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Vol 276 No 7388 p193
18 February 2006

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Pharmacists have role in patient safety, says NPSA

Claire Paxton and Jacqui Farrow/SPL

Intravenous drug infusions

Intravenous drug infusions are high risk

How pharmacists can help to improve patient safety is addressed in consultation documents released last week by the National Patient Safety Agency (NPSA).

The consultations will form the basis for four patient safety alerts to be issued in the second quarter of the year, focusing on anticoagulant therapy, wrong route administration errors, preparation and administration of injectable medicines, and paediatric infusion safety.

The draft document on the safe use of anticoagulant therapy highlights that not all workers involved with the prescribing and monitoring of anticoagulants have received the necessary level of training. The proposal suggests the employment of pharmacists and nurses — with specialist training in a specified range of competencies — to prescribe and adjust anticoagulant regimens.

Another area of concern is the potential for errors when inadequate safety checks have been carried out during repeat prescribing and repeat dispensing of anticoagulants in the community. Pharmacists will have a role in formalising the required safety checks when anticoagulants are being dispensed for patients, for example, ensuring that the international normalised ratio (INR) is being monitored regularly and that the INR is within range at the prescribed dose.

Several recommendations have been made in the draft document on preventing wrong route errors. If implemented, the recommendations would require that only oral syringes be used for measuring and administering oral liquid medicines and enteral feeds and flushes. Trusts would also be required to use enteral feeding tubes with safe ports that cannot connect to intravenous syringes, and the removal of any adaptors that enable oral syringes to connect to parenteral lines would be mandatory.

The NPSA has made proposals intended to improve the safe preparation and administration of injectable products in “near patient areas”. The recommendations include having a pharmacist and a senior practitioner undertake a standardised assessment of the risks involved in preparing and administering parenterals, as well as the risks presented by the individual injectable product. The NPSA plans to introduce a multiprofessional standard of practice for the preparation and administration of injectable medicines.

Paediatric infusion practices were also brought under scrutiny to produce the final draft patient safety alert. The NPSA calls for the introduction of clinical guidelines for the selection, management and monitoring of intravenous fluids in children and a review of training and supervision for all staff involved.

In terms of pharmacy involvement, the NPSA proposes that pharmacists oversee the removal of all hypotonic infusion fluids from general paediatric wards and restrict the use of these fluids to paediatric intensive care settings.

The NPSA welcomes comments and suggestions by 31 March. The consultation papers and feedback forms are available from the NPSA’s safer health care website where a forum has been set up for stakeholders to discuss the initiatives.

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