Evidence map›Paper›PMID 42715192›Full record

ArticlePloS one2026

Outcomes of immunocompromised and non-immunocompromised patients in the ICU diverge late in the pandemic.

Shreya Battu, Andrew R Moore, Katie Lebold, Ana Pacheco-Navarro, Shaun Pienkos, Christian O'Donnell, Pablo Sanchez, Caitlin Parmer-Chow, Jonasel Roque, Tara Ramaswamy and 4 more

Abstract read
In one paragraph

Article in PloS one, 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

14 authors.

Shreya BattuDivision of Pulmonary, Allergy and Critical Care Medicine, Stanford University School of Medicine, Stanford, California, United States of America.ORCID https://orcid.org/0009-0000-7515-7545
Andrew R MooreDivision of Pulmonary, Allergy and Critical Care Medicine, Stanford University School of Medicine, Stanford, California, United States of America.
Katie LeboldDivision of Pulmonary, Allergy and Critical Care Medicine, Oregon Health & Sciences University, Portland, Oregon, United States of America.
Ana Pacheco-NavarroDivision of Pulmonary, Allergy and Critical Care Medicine, Stanford University School of Medicine, Stanford, California, United States of America.
Shaun PienkosDivision of Pulmonary, Allergy and Critical Care Medicine, Stanford University School of Medicine, Stanford, California, United States of America.ORCID https://orcid.org/0009-0001-8409-4803
Christian O'DonnellDepartment of Medicine, Stanford University School of Medicine, Stanford, California, United States of America.ORCID https://orcid.org/0000-0002-4243-243X
Pablo SanchezDepartment of Medicine, University of California San Francisco, San Francisco, California, United States of America.
Caitlin Parmer-ChowDepartment of Medicine, Stanford University School of Medicine, Stanford, California, United States of America.ORCID https://orcid.org/0000-0003-0770-2286
Jonasel RoqueDivision of Pulmonary, Allergy and Critical Care Medicine, Stanford University School of Medicine, Stanford, California, United States of America.
Tara RamaswamyDepartment of Anesthesiology, Stanford University, Stanford, California, United States of America.
Jennifer G WilsonDepartment of Emergency Medicine, Stanford University, Stanford, California, United States of America.
Joseph E LevittDivision of Pulmonary, Allergy and Critical Care Medicine, Stanford University School of Medicine, Stanford, California, United States of America.
William CollinsDivision of Hospital Medicine, Stanford University, Stanford, California, United States of America.ORCID https://orcid.org/0000-0003-0974-2599
Angela J RogersDivision of Pulmonary, Allergy and Critical Care Medicine, Stanford University School of Medicine, Stanford, California, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleThe impact of immunocompromising conditions on outcomes in critically ill patients with COVID-19 remains poorly characterized. We hypothesized that disparities in COVID-19 outcomes in immunocompromised patients may differ by viral strain and time course of the pandemic.

methodsWe retrospectively reviewed SARS-CoV-2 RT-PCR positive patients admitted to intensive care (ICU) at Stanford from March 2020 to July 2022 using electronic medical records. Immunocompromised status included solid organ transplant; hematologic malignancy/transplant; solid cancer with metastases and recent chemotherapy; HIV/AIDS; and connective tissue disease on immunosuppression. SARS-CoV-2 strain periods were classified as pre-Delta (3/2020-8/2021), Delta (9/2021-12/2021), and Omicron (1/2022-7/2022). We assessed 90-day survival differences between immunocompromised and non-immunocompromised patients by strain using Cox-proportional hazards, adjusted for age, sex, and APACHE II score.

resultsA total of 791 patients were included, 450 from the pre-Delta period, 114 from the Delta period, and 227 from the Omicron period. We compared 633 non-immunocompromised patients with 158 immunocompromised patients (77 during the pre-Delta, 22 Delta, and 59 Omicron periods). Patients admitted during the Omicron period were more likely to be immunocompromised (26%) compared to pre-Delta (17%) or Delta periods (19%; p = 0.008). Immunocompromise was associated with worse outcomes in the entire cohort after adjustment (HR 1.68, 95% CI 1.2-2.3, p < 0.001). However, when stratified by strain period, immunocompromised status was only significantly associated with higher 90-day mortality in patients from the Omicron period (42% vs 17%, HR 2.9, CI% 1.7-5.0, p < 0.001). Differences in mortality between immunocompromised and immunocompetent patients were not statistically different in either the pre-Delta (34% vs. 23%, HR 1.4, 95% CI 0.9-2.1, p = 0.15) or Delta periods (32% vs. 28% HR 1.0, 95% CI 0.4-2.5, p = 0.92). Notably, survival was significantly improved during the Omicron period compared to earlier strain periods in immunocompetent patients (HR 0.6, 95% CI 0.4-0.9, p = 0.02) but not for immunocompromised patients (HR 1.4, 95% CI 0.80-2.44, p = 0.24).

conclusionIn this retrospective cohort analysis of patients admitted to the ICU due to SARS-CoV-2 infection, we found that lower survival among immunocompromised patients was due to higher mortality during the Omicron period, with similar mortality between immunocompetent and immunocompromised patients during other periods.

Indexed as

COVID-19Immunocompromised HostIntensive Care UnitsAgedCritical IllnessFemaleHumansMaleMiddle AgedPandemicsRetrospective StudiesSARS-CoV-2

Identifiers

PMID42715192
PMCPMC13557382

What OpenQuestion holds

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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.