Reducing the Incidence of PostOperative Residual Curarization

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

COMPLETED

Total Enrollment

2314 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-06-20

Study Completion Date

2018-12-31

Brief Summary

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The NMB (Neuromuscular Blockade) is the most frequent complication in anesthesiology associated with an increase in adverse respiratory events in the postoperative period. Its appearance depends on multiple factors. The introduction of a comprehensive educational strategy aimed at promoting the proper management of NMB in the intraoperative period and a package of measures that must be performed (intraoperative neuromuscular monitoring and reversal of the effect of neuromuscular blockers) may contribute to a decrease in the incidence of NMB, Increase safety in the surgical patient and decrease associated costs.

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Detailed Description

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Multicenter, epidemiological, prospective, randomized, sequential study. The introduction of an educational program and a package of clinical measures (specific monitoring and pharmacological reversion) in the incidence of NMB will be evaluated by evaluating variations in this incidence of NMB, the rate of compliance with the preventive measures and the perception of the Safety in the perioperative, through pre and postoperative survey.

Conditions

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Neuromuscular Blockade

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Study group

Intraoperative neuromuscular monitoring and pharmacological reversion according to data sheet

Educational program for clinicians: implementation of a package of clinical prevention measures of NMB

Intervention Type BEHAVIORAL

Intraoperative neuromuscular monitoring and pharmacological reversion of NMB according to data sheet

Control group

Treated according to usual clinical practice

No interventions assigned to this group

Interventions

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Educational program for clinicians: implementation of a package of clinical prevention measures of NMB

Intraoperative neuromuscular monitoring and pharmacological reversion of NMB according to data sheet

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Patients older than 18 years.
* Classification of the American Society of Anesthesiologists (ASA I-III).
* Patients with absence of cognitive deficit.
* Informed informed consent prior to surgery

Exclusion Criteria

* Negative of the patient to participate in the study
* Patients under the age of 18 or incapable of giving their consent
* ASA IV-V
* Pregnancy or breastfeeding
* Associated neuromuscular disorders
* Diabetes mellitus with diagnosed neuropathy

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No