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5th case of Legionnaires identified in Sydney

Two more people have been diagnosed with the potentially deadly Legionnaires’ disease after another outbreak was announced last week.

The men in their 40s and 50s were in the CBD at the same time as the other three patients identified.

The original cases included two women and an elderly man. A woman in her 30s is still in a critical condition in hospital.

According to the director of the NSW Health Communicable Diseases Branch, Dr Vicky Sheppeard, five cooling towers have tested positive to legionella however it’s possible that the actual source of the outbreak won’t be found as they may have already cleaned the building prior to authorities gaining access.

Related: Legionnaires strikes Sydney again

“We’ve already taken regulatory action against those five towers and ordered cleaning and disinfection,” Dr Sheppeard said. “We don’t believe there is an ongoing risk in the city of Sydney.”

The five people all spent time in the area of the city bordered by Market, George, King and Kent streets since Anzac Day.

Legionnaires is an infection of the lungs (pneumonia) that is caused by bacteria of the Legionella family which is caused by when a person breathes in the affected bacteria. Legionnaires disease most often affects middle-aged and older people, those who are heavy smokers or who have a chronic lung disease. People with suppressed immunity are also more at risk.

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New prostate cancer guidelines endorsed by RACGP

Evidence-based guidelines launched earlier this year for using the prostate specific antigen (PSA) blood test to assess prostate cancer risk in patients have been endorsed by the Royal Australian College of General Practitioners.

The PSA Testing and Early Management of Test-detected Prostate Cancer: Guidelines for health professionals were developed in partnership with the Prostate Cancer Foundation of Australia (PCFA) and Cancer Council Australia and were approved by the National Health and Medical Research Council (NHMRC).

The guidelines align with the RACGP view that using either the PSA test or a digital rectal examination is unreliable and not recommended.

According to RACGP President Dr Frank R Jones:  “The best way to approach prostate health is for the patient to discuss his concerns with his general practitioner who after careful deliberation, will determine the need for testing or not. In the vast majority of cases it is unnecessary.”

Related: New guidelines but prostate testing still complex

Evidence has found the harm of a false positive outweighs the possible benefit. For every 1000 men aged 55-65 who had an annual PSA screening test, 87 will find out through an invasive biopsy that they have received a false positive. 4 of the 1000 men screened will eventually die of prostate cancer and only one man will be saved through PSA testing.

The new guidelines include:

  • Men considering a PSA should be given information about the benefits and harms of testing.
  • Men with an average risk who have decided to undergo regular testing after being informed of the benefits and harms should be offered PSA testing every 2 years from age 50-69. If the total PSA concentration is greater than 3ng/mL then further investigation should be offered.
  • Men over 70 who have been informed of the benefits and harms of testing and who wish to start or continue regular testing should be informed that the harms of PSA testing may be greater than the benefits of testing in their age group.
  • Men with a father or one brother who has been diagnosed with prostate cancer has 2.5 – 3 times higher than average risk of developing the disease. If these men have decided to undergo regular testing after being informed of the benefits and harms, they should be offered PSA testing every 2 years from age 45 to 69.
  • Men with a father and two or more brothers who have been diagnosed with prostate cancer have at least 9 to 10 times higher than average risk of developing the disease. If these men have decided to undergo regular testing after being informed of the benefits and harms, they should be offered PSA testing every 2 years from age 40 to 69.
  • In a primary care setting, digital rectal examination is not recommended for asymptomatic men in addition to PSA testing however this may be an important assessment procedure if referred to a urologist or other specialist for further investigation.
  • Mortality benefit due to an early diagnosis of prostate cancer due to PSA testing isn’t seen within less than 6-7 years of testing so PSA testing isn’t recommended for men who are unlikely to live another 7 years (subject to health status).
  • A PSA testing decision aid for men and their doctors is under development by PCFA and Cancer Council Australia.

Other recommendations also include further investigations if the PSA concentration is above 3 ng/mL; prostate biopsy and multiparametric MRI; active surveillance and watchful waiting.

PSA Testing and Early Management of Test-detected Prostate Cancer: A guideline for health professionals is available for download at www.pcfa.org.au and wiki.cancer.org.au/PSAguidelines.

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Probiotics – do they benefit healthy people?

A systematic review has found that probiotics have little effect on the gut microbiota of healthy people.

The study was undertaken by researchers at the Novo Nordisk Foundation Center for Basic Metabolic Research at the University of Copenhagen and published in Genome Medicine.

It involved a review of seven randomised controlled trials to investigate the effect of probiotics on the faecal microbiota of healthy adults. The probiotics products administered were biscuits, milk-based drinks, sachets, or capsules for periods of 21 to 42 days.

The researchers looked at reported effects on the overall structure of faecal microbiota including the number of species present, the evenness and whether the healthy people taking probiotics had different changes of bacteria living in their guts compared to the placebo groups.

Related: Patrick Charles: Power of poo

The researchers investigated the trials for reported effects of probiotics on the overall structure of the fecal microbiota of healthy adults, including the number of species present, the evenness (distribution of species within the populations) and whether the probiotics groups of study participants as a result of the intervention had different changes in bacteria living in their gut than the placebo groups.

“According to our systematic review, no convincing evidence exists for consistent effects of examined probiotics on fecal microbiota composition in healthy adults, despite probiotic products being consumed to a large extent by the general population,” PhD student and junior author Nadja Buus Kristensen said.

Of the seven original trials, only one found observed changes in the bacterial composition of faecal microbiota.

Related: John Dwyer: Promoting wellness

The authors note that various limitations include small sample size, use of different probiotic strains, variations of diet and variation in susceptibility of probiotics between individuals could mask the true impact of probiotic intake.

Oluf Pedersen, professor at the University of Copenhagen and senior author of the paper said: “While there is some evidence from previous reviews that probiotic interventions may benefit those with disease-associated imbalances of the gut microbiota, there is little evidence of an effect in healthy individuals. To explore the potential of probiotics to contribute to disease prevention in healthy people there is a major need for much larger, carefully designed and carefully conducted clinical trials. These should include ideal composition and dosage of known and newly developed probiotics combined with specified dietary advice, optimal trial duration and relevant monitoring of host health status.”

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New cosmetic surgery guidelines encourage cooling off periods

The Medical Board of Australia has introduced a range of new guidelines in a bid to crackdown on the cosmetic surgery industry.

The guidelines aim to inform medical professionals and the community about the expectations the Board has for doctors who perform cosmetic surgery procedures.

According to Board Chair, Dr Joanna Flynn, “The guidelines will help keep patients safe, without imposing an unreasonable regulatory burden on practitioners.”

Related: Delay implants, women advised

The 6 page guidelines were developed after draft guidelines were circulated in March 2015.

“The Board listened to stakeholder feedback, and responded with a new set of guidelines that will best keep patients safe,” Dr Flynn said.

“The changes prioritise patient safety and reduce some of the regulatory requirements proposed in the previous draft guidelines, when either there was no evidence of improved safety or the costs significantly outweighed the benefits of a proposal,” she said.

Related: Cosmetic clinic under fire over surgeries

9 key points from the guidelines include:

  • There should be a 7 day cooling off period for all adults before any major procedure (anything that involves cutting beneath the skin);
  • Adult patients should be referred to a psychologist, psychiatrist or general practitioner if there are any indications of underlying psychological problems;
  • There should be a 3 month cooling off period for all under 18s before major procedures and a mandatory evaluation from a registered psychiatrist, psychologist or general practitioner;
  • There should be a 7 day cooling off period for all under 18s before minor procedures (cosmetic medical procedures that do not involve cutting beneath the skin but may involve piercing the skin);
  • The treating medical practitioner must take responsibility for any post-operative care;
  • The treating medical practitioner must make sure there are emergency facilities when using sedation, anaesthesia or analgesia;
  • There needs to be a mandatory consultation (either by person or by video conference) before medical practitioner prescribes schedule 4 cosmetic injectables;
  • Medical practioners need to provide detailed, written information to the patient to ensure they are making informed consent. Information should include the range of possible outcomes, complications and recovery times associated with the procedure and the qualifications and experience of the medical practioner;
  • Medical practitioners need to provide patients with detailed written information about costs including any costs for follow-up care or any potential revision surgery or treatment.

The new guidelines will take effect on 1 October 2016. Read the Cosmetic Surgery Guidelines.

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Don’t shoot the messenger

 

The Turnbull Government, led by Health Minister Sussan Ley, has recently made a habit of launching attacks on health professionals to justify its health policy decisions, especially the cuts to funding and services and the cost shifting.

It has not just been doctors in the firing line, although the Government has made a habit of demonising GPs, surgeons, radiologists, pathologists, and anaesthetists on a regular basis.

If not through direct attack, it has been via friendly journalists on the drip, or under cover of disenchanted private health insurers desperate to avoid the spotlight as their own sector is under forensic review.

Dentists have been copping it lately, joining the growing queue of health professionals being blamed for the Government’s health policy mistakes and misadventures. Pharmacists and nurses have also come under attack, and they are not amused, and do not take these attacks lightly.

None of the health professions appreciate being criticised publicly in the media, especially when these attacks do not reflect what is discussed in private meetings.

The public – voters – do not like it, either.

Every poll of the professions in living memory has doctors, nurses, and pharmacists rated as the most trusted professions in the community. People trust their doctors and other health professionals. They do not like the ugly spectacle of politicians and some in the media attacking the integrity of health professionals. Needless to say, politicians rate very low on the trusted profession scale.

So, what is behind the misguided strategy of demonising doctors and other health professionals so close to an election? There can’t be any votes in it.

You would think that an incumbent Government would want to win the hearts and minds of health sector leaders in the months ahead of a Federal Election, and on the eve of the Federal Budget, which will shape the direction of the Coalition’s election health policies.

But this is not the case.

Doctors, pharmacists, nurses, Aboriginal health services, and even medical receptionists, have in the past week been blamed for rorts and waste in the system, with incorrect and inaccurate statistics being used to push these mischievous claims.

This is all subterfuge to keep the public focus off the main game – the fact that the Government’s health policies, in the main, are all about making savings to the Budget, not improving access to quality affordable health care for all Australians.

The Government’s ongoing justification for its extreme health savings measures, including cuts to public hospital funding, has been that Australia’s health spending is unsustainable. This is simply not true.

The most recent comparative figures reported by the OECD show Australia’s health expenditure as a proportion of GDP was below the OECD average and lower than 18 other OECD countries.

Australia’s health costs (8.8 per cent), as assessed by the OECD, were just over half the corresponding proportion for the USA (16.4 per cent). Australia achieves better health outcomes for its significantly lower proportional spend than the USA and many other countries, with the second highest life expectancy in the world, with the exception of Indigenous Australians.

Moreover, the Commonwealth Government’s total health expenditure is reducing as a percentage of the total Commonwealth Budget. In the 2014-15 Commonwealth Budget, health was 16.13 per cent of the total, down from 18.09 per cent in 2006-07. It reduced further in the 2015-16 Budget, representing only 15.97 per cent of the total Commonwealth Budget.

Clearly, total health spending is not out of control. Nor is spending on medical services.

The reality is that today we are not spending any more on medical services as a proportion of total health spending than we were a decade ago.

The proportion today is 18.2 per cent, compared with 18.5 per cent a decade ago. While we are spending more on health in total, we are spending less on medical services.

Today, 86 per cent of privately insured medical services are charged at no gap by the doctor – which means that the doctor accepts the fee level set by the patient’s private health insurer.

A further 6.4 per cent are charged under ‘known’ gap arrangements. This means that less than 8 per cent of privately insured patients may be charged fees exceeding private health insurance levels, including known gap amounts.

The number of doctors charging ‘excessive’ fees is in the absolute minority, and the AMA continues to work with the relevant specialist colleges, associations and societies to address this.

Nor are doctors’ fees contributing to Budget woes, with specialist fees in many cases not being indexed for up to a decade.

Contrary to the line being pushed by the Government and the private health insurers, medical services are not an issue for the insurers or for patients.

Some insurers have been only too eager to vilify doctors even though the publicly listed PHIs have posted record profits, their executives are paid multimillion dollar salaries, and when doctors charge above the PHI schedule, i.e. a gap, the PHI contribution falls to 25 per cent of the scheduled fee.

During the December 2015 quarter, insurers paid $3,542 million in hospital treatment benefits. This was broken down into 70 per cent on hospital services such as accommodation and nursing, approximately 15 per cent on medical services, and 14 per cent on prostheses.

General practice, too, has demonstrated a real willingness to work with the Government to deliver high quality reforms, particularly in relation to the treatment of patients with complex and chronic disease.

The 2016 Budget provided the Government with a real opportunity to steer a new course and a new strategy of health policy and health sector engagement, but they passed on this opportunity. We can only hope the Government is saving some health largesse to be announced ahead of the election.

Doctors and the other health professions are restless and demanding better health policy, better consultation, and greater respect in public conversations and pronouncements. We need a mature and honest exchanges of views, not sneaky media leaks and cheap attacks on our integrity and professionalism.

Doctors see millions of Australians face-to-face every day. Multiply that number when you count radiology and pathology centres, pharmacies, and other health professionals.

Some groups have already commenced campaigns against Government health policies. More will join them if there is not a change in policy direction and a change in the Government’s public relationship with the health sector.

* An edited version of this column first appeared in the Australian Financial Review on 4 May 2016.

 

Using opioids in general practice for chronic non-cancer pain: an overview of current evidence

Chronic non-cancer pain is highly prevalent in our communities and its optimal management is crucial to the health and wellbeing of the community.1 Without good control of chronic pain, our community faces a level of avoidable suffering that cannot be justified, with costs of uncontrolled chronic pain borne across society by individuals, health services and businesses.2,3 At both the level of the individual patient and the community, there needs to be focus on using the best available evidence to assess and manage this overwhelming problem. Part of the appropriate treatment for many people will include opioid analgesics for acute pain at least for days to weeks.4 Simultaneously there is increasing pressure to ensure that prescribing of opioid analgesics is minimised to reduce the risk of dependence and illicit diversion. This is a difficult balance to strike, even with initiatives such as prescription drug monitoring programs.5

This article provides a brief overview of the current evidence to guide opioid use for chronic non-cancer pain in general practice.

Chronic pain: definitions and epidemiology

The International Association for the Study of Pain defines chronic pain as that which has persisted beyond normal tissue healing time; by convention, this is usually interpreted as pain that lasts for more than 3 months.6 Definitions for the duration of pain, intensity and level of interference with daily activities vary around the world. In the adult Australian population, pain has been defined as chronic if experienced daily for three of the past 6 months.1 Prevalence varies with the definition of chronicity.7,8

Chronic non-cancer pain is a major health problem around the world with prevalence rates as high as 33% of the population in western populations.9 It is prevalent across our communities, with up to 17.1% of men and 20.0% of women in Australia likely to experience the problem.1 These rates are comparable to those found in Denmark and Canada.10 Much higher rates have been reported from the United Kingdom, where rates may be as high as 46.5% of the population.11 Pain that interferes markedly with daily functioning has a rate in Australia of 5.0% of the population, with the strongest predictor being a work-related injury in an adjusted model with an odds ratio of 19.3 (95% CI 7.30–51.30; P < 0.001).12

The most frequently identified pains are those affecting the lower back and from osteoarthritis.11 As expected, the prevalence of pain increases with age, with some of the highest rates seen in residential aged care facilities.13 Chronic neuropathic pain is estimated to occur in one in 11 people.14

Chronic prescribing has been defined as 90 days or more of opioid prescribing in the past 120 days;15 this definition is congruent with that of the International Association for the Study of Pain.6

Current guidelines for safe prescribing of opioids for chronic non-malignant pain

The two most current and comprehensive evidence-based guidelines for the use of opioids for chronic non-cancer pain come from the United States and Canada.16,17 They share the stated purpose of ensuring the appropriate management of chronic non-cancer pain while minimising abuse of opioids.

The Canadian guideline is for all practitioners working with chronic non-cancer pain, not just clinicians in specialist pain practice (Box 1).17 Major domains in considering such therapy are outlined in the document: assessing patients for the suitability for opioids; initiating a therapeutic trial of opioids and monitoring long term use. Sections are devoted to particular patient populations. One recurring theme in the clinical recommendations is to treat only “well defined somatic or neuropathic pain conditions when non-opioid alternatives have failed”.17 Care needs to be taken when deciding to initiate or titrate opioids, especially in more vulnerable populations who have relevant comorbid conditions, and great care is necessary if people require more than 200 mg of oral morphine equivalents. Another key theme is the need for the clinicians involved in a patient’s care to have clear lines of accountability with each other and for agreed communication strategies among treating clinicians.

Guidelines from the US stress that the use in the longer term (more than 3 months) of opioids for chronic non-cancer pain has little data to support the practice.16 However, in contrast to the Canadian guideline, the US guidelines suggest that doses of greater than 91 mg of morphine equivalent should be treated with caution and specialist advice sought. There is some evidence to support prescription drug monitoring programs and urine drug testing as mechanisms to reduce abuse potential. Less robust evidence supports a thorough patient assessment, risk-screening tools, controlled-substance agreements, careful dose titration, opioid dose ceilings, and adherence to practice guidelines reduces the risk of aberrant prescription drug-related behaviours.18

With respect to Australian recommendations, most recently the National Prescribing Service (NPS) has released a series of documents providing clinical advice for health professionals engaged in the care of people with chronic pain. This includes a section titled “Best practice opioid analgesic prescribing for chronic pain”, with the Australian recommendations similar to those of the US suggesting that daily doses above 100 mg morphine equivalent should be avoided. Further, recommendations made by the NPS include the fact that when commencing opioids, initial doses should be low with careful and supervised titration.19 A summary of the NPS recommendations is included in Box 2.

Current prescribing trends in Australia

Australia continues to experience rising rates of opioid prescription.20 Between 1992 and 2012, Australian opioid dispensing episodes increased from 0.5 million prescriptions to 7.5 million, with no evidence to suggest that these figures are reaching a plateau.21 There has also been an increase in the number of opioid preparations available (n = 241), including morphine (n = 87), fentanyl (n = 43) and oxycodone (n = 37) as the largest three groups.21 The indication on the Pharmaceutical Benefits Scheme generally includes use for chronic severe disabling pain that is not responsive to non-opioids. The variation in opioid prescribing across Australia has recently been highlighted in the Australian Atlas of Healthcare Variation published by the Australian Commission on Safety and Quality in Health Care (http://www.safetyandquality.gov.au/atlas).

The overall increase in opioids in Australia likely reflects a population that continues to grow rapidly in part because of increasing life expectancy with chronic illnesses of ageing often associated with pain, previous under-prescribing, increasing incidence and survival from cancer, increased numbers of preparations available, poor access to allied health for non-pharmacological interventions, poor undergraduate and postgraduate education about opioid prescribing, aggressive marketing and the imperative for health professionals to better manage pain.20

Clinical consequences of opioid use

Despite the prevalence of pain across the community, overall chronic non-cancer pain generally remains poorly treated, resulting in limitations in activity and diminished quality of life. Although there are a variety of strategies available to help manage chronic non-cancer pain, for many people opioids are prescribed long term. While some patients do achieve effective analgesia, an estimated 40–70% of people with chronic pain do not,22 with the balance towards those who appear not to benefit from opioids in the long term.23 It is important to consider how the long term use is balanced with the risk of short and long term adverse effects of opioids.

Shorter term harms

Typically shorter term side effects are considered unpleasant but unlikely to lead to long term consequences (Box 3). Data from a systematic review suggest that for every four patients commenced on opioids, at least one person would experience at least one of these effects in a 1–8-week period.24

Longer term harms

Longer term harms may include physical and psychological issues and dependence. (Box 4) While most of the adverse effects that occur when opioids are commenced are expected to resolve rapidly,25 the adverse effects of constipation, sedation or dizziness for some people may not settle, all of which can cause significant morbidity. Older patients taking the equivalent of at least 50 mg of morphine daily have a twofold risk of sustaining a fracture as a result of a fall.26

Opioids may contribute to acceleration of loss of bone mineral density in the long term and to hypogonadism because of their suppression of hypothalamic gonadotrophin-releasing hormone. This can lead to amenorrhea or oligomenorrhea in premenopausal women and erectile dysfunction in men.27 There is also a 28% increase in the risk of myocardial infarction for people taking opioids long term.28

Psychological impacts include higher rates of depression after chronic opioid therapy is initiated in people who were not previously depressed. In this same cohort, higher rates of anxiety, lower self-efficacy and a tendency towards catastrophising were seen regardless of the opioid doses.29

People who use opioids long term for chronic non-cancer pain are at greater risk of misusing them, including through psychological dependency and overdose. These problems are prevalent in this cohort, with rates of misuse (21–29%) and addiction (8–12%) a cause for grave concern.30

The risk of sudden death due to opioids is amplified in the context of concurrent benzodiazepine and/or alcohol (mis)use.31

Aside from the direct adverse effects of opioids, there are several other potential negative consequences. There is a subset of people who are not concurrently using other agents such as alcohol, who are on modest doses of opioids and not currently experiencing high levels of pain, for whom driving is likely be to be safe.32 In Australia, recommendations include the suggestion that people should not drive if they feel drowsy or impaired. Further, due to the persistent miotic effects, driving at night is discouraged. If there are concerns regarding capacity, a practical driving assessment may be requested by health professionals with the details as to how to achieve this in each state, dependent on the local driver-licensing authority.33 Proper assessments of capacity are important given that health service use increases with opioid use. Higher rates of hospitalisations, emergency department presentations and even unintentional death have been recorded.31,34 The evidence that supports the benefits outweighing the risks of long term opioids for chronic pain is very poor. There is real need for further research to most clearly define which patients are most likely to benefit from opioids and what are the most suitable precautions to safeguard them from harm.35

GPs’ attitudes to prescribing opioids for chronic non-cancer pain

Despite the development of various guidance documents for the safe and effective use of opioids,17,19,36,37 GPs continue to be concerned about the risk of opioid dependence and misuse for patients with chronic non-cancer pain. There are also concerns expressed by GPs about their capacity to manage the complex physical and psychological needs of this patient cohort, and their role in long term prescribing and the limitations of available treatment approaches.3841 Regional difference in opioid-prescribing confidence has been noted in a pan-European online survey of primary care pain management practices.41 GPs in Norway (46%), Sweden (43%) and Poland (37%) reported lower levels of opioid-prescribing confidence, which they attributed to fears of addiction and adverse events.41 GPs in the UK, the Netherlands, France and Italy were more confident about prescribing opioids for patients with chronic non-cancer pain, which they attributed to their experience and the therapeutic treatment choices available.41

Opioid prescribing in primary care is complex because of the need to optimise pain management while balancing the risks of tolerance and addiction.37 Inappropriate prescribing is more likely when patients are exposed to repeated consultations that do not meet their needs and if GPs feel powerless to negotiate an alternative plan of care and set appropriate boundaries.38,42 If there is a perceived paucity of treatment alternatives, opioid prescribing can occur as a default decision.38 Variations in opioid prescribing have previously been linked to GPs’ pain management training, experience and exposure to adverse opiate-related events.43

What can be done to reduce inappropriate prescribing?

While there are opportunities to address inappropriate prescribing at the system, provider and patient levels, one of the most immediate changes could be achieved simply by supporting GPs to manage patients’ chronic non-cancer pain in accordance with recommended guidelines.39

Evidence-based guidelines provide GPs with an evidence-based framework for the collaborative development of a treatment plan with the patient.37 There are also opportunities to strengthen safe opioid prescribing by GPs for non-malignant pain through specific education programs.44 Combining clinician education with an opioid dose limitation practice policy45 and implementing a practice policy of not providing repeat opioid prescriptions or authorising a dose increase without a formal medical review may reduce the risk of inappropriate dose escalation.38

High level evidence supports the use of methadone or buprenorphine in patients with chronic non-cancer pain who are addicted to opioids (high level evidence).17

Indications to prescribe or not prescribe chronic opioids

Only carefully selected patients should be considered for long term opioids for chronic non-cancer pain that is moderate to severe, has led to substantial negative impacts on daily living and has failed all other analgesic modalities and adequate allied health assessments.46 Any concerns about the prevalence of opioid prescribing must be balanced with ensuring that people with opioid-responsive pain are adequately treated.47 Evidence is slowly building to refine prescribing guidelines, maximising benefits and minimising harms.48 Many of the more routine pain problems such as chronic back pain or chronic headaches are unlikely to respond to opioids, in contrast to more severe and physically disabling problems such as destructive rheumatoid arthritis.34

Managing aberrant patient behaviour

Aberrant behaviour related to prescription medications includes any behaviour that suggests non-medical use of a drug or evidence of addiction, such as drug-seeking behaviour, alternative routes of delivery, obtaining opioids from other sources or unsanctioned use.39 Preventing aberrant drug-related behaviour requires minimising the risk of opioid misuse while optimising the best evidenced-based treatments for patients with chronic non-cancer pain. In order to minimise harm, these patients require an approach that is similar to other chronic illness interventions, which includes appropriate non-pharmacological and pharmacological approaches, and an individualised evidence-based risk-mitigation plan to optimise adherence.39 There is good evidence that determining the treatment goals of pain relief and improved function can minimise the risk of aberrant behaviour.37 Prescribing tamper-resistant opioids currently offers the highest level of prevention of opioid misuse.18

If a patient with chronic non-cancer pain requests an early opioid prescription, it is important to consider the possibility that the patient may have developed tolerance to the opioid, thus requiring a higher dose to maintain the same level of pain control; developed physical dependence and is experiencing early withdrawal symptoms; diverted some or all of his or her opioids for financial gain; or that a third party may have diverted the prescribed opioids.49 Once aberrant behaviour has developed, management becomes more complex and is likely to require a range of responses including urgent referral to specialist services, urine drug screening and other compliance monitoring, treatment agreements, and patient education. High level evidence suggests that when combined, these measures can reduce substance misuse by 50%.50

Ensuring adequate prescribing when indicated

Promoting and implementing the guidance offered by recently updated guidelines and providing clinicians with point-of-care resources can help to ensure adequate and safe opioid prescribing for patients where opioids are indicated. In patients with acute pain, both the US and Canadian guidelines suggest that opioid therapy may be initiated with low doses and short-acting drugs with appropriate monitoring to provide effective relief and avoid side effects.17,48 Further, the US guidelines suggest that in well selected populations, chronic opioid therapy may be continued (≥ 90 days), with continuous adherence monitoring, in conjunction with or after failure of other modalities of treatments, with improvement in physical and functional status and minimal adverse effects.37

In addition to prescribing practices, greater emphasis on chronic pain management during initial medical training programs and access to point-of care pain management guidelines is required to better support GPs to manage opioid prescribing for people with non-malignant pain.40,41 Improved access to allied health services when pain is still acute is crucial if the prevalence of chronic, non-cancer pain is to be reduced substantially.

Box 1 –
Roadmap for safe and effective use of opioids for chronic non-cancer pain: Canadian guideline17


Reprinted with permission.

Box 2 –
Best practice opioid analgesic prescribing for chronic pain: National Prescribing Service19

When trialling an opioid:

  • limit the trial to 4 weeks and only after exploring all other treatment options, both physical and psychological
  • review weekly preferably with a family member
  • encourage the use of a pain diary with a validated pain assessment tool such as the Brief Pain Inventory
  • assess for measureable improvements in quality of life (sleep, mood, libido), function (activities) and pain scores to gauge the effectiveness of opioids during the trial phase
  • along with monitoring physical and mental condition, monitor other key areas of function such as fitness for driving, work and other activities, and check for aberrant drug-related behaviours
  • avoid short-acting opioids

Dosing:

  • start with low doses and titrate according to response and adverse effects
  • doses above the equivalent of 100 mg morphine per day require reassessment, including specialist advice if possible
  • exercise caution with older patients

Management plans and contracts:

  • an opioid contract that summarises conditions of use along with a management plan that outlines other activities can help set realistic goals and expectations of behaviour while undertaking an opioids trial

Box 3 –
Frequently encountered effects of opioids compared with placebo in short term use24

No. of trials

No. of participants

Side effect

Participants experiencing side effect


No. needed to harm*

Opioids

Placebo


8

1114

Constipation

41%

11%

3.4

8

1114

Nausea

32%

12%

5.0

7

1022

Sedation

29%

10%

5.3

7

972

Vomiting

15%

3%

8.1

8

1114

Dizziness

20%

7%

8.2

6

981

Itching

15%

7%

1.3

7

677

Dry mouth

13%

9


* Short term; reverses immediately with cessation.

Box 4 –
Definitions of misuse, abuse and addiction30

Term

Definition


Misuse

Opioid use contrary to the directed or prescribed pattern regardless of the presence or absence of harm or adverse effects

Abuse

Intentional use of the opioid for a non-medical purpose such as euphoria or altering of one’s state of consciousness

Addiction

Pattern of continued use with experience of, or demonstrated potential for harm with a psychological dependence


[Editorial] Transforming primary care

Last week saw two important publications on primary care in the UK. The General Practice Forward View, published by NHS England and developed in partnership with the Royal College of General Practitioners and Health Education England, sets out a plan to transform general practice over the next 5 years. Backed by an extra £2·4 billion a year, the plan outlines steps to increase the number of general practitioners (GPs) and co-workers, as well as measures to reduce workload stresses, develop infrastructure, and support care redesign to enable increased access to GPs.

Flu vaccine more effective in the morning: study

Research has shown administering the flu vaccine in the morning could be more effective for immunity than in the afternoon.

The research, published in Vaccine, was conducted on 24 general practices in the UK, and involved 276 adults over the age of 65.

The adults were vaccinated for three strains of influenza in two time slots, either 9-11am or 3-5pm.

For two of the strains, there was a significantly larger increase in antibody concentration detected a month later for the group who were vaccinated in the morning compared to those who were vaccinated in the afternoon. There was no difference in antibodies for the third strain.

Related: MJA – Influenza vaccine effectiveness in general practice and in hospital patients in Victoria, 2011–2013

According to Principal Investigator of the study from the University of Birmingham, Dr Anna Phillips, “We know that there are fluctuations in immune responses throughout the day and wanted to examine whether this would extend to the antibody response to vaccination. Being able to see that morning vaccinations yield a more efficient response will not only help in strategies for flu vaccination, but might provide clues to improve vaccination strategies more generally.”

Co-investigator Professor Janet Lordsaid, “Our results suggest that by shifting the time of those vaccinations to the morning we can improve their efficiency with no extra cost to the health service.”

A larger scale study will investigate whether vaccinating in the morning would benefit people with impaired immunity, such as those with diabetes, liver and kidney disease.

Future research will also look at whether the time of day may vary for different vaccines, as they stimulate diverse immune responses for protection.

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Low back pain enhanced by psychological factors

Psychological and social stressors often enhance the symptoms of low back pain, experts say.

Associate Professors Leigh Atkinson, from Wesley Pain and Spine Centre in Brisbane, and Andrew Zacest from Royal Adelaide Hospital wrote in the Medical Journal of Australia that the high incident of low back pain is best understood in a biopsychosocial framework.

They say the pain from an injury is compounded by other issues such as work dissatisfaction, family stress, depression and at times secondary gain.

Compensation and third party insurance can impact pain and prolong rehabilitation. Furthermore, a study of workers compensation patients receiving surgery found the outcomes were poor.

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“The incidence of persistent post-operative pain syndrome was as high as 40% and … there was a 50% success rate, at best, from the first operation, 30% from the second and 15% from the third,” the authors explained.

High expectation of successful surgical outcomes

Low back pain in the most common symptom seen in primary care, however patients often have high expectations from modern medicine.

“Not uncommonly, the patient attends the surgical consultation with an expectation that the problems can be fixed,” the authors wrote.

However despite an escalation in numbers performed, surgeries on low back pain remain controversial.

In the past 11 years, there has been a 267% increase of spinal fusion surgeries in the US and there has also been a disproportionate increase of surgeries in private hospitals compared to public.

There is a large array of techniques for spinal fusion however despite them all having different technical complications, there is little evidence of one providing better outcomes than another.

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Multiple Cochrane studies have confirmed insufficient evidence of the effectiveness of spinal fusions, one in 2005 finding “variable clinical outcomes ranging between 16% and 95%.”

The authors believe an increased there needs to be a national audit of patient centred outcomes for spinal fusion.

“While the spinal fusion procedure remains controversial, it would be valuable for spinal surgeons to undertake a national audit of patient-centred outcomes for the procedure, similar to the excellent audit carried out for hip and knee arthroplasties by the Australian orthopaedic surgeons,” they concluded.

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