[Clinical application study of midline catheter in vasopressor therapy].

Q3 Medicine
Runling Guo, Jianhua Wu, Xiaoying Ren, Chaoli Guo
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引用次数: 0

Abstract

Objective: To evaluate the safety and necessity of vasopressor infusion through midline catheter.

Methods: A convenient sampling method was used for a controlled study. A total of 88 adult patients who used vasopressors admitted to respiratory intensive care unit (RICU) of Fenyang Hospital in Shanxi Province from June 2022 to June 2023 were enrolled as the research subjects. A total of 44 patients who were infused with vasopressors through peripherally inserted central venous catheter (PICC) from June to December 2022 were enrolled as the PICC group, and 44 patients who were infused with vasopressors through midline catheter from January to June 2023 were enrolled as the midline catheter group. Both groups of patients used the modified Sedinger technique under the guidance of B-ultrasound for puncture and catheter placement. The middle 1/3 site between the cubital fossa and the axilla was selected. The catheters were 5 Fr double lumen. After catheter placement, the patients were followed until catheter removal, death, or 30 days (whichever came first). Based on the Infusion therapy standards of practice revised by American Infusion Nurses Society (INS), and combined with the results of previous preliminary tests, the safety evaluation was conducted on incomplete catheter obstruction, catheter-related bloodstream infection (CRBSI), phlebitis, thrombus within the catheter during extubation, redness of the puncture site (but no infection), and exudation of the puncture site in the two groups of patients.

Results: There were no statistical differences in gender, age, catheter indwelling time, and primary disease between the two groups, indicating that the baseline data of the two groups were balanced and comparable. No CRBSI or phlebitis occurred in both groups during the observation period after catheterization. One patient in both groups had exudation at the puncture site [both were 2.27% (1/44)]. Compared with the PICC group, the incidence of incomplete catheter obstruction, thrombus within the catheter during extubation, redness of the puncture site (but no infection) in the midline catheter group were lowered [incomplete catheter obstruction: 4.55% (2/44) vs. 6.82% (3/44), thrombus within the catheter during extubation: 0% (0/44) vs. 2.27% (1/44), redness of the puncture site (but no infection): 0% (0/44) vs. 4.55% (2/44)], the overall incidence was significantly decreased [6.82% (3/44) vs. 15.91% (7/44), P < 0.01].

Conclusions: Administering vasopressor through a midline catheter can reduce the incidence of catheter-related complications, decrease the rate of central venous catheterization, and reduce the financial burden on patients.

[中线导管在血管加压疗法中的临床应用研究]。
目的:评估通过中线导管输注血管加压素的安全性和必要性:评估通过中线导管输注血管加压素的安全性和必要性:方法:采用方便抽样法进行对照研究。研究对象为 2022 年 6 月至 2023 年 6 月入住山西省汾阳医院呼吸重症监护室(RICU)的 88 例使用血管加压素的成年患者。2022年6月至12月通过外周置入中心静脉导管(PICC)输注血管加压素的44例患者为PICC组,2023年1月至6月通过中线导管输注血管加压素的44例患者为中线导管组。两组患者均在 B 超引导下使用改良 Sedinger 技术进行穿刺和导管置入。选择肘窝和腋窝之间的中间 1/3 位置。导管为 5 Fr 双腔导管。置入导管后,对患者进行随访,直至导管拔出、死亡或 30 天(以先到者为准)。根据美国输液护士协会(INS)修订的输液治疗实践标准,并结合之前的初步测试结果,对两组患者的导管不完全阻塞、导管相关血流感染(CRBSI)、静脉炎、拔管时导管内血栓、穿刺部位发红(但无感染)、穿刺部位渗出等情况进行了安全性评估:两组患者在性别、年龄、导管留置时间和原发疾病方面均无统计学差异,表明两组患者的基线数据均衡且具有可比性。在导管插入后的观察期内,两组患者均未发生 CRBSI 或静脉炎。两组均有一名患者出现穿刺部位渗液[均为 2.27%(1/44)]。与 PICC 组相比,中线导管组导管不完全阻塞、拔管时导管内血栓、穿刺部位发红(但无感染)的发生率降低[导管不完全阻塞:4.55%(2/44)]:4.55% (2/44) vs. 6.82% (3/44),拔管时导管内有血栓:0% (0/44) vs. 2.27% (1/44),穿刺部位发红(但无感染):0% (0/44) vs. 4.55% (2/44)],总发生率显著下降[6.82% (3/44) vs. 15.91% (7/44),P <0.01]:通过中线导管给予血管加压素可减少导管相关并发症的发生率,降低中心静脉导管插入率,减轻患者的经济负担。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Zhonghua wei zhong bing ji jiu yi xue
Zhonghua wei zhong bing ji jiu yi xue Medicine-Critical Care and Intensive Care Medicine
CiteScore
1.00
自引率
0.00%
发文量
42
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