Sodium Bicarbonate (sodium bicarbonate)
Bicarbonates Intravenous Syringe (Ml)
Last reviewed · Source: First Databank (FDB) drug data
Overview
Sodium bicarbonate is an alkalinizing agent.
Sodium bicarbonate is a systemic alkalizer and electrolyte replenisher. IV administration of sodium bicarbonate elevates plasma bicarbonate concentrations, buffers excess hydrogen ions, increases systemic pH, and reverses the clinical manifestations of acidosis.
In aqueous solution, sodium bicarbonate dissociates into sodium (Na+) and bicarbonate (HCO3-) ions. Sodium, the predominant extracellular cation, plays a critical role in the management of fluid and electrolyte disturbances. Bicarbonate is an endogenous constituent of body fluids, with normal plasma concentrations ranging from 24-31 mEq/L.
Plasma concentrations are maintained by renal mechanisms, through urinary acidification in states of deficit or urinary alkalinization in states of excess.
Sodium bicarbonate solution has an approximate pH of 8.0 (7.0-8.5). Sodium bicarbonate solutions contain equal amounts (mEq/mL) each of sodium and bicarbonate ions. The 8.4, 7.5, and 4.2% concentration solutions contain 1 mEq/mL, 0.892 mEq/mL, and 0.5 mEq/mL, respectively, of each ion.
These solutions are very hyperosmolar-- 2000 mOsm/L for the 8.4% concentration and 1786 mOsm/L for the 7.5% concentration.
The bicarbonate anion is considered chemically labile, as it may combine with hydrogen ions to form carbonic acid (H2CO3), which subsequently converts to its volatile form, carbon dioxide (CO2), which is excreted by the lungs. Under physiologic conditions, the extracellular fluid maintains a 1:20 ratio of carbonic acid to bicarbonate. In adults with normal renal function, virtually all bicarbonate filtered at the glomerulus is reabsorbed, with urinary excretion typically accounting for <1%.
Oral administration of sodium bicarbonate leads to systemic absorption of excess bicarbonate, which induces metabolic alkalosis and promotes urinary alkalinization. IV administration achieves complete bioavailability. The onset of action after an IV push is rapid, with a mean onset of 8-10 minutes.
Sodium bicarbonate is extensively distributed within the extracellular fluid compartment. The elimination half-life of sodium bicarbonate is unknown.
Sodium bicarbonate is used parenterally as an alkalinizing agent in the treatment of metabolic acidosis, which may occur in severe renal disease, uncontrolled diabetes, circulatory insufficiency due to shock or severe dehydration, extracorporeal circulation of blood, cardiac arrest, and severe primary lactic acidosis. Sodium bicarbonate is also used parenterally for the treatment of certain drug intoxications, including barbiturates, salicylate or methyl alcohol poisoning, and in the treatment of hemolytic reactions requiring alkalinization of the urine to diminish the nephrotoxic effects of blood pigments. In addition, sodium bicarbonate is used parenterally in the treatment of severe diarrhea accompanied by substantial GI bicarbonate loss.
Generic name: sodium bicarbonate
Drug class: Bicarbonates
Therapeutic class: Electrolyte Balance-Nutritional Products
Reference product & biosimilars
No reference, biosimilar or interchangeable associated with this drug.
Today’s intelligence on Sodium Bicarbonate
Indications
The following indications are listed for Sodium Bicarbonate:
- Metabolic Acidosis
- Salicylate Intoxication
- Severe Diarrhea
- Toxic Phenobarbital Serum Level
- Tricyclic Antidepressant Overdose
- Urine Alkalinization
Also known as: Alkalinize The Urine, Aspirin Overdose, Overdose Of Phenobarbital, Phenobarbital Intoxication, Profuse Diarrhea, Salicylate Overdose, Secretory Diarrhea, Toxic Phenobarbital Concentration, Tricyclic Antidepressant Drug Intoxication, Tricyclic Antidepressant Drug Overdose.
Dosing
Sodium bicarbonate 42 mg is equal to 0.5 mEq each of sodium (Na+) and bicarbonate (HCO3-). Sodium bicarbonate 75 mg is equal to 0.892 mEq each of Na+ and HCO3-. Sodium bicarbonate 84 mg is equal to 1 mEq each of Na+ and HCO3-.
Dosage of sodium bicarbonate injection is determined by severity of the acidosis, appropriate laboratory determinations, and the patient's age, weight, and clinical condition. Frequent laboratory determinations and clinical evaluation of the patient are essential during therapy with sodium bicarbonate, especially during prolonged therapy, to monitor changes in fluid and electrolyte and acid-base balance.
Generally, full correction of bicarbonate deficit should not be attempted during the first 24 hours of sodium bicarbonate therapy, since this may result in precipitation of metabolic alkalosis because of delayed physiologic compensatory mechanisms. Due to this delay, reaching a total CO2 content of approximately 20 mEq/liter by the end of the first day of treatment is typically linked to a normal blood pH. Further correction of the acidosis to fully normal levels usually happens if the kidney function is normal and if and when the underlying cause of the acidosis can be controlled. If total CO2 levels are normalized or brought above normal within the first day, this may likely result in an excessively high (alkaline) blood pH, which can lead to undesired side effects.
In cases of metabolic acidosis associated with shock, monitor therapy by assessing blood gases, plasma osmolarity, arterial blood lactate, hemodynamic status, and cardiac rhythm. Bicarbonate therapy should always be administered gradually and in stages since the degree of response from a specific dose is not precisely predictable.
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Drug interactions
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Contraindicated Drug Combination: This drug combination is contraindicated and generally should not be dispensed or administered to the same patient.
Urinary Alkalinizers/Methenamine
SEVERITY LEVEL: 1-Contraindicated Drug Combination: This drug combination is contraindicated and generally should not be dispensed or administered to the same patient.
MECHANISM OF ACTION: Urinary alkalinizers may elevate urinary ph preventing the conversion of methenamine to formaldehyde and mandelic acid.(1)
CLINICAL EFFECTS: Concurrent administration may result in alkalinization of the urine causing methenamine to be less effective.(1)
PREDISPOSING FACTORS: None determined.
PATIENT MANAGEMENT: The Australian and UK manufacturers of methenamine state that concurrent use with agents that make urine alkaline or urine alkalinizing agents should be avoided.(2,3) Patients receiving concurrent therapy should be monitored for urinary ph and any worsening symptoms of their infection, including dysuria, flank pain, or fever.(1)
DISCUSSION: Administration of urinary alkalinizers may result in alkalinization of the urine resulting in therapeutic failure of methenamine. Formaldehyde is released by acid hydrolysis from methenamine resulting in bactericidal concentrations at urinary ph 5.0 to 5.5. Above urinary ph 6.0 there is insufficient quantities of formaldehyde and methenamine released to achieve a therapeutic response.(1) An in vitro study showed that methenamine efficacy is achieved when the urine pH is less than 5.7 to 5.85.(4)
Severe Interaction: Action is required to reduce the risk of severe adverse interaction.
Urinary Alkalinizers/Dextroamphetamine Transdermal
SEVERITY LEVEL: 2-Severe Interaction: Action is required to reduce the risk of severe adverse interaction.
MECHANISM OF ACTION: Urinary alkalinizers decrease the renal elimination of dextroamphetamine.(1)
CLINICAL EFFECTS: Concurrent use of dextroamphetamine and urinary alkalinizers may result in increased dextroamphetamine levels and side effects.
PREDISPOSING FACTORS: None determined.
PATIENT MANAGEMENT: Coadministration of dextroamphetamine with urinary alkalinizing agents should be avoided.(1)
DISCUSSION: Concurrent use of alkalinizing agents with dextroamphetamine decreases the renal elimination of dextroamphetamine. Co-administration of these should be avoided because of the potential of increased actions of dextroamphetamine.(1)
Moderate Interaction: Assess the risk to the patient and take action as needed.
Urinary Alkalinizers/Memantine; Amantadine
SEVERITY LEVEL: 3-Moderate Interaction: Assess the risk to the patient and take action as needed.
MECHANISM OF ACTION: Memantine and amantadine elimination is impaired by urinary alkalinization.(1,2)
CLINICAL EFFECTS: Potentiation of memantine or amantadine effects may be observed.
PREDISPOSING FACTORS: None determined.
PATIENT MANAGEMENT: Monitor patient for adverse reactions such as dizziness, headache, or confusion if a urinary alkalinizer is required. The memantine or amantadine dose may need to be adjusted when a urinary alkalinizer is started or stopped.(1,2)
DISCUSSION: The clearance of memantine was reduced by about 80% under alkaline urine conditions at pH 8. Urine alkalinization may lead to an accumulation of memantine with a possible increase in adverse effects. Urine pH is also altered by diet and clinical state of the patient (e.g., renal tubular acidosis or severe infections of the urinary tract). Hence, memantine should be used with caution under these conditions.(1) A study in rats showed that concomitant administration of sodium bicarbonate with amantadine caused a decrease in amantadine renal clearance (1.16 vs. 0.76). Amantadine's area-under-the-curve (AUC) was increased approximately 78%.(3) A study in 12 healthy subjects showed that plasma concentrations of memantine are dependent on urine pH. Alkaline urine pH caused a 79% reduction in renal clearance.(4)
Urinary Alkalinizers/Quinidine
SEVERITY LEVEL: 3-Moderate Interaction: Assess the risk to the patient and take action as needed.
MECHANISM OF ACTION: Quinidine elimination is impaired by urinary alkalinization.
CLINICAL EFFECTS: Potentiation of quinidine effects may be observed.
PREDISPOSING FACTORS: None determined.
PATIENT MANAGEMENT: Monitoring quinidine levels and cardiac function may be indicated. The quinidine dose may need to be adjusted when a urinary alkalinizer is started or stopped.
DISCUSSION: Additional documentation is necessary to confirm this potential interaction.
Urinary Alkalinizers/Sympathomimetics
SEVERITY LEVEL: 3-Moderate Interaction: Assess the risk to the patient and take action as needed.
MECHANISM OF ACTION: Unionized sympathomimetic amines will be reabsorbed into systemic circulation from the distal tubules of the kidneys.
CLINICAL EFFECTS: Enhanced sympathomimetic activity and increased risk of sympathomimetic toxicity.
PREDISPOSING FACTORS: None determined.
PATIENT MANAGEMENT: Watch patient for enhanced sympathomimetic side effects when urinary alkalinizers are concomitantly used. A lower dose of certain sympathomimetics may be required.
DISCUSSION: Signs and symptoms of sympathomimetic toxicity include euphoria, confusion, delirium, hallucinations and nervousness.
Contraindications
*Patients with excessive chloride loss from vomiting or continuous GI suctioning.
*Patients at risk of developing diuretic-induced hypochloremic alkalosis.
- Hypochloremia
- Metabolic alkalosis
- Anuria
- Chronic heart failure
- Edema
- Hypocalcemia
- Hypokalemia
- Severe renal impairment
- Oliguria
Adverse reactions
Adverse effects from IV sodium bicarbonate treatment include manifestations of metabolic alkalosis (muscular twitching, irritability, and tetany); hypernatremia; and chemical cellulitis with tissue necrosis, ulceration or sloughing at the site of infiltration from extravasation.
Rare or Very Rare
- Hypocalcemia
- Hypokalemia
- Metabolic alkalosis
Rare or Very Rare
- Cellulitis
- Edema
Precautions
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Rapid injection (10 mL/minute) of hypertonic sodium bicarbonate solutions in neonates and children younger than 2 years of age may produce hypernatremia, decreased CSF pressure, and possible intracranial hemorrhage. It is recommended that the rate of IV administration in these children not exceed 8 mEq/kg daily and that slow IV administration of a 4.2% solution may be preferred. In emergencies such as cardiac arrest, the risk of rapid infusion of the drug in these children must be weighed against the potential for death from acidosis.
Animal reproduction studies have not been performed with sodium bicarbonate. It is also not known whether sodium bicarbonate can cause fetal harm when administered to pregnant women. Sodium bicarbonate should be used during pregnancy only when clearly needed.
The manufacturer provides no specific information for use of sodium bicarbonate during breast-feeding.
The manufacturer makes no specific dosage recommendations for geriatric patients. In general, dosage selection for geriatric patients should be cautious, usually starting at the low end of the dosing range, reflecting the higher incidence of decreased hepatic, renal, or cardiac function and of concomitant disease or other drug therapy.
Clinical studies of sodium bicarbonate did not include sufficient numbers of patients >=65 years of age to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between geriatric and younger patients.
In general, dosage selection for geriatric patients should be cautious, usually starting at the low end of the dosing range, reflecting the higher incidence of decreased hepatic, renal, or cardiac function and of concomitant disease or other drug therapy.
ICD codes
| Code | Type | Description |
|---|---|---|
| Metabolic acidosis | ||
| E08.1 | ICD10CM | Diabetes mellitus due to underlying condition with ketoacidosis |
| E08.10 | ICD10CM | Diabetes mellitus due to underlying condition with ketoacidosis without coma |
| E08.11 | ICD10CM | Diabetes mellitus due to underlying condition with ketoacidosis with coma |
| E09.1 | ICD10CM | Drug or chemical induced diabetes mellitus with ketoacidosis |
| E09.10 | ICD10CM | Drug or chemical induced diabetes mellitus with ketoacidosis without coma |
| E09.11 | ICD10CM | Drug or chemical induced diabetes mellitus with ketoacidosis with coma |
| E10.1 | ICD10CM | Type 1 diabetes mellitus with ketoacidosis |
| E10.10 | ICD10CM | Type 1 diabetes mellitus with ketoacidosis without coma |
| E10.11 | ICD10CM | Type 1 diabetes mellitus with ketoacidosis with coma |
| E11.1 | ICD10CM | Type 2 diabetes mellitus with ketoacidosis |
| E11.10 | ICD10CM | Type 2 diabetes mellitus with ketoacidosis without coma |
| E11.11 | ICD10CM | Type 2 diabetes mellitus with ketoacidosis with coma |
| E13.1 | ICD10CM | Other specified diabetes mellitus with ketoacidosis |
| E13.10 | ICD10CM | Other specified diabetes mellitus with ketoacidosis without coma |
| E13.11 | ICD10CM | Other specified diabetes mellitus with ketoacidosis with coma |
| E87.2 | ICD10CM | Acidosis |
| E87.20 | ICD10CM | Acidosis, unspecified |
| E87.21 | ICD10CM | Acute metabolic acidosis |
| E87.22 | ICD10CM | Chronic metabolic acidosis |
| E87.29 | ICD10CM | Other acidosis |
| P19 | ICD10CM | Metabolic acidemia in newborn |
| P19.0 | ICD10CM | Metabolic acidemia in newborn first noted before onset of labor |
| P19.1 | ICD10CM | Metabolic acidemia in newborn first noted during labor |
| P19.2 | ICD10CM | Metabolic acidemia noted at birth |
| P19.9 | ICD10CM | Metabolic acidemia in newborn, unspecified |
| P74.0 | ICD10CM | Late metabolic acidosis of newborn |
| Salicylate intoxication | ||
| T39.011 | ICD10CM | Poisoning by aspirin, accidental (unintentional) |
| T39.011A | ICD10CM | Poisoning by aspirin, accidental (unintentional), initial encounter |
| T39.012 | ICD10CM | Poisoning by aspirin, intentional self-harm |
| T39.012A | ICD10CM | Poisoning by aspirin, intentional self-harm, initial encounter |
| T39.013 | ICD10CM | Poisoning by aspirin, assault |
| T39.013A | ICD10CM | Poisoning by aspirin, assault, initial encounter |
| T39.014 | ICD10CM | Poisoning by aspirin, undetermined |
| T39.014A | ICD10CM | Poisoning by aspirin, undetermined, initial encounter |
| T39.091 | ICD10CM | Poisoning by salicylates, accidental (unintentional) |
| T39.091A | ICD10CM | Poisoning by salicylates, accidental (unintentional), initial encounter |
| T39.092 | ICD10CM | Poisoning by salicylates, intentional self-harm |
| T39.092A | ICD10CM | Poisoning by salicylates, intentional self-harm, initial encounter |
| T39.093 | ICD10CM | Poisoning by salicylates, assault |
| T39.093A | ICD10CM | Poisoning by salicylates, assault, initial encounter |
| T39.094 | ICD10CM | Poisoning by salicylates, undetermined |
| T39.094A | ICD10CM | Poisoning by salicylates, undetermined, initial encounter |
| Severe diarrhea | ||
| R19.7 | ICD10CM | Diarrhea, unspecified |
| Toxic phenobarbital serum level | ||
| T42.3x1 | ICD10CM | Poisoning by barbiturates, accidental (unintentional) |
| T42.3x1A | ICD10CM | Poisoning by barbiturates, accidental (unintentional), initial encounter |
| T42.3x2A | ICD10CM | Poisoning by barbiturates, intentional self-harm, initial encounter |
| T42.3x3A | ICD10CM | Poisoning by barbiturates, assault, initial encounter |
| T42.3x4A | ICD10CM | Poisoning by barbiturates, undetermined, initial encounter |
| Tricyclic antidepressant overdose | ||
| T43.011A | ICD10CM | Poisoning by tricyclic antidepressants, accidental (unintentional), initial encounter |
| T43.012A | ICD10CM | Poisoning by tricyclic antidepressants, intentional self-harm, initial encounter |
| T43.013A | ICD10CM | Poisoning by tricyclic antidepressants, assault, initial encounter |
| T43.014A | ICD10CM | Poisoning by tricyclic antidepressants, undetermined, initial encounter |
ICD code information from First Databank (FDB).
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Last reviewed · Source: First Databank (FDB) drug data
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