Anemia - Nursing Case Study

Pathophysiology

• Primary mechanism: Reduced erythropoiesis due to deficient nutrients like iron, vitamin B12, or folate, limits the bone marrow's ability to produce healthy red blood cells, leading to decreased oxygen-carrying capacity in the blood.

• Secondary mechanism: Hemolysis, or the premature destruction of red blood cells, can be caused by autoimmune disorders, inherited conditions (like sickle cell disease), or external factors (such as certain medications), resulting in anemia when the bone marrow cannot compensate for the loss.

• Key complication: Hypoxia from impaired oxygen delivery can lead to fatigue, weakness, and organ dysfunction, emphasizing the importance of early detection and management to prevent severe systemic effects.

Patient Profile

Demographics:

42-year-old female, office manager

History:

• Key past medical history: Iron-deficiency anemia diagnosed 2 years ago, hypothyroidism

• Current medications: Ferrous sulfate, levothyroxine

• Allergies: Penicillin

Current Presentation:

• Chief complaint: Fatigue and shortness of breath

• Key symptoms: Dizziness, palpitations, pale skin, mild chest discomfort

• Vital signs: Blood pressure 98/60 mmHg, heart rate 105 bpm, respiratory rate 22 breaths per minute, temperature 98.2°F

Section 1

As the medical team proceeds with the initial assessment of the 42-year-old female patient, additional findings raise concerns about her current condition. During the physical examination, the patient exhibits more pronounced pallor, particularly noticeable in the conjunctiva and nail beds, suggesting a significant drop in hemoglobin levels. Auscultation reveals a systolic heart murmur, likely from increased cardiac output to compensate for the reduced oxygen-carrying capacity. The patient also reports intermittent lightheadedness and has difficulty with prolonged standing, indicative of orthostatic hypotension. These signs align with the presenting symptoms of dizziness and palpitations and suggest a potential worsening of her anemia.

Further laboratory tests are ordered to elucidate the cause of her exacerbating symptoms. The complete blood count (CBC) reveals a hemoglobin level of 7.8 g/dL, a decrease from her baseline of 10 g/dL. The mean corpuscular volume (MCV) is 72 fL, consistent with microcytic anemia, and the red blood cell distribution width (RDW) is elevated, indicating variation in red blood cell size. Iron studies show ferritin levels of 10 ng/mL, serum iron of 30 µg/dL, and total iron binding capacity (TIBC) of 450 µg/dL, confirming ongoing iron deficiency. Additionally, a peripheral blood smear shows hypochromic, microcytic red blood cells, with no evidence of hemolysis. These results suggest that the patient's iron deficiency anemia has progressed, possibly due to inadequate iron absorption or increased physiological needs.

In response to these findings, clinicians consider the possibility of an underlying gastrointestinal source of blood loss or malabsorption. A referral to a gastroenterologist is made for further evaluation, including endoscopy, to rule out peptic ulcer disease or other potential causes of chronic blood loss. The treatment plan is adjusted to include intravenous iron supplementation to address the acute deficiency more rapidly, given the patient's symptomatic anemia and inability to tolerate oral iron effectively. As the patient begins this intervention, careful monitoring of her response, including symptom resolution and improvement in hemoglobin levels, will be critical to guide ongoing management and prevent further complications.

Section 2

As the patient begins intravenous iron supplementation, her initial response appears promising, with some improvement in her energy levels and a reduction in lightheadedness. However, during a follow-up visit a week later, the medical team notes a concerning change in her status. The patient reports new symptoms of abdominal discomfort and dark, tarry stools, raising suspicion for gastrointestinal bleeding. Vital signs at this visit show blood pressure at 100/60 mmHg, heart rate of 110 beats per minute, and a respiratory rate of 22 breaths per minute, indicating potential hemodynamic instability.

Given these developments, the gastroenterologist prioritizes an expedited endoscopic evaluation. The upper endoscopy reveals the presence of multiple gastric ulcers, with evidence of recent bleeding as indicated by fresh blood and clots in the gastric lumen. This finding suggests that the patient's anemia is likely exacerbated by chronic blood loss from the gastrointestinal tract, possibly linked to the underlying ulcerative condition. The medical team collaborates to initiate treatment for peptic ulcer disease, including proton pump inhibitors and lifestyle modifications, while continuing the intravenous iron therapy to address the acute iron deficiency.

These new complications underscore the importance of comprehensive and timely interventions. The medical team emphasizes the need for ongoing monitoring of the patient's hemoglobin levels, vital signs, and symptoms to assess the effectiveness of the treatment plan and to prevent further deterioration. The patient's journey will require careful coordination among specialists to address both the iron deficiency anemia and the underlying gastrointestinal pathology, ensuring a holistic approach to her care and recovery.

Section 3

In the days following the initiation of treatment for peptic ulcer disease, the patient's clinical status shows both promising signs of recovery and emerging challenges. Her energy levels continue to improve modestly with ongoing intravenous iron supplementation, and she reports less frequent episodes of dizziness. However, a subsequent laboratory panel reveals concerning trends: her hemoglobin has only modestly improved to 9.0 g/dL, while her hematocrit remains low at 28%. The stool guaiac test returns positive, confirming the presence of occult blood, indicative of continued gastrointestinal bleeding.

The medical team, taking these findings into account, deliberates on the next steps. They highlight the necessity of refining the treatment strategy to address not only the anemia but also the ongoing gastrointestinal bleeding. A repeat endoscopic examination is considered to reassess the gastric mucosa and the effectiveness of the proton pump inhibitor therapy. Meanwhile, the patient's vital signs warrant close observation; her blood pressure fluctuates at borderline levels, with systolic readings occasionally dipping below 100 mmHg, and her heart rate remains elevated, suggesting persistent hemodynamic stress.

This phase of the patient's care journey underscores the complexity of managing concurrent conditions. The team considers the potential for additional pharmacologic interventions, such as the introduction of sucralfate to protect the gastric lining, and explores the feasibility of lifestyle modifications, including dietary changes and smoking cessation, to facilitate healing of the gastric ulcers. As they devise a comprehensive plan, the necessity for interdisciplinary collaboration becomes evident, with the gastroenterologist, hematologist, and primary care provider working in concert to optimize outcomes and prevent further complications.

Section 4

As the medical team proceeds with the repeat endoscopic examination, new diagnostic findings emerge that provide further insight into the patient's condition. The endoscopy reveals multiple small, actively bleeding ulcers in the gastric antrum, despite ongoing proton pump inhibitor therapy. Biopsies are taken to rule out Helicobacter pylori infection, and the team considers whether the ulcers might be stress-related or exacerbated by other factors, such as medication use or underlying coagulopathy. The presence of these ulcers suggests that the initial treatment regimen needs adjustment to effectively control the bleeding and promote ulcer healing.

In response to these findings, the team decides to augment the treatment plan. Sucralfate is initiated to create a protective barrier over the gastric mucosa, reducing further irritation and promoting healing. Additionally, the patient is started on a high-dose intravenous proton pump inhibitor drip to more aggressively suppress gastric acid secretion. The medical team also reviews her medication list, identifying and discontinuing any non-essential medications that might contribute to bleeding risk, such as NSAIDs.

Despite these interventions, the patient's clinical status shows subtle signs of deterioration. Her blood pressure continues to exhibit periodic hypotensive episodes, with systolic values occasionally dropping to 90 mmHg, and her heart rate remains elevated, often exceeding 110 beats per minute. These hemodynamic changes suggest the possibility of ongoing blood loss or inadequate compensation for the existing anemia. The team decides to increase the frequency of hemoglobin monitoring and contemplates the need for a blood transfusion to stabilize her condition. Recognizing the importance of a multidisciplinary approach, they engage the expertise of a hematologist to evaluate potential hematological causes for her persistent anemia and guide further management. This collaborative effort aims to stabilize the patient's condition while addressing the root causes of her gastrointestinal bleeding and anemia.

Section 5

As the medical team continues to monitor the patient closely, new diagnostic results from the endoscopic biopsies return, confirming the presence of Helicobacter pylori infection. This finding provides a crucial piece of the puzzle, suggesting that the gastric ulcers may be partially driven by the infection. In light of this, the treatment plan is revised to include a combination of antibiotics, specifically clarithromycin and amoxicillin, alongside the ongoing high-dose intravenous proton pump inhibitor therapy. This triple therapy is intended to eradicate the infection and further promote ulcer healing.

Despite these targeted interventions, the patient's condition remains precarious. Her laboratory results reveal a hemoglobin level that has dropped to 7.8 g/dL, indicating significant anemia. The persistent tachycardia and hypotensive episodes, alongside her pallor and fatigue, underscore the need for immediate action. Recognizing the urgency, the medical team decides to proceed with a blood transfusion to promptly address the severe anemia and stabilize her hemodynamic status. Concurrently, the hematologist initiates a workup to explore additional causes of anemia, including possible vitamin B12 deficiency or underlying bone marrow issues, given the patient's inadequate response to the initial treatment.

The patient's response to the blood transfusion is closely monitored, with her vital signs showing a temporary improvement as her systolic blood pressure rises to 105 mmHg and her heart rate decreases to 95 beats per minute. However, the team remains vigilant for any signs of transfusion reactions or further complications. The multidisciplinary approach continues to be crucial, as the team prepares to reassess the patient's condition following the completion of the Helicobacter pylori eradication therapy. Through this ongoing, dynamic management, the goal is to achieve stable hemodynamics and resolve the underlying causes of her anemia, ultimately paving the way for recovery and discharge planning.