Prevalence and Predictors of CCI in Patients With Acute Respiratory Failure (CCI)

NCT ID: NCT03851822

Last Updated: 2022-03-23

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

127 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-01-01

Study Completion Date

2022-01-01

Brief Summary

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Chronic Critical Illness (CCI) is a condition associated to patients surviving an acute phase of disease and respiratory failure (ARF) although remaining dependent on mechanical ventilation (MV). The prevalence and the underlying mechanisms of CCI have not been elucidated in this population.An observational prospective cohort study was undertaken at the Respiratory Intensive Care Unit (RICU) of the University Hospital of Modena (Italy) from January 2016 to January 2018. Patients mechanically ventilated with ARF in this unit were enrolled. Demographics, diagnosis, severity scores (APACHEII, SOFA, SAPSII) and clinical conditions (septic shock, infections, acute respiratory distress syndrome \[ARDS\]) were recorded on admission. Respiratory mechanics and inflammatory-metabolic blood parameters were recorded on admission and within the first seven days of stay. All these variables were tested as potential predictors of CCI through appropriate univariate and multivariate analysis.

Detailed Description

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Conditions

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Critical Illness

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* older than 18 years of age
* consecutively admitted to RICU due to acute respiratory failure (ARF) requiring mechanical ventilation.

Exclusion Criteria

* refractory shock (death \< 24h)
* patient goals of care not consistent with aggressive management
* end stage COPD requiring home oxygen long term therapy or home non invasive ventilation support
* presence of interstitial lung disease
* history of neuromuscular disease
* chest wall deformities
* pregnancy
* chemotherapy or radiotherapy within the past 30 days
* evidence of neurologic injury on CT scan and GCS \< 8
* tracheostomy.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Modena and Reggio Emilia

OTHER

Sponsor Role lead

Responsible Party

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Alessandro Marchioni

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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UModenaReggio3

Identifier Type: -

Identifier Source: org_study_id

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