MJA 217 5 5 Sept cover

Issues

Volume 217 Issue 5

5 September 2022

News

5 September 2022 Free

News briefs

COVID‐19 during pregnancy: increased risk of severe illness Coronavirus disease 2019 (COVID‐19) infection in pregnant women is associated with increased risk of adverse outcomes compared with women who are not pregnant, according to a review published in JACC: Advances. Cardiovascular complications include heart attack, arrythmias, heart failure and long‐haul symptoms that may be difficult to distinguish from other cardiac complications of pregnancy and require the cardiovascular care team to be vigilant when assessing pregnant women with COVID‐19. The Centers for Disease Control and Prevention (CDC) found pregnant women are at increased risk of adverse outcomes with COVID‐19, including severe infection (10%), intensive care unit admission (4%), mechanical ventilation (3%), and use of extracorporeal membrane oxygenation haemodynamic support (0.2%), compared with non‐pregnant women of reproductive age. Additionally, pregnant patients who were of increased maternal age, high body mass index or had other pre‐existing conditions, such as chronic hypertension, pre‐eclampsia and pre‐existing diabetes, were at even higher risk for severe infection. When compared with pregnant women without COVID‐19, pregnant patients with COVID‐19 were at higher risk for pre‐term birth and stillbirth. Overall, 33% of infants born to patients with COVID‐19 were admitted to the neonatal intensive care unit. No other differences have been found for perinatal outcomes. According to the authors, a reason for increased risk of cardiovascular complications is the low vaccination rate in pregnant women compared with other groups. In a recent study of over 130 000 pregnant people, over three‐quarters of those requiring hospital admission, most patients requiring critical care, and all fetal deaths occurred in unvaccinated compared with vaccinated women. The authors suggest management of cardiac complications in pregnant patients with COVID‐19 requires the creation of a “pregnancy heart team” to optimise care, which may include providers comfortable with high risk pregnancy, obstetric anaesthesia, cardiology, critical care and neonatal care, depending on the nature of the complication, stage of pregnancy and severity of infection. https://www.sciencedirect.com/science/article/pii/S2772963X22000618?via%3Dihub Mystery gene that helps mice survive virus infections Researchers from UNSW Sydney have discovered that a particular transposable element, or jumping gene, in the genome has a profound effect on the immune response to virus infection. The findings in mice, published in Nature, provide new information about how the immune system is regulated, and have potential ramifications for the treatment of virus infections that can lead to an overactive immune response. Up to two‐thirds of a mammal’s genome are obtained from transposable elements. But apart from some consensus that transposable elements negatively or positively affect gene transcription — a fundamental process in our genome where DNA gets copied into RNA — scientists do not fully understand what these jumping genes do. The authors say to really understand their function, researchers needed to observe what happens when they remove one of these transposable elements from an animal. This particular transposable element is located near one of the most highly expressed genes following virus infection, in the Schlafen gene family. There are ten Schlafen genes in mice and seven in humans and they are critically important as they encourage cell proliferation in response to viruses and inhibit virus replication. After knocking out one of the transposable elements — called Lx9c11 — from mice, the researchers infected the animals with Coxsackievirus B4, a virus that largely affects the pancreas and some other tissues. But instead of usually clearing the virus, the mice who had lost the Lx9c11 element died. The researchers discovered the Lx9c11 deficient mice had an exaggerated immune response, similar to what is rarely experienced by patients with influenza and more commonly experienced by people with severe COVID‐19. And the data indicated that the lethality was host induced. When they put the transposable element back into other still‐living mice that had been infected with Coxsackievirus B4, those mice survived the infection. https://www.nature.com/articles/s41586‐022‐05054‐9

Perspectives

Medical education

Editorials

Research

Research letter

Narrative review

Surgery 22 August 2022 Open Access

Breast surgery: a narrative review

Increased understanding of how to predict who is most at risk of breast cancer is leading to the possibility of risk-based screening, allowing better and more targeted early detection and treatment for women at high risk

Christobel M Saunders

Letters

Musculoskeletal diseases 5 September 2022 Free

Vertebral fractures after denosumab discontinuation for dental procedures: a consequence of distorted perceptions of risk

To the Editor: Khatri’s and Stuckey’s1 article, Vertebral fractures after denosumab discontinuation for dental procedures: a consequence of distorted perceptions of risk, sums up the authors’ knowledge and experience of medication‐related osteonecrosis of the jaws (MRONJ) in the latter part of the title. They quote the risk of MRONJ as being very low and equal for denosumab and oral bisphosphonates. This is incorrect. The risk of MRONJ is 0.3%.2 In our study we found the risk following extractions at 1.8%.3 The recent 2022 update of the position paper on MRONJ4 found that the risk with denosumab is an order of magnitude higher than for bisphosphonates. There is no discussion in Khatri’s and Stuckey’s article1 of the effect of MRONJ on patients. A patient with stage 3 or end‐stage MRONJ has months of severe pain and requires jaw resection with or without microvascular reconstruction similar to that required for advanced jaw cancer.4,5 The impact of this is similar to vertebral collapse, both largely avoidable disasters. The current Australian recommendations for dental extractions for patients taking denosumab for osteoporosis are to delay extractions to 6 months after the last injection of denosumab and then to allow 4weeks for initial socket healing before the next injection.6 The risk is greater if the patient has been taking antiresorptives for more than 4years and if they are immunocompromised.4,7 We would agree that education and communication between prescribers, patients and dentists are key. This can only be achieved by close, mutually respectful communication and understanding between medical, dental, oral and maxillofacial surgeons and patients. However, this is easier to say than put into meaningful practice. Most definitive articles on MRONJ are in oral and maxillofacial surgery journals, which are not commonly read by physicians who prescribe antiresorptives. The most likely reason that the patient was taken off denosumab for 5 months was that the dental plan was not only to extract the teeth but to replace them with dental implants. Implants require time for osseointegration.8 Hopefully, this letter helps correct the distorted precepts expressed by Khatri and Stuckey for prescribers of this, otherwise, useful drug.

Alastair Goss

Infectious diseases 5 September 2022 Free

Congenital cytomegalovirus: the case for targeted infant screening in Australia

To the Editor: We write in response to Reid and colleagues’1 article on congenital cytomegalovirus (CMV). While many countries worldwide have established congenital CMV screening programs, Australia urgently needs to recognise the importance of targeted congenital CMV screening and tracking its outcomes. Our 2019–2020 study tested the feasibility and acceptability of a parent‐completed targeted congenital CMV saliva polymerase chain reaction (PCR) screening program in Victoria.2 Parents of infants who did not pass their newborn hearing screening at four Victorian maternity hospitals completed their infants’ saliva swabs in the hospital or at home. The program was feasible with a 76% participation rate, and all 96 swabs (100%) were completed within the required 21days from birth, despite the majority being completed at home. Furthermore, more than 90% of families found the screen easy to do, thought it was a good idea, and were glad their baby had congenital CMV screening. However, there were challenges: false positive screens due to CMV contamination in breast milk, and excessive time taken from completing the screen to return of results due to reliance on the only laboratory in the state accredited to process saliva CMV PCR. We now have the means to overcome these challenges, determine whether universal congenital CMV screening in Australia is warranted, and systematically track outcomes of targeted congenital CMV screening. For 2years from October 2021, Murdoch Children’s Research Institute’s Generation Victoria (GenV) is recruiting a whole‐of‐state infant–parent cohort, collecting over 110000 saliva swabs from newborns to test for CMV using novel CRISPR technology at the Walter and Eliza Hall Institute of Medical Research.3 Our study, funded by the National Health and Medical Research Council, will determine the population prevalence of congenital CMV, develop a rapid bedside point‐of‐care test for congenital CMV screening, and establish whether universal congenital CMV screening is cost‐effective. In addition, the Australasian Congenital CMV Registry has been recently established to track outcomes of congenital CMV.4 These initiatives will pave the way for Australia to emerge as a leader in congenital CMV screening, better recognise this undetected condition of public health importance, and provide personalised care to affected children.

Emma Webb · Cheryl A Jones · Valerie Sung

Next Issue Volume 217 Issue 6

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MJA20217 6 1920 Sept20cover
News 19 September 2022 Free

News briefs

Perspectives 5 September 2022 Open Access

Assessing the value of precision medicine health technologies to detect and manage melanoma

Rashidul A Mahumud · Monika Janda · H Peter Soyer · Pablo Fernández‐Peñas · Victoria J Mar · Rachael L Morton

Perspectives 19 September 2022 Open Access

Roadmap to incorporating group A Streptococcus molecular point‐of‐care testing for remote Australia: a key activity to eliminate rheumatic heart disease

Dylan D Barth · Gelsa Cinanni · Jonathan R Carapetis · Rosemary Wyber · Louise Causer · Caroline Watts · Belinda Hengel · Susan Matthews · Anna P Ralph · Janessa Pickering · Jeffrey W Cannon · Lorraine Anderson · Vicki Wade · Rebecca J Guy · Asha C Bowen

Perspectives 29 August 2022 Open Access

Establishing the worth of deprescribing inappropriate medications: are we there yet?

Ian A Scott · Emily Reeve · Sarah N Hilmer

Previous Issue Volume 217 Issue 4

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MJA 217 4 15 Aug cover
News 15 August 2022 Free

News briefs

Perspectives 1 August 2022 Open Access

Making everyone count: it is time to improve the visibility of people with disability in primary care

Jodie Bailie · Nicola Fortune · Julie Gordon · Richard C Madden · Gwynnyth Llewellyn

Perspectives 1 August 2022 Open Access

More than a fleeting conversation: managing medication communication across transitions of care

Elizabeth Manias · Carmel Hughes · Robyn E Woodward‐Kron · Christine M Jorm · Guncag Ozavci · Tracey K Bucknall

Perspectives 25 July 2022 Open Access

Voluntary assisted dying: estimating life expectancy to determine eligibility

Sharon H Nahm · Martin R Stockler · Belinda E Kiely

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