Ultrasound Assessment of Gastric Content Before Anesthesia for Appendectomy

NCT ID: NCT02983175

Last Updated: 2016-12-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

150 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-12-31

Study Completion Date

2017-09-30

Brief Summary

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Performing anesthetic induction for appendicectomy has two main risks : first aspiraion of gastric content causing pneumonia. Otherwise, anaphylactic risk to drugs used during anesthetic induction. Indeed, the guidelines recommend an anesthetic induction protocol qualified "full stomach" whatever the patient and the preoperative fasting period are. This protocol provides the use of fast-acting neuromuscular blocking agents (succinylcholine or rocuronium). However, these neuromuscular blocking agents are ten times more at allergic risk than others. Ultrasound assessment of gastric content before rapid sequence induction of anesthesia is a reproducible, non-invasive, inexpensive and quickly achievable bedside technique. Furthermore, the correlations between gastric volume and risk of a full stomach and also between the cross-section antral area (CSA) and the risk of a full stomach have been validated on several patient cohorts. We formulate the hypothesis that the achievement of a gastric ultrasound before anesthetic induction for appendectomy could allow to identify "full stomach" patients who actually justify rapid sequence induction of anesthesia with exposure to fast-acting neuromuscular blocking agents that implies.

Primary endpoint is to determine te percentage of patients who have a gastric content before appendectomy. Secondary endpoint is to determine the incidenc of aspiration pneumonia and anaphylactic shock. Another secondary endpoint is to determine the percentage of patient with gastric content with the antral grading system (Perlas method) and to evaluate the concordance between this methode and the cross-section antral area.

Detailed Description

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Conditions

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Appendectomy

Keywords

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ultrasonogaphy full stomach pulmonary aspiration anaesthesia

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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ultrasound assessment of gastric content

Group Type EXPERIMENTAL

ultrasound assessment of gastric content

Intervention Type OTHER

Achievement of gastric ultrasound (specific procedure) :

Gastric ultrasound is performed specifically for the study by a senior anesthetist physician in a patient placed supine, semi-sitting by an angle of 45 ° relative to the horizontal.

Standardised achievement of the antral ultrasound by the following method:

* First, a qualitative assessment of antral contents in 3 grades according to the "Perlas" method \[24\].
* Second, performing a quantitative analysis of antral contents calculating the CSA.
* Then, volume of gastric contents calculation as from the CSA.

Interventions

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ultrasound assessment of gastric content

Achievement of gastric ultrasound (specific procedure) :

Gastric ultrasound is performed specifically for the study by a senior anesthetist physician in a patient placed supine, semi-sitting by an angle of 45 ° relative to the horizontal.

Standardised achievement of the antral ultrasound by the following method:

* First, a qualitative assessment of antral contents in 3 grades according to the "Perlas" method \[24\].
* Second, performing a quantitative analysis of antral contents calculating the CSA.
* Then, volume of gastric contents calculation as from the CSA.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patient admitted to the operating room for appendectomy.
* Major or minor patient (higher than 16) affiliated to a social security scheme.
* Patient or parents of minor patient who received the full information relative to the organization of the study and who signed his/their informed consent(s).

Exclusion Criteria

* Pregnant women.
* Childbearing age patient does not have effective contraception.
* Breastfeeding woman.
* Minor patient under 16.
* Major patient subject to a measure of legal protection or unable to consent.
* Persons deprived of liberty by a judicial or an administrative decision.
* Patient with gastric and/or esophagus surgery history.
Minimum Eligible Age

16 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Central Hospital, Nancy, France

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Central Contacts

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Marie-Alix REGNIER-KIMMOUN, PH

Role: CONTACT

Phone: 03.83.85.14.03

Email: [email protected]

References

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Bouvet L, Mazoit JX, Chassard D, Allaouchiche B, Boselli E, Benhamou D. Clinical assessment of the ultrasonographic measurement of antral area for estimating preoperative gastric content and volume. Anesthesiology. 2011 May;114(5):1086-92. doi: 10.1097/ALN.0b013e31820dee48.

Reference Type RESULT
PMID: 21364462 (View on PubMed)

Perlas A, Chan VW, Lupu CM, Mitsakakis N, Hanbidge A. Ultrasound assessment of gastric content and volume. Anesthesiology. 2009 Jul;111(1):82-9. doi: 10.1097/ALN.0b013e3181a97250.

Reference Type RESULT
PMID: 19512861 (View on PubMed)

Reddy JI, Cooke PJ, van Schalkwyk JM, Hannam JA, Fitzharris P, Mitchell SJ. Anaphylaxis is more common with rocuronium and succinylcholine than with atracurium. Anesthesiology. 2015 Jan;122(1):39-45. doi: 10.1097/ALN.0000000000000512.

Reference Type RESULT
PMID: 25405395 (View on PubMed)

Other Identifiers

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2016-A01501-50

Identifier Type: -

Identifier Source: org_study_id