No anxiolytic premedication was given to the patient before surgery. Anaesthetic induction was performed with Propofol + Sufentanil + Atracurium. Patients had standard monitoring including depth of anaesthesia using the Bispectral (BIS®) index. Hypothermia was prevented by using warming blankets.
All patients were intubated and ventilated with a mixture of O2/N2O: 50/50%. Fluid loading was achieved with crystalloids and/or colloids depending on requirements.
According to randomization, patients were allocated to receive either Desflurane (Group D) or Propofol (Group P) for anaesthesia maintenance.

Group D: Desflurane

Induction with a bolus of Propofol 2–3 mg/kg

Maintenance with a closed circuit of Desflurane with minimal alveolar concentration adapted to maintain a BIS value between 40 and 60.

Group P: Propofol

Target controlled administration of Propofol at 2 and 4 μg/ml to be adjusted to maintain a BIS value between 40 and 60.

Supplemental boluses of Sufentanil and Atracurium were given as required. At the end of surgery (T0), the patient was transferred to the post-anaesthesia care unit (PACU). Tracheal extubation was carried out when the patient was conscious, with a respiratory rate above 12.min− 1, a core temperature > 36 °C, and without residual muscle weakness (residual curarization was assessed with Double-Burst Stimulation and antagonized if necessary).
Post-operative pain intensity at rest was evaluated using the Numerical Rating Scale (NRS) with 0 = no pain and 10 = maximal imaginable pain intensity. Post-operative analgesia was multimodal. The use of locoregional techniques for post-operative analgesia was encouraged (nerve block, trunk block +/− placement of a perineural catheter +/− wound infiltration). During the stay in PACU, if NRS ≥ 3, morphine was administered by titration (bolus of 1 mg IV repeated every 5 min until NRS at rest < 3).
After arrival in the PACU, the Aldrete score was checked every 5 min. Once the score of ≥9 had been attained, the cognitive tests were carried out for a second time.
The data from these tests was collected by the same investigator as the day before surgery in the case report form.
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