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Preoperative Glucocorticoid Use in Major Hepatectomy

2021年4月27日 更新者:Dr. Chad G. Ball、University of Calgary

Preoperative Glucocorticoid Use in Major Hepatectomy - A Randomized Controlled Trial

Background: Reducing postoperative complications remains a dominant challenge for all clinicians. By minimizing the incidence of adverse outcomes, health care costs and patient recovery can be improved. A number of studies have documented that fewer postoperative adverse events occur with the preoperative use of glucocorticoids (GC). Two small manuscripts support the use of GC with particular reference to liver resection.

Major hepatectomy can be associated with numerous adverse outcomes (hemorrhage, bile leak, liver failure, wound infection other infectious complications). This rate approaches 54% in some trials. Additionally, the liver is responsible for numerous metabolic functions and actively participates in the acute phase response via the generation of inflammatory mediators and cytokines. Glucocorticoids play an important role in suppressing the over-synthesis of pro-inflammatory cytokines and therefore may assist in reducing postoperative complications. These pro-inflammatory cytokines recruit leukocytes at the site of injury, leading to hepatic parenchymal cell damage. Decreasing pro-inflammatory cytokine ratio may therefore reduce hepatic damage.

Methods: The investigators will complete a randomized controlled trial evaluating the incidence of postoperative complications and overall hospital length of stay in adult patients following preoperative vs. no administration of 500 mg of methylprednisolone (MP) within 30 minutes of starting a hepatectomy. This trial will employ block randomization and intention to treat protocols. Four HPB surgeons at University of Calgary will participate in the trial with a planned inclusion of all patients scheduled to undergo hepatectomy in a period of 2 years.

Analysis: Standard statistical analysis will include normally or near-normally distributed variables reported as means and non-normally distributed variables as medians. Means will be compared using the student's t test and medians using the Mann-Whitney U test. Differences in proportions among categorical data will be assessed using Fischer's exact test. A p value < 0.05 will represent statistical significance for all comparisons.

Hypothesis: Preoperative GC administration will decrease the incidence of postoperative complications and overall hospital length of stay following hepatectomy.

Potential Impact: Health care utilization and economics are an expanding area of importance. Reducing post-hepatectomy complications are crucial to this end.

研究概览

地位

完全的

条件

详细说明

Introduction:

Major hepatectomy lead to significant postoperative anatomical and physiological changes. The liver dictates the systemic metabolic environment and helps maintain homeostasis. When segments of liver are removed, it is challenged to regenerate and restore cellular volume, as well as continuing to perform mandated metabolic functions. Major hepatectomy can result in multiple complications (hemorrhage, biliary fistulae, wound infection, liver failure) with an overall complication rate up to 54% in some studies.

Recent studies purport that preoperative administration of GC may suppress the acute phase response during the early postoperative period. GCs are steroid hormones with a variety of immunological and biochemical functions (anti-inflammatory attenuation of the acute phase response by binding to intra-cytoplasmic GC receptors and therefore increased transcription of anti-inflammatory proteins interleukin-10 (IL-10), IL-1-receptor antagonist (IL-Ra), lipocortin-1 and neutral endopeptidase, or direct inhibition of activated transcription factors (nuclear factor kB, activator protein-1)). GC can also suppress gene expression by altering the chromatin structure and tightening DNA coils.

The acute phase response is a neuro-humoral and time-limited defensive mechanism, which aims to restore homeostasis. It is characterized by fever, leukocytosis, gluconeogenesis, as well as changes in lipid, carbohydrate and protein metabolism. Activation of the hypothalamus-pituitary-adrenal axis, coagulation and compliment pathways is also one of the salient features of the acute phase response. It is regulated by cytokine receptor antagonists (IL-1Ra) and soluble cytokine receptors. Cytokines are soluble, low molecular weight glycoproteins that act as inflammatory mediators and can be broadly divided into pro and anti-inflammatory cytokines. At low concentrations, they have a paracrine effect, while in high concentrations they act systemically. These pro-inflammatory cytokines (IL-1, IL-2, IL-6 and tumor necrosis factor (TNF) alpha) remain in the plasma for at least 24 hours after generation. They also attract leukocytes (neutrophils and macrophages) to the site of injury and are detrimental if produced in large amounts. Oka et al have demonstrated that increasing levels of IL-6 are directly related to an increased rate of postoperative complications.

In low doses, GC reduce short term mortality, reverse the shock process and improve hemodynamics in septic shock patients. In a meta-analysis of 17 RCTs, Annane et al found that 28-day mortality for a low-dose dexamethasone (DXA) group, versus control group was 35.3% vs. 38.5%. Shock reversal was also increased in the DXA group (66.9% vs. 58.6%) and the ICU stay was decreased by 4.49 days.

Preoperative use of GC improves cardiac functions after coronary artery bypass grafting. The likely underlying mechanism for this cardio-protective effect is reduced release of pro-inflammatory cytokines IL-6, IL-8, and TNF-alpha with a concurrent increased release of anti-inflammatory cytokine IL-10.

In cases of laparoscopic cholecystectomy, 50% to 75% of patients express nausea and vomiting in the early postoperative period. In a meta-analysis, Karanicolas et al found that the absolute risk of nausea in low risk patients. Similarly DXA decreases the absolute risk of vomiting from 12% to 5% in low risk and 30% to 12% in high risk groups as compared to placebo. Although the quality of evidence is low regarding postoperative pain in post-cholecystectomy patients, researchers have found less postoperative pain in the DXA group.

Gomez-Hernandez et al also suggested that a preoperative single dose of DXA decreased postoperative nausea, vomiting and pain in patients undergoing mastectomy (28.6% vs. 60% in the early postoperative period). The patients in placebo group required more anti-emetic medications. DXA reduced postoperative pain significantly and fewer patients requested analgesia (10 vs. 21). Additionally there was no increase in adverse events, morbidity and mortality in the steroid group.

Preoperative use of DXA significantly improves postoperative pain, nausea, vomiting and vocal function within the first 48 hours after thyroid surgery.

Subclinical renal dysfunction is frequently noted following liver transplantation. This occurs mainly due to hepatic ischemia/reperfusion injury. Turner et al suggested that GC decrease the incidence of renal tubular dysfunction when given at the time of induction of anesthesia. The main difference in serum creatinine level was noted on postoperative day 3 (164.8 mumol/L in the saline group vs. 88.5 mumol/L in the MP group). Additionally, patients in the saline group suffered from more complications (47% vs. 12%).

Studies have suggested that GC limit the peritoneal inflammatory response and therefore help in recovery and fatigue in the early postoperative period. Low levels of IL-6 and IL-13 were found in the peritoneal fluid of patients receiving GC on postoperative day 1. Schulze et al observed improved pulmonary function and early mobilization in a MP group, as compared to placebo, in colon surgery patients. Furthermore, they noted a significant decrease in IL-6, C reactive protein and pain scores. The appetite was increased significantly in patients on GC, however there was no difference in wound healing and other infectious complications (including anastomotic leaks). In colorectal surgery, GC do not appear to increase postoperative complications. A double blind, randomized clinical trial consisting of 30 patients undergoing colonic surgery, showed that there was no significant difference in postoperative IL-6, C reactive protein, pain scores, bowel functions, mobilization, hospital length of stay, complications and readmission rates between the two groups when a single 8 mg preoperative dose of DXA was given to the interventional group.

A recent systematic review and meta-analysis of 11 moderate quality RCTs suggested decreased postoperative complications and hospital length of stay of patients undergoing major abdominal surgery following preoperative use of GC. In the case of liver resection surgery, Aldrighetti et al found decreased serum ALT, AST, total bilirubin, IL-6, TNF-alpha, hospital length of stay and postoperative complications following a single preoperative GC dose.

The dominant clinical rationale for not using preoperative steroids is to avoid related side effects. A substantial number of studies have documented fewer adverse events in MP groups as compared to placebo, suggesting there is a need to reconsider the steroid-free protocol in the preoperative period. Further appropriately designed and well-powered studies are urgently needed to evaluate the effects of preoperative GC use. As a result, we have planned a prospective RCT at the University of Calgary to determine the role of GC in reducing postoperative complications and hospital length of stay for patients undergoing partial hepatectomy.

Recruitment:

Contact information for study candidates will be obtained by the project's research staff from the offices of the four participating surgeons. Patients will be contacted prior to surgery by the research staff and will be provided information regarding the study. Patients who consent to participate will be randomized (the clinic at the time of consent completion and operative scheduling).

Data collection:

Patients will be tracked postoperatively for the development of complications and overall length of hospital stay. Information will be collected by chart review from the operative report and patient record by research staff.

Data elements to be collected will include, but not be limited to:

  • Date of birth, Gender
  • Surgeon, procedure, surgery duration
  • Antibiotic prophylaxis
  • Estimated blood loss, Transfusion
  • Wound closure technique, peroperative drain, Wound infection or disruption
  • Hepatic failure
  • Acute kidney injury
  • Intraperitoneal abscess, surgical site infection
  • Pneumonia, Blood stream infection, Pulmonary embolism, Deep venous thrombosis
  • Hypoglycemic incidents
  • Bile leak (requiring percutaneous drainage or via an operatively placed drain)
  • Anastomotic gastrointestinal leaks (combined colorectal / hepatic resection)
  • Preparation type (ETOH based, chlorhexidine or iodine based)
  • Time to oral intake

Patient records:

  • Preoperative chemotherapy
  • Preoperative albumin level
  • Preoperative PVE and /or TACE
  • Underlying liver disease (cirrhosis)
  • ASA score
  • Length (if any) of hepatic inflow occlusion,
  • Length of hospital stay & mortality
  • Co-morbidities (smoking, diabetes, hypertension, COPD, Ischemic heart disease, arrhythmias, metastatic cancer, AIDS, obesity, alcohol abuse,psychosis, anemias etc.)
  • Glucocorticoids - methylprednisolone given, dose, route of administration and time before starting surgery.

The investigators will also track IL-6 and C-Reactive protein (CRP) levels on postoperative day 1 (with daily blood work) as a marker of global immune function. Definition of complications can be found in appendix 2.

Power calculation to determine sample size:

The largest surgical trial to date recruited a total of 73 patients. There are 5 small hepatic resection RCTs available for analysis (all trials utilized MP). The largest of these studies noted a decrease in overall complications from 54% to 14% with GC use. With a consistent volume of hepatectomies (100+ per year at FMC), and a planned inclusion/capture for our group's resections of nearly 100%, we expect to randomize over 100 patients in each arm in 2 full years. With an alpha = 0.5, probability = 80%, predicted effect size of 0.30 (2-tailed test), the sample size required would be 84 patients.

Additional comments:

Methylprednisolone (MP) is the best choice of GC because it: (1) has a 5-fold higher anti-inflammatory action compared to cortisol, (2) has reduced effects on electrolytes, (3) duration of MP biologic action is 36 hrs (half life = 2.8 hrs) so both phases of ischemia-reperfusion injury will be covered, and (4) 500 mg of MP results in a defined and predictable response of >1 ug/ml in blood and >10 ug/ml in liver tissue.

Resources:

This project is built on an existing research team who work collaboratively with the Principal Investigator to carry out the project effectively and efficiently. An experienced research assistant will assist in data collection, analysis, preparing reports for publications and organizing research meetings.

Appendix 2:

Hepatic failure; Hyperacute and/or acute onset of coagulopathy (INR>1.5), reduction in synthetic function, and encephalopathy requiring therapy.

Acute kidney injury; An abrupt (<48 hrs) reduction in kidney function (absolute increase in serum creatinine > or equal to 26.4 umol/L, a > 50% increase in serum creatinine or a reduction in urine output of less than 0.5 ml/kg per hour for more than six hours.

Intraperitoneal abscess; Identified on cross-sectional imaging. Bile leak; Either requiring percutaneous drainage or evidence of bile in an operatively placed closed suction drain.

Wound disruption, dehiscence or hernia Pneumonia; Blood stream infection; Urinary tract infection; Surgical site infection.

Anastomotic gastrointestinal leaks (combined colorectal/hepatic resections); GI leak confirmed by imaging (fistulogram, CT) and requiring intervention.

Deep venous thrombosis; Identified on ultrasonography or cross sectional imaging prompted by clinician suspicion or incidental imaging.

Pulmonary embolus; Identified on cross-sectional or V/Q scan imaging. Hypoglycemic incidents; Blood glucose <3.0 mm/L with concurrent patient symptoms of hypoglycemia.

研究类型

介入性

注册 (实际的)

200

阶段

  • 阶段2
  • 第三阶段

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Alberta
      • Calgary、Alberta、加拿大、T2N2T9
        • Foothills Medical Centre

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

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Elective surgery patients (adults) scheduled to undergo hepatectomy at FMC from May 2013 to May 2015.

Exclusion Criteria:

  • Patients will be excluded if they are unable to give informed consent.

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:三倍

武器和干预

参与者组/臂
干预/治疗
实验性的:Methylprednisolone
Injection, 500 mg, single use, over 15 to 20 minutes.
Patients in Methylprednisolone arm will receive injection methylprednisolone 500 mg I/V over 15 to 20 minutes, single dose, 30 minutes before starting surgery.
其他名称:
  • 溶液-美多尔
安慰剂比较:Control
In Control arm, patients will receive the standardized surgical treatment without receiving methylprednisolone preoperatively (placebo).
Patients in the placebo group will receive standard perioperative care and surgery, without preoperative administration of methylprednisolone.
其他名称:
  • Standard surgical care

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Total Complication rate
大体时间:1 month
1 month

次要结果测量

结果测量
大体时间
Total length of hospital stay
大体时间:3 months
3 months

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。

调查人员

  • 首席研究员:Chad G. Ball, MD,MSc,FRCSC、University of Calgary, Calgary, Alberta, Canada.

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

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

2014年10月1日

初级完成 (实际的)

2018年10月30日

研究完成 (实际的)

2018年10月30日

研究注册日期

首次提交

2013年5月14日

首先提交符合 QC 标准的

2013年11月22日

首次发布 (估计)

2013年11月28日

研究记录更新

最后更新发布 (实际的)

2021年4月28日

上次提交的符合 QC 标准的更新

2021年4月27日

最后验证

2021年4月1日

更多信息

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.

Methylprednisolone的临床试验

  • Barbara Ann Karmanos Cancer Institute
    National Cancer Institute (NCI)
    招聘中
    弥漫性大 B 细胞淋巴瘤 | 高级别 B 细胞淋巴瘤 | 双表达淋巴瘤 | 具有 MYC 和 BCL2 或 BCL6 重排的高级别 B 细胞淋巴瘤 | 具有 MYC、BCL2 和 BCL6 重排的高级别 B 细胞淋巴瘤
    美国
3
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