Thromb Haemost 2004; 91(03): 553-557
DOI: 10.1160/TH03-07-0489
Platelets and Blood Cells
Schattauer GmbH

Platelet kinetics and scintigraphic imaging in thrombocytopenic malaria patients

Georgios Karanikas
1   Department of Nuclear Medicine, University of Vienna, Austria
,
Konstantin Zedwitz-Liebenstein
2   Department of Internal Medicine I, Division of Infectious Diseases, University of Vienna, Austria
,
Harald Eidherr
1   Department of Nuclear Medicine, University of Vienna, Austria
,
Matthias Schuetz
1   Department of Nuclear Medicine, University of Vienna, Austria
,
Robert Sauerman
2   Department of Internal Medicine I, Division of Infectious Diseases, University of Vienna, Austria
,
Robert Dudczak
1   Department of Nuclear Medicine, University of Vienna, Austria
,
Stefan Winkler
2   Department of Internal Medicine I, Division of Infectious Diseases, University of Vienna, Austria
,
Ingrid Pabinger
3   Department of Internal Medicine I, Division of Hematology, University of Vienna, Austria
,
Kurt Kletter
1   Department of Nuclear Medicine, University of Vienna, Austria
› Institutsangaben
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Publikationsverlauf

Received 28. Juli 2003

Accepted after resubmission 04. Februar 2003

Publikationsdatum:
05. Dezember 2017 (online)

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Summary

Thrombocytopenia is a common occurrence in acute malaria. It is attributed, among other factors, to excessive splenic platelet pooling and a shortened platelet lifespan. The aim of our study was to evaluate the platelet kinetics and sequestration site by isotopic studies in uncomplicated malaria-induced thrombocytopenia. Seven thrombocytopenic malaria patients (74,000±36,000 platelets/µl) were included in the study. Autologous 111In-labeled platelet scintigraphy was performed up to 96 hours (h) post injection (p.i.) to evaluate the platelet sequestration site. Late sequestration for the spleen (S) and the liver (L) was analyzed according to the following activity ratios: S (spleen count on the last day of the platelet lifespan / spleen count at 30 min) and L (liver count on the last day of the platelet lifespan / liver count at 30 min). Additionally, platelet survival studies were performed. A normal late sequestration (S: 0.95±0.06 and L: 1.04±0.08; normal values, S and L: 1 ± 0.2.) was observed in all of our patients. The platelet lifespan was reduced (1 to 4 days; normal range, 7-9 days), recovery was normal (mean, 63±6%; normal range, 55-75%), and the turnover rate was enhanced (mean, 95,000±80,000/µl/day; normal value, 35,000±4,500/µl/ day). According to the results of scintigraphy, the sequestration site by uncomplicated malaria-induced thrombocytopenia appears to be non-splenic and/or hepatic, yet diffuse.