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Safe prescription verification of Systemic Anti …

safe prescription verification of Systemic anti -cancer Therapies (SACT) by pharmacists May 2015 Version TRAINEE WORKBOOK 2 Name of Pharmacist: .. GPhC no.: .. Job Title: .. Hospital Start Date: .. Department Start Date: .. Level of Practitioner ( 6) .. TRAINEE WORKBOOK 3 LCA safe prescription verification by pharmacists: Accreditation Checklist .. 4 LCA SACT dose calculation examples and competency .. 5 SACT mock prescription verification examples and competency .. 10 SACT prescription verification Multiple Choice Question (MCQ) Test .. 44 SACT Supervised prescription verification 49 LCA SACT pharmacist competency framework.

Safe prescription verification of Systemic Anti-cancer Therapies (SACT) by pharmacists May 2015 Version 5.0

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1 safe prescription verification of Systemic anti -cancer Therapies (SACT) by pharmacists May 2015 Version TRAINEE WORKBOOK 2 Name of Pharmacist: .. GPhC no.: .. Job Title: .. Hospital Start Date: .. Department Start Date: .. Level of Practitioner ( 6) .. TRAINEE WORKBOOK 3 LCA safe prescription verification by pharmacists: Accreditation Checklist .. 4 LCA SACT dose calculation examples and competency .. 5 SACT mock prescription verification examples and competency .. 10 SACT prescription verification Multiple Choice Question (MCQ) Test .. 44 SACT Supervised prescription verification 49 LCA SACT pharmacist competency framework.

2 50 Clinical verification Standards .. 56 TRAINEE WORKBOOK 4 The checklist below details the requirements for both local and LCA accreditation/sign-off. A Pharmacist can be assessed as competent to verify SACT by designated assessors. Each Trust will have a local list of accredited assessors. MOCK PRESCRIPTIONS AND WORKED EXAMPLES Completed examples in the LCA Trainee Workbook: Assessor s details: Date: Correctly completed mock prescriptions in workbook Name: Signature: Job Title: Correctly completed calculations in workbook (Pass mark 100%) Name: Signature: Job Title: Completed MCQ test (Pass mark 80%) Name: Signature: Job Title: SCREENING LOG Log of supervised SACT prescriptions completed to LCA criteria (refer to Passport accreditation programme guidance): Solid tumour First cycles Haemato-oncology Clinical Trials Oral Paediatrics Assessor s details.

3 Name: Signature: Job Title: LOCAL REGISTER Pharmacist s name added to the local register for clinical verification of SACT Assessor s details: Name: Signature: Job Title: If the above has been successfully completed, please ensure the LCA-assessor for your Trust is given the paperwork to review and assess for LCA Passport competency. TRAINEE WORKBOOK 5 Pharmacists are required to achieve 100% accuracy in the calculations section in order to continue with the accreditation programme. In clinical practice if in any doubt with calculations please seek advice from a senior colleague. You should attempt all questions and seek support where needed.

4 1. A 50 year old woman, diagnosed with metastatic breast cancer (bone and liver) presents for chemotherapy treatment. She has been assessed as fit for treatment and you are happy her FBC is acceptable. Doxorubicin 60mg/m2 and Cyclophosphamide 600mg/m2 have been prescribed. Calculate the dose of both drugs to be given if the patient s Body Surface Area (BSA) is a) Doxorubicin dose: .. b) Cyclophosphamide dose: .. 2. You are in clinic verifying prescriptions and need to check the correct dose has been calculated by the prescriber: a) For a drug that is usually prescribed at 75mg per kg; if the patient weighs 60kg, what should the dose of the drug be in grams?

5 B) For a drug that is usually prescribed at ; if the patient weighs 72kg, what should the dose of the drug be in milligrams? 3. A patient is due to receive Rituximab, for the treatment of lymphoma, as part of R-CHOP 21 regimen at a dose of 375mg/m2 three-weekly. This drug is a monoclonal antibody and the risk of a hypersensitivity reaction is high, it is therefore given with paracetamol, chlorphenamine and prednisolone pre-medications. To reduce the risk of a reaction the drip rate for the infusion is slowly titrated upwards. The following instruction for the first dose at cycle 1 is given: Infuse at a rate of 50mg/hour for 30 minutes and if tolerated increase by 50mg/hour every 30 minutes, to a maximum dose of 400mg/hour.

6 A) What is the dose of Rituximab the patient should be receiving (BSA )? Use the dose banding table below: BSA (m2) Dose (mg) 500 550 550 600 650 700 750 800 Rituximab dose: TRAINEE WORKBOOK 6 b) What does your local Intravenous (IV) guide or chemotherapy guide suggest is an adequate diluent volume for Rituximab for most patients? c) Based on your answers from above, what rate should be entered on the infusion pump in mL/hour for a bag of Rituximab? Please complete this without reference to a local standardised table. Please show your workings and round answers to the nearest whole number.

7 Vial concentration =10mg/mL Extra volume added to bag = 65mL Total bag volume= 565 mL Final bag concentration = 4. Looking at the dose banding table below what would the dose of Rituximab be for a patient with a BSA of BSA (m2) Dose (mg) 500 550 550 600 650 700 750 800 Rituximab dose: TRAINEE WORKBOOK 7 5. You need to mix a drug which is prescribed at a dose of 675mg and the instruction indicates to dilute to a concentration of 2mg/mL with either Sodium Chloride or Glucose 5%. a) What volume of diluent should be used? b) What would be the volume of diluent if the final concentration was to be 4mg/mL?

8 6. A patient develops haematological toxicities and requires a dose reduction of 25%. If the starting dose was 175mg what will the new dose be? 7. A patient has been dose reduced by 75% and the dose is now What was the original dose? 8. You are asked to commence a drug for a patient who is participating in a clinical trial. The drug needs to be administered at a rate of 2mg per minute for 15 minutes and then increase if tolerated to 4mg per minute. Calculate the rate to be administered in mL/hr. The drug dose is 150mg and the bag contains 75mL. (NB: you will need to sit with the patient and press stop on the pump at the end of 15 minutes) 9.

9 You are asked to commence a drug for a patient who is participating in a clinical trial. The drug needs to be administered at a rate of 1mg per minute for 15 minutes and then increased if tolerated to 3mg per minute. Calculate the rate to be administered in mL/hr. The drug dose is 145mg and the bag contains 58mL. (NB: you will need to sit with the patient and press stop on the pump at the end of 15 minutes) 10. You need to give atropine as a part of the pre-medication for Irinotecan. The drug comes in 600 micrograms in 1mL. The dose prescribed is , how many mLs need to be administered so the patient receives the correct dose?

10 11. What volume of diluent [Water For Injections (WFI)] needs to be added to reconstitute a 150mg powder vial to achieve a concentration of 21mg/mL considering the displacement value of per vial: TRAINEE WORKBOOK 8 12. a) What volume of diluent (WFI) needs to be added to reconstitute a 500mg powder vial to achieve a concentration of 50mg/mL b) For the above question how many mL are needed if the displacement value of is taken to achieve the 50mg/mL concentration c) The above drug needs further dilution to achieve a maximum concentration of 5mg/ml. What volume should this dose be made up to if the dose to be given is 750mg?


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