An audit carried out by the author on her recent practice placement. The practice placement was in a continuing care unit which cared mainly for patients who were at the end stages of life. The author decided to choose safe drug administration

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Clinical Audit.

This essay intends to focus upon an audit carried out by the author on her recent practice placement. The practice placement was in a continuing care unit which cared mainly for patients who were at the end stages of life. The author decided to choose safe drug administration for her audit for a number of reasons.

The unit had 24 beds with one qualified nurse caring for 12 patients each. Due to the complex health needs of individuals, many patients required several medicines at varying times of the day. The author felt that as these patients required more complex drugs regimes this gave a greater scope for drug errors to occur. Looking along the lines of human error, the author noted that the staff nurse on duty often worked 14 hour days and Fitzpatrick and While (1999) report that nurses overall clinical performance is significantly greater when working a traditional 8 hour shift compared to a 12+ hour shift.

Medication errors can not only be harmful to the patient but it is estimated that inpatient drug errors can cost the NHS £410 million per year. This figure does not include litigation costs which are thought to be conservative at £750 million per year (National Patient Safety Agency, 2007).

To ascertain what the standards should be for the clinical audit the author first looked at current guidelines and policy from varying sources and then applied them to her area of clinical practice. To keep the audit manageable, the administration of regular drugs was chosen as the area to be audited and only drugs give orally was monitored. The administration of controlled drugs or 'as required' drugs was not observed. Different criteria would have had to have been observed if taking in to account various routes of administration and whether the drug was controlled or not.

The author chose to break down the process of regular, oral drug administration in to 5 areas and looked at relevant literature to support each individual standard. The audit itself was carried out over 2 drugs rounds at different times of the day and by 2 different staff nurses. Each drug round consisted of 12 patients.

Standard 1 - Wash hands with both soap and water or bactericidal alcohol hand rub before administering drug to patient.

The rationale behind standard 1 is to minimize the risk of cross infection. The NMC (2006) reasons that infection control precautions underpin safe clinical practice. The Department of Health (DoH) (2006) specifies further that hand hygiene should be carried out immediately before contact with every patient and that the very old and the chronically sick are more susceptible to infection.
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Standard 2 - Before administration of any drug, check the medicine kardex for the following: the drug is due, has not been given already, information is complete, correct and legible.

Within this standard there are many factors to be checked and these should include the dose, the drug, date and time of administration, validity of prescription, signature of doctor and that the kardex is legible. Dougherty and Mallett (2001) state that the kardex should be checked thoroughly on every occasion to prevent harm to the patient; to ensure that the patient is given the correct drug, via ...

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