WGU D115 Pathophysiology OA Exam: 400+ Questions & Answers (Units 2-7) – 2025/2026

WGU D115 – POST PA STUDY EXAM (UNIT 2, 3, 4, 5, 6 & 7)
PATHOPHYSIOLOGY TEST BANK NEWEST 2025/2026 TESTING
ACTUAL EXAM WITH 400+ QUESTIONS AND CORRECT
DETAILED ANSWERS (VERIFIED ANSWERS) ALREADY GRADED
A+ / WGU D115 OA AND PRE-OA REVIEW (BRAND NEW)
GUARANTEED PASS



The nurse practitioner is caring for a patient who was rewarmed after suffering
J. J. J. J. J. J. J. J. J. J. J. J.




from hypothermia. What possible long-term complication should the NP continue to
J. J. J. J. J. J. J. J. J. J.




assess the patient for?
J. J. J. J.




Acidosis
Dysrhythmias
Shock
J.




Renal failure - ✔✔✔Correct Answer > Renal failure
J. J. J. J. J. J. J. J.




J. Feedback:
The long term complications of rewarming include congestive heart failure, renal
J. J. J. J. J. J. J. J. J. J.




and hepatic failure, abnormal erythropoiesis, myocardial infarction, pancreatitis,
J. J. J. J. J. J. J. J.




and neurologic dysfunction.
J. J. J.




The APN is evaluating a client for compartment IV primary amenorrhea. Which
J. J. J. J. J. J. J. J. J. J. J.




assessments would the APN perform as priorities? Select all that apply.
J. J. J. J. J. J. J. J. J. J. J.




Weight andBMI J. J.

,Signs of systemic infection
J. J. J.




Stress self-assessment questionnaire
J. J.




Genetic family history
J. J. J.




Presence of secondary sex characteristics - ✔✔✔Correct Answer > Weight and BMI
J. J. J. J. J. J. J. J. J. J. J. J.




Signs of systemic infection
J. J. J.




Stressself-assessment questionnaire
J. J.




Presence of secondary sex characteristics J. J. J. J.




Which of the following statements is false regarding the spleen?
J. J. J. J. J. J. J. J. J.




J. Divided up into lobules J. J. J.




Similar to a large lymph node Contains
J. J. J. J. J. J.




J. macrophages

Limited blood within the lobules - ✔✔✔Correct Answer > Limited blood within the
J. J. J. J. J. J. J. J. J. J. J. J. J.




lobules
J.




Feedback:
The sinuses in the spleen are a reservoir for blood. In emergencies such as
J. J. J. J. J. J. J. J. J. J. J. J. J.




hemorrhage, smooth muscle in the vessel walls and in the capsule of the spleen J. J. J. J. J. J. J. J. J. J. J. J. J.




contracts. This squeezes the blood out of the spleen into the general circulation.
J. J. J. J. J. J. J. J. J. J. J. J. J.




Which of the following is not considered a central location of lymph nodes? Cervical
J. J. J. J. J. J. J. J. J. J. J. J. J.




Axillary
Inguina
J.




l

,Tibial - ✔✔✔Correct Answer > Tibial
J. J. J. J. J. J.




J. Feedback:
There are three superficial regions on each side of the body where lymph nodes
J. J. J. J. J. J. J. J. J. J. J. J. J.




tend to cluster. These areas are the inguinal nodes in the groin, the axillary
J. J. J. J. J. J. J. J. J. J. J. J. J. J.




nodes in the armpit, and the cervical nodes in the neck.
J. J. J. J. J. J. J. J. J. J.




Lymphocytes that reach the thymus become J. J. J. J. J. J. .
T-cells
J.




B- cells
J.




J. Plasmacells J.




Beta cells - ✔✔✔Correct Answer > T-cells Feedback:
J. J. J. J. J. J. J. J.




The thymus reaches its maximum weight (about 1 ounce) during puberty.
J. J. J. J. J. J. J. J. J. J.




Thymosin stimulates the development of T cells. Throughout your childhood J. J. J. J. J. J. J. J. J.




years, white blood cells called lymphocytes pass through the thymus, where
J. J. J. J. J. J. J. J. J. J. J.




they are transformed into T cells.
J. J. J. J. J. J.




Lymphocytes that do not reach the thymus become J. J. J. J. J. J. J. J. .
T-cells
J.




B-cells
J. Plasmacells J.




Beta cells - ✔✔✔Correct Answer > B-cells
J. J. J. J. J. J. J.




Which of the following is associated with a B cell deficiency?
J. J. J. J. J. J. J. J. J. J.

, Job's syndrome J.




Chronicgranulomatousdisease J. J.




Bruton's agammaglobulinemia
J. J.




Wiskott-Aldrichsyndrome- ✔✔✔Correct Answer > Bruton's J. J. J. J. J. J. J.




agammaglobulinemia
J.




Feedback:
Bruton agammaglobulinemia, also known as X-linked agammaglobulinemia (XLA)
J. J. J. J. J. J. J.




or Bruton's agammaglobulinemia, is an inherited immunodeficiency
J. J. J. J. J. J. J.




disorder. It is characterized by the absence of mature B cells which in turn leads to
J. J. J. J. J. J. J. J. J. J. J. J. J. J. J.




severe antibody deficiency and recurrent infections. It can manifest in an
J. J. J. J. J. J. J. J. J. J. J.




infant as soon as the protective effect of maternal immunoglobulins wanes at
J. J. J. J. J. J. J. J. J. J. J.




around six months of age. Job Syndrome (Hyper-IgE syndrome) is a rare, primary
J. J. J. J. J. J. J. J. J. J. J. J. J.




immunodeficiency distinguished by the clinical triad of atopic dermatitis,
J. J. J. J. J. J. J. J. J.




recurrent skin staphylococcal infections, and recurrent pulmonary infections.
J. J. J. J. J. J. J.




The disease is characterized by elevated IgE levels with an early onset in primary
J. J. J. J. J. J. J. J. J. J. J. J. J. J.




childhood Chronic granulomatous disease (CGD) is an inherited disorder that
J. J. J. J. J. J. J. J. J. J.




occurs when a type of white blood cell (phagocyte) that usually helps your body
J. J. J. J. J. J. J. J. J. J. J. J. J.




fight infections doesn't work properly. As a result, the phagocytes can't protect
J. J. J. J. J. J. J. J. J. J. J. J.




your body from bacterial and fungal infections Wiskott-Aldrich syndrome is a
J. J. J. J. J. J. J. J. J. J. J.




rare genetic immunodeficiency that keeps a child's immune system from
J. J. J. J. J. J. J. J. J. J.




functioning properly. It also makes it difficult for a child's bone marrow to J. J. J. J. J. J. J. J. J. J. J. J.




produce platelets, making a child prone to bleeding. It occurs mostly in males.
J. J. J. J. J. J. J. J. J. J. J. J.




Which of the following is the autoantibody for systemic lupus?
J. J. J. J. J. J. J. J. J.




Anti-microsomal
J.




Antinuclearantibodies J.




Anti-gliadin
J.




Anti-histone- ✔✔✔Correct Answer > Antinuclear antibodies. J. J. J. J. J. J. J.