AmbuCineView: Evaluation of Immersive Audiovisual Distraction Impact on Peroperative Opioid Consumption.
Study Details
Study Description
Brief Summary
This study evaluate the impact of an audiovisual distraction device on the peroperative opioid consumption for outpatient procedures with Remifentanil added to local anesthesia.
Half of patients will receive an audiovisual distraction device while the other half not.
Condition or Disease | Intervention/Treatment | Phase |
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N/A |
Detailed Description
Early recovery for patients undergoing surgery is the key factor for an outpatient procedure.
The technique of adding remifentanil to a local anesthesia is used in 22% of the procedures realized in The CHU de Caen Outpatient unit. Decreasing opioid dose, whose side effects are numerous and widely described, as well as reducing anxiety are daily challenges to ensure comfort and successful care.
We propose a prospective, randomized, monocentric, open label study to evaluate the impact of the use of an audiovisual distraction device on the intraoperative consumption of opioids, on the patient's pain and peroperative anxiety.
ANI (Analgesia Nociception Index) will be used for peroperative overall comfort measurement. We will analyze if audiovisual distraction can integrate existing techniques such as hypnosis.
Finally, we will also assess the medico-economic impact of this technique in order to establish a benefit / cost ratio.
Study Design
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
Experimental: Audiovisual distraction device Audiovisual distraction device, analgesia nociception index monitoring, remifentanil added to local anesthesia technique |
Device: Audiovisual distraction device
Evaluate the impact of an audiovisual distraction device on the peroperative opioid consumption
Device: Analgesia nociception index
ANI (Analgesia Nociception Index) will be used for peroperative overall comfort measurement
|
Active Comparator: Active comparator group Analgesia nociception index monitoring, remifentanil added to local anesthesia technique |
Device: Analgesia nociception index
ANI (Analgesia Nociception Index) will be used for peroperative overall comfort measurement
|
Outcome Measures
Primary Outcome Measures
- Intraoperative Remifentanil dose [1 hour]
μg/kg/min
Secondary Outcome Measures
- Preoperative pain measured with a numeric pain rating scale (NRS) [1 hour]
Numeric pain rating scale (0 = No pain to 10 = Worst pain imaginable)
- Preoperative anxiety measured by the Amsterdam Preoperative Anxiety and Information Scale (APAIS) [1 hour]
APAIS measures the need-for-information with 6 items. Each one is rated from 1 = Not at all to 5 = Extremely. There is positive and significant correlation between the ned-for-information and anxiety.
- Preoperative anxiety measured by a visual analogue scale (VAS) [1 hour]
Visual analogue scale is a 100mm horizontal line. At the left hand (0mm) the statement "not anxious at all" and at the right hand (100mm) the statement "most anxious I can imagine"
- Per operative Analgesia nociception index (ANI) value [1 hour]
From 0 = Predominant sympathetic tone, pain and anxiety to 100 = Predominant parasympathetic tone, good analgesia. Negative linear Relationship between analgesia nociception index and pain scores
- Post operative anxiety measured by a visual analogue scale (VAS) [1 hour]
Visual analogue scale is a 100mm horizontal line. At the left hand (0mm) the statement "not anxious at all" and at the right hand (100mm) the statement "most anxious I can imagine"
- Postoperative pain measured with a numeric pain rating scale (NRS) [1 hour]
Numeric pain rating scale (0 = No pain to 10 = Worst pain imaginable)
Eligibility Criteria
Criteria
Inclusion Criteria:
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Adult patient
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Signed consent
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Outpatient surgery eligibility
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Patient covered by social security
Exclusion Criteria:
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Unsigned consent
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Study participation refusal
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Deafness, blindness
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Claustrophobia
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ANI contraindication (atrial fibrillation, pace maker, severe autonomic system dysfunction)
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Contraindication or impossibility to use the audiovisual distraction device
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Caen University Hospital | Caen | Calvados | France | 14000 |
Sponsors and Collaborators
- University Hospital, Caen
Investigators
- Study Chair: Clément Buléon, MD, Caen UH
Study Documents (Full-Text)
None provided.More Information
Publications
- Abend R, Dan O, Maoz K, Raz S, Bar-Haim Y. Reliability, validity and sensitivity of a computerized visual analog scale measuring state anxiety. J Behav Ther Exp Psychiatry. 2014 Dec;45(4):447-53. doi: 10.1016/j.jbtep.2014.06.004. Epub 2014 Jun 18.
- Boselli E, Musellec H, Martin L, Bernard F, Fusco N, Guillou N, Hugot P, Paqueron X, Yven T, Virot C. Effects of hypnosis on the relative parasympathetic tone assessed by ANI (Analgesia/Nociception Index) in healthy volunteers: a prospective observational study. J Clin Monit Comput. 2018 Jun;32(3):487-492. doi: 10.1007/s10877-017-0056-5. Epub 2017 Aug 20.
- Boselli E. Interest of Analgesia/Nociception Index (ANI) for monitoring the relative parasympathetic tone in anesthetized and awake patients. Douleurs (Paris) (2018)
- Boselli et al. Analgesia monitoring using Analgesia/Nociception Index: Results of clinical studies in awake and anesthetized patients. Le Praticien en anesthésie réanimation. 2015;19:78-86
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- 2019-A01243-54