MJA
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International vascularised composite allotransplantation activity: implications for Australia

Karen M Dwyer, James D Burt and Tim Bennett
Med J Aust 2019; 210 (2): . || doi: 10.5694/mja2.12068
Published online: 4 February 2019

Although hand transplantation has the potential to transform lives, the procedure is not without risk

March 2018 heralded 7 years since the only Australian to date received a hand transplant. The recipient has physically and psychologically integrated the transplanted hand and reports significantly improved quality of life;1 motor and sensory functions continue to improve incrementally with ongoing hand therapy. The Transplantation Society of Australia and New Zealand (TSANZ) Vascular Composite Allograft (VCA) Advisory Committee met during the TSANZ annual scientific meeting held in Melbourne in April 2018. Transplant physicians and surgeons and reconstructive microsurgeons comprise the advisory committee, with scope to co‐opt expert members (eg, in bioethics) as required. Despite the success of the seminal hand transplant in Australia, no further patients have progressed to the transplant waiting list. In light of this, the Advisory Committee reflects in this article on the status of hand transplantation internationally and considers its relevance for Australia.

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Recruiting general practice patients for large clinical trials: lessons from the Aspirin in Reducing Events in the Elderly (ASPREE) study

Jessica E Lockery, Taya A Collyer, Walter P Abhayaratna, Sharyn M Fitzgerald, John J McNeil, Mark R Nelson, Suzanne G Orchard, Christopher Reid, Nigel P Stocks, Ruth E Trevaks and Robyn Woods
Med J Aust 2019; 210 (4): . || doi: 10.5694/mja2.12060
Published online: 28 January 2019

Abstract

Objective: To assess the factors that contributed to the successful completion of recruitment for the largest clinical trial ever conducted in Australia, the Aspirin in Reducing Events in the Elderly (ASPREE) study.

Design: Enrolment of GPs; identification of potential participants in general practice databases; screening of participants.

Setting, participants: Selected general practices across southeast Australia (Tasmania, Victoria, Australian Capital Territory, New South Wales, South Australia).

Major outcomes: Numbers of patients per GP screened and randomised to participation; geographic and demographic factors that influenced screening and randomising of patients.

Results: 2717 of 5833 GPs approached (47%) enrolled to recruit patients for the study; 2053 (76%) recruited at least one randomised participant. The highest randomised participant rate per GP was for Tasmania (median, 5; IQR, 1–11), driven by the high rate of participant inclusion at phone screening. GPs in inner regional (adjusted odds ratio [aOR], 1.45; 95% CI, 1.14–1.84) and outer regional areas (aOR, 1.86; 95% CI, 1.19–2.88) were more likely than GPs in major cities to recruit at least one randomised participant. GPs in areas with a high proportion of people aged 70 years or more were more likely to randomise at least one participant (per percentage point increase: aOR, 1.10; 95% CI, 1.05–1.15). The number of randomised patients declined with time from GP enrolment to first randomisation.

Conclusion: General practice can be a rich environment for research when barriers to recruitment are overcome. Including regional GPs and focusing efforts in areas with the highest proportions of potentially eligible participants improves recruitment. The success of ASPREE attests to the clinical importance of its research question for Australian GPs.

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  • 1 Monash University, Melbourne, VIC
  • 2 College of Health and Medicine, Australian National University School of Clinical Medicine, Canberra, ACT
  • 3 Canberra Hospital, Canberra, ACT
  • 4 University of Tasmania, Hobart, TAS
  • 5 Curtin University, Perth, WA
  • 6 University of Adelaide, Adelaide, SA


Correspondence: jessica.lockery@monash.edu

Acknowledgements: 

The ASPREE study, including the design and implementation of the recruitment strategy, was supported by the National Institute on Aging and the National Cancer Institute at the National Institutes of Health in the United States (U01AG029824), the National Health and Medical Research Council (334047 and 1127060), Monash University, and the Victorian Cancer Agency. Bayer provided aspirin and the matching placebo. We acknowledge the dedicated and skilled staff in Australia and the Unites States who undertook the ASPREE trial. We are also most grateful to the ASPREE participants who so willingly volunteered for this study, and the general practitioners and medical clinics who supported the participants in the ASPREE study., (ASPREE): International Standard Randomized Controlled Trial Number Register (ISRCTN83772183) and clinicaltrials.gov (NCT01038583).

Competing interests:

No relevant disclosures.

  • 1. Foster JM, Sawyer SM, Smith L, et al. Barriers and facilitators to patient recruitment to a cluster randomized controlled trial in primary care: lessons for future trials. BMC Med Res Methodol 2015; 15: 18.
  • 2. Australian Bureau of Statistics. 4839.0. Patient experiences in Australia: summary of findings, 2015–16. Nov 2017. http://www.abs.gov.au/ausstats/abs@.nsf/mf/4839.0 (viewed Oct 2017).
  • 3. Newington L, Metcalfe A. Factors influencing recruitment to research: qualitative study of the experiences and perceptions of research teams. BMC Med Res Methodol 2014; 14: 10.
  • 4. Wing LMH, Reid CM, Ryan P, et al. A comparison of outcomes with angiotensin‐converting‐enzyme inhibitors and diuretics for hypertension in the elderly. N Engl J Med 2003; 348: 583–592.
  • 5. Reid CM, Ryan P, Nelson M, et al. General practitioner participation in the second Australian national blood pressure study (ANBP2). Clin Exp Pharmacol Physiol 2001; 28: 663–667.
  • 6. Hunt CJ, Shepherd LM, Andrews G. Do doctors know best? Comments on a failed trial. Med J Aust 2001; 174: 144–146. https://www.mja.com.au/journal/2001/174/3/do-doctors-know-best-comments-failed-trial
  • 7. Goodyear‐Smith F, York D, Petousis‐Harris H, et al. Recruitment of practices in primary care research: the long and the short of it. Fam Pract 2009; 26: 128–136.
  • 8. Page MJ, French SD, McKenzie JE, et al. Recruitment difficulties in a primary care cluster randomised trial: investigating factors contributing to general practitioners’ recruitment of patients. BMC Med Res Methodol 2011; 11: 35.
  • 9. Paul CL, Piterman L, Shaw JE, et al. Poor uptake of an online intervention in a cluster randomised controlled trial of online diabetes education for rural general practitioners. Trials 2017; 18: 137.
  • 10. Yallop JJ, McAvoy BR, Croucher JL, et al. Primary health care research — essential but disadvantaged. Med J Aust 2006; 185: 118–120. https://www.mja.com.au/journal/2006/185/2/primary-health-care-research-essential-disadvantaged
  • 11. Askew DA, Clavarino AM, Glasziou PP, Del Mar CB. General practice research: attitudes and involvement of Queensland general practitioners. Med J Aust 2002; 177: 74–77. https://www.mja.com.au/journal/2002/177/2/general-practice-research-attitudes-and-involvement-queensland-general
  • 12. Zwar NA, Weller DP, McCloughan L, Traynor VJ. Supporting research in primary care: are practice‐based research networks the missing link? Med J Aust 2006; 185: 110–113. https://www.mja.com.au/journal/2006/185/2/supporting-research-primary-care-are-practice-based-research-networks-missing
  • 13. Winzenberg TM, Gill GF. Prioritising general practice research. Med J Aust 2016; 205: 55–57. https://www.mja.com.au/journal/2016/205/2/prioritising-general-practice-research
  • 14. McNeil JJ, Woods RL, Nelson MR, et al. Baseline characteristics of participants in the ASPREE (ASPirin in Reducing Events in the Elderly) study. J Gerontol A Biol Sci Med Sci 2017; 72: 1586–1593.
  • 15. McNeil JJ, Woods RL, Nelson MR, et al. Effect of aspirin on disability‐free survival in the healthy elderly. N Engl J Med 2018; 379: 1499–1508.
  • 16. Williams CM, Maher CG, Hancock MJ, et al. Recruitment rate for a clinical trial was associated with particular operational procedures and clinician characteristics. J Clin Epidemiol 2014; 67: 169–175.
  • 17. Silagy CA, Carson NE. Factors affecting the level of interest and activity in primary care research among general practitioners. Fam Pract 1989; 6: 173–176.
  • 18. Nelson MR, Reid CM, Ames D, et al. Feasibility of conducting a primary prevention trial of low‐dose aspirin for major adverse cardiovascular events in older people in Australia: results from the ASPirin in Reducing Events in the Elderly (ASPREE) pilot study. Med J Aust 2008; 189: 105–109. https://www.mja.com.au/journal/2008/189/2/feasibility-conducting-primary-prevention-trial-low-dose-aspirin-major-adverse
  • 19. Australian Bureau of Statistics. 2033.0.55.001. Census of population and housing: Socio‐Economic Indexes for Areas (SEIFA), Australia, 2016. IRSAD. http://www.abs.gov.au/ausstats/abs@.nsf/Lookup/by%20Subject/2033.0.55.001=2016=Main%20Features=IRSAD=20 (viewed Oct 2018).
  • 20. Australian Bureau of Statistics. 1270.0.55.005. Australian Statistical Geography Standard (ASGS): Volume 5 — remoteness structure, July 2016. Mar 2018. http://www.abs.gov.au/ausstats/abs@.nsf/Latestproducts/1270.0.55.005Main%20Features15July%202016?opendocument&tabname=Summary&prodno=1270.0.55.005&issue=July%202016&num=&view (viewed Oct 2018).
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  • 22. Borgiel AEM, Dunn EV, Lamont CT, et al. Recruiting family physicians as participants in research. Fam Pract 1989; 6: 168–172.
  • 23. Freedman B. Equipoise and the ethics of clinical research. N Engl J Med 1987; 317: 141–145.
  • 24. Nuttall J, Hood K, Verheij TJ, et al. Building an international network for a primary care research program: reflections on challenges and solutions in the set‐up and delivery of a prospective observational study of acute cough in 13 European countries. BMC Fam Pract 2011; 12: 78.
  • 25. Peterson KA, Lipman PD, Lange CJ, et al. Supporting better science in primary care: a description of practice‐based research networks (PBRNs) in 2011. J Am Board Fam Med 2012; 25: 565–571.
  • 26. Gunn JM. Should Australia develop primary care research networks? Med J Aust 2002; 177: 63–66. https://www.mja.com.au/journal/2002/177/2/should-australia-develop-primary-care-research-networks
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Exposures to e‐cigarettes and their refills: calls to Australian Poisons Information Centres, 2009–2016

Carol Wylie, Aaron Heffernan, Jared A Brown, Rose Cairns, Ann‐Maree Lynch and Jeff Robinson
Med J Aust 2019; 210 (3): . || doi: 10.5694/mja2.12032
Published online: 28 January 2019

The popularity of e‐cigarettes has increased in Australia since they first became available as smoking cessation tools; an estimated 1.3% of the New South Wales population used them in 2015, and as many as 8.4% had experimented with them.1 E‐cigarettes have been recommended by Public Health England and the Royal College of Physicians as safe smoking cessation tools.2,3 In Australia, a prescription is required for legally importing nicotine‐containing e‐cigarettes.4 The safety of these products for users and the risks for members of their households have not been established. Imported products may not conform to Australian standards, including having child‐resistant closures and appropriate labelling, and refill bottles containing highly concentrated nicotine solutions — one millilitre of which can be lethal if ingested by a child — can be purchased online.

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  • 1 Queensland Poisons Information Centre, Lady Cilento Children's Hospital, Brisbane, QLD
  • 2 Griffith University, Gold Coast, QLD
  • 3 New South Wales Poisons Information Centre, The Children's Hospital at Westmead, Sydney, NSW
  • 4 University of Sydney, Sydney, NSW
  • 5 Western Australian Poisons Information Centre, Sir Charles Gairdner Hospital, Perth, WA
  • 6 Victorian Poisons Information Centre, Austin Health, Melbourne, VIC



Acknowledgements: 

We thank the poisons information specialists from the Queensland, New South Wales, Victorian and Western Australian centres.

Competing interests:

Jared Brown has received consultancy fees from GlaxoSmithKline Consumer for sitting on an advisory board regarding paracetamol.

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Medical assistance in dying: a disruption of therapeutic relationships

Douglas T Bridge, Sinead M Donnelly and Frank P Brennan
Med J Aust 2019; 210 (4): . || doi: 10.5694/mja2.12105
Published online: 21 January 2019

To the Editor: We commend William1 for his perceptive review of the complex issues involved in euthanasia and assisted suicide (EAS).1 In contrast to the euphemisms in the popular media, he confronts us with some uncomfortable realities: EAS is the intentional taking of a person's life (E) or facilitating suicide (AS); doctors considering EAS may be (unconsciously) demonstrating “countertransference of their helplessness onto the patient;” and relief of all suffering is a fantasy beyond the ability of doctors, politicians and lawyers.


  • 1 Royal Perth Hospital, Perth, WA.
  • 2 Capital and Coast District Health Board, Wellington, New Zealand.
  • 3 Calvary Hospital, Sydney, NSW.


Correspondence: dtbridge@iinet.net.au

Competing interests:

No relevant disclosures.

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Medical assistance in dying: a disruption of therapeutic relationships

Peter G Beahan
Med J Aust 2019; 210 (4): . || doi: 10.5694/mja2.12104
Published online: 21 January 2019

To the Editor: The Perspectives article by William1 states that medical assistance in dying may disrupt therapeutic relationships and will challenge beliefs.


  • Perth, WA


Correspondence: pbeahan@optusnet.com.au

Competing interests:

No relevant disclosures.

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Increased incidence of community‐associated Staphylococcus aureus bloodstream infections in Victoria and Western Australia, 2011–2016

Nabeel Imam, Simone Tempone, Paul K Armstrong, Rebecca McCann, Sandra Johnson, Leon J Worth and Michael J Richards
Med J Aust 2019; 210 (2): . || doi: 10.5694/mja2.12057
Published online: 21 January 2019

Standardised national surveillance of health care‐associated Staphylococcus aureus bloodstream infections (HA‐SABs)1 has found that rates are declining in Australia.2 The incidence of community‐associated SABs (CA‐SABs), however, has not been investigated. These infections frequently have complicated courses (eg, metastatic sites of infection)3 and high mortality (about 20%).4

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  • 1 Victorian Healthcare Associated Infection Surveillance System (VICNISS) Coordinating Centre, The Peter Doherty Institute for Infection and Immunity, Melbourne, VIC
  • 2 Western Australia Department of Health, Perth, WA
  • 3 Royal Melbourne Hospital, Melbourne, VIC


Correspondence: nabeel.imam@mh.org.au

Acknowledgements: 

We acknowledge the infection control consultants in Victorian and Western Australian hospitals who collected the data we analysed. VICNISS is fully funded by the Victorian Department of Health and Human Services; HISWA is a program in the Public Health Division of the Department of Health Western Australia.

Competing interests:

No relevant disclosures.

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Nicotine and other potentially harmful compounds in “nicotine‐free” e‐cigarette liquids in Australia

Emily Chivers, Maxine Janka, Peter Franklin, Benjamin Mullins and Alexander Larcombe
Med J Aust 2019; 210 (3): . || doi: 10.5694/mja2.12059
Published online: 14 January 2019

Awareness and use of e‐cigarettes is increasing in Australia.1 The thousands of available e‐liquids contain various excipients, nicotine, flavourings, and other additives. There is little to no regulation of their manufacture, and potentially dangerous ingredients and incorrect nicotine levels have been identified.2 Of particular concern is the frequency with which nicotine is detected in e‐liquids labelled “nicotine‐free”.2 E‐liquids containing nicotine cannot legally be sold in Australia,3 but inaccurate labelling means that users may unwittingly inhale this addictive substance, or retailers may sell incorrectly labelled nicotine‐containing e‐liquids to willing customers. The aim of our investigation was to assess the chemical composition of a range of e‐liquids available in Australia, focusing on nicotine and other potentially harmful compounds. Formal ethics approval was not required for this study.

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  • 1 Telethon Kids Institute, Perth, WA
  • 2 University of Western Australia, Perth, WA
  • 3 Curtin University, Perth, WA



Acknowledgements: 

We acknowledge funding from the Australian Competition and Consumer Commission, Health Department of Western Australia, and from the National Health and Medical Research Council (APP1128231).

Competing interests:

No relevant disclosures.

  • 1. Yong HH, Borland R, Balmford J, et al. Trends in e‐cigarette awareness, trial, and use under the different regulatory environments of Australia and the United Kingdom. Nicotine Tob Res 2015; 17: 1203–1211.
  • 2. Trehy ML, Ye W, Hadwiger ME, et al. Analysis of electronic cigarette cartridges, refill solutions, and smoke for nicotine and nicotine related impurities. J Liq Chromatogr R T 2011; 34: 1442–1458.
  • 3. Douglas H, Hall W, Gartner C. E‐cigarettes and the law in Australia. Aust Fam Physician 2015; 44: 415–418.
  • 4. Goniewicz ML, Gupta R, Lee YH, et al. Nicotine levels in electronic cigarette refill solutions: a comparative analysis of products from the US, Korea, and Poland. Int J Drug Policy 2015; 26: 583–588.
  • 5. Abdel‐Gawad H, Hegazi B. Fate of 14C‐ethyl prothiofos insecticide in canola seeds and oils. J Environ Sci Health B 2010; 45: 116–122.
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The Australasian Society of Clinical Immunology and Allergy infant feeding for allergy prevention guidelines

Preeti A Joshi, Jill Smith, Sandra Vale and Dianne E Campbell
Med J Aust 2019; 210 (2): . || doi: 10.5694/mja2.12102
Published online: 14 January 2019

Abstract

Introduction: The Australasian Society of Clinical Immunology and Allergy, the peak professional body for clinical immunology and allergy in Australia and New Zealand, develops and provides information on a wide range of immune‐mediated disorders, including advice about infant feeding and allergy prevention for health professionals and families. Guidelines for infant feeding and early onset allergy prevention were published in 2016, with additional guidance published in 2017 and 2018, based on emerging evidence.

Main recommendations:

  • When the infant is ready, at around 6 months, but not before 4 months, start to introduce a variety of solid foods. (This is not a strict window of introduction but rather a recommendation not to delay the introduction of solid foods beyond 12 months.)
  • Introduce peanut and egg in the first year of life in all infants, regardless of their allergy risk factors.
  • Hydrolysed (partially and extensively) formula is no longer recommended for the prevention of allergic disease.

 

Changes in management a result of the guidelines: The guidelines specifically recommend introducing solid foods at around 6 months of age and introducing peanut and egg in the first year of life in all infants to prevent allergy development. Hydrolysed formula is no longer recommended for prevention of allergic disease. A new document outlining the reasons for and the method of peanut introduction to high risk infants is available for health professionals.


  • 1 Australasian Society of Clinical Immunology and Allergy, Sydney, NSW
  • 2 The Children's Hospital at Westmead, Sydney, NSW
  • 3 University of Sydney, Sydney, NSW



Competing interests:

Preeti Joshi is currently the chair of the ASCIA paediatric committee and the deputy chair of the National Allergy Strategy allergy prevention project. Sandra Vale is coordinator of the National Allergy Strategy. Jill Smith is the ASCIA CEO and company secretary. Dianne Campbell was chair of the ASCIA paediatric committee from 2011 to 2017, has received funding for unrelated research from the NHMRC, the Allergy and Immunology Foundation of Australasia and the Australian Food Allergy Foundation, and has received travel expenses to attend investigator meetings from DBV Technologies.

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Baby boomers and booze: we should be worried about how older Australians are drinking

Ann M Roche and Victoria Kostadinov
Med J Aust 2019; 210 (1): . || doi: 10.5694/mja2.12025
Published online: 14 January 2019

Alcohol research has traditionally focused on younger age groups; consumption patterns and predictors for older people have received only limited attention. However, the number of older Australians has increased substantially in recent years, accompanied by unprecedented changes in their alcohol consumption patterns. Older people are vulnerable to a range of alcohol‐related adverse effects, including falls and other injuries, diabetes, cardiovascular disease, cancer, mental health problems, obesity, liver disease, and early onset dementia and other brain injury.1,2,3 These vulnerabilities are a cause for clinical concern.

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  • National Centre for Education and Training on Addiction, Flinders University, Adelaide, SA


Correspondence: ann.roche@flinders.edu.au

Competing interests:

No relevant disclosures.

  • 1. Crome I, Dar K, Janikiewicz S, et al. Our invisible addicts: first report of the Older Persons’ Substance Misuse Working Group of the Royal College of Psychiatrists. Second edition (College Report CR211). London: Royal College of Psychiatrists, 2018. https://www.rcpsych.ac.uk/files/pdfversion/CR211.pdf (viewed Aug 2018).
  • 2. Scoccianti C, Cecchini M, Anderson AS, et al. European Code against Cancer 4th edition. Alcohol drinking and cancer. Cancer Epidemiol 2015; 39: S67–S74.
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Screening for perinatal depression and predictors of underscreening: findings of the Born in Queensland study

Macarena A San Martin Porter, Kim Betts, Steve Kisely, Gino Pecoraro and Rosa Alati
Med J Aust 2019; 210 (1): . || doi: 10.5694/mja2.12030
Published online: 14 January 2019

Abstract

Objectives: To investigate screening with the Edinburgh Postnatal Depression Scale (EPDS) as part of Queensland prenatal care services, as well as maternal and socio‐demographic factors associated with not being screened.

Design, setting: Cross‐sectional retrospective analysis of data from the Queensland population‐based Perinatal Data Collection for July 2015 – December 2015.

Participants: All women giving birth in Queensland during the second half of 2015.

Main outcome measures: Screening with the EPDS, with the values “yes” (health professional recorded an EPDS score), “no” (health professional reported it was not performed), and “not stated”.

Results: Of 30 468 women who gave birth in Queensland, 21 735 (71.3%) completed the EPDS during pregnancy; 18 942 pregnant women were enrolled as public patients (91.0%) and 2762 as private patients (28.8%). After adjusting for other socio‐demographic factors, screening was less likely for women who were aged 36 years or more (v 25 years or younger: adjusted odds ratio [OR], 0.69; 95% CI, 0.60–0.79), enrolled as private patients (aOR, 0.05; 95% CI, 0.05–0.06), born overseas (aOR, 0.75; 95% CI, 0.68–0.82), Indigenous Australians (aOR, 0.47; 95% CI, 0.39–0.56), single or separated (aOR, 0.83; 95% CI, 0.73–0.94), or of higher socio‐economic status.

Conclusions: Four years after clinical guidelines recommending universal screening with the EPDS were published, screening rates for private and public health care patients differed markedly. Our results may inform future comparisons and analyses of the impact on screening of recent changes to Medicare definitions intended to increase that of women in private health care.

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  • 1 Institute for Social Science Research, University of Queensland, Brisbane, QLD
  • 2 University of Queensland, Brisbane, QLD
  • 3 Curtin University, Perth, WA


Correspondence: m.sanmartinporter@uq.edu.au

Competing interests:

No relevant disclosures.

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