Early Antibiotic Exposure and Bronchopulmonary Dysplasia in Very Preterm Infants at Low Risk of Early-Onset Sepsis

被引:1
|
作者
Shi, Wei [1 ,2 ]
Chen, Zheng [1 ,2 ]
Shi, Liping [1 ,2 ]
Jiang, Siyuan [3 ,4 ]
Zhou, Jianguo [3 ,4 ]
Gu, Xinyue [4 ]
Lei, Xiaoping [5 ]
Xiao, Tiantian [6 ]
Zhu, Yanping [7 ]
Qian, Aimin [8 ]
Zhou, Wenhao [3 ,4 ]
Lee, Shoo K. [9 ,10 ]
Du, Lizhong [1 ,2 ]
Yang, Jie [4 ]
Ma, Xiaolu [1 ,2 ]
Hu, Liyuan [3 ,4 ]
机构
[1] Zhejiang Univ, Childrens Hosp, Sch Med, Neonatal Intens Care Unit, 3333 Binsheng Rd, Hangzhou 310052, Peoples R China
[2] Natl Clin Res Ctr Child Hlth, Hangzhou, Peoples R China
[3] Fudan Univ, Childrens Hosp, Dept Neonatol, 399 Wanyuan Rd, Shanghai 201102, Peoples R China
[4] Fudan Univ, Childrens Hosp, Natl Hlth Commiss Key Lab Neonatal Dis, Shanghai, Peoples R China
[5] Southwest Med Univ, Affiliated Hosp, Dept Pediat, Div Neonatol, Luzhou, Peoples R China
[6] Univ Elect Sci & Technol China, Chengdu Womens & Childrens Cent Hosp, Sch Med, Dept Neonatol, Chengdu, Peoples R China
[7] Xinjiang Med Univ, Affiliated Hosp 1, Dept Neonatol, Urumqi, Peoples R China
[8] Nanjing Med Univ, Childrens Hosp, Dept Neonatol, Nanjing, Peoples R China
[9] Mt Sinai Hosp, Maternal Infant Care Res Ctr, Toronto, ON, Canada
[10] Mt Sinai Hosp, Dept Pediat, Toronto, ON, Canada
基金
加拿大健康研究院;
关键词
BIRTH-WEIGHT INFANTS; NECROTIZING ENTEROCOLITIS; ASSOCIATION; OUTCOMES; DEATH;
D O I
10.1001/jamanetworkopen.2024.18831
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ImportanceThe overutilization of antibiotics in very preterm infants (VPIs) at low risk of early-onset sepsis (EOS) is associated with increased mortality and morbidities. Nevertheless, the association of early antibiotic exposure with bronchopulmonary dysplasia (BPD) remains equivocal. ObjectiveTo evaluate the association of varying durations and types of early antibiotic exposure with the incidence of BPD in VPIs at low risk of EOS. Design, Setting, and ParticipantsThis national multicenter cohort study utilized data from the Chinese Neonatal Network (CHNN) which prospectively collected data from January 1, 2019, to December 31, 2021. VPIs less than 32 weeks' gestational age or with birth weight less than 1500 g at low risk of EOS, defined as those born via cesarean delivery, without labor or rupture of membranes, and no clinical evidence of chorioamnionitis, were included. Data analysis was conducted from October 2022 to December 2023. ExposureEarly antibiotic exposure was defined as the total number of calendar days antibiotics were administered within the first week of life, which were further categorized as no exposure, 1 to 4 days of exposure, and 5 to 7 days of exposure. Main Outcomes and MeasuresThe primary outcome was the composite of moderate to severe BPD or mortality at 36 weeks' post menstrual age (PMA). Logistic regression was employed to assess factors associated with BPD or mortality using 2 different models. ResultsOf the 27 176 VPIs included in the CHNN during the study period (14 874 male [54.7%] and 12 302 female [45.3%]), 6510 (23.9%; 3373 male [51.8%] and 3137 female [48.2.%]) were categorized as low risk for EOS. Among them, 1324 (20.3%) had no antibiotic exposure, 1134 (17.4%) received 1 to 4 days of antibiotics treatment, and 4052 (62.2%) received 5 to 7 days of antibiotics treatment. Of the 5186 VPIs who received antibiotics, 4098 (79.0%) received broad-spectrum antibiotics, 888 (17.1%) received narrow-spectrum antibiotics, and 200 (3.9%) received antifungals or other antibiotics. Prolonged exposure (5-7 days) was associated with increased likelihood of moderate to severe BPD or death (adjusted odds ratio [aOR], 1.23; 95% CI, 1.01-1.50). The use of broad-spectrum antibiotics (1-7 days) was also associated with a higher risk of moderate to severe BPD or death (aOR, 1.27; 95% CI, 1.04-1.55). Conclusions and RelevanceIn this cohort study of VPIs at low risk for EOS, exposure to prolonged or broad-spectrum antibiotics was associated with increased risk of developing moderate to severe BPD or mortality. These findings suggest that VPIs exposed to prolonged or broad-spectrum antibiotics early in life should be monitored for adverse outcomes.
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