TY - JOUR
T1 - Effect of goal-directed haemodynamic therapy on postoperative complications in low–moderate risk surgical patients
T2 - a multicentre randomised controlled trial (FEDORA trial)
AU - FEDORA Trial Investigators Group
AU - Calvo-Vecino, J. M.
AU - Ripollés-Melchor, J.
AU - Mythen, M. G.
AU - Casans-Francés, R.
AU - Balik, A.
AU - Artacho, J. P.
AU - Martínez-Hurtado, E.
AU - Serrano Romero, A.
AU - Fernández Pérez, C.
AU - Asuero de Lis, S.
AU - Errazquin, Ana Tirado
AU - Gil Lapetra, Cristina
AU - Motos, Ane Abad
AU - Reche, Elena Garrido
AU - Medraño Viñas, Cristina
AU - Villaba, Raúl
AU - Cobeta, Pilar
AU - Ureta, Eva
AU - Montiel, María
AU - Mané, Nuria
AU - Martínez Castro, Nilda
AU - Horno, Gema Aleson
AU - Salas, Rebeca Alonso
AU - Bona García, Carmen
AU - Ferrer Ferrer, Marta L.
AU - Franco Abad, Marta
AU - García Lecina, Ana C.
AU - Antón, Julia Guillén
AU - Gascón, Guillermo Hojas
AU - Peligro Deza, Javier
AU - Pascual, Leticia Pérez
AU - Ruiz Garcés, Tomás
AU - Roberto Alcácer, Ana T.
AU - Badura, Marek
AU - Terrer Galera, Eduardo
AU - Fernández Casares, Antonio
AU - Martínez Fernández, Maria Carmen
AU - Espinosa, Ángel
AU - Abad-Gurumeta, Alfredo
AU - Feldheiser, Aarne
AU - López Timoneda, Francisco
AU - Zuleta-Alarcón, Alix
AU - Bergese, Sergio
N1 - Publisher Copyright:
© 2017 British Journal of Anaesthesia
PY - 2018/4
Y1 - 2018/4
N2 - Background: The aim of this study was to evaluate postoperative complications in patients having major elective surgery using oesophageal Doppler monitor-guided goal-directed haemodynamic therapy (GDHT), in which administration of fluids, inotropes, and vasopressors was guided by stroke volume, mean arterial pressure, and cardiac index. Methods: The FEDORA trial was a prospective, multicentre, randomised, parallel-group, controlled patient- and observer-blind trial conducted in adults scheduled for major elective surgery. Randomization and allocation were carried out by a central computer system. In the control group, intraoperative fluids were given based on traditional principles. In the GDHT group, the intraoperative goals were to maintain a maximal stroke volume, with mean arterial pressure >70 mm Hg, and cardiac index ≥2.5 litres min−1 m−2. The primary outcome was percentage of patients with moderate or severe postoperative complications during the first 180 days after surgery. Results: In total, 450 patients were randomized to the GDHT group (n=224) or control group (n=226). Data from 420 subjects were analysed. There were significantly fewer with complications in the GDHT group (8.6% vs 16.6%, P=0.018). There were also fewer complications (acute kidney disease, pulmonary oedema, respiratory distress syndrome, wound infections, etc.), and length of hospital stay was shorter in the GDHT group. There was no significant difference in mortality between groups. Conclusions: Oesophageal Doppler monitor-guided GDHT reduced postoperative complications and hospital length of stay in low–moderate risk patients undergoing intermediate risk surgery, with no difference in mortality at 180 days. Clinical trial registration: ISRCTN93543537.
AB - Background: The aim of this study was to evaluate postoperative complications in patients having major elective surgery using oesophageal Doppler monitor-guided goal-directed haemodynamic therapy (GDHT), in which administration of fluids, inotropes, and vasopressors was guided by stroke volume, mean arterial pressure, and cardiac index. Methods: The FEDORA trial was a prospective, multicentre, randomised, parallel-group, controlled patient- and observer-blind trial conducted in adults scheduled for major elective surgery. Randomization and allocation were carried out by a central computer system. In the control group, intraoperative fluids were given based on traditional principles. In the GDHT group, the intraoperative goals were to maintain a maximal stroke volume, with mean arterial pressure >70 mm Hg, and cardiac index ≥2.5 litres min−1 m−2. The primary outcome was percentage of patients with moderate or severe postoperative complications during the first 180 days after surgery. Results: In total, 450 patients were randomized to the GDHT group (n=224) or control group (n=226). Data from 420 subjects were analysed. There were significantly fewer with complications in the GDHT group (8.6% vs 16.6%, P=0.018). There were also fewer complications (acute kidney disease, pulmonary oedema, respiratory distress syndrome, wound infections, etc.), and length of hospital stay was shorter in the GDHT group. There was no significant difference in mortality between groups. Conclusions: Oesophageal Doppler monitor-guided GDHT reduced postoperative complications and hospital length of stay in low–moderate risk patients undergoing intermediate risk surgery, with no difference in mortality at 180 days. Clinical trial registration: ISRCTN93543537.
KW - Elective Surgical Procedures/adverse effects
KW - Hemodynamics/physiology
KW - Intraoperative/methods
KW - Postoperative Complications/prevention & control
KW - Prospective Studies
UR - https://www.scopus.com/pages/publications/85045942108
U2 - 10.1016/j.bja.2017.12.018
DO - 10.1016/j.bja.2017.12.018
M3 - Article
C2 - 29576114
AN - SCOPUS:85045942108
SN - 0007-0912
VL - 120
SP - 734
EP - 744
JO - British Journal of Anaesthesia
JF - British Journal of Anaesthesia
IS - 4
ER -