A stain on iron therapy.

Iron staining is an unwanted and in some cases permanent adverse effect of intravenous iron administration. Cosmetically unacceptable staining may cause distress and have psychological implications for the patient There should be a suitable indication for parenteral iron therapy. Patients must be advised of the risk of harm and give their informed consent before receiving parenteral iron Strategies to minimise the risks of staining with intravenous iron include appropriate cannulation and close monitoring of the infusion. Stop the infusion if there are signs of extravasation Laser therapy may be a treatment option in cases of persistent discolouration due to iron staining (c) NPS MedicineWise.

Introduction

Iron deficiency is a common condition and a large contributor to anaemia.1 The prevalence of iron deficiency anaemia is high in younger women and indigenous Australians.2 Treatment options to correct iron deficiency in Australia include oral and parenteral iron.3 Within the last decade the use of intravenous iron has been increasing,4 particularly in the community. This is because of newer iron salts with favourable adverse effect profiles and shorter infusion times for intravenous formulations. These include ferric carboxymaltose and ferric derisomaltose. For patients in hospital, iron polymaltose or iron sucrose can also be used.

An uncommon adverse effect of parenteral iron is skin staining (see Fig.). This is not a new phenomenon as it is a well-known adverse effect of intramuscular iron.5 Iron staining can occur with intravenous infusions if there is extravasation into the surrounding tissue. The use of intramuscular iron administration is limited in practice,3 but the injection can be given into an unexposed site. However, administration at an unexposed site is not necessarily possible when giving iron intravenously. A rise in reports of iron staining6-10 may correspond with the increasing use of intravenous iron in clinical practice.6-13

Fig.

Iron stain

Incidence of skin staining

The rate of skin discolouration with intravenous iron preparations has been reported in clinical trials as 0.68%14 to 1.3%.15 Postmarketing reports suggest the incidence may be lower and skin necrosis has not been reported. However, iron staining may be under-reported to pharmacovigilance databases. A review of the French pharmacovigilance database from 2000 to 2016 found only 51 cases of cutaneous pigmentation with iron.12

Postmarketing reports to the Therapeutic Goods Administration (TGA) Database of Adverse Event Notifications,16 from March 2014 to October 2019, included 27 cases for ferric carboxymaltose. These reports included the terms skin discolouration or hyperpigmentation, haemosiderin stain, pigmentation disorder, infusion/injection/administration site discolouration, or extravasation. The TGA data include eight cases of pigmentation disorder or skin discolouration with iron polymaltose, with the first report in 2005. There are currently no reports for ferric derisomaltose, but this adverse effect is included in the product information.

Minimising harm

Specific definitive risk factors for extravasation of intravenous iron have not been published. The principles for minimising the harm associated with intravenous iron preparations have been adapted from those applied to intramuscular iron (Box 1).5 They include a good infusion technique (Box 2).

Is parenteral iron indicated?

Once iron deficiency is diagnosed, establish the cause. The decision on appropriate treatment should then consider the patient’s treatment goals. This includes assessing the options for correcting the iron deficiency and their potential adverse effects. Dietary intake, oral supplements or parenteral iron are suitable options.3

Parenteral iron is usually only indicated when oral iron therapy has failed.3 However, there are some patient cohorts who may benefit from intravenous iron without a trial of oral therapy. They include patients who have heart failure with a reduced ejection fraction,15 those undergoing haemodialysis,17 and pregnant women in their second or third trimester requiring rapid iron replenishment.18

Inform patients about skin staining

Although the incidence of iron staining appears to be relatively low, its potential irreversibility and the cosmetic impact it may have warrant discussion with patients. The Medical Board of Australia has reminded medical practitioners to advise patients about the risk so that they can give informed consent to treatment.19 Using a patient information brochure about iron staining may assist with this. The BloodSafe organisation has a useful leaflet available in English and other languages.20 When intravenous iron is indicated and patients choose to receive an infusion, it is advisable to document the content and outcome of the discussion about risks including discolouration or staining.

Correct injection site and infusion technique

The infusion sites used for intravenous therapy may influence the rate of extravasation due to the potential for vessel damage related to movement of the cannula.21,22 Administration of intravenous iron via cannulation at sites of flexion (e.g. antecubital fossa, wrist) or on the back of the hand should be avoided when possible. If these sites must be used, the smallest suitable cannula size may reduce the likelihood of vessel trauma.22 Try to minimise catheter movement by securing the cannula21-23 and using an extension set.24 When using smaller gauge devices, it may be necessary to slow the infusion to minimise the risk of dislodgement.25

The number of attempts at cannulation should be minimised as there is an increased risk of extravasation due to multiple venous punctures.21,22 For patients who are difficult to cannulate, seek the expertise of more experienced staff. Although postponing intravenous iron therapy may inconvenience the patient, it is unlikely to result in adverse clinical outcomes. Intravenous iron infusion is rarely urgent.

The patency of the cannula should be checked by giving 5–10 mL of sodium chloride 0.9% before the infusion.21

Monitor for extravasation

The review of cutaneous pigmentation reported to the French pharmacovigilance database suggested improvements in monitoring are necessary to detect extravasation.12 Patients who experience iron extravasation resulting in staining may describe pain, swelling, and feelings of pressure or pricking at the infusion site.13 Patients should therefore be told to notify staff of any of these symptoms (Box 3). This is an important consideration for patients who do not understand English. Administration of intravenous iron must be avoided if the patient’s ability to report these symptoms is reduced (e.g. anaesthetised patients). Early cessation of the infusion may limit the amount of solution that enters the tissues and could minimise the extent of staining.

Close assessment of the cannula site during infusion is essential to enable early identification of extravasation. The site should never be covered up with a bandage. Observations of the cannula site should be timed to correspond with monitoring of the patient’s other vital signs in accordance with local protocols for infusions.26 Giving intravenous iron infusions overnight must be avoided as it is more difficult to observe extravasation and staining in the dark.

Staff training

In order to ensure the best outcomes for patients, health professionals involved with the prescribing, administration and monitoring of intravenous iron must be adequately trained and competent. A set protocol that outlines best practice for intravenous iron administration, including cannulation, should be followed. Staff must be aware of the monitoring requirements and the symptoms of potential adverse effects.

Management of iron staining

There are no published guidelines outlining how to manage iron extravasation or skin discolouration following iron infusions. Box 4 gives the best available guidance for acute management to limit the potential for further staining. Clinical photographs should also be taken to capture the extent of the extravasation and to help with monitoring the success of subsequent treatments.

There are limited options to reverse iron staining. opical therapies, lymphatic drainage and massages have been tried without success.9,13 The most evidence for successful reversal of iron staining is with laser therapy.

One review assessed 29 patients who had reported accidental staining from iron infusions over a nine-year period.13 Thirteen patients had laser therapy and eight completed treatment. Regression of iron staining took an average of 5.6 laser sessions over one to two years. The type of laser is important with most evidence being for quality-switched Nd:YAG or picosecond. The patient’s individual skin type may also influence the success of laser treatment. In general, laser therapy was well tolerated.

Laser therapy is available in Australia, but there may be significant financial barriers as repeated applications are required. If the patient is concerned about the staining, early referral to a dermatologist with a laser clinic specialising in quality-switched Nd:YAG and picosecond laser is appropriate.

Review cases to improve patient safety

When extravasation occurs, prudent review of the patient is warranted. Consider likely contributing factors, such as whether there was a suitable indication for intravenous iron, poor techniques in cannulation, the patient’s own vasculature and any lack of monitoring. Report these cases to the TGA.

Conclusion

There should be a clear indication for using intravenous iron. Patients need to give informed consent for the infusion.

Iron extravasation can be cosmetically unacceptable for patients so strategies should be put in place to prevent it from occurring. These include appropriate vein selection, securing the cannula and close monitoring during the infusion. In addition, the patient should be advised to report any pain, irritation or swelling at the infusion site.

In the event of extravasation and persistent staining, repeated laser sessions over one to two years may be required. However, iron staining can be permanent.

Ensure an appropriate indication for parenteral ironInform the patient of the risk of skin staining at the initial consultationEnsure the correct injection site and administration technique is usedMonitor closely for signs and symptoms of extravasation

Avoid intravenous iron administration via cannulation at sites of flexion (e.g. antecubital fossa, wrist) or on the back of the handThe distal veins of the forearm are the preferred siteUse an appropriate cannula size (20- to 24-gauge)Secure the cannula and use an extension set to minimise catheter movementDo not cover the injection site with a bandageMinimise the number of cannulation attemptsEnsure the patency of the vein before administration. If patency is uncertain, do not administer intravenous ironDo not give infusions at night-timeDo not give infusions to patients unable to report symptoms (e.g. anaesthetised)

Symptoms during infusionPain, swelling, feeling of pressure, prickling on the injection site and immediately observable staining. Note: some patients report no pain or other symptoms during the infusion and the discolouration appears hours or days laterExtent of skin discolourationCan be localised to around the injection site or extend along the length of the arm. May be patchy or consistent discolourationColour changesMost common – light to dark brownLess common – black, bluish, purple, greySymptoms in the longer termGenerally, discolouration is asymptomatic, but some patients complain of aching, changed sensitivity in the affected area or tenderness on palpationOutcomeIn many cases, iron staining is permanent. Some patients report fading of the stain over time or successful treatment with laser therapy

If the patient complains of pain, swelling, soreness at the injection site or there is any obvious swelling or discolouration, stop the infusion immediately and assess the siteDisconnect the giving setAspirate any residual drug from the cannulaRemove the cannulaApply a cold pack if there is swelling or soreness, however this does not appear to prevent the spread of the stain