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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 Letters to the Editor are reviewed by JBJS editors but are not peer-reviewed.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:
Hari P. Bezwada, David G. Nazarian, David H. Henry, and Robert E. Booth, Jr.
- Preoperative Use of Recombinant Human Erythropoietin Before Total Joint Arthroplasty
J Bone Joint Surg Am 2003; 85: 1795-1800
[Abstract]
[Full text]
[PDF]
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Electronic letters published:
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Dr Bezwada and colleagues respond to Dr. Salot
- Hari P. Bezwada, Nazarian, Henry, Booth
(18 December 2003)
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Guidelines Regarding the Use of Erythropoietin Before Total Joint Arthroplasty
- William H. Salot, M.D.
(4 December 2003)
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Dr Bezwada and colleagues respond to Dr. Salot |
18 December 2003 |
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Hari P. Bezwada, Orthopaedic Surgeon Pennsylvania Hospital, Nazarian, Henry, Booth
Send letter to journal:
Re: Dr Bezwada and colleagues respond to Dr. Salot
hbezwada{at}yahoo.com Hari P. Bezwada, et al.
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We appreciate the comments from Dr. Salot. We will respond to his
points individually.
1) While it is true that the combination of recombinant human
erythropoietin with preoperative autologous donation might not necessarily
be in conformity with medicare regulations; Goodnough et al noted the
ability to increase the amount of autologous donation with recombinant
erythropoietin. Furthermore, peroperative autologous donation only leads
to preoperative anemia, as noted by several authors. The combination of
erythropoietin and preoperative autologous donation allows the patient to
preoperatively donate without the development of a significant
preoperative anemia.
2) This particular study did not address the issue of cost. While it
is true that the combination of autologous blood and recombinant
erythropoietin remains costly, this study addresses the issue of efficacy
not cost. The selection of a hemoglobin of 140 g/l as an inclusion
criteria was at the suggestion of our hematologist (DHH). This was a
hemoglobin level selected for other cases in which erythropoietin was
utilized.
3) While it is true that not many patients with a baseline
hemoglobin of >130 g/l will require allogeneic transfusions. Previous
studies have suggested that they have to be healthy patients, generally
under 60 years of age, and be undergoing primary unilateral total joint
arthroplasty. This study combined a large number of bilateral and
revision arthroplasties. There should be no dispute that bilateral and
revision arthroplasties have a greater allogeneic blood requirements than
primary unilateral arthroplasty. A baseline hemoglobin of 140 g/l may not
be sufficient to avoid allogeneic blood transfusions in bilateral and
revision arthroplasties. |
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Guidelines Regarding the Use of Erythropoietin Before Total Joint Arthroplasty |
4 December 2003 |
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William H. Salot, M.D., Orthopedist Associated Orthopedists of Detroit, P.C.
Send letter to journal:
Re: Guidelines Regarding the Use of Erythropoietin Before Total Joint Arthroplasty
wsalot{at}earthlink.net William H. Salot, M.D.
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To the Editor;
I was impressed by the efficacy of recombinant human erythropoietin
when used with autologous blood donation to reduce the need for perioperative allogeneic blood transfusion in total joint arthroplasty. However, your readership should be aware that the
protocol followed in this study was not in conformity with current
Medicare guidelines.
These guidelines restrict the surgical use of recombinant
erythropoietin to patients whose preoperative hemoglobin range lies
between 100 g/L and 130 g/L, and who are not candidates for autologous
blood donation. The authors’ selection of 140 g/L as the upper limit of
preoperative hemoglobin, as well as their addition of autologous blood
donation to the treatment regimen, if adopted by others, could lead to
challenges of reimbursement for these expensive programs.
The use of 140 g/L as the upper limit of preop hemoglobin is
puzzling, as a number of those patients between 130 g/l and
140 g/L probably need no preoperative treatment at all. Faris et al (1)
demonstrated that patients whose hemoglobin was > 130g/L were only half
as likely to require allogeneic blood in primary joint replacement as
those with levels < 130g/L.
William H. Salot, M.D.
Associated Orthopedists of Detroit,P.C.
24715 Little Mack St.
St. Clair Shores, Michigan 48080
wsalot@earthlink.net
1) Faris,P.M., Spence, R.K., Larholt, K.M., Sampson, A.R., Frei,
D. The predictive power of baseline hemoglobin for transfusion risk in
surgery patients Orthopedics 1999 January:22 (1 suppl.) s 135-40 |
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