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GUIDELINES AND AUDIT IMPLEMENTATION NETWORK General Palliative Care Guidelines The Management of Pain at the End Of Life November 2010

Aim To provide a user friendly, evidence based guide for the management of pain at the end of life in adult patients with advanced life limiting conditions

Pain An unpleasant sensory and emotional experience associated with actual or potential tissue damage, or described in terms of such damage. International Association of Pain 1986 An experience that affects, and is affected by, both the mind and the body. It involves the perception of a painful stimulus by the nervous system and the reaction of a person to this. Stannard and Booth 2004

Definitions and Terminology Acute pain Pain with well defined onset Associated with subjective and objective physical signs and with hyperactivity of the autonomic nervous system Usually responds to analgesic drug therapy and treatment of its underlying cause.

Definitions and Terminology Chronic pain Persists over weeks or months May be associated with significant changes in lifestyle, functional ability and personality Requires careful assessment, not only of the nature and intensity of pain, but also of the degree of psychological distress Management is challenging

Impact of acute and chronic pain ACUTE PAIN CHRONIC PAIN Meaningful Defined Onset Usually single pain Easy to describe Clinical signs of pain evident (tachycardia, sweating, rapid respirations) Pain behaviour apparent e.g. crying out, moaning, rubbing, rocking, protecting painful area Meaningless Often gradual onset May be multiple pains Difficult to describe Clinical signs of pain not maintained over time May not demonstrate overt pain behaviour but may become withdrawn, depressed and hopeless

Types of Pain- Nociceptive Pain Somatic pain Visceral pain

Types of Pain- Neuropathic Pain Differentiation pain Central pain Sympathetic-maintained pain Complex regional pain syndrome (CRPS) Referred pain

Patterns of Pain Background pain Breakthrough pain Incident pain Idiopathic/ spontaneous pain Total pain

Principles of Pain Management An understanding that pain is a subjective experience Aetiology should be considered to optimise pain management Comprehensive, individualised and holistic assessment and treatment planning Regular review and reassessment with involvement of the wider multiprofessional team as appropriate Patient and carer involvement

Principles of Pain Management Treatment should start at the level of the World Health Organisation (WHO) analgesic ladder appropriate for the severity of the pain Oral analgesia should be the preferred form of medication delivery Morphine is currently considered to be the strong opioid of choice Analgesia for continuous pain should be prescribed on a regular basis, and also prescribed as needed for "breakthrough pain" in appropriate dosages Adjuvant analgesics should be considered where appropriate as per WHO ladder.

Assessment of Pain Dimensions of Pain can be classified under the following headings Physical Psychosocial Spiritual

Pain Assessment A detailed pain assessment should include Clinical History Physical examination Identification of likely cause of pain and classify the type of pain Arrangement for appropriate diagnostic investigations Arrangement for multidisciplinary professional assessment Regular Review to determine effectiveness of treatment

Pain Assessment No universally accepted tool for the assessment of pain although there are many different pain assessment tools available

General Principles of Analgesic Prescribing By the mouth By the clock By the ladder (see WHO Ladder) Individual dose titration Use of adjuvants Attention to detail

WHO Analgesic Ladder Pain persists or increases Step Opioid for moderate to severe pain ± non-opioid ± adjuvant analgesic Step Opioid for mild to moderate pain ± non-opioid ± adjuvant analgesic Non-opioid ± adjuvant analgesic Step Ref: GAIN guidelines (2010)

WHO Analgesic Ladder (contd) Step 1: Drug Options - Non-Opioid +/- Adjuvants Paracetamol 1 g QDS Non-Steroidal anti-inflammatory drugs (NSAIDS) Step 2: Drug Options-Opioid for mild to moderate pain + Non-Opioid +/- Adjuvants Co-codamol (30/500 max 8 tablets in 24 hrs) Tramadol- up to 400mg/24hrs

WHO Analgesic Ladder (contd) Step 3: Drug Options-Opioid for moderate to severe pain + Non Opoid +/- Adjuvants Oral 1 st line Morphine Oral 2 nd Line Oxycodone Subcutaneous opioid 1 st Line Diamorphine/morphine 2 nd Line Oxycoden

Opioid Choice The decision to use a specific opioid preparation should be based on a combination of factors: pain characteristics the product characteristics the patient s previous response to opioids the patient s preference It is extremely unlikely that any one opioid preparation will be suitable for all patients with breakthrough pain.

Opioid Routes Oral Parenteral Transdermal

First Line- Oral Strong Opioids First Line- Morphine Sulphate Opioid with most evidence supporting its use and is therefore considered the first line oral strong opioid when renal and hepatic function is normal Morphine is available in a variety of formulations

First Line- Oral Strong Opioids Two commonly used approaches to initiating opioid therapy - Using immediate release (short-acting) morphine (preferred option) or - Using modified and immediate release morphine (alternative option)

Second Line- Oral Strong Opioids Alternative opioids may be considered if a patient develops intolerable adverse effects with their current opioid without achieving adequate pain relief This decision is optimally made in conjunction with a specialist in palliative medicine Where this is not possible the opioid conversion tables can be used to calculate the dose of an alternative opioid. Equi-analgesic doses can only be taken as an approximate guide when switching patients from one opioid to another and careful clinical observation is required when changing between opioids. Caution- consider dose reduction for first 12-24 hours of alternative opioid, especially when converting between high doses.

Approximate Equivalent Doses of Opioid Analgesic for Adults Caution should be used when converting opioids in opposite directions as potency ratios may be different Where there is no direct conversion between opioids,it is conventional practice to use Oral Morphine equivalents ALWAYS REVIEW PATIENT REGULARLY AFTER ANY OPIOID SWITCH AS CONVERSION RATIOS ARE APPROXIMATE AND CONSIDERABLE INTER- PATIENT VARIATION MAY OCCUR.

Approximate Equivalent Doses of Opioid Analgesic for Adults- Guiding Principles Suggested current practice guidelines are: Oral Morphine to Subcutaneous (SC) Diamorphine Divide by 3 Oral Morphine to Oral Oxycodone Divide by 2 Oral Morphine to SC Morphine- Divide by 2 Oral Morphine to Oral Hydromorphine Divide by 7.5 Oral Oxycodone to SC Oxycodone- Divide by 2 (Suggested safe practice) Oral Oxycodone to SC Diamorphine Divide by 1.5 (Suggested safe practice)* Oral Hydromorphine to SC Hydromorphine Divide by 2

Approximate Equivalent Doses of Opioid Analgesic for Adults- Guiding Principles Suggested current practice guidelines are SC Diamorphine to SC Oxycodone Treat as equivalent up to doses of 60mg/24hrs. Use caution when converting higher doses. Calculate by using oral morphine equivalents SC Diamorphine to SC Alfentanil- Divide by 10 SC Diamorphine to SC Morphine- ratio is 1:1.5 and 1:2 Multiply by 1.5 Oral Tramadol to Oral Morphine Divide by 10 (Suggested safe practice)** Oral Codeine/ Dihydrocodeine to Oral Morphine Divide by 10 November 2010

Parenteral Opioids First Line Diamorphine Morphine Sulphate Second Line Oxycodone Alfentanil Fentanyl Hydromorphone November 2010

Transdermal Opioids Indications for Use Patients who have difficulty with the oral route Unacceptable side- effects with other opioids Renal impairment Medication compliance Patient preference Transdermal preparations should not be commenced in patients with uncontrolled pain or who are moribund.

Breakthrough Pain A transient exacerbation of pain that occurs either spontaneously, or in relation to a specific predictable or unpredictable trigger, despite relatively stable and adequately controlled background pain Davis et al 2009

Managing Breakthrough Pain Patients with pain should be assessed for the presence of breakthrough pain and breakthrough pain should be specifically assessed Management of breakthrough pain should be individualised Consideration should be given to: treatment of the underlying cause of the pain e.g. radiotherapy avoidance/ treatment of the precipitating factors of the pain modification of the background analgesic regimen which may include titration of opioid analgesics, switching of opioid analgesics, or the addition of adjuvant analgesics November 2010

Managing Breakthrough Pain Opioids are the rescue medication of choice in the management of breakthrough pain episodes. Dose of opioid rescue medication should be determined by individual titration Non-opioid analgesics may be useful in the management of breakthrough pain episodes e.g. paracetamol, NSAIDs Interventional techniques and non-pharmacological methods may be useful in the management of breakthrough pain

Fentanyl Preparations These preparations have been developed specifically for breakthrough cancer pain ( BTcP) Have faster onset of action and shorter duration of effect, making them more suitable for traditional BTcP management They should only be used in patients who are on a daily minimum of 60mg PO morphine equivalent Currently available in oral transmucosal, buccal and intranasal preparations Dose of all short acting fentanyl preparations should be determined by individual titration as data suggests that there is no relationship between the most effective dose of these preparations and the effective dose of the background opioid medication

Opioid Adverse Effects Constipation Nausea and vomiting Sedation Dry mouth Opioid Toxicity

Adjuvant/Co Analgesics Medications whose prime function are not analgesic but which can enhance the management of pain Neuropathic pain First line Tricyclic Antidepressants Anticonvulsants Neuropathic pain Second line Combination of tricyclic and antidepressant November 2010

Adjuvant/Co Analgesics Neuropathic pain Second line Consider use of Lidocaine 5% patches Capsaicin Corticosteriods Neuropathic agents which may be used by specialists e.g selective noradrenaline reuptake inhibitors, selective serontonin reuptake inhibitors, clonazepam, ketamine,parental lidocaine

Adjuvant/Co Analgesics Bone Metastases- Bisphosphonates Muscle Spasm-Antispasmodics. Muscle relaxants (limited evidence) Liver capsule pain- Corticosteroids or NSAIDS The use of other drugs under specialist supervision only e.g topical opoids and cannabinoids may be indicated

Adjuvant/Co Analgesics Bone Metastases- Bisphosphonates Muscle Spasm-Antispasmodics. Muscle relaxants (limited evidence) Liver capsule pain- Corticosteroids or NSAIDS

Pain Management - Other Interventions Complementary therapies Transcutaneous electrical nerve stimulation (TENS) Acupuncture Creative Therapies Occupational Therapy Anti-cancer therapy

Pain Management - Other Interventions Anaesthetic Procedures Local nerve blocks Neuroaxial techniques Chemical neurolysis Spinal cord compression Vertebroplasty

Challenges in Managing Pain Assessing and managing pain in patients who are - cognitively impaired - have a learning disability Prescribing analgesics in patients with - Renal impairment - Renal replacement - Hepatic impairment - Respiratory impairment - Cardiac failure - Neurological conditions

References Davies AN, Dickman A, Reid C, Stevens AM, Zeppetella G.(2009) The management of cancer-related breakthrough pain: recommendations of a task group of the Science Committee of the Association for Palliative Medicine of Great Britain and Ireland. European Journal of Pain. 13(4):331-8 International Association for the Study of Pain, Subcommittee on Taxonomy. Pain 1986 (Suppl 3): S1-226 Classification of chronic pain. Descriptions of chronic pain syndromes and definitions of pain terms. Northern Ireland Cancer Network (2010) General Palliative Care Guidelines for the management of Pain at the End of Life Stannard C and Booth S.(2004) Pain. Churchill Livingstone. 183-6