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ARTICLE |

Haptoglobin and Hemolytic Disease FREE

Jorg Fehr, MD
JAMA. 1981;245(20):2028-2028. doi:10.1001/jama.1981.03310450022012
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To the Editor.—  The article by Marchand et al (1980;243:1909) provides too much hope for a resurrection of haptoglobin determinations as a reliable indicator of hemolytic diseases. First, the introduction of any new or renewed diagnostic measurement should be based on a reliable diagnosis. In the case of hemolysis, the standard reference method to establish the firm diagnosis of a reduction in the RBC survival relies on studies with radiolabeled autologous erythrocytes. Since the reticulocyte count, on which Marchand et al based their diagnosis, is an unreliable method for establishing a hemolytic process,1 at least in its milder form, their data lack the important prerequisite, and any conclusions derived thereof must remain in doubt.Second, even using the most sensitive assay for haptoglobin determination, one has to respect the fact that hemolytic diseases are often accompanied by inflammatory processes. Being an acute-phase reactant protein, increased haptoglobin levels are—in our

REFERENCES

Fehr J, Knob M:  Comparison of red cell creatine level and reticulocyte count in appraising the severity of hemolytic processes . Blood 1979;;53:966-976.
Tarukoski PH:  Quantitative spectrophotometric determination of haptoglobin . Scand J Clin Lab Invest 1966;;18:80-86.

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Country-Specific Mortality and Growth Failure in Infancy and Yound Children and Association With Material Stature

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Fehr J, Knob M:  Comparison of red cell creatine level and reticulocyte count in appraising the severity of hemolytic processes . Blood 1979;;53:966-976.
Tarukoski PH:  Quantitative spectrophotometric determination of haptoglobin . Scand J Clin Lab Invest 1966;;18:80-86.
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