Evidence map›Paper›PMID 32301846›Full record

ArticleCritical care medicine2020

Risk of Mortality in Immunocompromised Children With Severe Sepsis and Septic Shock.

Robert B Lindell, Akira Nishisaki, Scott L Weiss, Danielle M Traynor, Julie C Fitzgerald

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in Critical care medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 49 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

5 authors at 2 institutions in 1 country.

Robert B LindellDepartment of Anesthesiology and Critical Care Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.
Akira NishisakiDepartment of Anesthesiology and Critical Care Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.
Scott L WeissDepartment of Anesthesiology and Critical Care Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.
Danielle M TraynorDepartment of Anesthesiology and Critical Care Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.
Julie C FitzgeraldDepartment of Anesthesiology and Critical Care Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.
University of Pennsylvania · USChildren's Hospital of Philadelphia · US

Funding

Improving the Safety of Pediatric Tracheal Intubations in ICUs with Apneic Oxygenation and Video LaryngoscopesR18HS024511 · AHRQ · CHILDREN'S HOSP OF PHILADELPHIA · PI NISHISAKI, AKIRA · 2016 to 2019
$996k
Pediatric septic acute kidney injury: personalizing antibiotic dosing through understanding acute kidney injury risk factors and biomarker profilesK23DK119463 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI FITZGERALD, JULIE C. HOLLOWS · 2020 to 2024
$810k
Mitochondrial Dysfunction in Pediatric SepsisK23GM110496 · NIGMS · CHILDREN'S HOSP OF PHILADELPHIA · PI WEISS, SCOTT L · 2015 to 2018
$723k
Improving the safety and quality of tracheal intubation in pediatric ICUsR18HS022464 · AHRQ · CHILDREN'S HOSP OF PHILADELPHIA · PI NISHISAKI, AKIRA · 2013 to 2014
$499k
Improving safety and quality of tracheal intubations in neonatal ICUsR21HD089151 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI NISHISAKI, AKIRA · 2017 to 2018
$470k
Quality of bag mask ventilation in critically ill childrenR03HS026939 · AHRQ · CHILDREN'S HOSP OF PHILADELPHIA · PI NISHISAKI, AKIRA · 2019 to 2019
$100k
Evaluating safety and quality of tracheal intubation in pediatric ICUsR03HS021583 · AHRQ · CHILDREN'S HOSP OF PHILADELPHIA · PI NISHISAKI, AKIRA · 2012 to 2012
$98k
AHRQ HHS R03 HS021583AHRQ HHS R03 HS026939AHRQ HHS R18 HS022464AHRQ HHS R18 HS024511NICHD NIH HHS R21 HD089151NIDDK NIH HHS K23 DK119463NIDDK NIH HHS L40 DK103341NIGMS NIH HHS K23 GM110496NIGMS NIH HHS L40 GM102883
6 · The paper itself

Abstract

objectivesTo assess the prevalence of immunocompromised diagnoses among children with severe sepsis and septic shock, and to determine the association between immunocompromised diagnoses and clinical outcomes after adjustment for demographics and illness severity.

designRetrospective multicenter cohort study.

settingEighty-three centers in the Virtual Pediatric Systems database. PATIENTS: Children with severe sepsis or septic shock admitted to a participating PICU between January 1, 2012, and December 31, 2016.

interventionsNone. MEASUREMENTS AND MAIN

resultsAcross 83 centers, we identified 10,768 PICU admissions with an International Classification of Diseases, 9th Revision, Clinical Modification code for severe sepsis or septic shock; 3,021 of these patients (28%) had an immunocompromised diagnosis. To evaluate variation across centers and determine factors associated with PICU mortality, we used mixed-effect logistic regression models. Among patients without hematopoietic cell transplant, congenital immunodeficiency (adjusted odds ratio, 1.90; 95% CI, 1.24-2.92), multiple prior malignancies (adjusted odds ratio, 1.86; 95% CI, 1.15-2.99), and hemophagocytic lymphohistiocytosis (adjusted odds ratio, 3.09; 95% CI, 1.91-4.98) were associated with an increased odds of PICU mortality. Among patients with prior hematopoietic cell transplant, liquid malignancy (adjusted odds ratio, 3.15; 95% CI, 2.09-4.74), congenital immunodeficiency (adjusted odds ratio, 6.94; 95% CI, 3.84-12.53), multiple prior malignancies (adjusted odds ratio, 3.54; 95% CI, 1.80-6.95), and hemophagocytic lymphohistiocytosis (adjusted odds ratio, 2.79; 95% CI, 1.36-5.71) were associated with an increased odds of PICU mortality. PICU mortality varied significantly by center, and a higher mean number of sepsis patients per month in a center was associated with lower PICU mortality (adjusted odds ratio, 0.94; 95% CI, 0.90-0.98). PICU resource utilization varied by immunocompromised diagnosis and history of hematopoietic cell transplant, and among survivors immunocompromised patients have shorter median PICU length of stay compared with patients without immunocompromised diagnoses (p < 0.001).

conclusionsImmunocompromised diagnoses are present in 28% of children with severe sepsis or septic shock. Multiple prior malignancies, hemophagocytic lymphohistiocytosis, congenital immunodeficiency, and hematopoietic cell transplant are independently associated with an increased odds of PICU mortality in children with severe sepsis or septic shock. Significant variation exists in PICU mortality among centers despite adjustment for immunocompromised diagnoses, known risk factors for sepsis-related mortality, and center-level sepsis volume.

Indexed as

Immunocompromised HostAdolescentChildChild, PreschoolFemaleHumansInfantInfant, NewbornIntensive Care Units, PediatricMaleRetrospective StudiesRisk FactorsSepsisShock, Septic

Identifiers

PMID32301846
PMCPMC7311286
OpenAlexW2904240325

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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.