Characteristics of Emergency Department Visits Made by Individuals With Sickle Cell Disease in the U.S., 1999-2020

被引:10
作者
Attell, Brandon K. [1 ]
Barrett, Patricia M. [1 ]
Pace, Betty S. [2 ]
Mclemore, Morgan L. [3 ]
Mcgee, Blake T. [4 ]
Oshe, Rewo [5 ]
Digirolamo, Ann M. [1 ]
Cohen, Lindsey L. [5 ]
Snyder, Angela B. [1 ]
机构
[1] Georgia State Univ, Georgia Hlth Policy Ctr, POB 3992, Atlanta, GA 30302 USA
[2] Augusta Univ, Dept Pediat, Med Coll Georgia, Augusta, GA USA
[3] Emory Univ, Sch Med, Dept Hematol & Med Oncol, Atlanta, GA USA
[4] Georgia State Univ, Sch Nursing, Atlanta, GA USA
[5] Georgia State Univ, Coll Arts & Sci, Dept Psychol, Atlanta, GA USA
来源
AJPM FOCUS | 2024年 / 3卷 / 01期
关键词
UNITED-STATES; PAIN; CARE; IMPACT; SURVEILLANCE; TRANSITION; MANAGEMENT; CHILDREN; SURVIVAL; TRENDS;
D O I
10.1016/j.focus.2023.100158
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Introduction: Individuals living with sickle cell disease experience high levels of morbidity that result in frequent utilization of the emergency department. The objective of this study was to provide updated national estimates of emergency department utilization associated with sickle cell disease in the U.S. Methods: Data from the National Hospital Ambulatory Medical Care Survey for the years 1999-2020 were analyzed. Complex survey analysis was utilized to produce national estimates overall and by patient age groups. Results: On average, approximately 222,612 emergency department visits occurred annually among individuals with sickle cell disease, a nearly 13% increase from prior estimates. The annual volume of emergency department visits steadily increased over time, and pain remains the most common patient-cited reason for visiting the emergency department. Patient-reported pain levels for individuals with sickle cell disease were high, with 64% of visits associated with severe pain and 21% associated with moderate pain. Public insurance sources continue to cover most visits, with Medicaid paying for 60% of visits and Medicare paying for 12% of visits. The average time spent in the emergency department increased from previous estimates by about an hour, rising to approximately 6 hours. The average wait time to see a provider was 53 minutes. Conclusions: Utilization of the emergency department by individuals living with sickle cell disease remains high, especially for pain. With more than half of patients with sickle cell disease reporting severe pain levels, emergency department staff should be prepared to assess and treat sickle cell disease-related pain following evidence-based guidelines and recommendations. The findings of this study can help improve care in this population. AJPM Focus 2024;3(1):100158. (c) 2023 The Authors. Published by Elsevier Inc. on behalf of The American Journal of Preventive Medicine Board of Governors. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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页数:10
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