Yes This controlled document shall not be copied in part or whole without the express permission of the author or the author s representative.



Similar documents
NHSG/PGD/lido_eton/MGPG412 Organisation Wide

Patient Group Direction For The Administration Of Rotavirus Vaccine Rotarix By Nurses, Midwives and Health Visitors Working Within NHS Grampian

NHSG/PGD/SteroidInj/MGPG633. NHSG/PGD/SteroidInj/MGPG507

Yes This controlled document shall not be copied in part or whole without the express permission of the author or the author s representative.

Clinical Performance Director of Nursing Allison Bussey

Emergency Treatment of an Anaphylactic Reaction in the Community Protocol

Medicines Management

Developed / Reviewed by the Collaborative Provider PGD (Patient Group Direction) Group (CPPGDG) and approved by the following members of the CPPGDG:

Review Group: Mental Health Operational Medicines Management Group. Signature Signature Signature. Review Date: December 2014

Combined Child Diabetes

1. What Xylocaine with adrenaline is and what it is used for

CLINICAL PROTOCOL FOR THE USE OF INJECTED LOCAL ANAESTHETICS IN COMMUNITY TRUST SERVICES

Emergency Treatment of Anaphylactic Reactions

Version Number: 5. Patient Group Direction originally drawn up by: Reviewed by: Patient Group direction authorised by: Medical Lead

Lidocaine 2% w/v solution for injection Summary of Product Characteristics

Public Assessment Report. Table of Contents

Document Title: Patient Group Direction for Adrenaline (Epinephrine) 1:

UBISTESIN 1:200,000 and UBISTESIN FORTE 1:100,000

Patient Group Direction Hospital: Bristol Royal Infirmary Department: UHBristol Thrombosis Service University Hospitals Bristol NHS Foundation Trust.

St Bernard s Catholic School. Administration of Medicine Policy

MULTI AGENCY POLICY FOR THE ADMINISTRATION OF MEDICATION AND HEALTH CARE PROCEDURES:

patient group direction

PACKAGE LEAFLET: INFORMATION FOR THE USER. ADRENALINE (HCl) STEROP 0,8mg/1ml. Solution for injection. Adrenaline (Levorenine, Epinephrine)

Anaphylaxis and other adverse events

Uncontrolled When Printed. Version 1.1. Consultation Group: Approver: Co-ordinators: Grampian Medicines Management Group. Deputy Director of Pharmacy

Table of Contents. Page

Vaccine Protocol Agreement. Name of Pharmacy: Address: City, State, Zip:

Package leaflet : information for the user. Dilute Adrenaline/Epinephrine Injection 1:10,000 adrenaline (epinephrine) (as acid tartrate) 0.

Uncontrolled when printed. Version 1.1. Acute Sector. Lead Author/Co-ordinator: Mr Simon Barker Consultant Orthopaedic Surgeon Julie Fraser

PACKAGE LEAFLET: INFORMATION FOR THE USER. ADRENALINE (TARTRATE) STEROP 1 mg/1 ml Solution for injection. Adrenaline (Levorenine, Epinephrine)

Care Pathway for the Administration of Intravenous Iron Sucrose (Venofer )

PRIMARY CARE PRACTICE GUIDELINES

Influenza Vaccine Protocol Agreement (O.C.G.A. Section )

Package leaflet: Information for the patient. Naloxone Hydrochloride 20 micrograms / ml Solution for Injection Naloxone hydrochloride

Patient Group Directions. Guidance and information for nurses

Stowe School Medications Policy

Recommended guidelines for. schools

Suturing Policy for Nurses in Emergency Departments

PHENYLEPHRINE HYDROCHLORIDE INJECTION USP

National Chlamydia Screening Programme September 2012 PATIENT GROUP DIRECTION FOR THE ADMINISTRATION OF AZITHROMYCIN FOR CHLAMYDIA TRACHOMATIS

Direction Number: - NECSAT 2014/008

Children & Young People s Directorate. School Nursing Procedure For Administration of Immunisations

Administration of Medications & Fluids via a Peripheral Intravenous Cannula

2014 Supporting Students at School with Medical Conditions Policy

1 What Anapen is and what it is used for?

2. Characteristics of staff Qualifications required. Additional requirements. Continued education & training requirements

1.4.4 Oxyhemoglobin desaturation

PACKAGE LEAFLET: INFORMATION FOR THE USER. VITAMINE B12 STEROP 1mg/1ml Solution for injection / oral solution. Cyanocobalamin

Intraosseous Vascular Access and Lidocaine

NHS Professionals. Guidelines for the Administration of Medicines

NEW ZEALAND DATA SHEET NAPHCON-A Naphazoline hydrochloride and pheniramine maleate.

Data Sheet 2% Xylocaine DENTAL with Adrenaline 1:80,000

Influence of ph Most local anesthetics are weak bases.

Cardiac Catheter Lab Information for patients having a Coronary Angiogram

STANDARD OPERATING PROCEDURE. Administration of High Dose Muscular Vitamin Supplements for Undergoing Alcohol

Administration of Medicines and Healthcare Needs Policy

PACKAGE LEAFLET: INFORMATION FOR THE USER. PARACETAMOL MACOPHARMA 10 mg/ml, solution for infusion. Paracetamol

Management of an anaphylactic reaction to Omalizumab (Xolair) drug therapy

Sign up to receive ATOTW weekly - worldanaesthesia@mac.com

Document Title: PCT Doc Ref.: Version No.: 1/2014. Local Doc Ref.:

Shared Care Agreement Insulin Degludec (Tresiba )

Anaphylaxis. Exceptional healthcare, personally delivered

ANAPHYLAXIS. Introduction. Differential Diagnosis. Starship Children s Health Clinical Guideline

Protocol for Management of Suspected Anaphylactic Shock

Guidance for the Detoxification of Alcohol Dependent Patients in Community or Outpatient Settings

Donepezil (Aricept ), Galantamine (Reminyl XL ), Rivastigmine (Exelon ) and Memantine (Ebixa )

Rivaroxaban: Amber Drug Guidance for the prevention of stroke and systemic embolism in patients with non-valvular AF

Department of Education and Children Rheynn Ynsee as Paitchyn. Guidance for Schools on the Administration of Medication and Medical Care

2 QUALITATIVE AND QUANTITATIVE COMPOSITION

A. ADMINISTERING SUBCUTANEOUS MEDICATIONS INTERMITTENTLY/CONTINUOUSLY B. (SUBCUTANEOUS INFUSION) HYDRODERMOCLYSIS

Administration of Medicines and Healthcare Needs in Schools

SUMMARY OF PRODUCT CHARACTERISTICS. Albuman 200 g/l is a solution containing 200 g/l (20%) of total protein of which at least 95% is human albumin.

EMERGENCY TREATMENT OF ANAPHYLAXIS EPINEPHRINE AUTO-INJECTOR

The format of this leaflet was determined by the Ministry of Health and its content was checked and approved in May 2013.

3% Citanest Dental with Octapressin PRODUCT INFORMATION

Brewton City Schools Anaphylaxis Preparedness Guidelines

DERBYSHIRE JOINT AREA PRESCRIBING COMMITTEE (JAPC) SHARED CARE AGREEMENT FRAMEWORK

Adjunctive psychosocial intervention. Conditions requiring dose reduction. Immediate, peak plasma concentration is reached within 1 hour.

EMS Branch / Office of the Medical Director. Active Seziures (d) Yes Yes Yes Yes. Yes Yes No No. Agitation (f) No Yes Yes No.

Beaumont Hospital Department of Nephrology and Renal Nursing. Guideline for administering Ferinject

MEDICATION MANUAL Policy & Procedure

Version 2 This guideline describes how to manage patients who are showing signs and symptoms of alcohol withdrawal and Wernicke s Encephalopathy.

Introduction. Definition

8/6/2010. Name of medication Concentration (1:1,000 or 1mg/1ml) Expiration date

Medications or therapeutic solutions may be injected directly into the bloodstream

BEAUMONT HOSPITAL DEPARTMENT OF NEPHROLOGY RENAL BIOPSY

P AC K AG E L E AF L E T: INFORMAT I ON FO R THE USER. 500 mg, film-coated tablet Active substance: metformin hydrochloride

William MacGregor Primary School. Medical Administration Policy

ADMINISTRATION OF DRUG PRODUCTS/MEDICATIONS TO STUDENTS

Epipen Junior 150 micrograms solution for injection in pre-filled pen

Section 400: Code # 453.4R

Emergency Treatment of Anaphylaxis Policy and Guidelines

Medication Administration Guidelines for Child Care Programs

PRESCRIBING INFORMATION PRODUCT MONOGRAPH ADRENALIN* Adrenalin* Chloride Solution (Epinephrine Injection U.S.P) 1:1000 (1 mg/ml)

WIMBLEDON CHASE PRIMARY SCHOOL POLICY AND PROCEDURE FOR ADMINISTRATION OF MEDICATION AND FIRST AID AT SCHOOL

VISTARIL (hydroxyzine pamoate) Capsules and Oral Suspension

Central Alert System (CAS) Policy and Procedure Document Summary

Clinical Guideline For The Use of Rectus Sheath Catheters For The Management of Pain Following Laparotomy. 1. Aim/Purpose of this Guideline

PROPOSALS FOR AMENDMENTS TO THE HUMAN MEDICINES REGULATIONS 2012 TO ALLOW WIDER ACCESS TO NALOXONE FOR USE IN EMERGENCIES

White, circular, biconvex, uncoated tablets with a score line on one side, plain on the other.

Transcription:

Title: Patient Group Direction for the administration of lidocaine hydrochloride 1% injection as infiltration anaesthesia for insertion/removal of central venous catheters by nurses/radiographers working within the radiology departments, NHS Grampian Identifier: Replaces: Across NHS Boards NHSG/PGD/lidoCVC/MGPG729 NHSG/PGD/lidoCVC/MGPG625 Organisation Directorate Clinical Service Sub Wide Department Area Yes This controlled document shall not be copied in part or whole without the express permission of the author or the author s representative. Author: Subject Key word(s): Policy application: Purpose: Senior Charge Nurse, Radiology Patient Group Direction Patient Group Direction, PGD, lidocaine, injection, nurse, local anaesthetic, central venous catheter lignocaine radiographer NHS Grampian This Patient Group Direction (PGD) authorises appropriately qualified and trained nurses / radiographers working in the radiology departments to administer lidocaine hydrochloride 1% injection to individuals without the requirement for a patient specific prescription written by a medical practitioner. Responsibilities for implementation: Organisational: Corporate: Departmental: Area: Hospital/Interface services: Operational Management Unit: Policy statement: Review: Chief Executive and Management Teams Senior Managers Heads of Service/Clinical Leads Line Managers Deputy General Managers and Group Clinical Directors Unit Operational Managers It is the responsibility of individual nurses/radiographers and their line managers to ensure that they work within the terms laid down in this PGD and to ensure that staff are working to the most up to date PGD. By doing so, the quality of the services offered will be maintained, and the chances of staff making erroneous decisions which may affect patient, staff or visitor safety and comfort will be reduced. Supervisory staff at all levels must ensure that staff using this PGD act within their own level of competence. This policy will be reviewed at least every two years or sooner if current treatment recommendations change. UNCONTROLLED WHEN PRINTED Review Date: April 2017 Identifier: NHSG/PGD/lidoCVC/MGPG729 - i -

This document is also available in large print and other formats and languages, upon request. Please call NHS Grampian Corporate Communications on (01224) 551116 or (01224) 552245. Responsible for review of this document: Responsible for ensuring Registration of this document on the NHS Grampian Information/ Document Silo: Physical location of the original of this document: Job/group title of those who have control over this document: Responsible for disseminating document as per distribution list: Nurse/Radiographer led central venous catheter service Medicines Management Pharmacist, Westholme, Woodend. Medicines Information Office, Aberdeen Royal Infirmary Nurse/Radiographer led central venous catheter service Nurse/Radiographer led central venous catheter service Revision History: Date of change Approval date of PGD that is being superseded Summary of Changes Section heading Jan 2015 Jan 2014 Radiographer added to PGD Throughout Jan 2015 Jan 2014 2 Yearly update into new template April 2015 Jan 2014 Addition of working in the radiology departments Throughout UNCONTROLLED WHEN PRINTED Review Date: April 2017 Identifier: NHSG/PGD/lidoCVC/MGPG729 - ii -

Patient Group Direction for the administration of lidocaine hydrochloride 1% injection as infiltration anaesthesia for insertion / removal of central venous catheters by nurses/radiographers working within the radiology departments, NHS Grampian Part A... 2 1. Introduction... 2 2. Clinical Decision Making... 2 2.1. Patients who may be considered for the administration of lidocaine hydrochloride 1% injection as infiltration anaesthesia for the insertion/removal of central venous catheters... 2 2.2. Patients who may receive the administration of lidocaine hydrochloride 1% injection.... 2 2.3. Contraindications... 2 2.4. Precautions... 3 2.5. Action to be taken when a patient is excluded from treatment under this PGD 3 2.6. Action to be taken when a patient/parent/guardian or person with parental responsibility does not wish the treatment to be received under this PGD... 3 3. Description Of Treatment Available Under This Direction... 3 3.1. Lidocaine hydrochloride 1% injection... 3 3.2. Dose, route and frequency... 3 3.3. Concurrent medication... 4 3.4. Adverse effects... 4 3.5. Advice to patient... 5 3.6. Follow up treatment... 5 Part B... 6 4. Designated Staff Authorised To Administer Under This PGD... 6 5. Documentation... 7 5.1. Authorisation of administration... 7 5.2. Record of administration... 7 5.3. Consent... 8 6. Further Points... 8 7. Facilities And Supplies To Be Available At Sites For The Administration Of The Drug Specified In The PGD... 8 8. Audit... 8 Part C... 9 9. Management And Monitoring Of Patient Group Direction... 9 9.1. Consultative group... 9 9.2. Professional advisory group approving PGD... 9 9.3. Authorising managers... 9 10. References... 9 Appendix 1... 10 Appendix 2... 11 UNCONTROLLED WHEN PRINTED Review Date: April 2017 Identifier: NHSG/PGD/lidoCVC/MGPG729-1 -

Patient Group Direction For The Administration Of Lidocaine Hydrochloride 1% Injection As Infiltration Anaesthesia For Insertion /Removal Of Central Venous Catheters By Nurses/Radiographers Working Within The radiology Departments, NHS Grampian 1. Introduction Part A This patient group direction (PGD) will authorise nurses/radiographers working within the radiology departments to administer lidocaine hydrochloride 1% injection for infiltration anaesthesia by subcutaneous and intramuscular injection prior to the insertion/removal of central venous catheters to individuals aged over 16 years. This PGD should be used in conjunction with the Departmental Guidelines for Nurse/Radiographer Led Central Venous Catheter Insertion/Removal. 2. Clinical Decision Making 2.1. Patients who may be considered for the administration of lidocaine hydrochloride 1% injection as infiltration anaesthesia for the insertion/removal of central venous catheters Patients aged over 16 years of age who require insertion/removal of a central venous catheter in accordance with the Departmental Guidelines for Nurse/Radiographer Led Central Venous Catheter Insertion/Removal. 2.2. Patients who may receive the administration of lidocaine hydrochloride 1% injection. All patients in 2.1 above, where they, their parent, guardian or person with parental responsibility does not want specifically to consult with a doctor and are happy for the administration to be given by the nurse/radiographer. 2.3. Contraindications Patients may be administered lidocaine hydrochloride 1% injection under this PGD unless they: (i) (ii) (iii) (iv) (v) Have complete heart block. Have hypovolaemia. Have known hypersensitivity to local anaesthetics of the amide type. Have infection/ inflammation at the site of injection. Are aged under 16 years of age. UNCONTROLLED WHEN PRINTED Review Date: April 2017 Identifier: NHSG/PGD/lidoCVC/MGPG729-2 -

2.4. Precautions Lidocaine should be used with caution in patients with epilepsy, myasthenia gravis, cardiac conduction disturbances, congestive heart failure, bradycardia or impaired respiratory function. Lidocaine is metabolised in the liver and it should be used with caution in patients with impaired hepatic function. 2.5. Action to be taken when a patient is excluded from treatment under this PGD If a patient is excluded from treatment under this PGD, medical advice should be sought refer to a doctor. 2.6. Action to be taken when a patient/parent/guardian or person with parental responsibility does not wish the treatment to be received under this PGD This patient should be referred to a doctor. 3. Description Of Treatment Available Under This Direction 3.1. Lidocaine hydrochloride 1% injection Lidocaine hydrochloride injection 1% w/v is available in ampoules of 2mL, 5mL, 10mL and 20ML. Excipients may include water for injection, sodium hydroxide and sodium chloride or hydrochloric acid depending on the manufacturer (check the packaging and package insert for details). Store in a locked cupboard below 25 C, protected from light. Lidocaine hydrochloride 1% injection is a Prescription-only Medicine (PoM). 3.2. Dose, route and frequency Single doses of lidocaine (for anaesthesia other than spinal) should not exceed 4.5 mg/kg (or 200mg). Central Venous Catheter Insertion: Lidocaine hydrochloride 1% injection is injected subcutaneously in approximately 3mL increments (maximum of 20mL) along the planned line of the central venous catheter and overlying the vein to be punctured. The needle should be inserted subcutaneously and lidocaine hydrochloride 1% injection injected slowly, allowing 60 seconds for the injection to take effect. Each injection of lidocaine hydrochloride 1% injection must be preceded by aspiration to ensure needle is not intravascular. UNCONTROLLED WHEN PRINTED Review Date: April 2017 Identifier: NHSG/PGD/lidoCVC/MGPG729-3 -

Where lidocaine hydrochloride 1% injection is to be infiltrated intramuscularly, for example subclavian punctures, the needle must be visualised using ultrasound to ensure the needle is not intravascular. No more than 20mL (200mg) of lidocaine hydrochloride 1% injection should be used. The lowest possible volume should be used. Central Venous Catheter Removal: Lidocaine hydrochloride 1% injection is injected subcutaneously in approximately 3mL increments (maximum of 10mL) around the exit site. No more than 10mL (100mg) of lidocaine hydrochloride 1% injection should be used. The lowest possible volume should be used. 3.3. Concurrent medication No significant medicine interactions are expected with infiltration anaesthesia. 3.4. Adverse effects Adverse effects are rare and usually the result of excessively high blood concentration due to inadvertent intravascular injection, excessive dosage, rapid absorption or occasionally due to hypersensitivity. Side effects include nervousness, dizziness, confusion, respiratory depression, convulsions, hypotension and bradycardia. Allergic reactions can include urticaria, oedema and anaphylactic reactions. All serious suspected adverse reactions must be reported to the MHRA via the yellow card system https://yellowcard.mhra.gov.uk/ and to the local risk management scheme. Medical advice in cases of anaphylaxis Injections of IM adrenaline/epinephrine 1:1000 must be available to treat an anaphylactic reaction should this occur. Medical advice must be sought as soon as possible from a doctor if any patient develops any signs of hypersensitivity. If there is a delay in medical support arriving and the condition of the patient is deteriorating then an emergency ambulance must be called on 999 or direct via ambulance control or dial 2222 (hospital internal) according to local procedure, or seek urgent medical advice. (Refer to Patient Group Direction for the administration of adrenaline (epinephrine) in cases of suspected anaphylactic reactions by qualified health professionals). Overdose Stop administration immediately. Medical advice must be sought as soon as possible from a doctor if any patient develops any sign of overdosage. If there is any delay in medical support arriving and the condition of the patient is deteriorating then dial 2222 (hospital internal) according to local procedure, or seek urgent medical advice. UNCONTROLLED WHEN PRINTED Review Date: April 2017 Identifier: NHSG/PGD/lidoCVC/MGPG729-4 -

Maintain airway, supporting breathing and circulation as necessary. 3.5. Advice to patient (i) Advice should be given on what to expect and what to do for major and minor reactions. (ii) The patient should be made aware that there may be initial stinging, transient local swelling and erythema associated with the injection followed by a loss of sensation which may last for 30 60 minutes. There may be a continued sensitivity and awareness of touch/pressure at the injection site. (iii) The patient information leaflet contained in the medicine(s) should be made accessible to the patient/parent/guardian or person with parental responsibility. Where this is unavailable, or unsuitable, sufficient information should be given to the patient/parent/guardian or person with parental responsibility in a language that they can understand. 3.6. Follow up treatment Patients should not leave if they are feeling at all unwell without speaking to the nurse/radiographer first. If necessary a doctor or the patient s GP should be contacted for advice. UNCONTROLLED WHEN PRINTED Review Date: April 2017 Identifier: NHSG/PGD/lidoCVC/MGPG729-5 -

4. Designated Staff Authorised To Administer Under This PGD Part B The following staff are authorised to administer the drug specified in this PGD without an individual medical prescription providing the patient falls into one of the categories listed in 2.2 of this PGD. Staff must be employed either directly by NHS Grampian, or contracted to provide NHS services, or providing services in partnership with NHS Grampian under the direction of this authorised PGD and working within an NHSG Radiology Department. (i) (ii) Registered Nurse as recognised by the NMC. Registered Radiographer as recognised by the HCPC. In addition the following requirements are necessary. Staff must: (i) agree to be professionally accountable for their work (Appendix 1). (ii) be competent to assess the patient s capacity to understand the nature and purpose of the administration in order for the patient to give or refuse consent. (iii) be aware of current treatment recommendations and be competent to discuss issues about the drug with the patient. (iv) have been trained and assessed as being competent in the administration of the drug. All staff will have access to the current PGD. (v) have received central venous access training. (vi) have undertaken an NHS e-anaphylaxis training session which covers all aspects of the identification and management of anaphylaxis. This can be accessed via eksf or the AT Learning tool. (vii) be competent in basic life support which is required to be updated annually. (viii) have immediate access to the appropriate equipment and drugs to treat anaphylaxis and have access to the current PGD for the management and treatment of anaphylaxis should this occur. (ix) maintain their skills, knowledge and their own professional level of competence in this area according to their individual Code of Professional Conduct. (x) agree to work within the terms of the NHS Grampian PGD. Professional Managers/Nurse managers/lead nurses will be responsible for: (i) Ensuring that the current PGD is available to staff providing care under this direction. (ii) Ensuring that the staff have access to all relevant Scottish Government Health Directorate advice, including any relevant CMO letter(s). UNCONTROLLED WHEN PRINTED Review Date: April 2017 Identifier: NHSG/PGD/lidoCVC/MGPG729-6 -

(iii) Ensuring that staff have received adequate training in all areas relevant to this PGD and meet the requirements above. (iv) Maintaining a current record of all staff authorised to administer the drug specified in this PGD. 5. Documentation 5.1. Authorisation of administration Nurses/Radiographers working within NHS Grampian can be authorised to administer the drug specified in this PGD by their nurse manager/radiology manager. A certificate of authorisation (Appendix 2) signed by the authorising doctor/manager should be supplied. This should be held in the individual staff records or as agreed locally. 5.2. Record of administration An electronic or paper record for recording the screening of patients and the subsequent administration of the drug specified in this PGD must be completed in order to allow audit of practice. This should include: (i) Name and address of patient/parent/guardian or person with parental responsibility, patient CHI No (ii) Date of birth (iii) Consultant/General Practitioner details (iv) Risk group, if appropriate (v) Physical examination required, if appropriate (vi) Exclusion criteria, record why drug not administered (vii) Reason for giving (viii) Consent to the administration (if not obtained elsewhere) (ix) Drug manufacturer, batch number, expiry date (x) Site where drug administered, dose and route of administration (xi) Signature and name in capital letters of practitioner who administered the drug (xii) Date drug given (xiii) Record of adverse effects (advise patient s doctor). These records should be retained: For children and young people, retain until the patient's 25th birthday or 26th if the young person was 17 at the conclusion of treatment. For 17 years and over retain for 10 years after conclusion of treatment. Or for 3 years after death, or in accordance with local policy, where this is greater than above. UNCONTROLLED WHEN PRINTED Review Date: April 2017 Identifier: NHSG/PGD/lidoCVC/MGPG729-7 -

5.3. Consent Prior to the administration of the drug, consent must be obtained, preferably written, either from the patient, parent, guardian or person with parental responsibility and documented either in the patient s medical records/notes or on an administration form (see section 5.2). Consent must be in line with current NHSG Staff Policy for Obtaining Consent for Clinical Procedures and Healthcare Interventions. See link below. http://intranet.grampian.scot.nhs.uk/ccc_nhsg/15692.html?pmenuid=460& 6. Further Points The manufacturers leaflet inside boxes of drug should be read and advice from them taken into consideration. 7. Facilities And Supplies To Be Available At Sites For The Administration Of The Drug Specified In The PGD The following should be available at sites where the drug is to be administered: (i) Resuscitation equipment. (ii) Access to medical support (this may be via telephone). (iii) Safe storage areas for medicines and equipment. (iv) Approved equipment for the disposal of used materials. (v) Clean and tidy work areas. (vi) Copies of the current PGD for the drug specified in the PGD (vii) PGD for the administration of adrenaline (epinephrine) in cases of suspected anaphylactic reactions by qualified health professionals. 8. Audit All records of administration of the drug specified in this PGD will be filed with the normal records of medicines administration in each practice/service. A designated person within each CHP/practice/service will be responsible for auditing completion of drug forms and collation of data. UNCONTROLLED WHEN PRINTED Review Date: April 2017 Identifier: NHSG/PGD/lidoCVC/MGPG729-8 -

Appendix 1 Health Care Professional Agreement To Administer Medicines Under Patient Group Direction I: (Insert name) Working within: e.g. CHP, Practice Agree to administer medicines under the direction contained within the following Patient Group Direction Patient Group Direction for the administration of lidocaine hydrochloride 1% injection as infiltration anaesthesia for insertion/ removal of central venous catheters by nurses/radiographers working within the radiology departments, NHS Grampian I have completed the appropriate training to my professional standards enabling me to administer medicines under the above Patient Group Direction. I agree not to act beyond my professional competence nor outwith the recommendations of the Patient Group Direction. Signed: Print Name: Date: Professional Registration No: UNCONTROLLED WHEN PRINTED Review Date: April 2017 Identifier: NHSG/PGD/lidoCVC/MGPG729-10 -

Appendix 2 Certificate Of Authorisation To Administer Medicines Under Patient Group Direction This authorises: Working within: e.g. CHP, Practice To administer medicines under the following Patient Group Direction Patient Group Direction for the administration of lidocaine hydrochloride 1% injection as infiltration anaesthesia for insertion / removal of central venous catheters by nurses/radiographers working within the radiology departments, NHS Grampian The above named person has satisfied the training requirements and is authorised to administer medicines under the above Patient Group Direction. The above named person has agreed not to act beyond their professional competence nor outwith the recommendations of the Patient Group Direction Signed: Authorising Manager/Doctor Print Name: Date: UNCONTROLLED WHEN PRINTED Review Date: April 2017 Identifier: NHSG/PGD/lidoCVC/MGPG729-11 -