# A patient arrives at the emergency department after ingesting an unknown amount of acetaminophen 4 hours ago. The patient's serum acetaminophen level is 180 mcg/mL. Which antidote should the nurse prepare to administer?

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## 문제

A patient arrives at the emergency department after ingesting an unknown amount of acetaminophen 4 hours ago. The patient's serum acetaminophen level is 180 mcg/mL. Which antidote should the nurse prepare to administer?

## 보기

1. Flumazenil
2. Naloxone
3. Activated charcoal
4. N-acetylcysteine **✔ 정답**

**정답: 4**

## 해설

N-acetylcysteine is the specific antidote for acetaminophen overdose and should be administered when serum levels exceed 150 mcg/mL at 4 hours post-ingestion.

Acetaminophen overdose is a medical emergency that can cause severe liver toxicity and liver failure if not promptly treated with the appropriate antidote. The toxicity threshold for acetaminophen is determined by the Rumack-Matthew nomogram, which correlates serum acetaminophen levels with the time elapsed since ingestion to predict the risk of liver toxicity.

In this patient's case, the serum acetaminophen level at 4 hours post-ingestion is 180 mcg/mL, which far exceeds the treatment threshold of 150 mcg/mL at the 4-hour mark, indicating a high risk of liver toxicity. N-acetylcysteine (NAC) is the specific antidote for acetaminophen poisoning, and it works by replenishing the liver's glutathione stores, which become depleted during acetaminophen metabolism.

The mechanism of acetaminophen toxicity involves the formation of a toxic metabolite (NAPQI) when the normal conjugation pathways become saturated. This toxic metabolite binds to liver cells, causing cellular damage. NAC provides cysteine, a precursor to glutathione, which neutralizes the toxic metabolite and prevents further liver injury.

NAC is most effective when administered within 8-10 hours of ingestion, but it can still provide benefit up to 24 hours post-ingestion. The standard protocol involves oral or intravenous administration over 20-21 hours. Early recognition and prompt treatment with NAC can prevent progression to fulminant hepatic failure and significantly improve patient outcomes.

The other options are not appropriate for acetaminophen overdose. Flumazenil is a benzodiazepine antidote, naloxone is an opioid antidote, and activated charcoal is only effective within 1 hour of ingestion.

## 심화 해설

Clinical Context and Pathophysiology

The patient’s presentation—ingestion of an unknown amount of acetaminophen approximately 4 hours prior, accompanied by nausea and vomiting—is a classic early manifestation of acetaminophen toxicity. Acetaminophen is responsible for more pharmaceutical overdoses than any other medication in the United States and is the leading cause of acute liver failure [3]. In therapeutic doses, acetaminophen is primarily metabolized via glucuronidation and sulfation. However, in overdose, these pathways become saturated, shunting metabolism toward the cytochrome P450 system, which produces the highly reactive and hepatotoxic metabolite N-acetyl-p-benzoquinone imine (NAPQI). NAPQI is normally detoxified by conjugation with hepatic glutathione, but once glutathione stores are depleted, NAPQI binds to hepatocellular proteins, causing centrilobular necrosis and potentially severe acute liver failure [1].

Antidote Mechanism and Rationale

The correct antidote is N-acetylcysteine (NAC). Introduced as an antidote in 1974, NAC has revolutionized the management of acetaminophen poisoning by significantly reducing hepatotoxicity and associated mortality [1]. NAC works through multiple mechanisms: it serves as a glutathione precursor, replenishing depleted hepatic glutathione stores to detoxify NAPQI; it directly conjugates with NAPQI; and it may have antioxidant and hemodynamic effects. The standard treatment involves a three-bag intravenous protocol, though recent research has explored abbreviated 12-hour infusions compared to the traditional 20-hour regimen [4]. While NAC is widely considered safe when administered appropriately, the nurse must be vigilant, as improper administration—such as iatrogenic overdose—has been associated with serious adverse outcomes including cerebral edema and hemolytic uremic syndrome [2].

Analysis of Incorrect Options

- Flumazenil is a benzodiazepine receptor antagonist used to reverse benzodiazepine overdose. It has no role in acetaminophen toxicity and could precipitate seizures in patients with unknown co-ingestions.

- Naloxone is an opioid receptor antagonist indicated for opioid overdose. While many combination products contain both acetaminophen and opioids, naloxone does not address the hepatotoxic threat of acetaminophen itself [3].

- Activated charcoal may be considered for gastrointestinal decontamination if the patient presents within 1 to 2 hours of ingestion. At 4 hours post-ingestion, its benefit is significantly diminished, and it is not an antidote for the systemic toxicity that has already begun. NAC remains the priority intervention.

Nursing Considerations and Clinical Judgment

The nurse should anticipate preparing NAC for intravenous administration based on the patient’s weight and the institution’s protocol. Given the patient’s persistent nausea and vomiting, the nurse must recognize that antiemetic administration may be necessary to facilitate NAC tolerance, as vomiting is a common side effect of both the toxicity and the antidote infusion. The nurse should also prepare to draw a serum acetaminophen level, liver function tests, and coagulation studies to plot on the Rumack-Matthew nomogram, which guides the necessity and duration of NAC therapy. The presence of acetaminophen protein adducts in circulation serves as a highly sensitive biomarker of oxidation and potential hepatic injury, confirming the need for continued monitoring even after antidote completion [4].References (research sources)

- [1][Translated article] N-acetylcysteine: 50 years since the discovery of an antidote that has changed the prognosis of acetaminophen poisoning.Research articleNogué-Xarau S, Martínez-Sánchez L, García-Peláez M, Fernández de Gamarra-Martínez E, Pi-Sala N, Gispert-Ametller À, Salgado-García E, Aguilar-Salmerón R. (2026) · DOI: 10.1016/j.farma.2025.10.015

- [2]Safety of acetylcysteine: a scoping review of iatrogenic overdose cases and their associated complications.Research articleBaker MB, Young J, Binda DD, Dienes E, Kennedy JM. (2026) · DOI: 10.1080/15563650.2026.2673132

- [3]Acetaminophen ToxicityResearch articleSchaffer DH, Murray BP, Khazaeni B. (2026)

- [4]Paracetamol adducts following overdose treated with a shorter acetylcysteine infusion: findings from the NACSTOP 2 trial.Research articleWong A, James LP, McNulty R, Gunja N, Graudins A. (2026) · DOI: 10.1080/15563650.2026.2655388

## 임상 시나리오

Clinical Practice Guide: Acetaminophen Overdose Management

Assessment & Diagnosis

Obtain a serum acetaminophen level at least 4 hours post-ingestion for accurate plotting on the Rumack-Matthew nomogram. A level of 180 mcg/mL at 4 hours indicates probable hepatotoxicity and necessitates immediate antidotal therapy. Monitor liver function tests (AST, ALT), PT/INR, and renal function. Assess for clinical signs of hepatic injury, including right upper quadrant pain, nausea, vomiting, and altered mental status.

Antidote Administration

Administer N-acetylcysteine (NAC) as the definitive antidote. The standard IV protocol involves a loading dose of 150 mg/kg over 1 hour, followed by 50 mg/kg over 4 hours, then 100 mg/kg over 16 hours. Oral NAC may be used as an alternative. Treatment is most effective when initiated within 8 hours of ingestion. Monitor for anaphylactoid reactions during IV infusion, which can be managed by slowing the rate and administering antihistamines.

Nursing Considerations

Ensure accurate weight-based dosing. Monitor for adverse effects of NAC, including nausea, vomiting, and urticaria. Provide supportive care, including antiemetics as needed. Educate the patient on the importance of completing the full course of therapy. Coordinate with the poison control center for ongoing management guidance. Evaluate for intentional overdose and initiate appropriate psychiatric consultation.

## 핵심 개념

- **N-acetylcysteine (NAC)** — The specific antidote for acetaminophen poisoning that acts as a glutathione precursor to detoxify the hepatotoxic metabolite NAPQI.
- **NAPQI** — N-acetyl-p-benzoquinone imine, the toxic metabolite of acetaminophen produced via the CYP2E1 pathway that causes hepatic necrosis when glutathione is depleted.
- **Rumack-Matthew nomogram** — A tool used to assess the risk of hepatotoxicity after acute acetaminophen ingestion based on serum drug levels and time since ingestion.
- **Glutathione** — A critical endogenous antioxidant that conjugates and neutralizes NAPQI; stores are depleted in acetaminophen overdose.
- **Hepatotoxicity** — Chemical-driven liver damage, which in acetaminophen overdose results from centrilobular necrosis caused by unbound NAPQI.

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