Thrombosis Research
Volume 118, Issue 4 , Pages 463-469, 2006

A simple technique to determine thrombopoiesis level using immature platelet fraction (IPF)

  • Yasunori Abe

      Affiliations

    • Central Clinical Laboratories, Mie University Hospital, Tsu-city, Mie, Japan
  • ,
  • Hideo Wada

      Affiliations

    • Department of Laboratory Medicine, Mie University School of Medicine, 2-174 Edobashi, Tsu-city, Mie 514-8507, Japan
    • Corresponding Author InformationCorresponding author. Tel.: +81 59 232 1111; fax: +81 59 231 5204.
  • ,
  • Hiroaki Tomatsu

      Affiliations

    • Central Clinical Laboratories, Mie University Hospital, Tsu-city, Mie, Japan
  • ,
  • Akane Sakaguchi

      Affiliations

    • Central Clinical Laboratories, Mie University Hospital, Tsu-city, Mie, Japan
  • ,
  • Junji Nishioka

      Affiliations

    • Central Clinical Laboratories, Mie University Hospital, Tsu-city, Mie, Japan
  • ,
  • Yasunori Yabu

      Affiliations

    • Department of Laboratory Medicine, Mie University School of Medicine, 2-174 Edobashi, Tsu-city, Mie 514-8507, Japan
  • ,
  • Katsuya Onishi

      Affiliations

    • Department of Laboratory Medicine, Mie University School of Medicine, 2-174 Edobashi, Tsu-city, Mie 514-8507, Japan
  • ,
  • Kaname Nakatani

      Affiliations

    • Department of Laboratory Medicine, Mie University School of Medicine, 2-174 Edobashi, Tsu-city, Mie 514-8507, Japan
  • ,
  • Yoshitaka Morishita

      Affiliations

    • Central Clinical Laboratories, Mie University Hospital, Tsu-city, Mie, Japan
  • ,
  • Shinichiro Oguni

      Affiliations

    • Sysmex Corporation, Product Development, Kobe, Japan
  • ,
  • Tsutomu Nobori

      Affiliations

    • Department of Laboratory Medicine, Mie University School of Medicine, 2-174 Edobashi, Tsu-city, Mie 514-8507, Japan

Received 26 April 2005; received in revised form 27 August 2005; accepted 15 September 2005.

Abstract 

Immature platelet fraction (IPF) has been measured by fully automated analyzer (XE-2100) as reticulated platelet (RP) which is reflected with thrombopoiesis in bone marrow.

IPF value in the healthy volunteers was 3.3% (1.0–10.3) and upper 95% confidential interval (95% CI) of IPF was determined as 7.7%. IPF was significantly high in the patients with idiopathic thrombocytopenic purpura (ITP; 17.4%, 1.2–53.2%) and recovery phase of post-chemotherapy, and significantly low in nadir phase of post-chemotherapy, and within normal range in the patients with ITP in complete remission (CR) and with aplastic anemia (AA). Total count of IPF was significantly low in patients with ITP, AA or post-chemotherapy. Mean platelet volume (MPV) was significantly high in only patients with ITP.

IPF 7.7% is best point for highest sensitivity (86.8%) and specificity (92.6%) in diagnosis of ITP and recovery phase of post-chemotherapy. In receiver operating characteristic curve for diagnosis of ITP and recovery phase of post-chemotherapy, IPF was significantly more useful than MPV.

These results show that IPF reflects the pathology of thrombocytopenic disorders, and that measurement of IPF is useful for the differential diagnosis and analysis of platelet kinetics.

Keywords: IPF (immature platelet fraction), Reticulated platelet, ITP (idiopathic thrombocytopenic purpura), AA (aplastic anemia)

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0049-3848(05)00385-3

doi:10.1016/j.thromres.2005.09.007

Thrombosis Research
Volume 118, Issue 4 , Pages 463-469, 2006