Perioperative omega-3 fatty acids fail to confer protection in liver surgery: Results of a multicentric, double-blind, randomized controlled trial

[Display omitted] •Perioperative intravenous infusions of omega-3 fatty acids failed to confer a benefit in this RCT.•No differences in complications were evident in the Omegaven vs. Placebo groups.•Subgroup analyses likewise did not detect differences in outcomes after liver resection. In a variety...

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Veröffentlicht in:Journal of hepatology 2020-03, Vol.72 (3), p.498-505
Hauptverfasser: Linecker, Michael, Botea, Florin, Aristotele Raptis, Dimitri, Nicolaescu, Diana, Limani, Përparim, Alikhanov, Ruslan, Kim, Pavel, Wirsching, Andrea, Kron, Philipp, Schneider, Marcel A., Tschuor, Christoph, Kambakamba, Patryk, Oberkofler, Christian, De Oliveira, Michelle L., Bonvini, John, Efanov, Michail, Graf, Rolf, Petrowsky, Henrik, Khatkov, Igor, Clavien, Pierre-Alain, Popescu, Irinel
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Sprache:eng
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Zusammenfassung:[Display omitted] •Perioperative intravenous infusions of omega-3 fatty acids failed to confer a benefit in this RCT.•No differences in complications were evident in the Omegaven vs. Placebo groups.•Subgroup analyses likewise did not detect differences in outcomes after liver resection. In a variety of animal models, omega-3 polyunsaturated fatty acids (Ω3-FAs) conferred strong protective effects, alleviating hepatic ischemia/reperfusion injury and steatosis, as well as enhancing regeneration after major tissue loss. Given these benefits along with its safety profile, we hypothesized that perioperative administration of Ω3-FAs in patients undergoing liver surgery may ameliorate the postoperative course. The aim of this study was to investigate the perioperative use of Ω3-FAs to reduce postoperative complications after liver surgery. Between July 2013 and July 2018, we carried out a multicentric, double-blind, randomized, placebo-controlled trial designed to test whether 2 single intravenous infusions of Omegaven® (Ω3-FAs) vs. placebo may decrease morbidity. The primary endpoints were postoperative complications by severity (Clavien-Dindo classification) integrated within the comprehensive complication index (CCI). A total of 261 patients (132 in the Omegaven and 129 in the placebo groups) from 3 centers were included in the trial. Most cases (87%, n = 227) underwent open liver surgery and 56% (n = 105) were major resections (≥3 segments). In an intention-to-treat analysis including the dropout cases, the mortality rate was 4% and 2% in the Omegaven and placebo groups (odds ratio0.40;95% CI 0.04–2.51; p = 0.447), respectively. Any complications and major complications (Clavien-Dindo ≥ 3b) occurred in 46% vs. 43% (p = 0.709) and 12% vs. 10% (p = 0.69) in the Omegaven and placebo groups, respectively. The mean CCI was 17 (±23) vs.14 (±20) (p = 0.417). An analysis excluding the dropouts provided similar results. The routine perioperative use of 2 single doses of intravenous Ω3-FAs (100 ml Omegaven) cannot be recommended in patients undergoing liver surgery (Grade A recommendation). Despite strong evidence of omega-3 fatty acids having liver-directed, anti-inflammatory and pro-regenerative action in various rodent models, 2 single omega-3 fatty acid infusions given to patients before and during liver surgery failed to reduce complications. Because single omega-3 fatty acid infusions failed to confer liver protection in this trial, they cannot currently be recom
ISSN:0168-8278
1600-0641
DOI:10.1016/j.jhep.2019.10.004