Evidence map›Paper›PMID 38935248›Full record

ArticleInfection2024

Epidemiology and risk factors of community-acquired pneumonia in patients with different causes of immunosuppression.

Fabian Reichel, Falko Tesch, Saskia Berger, Martin Seifert, Dirk Koschel, Jochen Schmitt, Martin Kolditz

Abstract read
In one paragraph

Article in Infection, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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

7 authors.

Fabian ReichelMedical Department I, Division of Pneumology, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany. fabian.reichel@ukdd.de.ORCID http://orcid.org/0009-0007-7905-1060
Falko TeschCenter for Evidence-Based Healthcare, University Hospital and Faculty of Medicine Carl Gustav Carus at TU Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0001-8933-643X
Saskia BergerCenter for Evidence-Based Healthcare, University Hospital and Faculty of Medicine Carl Gustav Carus at TU Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0002-6806-3257
Martin SeifertCenter for Evidence-Based Healthcare, University Hospital and Faculty of Medicine Carl Gustav Carus at TU Dresden, Dresden, Germany.
Dirk KoschelMedical Department I, Division of Pneumology, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0002-5609-4574
Jochen SchmittCenter for Evidence-Based Healthcare, University Hospital and Faculty of Medicine Carl Gustav Carus at TU Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0003-0264-0960
Martin KolditzMedical Department I, Division of Pneumology, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0001-6022-6827

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunosuppression constitutes a significant risk for community-acquired pneumonia (CAP). Nevertheless, specific causes of immunosuppression and their relevance for incidence, etiology and prognosis of CAP are insufficiently investigated.We conducted a population-based cohort study within a statutory health insurance in Germany from 2015 to 2018. CAP was retrieved by ICD-10-GM codes. Episodes of immunosuppression were identified by coded conditions (hematologic neoplasms, stem cell or organ transplantation, neutropenia, HIV, primary immunosuppressive syndromes) or treatments (immunosuppressants, antineoplastic drugs, systemic steroids). Endpoints were defined as occurrence of CAP (primary), hospitalization, 30-day mortality and CAP associated with rare pathogens. Our analysis utilized the Andersen-Gill model adjusted for sex, age, level of long-term care, vaccination status, community type and comorbidities.942,008 individuals with 54,781 CAPs were included (hospitalization 55%, 30-day mortality 14.5%). 6% of individuals showed at least one episode of immunosuppression during the study period with systemic steroids (39.8%) and hematologic neoplasms (26.7%) being most common. Immunosuppression was recorded in 7.7% of CAPs. Besides classical risk factors such as age and level of long-term care, immunosuppressed patients were most prone to CAP (HR 2.4[2.3-2.5]) and consecutive death (HR 1.9[1.8-2.1]). Organ and stem cell transplantation (HR 3.2[2.6-4.0] and 2.8[2.1-3.7], respectively), HIV (HR 3.2[1.9-5.4]) and systemic steroids (> 20 mg prednisone daily dose equivalent (HR 2.7[2.4-3.1])) showed the highest risk for contracting CAP. CAP by rare pathogens was strongly associated with immunosuppression (HR 17.1[12.0-24.5]), especially HIV (HR 34.1[7.6-153]) and systemic steroids (HR 8.2[4.6-14.8]).Our study elucidates the relevance of particular immunosuppressive conditions including systemic steroids for occurrence and prognosis of CAP.

Indexed as

Community-Acquired InfectionsImmunocompromised HostPneumoniaAdolescentAdultAgedAged, 80 and overChildChild, PreschoolCohort StudiesFemaleGermanyHumansImmunosuppression TherapyImmunosuppressive AgentsIncidenceImmunosuppressive AgentsCommunity-acquired pneumoniaHospitalizationImmunosuppressionMortalityRiskSteroids

Identifiers

PMID38935248
PMCPMC11621203

What OpenQuestion holds

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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.