Javascript must be enabled to continue!
Sickle cell disease complications: prevalence and resource utilization
View through CrossRef
Abstract
This study evaluated the prevalence rate of vaso-occlusive crisis (VOC) episodes, rates of uncomplicated and complicated VOC episodes, and the primary reasons for emergency room (ER) visits and inpatient admissions for sickle cell disease (SCD) patients. The Medicaid Analytic extracts database was used to identify adult SCD patients using claims from 01JUL2009-31DEC2012. The date of the first observed SCD claim was designated as the index date. Patients were required to have continuous medical and pharmacy benefits for ≥6 months baseline and ≥12 months follow-up period. Patient demographics, baseline clinical characteristics, the rate of uncomplicated and complicated VOC (VOC with concomitant SCD complications) episodes, and reasons for ER visits and inpatient stays were analyzed descriptively. A total of 8,521 patients were included in the analysis, with a median age of 30 years. The average follow-up period was 2.7 years. The rate of VOC episodes anytime in the follow-up was 3.31 in person-years. During the first-year follow-up period, an average of 2.79 VOC episodes were identified per SCD patients, with 1.06 VOC episodes treated in inpatient setting and 0.90 VOC episodes in ER without admission. A total of 76,154 VOC episodes were identified during the entire follow-up period for the overall SCD patients. Most of the VOC episodes (70.3% [n=53,523]) were uncomplicated episodes, and 29.7% were complicated episodes. Using primary diagnosis claims only, the most frequent complications during the VOC episode were infectious diseases (25.9%), fever (21.8%), and pulmonary disorders (16.2%). Among ER and hospitalizations related to VOC or SCD complication, ~85.0% had VOCs as the primary reason for admission; 15.0% had SCD complications as the primary reason. In summary, SCD and its related comorbidities and complications result in high acute health care utilization. In addition, VOC remains the primary reason for SCD patients’ ER visits and inpatient admissions.
Title: Sickle cell disease complications: prevalence and resource utilization
Description:
Abstract
This study evaluated the prevalence rate of vaso-occlusive crisis (VOC) episodes, rates of uncomplicated and complicated VOC episodes, and the primary reasons for emergency room (ER) visits and inpatient admissions for sickle cell disease (SCD) patients.
The Medicaid Analytic extracts database was used to identify adult SCD patients using claims from 01JUL2009-31DEC2012.
The date of the first observed SCD claim was designated as the index date.
Patients were required to have continuous medical and pharmacy benefits for ≥6 months baseline and ≥12 months follow-up period.
Patient demographics, baseline clinical characteristics, the rate of uncomplicated and complicated VOC (VOC with concomitant SCD complications) episodes, and reasons for ER visits and inpatient stays were analyzed descriptively.
A total of 8,521 patients were included in the analysis, with a median age of 30 years.
The average follow-up period was 2.
7 years.
The rate of VOC episodes anytime in the follow-up was 3.
31 in person-years.
During the first-year follow-up period, an average of 2.
79 VOC episodes were identified per SCD patients, with 1.
06 VOC episodes treated in inpatient setting and 0.
90 VOC episodes in ER without admission.
A total of 76,154 VOC episodes were identified during the entire follow-up period for the overall SCD patients.
Most of the VOC episodes (70.
3% [n=53,523]) were uncomplicated episodes, and 29.
7% were complicated episodes.
Using primary diagnosis claims only, the most frequent complications during the VOC episode were infectious diseases (25.
9%), fever (21.
8%), and pulmonary disorders (16.
2%).
Among ER and hospitalizations related to VOC or SCD complication, ~85.
0% had VOCs as the primary reason for admission; 15.
0% had SCD complications as the primary reason.
In summary, SCD and its related comorbidities and complications result in high acute health care utilization.
In addition, VOC remains the primary reason for SCD patients’ ER visits and inpatient admissions.
Related Results
Adverse pregnancy, fetal and neonatal outcomes in women with sickle cell disease in a Middle Eastern country
Adverse pregnancy, fetal and neonatal outcomes in women with sickle cell disease in a Middle Eastern country
Background: Sickle cell disease in pregnancy is associated with high maternal and fetal mortality. However, studies reporting pregnancy, fetal, and neonatal outcomes in women with ...
Complex Collision Tumors: A Systematic Review
Complex Collision Tumors: A Systematic Review
Abstract
Introduction: A collision tumor consists of two distinct neoplastic components located within the same organ, separated by stromal tissue, without histological intermixing...
Selected Testing of Newborns for Sickle Cell Disease
Selected Testing of Newborns for Sickle Cell Disease
There are two main reasons for sickle cell testing: the early detection of those with sickle cell disease and the detection of the carrier state, sickle cell trait. The mortality o...
Microalbuminuria among Egyptian Children and Adult with Sickle Cell Hemoglobinopathy, Single Institution Study.
Microalbuminuria among Egyptian Children and Adult with Sickle Cell Hemoglobinopathy, Single Institution Study.
Abstract
Introduction: Renal failure is one of the most serious complications of sickle cell diseases; it affects 5% – 18% and leads to early death. Protienuria is h...
Sickle Cell Disease and Uterine Fibroids: Evaluation of the Prevalence of Fibroids across Sickle Cell Genotypes
Sickle Cell Disease and Uterine Fibroids: Evaluation of the Prevalence of Fibroids across Sickle Cell Genotypes
ABSTRACT
Introduction
Uterine fibroids are known to affect >80% of premenopausal American women of African descent, and sick...
Systematic Evaluation of Sickle Cell-Related Organ Damage and Complications: Implications for Sickle Cell Disease Management.
Systematic Evaluation of Sickle Cell-Related Organ Damage and Complications: Implications for Sickle Cell Disease Management.
Abstract
Sickle cell disease (SCD) is characterised by acute complications such as the painful vaso-occlusive crisis, acute chest syndrome and stroke. Although these...
Frequency of Common Chromosomal Abnormalities in Patients with Idiopathic Acquired Aplastic Anemia
Frequency of Common Chromosomal Abnormalities in Patients with Idiopathic Acquired Aplastic Anemia
Objective: To determine the frequency of common chromosomal aberrations in local population idiopathic determine the frequency of common chromosomal aberrations in local population...
Exchange Transfusion In Adult Patients With Sickle Cell Disease With Refractory Vaso-Occlusive Crises
Exchange Transfusion In Adult Patients With Sickle Cell Disease With Refractory Vaso-Occlusive Crises
Sickle cell disease occurs in 1/500 African-American births. Pain is one of the most common complications of sickle cell disease and is associated with depression, anxiety, decreas...

