Evidence map›Paper›PMID 40464592›Full record

ArticleCancer research communications2025

Real-world Data on Risk Factors for Emergency Department Visits to Treat Outpatient Chemotherapy-Associated Toxicities.

Sanja Karovic, Erik Dvergsten, Chiara Pierattini, Ana Barac, Lauren Fay, Timothy L Cannon, Kathleen K Harnden, Jeanny B Aragon-Ching, Raymund S Cuevo, Michael L Maitland and 1 more

Abstract read
In one paragraph

Article in Cancer research communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Observational
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.

Sanja KarovicInova Schar Cancer Institute, Fairfax, Virginia.ORCID 0000-0003-4633-8114
Erik DvergstenInova Schar Cancer Institute, Fairfax, Virginia.ORCID 0000-0003-3324-6413
Chiara PierattiniInova Schar Cancer Institute, Fairfax, Virginia.ORCID 0000-0002-2547-2544
Ana BaracInova Schar Heart and Vascular, Inova Health System, Falls Church, Virginia.ORCID 0000-0002-9935-8904
Lauren FayInova Schar Cancer Institute, Fairfax, Virginia.ORCID 0009-0008-5284-9440
Timothy L CannonInova Schar Cancer Institute, Fairfax, Virginia.ORCID 0000-0001-5033-3071
Kathleen K HarndenInova Schar Cancer Institute, Fairfax, Virginia.ORCID 0009-0009-1152-3484
Jeanny B Aragon-ChingInova Schar Cancer Institute, Fairfax, Virginia.ORCID 0000-0002-6714-141X
Raymund S CuevoInova Schar Cancer Institute, Fairfax, Virginia.ORCID 0009-0001-5357-5831
Michael L MaitlandInova Schar Cancer Institute, Fairfax, Virginia.ORCID 0000-0002-2476-5732
John F DeekenInova Schar Cancer Institute, Fairfax, Virginia.ORCID 0000-0001-8414-1553

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Centers for Medicare & Medicaid Services Hospital Outpatient Quality Reporting Program's OP-35 rule penalizes health systems that have a higher-than-expected rate of emergency department (ED) visits or inpatient admissions for 10 potentially preventable conditions within 30 days of receiving chemotherapy. Identifying patients at risk for toxicities and resultant acute care could lead to reducing the rate of such events, improving patient care, and reducing costs. We identified patients with cancer seen in the ED at our institution between January 1, 2018, and December 31, 2021, for one of the OP-35 toxicities who had received chemotherapy within the previous 30 days and analyzed demographic factors using zero-truncated Poisson regression. We further analyzed comorbid conditions for risk factors by matching by demographics and cancer type a cohort of patients without ED visits due to OP-35 events. A total of 1,618 patients were identified. The most frequent events were pain, sepsis, and fever. Thirty-nine percent had two or more visits during the study, and among those patients, the most frequent cancer types were gastrointestinal (32%) and breast (22%) cancers. Race, age, and sex were associated with an increased risk of events. In the matched cohort analysis, five comorbidities were statistically significant (P < 0.05) with event risk: history of coagulopathy/pulmonary emboli, myocardial infarction, cardiac arrhythmias, depression, and weight loss (concordance = 0.58). Forty-seven percent of patients with an event had at least one of these five comorbidities. Future interventions may concentrate on resources to monitor patients based on the risk assessment established in this study. SIGNIFICANCE: Cardiovascular comorbidities, cancer cachexia, and depression were associated with increased risk for ED visits due to OP-35 events throughout cancer treatment. Future interventions may concentrate on resources to monitor patients based on the risk assessment established in this real-world data study.

Indexed as

Antineoplastic AgentsDrug-Related Side Effects and Adverse ReactionsEmergency Service, HospitalNeoplasmsAdultAgedAged, 80 and overComorbidityEmergency Room VisitsFemaleHumansMaleMiddle AgedOutpatientsRisk FactorsAntineoplastic Agents

Identifiers

PMID40464592
PMCPMC12169210

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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.