Evidence map›Paper›PMID 35296445›Full record

ArticleTransplantation and cellular therapy2022

High Mortality of COVID-19 Early after Allogeneic Stem Cell Transplantation: A Retrospective Multicenter Analysis on Behalf of the German Cooperative Transplant Study Group.

Judith Schaffrath, Christina Brummer, Daniel Wolff, Udo Holtick, Nicolaus Kröger, Martin Bornhäuser, Sabrina Kraus, Inken Hilgendorf, Igor-Wolfgang Blau, Olaf Penack and 9 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Transplantation and cellular therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 9% of its field
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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

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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

19 authors at 14 institutions in 2 countries.

Judith SchaffrathDepartment of Internal Medicine IV - Hematology and Oncology, Martin Luther University Halle-Wittenberg, Halle (Saale), Germany. Electronic address: judith.schaffrath@uk-halle.de.
Christina BrummerDepartment of Internal Medicine III, University Hospital of Regensburg, Regensburg, Germany.
Daniel WolffDepartment of Internal Medicine III, University Hospital of Regensburg, Regensburg, Germany.
Udo HoltickDepartment I of Internal Medicine, University of Cologne, Faculty of Medicine and University Hospital, Cologne, Germany.
Nicolaus KrögerDepartment of Stem Cell Transplantation, University Hospital Hamburg-Eppendorf, Hamburg, Germany.
Martin BornhäuserDepartment of Internal Medicine I, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.
Sabrina KrausDepartment of Internal Medicine II, University Hospital of Würzburg, Würzburg, Germany.
Inken HilgendorfDepartment of Internal Medicine II, University Hospital of Jena, Jena, Germany.
Igor-Wolfgang BlauDepartment of Hematology, Oncology and Tumorimmunology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
Olaf PenackDepartment of Hematology, Oncology and Tumorimmunology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
Christoph WittkeDepartment of Internal Medicine III, University Hospital of Rostock, Rostock, Germany.
Normann SteinerUniversity Hospital of Internal Medicine V, Innsbruck Medical University, Innsbruck, Austria.
David NachbaurUniversity Hospital of Internal Medicine V, Innsbruck Medical University, Innsbruck, Austria.
Lorenz ThurnerDepartment of Internal Medicine I, Saarland University, Homburg, Germany.
Heidrun HindahlDepartment of Internal Medicine II, St.-Johannes-Hospital Dortmund, Dortmund, Germany.
Robert ZeiserDepartment of Internal Medicine I, Medical Center - University of Freiburg, Faculty of Medicine, Freiburg, Germany.
Claus-Philipp MaierDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tuebingen, Tuebingen, Germany.
Wolfgang BethgeDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tuebingen, Tuebingen, Germany.
Lutz P MüllerDepartment of Internal Medicine IV - Hematology and Oncology, Martin Luther University Halle-Wittenberg, Halle (Saale), Germany.
Humboldt-Universität zu Berlin · DEInnsbruck Medical University · ATMartin Luther University Halle-Wittenberg · DEUniversity Hospital Regensburg · DEUniversity of Tübingen · DEJena University Hospital · DESaarland University · DESt.-Johannes-Hospital Dortmund · DEUniversität Hamburg · DEUniversitätsklinikum Würzburg · DEUniversity Hospital Carl Gustav Carus · DEUniversity of Cologne · DEUniversity of Freiburg · DEUniversity of Rostock · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recipients of allogeneic stem cell transplantation (alloSCT) are at high risk for contracting infectious diseases with high morbidity and mortality. Coronavirus disease 2019 (COVID-19) is a viral respiratory disease that can lead to severe pneumonia and acute respiratory distress syndrome, with a potentially fatal outcome. In this retrospective study conducted on behalf of the German Cooperative Transplant Study Group, we aimed to analyze risk factors, disease course, and outcomes of COVID-19 in patients who underwent alloSCT. AlloSCT recipients who became infected with SARS-CoV-2 at German and Austrian transplant centers between February 2020 and July 2021 were included. Classification of COVID-19 severity into mild, moderate-severe, or critical disease and division of the course of the pandemic into 4 phases were done according to the German Robert Koch Institute. The main endpoint was overall mortality at the end of follow-up. We further analyzed the need for treatment in an intensive care unit (ICU) and the severity of disease. Risk factors were evaluated using univariate and multivariate analyses, and survival analysis was performed using Kaplan-Meier method. The study cohort comprised 130 patients from 14 transplant centers, with a median age at diagnosis of COVID-19 of 59 years (range, 20 to 81 years) and a median interval between alloSCT and COVID-19 of 787 days (range, 19 to 8138 days). The most common underlying diseases were acute myeloid leukemia (45.4%) and lymphoma (10.8%). The majority of patients (84.9%) were infected in the later phases of the pandemic; 20.8% had moderate-severe disease, 12.3% had critical disease, and 19.2% were treated in an ICU. After a median follow-up of 127 days, overall mortality was 16.2%, 52.0% among patients treated in an ICU. Risk factors for mortality in multivariate analysis were active disease (odds ratio [OR], 4.46), infection with SARS-CoV-2 ≤365 days after alloSCT (OR, 5.60), age >60 years (OR, 5.39), and ongoing immunosuppression with cyclosporine (OR, 8.55). Risk factors for developing moderate-severe or critical disease were concurrent immunosuppression (OR, 4.06) and age >40 years (OR, 4.08). Patients after alloSCT exhibit a substantially increased mortality risk after COVID-19 infection compared with the normal population, without considerable improvement over the course of the pandemic. Risk factors include age, early infection post-alloSCT, and active immunosuppression. Further studies are needed to improve prevention and treatment in this high-risk patient group.

Indexed as

COVID-19Hematopoietic Stem Cell TransplantationAdultAgedAged, 80 and overHumansMiddle AgedPandemicsRetrospective StudiesSARS-CoV-2Young AdultAllogeneic stem cell transplantationCOVID-19SARS-CoV-2

Identifiers

PMID35296445
PMCPMC8918088
OpenAlexW4220998395

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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.