Evidence map›Paper›PMID 41216418›Full record

ArticleOpen forum infectious diseases2025

Mortality and Causes of Death in Patients With

Victor N Dahl, Andreas A Pedersen, Isik S Johansen, Michael H Ibsen, Andreas Fløe, Anders Løkke, Ole Hilberg, Aase B Andersen, Christian M Wejse, Troels Lillebaek

Abstract read
In one paragraph

Article in Open forum infectious diseases, 2025. 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

10 authors.

Victor N DahlDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.ORCID https://orcid.org/0000-0003-2965-6348
Andreas A PedersenDepartment of Infectious Diseases, Odense University Hospital, Odense, Denmark.ORCID https://orcid.org/0000-0003-0751-6918
Isik S JohansenDepartment of Infectious Diseases, Odense University Hospital, Odense, Denmark.ORCID https://orcid.org/0000-0002-2189-9823
Michael H Ibseni2minds, Aarhus, Denmark.ORCID https://orcid.org/0000-0002-7350-9196
Andreas FløeDepartment of Respiratory Diseases and Allergy, Aarhus University Hospital, Aarhus, Denmark.ORCID https://orcid.org/0000-0003-2787-0041
Anders LøkkeDepartment of Medicine, Lillebaelt Hospital, Vejle, Denmark.ORCID https://orcid.org/0000-0002-6905-4141
Ole HilbergMycobacterial Center for Research Southern Denmark (MyCRESD), University of Southern Denmark, Odense, Denmark.ORCID https://orcid.org/0000-0002-3075-3463
Aase B AndersenDepartment of Infectious Diseases, Rigshospitalet, Copenhagen, Denmark.ORCID https://orcid.org/0000-0003-4779-7603
Christian M WejseDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.ORCID https://orcid.org/0000-0002-2534-2942
Troels LillebaekInternational Reference Laboratory of Mycobacteriology, Statens Serum Institut, Copenhagen, Denmark.ORCID https://orcid.org/0000-0002-2601-2718

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Nontuberculous mycobacterial (NTM) disease, predominantly caused by Methods: A nationwide study in Denmark (1991-2018) included all patients with MAC isolates, excluding those identified using gastric lavages alone. Data from the International Reference Laboratory of Mycobacteriology, Statens Serum Institut, Copenhagen, were linked with national registries. Patients were classified as having pulmonary (PMAC), extrapulmonary (EMAC), or disseminated MAC (DMAC) disease. Cumulative mortality rates were calculated, and adjusted hazard ratios (aHR) for mortality were estimated using Cox models, adjusting for age, sex, disease manifestation, and comorbidities. Results: Among 2,027 patients, 1-year mortality rates were 19% (PMAC), 15% (EMAC), and 52% (DMAC), increasing to 68%, 22%, and 84% at 10 years, respectively. Mortality decreased over time, especially for EMAC and DMAC. The risk factors for higher mortality included older age (aHR 1.04), male sex (aHR 1.85), DMAC (aHR 2.66), and higher comorbidity (aHR 1.21). Over time, age-related mortality hazards increased (0.4%/year on average), while hazards related to EMAC (-9%/year), DMAC (-13%/year), and comorbidities (-1%/year) declined. Chronic respiratory disease and HIV were the leading causes of death. Conclusions: Despite improvements over nearly three decades, PMAC remains associated with substantial mortality. This study offers valuable insights into mortality trends and risk factors for MAC disease, providing findings that can assist clinicians in delivering more accurate prognoses for different patient groups.

Indexed as

epidemiologymortalitymycobacterium avium complexnontuberculous mycobacteriaprognosis

Identifiers

PMID41216418
PMCPMC12596373

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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.