9.1.1 Iron-deficiency anaemias
Treat demonstrable iron-deficiency state only. Use prophylactically in some situations.
Patients should be directed to purchase nutritional supplements (including iron) over the counter post bariatric surgery. See Guideline
9.1.1.1 Oral Iron
Treatment needs 100-200mg elemental iron per day. Prophylaxis 50-100mg elemental iron per day. When treating iron-deficiency anaemia, haemoglobin should rise by approximately 100-200mg/100ml (1-2g/litre) per day or 2g/100ml (20g/litre) over 3-4 weeks. Once it has reached reference range, treatment should be continued for a further 3 months in order to replenish iron stores, and then stopped.
GREEN Ferrous sulphate tablets 200mg provide 65mg iron
GREEN Ferrous fumarate tablets 210mg provide 68mg iron
GREEN Sodium feredetate elixir (Sytron®) provides 27.5mg iron/5mL
GREEN Ferrous fumarate syrup 140mg/5ml provides 45mg iron/5mlL
Modified release preparations give a reduced total daily dose of iron, and are less efficacious as they carry iron past the duodenum where absorption may be poor. They should therefore only ever be used for low dose prophylaxis, not for treatment of iron-deficiency states.
GREEN Ferrous sulphate modified release tablets 325mg (Ferrograd®) provides 105mg iron (give once daily)
Iron and folic acid
GREEN Pregaday® tablets provide 100mg iron + 350microgram folic acid
9.1.1.2 Parenteral Iron
The only valid reason for administering iron parenterally is non-tolerance of oral therapy, continuing blood loss or malabsorption. If oral preparations are taken reliably and are absorbed, the haemoglobin response is not significantly faster with the parenteral route.
CosmoFer® (iron dextran injection) has the advantage of being licensed for administration as a single total dose infusion, and can also be given IM. Due to the association of administration of parenteral iron preparations with severe anaphylactoid reactions prescribers are reminded to test dose patients and have anaphylactic emergency kits close to hand when giving either Cosmofer® or Venofer®.
First Line
AMBER Iron dextran injection (CosmoFer®) 2ml provides 50mg/mL iron
Second Line
AMBER Iron sucrose injection (Venofer®) 5ml provides 20mg/mL iron
RED Ferric Carboxymaltose (Ferinject®) 50mg/mL * as a second line treatment when there is hypersensitivity to iron dextran.
* Can be considered as a cost effective option where IV iron is required - shorter infusion time , reduced adverse effects
Megaloblastic anaemia is usually due to vitamin B12 or folate deficiency; the specific deficiency and underlying cause must be identified. Treatment is usually only begun once a firm diagnosis is made. In emergencies, where delayed treatment may be dangerous, both folate and vitamin B12 may be required initially, until assay results are known. Folate must not be used alone in undiagnosed megaloblastic anaemia due to the risk of B12 deficiency leading to peripheral neuropathy.
During pregnancy the prevention of a first occurrence of neural tube defects is with 400 microgram/day. A higher dose of folic acid at 5mg/day is used for folate deficiency and prevention of recurrence of neural tube defects. Both should be continued for the first twelve weeks of pregnancy.
GREEN Folic Acid
tablets 5mg
tablets 400 microgram
syrup 2.5mg/5mL
RED Folic acid injection 15mg/ml (unlicensed)
GREEN Hydroxocobalamin injection 1mg/mL
There is little place for use of low dose vitamin B12 orally. However, cyanocobalamin tablets can be used in doses of 50-150micrograms daily for vegans or patients who have proven dietary deficiency (prescription must be endorsed SLS).
Epoetin for use in patients with renal disease will be supplied from the tertiary referral centre. For all other indications supply will usually be organised through a home delivery company.
RED Darbepoetin alfa (Aranesp®) Prefilled disposable SureClick™ devices
100micrograms, 150micrograms, 300micrograms, 500micrograms.
RED Epoetin alfa (Eprex®)
Vial 40 000unit/ml 1mL Prefilled syringes 1000units, 2000units, 4000units, 5000units, 6000units, 8000units, 10,000units.
Iron Overload
Iron overload is the result of many disorders and can lead per se to the development of organ damage and increased mortality. In humans total body iron stores is maintained within the range of 200-1500 mg by adequate adjustment of intestinal iron absorption, since no excretory mechanisms exist.
Frequent blood transfusions lead to excessive accumulation of iron with a toxic accumulation in 3 to 10 years. The toxicity of iron results from two related events:
1. excess iron deposits in various tissues of the body, particularly in liver, heart and endocrine organs with the consequence of liver diseases, diabetes mellitus and other complications, and
2. free iron that catalyzes the formation of highly reactive hydroxyl radicals which lead to membrane damage and denaturation of proteins.
Once iron exceeds a certain level, these effects lead to significant morbidity and mortality. Without specific chelation therapy to remove the iron, in 3 to 10 years almost all regularly transfused patients will have acquired a toxic accumulation of iron. The main cause of death is due to cardiac complications.
The management of established iron overload also involves venesection which is not always possible. The subsequent aim is to make the iron as safe as possible by binding the toxic iron pools responsible for causing tissue damage. Iron chelation therapy reduces iron-related morbidity, reduces and retards liver diseases, diabetes and other endocrine failures, normalizes growth and sexual development, prevents, and in some cases reverses, cardiac insufficiency and improves quality of life. Consequently iron chelation therapy dramatically reduces mortality.
Deferasirox
Deferasirox should only be initiated and prescribed by a haematologist or paediatrician for the management of patients with chronic iron overload. It can be used as a first line therapy for all beta thalassaemia patients aged 6yrs and older requiring frequent blood transfusions (>7 ml/kg/month packed red blood cells).
It should be used as a second or third line therapy in the following groups:
- patients with beta thalassemia major 2-5 yrs, patients with beta thalassemia requiring infrequent blood transfusions, or
- those patients with other rare anaemias where desferrioxamine (DFO) and/or deferiprone are contra-indicated, not tolerated or insufficiently effective.
Deferasirox should only be used in those patients with myelodyslplastic syndrome (MDS) requiring long term blood transfusions such as those with sideroblastic anaemia or 5q-- syndrome where concurrent immunosuppression prevents the use of DFO. Treatment should be regularly monitored by the specialist according to the SPC. Desferasirox should be funded by the patients PCT under ‘pass through’ funding. Deferasirox requires intensive monitoring - consult the SPC. A new drug review is available online - click here to access it.
RED Deferasirox dispersible tablets 125mg, 250mg, 500mg (Exjade®)
Desferrioxamine
Desferrioxamine (deferoxamine) is given by sub-cutaneous infusion, usually over 12hrs for a certain number of days per week. It is an alternative to desferasirox, where this cannot be used. Supplies are made direct to the patients home through a homecare delivery service, funded by the patients PCT. Contact pharmacy before prescribing. Specialist use only.
RED Desferrioxamine mesilate 500mg, 2gram vial
Deferiprone
Deferiprone is only used in thalassaemia major where desferrioxamine is contra-indicated or is not tolerated. Blood dyscrasias, particularly agranulocytosis have been reported with its use. Specialist use only.
RED Deferiprone tablets 500mg
RED Deferiprone suspension 750mg/5ml (unlicensed special)
Idiopathic thrombocytopenic purpura
Romiplostim is recommended by NICE TAG221 for the treatment of adults with chronic immune (idiopathic) thromboycytopenic purpura:
- whose condition is refractory to standard active treatments and rescue therapies or
- who have severe disease and a high risk of bleeding that needs frequent courses of rescue therapy and
- if the manufacturer makes romiplostim available with the discount agreed as part of the patient access scheme
RED Romiplostim (Nplate®) 250mcg vial
Eltrombopag is recommended as an option by NICE (TAG293) for treating adults with chronic immune (idiopathic) thrombocytopenic purpura, within its marketing authorisation (that is, in adults who have had a splenectomy and whose condition is refractory to other treatments, or as a second-line treatment in adults who have not had a splenectomy because surgery is contraindicated), only if:
- their condition is refractory to standard active treatments and rescue therapies, or
- they have severe disease and a high risk of bleeding that needs frequent courses of rescue therapies and
- the manufacturer provides eltrombopag with the discount agreed in the patient access scheme
RED Eltrombopag (Revolade®) tablets 25mg, 50mg
Essential thrombocythaemia
In thrombocythaemia, Anagrelide is recommended to be initiated for patients who have failed two previous treatments to control platelet counts and who have one or more of the following features:
- >60 years of age, or
- a platelet count >1,000 x 109/l, or
- a history of thrombo-haemorrhagic events.
Anagrelide treatment should be initiated by a clinician with experience in the management of essential thrombocythaemia.
RED Anagrelide capsules 500micrograms
9.1.6 Drugs used in neutropenia
Single dose pegfilgrastim is to replace the use of daily filgrastim (G-CSF) to reduce chemotherapy induced neutropenia in cancer patients who would normally receive 5 or more days of daily filgrastim (G-CSF) following chemotherapy (except chronic myeloid leukaemia and myelodysplastic syndrome patients).
RED Pegfilgrastim prefilled syringe 6mg
Pegfilgrastim is not licensed for the following indications:
- Mobilisation of peripheral blood progenitor cells (PBPCs)
- To reduce duration of neutropenia post transplant of PBPCs
- To support weekly chemotherapy regimes
Filgrastim will continue to be used for these three indications.
RED Filgrastim
Injection 300micrograms 1mL vial
Prefilled syringes 300microgram, 480microgram