GI Dysfunction Flashcards
1
Q
Dehydration
A
- Incrd risk for dehydration due to high % of water in body
- Kidneys don’t reutake water like adults
-
Causes
> diarrhea, N/V
> dcrd intake
> sweating w/ fevers
2
Q
Dehydration - CMs
A
- No forming tears
- Wt loss
- Incrd respirations
- Incrd pulses
- Dcrd BP
- Limited urine output
- Dcrd skin turgor
- Sunken eyes
-
Sunken fontanels
want to correct before it causes shock
3
Q
Correcting Fluid Imbalance
A
-
IV hydration
> not 1st option -
Oral rehydration solution
> pedialyte; electrolyes, low sugar
> give small amnt
> popsicles
4
Q
Cleft Lip & Palate
A
- Facial malformations tht occur during embryonic development
-
Bones & tissue fail to fuse completely at midline
> 1st trimester
5
Q
Cleft Lip & Palate - Risk Factors
A
- Syndromes
- Genetics
- Mom has dcr in folic acid during pregnancy
- Alcohol
- Smoking
-
Anticonvulsants, steroids, retinols
> incr change
6
Q
Interprofessional Management
A
-
Can have cleft lip & palate at same time
> can have one or the other -
Cleft lip easier to treat
> don’t usually need more than 1 surgery -
Cleft palate more difficult
> can be a couple of surgeries, around 12-18 months
7
Q
Cleft Lip & Palate - Nursing Interventions
A
-
Feeding
> difficulty suctioning
> want longer nipple, Haberman - Pre & post op care
-
Long-term care
> monitor palate as they grow -
At higher risk for ear infections
> tubes may be placed during correction surgeries
8
Q
Esophageal Atresia & Tracheoesophageal Fistual (TEF)
A
-
Esophageal Atresia: Failure of esophagus to develop as a continuous passage
> esophagus doesn’t attach to stomach or anything, or attaches to trachea - TEF: Failure of trachea to separate into a distinct structure
- Seen on ultrasound
- **Fluid going to lungs or straight back out
9
Q
Esophageal Atresia & Tracheoesophageal Fistual (TEF) - Manifs
A
- Coughing
- Choking
- Cyanosis
10
Q
Esophageal Atresia & Tracheoesophageal Fistual (TEF) - Nursing Interventions
A
- Have continuous suction set up
-
Prepared for surgery
> pretty quickly after birth
> goal: reattach esophagus to stomach & separate from trachea - Maintain airway
-
Feedings through IV
> NOT NG until after surgery
11
Q
Pyloric Stenosis
A
-
Constiction of pyloric sphincter w/ obstruction of gastric outlet
> result of the thickening of pyloric sphincter which leads to obstruction - Not always present at delivery, happens w/in 1st few wks
- Not usually seen on ultrasound before brith
12
Q
Pyloric Stenosis - Manifs
A
-
Vomit after feedings
> projectile; entire feeding - Act very hungry
- Dehydration
- Failure to thrive
-
Peristaltic waves
> left to right - Oval shaped mass
13
Q
Pyloric Stenosis - Treatment
A
Surgery
14
Q
Pyloric Stenosis - Nursing Interventions
A
- Gain IV access to correct hydration
-
Postop, kids usually progress great
> usually no long term effects
15
Q
Hirschsprung’s
A
-
AKA “congenital aganglionic megacolon”
> congenital anomaly
> usually seen after they are born -
Mechanical obstruction from inadequate motility (peristalsis) of intestine
> absence of ganglion cells in colon
> leads to a blockage above area