The Journal of Bone and Joint Surgery (American). 2007;89:1818-1825.
doi:10.2106/JBJS.E.01305
© 2007 The Journal of Bone and Joint Surgery, Inc.
Progression of Acetabular Periprosthetic Osteolytic Lesions Measured with Computed Tomography
Donald W. Howie, MBBS, PhD, FRACS1,
Susan D. Neale, MSc1,
Roumen Stamenkov, MD1,
Margaret A. McGee, BSc, MPH1,
David J. Taylor, MBBS2 and
David M. Findlay, MSc, PhD1
1 Department of Orthopaedics and Trauma, Level 4, Bice Building, Royal Adelaide
Hospital, North Terrace, Adelaide, 5000, Australia. E-mail address for S.
Neale:
susan.neale{at}health.sa.gov.au
2 Department of Radiology, Level 3, Royal Adelaide Hospital, North Terrace,
Adelaide, 5000, Australia
Investigation performed at the Department of Orthopaedics and Trauma
and the Department of Radiology, Royal Adelaide Hospital, and the Discipline
of Orthopaedics and Trauma, University of Adelaide, Adelaide,
Australia
Disclosure: In support of their research for or preparation of this
work, one or more of the authors received, in any one year, outside funding or
grants in excess of $10,000 from the National Health and Medical Research
Council, Novartis Pharmaceuticals, Royal Adelaide Hospital, and Bristol-Myers
Squibb/Zimmer. Neither they nor a member of their immediate families received
payments or other benefits or a commitment or agreement to provide such
benefits from a commercial entity. A commercial entity (Novartis
Pharmaceuticals Australia Pty Ltd and Bristol-Myers Squibb/Zimmer) paid or
directed in any one year, or agreed to pay or direct, benefits in excess of
$10,000 to a research fund, foundation, division, center, clinical practice,
or other charitable or nonprofit organization with which one or more of the
authors, or a member of his or her immediate family, is affiliated or
associated.
Background: A better understanding of the factors associated with
the size and/or progression of osteolytic lesions has been hampered by a lack
of sensitivity of radiographic measurement techniques.
Methods: We retrospectively analyzed quantitative computed
tomography scans that had been made with use of a high-resolution multi-slice
scanner with a metal artifact-suppression protocol. The scans had been made to
determine the volume of osteolytic lesions around thirty-five cementless
Harris-Galante acetabular components that had been in situ for at least ten
years. Repeat scans of thirty hips allowed for the measurement of progression
in the size of osteolytic lesions over a one-year period. Associations between
the volume of osteolytic lesions, progression in the size of the lesions,
polyethylene wear since the time of implantation, change in component
position, and patient-related variables (age, gender, body mass index,
activity level, walking limitations, joint pain, and function) were
determined.
Results: In sixteen of the thirty hips that had repeat computed
tomography scans, the lesions progressed in size during the study period. The
median size of the lesions in these sixteen hips was 10.3 cm3 at
the time of the initial scan, compared with 13.3 cm3 at a median of
fifteen months later (p = 0.001). Osteolytic lesions measuring >10
cm3 in volume on the initial scan were 2.5 times (95% confidence
interval 1.3 to 4.8 times) more likely to progress in size over one year than
smaller lesions were. Patients with greater polyethylene wear rates, higher
activity levels, no walking limitations, and larger prosthetic femoral head
dimensions (26 or 28 mm) had significantly larger osteolytic lesions (p <
0.0001, p = 0.009, p = 0.006, and p = 0.028, respectively). Progression in the
size of the osteolytic lesions over one year was significantly associated with
larger initial osteolytic lesions (p = 0.002), greater polyethylene wear rates
(p = 0.009), and larger (26 or 28-mm) prosthetic femoral head dimensions (p =
0.019).
Conclusions: There is considerable variation in the rates of
progression of the size of osteolytic lesions around stable acetabular
components. Lesion size and the progression of lesion size are generally
related to polyethylene wear rates, higher patient activity levels, and
larger-diameter femoral heads. Osteolytic lesions measuring >10
cm3 in volume are associated with a high rate of progression.
Level of Evidence: Prognostic Level III. See Instructions
to Authors for a complete description of levels of evidence.

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