Habib Mohammed
Alshifa Hospital, Gaza, Palestine.
Arch Med Sci Atheroscler Dis. 2024 Dec 31;9:e207-e211. doi: 10.5114/amsad/195767. eCollection 2024.
Contrast-induced acute renal injury is the third leading cause of hospital-acquired acute kidney injury. Our trial aimed to compare high-dose statin versus statin plus N-acetylcysteine (NAC) to prevent contrast-induced nephropathy.
Randomized control trial included patients who undergoing elective percutaneous coronary intervention (PCI) at Alshifa Hospital in Gaza, the first group (statin: 50 patients) received 80 mg of atorvastatin orally once daily for 3 days. The second group (statin + NAC: 50 patients) received 80 mg of atorvastatin orally once daily for 3 days, plus NAC 1200 mg orally twice daily every 12 h for 2 days. All patients underwent measurement of serum creatinine and urea level before PCI and 2-3 days after the procedure. The primary endpoint was to compare development of contrast-induced nephropathy between the two groups.
The total group comprised 100 patients: 71 male patients and 29 female patients. Mean age was 59 ±9.8 years. After intervention serum creatinine decreased from 1.02 ±0.27 mg/dl to1.01 ±0.29 mg/dl in the statin group, while it decreased from 1.08 ±0.36 mg/dl to 0.92 ±0.13 mg/dl in the statin + NAC group. The difference between the two groups was significant ( = 0.048). Also, the urea plasma level in the statin group decreased from 34.5 ±9.7 mmol/l to 30.6 ±8.7 mmol/l after PCI, while in the statin + NAC group it decreased from 36.4 ±9.9 mmol/l to 26.2 ±10.6 mmol/l; the difference between the two groups was significant ( = 0.017). Contrast-induced nephropathy was seen in 9 (18%) patients in the statin group and in 2 (4%) patients in the statin + NAC group ( = 0.025).
The combination of high-dose atorvastatin plus NAC compared to atorvastatin alone was associated with a significant reduction of contrast-induced nephropathy in patients undergoing PCI.
对比剂诱导的急性肾损伤是医院获得性急性肾损伤的第三大主要原因。我们的试验旨在比较高剂量他汀类药物与他汀类药物加N-乙酰半胱氨酸(NAC)预防对比剂肾病的效果。
随机对照试验纳入了在加沙的阿尔希法医院接受择期经皮冠状动脉介入治疗(PCI)的患者,第一组(他汀类药物组:50例患者)每天口服一次80毫克阿托伐他汀,共3天。第二组(他汀类药物+NAC组:50例患者)每天口服一次80毫克阿托伐他汀,共3天,外加NAC 1200毫克,每12小时口服两次,共2天。所有患者在PCI术前及术后2 - 3天测量血清肌酐和尿素水平。主要终点是比较两组对比剂肾病的发生情况。
总共有100例患者,其中男性71例,女性29例。平均年龄为59±9.8岁。干预后,他汀类药物组血清肌酐从1.02±0.27毫克/分升降至1.01±0.29毫克/分升,而他汀类药物+NAC组从1.08±0.36毫克/分升降至0.92±0.13毫克/分升。两组间差异有统计学意义(=0.048)。此外,他汀类药物组PCI术后尿素血浆水平从34.5±9.7毫摩尔/升降至30.6±8.7毫摩尔/升,而他汀类药物+NAC组从36.4±9.9毫摩尔/升降至26.2±10.6毫摩尔/升;两组间差异有统计学意义(=0.017)。他汀类药物组有9例(18%)患者发生对比剂肾病,他汀类药物+NAC组有2例(4%)患者发生(=0.025)。
与单独使用阿托伐他汀相比,高剂量阿托伐他汀加NAC的联合用药可使接受PCI的患者对比剂肾病显著减少。