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.
Przegląd badań
Status
Warunki
Interwencja / Leczenie
Typ studiów
Zapisy (Rzeczywisty)
Kontakty i lokalizacje
Lokalizacje studiów
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Lyon, Francja
- Intensive care and anesthesiology department, Hôpital Louis Pradel.
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Lyon, Francja
- Pediatric Intensive care, Hôpital Femme Mère Enfant
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Metoda próbkowania
Badana populacja
Opis
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
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Ability of the stroke volume variation after abdominal compression to predict fluid responsiveness
Ramy czasowe: 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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Miary wyników drugorzędnych
Miara wyniku |
Ramy czasowe |
|---|---|
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Ability of the pulse pressure variation after abdominal compression to predict fluid responsiveness
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 30 minutes
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30 minutes
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Współpracownicy i badacze
Sponsor
Śledczy
- Dyrektor Studium: Jean-Luc Fellahi, MD, PhD, Hôpital Louis Pradel, Hospice Civil de Lyon
Publikacje i pomocne linki
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Oszacować)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Oszacować)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- EudraCT/ANSM 2015-A00388-41
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