Related Experiment Video
Updated: Aug 10, 2026

Characterization of Sickling During Controlled Automated Deoxygenation with Oxygen Gradient Ektacytometry
Published on: November 5, 2019
Fall Risk Factors in Older Patients with Sickle Cell Disease (SCD): A Narrative Review
Salome Bwayo Weaver1, E'Shay Winfield Winfield1, Dhakrit Rungkittawattanakul1
11Howard University College of Pharmacy, Washington DC.
Insights
Older adults with sickle cell disease (SCD) face increased fall risks due to factors like poor physical function and cognitive issues. Early identification of these risks is crucial for prevention and management.
Area of Science:
- Geriatrics
- Hematology
- Neurology
Background:
- Sickle cell disease (SCD) affects over 100,000 Black individuals in the US.
- Fall risk in older adults with SCD is understudied, despite overlapping risk factors with the general geriatric population.
- Existing literature primarily focuses on fall risks in adults aged 65+, leaving a gap for older SCD patients.
Purpose of the Study:
- To identify and describe factors contributing to increased fall risk in older patients diagnosed with sickle cell disease.
- To synthesize current evidence on fall risk factors specific to the aging SCD population.
Main Methods:
- A comprehensive literature search was conducted on PubMed and MEDLINE.
- Keywords included "sickle cell disease," "falls," "risk factors," "older adults," "management," and "prevention."
- Fifteen relevant studies were identified and synthesized.
Main Results:
- Key fall risk factors identified in older adults with SCD include reduced physical functioning, dizziness, imbalance, and cognitive impairment.
- Visual deficits, vitamin D deficiency, osteoporosis, polypharmacy, and silent cerebral ischemia (SCI) were also significant risk factors.
- These factors highlight a complex interplay of physiological and medical issues.
Conclusions:
- Falls in older adults with SCD result from a combination of neuromusculoskeletal issues, sensory deficits, cognitive vulnerability, and medication effects.
- Current evidence is limited, and specific clinical guidelines for SCD fall prevention are lacking.
- Clinicians should proactively assess older SCD patients for identified fall risk factors.
Abstract:
Background: Sickle cell disease (SCD) is a hematologic disorder that affects approximately 100,000 Black individuals in the United States. Although extensive literature describes fall risk factors in adults 65 years and older, evidence regarding fall risk in older adults with SCD remains limited and largely anecdotal. Risk factors for falls in adults aged 50 years and older with SCD overlap with those observed in the general geriatric population aged 65 years and older. Objective: The objective of this study was to describe factors associated with increased fall risk in older patients with SCD. Data Sources: A literature search of PubMed and MEDLINE was performed using the following search terms: "sickle cell disease", "falls", "risk factors", "older adults", "management," and "prevention," as well as combinations of these terms. Data Synthesis: Fifteen studies were identified. Reduced physical functioning, dizziness/imbalance, cognitive impairment, visual deficits, vitamin D deficiency, osteoporosis, polypharmacy, and silent cerebral ischemia (SCI) were identified as risk factors for SCD-related falls. Discussion: Fall risk factors, prevention, and management strategies in patients are understudied and complex. Fall-prevention strategies used for older adults are also important for patients with SCD. Conclusion: Falls in older adults with SCD appear to reflect a convergence of neuromusculoskeletal complications, sensory deficits, cognitive vulnerability, and medication-related effects; however, the evidence base remains limited, and SCD-specific guidance is lacking. Clinicians should evaluate older adults with SCD for the aforementioned fall risk factors.
Related Concept Videos
Venous Thrombosis IV: Nursing Management
Peripheral Artery Disease IV: Nursing Management
Degenerative Disc Disease I: Introduction
