There is no treatment for [disease name]; the mainstay of therapy is supportive care.
OR
Supportive therapy for [disease name] includes [therapy 1], [therapy 2], and [therapy 3].
OR
The majority of cases of [disease name] are self-limited and require only supportive care.
OR
[Disease name] is a medical emergency and requires prompt treatment.
OR
The mainstay of treatment for [disease name] is [therapy].
OR
The optimal therapy for [malignancy name] depends on the stage at diagnosis.
OR
[Therapy] is recommended among all patients who develop [disease name].
OR
Pharmacologic medical therapy is recommended among patients with [disease subclass 1], [disease subclass 2], and [disease subclass 3].
OR
Pharmacologic medical therapies for [disease name] include (either) [therapy 1], [therapy 2], and/or [therapy 3].
OR
Empiric therapy for [disease name] depends on [disease factor 1] and [disease factor 2].
OR
Patients with [disease subclass 1] are treated with [therapy 1], whereas patients with [disease subclass 2] are treated with [therapy 2].
Medical Therapy
Hyponatremia must be corrected slowly in order to lessen the chance of the development of central pontine myelinolysis (CPM), a severe neurological disease. In fact, overly rapid correction of hyponatremia is the most common cause of that potentially devastating disorder.[1] During treatment of hyponatremia, the serum sodium should not be allowed to rise by more than 8 mmol/l over 24 hours (i.e. 0.33 mmol/l/h rate of rise). In practice, too rapid correction of hyponatremia and thence CPM is most likely to occur during the treatment of hypovolemic hyponatremia. In particular, once the hypovolemic state has been corrected, the signal for ADH release disappears. At that point, there will be an abrupt water diuresis (since there is no longer any ADH acting to retain the water). A rapid and profound rise in serum sodium can then occur. Should the rate of rising of serum sodium exceed 0.33 mmol/l/h over several hours, vasopressin may be administered to prevent ongoing rapid water diuresis.[2]
Renal failure (acute or chronic),Nephrotic syndrome : Correct underlying disease with angiotensin-converting enzyme inhibitors or angiotensin receptor blockers,treat underlying cause for nephrotic syndrome
Euvolemic
Hyponatremia
Drugs :Stop causative medications
SIADH/SIAD : Fluid restriction, consider vaptans
Nephrogenic SIAD : Fluid restriction, loop diuretics
Hospitalize the patients if • The patient is symptomatic regardless of duration • Serum sodium < 125 mEq/L • Acute hyponatremia
Chronic
Acute
Is the patient symptomatic ( Whether mild, moderate, severe)
Hospitalize the patient and check for symptoms of hyponatremia ( Whether mild, moderate, severe)
Asymptomatic but serum sodium level < 120 mEq/L
Symptomatic patients must be admitted
No
Are the symptoms severe?
Recheck serum Na still hyponatremia( incase of water diuresis autocorrectiom may happen
Yes
Yes
Yes
No
No
Manage the patient in the hospital • Primary management‡ • Monitor serum Na every 4 hours to ensure appropriate rate of correction ≤ 8 mEq/L in 24 hours
• 100 ml bolus of 3% saline,repeat as needed if symptoms persist • Monitor serum Na hourly till it is increased by 4 to 6 mEq/L • Primary management‡
Primary management‡ Monitor serum Na every 4 hour (Na rise ≤ 8 mEq/L in 24 h)
If no, Primary management‡
Yes
Is there any history of intracranial pathology? Trauma, surgery, hemorrhage, neoplasm, SOP
• Monitor serum Na hourly till it is increased by 4 to 6 mEq/L • Further decline in serum Na means delayed water absorbtion • If serum Na declines give 50ml bolus of 3% saline • Primary management‡
No
Yes
Is the serum Na < 120 mEq/L?
Yes
No
Is the hyponatremia due to self-induced water intoxication?
• Primary management‡ • Monitor serum Na every 6-12 hours
Yes
No
• Primary management‡ • Monitor serum Na every 6-12 hours
Is the patient hypervolemic/edematous (CHF,RF,cirrhosis)
Yes
No
• Primary management‡ • Infusion of 3% saline at the rate of 15-30 ml/hour plus IV furosemide(40 mg or higher)twice daily• Monitor serum Na frequently to adjust rate of furosemide and saline to achieve 4-6mEq/L rise in serum Na• Discontinue regimen when serum Na is at least 125 mEq/L
Is the cause of hyponatremia reversible? (True hypovolemia, adrenal insufficiency, transient SIADH)
No
Yes
Evaluate the risk for osmotic demyelination syndrome
• Primary management‡• Infusion of 3% salin at 15-30 ml/hour • Monitor serum Na to achieve rate of correction 4-6 mEq/L • Discontinue regimen when serum Na is atleast 125 mEq/L
• Infusion of 3% saline at 15-30 ml/hour plus IV or subcutaneous desmopressin 1 to 2 mcg every 6-8 hours • Monitor serum Na to achieve rate of correction 4-6 mEq/L • Discontinue regimen when serum Na is atleast 125 mEq/L • Primary management‡
‡ Primary management:
Treat the underlying cause of hyponatremia
Discontinue responsible drugs unless there is no other substitute
Treat chronic hyponatremia and SIADH with loop diuretics, oral salt tablets, urea
Reduce intake of electrolyte-free water(IV fluid, oral intake)
$$$$$
Hyponatremia serum sodium < 135 mEq/L
check for pseudohyponatremia (Hyperglycemia, Hyperlipidemia, Hyperproteinemia, lab errors)
Infuse 3% saline (1 to 2 mL per kg per hour) with goal of increasing serum sodium level by 6 to 8 mEq per L (not to exceed 10 to 12 mEq per L in the first 24 hours or 18 mEq per L in 48 hours) Consider desmopressin, 1 to 2 mcg every four to six hours
Give single intravenous bolus of 100 to 150 mL 3% saline with goal of increasing serum sodium level by 2 to 3 mEq per L; check sodium level every 20 minutes until symptoms resolve; may repeat bolus twice if symptoms do not resolve
Normal 275-295 mOsm/kg Isotonic hyponatremia (pseudohyponatremia)
Low <275mOsm/kg Hypotonic hyponatremia
High >295 mOsm/kg Hypertonic hyponatremia
Assess for hyperproteinuria or hyperlipidemia
Assess volume status
Assess for hyperglycemia, check for mannitol or sorbitol use or recent administration of radiocontrast media
The “vaptan” class of drugs contains a number of compounds with varying selectivity, several of which are either already in clinical use or in clinical trials as of 2010.
The V2-receptor antagonists tolvaptan and conivaptan allow excretion of electrolyte free water and are effective in increasing serum sodium in euvolemic and hypervolemic hyponatremia.[6]
Rate of Na Correction
The rate of correction of hyponatremia should be 0.5-1.0meq/L/hr, with not more than a 12 meq/l correction in 24 hrs. If the patient has ongoing seizures (or [Na+]<115 meq/li), correction can be attempted at up to 2 meq/L/hr, but only while seizure activity lasts and the [Na+] exceeds 125-130 meq/Li.
Contraindicated medications
Hyponatremia is considered an absolute contraindication to the use of the following medications:
Preferred regimen (1): drug name 50 mg/kg/day PO q8h (maximum, 500 mg per dose)
2 Stage 2 - Name of stage
2.1 Specific Organ system involved 1
Note (1):
Note (2):
Note (3):
2.1.1 Adult
Parenteral regimen
Preferred regimen (1): drug name 2 g IV q24h for 14 (14–21) days
Alternative regimen (1): drug name 2 g IV q8h for 14 (14–21) days
Alternative regimen (2): drug name 18–24 MU/day IV q4h for 14 (14–21) days
Oral regimen
Preferred regimen (1): drug name 500 mg PO q8h for 14 (14–21) days
Preferred regimen (2): drug name 100 mg PO q12h for 14 (14–21) days
Preferred regimen (3): drug name 500 mg PO q12h for 14 (14–21) days
Alternative regimen (1): drug name 500 mg PO q6h for 7–10 days
Alternative regimen (2): drug name 500 mg PO q12h for 14–21 days
Alternative regimen (3):drug name 500 mg PO q6h for 14–21 days
2.1.2 Pediatric
Parenteral regimen
Preferred regimen (1): drug name 50–75 mg/kg IV q24h for 14 (14–21) days (maximum, 2 g)
Alternative regimen (1): drug name 150–200 mg/kg/day IV q6–8h for 14 (14–21) days (maximum, 6 g per day)
Alternative regimen (2): drug name 200,000–400,000 U/kg/day IV q4h for 14 (14–21) days (maximum, 18–24 million U per day) '(Contraindications/specific instructions)'
Oral regimen
Preferred regimen (1): drug name 50 mg/kg/day PO q8h for 14 (14–21) days (maximum, 500 mg per dose)
Preferred regimen (2): drug name(for children aged ≥ 8 years) 4 mg/kg/day PO q12h for 14 (14–21) days (maximum, 100 mg per dose)
Preferred regimen (3): drug name 30 mg/kg/day PO q12h for 14 (14–21) days (maximum, 500 mg per dose)
Alternative regimen (1): drug name 10 mg/kg PO q6h 7–10 days (maximum, 500 mg per day)
Alternative regimen (2): drug name 7.5 mg/kg PO q12h for 14–21 days (maximum, 500 mg per dose)
Alternative regimen (3): drug name 12.5 mg/kg PO q6h for 14–21 days (maximum,500 mg per dose)
2.2 'Other Organ system involved 2'
Note (1):
Note (2):
Note (3):
2.2.1 Adult
Parenteral regimen
Preferred regimen (1): drug name 2 g IV q24h for 14 (14–21) days
Alternative regimen (1): drug name 2 g IV q8h for 14 (14–21) days
Alternative regimen (2): drug name 18–24 MU/day IV q4h for 14 (14–21) days
Oral regimen
Preferred regimen (1): drug name 500 mg PO q8h for 14 (14–21) days
Preferred regimen (2): drug name 100 mg PO q12h for 14 (14–21) days
Preferred regimen (3): drug name 500 mg PO q12h for 14 (14–21) days
Alternative regimen (1): drug name 500 mg PO q6h for 7–10 days
Alternative regimen (2): drug name 500 mg PO q12h for 14–21 days
Alternative regimen (3):drug name 500 mg PO q6h for 14–21 days
2.2.2 Pediatric
Parenteral regimen
Preferred regimen (1): drug name 50–75 mg/kg IV q24h for 14 (14–21) days (maximum, 2 g)
Alternative regimen (1): drug name 150–200 mg/kg/day IV q6–8h for 14 (14–21) days (maximum, 6 g per day)
Alternative regimen (2): drug name 200,000–400,000 U/kg/day IV q4h for 14 (14–21) days (maximum, 18–24 million U per day)
Oral regimen
Preferred regimen (1): drug name 50 mg/kg/day PO q8h for 14 (14–21) days (maximum, 500 mg per dose)
Preferred regimen (2): drug name 4 mg/kg/day PO q12h for 14 (14–21) days (maximum, 100 mg per dose)
Preferred regimen (3): drug name 30 mg/kg/day PO q12h for 14 (14–21) days (maximum, 500 mg per dose)
Alternative regimen (1): drug name 10 mg/kg PO q6h 7–10 days (maximum, 500 mg per day)
Alternative regimen (2): drug name 7.5 mg/kg PO q12h for 14–21 days (maximum, 500 mg per dose)
Alternative regimen (3): drug name 12.5 mg/kg PO q6h for 14–21 days (maximum,500 mg per dose)
References
↑Bernsen HJ, Prick MJ (1999). "Improvement of central pontine myelinolysis as demonstrated by repeated magnetic resonance imaging in a patient without evidence of hyponatremia". Acta Neurol Belg. 99 (3): 189–93. PMID10544728. Unknown parameter |month= ignored (help)