Evidence map›Paper›PMID 31022253›Full record

ArticlePloS one2019

Retrospective evaluation of natural course in mild cases of Mycobacterium avium complex pulmonary disease.

Yoshifumi Kimizuka, Yoshihiko Hoshino, Tomoyasu Nishimura, Takahiro Asami, Yumi Sakakibara, Kozo Morimoto, Shinji Maeda, Noboru Nakata, Takayuki Abe, Shunsuke Uno and 12 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 13% 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, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
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  9. Observational
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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

22 authors at 5 institutions in 1 country.

Yoshifumi KimizukaDivision of Pulmonary Medicine, Department of Medicine, School of Medicine, Keio University, Shinjuku, Tokyo, Japan.ORCID 0000-0002-4026-7506
Yoshihiko HoshinoLeprosy Research Center, National Institute of Infectious Diseases, Higashimurayama, Tokyo, Japan.
Tomoyasu NishimuraHealth Center, Keio University, Shinjuku, Tokyo, Japan.
Takahiro AsamiDivision of Pulmonary Medicine, Department of Medicine, School of Medicine, Keio University, Shinjuku, Tokyo, Japan.
Yumi SakakibaraDepartment of Integrated Pulmonology, Tokyo Medical and Dental University, Bunkyo, Tokyo, Japan.
Kozo MorimotoRespiratory Disease Center, Fukujuji Hospital, Anti-tuberculosis Association, Kiyose, Tokyo, Japan.
Shinji MaedaFaculty of Pharmaceutical Sciences, Hokkaido University of Science, Sapporo, Hokkaido, Japan.
Noboru NakataLeprosy Research Center, National Institute of Infectious Diseases, Higashimurayama, Tokyo, Japan.
Takayuki AbeDepartment of Preventive Medicine and Public Health, Biostatistics Unit at Clinical and Translational Research Center, School of Medicine, Keio University, Shinjuku, Tokyo, Japan.
Shunsuke UnoCenter for Infectious Diseases and Infection Control, School of Medicine, Keio University, Shinjuku, Tokyo, Japan.
Ho NamkoongDivision of Pulmonary Medicine, Department of Medicine, School of Medicine, Keio University, Shinjuku, Tokyo, Japan.ORCID 0000-0001-6181-4284
Hiroshi FujiwaraCenter for Infectious Diseases and Infection Control, School of Medicine, Keio University, Shinjuku, Tokyo, Japan.
Yohei FunatsuDivision of Pulmonary Medicine, Department of Medicine, School of Medicine, Keio University, Shinjuku, Tokyo, Japan.
Kazuma YagiDivision of Pulmonary Medicine, Department of Medicine, School of Medicine, Keio University, Shinjuku, Tokyo, Japan.
Toshihide FujieDepartment of Integrated Pulmonology, Tokyo Medical and Dental University, Bunkyo, Tokyo, Japan.
Makoto IshiiDivision of Pulmonary Medicine, Department of Medicine, School of Medicine, Keio University, Shinjuku, Tokyo, Japan.
Naohiko InaseDepartment of Integrated Pulmonology, Tokyo Medical and Dental University, Bunkyo, Tokyo, Japan.
Satoshi IwataDepartment of Infectious Diseases, Keio University School of Medicine, Shinjuku, Tokyo, Japan.
Atsuyuki KurashimaRespiratory Disease Center, Fukujuji Hospital, Anti-tuberculosis Association, Kiyose, Tokyo, Japan.
Tomoko BetsuyakuDivision of Pulmonary Medicine, Department of Medicine, School of Medicine, Keio University, Shinjuku, Tokyo, Japan.
Naoki HasegawaCenter for Infectious Diseases and Infection Control, School of Medicine, Keio University, Shinjuku, Tokyo, Japan.
Non-Tuberculous Mycobacteriosis-Japan Research Consortium (NTM-JRC)
Keio University · JPTokyo Medical and Dental University · JPFukujuji Hospital · JPNational Institute of Infectious Diseases · JPHokkaido University of Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere is no proven management for mild cases of Mycobacterium avium complex (MAC) pulmonary disease, who do not immediately receive treatment and are managed with observation alone, because its long term-natural course, factors predictive of deterioration, and the effect of treating the disease remain unclear. Thus, we sought to investigate the natural course of mild cases of MAC pulmonary disease.

methodsWe conducted a multicenter retrospective study. Sixty-five patients with mild MAC pulmonary disease in whom treatment was withheld for at least 6 months after diagnosis were retrospectively recruited after a review of 747 medical records. Longitudinal changes in clinical features were evaluated by using a mixed effects model.

resultsMean follow-up was 6.9 ± 5.7 years. During the follow-up period, 15 patients (23%) required treatment and 50 (77%) were managed with observation alone. At diagnosis, 65 patients had nodular bronchiectatic disease without fibrocavitary lesions. Among clinical features, mean body mass index (BMI), forced expiratory volume in 1 second as percent of forced vital capacity (%FEV1), nodular lung lesions, and bronchiectasis worsened significantly in the observation group during follow-up. In the treatment group, BMI, and %FEV1 were stable, but bronchiectasis significantly worsened. At diagnosis, the polyclonal MAC infection rate in the treatment group was higher than that in the observation group. Other microbiological factors, such as insertion sequences, did not differ significantly between the groups.

conclusionsMild MAC pulmonary disease progresses slowly but substantially without treatment. Treatment prevents the deterioration of the disease but not the progression of bronchiectasis. Polyclonal MAC infection is a predictor of disease progression.

Indexed as

Disease ProgressionAgedFemaleHumansLung DiseasesMaleMiddle AgedMycobacterium avium ComplexMycobacterium avium-intracellulare InfectionRetrospective Studies

Identifiers

PMID31022253
PMCPMC6483267
OpenAlexW2940861929

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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.