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JBJS welcomes reader comments on published articles. Letters to the Editor are reviewed by JBJS editors but are not peer-reviewed. To submit your letter, please follow the "submit a response" link that appears in the content box at the upper right of the full text of the article.
Letters to the Editor to:
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- Scientific Articles:
Yuichi Mochida, Thomas W. Bauer, Toshihiro Akisue, and Phillip R. Brown
- Alendronate Does Not Inhibit Early Bone Apposition to Hydroxyapatite-Coated Total Joint Implants : A Preliminary Study
J Bone Joint Surg Am 2002; 84: 226-235
[Abstract]
[Full text]
[PDF]
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Electronic letters published:
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UPDATE: bisphosphonates and osteoporosis
- Robert Poss
(5 March 2002)
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Bisphosphonates in Total Hip Arthroplasty--A Response to Dr. Cottrell
- Thomas A. Einhorn, MD
(4 March 2002)
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Bone Density, ALN, Total Jt. Arthroplasty
- William Cottrell
(28 February 2002)
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UPDATE: bisphosphonates and osteoporosis |
5 March 2002 |
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Robert Poss, MD deputy editor for electronic media, JBJS
Send letter to journal:
Re: UPDATE: bisphosphonates and osteoporosis
possr{at}jbjs.org Robert Poss
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For a perspective on the status of using bisphsophonates to treat
osteoporosis, see New England Journal of Medicine:346, page642, February
28, 2002.
In the same issue, there is a report on the use of a bisphosphonate,
zoledronic acid, that when given intermittently via an intravenous route
is effective in promoting increased bone density. (Reid, IR, et.al,
Intravenous Zoledronic Acid In Postmenopausal Women With Low Bone Mineral
Density, NEJM,346:653-661 |
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Bisphosphonates in Total Hip Arthroplasty--A Response to Dr. Cottrell |
4 March 2002 |
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Thomas A. Einhorn, MD, Chairman, Department of Orthopaedic Surgery Boston University School of Medicine
Send letter to journal:
Re: Bisphosphonates in Total Hip Arthroplasty--A Response to Dr. Cottrell
thomas.einhorn{at}bmc.org Thomas A. Einhorn, MD
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Although there have been no peer-reviewed reports demonstrating poor
results of total joint arthroplasties performed in patients with
documented osteoporosis, the notion that an individual should have healthy
bone mass before undergoing such a procedure certainly makes sense. The
best way to determine this is to perform a bone density examination.
However, to my knowledge there is no consensus that all patients should
undergo bone density testing prior to being indicated for total joint
arthroplasty. Furthermore, I believe that if a patient has had
radiographs taken with a standardized technique, and if there is neither
visible evidence of osteopenia nor a medical history of metabolic disease,
the measurement of bone mass is probably unnecessary.
The use of alendronate in the management of patients who have
documented prosthetic loosening secondary to the presence of particulate
wear debris is very intriguing. Several pre-clinical animal studies have
addressed this question and all seem to support the concept that effective
anti-osteoclastic therapy, using a bisphosphonate such as alendronate,
could limit the resorption of bone in the vicinity of an implant. The
pathophysiological basis for this concept is that wear debris elaborated
from articulating prosthetic joint surfaces is phagocytized by synovial
macrophages and these cells respond by secreting a variety of cytokines
which activate osteoclastic activity. Alendronate, a bisphosphonate
approved for the treatment of osteoporosis and Paget's disease, has a
direct action on the osteoclast to inhibit its activity and possibly
induce apoptosis(programmed cell death). Thus, without having to modify
the wear-generating process or the production of cytokines, prosthetic
loosening could potentially be managed by inhibiting the final step in the
pathway to osteolysis, osteoclast-mediated bone resorption. Thus far, a
handful of clinical studies have reported improved proximal femoral bone
mass following total hip arthroplasty in patients treated with different
bisphosphonates over the first twenty-four months after surgery. In
addition, prospective studies are now underway to test the hypothesis that
prosthetic loosening can be prevented or arrested in patients treated with
alendronate. At this time, the use of these pharmaceutical agents in the
management of patients with joint prostheses would be considered an off-
label use. However, as new drugs become available for the treatment of
bone diseases, there may be numerous ways that they can be used to enhance
the results of orthopaedic surgery. |
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Bone Density, ALN, Total Jt. Arthroplasty |
28 February 2002 |
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William Cottrell, orthopaedist
Send letter to journal:
Re: Bone Density, ALN, Total Jt. Arthroplasty
whc{at}innercite.com William Cottrell
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The literature seems to support the concept that
patients anticipating total joint arthroplasty should have a bone mineral density prior to surgery.
If bone is osteoporotic, I would consider treating
with alendronate for 1-2 years. The literature also supports the concept that prosthetic loosening secondary to the sequelae of particulate debris might be limited by alendronate also.
I would appreciate comments from experts in the field. |
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