The Effectiveness of Measuring for Fragmented Red Cells Using an Automated Hematology Analyzer in Patients With Thrombotic Microangiopathy

Author:

Abe Yasunori1,Wada Hideo2,Yamada Eri1,Noda Maki1,Ikejiri Makoto1,Nishioka Junji1,Kobayashi Toshihiko3,Matsumoto Takeshi3,Masuya Masahiro3,Isaji Syuji4,Usui Masanobu4,Uemoto Sinji5,Katayama Naoyuki6,Nobori Tsutomu7

Affiliation:

1. Central Laboratory, Mie University Graduate School of Medicine, Tsu

2. Department of Molecular and Laboratory Medicine, Mie University Graduate School of Medicine, Tsu, .mie-u.ac.jp

3. Department of Hematology, Mie University Graduate School of Medicine, Tsu

4. The First Department of Surgery, Mie University Graduate School of Medicine, Tsu

5. Hepatobiliary Pancreatic Surgery and Transplantation, Kyoto University Graduate School, Kyoto Japan

6. Department of Hematology,

7. Department of Molecular and Laboratory Medicine, Mie University Graduate School of Medicine, Tsu

Abstract

Thrombotic microangiopathy (TMA) or thrombotic thrombocytopenic purpura (TTP) is a life-threatening syndrome characterized by increased number of fragmented red cells (FRCs) and thrombocytopenia. FRCs can be measured using the recently developed automated hematology analyzer XE-2100. The normal range for FRCs is 0% to 0.205%, as determined by the automated hematology analyzer XE-2100. The FRC count is significantly elevated in patients with TMA associated with liver transplantation, bone marrow transplantation, or TTP. In patients with TMA after liver transplantation, the FRC count is significantly higher than in those without TMA. In receiver operating characteristic analysis for the diagnosis of TMA, the area under the curve is 0.986, suggesting that FRC is a useful marker for the diagnosis of TMA. When the cutoff value of FRC for TMA is 1.2%, the sensitivity is 90% and the specificity is 96%, indicating that FRC is the most useful screening test for the diagnosis of TMA.

Publisher

SAGE Publications

Subject

Hematology,General Medicine

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