Skip to main content

Table 1 Details of the donors and of the implanted stems. GROUP A (top) contained paired femurs where one femur of each donor was implanted with the commercial stem, and the contralateral one with the OsteoCustom stem; GROUP B (bottom) consisted of femurs whose anatomy could not meet the eligibility criteria of the commercial stem and were implanted (unpaired) only with the OsteoCustom one. The right column reports the size of the stem. For the OFI-C the nominal diameter is indicated. For the OsteoCustom stems the size is indicated by five numbers: the first number indicates the diameter (in mm) of the proximal portion of the stem, the second and third numbers indicate the major and minor axes (in mm) of the elliptical distal section; the fourth number indicates the radius of curvature of the stem (in mm), the fourth number indicates the angle of internal/external rotation of the plane of curvature with respect to the major axis of the elliptical cross-section)

From: Improved primary stability and load transfer of a customized osseointegrated transfemoral prosthesis compared to a commercial one

Group A

Type of

prosthesis

Donor ID

Side

Age

(year)

Sex

BMI

(kg/m2)

Weight (kg)

Height (cm)

Prosthesis

(size)

Commercial stem

#1 (*)

Left

58

M

34

100

170

15

#2

Right

52

M

24

72

172

16

#3

Right

56

M

35

113

180

16

#4

Left

57

F

44

127

170

15

#5 (*)

Right

44

F

21

54

163

15

#6

Right

27

M

42

142

183

17

OsteoCustom stem

#1

Left

58

M

34

100

170

15-18-15-849-69

#2

Right

52

M

24

72

172

16-19-16-664-33

#3

Right

56

M

35

113

180

16-23-20-739-47

#4

Right

57

F

44

127

170

15-18-15-632-17

#5

Left

44

F

21

54

163

16-19-16-664-33

#6

Left

27

M

42

142

183

16-23-20-944-17

Group B

OsteoCustom stem

#7

Right

44

M

32

82

160

12-16-15-641-10

#8

Left

59

M

33

109

183

12-16-15-695-18

#9

Left

58

F

32

81.6

160

13-19-15-683-3

  1. Note (*): For the commercial stem, the Specimens from donors 1, and 5, were previously tested as part of the study where the experimental protocol was developed and validated [18]