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Assessment of Analgesia, Sedation, Physical Restraints and Delirium in Spanish Intensive Care Units

Assessment of Analgesia, Sedation, Physical Restraints and Delirium in Patients Admitted to Spanish Intensive Care Units. ASCyD Project

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03773874
Acronym
ASCyD
Enrollment
1574
Registered
2018-12-12
Start date
2018-02-12
Completion date
2018-03-11
Last updated
2018-12-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Agitation, Critical Care, Delirium, Nursing Assessment, Pain, Restraint, Physical, Sedation

Brief summary

This study assess which Spanish intensive care units evaluate and record, in a standardized way, levels of pain, sedation / agitation, use of physical restraints and prevalence of delirium. Also determine the use of validated assessment tools and explore levels of pain and sedation / agitation, use of physical restraints and prevalence of delirium.

Detailed description

An observational, descriptive, cross-sectional, prospective and multicenter study was conducted to know the usual practice (audit) in critical care units and about the assessment of pain, sedation, delirium and the use of mechanical restraints. At the same time, the level of pain, sedation / agitation and presence of delirium were evaluated in all adult patients who were admitted to the participating units with a minimum stay of 24 hours in the unit. Process In order to obtain the largest representation of Spanish Intensive Care Units, a network of research nurses was created with coordinators in each autonomous community. The function of the coordinators was to contact and recruit units of adult critical patients within their community. Each coordinator contacted the centers (public and private), creating a network of collaborating nurses from those units who expressed their willingness to participate and who obtained the authorization of their Research Ethics Committee. Each unit was asked to contact a collaborating nurse for the project. Once the national network of collaborating nurses was created, through the community coordinators, each password was given to each nurse to access the platform created for data entry. The platform offered access to all the documents (methodology, timeline, recommended assessment tools, navigation tutorial for the platform). Data collection The tool used was an ad hoc survey with online access which consisted of 2 blocks. The first block asked about the characteristics of the units, the nurse-patient ratio, the existence of protocols and the usual practice for the control of pain, sedation / agitation, delirium and the use of mechanical restraints in the unit. In the second block, questions were asked about aspects of direct assistance to patients, and direct evaluation of pain level, sedation / agitation of patients as well as the presence of delirium and mechanical containment. Evaluation of patients included The data collection was done by direct observation and in the same period in all participating units. These data were entered into the platform through a Patient Code, created automatically by the system. To assess pain in patients, the investigators used two scales, for patients with the ability to communicate, the Visual Analogue Scale (VAS) scale was recommended and for patients without the ability to communicate the Scale of Behavioral Indicators of Pain (ESCID). The evaluation of the level of sedation / agitation was recommended to be carried out with the Richmond Agitation Sedation Scale (RASS) and delirium with the Confusion Assessment Method for the Intensive Care Unit (CAM-ICU). The data on the use of tools to assess pain, sedation / agitation and delirium, as well as the recording of the use of mechanical restraints, were collected retrospectively on the nursing records of the patients evaluated, the day after their assessment. Statistic analysis First, a descriptive analysis was made of the general characteristics of the participating units and the study population, presenting the data with means and standard deviations (SD) or medians and interquartile ranges (RIC), as appropriate. Group comparison was performed with the Student t test for quantitative variables or nonparametric tests, as appropriate, and Fischer's test or chi-square for qualitative variables. The data was analyzed with the statistical package IBM SPSS Statistics 21.0 for Windows

Interventions

OTHERAssessment

Evaluation

Sponsors

Hospital Universitario Getafe
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All adult patients who were admitted to the participating units at the time of the audit and had a minimum stay of 24 hours in the unit.

Exclusion criteria

* no criteria

Design outcomes

Primary

MeasureTime frameDescription
Communicative patient's pain with Numeric Rating Scale (NRS) in critical care units.one dayPrimary assessment of pain. NRS scale's range from 0 to 10. 0: no pain; 1-3: light pain; 4-6: moderate pain; 7-10: severe pain
Non communicative patient's pain with Behavioural Indicators of Pain Scale (ESCID) in critical care units.one dayPrimary assessment of pain ESCID scale's range from 0 to 10. 0: no pain; 1-3: light pain; 4-6: moderate pain; 7-10: severe pain
Communicative and no communicative patient's sedation/agitation level's with Richmond Agitation Sedation Scale (RASS) in critcal care units.one dayPrimary assessment of sedation/agitation level' s. RASS scale range from -5 to +5. -4 to -5: depth sedation; -3 to -1: light sedation; 0: aware; +1 to +4: agitation.
Communicative and no communicative patient's delirium prevalence with Confusion Assessment Method for the Intensive Care Unit (CAM-ICU) in critical care unitsone dayPrimary assessment of delirium
Use of physical restraints on Communicative and no communicative patient's in critical care unitsone dayPrimary assessment of use of physical restraints

Secondary

MeasureTime frameDescription
use of validated scales of pain: Critical-Care Pain Observation Tool (CPOT)one dayuse of validated scales of pain for non communicative patients. CPOT: range from 0 to 8; 0-2: no pain, \> 2 pain.
use of validated scales of sedation/agitation (RASS)one dayuse of validated scales of sedation/agitation patients. RASS scale range from -5 to +5. -4 to -5: depth sedation; -3 to -1: light sedation; 0: aware; +1 to +4: agitation.
use of validated scales of sedation/agitation (Ramsay scale)one dayuse of validated scales of sedation/agitation patients. Ramsay score from 1 to 6; 1: anxious, agitated restless, 2: cooperative, oriented, tranquil, 3: responsive to commands only, 4: brisk response to light glabellar tap or loud auditory stimulus, 5: sluggish response to light glabellar tap or loud auditory stimulus, 6: no response to light glabellar tap or loud auditory stimulus.
use of validated scales of delirium (Intensive Care Delirium Screening Checklist (ICDSC))one dayUse of validated scales of delirium. ICDSC is positive (delirium present) or negative (no delirium).
use of validated scale of pain: Numeric Rating Scale (NRS)one dayuse of validated scales of pain for communicative patients. NRS scale's range from 0 to 10. 0: no pain; 1-3: light pain; 4-6: moderate pain; 7-10: severe pain.
protocols of pain and sedationone dayPresence of protocols in the critical care units
protocols of use of physical restraintsone dayPresence of protocols in the critical care units
protocols of management of deliriumone dayPresence of protocols in the critical care units
use of validated scales of delirium (CAM-ICU)one dayUse of validated scales of delirium. CAM-ICU is positive (delirium present) or negative (no delirium).
use of validated scale of pain: Visual Analog Scale (VAS)one dayuse of validated scales of pain for communicative patients. VAS, scale's range from 0 to 10. 0: no pain; 1-3: light pain; 4-6: moderate pain; 7-10: severe pain.
use of validated scale of pain: Campbell scaleone dayuse of validated scales of pain for non communicative patients. Campbell scale's range from 0 to 10. 0: no pain; 1-3: light pain; 4-6: moderate pain; 7-10: severe pain.
use of validated scale of pain: Behavioural Indicators of Pain Scale (ESCID)one dayuse of validated scales of pain for non communicative patients. ESCID scale's range from 0 to 10. 0: no pain; 1-3: light pain; 4-6: moderate pain; 7-10: severe pain.
use of validated scales of pain: Behavioral Pain Scale (BPS)one dayuse of validated scales of pain for non communicative patients. scale's range from 3 to 12; 3: no pain, high number more pain.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026