MJA 212 4 2 Mar cover

Issues

Volume 212 Issue 4

2 March 2020

News

2 March 2020 Free

News briefs

Further evidence linking diabetes drug to heart problems Research published by The BMJ adds to evidence that rosiglitazone, used to treat type 2 diabetes, is associated with increased risk of heart problems, especially heart failure. Rosiglitazone, a thiazolidinedione, helps control blood sugar levels in patients with type 2 diabetes, but can also increase the risk of serious heart problems, leading to suspension of its use in Europe and to earlier restrictions in the US. However, conflicting findings have been reported since 2007 of meta‐analyses of studies investigating whether rosiglitazone increases the risk of heart attack. The relevant studies did not have access to individual patient level data from clinical trials, instead relying on summary level data (ie, results reported in publications and clinical trial registries), which are not as reliable for assessing the safety profile of drugs. US researchers have now analysed the results of more than 130 trials, involving more than 48 000 adult patients, that compared rosiglitazone with any control for at least 24 weeks. Individual patient level data were available for 33 of the trials (21 156 patients), analysis of which indicated that rosiglitazone was associated with a 33% higher risk of a composite cardiovascular event (heart attack, heart failure, cardiovascular‐ and non‐cardiovascular‐related death) compared with controls (274 events among 11 837 patients taking rosiglitazone and 219 events among 9319 control patients). In particular, analysis of the 33 trials with individual patient level data yielded higher estimates of the risk of heart attacks than did those of trials reporting patient or summary level data. These findings highlight the potential for differing results to be derived from different types of data, and underline the need for greater clinical trial transparency and data sharing to accurately assess the safety of drugs, say the researchers. https://www.bmj.com/content/368/bmj.l7078 Mental health‐related tweets associated with crisis referrals Referrals for patients requiring urgent help to two mental health care providers in London were significantly more frequent on days with a higher than average number of tweets discussing mental health topics, according to an article published in Scientific Reports. Earlier studies had found that social media use, depiction of mental illness in the media, and public discussions about mental health may be associated with negative mental health outcomes. Research has primarily focused on high profile events reported by news media, while associations with references to mental health in social media are less well studied. The researchers compared the number of tweets including keywords associated with two important mental health disorders ― depression and schizophrenia ― with recorded referrals for “crisis episodes”. Between January 2010 and December 2014, 48 691 and 32 689 crisis episodes were respectively recorded by the two mental health providers. On days with a higher than average number of tweets mentioning depression or schizophrenia or showing support for people with either illness, the authors observed a 5–15% increase in the number of people referred with mental health‐related crisis episodes. The authors suggested that the factors underlying these associations should be further investigated, as should whether social media platforms could be monitored by health care services to identify vulnerable groups and predict times of higher risk. https://www.nature.com/articles/s41598-020-57835-9

Perspectives

Medical education

Cancer 2 March 2020 Lessons from Practice Free

Hidden in plain sight: umbilical melanoma

A 74-year-old Caucasian woman was referred for hirsutism over the abdomen and was incidentally found to have a 21 × 25mm ulcerated nodule over the umbilicus

Tom Kovitwanichkanont · Shoba Joseph · Leona Yip

Dermatology 2 March 2020 Clinical skills Free

How to perform a skin biopsy

The skin has more disease processes than any other organ system in medicine, with over 3000 dermatological conditions described

Kirsty JL Wark · Saxon D Smith · Deshan F Sebaratnam

Editorials

Research

Guideline summary

Narrative review

Letters

Neurology 2 March 2020 Free

Expanding the availability of medications for amyotrophic lateral sclerosis in Australia

To the Editor: Amyotrophic lateral sclerosis (ALS) is a rapidly progressive and fatal neurodegenerative condition with no cure. Only two treatments with class I evidence exist — riluzole1 and edaravone2 — both with unclear mechanisms of action and modest survival benefits. In Australia, riluzole remains the only treatment approved by the Therapeutic Goods Administration. The Pharmaceutical Benefits Scheme limits initiation of riluzole to patients with at least 60% of predicted forced vital capacity, although facial weakness may make this an unreliable target. Initial and continuing treatment requires patients to be ambulant; or to have good upper limb function or to be able to swallow; and not to have respiratory failure. A recent retrospective study classified patients into different disease severity stages, ranging from 1 (one region involved) to 5 (death); patients with respiratory and nutritional failure were assigned to stage 4.3 The study identified that patients in stage 4 receiving 100 mg of riluzole daily did not progress to the next clinical stage (ie, death) as rapidly as those in milder stages. This suggests that the modest survival benefit experienced by patients taking riluzole comes about by extending the time spent at this stage. A quarter of patients present with bulbar or respiratory onset,4 making many ineligible for treatment, despite data suggesting they may benefit most.5 Mean survival in these forms of ALS is particularly short, meaning the modest survival benefit offered should be considered, as a majority of patients with advanced ALS do not wish to hasten death.6 A recent study of over 4000 trial participants confirmed benefit in both early and late stages,7 supporting use of riluzole throughout the disease. Few prospective studies on late‐stage treatments exist; patient choice in continuing treatment during advanced stages therefore remains paramount. Prospective studies are needed to establish whether the benefit of riluzole is weighted towards more advanced disease. However, recent studies, along with the recognition of the clinical spectrum of ALS, indicate that the current Pharmaceutical Benefits Scheme criteria are too stringent. As we move towards precision‐based medicine, different profiles of therapeutic response are likely. Regulators will be required to rapidly respond to emerging data to ensure the right patients can access the right medications.

Colin J Mahoney · Matthew C Kiernan

Advancing women in medical leadership

To the Editor: We applaud the astute perspective of Teede in relation to gender equity in medical leadership.1 Organisational culture that promotes male leadership styles is self‐perpetuating and this has implications for our specialty of endocrinology, which is rapidly becoming “feminised”. About 80% of physician advanced trainees in endocrinology are female and yet only 20% of heads of endocrinology departments in Australian training hospitals are women (Royal Australasian College of Physicians Advanced Training in Endocrinology Program, unpublished data). Waseem and colleagues2 documented significant under‐representation of women at higher academic levels in endocrinology societies internationally. Only 23% of full professors and 31% of board members were female. Women have fewer publications or research citations, but their skill sets are diverse and they bring value to executive boards through negotiation and problem solving skills. The historical biases around the expectations of women are perpetuated by male powerbrokers. Unconscious bias can be subtle. Duma and colleagues3 reported that when introducing female speakers at an international conference, men were more likely to use a woman's first name alone, but male speakers were introduced with full professorial title and surname. This undervalues the women who already tend to underplay their own skills. Part‐time employment may be supported in theory, but it is left up to the woman to find a solution. Women fear that part‐time work may challenge perceptions of competence. A healthy endocrinology training scheme must support our significant female workforce and serve the 70% of endocrinology outpatients who are women. We have wonderful male colleagues who are willing to support progress, but they may be deterred by the stigma attached to issues such as paternity leave. The current chair of the Royal Australasian College of Physicians Advanced Training Committee and the coordinator of the Advanced Training in Endocrinology Program are both women, so we do see a bright future ahead. This is an important issue for our patients, for women and for men.

Diana L Learoyd · Jane Holmes‐Walker

Advancing women in medical leadership

To the Editor: Teede's inspirational, forward‐looking review1 should also prompt scrutiny of the philosophical constructs underpinning gender equity. “Unconscious bias” is raised four times but does not appear to be supported by referencing, apart from a qualitative survey which reports the perception of unconscious bias.1 Some critics have argued2,3,4 that implicit (unconscious) bias as a factor in creating gender or other types of societal inequity is not proven, and that the Implicit Association Test, which has been used to support the concept of implicit bias, does not meet criteria for reliability and validity.2,3 Substantive equality allows different groups to be treated differently to enable members of these groups to enjoy equal human rights. It is the philosophical justification for the legal instrument of “special measures”, as described in the Australian Human Rights Commission guidelines on special measures under the Sex Discrimination Act 1984 (Cth).4 Special measures allow for “lawful” discrimination, without which, for example, leadership programs for women and quotas would be unlawful under anti‐discrimination legislation. However, there is no strict legal definition of special measures and the guidelines do not provide a definitive legal clarification of the special measures allowed under the Sex Discrimination Act.5 This leads to the question of how individuals, institutions and the legal system can determine if substantive equality has been achieved and whether this has led to gender equity. Although statistics are frequently used to support either the attainment of gender equity, as they are in Teede's article,1 or the lack of it, the concept of “disparate impact” needs to be considered. This describes the situation where groups which have protection under the law (eg, for race or gender) experience disadvantage despite all the rules being formally neutral. The United States Supreme Court6 found in 2015 that a “disparate‐impact claim relying on a statistical disparity must fail if the plaintiff cannot point to a defendant's policy or policies causing that disparity”. That is, a statistical variation alone cannot prove discrimination. Such findings are also likely to partly shape debate in Australia. In summary, justifying otherwise discriminatory means of redress using the unjustifiably blunt dichotomous test of “gender” creates untenable rankings of individual disadvantage.7 How does this deal with the situation where, for example, a man wishes to make career sacrifices for childrearing. Should this situation be included in special measures?

Michael Keane

Careers

14 February 2020 Free

Leading a Thursday Island life

Dr Allison Hempenstall left herself open to all career possibilities and so far, things are working out well …

Cate Swannell

Next Issue Volume 212 Issue 5

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MJA 212 5 16 Mar cover
News 16 March 2020 Free

News briefs

Perspectives 16 March 2020 Free

More than a refresh required for closing the gap of Indigenous health inequality

Chelsea J Bond · David Singh

Perspectives 16 March 2020 Free

Lessons learned in genetic research with Indigenous Australian participants

Steven YC Tong · Heather D'Antoine · Melita McKinnon · Kyle Turner · Maui Hudson · Ngiare Brown · Jonathan R Carapetis · Dawn C Bessarab

Perspectives 16 March 2020 Free

Investing in the health of Aboriginal and Torres Strait Islander adolescents: a foundation for achieving health equity

Peter Azzopardi · Ngaree Blow · Tara Purcell · Ngiare Brown · Tirritpa Ritchie · Alex Brown

Previous Issue Volume 212 Issue 3

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MJA 212 3 17 Feb cover
Perspectives 17 February 2020 Free

Exploring the role of a recently licensed dengue vaccine in Australian travellers

Irani Thevarajan · Joseph Torresi · Cameron Simmons

Perspectives 17 February 2020 Free

Implementing value‐based health care at scale: the NSW experience

Elizabeth Koff · Nigel Lyons

Medical education 3 February 2020 Lessons from practice Free

HPV swab self‐collection and cervical cancer in women who have sex with women

Monica FG McGauran · Adam Pendlebury

Medical education 17 February 2020 Snapshot Free

Eumycetoma diagnosed in urban Australia

Lakshana Kalatharan · Peter Kelley

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