A Brief Intervention by Nurses to Reduce the Prescribing of Occluded Peripheral Venous Catheters in the Emergency Department
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 1,680
- 试验地点
- 16
研究概览
简要总结
Peripheral venous catheters are frequently inserted in hospitals, with approximately 25 million placed annually in France (HAS data, 2005). The occluded peripheral venous catheter with extension tubing has become the standard in some emergency departments, offering advantages such as patient mobility, the ability to perform repeated blood draws, and the administration of intravenous medications. A 2018 meta-analysis revealed that one in three devices was unnecessary. The placement of a occluded peripheral venous is associated with a more painful insertion, higher cost, and an increased risk of infection and thromboembolism, and blood samples obtained via the occluded peripheral venous catheter are more often hemolyzed than those obtained by direct venipuncture.
Communication between physicians and nurses is essential to ensure optimal patient care. A brief intervention by the nurse when a physician prescribes a occluded peripheral venous catheter can help clarify the appropriateness of this prescription, which could lead to reduced pain for the patient, time savings for healthcare providers, and material cost savings for the hospital.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Sequential
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients assigned a triage score of 3A, 3B, or 4 according to the French triage scale, or 3 or 4 according to the CIMU triage scale, by the triage nurse
- •Patients with a blood draw order involving the placement of an occluded catheter
- •Age 18 years or older
- •Patients who have read and understood the information sheet
- •Patients who have given their verbal consent to participate in the study
- •Patients enrolled in a social security program
排除标准
- •Patients admitted to the emergency department with a pre-existing intravenous line
- •Patients treated by the Mobile Emergency and Resuscitation Unit outside the hospital
- •Patients with a blocked catheter who did not undergo an initial blood draw
- •Patient with known neurocognitive disorders incompatible with informed consent
- •Pregnant or breastfeeding woman
- •Patient under legal guardianship (guardianship or conservatorship) or patient deprived of liberty
- •Patient refusing to participate in the study
- •Patient participating in another interventional research study
