Background
IVIg is a concentrated solution of immune-supporting antibodies, given as an infusion. It is a blood product and must be managed as such.
IVIg is not routinely given in the ED - the usual setting is Wards 1A, 3A or 3D.
Departmental Position
- In the ED, IVIg is only given for life-threatening indications, as outlined in table below
- It should only be given if agreed by the CNM, and administered in Resus or Majors
- Medical and nursing staff should seek support if unfamiliar with prescribing or administering IVIg
Indications
| Specialty | Indication |
|---|---|
| Haematology | Severe thrombocytopaenia in ITP with platelets <10 Severe refractory AIHA with Hb <7 |
| Rheumatology | Myositis (particularly with dysphagia) Haemophagocytic lymphohistiocytosis (HLH) |
| Neurology | Severe Guillain-Barré syndrome Relapse of CIDP Myasthenia Gravis crisis - give within 12 hours of admission |
Contraindications
- Patient is acutely unwell with untreated infection - wait until infection is controlled and the patient is improving clinically
Prescriber Protocol
- Verbal consent, documented in the notes - indication, possible side-effects, and blood component/haemovigilance discussed
- Pre-treatment bloods: FBC, U&E, creatinine must be back before treatment; LFTs and HepB/C/HIV serology also taken
- Prescribe on Form 15B (Intravenous Immunoglobulin Prescription and Administration Record)
Caution
- Kiovig® and Flebogamma® are not interchangeable
- Contact Pharmacy to confirm stock, dose rounding, and the patient's IVIg brand history
Dose
Dose is calculated using an adjusted body weight for overweight or obese adults, not actual weight:
- Dosing weight = IBW + [0.4 × (Actual weight − IBW)] (if actual weight is less than IBW, use actual weight)
- IBW (Devine formula, using cm):
- Male: 50 + 0.91 × (height cm − 152.4)
- Female: 45.5 + 0.91 × (height cm − 152.4)
Round the dose down to the nearest whole vial to minimise waste - never use part vials in adults. If the dose is split over several days, the daily amount may vary.
| Stage | Rate |
|---|---|
| Start (first 30 min) | 0.5 ml/kg/hr |
| Then, every 30 min as tolerated | increase by 0.5 ml/kg/hr |
| Maximum | 6 ml/kg/hr (rarely >4 ml/kg/hr for inpatients) |
The Alberta Health Services IVIg calculator can be used to assist with calculations
Two nurses must independently double-check the dose and preparation before it is connected.
Monitoring
- Observations (temp, pulse, sats, BP) at the start, at every rate change, and at the end - document on the INEWS chart
- Ensure adequate hydration before starting, and monitor urine output and creatinine throughout
- Watch for signs and symptoms of thrombosis
- First infusion, a switched product, or a long gap since the last dose: monitor throughout and for 1 hour after. All other patients: observe for at least 20 minutes after
Adverse Reaction
- Stop the infusion immediately
- Contact a member of the medical team
- Please report any suspected adverse reactions
Links
- Full SOP for the Management of Intravenous Immunoglobulin (Rev.1, 14.11.2025) local copy
- HSE Guidelines for Immunoglobulin Use in Neurological Conditions