Relationship between intra-operative vein graft treatment with DuraGraft® or saline and clinical outcomes after coronary artery bypass grafting

Autor: Nicole M Kosik, Maximilian Y. Emmert, Michael Gaziano, David R. Gagnon, Katherine E. Kurgansky, Robert R. McLean, Kelly Cho, Constance Nelson, Miguel Haime
Přispěvatelé: University of Zurich, Haime, Miguel
Rok vydání: 2018
Předmět:
Adult
Male
CABG myocardial infarction patency repeat revascularization vein graft failure
medicine.medical_specialty
Intimal hyperplasia
Bypass grafting
medicine.medical_treatment
Myocardial Infarction
610 Medicine & health
Vein graft
030204 cardiovascular system & hematology
2705 Cardiology and Cardiovascular Medicine
03 medical and health sciences
Postoperative Complications
0302 clinical medicine
Internal Medicine
medicine
Clinical endpoint
Humans
Saphenous Vein
Myocardial infarction
Coronary Artery Bypass
Saline
Aged
Proportional Hazards Models
Retrospective Studies
Aged
80 and over

business.industry
11359 Institute for Regenerative Medicine (IREM)
General Medicine
Middle Aged
medicine.disease
10020 Clinic for Cardiac Surgery
Surgery
Treatment Outcome
surgical procedures
operative

medicine.anatomical_structure
2724 Internal Medicine
030220 oncology & carcinogenesis
Female
Cardiology and Cardiovascular Medicine
business
Mace
Follow-Up Studies
Artery
Zdroj: Expert Review of Cardiovascular Therapy. 16:963-970
ISSN: 1744-8344
1477-9072
2001-2004
Popis: Saphenous vein grafts (SVGs) remain the most often used conduits for coronary bypass grafting (CABG). Progressive intimal hyperplasia contributes to vein-graft disease and vein-graft failure (VGF). We compared the impact of intraoperative preservation of SVGs in a storage solution (DuraGraft®) versus heparinized saline on VGF-related outcomes after CABG.From 1996 to 2004, 2436 patients underwent isolated CABG with ≥ 1 SVG. SVGs were consecutively treated with DuraGraft in 1036 patients (2001-2004) and heparinized saline in 1400 patients (1996-1999). Short- ( 30 days) and long-term (≥ 1000 days) outcomes were assessed using repeat revascularization (primary end point), and major adverse cardiac events (MACE) consisting of the composite of death, nonfatal myocardial infarction, or repeat revascularization.Mean follow-up in the DuraGraft group was 8.5 ± 4.2 years and 9.9 ± 5.6 years in controls. Short-term event rates were low and generally did not differ between groups. DuraGraft was associated with a 45% lower occurrence of nonfatal myocardial infarction after 1000 days (hazard ratio 0.55, 95% CI 0.41-0.74; P 0.0001). There was 35% and 19% lower long-term risk for revascularization (HR 0.65, 95% CI 0.44-0.97; P = 0.037) and MACE (HR 0.81, 95% CI 0.70-0.94; P = 0.0051), respectively, after DuraGraft. Mortality was comparable between both groups at 1, 5, and 10 years. There was no statistically significant association between DuraGraft exposure and time to death starting at 30 or 1000 days (HR 0.91, 95% CI 0.76-1.09; P = 0.29).In this study, intraoperative treatment of SVGs with DuraGraft was associated with a lower risk of long-term adverse events suggesting that efficient intraoperative SVG treatment may reduce VGF-related complications post-CABG. These data warrant randomized clinical trials to validate these findings.
Databáze: OpenAIRE