Written by students who passed Immediately available after payment Read online or as PDF Wrong document? Swap it for free 4.6 TrustPilot
logo-home
Document preview thumbnail
Preview 4 out of 34 pages
Exam (elaborations)

NR 507 Exam 3: Advanced Pathophysiology V3 Updated and Latest Questions and Correct Answers with Rationale

Document preview thumbnail
Preview 4 out of 34 pages

NR 507 Exam 3: Advanced Pathophysiology V3 Updated and Latest Questions and Correct Answers with Rationale

Content preview

NR 507 Exam 3: Advanced Pathophysiology V3 Updated
and Latest Questions and Correct Answers with Rationale
1. Which electrolyte imbalance is a hallmark feature of the Syndrome of Inappropriate

Antidiuretic Hormone (SIADH)?


A. Hypernatremia


B. Hypokalemia


C. Hyponatremia


D. Hypercalcemia



Ans: C


Rationale: SIADH involves the excessive release of antidiuretic hormone which promotes significant

water reabsorption in the kidneys. This extra water expands the extracellular fluid volume and leads to a

dilutional effect on sodium. Consequently, serum sodium levels drop below the normal range resulting in

hyponatremia. Patients may experience neurological symptoms as water shifts into brain cells causing

edema. The condition is often associated with small cell lung cancer or traumatic brain injuries.

Treatment involves fluid restriction to normalize the sodium concentration in the blood.

,2. In Type 1 Diabetes Mellitus, the primary underlying mechanism is:


A. Insulin resistance in peripheral tissues


B. Excessive glucagon production from alpha cells


C. Autoimmune destruction of pancreatic beta cells


D. Decreased glucose absorption in the gut



Ans: C


Rationale: Type 1 diabetes is characterized by an absolute insulin deficiency due to the loss of beta cells.

This destruction is typically mediated by an autoimmune response involving T-cells and various

autoantibodies. Without insulin, glucose cannot enter cells for energy, leading to hyperglycemia and

metabolic distress. The body compensates by breaking down fats, which often leads to the development

of ketoacidosis. Genetic susceptibility and environmental triggers are considered the primary drivers of

this immune dysfunction. Clinical presentation usually occurs abruptly in children or young adults with

classic symptoms of polyuria and polydipsia.


3. Which clinical manifestation is most characteristic of Cushing Syndrome?


A. Hyperpigmentation and weight loss


B. Cold intolerance and bradycardia


C. Postural hypotension and tachycardia


D. Central obesity and a ‘buffalo hump’



Ans: D

,Rationale: Cushing syndrome results from chronic exposure to excessive levels of cortisol in the body.

Cortisol promotes lipogenesis in the trunk while causing muscle wasting in the extremities. This leads to

the classic physical appearance of a rounded ‘moon face’ and a fat pad on the upper back. High cortisol

levels also interfere with collagen synthesis, resulting in thin skin and purple striae. Bone density often

decreases because cortisol inhibits osteoblast activity and calcium absorption. Metabolic consequences

include glucose intolerance and potential development of secondary diabetes mellitus.


4. The most common cause of hypothyroidism worldwide is:


A. Pituitary adenoma


B. Hashimoto thyroiditis


C. Iodine deficiency


D. Graves disease



Ans: C


Rationale: Hypothyroidism occurs when the thyroid gland fails to produce sufficient levels of T3 and T4

hormones. Globally, the lack of dietary iodine remains the most prevalent cause of this condition. In

regions with adequate iodine, Hashimoto thyroiditis, an autoimmune disorder, becomes the leading

cause. Symptoms typically include fatigue, weight gain, and cold intolerance due to a lowered metabolic

rate. Elevated levels of Thyroid Stimulating Hormone are usually found as the pituitary tries to

compensate. Long-term untreated hypothyroidism can lead to severe complications like myxedema

coma.

, 5. Which hormone is responsible for stimulating the contraction of the gallbladder and the

release of pancreatic enzymes?


A. Gastrin


B. Secretin


C. Cholecystokinin (CCK)


D. Somatostatin



Ans: C


Rationale: Cholecystokinin is a peptide hormone produced by the I-cells in the duodenum and jejunum.

It is released in response to the presence of fats and proteins in the small intestine. CCK triggers the

gallbladder to contract, which moves bile into the common bile duct. Simultaneously, it stimulates the

pancreas to secrete digestive enzymes into the duodenum. This hormone also plays a role in slowing

gastric emptying to ensure efficient digestion. Understanding CCK is vital for diagnosing disorders like

biliary dyskinesia or chronic pancreatitis.


6. Gastroesophageal reflux disease (GERD) is primarily caused by:


A. Excessive production of hydrochloric acid


B. Incompetence of the lower esophageal sphincter


C. Rapid gastric emptying into the duodenum


D. Infection with Helicobacter pylori



Ans: B

Document information

Uploaded on
April 1, 2026
Number of pages
34
Written in
2025/2026
Type
Exam (elaborations)
Contains
Questions & answers
$17.99

Wrong document? Swap it for free Within 14 days of purchase and before downloading, you can choose a different document. You can simply spend the amount again.
Written by students who passed
Immediately available after payment
Read online or as PDF

Seller avatar
Reputation scores are based on the amount of documents a seller has sold for a fee and the reviews they have received for those documents. There are three levels: Bronze, Silver and Gold. The better the reputation, the more your can rely on the quality of the sellers work.
Axpert
3.8
(126)
Sold
560
Followers
167
Items
29683
Last sold
1 week ago



Why students choose Stuvia

Created by fellow students, verified by reviews

Quality you can trust: written by students who passed their tests and reviewed by others who've used these notes.

Didn't get what you expected? Choose another document

No worries! You can instantly pick a different document that better fits what you're looking for.

Pay as you like, start learning right away

No subscription, no commitments. Pay the way you're used to via credit card and download your PDF document instantly.

Student with book image

“Bought, downloaded, and aced it. It really can be that simple.”

Alisha Student

Working on your references?

Create accurate citations in APA, MLA and Harvard with our free citation generator.

Working on your references?

Frequently asked questions