Overview

The Effect of Fluid Resuscitation With 0.9% Sodium Chloride Versus Balanced Crystalloid Solution on Renal Function of Sepsis Patients

Status:
Completed
Trial end date:
2021-03-01
Target enrollment:
0
Participant gender:
All
Summary
The high chloride content of 0.9%sodium chloride (0.9%NaCl) leads to adverse pathophysiological effects in both animals and healthy human volunteers. Small randomized trials confirm that the hyperchloremic acidosis induced by 0.9%NaCl also occurs in patients. A strong signal is emerging from recent large propensity-matched and cohort studies for the adverse effects that 0.9% NaCl has on the clinical outcome in surgical and critically ill patients when compared with balanced crystalloids. Major complications are the increased incidences of acute kidney injury and the need for renal replacement therapy, and that pathological hyperchloremia may increase postoperative mortality. Fluid resuscitation with 0.9% NaCl in animals with sepsis resulted in hyperchloremic metabolic acidosis, worsened AKI, and increased mortality when compared with resuscitation with a balanced crystalloid solution. Furthermore, hyperchloremic acidosis also resulted in increased concentrations of circulating inflammatory mediators in an experimental model of severe sepsis in rats, with a dose-dependent increase in circulating interleukin-6, tumor necrosis factor-a, and interleukin-10 concentrations with increasing acidosis. Thus, in this study, investigators compared the effects of a balanced crystalloid solution with 0.9% NaCl on the renal function in severe sepsis/septic shock patients. Investigators hypothesized that balanced crystalloid solution resuscitation would decrease AKI incidence and severity and would improve immunomodulatory effect when compared with 0.9% NaCl resuscitation.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Chulalongkorn University
Treatments:
Pharmaceutical Solutions
Criteria
Inclusion Criteria:

- Age ≥ 18 years old

- Who need fluid resuscitation in the Emergency Room (ER).

- Who have fulfilled the criteria for sepsis/septic shock within the previous 24 hours
according to sepsis is defined as life-threatening organ dysfunction caused by a
dysregulated host response to infection.

o Patients with infection and resulted from a host's systemic inflammatory response
syndrome (SIRS) to infection are defined as sepsis if meet the criteria 2 or more of

- Temperature >38°C or <36°C

- Heart rate >90/min

- Respiratory rate >20/min or PaCo2 <32 mm Hg (4.3 kPa)

- White blood cell count >12000/mm3 or <4000/mm3 or >10% immature bands.

- Patient who have Septic shock is a subset of sepsis in which underlying circulatory
and cellular/metabolic abnormalities are profound enough to substantially increase
mortality.

o Patients with septic shock can be identified with a clinical construct of sepsis
with persisting hypotension requiring vasopressors to maintain MAP ≥65 mm Hg and
having a serum lactate level >2 mmol/L (18 mg/dL) despite adequate volume
resuscitation.

- AND where informed consent is obtainable either from the patient or by proxy (first
degree relative, spouse) if patients aren't in fully conscious status (eg.comatose,
drowsiness, irritable).

Exclusion criteria

Exclusion Criteria:

- Patients with chronic kidney disease (CKD) defined by baseline serum creatinine > 2.0
in male and 1.5 in female.

- Patients with End stage renal disease (ESRD) with or without renal replacement
therapy.

- Patients with active cardiac disease : severe valvular heart, cardiomyopathy,
decompensated heart failure NYHA II-IV, severe pulmonary hypertension.

- HIV/AIDs Patients.

- Allergy towards 0.9% NaCl or Ringer's Acetate.

- Any form of renal replacement therapy.

- Intracranial bleeding within current hospitalization.

- Therapy with corticosteroid or non steroidal anti-inflammatory substance.

- Patients who predicted not to survive more than 24 hours.

- Pregnant and lactating patients.

- Withdrawal of active therapy.