Lecture 3 (Part 1)-Peds GI Surgeries Flashcards

1
Q

What are two types of abdominal wall defects in peds?

A
  • Gastrochisis

- Omphalocele

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2
Q

What is the following describing?—defect of the anterior abdominal wall to the right of the umbilical cord; no sac, bowel is exposed to the intrauterine environment; bowel is matted, thickened, covered with an inflammatory coating

A

Gastroschisis

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3
Q

Newborns with gastroschisis have ___ issues

A

Malabsorption

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4
Q

Gastroschisis results in ___itis, ___cellular fluid loss, significant ___ loss

A

Peritonitis, extracellular fluid loss, significant heat loss

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5
Q

Fascial defect in gastroschisis is ___-___ cm

A

2-5 cm

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6
Q

Umbilical cord in gastroschisis is normal—T/F?

A

True

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7
Q

Gastroschisis usually involves ___ and ___

A

Large and small intestines

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8
Q

Gastroschisis is a ___ event, resulting from an abnormality of ___ (right/left) omphalomesenteric artery or ___ (right/left) umbilical vein

A

Vascular event, right omphalomesenteric artery or right umbilical vein

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9
Q

Gastroschisis results in ischemia to ___ (right/left) periumbilical area and dysplastic abdominal wall growth

A

Right

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10
Q

In gastroschisis, weakened area ___ as abdominal organs grow

A

Ruptures

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11
Q

Gastroschisis results from a ___ (increased/decreased) blood supply during development

A

Decreased blood supply

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12
Q

Risk factors for gastroschisis = ___ maternal age, exposure to ___ and ___ during development

A

Young maternal age, exposure to tobacco and alcohol during development

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13
Q

Diagnosis of gastroschisis is done ___ birth via ___

A

Before birth via ultrasound

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14
Q

Omphalocele is more associated with increased maternal serum alpha fetoprotein than is gastroschisis—T/F?

A

False—gastroschisis has a higher incidence in mothers with increased maternal serum alpha fetoprotein

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15
Q

What is this describing?—central defect of umbilical ring/base of umbilical cord; abdominal contents are within a sac; umbilical cord embedded in a sac

A

Omphalocele

C in Omphalocele = central defect

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16
Q

Fascial defect in Omphalocele is > ___ cm

A

> 4 cm

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17
Q

Omphalocele—sac contains ___, ___ and ___, ___ (30-50%)

A

Stomach, large and small intestine, liver

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18
Q

Omphalocele—if fascial defect is < 4 cm, then it is considered ___

A

Umbilical hernia

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19
Q

Omphalocele results from a failure of ___

A

The gut to return to abdominal cavity

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20
Q

Embryology of Omphalocele—weeks ___: midgut herniates into umbilical cord

A

7-12

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21
Q

Embryology of Omphalocele—week ___, abdominal cavity is large enough and gut re-enters the abdomen

A

12…in Omphalocele, the gut does NOT return back into the abdominal cavity

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22
Q

Which has associated anomalies—gastroschisis or Omphalocele?

A

Omphalocele

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23
Q

Gastroschisis or omphalocele—isolated lesion

A

Gastroschisis

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24
Q

Gastroschisis or omphalocele—associated anomalies common

A

Omphalocele

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25
Q

Gastroschisis or omphalocele—central defect

A

Omphalocele

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26
Q

Gastroschisis or omphalocele—lateral defect

A

Gastroschisis

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27
Q

Gastroschisis or omphalocele—umbilical cord within defect

A

Omphalocele

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28
Q

Gastroschisis or omphalocele—umbilical cord normal

A

Gastroschisis

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29
Q

Gastroschisis or omphalocele—bowel exposed, thickened, edematous

A

Gastroschisis

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30
Q

Gastroschisis or omphalocele—sac covers organs, bowl normal

A

Omphalocele

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31
Q

Which is more common—gastroschisis or omphalocele?

A

Omphalocele = 1:4,000-7,000

Gastroschisis = 1:10,000

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32
Q

Surgical management of omphalocele—in some cases with very large omphalocele in which the organs are so large they will not fit into the abdominal cavity, a “paint and wait” method is done. Eventually, skin will grow over the sac and after the baby grows, the surgeon can discuss a procedure to finish closing what remains—T/F?

A

True

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33
Q

If primary closure is to be done for omphalocele, the peritoneal cavity must be able to accommodate abdominal viscera without compromising ___ and ___

A

Ventilation and circulation

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34
Q

Negative effects of tight abdominal closure—impairs diaphragmatic excursion, resulting in inadequate ___ and ___ (increased/decreased) airway pressure

A

Inadequate ventilation and increased airway pressure

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35
Q

Negative effects of tight abdominal closure—impaired ___ return, leading to profound ___tension

A

Impaired venous return, leading to profound hypotension

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36
Q

Negative effects of tight abdominal closure—aortocaval compression, leading to bowel ___, ___ (increased/decreased) CO, and renal and hepatic dysfunction

A

Bowel ischemia, decreased CO

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37
Q

If tight abdominal closure is done, ___ syndrome can occur

A

Abdominal compartment syndrome

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38
Q

Abdominal wall defects—unsafe for primary closure = intragastric pressure > ___ mm Hg

A

> 20 mm Hg

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39
Q

Abdominal wall defects—unsafe for primary closure = change in CVP > ___ mm Hg above baseline

A

CVP > 4 mm Hg

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40
Q

Abdominal wall defects—unsafe for primary closure = ETCO2 > ___ mm Hg

A

ETCO2 > 50 mm Hg

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41
Q

Abdominal wall defects—unsafe for primary closure = peak inspiratory pressure > ___ cm H2O

A

PIP > 35 cm H2O

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42
Q

Abdominal wall defects—CVP change > 4 mm Hg above baseline can indicate reductions in ___ and ___

A

Venous return and cardiac index

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43
Q

Abdominal wall defects pre-op—fluid resuscitation—maintenance fluid = __ or ___ in 0.2 NS

A

D5 or D10 in 0.2 NS

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44
Q

Abdominal wall defects pre-op—replacement fluid—___ solution at ___-___ times maintenance rate

A

Isotonic solution (NS or LR) at 2-4 times maintenance rate (8-15 cc/kg/hr)

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45
Q

Abdominal wall defects pre-op—urine output goal ___-___ cc/kg/hr

A

1-2 cc/kg/hr

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46
Q

Abdominal wall defects pre-op—monitor ___ose, ___lytes, ___ status

A

Glucose, electrolytes, acid/base status

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47
Q

Abdominal wall defects pre-op—maintain ___thermia and prevent ___ from exposed viscera; cover abdominal contents with ___ gauze and ___ bag

A

Maintain normothermia and prevent heat loss from exposed viscera; cover abdominal contents with warm, saline soaked gauze and plastic bowel bag

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48
Q

Abdominal wall defects—a lot of heat loss can happen through wet gauze dressing, so plastic bowel bag is imperative to prevent heat loss—T/F?

A

True

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49
Q

Abdominal wall defects pre-op—treat sepsis with ___

A

Broad spectrum antibiotics

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50
Q

Abdominal wall defects—prevent aspiration by ___

A

Decompressing the stomach with orogastric tube

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51
Q

Anesthetic management of abdominal wall defects—ASA standard monitors; ___ pulse oximeters—right ___ (pre-ductal) and left ___ (post-ducal); ___ large bore IVs above diaphragm; ___ line if hemodynamically unstable; foley; monitor airway ___; CVP to assess changes in blood ___, magnitude of visceral compression

A

2 pulse oximeters—right arm (pre-ducal) and left foot (post-ducal); 2 large bore IVs above diaphragm; arterial line if HD unstable; foley; monitor airway pressures; CVP to assess changes in blood volume, magnitude of visceral compression

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52
Q

Abdominal wall defects—avoid ___ because it can cause bowel distention

A

Nitrous oxide

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53
Q

Abdominal wall defects—set FiO2 to maintain SPO2 ___-___%, PaO2 ___-___ mm Hg

A

Sat 95-97%, PaO2 50-70 mm Hg

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54
Q

Abdominal wall defects—maintenance fluid = ___

A

D5.2 NS

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55
Q

Abdominal wall defects—replacement fluid = ___ at ___-___ ml/kg/hr

A

Isotonic fluid at 8-15 ml/kg/hr

Replace third space losses with this*

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56
Q

Abdominal wall defects—replace blood loss with ___ PRBCs

A

Washed PRBCs (decreased K in washed)

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57
Q

Abdominal wall defects—maintain normothermia; room temp ___ degrees

A

80 degrees

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58
Q

NICU often prefers to receive patient ___ post-op because they can more easily control pain and ensure baby maintains adequate ventilation support while receiving narcotics

A

Intubated post-op

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59
Q

Post-op abdominal wall defects—___ required for days to weeks d/t prolonged postoperative ileus

A

TPN

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60
Q

Postoperative complications after abdominal wall repair—___onia, ___ (NEC), ___ insufficiency, ___ breakdown, ___ reflux

A

Pneumonia, necrotizing enterocolitis, renal insufficiency, abdominal wall breakdown, gastroesophageal reflux

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61
Q

What is this describing?—defect in the diaphragm that allows herniation of abdominal organs into the thoracic cavity

A

Congenital diaphragmatic hernia

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62
Q

Congenital diaphragmatic hernia usually occurs if there is a prenatal history of ___

A

Polyhydramnios

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63
Q

(3) CDH Classifications:

A
  • Posterolateral (80-90%, left 75%)
  • Anteromedial (2%)
  • Paraesophageal (15-20%)
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64
Q

Which CDH classification occurs most commonly?

A

Posterolateral—80-90%, left 75%

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65
Q

CDH complications—bilateral lung ___plasia; pulmonary ___tension and arteriolar ___; ___ ventricular dysfunction

A

Bilateral lung hypoplasia; pulmonary hypertension and arteriolar reactivity; left ventricular dysfunction

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66
Q

CDH—the degree of pulmonary hypoplasia and hypertension is predictive of mortality and long-term sequelae—T/F?

A

True

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67
Q

Pathophysiology of CDH—abdominal viscera (midgut, stomach, parts of descending colon, L kidney, L lobe of liver) occupy the ___ thoracic cavity and interfere with the development of the lung, resulting in pulmonary hypoplasia

A

Left thoracic cavity

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68
Q

Patho of CDH—herniation of abdominal contents shifts mediastinum to the ___, resulting in ___ and ___plasia of the contralateral lung

A

Shifts mediastinum to the right, resulting in compression and hypoplasia of the contralateral lung

69
Q

Patho of CDH—CDH causes structural abnormalities of pulmonary vasculature, which results in ___ lung disease—___ number of airways; simple arterial branching pattern; ___ (increased/decreased) smooth muscle mass in resistance vessels; left ventricular abnormalities

A

Chronic lung disease—small number of airways; simple arterial branching pattern; increased smooth muscle mass in resistance vessels; left ventricular abnormalities

70
Q

CDH—compressed lungs leads to hindered development of ___

A

Hindered development of alveoli—there are less of them overall

71
Q

CDH—smaller alveolar gas exchange ___

A

Surface area

72
Q

CDH—___ is usually the problem d/t rising ___; ___ is okay

A

Ventilation is usually the problem d/t rising CO2; oxygenation is okay

73
Q

Clinical presentation of CDH—symptoms appear within ___ to ___

A

Minutes to hours

74
Q

CDH classic triad of symptoms =

A
  • Dyspnea
  • Cyanosis
  • Apparent dextrocardia (heart points to the right instead of left)
75
Q

CDH physical exam—___ chest and ___ abdomen; ___ (increased/decreased) breath sounds; ___ or ___ (right/left) displaced heart sounds; ___ sounds in the chest; chest x-ray shows ___ loops in the chest and ___ shift

A

Bulging chest and scaphoid abdomen; decreased breath sounds; distant or left displaced heart sounds; bowel sounds in the chest; chest x-ray shows bowel loops in the chest and mediastinal shift

76
Q

Key to survival of CDH = ___ diagnosis which can allow the birth to occur in a center with a high level NICU and experienced surgeons

A

Prenatal diagnosis—can see bowel in the thoracic cavity on ultrasound

77
Q

Old school of thought—CDH was considered a neonatal surgical emergency; surgical repair was performed immediately; goal was ___ventilation with ___% O2 to produce pulmonary vaso___ with ___oxia and respiratory ___osis

A

Goal was hyperventilation with 100% O2 to produce pulmonary vasodilation with hyperoxia and respiratory alkalosis

78
Q

Result of former CDH interventions was repeated over distention of the lung tissue and damage to the alveolar and capillary membranes; net effect of hyperventilation/oxygenation was an ___ response that caused the release of vasoactive mediators, worsening pulmonary vaso___ and pulmonary ___tension

A

Inflammatory response that caused the release of vasoactive mediators, worsening pulmonary vasoconstriction and pulmonary hypertension

79
Q

Goals of medical management of CDH—current wisdom is that these patients benefit from 24-48 hours of medical stabilization prior to surgery—T/F?

A

True

80
Q

4 goals of medical management for CDH—maximize arterial ___; correct ___osis; prevent ___thermia; and prevent ___

A

Maximize arterial oxygenation; correct acidosis; prevent hypothermia; and prevent pain!

81
Q

CDH maximize arterial oxygenation—intubation; mechanical ventilation with low inflating pressures (< ___-___ cm H2O); maintain muscle ___

A

Inflating pressures < 20-30 cm H2O; maintain muscle relaxation

82
Q

CDH surgery can occur when ___ is normal for age and stable for 24 hours; pre-ductal sat > ___ (preferably ___ to ___) with FiO2 less than ___; no ___osis; lactate < ___; urine output ___-___ ml/kg/hr

A

When BP is normal for age and stable for 24 hours; pre-ductal sat > 85 (preferably 90 to 95) with FiO2 less than 0.5; no acidosis; lactate < 3; urine output 1-2 ml/kg/hr

83
Q

CDH intubation diminishes the danger of ___

A

Pneumothorax

84
Q

CDH intubation—minimize ___trauma/___trauma from positive pressure ventilation, thereby minimizing further lung damage

A

Minimize barotrauma/volutrauma

85
Q

CDH—bag mask ventilation has the potential to create distention of the stomach and intestines, resulting in ___ (increased/decreased) chest compliance

A

Decreased chest compliance

86
Q

CDH—important to improve pulmonary perfusion—___ventilation (maintain PaCO2 ___-___ mm Hg); ___ infusion to maintain sedation and limit spikes in PVR from irritability; minimal handling

A

Hyperventilation (maintain PaCO2 25-30 mm Hg); fentanyl infusion

87
Q

CDH—use ___ because it allows for vascular smooth muscle relaxation and decreases PVR

A

Nitric oxide

88
Q

ECMO for CDH—blood removed via ___ cannula, passed through membrane oxygenator, returned via ___ cannula; common sites for cannulation = ___ and ___

A

Blood removed via venous cannula, passed through membrane oxygenator, returned via arterial cannula; common sites for cannulation = IJ and common carotid

89
Q

CDH—since spontaneous ventilatory efforts are usually inadequate, early ___ and ___ of the stomach are critical initial steps to prevent further distention of abdominal organs and pulmonary compression by abdominal viscera

A

Early intubation and decompression of the stomach

90
Q

CDH—unless right to left shunting has occurred, permissive ___capnea should occur to PaCO2 of ___-___, helping to provide less aggressive ventilatory support resulting in secondary lung injury

A

Permissive hypercapnea should occur to PaCO2 55-60

91
Q

Complications of ECMO—___ at cannulation sites; ___ hemorrhage; ___sis; ___tension; ___ death

A

Bleeding at cannulation sites; intracranial hemorrhage; sepsis; hypertension; brain death

92
Q

Criteria for ECMO—weight more than ___ kg; gestation > ___ weeks

A

Weight more than 2.0 kg; gestation > 35 weeks

93
Q

CDH preoperative prep—IV access in ___ extremities (because vena cava is sometimes compressed after reduction of hernia); prevent ___thermia

A

IV access in upper extremities; prevent hypothermia

94
Q

CDH preoperative management—___ support; meticulous management of ___ and ___; hemodynamic monitoring

A

Ventilatory support; meticulous management of fluids and nutrition; hemodynamic monitoring

95
Q

CDH preoperative management—often there is a ___ period followed by rapid ___

A

Honeymoon period followed by rapid deterioration—mild ventilatory/hemodynamic support, then quickly deteriorate requiring NO or ECMO—unexplained reasons

96
Q

CDH signs of deterioration—___ (increased/decreased) intraabdominal pressure; ___ (increased/decreased) perfusion of the viscera and periphery; ___ (increased/decreased) diaphragmatic excursion; ___ pulmonary compliance

A

Increased intraabdominal pressure; decreased perfusion of the viscera and periphery; decreased diaphragmatic excursion; worsening pulmonary compliance

97
Q

CDH anesthetic management—ASA standard monitors; arterial line; foley; precordial stethoscope at ___ axilla; ___ to decompress stomach; IV access; core temp management to prevent ___thermia

A

Precordial stethoscope at right axilla; NGT to decompress stomach; IV access; core temp management to prevent hypothermia

98
Q

CDH induction—___ intubation; ___ induction; avoid ___ ventilation or ___ pressure ventilation before intubation

A

Awake intubation; rapid sequence induction; avoid mask ventilation or positive pressure ventilation before intubation

99
Q

CDH anesthetic maintenance—avoid ___ because it increases oxygen concentration required and can expand viscera and cause further compression of the lungs

A

Nitrous oxide

100
Q

CDH anesthetic maintenance—TIVA can be done with ___ infusion and muscle relaxation

A

Remifentanil infusion

101
Q

CDH anesthetic maintenance—inhaled agents can be used, but will ___ (increase/decrease) PVR; ___ decreases more than PVR, which could cause right to left shunting

A

Decrease PVR; SVR decreases more than PVR, which could cause right to left shunting

102
Q

What may be the best anesthetic maintenance for CDH?

A

Narcotics and muscle relaxants

103
Q

CDH anesthetic maintenance—avoid ___ia and ___osis, which ___ (increase/decrease) PVR and cause R to L shunting

A

Hypoxia and acidosis, which increase PVR and cause R to L shunting

104
Q

CDH—hypothermia ___ (increases/decreases) PVR, which increases R to L shunting through PDA or patent foramen ovale; also increases oxygen consumption

A

Increases PVR

105
Q

CDH—have ___ and ___ in the room

A

Nitrous oxide and ECMO

106
Q

CDH surgical complications—___emia; pulmonary ___plasia; pulmonary ___tension; respiratory ___ from distention of stomach, ___ intraabdominal pressure; contralateral ___; ___ compression; ___tension

A

Hypoxemia; pulmonary hypoplasia; pulmonary hypertension; respiratory compromise from distention of stomach, increased intraabdominal pressure; contralateral pneumothorax; IVC compression; hypotension

107
Q

CDH—during surgery, if hemodynamics/ventilatory status quickly deteriorates, must be able to differentiate between ___ crisis or ___

A

Pulmonary hypertensive crisis or pneumothorax

Pulmonary HTN = nitrous + hyperventilate

Pneumothorax = needle decompression + chest tube placement

108
Q

CDH outcomes—pulmonary = the first year post-op consists of multiple respiratory ___; need for ___, inhaled ___; however, by childhood and late adolescence, survivors achieve near normal lung ___ and ___ with minimal obstructive or restrictive lung disease/without pulmonary HTN

A

The first year post-op consists of multiple respiratory infections; need for bronchodilators, inhaled steroids; however, by childhood and late adolescence, survivors achieve near normal lung volumes and mechanics with minimal obstructive or restrictive lung disease/without pulmonary HTN

109
Q

CDH outcomes—MSK = mild ___ abnormalities can be noted—pectus ___ or ___ can be noted in 7-9%

A

Mild chest abnormalities can be noted—pectus excavatum or scoliosis can be noted in 7-9%

110
Q

CDH outcomes—GI dysfunction = GERD, can later do ___ fundoplication; bowel ___ or ___ (d/t lack of fixation to abdominal cavity)

A

GERD, can later do nissen fundoplication; bowel obstruction or malrotation (d/t lack of fixation to abdominal wall)

111
Q

CDH outcomes—neuro = cerebral ___regulation is affected d/t pulmonary ___tension and hemodynamic instability; ultimately leads to cognitive issues d/t lack of ___

A

Cerebral autoregulation is affected d/t pulmonary hypertension and hemodynamic instability; ultimately leads to cognitive issues d/t lack of perfusion

112
Q

Pyloric stenosis occurs in 1 in ___ live births; occurs 4 times more often in ___

A

Occurs in 1 in 500 live births; occurs 4 times more often in males

113
Q

Pyloric stenosis is ___, not congenital; occurs more often if ___

A

Acquired; occurs more often if a parent had the same condition

114
Q

Patho of pyloric stenosis = gross thickening of the circular smooth muscle of the ___; results in gradual ___ of the gastric outlet; causes ___, ___, nonbilious vomiting

A

Gross thickening of the circular smooth muscle of the pylorus; results in gradual obstruction of the gastric outlet; causes forceful, projectile, nonbilious vomiting

115
Q

What disease is this characteristic of?—vomiting “across the room and hitting the wall”

A

Pyloric stenosis

116
Q

Pyloric stenosis typically presents between ___-___ weeks of life; most commonly ___ weeks and ___ kg

A

2-8 weeks of life; most commonly 4 weeks and 4 kg

117
Q

Pyloric stenosis diagnosis = palpation of ___-sized mass in the ___ aspect of the abdomen; verified by upper GI series with ___, ___, or abdominal ___

A

Palpation of olive-sized mass in the upper aspect of the abdomen; verified by upper GI series with barium, x-ray, or abdominal ultrasound

118
Q

Pyloric stenosis clinical presentation—persistent vomiting results in the loss of ___ gastric juices rich in ___, ___, and to a lesser degree ___ ions

A

Persistent vomiting results in the loss of acidic gastric juices rich in hydrogen, chloride, and to a lesser degree sodium ions

119
Q

Pyloric stenosis—vomitus does not contain the ___ secretions of the duodenum

A

Vomitus does not contain the alkaline secretions of the duodenum

120
Q

Pyloric stenosis—kidneys begin secreting ___ ions in exchange for hydrogen in an attempt to maintain normal arterial pH

A

Potassium ions

121
Q

Pyloric stenosis—patient develops a ___ ___osis— decreased ___ and ___

A

Metabolic alkalosis—decreased Na and Cl

122
Q

Pyloric stenosis—after vomiting, patient is ___

A

Hungry again

123
Q

The result of pyloric stenosis is a ___ infant with a ___natremic, ___kalemic, ___chloremic metabolic ___osis

A

Dehydrated infant with a hyponatremic, hypokalemic, hypochloremic metabolic alkalosis

124
Q

Severe cases of pyloric stenosis can manifest as a metabolic ___osis, secondary to severe ___ and ___perfusion

A

Metabolic acidosis secondary to severe dehydration and hypoperfusion

125
Q

Pyloric stenosis is a ___ emergency, NOT a ___ emergency!

A

Medical emergency…NOT a surgical emergency!

126
Q

Initial treatment of pyloric stenosis is aimed at correcting the ___ and ___ disturbances; administration of IV fluid containing ___, ___, and ___

A

Correcting the fluid and electrolyte disturbances; administration of IV fluid containing Na, KCl, and glucose—D5 0.45% NSS with KCl meq/L for 12-48 hours

127
Q

What is the primary concern of pyloric stenosis?

A

Aspiration of gastric fluid

128
Q

Pyloric stenosis induction—IV in place; O2 by mask, atropine 10-20 mcg/kg; ___ stomach with large bore (14 Fr) catheter at least ___ times; give O2 inbetween; ___ induction—propofol, succs (roc), styletted ETT, do NOT ___

A

IV in place; O2 by mask, atropine 10-20 mcg/kg; suction stomach with large bore (14 Fr) catheter at least 3 times; give O2 inbetween; rapid sequence induction—propofol, succs (roc), styletted ETT, do NOT ventilate

129
Q

Pyloric stenosis maintenance—O2, ___, low dose ___ agent; “short-acting” ___ muscle relaxant; no ___; ___ anesthetic at the surgical site

A

O2, N2O, low dose inhalation agent; “short-acting” non-depolarizing muscle relaxant; no narcotics; local anesthetic at the surgical site—bupivicaine 0.25%

130
Q

Pyloric stenosis emergence—patients are prone to post-operative respiratory ___ related to preexisting central ___osis; patient must be fully ___ and demonstrating acceptable patterns of ___ before extubation—adequate ___ volume, movement of extremities, protective reflexes intact, absence of breath ___ and ___

A

Patients are prone to post-operative respiratory alkalosis related to preexisting central alkalosis (because body will want to hold onto CO2 to normalize pH); patient must be fully awake and demonstrating acceptable patterns of ventilation before extubation—adequate tidal volume, movement of extremities, protective reflexes intact, absence of breath holding and apnea

131
Q

Pyloric stenosis—the alkalosis can reset the respiratory drive, and the CO2 may need to be in the ___ in order for the baby to breathe

A

CO2 may need to be in the 40s

132
Q

Pyloric stenosis—why don’t we use narcotics for these patients? What can be used alternatively?

A

Narcotics can cause gastroparesis, slow the gut; consider IV or rectal Tylenol

133
Q

What condition is this describing?—condition characterized by esophageal atresia with or without a communication (fistula) between the esophagus and trachea; it is the most common esophageal anomaly, 1:3,000-4,500 live births

A

Tracheoesophageal fistula

134
Q

Tracheoesophageal fistula is common with ___ and ___

A

Prematurity (20-40%) and polyhydramnios (60%)

135
Q

TEF—associated anomalies occur in ___-___% of patients

A

20-50% of patients

136
Q

TEF survival rate is > ___%

A

> 90%

137
Q

Types of TEF; most common?

A

Types A-E; C is most common

138
Q

What type of TEF often escapes diagnosis until later in life when recurrent pneumonias occur?

A

Type E

139
Q

TEF clinical presentation—inability to manage ___ secretions; excessive ___; ___ on first feed; ___ing; ___nosis; ___ation; gastric ___; ___monia

A

Inability to manage oral secretions; excessive salivation; choking on first feed; coughing; cyanosis; aspiration; gastric distention; pneumonia

140
Q

Gastric distention is very common with type ___ TEF

A

Type C TEF—because the lower esophagus connects to the trachea

141
Q

If TEF is not diagnosed prenatally, it is usually diagnosed ___

A

In the first few hours after birth

142
Q

TEF diagnosis—inability to pass ___ catheter or ___ tube into the stomach; chest x-ray confirming position of catheter in ___ pouch, ___ in the stomach and intestines

A

Inability to pass suction catheter or orogastric tube into the stomach; chest x-ray confirming position of catheter in esophageal pouch, air in stomach and intestines

143
Q

TEF associated anomalies—incidence 35-65%, VATER or VACTERL

A
V = vertebral anomalies
A = anorectal anomalies
C = cardiac anomalies, 20-25%
T = TEF
E = esophageal atresia
R = renal anomalies
L = limb anomalies
144
Q

TEF surgical repair—identification and ligation of the fistula; esophageal repair—primary or staged using stomach or intestine; placement of feeding ___ and ___ tube

A

Placement of feeding gastrostomy and chest tube

145
Q

TEF preop preparation—minimize ___ complications—keep patient ___; HOB elevated ___, consider ___ or ___ position; esophageal ___ to low continuous suction

A

Minimize pulmonary complications—keep patient NPO; HOB elevated 30 degrees, consider prone or lateral position; esophageal sump to low continuous suction

146
Q

TEF preop preparation—___ x-ray, ___ x-ray, ___ ultrasound; 12 lead ECG, echocardiogram—___; central IV access for ___; medical stabilization—treat ___monia and optimize volume and acid/base status

A

Chest x-ray, abdominal x-ray, renal ultrasound; 12 lead ECG, echocardiogram—mandatory; central IV access for TPN; medical stabilization—treat pneumonia and optimize volume and acid/base status

147
Q

TEF anesthetic management—priorities = ___ation, ___ation, securing the ___, prevention of ___

A

Oxygenation, ventilation, securing the airway, prevention of aspiration

148
Q

TEF anesthetic management—monitors = ASA standard, precordial stethoscope over ___ chest, ___ line

A

ASA standard, precordial stethoscope over left chest, arterial line

149
Q

TEF—precordial stethoscope can allow breath to breath monitoring to determine ventilation of ___ lung

A

Dependent lung

150
Q

TEF induction—concerns are ___, gastric ___, respiratory ___

A

Aspiration, gastric distention, respiratory compromise

151
Q

TEF induction for unstable infants—consider ___ insertion and ___ intubation—this allows ETT positioning without ___ ventilation

A

Consider gastrostomy insertion and awake intubation—this allows ETT positioning without positive pressure ventilation

152
Q

TEF induction for stable infants—___ induction with spontaneous ventilation vs. ___ induction; avoid or minimize ___ ventilation—___ tidal volumes, ___ peak inspiratory pressures

A

Inhalation induction with spontaneous ventilation vs. IV induction; avoid or minimize positive pressure ventilation—small tidal volumes, low peak inspiratory pressures

153
Q

TEF—surgery may begin with ___ to evaluate where the lesion is—keep patient ___ ventilating during this

A

Surgery may begin with rigid Bronchoscopy to evaluate where the lesion is—keep patient spontaneously ventilating during this

154
Q

TEF—surgeon should be available because in an emergency, gastric ___ may need to occur via insertion of transcutaneous needle or catheter

A

Gastric decompression

155
Q

TEF—assessment of ETT position—goal = above the ___, below the ___

A

Above the carina, below the fistula

156
Q

TEF technique for intubation = ___ intubation; withdraw ETT until breath sounds are confirmed at the ___

A

Right mainstem intubation; withdraw ETT until breath sounds are confirmed at the left axilla

157
Q

TEF anesthetic management—minimize gastric ___; avoid or minimize ___ ventilation—small ___ volumes, low ___ pressures

A

Minimize gastric distention; avoid or minimize positive pressure ventilation—small tidal volumes, low peak inspiratory pressures

158
Q

Anesthetic maintenance for TEF—___ position for R thoracotomy

A

Left lateral decubitus position for R thoracotomy

159
Q

Anesthetic maintenance for TEF—after ligation of fistula, ___ relaxation and controlled ___; use ___ agent and ___ to maintain anesthesia; avoid ___

A

After ligation of fistula, muscle relaxation and controlled ventilation; use inhalation agent and opioids to maintain anesthesia; avoid nitrous oxide

160
Q

TEF intraoperative complications—___ intubation; intubation of ___; ___ of ETT from secretions, blood, infectious material; obstruction/compression of ___ or ___ by surgeon; atelectasis, lung retraction; ___thermia; ___glycemia; resumption of ___ circulation—___ shunting

A

Right mainstem intubation; intubation of fistula; obstruction of ETT from secretions, blood, infectious material; obstruction/compression of trachea or bronchus by surgeon; atelectasis, lung retraction; hypothermia; hypoglycemia; resumption of fetal circulation—R to L shunting

161
Q

TEF emergence—goal is ___ at the end of surgery to prevent manipulation of anastamosis from ETT; patient must be able to maintain airway ___ because reintubation could damage repair; consider that the patient may have tracheo___ or tracheal ___

A

Goal is extubation at the end of surgery to prevent manipulation of anastamosis from ETT; patient must be able to maintain airway patency because reintubation could damage repair; consider that the patient may have tracheomalacia or tracheal collapse

162
Q

TEF—sometimes exubation is not possible d/t issues with ___ control and ___ complications—sometimes safer to leave patient intubated to allow them more time to heal

A

D/t issues with pain control and pulmonary complications

163
Q

TEF post-op—___ should be avoided if possible during first several days post-op

A

Bag valve mask

164
Q

TEF postop—no ___ of the head because it puts tension on the anastomosis; no ___ suctioning beyond the level of the esophageal anastomosis

A

No extension of the head; no esophageal suctioning

165
Q

Long-term complications from TEF = esophageal ___, tracheo___, gastroesophageal ___

A

Esophageal stricture; tracheomalacia; gastroesophageal reflux

166
Q

Esophageal strictures post-TEF may require serial ___

A

Dilations

167
Q

Tracheomalacia post-TEF usually occurs in the ___ one third of the trachea just above the fistula; other respiratory issues = chronic ___, ___, exercise ___

A

Usually occurs in the lower one third of the trachea just above the fistula; other respiratory issues = chronic cough, wheezing, exercise intolerance

168
Q

GERD occurs in ___ to ___% of patients with TEF

A

40 to 65%