Propofol and Halothane versus Sevoflurane in paediatric day-case surgery :induction and recovery characteristic from British Journal of Anaesthesia April.

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Propofol and Halothane versus Sevoflurane in paediatric day-case surgery :induction and recovery characteristic from British Journal of Anaesthesia April 2003

Economic pressure Increase in day-case elective surgery In UK > 50 % elective surgery Day-case surgery Avoidance of an overnight admission Minimal lifestyle dsruption

Day-case Surgery : Highest quality during and aftersurgery care : Minimized postoperative morbidity - Pain - nausea and vomitting ( PONV)

Halothane Sevoflurane/Propofol Sevoflurane Low blood-gas solubility Non pungent smell Rapid induction of,emergence from anaethesia Propofol Rapid emergence PONV Propofol < Sevoflurane

Methods Population : Aged 3-12 yr, General/ENT surgery October January 2001 To detect a reduction of PONV 20  10 % Required 440 population Fit to Hospital Day-case protocol

Precluded Factor History of Allergic or other serious adverse experience of anaesthesia Severe cardiovascular Respiratory, Metabolic, Central nervous system disease anticipated airway management problem anaesthetic regimen include Succinylcholine

322 children were studied Randomise to one of two study group Group P/H : iv Propofol(+lidocaine) induction Halothane/Nitrous oxide maintenance Group S : Sevoflurane /Nitrous oxide induction and maintenance

On admission - topical anaesthetic cream apply to both hand - Parents were present during induction - routine monitoring : NIBP, EKG, Pulse oximetry : Gas monitoring (inspire+expire) - carbon dioxide - volatile agent concentration

Can’t blind Anaesthetist Drug dose individual Anaesthetist FGS was fixed at ml/kg/min via Mapleson A/F 50-70% Nitrous Oxide

Airway maintenance Non-depolarizing neuromuscular blocking agent Individual to Anaesthetist

After Induction Diclofenac 12.5/25 mg suppository (Acetaminophen if allergr to DCF) Intra operative opioid analgesia : Fentanyl / Alfentanyl ( exclude if use Morphine ) Prophylactic antiemetic drugs were not permitted

All datas were collected Children can leave RR when awake Return to community was allow when The children were ambulatory

The Primary outcome measure was PONV PONV SCORE 0 = absence 1 = nausea only 2 = one emetic episode 3 = multipleemetic episode

In recovery room Nurse was asked to judge mental stage alert and awake drowsy agited and distressed

After discharge Parent was interviewed by phone :economic evaluation :future for anaesthetic induction technic, shoud their child again require

Analysis SAS 6.12 and SPSS 10 Chi-square PONV Mann-Whitney U-test Logistic regression analysis

Table 1 Time measures employed with their definitions Time Definition Induction Time from commencing induction to patient entering theatre Maintenance Time from entering theatre to time when maintenance agents discontinued Recovery Time from maintenance agent discontinuation to leaving the anaesthetic recovery room to return to the postoperative ward Discharge Time from return to the postoperative ward to discharge home

Table 2 Number of parents/guardians declining to take part in the trial with their reasons Reason for refusal n Do not want volatile induction 59 No reason/‘don’t like the idea’ 19 No time 12 I want anaesthetist to choose anaesthetic 7 Do not want i.v. induction 6 Been in study before 5 Legal reasons 4 Concurrent disease 3 Want same anaesthetic as previously 3 Total 118

Table 3 Patients withdrawn from trial after randomization,with reasons Reason for withdrawal n Protocol violation 15 Operation cancelled 5 Withdrawal of consent 5 Total 25

Table 4 Patient’s age, sex, and surgery type with randomization group ( 2 -test) Group P/H Group S P-value N Age in years, mean (range)7.2 (3.0–13.0) 7.1 (2.9–12.9) n.s. Female ENT n.s. Male ENT n.s. Female general surgery 7 6 n.s. Male general surgery n.s. Intraoperative opioids n.s.

Table 5 Induction time, maintenance time, total anaesthesia time, time in recovery, and time from recovery to ready for home discharge, in minutes, by randomization group. Values are mean (SD). (Student’s t-test) Group P/H Group S P-value Induction time 3.1 (1.9) 5.0 (2.3) <0.001 Maintenance time 9.5 (7.1) 10.1 (6.7) 0.45 Total anaesthesia time 12.6 (7.8) 15.1 (7.7) <0.01 Recovery time 26.4 (8.9) 23.2 (8.8) Time to discharge (127.2) (96.4) 0.976

Table 6 Induction adverse events by randomization group Group P/H Group S P-value Pain on injection 22 0 <0.001 Excitatory movement Laryngospasm Breath-holding Cough test, Fisher’s exact test.

Table 7 Recovery mental state by randomization group. ( 2 -test) Group P/H Group S P-value Alert and awake Drowsy <0.001 Agitated and distressed <0.001

Table 8 Nausea and vomiting in recovery and on the postoperative ward by randomization group. (Mann–Whitney U-test) Group P/H Group S P-value Recovery None Nausea 2 3 One emetic episode 1 6 Multiple emetic episodes 0 0 Postoperative ward None Nausea 4 11 One emetic episode 2 6 Multiple emetic episodes 1 2

Table 8 Nausea and vomiting in recovery and on the postoperative ward by randomization group. (Mann–Whitney U-test) Group P/H Group S P-value Recovery None Nausea 2 3 One emetic episode 1 6 Multiple emetic episodes 0 0 Postoperative ward None Nausea 4 11 One emetic episode 2 6 Multiple emetic episodes 1 2

Table 9 Logistic regression for any nausea or vomiting on the postoperative ward, by randomization group, sex, surgical speciality and age P-value Randomization group Sex Surgical speciality Age 0.498

Table 10 Parental preference for future anaesthetic induction by randomization group. ( 2 -test) Group P/H Group S P-value Lost to follow up 62 I.V <0.001 Volatile No preference 1 0