Postoperative complications are major healthcare problems and are associated with a reduced short-term and long-term survival after surgery. Major surgery is associated with a predictable and usually transient Systemic Inflammatory Response (SIRS), depending on the magnitude of the surgical trauma. An excessive SIRS syndrome participates to the development of postoperative organ dysfunction, infection and mortality. Corticosteroids may decrease the postsurgical SIRS in cardiac surgery: in a large multicenter randomized trial, a single intravenous administration of high-dose dexamethasone did not reduce the incidence of a composite endpoint of adverse events but was associated with a reduced incidence of postoperative pulmonary complications and infections and with a reduction in hospital stay. However, a similar study, recently published in the Lancet was negative. Evidences from one meta-analysis, including 11 studies of moderate quality (439 patients in total), suggest that intraoperative administration of corticosteroids during major abdominal surgery decreases postoperative complications, including infectious complications, without significant risk of anastomotic leakage. At present, no large randomized controlled trial has been performed in patients undergoing major non-cardiac surgery. In acute medicine, several lines of evidence have shown that low to moderate doses of corticosteroids decrease the excessive inflammatory response, without inducing immuno suppression. However, despite the widespread use of corticosteroids to reduce postoperative nausea and vomiting and to improve analgesia, concerns continue to be raised about their safety, especially regarding an increased risk of postoperative infection. We hypothesize that the perioperative administration of glucocorticoids would reduce postoperative morbidity after major non-cardiac surgery through dampening of the inflammatory response. Given the number of surgical patients for whom the question applies, the study is of significant clinical importance
Background : Postoperative complications are major healthcare problems and are associated with a reduced short-term and long-term survival after surgery. Corticosteroids may decrease the postsurgical SIRS in cardiac surgery, but this treatment is not recommended yet. The aim of the current study is to assess the efficiency and the safety of dexamethasone to prevent on postoperative complications. Methods : The PACMAN trial is a multicenter, randomized, controlled, double-blind, two-arms study. 1222 patients undergoing major surgery (duration \>90 minutes and one or more risk factor of postoperative complication) are randomized to dexamethasone (0.2mg/kg at the end of the surgery and at day1) or to placebo. The primary outcome is a composite outcome of major postoperative complication during 14 days after the surgery. Analyzes will be conducted, first, on data from the intention-to-treat (ITT) population, second, in the modified intention-to-treat (mITT) population as well as in the per-protocol population. All statistical analyzes will take into account stratified randomization (cancer and type of surgery) and will be adjusted on the center as random effect as. Discussion : The PACMAN trial is the first randomized controlled trial powered to investigate whether perioperative administration of dexamethasone in high risk patients improve outcomes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
1,222
Dexamethasone : first dose : 0,2mg.kg-1 at the end of the surgical procedure, second dose (0,2 mg.kg-1) 24 hours after the surgery
placebo : first infusion at the end of the surgical procedure, second 24 hours after the surgery
CHU Angers
Angers, France
CHU La Cavale Blanche
Brest, France
Hôpital Estaing, CHU de Clermont Ferrand
Clermont-Ferrand, France
Hôpital Beaujon
Clichy, France
CHD Vendée
La Roche-sur-Yon, France
Centre Hospitalier Du Mans
Le Mans, France
Hôpital Claude Huriez
Lille, France
Hopital Edouard Herriot
Lyon, France
Institut Paoli Calmettes
Marseille, France
Hôpital Timone
Marseille, France
...and 19 more locations
Composite outcome at least one item among the following:-Postoperative sepsis, severe sepsis, septic shock-Postoperative pulmonary complication: pneumonia, need for invasive and/or noninvasive ventilation for respiratory failure-All-cause mortality
Time frame: 14 days
All cause mortality
Time frame: 28 days
Hospital free days
Time frame: 28 days
Rate of patients with post operative sepsis
Time frame: 28 days
Postoperative intubation rate for respiratory failure
Postoperative respiratory failure requiring invasive ventilation
Time frame: 28 days
Rate of patients with postoperative respiratory failure requiring non-invasive ventilation
Time frame: 28 days
Surgical complications
The Clavien-Dindo classification
Time frame: 28 days
Duration of hospitalization
Time frame: 28 days
Rate of unplanned hospitalization in intensive care unit
Time frame: 28 days
Rate of patients developing postoperative organ failures
Time frame: 28 days
Blood level of marker of inflammation (C Reactive protein)
Time frame: 28 days
Delayed healing defined as non hermetic scar
Time frame: 28 days
ICU length of stay
Time frame: 28 days
Rate of patients with Gastric ulcer
Time frame: 28 days
Rate of patients with Digestive bleeding
Time frame: 28 days
Rate of patients with Anastomotic leakage
Time frame: 28 days
Dose of insulin
Time frame: 3 days
Rate of patients with Hypokaliemia (< 4 mmol/l)
Time frame: 28 days
Rate of patients with Dysnatremia (<139 mmol/l or > 145 mmol/l)
Time frame: 28 days
Rate of patients with Hypocalcemia (<2.2 mmol/l)
Time frame: 28 days
Rate of patients with Cardiac events (Atrial fibrillation / cardiac flutter, Acute coronary syndrome or Cardiac failure)
Time frame: 28 days
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