Abstract
Cognitive deficit after coronary artery bypass surgery (CABG) has a high prevalence and is persistent. Meta-analysis of clinical trials demonstrates a decreased incidence of stroke after CABG when aprotinin is administrated perioperatively. We hypothesized that aprotinin administration would decrease the incidence of cognitive deficit after CABG.
Thirty-six ASA III-IV patients undergoing elective CABG were included in a prospective, randomized, single-blinded pilot study. Eighteen patients received aprotinin 2 x 10(6) KIU (loading dose), 2 x 10(6) KIU (added to circuit prime) and a continuous infusion of 5 x 10(5) KIU.hr(-1). A battery of cognitive tests was administered to patients and spouses (n = 18) the day before surgery, four days and six weeks postoperatively.
Four days postoperatively new cognitive deficit (defined by a change in one or more cognitive domains using the Reliable Change Index method) was present in ten (58%) patients in the aprotinin group compared to 17 (94%) in the placebo group [95% confidence interval (CI) 0.10-0.62, P = 0.005); (P = 0.01)]. Six weeks postoperatively, four (23%) patients in the aprotinin group had cognitive deficit compared to ten (55%) in the placebo group (95% CI 0.80-0.16, P = 0.005); (P = 0.05).
In this prospective pilot study, the incidence of cognitive deficit after CABG and cardiopulmonary bypass is decreased by the administration of high-dose aprotinin.
Thirty-six ASA III-IV patients undergoing elective CABG were included in a prospective, randomized, single-blinded pilot study. Eighteen patients received aprotinin 2 x 10(6) KIU (loading dose), 2 x 10(6) KIU (added to circuit prime) and a continuous infusion of 5 x 10(5) KIU.hr(-1). A battery of cognitive tests was administered to patients and spouses (n = 18) the day before surgery, four days and six weeks postoperatively.
Four days postoperatively new cognitive deficit (defined by a change in one or more cognitive domains using the Reliable Change Index method) was present in ten (58%) patients in the aprotinin group compared to 17 (94%) in the placebo group [95% confidence interval (CI) 0.10-0.62, P = 0.005); (P = 0.01)]. Six weeks postoperatively, four (23%) patients in the aprotinin group had cognitive deficit compared to ten (55%) in the placebo group (95% CI 0.80-0.16, P = 0.005); (P = 0.05).
In this prospective pilot study, the incidence of cognitive deficit after CABG and cardiopulmonary bypass is decreased by the administration of high-dose aprotinin.
| Original language | English |
|---|---|
| Pages (from-to) | 1002-9 |
| Number of pages | 8 |
| Journal | Canadian Journal of Anesthesia |
| Volume | 51 |
| Issue number | 10 |
| DOIs | |
| Publication status | Published - 1 Dec 2004 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Cardiopulmonary Bypass methods
- Cardiopulmonary Bypass psychology
- Cognition Disorders etiology
- Cognition Disorders psychology
- Coronary Artery Bypass methods
- Coronary Artery Bypass psychology
- Dose-Response Relationship, Drug
- Female
- Humans
- Incidence
- Male
- Middle Aged
- Neuropsychological Tests statistics & numerical data
- Pilot Projects
- Postoperative Complications etiology
- Postoperative Complications prevention & control
- Postoperative Complications psychology
- Prospective Studies
- Psychiatric Status Rating Scales statistics & numerical data
- Single-Blind Method
- Time Factors
- Aprotinin therapeutic use
- Cardiopulmonary Bypass adverse effects
- Cognition Disorders prevention & control
- Coronary Artery Bypass adverse effects
- Hemostatics therapeutic use
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