eMedicine Specialties > Pediatrics: Cardiac Disease and Critical Care Medicine > Critical Care

Hypernatremia: Treatment & Medication

Author: Ewa Elenberg, MD, Assistant Professor, Department of Pediatrics, Renal Section, Texas Children's Hospital, Baylor College of Medicine
Coauthor(s): Muthukumar Vellaichamy, MD, FAAP, Clinical Assistant Professor, Department of Pediatrics, University of Kansas School of Medicine-Wichita, Wesley Medical Center
Contributor Information and Disclosures

Updated: Nov 2, 2009

Treatment

Medical Care

Medical care involves the correction of hypernatremia. In correcting hypernatremia, do not rapidly decrease the sodium level because a rapid decline in the serum sodium concentration can cause cerebral edema. The recommended rate of sodium correction is 0.5 mEq/h or as much as 10-12 mEq/L in 24 hours. Dehydration should be corrected over 48-72 hours. Guidelines for hydration management have been established.4 If the serum sodium concentration is more than 200 mEq/L, peritoneal dialysis should be performed using a high-glucose, low-sodium dialysate.

  • One of the following equations may be used to calculate body water deficit:
    • The equations are based on a goal of plasma sodium concentration of 145 mEq/L. In children, total body water (TBW) is 60% of their lean body weight. Therefore, TBW = 0.6 X weight. Babies are an exception to these equations and may have a TBW as much as 80% of their body weight.
      • Water deficit (in L) = [(current Na level in mEq/L ÷ 145 mEq/L) - 1] X 0.6 X weight (in kg)
      • Water deficit (in L) = [(current Na level in mEq/L - 145 mEq/L)/145 mEq/L)] X 0.6 X weight (in kg)
      • Water deficit (in L) = [1- (145 mEq/L ÷ current Na level in mEq/L)] X 0.6 X weight (in kg)
    • Example calculation: A child weighs 10 kg and has a plasma sodium concentration of 160 mEq/L. By using the first equation, water deficit (in L) = [(160 mEq/L ÷ 145 mEq/L) - 1] X 0.6 X 10 = 0.62 L.
  • The volume of replacement fluid needed to correct the water deficit is determined by using the concentration of sodium in the replacement fluid. The replacement volume can be determined as follows:
    • Replacement volume (in L) = TBW deficit X [1 ÷ 1 - (Na concentration in replacement fluid in mEq/L ÷ 154 mEq/L)]
    • Example calculation: If the patient from the example calculation above has a TBW of 0.62, and if the replacement fluid contains 0.2% NaCl (Na concentration of 34 mEq/L), the replacement volume (in L) = 0.62 L X [1 ÷ 1 - (34 mEq/L ÷ 154 mEq/L)] = 0.79 L. This volume has to be replaced slowly over 48-72 hours.
  • The election of intravenous fluid is based on the following:
    • If the patient is hypotensive, normal saline (lactated Ringer solution, or 5% albumin solution) should be used regardless of a high serum sodium concentration.
    • In hypernatremic dehydration, 0.45% or 0.2% NaCl should be used as a replacement fluid to prevent excessive delivery of free water and a too-rapid decrease in the serum sodium concentration.
    • In cases of hypernatremia caused by sodium overload, sodium-free intravenous fluid (eg, 5% dextrose in water) may be used, and a loop diuretic may be added.
    • The serum sodium concentration should be monitored frequently to avoid too-rapid correction of hypernatremia.
    • In cases of associated hyperglycemia, 2.5% dextrose solution may be given. Insulin treatment is not recommended because the acute decrease in glucose, which lowers plasma osmolality, may precipitate cerebral edema.
    • Once the child is urinating, add 40 mEq/L KCl to fluids to aid water absorption into cells.
    • Calcium may be added if the patient has an associated low serum calcium level.
  • Serum sodium levels should be monitored every 4 hours.

Consultations

Consultation is also recommended for patients with renal dysplasia, medullary cystic disease, reflux nephropathy, or polycystic disease.

  • Critical care specialist: Patients with symptomatic hypernatremia may need to be transferred to a pediatric ICU for appropriate treatment and monitoring.
  • Endocrinologist: Consult an endocrinologist for patients with primary hyperaldosteronism.
  • Nephrologist: Consult a nephrologist in cases of renal failure, obstructive uropathy, and serum sodium levels of more than 180 mEq/L for possible peritoneal dialysis.

Diet

  • In diabetes insipidus, a sodium-restricted and protein-restricted diet should be prescribed.

Medication

The medications described below are used in patients with diabetes insipidus who have hypernatremia.

Vasopressin and vasopressin analogs

Desmopressin is a synthetic ADH with actions mimicking vasopressin. These agents are used to treat diabetes insipidus, which deprives the kidney of its capacity to produce concentrated urine. This effect results in large volumes of dilute urine (polyuria) and excessive thirst (polydipsia). Serum sodium concentrations may be elevated, but hypernatremia is most likely to be severe when fluid is restricted.


Desmopressin acetate (DDAVP)

Structural analog of vasopressin (ADH), the endogenous posterior pituitary hormone that maintains serum osmolality in a physiologically acceptable range. Works in neurohypophysial (eg, central) diabetes insipidus. Exerts similar antidiuretic effects. Vasopressin increases resorption of water at level of renal collecting duct, reducing urinary flow and increasing urine osmolality.

Adult

PO: 0.05 mg PO bid initially; titrate to effect; usual range 0.1-0.2 mg/d divided bid/tid
Intranasal: 10-40 mcg/d divided qd/bid; titrate dose to achieve control of excessive thirst and urination; not to exceed 40 mcg/d
Note: The nasal spray pump can only deliver doses of 10 mcg (0.1 mL) or multiples of 10 mcg (0.1 mL); if doses other than this are needed, the rhinal tube delivery system is preferred

Pediatric

PO: 0.05 mg PO divided bid initially; titrate to effect
Intranasal: 3 months to 12 years: 5-30 mcg/d divided qd/bid
Note: The nasal spray pump can only deliver doses of 10 mcg (0.1 mL) or multiples of 10 mcg (0.1 mL); if doses other than this are needed, the rhinal tube delivery system is preferred

Coadministration with demeclocycline and lithium decrease effects; fludrocortisone and chlorpropamide increase effects

Documented hypersensitivity; platelet-type von Willebrand disease

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Avoid overhydration in patients to benefit from its hemostatic effects


Vasopressin (Pitressin)

Exogenous, parenteral form of ADH. Antidiuretic and increases resorption of water at renal collecting ducts.

Adult

5-10 U IM/SC bid/qid; titrate to effect
Continuous IV infusion: 0.5 mU/kg/h (ie, 0.0005 U/kg/h) IV initially; double dosage every 30 min prn, not to exceed 10 mU/kg/h IV (ie, 0.01 U/kg/h)

Pediatric

2.5–10 U IM/SC bid/qid; titrate to effect
Continuous IV infusion: Administer as in adults

Lithium, epinephrine, demeclocycline, heparin, and alcohol may decrease effects; chlorpropamide, urea, fludrocortisone, and carbamazepine may potentiate effects

Documented hypersensitivity; coronary artery disease

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Caution in cardiovascular disease, seizure disorders, nitrogen retention, asthma, or migraine; excessive doses may result in hyponatremia

Diuretics

These drugs promote the excretion of water and electrolytes by the kidneys. They are used in patients with nephrogenic diabetes insipidus.


Hydrochlorothiazide (Esidrix, HydroDIURIL)

Works by increasing excretion of sodium, chloride, and water by inhibiting sodium ion transport across renal tubular epithelium. Resulting sodium depletion reduces glomerular filtration rate, enhancing reabsorption of fluid in proximal portion of nephron, decreasing delivery of sodium to ascending limb of loop of Henle and consequently reducing capacity to dilute urine.

Adult

25-100 mg/d PO qd or intermittently

Pediatric

Infants <6 months: Up to 3 mg/kg/d PO divided bid, total range 12.5-37.5 mg/d
Children 6 months to 2 years: 1-2 mg/kg/d PO divided qd/bid, total range 12.5-37.5 mg/d
Children 2-12 years: 1-2 mg/kg/d PO divided qd/bid, not to exceed 37.5-100 mg/d

Thiazides may decrease effects of anticoagulants, antigout agents and sulfonylureas; thiazides may increase toxicity of allopurinol, anesthetics, antineoplastics, calcium salts, loop diuretics, lithium, diazoxide, digitalis, amphotericin B, and nondepolarizing muscle relaxants

Documented hypersensitivity; anuria or renal decompensation

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Caution in renal disease, hepatic disease, gout, diabetes mellitus, and erythematosus

More on Hypernatremia

Overview: Hypernatremia
Differential Diagnoses & Workup: Hypernatremia
Treatment & Medication: Hypernatremia
Follow-up: Hypernatremia
Multimedia: Hypernatremia
References

References

  1. Conley SB. Hypernatremia. Pediatr Clin North Am. Apr 1990;37(2):365-72. [Medline].

  2. Abramovici MI, Singhal PC, Trachtman H. Hypernatremia and rhabdomyolysis. J Med. 1992;23(1):17-28. [Medline].

  3. Yang TY, Chang JW, Tseng MH, Wang HH, Niu DM, Yang LY. Extreme hypernatremia combined with rhabdomyolysis and acute renal failure. J Chin Med Assoc. Oct 2009;72(10):555-8. [Medline].

  4. [Guideline] Mentes JC. Hydration management. Iowa City (IA): University of Iowa Gerontological Nursing Interventions Research Center, Research Dissemination Core; 2004 Feb. [Full Text].

  5. Konetzny G, Bucher HU, Arlettaz R. Prevention of hypernatraemic dehydration in breastfed newborn infants by daily weighing. Eur J Pediatr. Sep 26 2008;[Medline].

  6. Avner ED. Clinical disorders of water metabolism: hyponatremia and hypernatremia. Pediatr Ann. Jan 1995;24(1):23-30. [Medline].

  7. Berl T. Disorders of water metabolism. In: Schrier RW, ed. Renal and Electrolyte Disorders. 5th ed. Lippincott-Raven; 1997.

  8. Brown RG. Disorders of water and sodium balance. Postgrad Med. Mar 1993;93(4):227-8, 231-4, 239-40 passim. [Medline].

  9. DeVita MV, Michelis MF. Perturbations in sodium balance. Hyponatremia and hypernatremia. Clin Lab Med. Mar 1993;13(1):135-48. [Medline].

  10. Finberg L. Hypernatremic (hypertonic) dehydration in infants. N Engl J Med. Jul 26 1973;DA - 19730822(4):196-8. [Medline].

  11. Ho L, Bradford BJ. Hypernatremic dehydration and rotavirus enteritis. Clin Pediatr (Phila). Aug 1995;34(8):440-1. [Medline].

  12. Lin M, Liu SJ, Lim IT. Disorders of water imbalance. Emerg Med Clin North Am. Aug 2005;23(3):749-70, ix. [Medline].

  13. Molteni KH. Initial management of hypernatremic dehydration in the breastfed infant. Clin Pediatr (Phila). Dec 1994;33(12):731-40. [Medline].

  14. Moritz ML, Ayus JC. Preventing neurological complications from dysnatremias in children. Pediatr Nephrol. Dec 2005;20(12):1687-700. [Medline].

  15. Moritz ML, Ayus JC. The changing pattern of hypernatremia in hospitalized children. Pediatrics. Sep 1999;104(3 Pt 1):435-9. [Medline].

  16. Moritz ML, Manole MD, Bogen DL, Ayus JC. Breastfeeding-associated hypernatremia: are we missing the diagnosis?. Pediatrics. Sep 2005;116(3):e343-7. [Medline].

  17. Palevsky PM. Hypernatremia. Semin Nephrol. Jan 1998;18(1):20-30. [Medline].

  18. Paneth N. Hypernatremic dehydration of infancy: an epidemiologic review. Am J Dis Child. Aug 1980;134(8):785-92. [Medline].

  19. Roscelli JD, Yu CE, Southgate WM. Management of salt poisoning in an extremely low birth weight infant. Pediatr Nephrol. Apr 1994;8(2):172-4. [Medline].

  20. Trachtman H. Cell volume regulation: a review of cerebral adaptive mechanisms and implications for clinical treatment of osmolal disturbances: II. Pediatr Nephrol. Jan 1992;6(1):104-12. [Medline].

  21. Visser L, Devuyst O. Physiopathology of hypernatremia following relief of urinary tract obstruction. Acta Clin Belg. 1994;49(6):290-5. [Medline].

Further Reading

Keywords

hypernatremia, high serum sodium, pure water depletion, sodium excess, water depletion exceeding sodium depletion, total body water, TBW, Na, salt poisoning, dehydration, thirst, sodium loading, diabetes insipidus, diarrhea, gastroenteritis, dysplasia, medullary cystic, polycystic, tubulointerstitial disease, obstructive uropathy, heat stroke, rhabdomyolysis, oligoanuria, craniopharyngioma, pinealoma, sarcoid, tuberculosis, Wegener granulomatosis, histiocytosis, sickle cell disease, meningitis, encephalitis, cleft lip and palate, amyloidosis

Contributor Information and Disclosures

Author

Ewa Elenberg, MD, Assistant Professor, Department of Pediatrics, Renal Section, Texas Children's Hospital, Baylor College of Medicine
Ewa Elenberg, MD is a member of the following medical societies: American Academy of Pediatrics, American Medical Association, and American Society of Nephrology
Disclosure: Nothing to disclose.

Coauthor(s)

Muthukumar Vellaichamy, MD, FAAP, Clinical Assistant Professor, Department of Pediatrics, University of Kansas School of Medicine-Wichita, Wesley Medical Center
Muthukumar Vellaichamy, MD, FAAP is a member of the following medical societies: American Academy of Pediatrics and Society of Critical Care Medicine
Disclosure: Nothing to disclose.

Medical Editor

G Patricia Cantwell, MD, Associate Clinical Professor, Department of Pediatrics, University of Miami; Director of Pediatric Critical Care Medicine, Miller School of Medicine, Jackson Children's Hospital
G Patricia Cantwell, MD is a member of the following medical societies: American Academy of Pediatrics, American College of Emergency Physicians, American Heart Association, American Trauma Society, National Association of EMS Physicians, Society of Critical Care Medicine, and Wilderness Medical Society
Disclosure: Nothing to disclose.

Pharmacy Editor

Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine
Disclosure: Pfizer Inc Stock Investment from financial planner; Avanir Pharma Stock Investment from financial planner ; WebMD Salary and stock Employment and investment from financial planner

Managing Editor

Barry J Evans, MD, Assistant Professor of Pediatrics, Temple University Medical School; Director of Pediatric Critical Care and Pulmonology, Associate Chair for Pediatric Education, Temple University Children's Medical Center
Barry J Evans, MD is a member of the following medical societies: American Academy of Pediatrics, American College of Chest Physicians, American Thoracic Society, and Society of Critical Care Medicine
Disclosure: Nothing to disclose.

CME Editor

Mary E Cataletto, MD, Associate Director, Division of Pediatric Pulmonology, Winthrop University Hospital; Professor of Clinical Pediatrics, State University of New York at Stony Brook; Director of Children's Sleep Services, Winthrop University Hospital
Mary E Cataletto, MD is a member of the following medical societies: American Academy of Pediatrics and American College of Chest Physicians
Disclosure: Shering Plough Pharmaceuticals Honoraria Consulting

Chief Editor

Timothy E Corden, MD, Associate Professor of Pediatrics, Co-Director, Policy Core, Injury Research Center, Medical College of Wisconsin; Associate Director, PICU, Children's Hospital of Wisconsin
Timothy E Corden, MD is a member of the following medical societies: American Academy of Pediatrics, Phi Beta Kappa, Society of Critical Care Medicine, and Wisconsin Medical Society
Disclosure: Nothing to disclose.

 
 
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