Pathophysiology

Metabolic and Cardiac

With contributions from Jennifer Ring, AGPCNP-C

Case Study

Patient Profile

Name: Cat Stevorski

Age: 72 years old

Gender: female

History of Present Illness

C.T. is a 72-year-old woman who presents with increasing fatigue, occasional palpitations, and mild swelling in her ankles.

Past Medical History

  • Hypertension
  • Type 2 Diabetes Mellitus (T2DM) HbA1c: 7.5%
  • Atrial Fibrillation (AF) diagnosed 3 years ago
  • Osteoporosis

Social History

  • Retired accountant
  • Single
  • Volunteers for Meals on Wheels
    Consumes alcohol 1x/month
  • No drug or tobacco use

Current Medications

  • Metformin 1000 mg twice daily
  • Lisinopril 20 mg daily
  • Apixaban 5 mg twice daily
  • Alendronate 70 mg weekly

Physical Assessment

General Appearance: Ms. Stevorski is alert and oriented to person, place, and time. Her overall appearance suggests mild discomfort and fatigue. She has a slightly stooped posture.

Vitals

  • Blood Pressure: 138/82 mm Hg (right arm, seated position)
  • Heart Rate: 84 bpm, irregularly irregular
  • Respiratory Rate: 18 bpm
  • Temperature: 97.9°F (36.6°C) (oral)
  • Oxygen Saturation: 96% on room air

Cardiovascular Examination

  • Jugular venous pressure (JVP) is slightly elevated at 4 cm above the sternal angle in a 30-degree position. No visible carotid pulsations or abnormal pulsations in the chest wall.
  • Mild bilateral ankle edema is noted.
  • Apical impulse is displaced laterally and diffuse, suggesting left ventricular enlargement.
  • Peripheral pulses:
    • Carotid: 2+ bilaterally, no bruits
    • Radial: 2+ bilaterally, irregularly irregular
    • Femoral: 1+ bilaterally
    • Dorsalis pedis: 1+ bilaterally
    • Posterior tibial: 1+ bilaterally
    • Capillary refill time is 3 seconds in both feet, slightly delayed
    • Heart sounds: S1 and S2 are irregular in rhythm, consistent with AF. A soft (grade 2/6) systolic murmur is heard at the apex, radiating to the axilla, suggestive of mitral valve regurgitation. No S3 or S4 gallop is appreciated

Respiratory Examination

  • Lung fields are clear to auscultation bilaterally, with no rales or wheezes.
  • Chest expansion is symmetric.
  • No use of accessory muscles for breathing.
  • Percussion reveals resonance throughout all lung fields.
  • Breath sounds are vesicular and equal bilaterally, without adventitious sounds.

Abdominal Examination

  • Abdomen is soft, non-tender, and non-distended.
  • No hepatomegaly or splenomegaly is appreciated.
  • No abdominal bruits are auscultated.

Neurological Examination

  • Cranial nerves II-XII are grossly intact.
  • Motor strength is 5/5 in all extremities.
  • Deep tendon reflexes are +2 in upper extremities and +1 in lower extremities.
  • Sensation to light touch and pinprick is diminished in a stocking distribution bilaterally.
  • Proprioception is intact in the upper extremities but diminished in the toes.
  • Romberg test is positive.

Musculoskeletal Examination

  • Mild kyphosis of the thoracic spine is observed.
  • Range of motion in the cervical and lumbar spine is limited and accompanied by discomfort.
  • No joint swelling, erythema, or warmth is noted in the peripheral joints.
  • Mild tenderness is elicited on palpation of the thoracic spine.

Skin Examination

  • Skin is warm and dry with normal turgor.
  • No rashes, lesions, or ulcerations are observed.
  • There is no evidence of acanthosis nigricans.

Foot Examination

  • Mild callus formation is noted on the plantar surface of both feet.
  • No open wounds or ulcerations are present.
  • Monofilament testing reveals decreased sensation in both feet.

Ophthalmologic Examination

  • Visual acuity is 20/40 in both eyes with corrective lenses.
  • Fundoscopic examination report indicates mild arteriolar narrowing and arteriovenous nicking.
  • No evidence of diabetic retinopathy is observed at this time.

Diagnosis

  • AF: Confirmed by irregularly irregular heart rhythm on examination and previous diagnosis.
  • Hypertension: Currently controlled with medication, but requires ongoing management.
  • T2DM: Suboptimal control based on HbA1c of 7.5% and evidence of diabetic neuropathy.
  • Osteoporosis: Previously diagnosed, with physical examination findings consistent with the condition.
  • Early Signs of Heart Failure: Suggested by mild ankle edema, elevated JVP, and displaced apical impulse.
  • Mitral Regurgitation: Indicated by the systolic murmur heard on auscultation.
  • Peripheral Arterial Disease: Suggested by diminished peripheral pulses in the lower extremities.
  • Diabetic Peripheral Neuropathy: Evidenced by diminished sensation and absent ankle reflexes.
  • Hypertensive Retinopathy: Mild changes observed on fundoscopic examination.

Treatment Plan

AF Management

  • Anticoagulation: Continue apixaban 5 mg twice daily for stroke prevention.
  • Rate Control: Initiate metoprolol 25 mg twice daily for rate control.
  • Monitoring: Schedule regular electrocardiogram (ECG) monitoring to assess AF burden and effectiveness of rate/rhythm control. Consider home monitoring with wearable devices if appropriate for the patient.

Hypertension Management

  • Medication: Continue lisinopril 20 mg daily, may increase if blood pressure remains above target after 2-4 weeks.
  • Home Blood Pressure Monitoring: Encourage home blood pressure monitoring and maintain a log.
  • Lifestyle Modifications: Recommend sodium restriction (<2300 mg/day) and adoption of the dietary approaches to stop hypertension (DASH) diet, with physical activity as tolerated.

T2DM Management

  • Glycemic Target: Set an individualized HbA1c target of <7.5% to balance glycemic control with the risk of hypoglycemia.
  • Medication: Continue metformin 1000 mg twice daily.
    • Add an SGLT2 inhibitor (e.g., empagliflozin 10 mg daily) as a second-line agent.
  • Blood Glucose Monitoring: Implement a structured self-monitoring blood glucose plan. Educate on recognition and management of hypoglycemia. Focus on nutrition, foot care, and the importance of glycemic control in preventing complications.
  • Screening:
    • Schedule annual comprehensive foot exams and eye examinations.
    • Monitor renal function and urine albumin-to-creatinine ratio regularly.

Osteoporosis Management

  • Medication: Continue alendronate 70 mg weekly. Ensure adequate calcium (1200 mg/day) and vitamin D (800-1000 IU/day) supplementation.
  • Fall Prevention: Implement a multifactorial fall prevention program, including:
    • Home safety assessment and modification.
    • Balance and strength training exercises.
    • Review of medications that may increase fall risk.
  • Bone Density Monitoring: Schedule a follow-up DXA scan to assess treatment efficacy and monitor for progression.
  • Physical Therapy: Refer for physical therapy to improve posture, spinal mobility, and overall strength.

Heart Failure Prevention and Management

  • Diagnostic Evaluation: Echocardiogram to assess left ventricular function, valvular status, and confirm the presence of mitral regurgitation. Measure B-type natriuretic peptide (BNP) levels to aid in diagnosis and prognosis.
  • Medication Optimization: The current regimen of lisinopril and planned addition of metoprolol aligns with heart failure management.
  • Fluid Management: Educate on daily weight monitoring and when to report changes. Recommend sodium and fluid restriction if heart failure is confirmed.
  • Multidisciplinary Team: Continue communication and collaboration between cardiology, endocrinology, and PCP.

Activity: Pathophysiology of Atrial Fibrillation

Fill in the blanks with the correct term: sinoatrial node, atrioventricular node, ventricular, thrombus, uncoordinated, coordinated, Purkinje fibers.

AF is a cardiac arrhythmia that involves rapid and unorganized electrical activity in the atria that alters normal cardiac conduction, producing ____________________ contractions between the atria and ventricles. Typically, the ____________________ is the heart’s pacemaker.  However, during AF, irregular electrical impulses-often from the pulmonary veins-can travel through the ____________________ node, initiating heartbeats. This produces an abnormal rate and rhythm, ineffective atrial contraction, irregular ____________________ activation, and structural changes, such as fibrosis, wall thinning, and hypertrophy in the atria.  The condition can be triggered or exacerbated by various factors, including autonomic nervous system changes, inflammation, and activation of molecular pathways like the renin-angiotensin-aldosterone system. If left untreated, this can lead to progression from paroxysmal AF to a more persistent form of AF.  AF increases the risk of ____________________ formation, heart failure, and stroke.

Review Questions

Click the arrow to expand the section and view the correct answers.

  1. As a nurse practitioner, you’re assessing Mrs. Stevorski’s risk factors for AF progression. Which of the following mechanisms best explains how her diabetes contributes to her AF?
    1. Decreases inflammation in the atria.
    2. Improves autonomic function.
    3. Promotes atrial fibrosis.
    4. Reduces oxidative stress in cardiac tissue.
Answer:

C) Promotes atrial fibrosis.

Feedback: Diabetes contributes to AF progression by promoting atrial fibrosis through the formation of advanced glycation end products and increasing oxidative stress. This process leads to structural changes in the atria that maintains AF.

  1. In patients with T2DM, hyperglycemia combines with which factors to contribute to the development of atherosclerosis?
    1. Inflammation and endothelial dysfunction.
    2. Increased HDL cholesterol and vasodilation.
    3. Decreased LDL cholesterol and normal blood pressure.
    4. Inflammation and reduced oxidative stress.
Answer:

A) Inflammation and endothelial dysfunction.

Feedback: In T2DM, hyperglycemia promotes oxidative stress and inflammation, contributing to endothelial dysfunction and plaque formation, which are key factors in the development of atherosclerosis.

  1. During a follow-up visit, Mrs. Stevorski reports feeling occasional rapid heartbeats. As her nurse practitioner, which diagnostic tool would you most likely use to assess her heart’s electrical activity and confirm these episodes?
    1. Chest X-ray
    2. Echocardiogram
    3. ECG
    4. Cardiac MRI
Answer:

C) ECG

Feedback: An ECG is the primary diagnostic tool used to assess the heart’s electrical activity and confirm episodes of AF. It provides immediate information about heart rhythm and rate, which is crucial for managing AF.

  1. Mrs. Stevorski asks about the long-term effects of her AF. Which of the following is the most accurate response from the nurse practitioner regarding potential cardiac complications of prolonged AF?
    1. Decreased cardiac output.
    2. Heart failure.
    3. Blood clots.
    4. All of these are potential complications associated with AF.
Answer:

D) All of these are potential complications associated with AF.

Feedback: Prolonged periods of rapid ventricular rates in AF can lead to tachycardia-induced cardiomyopathy, which is characterized by left ventricular dysfunction and can progress to heart failure. The loss of effective atrial contraction leads to blood stasis, increasing the risk of clot formation and stroke. Irregular ventricular rates and loss of atrial kick (the contribution of atrial contraction to ventricular filling) can decrease cardiac output.

  1. Considering Mrs. Stevorski’s postmenopausal status, which age-related cardiovascular change is most likely to impact her AF management?
    1. Decreased arterial stiffness.
    2. Improved vascular compliance.
    3. Enhanced baroreceptor sensitivity.
    4. Increased left ventricular wall thickness.
Answer:

D) Increased left ventricular wall thickness.

Feedback: Postmenopausal women experience age-related structural changes in the heart, including increased left ventricular wall thickness. This change, along with reduced elasticity of large arteries, can affect AF management by altering cardiac function and response to treatment.

  1. A 70-year-old male patient with persistent AF reports feeling increasingly fatigued over the past few months. As a nurse practitioner, which pathophysiological mechanism would you consider most likely responsible for his symptoms?
    1. Increased parasympathetic tone.
    2. Enhanced atrial kick.
    3. Reduced cardiac output due to irregular ventricular rates.
    4. Improved diastolic filling time.
Answer:

C) Reduced cardiac output due to irregular ventricular rates.

Feedback: In AF, irregular ventricular rates and loss of atrial kick can lead to reduced cardiac output. This reduction in cardiac output can manifest as fatigue, especially during physical exertion. The irregular heart rhythm and potentially rapid ventricular response in AF can compromise the heart’s ability to pump blood effectively, leading to symptoms such as fatigue, shortness of breath, and reduced exercise tolerance.

  1. Which of the following statements best describes the relationship between age and AF risk?
    1. AF risk decreases with age
    2. AF risk remains constant throughout adulthood
    3. AF risk increases significantly after age 65
    4. Age has no impact on AF risk
Answer:

C) AF risk increases significantly after age 65

Feedback: Age is a well-established non-modifiable risk factor for atrial fibrillation. The prevalence of AF increases significantly with age, particularly in individuals over 65 years.

References

Fuehrer, M. (2024). Lecture on the cardiac system. [Transcript].

Fuehrer, M. (2024). Lecture on the endocrine system. [Transcript].

Kumar, K.(2023). Up to Date. Management of Atrial Fibrillation. Available at: https://www.uptodate.com/contents/management-of-atrial-fibrillation-rhythm-control-versus-rate-control

Tkacs, N. (Ed.). (2020). Advanced physiology and pathophysiology: Essentials for clinical practice. Springer Publishing Company.

You.com. (n.d.). ARI. You.com. Retrieved March 1, 2025, from https://www.you.com

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Be Prepared for Your Nurse Practitioner Clinical Readiness Exam Copyright © 2026 by Elizabeth Heavey, Renee Biedlingmaier, Colleen Burgoyne and Carnel C. Jackson is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, except where otherwise noted.