FIDLINE: femorally inserted midline catheter. Retrospective evaluation of clinical outcomes in acute care patients

医学 回顾性队列研究 导管 外科 病历 血栓形成 静脉血栓形成 中心线 中心静脉导管 急症护理 外周穿刺中心静脉导管 静脉通路 镶边技术 并发症 深静脉 锁骨下静脉 外围设备
作者
Genesio Puzio,E. Landolfi,Maria Segneri,Giovanna Passaro
出处
期刊:Journal of Vascular Access [SAGE Publishing]
卷期号:: 11297298261486394-11297298261486394
标识
DOI:10.1177/11297298261486394
摘要

INTRODUCTION: Venous access device (VAD) placement is essential for inpatient care but may be challenging when upper extremity veins are unavailable. Although femorally inserted central catheters are frequently used, a central device is not always required. Femorally inserted midline catheters with a peripheral tip represent a feasible alternative in selected patients. Given the absence of standardized nomenclature, the term "Fidline" was introduced as a fusion of "Femorally inserted peripheral catheter" and "Midline." This retrospective study evaluates indications, feasibility, and complications associated with this device. METHODS: A retrospective case series was conducted using the institutional database to identify all Fidline catheters (FCs) inserted over a 12-month period. A total of 57 patients underwent FC placement; three were excluded because of unavailable post-implantation clinical documentation, leaving 54 patients for analysis. Clinical records were reviewed to collect data on catheter related thrombosis (CRT) and catheter-associated bloodstream infection (CABSI). All FCs (midline, 25 cm length 4 FR single lumen) were implanted in the "superficial femoral vein" at mid-thigh according to the SIF protocol. RESULTS: Fifty-four patients were included (median age 85 years; IQR 69.8-88), with a female predominance (53.7%) and the median length of hospital stay was 17.5 days (IQR, 11.0-32.3). Most patients were admitted to medical wards (57.4%) and 50% had a previously placed VAD. Median catheter dwell time was 8 days (IQR 4.0-13.0), with a median of 5.5 days from admission to catheter placement. During 506 catheter-days, one symptomatic CRT and one CABSI occurred (1.97/1000 catheter-days). At hospital discharge, the catheter remained in situ in 26 patients (48.1%). CONCLUSIONS: FC appears to be a safe and viable VAD option, associated with a low observed rate of major complications in this cohort.
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