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Send Sub-Q to the rescue

Timing

Initiating rehydration was quick with hylenex recombinant-facilitated Sub-Q rehydration

In the INFUSE PEDS 1 Study :

The median time from catheter insertion to start of Sub-Q fluids was 2 minutes1

Timing
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In the Spandorfer Study :

(Conducted at Children’s Hospital of Philadelphia)
  • The mean time to initiate IV infusion was 41.2 ± 29.4 minutes. 2
Time to Initiate IV
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Median Stay

In the INFUSE PEDS 1 Study :

  • Multicenter trial, n = 51
  • Children with mild-to-moderate dehydration
  • Time from trial enrollment to discharge
  • Patients discharged to home (45/51)
Median Stay
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In the Bender Study

(Conducted at Albert Einstein College of Medicine Chidren's Hospital4)
  • Single center trial, n = 549
  • Children with dehydration secondary to gastroenteritis
  • Time from placement in emergency department room to discharge
  • Patients discharged to home
Median Stay
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Important Risk Information

Special care must be taken in pediatric patients to avoid over hydration by controlling the rate and total volume of the infusion. Please refer to Indication and Important Risk Information below.

Click here for full Prescribing Information

1. Allen C, Etzwiler L, Miller M, Maher G, Mace S. Recombinant Human Hyaluronidase-Enabled Subcutaneous Pediatric Rehydration. PEDIATRICS Volume 124, Number 5, November 2009.
2. Spandorfer PR, Alessandrini EA, Joffe MD, Localio R, Shaw KN. Oral versus intravenous rehydration of moderately dehydrated children: a randomized, controlled trial. Pediatrics. 2005;115(2):295-301.
3.
American Academy of Pediatrics. Practice parameter: the management of acute gastroenteritis in young children. Pediatrics. 1996;97(3):424-435.
4.
Bender BJ, Ozuah PO. Intravenous rehydration for gastroenteritis: how long does it really take? Pediatr Emerg Care.2004; 20(4):215-218.

Important Risk Information for Healthcare Professionals
Indications

HYLENEX recombinant (hyaluronidase human injection) is indicated as an adjuvant to increase the absorption and dispersion of other injected drugs; for subcutaneous fluid administration; and as an adjunct in subcutaneous urography for improving resorption of radiopaque agents.

Important Risk Information
  • Hypersensitivity to hyaluronidase or any other ingredient in the formulation is a contraindication to the use of this product.
  • Discontinue HYLENEX recombinant (hyaluronidase human injection) if sensitization occurs.
  • Hyaluronidase should not be used to enhance the absorption and dispersion of dopamine and/or alpha agonist drugs.
  • Hyaluronidase should not be injected into or around an infected or acutely inflamed area because of the danger of spreading a localized infection.
  • Hyaluronidase should not be used to reduce the swelling of bites or stings.
  • Hyaluronidase should not be applied directly to the cornea.
  • Hyaluronidase should not be used for intravenous injections because the enzyme is rapidly inactivated.
  • Furosemide, the benzodiazepines and phenytoin have been found to be incompatible with hyaluronidase.
  • The most frequently reported adverse experiences have been mild local injection site reactions, such as erythema and pain.
  • Hyaluronidase has been reported to enhance the adverse events associated with co-administered drug products.
  • Allergic reactions (urticaria or angioedema) have been reported in less than 0.1% of patients receiving hyaluronidase.
  • Anaphylactic-like reactions following retrobulbar block or intravenous injections have occurred, rarely.
  • When hyaluronidase is added to a local anesthetic agent, it hastens the onset of analgesia and tends to reduce the swelling caused by local infiltration, but the wider spread of the local anesthetic solution increases its absorption; this shortens its duration of action and tends to increase the incidence of systemic reaction.
  • Edema has been reported most frequently in association with subcutaneous fluid administration.
  • The rate and volume of subcutaneous fluid administration should not exceed those employed for intravenous infusion. As with all parenteral fluid therapy, use the same precautions for restoring fluid and electrolyte balance.
  • During subcutaneous fluid administration, special care must be taken in pediatric patients to avoid over hydration by controlling the rate and total volume of the infusion.
  • When solutions devoid of inorganic electrolytes are given subcutaneously, hypovolemia may occur.
Timing
Median Stay
Time to Initiate IV
Median Stay