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Dehydration

Last Updated: March 30, 2006
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Synonyms and related keywords: dehydration, negative fluid balance, diarrheal illness, diarrhea, isonatremic dehydration, hypernatremic dehydration, hyponatremic dehydration

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Author: Dan L Ellsbury, MD, FAAP, Consulting Staff, Pediatrix Medical Group of Iowa; Consulting Staff, Department of Pediatrics, Neonatology Intensive Care Unit, Mercy Medical Center of Des Moines

Coauthor(s): Caroline S George, MD, Assistant Professor, Department of Pediatrics, Division of Pediatric Critical Care, Children's Hospital of Iowa, University of Iowa Hospital and Clinics

Dan L Ellsbury, MD, FAAP, is a member of the following medical societies: American Academy of Pediatrics

Editor(s): G Patricia Cantwell, MD, Associate Clinical Professor, Department of Pediatrics, Miller School of Medicine, University of Miami; Director of Pediatric Critical Care Medicine, Jackson Children's Hospital; Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine.com, Inc; Barry 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; Mary E Cataletto, MD, Associate Director, Division of Pediatric Pulmonology, Winthrop University Hospital; Associate Professor, Department of Clinical Pediatrics, State University of New York at Stony Brook; and Maureen Strafford, MD, Arnold P Gold Foundation Associate Professor, Departments of Anesthesiology and Pediatrics, Tufts University and Tufts-New England Medical Center

Disclosure


  INTRODUCTION Section 2 of 9   Click here to go to the previous section in this topic Click here to go to the top of this page Click here to go to the next section in this topic
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Background: Dehydration describes a state of negative fluid balance that may be caused by a number of disease entities. Diarrheal illnesses are the most common etiologies. Worldwide, dehydration secondary to diarrheal illness is the leading cause of infant and child mortality.

Pathophysiology: The negative fluid balance causing dehydration results from decreased intake, increased output (renal, gastrointestinal, or insensible losses), or fluid shift (ascites, effusions, and capillary leak states such as burns and sepsis). The decrease in total body water causes reductions in both the intracellular and extracellular fluid volumes. Clinical manifestations of dehydration are most closely related to intravascular volume depletion. As dehydration progresses, hypovolemic shock ultimately ensues, resulting in end organ failure and death.

Dehydration is often categorized according to serum sodium concentration as isonatremic (130-150 mEq/L), hyponatremic (<130 mEq/L), or hypernatremic (>150 mEq/L). Isonatremic dehydration is the most common (80%). Hypernatremic and hyponatremic dehydration each comprise 5-10% of cases. Variations in serum sodium reflect the composition of the fluids lost and have different pathophysiologic effects.

Isonatremic (isotonic) dehydration occurs when the lost fluid is similar in sodium concentration to the blood. Sodium and water losses are of the same relative magnitude in both the intravascular and extravascular fluid compartments.

Hyponatremic (hypotonic) dehydration occurs when the lost fluid contains more sodium than the blood (loss of hypertonic fluid). Relatively more sodium than water is lost. Because the serum sodium is low, intravascular water shifts to the extravascular space, exaggerating intravascular volume depletion for a given amount of total body water loss.

Hypernatremic (hypertonic) dehydration occurs when the lost fluid contains less sodium than the blood (loss of hypotonic fluid). Relatively less sodium than water is lost. Because the serum sodium is high, extravascular water shifts to the intravascular space, minimizing intravascular volume depletion for a given amount of total body water loss.

Neurologic complications can occur in hyponatremic and hypernatremic states. Rapid correction of chronic hyponatremia (>2 mEq/L/h) has been associated with central pontine myelinolysis. During hypernatremic dehydration, water is osmotically pulled from cells into the extracellular space. To compensate, cells can generate osmotically active particles (idiogenic osmoles) that pull water back into the cell and maintain cellular fluid volume. During rapid rehydration of hypernatremia, the increased osmotic activity of these cells can result in a large influx of water, causing cellular swelling and rupture, with cerebral edema being the most devastating consequence. Slow rehydration over 48 hours generally minimizes this risk.

Frequency:

  • In the US: Diarrheal illnesses in children causes 3 million physician visits, 220,000 hospitalizations (10% of all children who require hospitalization), and 400 deaths per year.
  • Internationally: Diarrheal illnesses with subsequent dehydration account for nearly 4 million deaths per year in infants and children.

Mortality/Morbidity: Mortality and morbidity are generally dependent upon the severity of dehydration and the promptness of oral or intravenous rehydration. If treatment is rapidly and appropriately obtained, morbidity and mortality are low.

Age: Children younger than 5 years are at the highest risk.


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History:

  • Intake of fluids, including the volume, type (hypertonic or hypotonic), and frequency
  • Urine output, including the frequency of voiding, presence of concentrated or dilute urine, hematuria
  • Stool output, frequency of stools, stool consistency, presence of blood or mucus in stools
  • Emesis, including frequency and volume and whether bilious or nonbilious, hematemesis
  • Contact with ill people, especially others with gastroenteritis
  • Underlying illnesses, especially cystic fibrosis, diabetes mellitus, hyperthyroidism, renal disease
  • Fever
  • Appetite patterns
  • Weight loss
  • Travel
  • Recent antibiotic use
  • Possible ingestions

Physical: A complete physical examination is essential to determine the underlying cause of the patient's dehydration and to define the severity of dehydration. The clinical assessment of severity of dehydration determines the approach to management.

Table 1. Clinical Findings of Dehydration
Symptom/SignMild DehydrationModerate DehydrationSevere Dehydration
Level of consciousness*AlertLethargicObtunded
Capillary refill*2 Seconds2-4 Seconds Greater than 4 seconds, cool limbs
Mucous membranes*NormalDryParched, cracked
Tears*NormalDecreasedAbsent
Heart rateSlight increaseIncreasedVery increased
Respiratory rateNormalIncreasedIncreased and hyperpnea
Blood pressureNormalNormal, but orthostasisDecreased
PulseNormalThreadyFaint or impalpable
Skin turgorNormalSlowTenting
Fontanel NormalDepressedSunken
EyesNormalSunkenVery sunken
Urine outputDecreasedOliguria Oliguria/anuria
* Best indicators of hydration status

Table 2. Estimated Fluid Deficit
SeverityInfants (weight <10 kg)Children (weight >10 kg)
Mild dehydration5% or 50 mL/kg3% or 30 mL/kg
Moderate dehydration10% or 100 mL/kg6% or 60 mL/kg
Severe dehydration 15% or 150 mL/kg9% or 90 mL/kg

Causes: Determination of the cause of dehydration is essential. Poor fluid intake, excessive fluid output and increased insensible fluid losses all may cause intravascular volume depletion. Successful treatment requires identification of the underlying disease state.

    • Febrile illness: Fever causes increased insensible fluid losses and may affect appetite.

    • Pharyngitis: This may decrease oral intake.
  • Life-threatening causes
    • Gastroenteritis
    • Diabetic ketoacidosis
    • Burns: Fluid losses may be extreme. Very aggressive fluid management is required (see Burns, Thermal).
    • Congenital adrenal hyperplasia: This may have associated hypoglycemia, hypotension, hyperkalemia, and hyponatremia.
    • Gastrointestinal obstruction: This is often associated with poor intake and emesis. Bowel ischemia can result in extensive capillary leak and shock.
    • Heat stroke: Hyperpyrexia, dry skin, and mental status changes may occur.
    • Cystic fibrosis: This results in excessive sodium and chloride losses in sweat, placing patients at risk for severe hyponatremic hypochloremic dehydration.
    • Diabetes insipidus: Excessive output of very dilute urine can result in large free water losses and severe hypernatremic dehydration.
    • Thyrotoxicosis: Weight loss is observed, despite increased appetite. Diarrhea occurs.
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Acidosis, Metabolic
Adrenal Insufficiency
Alkalosis, Metabolic
Bowel Obstruction in the Newborn
Burns, Thermal
Congenital Adrenal Hyperplasia
Dehydration
Diabetes Insipidus
Diabetic Ketoacidosis
Diarrhea
Eating Disorder: Anorexia
Enteroviral Infections
Fluid, Electrolyte, and Nutrition Management of the Newborn
Gastroenteritis
Hyperkalemia
Hypernatremia
Hypochloremic Alkalosis
Hypoglycemia
Hypokalemia
Hyponatremia
Intestinal Malrotation
Intestinal Volvulus
Intussusception
Neonatal Sepsis
Oliguria
Pyloric Stenosis, Hypertrophic
Shock
Shock and Hypotension in the Newborn
Small-Bowel Obstruction


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Related Articles
Acidosis, Metabolic

Adrenal Insufficiency

Alkalosis, Metabolic

Bowel Obstruction in the Newborn

Burns, Thermal

Congenital Adrenal Hyperplasia

Dehydration

Diabetes Insipidus

Diabetic Ketoacidosis

Diarrhea

Eating Disorder: Anorexia

Enteroviral Infections

Fluid, Electrolyte, and Nutrition Management of the Newborn

Gastroenteritis

Hyperkalemia

Hypernatremia

Hypochloremic Alkalosis

Hypoglycemia

Hypokalemia

Hyponatremia

Intestinal Malrotation

Intestinal Volvulus

Intussusception

Neonatal Sepsis

Oliguria

Pyloric Stenosis, Hypertrophic

Shock

Shock and Hypotension in the Newborn

Small-Bowel Obstruction


Patient Education



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Lab Studies:

  • Laboratory data are generally not required if the etiology is apparent and mild-to-moderate dehydration is present.
  • With severe dehydration, the following laboratory studies are suggested:
    • Serum sodium should be determined because hyponatremia (Na <130 mEq/L) and hypernatremia (Na >150 mEq/L) require specific treatment regimens.
    • Potassium may be elevated (eg, congenital adrenal hyperplasia, renal failure) or low (eg, pyloric stenosis, alkalosis).
    • Chloride may be low in pyloric stenosis (eg, hypochloremic, hypokalemic, or metabolic alkalosis).
    • Poor tissue perfusion in dehydration results in production of lactic acid. Bicarbonate is consumed as lactic acid levels increase. In DKA, ketoacids also consume bicarbonate. Bicarbonate levels can also be reduced because of loss of bicarbonate in diarrheal stools.
    • Glucose may be dangerously low because of poor intake or extremely elevated in DKA.
    • Blood urea nitrogen and creatinine may be elevated because of renal hypoperfusion.
    • Urine specific gravity may be elevated; diabetes insipidus causes the urine to be dilute.
    • Urinalysis may show findings of DKA (eg, ketones, glucose).
    • Electrolyte analysis of any fluid that is lost (eg, urine, stool, gastric fluid) can be performed to further refine the composition of replacement fluids.

Procedures:

  • Intravenous line
    • If severe dehydration is present, peripheral intravenous line insertion may be difficult. The preferred sites for initial insertion attempts include the basilic and cephalic veins in the antecubital fossa and the saphenous veins near the ankle. Transillumination of the insertion site with a fiberoptic light source may be used to facilitate locating the desired vein.
    • If peripheral intravenous access cannot be rapidly achieved (<90 s) in a child with severe dehydration and shock, intraosseous cannulation should be attempted. If the child is not in extremis, more time may be taken to establish central venous access percutaneously (eg, femoral, subclavian, internal, external jugular).
  • Intraosseous line: Intraosseous cannulation can easily and rapidly be achieved in children younger than 6 years. Specially designed intraosseous infusion needles or Jamshidi-type bone marrow aspiration needles may be used. Short large-bore spinal needles may also be used but often bend during placement. The ideal site of insertion is the anteromedial surface of the tibia, 1-3 cm below the anterior tibial tuberosity.
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Medical Care: Medications such as loperamide, opiates, anticholinergics, bismuth subsalicylate, and adsorbents are not recommended because of questionable efficacy and potential adverse effects.

Oral rehydration solutions

During gastroenteritis, the intestinal mucosa retains absorptive capacity. Sodium and glucose in the correct proportions can be passively cotransported with fluid from the gut lumen into the circulation. Rapid oral rehydration with the appropriate solution has been shown to be as effective as intravenous fluid therapy in restoring intravascular volume and correcting acidosis.

Table 3. Composition of Appropriate Oral Rehydration Solutions
SolutionCHO*, g/dLNa, mEq/LK, mEq/LBase, mEq/L Osmolality
Pedialyte2.5452030250
Infalyte3 5025 30 200
Rehydralyte2.5 75 20 30 310
WHO/UNICEF290 20 30 310
*Carbohydrate
World Health Organization/United Nations Children's Fund

All of the commercially available rehydration fluids are acceptable for oral rehydration therapy (ORT). They contain 2-3 g/dL of glucose, 45-90 mEq/L of sodium, 30 mEq/L of base, and 20-25 mEq/L of potassium. Osmolality is 200-310 mOsm/L.

Table 4. Composition of Inappropriate Oral Rehydration Solutions
SolutionCHO, g/dLNa, mEq/LK, mEq/LBase, mEq/LOsmolality
Apple juice120.4260700
Ginger ale93.50.1 3.6565
Milk4.9 2236 30260
Chicken broth0 2 3 3 330

Traditional clear fluids are not appropriate for ORT. Many contain excessive concentrations of CHO and low concentrations of sodium. The inappropriate glucose-to-sodium ratio impairs water absorption, and the large osmotic load creates an osmotic diarrhea, further worsening the degree of dehydration.

  • Oral rehydration therapy for mild or moderate dehydration
    • Mild or moderate dehydration can usually be treated very effectively with ORT.

    • Vomiting is generally not a contraindication to ORT. If evidence of bowel obstruction, ileus, or acute abdomen exists, then intravenous rehydration is indicated.

    • Calculate fluid deficit. Physical findings consistent with mild dehydration suggest a fluid deficit of 5% of body weight in infants and 3% in children. Moderate dehydration occurs with a fluid deficit of 5-10% in infants and 3-6% in children (see Table 1 and Table 2). The fluid deficit should be replaced over 4 hours.

    • The oral rehydration solution should be administered in small volumes very frequently to minimize gastric distention and reflex vomiting. Generally, 5 mL of oral rehydration solution every minute is well tolerated. Hourly intake and output should be recorded by the caregiver. As the child becomes rehydrated, vomiting often decreases and larger fluid volumes may be used.

    • If vomiting persists, infusion of oral rehydration solution via a nasogastric tube may be temporarily used to achieve rehydration. Intravenous fluid administration (20-30 mL/kg of isotonic sodium chloride solution over 1-2 h) may also be used until oral rehydration is tolerated.

    • Replace ongoing losses from stools and emesis (estimate volume and replace) in addition to replacing the calculated fluid deficit.

    • Once the child is rehydrated, start an age-appropriate diet (see below).
  • Severe dehydration
    • Laboratory evaluation and intravenous rehydration are required. The underlying cause of the dehydration must be determined and treated appropriately.

    • Phase 1 focuses on emergency management. Severe dehydration is characterized by a state of hypovolemic shock requiring rapid treatment. Initial management includes placement of an intravenous or intraosseous line and rapid administration of 20 mL/kg of lactated Ringer solution or isotonic sodium chloride solution. Additional fluid boluses may be required depending on the severity of the dehydration. The child should be frequently reassessed to determine the response to treatment. As intravascular volume is replenished, tachycardia, capillary refill, urine output, and mental status all should improve. If improvement is not observed after 60 mL/kg of fluid administration, other etiologies of shock (eg, cardiac, anaphylactic, septic) should be considered. Hemodynamic monitoring and inotropic support may be indicated.

    • Phase 2 focuses on deficit replacement, provision of maintenance fluids, and replacement of ongoing losses. Daily maintenance fluid requirements may calculated as follows:

      • Less than 10 kg = 100 mL/kg

      • 10-20 kg = 1000 + 50 mL/kg for each kg over 10 kg

      • Greater than 20 kg = 1500 + 20 mL/kg for each kg over 20 kg

    • Severe dehydration by clinical examination suggests a fluid deficit of 10-15% of body weight in infants and 6-9% of body weight in older children. The daily maintenance fluid is added to the fluid deficit. In general, the recommended administration is one half of this volume administered over 8 hours and administration of the remainder over the following 16 hours. Continued losses (eg, emesis, diarrhea) must be replaced promptly.

    • If the child is isonatremic (130-150 mEq/L), the sodium deficit incurred can generally be corrected by administering the fluid deficit plus maintenance as 5% dextrose in 0.45% NaCl. Potassium (20 mEq/L KCl) may be added once urine output is established.

    • An alternative approach to the deficit therapy approach is rapid replacement therapy. With this approach, a child with severe isonatremic dehydration is administered 20-40 mL/kg of isotonic sodium chloride solution or lactated Ringer solution over 15-60 minutes. As perfusion is restored, the child improves and is able to tolerate an oral rehydration solution for the remainder of his rehydration. This approach is not appropriate for hypernatremic or hyponatremic dehydration.
  • Hyponatremic dehydration

    • Phase 1 management of hyponatremic dehydration is identical to that of isonatremic dehydration. Rapid volume expansion with 20 mL/kg of isotonic sodium chloride solution or lactated Ringer solution should be administered and repeated until perfusion is restored.

    • Severe hyponatremia (<130 mEq/L) indicates additional sodium loss. In phase 2 management, rehydration is calculated as for isonatremic dehydration. The additional sodium deficit must be calculated and added to the rehydration fluids. The deficit may be calculated to restore the sodium to 130 mEq/L and administered over 24 hours.

      • Sodium deficit = (sodium desired - sodium actual) X volume of distribution X weight (kg)

      • Example: Na = 123, weight = 10 kg, assumed volume of distribution of 0.6; Na deficit = (130-123) X 0.6 X 10 kg = 42 mEq Na

    • A simplified approach is to use 5% dextrose in 0.9% NaCl or 0.45% NaCl as the replacement fluid. The sodium is monitored closely, and the amount of sodium in the fluid is adjusted to maintain a slow correction (<0.5 mEq/L/h).

    • Frequently reassessing the serum sodium level during correction is imperative. Rapid correction of chronic hyponatremia (>2 mEq/L/h) has been associated with central pontine myelinolysis. Rapid partial correction of symptomatic hyponatremia has not been associated with adverse effects. Therefore, if the child is symptomatic (seizures), a more rapid partial correction is indicated. Hypertonic (3%) isotonic sodium chloride solution (0.5 mEq/mL) may be used for rapid partial correction of symptomatic hyponatremia. A dose of 4 mL/kg raises the serum sodium by 3-4 mEq/L.
  • Hypernatremic dehydration

    • Phase 1 management of hypernatremic dehydration is identical to that of isonatremic dehydration. Rapid volume expansion with 20 mL/kg of isotonic sodium chloride solution or lactated Ringer solution should be administered and repeated until perfusion is restored.

    • Varied regimens may be successfully followed to achieve correction of severe hypernatremia (>150 mEq/L). In phase 2 management, the most important goal is to reestablish intravascular volume and return serum sodium levels toward the reference range by not more than 10 mEq/L/24 h. Rapid correction of hypernatremic dehydration can have disastrous neurologic consequences, including cerebral edema and death.

    • The most cautious approach is to plan a slow correction of the fluid deficit over 48 hours. Following adequate intravascular volume expansion, rehydration fluids should be initiated with 5% dextrose in 0.9% NaCl. Serum sodium levels should be assessed every 4 hours. If the sodium has decreased by less than 0.5 mEq/L/h, then the sodium content of the rehydration fluid is decreased. This allows for a slow controlled correction of the hypernatremic state.

    • Hyperglycemia and hypocalcemia are sometimes associated with hypernatremic dehydration. Serum glucose and calcium levels should be monitored closely.

Diet:

  • Once the child is rehydrated, an age-appropriate diet should be started. Children with dehydration from gastroenteritis have decreased duration of diarrhea when feedings are rapidly restarted.
  • Diluting milk or formula is not indicated. Breast-feeding should be resumed as soon as possible.
  • Foods containing complex carbohydrates (eg, rice, wheat, potatoes, bread, cereals), lean meats, fruits, and vegetables are encouraged. Fatty foods and simple carbohydrates should be avoided.
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Further Inpatient Care:

  • Severe dehydration warrants hospital admission for rehydration, as do hypernatremic or hyponatremic states.
  • Inability to tolerate oral rehydration therapy may necessitate hospital admission for nasogastric or intravenous fluid therapy.

Further Outpatient Care:

  • ORT may be continued at home if clear instructions are provided for the family and if the family members can be relied upon to carry out the hydration regimen. Close follow-up by the primary physician is recommended.

Complications:

  • Complications may include irreversible shock, sagittal or other venous sinus thrombosis, intractable seizures, and renal failure.

Prognosis:

  • Prognosis is excellent if the child is promptly and effectively treated. However, the child with severe dehydration and hypovolemic shock can have significant morbidity and mortality if treatment is delayed.

Patient Education:

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Medical/Legal Pitfalls:

  • Failure to recognize and appropriately treat DKA
  • Failure to recognize hypoglycemia
  • Failure to recognize severe hyponatremia or hypernatremia
  • Failure to recognize an acute abdomen
  • Inadequate volume administration (too slow, not enough) for the child with severe dehydration
  • Failure to recognize cardiogenic shock (gallop rhythm, hepatomegaly): Rapid fluid resuscitation may further impair cardiac output.
  BIBLIOGRAPHY Section 9 of 9   Click here to go to the previous section in this topic Click here to go to the top of this page
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  • AdroguĂ© HJ, Madias NE: Hypernatremia. N Engl J Med 2000 May 18; 342(20): 1493-9[Medline].
  • Atherly-John YC, Cunningham SJ, Crain EF: A randomized trial of oral vs intravenous rehydration in a pediatric emergency department. Arch Pediatr Adolesc Med 2002 Dec; 156(12): 1240-3[Medline].
  • Bellemare S, Hartling L, Wiebe N, et al: Oral rehydration versus intravenous therapy for treating dehydration due to gastroenteritis in children: a meta-analysis of randomised controlled trials. BMC Med 2004 Apr 15; 2: 11[Medline].
  • Bhatnagar S, Bahl R, Sharma PK, et al: Zinc with oral rehydration therapy reduces stool output and duration of diarrhea in hospitalized children: a randomized controlled trial. J Pediatr Gastroenterol Nutr 2004 Jan; 38(1): 34-40[Medline].
  • Choice Study Group: Multicenter, randomized, double-blind clinical trial to evaluate the efficacy and safety of a reduced osmolarity oral rehydration salts solution in children with acute watery diarrhea. Pediatrics 2001 Apr; 107(4): 613-8[Medline].
  • Dale J: Oral rehydration solutions in the management of acute gastroenteritis among children. J Pediatr Health Care 2004 Jul-Aug; 18(4): 211-2[Medline].
  • Duggan C, Refat M, Hashem M, et al: How valid are clinical signs of dehydration in infants? J Pediatr Gastroenterol Nutr 1996 Jan; 22(1): 56-61[Medline].
  • Duggan C, Fontaine O, Pierce NF, et al: Scientific rationale for a change in the composition of oral rehydration solution. JAMA 2004 Jun 2; 291(21): 2628-31[Medline].
  • Duke T, Molyneux EM: Intravenous fluids for seriously ill children: time to reconsider. Lancet 2003 Oct 18; 362(9392): 1320-3[Medline].
  • Fonseca BK, Holdgate A, Craig JC: Enteral vs intravenous rehydration therapy for children with gastroenteritis: a meta-analysis of randomized controlled trials. Arch Pediatr Adolesc Med 2004 May; 158(5): 483-90[Medline].
  • Gorelick MH, Shaw, KN, Murphy, KO: Validity and reliability of clinical signs in the diagnosis of dehydration in children. Pediatrics. 1997; May;(5):99: E6[Medline].
  • Holliday M: The evolution of therapy for dehydration: should deficit therapy still be taught? Pediatrics 1996 Aug; 98(2 Pt 1): 171-7[Medline].
  • Holliday MA, Friedman AL, Wassner SJ: Extracellular fluid restoration in dehydration: a critique of rapid versus slow. Pediatr Nephrol 1999 May; (4): 292-7[Medline].
  • Holliday MA, Friedman AL, Segar WE, et al: Acute hospital-induced hyponatremia in children: a physiologic approach. J Pediatr 2004 Nov; 145(5): 584-7[Medline].
  • Hoorn EJ, Geary D, Robb M, et al: Acute hyponatremia related to intravenous fluid administration in hospitalized children: an observational study. Pediatrics 2004 May; 113(5): 1279-84[Medline].
  • King CK, Glass R, Bresee JS, et al: Managing acute gastroenteritis among children: oral rehydration, maintenance, and nutritional therapy. MMWR Recomm Rep 2003 Nov 21; 52(RR-16): 1-16[Medline].
  • Miyasaka K, Shimizu N, Kojima J: Recent trends in pediatric fluid therapy. Methods Find Exp Clin Pharmacol 2004 May; 26(4): 287-94[Medline].
  • Moritz ML, Ayus JC: Prevention of hospital-acquired hyponatremia: a case for using isotonic saline. Pediatrics 2003 Feb; 111(2): 227-30[Medline].
  • Moritz ML, Ayus JC: Preventing neurological complications from dysnatremias in children. Pediatr Nephrol 2005 Aug 4;[Medline].
  • Moritz ML, Manole MD, Bogen DL, Ayus JC: Breastfeeding-associated hypernatremia: are we missing the diagnosis?. Pediatrics 2005 Sep; 116(3): e343-7[Medline].
  • Murphy C, Hahn S, Volmink J: Reduced osmolarity oral rehydration solution for treating cholera. Cochrane Database Syst Rev 2004; CD003754[Medline].
  • Nager AL, Wang VJ: Comparison of nasogastric and intravenous methods of rehydration in pediatric patients with acute dehydration. Pediatrics 2002 Apr; 109(4): 566-72[Medline].
  • Nalin DR, Hirschhorn N, Greenough W, et al: Clinical concerns about reduced-osmolarity oral rehydration solution. JAMA 2004 Jun 2; 291(21): 2632-5[Medline].
  • Ozuah PO, Avner JR, Stein RE: Oral rehydration, emergency physicians, and practice parameters: a national survey. Pediatrics 2002 Feb; 109(2): 259-61[Medline].
  • Phin SJ, McCaskill ME, Browne GJ, Lam LT: Clinical pathway using rapid rehydration for children with gastroenteritis. J Paediatr Child Health 2003 Jul; 39(5): 343-8[Medline].
  • Playfor SD: Hypotonic intravenous solutions in children. Expert Opin Drug Saf 2004 Jan; 3(1): 67-73[Medline].
  • Reid SR, Bonadio WA: Outpatient rapid intravenous rehydration to correct dehydration and resolve vomiting in children with acute gastroenteritis. Ann Emerg Med 1996 Sep; 28(3): 318-23[Medline].
  • Santosham M, Keenan EM, Tulloch J, et al: Oral rehydration therapy for diarrhea: an example of reverse transfer of technology. Pediatrics 1997 Nov; 100(5): E10[Medline].
  • Sarnaik AP, Meert K, Hackbarth R, Fleischmann L: Management of hyponatremic seizures in children with hypertonic saline: a safe and effective strategy. Crit Care Med. 1991; Jun;19(6): 758-62[Medline].
  • Spandorfer PR, Alessandrini EA, Joffe MD, et al: Oral versus intravenous rehydration of moderately dehydrated children: a randomized, controlled trial. Pediatrics 2005 Feb; 115(2): 295-301[Medline].
  • Steiner MJ, DeWalt DA, Byerley JS: Is this child dehydrated?. JAMA 2004 Jun 9; 291(22): 2746-54[Medline].
  • Wathen JE, MacKenzie T, Bothner JP: Usefulness of the serum electrolyte panel in the management of pediatric dehydration treated with intravenously administered fluids. Pediatrics 2004 Nov; 114(5): 1227-34[Medline].

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