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. 2014 Dec 17;96(Suppl 1):73–78. doi: 10.2106/JBJS.N.00541

TABLE I.

Overview of the Literature Focused on THA in Cohorts That Included Patients Younger Than Thirty-one Years of Age*

Authors Year No. of Patients/Hips Revision Rate (%) Mean Follow-up (yr) Mean Age at Surgery (Range) (yr) Most Common Stated Diagnoses
Roach and Paradies15 1984 6/10 33.0 7.9 13.2 (9-16) Arthritis
Ruddlesdin et al.16 1986 42/75 14.0 5.4 14 (11-17) JCA
Lachiewicz et al.17 1986 34/62 3.0 6.0 26 (NR) JRA
Learmonth et al.18 1989 7/14 0 8.5 16 (12-22) JCA
Witt et al.19 1991 54/96 25.0 11.5 16.7 (NR) JCA
Cage et al.20 1992 17/22 3.4 10.6 18.4 (14-20) NR
Maric and Haynes21 1993 17/17 7.7 9.3 18 (14-20) NR
Hyder et al.22 1996 22/26 7.7 6.5 24 (17-30) Perthes, PTA
Torchia et al.13 1996 50/63 42.9 11.0 17 (11-19) JRA, CD, trauma, tumors
Chmell et al.14 1997 39/66 35.0 15.1 19.9 (11-29) JRA
Kumar and Swann23 1998 16/25 12.0 4.5 24.9 (15-39) SOD, JCA
Sochart and Porter24 1998 55/83 30.0 20.0 24.9 (17-29) AS, CD, JRA, OA
Bessette et al.25 2003 11/15 33.0 13.6 16.5 (10-20) NR
Dudkiewicz et al.26 2003 56/69 11.6 7.4 23.2 (14-29) JRA, TA, DDH
Kitsoulis et al.27 2006 10/20 1.5 9.2 15.8 (13-24) JCA
Restrepo et al.28 2008 25/35 3.0 6.6 17.6 (13.5-20) AVN, JRA, DDH, SD, Perthes, OA, PTA, PRC
Wangen et al.29 2008 44/49 48.9 13 25 (15-30) OA
Busch et al.30 2010 48/69 11.6 2.0 24.6 (16-29) JRA, OFH
Clohisy et al.5 2010 88/102 7.0 2.0 20.0 (12-25) ON, OA
Girard et al.31 2010 35/48 8.3 9.0 25 (15-30) OFH
Finkbone et al.32 2012 19/24 4.0 2.4 16.4 (12-20) AVN, JRA
Kamath et al.33 2012 18/21 5.5 4.1 18 (13-20) CIO, SIO, SCD
*

JCA = juvenile chronic arthritis, NR = not reported, JRA = juvenile rheumatoid arthritis, Perthes = Legg-Calvé-Perthes disease, PTA = posttraumatic arthritis, CD = congenital dysplasia, SOD = systemic onset disease, AS = ankylosing spondylitis, OA = osteoarthritis, TA = traumatic arthritis, DDH = developmental dislocation (dysplasia) of the hip, AVN = avascular necrosis, SD = spondyloepiphyseal dysplasia, PRC = pseudo rheumatoid chondrodysplasia, ON = osteonecrosis, OFH = osteonecrosis of femoral head, CIO = chemotherapy-induced osteonecrosis, SIO = steroid-induced osteonecrosis, and SCD = sickle cell disease. Note that some of the stated diagnoses (e.g., avascular necrosis and osteonecrosis) are equivalent.

Ruddlesdin et al. reported on twenty-nine of these cases in 1986.