HEPATITIS A + TYPHOID VACCINE

Transcription

1 GG&C PGD ref no: 2017/1522 YOU MUST BE AUTHORISED BY NAME, UNDER THE CURRENT VERSION OF THIS PGD BEFORE YOU ATTEMPT TO WORK ACCORDING TO IT Clinical Condition Indication: Indicated for active immunisation against hepatitis A virus infection and typhoid fever in adults and adolescents. Inclusion criteria: Travellers going to areas of high or moderate prevalence of hepatitis A virus and typhoid fever. Long stay travellers or travellers to low to moderate risk areas of hepatitis A virus and typhoid fever who are unable to take reasonable precautions with food and water hygiene. Travellers staying with or visiting local populations where there is a high or moderate risk of hepatitis A virus and typhoid fever. Injecting drug users. Individuals at high risk because of sexual practices. Laboratory staff working with hepatitis A virus and S. typhi in the course of their work. Occupational exposure e.g. workers in contact with sewage. During an outbreak. Patients with chronic liver disease. Close contacts of hepatitis A cases. Those groups which under certain circumstances could be at increased risk of infection or transmission of hepatitis A virus. Exclusion criteria: Children aged 15 or below (Hepatyrix ) Children aged 16 or below (Viatim ) Anaphylactic reaction to a previous dose of hepatitis A or typhoid vaccine. Anaphylactic reaction or severe sensitivity to any component of hepatitis A or typhoid vaccine. Evolving neurological condition, immunisation should be deferred until resolved or stabilised. History of severe reaction (i.e. anaphylactic reaction) to latex where vaccine is not latex free. Acute illness or fever, immunisation should be postponed until fully recovered. Non consent. Template Version: 2017 Page 1 of 10

2 Cautions/Need for further advice/ Circumstances when further advice should be sought from the prescriber: Action if patient declines or is excluded: Further advice should be sought for: Pregnant women and breast-feeding mothers should only be given pre-exposure vaccination where the risk of disease is high and when it is considered that the potential benefit outweighs any possible risk to foetus/infant. Those suffering from auto-immune disease or undergoing immunosuppressive therapy. Known bleeding disorder administer subcutaneously. Refer to appropriate clinician e.g. GP, Travel Health Consultant, Sexual Health, GUM or ID Consultant. If declined advise regarding protective effect of immunisation and potential disease complications. Document advice given and refer to appropriate clinician. Referral arrangements for further advice / cautions As above. Template Version: 2017 Page 2 of 10

3 Drug Details Name, form & strength of medicine: Route/Method of administration: Dosage (include maximum dose if appropriate): Frequency: Duration of treatment: Hepatitis A (Inactivated) and Typhoid Polysaccharide vaccine (adsorbed) Intramuscular injection into deltoid muscle.deep subcutaneous injection for individuals with a bleeding disorder (caution possibility of reduced immunogenicity with this route). One single dose of vaccine (1ml) to be administered per occasion. Primary immunisation consists of one dose of the vaccine. Single dose only. (NB A reinforcing dose of single hepatitis A vaccine should be administered 6-12 mths following primary dose. This PGD does NOT cover the reinforcing dose, please refer to single hepatitis A or typhoid PGD for information). Maximum or minimum treatment period: Quantity to supply/administer: Supply, Administer or Both: Additional monitoring:* Legal Category: Is the use outwith the SPC:** Storage requirements: 1 dose only. 1 dose. Administer only. No. POM No. Store between 2 0 C-8 0 C in locked storage. NHS GG&C Vaccine Ordering, Storage and Handling Guidelines should be observed ocedures/ggcclinicalguidelines/ggc%20clinical%20guidel ines%20electronic%20resource%20direct/vaccine%20orde ring%20storage%20and%20handling%20guideline.pdf Vaccine storage history e.g. temperature charts must be checked and deemed satisfactory before administration to patient. * The black triangle symbol has now been replaced by European additional monitoring ( ) **Summary of Product Characteristics Template Version: 2017 Page 3 of 10

4 Warnings including possible adverse reactions and management of these: Awareness of potential side effects as listed below: Minor Local Reactions mild transient soreness, erythema, induration at the injection site. Less Common headache, fatigue, fever, nausea, vomiting, diarrhoea, loss of appetite and rash. o Very Rarely - anaphylactic reactions, arthralgia, myalgia, convulsions. Hepatyrix only: Neurological manifestations including transverse myelitis, Guillain-Barre syndrome and neuralgic amyotrophy, convulsions. Please refer to current BNF, ebnf or SPC at for full details. Use the Yellow Card System to report adverse drug reactions. Yellow Cards and guidance on their use are available at the back of the BNF or online at Assessment of patients pre and post immunisation. Any adverse event to be recorded and highlighted within patients individual record. Advice to patient/carer including written information provided: Monitoring (if applicable): Follow up: Explain treatment and course of action. If appropriate give patient a copy of relevant patient information leaflet PIL available at If severe reaction with persisiting symptoms seek medical advice. Further Information available to patients at or n/a See advice to patient/carer. Template Version: 2017 Page 4 of 10

5 Staff Characteristics Professional qualifications: Specialist competencies or qualifications: Continuing education & training: Those registered health care professionals that are listed and approved in legislation as able to operate under patient group directions and have current registration. Has undertaken appropriate training and competence to undertake immunisation including recognition and treatment of anaphylaxis. Has undertaken appropriate training for working under PGDs for the supply and administration of medicines. All health care professionals working under the direction will be expected to maintain their competence as specified in hospital, local and national policies e.g. Nursing & Midwifery Council guidelines. Referral Arrangements and Audit Trail Referral arrangements The practitioner should be aware of any change to the recommendations for the medicine listed. It is the responsibility of the individual to keep up-to-date with continued professional development in all aspects of immunisation including recognition and treatment of anaphylaxis. Any prolonged reaction, whether mild or severe must be reported to an appropriate clinician for the department administering vaccination. Records/audit trail: Patient s name, address, date of birth and consent given; Contact details of GP (if registered); Dose and form administered (batch details and expiry date); Advice given to patient (including side effects); Signature/name of staff who administered or supplied the medication, and also, if relevant, signature/name of staff who removed/discontinued the treatment; Details of any adverse drug reaction and actions taken including documentation in the patient s medical record; Referral arrangements (including self-care); Administration must be recorded on the SIRS sheet, GP, Travel Health clinic or Primary Care clinic record as appropriate. Template Version: 2017 Page 5 of 10

6 References/Resources and comments: Notes: SPC Summary of Product Characteristics BNF British National Formulary TRAVAX NMC (2015) Standards for Medicines Management NMC (2015) The NMC Code of Professional Conduct: standards for conduct, performance and ethics NHS GG&C Immunisation Best Practice Guideline cedures/ggcclinicalguidelines/ggc%20clinical%20guidelin es%20electronic%20resource%20direct/immunisation%20an d%20best%20practice.pdf NHS GG&C Vaccine Ordering Storage and Handling Guidelines cedures/ggcclinicalguidelines/ggc%20clinical%20guidelin es%20electronic%20resource%20direct/vaccine%20orderin g%20storage%20and%20handling%20guideline.pdf Immunisation against Infectious Diseases (2006). DOH (green book) always refer to on-line version NHS HealthScotland website x.aspx Health Protection Scotland Immunisation and Vaccine Preventable Diseases website Immunisation Scotland Template Version: 2017 Page 6 of 10

7 This Patient Group Direction must be agreed to and signed by all healthcare professionals involved in its use. The original signed copy will be held at PPSU, Queens Park House, Victoria Infirmary. The PGD must be easily accessible in the clinical setting. Organisation: NHS Greater Glasgow & Clyde Professionals drawing up PGD/Authors Designation and Contact Details Name: Clare Walker Designation: Nurse Specialist in Travel Health, Health Protection Scotland. Signature: Date: 30/11/2017 *Name: Val Reilly address: Designation: Public Health Pharmacist Signature: Date: 30/11/2017 Name: Alisdair MacConnachie address: Designation: Consultant Physician, Brownlee Clinic Signature: Date: 10/01/2018 address: * Lead Author Template Version: 2017 Page 7 of 10

8 AUTHORISATION: NHSGG&C PGD & Non-medical Prescribing Sub-Committee of ADTC Signature: Date: Chairman in BLOCK CAPITALS Dr Craig Harrow 30/11/2017 Lead of the professional group to which this PGD refers: Signature: Name: in BLOCK CAPITALS Gavin Gorman 30/11/2017 Date: Pharmacist representative of PGD & Non-Medical Sub-Committee of ADTC Signature: Date: Name: in BLOCK CAPITALS Mairi McGinnes 30/11/2017 Template Version: 2017 Page 8 of 10

9 Local Authorisation: Service Area for which PGD is applicable: I authorise the supply/administer medicines in accordance with this PGD to patients cared for in this service area. Lead Clinician for the service area (Doctor) Name: Signature: Designation: Date: contact address: I agree that only fully competent, qualified and trained professionals are authorised to operate under the PGD. Records of nominated individuals will be kept for audit purposes. Name (Lead Professional): Signature: Designation: Date: contact address: Description of Audit arrangements: Frequency of checks: (Generally annually) Names of auditor(s): PGDs DO NOT REMOVE INHERENT PROFESSIONAL OBLIGATIONS OR ACCOUNTABILITY. It is the responsibility of each professional to practice only within the bounds of their own competence and in accordance with their own Code of Professional Conduct. Note to Authorising Managers: authorised staff should be provided with an individual copy of the clinical content of the PGD and a photocopy of the document showing their authorisation. I have read and understood the Patient Group Direction. I acknowledge that it is a legal document and agree to supply/administer this medicine only in accordance with this PGD. Name of Professional Signature Date Template Version: 2017 Page 9 of 10

10 Patient Group Direction Audit Form Form for the audit of compliance with PGD or PGDs To ensure best practice all PGDs should be audited on a 6 monthly basis. Name and post of Designated Lead person within each practice/clinic base: Location/Clinic Base: Date of audit: Tick as appropriate. If no, state action required Y N Action Is the PGD or PGDs utilised within the clinical area? Has the PGD or PGDs been reviewed within the 2 year limit? Do the managers listed on the PGD or PGDs hold a current list of authorised staff? Are all staff authorised to work under the PGD or PGDs members of one of the health professions listed in the PGD? Do all staff meet the training requirements identified within the PGD? Are you confident that all medicines supplied or administered under the PGD or PGDs are stored according to the PGD where this is specified? Do the staff working under the PGD or PGDs have a copy of the PGD which has governance sign off and is in date and, available for reference at the time of consultation? Where the medicine requires refrigeration. (Delete if not required). Is there a designated person responsible for ensuring that the cold chain is maintained? Is there a record that the fridge temperature has been monitored to required levels? If there is regular and sustained reliance on PGDs for service provision has a Non Medical Prescribing approach been considered as an alternative? (Please note reasons for either a Y/N response). Name: Date of audit: Keep copies of completed audits alongside your PGD for local reference. Please retain at local level and ensure audit forms are readily available as they may be required for clinical governance audit purposes. Template Version: 2017 Page 10 of 10