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Updated: Jul 27, 2026

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Risk Factors for 30-Day Readmission in Adults with Sickle Cell Disease
Max A Brodsky1, Mark Rodeghier2, Maureen Sanger3
1College of Medicine MD Program, Drexel University, Philadelphia, Pa.
Identifying modifiable risk factors for hospital readmission in sickle cell disease (SCD) is crucial. Ensuring access to a primary care provider and improving discharge planning can significantly reduce 30-day readmissions for SCD patients.
Area of Science:
- Hematology
- Public Health
- Clinical Medicine
Background:
- Hospital readmission within 30 days is a key quality indicator.
- Few modifiable risk factors for 30-day readmissions in adults with sickle cell disease (SCD) are identified.
- Vasoocclusive pain episodes are a common reason for SCD readmissions.
Purpose of the Study:
- To identify potentially modifiable risk factors for 30-day hospital readmission in adults with SCD.
- To analyze risk factors specifically for readmission due to vasoocclusive pain episodes.
- To inform strategies for reducing readmission rates in SCD patients.
Main Methods:
- Retrospective review of medical records of 88 adult SCD patients over 3.5 years.
- Analysis of 158 first admissions for vasoocclusive pain episodes.
- Multivariable modeling of seven risk factors including PCP listing and prior hospitalization history.
Main Results:
- Absence of a listed primary care provider (PCP) was associated with lower readmission risk (OR 0.38).
- Higher number of prior hospitalizations for vasoocclusive pain episodes significantly increased readmission risk (OR 1.30).
- Median time to readmission was 11 days.
Conclusions:
- Ensuring access to a primary care provider may reduce 30-day readmissions in adults with SCD.
- Improved discharge planning is recommended to decrease readmission rates.
- Targeting patients with frequent prior hospitalizations may be beneficial.
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