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134<br />

Appendix 4<br />

TABLE 66 contd Summary of adult clinical outcomes studies<br />

Study Investigations and subjects Outcome Results Conclusions and<br />

measures grade of evidence<br />

Short et al.,<br />

1985,<br />

(1) Methohexitone, alfentanil, N2O, O2 (a) Time to Group 2 abandoned after Grade I<br />

122 UK (n = 20: 14 women, 6 men) open eyes 11 patients due to poor<br />

conditions during induction Method of randomisation<br />

RCT (2) Methohexitone, isoflurane, O2 (n = 20: 8 women, 3 men)<br />

(b) Time to<br />

recall date (a): (1) 9.2, (3) 9.1 min;<br />

not reported<br />

of birth p < 0.01 Not blind<br />

(3) Methohexitone, isoflurane, N2O, O2 (n = 20: 10 women, 10 men) (c) Time to (b): (1) 9.9, (3) 9.7 min; The majority of group 2<br />

recall name p < 0.01 patients were not able to<br />

N2O: given in groups 1 and 3 complete the trial<br />

(d) Post-box (c): (1) 9.5, (3) 9.6 min;<br />

Premedication: none test p < 0.01<br />

Procedures: D&C, cystourethroscopy (e) P-deletion (d): (1) 34.3, (2) 44.3, (3) 40.3;<br />

Age: > 18 years; mean (1) 45, (2) 46,<br />

test p < 0.01 group 2<br />

(3) 43 years (e): (1) 4; (2) 2; (3) 2; NS<br />

Sivalingam ASA grade I or II LMA insertion Satisfactory or excellent: (1) Grade I<br />

et al., 1999, 123<br />

(quality <strong>for</strong> 64%, (2) 64%, (3) 100%, (4)<br />

Singapore (1) Propofol 2.5 mg/kg + 10 mg induction only): 88%; p < 0.001 Method of randomisation<br />

increments i.v. (n = 25) excellent, not reported<br />

RCT satisfactory<br />

(2) Sevoflurane 8% + 60% N 2O vital or poor Open<br />

capacity breath (n = 25)<br />

(3) Sevoflurane as (2) + alfentanil<br />

5 µg/kg (n = 25)<br />

(4) Propofol as (1) + alfentanil 5 µg/kg (n = 25)<br />

N 2O: given in groups 2 and 3<br />

Premedication: none<br />

Procedures: mixed<br />

Gender: 55% men<br />

Sloan et al.,<br />

1996,<br />

Age: 16–65 years<br />

(1) Sevoflurane/sevoflurane + N2O (n = 25) (a) Open eyes (a): (1) 8.1, (2) 10.6 min Grade I<br />

124 USA<br />

(2) Isoflurane/isoflurane + N2O (n = 25) (b) Obey (b): (1) 8.0, (2) 9.9 min Method of randomisation<br />

RCT command not reported<br />

N2O: given (c): (1) 9.9, (2) 12.6 min<br />

(c) Orientation Not blind<br />

Premedication: none (d): (1) 120, (2) 133 min<br />

(d) Discharge<br />

Procedures: not reported (e): Data not given<br />

(e) DSST<br />

Age: 18–76 years No difference between groups<br />

Smith and<br />

Thwaites,<br />

(1) Sevoflurane./sevoflurane (n = 30) (a) Open eyes (a): 7.1 min; p = 0.027 Grade I<br />

1999, 125<br />

(2) Propofol TCI (n = 31) (b) Date of (b): 8.1 min; NS Method of randomisation:<br />

England birth computer-generated<br />

N2O: not given (c): 100 min; p = 0.024 random numbers<br />

RCT (c) Sit up<br />

Premedication: none<br />

(d) Walk<br />

(d): 175 min; NS Blind<br />

Procedures: mixed<br />

(e) Street fit<br />

(e): 193 min; p = 0.005<br />

Gender: 66% women<br />

Age: 18–73 years<br />

(f) PONV<br />

(f): (1) 9%; (2) 1%; p = 0.006<br />

continued

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