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Article: Acetylcysteine for Prevention of Acute Deterioration of Renal Function Following Elective Coronary Angiography and Intervention: A Randomized Controlled Trial
Title | Acetylcysteine for Prevention of Acute Deterioration of Renal Function Following Elective Coronary Angiography and Intervention: A Randomized Controlled Trial |
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Authors | |
Issue Date | 2003 |
Publisher | American Medical Association. The Journal's web site is located at http://jama.ama-assn.org/index.dtl |
Citation | Journal Of The American Medical Association, 2003, v. 289 n. 5, p. 553-558 How to Cite? |
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 μmol/L]; 95% CI, 1.11-1.33 mg/dL vs 1.38 mg/dL [122.9 μmol/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. |
Persistent Identifier | http://hdl.handle.net/10722/162682 |
ISSN | 2023 Impact Factor: 63.1 2023 SCImago Journal Rankings: 5.928 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kay, J | en_US |
dc.contributor.author | Chow, WH | en_US |
dc.contributor.author | Chan, TM | en_US |
dc.contributor.author | Lo, SK | en_US |
dc.contributor.author | Kwok, OH | en_US |
dc.contributor.author | Yip, A | en_US |
dc.contributor.author | Fan, K | en_US |
dc.contributor.author | Lee, CH | en_US |
dc.contributor.author | Lam, WF | en_US |
dc.date.accessioned | 2012-09-05T05:22:19Z | - |
dc.date.available | 2012-09-05T05:22:19Z | - |
dc.date.issued | 2003 | en_US |
dc.identifier.citation | Journal Of The American Medical Association, 2003, v. 289 n. 5, p. 553-558 | en_US |
dc.identifier.issn | 0098-7484 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/162682 | - |
dc.description.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 μmol/L]; 95% CI, 1.11-1.33 mg/dL vs 1.38 mg/dL [122.9 μmol/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. | en_US |
dc.language | eng | en_US |
dc.publisher | American Medical Association. The Journal's web site is located at http://jama.ama-assn.org/index.dtl | en_US |
dc.relation.ispartof | Journal of the American Medical Association | en_US |
dc.title | Acetylcysteine for Prevention of Acute Deterioration of Renal Function Following Elective Coronary Angiography and Intervention: A Randomized Controlled Trial | en_US |
dc.type | Article | en_US |
dc.identifier.email | Chan, TM:dtmchan@hku.hk | en_US |
dc.identifier.authority | Chan, TM=rp00394 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1001/jama.289.5.553 | en_US |
dc.identifier.pmid | 12578487 | - |
dc.identifier.scopus | eid_2-s2.0-0037419923 | en_US |
dc.identifier.hkuros | 79061 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0037419923&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 289 | en_US |
dc.identifier.issue | 5 | en_US |
dc.identifier.spage | 553 | en_US |
dc.identifier.epage | 558 | en_US |
dc.identifier.isi | WOS:000180787500025 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Kay, J=19835646800 | en_US |
dc.identifier.scopusauthorid | Chow, WH=7402281062 | en_US |
dc.identifier.scopusauthorid | Chan, TM=7402687700 | en_US |
dc.identifier.scopusauthorid | Lo, SK=7401542391 | en_US |
dc.identifier.scopusauthorid | Kwok, OH=7004955826 | en_US |
dc.identifier.scopusauthorid | Yip, A=7004871382 | en_US |
dc.identifier.scopusauthorid | Fan, K=7202978353 | en_US |
dc.identifier.scopusauthorid | Lee, CH=7410141524 | en_US |
dc.identifier.scopusauthorid | Lam, WF=19835820000 | en_US |
dc.identifier.issnl | 0098-7484 | - |