» Articles » PMID: 33294890

The Relation Between Regular Outpatient Follow-up and Frequency of Emergency Department Visits in Sickle Cell Pediatric Patients

Overview
Journal Saudi Med J
Specialty General Medicine
Date 2020 Dec 9
PMID 33294890
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: To evaluate the relationship between the frequency of ED visits and outpatient department (OPD) follow-up in sickle cell disease (SCD) pediatric patients.

Methods:   A retrospective cohort study included 247 SCD pediatric patients between January 2016 and December 2018 at the Maternity and Children Hospital, Department of Pediatrics, Al Medinah Al Munawarah, Saudi Arabia. Data were extracted from electronic medical record system; patient demographics, medications, frequency of emergency department (ED) and OPD visits. Pearson correlation coefficient, linear regression and independent sample t-test were applied.

Results: There was no significant correlation (95% CI [-0.013- 0.233]; p=0.07) between the frequency of ED and OPD visits. However, a significant correlation was found between ED visits and missed OPD appointments. Thus, linear regression was applied and indicated that one missed OPD appointment is associated with 1.92 ED visits, (95% CI: 0.19-0.42; p less than 0.001). Also, a higher rate of ED visits was observed when compared with other studies, with a high ED reliance of 43%.

Conclusion: This study found that regular OPD visits could improve SCD management, as a directly proportional relationship between the frequency of ED visits and missed OPD appointments along with high ED reliance.

Citing Articles

Outcome of Pediatric Patients With Sickle Cell Anemia Admitted With Fever: A Retrospective Single-Center Study.

Zolaly M, Alharbi A, Algrafi S, Balkhair M, Aljohani J, Quordi M Cureus. 2024; 16(9):e69570.

PMID: 39421130 PMC: 11483867. DOI: 10.7759/cureus.69570.


Gaps during pediatric to adult care transfer escalate acute resource utilization in sickle cell disease.

Howell K, Kayle M, Smeltzer M, Nolan V, Mathias J, Nelson M Blood Adv. 2024; 8(14):3679-3685.

PMID: 38809136 PMC: 11284702. DOI: 10.1182/bloodadvances.2023011268.


The Health Belief Model Modifying Factors Associated with Missed Clinic Appointments among Individuals with Sickle Cell Disease in the Jazan Province, Saudi Arabia.

Alhazmi S, Maashi A, Shabaan S, Majrashi A, Thakir M, Almetahr S Healthcare (Basel). 2022; 10(12).

PMID: 36553900 PMC: 9778402. DOI: 10.3390/healthcare10122376.


Treatment Options That Reduce the Duration of Sickle Cell Vaso-Occlusive Crises: A Systematic Review.

Akindele A, Jalkh A, Eastmond A, Shetty C, Rizvi S, Sharaf J Cureus. 2022; 14(8):e28337.

PMID: 36176876 PMC: 9510888. DOI: 10.7759/cureus.28337.

References
1.
Keikhaei B, Yousefi H, Bahadoram M . Hydroxyurea: Clinical and Hematological Effects in Patients With Sickle Cell Anemia. Glob J Health Sci. 2015; 8(3):252-6. PMC: 4803938. DOI: 10.5539/gjhs.v8n3p252. View

2.
Morgan S, Chang A, Alqatari M, Pines J . Non-emergency department interventions to reduce ED utilization: a systematic review. Acad Emerg Med. 2013; 20(10):969-85. PMC: 4038086. DOI: 10.1111/acem.12219. View

3.
Kroner E, Hoffmann R, Brousseau D . Emergency department reliance: a discriminatory measure of frequent emergency department users. Pediatrics. 2009; 125(1):133-8. DOI: 10.1542/peds.2009-0960. View

4.
Alsaeed E, Farhat G, Assiri A, Memish Z, Ahmed E, Saeedi M . Distribution of hemoglobinopathy disorders in Saudi Arabia based on data from the premarital screening and genetic counseling program, 2011-2015. J Epidemiol Glob Health. 2018; 7 Suppl 1:S41-S47. PMC: 7386442. DOI: 10.1016/j.jegh.2017.12.001. View

5.
Nietert P, Silverstein M, Abboud M . Sickle cell anaemia: epidemiology and cost of illness. Pharmacoeconomics. 2002; 20(6):357-66. DOI: 10.2165/00019053-200220060-00001. View