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. 2015 Oct 5;5(10):e008344. doi: 10.1136/bmjopen-2015-008344

Table 1.

Baseline characteristics of participants in the ISS and OSS groups (n=100)

  ISS group OSS group
Number of participants 48* 49†
Number of females/males 42/6 43/6
Median age (range) 44.5 (26–63) 42 (27–65)
Median years of obstetric work experiences (range)  7 (0.6–38)  7 (0.6–39)
Previous simulation experiences‡
 No experience  8 10
 Simple simulation 25 24
 Full-scale simulation 15 15
Pregnant participants  2  2
Participants on any kind of medication 19 20
Participants on medication with no expected influence on cortisol measurement§ 12  9
Participants on medication with potential influence on cortisol measurement  7 11
   Intranasal and inhaled corticosteroids (mometasone furoate, budesonide/formoterol, budesonide, fluticasone/salmeterol)    2    3
   Levothyroxine    1    2
   Metformin    1    1
   Norethisterone/estradiol acetate    0    1
   Oral contraceptives    1    3
   Beta blockers (metoprolol)    0    1
   Antidepressants (nortriptyline, fluoxetine)    2    0

*Not included due to illness: A consultant obstetrician and an operating room nurse (n=2).

†Not included due to illness: An auxiliary nurse (n=1).

‡A simple simulation experience is, for example, skills training using a low-tech delivery mannequin and no video recording of the simulation scenario. Full-scale simulation is, for example, done in teams with fully interactive mannequins and video recorded scenarios.

§Intrauterine contraceptive devices, angiotensin II receptor antagonists, angiotensin-converting-enzyme inhibitors, simvastatin, alendronate, pantoprazole, antihistamine and tinzaparine.

ISS, in situ simulation; OSS, off-site simulation.