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  • Version 2 * National Standard 4 - Medication Safety Standard

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Standard 4 - Audit Report

CLINICAL GOVERNANCE AND QUALITY IMPROVEMENT TO SUPPORT MEDICATION MANAGEMENT

Integrating clinical governance

  • 4.1 Clinicians use the safety and quality systems from the Clinical Governance Standard when:<br>a. Implementing policies and procedures for medication management<br>b. Managing risks associated with medication management<br>c. Identifying training requirements for medication management

Applying quality improvement systems

  • 4.2 The health service organisation applies the quality improvement system from the Clinical Governance Standard when:<br>a. Monitoring the effectiveness and performance of medication management<br>b. Implementing strategies to improve medication management outcomes and associated processes<br>c. Reporting on outcomes for medication management

Partnering with consumers

  • 4.3 Clinicians use organisational processes from the Partnering with Consumers Standard in medication management to:<br>a. Actively involve patients in their own care<br>b. Meet the patient’s information needs<br>c. Share decision-making

Medicines scope of clinical practice

  • 4.4 The health service organisation has processes to define and verify the scope of clinical practice for prescribing, dispensing and administering medicines for relevant clinicians

DOCUMENTATION OF PATIENT INFORMATION

Medication reconciliation

  • 4.5 Clinicians take a best possible medication history, which is documented in the healthcare record on presentation or as early as possible in the episode of care

  • 4.6 Clinicians review a patient’s current medication orders against their best possible medication history and the documented treatment plan, and reconcile any discrepancies on presentation and at transitions of care

Adverse drug reactions

  • 4.7 The health service organisation has processes for documenting a patient’s history of medicine allergies and adverse drug reactions in the healthcare record on presentation

  • 4.8 The health service organisation has processes for documenting adverse drug reactions experienced by patients during an episode of care in the healthcare record and in the organisation-wide incident reporting system

  • 4.9 The health service organisation has processes for reporting adverse drug reactions experienced by patients to the Therapeutic Goods Administration, in accordance with its requirements

CONTINUITY OF MEDICATON MANAGMENT

Medication review

  • 4.10 The health service organisation has processes:<br>a. To perform medication reviews for patients, in line with evidence and best practice<br>b. To prioritise medication reviews, based on a patient’s clinical needs and minimising the risk of medication-related problems<br>c. That specify the requirements for documentation of medication reviews, including actions taken as a result

Information for patients

  • 4.11 The health service organisation has processes to support clinicians to provide patients with information about their individual medicines needs and risks

Provision of a medicines list

  • 4.12 The health service organisation has processes to:<br>a. Generate a current medicines list and the reasons for any changes <br>b. Distribute the current medicines list to receiving clinicians at transitions of care<br>c. Provide patients on discharge with a current medicines list and the reasons for any changes

MEDICATION MANAGEMENT PROCESSES

Information and decision support tools for medicines

  • 4.13 The health service organisation ensures that information and decision support tools for medicines are available to clinicians

Safe and secure storage and distribution of medicines

  • 4.14 The health service organisation complies with manufacturers’ directions, legislation, and jurisdictional requirements for the:<br>a. Safe and secure storage and distribution of medicines<br>b. Storage of temperature-sensitive medicines and cold chain management<br>c. Disposal of unused, unwanted or expired medicines

High-risk medicines

  • 4.15 The health service organisation:<br>a. Identifies high-risk medicines used within the organisation<br>b. Has a system to store, prescribe, dispense and administer high-risk medicines safely

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