100% satisfaction guarantee Immediately available after payment Both online and in PDF No strings attached
logo-home
RNC-NIC QUESTIONS AND ANSWERS £9.95   Add to cart

Exam (elaborations)

RNC-NIC QUESTIONS AND ANSWERS

 10 views  0 purchase
  • Module
  • RNC-NIC
  • Institution
  • RNC-NIC

RNC-NIC QUESTIONS AND ANSWERS

Preview 3 out of 16  pages

  • September 2, 2024
  • 16
  • 2024/2025
  • Exam (elaborations)
  • Questions & answers
  • RNC-NIC
  • RNC-NIC
avatar-seller
RNC-NIC QUESTIONS AND ANSWERS
"Double bubble" on xray - Answers -Duodenal atresia

4 pulmonary veins attached to the venous system, returning oxygenated blood to the
right side of the heart instead of left atrium - Answers -TAPVR

Adrenal crisis and signs of cortisol insufficiency - Answers -Complication of CAH
S/S include shock, low blood pressure, acidosis, low glucose, seizures, sodium
depletion

Albumin - Answers --Synthesized in the liver
-decreased in hepatocellular injury

Alk Phos - Answers --derived from liver, also found in bone, kidney, and small intestine
-increased an obstructed bile disease, hepatitis, bone disease

Anencephaly - Answers -A primary defect of anterior neural tube closure

Anomalies associated with esophageal atresia - Answers -SGA
VATER synd.
-vertebral
-imperf anus
-renal dysplasia

Aortic stenosis signs/symptoms - Answers -None at birth
Grade 2-6 harsh systolic murmur in upper RSB
CHF S/S delayed by weeks but progresses rapidly

Components of TOF - Answers -1) pulmonary stenosis
2) VSD
3) aorta overrides VSD
4) RV hypertrophy

Congenital adrenal hyperplasia (CAH)
Treatment - Answers -1) Restore physiological levels of cortisol
2) suppress ACTH & androgen overproduction
3) Watch fluid and electrolytes (esp low Na)
4) lifelong here, may need increased doses of cortisol with illness

Congenital adrenal hyperplasia (CAH) - Answers -A group of autosomal recessive
genetic disorders resulting from deficient activity of enzyme required to synthesize
cortisol from cholesterol in adrenal cortex

Most common cause of ambiguous genitalia

,Congenital diaphragmatic hernia
Associated with - Answers -Trisomy 13
Trisomy 18
Trisomy 21,
Trisomy 45
Trisomy X
Intestinal malrotation

Congenital diaphragmatic hernia
Care - Answers -NPO, gastric decompression
Avoid BVM, intubate
Watch for pulmonary air leaks
May need HFOV, INO, ECMO

Congenital Diaphragmatic hernia
S/s - Answers -Hallmark finding-
fluid filled stomach just below left atrium

Consistent finding that reflects RV volume overload - Answers -Hyperdynamic
precordial activity

Correct ETT placement - Answers -T1-T2
level of clavicles

Correct PICC placement - Answers -T3-5
Lower 1/3 of s. Vena cava

Correct UAC placement - Answers -Low-L3-4
Below renal arteries

High-T6-10

Correct UVC placement - Answers -T 8-9
0.5-1 cm above diaphragm
Tip in inf. vena cava

Cri du chat syndrome - Answers -

CXR heart has appearance of "egg on a string" - Answers -TGV

Dexamethasone adverse effects - Answers --increased glucose levels
-increase blood pressure
-Poor weight gain
-Increased risk of sepsis

, Di George syndrome (22q11.2 deletion syndrome) - Answers -Inherited Autosomal
dominant trait
Short stature
Hypogonadism
Hypoplasia or aplasia of thymus and parathyroid
Associated heart defects
Microcephaly
Palatial anomalies and small mouth
Hypotonia
Can have later schizophrenia & depression

Diagnosis of gastroschisis or omphalocele - Answers -Elevated AFP

DIC Labs - Answers --Low platelets
-prolonged PT and PTT
-increased FSP
-decreased fibrinogen
-increased d-dimer which is the marker DIC

Difference in PaO2 of________ or greater documents ductal shunting - Answers -15%

Digoxin works by - Answers -Increasing intracellular calcium leading to a +inotropic
effect which increases contractility

Duodenal atresia stenosis s/s - Answers -Polyhydramnios
Abdominal distention
No stools
Bilious vomiting within 24 hours

Duodenal stenosis atresia associated with - Answers -Trisomy 21
CHD
Intestinal malrotation
TE abnormalities
Anorectal defects

Eagle-Barrett Syndrome - Answers -1) absent abdominal musculature
2) GU tract abnormalities
3) undescended testicles

Oligohydramnios

Encephalocele - Answers -Failure of closure resulting in extension of brain tissue
through defect in skull
Often occipital

Erb's palsy - Answers -Brachioplexus injury involving cranial n. V & VI

The benefits of buying summaries with Stuvia:

Guaranteed quality through customer reviews

Guaranteed quality through customer reviews

Stuvia customers have reviewed more than 700,000 summaries. This how you know that you are buying the best documents.

Quick and easy check-out

Quick and easy check-out

You can quickly pay through credit card for the summaries. There is no membership needed.

Focus on what matters

Focus on what matters

Your fellow students write the study notes themselves, which is why the documents are always reliable and up-to-date. This ensures you quickly get to the core!

Frequently asked questions

What do I get when I buy this document?

You get a PDF, available immediately after your purchase. The purchased document is accessible anytime, anywhere and indefinitely through your profile.

Satisfaction guarantee: how does it work?

Our satisfaction guarantee ensures that you always find a study document that suits you well. You fill out a form, and our customer service team takes care of the rest.

Who am I buying these notes from?

Stuvia is a marketplace, so you are not buying this document from us, but from seller GEEKA. Stuvia facilitates payment to the seller.

Will I be stuck with a subscription?

No, you only buy these notes for £9.95. You're not tied to anything after your purchase.

Can Stuvia be trusted?

4.6 stars on Google & Trustpilot (+1000 reviews)

84866 documents were sold in the last 30 days

Founded in 2010, the go-to place to buy revision notes and other study material for 14 years now

Start selling
£9.95
  • (0)
  Add to cart