Medical Chronicle November/December 2013 | Page 38

PAIN Acute pain: The role of opioids “By any reasonable code, freedom from pain should be a basic human right, limited only by our knowledge to achieve it.” DR ERIC HODGSON Chief Specialist Anaesthesiologist, Inkosi Albert Luthuli Central Hospital and Honorary Lecturer, Department of Anaesthesia, Critical Care and Pain Management, Nelson R Mandela School of Medicine, University of KwaZulu-Natal There has been strong evidence of oligoanalgesia in acute pain management since a landmark article by Marks and Sachar in 1973. They were psychiatrists routinely called on to evaluate drug-seeking behaviour and addiction in hospitalised medical patients, and concluded that the majority of the patients they examined simply had severe untreated pain. A recent review article in 2013 confirms that oligoanalgesia still exists today in 20%-75% of patients in hospital for various diseases. Usually, the cause of acute pain in the emergency department (ED) or surgical ward is obvious but appropriate treatment is less well understood. Pain arises from trauma as a result of injury, disease or surgery. Pain resolves as the injury heals so that treatment is only required for a short period. Treatment of acute pain Fear of side effects leads to inappropriate withholding and/ or inadequate prescription of pain medication as revealed by the following studies: • Less than 2% of long bone fractures received analgesia • Only 26% of children with second-degree burns received analgesia • Less than 50% of patients discharged were satisfied with their pain management. Treatment of acute pain is improved by a systematic approach that emphasises: Monitoring - Measurement of level of consciousness A sleeping patient with a respiratory rate >10/min does not need to be woken to be asked if they are in pain. If the respiratory rate is <10/min, the patient should be roused and not asked about pain but to assess the requirement for administration of naloxone and closer monitoring in a monitored/intensive care environment. Rousability is best assessed by the AVPU score: A - Awake & Able to assess V - Rouses to Verbal stimulus P - Rouses to Painful (Noxious) stimulus: Glabellar ta p, Trapezius pinch, nailbed pressure/jaw thrust. Not: Sternal rub/nipple twist. U - Unresponsive = General anaesthesia Measurement of pain level in conscious patients: A simple four-point score is most useful in the ward/ER: 1 - No pain 2 - Discomfort NOT needing added therapy 3 - Pain requiring therapy 4 - Severe pain despite therapy • Anti-hyperalgesic drugs hyperalgesia is a prominent feature of acute nociceptive pain, especially dynamic pain. Adequate treatment of dynamic pain with antihyperalgesic drugs is essential to allow adequate breathing and coughing and to allow mobilisation after injury. • Paracetamol has few contraindications, with IV paracetamol providing excellent initial pain relief. • Non-steroidal anti-inflammatory drugs (NSAIDs) have numerous contraindications relevant to acute pain management including: dehydration/hypovolaemia, renal dysfunction, wound and gastrointestinal bleeding, allergy and cardiovascular (CV) thrombosis. CV thrombosis is associated not only with the coxibs (like rofecoxib) but also the nonaspirin NSAIDs such as diclofenac and ibuprofen. • Local anaesthetics are also extremely effective for ED pain management by various routes, including infiltration, nerve and plexus blocks. • Analgesic drugs are drugs that increase, rather than normalise, the Appropriate drugs 38 MEDICAL CHRONICLE NOVEMBER/DECEMBER 2013 pain threshold. The most commonly used drugs in this group are the opioids analgesics. Appropriate prescriptions will use regular antihyperalgesic drugs, in the absence of contraindications, to minimise opioids requirements. Despite having many registered compound analgesics with many inappropriate drugs included, there have been a limited number of opioid analgesics available to South African clinicians treating acute pain. The selection was further reduced by the withdrawal of SA’s most widely used opioid analgesic, dextropropoxyphene, due to concerns regarding cardiac toxicity and use in suicide attempts. Codeine remains available but relies on metabolism by cytochrome to morphine by three enzymatic variants as follows: 1. Ultra-rapid: Resulting in potentially fatal levels of morphine that may result in death as seen in a child post-tonsillectomy in the US, leading to a recommendation from the FDA that codeine be withheld from paediatric pain management. 2. Normal metabolism: Seen in the majority of persons taking codeine, resulting in morphine analgesia with varying onset and duration. 3. Slow metabolism: Patients will characteristically complain of inadequate pain relief with codeine but still experiencing constipation, caused by unmetabolised codeine. Analgesic drugs Oxycodone was registered for use in SA in 2012. Oxycodone provides opioid analgesia without a ceiling effect at clinically achievable concentrations. Oxycodone has twice the potency of morphine and has an oral bioavailability of 60% as opposed Oxycodone to 30% for morphine. Oxycodone dosing is thus 30%-40% of that required for morphine. A safe dose in healthy volunteers is 0.2mg/kg of an immediate-release preparation (Oxynorm®). The dose can be repeated every 2-4 hours until pain relief is achieved. Where pain could be expected to persist for more than 48 hours, a slowrelease preparation (OxyContin®) may be used at a dose of 0.2-0.4mg/ kg 12 hourly, with immediate-release oxycodone given at 2-4 hourly intervals at a dose of 0.2mg/kg for breakthrough pain. OxyContin is formulated to release 40% of the dose immediately with delayed release of the remaining 60% from a matrix that remains intact and may be passed in the stool. The matrix also hinders the abuse of OxyContin by preventing crushing and dissolving of the oxycodone for illicit IV administration. The FDA has recently banned the manufacture of generics without this tamper-proof matrix. The aim of pain management with oxycodone should be to administer 60%-80% of oxycodone required as slow-release preparation, which provides excellent pain relief, without the euphoria that may predispose to abuse. There is no reason for patients admitted to a modern ED or surgical ward to suffer inadequate pain management with the many and varied options available for relief. Conclusion References available on request.