a Department of Medicine, School of Clinical Sciences , Monash University , Victoria , Australia.
b Victorian Poisons Centre and Austin Toxicology Service , Heidelberg , Australia.
Clin Toxicol (Phila). 2018 Mar;56(3):199-203. doi: 10.1080/15563650.2017.1359620. Epub 2017 Aug 16.
In Australia, the treatment guideline for patients with repeated supratherapeutic ingestion (RSTI) of paracetamol recommends an abbreviated acetylcysteine regimen if the paracetamol concentration is low (<10 mg/L) and alanine aminotransferase (ALT) is normal or static after 8 hours of infusion. There are currently no studies of this recommendation.
A retrospective review of paracetamol overdose presentations from October 2009 to August 2016 in two hospital toxicology networks was performed. All cases of RSTI treated with acetylcysteine were extracted.
Of the 2249 paracetamol overdose presentations, 91 cases of RSTI were treated with acetylcysteine. Median time to initial blood tests was 6 hours post-last paracetamol dose (IQR 4-6). Sixty-three (69%) presentations had an initial detectable paracetamol concentration, median 30 mg/L (IQR 18-60). Median ALT on presentation was 48 IU/L (IQR 18-109). After 8 hours of acetylcysteine infusion, median ALT was 34 IU/L (IQR 16-71) in those receiving abbreviated treatment and 74 IU/L (IQR 40-231) in those continuing acetylcysteine. Thirty-nine presentations (43%) had an abbreviated regimen. Nine (10%) patients had an initial ALT ≥50 IU/L and subsequently developed hepatotoxicity (ALT >1000 IU/L). No patients with an initial ALT <50 IU/L developed hepatotoxicity. Median duration of acetylcysteine infusion for those receiving a non-abbreviated regimen was 20 hours (IQR 20-25) vs. 10.4 hours (IQR 4.8-12.0) who received an abbreviated regimen. There were no re-presentations with hepatotoxicity.
An 8-hour acetylcysteine infusion regimen for treatment of paracetamol RSTI may be safe and is likely to reduce length of stay for patients at low risk of hepatotoxicity. Larger prospective studies are needed to examine the efficacy of this abbreviated acetylcysteine protocol.
在澳大利亚,对于反复摄入(RSTI)超治疗剂量扑热息痛的患者,若血药浓度<10mg/L,且输注 8 小时后丙氨酸氨基转移酶(ALT)正常或无变化,建议采用简化的乙酰半胱氨酸方案。目前尚未对此建议进行研究。
对 2009 年 10 月至 2016 年 8 月期间两个医院毒物网络中扑热息痛过量的病例进行回顾性分析。提取所有接受乙酰半胱氨酸治疗的 RSTI 病例。
在 2249 例扑热息痛过量的病例中,有 91 例 RSTI 患者接受了乙酰半胱氨酸治疗。首次血检时间中位数为末次扑热息痛剂量后 6 小时(IQR 4-6)。63 例(69%)患者的初始可检测扑热息痛浓度中位数为 30mg/L(IQR 18-60)。就诊时的中位 ALT 为 48IU/L(IQR 18-109)。在接受简化治疗的患者中,乙酰半胱氨酸输注 8 小时后,中位 ALT 为 34IU/L(IQR 16-71),而继续使用乙酰半胱氨酸的患者为 74IU/L(IQR 40-231)。39 例(43%)患者采用了简化方案。9 例(10%)患者初始 ALT≥50IU/L,随后出现肝毒性(ALT>1000IU/L)。初始 ALT<50IU/L 的患者无一例发生肝毒性。未接受简化治疗的患者乙酰半胱氨酸输注时间中位数为 20 小时(IQR 20-25),而接受简化治疗的患者为 10.4 小时(IQR 4.8-12.0)。无再次出现肝毒性的病例。
RSTI 患者接受 8 小时乙酰半胱氨酸输注治疗方案可能是安全的,并且可能降低低肝毒性风险患者的住院时间。需要更大规模的前瞻性研究来检验该简化乙酰半胱氨酸方案的疗效。