Perry H E, Shannon M W
Division of Emergency Medicine, Children's Hospital, Boston, Massachusetts, USA.
J Pediatr. 1998 Jan;132(1):149-52. doi: 10.1016/s0022-3476(98)70501-3.
We compared the clinical course of pediatric patients (n = 25) with acetaminophen poisoning treated with an investigational intravenous preparation of N-acetylcysteine (IV-NAC) with that of historical control subjects (n = 29) treated with conventional oral NAC (O-NAC) therapy. Patients received IV-NAC for 52 hours; historical control subjects received O-NAC (72 hours). There were no significant intergroup differences between treatment groups in age (15.5 vs 15.9 years), gender (88% vs 90% female) or distribution of risk categories (probable risk, 12 vs 15; high risk; 13 vs 14). The peak prothrombin time was significantly higher in the IV-NAC group (14.2 vs 13.6 seconds; p = 0.048). Mean treatment delay was significantly longer in the IV-NAC group (14.4 vs 10.4 hours; p = 0.001). Hepatoxicity was noted in two (8.0%) patients in the IV-NAC treatment group and two (6.9%) patients in the O-NAC group. All patients recovered. Our results indicate that 52 hours of intravenous NAC is as effective as 72 hours of oral NAC.
我们将使用研究性静脉注射用N-乙酰半胱氨酸(IV-NAC)治疗的对乙酰氨基酚中毒儿科患者(n = 25)的临床病程与接受传统口服NAC(O-NAC)治疗的历史对照受试者(n = 29)的临床病程进行了比较。患者接受IV-NAC治疗52小时;历史对照受试者接受O-NAC治疗(72小时)。治疗组之间在年龄(15.5岁对15.9岁)、性别(女性占88%对90%)或风险类别分布(可能风险,12例对15例;高风险,13例对14例)方面无显著组间差异。IV-NAC组的凝血酶原时间峰值显著更高(14.2秒对13.6秒;p = 0.048)。IV-NAC组的平均治疗延迟显著更长(14.4小时对10.4小时;p = 0.001)。IV-NAC治疗组有2例(8.0%)患者出现肝毒性,O-NAC组有2例(6.9%)患者出现肝毒性。所有患者均康复。我们的结果表明,52小时的静脉注射NAC与72小时的口服NAC效果相同。