Evidence map›Paper›PMID 39488718›Full record

ArticleBMC infectious diseases2024

Effectiveness of pulse methylprednisolone in patients with non-human immunodeficiency virus pneumocystis pneumonia: a multicentre, retrospective registry-based cohort study.

Yasuhiro Morimoto, Hiroki Matsui, Haruka Fujioka, Yuya Homma, Tatsuya Nagai, Ayumu Otsuki, Hiroyuki Ito, Shin-Ichiro Ohmura, Toshiaki Miyamoto, Daisuke Shichi and 3 more

Abstract readMulticenter Study
In one paragraph

Article in BMC infectious diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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

13 authors.

Yasuhiro MorimotoDepartment of Pulmonology, Kameda Medical Center, 929 Higashi-cho, Kamogawa, 296-8602, Chiba, Japan.
Hiroki MatsuiDepartment of Clinical Epidemiology and Health Economics, School of Public Health, the University of Tokyo, Tokyo, Japan.
Haruka FujiokaDepartment of Pulmonology, Kameda Medical Center, 929 Higashi-cho, Kamogawa, 296-8602, Chiba, Japan.
Yuya HommaDepartment of Pulmonology, Kameda Medical Center, 929 Higashi-cho, Kamogawa, 296-8602, Chiba, Japan.
Tatsuya NagaiDepartment of Pulmonology, Kameda Medical Center, 929 Higashi-cho, Kamogawa, 296-8602, Chiba, Japan.
Ayumu OtsukiDepartment of Pulmonology, Kameda Medical Center, 929 Higashi-cho, Kamogawa, 296-8602, Chiba, Japan.
Hiroyuki ItoDepartment of Pulmonology, Kameda Medical Center, 929 Higashi-cho, Kamogawa, 296-8602, Chiba, Japan.
Shin-Ichiro OhmuraDepartment of Rheumatology, Seirei Hamamatsu General Hospital, Hamamatsu, Shizuoka, Japan.
Toshiaki MiyamotoDepartment of Rheumatology, Seirei Hamamatsu General Hospital, Hamamatsu, Shizuoka, Japan.
Daisuke ShichiDepartment of Infectious Diseases and Rheumatology, Seirei Mikatahara General Hospital, Hamamatsu, Shizuoka, Japan.
Tomohisa WatariDepartment of Laboratory Medicine, Kameda Medical Center, Kamogawa, Chiba, Japan.
Yoshihito OtsukaDepartment of Laboratory Medicine, Kameda Medical Center, Kamogawa, Chiba, Japan.
Kei NakashimaDepartment of Pulmonology, Kameda Medical Center, 929 Higashi-cho, Kamogawa, 296-8602, Chiba, Japan. kei.7.nakashima@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA recent database study and meta-analysis reported that adjunctive glucocorticoid therapy reduces mortality in patients with non-human immunodeficiency virus-associated (non-HIV) Pneumocystis jirovecii pneumonia (PCP), having hypoxemia. However, the optimal glucocorticoid dose remains unclear. Our study aimed to evaluate the effectiveness of pulse methylprednisolone compared with mild-to-moderate steroid doses in patients with non-HIV PCP.

methodsThis multicentre retrospective cohort study included adults with non-HIV PCP receiving adjunctive steroids at three Japanese tertiary care hospitals from June 2006 to March 2021. Patients were categorised into pulse methylprednisolone and mild-to-moderate dose groups. Pulse methylprednisolone involved an initial intravenous infusion of 500-1000 mg methylprednisolone daily, while the mild-to-moderate dose was lower. Primary and secondary outcomes were 30-day and 180-day mortality from treatment initiation. Patient characteristics were adjusted using propensity score analysis with overlap weighting. Subgroup analysis focused on patients with respiratory failure.

resultsThe study included 139 patients with non-HIV PCP: 55 in the pulse methylprednisolone group and 84 in the mild-to-moderate dose group. After adjusting for patient background, 30-day mortality (14.2% vs. 15.5%, P = 0.850) and 180-day mortality (33.5% vs. 27.3%, P = 0.516) did not differ significantly between groups. Subgroup analysis revealed no significant associations among patients with respiratory failure.

conclusionsAfter adjusting for patient characteristics, no difference in prognosis was observed between pulse methylprednisolone and mild-to-moderate dose groups in patients with non-HIV PCP. A mild-to-moderate dose of adjunctive corticosteroid may suffice for treating non-HIV PCP.

Indexed as

MethylprednisolonePneumonia, PneumocystisAdultAgedFemaleGlucocorticoidsHumansJapanMaleMiddle AgedPneumocystis cariniiRegistriesRetrospective StudiesTreatment OutcomeGlucocorticoidsMethylprednisoloneAdjunctive corticosteroid treatmentNon-human immunodeficiency virus-infected patientPneumocystis pneumoniaPulse methylprednisolone

Identifiers

PMID39488718
PMCPMC11531689

What Socratic holds

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LicenceCC BY
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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 Socratic graph.