Immunization adherence among children with sickle cell disease and sickle cell trait: Results of a population‐based study

Author:

Shi Jiajing Scarlette1ORCID,Sutaria Ankit2,Lakshmanan Sangeetha1,Attell Brandon1,Zhou Mei1,Tang Amy34ORCID,Eckman James4,Snyder Angela1ORCID

Affiliation:

1. Georgia Health Policy Center Andrew Young School of Policy Studies Georgia State University Atlanta Georgia USA

2. Georgia Department of Public Health Atlanta Georgia USA

3. Aflac Cancer and Blood Disorders Center Children's Healthcare of Atlanta Atlanta Georgia USA

4. Emory University School of Medicine Atlanta Georgia USA

Abstract

AbstractIntroductionDespite the importance of timely vaccine completion for protection from infectious disease, there is limited knowledge of the immunization adherence rates of children with sickle cell disease (SCD).MethodsThis is a retrospective cohort study comparing the immunization rates of children with SCD to those with sickle cell trait between 2008 and 2019 in Georgia. Completion rates for each vaccine and the proportion of children with up‐to‐date status at 24 and 35 months were calculated and compared between the cohorts. Chi‐square tests with odds ratios (OR) for differences and 95% confidence intervals (CIs) were reported on the overall up‐to‐date rates and rates for individual vaccines at 24 and 35 months for the two cohorts.ResultsChildren with SCD had higher up‐to‐date rates than children with sickle cell trait at 24 and 35 months. At 35 months, the overall up‐to‐date rates (OR = 1.17; 95% CI, 1.04‐1.31; = .004) and the four‐dose pneumococcal conjugate vaccine series (OR = 1.36; 95% CI, 1.18‐1.57; < .001) were significantly different between the groups. Both cohorts had the highest completion rates for the hepatitis B series and the lowest rates for the varicella vaccine. Doses of diphtheria, tetanus, and acellular pertussis vaccine; varicella; and pneumococcal conjugate vaccines were most commonly missed by children in both cohorts.ConclusionsChildren with SCD have better immunization coverage than children with sickle cell trait, but there is an opportunity for improvement. Policymakers and healthcare professionals should focus on increasing access to care coordination services among children with SCD to ensure on‐time and preventive healthcare services.

Funder

Centers for Disease Control and Prevention

Publisher

Wiley

Reference59 articles.

1. Reducing Health Care Disparities in Sickle Cell Disease: A Review

2. Trends in Sickle Cell Disease–Related Mortality in the United States, 1979 to 2017

3. Centers for Disease Control and Prevention.What is sickle cell disease? Centers for Disease Control and Prevention. August 18 2022. Accessed September 26 2022.https://www.cdc.gov/ncbddd/sicklecell/facts.html

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