Inhalative Sedation in ICU With Sevoflurane Via Anaesthetic Conserving Device Compared to Propofol
Information source: Klinikum Ludwigshafen
Information obtained from ClinicalTrials.gov on June 20, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Recovery From Sedation; Sevoflurane Consumption; Renal Function; Hepatic Function; Cardioprotection
Intervention: Sevoflurane (Drug); Propofol (Drug)
Phase: N/A
Status: Completed
Sponsored by: Klinikum Ludwigshafen Official(s) and/or principal investigator(s): Kerstin D. Röhm, Dr. med., Principal Investigator, Affiliation: Klinikum Ludwigshafen, Department of Anaesthesiology, Ludwigshafen, Germany
Summary
The evaluation of the presented study will work on the practicability of inhalative sedation
on the ICU, potential benefits and limitations of the ACD system in a postoperative sedated
patient population in comparison to a standard intravenous sedation regimen with propofol,
and focus on renal and hepatic function, cardioprotection and pharmacoeconomics
Clinical Details
Study design: Case Control, Prospective
Primary outcome: Extubation time
Secondary outcome: Consumption of anaestheticsRenal function Hepatic function Cardioprotection Costs
Detailed description:
A goal-oriented sedation complies the ability to sedate the patient as deeply as necessary,
and allow a modern ventilation regimen with early spontaneous breathing and a pain-free
cooperative patient. The ideal sedative agent - with a short duration of action, predictable
wake-up times, low drug toxicity, haemodynamic stability and less side effects, and a
rational pharmacoeconomic impact nowadays - has still to be found. Inhalative anaesthetics
show these properties, but until the introduction of AnaConDa© (Anesthetic Conserving Device,
ACD) in 2005, the use of volatile anaesthetics on the intensive care unit (ICU) required
specific evaporating devices or scavenging systems. The ACD, a modified heat- moisture
filter, is connected to the breathing circuit of conventional ICU ventilators and a syringe
pump delivers the volatile anaesthetic to the ACD where it is vaporized through a rod. Most
of the exhaled gas is absorbed in a charcoal filter's membrane and reflected to the patient
in the following inspiration. Randomised, controlled and comparative studies to the use of
volatile anaesthetics in ICU via this innovative device are still missing. Isoflurane has
been studied in small patient populations and in comparison to midazolam, while Sevoflurane
- a newer volatile agent with short action, brief elimination time, and low hepatic biodegradation - has only been studied intraoperatively and in short-term sedation. This is
the first prospective, randomised, clinical study on the feasibility of sevoflurane via the
ACD for sedation in ICU patients until 72 hours in comparison to a standard intravenous
sedation with propofol. The investigation will work on potential benefits and limitations of
the use of volatile agents on the ICU, the quality of sedation (Richmond Agitation Sedation
Scale, BIS), infusion rate stability of sevoflurane and respiratory parameters, short-term
recovery (time from discontinuation of infusion until following verbal commands and
extubation), haemodynamics, renal and hepatic function and adverse side effects.
Eligibility
Minimum age: 18 Years.
Maximum age: 80 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- 18-80 years
- elective operative procedure, and indication for admission to the ICU for
postoperative sedation
- ASA I-III
- weight 50-120 kg
- Haemoglobin > 10 g/dl
- ability and acceptance to agree to the study participation
Exclusion Criteria:
- malignant hyperthermia
- muscle diseases or weakness
- liver insufficiency (ASAT, ALAT > 40 U/min)
- pancreas insufficiency
- emergencies
- women in child bearing age and missing negative pregnancy test, pregnancy or
lactation
- diseases from the central nervous system (such as M. Parkinson and multiple
sclerosis)
- increased intracranial pressure, head trauma
- pre-existing delirium, agitation and psychiatric derangements
- alcohol and drug abuse (including opioid abuse)
- allergy to any of the study agents
- refusal from the patient to participate in the study
- participation in another study project.
Locations and Contacts
Additional Information
Related publications: Sackey PV, Martling CR, Nise G, Radell PJ. Ambient isoflurane pollution and isoflurane consumption during intensive care unit sedation with the Anesthetic Conserving Device. Crit Care Med. 2005 Mar;33(3):585-90. Sackey PV, Martling CR, Granath F, Radell PJ. Prolonged isoflurane sedation of intensive care unit patients with the Anesthetic Conserving Device. Crit Care Med. 2004 Nov;32(11):2241-6. Berton J, Sargentini C, Nguyen JL, Belii A, Beydon L. AnaConDa reflection filter: bench and patient evaluation of safety and volatile anesthetic conservation. Anesth Analg. 2007 Jan;104(1):130-4.
Starting date: December 2006
Ending date: December 2007
Last updated: January 3, 2008
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