Evidence map›Paper›PMID 40526379›Full record

ArticleJAMA network open2025

Hospital Readmissions Among People With Sickle Cell Disease.

Ruchika Goel, Ping Yang, Xianming Zhu, Eshan U Patel, Elizabeth P Crowe, Herleen Rai, Evan M Bloch, Aaron A R Tobian

Abstract read
In one paragraph

Article in JAMA network open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

8 authors.

Ruchika GoelDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Ping YangDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Xianming ZhuDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Eshan U PatelDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Elizabeth P CroweDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Herleen RaiDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Evan M BlochDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Aaron A R TobianDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Funding

T-cell depletion and maintenance of the HIV-1 latent reservoir in distinct tissue compartmentsR01DK131926 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI Melissa Laird Smith, AARON A TOBIAN · 2022 to 2026
$3.6M
NIDDK NIH HHS R01 DK131926
6 · The paper itself

Abstract

Importance: While advances in the management and treatment of sickle cell disease (SCD), the most common inherited disorder in the United States, have improved outcomes, hospital readmissions remain a significant concern. Thirty-day hospital readmissions is a key quality-of-care indicator; however, there are limited contemporary nationally representative data on SCD readmissions. Objective: To characterize national trends in SCD-related readmissions in the United States and describe factors associated with readmission among patients with SCD. Design, Setting, and Participants: This cohort study included patients with SCD aged 18 years and older. Patients were identified in the Nationwide Readmissions Database (NRD), an all-payer database of US hospitalizations, using International Statistical Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) codes. Data were collected from January 2016 to December 2021 and analyzed from May to September 2024. Main Outcomes and Measures: Readmission was defined as subsequent admission within 30 days of hospitalization discharge using the Centers for Medicare & Medicaid Services methodology. The 30-day all-cause unplanned readmission risk among adults with SCD was estimated, and the trend in 30-day readmissions among adults with and without SCD was assessed by calendar year from 2016 to 2021. Survey-weighted mixed-effect Poisson regressions were used to identify factors associated with readmission. Results: From 2016 to 2021, 140 096 807 all-cause index hospitalizations and 592 951 SCD-related index hospitalizations were analyzed. Patients with SCD had a stable readmission risk of approximately 34% (annual range, 32.6%-34.3%), significantly higher per year than the approximately 12% readmission risk among patients without SCD (annual range, 12.0%-12.2%) (P < .001). In 2021, there were 92 536 index admissions from 37 410 unique patients with SCD (median [IQR] age, 34 [26-46] years; 22 484 [60.1%] female), with 30 467 readmissions. Younger patients (aged 18-29 years) had the highest readmission risk at 35.1%. In multivariable model among patients with SCD, patients from the highest-income zip codes had lower readmission risk than those from lower-income areas (adjusted risk ratio [aRR], 0.90; 95% CI, 0.84-0.97). Admissions paid by Medicare and Medicaid were associated with higher readmission risk than private insurance (Medicare: aRR, 1.67; 95% CI, 1.56-1.78; Medicaid: aRR,1.53; 95% CI, 1.43-1.63). Vaso-occlusive crises at index admission were associated with higher readmission risk (aRR, 1.31; 95% CI, 1.25-1.37). Fewer readmissions were observed in patients receiving simple (aRR, 0.86; 95% CI, 0.82-0.91) and exchange (aRR, 0.78; 95% CI, 0.61-0.99) red blood cell transfusions. Conclusions and Relevance: In this cohort study with nationally representative data, patients with SCD had a significantly higher readmission risk than patients without SCD. Preventative, disease-modifying, and curative interventions are needed to reduce readmission risks and improve outcomes for patients with SCD.

Indexed as

Anemia, Sickle CellPatient ReadmissionAdolescentAdultCohort StudiesFemaleHumansMaleMiddle AgedRisk FactorsUnited StatesYoung Adult

Identifiers

PMID40526379
PMCPMC12175023

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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.