Evidence map›Paper›PMID 36265823›Full record

ArticleJournal of the American Academy of Dermatology2023

Retrospective analysis of sepsis in cutaneous T-cell lymphoma reveals significantly greater risk in Black patients.

Madeline J Hooper, Francesca L Veon, Gail L Enriquez, Morgan Nguyen, Cameron B Grimes, Tessa M LeWitt, Yanzhen Pang, Slaton Case, Jaehyuk Choi, Joan Guitart and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Academy of Dermatology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Observational
  6. Role of Antigenic Stimulation in Cutaneous T-Cell Lymphomas.The Journal of investigative dermatology · 2024
    Review
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 1 country.

Madeline J HooperDepartment of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Francesca L VeonDepartment of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Gail L EnriquezDepartment of Biology, Loyola University Chicago, Chicago, Illinois.
Morgan NguyenDepartment of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Cameron B GrimesDepartment of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Tessa M LeWittDepartment of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Yanzhen PangDepartment of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Slaton CaseDepartment of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Jaehyuk ChoiDepartment of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Joan GuitartDepartment of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Michael B BurnsDepartment of Biology, Loyola University Chicago, Chicago, Illinois.
Xiaolong A ZhouDepartment of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois. Electronic address: alan.zhou@northwestern.edu.
Northwestern University · USLoyola University Chicago · US

Funding

Northwestern University Clinical and Translational Science Institute (NUCATS)KL2TR001424 · NCATS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SHARMA, LEENA · 2015 to 2023
$8.1M
NCATS NIH HHS KL2 TR001424NCI NIH HHS L30 CA231686
6 · The paper itself

Abstract

backgroundSepsis is a leading cause of morbidity, mortality, and resource utilization among patients with cutaneous T-cell lymphoma (CTCL).

objectiveTo characterize the demographic, clinical, and microbial attributes distinguishing patients with CTCL sepsis from other patients with non-Hodgkin lymphoma (NHL) sepsis and patients with CTCL in general.

methodsTwo-part retrospective cohort study at an academic medical center from 2001-2019 involving patients with CTCL (n = 97) and non-CTCL NHL (n = 88) admitted with sepsis, and a same-institution CTCL patient database (n = 1094). Overall survival was estimated by Kaplan-Meier analyses.

resultsPatients with CTCL sepsis were more likely to be older, Black, experience more sepsis episodes, die or be readmitted within 30 days of an inpatient sepsis episode, and develop Gram-positive bacteremia than patients with non-CTCL NHL sepsis. Staphylococcus aureus and Escherichia coli were the most frequently speciated organisms in CTCL (26%) and non-CTCL NHL (14%), respectively. No between-group differences were identified regarding sex, presence of central line, chemotherapy use, or disease stage. Compared with general patients with CTCL, patients with sepsis were Black and exhibited advanced-stage disease, higher body surface area involvement, and higher lactate dehydrogenase levels. LIMITATIONS: Single institution, retrospective nature may limit generalizability.

conclusionAwareness of CTCL-specific risk factors is crucial for guiding sepsis prevention and improving patient outcomes.

Indexed as

Lymphoma, Non-HodgkinLymphoma, T-Cell, CutaneousSepsisSkin NeoplasmsHumansRetrospective StudiesbacteremiaBlack patientscutaneous T-cell lymphomanon-Hodgkin lymphomaoutcomesracerisk factorssepsis

Identifiers

PMID36265823
PMCPMC9839541
OpenAlexW4306654979

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.