Evidence map›Paper›PMID 29963516›Full record

ArticleBlood research2018

Clinical characteristics and treatment courses for cytomegalovirus-associated thrombocytopenia in immunocompetent children after neonatal period.

Min Ji Jin, Yunkyum Kim, Eun Mi Choi, Ye Jee Shim, Heung Sik Kim, Jin Kyung Suh, Ji Yoon Kim, Kun Soo Lee, Sun Young Park, Jae Min Lee and 1 more

Open access · diamondAbstract read
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Article in Blood research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

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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

11 authors at 5 institutions in 1 country.

Min Ji JinDepartment of Pediatrics, Keimyung University School of Medicine and Dongsan Medical Center, Daegu, Korea.
Yunkyum KimDepartment of Pediatrics, Keimyung University School of Medicine and Dongsan Medical Center, Daegu, Korea.
Eun Mi ChoiDepartment of Pediatrics, Keimyung University School of Medicine and Dongsan Medical Center, Daegu, Korea.
Ye Jee ShimDepartment of Pediatrics, Keimyung University School of Medicine and Dongsan Medical Center, Daegu, Korea.
Heung Sik KimDepartment of Pediatrics, Keimyung University School of Medicine and Dongsan Medical Center, Daegu, Korea.
Jin Kyung SuhDepartment of Pediatrics, Gachon University Gil Medical Center, Incheon, Korea.
Ji Yoon KimDepartment of Pediatrics, School of Medicine, Kyungpook National University, Kyungpook National University Hospital, Daegu, Korea.
Kun Soo LeeDepartment of Pediatrics, School of Medicine, Kyungpook National University, Kyungpook National University Hospital, Daegu, Korea.
Sun Young ParkDepartment of Pediatrics, College of Medicine, Yeungnam University, Daegu, Korea.
Jae Min LeeDepartment of Pediatrics, College of Medicine, Yeungnam University, Daegu, Korea.
Jeong Ok HahDepartment of Pediatrics, Fatima Hospital, Daegu, Korea.
Keimyung University Dongsan Medical Center · KRKyungpook National University Hospital · KRYeungnam University · KRDaegu Fatima Hospital · KRGachon University Gil Medical Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCytomegalovirus (CMV) causes severe diseases in premature infants and immunocompromised hosts, and antiviral therapy is often required for disease control. However, the clinical manifestations and treatment courses for CMV-associated thrombocytopenia in immunocompetent children are unclear.

methodsMedical records of the children who suffered from thrombocytopenia, and showed positive CMV polymerase chain reaction and CMV-like symptoms were retrospectively analyzed at three university hospitals in Daegu from January 2000 to March 2017. Patients suffering from leukemia, immunodeficiency, and other infections were excluded.

resultsAmong 1,065 children with thrombocytopenia, 29 (2.7%) displayed CMV-associated thrombocytopenia. The median age at diagnosis was 15 months and the median platelet count was 26,000/µL. They were classified into the CMV-induced thrombocytopenia (23/29) and CMV-related secondary immune thrombocytopenia (ITP, 6/29) groups. Fourteen subjects had hepatic dysfunction, four had Evans syndrome, two had pneumonitis, and one had gastritis. IVIG was used for 21 patients, and six patients among them showed recurrence, for whom IVIG or antiviral therapy was used. All, except one, recurrent or chronic cases belonged to the CMV-induced thrombocytopenia group. Antiviral therapy was used more frequently for the CMV-induced thrombocytopenia group (8/23, 34.8%) than for the CMV-related secondary ITP group (0/6); however, the results were not statistically significant (

conclusionCMV is a rare but unique etiology of thrombocytopenia, and observed even in healthy children after the neonatal period. About one-third patients need antiviral therapy for disease control. Further, CMV-induced thrombocytopenia is more complex than CMV-related secondary ITP.

Indexed as

CytomegalovirusGanciclovirImmune thrombocytopeniaImmunocompetentValganciclovir

Identifiers

PMID29963516
PMCPMC6021578
OpenAlexW2810950530

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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.