Evidence map›Paper›PMID 32264655›Full record

ArticleThe Korean journal of internal medicine2020

Immature platelet fraction based diagnostic predictive scoring model for immune thrombocytopenia.

Min Ji Jeon, Eun Sang Yu, Ka-Won Kang, Byung-Hyun Lee, Yong Park, Se Ryeon Lee, Hwa Jung Sung, Soo Yong Yoon, Chul Won Choi, Byung Soo Kim and 1 more

Open access · goldAbstract read
In one paragraph

Article in The Korean journal of internal medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Cytopenias in Autoimmune Liver Diseases-A Review.Journal of clinical medicine · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Min Ji JeonDivision of Hematology-Oncology, Department of Internal Medicine, Korea University Guro Hospital, Seoul, Korea.
Eun Sang YuDivision of Hematology-Oncology, Department of Internal Medicine, Korea University Guro Hospital, Seoul, Korea.
Ka-Won KangDivision of Hematology-Oncology, Department of Internal Medicine, Korea University Anam Hospital, Seoul, Korea.
Byung-Hyun LeeDivision of Hematology-Oncology, Department of Internal Medicine, Korea University Anam Hospital, Seoul, Korea.
Yong ParkDivision of Hematology-Oncology, Department of Internal Medicine, Korea University Anam Hospital, Seoul, Korea.
Se Ryeon LeeDivision of Hematology-Oncology, Department of Internal Medicine, Korea University Ansan Hospital, Ansan, Korea.
Hwa Jung SungDivision of Hematology-Oncology, Department of Internal Medicine, Korea University Ansan Hospital, Ansan, Korea.
Soo Yong YoonDepartment of Laboratory Medicine, Korea University Guro Hospital, Seoul, Korea.
Chul Won ChoiDivision of Hematology-Oncology, Department of Internal Medicine, Korea University Guro Hospital, Seoul, Korea.
Byung Soo KimDivision of Hematology-Oncology, Department of Internal Medicine, Korea University Anam Hospital, Seoul, Korea.
Dae Sik KimDivision of Hematology-Oncology, Department of Internal Medicine, Korea University Guro Hospital, Seoul, Korea.
Korea University · KRKorea University Medical Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimsThe diagnosis of immune thrombocytopenia (ITP) is based on clinical manifestations and there is no gold standard. Thus, even hematologic malignancy is sometimes misdiagnosed as ITP and adequate treatment is delayed. Therefore, novel diagnostic parameters are needed to distinguish ITP from other causes of thrombocytopenia. Immature platelet fraction (IPF) has been proposed as one of new parameters. In this study, we assessed the usefulness of IPF and developed a diagnostic predictive scoring model for ITP.

methodsWe retrospectively studied 568 patients with thrombocytopenia. Blood samples were collected and IPF quantified using a fully-automated hematology analyzer. We also estimated other variables that could affect thrombocytopenia by logistic regression analysis.

resultsThe median IPF was significantly higher in the ITP group than in the non-ITP group (8.7% vs. 5.1%). The optimal cut-off value of IPF for differentiating ITP was 7.0%. We evaluated other laboratory variables via logistic regression analysis. IPF, hemoglobin, lactate dehydrogenase (LDH), and ferritin were statistically significant and comprised a diagnostic predictive scoring model. Our model gave points to each of variables: 1 to high hemoglobin (> 12 g/dL), low ferritin (≤ 177 ng/ mL), normal LDH (≤ upper limit of normal) and IPF ≥ 7 and < 10, 2 to IPF ≥ 10. The final score was obtained by summing the points. We defined that ITP could be predicted in patients with more than 3 points.

conclusionIPF could be a useful parameter to distinguish ITP from other causes of thrombocytopenia. We developed the predictive scoring model. This model could predict ITP with high probability.

Indexed as

Purpura, Thrombocytopenic, IdiopathicThrombocytopeniaBlood PlateletsHumansPlatelet CountRetrospective StudiesImmature platelet fractionImmune thrombocytopeniaThrombocytopenia

Identifiers

PMID32264655
PMCPMC7373978
OpenAlexW3015187453

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.