# A nurse in the intensive care unit is caring for a client with type 1 diabetes mellitus who presents with a blood glucose level of 480 mg/dL, large ketones in the urine, and an arterial blood pH of 7.25. To prevent life-threatening complications, which intervention should the nurse prioritize?

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## 문제

A nurse in the intensive care unit is caring for a client with type 1 diabetes mellitus who presents with a blood glucose level of 480 mg/dL, large ketones in the urine, and an arterial blood pH of 7.25. To prevent life-threatening complications, which intervention should the nurse prioritize?

## 보기

1. Administer prescribed IV regular insulin as ordered **✔ 정답**
2. Encourage oral fluid intake to prevent dehydration
3. Administer sodium bicarbonate to correct acidosis
4. Monitor blood glucose levels every 4 hours

**정답: 1**

## 해설

In DKA, the priority intervention is administering IV regular insulin to stop ketone production and reduce blood glucose levels. This addresses the underlying pathophysiology of DKA.

Diabetic ketoacidosis (DKA) is a life-threatening acute complication of diabetes, characterized by hyperglycemia, ketosis, and metabolic acidosis. Pathophysiologically, insulin deficiency leads to increased glucose production and decreased glucose utilization, resulting in hyperglycemia. At the same time, the body breaks down fat for energy, producing ketones, which cause metabolic acidosis.

The priority nursing intervention is administering prescribed intravenous regular insulin. This is because it directly addresses the root cause of DKA. Insulin halts lipolysis and ketogenesis, reduces blood glucose levels, and helps correct metabolic acidosis. Regular insulin is the only type of insulin used in DKA management due to its rapid onset and short duration, allowing precise dose titration.

The correct answer (option 1) is the priority because insulin administration is the definitive treatment that addresses the underlying cause of DKA. Without insulin, ketone production continues, acidosis worsens, and the patient's condition deteriorates rapidly. Intravenous administration ensures immediate bioavailability and enables the continuous infusion protocols commonly used in DKA management.

Option 2 (encouraging oral fluid intake) is inappropriate because DKA patients often have altered levels of consciousness and are at risk for vomiting. Option 3 (administering sodium bicarbonate) is generally not recommended and may increase the risk of cerebral edema. Option 4 (monitoring blood glucose every 4 hours) is too infrequent in DKA, where monitoring is typically needed every hour.

This intervention aligns with the NCLEX-RN emphasis on prioritization and understanding pathophysiology. Nurses must recognize that while supportive care is important, addressing the fundamental metabolic derangement through insulin therapy is the most critical intervention to prevent complications such as cerebral edema, cardiac arrhythmias, and death.

## 심화 해설

Clinical Presentation Analysis

The client's presentation—marked hyperglycemia (480 mg/dL), ketonuria, and a low arterial pH of 7.25—is a classic triad for diabetic ketoacidosis (DKA). DKA is a life-threatening metabolic emergency resulting from an absolute or relative insulin deficiency. This deficiency prevents glucose from entering cells, leading to cellular starvation. In response, the body shifts to lipolysis for energy, producing free fatty acids that the liver converts into ketone bodies (beta-hydroxybutyrate, acetoacetate). The accumulation of these strong acids overwhelms the body’s bicarbonate buffer system, causing a high anion gap metabolic acidosis [1].

Prioritization and Rationale for IV Insulin

In the hierarchy of DKA management, the immediate priority is to halt the production of ketone bodies and reverse the acidosis. The cornerstone of this process is the administration of intravenous regular insulin. Insulin suppresses lipolysis and hepatic ketogenesis while promoting peripheral glucose uptake [1]. A foundational principle in DKA treatment is that the insulin deficit must be corrected to resolve both the hyperglycemia and the acidosis; aggressive fluid replacement alone is insufficient [1]. By selecting the prescribed IV regular insulin as the first action, the nurse directly targets the underlying pathophysiology. The standard of care involves a continuous IV insulin infusion, typically at a rate of 0.1 units/kg/h, which effectively and predictably lowers serum glucose and clears ketones [3]. While recent research explores early co-administration of subcutaneous basal insulin (e.g., glargine) to shorten the duration of IV infusion, the initial and most critical step remains the initiation of IV insulin to stabilize the patient [1].

Analysis of Incorrect Options

- Option 2: Encourage oral fluid intake. Oral hydration is contraindicated in a patient with an altered level of consciousness or severe acidosis due to the risk of aspiration. More critically, fluid resuscitation in DKA must be precisely controlled using isotonic IV fluids to expand intravascular volume and correct dehydration, which cannot be achieved through the oral route [1].

- Option 3: Administer sodium bicarbonate. The use of bicarbonate in DKA is controversial and reserved only for extreme, life-threatening acidosis (typically a pH less than 6.9). Routine administration is not recommended because it can cause paradoxical cerebrospinal fluid acidosis, hypokalemia, and a delay in the clearance of ketone bodies. The primary treatment for DKA-related acidosis is insulin, which stops the production of ketoacids [1].

- Option 4: Monitor blood glucose every 4 hours. While glucose monitoring is an essential component of DKA management, a frequency of every 4 hours is dangerously infrequent during the acute phase. Standard protocols require hourly blood glucose monitoring to titrate the insulin infusion and prevent hypoglycemia. This intervention is important but does not take precedence over initiating the treatment that will resolve the crisis [1].References (research sources)

- [1]Retrospective Evaluation of Early Glargine Administration in Adults With Diabetic Ketoacidosis.Research articleLesniak C, Gonzalez Espinosa P, Philip R, Farhat F, Ashan E, Murshad M, Gupta A, Hossain MA, Cheng J, Ong R, Chalasani K, Hu K, Akula M, Holland S. (2025) · DOI: 10.7759/cureus.90566

- [3]Eﬃcacy and safety of reduced-dose insulin infusion in pediatric diabetic ketoacidosis: a randomized clinical trial.RCT/clinical trialAtwa H, Ali M, Ibrahim A. (2026) · DOI: 10.1297/cpe.2025-0072

## 임상 시나리오

DKA Management: Insulin FirstPrioritizing IV Insulin to Reverse Ketogenesis
The immediate priority in Diabetic Ketoacidosis (DKA) is to stop ketone production and reverse acidosis. This is achieved by administering IV regular insulin to suppress lipolysis and hepatic ketogenesis. Fluid resuscitation alone will not correct the underlying metabolic defect.

A continuous IV insulin infusion is typically started at a rate of 0.1 units/kg/h. The goal is to reduce blood glucose by 50 to 75 mg/dL per hour. Insulin must be continued until the anion gap closes, not just when blood glucose normalizes.

CautionDo not administer sodium bicarbonate routinely for pH > 6.9; it can cause paradoxical CNS acidosis and hypokalemia. Avoid oral fluids in patients with altered mental status due to aspiration risk. Never delay insulin initiation for monitoring tasks.

## 핵심 개념

- **Diabetic Ketoacidosis (DKA)** — A life-threatening metabolic emergency caused by absolute or relative insulin deficiency, leading to hyperglycemia, ketone body formation, and high anion gap metabolic acidosis.
- **Anion Gap Metabolic Acidosis** — A type of acidosis where the calculated anion gap is elevated due to the accumulation of unmeasured anions such as ketoacids, commonly seen in DKA.
- **Ketogenesis** — The hepatic production of ketone bodies from free fatty acids, which is stimulated by insulin deficiency and suppressed by insulin administration.
- **Regular Insulin (IV)** — The only type of insulin used for continuous intravenous infusion in DKA management due to its rapid onset and short half-life, allowing for precise titration.

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