Molnar Z, MacKinnon K L, Shearer E, Lowe D, Watson I D
Department of Anaesthesia and Intensive Care, Medical University of Pécs, Hungary.
Intensive Care Med. 1998 Mar;24(3):230-5. doi: 10.1007/s001340050555.
To investigate the effects of N-acetylcysteine (NAC) when given as an early treatment to critically ill patients on the serum total anti-oxidant potential (TAP) and urine micro-albumin:creatinine (M:Cr) ratio.
Prospective, placebo controlled double blinded clinical trial.
General intensive care unit in a teaching hospital.
Sixty critically ill patients were recruited but ten were withdrawn due to less than 48 h of ICU stay.
After envelope randomisation, patients received either NAC (n = 23): a bolus of 150 mg/kg in 250 ml of 5% dextrose followed by a continuous infusion of 12 mg/kg per h in 500 ml of 5% dextrose over 24 h or, as controls (n = 27), the equal volume of placebo. Treatment lasted for a minimum of 3, up to a maximum of 5, days. Blood and urine samples were collected on admission (0 h) and then 6 hourly up 18 h.
There was no significant difference between NAC and placebo groups regarding the required length of inotropic support, mechanical ventilation and ICU stay. There was no significant difference in TAP or M:Cr ratio over 18 h or between the groups.
Our results suggest that NAC had no significant effects on the progress of the TAP and the urinary albumin excretion in our patients, which may suggest that NAC at the given dose has no clinical relevance as an early treatment in the critically ill.
研究N-乙酰半胱氨酸(NAC)早期治疗重症患者对血清总抗氧化能力(TAP)及尿微量白蛋白与肌酐比值(M:Cr)的影响。
前瞻性、安慰剂对照双盲临床试验。
一所教学医院的综合重症监护病房。
招募了60例重症患者,但10例因在重症监护病房停留时间不足48小时而退出。
经信封随机分组后,患者接受NAC治疗(n = 23):先在250 ml 5%葡萄糖溶液中静脉推注150 mg/kg,随后在24小时内于500 ml 5%葡萄糖溶液中以12 mg/kg每小时的速度持续输注;或作为对照(n = 27)接受等体积的安慰剂。治疗持续至少3天,最长5天。入院时(0小时)采集血样和尿样,随后每6小时采集一次,共采集18小时。
NAC组和安慰剂组在血管活性药物支持、机械通气所需时间及重症监护病房停留时间方面无显著差异。18小时内及两组间的TAP或M:Cr比值均无显著差异。
我们的结果表明,NAC对我们研究患者的TAP进展及尿白蛋白排泄无显著影响,这可能提示给定剂量的NAC作为重症患者的早期治疗无临床意义。