Gidaro Antonio, Samartin Federica, Salvi Emanuele, Casella Francesco, Cogliati Chiara, Giustivi Davide, Lugli Francesca, Trione Chiara, Melchionda Chiara, Bartoli Arianna, Foschi Antonella, Schiavini Monica, Schiuma Marco, Castelli Roberto, Calloni Maria
Department of Biomedical and Clinical Sciences "Luigi Sacco," University of Milan, Luigi Sacco Hospital, Milan, Italy.
Emergency Department ASST Lodi, Lodi, Italy.
J Vasc Access. 2023 Nov;24(6):1469-1476. doi: 10.1177/11297298221085450. Epub 2022 May 2.
During coronavirus disease 2019 (COVID-19) pandemic, Helmet Continuous Positive Airway Pressure (h-CPAP) has been widely used to treat Acute Hypoxemic Respiratory Failure (AHRF). In COVID-19 patients undergoing h-CPAP a simple short peripheral catheter could be insufficient. According to the European Recommendations for Proper Indication and Use of Peripheral venous access consensus, a stable peripheral Vascular Access Device is indicated for intravenous treatment compatible with the peripheral route scheduled for more than 1 week.
The aim of this prospective study was to evaluate the performance and the potential complications of superficial femoral midline catheters (SFMC) inserted in the Superficial Femoral Vein by direct Seldinger technique with peripheral tip (Arrow®, Teleflex; 20 cm length four FR single lumen and seven FR dual lumen) in AHRF COVID-19 patient. Complications were divided in early (accidental puncture of superficial femoral artery (APSFA); accidental saphenous nerve puncture (ASNP); bleeding) and late (Catheter Related Thrombosis (CRT); Catheter-Related Bloodstream Infections (CRBSI); Accidental Removal (AR); persistent withdrawal occlusion (PWO)).
From 1 October 2020 to 30 June 2021 we conducted a prospective observational study in COVID-19 sub-intensive wards at Luigi Sacco Hospital (Milan).
Hundred seventy five SFMC (mean dwell time 11.1 ± 9.8 days) were implanted in COVID-19 patients, 107 (61.1%) during h-CPAP treatment (10.5 ± 8.9 days), the remaining 68 (38.9%) in patients with severe disease. We recorded two minor immediate/early complications (APSFA without sequelae) and no major complications.The long-term follow-up registered four CRBSI (2.3%-2.5/1000 catheters days (CD)), five CRT (2.9%: 2.6/1000 CD), 22 AR (12.6%; 11.4/1000 CD), 38 PWO (36.5%), 34 of which occurred due to fibroblastic sleeve (32.7%).
SFMC proved to be safe, easy and time-saving. It could be implemented, after a careful benefits and risks evaluation, in particular settings such as h-CPAP, delirium, bleeding risk factors and palliative care patients.
在2019冠状病毒病(COVID-19)大流行期间,头盔式持续气道正压通气(h-CPAP)已被广泛用于治疗急性低氧性呼吸衰竭(AHRF)。在接受h-CPAP治疗的COVID-19患者中,一根简单的短外周导管可能不够用。根据欧洲关于外周静脉通路正确指征和使用的共识建议,对于计划持续超过1周的外周途径兼容的静脉治疗,应使用稳定的外周血管通路装置。
本前瞻性研究的目的是评估在AHRF COVID-19患者中,通过直接塞丁格技术在外股浅静脉插入的外周尖端(Arrow®,Teleflex;20厘米长,四法国规格单腔和七法国规格双腔)股浅中线导管(SFMC)的性能和潜在并发症。并发症分为早期(股浅动脉意外穿刺(APSFA);隐神经意外穿刺(ASNP);出血)和晚期(导管相关血栓形成(CRT);导管相关血流感染(CRBSI);意外拔除(AR);持续性回撤阻塞(PWO))。
2020年10月1日至2021年6月30日,我们在路易吉·萨科医院(米兰)的COVID-19亚重症病房进行了一项前瞻性观察研究。
175根SFMC(平均留置时间11.1±9.8天)植入COVID-19患者体内,107根(61.1%)在h-CPAP治疗期间(10.5±8.9天),其余68根(38.9%)植入重症患者体内。我们记录了2例轻微的即刻/早期并发症(APSFA,无后遗症),无重大并发症。长期随访记录了4例CRBSI(2.3%-2.5/1000导管日(CD)),5例CRT(2.9%:2.6/1000 CD),22例AR(12.6%;11.4/1000 CD),38例PWO(36.5%),其中34例是由于纤维母细胞套形成(32.7%)。
SFMC被证明是安全、简便且省时的。在仔细评估利弊后,它可在特定情况下实施,特别是在h-CPAP、谵妄、出血风险因素和姑息治疗患者等情况下。