Fluid Responsiveness Evaluation by AbdomiNal Compression in Kids Based on the STARLING Concept (FRANCK)
Purpose:
Fluid responsiveness in a context of circulatory failure can be predicted by different way. Dynamic criteria such as pulse pressure variation, stroke volume variation during an end-expiratory occlusion maneuver or a passive leg raising have been reported to predict fluid responsiveness. Only aortic velocity peak variation measured with transthoracic echocardiography during mechanical ventilation has been reported to predict fluid responsiveness in children. Besides some physician use a maneuver of abdominal compression to predict fluid responsiveness in children with circulatory failure. This strategy has never been formally evaluated.
The investigators will study the diagnosis accuracy of the stroke volume variation induced by an abdominal compression to predict stroke volume variation after 10 ml/kg fluid load in children with circulatory failure.
Thirty-eight pediatric patients under eight years old in circulatory failure, for whom the attending physician has decided a fluid load will be included. Hemodynamic parameters: arterial pressure, heart rate, stroke volume measured with echocardiography; will be recorded. This data collection will be performed before, after abdominal compression and after a fluid load of 10 ml/kg.
Patients will be aposteriori sorted in two groups: Fluid responders and Fluid non-responders. Fluid responders are defined as patients that show an increase greater than 15 % in stroke volume. The diagnosis ability of the Stroke volume variation after an abdominal compression to predict fluid responsiveness will be investigate and receiving operative characteristic (ROC) curve will be built. The correlation between the variation of stroke volume during abdominal compression and during the fluid load will be studied. Other parameters such as arterial pressure and heart rate will also be investigated.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Studientyp
Einschreibung (Tatsächlich)
Kontakte und Standorte
Studienorte
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Lyon, Frankreich
- Intensive care and anesthesiology department, Hôpital Louis Pradel.
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Lyon, Frankreich
- Pediatric Intensive care, Hôpital Femme Mère Enfant
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Probenahmeverfahren
Studienpopulation
Beschreibung
Inclusion Criteria:
- Age < 8 years old
- Patient with a circulatory failure defined as follow :
Treatment including vasopressor or inotrope
OR macrocirculatory failure
- Heart rate > 2 Standard Deviation (SD)
- Systolic arterial pressure < 2 SD
- Mean arterial pressure < 2 SD
- Diastolic arterial pressure < 2 SD
WITH signs of microcirculatory failure
- Capillary refill time > 2 secondes
- Blotch
- Organ dysfunction due to the circulatory failure (Oliguria < 0,5 ml/kg/h, acute lung injury, encephalopathy)
Exclusion Criteria:
- Opposition from the parents or the one who holds the parental authority
- Cardiogenic acute pulmonary edema,
- Extreme hemodynamic instability,
- Intra-abdominal hypertension,
- Recent abdominal surgery that does not permit an abdominal compression without causing pain.
- Patient with mechanical circulatory support, such as Extra Corporal Life Support or Berlin-Heart
- Patient with congenital cardiopathy with a palliative correction or an incomplete correction
- Open thorax
- Prone position
- Investigators not available
- No security number registration.
- Moribund patient
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
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Ability of the stroke volume variation after abdominal compression to predict fluid responsiveness
Zeitfenster: 30 minutes
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Stroke volume will be measured before and after a calibrated abdominal compression and after a fluid load.
Patient will then be sorted in two groups.
Responders defined as patient that show an increase in stroke volume after a 10ml/kg fluid load and Fluid non responders, defined as patient that show an increase of less than 15 % in stroke volume.
The ROC curve will investigate the ability of stroke volume variation after abdominal compression to predict fluid responsiveness.
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30 minutes
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
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Ability of the pulse pressure variation after abdominal compression to predict fluid responsiveness
Zeitfenster: 30 minutes
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30 minutes
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Ability of the heart rate variation after abdominal compression to predict fluid responsiveness
Zeitfenster: 30 minutes
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30 minutes
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Correlation between stroke volume variation, heart rate variation, pulse pressure variation between the abdominal compression and the fluid load
Zeitfenster: 30 minutes
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30 minutes
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Mitarbeiter und Ermittler
Sponsor
Ermittler
- Studienleiter: Jean-Luc Fellahi, MD, PhD, Hôpital Louis Pradel, Hospice Civil de Lyon
Publikationen und hilfreiche Links
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Schätzen)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- EudraCT/ANSM 2015-A00388-41
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