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down Stephen A. Mikulak, Ormonde M. Mahoney, Mylene A. delaRosa, and Thomas P. Schmalzried
Loosening and Osteolysis with the Press-Fit Condylar Posterior-Cruciate-Substituting Total Knee Replacement
J. Bone Joint Surg. Am. 83: 398.

down OM Mahoney, and JH Dimon
Unsatisfactory results with a ceramic total hip prosthesis
J. Bone Joint Surg. Am. 72: 663-671.

down TE Bailey, and OM Mahoney
The use of banked autologous blood in patients undergoing surgery for spinal deformity
J. Bone Joint Surg. Am. 69: 329-332.


Abstract 1 of 3 back The Journal of Bone and Joint Surgery 83:398 (2001)
© 2001 The Journal of Bone and Joint Surgery, Inc.

Loosening and Osteolysis with the Press-Fit Condylar Posterior-Cruciate-Substituting Total Knee Replacement

Stephen A. Mikulak, MD, Ormonde M. Mahoney, MD, Mylene A. delaRosa, BS and Thomas P. Schmalzried, MD

Investigation performed at the Joint Replacement Institute at Orthopaedic Hospital, Los Angeles, California
Stephen A. Mikulak, MD Ormonde M. Mahoney, MD Mylene A. dela Rosa, BS Thomas P. Schmalzried, MD Joint Replacement Institute at Orthopaedic Hospital, 2400 South Flower Street, Los Angeles, CA 90007
One or more of the authors has received or will receive benefits for personal or professional use from a commercial party related directly or indirectly to the subject of this article. Funds were received in total or partial support of the research or clinical study presented in this article. The funding source was the Los Angeles Orthopaedic Foundation.

Background: Aseptic loosening and osteolysis are rarely associated with cemented posterior-cruciate-substituting total knee replacements. Consequently, there is a paucity of information on this topic.

Methods: After a mean follow-up interval of fifty-six months (range, thirty-seven to eighty-nine months), sixteen (2.9%) of 557 posterior-cruciate-substituting primary total knee replacements were revised by a single surgeon because of loosening and osteolysis. Clinical, radiographic, and retrieval analyses were conducted to determine the mechanism of loosening and to identify associated risk factors.

Results: All sixteen knees (fifteen patients) were rated as good or excellent at one year after the primary replacement, with mean clinical and functional Knee Society scores of 95 and 86 points, respectively. Nine of the fifteen patients who had a revision because of loosening and osteolysis had had a total knee arthroplasty on the contralateral side compared with only 18% of the patients who did not have a revision (p = 0.026). No evidence of transmission of substantial anteroposterior stresses from the posterior-cruciate-substituting mechanism was found. All twelve retrieved knee implants, however, had damage to the lateral and medial side walls of the polyethylene posterior-cruciate-substituting post. Damage to the inferior surface of the polyethylene inserts had a rotational pattern, with the axis of rotation in the medial compartment. Surface damage in a rotational pattern was also present on the superior and inferior surfaces of the titanium tibial base-plates.

Conclusions: In the knees in our study, rotational forces were generated by impingement of the side walls of the intercondylar box on the polyethylene post. Such box-post impingement can occur throughout the range of motion. Rotational stresses are transmitted to the modular interfaces and to the metal-cement interfaces, resulting in loosening and osteolysis. A reduction in rotational constraint would be desirable. Patients with bilateral total knee replacement may be at increased risk for this type of loosening.

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Abstract 2 of 3 back

The Journal of Bone and Joint Surgery, Vol 72, Issue 5 663-671, Copyright © 1990 by Journal of Bone and Joint Surgery, Inc


JOURNAL CONTENTS

Unsatisfactory results with a ceramic total hip prosthesis

OM Mahoney and JH Dimon
Peachtree Orthopaedic Clinic, Piedmont Hospital, Atlanta, Georgia 30367.

We reviewed the results of forty-two total hip replacements that had been done with the self-locking Autophor ceramic total hip prosthesis in thirty-four patients. The patients ranged in age from twenty-five to sixty-seven years (average, forty-eight years). The diagnoses were avascular necrosis (eight patients), degenerative arthritis (nineteen patients), ankylosing spondylitis (one patient), post-traumatic arthritis (two patients), and rheumatoid arthritis (four patients). Seven procedures were revisions: five, of a loose cemented total hip prosthesis and two, of a loose noncemented endoprosthesis. No revision was done for infection. The length of follow-up ranged from twenty-seven to sixty-six months (average, fifty-one months). The patients were evaluated by physical examination, serial radiographs, and questionnaires. The hips were rated with the modified Harris hip score. At the time of follow-up, eleven of the twenty-seven patients who had had a primary hip replacement complained of at least moderate pain that limited activities; however, only three patients had to have a revision. The femoral components had a notable tendency to subside more than five millimeters, and in fifteen hips there was radiographic evidence of progressive loosening. Our experience with the self-locking Autophor ceramic total hip prosthesis has been disappointing. We no longer use it.

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Abstract 3 of 3 back

The Journal of Bone and Joint Surgery, Vol 69, Issue 3 329-332, Copyright © 1987 by Journal of Bone and Joint Surgery, Inc


JOURNAL CONTENTS

The use of banked autologous blood in patients undergoing surgery for spinal deformity

TE Bailey and OM Mahoney

The cases of fifty-two patients who underwent sixty elective spinal fusions for spinal deformity were studied to evaluate the efficacy of the use of banked autologous blood to replace operative loss of blood. The patients ranged in age from ten to forty-nine years. Each patient began to take 325 milligrams of ferrous sulphate, three times a day, as soon as surgery was scheduled, and was evaluated weekly at the Shepeard Community Blood Bank. If a patient's hemoglobin level was more than eleven milligrams per 100 milliliters, either a whole unit of blood or a half-unit was drawn at each visit. An average of 3.3 units of blood (range, 1.5 to 6.0 units) was obtained and was stored for as long as forty-two days. Either citrate phosphate dextrose with adenine (CPDA-1) or adenine, dextrose, and mannitol (ADSOL) was used as a preservative. In 85 per cent of the procedures only autologous blood was required for transfusion. This method proved to be simple, safe, and very well accepted.

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