Microsoft word - edwards palliative care nurse practitioner formulary v6
Palliative Care Nurse Practitioner Sydney Adventist Hospital
DRUG FORMULARY for JULIE EDWARDS
Palliative Care Nurse Practitioner
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The formulary provides for the poisons and restricted substances that may be possessed, used, supplied or prescribed by JULIE EDWARDS as a Nurse
Practitioner under Section 17A of the Poisons and Therapeutic Goods Act 1966 (1) and the Poisons and Therapeutics Goods Regulation 2008 (2) It is the
Nurse Practitioners responsibility to use this formulary in conjunction with the most recent MIMS/MIMS Online (3), Australian Medicines Handbook (4) and
Therapeutic Guidelines: Palliative Care (5).
Any alteration must be submitted to the Chief Nursing and Midwifery Officer (CNMO) NSW for approval. This document is invalid if any alterations or
amendments are made without the approval from the CNMO NSW.
Introduction: The Palliative Care Nurse Practitioner (PCNP):
Has the authority to prescribe, administer, use, supply and possess medications detailed in this PCNP Drug Formulary.
Will utilise the most recent and appropriate resources to obtain information on compatibilities of drugs used in continuous subcutaneous infusions.
May prescribe end of life medications on the community medication chart prior to discharge, for patients returning home, after consultation with and approval from the patients treating specialist.
May convert routes of administration
Will document in the medical records whenever a medication change is made. A physical assessment will be included as part of the documentation process.
Will seek advice from the palliative care consultant to discuss appropriate management for complex patients and for those patients not responding as expected to treatment changes.
Acknowledgement:This Formulary has been adapted from previous work developed by Judith Jacques - Nurse Practitioner Palliative Care - CCLHD;
Pauline Davis – Nurse Practitioner Palliative Care SWSLHD;Debbie White – Nurse Practitioner Palliative Care MNCLHD; Pauline Wilson - Palliative Care
Nurse Practitioner SWCN.
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Dosages are in accordance with the Therapeutic Guidelines Palliative Care and Australian Medicines Handbook.
PO = Oral; SL = Sublingual; SC = Subcutaneous; IM = Intramuscular; IV = Intravenous; PR = Per Rectum; TOP = Topical.
Drug (Generic name)
Therapeutic Class
Clinical Presentation
Schedule
Analgesia
Non-opioid
Simple analgesic
Simple analgesic
1. Mild to moderate pain
2. Osteoarthritis
(modified release 665mg)
Simple analgesic
1. Mild to moderate pain (when oral route not available)
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Drug (Generic name)
Therapeutic Class
Clinical Presentation
Schedule
Analgesia
Paracetamol/Codeine
Combination Simple Analgesic
Mild to moderate pain
Paracetamol/Codeine
Opioid analgesic
Moderate – Severe Pain
Opioid Analgesic
Moderate – severe breakthrough pain
Various strengths
Opioid Analgesic
Transdermal Patch
Patient education on placement and changing of patch.
Various strengths
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Drug (Generic name)
Therapeutic Class
Clinical Presentation
Schedule
Opioid Analgesic
2. Breakthrough pain
Opioid Analgesic
Sustained release tablet
Opioid Analgesic
2. Breakthrough pain
3.Pain management; end of life care
Opioid Analgesic
1. Moderate to severe pain
(Immediate Release)
2. Breakthrough pain
Opioid Analgesic
1. Moderate to severe pain
(Sustained Release)
Tablet / Granules
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Drug (Generic name)
Therapeutic Class
Clinical Presentation
Schedule
Morphine Sulphate
Opioid Analgesic
1.Moderate to severe pain
2. Breakthrough pain
Morphine Tartrate Injection
Opioid Analgesic
1. Moderate to severe pain
2. Breakthrough pain
Opioid Analgesic
1. Painful wound
Infused hydrogel
2. Painful pressure area
Opioid Analgesic
1. Moderate to severe pain
IR (immediate release)
2. Breakthrough pain
Tablet / capsule/ liquid
Various strengths
Opioid Analgesic
Moderate to severe pain
SR (sustained release)
Various strengths
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Drug (Generic name)
Therapeutic Class
Clinical Presentation
Schedule
Oxycodone hydrochloride
Opioid Analgesic
Moderate to severe pain
and naloxone hydrochloride dehydrate (Targin)
Various strengths
Opioid Antagonist
Opioid Antagonist
Reversal of opioid overdose; opioid induced respiratory S4 depression: respirations < 8 min
NB: Before use consider other causes of sedation or delirium (eg: sepsis) (American Pain Society)
Oral/oesophageal candidiasis
Systemic candidiasis
Miconazole 20mg/ ml
Oropharyngeal candidiasis
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Drug (Generic name)
Therapeutic Class
Clinical Presentation
Schedule
Nystatin 100,000 units/ml
Oral / oesophageal candidiasis
Sodium Bicarbonate
Oral candidiasis
Sodium Hyaluronate Gel
oral lesions, oral mucositis/stomatitis
Vulvovaginal candidiasis
Fungal infections, dermatitis
Hydrocortisone 1%
Metronidazole Gel
Malodorous malignant wounds
Exacerbation chronic bronchitis; pneumonia; sinusitis
Capsule, suspension
Amoxycillin with Clavulanic PO
URTI; Pneumonia, sinusitis,
Tablet; suspension
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Drug (Generic name)
Therapeutic Class
Clinical Presentation
Schedule
Staphylococcal and streptococcal infection in people S4 with mild – moderate penicillin allergy
Capsule; suspension
Moderate Spectrum
Systemic management of malignant malodorous S4 wounds
Tablet / suspension
Upper and lower respiratory tract infection
Acute uncomplicated urinary tract infection.
1. Patients not responding or unlikely to respond to S4 Hyoscine; for management of respiratory secretions in
the terminal phase.
2. Management of respiratory secretions in conscious and alert patients.
3. Management of drooling in MND patients
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Drug (Generic name)
Therapeutic Class
Clinical Presentation
Schedule
HyoscineButylbromide
Antispasmodic Anticholinergic
1. Management of respiratory secretions in the S4 conscious patient.
2. Management of painful colic in malignant bowel
3. Reduction of gastric secretions
HyoscineHydrobromide
Management of terminal respiratory secretions
Diphenoxylate 2.5 mg
Atropine Sulphate 25mcg
Antiemetics
Nausea and Vomiting
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Drug (Generic name)
Therapeutic Class
Clinical Presentation
Schedule
Nausea and vomiting
Tablet / Injection
Nausea and vomiting
Nausea and vomiting
Tablet / Injection
Anticipatory Nausea and vomiting
Antipsychotic, antiemetic
1. Nausea and Vomiting
2. Terminal agitation
1. Nausea and vomiting
Tablet / Injection
2. Persistent hiccups
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Drug (Generic name)
Therapeutic Class
Clinical Presentation
Schedule
Prochlorperazine
Nausea and vomiting
Tablet / Suppositories
2. Nausea and vomiting
Steroidal
1. Pain associated with tumour related oedema
2. Cerebral Oedema
3. Spinal cord compression
4. Superior vena cava obstruction
5. Acute airways obstruction / dyspnoea
6. Malignancy related gastrointestinal obstruction
7. Appetite stimulant and feeling of well being
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Drug (Generic name)
Therapeutic Class
Clinical Presentation
Schedule
1. Airways obstruction / dyspnoea
2. Inflammatory disease
3. Appetite stimulate
Anti-inflammatory Non
steroidal
Non-steroidal anti-inflammatory
Selective COX-2 Inhibitor
nausea and vomiting
Non-steroidal anti-inflammatory
Non-steroidal anti-inflammatory
Non-steroidal anti-inflammatory
2. Co-analgesic.
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Drug (Generic name)
Therapeutic Class
Clinical Presentation
Schedule
Non-steroidal anti-inflammatory
Always cover with PPI. Avoid if renal impairment, peptic ulcer, oesophagitis, GORD
Non-steroidal anti-inflammatory
Non-steroidal anti-inflammatory
Pain – co-analgesic
Related to inflammation, bony pain
Tablet / Injection
Hyoscinebutylbromide
Antispasmodic and motility agent
Colic related to bowel obstruction
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Drug (Generic name)
Therapeutic Class
Clinical Presentation
Schedule
Hyoscinebutylbromide
Antispasmodic and motility agent
Colic related to bowel obstruction
Anxiolytics
Anxiety or panic associated with dyspnoea
Anticipatory nausea
Liquid/ injectable
3. Seizure – prophylactic and acute treatment
4. Terminal agitation
2. Pain associated with skeletal muscle spasm
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Drug (Generic name)
Therapeutic Class
Clinical Presentation
Schedule
1. Anxiety or panic associated with dyspnoea
2. Agitation related to delirium not responding to Haloperidol alone
1. Terminal restlessness
4. Agitation related to delirium
5. Sudden catastrophic event
Laxatives
Always prescribed with Opioids
Prophylaxis and Treatment of Constipation
Soft faeces on rectal examination not responding to oral laxatives
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Drug (Generic name)
Therapeutic Class
Clinical Presentation
Schedule
Docusate + sennoside B PO
Softener+ stimulant
(Coloxyl with Senna) Tablet
Hard faeces on rectal examination
Macrogol 3350, Potassium PO
Polyethylene glycol
2. Faecal Impaction
(Movicol) Powder
2. Faecal impaction
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Drug (Generic name)
Therapeutic Class
Clinical Presentation
Schedule
Methylnaltrexone
Opioid induced constipation that has not responded to S4 other laxatives
citrate 450mg, sodium lauryl sulfoacetate
2. Faecal impaction
Sodium Phosphate
Constipation unresponsive to other treatments
(Fleet ready-to-use enema)
Neuropathic Agents
1. Refractory neuropathic pain
2. Uraemic pruritus 2° to renal failure
3. Restless legs syndrome 2° to renal failure
Neuropathic Pain
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Drug (Generic name)
Therapeutic Class
Clinical Presentation
Schedule
Neuropathic pain
Sodium Valproate
Neuropathic Pain
Protein-pump inhibitors
Proton Pump Inhibitor
1. Gastro-oesophageal reflux disease
Tablet/ Injection
2. Protection from gastrointestinal irritation from anti-inflammatory medication
Proton Pump Inhibitor
1. Gastro-oesophageal reflux disease
Tablet/ Injection
2. Protection from gastrointestinal irritation from anti-
inflammatory medication
Proton Pump Inhibitor
1. Gastro-oesophageal reflux disease
Tablet/ Injection
2. Protection from gastrointestinal irritation from anti-inflammatory medication
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Drug (Generic name)
Therapeutic Class
Clinical Presentation
Schedule
Skeletal muscle relaxant
1.Pain associated with skeletal muscle spasm – S4 particularly in MND
Normal Saline 0.9%
2. Comfort measures
Normal Saline 0.9%
2. Physiological K+ replacement
Dyspnoea, breathlessness
Antifibrinolytic
1. Profuse bleeding from malignant wound
2. Haemoptysis; vaginal or rectal bleeding secondary to local tumour invasion
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1. Patients in the terminal phase of their disease will have the reduced ability or inability to swallow medications. The Palliative Care Nurse Practitioner will reduce or cease oral medications and change to an alternate route as appropriate. This process is undertaken in an informative, collaborative manner with the patient, family, carers and the treating Medical Practitioner(s). The same approach will also be taken for the cessation of artificial nutrition and/or hydration.
References:
1. Poisons and Therapeutic Goods Act (1966) Section 17A http://www.austlii.edu.au/au/legis/nsw/consol_act/patga1966307/
2. Poisons and Therapeutic Regulation (2008) http://www.legislation.nsw.gov.au/sessionalview/sessional/sr/2008-392.pdf
3. MIMS Online: http://proxy36.use.hcn.com.au/Search/Search.aspx
4. Australian Medicines Handbook (2011) AMH Adelaide
5. Therapeutics Guidelines, Palliative Care Version 3 (2010)
eviQ Opioid Calculator https://www.eviq.org.au/OpioidCalculator.aspx
Therapeutic Guidelines, Analgesia Version 5 (2007)
Therapeutic Guidelines, Psychotropic Version 6 (2008)
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Available Opioid Formulations and Equivalency
The following is a list of the currently available opioid formulations in Australia. Preparations are available as immediate release or as modified released formulations.
Modified-release formulations should never be crushed or chewed, as this destroys their release properties and can result in a large dose being absorbed over a short period.
Please note that all conversions listed are a
guide only and may vary according to the clinical situation, condition of the patient and previous analgesic
requirements.
Trade name
Release Rate
Formulation
Oral morphine (PO) equivalent dose*
5, 10 and 20 mcg/hr transdermal (TD)
50 mg PO morphine = 20 mcg TD patch
7.5 mg PO morphine = 60 mg PO codeine
Codeine/Paracetamol Immediate
30/500 mg tablets
2 tablets = 7.5 mg PO morphine
eg.Panadeine Forte®**
Codeine/Paracetamol Immediate
8/500 mg tablets
2 tablets = 2 mg PO morphine
eg.Panadeine®**
Conversions from transdermal fentanyl to
12, 25, 50, 75 and 100 mcg/hr
other opioids are imprecise and poorly
transdermal (TD) patch
studied. The calculator uses conversion
figures provided by the manufacturer.
50 mcg/ml injection
25 mg PO morphine= 100 mcg fentanyl
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2, 4 and 8 mg tablets
10 mg PO morphine = 1.67 mg PO Dilaudid
1 mg/ml oral liquid
10 mg PO morphine = 1.67 mg PO Dilaudid
2 mg/ml and 10 mg/ml injection
20 mg PO morphine = 1 mg IV Dilaudid
10 mg/ml injection
20 mg PO morphine= 1 mg IV Dilaudid
4, 8, 16, 32 and 64 mg tablets
4 mg PO Jurnista = 24 mg PO morphine
10 and 20 mg tablets
Direct equivalent
Direct equivalent
1mg, 2mg, 5mg and 10mg/ml oral
Direct equivalent
10, 20, 50 and 100 mg capsules
Direct equivalent
10, 30, 60, 100 mg tablets
Direct equivalent
30, 60, 90 and 120 mg capsules
Direct equivalent
20, 30, 60, 100 and 200 mg sachets
Direct equivalent
5, 10, 15, 30, 60, 100 and 200 mg
Direct equivalent
Morphine sulfate
5, 10, 15, 30 mg/ml injection
25 mg PO morphine = 10 mg IV morphine
Morphine tartrate
80 mg/ml injection
25 mg PO morphine = 10 mg IV morphine
15 mg PO morphine = 10 mg PO Endone
5, 10, and 15 mg capsules
15 mg PO morphine = 10 mg PO OxyNorm
1 mg/ml oral solution
5, 10, 15, 20, 30, 40 and 80 mg
15 mg PO morphine = 10 mg PO OxyContin
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10 mg/ml and 20 mg/2ml injection
20 mg PO morphine = 8 mg IV OxyNorm
10 mg PO morphine = 50 mg PO Tramadol
50 mg/ml injection
10 mg PO morphine = 50 mg PO Tramadol
Tramal SR® Zydol®
50, 100, 150 and 200 mg tablets
10 mg PO morphine = 50 mg PO Tramadol
100, 200 and 300 mg tablets
10 mg PO morphine = 50 mg PO Tramadol
* Based on the conversions used in the eviQ Opioid Calculator
** Combination products are not in the eviQ calculator as there is no conclusive evidence that combination analgesics containing lower doses of codeine with paracetamol, aspirin or ibuprofen have any benefits over these non-opioids alone.
*** The safety and efficacy of Jurnista in children and adolescents under the age of 18 has not been established. Until further experience is gained, Jurnista must not be used in this population
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CONVERSION OF MORPHINE Q4H TO A FENTANYL PATCH
Oral morphine range q4h
Fentanyl dose mcg/hr
• Ensure patch is calculated using q4h morphine dose To determine the appropriate Fentanyl patch, divide the 24hr oral dose by 3
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NURSE PRACTITIONER FORMULARY ENDORSEMENT:
Approved By:
Name
Nursing Council Chairperson
Pharmacy and Drug
Dr Jeanette Conley
Committee Chairperson
Palliative Care Specialist
Dr Gillian Rothwell
(Collaborative arrangement)
Medical Advisory Committee
Executive Committee
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Source: http://www.sah.org.au/assets/files/PDFs/Nurse%20Practioners/EDWARDS%20Palliative%20Care%20Nurse%20Practitioner%20formulary%20v6%201.pdf
Viterol.A (viatrozene gel) 16% and patients with sunburn should beadvised not to use the product until ful y recovered. • Weather extremes, such as wind or cold, also may be irritating to patients under treatment with Viterol.A. Drug Interactions: Concomitant use of potential y irritating topical products (medicated or abrasive soaps and cleansers, soaps and cosmetics that have a strong drying ef ect, and products with high concentrations of alcohol, astringents, spices, or lime) should be approached with caution. Particular caution should be exercised in using preparations containing sulfur, resorcinol, or salicylic acid in combination with Viterol.A.
Heteronormativity in Action: Reproducing the Heterosexual Nuclear Family in After-hours Medical Calls CELIA KITZINGER, University of York Heterosexism has become a recognized social problem since the rise of lesbian, gay, bisexual, and transgen- dered (LGBT) activism in the 1970s. One of its manifestations is heteronormativity: the mundane production ofheterosexuality as the normal, natural, taken-for-granted sexuality. My research uses conversation analysis toexplore heteronormativity as an ongoing, situated, practical accomplishment by people oriented to other actionsentirely. I show that family reference terms—across a dataset of 59 after-hours calls to the doctor—are deployedso as to construct a normative version of the heterosexual nuclear family: a married couple, co-resident with theirbiological, dependent children. I examine the inferences normatively attached to family reference terms, considerhow these inferences are used interactionally, and document how this everyday talk-in-interaction both reflectsand reconstitutes the culturally normative definition of the family. This research advances our understanding ofnormativity by showing how a social problem can exist even when there is no orientation to "trouble" in inter-action. Here, the persistent and untroubled reproduction of a taken-for-granted heteronormative world bothreflects heterosexual privilege and (by extrapolation) perpetuates the oppression of non-heterosexual people,denied access to key social institutions such as marriage and unable to take for granted access to their culture'sfamily reference terms. The article shows how the heteronormative social order is reproduced at the level of mun-dane social interaction, through the everyday conversational practices of ordinary folk.