Diabetes Mellitus Type 2 - Nursing Case Study
Pathophysiology
• Primary mechanism: Insulin resistance - Cells in muscles, fat, and liver become less responsive to insulin, leading to impaired glucose uptake and increased blood glucose levels. This resistance is often linked to obesity and a sedentary lifestyle, affecting insulin's ability to facilitate glucose entry into cells.
• Secondary mechanism: Beta-cell dysfunction - Over time, pancreatic beta cells become unable to produce adequate insulin to overcome resistance. This dysfunction is often exacerbated by chronic hyperglycemia and increased demand for insulin, eventually leading to decreased insulin secretion.
• Key complication: Hyperglycemia-induced damage - Prolonged elevated blood glucose levels can lead to complications such as neuropathy, retinopathy, and nephropathy due to damage to blood vessels and nerves, emphasizing the importance of maintaining glucose control.
Patient Profile
Demographics:
54-year-old male, office manager
History:
• Key past medical history: Diagnosed with Type 2 Diabetes Mellitus 8 years ago, hypertension, hyperlipidemia
• Current medications: Metformin 1000 mg BID, Lisinopril 20 mg daily, Atorvastatin 40 mg daily, Aspirin 81 mg daily
• Allergies: Penicillin
Current Presentation:
• Chief complaint: Increasing fatigue and occasional blurred vision
• Key symptoms: Numbness and tingling in feet, frequent urination, increased thirst, recent unintentional weight loss
• Vital signs: Blood pressure 148/92 mmHg, heart rate 88 bpm, respiratory rate 18 breaths per minute, temperature 98.6°F, random blood glucose 210 mg/dL
Section 1
Following the initial presentation and concerns of the patient, the healthcare team conducted a thorough assessment, which included additional diagnostic tests to evaluate the extent of complications and guide further management. The patient's HbA1c was measured at 8.9%, indicating poor long-term glucose control. A comprehensive metabolic panel revealed elevated creatinine levels at 1.6 mg/dL, suggesting some degree of renal impairment, possibly early diabetic nephropathy. Urinalysis showed microalbuminuria, further supporting renal involvement. Additionally, a lipid panel showed a total cholesterol level of 230 mg/dL, with LDL cholesterol at 160 mg/dL, indicating that despite statin therapy, the patient’s lipid levels remained suboptimal.
During the neurological examination, a monofilament test indicated decreased sensation in the patient's feet, consistent with peripheral neuropathy. A dilated eye exam revealed signs of non-proliferative diabetic retinopathy, with the presence of microaneurysms and cotton wool spots. These findings suggest that the patient's diabetes management requires urgent optimization to prevent further progression of microvascular complications.
The clinical team initiated an adjustment in the patient's diabetes management plan, focusing on intensifying glycemic control. The introduction of a GLP-1 receptor agonist was considered to improve glucose regulation and provide cardiovascular benefits. The patient was also counseled on lifestyle modifications, emphasizing the importance of diet, weight loss, and increased physical activity to enhance insulin sensitivity and reduce cardiovascular risk. Regular follow-up appointments were scheduled to monitor the response to interventions and adjust the treatment plan as necessary. This approach aimed to address the immediate complications while preventing further deterioration, particularly in renal function and ocular health.
Section 2
Following the adjustment in the patient's diabetes management plan, the healthcare team closely monitored the patient's response to the interventions. During a follow-up appointment six weeks later, the patient reported feeling more energetic and noted a modest weight loss of 5 pounds. However, they also mentioned occasional episodes of nausea, a known side effect of the newly introduced GLP-1 receptor agonist. The healthcare provider reassured the patient and advised dietary modifications to help manage this side effect.
Vital signs taken during this visit showed a blood pressure of 148/88 mmHg, which, although slightly elevated, indicated a mild improvement from previous readings. Heart rate was stable at 78 beats per minute. Repeat laboratory tests revealed a decrease in HbA1c to 8.2%, demonstrating improved glycemic control, albeit still above the target range. The patient's creatinine level remained stable at 1.6 mg/dL, and microalbuminuria persisted, suggesting that renal function had not worsened but required continuous monitoring. Lipid levels showed a slight improvement with total cholesterol at 210 mg/dL and LDL cholesterol at 145 mg/dL, indicating progress but necessitating further optimization.
The clinical team recognized the need for sustained efforts to enhance the patient's health outcomes. They emphasized the importance of adherence to medications and lifestyle modifications, specifically targeting further weight reduction and increased physical activity. Given the moderate improvement in glycemic and lipid control, the team planned to continue the current regimen while considering additional therapies to address hypertension and further reduce cardiovascular risk. The patient was scheduled for a comprehensive review in three months, with interim check-ins to evaluate ongoing challenges and successes in their diabetes management journey.
Section 3
Three months later, the patient returned for their scheduled comprehensive review. Upon assessment, the patient reported increased fatigue and occasional dizziness, especially upon standing. They also mentioned experiencing more frequent nocturia and slight swelling in the ankles by the end of the day. Vital signs revealed a blood pressure of 152/94 mmHg, indicating a possible need for further intervention in managing hypertension. The heart rate remained stable at 76 beats per minute. A physical examination showed mild bilateral pedal edema, an important clinical finding given the patient's history and current symptoms.
Repeat laboratory tests brought new insights into the patient's condition. The HbA1c level had decreased slightly to 8.0%, showing continued, albeit slow, improvement in glycemic control. However, the creatinine level had increased to 1.8 mg/dL, raising concerns about declining renal function. Microalbuminuria persisted, reinforcing the need for intensified renal protection strategies. Lipid profile results showed marginal changes, with total cholesterol at 208 mg/dL and LDL cholesterol at 142 mg/dL, suggesting that while cardiovascular risks were being managed, they still required attention.
These findings prompted the clinical team to reassess the management plan. The increased creatinine level and persistent microalbuminuria highlighted the necessity for a more aggressive approach to renal protection, possibly through the introduction of an ACE inhibitor or angiotensin receptor blocker. Additionally, the team considered adjusting the current antihypertensive regimen to address the elevated blood pressure and prevent further cardiovascular complications. The patient's symptoms of fatigue and dizziness were discussed in the context of potential orthostatic hypotension and electrolyte imbalances, warranting closer monitoring and dietary adjustments. The team scheduled more frequent follow-up visits to closely monitor these developments and ensure timely interventions.
Section 4
Two months later, the patient returned for a follow-up appointment, prompted by a recent episode of severe dizziness and a near fall, which occurred while they were getting out of bed. During the visit, the patient reported that the dizziness had become more frequent, now accompanied by occasional palpitations and a persistent feeling of weakness. They also noted that the nocturia had increased, causing significant disruption to their sleep. The physical examination revealed an increase in bilateral pedal edema, now rated as moderate, with pitting observed upon palpation. Blood pressure readings taken in both sitting and standing positions indicated orthostatic hypotension, with seated blood pressure at 148/92 mmHg and standing blood pressure dropping to 118/78 mmHg. Heart rate was slightly elevated at 82 beats per minute, and the patient appeared fatigued.
Given these new developments, the clinical team ordered additional laboratory tests and imaging to investigate potential causes of the patient's worsening symptoms. Serum electrolyte levels revealed mild hyponatremia with a sodium level of 132 mmol/L, which could contribute to the dizziness and weakness. Additionally, a urinalysis showed an increase in proteinuria, emphasizing a potential exacerbation of renal issues. An echocardiogram was performed to assess cardiac function, revealing mild left ventricular hypertrophy, likely secondary to chronic hypertension, but no overt heart failure. These findings suggested a multifactorial origin of the patient's symptoms, including potential medication side effects, electrolyte imbalances, and underlying cardiovascular changes.
In response to these findings, the clinical team decided to modify the patient's treatment regimen. The patient's antihypertensive therapy was adjusted, switching from a thiazide diuretic to an ACE inhibitor to better manage blood pressure and provide renal protection while mitigating the risk of further electrolyte imbalances. Dietary counseling was provided to address sodium intake and fluid management, aiming to stabilize electrolyte levels. The patient was also scheduled for more frequent blood pressure monitoring and follow-ups to closely observe the response to these interventions. This proactive approach aimed to prevent further complications, improve the patient's quality of life, and maintain renal function, setting the stage for the next phase of management.
Section 5
Two weeks after the adjustments to the treatment regimen, the patient returned for a follow-up appointment. The clinical team was eager to assess the impact of the changes, particularly the switch to an ACE inhibitor and the dietary modifications. During this visit, the patient reported a slight improvement in dizziness, although palpitations and nocturnal disruptions persisted. More notably, the patient expressed concern over new symptoms of frequent headaches and increased thirst, which had developed over the past week. On physical examination, the bilateral pedal edema had slightly reduced to mild, but pitting was still present. Orthostatic blood pressure measurements showed some improvement, with seated blood pressure at 140/88 mmHg and standing blood pressure at 120/80 mmHg. The heart rate remained stable at 80 beats per minute. However, the patient appeared more fatigued than before, with noticeable pallor.
Laboratory tests were repeated to monitor the patient's status and response to the interventions. Serum sodium levels had improved slightly to 134 mmol/L, suggesting better electrolyte balance. However, fasting blood glucose was elevated at 146 mg/dL, indicating suboptimal glycemic control. Urinalysis still showed persistent proteinuria with a slight increase, signaling ongoing renal stress. Given these new findings, the team suspected that the patient’s diabetes management might need further optimization to prevent progression of renal complications and mitigate cardiovascular risks.
In light of these developments, the clinical team decided to intensify the patient's diabetes management. They introduced a sodium-glucose co-transporter-2 (SGLT2) inhibitor to improve glycemic control and offer additional renal protection. Dietary counseling was reinforced, emphasizing carbohydrate regulation to manage blood glucose levels effectively. The team also recommended routine home glucose monitoring to better track blood sugar trends. With these adjustments, the clinical team aimed to address the multifaceted challenges presented by the patient's condition, striving to balance glycemic control, blood pressure management, and renal protection while minimizing adverse effects. The next phase of management would focus on closely monitoring the patient's response to these changes, with the aim of preventing further complications and improving overall health outcomes.