Evidence map›Paper›PMID 42084230›Full record

ArticleCritical care explorations2026

Extracorporeal Membrane Oxygenation for Pneumocystis Pneumonia: Outcomes in Patients From the Extracorporeal Life Support Organization.

Kyle J Henry, Emily R Thompson, Kealy Ham, Holenarasipur R Vikram, Rodrigo Cartin-Ceba, Georges Khattar, Jonathan D'Cunha, Andrew H Limper, Ayan Sen, Bhavesh Patel and 1 more

Abstract read
In one paragraph

Article in Critical care explorations, 2026. 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

11 authors.

Kyle J HenryDepartment of Critical Care, Mayo Clinic, Phoenix, AZ.
Emily R ThompsonDivision of Clinical Trials and Biostatistics, Mayo Clinic Arizona, Phoenix, AZ.
Kealy HamDepartment of Critical Care, Mayo Clinic, Phoenix, AZ.
Holenarasipur R VikramDivision of Infectious Diseases and Transplant Center, Mayo Clinic, Phoenix, AZ.
Rodrigo Cartin-CebaDepartment of Critical Care, Mayo Clinic, Phoenix, AZ.
Georges KhattarDepartment of Critical Care, Mayo Clinic, Phoenix, AZ.
Jonathan D'CunhaDivision of Cardiothoracic Surgery, Mayo Clinic, Phoenix, AZ.
Andrew H LimperDivision of Pulmonary and Critical Care, Mayo Clinic, Rochester, MN.
Ayan SenDepartment of Critical Care, Mayo Clinic, Phoenix, AZ.
Bhavesh PatelDepartment of Critical Care, Mayo Clinic, Phoenix, AZ.
Aaron M PulsipherDepartment of Critical Care, Mayo Clinic, Phoenix, AZ.ORCID 0009-0000-8225-1361

Funding

Mayo Clinic Arizona Department of Critical Care Department Funds
6 · The paper itself

Abstract

objectivesPneumocystis jirovecii pneumonia (PCP) can cause severe hypoxemic respiratory failure in immunocompromised patients. Contemporary outcomes of venovenous extracorporeal membrane oxygenation (VV ECMO) support for PCP are poorly characterized, and existing reports are limited to small case series.

designRetrospective cohort study.

settingInternational registry study using the Extracorporeal Life Support Organization (ELSO) registry. PATIENTS/SUBJECTS: Adults with PCP-associated hypoxemic respiratory failure supported with VV ECMO between 2011 and 2024.

interventionsVV ECMO. MEASUREMENTS AND MAIN

resultsA total of 209 patients with PCP-associated respiratory failure supported with VV ECMO were identified. The overall in-hospital mortality was 60.8%. Survivors were younger than nonsurvivors (median age 41.9 vs. 46.8 yr; p = 0.047). Duration of mechanical ventilation before VV ECMO was longer among nonsurvivors (median 4.7 vs. 1.6 d; p = 0.019). The proportion of patients with HIV infection was similar among survivors and nonsurvivors (19.5% vs. 22.1%; p = 0.73). Pre-ECMO vasopressor use, prone positioning, and renal replacement therapy were common and did not differ between groups. Clinical course was characterized by prolonged VV ECMO support (median 18.6 d) and frequent complications, including pneumothorax (21.1%), renal replacement therapy during VV ECMO (31.6%), intracranial hemorrhage or stroke (7.7%), and major pulmonary or gastrointestinal hemorrhage (16.8%). PCP accounted for a small proportion of VV ECMO runs reported to the ELSO registry throughout the study period at 0.36% of reported cases. No significant temporal trend in mortality was observed.

conclusionsPCP-associated respiratory failure supported with VV ECMO is associated with substantial mortality and prolonged VV ECMO support. These findings provide contemporary benchmarks that may inform VV ECMO candidacy discussions and expectations in this challenging patient population.

Indexed as

Extracorporeal Membrane OxygenationPneumonia, PneumocystisRespiratory InsufficiencyAdultFemaleHospital MortalityHumansMaleMiddle AgedRegistriesRetrospective StudiesTreatment Outcomeacute respiratory distress syndromeimmunocompromised hostvenovenous extracorporeal membrane oxygenation

Identifiers

PMID42084230
PMCPMC13143505

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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.