Perfusion Parameters and Outcome During a Standardized Deresuscitation Strategy with Net Ultrafiltration: a Retrospective Cohort Study.
NCT ID: NCT06899880
Last Updated: 2025-03-28
Study Results
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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COMPLETED
120 participants
OBSERVATIONAL
2024-01-01
2024-04-01
Brief Summary
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The aim of the study was to describe perfusion during deresuscitation, and to determine whether it is associated with major adverse kidney events at day 30.
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Standardized deresuscitation strategy
Eligible patients without hypoperfusion benefited from: 1) a restrictive approach of intakes combining hypercaloric enteral or per os feeding with hydric restriction as much as possible and no fluid of maintenance, and 2) a systematic UFnet of 2 mL/kg/h until reaching dry weight and a systematic monitoring every 6 h of: peripheral perfusion by capillary refilling time and mottling score, arterial lactate level, and central venous oxygen saturation.
Describe the perfusion parameters during a deresuscitation strategy and their association with the outcome.
Arterial lactate, pCO2 gap, SvO2, capillary refill time and mottling score anomalies will be described during the first 5 days of the deresuscitation strategy.
Interventions
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Describe the perfusion parameters during a deresuscitation strategy and their association with the outcome.
Arterial lactate, pCO2 gap, SvO2, capillary refill time and mottling score anomalies will be described during the first 5 days of the deresuscitation strategy.
Eligibility Criteria
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Inclusion Criteria
* Acute kidney injury requiring continuous renal replacement therapy
* Standardized deresuscitation following a routine care protocol
Exclusion Criteria
* Advanced directives to withhold or withdraw life-sustaining treatment,
* Patient's opposition to the use of his/her personal health data
18 Years
ALL
No
Sponsors
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Hospices Civils de Lyon
OTHER
Responsible Party
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Locations
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Louis Pradel Hospital
France, Bron, France
Countries
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Other Identifiers
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24-5563
Identifier Type: -
Identifier Source: org_study_id
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