Evidence map›Paper›PMID 41178192›Full record

ArticleTurkish journal of haematology : official journal of Turkish Society of Haematology2025

All-Cause and Exacerbation-Related Readmissions in Thrombotic Microangiopathy Requiring Plasmapheresis: A Population-Based Cohort Study

Alexander R Thebert, Toru Yoshino, Sae X Morita, Misa Ito, Ayman Qasrawi, Hirotaka Kato

Abstract read
In one paragraph

Article in Turkish journal of haematology : official journal of Turkish Society of Haematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Alexander R ThebertUniversity of Kentucky College of Medicine, Department of Internal Medicine, Lexington, KY, United States
Toru YoshinoJacobi Medical Center, Albert Einstein College of Medicine, Department of Medicine, Bronx, NY, United StatesORCID 0000-0003-1586-2706
Sae X MoritaSBH Health System, Department of Medicine, Bronx, NY, United StatesORCID 0000-0002-6830-8672
Misa ItoUniversity of Kentucky College of Medicine, Department of Internal Medicine and Pediatrics, Lexington, KY, United StatesORCID 0000-0001-7712-5213
Ayman QasrawiUniversity of Kentucky College of Medicine and Markey Cancer Center, Division of Hematology, Bone Marrow Transplant & Cellular Therapy, Lexington, KY, United StatesORCID 0000-0002-2233-6539
Hirotaka KatoUniversity of Kentucky College of Medicine, Division of Hospital Medicine, Lexington, KY, United StatesORCID 0000-0002-2593-0795

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Thrombotic microangiopathy (TMA) is a serious condition characterized by microangiopathic hemolytic anemia and thrombocytopenia, with high exacerbation rates. This study examined all-cause and exacerbation-related readmission risks among patients hospitalized with TMA requiring plasmapheresis. Materials and Methods: Secondary analysis of the 2020 Nationwide Readmission Database was conducted, including discharge data from non-federal hospitals in 31 U.S. states. Patients aged 18 years or older admitted non-electively with a primary or secondary diagnosis of TMA requiring plasmapheresis were included. Exacerbation-related readmission was defined as subsequent admission requiring plasmapheresis within 7 or 30 days after the original discharge. Multivariable logistic regression and Cox proportional hazards models were used to assess readmission risks, adjusting for demographics, comorbidities, and predisposing factors. Results: Among an estimated 1393 patients, 791 (56.8%) had predisposing conditions. All-cause readmissions were more frequent in patients with predisposing conditions (26.2% vs. 21.9%), while exacerbation-related readmissions were more common in TMA-only patients (9.0% vs. 3.4% at 7 days; 13.7% vs. 6.4% at 30 days). Most exacerbations occurred within 14 days after discharge. No patients treated with caplacizumab experienced exacerbation. TMA-only patients had a 2.1-times higher risk of 30-day exacerbation-related readmissions (adjusted hazard ratio: 2.10, p=0.04). Rural residence and patient-directed discharge were potential risk factors for exacerbation-related readmissions. Conclusions: These findings highlight the need for improved post-discharge care and treatment strategies to prevent readmissions. Further studies should explore interventions to reduce exacerbation-related readmissions, particularly in high-risk populations.

Indexed as

Patient ReadmissionPlasmapheresisThrombotic MicroangiopathiesAdultAgedCohort StudiesFemaleHumansMaleMiddle AgedRisk FactorsUnited StatesDatabaseMicroangiopathyNationwideReadmissionThrombotic

Identifiers

PMID41178192
PMCPMC12671254

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