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Evaluating Adult Patient Temperatures During Lower Spinal Surgery

2018年5月3日 更新者:Jean M. Guyer、Mayo Clinic

Comparing Patient Temperatures in Adults During Lower Spinal Surgery Using Either a Heated Ventilator Circuit or a Standard Ventilator Circuit With a Heat-Moisture Exchanger

The purpose of this study is to evaluate patients' temperatures after using one of two ventilator circuits (breathing systems): the ANAPOD™ Heat and Humidification System (ANAPOD™ system) or the standard ventilator circuit with a heat-moisture exchanger (standard ventilator). The ANAPOD™ system will provide additional heat and humidity to patients through their breathing tube while the standard ventilator will not. The investigators are doing this research study to find out if the ventilator circuit providing additional heat and humidity will keep patients warmer during surgery and after surgery.

研究概览

详细说明

Patients were randomly assigned to either the treatment group or the control group prior to surgery. Prior to induction, patients in the control group were given inspiratory gas at ambient air temperature (20-22 degrees Celsius) and patients in the treatment group were given inspiratory gas at warmed temperatures (40-41 degrees Celsius). All patients were induced with general anesthesia in the supine position and repositioned prone following endotracheal intubation and placement of an esophageal stethoscope with a temperature sensor, as per usual hospital practice. Esophageal temperatures were recorded within 30 minutes of the baseline esophageal temperature and every 10 minutes thereafter for the first hour post-induction. All patients had a blanket and forced air warming applied to their lower extremities and upper back at 43 degrees Celsius after draping. All patients had esophageal temperature measurements recorded every 30 minutes until the patient was repositioned supine. Core temperatures were recorded four hours post-induction for those patients reaching that timeframe.

研究类型

介入性

注册 (实际的)

70

阶段

  • 不适用

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Elective spine surgery anticipated greater than three hours in duration
  • Posterior approach
  • An operative site between lumbar one and sacral one
  • Involving two or more levels with fusion and/or instrumentation and/or revisions
  • American Society of Anesthesiologists (ASA) Status of I-III

Exclusion Criteria:

  • Patients with a tracheostomy
  • Preoperative temperature >38°C or <36°C on the day of surgery
  • Active infection or erythema to the back
  • White blood cell count greater than 10,500/microliter (mcL)

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:预防
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
实验性的:Heated Ventilator Circuit
Heated and humidified inspired gases using the ANAPOD™ Heat and Humidification System (Westmed; Tucson, Arizona, USA) circuit prior to induction of general anesthesia in addition to standard ventilation and temperature management.
active heat and humidification during anesthesia by warming inspire gases without a heat-moisture exchanger
其他名称:
  • ANAPOD™ Heat and Humidification System
有源比较器:Standard Ventilator Circuit
Standard ventilation and temperature management.
no active heat and humidification during anesthesia
其他名称:
  • Thermovent 600; Portex

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Core Body Temperature
大体时间:Approximately four hours post-induction of general anesthesia (or last recorded temperature)
Core body temperature will be taken in the esophagus. The last recorded esophageal temperature will be used for surgeries not reaching 3 hours duration.
Approximately four hours post-induction of general anesthesia (or last recorded temperature)

次要结果测量

结果测量
措施说明
大体时间
Intraoperative Core Temperatures Post-induction
大体时间:Approximately 30 minutes, 60 minutes, 120 minutes post-induction of general anesthesia
Core body temperature will be taken in the esophagus after general anesthesia induction.
Approximately 30 minutes, 60 minutes, 120 minutes post-induction of general anesthesia
Number of Subjects With Post-operative Shivering
大体时间:Approximately 2 hours after completion of the surgery
Shivering in the post-anesthesia care unit will be assessed using the Bedside Shivering Assessment Scale. This is a 4 point scale and rate shivering as the following: absent, mild, moderate, or severe. Only the highest degree of patient shivering was used in the analysis.
Approximately 2 hours after completion of the surgery
Hospital Length of Stay
大体时间:Surgery to hospital discharge
Number of days in the hospital
Surgery to hospital discharge
Overall Post-operative Temperature
大体时间:PACU arrival
Temperature at Post Anesthesia Care Unit (PACU) arrival.
PACU arrival
Number of Participants With Transfusion Within 48 Hours of Surgery
大体时间:Within 48 hours of surgery
Requirement of blood transfusion within 48 hours of surgery
Within 48 hours of surgery
Estimated Blood Loss
大体时间:duration of surgery
The estimated blood loss per case was determined by the anesthesia provider by measuring the volume of blood in the suction canister while taking into account the amount of irrigation solution used.
duration of surgery

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

赞助

合作者

调查人员

  • 首席研究员:Jean M Guyer, DNP、Mayo Clinic

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2015年8月28日

初级完成 (实际的)

2017年2月5日

研究完成 (实际的)

2017年2月5日

研究注册日期

首次提交

2017年2月9日

首先提交符合 QC 标准的

2017年2月9日

首次发布 (实际的)

2017年2月13日

研究记录更新

最后更新发布 (实际的)

2018年5月7日

上次提交的符合 QC 标准的更新

2018年5月3日

最后验证

2018年5月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • 15-001604
  • UL1TR000135 (美国 NIH 拨款/合同)

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

是的

在美国制造并从美国出口的产品

是的

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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