Evidence map›Paper›PMID 37881854›Full record

ArticleHaematologica2024

A Japanese retrospective study of non-tuberculous mycobacterial infection in children, adolescents, and young adult patients with hematologic-oncologic diseases.

Yusuke Tsumura, Hideki Muramatsu, Nobuyuki Tetsuka, Takahiro Imaizumi, Kikue Sato, Kento Inoue, Yoshitomo Motomura, Yuko Cho, Daiki Yamashita, Daichi Sajiki and 14 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 3 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

24 authors at 7 institutions in 1 country.

Yusuke TsumuraDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya.
Hideki MuramatsuDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya. hideki-muramatsu@med.nagoya-u.ac.jp.
Nobuyuki TetsukaDepartment of Infection Control, Gifu University Graduate School of Medicine, Gifu.
Takahiro ImaizumiDepartment of Advanced Medicine, Nagoya University Hospital, Nagoya.
Kikue SatoMedical IT Center, Nagoya University Hospital, Nagoya.
Kento InoueDepartment of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo.
Yoshitomo MotomuraDepartment of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka.
Yuko ChoDepartment of Pediatrics, Hokkaido University Hospital, Sapporo.
Daiki YamashitaDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya.
Daichi SajikiDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya.
Ryo MaemuraDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya.
Ayako YamamoriDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya.
Masayuki ImayaDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya.
Manabu WakamatsuDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya.
Kotaro NaritaDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya.
Shinsuke KataokaDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya.
Motoharu HamadaDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya.
Rieko TaniguchiDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya.
Eri NishikawaDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya.
Atsushi NaritaDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya.
Nobuhiro NishioDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya.
Seiji KojimaDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya.
Yoshihiko HoshinoDepartment of Mycobacteriology, Leprosy Research Center, National Institute of Infectious Diseases, Tokyo.
Yoshiyuki TakahashiDepartment of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya. ytakaha@med.nagoya-u.ac.jp.
Nagoya University · JPNagoya University Hospital · JPGifu University · JPHokkaido University Hospital · JPKyushu University · JPNational Institute of Infectious Diseases · JPTokyo Medical and Dental University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-tuberculous mycobacterial infection (NTM) is rare in healthy children, with lymphadenitis being the most common presentation. Immunocompromised populations are known to be at high risk, but the clinical picture of NTM infection in pediatric hematology/oncology patients is unclear. In this nationwide retrospective analysis of patients under the age of 40 treated in Japanese pediatric hematology/oncology departments who developed NTM infection between January 2010 and December 2020, 36 patients were identified: 21 patients with hematopoietic stem cell transplantation (HSCT) and 15 non-transplant patients. Post-transplant patients were infected with NTM at 24 sites, including the lungs (N=12), skin and soft tissues (N=6), bloodstream (N=4), and others (N=2). Nine of 12 patients with pulmonary NTM infection had a history of pulmonary graft-versus-host disease (GvHD), and rapid-growing mycobacteria (RGM) were isolated from 5 of them. In non-transplant patients, the primary diseases were acute lymphoblastic leukemia (ALL; N=5), inborn errors of immunity (IEI; N=6), and others (N=4). All cases of ALL had bloodstream infections with RGM, whereas all cases of IEI were infected with slow-growing mycobacteria (SGM). In summary, 3 typical clinical scenarios for pediatric hematology/oncology patients have been established: RGM-induced pulmonary disease in patients with pulmonary GvHD, RGM bloodstream infection in patients with ALL, and SGM infection in patients with IEI. Our findings suggest that NTM must be regarded as a pathogen for infections in these high-risk patients, especially those with pulmonary GvHD, who may require active screening for NTM.

Indexed as

Hematopoietic Stem Cell TransplantationMycobacterium Infections, NontuberculousAdolescentAdultChildChild, PreschoolEast Asian PeopleFemaleHematologic NeoplasmsHumansInfantJapanMaleNontuberculous MycobacteriaRetrospective StudiesYoung Adult

Identifiers

PMID37881854
PMCPMC11367237
OpenAlexW4387948832

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LicenceCC BY-NC
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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.