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. 2008 Jun 4;467(2):485–492. doi: 10.1007/s11999-008-0329-x

Table 2.

Published results with rotating-hinge devices in nontumor use

Study Year Number of patients Number of knees Mean followup (months) Device* Postoperative Hospital for Special Surgery score (0–100) Postoperative Knee Society clinical score (0–200) Postoperative range of motion Survival free of open reoperation for any reason
Shindell et al. [30] 1986 14 18 60–75 Noiles 77 44%
Rand et al. [28] 1987 36 38 50 Kinematic 100° 48%
Berman et al. [5] 1996 9 9 24 Kinematic 71 93° 67%
Lombardi et al. [22] 1997 109 113 25 Endo-Model 73 95° 85%
Barrack et al. [4] 2000 15 16 51 S-ROM 131 93° 94%
Westrich et al. [37] 2000 21 24 33 Finn 128 92%
Barrack [3] 2001 22 23 58 S-ROM 133 95° 96%
Jones et al. [17] 2001 15 16 47 S-ROM 137 105° 88%
Jones et al. [18] 2001 29 30 49 S-ROM 134 100° 90%
Springer et al. [31] 2001 58 69 75 Kinematic 100 94° 67%
Springer et al. [32] 2004 25 26 59 Kinematic 101 97° 73%
Pradham et al. [27] 2004 50 51 48 Endo-Model 72 89°
Petrou et al. [25] 2004 80 100 132 Endo-Model 163 120° 87%
Utting and Newman [34] 2004 30 36 Custom Endo-Model (21 rotating; 9 fixed) 106 70%
Pour et al. [26] 2007 43 44 50 31 Kinematic; 13 Finn 117 70%
Back et al. [2] 2008 30 32 58 SMILES 95 88° 84%
Current study 2008 37 39 46 OSS 123 106° 87%

* Devices included Noiles™ (DePuy Orthopaedics, Inc, Warsaw, IN), Kinematic® (Stryker Orthopaedics, Mahwah, NJ), Endo-Model® (Waldemar Link, Hamburg, Germany), S-ROM® (DePuy Orthopaedics, Inc), Finn® (Biomet, Inc, Warsaw, IN), SMILES™ (Stanmore Implant Worldwide Ltd, Stanmore, UK), and OSS™ (Biomet, Inc).