In coronary bypass patients, high-dose acadesine mildly increased plasma uric acid without clinical sequelae, unlike placebo and low-dose acadesine.
In plain wordsIn coronary bypass patients, only high-dose acadesine mildly increased uric acid, without clinical consequences.
- Peptide
- AICAR (acadesine)
- Outcome
- IncreasePlasma uric acid
- Study
n: not reported in source
- Comparator
- Placebo
- Outcome group
- Adverse events · Whole body
- Studied dose
- High dose, amount not stated · Intravenous infusion and cardioplegia · 7 hAs given in this study (human).
Measurements
- Mean uric acid increase
- 1.6 mg/dL
- high-dose acadesine
- Reported uncertainty
- 0.2 mg/dL
- type not stated
Source sentences
The administration of acadesine was safe: mild increases in plasma uric acid (a metabolite of acadesine) occurred only in patients receiving high doses (mean increase 1.6 +/- 0.2 mg/dL) and were without clinical sequelae.
3 context sentences(design, population, supporting numbers)
Because patients undergoing coronary artery bypass graft (CABG) surgery are especially vulnerable to developing myocardial ischemia, we investigated whether perioperative use of this adenosine-regulating drug with potential anti-ischemic properties could modify the incidence and severity of perioper…
One hundred sixteen patients were randomized to receive one of three continuous intravenous dosing regimens (placebo [control] or one of two doses of acadesine [high- and low-dose infusion]) in double-blind fashion intraoperatively and in the early postoperative period (total infusion time was 7 h).
Multidose cold crystalloid cardioplegia (each containing either acadesine or placebo) was used for myocardial protection.