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Pilot Study for the SQUEEZE Trial

Phase 3
Completed
Conditions
Septic Shock
Interventions
Other: Fluid Sparing Resuscitation Strategy
Registration Number
NCT01973907
Lead Sponsor
McMaster Children's Hospital
Brief Summary

The purpose of the SQUEEZE Trial is to determine which fluid resuscitation strategy results in the best outcomes for children treated for suspected or confirmed septic shock. In this study, eligible children will be randomized to either the 'Usual Care Arm' or the 'Fluid Sparing Arm'. Children will receive treatment according to current ACCM Septic Shock Resuscitation Guidelines, with the assigned resuscitation strategy used to guide administration of further fluid boluses as well as the timing of initiation and escalation of vasoactive medications to achieve ACCM recommended hemodynamic targets.

Detailed Description

Current pediatric surviving sepsis guidelines from the American College of Critical Care Medicine (ACCM) emphasize an early and goal-directed approach to resuscitation. These guidelines suggest that fluid resuscitation should be aggressive with repeated intravenous (IV) fluid boluses of 20 mL/kg, such that some children may require as much as 200 mL/kg of fluid to achieve therapeutic endpoints. The guidelines also recommend the initiation of vasoactive agents at the stage of "fluid refractory shock", i.e. when there is persistent hypoperfusion despite at least 60 ml/kg IV fluid. Improvements in pediatric septic shock survival have been attributed to adherence to the first iteration of the ACCM septic shock guidelines, and the use of goal directed targets. However, the largest and most publicized pediatric trial of fluid resuscitation in children with suspected septic shock (FEAST Trial), published in NEJM in 2011, demonstrated an increased mortality among children treated with aggressive fluid resuscitation in comparison to the conservative fluid resuscitation arm. As a result, the pediatric critical care community clearly acknowledges that these results, while important, are not necessarily generalizable to developed countries such as Canada.

Emerging publications in the ICU literature suggest that excessive compared to conservative fluid administration in adults with septic shock worsens outcomes such as duration of mechanical ventilation, complications related to the third-spacing of fluids, length of ICU stay, and mortality. A systematic review published in August 2012 reveals a paucity of randomized controlled trial (RCT) evidence apart from the FEAST trial examining the impact of fluid resuscitation on mortality in children with septic shock. This raises the important question of whether children in developed countries would also benefit from a fluid sparing resuscitation strategy to achieve the ACCM goal-directed targets. Use of such a fluid sparing strategy would, by default, require earlier initiation and preferential escalation of vasoactive medications to meet ACCM hemodynamic goals. The optimal degree of fluid resuscitation and the timing of initiation of vasoactive support in order to achieve therapeutic targets in children with septic shock remains unanswered.

This Pilot Randomized Controlled Trial constitutes the first step in answering our research question of whether, in pediatric patients with septic shock, use of a fluid sparing strategy to achieve ACCM therapeutic goals, results in improved clinical outcomes without an increased risk of adverse events, compared to the usual care of aggressive fluid resuscitation as currently recommended by the ACCM guidelines. The purpose of the pilot study is to determine feasibility and inform the appropriate methodological design of the larger multi-centre RCT to fully answer our research question. The hypothesis of the pilot study is that the SQUEEZE Trial is feasible to conduct.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
53
Inclusion Criteria

Inclusion Criteria for 1 and 3 must be answered YES to be eligible for study.

  1. Age 29 days to less than 18 years of age

2a) Patient has Persistent Signs of Shock including one or more of the following: i) Vasoactive Medication Dependence ii) Hypotension (Systolic Blood Pressure and/or Mean Blood Pressure less than the 5th percentile for age) iii) Abnormal Perfusion (2 or more of: abnormal capillary refill, tachycardia, decreased level of consciousness, decreased urine output)

2b) Suspected or Confirmed Septic Shock (Shock due to Suspected or Confirmed Infectious Cause)

2c) Patient has received initial fluid resuscitation of: Minimum of 40 mL/kg of isotonic crystalloid (0.9% Normal Saline and/or Ringer's Lactate) and/or colloid (5% albumin) as fluid boluses within the previous 6 hours for patients weighing less than 50 kg, OR Minimum of 2 litres (2000 mL) of isotonic crystalloid (0.9% Normal Saline and/or Ringer's Lactate) and/or colloid (5% albumin) as fluid boluses within the previous 6 hours for patients weighing 50 kg or more

  1. Patient has Fluid Refractory Septic Shock as defined by the Presence of all of 2a, 2b, and 2c.
Exclusion Criteria
  • Patient admitted to the Neonatal Intensive Care Unit (NICU)
  • Patient requiring resuscitation in the Operating Room (OR) or Post-Anesthetic Care Unit (PACU)
  • Full active resuscitative treatment not within the goals of care
  • Shock Secondary to Cause other than Sepsis (i.e. obvious signs of cardiogenic shock, anaphylactic shock, hemorrhagic shock, spinal shock)
  • Previous enrolment in this trial, where known by the research team

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Fluid Sparing Resuscitation StrategyFluid Sparing Resuscitation StrategyThe treating physician and medical team are advised to follow the assigned Fluid Sparing Resuscitation Strategy to guide decisions regarding the IV/IO administration of further isotonic fluid boluses, and the timing of initiation and escalation of vasoactive medication infusions to target the therapeutic endpoints recommended in the ACCM guidelines for the resuscitation of neonatal and pediatric septic shock.
Primary Outcome Measures
NameTimeMethod
Feasibility of conducting the SQUEEZE TrialThe earliest of: 1. Recruitment of the planned 50 participants, or 2. 24 months following initiation of recruitment

The Primary Outcome of Feasibility of conducting the SQUEEZE Trial will be evaluated based on the following:

1. Participant enrolment rate: We will define success as an enrolment rate of at least 2 patients/month (recognizing that enrolment may be slower during the study run-in phase).

2. Protocol adherence: the ability to execute the study procedures. We will assess our ability to initiate study procedures in enrolled patients within 1 hour of randomization.

Secondary Outcome Measures
NameTimeMethod
Clinical outcomesThe earliest of: 1. Recruitment of the planned 50 participants, or 2. 24 months following initiation of recruitment

We will assess our ability to collect clinical outcome data of interest to determine the most appropriate outcomes, perform a sample size calculation, and inform the design of a definitive multi-centered RCT. Clinical outcomes include:

i) PICU admission rate, PICU Length of Stay, Ventilator Free Days, Acuity Scores (PRISM III), Organ Dysfunction scores (PELOD, PELOD 2), Vasoactive Medication Score, Mortality (28-day, 60-day, and 90-day), Hospital Mortality

ii) Adverse Events- complications which may be attributable to third spacing of fluid, or inotrope/vasopressor use, including: Intrabdominal Hypertension, Abdominal Compartment Syndrome, Pulmonary Edema, Pleural Effusion requiring drainage, Signs of Digital Ischemia, Digital/Limb Revision amputation, Bowel Ischemia

iii) Short term hemodynamic outcomes- time to shock reversal determined by freedom from vasoactive medication(s), bedside hemodynamic measurements (HR, MAP, CVP, and non-invasive CO (CI) measurement (USCOM)

Management FeasibilityThe earliest of: 1. Recruitment of the planned 50 participants, or 2. 24 months following initiation of recruitment

We will collect descriptive data related to study Management feasibility to inform conduct of a multi-centred RCT.

Appropriateness of eligibility criteriaThe earliest of: 1. Recruitment of the planned 50 participants, or 2. 24 months following initiation of recruitment

We will determine our ability to enroll patients based on the current eligibility criteria, to inform the design of a future multi-centered RCT.

Resource FeasibilityThe earliest of: 1. Recruitment of the planned 50 participants, or 2. 24 months following initiation of recruitment

We will collect descriptive data related to study Resource feasibility to inform conduct of a multi-centred RCT.

Process FeasibilityThe earliest of: 1. Recruitment of the planned 50 participants, or 2. 24 months following initiation of recruitment

We will collect descriptive data related to study Process feasibility to inform conduct of a multi-centred RCT

Trial Locations

Locations (1)

McMaster Children's Hospital

🇨🇦

Hamilton, Ontario, Canada

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