Evidence map›Paper›PMID 37338625›Full record

ArticleAnnals of hematology2023

Risk factors and outcome of Stenotrophomonas maltophilia infection after allogeneic hematopoietic stem cell transplantation: JSTCT, Transplant Complications Working Group.

Masuho Saburi, Kumi Oshima, Kuniko Takano, Yoshitaka Inoue, Kaito Harada, Naoyuki Uchida, Takahiro Fukuda, Noriko Doki, Kazuhiro Ikegame, Yayoi Matsuo and 12 more

Abstract read
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In one paragraph

Article in Annals of hematology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-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

7 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. The Other Face ofAntibiotics (Basel, Switzerland) · 2026
    Article
  4. Infection and drug resistance · 2026
    Review
  5. Aztreonam-Avibactam Successfully Treated SevereJournal of blood medicine · 2026
    Article
  6. Cefiderocol susceptibility of 146 Stenotrophomonas maltophilia strains clinically isolated from blood in two Japanese hospitals over a 10-year period.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2024
    Article
  7. Article
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 19 institutions in 1 country.

Masuho SaburiDepartment of Hematology, Oita Prefectural Hospital, 2-8-1 Bunyo, Oita City, Oita, 870-8511, Japan. masuho-saburi@oita-u.ac.jp.ORCID http://orcid.org/0000-0001-6097-5633
Kumi OshimaDepartment of Hematology, Jyoban Hospital, Tokiwa Foundation, Fukushima, Japan.
Kuniko TakanoDepartment of Hematology, Oita University Hospital, Oita, Japan.
Yoshitaka InoueDepartment of Hematology, Kumamoto University Hospital, Kumamoto, Japan.
Kaito HaradaDepartment of Hematology and Oncology, Tokai University, Isehara, Japan.
Naoyuki UchidaDepartment of Hematology, Toranomon Hospital, Tokyo, Japan.
Takahiro FukudaDepartment of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.
Noriko DokiHematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo, Japan.
Kazuhiro IkegameDivision of Hematology, Hyogo College of Medicine, Hyogo, Japan.
Yayoi MatsuoDepartment of Hematology, Hamanomachi Hospital, Fukuoka, Japan.
Yuta KatayamaDepartment of Hematology, Hiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital, Hiroshima, Japan.
Yukiyasu OzawaDepartment of Hematology, Japanese Red Cross Aichi Medical Center Nagoya Daiichi Hospital, Nagoya, Japan.
Ken-Ichi MatsuokaDepartment of Hematology and Oncology, Okayama University Hospital, Okayama, Japan.
Toshiro KawakitaDepartment of Hematology, National Hospital Organization Kumamoto Medical Center, Kumamoto, Japan.
Yasuo MoriHematology, Oncology & Cardiovascular medicine, Kyushu University Hospital, Fukuoka, Japan.
Takahide AraDepartment of Hematology, Hokkaido University Hospital, Hokkaido, Japan.
Hirohisa NakamaeDepartment of Hematology, Osaka Metropolitan University Hospital, Osaka, Japan.
Takafumi KimuraPreparation Department, Japanese Red Cross Kinki Block Blood Center, Osaka, Japan.
Yoshinobu KandaDivision of Hematology, Jichi Medical University, Tochigi, Japan.
Yoshiko AtsutaJapanese Data Center for Hematopoietic Cell Transplantation, Nagoya, Japan.
Masao OgataDepartment of Hematology, Oita University Hospital, Oita, Japan.
Transplant Complications Working Group of the Japanese Society for Transplantation and Cellular Therapy
Oita University Hospital · JPAichi Medical University · JPHamanomachi Hospital · JPHiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital · JPHokkaido University Hospital · JPHyogo Medical University · JPJapanese Red Cross Nagoya Daiichi Hospital · JPJapanese Red Cross Society, Japan · JPJichi Medical University · JPJyoban Hospital of Tokiwa Foundation · JPKumamoto Medical Center · JPKumamoto University Hospital · JPKyushu University Hospital · JPOita Prefectural Hospital · JPOkayama University Hospital · JPOsaka Metropolitan University · JPTokai University · JPTokyo Metropolitan Komagome Hospital · JPToranomon Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stenotrophomonas maltophilia (S. maltophilia) is an aerobic nonfermenting Gram-negative bacillus widely distributed in the environment that has inherent multidrug resistance to beta-lactam and carbapenem antibiotics. S. maltophilia infection (SMI) is known as an important fatal complication following allogeneic hematopoietic stem cell transplantation (HSCT), but its clinical characteristics have not been well clarified. A retrospective study to identify the incidence, risk factors, and outcomes of SMI after allogeneic HSCT was performed using the database of the Japanese nationwide registry, including 29,052 patients who received allogeneic HSCT in Japan between January 2007 and December 2016. A total of 665 patients developed SMI (sepsis/septic shock, 432; pneumonia, 171; other, 62). The cumulative incidence of SMI at 100 days after HSCT was 2.2%. Among risk factors identified for SMI (age ≥ 50 years, male, performance status 2-4, cord blood transplantation [CBT], myeloablative conditioning, Hematopoietic Cell Transplant-Comorbidity Index [HCT-CI] score 1-2, HCT-CI score ≥ 3, and active infectious disease at HSCT), CBT was the strongest risk factor (hazard ratio, 2.89; 95%CI, 1.94-4.32; p < 0.001). The survival rate at day 30 after SMI was 45.7%, and SMI before neutrophil engraftment was significantly associated with poor survival (survival rate 30 days after SMI, 40.1% and 53.8% in patients with SMI before and after engraftment, respectively; p = 0.002). SMI is rare after allogeneic HSCT, but its prognosis is extremely poor. CBT was a strong risk factor for SMI, and its development prior to neutrophil engraftment was associated with poor survival.

Indexed as

Gram-Negative Bacterial InfectionsHematopoietic Stem Cell TransplantationStenotrophomonas maltophiliaGram-Negative BacteriaHumansMaleMiddle AgedRetrospective StudiesRisk FactorsAllogeneic Hematopoietic Stem Cell transplantationCord blood transplantationPneumoniaSepsisStenotrophomonas maltophilia

Identifiers

PMID37338625
OpenAlexW4381308665

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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.