Unique characteristics of new complete blood count parameters, the Immature Platelet Fraction and the Immature Platelet Fraction Count, in dengue patients.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2021
Historique:
received: 28 05 2021
accepted: 11 10 2021
entrez: 1 11 2021
pubmed: 2 11 2021
medline: 22 12 2021
Statut: epublish

Résumé

The advanced platelet parameters Immature Platelet Fraction and Immature Platelet Fraction Count have been implemented in clinical practice as measures of thrombopoietic activity, mainly in hematologic disorders that cause thrombocytopenia. The purpose of this observational study was to examine thrombopoiesis as reflected by these 2 new CBC parameters in patients infected with dengue. The study was conducted in infectious disease referral hospital in Metro Manila, the Philippines. We enrolled hospitalized patients at admission who were diagnosed with acute dengue or community acquired bacterial infection (CABI). Immature Platelet Fraction (IPF) and Immature Platelet Fraction Count were evaluated at admission and during hospitalization. A total of 606 patients were enrolled from May 1, 2017 to June 1, 2018. The participants consisted of 152 patients with dengue infection, 180 confirmed CABI, and 274 suspected CABI patients. At admission, the percent IPF (IPF%) of the patients with dengue was significantly higher than that of the confirmed CABI patients (median 3.7% versus 1.9%; p <0.001). In a time course evaluation, there was no significant difference of IPF% between the patients with dengue infection and the confirmed CABI patients in the febrile phase (median 1.9% versus 2.4%; p = 0.488), however, the IPF% of the patients with dengue infection increased to be significantly higher than that of the confirmed CABI patients in the critical phase (median 5.2% versus 2.2%; p <0.001). Our study elucidated the unique characteristics and time-course trends of IPF percent and number (IPF#) in the patients with dengue infection. IPF% and IPF# are potentially valuable parameters in dengue and further investigation is required for the optimal use in clinical practice.

Identifiants

pubmed: 34723977
doi: 10.1371/journal.pone.0258936
pii: PONE-D-21-17692
pmc: PMC8559939
doi:

Banques de données

figshare
['10.6084/m9.figshare.16810771.v1']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0258936

Déclaration de conflit d'intérêts

The authors have no conflicts of interest associated with Sysmex Corporation relating to the employment, consultancy, patents, products in development, and marketed products. This does not alter our adherence to PLoS ONE policies on sharing data and materials.

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Auteurs

Ikkoh Yasuda (I)

School of Tropical Medicine and Global Health, Nagasaki University, Nagasaki, Japan.
Department of Clinical Medicine, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Department of General Internal Medicine and Clinical Infectious Diseases, Fukushima Medical University, Fukushima, Japan.

Nobuo Saito (N)

School of Tropical Medicine and Global Health, Nagasaki University, Nagasaki, Japan.
Department of Clinical Medicine, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Department of Microbiology, Oita University Faculty of Medicine, Oita, Japan.

Motoi Suzuki (M)

Department of Clinical Medicine, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Infectious Disease Surveillance Center, National Institute of Infectious Diseases, Tokyo, Japan.

Dorcas Valencia Umipig (DV)

San Lazaro Hospital, Manila, The Philippines.

Rontgene M Solante (RM)

San Lazaro Hospital, Manila, The Philippines.

Ferdinand De Guzman (F)

San Lazaro Hospital, Manila, The Philippines.

Ana Ria Sayo (AR)

San Lazaro Hospital, Manila, The Philippines.

Michio Yasunami (M)

Department of Clinical Medicine, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Saga-Ken Medical Centre Koseikan, Saga, Japan.

Nobuo Koizumi (N)

Department of Bacteriology I, National Institute of Infectious Diseases, Toyama, Shinjuku-ku, Tokyo, Japan.

Emi Kitashoji (E)

Department of Clinical Medicine, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.

Kentaro Sakashita (K)

School of Tropical Medicine and Global Health, Nagasaki University, Nagasaki, Japan.
Department of Basic Mycobacteriology, Graduate School of Biomedical Science, Nagasaki University, Nagasaki, Japan.

Chris Fook Sheng Ng (CFS)

School of Tropical Medicine and Global Health, Nagasaki University, Nagasaki, Japan.

Chris Smith (C)

School of Tropical Medicine and Global Health, Nagasaki University, Nagasaki, Japan.
Department of Clinical Research, London School of Hygiene and Tropical Medicine, London, United Kingdom.

Koya Ariyoshi (K)

School of Tropical Medicine and Global Health, Nagasaki University, Nagasaki, Japan.
Department of Clinical Medicine, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.

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