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. 2020 May 13;44(2):843–854. doi: 10.1007/s10143-020-01314-2

Table 2.

Further characteristics of the 19 papers included in the study

Authors OR baseline established Use of intraop. rating scale Recorded operative time Patient outcomes recorded Time spent on simulation training Control group training Clinically relevant effect Effect of training on patient outcome
Wooster et al. [27] No No Yes No Pre-op. rehearsal ≤ 24 h None No NA
Maertens et al. [41] No Yes Yes Yes Time until proficiency Continued conventional training Yes No
Zevin et al. [52] No Yes No No Time until proficiency Continued conventional training NA NA
Desender et al. [29] No Yes Yes Yes Pre-operative rehearsal once Rehearsal after procedure Yes No
Nilsson et al. [17] No Yes No No 2 h None No NA
Waterman et al. [46] Yes Yes Yes No 1 h Continued conventional training Yes NA
Shore et al. [15] No Yes Yes No 14 h Continued conventional training Yes NA
Patel et al. [6] Yes Yes No No 1.5 h Continued conventional training NA NA
Dunn et al. [47] Yes Yes Yes No 1 h Continued conventional training No NA
Peltan et al. [29] No Yes No Yes Time until proficiency Continued conventional training Yes No
Grover et al. [42] No Yes No No 8 h Simulation training without feedback Yes NA
Carlsen et al. [48] No Yes Yes No 1 day skills lab course Continued conventional training Yes NA
Koch et al. [49] Yes No No No Number of procedures** Number of procedures** Yes NA
Zendejas et al. [14] Yes Yes Yes Yes Time until proficiency Continued conventional training Yes Yes
Kessler et al. [6] No No No No Time until proficiency Continued conventional training Yes NA
Calatayud et al. [30] No Yes No No 0.75 h Surgeons served as own controls Yes NA
Haycock et al. [50] No Yes Yes No 16 h 16 h of practice on patients No NA
Ahlberg et al. [2] No No Yes No Time until proficiency Continued conventional training Yes NA
Cohen et al. [51] No No No No 10 h Continued conventional training Yes NA

*Study population refers to number of surgeons

**Number of completed VR cases; group i was tested twice in patient after 10, 30, and 50 VR cases completed; group ii was tested twice in patients after 20, 60, and 100 VR cases completed