Evidence map›Paper›PMID 24260127›Full record

Trial reportPloS one2013

Rates of serious intracellular infections in autoimmune disease patients receiving initial glucocorticoid therapy.

Kiyoshi Migita, Toru Arai, Naoki Ishizuka, Yuka Jiuchi, Yasuharu Sasaki, Yasumori Izumi, Tetsuyuki Kiyokawa, Eiichi Suematsu, Tomoya Miyamura, Hiroshi Tsutani and 19 more

Open access · goldAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.2field-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

20 citing papers in PubMed, 54 citations in OpenAlex.

  1. Trial
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  7. Review
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  13. Clinical Relevance of Steroid Use in Neuro-Oncology.Current neurology and neuroscience reports · 2017
    Review
  14. Infection and Lupus: Which Causes Which?Current rheumatology reports · 2016
    Review
  15. Article
  16. Article
  17. Review
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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

29 authors at 1 institution in 1 country.

Kiyoshi MigitaJapanese National Hospital Organization (NHO)-EBM study group for Adverse Effects of Corticosteroid Therapy (J-NHOSAC), Meguro, Tokyo, Japan.
Toru Arai
Naoki Ishizuka
Yuka Jiuchi
Yasuharu Sasaki
Yasumori Izumi
Tetsuyuki Kiyokawa
Eiichi Suematsu
Tomoya Miyamura
Hiroshi Tsutani
Yojiro Kawabe
Ryutaro Matsumura
Shunsuke Mori
Shiro Ohshima
Shigeru Yoshizawa
Kenji Kawakami
Yasuo Suenaga
Hideo Nishimura
Toyohiko Sugimoto
Hiroaki Iwase
Hideyuki Sawada
Haruhiro Yamashita
Shigeyuki Kuratsu
Fumitaka Ogushi
Masaharu Kawabata
Toshihiro Matsui
Hiroshi Furukawa
Seiji Bito
Shigeto Tohma
National Hospital Organization · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimsThe Japanese National Hospital Organization evidence-based medicine (EBM) Study group for Adverse effects of Corticosteroid therapy (J-NHOSAC) is a Japanese hospital-based cohort study investigating the safety of the initial use of glucocorticoids (GCs) in patients with newly diagnosed autoimmune diseases. Using the J-NHOSAC registry, the purpose of this observational study is to analyse the rates, characteristics and associated risk factors of intracellular infections in patients with newly diagnosed autoimmune diseases who were initially treated with GCs. METHODOLOGY/PRINCIPAL

findingsA total 604 patients with newly diagnosed autoimmune diseases treated with GCs were enrolled in this registry between April 2007 and March 2009. Cox proportional-hazards regression was used to determine independent risk factors for serious intracellular infections with covariates including sex, age, co-morbidity, laboratory data, use of immunosuppressants and dose of GCs. Survival was analysed according to the Kaplan-Meier method and was assessed by the log-rank test. There were 127 serious infections, including 43 intracellular infections, during 1105.8 patient-years of follow-up. The 43 serious intracellular infections resulted in 8 deaths. After adjustment for covariates, diabetes (Odds ratio [OR]: 2.5, 95% confidence interval [95% CI] 1.1-5.9), lymphocytopenia (≦1000/μl, OR: 2.5, 95% CI 1.2-5.2) and use of high-dose (≧30 mg/day) GCs (OR: 2.4, 95% CI 1.1-5.3) increased the risk of intracellular infections. Survival curves showed lower intracellular infection-free survival rate in patients with diabetes, lymphocytopaenia and high-dose GCs treatments. CONCLUSIONS/SIGNIFICANCE: Patients with newly diagnosed autoimmune diseases were at high risk of developing intracellular infection during initial treatment with GCs. Our findings provide background data on the risk of intracellular infections of patients with autoimmune diseases. Clinicians showed remain vigilant for intracellular infections in patients with autoimmune diseases who are treated with GCs.

Indexed as

Autoimmune DiseasesInfectionsRegistriesAdultAgedAsian PeopleFemaleFollow-Up StudiesGlucocorticoidsHumansJapanMaleMiddle AgedRisk FactorsGlucocorticoids

Identifiers

PMID24260127
PMCPMC3834005
OpenAlexW1972373948

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.