Webster-pak® Community Dispensing Procedures Manual Product Code: s153 ™ v 6.0 Webster-pak® Community Dispensing Manual Webster-pak® Community Dispensing Manual Contents Introduction to Webster-pak ____________________________________2 Essential Components for Webster-pak Community __________________3 Getting Started ______________________________________________6 Patient Profile _______________________________________________7 Medication ‘Not Suitable for Packing’ _____________________________7 Complying With PBS Requirements _______________________________8 Complying with other Guidelines _________________________________8 Packing and Sealing Webster-pak Community _______________________8 The Final Check _____________________________________________11 Having the Prescriptions When Needed ___________________________12 Re-Ordering Medication _______________________________________12 What About Dosage Changes? __________________________________12 What If The Patient Needs More Than One Pack? ___________________13 For More Information _________________________________________13 References _________________________________________________13 © (07/2013) Manrex Pty Ltd t/as Webstercare 2014. Webstercare, Webster-pak, Webstersystem and MedsPro are Registered Trade Marks of Manrex Pty Ltd t/as Webstercare. Blu-Lok, QA Sig Box device and Virtual Pill Count (VPC) are Trade Marks of Manrex Pty Ltd t/as Webstercare. ________________________________________________________________ © (07.2013) Manrex Pty/Ltd (ABN: 63 074 388 088) t/as Webstercare - 2014 17-19 Moore St, Leichhardt NSW 2040 Tel: (02) 9563 4900 Fax: (02) 9563 4955 Free Call: 1800 244 358 Page 1 Webster-pak® Community Dispensing Manual Introduction to Webster-pak Studies in Australia have shown that more than half of people on three or more medications do not take them as prescribed. The cost to the community as a result of a person’s unnecessary admission to a residential aged care facility or to hospital due to adherance errors is enormous and preventable. Webster-pak is a multi dose, dose administration aid designed to assist people to correctly take their medication as prescribed. An independent clinical trial 1 has shown Webster-pak to more than double the rate of adherance with elderly patients. Widespread usage in other areas also supports this improvement. It is suitable for anyone, who is taking routine medication (irrespective of age). Webstercare aims to; • Encourage a safe and responsible attitude towards use of medication • Minimise the likelihood of under and over use of medication • Optimise the possible health outcome through appropriate use of medication • Allow easy monitoring of medication use by a relative or carer Supply of Webster-pak is consistent with the concept of quality use of medicines, for both residential care and home care patients. The Webster-pak makes medication monitoring and medication review a practical and cost effective option for community patients. With Webster-pak Community the medication profile is printed onto the specially designed header card for laser and Ink Jet printers. A unique low temperature foil, or low-temp foil is used which makes the sealing process effortless and inexpensive. Once the pack is complete, the pack itself will serve as an effective complete medication profile as well as a dose administration aid. In the event of an emergency all the information is on hand for the doctor, ambulance officer or hospital staff. 1 Ware Gail J et al. New Zealand Medical Journal 27 November 1991, Vol 104, No 924: Pages 495-7 Unit Dose Calendar Packaging and Elderly Patient Compliance. © (07.2013) Manrex Pty/Ltd (ABN: 63 074 388 088) t/as Webstercare - 2014 17-19 Moore St, Leichhardt NSW 2040 Tel: (02) 9563 4900 Fax: (02) 9563 4955 Free Call: 1800 244 358 Page 2 Webster-pak® Community Dispensing Manual Essential Components for Webster-pak Community The following materials will be needed prior to starting. Some purchases for example Blisters, Foils and Header cards will be ongoing while other items are generally a oneoff purchase. Folders The side of the re-usable plastic folder is labelled with the days of the week: Monday at the top of the pack, following through to Sunday at the bottom. The folders are used in a colour coded system according the completed packs use or what type of medication is contained in the pack. Colour Coding System Blue Regular Weekly medication: Breakfast, Lunch, Dinner, Bedtime Black Regular Weekly medication Low Vision White When Necessary medication (PRN) Green Antibiotic & Short Term medication Mustard Warfarin medication Burgundy Special Dose Times & Before Meals medication Purple Special Alert, Accountable drugs, Cytotoxic and special precautions Blisters Through experience we have found that 60-80% of patient medication will fit into the small sized blister. If the dose or tablet size is too large, the next sized blister may be used. Small Concertina Blister (product code: 780 pack of 500) Medium Concertina Blister (product code: 787 pack of 500) Large Concertina Blister (product code: 782 pack of 500) King Concertina Blister (product code: 790 pack of 250) © (07.2013) Manrex Pty/Ltd (ABN: 63 074 388 088) t/as Webstercare - 2014 17-19 Moore St, Leichhardt NSW 2040 Tel: (02) 9563 4900 Fax: (02) 9563 4955 Free Call: 1800 244 358 Page 3 Webster-pak® Community Dispensing Manual Webster-pak Community Header Cards The Header Card contains the patient information and colour photograph, medication information, the dosage times as well as your pharmacy name and telephone number. All this information can be printed on the Header Card using a laser or ink jet printer together with Webstercare’ Medication Management Software (MMS). The Community Header Cards are available with pre-printed dosage times for Breakfast, Lunch, Dinner and Bedtime. Blank Header Cards are also available to allow you to tailor dosage times according to individual patient’s medication regimes. Laser Community Header Card (product code: 406 sold in pack of 250) Laser Blank Community Header Card (product code: 587 sold in pack of 250) Foil Due to the fact that printing is not required on the back of the pack, a pre-cut sheet of LoTemp foil (Product Code 366-S) is all you need for sealing a Community Webster-pak. Pre-cut sheets come in packs of 500 sheets and are packaged between thick pieces of cardboard to prevent the sheets from curling. Webstercare LoTemp foil is designed to seal at a low temperature. This ensures minimal heat, pressure and waiting time required to form an effective seal. Platen The Blu-Lok™ Platen is a silicon-moulded frame which is used to hold the blister whilst packing the medication. It has cut-out holes matching the Webster-pak blisters. The © (07.2013) Manrex Pty/Ltd (ABN: 63 074 388 088) t/as Webstercare - 2014 17-19 Moore St, Leichhardt NSW 2040 Tel: (02) 9563 4900 Fax: (02) 9563 4955 Free Call: 1800 244 358 Page 4 Webster-pak® Community Dispensing Manual Blu-lok Platen also has an interlocking feature allowing two or more platens to be secured together for packing more than one Webster-pak. Blu-Lok Platen (product code: 660 sold individually) Sealing Mouse The Sealing Mouse has been designed specifally for sealing LoTemp foil on the back of Webster-paks. Its ergonomic and compact design offers a flat sealing surface ensuring an even seal for each pack. Sealing Mouse (product code: 795 sold individually) Sealing Iron The Sealing Iron is a ‘dry’ or non-steam iron which can be used as an alternative to the Sealing Mouse to seal LoTemp foil on the back of Webster-paks. © (07.2013) Manrex Pty/Ltd (ABN: 63 074 388 088) t/as Webstercare - 2014 17-19 Moore St, Leichhardt NSW 2040 Tel: (02) 9563 4900 Fax: (02) 9563 4955 Free Call: 1800 244 358 Page 5 Webster-pak® Community Dispensing Manual Sealing Iron (product code: 320 sold individually) Webstercare Medication Management Software The Communty Webster-pak is available in all versions of the Webstercare Medication Management Software. Webster-pak is now available in 20 different languages, designed to cater for people whose first language is not English. This enables people from certain non-English speaking backgrounds to read the days of the week and the time of day in their own language to take their medication as prescribed. There are 2 parts: a tailored header card (Community style) for each language and tailored Monday to Sunday labels for each language. Please refer to your Webstercare order form for individual product codes. Getting Started It is most important that before you start to pack medication into a Webster-pak you have complete and accurate information. To record this, use the Doctor Order/Patient Medication Profile Form (Product Code 284 – pad of 100 sheets). Exact dosage times and complete profiles of all medication must be recorded and maintained. It is essential to check this information with the doctor or carer from written documentation supplied by the doctor. It is essential to cross check this information against the prescriptions. You may find discrepancies that will need to be discussed and resolved before commencing. At this time it is opportune to check for any potential drug/drug or drug/disease allergies, interactions or dosage discrepancies and take appropriate action. © (07.2013) Manrex Pty/Ltd (ABN: 63 074 388 088) t/as Webstercare - 2014 17-19 Moore St, Leichhardt NSW 2040 Tel: (02) 9563 4900 Fax: (02) 9563 4955 Free Call: 1800 244 358 Page 6 Webster-pak® Community Dispensing Manual Patient Profile All Webstercare systems including Webster-pak Community have been designed with specific steps to follow in order to minimise the risk of human error. It is important that ALL steps are followed EVERY time a Webster-pak is filled AND before it leaves the pharmacy. It is the pharmacist’s responsibility to ensure that the medication packed is correct against the very latest instructions from the doctor. To support this process, Webstercare advises that a hard copy profile be generated and maintained. For a new patient, confirm and enter the data from all original documentation which may include prescriptions etc. into Webstercare Medication Management Software (MMS). Once the data entry is completed in MMS print a hard copy profile by selecting ‘Patient Medication Record With Pill Images’. The hard copy profile is confirmed by the pharmacist against the original documentation. This is to check the accuracy of the data entry and that the correct medication profile has been entered. If possible request the prescriber to ‘sign off’ the completed profile. This becomes the hard copy profile which is used to check the Webster-pak system after packing is completed. The hard copy profile should be stored in a plastic sleeve in a folder with a copy of the prescriber’s original documentation, along with any previous versions of the hard copy profile to confirm its validity. As changes occur to the patient’s medication profile, they are hand-written on the hard copy profile. These are confirmed by a pharmacist and the client profile is updated in MMS. An updated copy is printed from MMS as needed. Store the previous version with all documentation behind the latest copy. All printed copies of the hard copy profile need to be checked by the pharmacist. For more information on patient profiles, please refer to the ‘Hard Copy Profile’ document in the back of this manual. Medication ‘Not Suitable for Packing’ Solid dose medication unsuitable for repackaging can be dispensed in their original containers. The header card, where “Also On” or “Non-packed” medication is printed, is a reference for when non-packed medication should be administered. This gives a complete record of all the medicines a person is taking. Some examples of medicines that may be unsuitable for repackaging include: effervescent tablets, dispersible tablets, buccal tablets, hygroscopic preparations and solid dose cytotoxic preparations. For more information, please refer to the Webstercare advice on ‘Medications not suitable for packing in a dose administration aid’ document in the back of this manual. © (07.2013) Manrex Pty/Ltd (ABN: 63 074 388 088) t/as Webstercare - 2014 17-19 Moore St, Leichhardt NSW 2040 Tel: (02) 9563 4900 Fax: (02) 9563 4955 Free Call: 1800 244 358 Page 7 Webster-pak® Community Dispensing Manual Complying With PBS Requirements Medications are dispensed via the PBS in the usual way. Once the dispensing is complete, a record of the dispensed medication for each patient must be maintained. This can be done through the use of the MedsPro® – Virtual Pill Count (VPC)™ system. A record of your patient’s medications is retained in the software. If at any time a patient requests their medications, you have a record of their balance held on their behalf and you can supply at short notice. Alternatively, Integrity bags can be used to store each patient’s medications with the identification similar to “this medication is the property of.............” Non-packed medication will be dispensed and labelled as normal and supplied as normal eg. Liquids, eye drops, ointments, PRNs. Complying with other Guidelines Pharmacists should also refer to the “guidelines for medication management in residential aged care facilities” released by the Australian Pharmaceutical Advisory Council (APAC). Other professional guidelines such as QCPP and PSA should also be taken into consideration. Packing and Sealing Webster-pak Community The Webster-pak Community is a quick and simple way for pharmacies to prepare a medication management system for community customers. For a quick reference guide on how to pack Webster-pak Community please refer to the ‘Packing Procedure’ document in the back of this manual. Preparation The Packing Technician: • Thoroughly washes hands prior to packing or uses gloves • Collects the first client’s medication • Ensures there are plenty of blisters for packing • Places the medication for the first client on their left. Once they have used the medication, it is placed on their right hand side until packing is complete to assist with workflow. STEP 1. Using the Webstercare Medication Managment Software (MMS) print the Community Header Cards. © (07.2013) Manrex Pty/Ltd (ABN: 63 074 388 088) t/as Webstercare - 2014 17-19 Moore St, Leichhardt NSW 2040 Tel: (02) 9563 4900 Fax: (02) 9563 4955 Free Call: 1800 244 358 Page 8 Webster-pak® Community Dispensing Manual The bottom panel of the header card On the front of the card you can print the patient’s name and photograph (Client Photo) as well as any other non-packed medication to be administered. You can also print your pharmacy name, logo and contact details. The centre panel of the header card You can print the complete patient profile onto the the Community Header card. Including: Patient’s Name, Doctor, Date and a reference to the profile number. The information on the centre panel of the header card is printed upside down. This is because the header card will be folded on the completed pack, so this information will appear the correct way up. The bedtime medications are also printed on the left hand side as this will be viewed from the back of the pack. The drug name, strength, dosage and description is also printed. STEP 2. Place an empty blister sheet in the Blu-Lok platen. Fold the header card along the perforations so the profile faces you and place it under the lip of the blister sheet. © (07.2013) Manrex Pty/Ltd (ABN: 63 074 388 088) t/as Webstercare - 2014 17-19 Moore St, Leichhardt NSW 2040 Tel: (02) 9563 4900 Fax: (02) 9563 4955 Free Call: 1800 244 358 Page 9 Webster-pak® Community Dispensing Manual STEP 3. Pack the medications from right to left into the blister sheet as per the medication profile printed on the header card. IMPORTANT: As you are viewing the blister sheet back to front, Breakfast is on the right, bedtime on the left. STEP 4. IMPORTANT: DOUBLE CHECK the filled blister against the header card, confirming packing accuracy before sealing the pack. Place a sheet of low-temp pre-cut foil over the back of the blister sheet. Making sure the shiny silver side of the foil is face down. Align the bottom corners of the foil with the bottom corners of the blister sheet. Note: the foil should overlap the header card towards the top of the pack by approximately 1cm. A Sealing Mouse or a dry (non-steam) iron on a low or “wool” temperature setting can be used to seal the foil. Make sure you run the Sealing Mouse or iron over the entire back surface of the foil. Particularly around the foil edges and where the foil overlaps onto the header card. The heat from the Sealing Mouse or Iron will activate the adhesive on the low-temp foil. As the adhesive cools, it will adhere to the blister sheet and header card making a single complete pack. For this reason applying slight pressure using the palm of your hand or a white board duster to the back of the foil as it cools will maximise the foil to blister seal. After sealing the pack, sign the ‘TECH’ box on the front of the header card to confirm packing accuracy. © (07.2013) Manrex Pty/Ltd (ABN: 63 074 388 088) t/as Webstercare - 2014 17-19 Moore St, Leichhardt NSW 2040 Tel: (02) 9563 4900 Fax: (02) 9563 4955 Free Call: 1800 244 358 Page 10 Webster-pak® Community Dispensing Manual Finally, place the sealed pack into the appropriate coloured folder and put aside for a pharmacist to check. For more information on sealing a Webster-pak, please refer to the ‘Webstercare Sealing Techniques’ document in the back of this manual. The Final Check STEP 5. The pharmacist arranges the packs to be checked on the left side of the checking area in a folder tray, with an empty folder tray on the right side of the checking area. Confirm the following are correct against the hard copy profile; • Information on the header card and the start date are accurate. • The pack is in the correct colour folder. • Confirm drug names and strengths in each blister from Mon-Sun for each meal time (column by column). Handy Hint: Check in reverse i.e. start from Bedtime working towards Breakfast. Working backwards breaks expected patterns and makes errors easier to detect. • Alternate-day doses schedule is correct as printed on the front of the header card. It is important to check the start date on the pack to confirm the correct week sequence. • The correct number of pieces are in each blister from top to bottom, this time from Breakfast to Bedtime. Again confirm the alternate dose schedule. STEP 6. After checking the pack the pharmacist initials the ‘PHARM’ box printed on the header card. Place this pack backwards in the empty folder tray to your right to indicate the pack has been checked while maintaining the order of the packs. For a quick reference guide on how to check a pack please refer to the ‘Multi Dose Websterpak Checking Guide’ document in the back of this manual. © (07.2013) Manrex Pty/Ltd (ABN: 63 074 388 088) t/as Webstercare - 2014 17-19 Moore St, Leichhardt NSW 2040 Tel: (02) 9563 4900 Fax: (02) 9563 4955 Free Call: 1800 244 358 Page 11 Webster-pak® Community Dispensing Manual Having the Prescriptions When Needed To comply with the PBS regulations you must ensure that prescriptions are available at the time of dispensing. It is unacceptable and illegal for there to be owing prescriptions unless in the case of an emergency order from the doctor. The Webster-pak makes it far easier for you to get prescriptions when you need them because you know exactly how much medication is on hand at any time. Depending on the normal response time and visiting patterns of the doctors, you need to order prescriptions in advance of them being required. This is very simple with the Webster-pak. You can tell at any time how much of any medication is left in any original pack or bottle. Once this gets down say for example between 1 and 2 weeks supply, you may need a new prescription. Re-Ordering Medication Re-Ordering medication is simple using the blue Pharmacy Order Sheet (Product Code 477) and Thermal Re-Order Labels. During the packing process, if less than one-week’s supply of a medication remains, remove the label’s lift-off tab and apply to the Order Sheet. Alternatively, orders can be handwritten onto the Order Sheet. The Pharmacy Order Sheet can then be actioned by either dispensing medication from an existing prescription, or sending a letter to the doctor informing them of the need for a new prescription. What About Dosage Changes? In a community setting a complete new pack may be supplied each time there is a change. The previous pack used must be returned to the pharmacy. © (07.2013) Manrex Pty/Ltd (ABN: 63 074 388 088) t/as Webstercare - 2014 17-19 Moore St, Leichhardt NSW 2040 Tel: (02) 9563 4900 Fax: (02) 9563 4955 Free Call: 1800 244 358 Page 12 Webster-pak® Community Dispensing Manual What If The Patient Needs More Than One Pack? There are a few occasions where a second pack may be required; • A patient may have too many medications to fit into one blister compartment • There are too many medications in the one compartment making it hard to check the pack • A patient may have more than four dosage times per day Once a second pack is prepared, attach them together with a split ring eg. shower curtain ring or similar device. For More Information Your success with Webster-pak depends on you understanding the procedures involved. Please feel free to contact us at any time if you need further assistance or advice on Free Call 1800 244 358. References PSA standard 7: http://www.psa.org.au/download/community-pharmacy-agreements/doseadministration-aids/professional-practice-standard-7.pdf APRAH guidelines on specialised supply of medicines: http://www.pharmacyboard.gov.au/Codes-Guidelines.aspx QCPP guidelines: http://www.guild.org.au/ Safe use of oral cytotoxic medicines: http://www.australianprescriber.com/magazine/36/1/article/1377.pdf © (07.2013) Manrex Pty/Ltd (ABN: 63 074 388 088) t/as Webstercare - 2014 17-19 Moore St, Leichhardt NSW 2040 Tel: (02) 9563 4900 Fax: (02) 9563 4955 Free Call: 1800 244 358 Page 13 Medications not suitable for packing in Webstercare® Systems Packing Cautions Pharmacy Board of Australia guidelines recommend pharmacies maintain a list of medicines or medicine types that should not be removed from the original manufacturer’s packaging for packing in a Dose Administration Aid1. A pharmacist must make an informal judgment as to the suitability of packing a medicine in a Webstercare system. It is recommended that the pharmacist use a ‘risk assessment’ approach utilising all available information. Included medicines may vary depending on the local prescribing preferences and climate. Consideration may also be given to the formulation used and the length of time the medicine is to be stored in the Webstercare system. If unsure, please contact the manufacturer for more information. Examples to consider include: Ÿ Ÿ Ÿ Ÿ Moisture sensitive or hygroscopic formulations Dispersible tablets A Webstercare system packed more than a week in advance Medicines packed in a PRN (when required medicine) Webstercare system Webstercare® recommends medication removed from a manufacturer’s original packaging should be: Ÿ Placed immediately in the Webstercare system using tweezers or Pil-Kot™ packing accessory Ÿ Sealed immediately after filling using the correct sealing technique* Medicines which must NOT be removed from the manufacturer’s packaging and packed in a Webstercare system include: Pradaxa: dabigatran etexilate capsules Anginine: glyceryl trinitrate tablets Wafer formulations: packed as a PRN pack The following medicines are not to be packed in this pharmacy unless the pharmacist has specified otherwise: T (02) 9563 4900 I FREE CALL 1800 244 358 I F (02) 9563 4955 I FREE FAX 1800 626 739 [email protected] I www.webstercare.com.au © (06/06) Manrex Pty Ltd (ABN: 63 074 388 088) t/as Webstercare - 2014. Webstercare and W-Device are Registered Trade Marks of Manrex Pty Ltd t/as Webstercare. Pil-Kot is a Trade Mark of Manrex Pty Ltd t/as Webstercare. v 4.0 1 Pharmacy Board Australia Guidelines on Specialised Supply Arrangements: March 2012 *Sealing technique information is available from Webstercare. Webster-pak Community ® PACKING PROCEDURES 4 1 Align a sheet of lowtemp pre-cut foil over the back of the blister sheet. The foil should overlap the header card by approximately 1cm. Seal the foil to the blister sheet. Using the Webstercare® Medication Management Software (MMS), print the Webster-pak® Community header cards. 5 Place an empty blister sheet into a Blu-Lok™ platen. Fold the header card so the profile faces you and place it under the lip of the blister sheet. 3 The packing technician checks the sealed pack and signs the square ‘TECH’ box to confirm packing accuracy. 6 Product Code: s165 Pack the medications into the blister sheet as per the medication profile printed on the header card as a guide. Check for accuracy before sealing. The pharmacist checks the pack against the hard copy medication profile. After placing the sealed pack into a Webster-pak folder, the pharmacist signs the ‘PHARM’ box on the completed pack to confirm that it has been audited. T (02) 9563 4900 I FREE CALL 1800 244 358 I F (02) 9563 4955 I FREE FAX 1800 626 739 [email protected] I www.webstercare.com.au © (02/08) Manrex Pty Ltd (ABN: 63 074 388 088) t/as Webstercare - 2013. Webstercare, Webster-pak and W-Device are Registered Trade Marks of Manrex Pty Ltd t/as Webstercare. Blu-Lok and the QA Sig Box device are Trade Marks of Manrex Pty Ltd t/as Webstercare. V 2.0 2 ® Webstercare Sealing Techniques Some simple tips to ensure a great seal everytime Webstercare® low temp foil is specifically designed to seal at a low temperature. This ensures minimal heat, pressure and waiting time is required to form an effective seal. 1 2 3 4 5 6 7 Turn the iron on and adjust temperature to a mid range setting. The Webstercare Sealing Mouse™ is recommended for use or a ‘Dry Iron’ (non-steam iron). Place the blister sheet in the Blu-Lok™ platen and pack medication. Align the foil (shiny side down) against the back of the filled blister sheet, holding it in position. Press the Sealing Mouse or iron against the top right corner to secure the foil in position. Run the Sealing Mouse or iron in a sweeping motion across the foil backing making contact with all areas of the foil. Immediately after the foil has been warmed, apply light pressure to the foil by rubbing with a white board duster. If rubbing by hand, wait a few seconds for foil to cool to the touch. Remove the sealed pack from the platen and lay the pack blister face down. int Handy H en essure wh r p ly p p A aximise m o t g n li coo , r contact e t s li b / il fo eat n more h a h t r e h t ra ressure. and no p T (02) 9563 4900 I FREE CALL 1800 244 358 I F (02) 9563 4955 I FREE FAX 1800 626 739 [email protected] I www.webstercare.com.au © (06/10) Manrex Pty Ltd (ABN: 63 074 388 088) t/as Webstercare - 2014. Webstercare and the W Device are Registered Trade Marks of Manrex Pty Ltd t/as Webstercare. Blu-Lok and Sealing Mouse is a Trade Mark of Manrex Pty Ltd t/as Webstercare. V 2.0 Product Code: s189 If you have any questions please call our Customer Service Team Ph: 1800 244 358 Multi Dose Webster-pak ® CHECKING GUIDE All Webstercare® systems including Multi Dose Webster-pak have been designed with specific steps to follow in order to minimise the risk of human error. It is important that ALL steps are followed EVERY time a Webster-pak® is filled AND before it leaves the pharmacy. It is the pharmacist's responsibility to ensure that the medication packed is correct against the very latest instructions from the doctor. To support this process, Webstercare advises that a hard copy profile be generated and maintained.* 1 If printing for the first time, print a hard copy profile using MMS. Select ‘Patient Medication Record With Pill Images’. This is stored in a plastic sleeve in a folder with a copy of the prescriber’s original order to confirm its validity. 2 3c Confirm drug names and strengths in each blister from Mon-Sun for each meal time (column by column). Handy Hint: Check in reverse i.e. start from Bedtime working towards Breakfast. Working backwards breaks expected patterns and makes errors easier to detect. 3d Arrange Multi Dose packs to be checked on the left side of the checking area in a folder tray, with an empty folder tray on the right side of the checking area. 3a Confirm the following (3a-3e) are correct against the hard copy profile: Alternate-day doses schedule is correct as printed on the front of the header card. It is important to check the start date on the pack to confirm the correct week sequence. 3e Information on the header card and the start date are accurate. 3b 4 PRN Medication Regular 7 Day Medication Antibiotic & Short Term Warfarin Medication Special Dose Times & Before Meals Medication The pack is in the correct colour folder. Special Alert e.g. Accountable drugs, Cytotoxic The correct number of pieces are in each blister from top to bottom, this time from Breakfast to Bedtime. Again confirm the alternate dose schedule. After checking the pack the pharmacist initials the PHARM box printed on the header card. Place this pack backwards in the empty folder tray to your right to indicate the pack has been checked while maintaining the order of the packs. Regular 7 day Low Vision T (02) 9563 4900 I FREE CALL 1800 244 358 I F (02) 9563 4955 I FREE FAX 1800 626 739 [email protected] I www.webstercare.com.au © (07/14) Manrex Pty Ltd (ABN: 63 074 388 088) t/as Webstercare - 2015. Webstercare, Webster-pak and W-Device are Registered Trade Marks of Manrex Pty Ltd t/as Webstercare. The QA Sig Box Device is a Trade Mark of Manrex Pty Ltd t/as Webstercare. v 2.0 *See over page Hard Copy Profile HOW TO CREATE AND MAINTAIN A HARD COPY PROFILE For a new patient, confirm and enter the data from all original documentation which may include prescriptions etc. into Webstercare® Medication Management Software (MMS). Once the data entry is completed in MMS print a hard copy of the profile by selecting ‘Patient Medication Record With Pill Images’. The hard copy profile is confirmed by the pharmacist against the original documentation. This is to check the accuracy of the data entry and that the correct medication profile has been entered. If possible request the prescriber to ‘sign off’ the completed profile. This becomes the hard copy profile which is used to check the Webster-pak® system after packing is completed. The hard copy profile should be stored in a plastic sleeve in a folder with a copy of the prescriber’s original documentation, along with any previous versions of the hard copy profile to confirm its validity. As changes occur to the patient’s medication profile, they are hand-written on the hard copy profile. These are confirmed by a pharmacist and the client profile is updated in MMS. An updated copy is printed from MMS as needed. Store the previous version with all original documentation behind the latest copy. All printed copies of the hard copy profile need to be checked by the pharmacist. T (02) 9563 4900 I FREE CALL 1800 244 358 I F (02) 9563 4955 I FREE FAX 1800 626 739 [email protected] I www.webstercare.com.au v 1.0 If you require any further assistance with creating or maintaining a hard copy profile, please call Customer Service on free call 1800 244 358. Managing oral cytotoxic medicines in Webstercare® systems Cytotoxic medicines management guide Methotrexate and other oral chemotherapy medicines are “high risk” medicines1. Serious toxicities and fatal outcomes have occurred as a result of incorrect prescribing, dispensing and misinterpretation of instructions2. Cytotoxic medicines should be administered in a safe environment where all healthcare professionals follow principles of the same medication practice. The Guiding principles for medication management in residential aged care facilities3 recommends that residential aged care facility (RACF) organisations develop a specific policy for the safe management of cytotoxic medicines and contaminated waste. The following suggested precautions are for consideration when developing a cytotoxic policy. When cytotoxic medicines are prescribed · Verify dose regime. If there is any doubt about the prescribed dose seek clarification from the prescriber. · Do not use “as directed” instructions, even if the instructions are recorded elsewhere. Pharmacy and packing cytotoxic medicines · Specify the cytotoxic drug name, dose and frequency of administration to print on Webster-pak®, medication chart and signing sheet. · The Webstercare Medication Management Software(MMS) will alert pharmacy staff when methotrexate and cytotoxic medicines are entered into a patient’s profile: “ALERT: Special conditions apply. Check with pharmacist.” · Specify the day of the week and include the term “once a week” instructions for methotrexate and other once a week cytotoxic medicines. · For cyclic doses of cytotoxic medicines include start and stop dates. · Ensure pharmacy staff are not exposed to skin contact or dust inhalation from the cytotoxic medication when packing a Webster-pak. · Pack methotrexate and other cytotoxic medicines in a separate purple Webster-pak folder. · Add CYTOTOXIC alert label to the Webster-pak, medication chart and signing sheet to identify the medicine as cytotoxic. · Seal the Webster-pak containing cytotoxic medicine into the cytotoxic delivery bag. This is a precaution in case the packaging is damaged in transit. T (02) 9563 4900 I FREE CALL 1800 244 358 I F (02) 9563 4955 I FREE FAX 1800 626 739 [email protected] I www.webstercare.com.au v 1.0 Please see over for references. Managing oral cytotoxic medicines in Webstercare® systems Cytotoxic medicines management guide Administration of a cytotoxic from a Webster-pak · Train and assess RACF staff as competent in administration of cytotoxic medicines. · Use disposable protective gloves to avoid direct contact with cytotoxic medicines and avoid contamination with other medicines. Use a mask if there is a risk of inhaling cytotoxic aerosol or dust. · Remove medicine from the Webster-pak using a dedicated purple cytotoxic Pil-Bob®. · Transfer cytotoxic medicine to disposable medicine cups for administration to resident – do not re-use medicine cups for other residents. · If a tablet is damaged do not open the blister - contact the pharmacy for advice. · DO NOT CRUSH cytotoxic medicines. · If a medicine is spilt or dropped, do not pick it up with your hands. Use a cytotoxic spill kit if available. · All staff should be alerted that the medicine is cytotoxic. Women who are pregnant or of childbearing age and who might come into contact with cytotoxic medicines should contact their own GP for further advice. · Unused tablets must be returned to the supply pharmacy and not disposed of at the RACF. · Refer to your relevant state and territory Work, Health Safety legislation for further information. Contact Customer Service to request the cytotoxic support products brochure or place an order on Freecall 1800 244 358 or [email protected] References: Pharmacy Board of Australia Guidelines for dispensing medicines 2 Safe use of oral cytotoxic medicines; Australian Prescriber; Vol 36; Feb 13 3 Guiding principles for medication management in residential aged care facilities; Dept Health and Aging; Oct 12 T (02) 9563 4900 I FREE CALL 1800 244 358 I F (02) 9563 4955 I FREE FAX 1800 626 739 [email protected] I www.webstercare.com.au © (06/06) Manrex Pty Ltd (ABN: 63 074 388 088) t/as Webstercare - 2014. Webstercare, Webster-pak, Webstersystem and W-Device are Registered Trade Marks of Manrex Pty Ltd t/as Webstercare. v 1.0 1 VOLUME 36 : NUMBER 1 : february 2013 article Safe use of oral cytotoxic medicines SUMMARY All health professionals involved should: •• The oral route is increasingly used to administer cytotoxic therapy for cancer and non-cancer conditions. have appropriate training and skills in the use of cytotoxic chemotherapy and cancer care, when therapy is being used in this context7 •• Oral cytotoxic therapy carries the same risk of medication errors as parenteral therapy. seek advice from a practitioner experienced in cytotoxic chemotherapy when required •• follow the principles of safe medication practices for oral cytotoxic medicines. It is essential that health professionals involved in providing oral cytotoxic therapies understand how they are used, what adverse effects can occur and how to minimise medication errors. Introduction Oral administration of cytotoxic therapy has increased over the past decade as newer drugs and formulations have become available (see Table). Cytotoxic chemotherapy is not restricted to cancer. Conditions including rheumatoid arthritis, psoriasis and other autoimmune diseases may be managed using oral medicines such as methotrexate. The pros and cons of oral cytotoxic therapy The oral route offers many advantages over the parenteral route of administration. Medicines can be administered in the community, without the need for venous access, and fewer visits to the hospital are needed. While self-administration at home is convenient for both patients and carers, it can present a risk for the patient. Adverse effects can go undetected unless appropriate steps are in place to monitor the patient. Cytotoxic chemotherapy has a narrow therapeutic index and a small increase in dose can result in toxic effects, while under-dosing can lead to failure of therapy. Serious toxicities and fatal outcomes have occurred as a result of incorrect prescribing and dispensing as well as patient misinterpretation of dosing instructions.1-6 Responsibilities of the healthcare team The safe delivery of oral cytotoxic therapy requires a multidisciplinary approach. Patients may be managed under shared-care arrangements between hospital specialists, general practitioners and community pharmacies. All patients should have a treatment plan. This is completed by the specialist who initiates the treatment7 and should be given to the patient and all the healthcare professionals involved in their treatment. It is important that the patient has the plan with them if they see a different doctor, for instance in an emergency. Christine Carrington Senior consultant pharmacist Princess Alexandra Hospital Assistant pharmacy director Cancer Services Royal Brisbane and Women’s Hospital Brisbane Key words capecitabine, methotrexate Aust Prescr 2013;36:9–12 For the treatment plan to be useful, it should be explicit about: •• •• the patient’s diagnosis •• the expected number of cycles and the intended duration of treatment •• other adjuvant or concurrent treatments the patient is receiving (for example radiation therapy or surgery for cancer patients) •• expected adverse effects and their management. the name of the chemotherapy protocol or specific cytotoxic medicine Prescribing Prescriptions for oral cytotoxic therapy should be clear and unambiguous. The term ‘as directed’ must not be used regardless of how long the patient has been on the therapy. Table Oral cytotoxic medicines Drug class Drugs Alkylating agents busulfan, chlorambucil, cyclophosphamide*, lomustine, melphalan, procarbazine, temozolomide Anthracyclines idarubicin Antimetabolites capecitabine, fludarabine, hydroxyurea*, mercaptopurine*, methotrexate*, thioguanine Podophyllotoxins etoposide Vinca alkaloids vinorelbine * currently used for both cancer and non-cancer indications Full text free online at www.australianprescriber.com 9 VOLUME 36 : NUMBER 1 : february 2013 article Oral cytotoxic medicines •• the generic drug name, number of tablets to be taken7 and frequency and duration of therapy (written in full) issued within the Pharmaceutical Benefits Scheme regulations, the patient should be directed to destroy any repeats or return them to the prescriber if treatment is changed or stopped. •• whether the medicine is given on a cyclical or continuous basis. For example, capecitabine is frequently administered for 14 days of a 21-day cycle while temozolomide may be administered for 5 days of a 28-day cycle. The start and stop dates for a cycle should be clear. Patients should always be advised on the action to take should they experience an adverse event – for example severe diarrhoea with capecitabine requires immediate cessation of therapy. Patients should be given the name of an accessible healthcare contact they can speak to regarding any concerns. •• the day on which tablets should be taken. For example, methotrexate is most commonly given as a once-weekly dose (Box).8 Fatal errors have occurred when methotrexate has been prescribed to be taken daily or when the incorrect strength of tablets has been prescribed.9 Dispensing and supplying oral cytotoxic treatment Prescriptions should specify: Wherever possible the quantity prescribed should be the quantity needed for one cycle (cancer chemotherapy) or one month (for example methotrexate for rheumatoid arthritis). Preferably, repeat prescriptions should not be issued as doses may change according to adverse effects and therapeutic response. If a repeat prescription is Box Safe prescribing of weekly methotrexate 8 Provide the patient with verbal and written information on the intended schedule of therapy including the dose as a quantity of tablets and the frequency of dosing Ensure handwritten prescriptions are complete and legible and include in full the form, strength, dose and directions Nominate on the prescription the day on which the dose should be taken Do not write ‘as directed’ on the prescription Consider limiting the prescribed quantity of methotrexate to four weeks Do not override warnings and flags for methotrexate in prescribing software Keep the strength of tablet supplied to the patient consistent to avoid confusion for the patient over the number of tablets they need to take Be aware of signs of methotrexate toxicity or intolerance, for example dry persistent cough, vomiting and diarrhoea Patients should be advised to contact their doctor or pharmacist straight away if a dose is missed, or they develop an infection such as gastroenteritis or fever If a patient is admitted to hospital, strike out the six days of the week when methotrexate is NOT required in the administration section of the inpatient medication chart 10 Full text free online at www.australianprescriber.com The dispensing of oral cytotoxic therapy includes verification of the prescription for the patient and their condition, and appropriate supply in a safe and timely manner.7 For cancer chemotherapy the pharmacist should have access to the treatment plan, the chemotherapy protocol and relevant patient parameters including height and weight and recent laboratory results.10 The pharmacist should ensure that the relevant supportive medicine has been prescribed or is available to the patient. Interactions between chemotherapy, other prescribed drugs, and over-the-counter and complementary medicines can cause changes in the efficacy and safety of oral chemotherapy.11 For example, analgesic doses of aspirin and non-steroidal anti-inflammatory drugs can increase the toxicity of methotrexate when they are used with cancer therapy. Low-dose aspirin can be used with weekly methotrexate. The risk associated with lower doses of methotrexate used in rheumatoid arthritis therapy is much less. Conversely cytotoxic chemotherapy can alter the effectiveness of other drugs. For example, capecitabine significantly reduces the metabolism of warfarin, increasing its anticoagulant effect. A complete medication history should be taken from the patient or carer before dispensing a prescription and potential interactions should be discussed. If a dose administration aid (for example a Websterpak) is required by the patient, then oral cytotoxics must be packed separately from the patient’s noncytotoxic medicines. Medicine labelling The labelling of oral cytotoxic therapy should clearly state the dose and the number of tablets to be taken. The label for weekly dosing for medicines such as methotrexate and vinorelbine should include the term ‘once a week’ and specify the day the dose should be taken. Cytotoxic chemotherapy can be carcinogenic, mutagenic and teratogenic. A warning sticker should be placed on all containers of cytotoxic chemotherapy tablets and capsules, in accordance with local health VOLUME 36 : NUMBER 1 : february 2013 article and safety policy. An adhesive purple sticker with the wording ‘cytotoxic, handle with care’ is recommended. A warning label must be placed on administration aid packs that identify the contents as cytotoxic. Oral cytotoxic tablets and capsules should not be broken or crushed as this can increase the risk of exposure and alter the bioavailability of the medicine. Information for the patient Patient information is paramount to support the safe use of oral cytotoxic therapy. Patients should be given verbal and written information that includes dose instructions (when the medicine should be taken and if it is required to be taken before or after food), adverse effects and safe storage instructions.7,12 Some oral cytotoxic medicines need to be stored securely in a refrigerator, for example chlorambucil and melphalan. Patients should be advised that oral cytotoxic medicine should only be taken out of the dispensed packaging immediately before a dose. To minimise exposure of carers and family members to cytotoxic medicines, patients should be advised that selfadministration is preferable. If administration by a carer is required then disposable gloves should be worn. Unused tablets must be returned to the local pharmacy or original supplier and not disposed of at home. The intermittent, cyclical treatment that is characteristic of many cancer chemotherapy protocols is difficult for some patients to understand and they may misinterpret instructions. Medication guides, patient calendars and dose administration aids are often useful to help patients follow complex dose regimens, particularly those on multiple medicines. Adherence to oral therapy is important to maximise the benefits and reduce the risks of treatment. This should be discussed with the patient. If appropriate, Consumer Medicine Information leaflets should be given to patients, however the context in which cytotoxic chemotherapy is used often limits their suitability. Patient information leaflets on many of the commonly used cancer chemotherapy protocols can be found on the eviQ Cancer Treatments Online website.13 This website also provides information about how to safely take oral chemotherapy treatments at home.* The Australian Rheumatology Association provides patient information on drugs such as methotrexate and cyclophosphamide.8 * www.eviq.org.au/Protocol/tabid/66/ categoryid/449/id/492/Patient+Information++Oral+Chemotherapy.aspx Patients should be advised of the importance of notifying dentists, doctors and other healthcare professionals who may be involved in their care about their cytotoxic therapy. Identifying and managing adverse effects Cytotoxic chemotherapy causes many adverse effects such as nausea, vomiting, bone marrow suppression, stomatitis, diarrhoea, hand-foot syndrome, peripheral and central neurotoxicity, renal and liver dysfunction and hair loss. The effects require careful monitoring, and supportive therapies Patient information is may be needed to minimise them. paramount to support Antiemetics should be prescribed the safe use of oral according to the emetogenic potential 14 of the chemotherapy. Nausea and cytotoxic therapy vomiting can continue for several days after a dose of chemotherapy and the duration of antiemetic therapy should take this into consideration. Guidelines exist for prescribing antiemetics with cancer chemotherapy.15,16 Blood counts need to be frequently checked with cytotoxic therapy. Patient monitoring, including laboratory tests and the parameters for initiating the next cycle of chemotherapy, should be clearly defined in the protocol or treatment plan. For example, a neutrophil count of greater than 1 x 109 is usually required for a cycle of cancer chemotherapy to proceed. Particular care should be taken with patients when the cytotoxic therapy is taken continuously, for example cyclophosphamide or chlorambucil, as severe myelosuppression can develop. Cytotoxic chemotherapy can adversely affect liver and renal function and these should be monitored before each course of therapy. Live vaccines are contraindicated in patients with impaired immune function which includes those receiving oral cytotoxic therapy. These vaccinations should usually be delayed until at least six months after the completion of any chemotherapy. Inactivated vaccines are generally safe, but patients may have a diminished immune response to the vaccine. The influenza vaccine should be administered before each influenza season and pneumococcal vaccine should be considered before starting therapy. Recommendations Despite the convenience that oral cytotoxic therapy offers, it carries the same risk of medication errors and adverse effects as parenteral therapy. Oral Full text free online at www.australianprescriber.com 11 VOLUME 36 : NUMBER 1 : february 2013 Oral cytotoxic medicines article cytotoxic medicines have a narrow therapeutic index and monitoring the patient for safety and efficacy is essential. Written and verbal communication with patients and carers is critical for the safe and appropriate use of cytotoxic therapy. If a patient unknown to the prescriber, pharmacist or healthcare professional presents for oral cytotoxic therapy, the risk of continuing therapy should be balanced against the risk of stopping therapy until a full history and safety checks are done. In many cases delaying therapy for a short time while a full patient review is conducted and laboratory counts are obtained is safer than continuing therapy. Dr Carrington served on advisory boards for Amgen and Merck Sharp & Dohme and has received honoraria from Roche and Merck Sharp & Dohme for educational presentations. References 1. 2. 3. 4. 5. 6. 7. 8. The Institute for Safe Medication Practices. Lowdown on lomustine: we’d hate CeeNU make this mistake. ISMP Safety Alert; 2004 Jul 15. www.ismp.org/Newsletters/acutecare/articles/20040715. asp [cited 2013 Jan 7] Holquist C, Phillips J. FDA Safety Page: fatal medication errors associated with Temodar. Drug Topics 2003;7:42. http://drugtopics.modernmedicine.com/drugtopics/ DrugInformation/ArticleStandard/article/detail/110864 [cited 2013 Jan 7] NHS National Patient Safety Agency UK. Rapid Response Report: risks of incorrect dosing of oral anti-cancer medicines. 2008 Jan 22:NPSA/2008/RRR001. www.nrls.npsa.nhs.uk/resources/?entryid45=59880 [cited 2013 Jan 7] Weingart SN, Spencer J, Buia S, Duncombe D, Singh P, Gadkari M, et al. Medication safety of five oral chemotherapies: a proactive risk assessment. J Oncol Pract 2011;7:2-6. Arnet I, Bernhardt V, Hersberger KE. Methotrexate intoxication: the Pharmaceutical Care process reveals a critical error. J Clin Pharm Ther 2012;37:242-4. Department of Health Victoria. Quality use of medicines notice: Caution with oral chemotherapy for cancer. 2010. www.safetyandquality.gov.au/wp-content/ uploads/2012/02/Oral-for-health-services-VictorianDepartment-of-Health.pdf [cited 2013 Jan 8] Carrington C, Stone L, Koczwara B, Searle C, Siderov J, Stevenson B, et al. The Clinical Oncological Society of Australia (COSA) guidelines for the safe prescribing, dispensing and administration of cancer chemotherapy. Asia Pac J Clin Oncol 2010;6:220-37. Australian Rheumatology Association. Patient Information. 2012. www.rheumatology.org.au/community/ PatientMedicineInformation.asp [cited 2013 Jan 7] 9. NHS National Patient Safety Agency UK. Improving compliance with oral methotrexate guidelines. 2006. NPSA/2006/13. www.nrls.npsa.nhs.uk/resources/healthcare-setting/ community-hospital/?entryid45=59800&cord=ASC [cited 2013 Jan 7] 10. Carrington C, Gilbar P, Wintraeken J; The Society of Hospital Pharmacists of Australia Committee of Specialty Practice in Cancer Services. Standards of practice for the provision of pharmaceutical care of patients receiving oral chemotherapy for the treatment of cancer. J Pharm Pract Res 2007;37:149-52. 11. Goodin S. Oral chemotherapeutic agents: understanding mechanisms of action and drug interactions. Am J Health Syst Pharm 2007;64 Suppl 5:S15-24. 12. Viele CS. Managing oral chemotherapy: the healthcare practitioner’s role. Am J Health Syst Pharm 2007;64 Suppl 5:S25-32. 13. Cancer Institute NSW. EviQ Cancer Treatments Online [website]. www.eviq.org.au [cited 2013 Jan 7] 14. Grunberg SM, Osoba D, Hesketh PJ, Gralla RJ, Borjeson S, Rapoport BL, et al. Evaluation of new antiemetic agents and definition of antineoplastic agent emetogenicity–an update. Support Care Cancer 2005;13:80-4. 15. Roila F, Herrstedt J, Gralla RJ, Tonato M. Prevention of chemotherapy- and radiotherapy-induced nausea and vomiting: guideline update and results of the Perugia consensus conference. Support Care Cancer 2011;19 Suppl 1:S63-5. 16. Basch E, Prestrud AA, Hesketh PJ, Kris MG, Feyer PC, Somerfield MR, et al. Antiemetics: American Society of Clinical Oncology clinical practice guideline update. J Clin Oncol 2011;29:4189-98. FURTHER READING Risks associated with prescribing oral methotrexate [media release]. NPS MedicineWise. 2011 Dec 20. www.nps.org.au/media-centre/media-releases/repository/ health-professionals-alert-to-the-risks-associated-with-oralmethotrexate [cited 2013 Jan 7] Dental note Safe use of oral cytotoxic drugs Michael McCullough Chair Therapeutics Committee Australian Dental Association 12 The increasing use of oral cytotoxic drugs for non-oncological diseases has resulted in an increased likelihood that dental patients will be taking them. The oral mucosa has a very high cell turnover rate and these drugs will invariably result in thinning of the mucosa, and often, concurrent salivary hypofunction. Full text free online at www.australianprescriber.com These patients are likely to require increased care and, if they have complex dental treatment needs, may require specialist management. Good communication with the treating doctors and appropriate referral where necessary will significantly help these patients.
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