A Double Blind, Randomized, Placebo-controlled Study to Investigate the Effectiveness of IV Acetominophen Administered During Functional Endoscopic Sinus Surgery in Reducing the Use of Opiates to Treat Postoperative Pain
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 62
- 试验地点
- 1
- 主要终点
- Pain Level Assessed Using a Visual Analogue Scale (VAS) Scale
研究概览
简要总结
The purpose of this study is to assess the use of IV acetaminophen (Ofirmev) as a and safe and efficacious agent in reducing post-operative pain; we hypothesize that its use will reduce post-operative pain when compared to a control group using the visual analogue score (VAS) analog pain scoring system.
详细描述
Unrelieved postoperative pain may result not only in suffering and discomfort, but may also lead to multiple physiological and psychological consequences which can contribute to adverse perioperative outcomes. Inadequate perioperative analgesia can potentially contribute to a higher incidence of myocardial ischemia. Additionally, the use of opioids has been associated with major side effects that can include impaired wound healing and delayed gastrointestinal (GI) motility that results in prolonged postoperative ileus.
Intravenous acetyl-para-aminophenol (APAP, also known as acetaminophen) is considered as the non-opioid analgesic of choice to treat postoperative mild and moderate pain, and has been demonstrated in several randomized trials to be both safe and effective at reducing acute post-operative pain in both children and adults. Furthermore, in the treatment of severe pain, it can reduce the need for opioid-analgesics while exhibiting a relatively limited side effect profile when compared to opioids and nonsteroidal anti-inflammatory drugs.
Chronic rhinosinusitis (CRS) describes a group of disorders characterized by inflammation of the nasal mucosa and/or paranasal sinuses for at least 12 consecutive weeks. In the United States, CRS affects approximately 30 million people, and represents 2% of the primary diagnoses in physician office visits, resulting in an estimated 200,000 sinus procedures annually. Patients suffering from CRS that is refractory to medical management complain of symptoms that include fatigue, headache, nasal drainage, facial pain and pressure, and decreased sense of smell. Functional endoscopic sinus surgery (FESS) represents a surgical approach to treating CRS that is unresponsive to medical management. Outcomes studies have identified FESS as efficacious at reducing the majority of symptoms related to CRS. Despite this, pain associated with CRS remains a significant co-morbidity that often is resistant to both medical and surgical management. Reducing the incidence and severity of acute post-operative pain is paramount to reducing the development of chronic pain that may exacerbate a patient's existing pain. The use of pre- and intra- operative IV acetaminophen thus serves as a unique pain management modality in this setting, as it has the potential for reducing post-operative complications and pain, with the additional benefit of minimal intraoperative bleeding, an undesirable complication often associated with FESS and with the use of non-steroidal anti-inflammatory drugs (NSAIDs).
The use of IV acetaminophen in ear, nose, and throat (ENT) surgery is not a novel endeavor. Indeed, studies have demonstrated the efficacy and safety of IV acetaminophen for use in tonsillectomy and FESS. We wish to provide a more comprehensive analysis of pain management in the setting of FESS in the following ways :
- by administering IV acetaminophen perioperatively (before start of surgery, and after surgery completion;
- by employing a pain score of 4 (whereas other studies use 3) as a cutoff for breakthrough pain; and,
- by addressing novel outcomes including patient sedation and patient satisfaction, in addition to opioid analgesic use.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 68 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- 未提供
研究组 & 干预措施
IV Acetaminophen
The experimental group will receive a preoperative dose of 1000mg IV acetaminophen over 15 minutes. This will occur at least 15 minutes before the start of surgery. Another 1000mg dose of IV acetaminophen will be administered 4 hours after the first dose. A rescue analgesic containing oxycodone will also be provided (with APAP concentrations of 325 mg per Hospital and FDA recommendations).
干预措施: IV Acetaminophen (Drug)
Control
The control group (Placebo) will receive 100 mL of 0.9% normal saline in place of IV acetaminophen in the same manner as the experimental group; the investigator/physician in question will be blinded to the agent that is being administered. Patients will be discharged with instruction to continue APAP 500 mg PO every 6-8 hours. A rescue analgesic containing oxycodone will also be provided (with APAP concentrations of 325 mg per Hospital and FDA recommendations).
干预措施: Placebo (Drug)
结局指标
主要结局
Pain Level Assessed Using a Visual Analogue Scale (VAS) Scale
时间窗: 15 minutes and 120 minutes Post-Operatively
VAS is a validated, self-reported data sheet assessing average pain intensity. Possible scores range from 0 (no pain) to 10 (highest level of pain).
次要结局
- Total Doses of Postoperative Opiate (Morphine) Use(During Postoperative Acute Care Unit (PACU) stay (up to 4 hours after surgery))
- Number of Participants Who Received Intraoperative Supplemental Fentanyl(During Postoperative Acute Care Unit (PACU) stay (up to 4 hours after surgery))
- Number of Participants Who Experienced Postoperative Morbidity (Nausea)(During Postoperative Acute Care Unit (PACU) stay (up to 4 hours after surgery))
- Postoperative Vital Sign (Systolic Blood Pressure)(During Postoperative Acute Care Unit (PACU) stay (up to 4 hours after surgery))
- Postoperative Vital Sign (Temperature)(During Postoperative Acute Care Unit (PACU) stay (up to 4 hours after surgery))
- Postoperative Vital Sign (Respiratory Rate)(During Postoperative Acute Care Unit (PACU) stay (up to 4 hours after surgery))
- Postoperative Vital Sign (Diastolic Blood Pressure)(During Postoperative Acute Care Unit (PACU) stay (up to 4 hours after surgery))
- Postoperative Vital Sign (Pulse)(During Postoperative Acute Care Unit (PACU) stay (up to 4 hours after surgery))
研究者
Davide Cattano
Associate Professor, Department of Anesthesia
The University of Texas Health Science Center, Houston
