Volume depletion in children
- Overview
- Theory
- Diagnosis
- Management
- Follow up
- Resources
Treatment algorithm
Please note that formulations/routes and doses may differ between drug names and brands, drug formularies, or locations. Treatment recommendations are specific to patient groups: see disclaimer
enteric losses
oral rehydration solution (oral route)
Mild to moderate volume depletion is indicated by normal mental status, hemodynamic stability, and only mildly altered vital signs (e.g., minor degree of tachycardia).
Enteral replacement of fluid volume deficit and ongoing losses is appropriate for patients with mild or moderate dehydration.
Commercially available oral rehydration solutions (ORS) have a formulation close to that of the WHO-recommended ORS and may be used. Fluids such as carbonated beverages, fruit juice, or plain water should not be used.
Frequent small volumes, with gradual advancement as tolerated, is preferred. A general guideline is to give 50-100 mL/kg of ORS over 2-4 hours.[13]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. http://www.cdc.gov/mmwr/preview/mmwrhtml/rr5216a1.htm http://www.ncbi.nlm.nih.gov/pubmed/14627948?tool=bestpractice.com [17]Freedman SB, Vandermeer B, Milne A, et al; Pediatric Emergency Research Canada Gastroenteritis Study Group. Diagnosing clinically significant dehydration in children with acute gastroenteritis using noninvasive methods: a meta-analysis. J Pediatr. 2015;166:908-916. http://www.ncbi.nlm.nih.gov/pubmed/25641247?tool=bestpractice.com
age-appropriate diet
Treatment recommended for ALL patients in selected patient group
"Gut rest" has no role in gastroenteritis. Breastfed infants should continue nursing in addition to receiving oral rehydration solution.
Age-appropriate diets should be instituted early in the course of gastroenteritis-associated mild or moderate volume depletion. Foods high in sugar and carbohydrates should be avoided.
antiemetic
Treatment recommended for SOME patients in selected patient group
Not commonly used in pediatric patients to treat vomiting related to acute gastroenteritis, but occasionally used in patients who are clinically stable and are unable to take adequate oral hydration.[31]Roslund G, Hepps TS, McQuillin KK. The role of oral ondansetron in children with vomiting as a result of acute gastritis/gastroenteritis who have failed oral rehydration therapy: a randomized controlled trial. Ann Emerg Med. 2008;52:22-29. http://www.ncbi.nlm.nih.gov/pubmed/18006189?tool=bestpractice.com [32]Freedman SB, Adler M, Seshadri R, et al. Oral ondansetron for gastroenteritis in a pediatric emergency department. N Engl J Med. 2006;354:1698-1705. http://www.nejm.org/doi/full/10.1056/NEJMoa055119#t=article http://www.ncbi.nlm.nih.gov/pubmed/16625009?tool=bestpractice.com
Ondansetron, in a disintegrating tablet formulation, has been studied for use in this clinical situation in a large, randomized, controlled study.[32]Freedman SB, Adler M, Seshadri R, et al. Oral ondansetron for gastroenteritis in a pediatric emergency department. N Engl J Med. 2006;354:1698-1705. http://www.nejm.org/doi/full/10.1056/NEJMoa055119#t=article http://www.ncbi.nlm.nih.gov/pubmed/16625009?tool=bestpractice.com
Although other antiemetics are sometimes used in pediatric patients, they are generally not substantiated in the literature.
Primary options
ondansetron: children 8-15 kg: 2 mg orally (disintegrating tablet) as a single dose; children 16-30 kg: 4 mg orally (disintegrating tablet) as a single dose; children >30 kg: 6-8 mg orally (disintegrating tablet) as a single dose
oral rehydration solution (nasogastric route)
Nasogastric administration of oral rehydration solution is rapid and efficacious for children who have mild to moderate volume depletion, and who are unable or unwilling to drink.
It may even be tolerated by many children with vomiting. Potential advantages of the nasogastric route include more rapid initiation of treatment, ease of nasogastric placement compared with intravenous placement (particularly in very young and dehydrated patients), and lower cost.
Potential disadvantages include risk for continued vomiting, ileus, displacement, and aspiration. Interestingly, parents are equally satisfied with nasogastric and intravenous treatments.[34]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. http://www.ncbi.nlm.nih.gov/pubmed/11927697?tool=bestpractice.com
antiemetic
Treatment recommended for SOME patients in selected patient group
Not commonly used in pediatric patients to treat vomiting related to acute gastroenteritis, but occasionally used in patients who are clinically stable and are unable to take adequate oral hydration.[31]Roslund G, Hepps TS, McQuillin KK. The role of oral ondansetron in children with vomiting as a result of acute gastritis/gastroenteritis who have failed oral rehydration therapy: a randomized controlled trial. Ann Emerg Med. 2008;52:22-29. http://www.ncbi.nlm.nih.gov/pubmed/18006189?tool=bestpractice.com [32]Freedman SB, Adler M, Seshadri R, et al. Oral ondansetron for gastroenteritis in a pediatric emergency department. N Engl J Med. 2006;354:1698-1705. http://www.nejm.org/doi/full/10.1056/NEJMoa055119#t=article http://www.ncbi.nlm.nih.gov/pubmed/16625009?tool=bestpractice.com
Antiemetics may be indicated even in children receiving nasogastric therapy.
Ondansetron, in a disintegrating tablet formulation, has been studied for use in this clinical situation in a large, randomized, controlled study.[32]Freedman SB, Adler M, Seshadri R, et al. Oral ondansetron for gastroenteritis in a pediatric emergency department. N Engl J Med. 2006;354:1698-1705. http://www.nejm.org/doi/full/10.1056/NEJMoa055119#t=article http://www.ncbi.nlm.nih.gov/pubmed/16625009?tool=bestpractice.com
Although other antiemetics are sometimes used in pediatric patients, they are generally not substantiated in the literature.
Primary options
ondansetron: children 8-15 kg: 2 mg orally (disintegrating tablet) as a single dose; children 16-30 kg: 4 mg orally (disintegrating tablet) as a single dose; children >30 kg: 6-8 mg orally (disintegrating tablet) as a single dose
intravenous isotonic crystalloid
Severe volume depletion, which is indicated by an altered mental status and hemodynamic instability, is a medical emergency and must be treated aggressively with intravenous isotonic crystalloid solutions. The intravenous route may be preferred if enteral administration is not tolerated.
Isotonic crystalloid is given in boluses of up to 20 mL/kg. This is repeated until the estimated deficit is restored or normal hemodynamic values, particularly heart rate and urine output, are well established.
If symptoms do not improve after 40-60 mL/kg of isotonic saline, other etiologies (e.g., anaphylaxis, hemorrhage, intoxication, concomitant cardiovascular dysfunction) should be considered. However, children presenting in hypovolemic shock may require additional fluid replacement before shock is reversed.[5]Carcillo JA, Wheeler DS, Kooy NW, et al. Shock: an overview. In: Wheeler DS, Wong HR, Shanley TP, eds. Pediatric critical care medicine: basic science and clinical evidence. London, UK: Springer-Verlag; 2007:274-298.[44]Davis AL, Carcillo JA, Aneja RK, et al. American College of Critical Care Medicine Clinical practice parameters for hemodynamic support of pediatric and neonatal septic shock. Crit Care Med. 2017 Jun;45(6):1061-93. https://www.doi.org/10.1097/CCM.0000000000002425 http://www.ncbi.nlm.nih.gov/pubmed/28509730?tool=bestpractice.com [45]de Oliveira CF, de Oliveira DS, Gottschald AF, et al. ACCM/PALS haemodynamic support guidelines for paediatric septic shock: an outcomes comparison with and without monitoring central venous oxygen saturation. Intensive Care Med. 2008;34:1065-1075. http://www.ncbi.nlm.nih.gov/pubmed/18369591?tool=bestpractice.com
Careful consideration of the individual circumstances of each patient and available resources should be part of the assessment of the risks versus the benefits of different strategies for volume repletion.
intraosseous isotonic crystalloid
If intravenous access cannot be obtained within the first 5 minutes, an intraosseous line should be placed. The proximal tibia and distal femur sites are frequently used.
Isotonic crystalloid is given in boluses of up to 20 mL/kg. This is repeated until the estimated deficit is restored or normal hemodynamic values, particularly heart rate and urine output, are well established. However, if symptoms do not improve after 40-60 mL/kg of isotonic saline, other etiologies (e.g., anaphylaxis, hemorrhage, intoxication, concomitant cardiovascular dysfunction) should be considered.
hemorrhagic losses
intravenous isotonic saline + surgical consultation
Initial treatment is with 20 mL/kg of isotonic crystalloid solution.[5]Carcillo JA, Wheeler DS, Kooy NW, et al. Shock: an overview. In: Wheeler DS, Wong HR, Shanley TP, eds. Pediatric critical care medicine: basic science and clinical evidence. London, UK: Springer-Verlag; 2007:274-298.[8]American Academy of Pediatrics. Management of pediatric trauma. Pediatrics. 2008;121:849-854. http://pediatrics.aappublications.org/cgi/content/full/121/4/849 http://www.ncbi.nlm.nih.gov/pubmed/18381551?tool=bestpractice.com This can be repeated until signs of hemodynamic instability are improved with potential need for blood products/transfusion.
In addition, hemostasis is essential for correcting volume depletion. Occult bleeding is more common in children, due to patterns of trauma injury.[8]American Academy of Pediatrics. Management of pediatric trauma. Pediatrics. 2008;121:849-854. http://pediatrics.aappublications.org/cgi/content/full/121/4/849 http://www.ncbi.nlm.nih.gov/pubmed/18381551?tool=bestpractice.com
Occult trauma should be considered in an infant or a young child presenting with altered mental status and signs of volume depletion who does not respond to crystalloid administration. A head and abdominal ultrasound or CT should be considered.
packed red blood cell transfusion
Treatment recommended for SOME patients in selected patient group
In cases of significant hemorrhagic losses when adequate oxygen delivery to vital organs is not maintained with crystalloid alone, blood products need to be repleted.
Generally, 5-10 mL/kg of cross-matched blood is given. In cases of active hemorrhage associated with hemodynamic instability, giving unmatched blood (trauma pack) may be necessary. Simultaneous consultation with a pediatric trauma team is indicated.
Attaining hemoglobin >10 mg/dL improves outcomes in children with shock.[24]American College of Surgeons. Advanced trauma life support. 7th ed. Chicago, IL: American College of Surgeons; 2004.[47]Rivers E, Nguyen B, Havstad S, et al. Early goal-directed therapy in the treatment of severe sepsis and septic shock. N Engl J Med. 2001 Nov 8;345(19):1368-77. http://www.nejm.org/doi/full/10.1056/NEJMoa010307#t=article http://www.ncbi.nlm.nih.gov/pubmed/11794169?tool=bestpractice.com
fresh frozen plasma + platelets
Treatment recommended for SOME patients in selected patient group
Coagulopathic patients with ongoing losses may require replacement of clotting factors for hemostasis. Platelets and fresh frozen plasma are given if bleeding is ongoing, blood loss is massive, or the patient has received massive transfusion (50% of total blood volume).
skin losses
enteral oral rehydration solution + environmental control
Mild to moderate volume depletion is indicated by normal mental status, hemodynamic stability, and only mildly altered vital signs (e.g., minor degree of tachycardia).
Initial management is with enteric replacement with oral rehydration solutions (ORS). Commercially available ORS have a formulation close to that of the WHO-recommended ORS and may be used.
Frequent small volumes, with gradual advancement as tolerated, is preferred. A general guideline is to give 50-100 mL/kg of ORS over 2-4 hours, similarly to treatment of mild to moderate volume depletion in children with enteral losses.[13]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. http://www.cdc.gov/mmwr/preview/mmwrhtml/rr5216a1.htm http://www.ncbi.nlm.nih.gov/pubmed/14627948?tool=bestpractice.com [17]Freedman SB, Vandermeer B, Milne A, et al; Pediatric Emergency Research Canada Gastroenteritis Study Group. Diagnosing clinically significant dehydration in children with acute gastroenteritis using noninvasive methods: a meta-analysis. J Pediatr. 2015;166:908-916. http://www.ncbi.nlm.nih.gov/pubmed/25641247?tool=bestpractice.com
In addition, environmental control is important. The patient should be moved to a neutral ambient temperature.
subsequent hypotonic oral solution
Treatment recommended for SOME patients in selected patient group
In cases of skin loss from excessive sweating, the fluid lost is relatively hypotonic. After intravascular volume is restored, relatively hypotonic solutions can be used to restore total body water deficit.
intravenous isotonic saline
Severe volume depletion is indicated by an altered mental status and hemodynamic instability.
Initial treatment is with intravenous isotonic saline 20 mL/kg, repeated as necessary to restore normal hemodynamics.
subsequent intravenous hypotonic saline
Treatment recommended for SOME patients in selected patient group
After intravascular volume is restored, in cases of skin loss from excessive sweating, relatively hypotonic solutions (e.g., 0.45% normal saline) can be used with caution to restore total body water deficit if indicated by persistent hypernatremia. Whenever hypotonic fluids are delivered, frequent monitoring of electrolytes to ensure detection of rapid changes in serum sodium is recommended.
intravenous isotonic saline
Volume losses can be extremely high in patients with significant burns, requiring urgent hemodynamic stabilization and transfer to highly specialized burn centers.[51]Mak GZ, Allen SR, Kagan RJ. Pediatric burns. In: Wheeler DS, Wong HR, Shanley TP, eds. Pediatric critical care medicine: basic science and clinical evidence. London, UK: Springer-Verlag; 2007:1597-1606.
All patients with burns >10% total body surface area (TBSA) should be resuscitated with isotonic saline solution delivered intravenously.
Advanced Burn Life Support (ABLS) Guidelines state that pediatric patients (12 years or younger) with nonelectrical burns should receive 3mL/kg/%TBSA of isotonic crystalloid (ideally lactated Ringer’s solution) in the first 24 hours. Pediatric electrical burns should receive 4mL/kg/%TBSA.[52]American Burn Association. Pediatric burn injuries. In: Thompson C, ed. Advanced burn life support course manual. Chicago, IL: American Burn Association; 2023:56-64. One half of this total volume should be delivered in the first 8 hours, and the remainder over the next 16 hours in addition to maintenance intravenous fluids.[53]Baxter CR, Shires T. Physiological response to crystalloid resuscitation of severe burns. Ann N Y Acad Sci. 1968;150:874-894. http://www.ncbi.nlm.nih.gov/pubmed/4973463?tool=bestpractice.com Maintenance fluids should include dextrose; 5% dextrose in lactated Ringer’s solution is recommended by ABLS Guidelines. Resuscitation should be titrated hourly to urine output (0.5 mL/kg/hour for children weighing >30 kg or 1 mL/kg/hour for children weighing ≤30 kg) until the fluid rate is decreased down to the maintenance rate.[52]American Burn Association. Pediatric burn injuries. In: Thompson C, ed. Advanced burn life support course manual. Chicago, IL: American Burn Association; 2023:56-64. Children with larger burns or who are hemodynamically unstable may require resuscitation in excess of these amounts.
Consultation with burn specialists and transfer to a burn unit for optimal care should be considered.
appropriate wound care
Treatment recommended for ALL patients in selected patient group
Appropriate wound care is required.
renal losses
intravenous isotonic saline
In these patients, volume depletion is mostly due to renal water loss associated with glycosuria. A reasonable approach is to administer 10-20 mL/kg of normal saline intravenously over the first 20-30 minutes, and the remaining fluid deficit plus the weight-based maintenance fluid requirement, with either 0.45% or 0.90% normal saline, over the next 24-48 hours while monitoring closely for signs of cerebral edema.[9]Glaser N, Fritsch M, Priyambada L, et al. ISPAD clinical practice consensus guidelines 2022: diabetic ketoacidosis and hyperglycemic hyperosmolar state. Pediatr Diabetes. 2022 Nov;23(7):835-56. http://www.ncbi.nlm.nih.gov/pubmed/36250645?tool=bestpractice.com [55]Rosenbloom AL. The management of diabetic ketoacidosis in children. Diabetes Ther. 2010 Dec;1(2):103-20. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3138479 http://www.ncbi.nlm.nih.gov/pubmed/22127748?tool=bestpractice.com [56]Canadian Paediatric Society. Current recommendations for management of paediatric diabetic ketoacidosis. Dec 2022 [internet publication]. https://cps.ca/en/documents/position/current-recommendations-for-management-of-paediatric-diabetic-ketoacidosis
Cerebral injury occurs frequently and with varying severity in children with DKA; however, evidence suggests that this is due to cerebral hypoperfusion and the hyperinflammatory state caused by DKA, rather than rapid fluid administration.[9]Glaser N, Fritsch M, Priyambada L, et al. ISPAD clinical practice consensus guidelines 2022: diabetic ketoacidosis and hyperglycemic hyperosmolar state. Pediatr Diabetes. 2022 Nov;23(7):835-56. http://www.ncbi.nlm.nih.gov/pubmed/36250645?tool=bestpractice.com [57]Kuppermann N, Ghetti S, Schunk JE, et al. Clinical trial of fluid infusion rates for pediatric diabetic ketoacidosis. N Engl J Med. 2018 Jun 14;378(24):2275-87. https://www.nejm.org/doi/10.1056/NEJMoa1716816 http://www.ncbi.nlm.nih.gov/pubmed/29897851?tool=bestpractice.com
Managing a young child in DKA can be complicated by late presentation, new diagnosis, underestimated degree of illness, and high insulin sensitivity leading to hypoglycemia.
intravenous insulin therapy
Treatment recommended for ALL patients in selected patient group
Insulin therapy guided by specialist protocols is required. Giving insulin subcutaneously to young children presenting in DKA, particularly with a new diagnosis of diabetes mellitus, is not advised.
Primary options
insulin regular: consult specialist for guidance on dose
enteral hypotonic oral rehydration
Volume depletion from renal losses other than DKA is uncommon. Of other rare causes, an unlikely but possible presentation is in children with central diabetes insipidus.
Volume depletion may present in children with known central diabetes insipidus because of interrupted normal treatment. Rarely, patients with history of head trauma or brain tumor are at risk of developing new central diabetes insipidus, which results in dehydration, sometimes associated with volume depletion.
Enteral replacement is generally sufficient. As water losses are primary, hypotonic solutions may be used.
desmopressin
Treatment recommended for SOME patients in selected patient group
The safety and efficacy of desmopressin injection for treating diabetes insipidus have not been established in children <12 years old. However, intranasal desmopressin therapy is given to patients previously known to have diabetes insipidus who present in hypovolemic shock that is clearly attributable to or complicated by unregulated diabetes insipidus.
Additional fluid therapy is discontinued as soon as volume is adequately replaced.
Primary options
desmopressin nasal: children 3 months to 12 years: 5-30 micrograms/day intranasally given in 1-2 divided doses; children ≥12 years: 10-40 micrograms/day intranasally given in 1-2 divided doses
intravenous hypotonic solution
If patients cannot tolerate oral replacement, intravenous hypotonic solution (e.g., one quarter normal saline) may be used.
desmopressin
Treatment recommended for SOME patients in selected patient group
The safety and efficacy of desmopressin injection for treating diabetes insipidus have not been established in children <12 years old. However, intranasal desmopressin therapy is given to patients previously known to have diabetes insipidus who present in hypovolemic shock that is clearly attributable to or complicated by unregulated diabetes insipidus.
Additional fluid therapy is discontinued as soon as volume is adequately replaced.
Primary options
desmopressin nasal: children 3 months to 12 years: 5-30 micrograms/day intranasally given in 1-2 divided doses; children ≥12 years: 10-40 micrograms/day intranasally given in 1-2 divided doses
enteral oral rehydration solution
Diuretic overuse can result from accidental ingestions in toddlers or rarely, Munchausen by proxy. These patients should be treated with enteral oral rehydration solution (ORS) (as for enteral losses).
Commercially available ORS have a formulation close to that of the WHO-recommended ORS and may be used.
Frequent small volumes, with gradual advancement as tolerated, is preferred. A general guideline is to give 50-100 mL/kg of ORS over 2-4 hours, similarly to treatment of mild to moderate volume depletion in children with enteral losses.[13]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. http://www.cdc.gov/mmwr/preview/mmwrhtml/rr5216a1.htm http://www.ncbi.nlm.nih.gov/pubmed/14627948?tool=bestpractice.com [17]Freedman SB, Vandermeer B, Milne A, et al; Pediatric Emergency Research Canada Gastroenteritis Study Group. Diagnosing clinically significant dehydration in children with acute gastroenteritis using noninvasive methods: a meta-analysis. J Pediatr. 2015;166:908-916. http://www.ncbi.nlm.nih.gov/pubmed/25641247?tool=bestpractice.com
Diuretic overdose may result in electrolyte abnormalities that require correction. Serum electrolytes should be monitored.
septic shock
intravenous isotonic crystalloid
Sepsis is usually associated with elements of hypovolemia from decreased intake, increased insensible losses, gastrointestinal losses, and third spacing (loss to the extravascular space).
Pediatric Surviving Sepsis Campaign guidelines recommend that if a critical care facility is available initial fluid resuscitation should be provided with intravenous isotonic crystalloid fluids in boluses of 10-20 mL/kg administered over the first hour until the patient has reversal of shock (i.e., a normal heart rate and BP for age, capillary refill less than 2 seconds, normal mental status, and adequate urinary output). If fluid resuscitation results in new hepatomegaly or pulmonary edema, or if there are persistent signs of shock after 40-60 mL/kg of isotonic fluid has been given, vasoactive therapy should be initiated.[22]Weiss SL, Peters MJ, Alhazzani W, et al. Surviving sepsis campaign international guidelines for the management of septic shock and sepsis-associated organ dysfunction in children. Intensive Care Med. 2020 Feb;46(suppl 1):10-67. https://www.doi.org/10.1007/s00134-019-05878-6 http://www.ncbi.nlm.nih.gov/pubmed/32030529?tool=bestpractice.com
If a critical care facility is not available and hypotension is present, pediatric Surviving Sepsis Campaign guidelines recommend that up to 40 mL/kg in bolus fluid (10-20 mL/kg per bolus) should be administered over the first hour with titration to clinical markers of cardiac output. Fluid boluses should be discontinued if signs of fluid overload develop. In the absence of hypotension, bolus fluid administration is not recommended and maintenance fluids should be started.[22]Weiss SL, Peters MJ, Alhazzani W, et al. Surviving sepsis campaign international guidelines for the management of septic shock and sepsis-associated organ dysfunction in children. Intensive Care Med. 2020 Feb;46(suppl 1):10-67. https://www.doi.org/10.1007/s00134-019-05878-6 http://www.ncbi.nlm.nih.gov/pubmed/32030529?tool=bestpractice.com
broad-spectrum antibiotics
Treatment recommended for ALL patients in selected patient group
After obtaining blood cultures, empiric broad-spectrum antibiotics, which take into account local susceptibility and infectious patterns, should be given promptly. It is important to give broad-spectrum antibiotics as soon as possible and always within 1 hour of recognition of septic shock.[22]Weiss SL, Peters MJ, Alhazzani W, et al. Surviving sepsis campaign international guidelines for the management of septic shock and sepsis-associated organ dysfunction in children. Intensive Care Med. 2020 Feb;46(suppl 1):10-67. https://www.doi.org/10.1007/s00134-019-05878-6 http://www.ncbi.nlm.nih.gov/pubmed/32030529?tool=bestpractice.com
Common regimens include ampicillin and gentamicin in neonates, and third-generation cephalosporins, such as ceftriaxone plus vancomycin, in older children. Additional coverage for gram-negative organisms, Pseudomonas species, fungal pathogens, and resistant Staphylococcus aureus will be guided by the patient's medical history and clinical presentation.
Primary options
ampicillin: consult specialist for guidance on neonatal doses
and
gentamicin: consult specialist for guidance on neonatal doses
OR
vancomycin: infants and children: 15 mg/kg intravenously every 6 hours
and
ceftriaxone: infants and children: 100 mg/kg intravenously every 24 hours
vasopressor + blood products + advanced monitoring
Treatment recommended for SOME patients in selected patient group
Hemodynamic support with infusion of vasopressor agents may be required. There is no adequate evidence that any one vasopressor agent is a superior choice compared with another and specific choice may be individualized.[59]Gamper G, Havel C, Arrich J, et al. Vasopressors for hypotensive shock. Cochrane Database Syst Rev. 2016;(2):CD003709. http://onlinelibrary.wiley.com/doi/10.1002/14651858.CD003709.pub4/full http://www.ncbi.nlm.nih.gov/pubmed/26878401?tool=bestpractice.com Consult a specialist for guidance on choice of vasopressor and dose.
Correcting coagulopathy and anemia may also be necessary for optimal management.
Patients requiring vasopressors or deteriorating despite crystalloid need to be transferred to ICU for advanced monitoring.
anaphylactic shock
epinephrine (adrenaline) + intravenous or intraosseous isotonic saline
Patients with anaphylaxis classically manifest in distributive shock, in which severe systemic vasodilation and capillary leak causes underperfusion of vital organs despite normal total body volume status. While not technically volume depletion, the clinical presentation of a child in anaphylaxis has some overlap with patients presenting in hypovolemic shock, with altered mental status, tachycardia, and low BP. Infants and toddlers may report age-specific symptoms of anaphylaxis that are different from older children and adults. For example, skin symptoms and subtle behavioral signs (pulling/scratching/fingers in ear, withdrawal, inconsolable crying, irritability, or clinging) may be more common in infants and younger children, while respiratory symptoms may be more common in older children.[60]Golden DBK, Wang J, Waserman S, et al. Anaphylaxis: a 2023 practice parameter update. Ann Allergy Asthma Immunol. 2024 Feb;132(2):124-76. https://www.annallergy.org/article/S1081-1206(23)01304-2/fulltext http://www.ncbi.nlm.nih.gov/pubmed/38108678?tool=bestpractice.com
Initial acute therapy is with intramuscular epinephrine. This may be given by a self-injectable device.[60]Golden DBK, Wang J, Waserman S, et al. Anaphylaxis: a 2023 practice parameter update. Ann Allergy Asthma Immunol. 2024 Feb;132(2):124-76. https://www.annallergy.org/article/S1081-1206(23)01304-2/fulltext http://www.ncbi.nlm.nih.gov/pubmed/38108678?tool=bestpractice.com [61]Muraro A, Worm M, Alviani C, et al. EAACI guidelines: anaphylaxis (2021 update). Allergy. 2022 Feb;77(2):357-77. https://onlinelibrary.wiley.com/doi/10.1111/all.15032 http://www.ncbi.nlm.nih.gov/pubmed/34343358?tool=bestpractice.com
In addition, intravenous saline 10 mL/kg is given (repeated as necessary to restore intravascular volume and hemodynamic stability).[61]Muraro A, Worm M, Alviani C, et al. EAACI guidelines: anaphylaxis (2021 update). Allergy. 2022 Feb;77(2):357-77. https://onlinelibrary.wiley.com/doi/10.1111/all.15032 http://www.ncbi.nlm.nih.gov/pubmed/34343358?tool=bestpractice.com [62]Resuscitation Council UK. Emergency treatment of anaphylactic reactions: guidelines for healthcare providers. 2021 [internet publication]. https://www.resus.org.uk/library/2021-resuscitation-guidelines The intraosseous route may be used if gaining intravenous access is not possible.
Corticosteroids and/or antihistamines are no longer recommended for the initial emergency treatment of anaphylaxis.[63]Shaker MS, Wallace DV, Golden DBK, et al. Anaphylaxis-a 2020 practice parameter update, systematic review, and Grading of Recommendations, Assessment, Development and Evaluation (GRADE) analysis. J Allergy Clin Immunol. 2020 Apr;145(4):1082-123. https://www.jacionline.org/article/S0091-6749(20)30105-6/fulltext http://www.ncbi.nlm.nih.gov/pubmed/32001253?tool=bestpractice.com
Primary options
epinephrine (adrenaline): 0.01 mg/kg (1 mg/mL solution) intramuscularly every 5-10 minutes according to response, maximum 0.3 mg/dose
OR
epinephrine (adrenaline): (auto-injector) children 7.5 to <15 kg body weight: 0.1 mg intramuscularly as a single dose, may repeat once after 5-15 minutes; children 15-30 kg body weight: 0.15 mg intramuscularly as a single dose, may repeat once after 5-15 minutes; children ≥30 kg body weight: 0.3 mg intramuscularly as a single dose, may repeat once after 5-15 minutes
More epinephrine (adrenaline)The 0.1 mg-dose applies to the Auvi-Q® brand of auto-injector only.
vasopressor + transfer to intensive care unit (ICU)
Treatment recommended for SOME patients in selected patient group
Refractory anaphylaxis may require ongoing vasopressor support. There is no adequate evidence that any one vasopressor agent is a superior choice compared with another.[59]Gamper G, Havel C, Arrich J, et al. Vasopressors for hypotensive shock. Cochrane Database Syst Rev. 2016;(2):CD003709. http://onlinelibrary.wiley.com/doi/10.1002/14651858.CD003709.pub4/full http://www.ncbi.nlm.nih.gov/pubmed/26878401?tool=bestpractice.com Consult a specialist for guidance on choice of vasopressor and dose. The patient is transferred to the ICU.
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Please note that formulations/routes and doses may differ between drug names and brands, drug formularies, or locations. Treatment recommendations are specific to patient groups. See disclaimer
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