一项随机对照试验:FemoStop装置和沙袋压力对经股动脉冠状动脉造影后脱鞘止血和减少穿刺部位并发症的效果比较

Hojjat Niknam Sarabi, Zahra Farsi, Younes Ghelich, Behzad Moradi, Seyyed Hossein Mousavi
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FemoStop devices and sandbags were used in the experimental and control groups to control angiography complications, respectively. The patient’s individual characteristics questionnaire, visual analog scale, checklist of complications, and laboratory indicators were used for data collection. Pain intensity, heart rate, respiratory rate, temperature, systolic and diastolic blood pressure, arterial oxygen saturation, and the amount of hematoma and bleeding of patients before, after 15 minutes, 1 h, 2 h, 2.5 h, 3 h, 3.5 h, 4 h, 4.5 h, 5 h, and 6 h were measured after the intervention. Results: The trend of changes in pain intensity (P < 0.001), heart rate (P = 0.036), and systolic blood pressure (P < 0.001) of patients in the experimental and control groups after the intervention was significant, and in patients who had used the FemoStop device, it was less than the control group. 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引用次数: 0

摘要

背景:处理动脉鞘切除术后常见和不愉快的并发症是血管造影患者护理的目标和重点之一。目的:本研究旨在设计和制造一种FemoStop装置,并比较其与沙袋压力在脱鞘止血和减少经股冠状动脉造影后穿刺部位并发症方面的效果。方法:该随机对照试验于2019 - 2021年进行。本研究采用方便抽样的方法,将80例在德黑兰一家心脏血管医院接受选择性经股冠状动脉造影的患者随机分为实验组(n = 40)和对照组(n = 40)。实验组和对照组分别采用FemoStop装置和沙袋控制血管造影并发症。采用患者个体特征问卷、视觉模拟量表、并发症清单和实验室指标进行数据收集。测量干预前、干预后15分钟、1小时、2小时、2.5小时、3小时、3.5小时、4小时、4.5小时、5小时、6小时患者的疼痛强度、心率、呼吸频率、体温、收缩压、舒张压、动脉血氧饱和度、血肿量、出血量。结果:疼痛强度变化趋势(P <0.001)、心率(P = 0.036)和收缩压(P <干预后实验组和对照组患者的差异有统计学意义(0.001),而使用FemoStop装置的患者的差异小于对照组。两组患者呼吸频率(P = 0.308)、舒张压(P = 0.089)、动脉血氧饱和度(P = 0.205)、体温(P = 0.195)变化均无统计学意义。两组在这些变量及12个测量阶段血肿出血量方面均无显著差异。结论:与经股动脉冠状动脉造影后使用沙袋相比,FemoStop装置可减少患者的并发症,如疼痛强度、较低的心率和收缩压。因此,考虑到并发症较少,建议进行更多的研究来证实该装置的使用对患者并发症的控制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of the Effectiveness of the FemoStop Device and Sandbag Pressure on Hemostasis During Sheath Removal and Reducing Puncture Site Complications Following Transfemoral Coronary Angiography: A Randomized Controlled Trial
Background: Management of common and unpleasant complications following the removal of the arterial sheath is one of the goals and priorities of nursing care in patients undergoing angiography. Objectives: This study aimed to design and manufacture a FemoStop device and compare its effectiveness with sandbag pressure on hemostasis during sheath removal and reducing puncture site complications following transfemoral coronary angiography. Methods: This randomized controlled trial was conducted between 2019 and 2021. Eighty patients undergoing elective transfemoral coronary angiography referred to a Heart and Vascular Hospital in Tehran were recruited by convenience sampling and were randomly assigned to experimental (n = 40) and control (n = 40) groups. FemoStop devices and sandbags were used in the experimental and control groups to control angiography complications, respectively. The patient’s individual characteristics questionnaire, visual analog scale, checklist of complications, and laboratory indicators were used for data collection. Pain intensity, heart rate, respiratory rate, temperature, systolic and diastolic blood pressure, arterial oxygen saturation, and the amount of hematoma and bleeding of patients before, after 15 minutes, 1 h, 2 h, 2.5 h, 3 h, 3.5 h, 4 h, 4.5 h, 5 h, and 6 h were measured after the intervention. Results: The trend of changes in pain intensity (P < 0.001), heart rate (P = 0.036), and systolic blood pressure (P < 0.001) of patients in the experimental and control groups after the intervention was significant, and in patients who had used the FemoStop device, it was less than the control group. However, the changes in respiratory rate (P = 0.308), diastolic blood pressure (P = 0.089), arterial oxygen saturation (P = 0.205), and temperature (P = 0.195) of patients in the 2 groups were not significant. The 2 groups were not significantly different in terms of these variables and the amount of hematoma and bleeding in the 12 stages of measurement. Conclusions: Compared to using a sandbag after transfemoral coronary angiography, the FemoStop device leads to fewer complications, such as pain intensity, lower heart rate, and systolic blood pressure in patients. Therefore, considering fewer complications, it is suggested to conduct more studies to confirm the use of this device to control complications in patients.
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