Evidence map›Paper›PMID 27375692›Full record

ArticlePakistan journal of medical sciences

Importance of immature platelet fraction as predictor of immune thrombocytopenic purpura.

Arshi Naz, Samina Naz Mukry, Mahwish Rauf Shaikh, Ali Raza Bukhari, Tahir Sultan Shamsi

Open access · goldAbstract read
In one paragraph

Article in Pakistan journal of medical sciences. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 31 citations in OpenAlex.

  1. Immature Platelet Fraction and Clinical Outcomes in Patients Undergoing Transcatheter Aortic Valve Implantation.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
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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

5 authors at 2 institutions in 1 country.

Arshi NazArshi Naz, Ph.D. National Institute of Blood Disease and Bone Marrow Transplantation, Karachi, Pakistan.
Samina Naz MukrySamina Naz Mukry, Ph.D. National Institute of Blood Disease and Bone Marrow Transplantation, Karachi, Pakistan.
Mahwish Rauf ShaikhMahwish Rauf Shaikh, M.Sc. Jinnah University for Women, Karachi, Pakistan.
Ali Raza BukhariAli Raza Bukhari, M.Sc. National Institute of Blood Disease and Bone Marrow Transplantation, Karachi, Pakistan.
Tahir Sultan ShamsiTahir Sultan Shamsi, FRCPath. National Institute of Blood Disease and Bone Marrow Transplantation, Karachi, Pakistan.
Jinnah University for Women · PKNational Institute Of Blood Disease and Bone Marrow Transplantation · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveImmune thrombocytopenic purpura (ITP) is a clinical syndrome in which a decreased number of circulating platelets (thrombocytopenia) manifests as a bleeding tendency, easy bruising (purpura) or extravasation of blood from capillaries into skin and mucous membranes (petechiae). The diagnosis of ITP can be made clinically on the basis of symptoms, we need to see if ITP can be confirmed in patients by quantification of residual RNA containing immature platelets (megakaryocytic mass) or immature platelets fraction (IPF) using automated hematology analyzers (Sysmex XE-2100).

methodsIn order to check the efficacy of IPF% parameter of Sysmex XE-2100 a total of 231 patients of thrombocytopenia were included in this study. Complete blood count (CBC) was estimated. The data was statistically analyzed by SPSS version 17.

resultsAbout 62 patients were diagnosed as ITP and 169 patients were diagnosed as non ITP on the basis of clinical history. The mean IPF % value of ITP patients was 16.39% and the IPF % value of Non ITP patients was ~7.69% respectively. There was no significant difference in IPF% values with respect to time between sampling and acquisition of complete blood count. The diagnostic sensitivity of IPF% as biomarker for ITP and non-ITP was 85.71% (95%CI: 84.04% to 85.96%) and 41.76% (95% CI: 39.87% to 43.65%).

conclusionThe mean IPF % value by Sysmex XE-2100 can be used to predict ITP.

Indexed as

immature platelet fraction (IPF)Immune thrombocytopenic purpura (ITP)

Identifiers

PMID27375692
PMCPMC4928401
OpenAlexW2341362200

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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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.