Evaluation of different safety-engineered protection mechanisms of port access needles using a lifelike model of vascular access routes.

IF 2.7 Q3 ENGINEERING, BIOMEDICAL
Frontiers in medical technology Pub Date : 2025-04-03 eCollection Date: 2025-01-01 DOI:10.3389/fmedt.2025.1505184
Feline Gabler, Pierre Heiden, Peter Deibert, Daniel Steinmann
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引用次数: 0

Abstract

Background: Preventing needlestick injuries caused by hypodermic needles is crucial for healthcare personnel. In this context, port access needles play an important role. However, systematic comparisons of different safety-engineered port access needles have not been conducted. Therefore, we evaluated differences in product characteristics and user preferences of safety-engineered protection mechanisms of port access needles.

Methods: Port puncture was performed using port access needles with four different safety mechanisms: (a) EZ Huber™ PFM Medical, (b) Gripstick® Safety OMT, (c) Gripper Micro® Smiths Medical and (d) pps ct® Vygon. Each needle type was used in three consecutive tries: an uninstructed first handling, after which instructions were given according to operating manual. Subsequently, a first and second trial were conducted. Study endpoints included successful activation, activation time, way of activation (one hand or two hands), correct activation, possible risk of needlestick injury, possibility of deactivation and preferred safety mechanism.

Results: Overall, successful activation rate during the second trial was equal for all four devices (100%). Median activation time was (a) 6 s, (b) 3 s, (c) 11 s and (d) 6 s. Single-handed activation during the second trial was (a) 0%, (b) 75%, (c) 1% and (d) 1%. Single-handed activation after further preparation with two hands during the second trial was (a) 0%, (b) 0%, (c) 0% and (d) 50%. Correct activation during the second trial was (a) 97%, (b) 66%, (c) 19% and (d) 44%. Possible risk of needlestick injury during the second trial was highest with (b). Possibility of deactivation was (a) 75%, (b) 94%, (c) 97% and (d) 22%. Individual preferences for each system were (a) n = 5, (b) n = 2, (c) n = 1 and (d) n = 24. The main written reasons given for preference were the safety protection mechanism and handling of the port needle.

Conclusion: We have shown significant differences regarding product characteristics of safety mechanisms of port access needles. Our evaluation approach provides specific data for both, technical (e.g., single-handed activation) and personal device selection criteria (e.g., preference of the safety mechanism).

利用血管通路的逼真模型评价不同安全工程的端口通路针保护机制。
背景:预防由皮下注射针头引起的针刺损伤对卫生保健人员至关重要。在这种情况下,端口访问针起着重要的作用。然而,系统比较不同的安全工程港口接入针尚未进行。因此,我们评估了产品特性的差异和用户偏好的安全工程保护机制的端口接入针。方法:使用具有四种不同安全机制的端口接入针进行端口穿刺:(a) EZ Huber™PFM Medical, (b) Gripstick®safety OMT, (c) Gripper Micro®Smiths Medical和(d) pps ct®Vygon。每种针型连续使用三次:第一次无指导操作,之后根据操作手册进行指导。随后进行了第一次和第二次试验。研究终点包括成功激活、激活时间、激活方式(单手或双手)、正确激活、针刺损伤的可能风险、失活的可能性和首选安全机制。结果:总体而言,在第二次试验期间,所有四个设备的成功激活率相同(100%)。中位激活时间为(a) 6 s, (b) 3 s, (c) 11 s, (d) 6 s。在第二次试验中,单手激活为(a) 0%, (b) 75%, (c) 1%和(d) 1%。在第二次试验中,双手进一步制备后的单手激活为(a) 0%, (b) 0%, (c) 0%和(d) 50%。第二次试验的正确激活率为(a) 97%, (b) 66%, (c) 19%, (d) 44%。在第二次试验中,针刺伤的可能风险最高(b)。失活可能性为(a) 75%, (b) 94%, (c) 97%, (d) 22%。每个系统的个体偏好分别为(a) n = 5, (b) n = 2, (c) n = 1, (d) n = 24。首选的主要书面理由是安全保护机制和端口针的处理。结论:我们在端口接入针的产品特性和安全机制方面存在显著差异。我们的评估方法为技术(例如,单手激活)和个人设备选择标准(例如,安全机制的偏好)提供了具体的数据。
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
CiteScore
3.70
自引率
0.00%
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审稿时长
13 weeks
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