TY - JOUR
T1 - Effect of lung ultrasound-guided fluid deresuscitation on duration of ventilation in intensive care unit patients (CONFIDENCE)
T2 - protocol for a multicentre randomised controlled trial
AU - Blok, Siebe G.
AU - Mousa, Amne
AU - Brouwer, Michelle G.
AU - de Grooth, Harm Jan
AU - Neto, Ary Serpa
AU - Blans, Michiel J.
AU - den Boer, Sylvia
AU - Dormans, Tom
AU - Endeman, Henrik
AU - Roeleveld, Timo
AU - Scholten, Harm
AU - van Slobbe-Bijlsma, Eline R.
AU - Scholten, Erik
AU - Touw, Hugo
AU - van der Ven, Fleur Stefanie L.I.M.
AU - Wils, Evert Jan
AU - van Westerloo, David J.
AU - Heunks, Leo M.A.
AU - Schultz, Marcus J.
AU - Paulus, Frederique
AU - Tuinman, Pieter R.
N1 - Funding Information:
This study is completely funded by The Netherlands Organisation for Health Research and Development (ZonMW). ZonMW does not have any role in the design of the study; collection, analysis, and interpretation of the data nor in writing the manuscript.
Publisher Copyright:
© 2023, The Author(s).
PY - 2023/3/24
Y1 - 2023/3/24
N2 - Background: Fluid therapy is a common intervention in critically ill patients. It is increasingly recognised that deresuscitation is an essential part of fluid therapy and delayed deresuscitation is associated with longer invasive ventilation and length of intensive care unit (ICU) stay. However, optimal timing and rate of deresuscitation remain unclear. Lung ultrasound (LUS) may be used to identify fluid overload. We hypothesise that daily LUS-guided deresuscitation is superior to deresuscitation without LUS in critically ill patients expected to undergo invasive ventilation for more than 24 h in terms of ventilator free-days and being alive at day 28. Methods: The “effect of lung ultrasound-guided fluid deresuscitation on duration of ventilation in intensive care unit patients” (CONFIDENCE) is a national, multicentre, open-label, randomised controlled trial (RCT) in adult critically ill patients that are expected to be invasively ventilated for at least 24 h. Patients with conditions that preclude a negative fluid balance or LUS examination are excluded. CONFIDENCE will operate in 10 ICUs in the Netherlands and enrol 1000 patients. After hemodynamic stabilisation, patients assigned to the intervention will receive daily LUS with fluid balance recommendations. Subjects in the control arm are deresuscitated at the physician’s discretion without the use of LUS. The primary endpoint is the number of ventilator-free days and being alive at day 28. Secondary endpoints include the duration of invasive ventilation; 28-day mortality; 90-day mortality; ICU, in hospital and total length of stay; cumulative fluid balance on days 1–7 after randomisation and on days 1–7 after start of LUS examination; mean serum lactate on days 1–7; the incidence of reintubations, chest drain placement, atrial fibrillation, kidney injury (KDIGO stadium ≥ 2) and hypernatremia; the use of invasive hemodynamic monitoring, and chest-X-ray; and quality of life at day 28. Discussion: The CONFIDENCE trial is the first RCT comparing the effect of LUS-guided deresuscitation to routine care in invasively ventilated ICU patients. If proven effective, LUS-guided deresuscitation could improve outcomes in some of the most vulnerable and resource-intensive patients in a manner that is non-invasive, easy to perform, and well-implementable. Trial registration: ClinicalTrials.gov NCT05188092.
AB - Background: Fluid therapy is a common intervention in critically ill patients. It is increasingly recognised that deresuscitation is an essential part of fluid therapy and delayed deresuscitation is associated with longer invasive ventilation and length of intensive care unit (ICU) stay. However, optimal timing and rate of deresuscitation remain unclear. Lung ultrasound (LUS) may be used to identify fluid overload. We hypothesise that daily LUS-guided deresuscitation is superior to deresuscitation without LUS in critically ill patients expected to undergo invasive ventilation for more than 24 h in terms of ventilator free-days and being alive at day 28. Methods: The “effect of lung ultrasound-guided fluid deresuscitation on duration of ventilation in intensive care unit patients” (CONFIDENCE) is a national, multicentre, open-label, randomised controlled trial (RCT) in adult critically ill patients that are expected to be invasively ventilated for at least 24 h. Patients with conditions that preclude a negative fluid balance or LUS examination are excluded. CONFIDENCE will operate in 10 ICUs in the Netherlands and enrol 1000 patients. After hemodynamic stabilisation, patients assigned to the intervention will receive daily LUS with fluid balance recommendations. Subjects in the control arm are deresuscitated at the physician’s discretion without the use of LUS. The primary endpoint is the number of ventilator-free days and being alive at day 28. Secondary endpoints include the duration of invasive ventilation; 28-day mortality; 90-day mortality; ICU, in hospital and total length of stay; cumulative fluid balance on days 1–7 after randomisation and on days 1–7 after start of LUS examination; mean serum lactate on days 1–7; the incidence of reintubations, chest drain placement, atrial fibrillation, kidney injury (KDIGO stadium ≥ 2) and hypernatremia; the use of invasive hemodynamic monitoring, and chest-X-ray; and quality of life at day 28. Discussion: The CONFIDENCE trial is the first RCT comparing the effect of LUS-guided deresuscitation to routine care in invasively ventilated ICU patients. If proven effective, LUS-guided deresuscitation could improve outcomes in some of the most vulnerable and resource-intensive patients in a manner that is non-invasive, easy to perform, and well-implementable. Trial registration: ClinicalTrials.gov NCT05188092.
KW - Critical care
KW - Deresuscitation
KW - Invasive ventilation
KW - Lung ultrasound
KW - Pulmonary oedema
KW - Randomised controlled trial
KW - Intensive Care Units
KW - Lung/diagnostic imaging
KW - Humans
KW - Ultrasonography, Interventional
KW - Critical Illness
KW - Randomized Controlled Trials as Topic
KW - Critical Care/methods
KW - Multicenter Studies as Topic
KW - Respiration, Artificial/methods
KW - Adult
UR - http://www.scopus.com/inward/record.url?scp=85150965075&partnerID=8YFLogxK
U2 - 10.1186/s13063-023-07171-w
DO - 10.1186/s13063-023-07171-w
M3 - Article
C2 - 36964614
AN - SCOPUS:85150965075
SN - 1745-6215
VL - 24
JO - Trials
JF - Trials
M1 - 226
ER -