Acute Neurological ICU Sedation Trial (ANIST)

Sedation Clinical Trial

— ANIST  

Official title:

Acute Neurological ICU Sedation Trial (ANIST)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00390871
• Other study ID #: ANIST
• Status: Completed
• Phase: Phase 2
• Start date: May 2005
• Est. completion date: December 2007

Study information

• Verified date: May 2019
• Source: Johns Hopkins University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Dexmedetomidine (Precedex, Hospira) is a "super" selective alpha2-agonist - 8-10x more avid binding to alpha2 receptors than clonidine - and may have particularly favorable characteristics as a continuous i.v. infusion sedative for critically ill neuroscience patients. Its combination of anxiolysis, analgesia, without undue lethargy may make it an ideal agent where frequent neurological examinations are important. Unclear, however, is whether Precedex is superior to current common i.v. sedation protocols, and if there are any undue concerns of this agent on cerebral physiology and cortical stimulation.

Description:

Dexmedetomidine has shown promise in small case series to be an efficacious sedative agent in the intensive care unit (ICU) setting, in both post-surgical and medical patients. A recent publication reported on the efficacy in a small series of medical patients (n=12), but as part of the exclusion criteria were any serious nervous system trauma or direct central nervous system (CNS) pathology.

A potential advantage of dexmedetomidine as a sedative agent compared to current popular classes of drugs, particularly propofol, benzodiazepines, and narcotics, is the nominal effect on reduction of level of arousal. Experience suggests that this agent may induce effective degrees of sedation without concomitant loss of attentive behavior and cognition following low levels of auditory or tactile stimulation. Thus, neurological assessment may be preserved while achieving the goal of a non-agitated or anxious patient. Additionally, the combination of both sedative/anxiolytic and analgesic action of dexmedetomidine may permit single drug use for both sedation and pain control during the post-operative and medical ICU period.

The cerebral effects of alpha2-agonists have been modestly studied in the clinical environment, and only in normal volunteers. As expected, cerebral blood flow decreased following initiation of the sedative, coincident with the expected diminishment of global cerebral metabolism. No studies have evaluated dexmedetomidine in patients suffering from neurological injury, the very population that may most benefit from the agent's sedative characteristics. Thus, it is imperative that a safety & efficacy study be carried out in a population of both medical and post-operative neuroscience patients. From an intraoperative perspective, dexmedetomidine has been effectively used as a sedative for both awake and sedation cases. Some evidence suggests prolonged cognitive deficits may persist beyond the sedative action of the drug.

One concern in the neuroscience patient population is laboratory evidence that alpha2-agonists may lower the seizure threshold. Such data has been shown for both clonidine and dexmedetomidine.

Therefore, to provide a comprehensive evaluation leading to successful safety and efficacy data for this sedative, it will be important to perform the following three studies. All three studies will be done concurrently but enrollment between the three studies will be mutually exclusive.

Objective 1: Evaluation of Quality of Sedation: Does dexmedetomidine provide superior sedative characteristics relative to current standard agents in patients with neurological dysfunction? The metrics for such a study will include -

1. Pharmacodynamic ease of sedation: time to goal, required nursing interventions to goal;

2. Quality & consistency of sedation: ability to examine the patient, number of required titration interventions;

3. Rapid weaning: time to off and no residual effect both hemodynamic and neurologic;

4. Systemic hemodynamic alterations requiring drug infusion adjustment or medical intervention;

5. Side effect and toxicity of sedative infusion: neurological dysfunction - cognitive, motor, sensory; electrolyte/hematological/metabolic disturbances, alteration of drug levels.

Objective 2: Alteration of Cerebral Physiology: Does Dexmedetomidine alter intracranial physiology either in a favorable or unfavorable manner? The metrics for such a study will include -

1. Measures of intracranial pressure (ICP), mean arterial pressure (MAP), cerebral perfusion pressure (CPP);

2. Cognitive neurological state;

3. Cerebral saturation (venous) or direct cerebral oximetry (oxygen tissue level) in a subset population with specific intracranial device.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 35
• Est. completion date: December 2007
• Est. primary completion date: December 2007
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Objective 1: Inclusion Criteria:

Neuroscience patients in the Neuro Critical Care Unit (NCCU) who are:

• 18-80 years of age;

• Mechanically ventilated patients;

• Requiring continuous sedation for a minimum of 9-11 hours (depending on whether or not pt is post-operative), yet frequent neurological examinations or Patients with a Nursing Instrument for Communication of Sedation Score (NICSS) > 0

• Patient or family able to provide consent.

• Considered to have guarded yet stable neurological state. Not fluctuating intracranial pressure (ICP), cerebral perfusion pressure (CPP), or ongoing known cerebral ischemia if ICP monitoring in place.

Objective 1: Exclusion Criteria:

• Pregnancy.

• ICP> 30 mm Hg despite therapy if ICP monitored.

• CPP <70 mm Hg if monitored.

• Occurrence of: new cerebral stroke, hemorrhage, or change in edema by CT, increase in ICP if monitored.

• Neuromuscular paralysis.

• Non-functional cognitive exam - not following commands.

• Renal insufficiency: Serum Creatinine >2.0 mg/dl or estimated Cr Clearance <40.0 ml/min.

• Hepatic disease: aspartate aminotransferase (AST), alanine aminotransferase (ALT) > 300, or international normalized ratio (INR) > 1.7 not on anticoagulants.

• Severe chronic obstructive pulmonary disease (COPD) with baseline arterial partial pressure of carbon dioxide (pCO2)>50.

• Suspected alcohol or substance withdrawal.

• Hypotension - requiring pressor therapy to maintain baseline adequate CPP or mean arterial pressure (MAP).

• Cardiac arrhythmia - sinus bradycardia (HR <60), atrial fibrillation (>6 PVC's/min)

• Bradycardia- heart rate less than 60 beats per minute.

• Patient does not require mechanical ventilation.

Objective 2: Inclusion Criteria:

Critically ill neuroscience patients who are:

• 18-80 years of age;

• Mechanically ventilated;

• Require Intracranial Pressure (ICP) monitoring by either subarachnoid bolt (SA bolt), or by an Intra-Ventricular Catheter (IVC).

• Amenable for placement of intra-cerebral oxygen sensor or jugular bulb catheter.

• Have glaucoma coma score (GCS) score > 5 that requires sedation.

• Requiring continuous sedation for minimum of 9-11 hours (depending on whether or not pt is post-operative) , yet frequent neurological examinations every 1-2 hours or Patients with a NICSS score > 0

• Patient or family able to provide consent.

Objective 2: Exclusion Criteria:

• Pregnancy;

• ICP> 30 mm Hg despite therapy; 3) CPP <70 mm Hg;

• Occurrence of: new cerebral stroke, hemorrhage, or change in edema by CT, increase in ICP if monitored.

• Continuous neuromuscular paralysis

• Renal insufficiency: Serum Creatinine >2.0 mg/dl or estimated Cr <40.0 Clearance ml/min.

• Hepatic disease: AST, ALT > 300, or INR > 1.7 not on anticoagulants.

• Severe COPD with baseline arterial pCO2>50.

• Suspected alcohol or substance withdrawal.

Related Conditions & MeSH terms

• Sedation

Intervention

Drug:
• Fentanyl/Dexmedetomidine

• Fentanyl/Propofol

• Fentanyl

Locations

Country	Name	City	State
United States	Johns Hopkins University	Baltimore	Maryland

Sponsors (1)

Lead Sponsor	Collaborator
Johns Hopkins University

Country where clinical trial is conducted

United States, 

References & Publications (1)

Lewin JJ 3rd, LeDroux SN, Shermock KM, Thompson CB, Goodwin HE, Mirski EA, Gill RS, Mirski MA. Validity and reliability of The Johns Hopkins Adapted Cognitive Exam for critically ill patients. Crit Care Med. 2012 Jan;40(1):139-44. doi: 10.1097/CCM.0b013e3 — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Johns Hopkins Adapted Cognitive Exam	Cognitive assessment tool	day of study
Primary	Confusion Assessment Method (CAM) for the Intensive Care Unit	CAM-ICU delirium assessment tool	day of study
Primary	Time from initiation of study drug to calm, non-anxious state	From control state to RASS Score or 0 to -1 (average=137 min)	day of study
Secondary	Therapy Intensity Level Scale (TIL)	Bedside assessment tool to quantify nursing effort	day of study
Secondary	Requirement for fluids, pressors	Documenting need for adjunctive treatment with vasoactive agents	day of study
Secondary	Toxicity/side effects	documenting drug toxicity - rash, angioedema, nausea, fever, etc.	day of study
Secondary	Numerical Pain Rating Scale	behavioral and numerical pain rating	day of study
Secondary	Need for less or more fentanyl during the infusion drug phase	assessment of fentanyl dosing required to maintain behavioral pain score at < 3	day of study