FC. feel free to change. -bri
65
Anestheitc Managment of Gastroschisis & Omphalocele: * Warm the room, have what available? * Aspirate the in situ gastric tube- place to suction prior to ____ and place to ____ throughout the case * Preoxygenate with 100% O2 as tolerated * RSI with cricoid pressure * Maintain with O2 and air * No ____ * ____ and ____ for surgical repair
* Warm the room, have **underbody bear hugger, lights, hat, in-line humidifier** * Aspirate the in situ gastric tube- place to suction prior to **intubation** and place to **continuous gravity drainage** throughout the case * Preoxygenate with 100% O2 as tolerated * RSI with cricoid pressure * Maintain with O2 and air * No **N2O** * **Narcotics and muscle relaxation** for surgical repair | pg 39
66
Anestheitc Managment of Gastroschisis & Omphalocele: * Preoperative ____ should be maintained throughout surgery and postoperatively * Monitor Peak Airway Pressure & maintain < ____ mmHg during primary closure * Watch for____ * What may be required during surgery? * ____ intubation and controlled ventilation
* Preoperative **dextrose IVF** should be maintained throughout surgery and postoperatively * Monitor Peak Airway Pressure & maintain **< 25mmHg** during primary closure * Watch for **hypotension** (increased abdominal P can decreased venous return) * Pulse ox on upper and lower extremity to watch venous return from the lower extremity * **Rehydration with crystalloid and colloid** may be required during surgery * **Post operative** intubation and controlled ventilation | pg 40