Division of Gastroenterology, Department of Internal Medicine, Glostrup Hospital, Glostrup, Denmark.
Clin Toxicol (Phila). 2013 Jul;51(6):467-72. doi: 10.3109/15563650.2013.799677. Epub 2013 May 23.
N-acetylcysteine (NAC) is acknowledged as an effective antidote for paracetamol overdose. However, adverse effects to NAC are common and may be a point of concern for the patient and the treating physician.
The aim of the present study was to further analyse possible risk factors of anaphylactoid adverse effects to intravenous NAC in order to identify individual patients or groups of patients at particular risk.
This study is an observational case series of adverse effects to NAC administered according to the standard guidelines in patients who presented with paracetamol overdose between March 1999 and September 2011.
A total of 1218 admissions for paracetamol overdose receiving intravenous NAC were recorded in 950 patients. Anaphylactoid adverse effects occurred in 18.6%. The proportion of cases with adverse effects gradually declined from 25.9% in cases with undetectable p-paracetamol to 6.3% in cases with p-paracetamol above 1.5 mmol/L (226 μg/mL) (Spearman Rank R-test: p < 0.00001). The proportion of cases with adverse effects was significantly higher in cases of non-Danish origin than that of Danish origin (28.5% vs. 15.1%; Chi-square: p < 0.00001). In patients with repeated exposure to NAC, the rate of adverse effects on re-exposure was significantly higher in patients with a previous reaction to NAC compared to those without a previous reaction (Rate Ratio 6.2; 95% CI 2.9-17.1).
The development of anaphylactoid adverse effects to intravenous NAC was strongly associated with a low p-paracetamol, non-Danish origin and a history of previous reaction to NAC. These adverse effects are common, but usually mild and easily manageable. The incidence of adverse effects may be reduced by pre-treating selected patients with antihistamines, in particular those with a previous reaction to NAC.
N-乙酰半胱氨酸(NAC)被认为是对乙酰氨基酚过量的有效解毒剂。然而,NAC 的不良反应很常见,这可能是患者和治疗医生关注的一个问题。
本研究旨在进一步分析静脉注射 NAC 引起类过敏不良反应的可能危险因素,以确定个体患者或特定风险群体。
这是一项观察性病例系列研究,研究对象为 1999 年 3 月至 2011 年 9 月期间因乙酰氨基酚过量而接受静脉注射 NAC 治疗的患者,共记录了 950 名患者的 1218 例乙酰氨基酚过量入院病例。
共记录了 950 名患者的 1218 例乙酰氨基酚过量接受静脉注射 NAC 的入院病例。发生类过敏不良反应的比例为 18.6%。不良反应的病例比例从 p-对乙酰氨基酚检测值为 0 到 1.5mmol/L(226μg/ml)的病例(Spearman 秩相关检验:p<0.00001)逐渐下降,从 25.9%下降到 6.3%。非丹麦原籍的病例发生不良反应的比例明显高于丹麦原籍的病例(28.5%比 15.1%;卡方检验:p<0.00001)。在重复接触 NAC 的患者中,与无既往 NAC 反应的患者相比,有既往 NAC 反应的患者再次接触 NAC 时不良反应的发生率明显更高(发生率比 6.2;95%CI 2.9-17.1)。
静脉注射 NAC 引起的类过敏不良反应与低 p-对乙酰氨基酚、非丹麦原籍和既往对 NAC 反应的病史密切相关。这些不良反应很常见,但通常是轻微的,易于管理。通过在特定患者中预先使用抗组胺药物治疗,特别是那些有既往 NAC 反应的患者,可能会降低不良反应的发生率。