妊娠期和产后暴露于野火烟雾以及早年长期使用呼吸道药物。

Environmental research, health : ERH Pub Date : 2024-12-01 Epub Date: 2024-09-11 DOI:10.1088/2752-5309/ad748c
Hanna Jardel, Kristen M Rappazzo, Thomas J Luben, Corinna Keeler, Brooke S Staley, Cavin K Ward-Caviness, Cassandra R O'Lenick, Meghan E Rebuli, Yuzhi Xi, Michelle Hernandez, Ann Chelminski, Ilona Jaspers, Ana G Rappold, Radhika Dhingra
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引用次数: 0

摘要

随着野火发生频率和严重程度的增加,烟雾暴露会对呼吸系统造成越来越多的不良影响。虽然烟雾暴露对儿童呼吸系统的急性影响已被记录在案,但对长期后遗症的研究却很少。在此,我们的目标是研究妊娠期和产后暴露于野火烟雾与幼儿期长期使用处方药治疗呼吸系统疾病之间的关联。利用 Merative MarketScan 索赔数据,我们对 2010 年 1 月 1 日至 2014 年 12 月 31 日期间在西部各州出生的足月儿童建立了至少跟踪三年的队列。利用 NOAA 危险绘图系统数据,我们确定了在每个暴露期内,大都会统计区 (MSA) 中大于 25% 的人口每周被烟雾覆盖的平均天数。烟雾暴露期按孕期和产后两个 12 周来定义。药物使用基于呼吸道适应症(上呼吸道、下呼吸道或任何呼吸道疾病),并分为长期使用(使用 30 天)(PU)和多次长期使用(至少两次长期使用)(MPU)两种结果。我们使用了带有随机截距的澳门金沙在线娱乐平台回归模型,并对儿童性别、出生季节和出生年份进行了调整。不同的暴露期和呼吸系统结果会产生不同的关联,在妊娠三个月和产后前 12 周暴露于下呼吸道药物后,发生 MPU 的风险升高(RR 分别为 1.15,95% CI 0.98,1.35;RR 分别为 1.21,95% CI 1.05,1.40)。只有男婴在妊娠三个月内接触任何呼吸道疾病,其死亡率才会增加(男婴 RR 1.22,95% CI 1.00,1.50;女婴 RR 0.93,95% CI 0.66,1.31)。通过对处方索赔数据的新颖利用,这项研究确定了怀孕三个月和产后前 12 周的关键发育窗口期,在此期间,环境吸入性灾难事件可能会影响较长期的呼吸系统健康。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gestational and postnatal exposure to wildfire smoke and prolonged use of respiratory medications in early life.

As wildfire frequency and severity increases, smoke exposures will cause increasingly more adverse respiratory effects. While acute respiratory effects of smoke exposure have been documented in children, longer term sequelae are largely unstudied. Our objective here was to examine the association between gestational and postnatal exposure to wildfire smoke and prolonged use of prescription medication for respiratory conditions in early childhood. Using Merative MarketScan claims data, we created cohorts of term children born in western states between 1 January 2010-31 December 2014 followed for at least three years. Using NOAA Hazard Mapping System data, we determined the average number of days a week that >25% of the population in a metropolitan statistical area (MSA) was covered by smoke within each exposure period. The exposure periods were defined by trimester and two 12 week postnatal periods. Medication use was based on respiratory indication (upper respiratory, lower respiratory, or any respiratory condition) and categorized into outcomes of prolonged use (⩾30 d use) (PU) and multiple prolonged uses (at least two prolonged uses) (MPU). We used logistic regression models with random intercepts for MSAs adjusted for child sex, birth season, and birth year. Associations differed by exposure period and respiratory outcome, with elevated risk of MPU of lower respiratory medications following exposure in the third trimester and the first 12 postnatal weeks (RR 1.15, 95% CI 0.98, 1.35; RR 1.21, 95% CI 1.05, 1.40, respectively). Exposure in the third trimester was associated with an increase in MPU of any respiratory among males infants only (male RR 1.22, 95% CI 1.00, 1.50; female RR 0.93, 95% CI 0.66, 1.31). Through novel use of prescription claims data, this work identifies critical developmental windows in the 3rd trimester and first 12 postnatal weeks during which environmental inhalational disaster events may impact longer-term respiratory health.

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