Princess Máxima Centre for Paediatric Oncology, Utrecht, The Netherlands.
Department of Immunology, Wilhelmina Children's Hospital, Utrecht, The Netherlands.
J Hosp Infect. 2024 Oct;152:56-65. doi: 10.1016/j.jhin.2024.06.009. Epub 2024 Jul 14.
Taurolidine-citrate(-heparin) lock solutions (TCHL) are suggested as a promising and safe method for the prevention of central-line-associated bloodstream infections (CLABSI).
To investigate the efficacy of TCHL for the prevention of CLABSI in paediatric oncology patients.
An assessor-blinded randomized controlled trial at the Princess Máxima Centre for paediatric oncology, the Netherlands, was performed from 2020 to 2023. Paediatric oncology patients receiving a tunnelled central venous access device (CVAD) were eligible. A total of 462 patients were required to compare the TCHL to the heparin-only lock (HL). Patients were followed-up for the first 90 days after CVAD insertion. The primary outcome was the incidence of the first CLABSI from CVAD insertion until the end of follow-up. Intention-to-treat and per-protocol analyses were performed.
In total, 232 were randomized in the HL and 231 in the TCHL group. A total of 47 CLABSIs were observed. The intention-to-treat analysis showed that a CLABSI was observed in 26 (11.2%) of the HL group patients versus 21 (9.1%) of the TCHL group patients; incidence rate ratio (IRR) of 0.81 (95% confidence interval (CI): 0.46-1.45) in favour of the TCHL group. The per-protocol analysis showed that a CLABSI was observed in 10 (7.9%) of the HL group patients versus 6 (4.8%) of the TCHL group patients; IRR of 0.59 (95% CI: 0.21-1.62) in favour of the TCHL group. Adverse events were more common in the TCHL group but rarely reported.
No difference was detected between the TCHL and HL in the incidence of CLABSI in paediatric oncology patients.
牛磺酸-柠檬酸盐(肝素)封管液(TCHL)被认为是预防中心静脉导管相关血流感染(CLABSI)的一种有前途且安全的方法。
研究 TCHL 预防儿科肿瘤患者 CLABSI 的效果。
荷兰马克西玛公主儿童医院进行了一项评估者设盲的随机对照试验,纳入 2020 年至 2023 年期间接受经皮隧道式中心静脉置管(CVAD)的儿科肿瘤患者。共需纳入 462 例患者,以比较 TCHL 与肝素单封管(HL)的效果。患者在 CVAD 植入后随访 90 天。主要结局为从 CVAD 植入到随访结束时首次发生 CLABSI 的发生率。采用意向治疗和方案分析。
共有 232 例患者被随机分入 HL 组,231 例患者分入 TCHL 组。共观察到 47 例 CLABSIs。意向治疗分析显示,HL 组有 26 例(11.2%)发生 CLABSI,TCHL 组有 21 例(9.1%);TCHL 组的发病率比(IRR)为 0.81(95%置信区间(CI):0.46-1.45)。方案分析显示,HL 组有 10 例(7.9%)发生 CLABSI,TCHL 组有 6 例(4.8%)发生 CLABSI;TCHL 组的 IRR 为 0.59(95% CI:0.21-1.62)。TCHL 组的不良事件更为常见,但很少报告。
在儿科肿瘤患者中,TCHL 与 HL 在 CLABSI 发生率方面无差异。