Nursing Elites

1. Which of the following is NOT a function of the integumentary system?

• A. Regulation of body temperature
• B. Protection from pathogens
• C. Synthesis of vitamin D
• D. Production of digestive enzymes

Correct answer: D

Rationale: The correct answer is D. The production of digestive enzymes is not a function of the integumentary system. The integumentary system is responsible for regulating body temperature, protecting the body from pathogens, and synthesizing vitamin D. Digestive enzymes are produced by organs in the digestive system, such as the pancreas and stomach, and not by the integumentary system.

2. How can you differentiate between a bacterial and viral infection based solely on symptoms?

• A. It's impossible to differentiate solely based on symptoms.
• B. Bacterial infections typically respond well to antibiotics, while viral infections don't.
• C. Bacterial infections usually cause fever, while viral infections don't.
• D. Viral infections often present with respiratory symptoms like a cough, while bacterial infections don't.

Correct answer: A

Rationale: It is impossible to differentiate between a bacterial and viral infection based solely on symptoms because many symptoms overlap between the two types of infections. Symptoms like fever, cough, and others can be present in both bacterial and viral infections. Additional diagnostic tests such as cultures or blood tests are often needed to determine the cause of the infection accurately. Relying only on symptoms can lead to misdiagnosis and inappropriate treatment. Choices B, C, and D are incorrect because they oversimplify the differentiation process and do not encompass the complexity of symptoms associated with bacterial and viral infections. While it is true that bacterial infections may respond to antibiotics and some differences in symptoms may be observed between bacterial and viral infections, these are not definitive indicators without proper diagnostic tests.

3. What is the process by which RNA molecules are modified after transcription but before translation?

• A. Replication
• B. Splicing
• C. Editing
• D. Packaging

Correct answer: B

Rationale: B) Splicing is the correct answer. Splicing is the process by which non-coding regions (introns) are removed from pre-mRNA, and the remaining coding regions (exons) are joined together to form mature mRNA. This modification occurs after transcription but before translation. A) Replication is incorrect as replication is the process by which DNA is copied to produce a new DNA molecule, not RNA modifications. C) Editing may involve RNA editing, but it is not commonly used to describe the modification of RNA molecules after transcription. D) Packaging is not the correct term as it refers to the condensation and organization of DNA into chromatin in eukaryotic cells, not the modification of RNA molecules.

4. Which of the following is specialized tissue in the right atrium that acts as the heart’s natural pacemaker by generating the electrical signal for the heartbeat?

• A. sinus venosus
• B. sinoatrial node
• C. atrioventricular node
• D. tricuspid valve

Correct answer: B

Rationale: The sinoatrial node, often referred to as the SA node, is specialized tissue located in the right atrium of the heart. It functions as the heart's natural pacemaker by generating the electrical signal that initiates each heartbeat. This electrical signal spreads to the atrial muscles and then to the atrioventricular node, causing the heart to contract rhythmically and efficiently. The other options listed do not serve as the heart's natural pacemaker responsible for generating the electrical signal for the heartbeat. Sinus venosus is a developmental structure in fetal hearts, the atrioventricular node delays the electrical signal, and the tricuspid valve is a heart valve that prevents backflow of blood from the right ventricle to the right atrium.

5. Which of the following antibodies can cross the placenta?

• A. IgA
• B. IgD
• C. IgG
• D. IgM

Correct answer: C

Rationale: The correct answer is IgG. IgG is the only antibody that can cross the placenta, providing passive immunity to the developing fetus. IgA, IgD, and IgM do not cross the placenta. IgA is mainly found in mucosal secretions, IgD is involved in the activation of B cells, and IgM is the first antibody produced in response to an infection, but it does not cross the placental barrier.

Similar Questions