Efficacy and Safety of Rapid Intermittent Compared With Slow Continuous Correction in Severe Hyponatremia Patients
Hyponatremia Symptomatic
About this trial
This is an interventional treatment trial for Hyponatremia Symptomatic focused on measuring Hyponatremia, Hypertonic saline, Treatment, Osmotic demyelination syndrome
Eligibility Criteria
Inclusion Criteria:
- In emergency setting (2016.6-) and/or inpatients at ward (2018.9-)
- Glucose corrected serum sodium ≤125 mmol/L
Patients with moderately severe or severe symptom
Moderately severe
:Nausea without vomiting Drowsy, Headache General weakness, myalgia
- Severe :Vomiting, Stupor, Seizures, Coma (Glasgow Coma Scale ≤8)
- written consent
Exclusion Criteria:
Pseudohyponatremia: serum osmolality > 275 mOsm/kg
- If the serum osmolality is > 275 mOsm/kg but the BUN is ≥ 30 mg/dL, the patients can be registered if calculated serum osmolality (2 x plasma [Na] + [Glucose]/18) is <275 mOsm/kg
- Primary polydipsia: urine osmolality ≤ 100 mOsm/kg
- Glucose corrected serum sodium >125 mmol/L
- Arterial hypotension (SBP <90mmHg and MAP <70mmHg)
- Anuria or urinary outlet obstruction
Liver disease
- transaminase levels >3 times the upper limit normal
- Known LC with ascites or diuretics use or PSE Hx or Varix Hx
- Uncontrolled diabetes mellitus (HbA1C > 9%)
- Women who are pregnant or breast feeding
- History of cardiac surgery excluding PCA, acute myocardial infarction, sustained ventricular tachycardia, ventricular fibrillation, acute coronary syndrome, cebrovascular trauma, and increased intracranial pressure within the 3 months prior to randomization
Sites / Locations
- Hallym University Dongtan Sacred Hospital
- Seoul National University Bundang Hospital Clinical Trial Center
- Seoul National University Boramae Hospital
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Intermittent bolus group
slow continuous infusion group
<<Within 6hr>> Moderately Severe : 3% saline 2ml/kg over 20min *1 (unknown bwt 100ml) Severe :3% saline 2ml/kg over 20min *2 (unknown bwt 100ml) <additional treatment> Repeat 3% saline 2ml/kg over 20min at every sample time point (at 1/6hr) till Na 5-9 mmol/L inc from initial Na and sx relief <<During 6-24hr>> - Moderately Severe or Severe : Repeat 3% saline 2ml/kg over 20min at every sample time point(at 12/18/24hr) till Na 5-9 mmol/L inc from initial Na and sx relief <<During 24-48hr>> Moderately Severe or Severe : Repeat 3% saline 2ml/kg over 20min at every sample time point (at 30/36/42/48hr) till Na 10-17 mmol/L inc from initial Na or Na ≥ 130mmol and sx relief
<<Within 24hr>> - Moderately Severe: 3% saline 0.5ml/kg/hr (unknown bwt 25ml/hr) - Severe: 3% saline 1ml/kg/hr (unknown bwt 50ml/hr) Infusion protocol modification as below by Na at every sample time point (at 1/6/12/18/24 hr) If Na 5-9 mmol/L inc from initial Na and sx relief : stop 3% saline infusion regardless of △ Na if △ Na inc <0.5mmol/hr or △ Na inc <3mmol/6hr : add 0.25ml/kg/hr, restart 0.5ml/kg/hr if previously stopped if △ Na inc ≥0.5mmol/hr or △ Na inc ≥ 3mmol/6hr : maintain infusion rate <<During 24-48hr>> - Moderately Severe and Severe Infusion protocol modification as below by Na at every sample time point (at 30/36/42/48hr) If Na 10-17 mmol/L inc from initial Na or Na ≥ 130mmol and sx relief : stop 3% saline infusion regardless of △ Na if △ Na inc <1.5mmol/6hr : add 0.25ml/kg/hr or restart 0.25ml/kg/hr if previously stopped if △ Na inc ≥ 1.5mmol/6hr : maintain infusion rate