Evidence map›Paper›PMID 42857200›Full record

ArticleCase reports in nephrology2026

Recurrent Invasive

Keisuke Ono, Nobuhiro Ayuzawa, Takahisa Kawakami, Koichi Taniwaki, Shiori Arai, Aoi Kanematsu, Yuki Suhara, Mitsumasa Kishimoto, Yoshinori Komagata

Abstract read
In one paragraph

Article in Case reports in nephrology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Keisuke OnoDepartment of Nephrology and Rheumatology Kyorin University School of Medicine Tokyo Japan kyorin-u.ac.jp.ORCID https://orcid.org/0000-0002-2651-1509
Nobuhiro AyuzawaDepartment of Nephrology and Rheumatology Kyorin University School of Medicine Tokyo Japan kyorin-u.ac.jp.
Takahisa KawakamiDepartment of Nephrology and Rheumatology Kyorin University School of Medicine Tokyo Japan kyorin-u.ac.jp.
Koichi TaniwakiDepartment of Nephrology and Rheumatology Kyorin University School of Medicine Tokyo Japan kyorin-u.ac.jp.
Shiori AraiDepartment of Nephrology and Rheumatology Kyorin University School of Medicine Tokyo Japan kyorin-u.ac.jp.ORCID https://orcid.org/0009-0008-6324-0286
Aoi KanematsuDepartment of Nephrology and Rheumatology Kyorin University School of Medicine Tokyo Japan kyorin-u.ac.jp.
Yuki SuharaDepartment of Nephrology and Rheumatology Kyorin University School of Medicine Tokyo Japan kyorin-u.ac.jp.
Mitsumasa KishimotoDepartment of Nephrology and Rheumatology Kyorin University School of Medicine Tokyo Japan kyorin-u.ac.jp.
Yoshinori KomagataDepartment of Nephrology and Rheumatology Kyorin University School of Medicine Tokyo Japan kyorin-u.ac.jp.ORCID https://orcid.org/0000-0003-2047-4900

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Myelodysplastic syndromes (MDS) may be overlooked in patients undergoing hemodialysis (HD) because anemia is commonly attributed to renal anemia and treated with erythropoiesis-stimulating agents. MDS is also associated with an increased risk of bacterial infections due to neutropenia and qualitative immune dysfunction. We report recurrent invasive methicillin-susceptible Case Presentation: The patient was a 76-year-old man undergoing HD for end-stage kidney disease due to nephrosclerosis who was referred to our hospital because of persistent anemia despite high-dose darbepoetin alfa therapy. He had a history of CHOP therapy for diffuse large B-cell lymphoma, and his MDS was considered possibly therapy related. Bone marrow aspiration revealed trilineage dysplasia and 3.4% blasts without chromosomal abnormalities, leading to a diagnosis of MDS with multilineage dysplasia. Approximately 1 year later, he developed persistent fever. Blood cultures yielded MSSA, and imaging studies revealed septic pulmonary embolism and multiple cerebral infarctions. He improved after intravenous cefepime therapy. Twenty-two months later, he developed fever and left shoulder pain. Contrast-enhanced computed tomography revealed an abscess in the left subscapularis muscle, and MSSA was isolated from the drainage fluid after CT-guided drainage. He improved with drainage and antibiotic therapy. In both episodes, the neutrophil count was preserved. Conclusion: This case illustrates recurrent invasive MSSA infections in a non-neutropenic HD patient with possibly therapy-related MDS. HD-related factors should be carefully evaluated as common causes of recurrent

Indexed as

hemodialysismyelodysplastic syndromeStaphylococcus aureus

Identifiers

PMID42857200
PMCPMC13651712

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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.