Effects of continuous venovenous hemofiltration on vancomycin trough concentrations in critically ill children

被引:1
|
作者
Peng, Lengyue [1 ]
Gao, Yawen [1 ]
Zhang, Guangli [1 ]
Tian, Xiaoyin [1 ]
Xu, Huiting [1 ]
Yu, Qinghong [1 ]
Cheng, Jie [1 ]
Li, Yuanyuan [1 ]
Li, Qinyuan [1 ]
Chen, Yingfu [2 ]
Zhao, Wei [3 ]
Luo, Zhengxiu [1 ]
机构
[1] Chongqing Med Univ, Natl Clin Res Ctr Child Hlth & Disorders, Childrens Hosp,Minist Educ,Key Lab Child Dev & Di, Dept Resp Med,Chongqing Key Lab Pediat, Chongqing, Peoples R China
[2] Chongqing Med Univ, Natl Clin Res Ctr Child Hlth & Disorders, Minist Educ,Key Lab Child Dev & Disorders,Childre, Chongqing Key Lab Pediat,Dept Pediat Intens Care, Chongqing, Peoples R China
[3] Shandong Univ, Sch Pharmaceut Sci, Dept Clin Pharm, Jinan, Peoples R China
关键词
Vancomycin; continuous venovenous hemofiltration (CVVH); children; concentration; RENAL REPLACEMENT THERAPY; INTENSIVE-CARE; RECOMMENDATIONS; GUIDELINES; MORTALITY; SEPSIS; RISK;
D O I
10.21037/atm-20-4005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Vancomycin trough concentrations are associated with clinical outcomes and drug adverse effects. This study investigates the effects of continuous venovenous hemofiltration (CVVH) on vancomycin trough concentrations in critically ill children with a vancomycin dosage of 40-60 mg/kg/day. Methods: Children with steady-state vancomycin trough concentrations admitted to the pediatric intensive care unit (PICU) between January 2016 and December 2019 were retrospectively enrolled. Patients were divided into CVVH and non-CVVH groups according to treatment differences and renal function. Vancomycin trough concentrations were then compared between the groups, and risk factors for supratherapeutic trough concentrations (>20 mg/L) were analyzed with logistic regression. Results: Of the 119 patients included, 35 were enrolled in the CVVH group and 84 in the non-CVVH group. Median vancomycin trough concentrations were significantly higher in the CVVH group than those in the non-CVVH group [14.9 (IQR =9.6-19.6) vs. 9.3 (IQR =7.0-13.4), P<0.001] and the proportion of therapeutic trough concentrations (10-20 mg/L) was similar between CVVH and non-CVVH groups (54.3% vs. 39.3%, P=0.133). However, CVVH therapy patients had a significantly higher proportion of supratherapeutic trough concentrations (20.0% vs. 1.2%, P=0.001) compared to the non-CVVH group. Multivariate analysis demonstrated that the Pediatric Risk of Mortality (PRISM) III score >= 28 (OR =13.7; 95% CI, 1.4-137.0; P=0.026] was an independent risk factor for supratherapeutic trough concentrations in critically ill patients. Conclusions: CVVH therapy affects vancomycin trough concentrations and is associated with supratherapeutic concentrations with a 40-60 mg/kg/day vancomycin dosage. PRISM III scores >= 28 may serve as an independent risk factor for supratherapeutic trough concentrations in children receiving CVVH therapy.
引用
收藏
页数:9
相关论文
共 50 条
  • [21] Continuous infusion versus intermittent infusion of vancomycin in critically ill patients undergoing continuous venovenous hemofiltration: a prospective interventional study
    Xu, Jinhui
    Duan, Lufen
    Li, Jiahui
    Chen, Fang
    Xu, Xiaowen
    Lu, Jian
    Zhuang, Zhiwei
    Cao, Yifei
    Yuan, Yunlong
    Liu, Xin
    Sun, Jiantong
    Zhou, Qin
    Shi, Lu
    Tang, Lian
    BMC INFECTIOUS DISEASES, 2022, 22 (01)
  • [22] Continuous infusion versus intermittent infusion of vancomycin in critically ill patients undergoing continuous venovenous hemofiltration: a prospective interventional study
    Jinhui Xu
    Lufen Duan
    Jiahui Li
    Fang Chen
    Xiaowen Xu
    Jian Lu
    Zhiwei Zhuang
    Yifei Cao
    Yunlong Yuan
    Xin Liu
    Jiantong Sun
    Qin Zhou
    Lu Shi
    Lian Tang
    BMC Infectious Diseases, 22
  • [23] CONTINUOUS ARTERIOVENOUS HEMOFILTRATION IN CRITICALLY ILL CHILDREN
    LATTA, K
    KRULL, F
    WILKEN, M
    BURDELSKI, M
    RODECK, B
    OFFNER, G
    PEDIATRIC NEPHROLOGY, 1994, 8 (03) : 334 - 337
  • [24] Determinants of vancomycin clearance by continuous venovenous hemofiltration and continuous venovenous hemodialysis
    Joy, MS
    Matzke, GR
    Frye, RF
    Palevsky, PM
    AMERICAN JOURNAL OF KIDNEY DISEASES, 1998, 31 (06) : 1019 - 1027
  • [25] Effect of continuous venovenous hemofiltration with dialysis on lactate clearance in critically ill patients
    Levraut, J
    Ciebiera, JP
    Jambou, P
    Ichai, C
    Labib, Y
    Grimaud, D
    CRITICAL CARE MEDICINE, 1997, 25 (01) : 58 - 62
  • [26] Amino Acid Loss during Continuous Venovenous Hemofiltration in Critically Ill Patients
    Stapel, Sandra N.
    de Boer, Ruben J.
    Thoral, Patrick J.
    Vervloet, Marc G.
    Girbes, Armand R. J.
    Oudemans-van Straaten, Heleen M.
    BLOOD PURIFICATION, 2019, 48 (04) : 321 - 329
  • [27] Pharmacokinetics of cefoperazone/sulbactam in critically ill patients receiving continuous venovenous hemofiltration
    Chunlu Gao
    Jing Tong
    Kaijiang Yu
    Zhidan Sun
    Ran An
    Zhimin Du
    European Journal of Clinical Pharmacology, 2016, 72 : 823 - 830
  • [28] GENTAMICIN AND VANCOMYCIN REMOVAL BY CONTINUOUS VENOVENOUS HEMOFILTRATION
    THOMSON, AH
    GRANT, AC
    RODGER, RSC
    HUGHES, RL
    DICP-THE ANNALS OF PHARMACOTHERAPY, 1991, 25 (02): : 127 - 129
  • [29] OPTIMIZE CEFEPIME DOSING IN CRITICALLY ILL PATIENTS RECEIVING CONTINUOUS VENOVENOUS HEMOFILTRATION
    Lin, Hsin
    Boidin, Clement
    Evans, Danielle
    Lopez, Natasha
    Healy, Daniel
    Serpico, Elena
    Goutelle, Sylvain
    Roberts, Jason
    CRITICAL CARE MEDICINE, 2019, 47
  • [30] Ceftolozane-Tazobactam Pharmacokinetics in a Critically Ill Patient on Continuous Venovenous Hemofiltration
    Oliver, Wesley D.
    Heil, Emily L.
    Gonzales, Jeffrey P.
    Mehrotra, Shailly
    Robinett, Kathryn
    Saleeb, Paul
    Nicolau, David P.
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2016, 60 (03) : 1899 - 1901