Multi-level determinants of timely routine childhood vaccinations in The Gambia: Findings from a nationwide analysis

IF 4.5 3区 医学 Q2 IMMUNOLOGY
Oghenebrume Wariri , Chigozie Edson Utazi , Uduak Okomo , Winfred Dotse-Gborgbortsi , Malick Sogur , Sidat Fofana , Kris A. Murray , Chris Grundy , Beate Kampmann
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引用次数: 0

Abstract

Introduction

Achieving the ambitious goals of the Immunisation Agenda 2030 (IA2030) requires a deeper understanding of factors influencing under-vaccination, including timely vaccination. This study investigates the demand- and supply-side determinants influencing the timely uptake of key childhood vaccines scheduled throughout the first year of life in The Gambia.

Methods

We used two nationally-representative datasets: the 2019–20 Gambian Demographic and Health Survey and the 2019 national immunisation facility mapping. Using Bayesian multi-level binary logistic regression models, we identified key factors significantly associated with timely vaccination for five key vaccines: birth dose of hepatitis-B (HepB0), first, second, and third doses of the pentavalent vaccine (Penta1, Penta2, Penta3), and first-dose of measles-containing vaccine (MCV1) in children aged 12–35 months. We report the adjusted Odds Ratios (aORs) and 95 % Credible Intervals (95 % CIs) in each case.

Results

We found that demand-side factors, such as ethnicity, household wealth status, maternal education, maternal parity, and the duration of the household's residency in its current location, were the most common drivers of timely childhood vaccination. However, supply-side factors such as travel time to the nearest immunisation clinic, availability of cold-storage and staffing numbers in the nearest immunisation clinic were also significant determinants. Furthermore, the determinants varied across specific vaccines and the timing of doses. For example, delivery in a health facility (aOR = 1.58, 95 %CI: 1.02–2.53), living less than 30 min (aOR = 2.11, 95 %CI: 1.2–8.84) and living between 30 and 60 min (aOR = 3.68, 95 %CI: 1.1–14.99) from a fixed-immunisation clinic was associated with timely HepB0, a time-sensitive vaccine that must be administered within 24 h of birth. On the other hand, children who received Penta1 and Penta2 on time were three- to five-fold more likely to receive subsequent doses on time (Penta2 and Penta3, respectively). Finally, proximity to an immunisation facility with functional vaccine cold-storage was a significant supply-side determinant of timely MCV1 (aOR = 1.4, 95 %CI: 1.09–1.99).

Conclusions

These findings provide valuable insights for programme managers and policymakers. By prioritising interventions and allocating scarce resources based on these identified determinants, they can maximize their impact and ensure children in The Gambia receive timely vaccinations throughout their first year of life, contributing to IA2030 goals.
冈比亚儿童及时接种常规疫苗的多层面决定因素:全国性分析结果。
导言:要实现《2030 年免疫议程》(IA2030)的宏伟目标,就必须深入了解接种不足的影响因素,包括及时接种疫苗。本研究调查了影响冈比亚儿童在出生后第一年及时接种主要儿童疫苗的需求方和供应方决定因素:我们使用了两个具有全国代表性的数据集:2019-20 年冈比亚人口与健康调查和 2019 年全国免疫接种设施分布图。利用贝叶斯多层次二元逻辑回归模型,我们确定了与及时接种五种关键疫苗显著相关的关键因素:出生时接种的乙肝疫苗(HepB0)、五价疫苗(Penta1、Penta2、Penta3)的第一、第二和第三剂,以及 12-35 个月儿童含麻疹成分疫苗(MCV1)的第一剂。我们报告了每种情况下调整后的几率比(aORs)和 95 % 可信区间(95 % CIs):我们发现,需求方因素,如种族、家庭财富状况、孕产妇教育程度、孕产妇均等以及家庭在当前地点的居住时间,是影响儿童及时接种疫苗的最常见因素。然而,供应方因素也是重要的决定因素,如前往最近免疫接种诊所的交通时间、冷藏库的可用性以及最近免疫接种诊所的工作人员数量。此外,不同疫苗和剂量时间的决定因素也各不相同。例如,在医疗机构分娩(aOR = 1.58,95 %CI:1.02-2.53)、距离固定免疫诊所不足 30 分钟(aOR = 2.11,95 %CI:1.2-8.84)和距离固定免疫诊所 30-60 分钟(aOR = 3.68,95 %CI:1.1-14.99)与及时接种乙肝疫苗(一种必须在出生后 24 小时内接种的时间敏感性疫苗)有关。另一方面,按时接种 Penta1 和 Penta2 的儿童按时接种后续剂量(分别为 Penta2 和 Penta3)的几率要高出三到五倍。最后,是否靠近具有疫苗冷藏功能的免疫接种设施是及时接种 MCV1 的一个重要供应方决定因素(aOR = 1.4,95 %CI: 1.09-1.99):这些发现为项目管理人员和政策制定者提供了宝贵的见解。通过根据这些已确定的决定因素确定干预措施的优先次序和分配稀缺资源,他们可以最大限度地发挥其影响,并确保冈比亚儿童在出生后第一年内及时接种疫苗,从而为实现 2030 年国际行动计划目标做出贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Vaccine
Vaccine 医学-免疫学
CiteScore
8.70
自引率
5.50%
发文量
992
审稿时长
131 days
期刊介绍: Vaccine is unique in publishing the highest quality science across all disciplines relevant to the field of vaccinology - all original article submissions across basic and clinical research, vaccine manufacturing, history, public policy, behavioral science and ethics, social sciences, safety, and many other related areas are welcomed. The submission categories as given in the Guide for Authors indicate where we receive the most papers. Papers outside these major areas are also welcome and authors are encouraged to contact us with specific questions.
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