Pediatrics, Neonatology, The Children's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA
Pediatrics, Neonatology, The Children's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Arch Dis Child Fetal Neonatal Ed. 2021 Sep;106(5):467-473. doi: 10.1136/archdischild-2020-320664. Epub 2021 Jan 21.
Determine risk of death or neurodevelopmental impairment (NDI) in infants with late-onset sepsis (LOS) versus late-onset, antibiotic-treated, blood culture-negative conditions (LOCNC).
Retrospective cohort study.
24 neonatal centres.
Infants born 1/1/2006-31/12/2014, at 22-26 weeks gestation, with birth weight 401-1000 g and surviving >7 days were included. Infants with early-onset sepsis, necrotising enterocolitis, intestinal perforation or both LOS and LOCNC were excluded.
LOS and LOCNC were defined as antibiotic administration for ≥5 days with and without a positive blood/cerebrospinal fluid culture, respectively. Infants with these diagnoses were also compared with infants with neither condition.
Death or NDI was assessed at 18-26 months corrected age follow-up. Modified Poisson regression models were used to estimate relative risks adjusting for covariates occurring ≤7 days of age.
Of 7354 eligible infants, 3940 met inclusion criteria: 786 (20%) with LOS, 1601 (41%) with LOCNC and 1553 (39%) with neither. Infants with LOS had higher adjusted relative risk (95% CI) for death/NDI (1.14 (1.05 to 1.25)) and death before follow-up (1.71 (1.44 to 2.03)) than those with LOCNC. Among survivors, risk for NDI did not differ between the two groups (0.99 (0.86 to 1.13)) but was higher for LOCNC infants (1.17 (1.04 to 1.31)) compared with unaffected infants.
Infants with LOS had higher risk of death, but not NDI, compared with infants with LOCNC. Surviving infants with LOCNC had higher risk of NDI compared with unaffected infants. Improving outcomes for infants with LOCNC requires study of the underlying conditions and the potential impact of antibiotic exposure.
确定晚发型败血症(LOS)与晚发型、抗生素治疗、血培养阴性的条件(LOCNC)相比,婴儿死亡或神经发育障碍(NDI)的风险。
回顾性队列研究。
24 个新生儿中心。
纳入 2006 年 1 月 1 日至 2014 年 12 月 31 日出生,胎龄 22-26 周,出生体重 401-1000g,存活>7 天的婴儿。排除早发型败血症、坏死性小肠结肠炎、肠穿孔或 LOS 和 LOCNC 均存在的婴儿。
LOS 和 LOCNC 的定义分别为抗生素治疗≥5 天,同时血/脑脊液培养阳性和阴性。这些诊断的婴儿也与没有这些条件的婴儿进行了比较。
在 18-26 个月的校正年龄随访中,评估了死亡或 NDI 的情况。使用修正泊松回归模型,在≤7 天龄时发生的协变量进行调整,以估计相对风险。
在 7354 名符合条件的婴儿中,有 3940 名符合纳入标准:786 名(20%)患有 LOS,1601 名(41%)患有 LOCNC,1553 名(39%)均未患有。与 LOCNC 相比,患有 LOS 的婴儿死亡/NDI 的调整后相对风险(95%CI)更高(1.14(1.05 至 1.25))和随访前死亡的风险更高(1.71(1.44 至 2.03))。在幸存者中,两组之间的 NDI 风险没有差异(0.99(0.86 至 1.13)),但 LOCNC 婴儿(1.17(1.04 至 1.31))的风险高于未受影响的婴儿。
与 LOCNC 婴儿相比,患有 LOS 的婴儿死亡风险更高,但 NDI 风险没有增加。与未受影响的婴儿相比,患有 LOCNC 的幸存婴儿发生 NDI 的风险更高。改善 LOCNC 婴儿的结局需要研究潜在疾病和抗生素暴露的潜在影响。