This study evaluates if improvement of renal resistive index when mean arterial pressure increase (at 65 mmHg to 85 mmHg) in early phase of septic shock is predictive of better renal survival.
Learned societes (survival sepsis campaign and ESICM) are currently recommending a mean arterial pressure (MAP) target at 65 mmHg in septic shoc with a potential increase to 85 mmHg in patients with medical history of arterial hypertension. A high renal resistive index on the first day of septic shock was associated with acute renal failure more frequently on the 5th day. A decrease in the renal resistance index was also objectified during the increase in MAP. The main objective of this trial is to study the relationship between the improvement of the resistance index during a test of increase in average blood pressure during septic shock and the improvement of renal function In this interventional monocenter trial, we will measure the renal resistive index after stabilization of the MAP at 65 mmHg for two hours, then after 2 hours of stabilization at 85 mmHg. This part allows us to define the patients "responding" to the renal resistive index (improvement of the resitive renal index when the MAP increases). Then, patients will be randomized into two groups : * first group with a MAP target at 65 mmHg * second group with a MAP target at 85 mmHg. There will be a stratification on the responder character to the renal resistance index. Finally, we will assess renal function on the 7th day (with the assessment of serum creatinine and the change of stage of the KDIGO classification)
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
80
increase of mean arterial pressure at 80-85 mmHg (with catecholamines or volemic expansion).
increase of mean arterial pressure at 65-70 mmHg (with catecholamines or volemic expansion).
CHU Angers. Médecine Intensive Réanimation et médecine hyperbare
Angers, France
changes of KDIGO stage
modification of the KDIGO classification stage (estimated based on serum creatinine and diuresis) between the group with low target of mean arterial pressure ( 65-70 mmHg) and high target MAP (80-85 mmHg)
Time frame: Inclusion and day 7
Renal resistive index
We will assess the evolution of the renal resistive index during an increase in the target of MAP in the early phase of septic shock . We will assess the evolution of renal resistive index according to the comorbidities, as a function of time in septic shock, according to the hemodynamic data, according to quantity of filling solution administered and catecholamine doses
Time frame: Inclusion, and 2 hours of mean arterial pressure stabilized at 85 mmHg and every day (day 1 to day 7)
Collection of all adverse event
Difference in sides effects between target at 65-70 mmHg of MAP and 80-85 mmHg.
Time frame: Day 1 to day 7
amount of fluids (unit = L or L/day)
Time frame: Inclusion, day 1 to day 7
catecholamines free days
Time frame: day 1 to day 7
extra renal replacement free days
Difference in need of renal replacement therapy between the group of 80-85mmHg and the groupe 65-70 mmHg, depending on the responder character
Time frame: Daily to day 1 to day 7, at day 28 and day 90
Number of day with supportive care in intensive care unit (renal replacement therapy, mechanical ventilation, extracorporeal membrane oxygenation)
Quantification of the number of days with supportive care (catecholamine,renal replacement therapy, mechanical ventilation, extracorporeal membrane oxygenation)
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Time frame: Collection daily between Day 1 and Day 7, at Day 28.
Number of day in intensive care unit
Quantification of the number of days hospitalized in intensive care unit
Time frame: Collection at Day 28 and Day 90
Number of day in hospital
Quantification of the number of days hospitalized.
Time frame: Collection at Day 28 and Day 90
hemodynamic data collected by swan ganz or PICCO catheter
Time frame: Inclusion and at 2 hours, daily between Day 1 and Day 7
quantity of nephrotoxic drugs
Time frame: Inclusion and daily between Day 1 and Day 7.
serum creatinine (unit = µmol/L)
Time frame: Inclusion and daily between Day 1 and Day 7
Diuresis (unit = mL per day)
Time frame: Daily between day 1 and day 7
Survival at day 28
Time frame: patient status (live or dead) at day 28
Survival at day 90
Time frame: patient status (live or dead) at day 90
Skin recoloration time evolution
measurement onto the right index finger by a standardized method after 2 hours of stabilization at 65 mmHg and after 2 hours of stabilization at 85 mmHg.
Time frame: Inclusion and at 2 hours, daily between Day 1 and Day 7
Skin recoloration time evolution
measurement onto the right index fingerby a standardized method depending on the randomization group.
Time frame: Inclusion and at 2 hours, daily between Day 1 and Day 7