Acetylcysteine for prevention of acute deterioration of renal function following elective coronary angiography and intervention: a randomized controlled trial
- PMID: 12578487
- DOI: 10.1001/jama.289.5.553
Acetylcysteine for prevention of acute deterioration of renal function following elective coronary angiography and intervention: a randomized controlled trial
Abstract
Context: The antioxidant acetylcysteine prevents acute contrast nephrotoxicity in patients with impaired renal function who undergo computed tomography scanning. However, its role in coronary angiography is unclear.
Objective: To determine whether oral acetylcysteine prevents acute deterioration in renal function in patients with moderate renal insufficiency who undergo elective coronary angiography.
Design and setting: Prospective, randomized, double-blind, placebo-controlled trial conducted from May 2000 to December 2001 at the Grantham Hospital at the University of Hong Kong.
Participants: Two hundred Chinese patients aged mean (SD) 68 (6.5) years with stable moderate renal insufficiency (creatinine clearance <60 mL/min [1.00 mL/s]) who were undergoing elective coronary angiography with or without intervention.
Intervention: Participants were randomly assigned to receive oral acetylcysteine(600 mg twice per day; n = 102) or matching placebo tablets (n = 98) on the day before and the day of angiography. All patients received low-osmolality contrast agent.
Main outcome measures: Occurrence of more than a 25% increase in serum creatinine level within 48 hours after contrast administration; change in creatinine clearance and serum creatinine level.
Results: Twelve control patients (12%) and 4 acetylcysteine patients (4%) developed a more than 25% increase in serum creatinine level within 48 hours after contrast administration (relative risk, 0.32; 95% confidence interval [CI], 0.10-0.96; P =.03). Serum creatinine was lower in the acetylcysteine group (1.22 mg/dL [107.8 micromol/L]; 95% CI, 1.11-1.33 mg/dL vs 1.38 mg/dL [122.9 micromol/L]; 95% CI, 1.27-1.49 mg/dL; P =.006) during the first 48 hours after angiography. Acetylcysteine treatment significantly increased creatinine clearance from 44.8 mL/min (0.75 mL/s) (95% CI, 42.7-47.6 mL/min) to 58.9 mL/min (0.98 mL/s) (95% CI, 55.6-62.3 mL/min) 2 days after the contrast administration (P<.001). The increase was not significant in the control group (from 42.1 to 44.1 mL/min [0.70 to 0.74 mL/s]; P =.15). The benefit of acetylcysteine was consistent among various patient subgroups and persistent for at least 7 days. There were no major treatment-related adverse events.
Conclusion: Acetylcysteine protects patients with moderate chronic renal insufficiency from contrast-induced deterioration in renal function after coronary angiographic procedures, with minimal adverse effects and at a low cost.
Comment in
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Prevention of contrast nephropathy.JAMA. 2003 Feb 5;289(5):606-8. doi: 10.1001/jama.289.5.606. JAMA. 2003. PMID: 12578494 No abstract available.
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Acetylcysteine and renal function following coronary angiographic procedures.JAMA. 2003 Jun 4;289(21):2794-5; author reply 2796. doi: 10.1001/jama.289.21.2794-c. JAMA. 2003. PMID: 12783905 No abstract available.
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Acetylcysteine and renal function following coronary angiographic procedures.JAMA. 2003 Jun 4;289(21):2795-6; author reply 2796. doi: 10.1001/jama.289.21.2795-b. JAMA. 2003. PMID: 12783907 No abstract available.
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Acetylcysteine and renal function following coronary angiographic procedures.JAMA. 2003 Jun 4;289(21):2795; author reply 2796. doi: 10.1001/jama.289.21.2795-a. JAMA. 2003. PMID: 12783908 No abstract available.
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Acetylcysteine for prevention of acute deterioration of renal function following elective coronary angiography and intervention: a randomized controlled trial.Vasc Med. 2002;7(4):337-8. doi: 10.1191/1358863x02vm459xx. Vasc Med. 2002. PMID: 12884839 No abstract available.
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Acetylcysteine prevented acute deterioration in renal function after coronary angiography in moderate renal insufficiency.ACP J Club. 2003 Sep-Oct;139(2):41. ACP J Club. 2003. PMID: 12954033 No abstract available.
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