PMID- 21542122 OWN - NLM STAT- MEDLINE DCOM- 20120813 LR - 20161125 IS - 1522-726X (Electronic) IS - 1522-1946 (Linking) VI - 79 IP - 6 DP - 2012 May 1 TI - A randomized trial of intravenous n-acetylcysteine to prevent contrast induced nephropathy in acute coronary syndromes. PG - 921-6 LID - 10.1002/ccd.23157 [doi] AB - BACKGROUND: Pharmacokinetic data suggests that the intravenous form of n-acetylcysteine (NAC) may be more effective than the oral formulation in preventing contrast induced nephropathy (CIN). NAC owing to its anti-oxidant properties might be beneficial for patients with acute coronary syndromes (ACS) who are at increased risk for CIN. The aim of this prospective randomized, single-center, double-blind, placebo controlled trial (NCT00939913) was to assess the effect of high-dose intravenous NAC on CIN in ACS patients undergoing coronary angiography and/or percutaneous coronary intervention (PCI). METHODS: We randomized 398 ACS patients scheduled for diagnostic angiography +/- PCI to an intravenous regimen of high-dose NAC (1,200 mg bolus followed by 200 mg/hr for 24 hr; n = 206) or placebo (n = 192). The primary end-point was incidence of CIN defined as an increase in serum creatinine concentration >/= 25% above the baseline level within 72 hr of the administration of intravenous contrast. RESULTS: There was no difference found for the primary end point with CIN in 16% of the NAC group and in 13% of the placebo group (p = 0.40). Change in serum cystatin-C, a sensitive marker for renal function, was 0.046 +/- 0.204 in the NAC group and 0.002 +/- 0.260 in the control group (p = 0.07). CONCLUSION: In ACS patients undergoing angiography +/- PCI, high-dose intravenous NAC failed to reduce the incidence of CIN. CI - Copyright (c) 2011 Wiley Periodicals, Inc. FAU - Jaffery, Zehra AU - Jaffery Z AD - Department of Cardiovascular Diseases, The John Ochsner Heart & Vascular Institute, Ochsner Clinic Foundation, New Orleans, Louisiana, USA. zjaffery@ochsner.org FAU - Verma, Anil AU - Verma A FAU - White, Christopher J AU - White CJ FAU - Grant, Arthur G AU - Grant AG FAU - Collins, Tyrone J AU - Collins TJ FAU - Grise, Mark A AU - Grise MA FAU - Jenkins, James S AU - Jenkins JS FAU - McMullan, Paul W AU - McMullan PW FAU - Patel, Rajan A AU - Patel RA FAU - Reilly, John P AU - Reilly JP FAU - Thornton, Stanley N AU - Thornton SN FAU - Ramee, Stephen R AU - Ramee SR LA - eng SI - ClinicalTrials.gov/NCT00939913 PT - Journal Article PT - Randomized Controlled Trial DEP - 20111130 PL - United States TA - Catheter Cardiovasc Interv JT - Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions JID - 100884139 RN - 0 (Antioxidants) RN - 0 (Biomarkers) RN - 0 (CST3 protein, human) RN - 0 (Contrast Media) RN - 0 (Cystatin C) RN - 0 (Placebos) RN - AYI8EX34EU (Creatinine) RN - WYQ7N0BPYC (Acetylcysteine) SB - IM CIN - Catheter Cardiovasc Interv. 2012 May 1;79(6):927-8. PMID: 22511379 MH - Acetylcysteine/*administration & dosage MH - Acute Coronary Syndrome/*diagnostic imaging/therapy MH - Aged MH - *Angioplasty, Balloon, Coronary MH - Antioxidants/*administration & dosage MH - Biomarkers/blood MH - Chi-Square Distribution MH - Contrast Media/*adverse effects MH - Coronary Angiography/*adverse effects MH - Creatinine/blood MH - Cystatin C/blood MH - Double-Blind Method MH - Female MH - Humans MH - Infusions, Intravenous MH - Kidney Diseases/blood/chemically induced/diagnosis/*prevention & control MH - Male MH - Middle Aged MH - New Orleans MH - Placebos MH - Prospective Studies MH - Risk Assessment MH - Risk Factors MH - Time Factors MH - Treatment Outcome EDAT- 2011/05/05 06:00 MHDA- 2012/08/14 06:00 CRDT- 2011/05/05 06:00 PHST- 2011/03/17 00:00 [received] PHST- 2011/03/19 00:00 [accepted] PHST- 2011/05/05 06:00 [entrez] PHST- 2011/05/05 06:00 [pubmed] PHST- 2012/08/14 06:00 [medline] AID - 10.1002/ccd.23157 [doi] PST - ppublish SO - Catheter Cardiovasc Interv. 2012 May 1;79(6):921-6. doi: 10.1002/ccd.23157. Epub 2011 Nov 30.