TY - JOUR
T1 - Effects of fine particulate matter and its components on emergency room visits for pediatric pneumonia
T2 - A time-stratified case-crossover study
AU - Tsai, Ming Ta
AU - Ho, Yu Ni
AU - Chiang, Charng Yen
AU - Chuang, Po Chun
AU - Pan, Hsiu Yung
AU - Chiu, I. Min
AU - Tsai, Chih Min
AU - Cheng, Fu Jen
N1 - Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/10/2
Y1 - 2021/10/2
N2 - Pneumonia, one of the important causes of death in children, may be induced or aggra-vated by particulate matter (PM). Limited research has examined the association between PM and its constituents and pediatric pneumonia-related emergency department (ED) visits. Measurements of PM2.5, PM10, and four PM2.5 constituents, including elemental carbon (EC), organic carbon (OC), nitrate, and sulfate, were extracted from 2007 to 2010 from one core station and two satellite stations in Kaohsiung City, Taiwan. Furthermore, the medical records of patients under 17 years old who had visited the ED in a medical center and had a diagnosis of pneumonia were collected. We used a time-stratified, case-crossover study design to estimate the effect of PM. The single-pollutant model demonstrated interquartile range increase in PM2.5, PM10, nitrate, OC, and EC on lag 3, which increased the risk of pediatric pneumonia by 18.2% (95% confidence interval (Cl), 8.8‒28.4%), 13.1% (95% CI, 5.1‒21.7%), 29.7% (95% CI, 16.4‒44.5%), 16.8% (95% CI, 4.6‒30.4%), and 14.4% (95% Cl, 6.5‒ 22.9%), respectively. After PM2.5, PM10, and OC were adjusted for, nitrate and EC remained signifi-cant in two-pollutant models. Subgroup analyses revealed that nitrate had a greater effect on children during the warm season (April to September, interaction p = 0.035). In conclusion, pediatric pneumonia ED visit was related to PM2.5 and its constituents. Moreover, PM2.5 constituents, nitrate and EC, were more closely associated with ED visits for pediatric pneumonia, and children seemed to be more susceptible to nitrate during the warm season.
AB - Pneumonia, one of the important causes of death in children, may be induced or aggra-vated by particulate matter (PM). Limited research has examined the association between PM and its constituents and pediatric pneumonia-related emergency department (ED) visits. Measurements of PM2.5, PM10, and four PM2.5 constituents, including elemental carbon (EC), organic carbon (OC), nitrate, and sulfate, were extracted from 2007 to 2010 from one core station and two satellite stations in Kaohsiung City, Taiwan. Furthermore, the medical records of patients under 17 years old who had visited the ED in a medical center and had a diagnosis of pneumonia were collected. We used a time-stratified, case-crossover study design to estimate the effect of PM. The single-pollutant model demonstrated interquartile range increase in PM2.5, PM10, nitrate, OC, and EC on lag 3, which increased the risk of pediatric pneumonia by 18.2% (95% confidence interval (Cl), 8.8‒28.4%), 13.1% (95% CI, 5.1‒21.7%), 29.7% (95% CI, 16.4‒44.5%), 16.8% (95% CI, 4.6‒30.4%), and 14.4% (95% Cl, 6.5‒ 22.9%), respectively. After PM2.5, PM10, and OC were adjusted for, nitrate and EC remained signifi-cant in two-pollutant models. Subgroup analyses revealed that nitrate had a greater effect on children during the warm season (April to September, interaction p = 0.035). In conclusion, pediatric pneumonia ED visit was related to PM2.5 and its constituents. Moreover, PM2.5 constituents, nitrate and EC, were more closely associated with ED visits for pediatric pneumonia, and children seemed to be more susceptible to nitrate during the warm season.
KW - Air pollution
KW - Particulate matter
KW - Particulate matter component
KW - Pediatric
KW - Pneumonia
UR - http://www.scopus.com/inward/record.url?scp=85116669393&partnerID=8YFLogxK
U2 - 10.3390/ijerph182010599
DO - 10.3390/ijerph182010599
M3 - 文章
C2 - 34682345
AN - SCOPUS:85116669393
SN - 1661-7827
VL - 18
JO - International Journal of Environmental Research and Public Health
JF - International Journal of Environmental Research and Public Health
IS - 20
M1 - 599
ER -