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High dose intra muscular vitamin supplements for patients undergoing alcohol detoxification SOP

Contents

1 Aim

The aim is to outline some of the potential problems associated with alcohol detoxification related to thiamine deficiency and possibility of the patient developing Wernicke’s encephalopathy, a potentially serious condition, and the prophylactic treatments available to reduce the likelihood of this occurring.

Due to the nature of the treatment provided (intramuscular injection) and the remote (but with potentially serious consequence) risk of anaphylactic reaction to the treatment, the protocol aims to outline best and standard practice for managing this treatment.

2 Scope

This standard operating procedure (SOP) is applicable to all patients undergoing treatment for alcohol dependence whether in the care of substance misuse services or in other directorates (for example, adult or older adult mental health services). In the latter cases, it is suggested that advice be sought from the locality’s substance misuse consultant on patient management.

This protocol is applicable both to treatment in the community under the direct care of the relevant Substance Misuse team (in circumstances detailed later in this document) and, more specifically, in the adult inpatient units in Rotherham, Doncaster and Scunthorpe where the mental health ward nursing staff will also be involved in the provision of this treatment.

3 Link To overarching policy

This SOP is overarched by and to be used in conjunction with the trust’s safe and secure handling of medicines manual.

4 Procedure

4.1 Presentation of Wernicke’s encephalopathy

The classic triad of confusion, ataxia, and ophthalmoplegia occurs in only 10% of cases. Difficulties in diagnosis occur due the fact that alcohol intoxication or withdrawal and common co-morbidities, such as head injury, share many of the features of Wernicke’s encephalopathy. A high index of suspicion should be maintained for any patient with alcohol dependence that also exhibits acute confusion, decreased level of consciousness, ophthalmoplegia, ataxia, memory disturbance, hypothermia with hypotension or delirium tremens.

4.2 Prophylaxis

Prophylactic treatment with parental thiamine is routinely recommended for those clients with a high risk of developing thiamine deficiency, for example, those with severe alcohol dependence, history of seizures or delirium tremens, diarrhoea, vomiting, physical illness, malnourished, poor diet and weight loss.

In the UK, Pabrinex is the only parenteral high-potency B-complex vitamin therapy available. Two ampoules contain thiamine hydrochloride 250mg in combination with ascorbic acid 500mg, nicotinamide 160mg, pyridoxine hydrochloride 50mg and riboflavin 4mg. This protocol therefore refers to “Pabrinex” but could be taken as referring to any parenteral high dose B complex vitamin injection marketed under any other name.

Clients admitted for an inpatient detoxification should routinely receive Pabrinex. The only contra-indication to parenteral thiamine would be a previous allergic reaction.

For those clients receiving a community detoxification an assessment needs to be made as to whether parental Pabrinex is required using the above criteria as a guide. If Pabrinex is not required then the client should receive oral thiamine (see below).

4.3 Intramuscular Pabrinex

Administer one pair of Pabrinex ampoules (thiamine 250mg) once daily for three to five days via deep intramuscular injection into the gluteal muscle as outlined in section 5.

4.4 Oral vitamin prophylaxis

The role of oral supplementation is unclear and clinical practice varies. Prescribing and administration of oral vitamins for this patient group is outside the scope of this protocol, however, the information below is included for reference.

BNF guidance, ‘Thiamine 200 to 300mg daily in divided doses during detoxification is recommended in addition to Pabrinex or instead of if parental thiamine is not required (see above). Continue thiamine post discharge if there is cognitive impairment.’

4.5 Treatment of suspected or diagnosed Wernicke’s encephalopathy

Wernicke’s encephalopathy is a medical emergency. If suspected an assessment of the client must be made immediately to consider transfer to a medical ward. As well as examining the client for Wernicke’s an assessment should include possibilities of co-morbid physical health problems for example, infection, dehydration, head injury and so on.

4.6 Risk of anaphylaxis

This should not preclude the use of parenteral thiamine in patients where this route of administration is required, particularly those at risk of Wernicke-Korsakoff syndrome where treatment with thiamine is essential. Facilities for treating anaphylaxis (including resuscitation facilities) should be available when parenteral thiamine is administered.

5 Administration of Pabrinex

The scope of this procedure is to standardise the nursing administration of medication as trust’s intramuscular injection policy.

The appropriate site for this type of administration is the Gluteus Medius or ventrogluteal used for deep intramuscular (I.M) using the Z track injections technique. This is identified as the upper outer quadrant of the buttock. This site is used to lower risk of hitting the sciatic nerve and the superior gluteal arteries. The Z-tracking method involves pulling the underlying skin down wards or on to one side of the injection site, inserting the needle at a right angle to the skin, which moves the subcutaneous and cutaneous muscle tissues by approximately 1 to 2 cm. The injection is given and the needle withdrawn, whilst releasing and retracting the skin at the same time. This manoeuvre seals of the puncture tract at the junction at each tissue layer.

It is generally recommended that IM injection cannot be administered in volumes larger than 5mls, but the preferred volume is not larger than 4mls.

Therefore for Pabrinex, the 7ml volume should be split in to two administrations. The same barrel and needle should not be withdrawn and re-sited. Please refer to the Royal Marsden (staff access only) (opens in new window).

Some patients may prefer to have their injection on a single site and this option can be discussed with them.

5.1 Procedure

Equipment to be in date and sterile, where appropriate:

  • recently prescribed medication, supplied in two vials
  • 10ml syringe
  • 5ml syringe
  • filter needle
  • 2 needles for administration, long enough to ensure I.M injection 20G
  • gloves
  • swabs for site cleaning
  • plasters
  • sharps bin
  • appropriate equipment (‘shock pack’) for the management of anaphylaxis (containing adrenaline 1:1000 1mg/ml)

5.2 Preparation

  • Check dates on vials.
  • Snap open tops.
  • Draw contents in to 10 ml syringe to mix. Total volume 7mls.
  • Divide half to 5ml syringe (if patient has indicated preference for two injections).
  • Renew the needle on to the barrel so that both syringes have fresh needles.

5.3 Implementation

  • Confirm patient identity and script validity.
  • Obtain consent for procedure.
  • Ask patient to lie on bed in prone position.
  • Select and prepare injection site.
  • Clean site using alcohol swab in circular motion of 5cm, for 30 seconds. Allow to dry.
  • Put gloves on. With thumb and finger of non-dominant hand gently stretch back skin and hold taut.
  • Remove needle sheath. Position at 90 degree to skin surface away from skin.
  • Inform patient they will notice injection.
  • Quickly and smoothly thrust the needle through the skin and subcutaneous tissue in to the deep muscle.
  • Support syringe and check for blood by slowly pulling back plunger, if no blood appears slowly inject the appropriate volume.
  • Remove needle and allow skin to relax.
  • Apply plaster.
  • Consider slow massage to help distribute the drug.
  • Repeat procedure for 2nd half of the injection at opposite side of body (if appropriate).

5.4 Aftercare

  • Discard of equipment safely.
  • Observe for anaphylactic-type reaction for 30 minutes.
  • Sign medication card and make entry in patient records.
  • If repeatedly injecting vary sites as much as possible and avoid previous sites by 2.5cm.
  • Ice can be used to numb the injection site, or lower pain if appropriate for patient comfort.

The UK Resuscitation Council states that staff administering parental medication should be trained in the management of anaphylaxis. All staff working within RDASH should receive training in immediate life support (annually), which includes the treatment of anaphylaxis. Staff should follow existing trust protocols. This includes a requirement to be aware and competent as an authorised nurse in the guideline adrenaline for the emergency management of Anaphylaxis. There is no requirement that medical staff have to be present whilst Pabrinex is administered (previously nursing staff have waited for a doctor to be present which has led to treatment being delayed unnecessarily). Equipment for the management of anaphylaxis (including adrenaline injection 1:1000 1mg/ml).


Document control

  • Version: 4.
  • Unique reference number: 142.
  • Date ratified: 5 January 2021.
  • Ratified by: Clinical policy review and approval group.
  • Name of originator or author: Consultant psychiatrist.
  • Name of responsible individual: Medicines management committee.
  • Date issued: 29 January 2021.
  • Review date: January 2024.
  • Target audience: All clinical staff treating patients undergoing treatment for alcohol dependence whether in the care of substance misuse services or in other directorates (for example, adult or older adult mental health services).

Page last reviewed: April 24, 2024
Next review due: April 24, 2025

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