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Infectious diseases

Neglected tropical diseases in Australia: a narrative review

Neglected tropical diseases represent a threat to the health, wellbeing and economic prosperity of billions of people worldwide, often causing serious disease or death

Johanna Kurcheid · Catherine A Gordon · Naomi E Clarke · Kinley Wangdi · Matthew Kelly · Aparna Lal · Polydor N Mutombo · Dongxu Wang · Mary L Mationg · Archie CA Clements · Stephen Muhi · Richard S Bradbury · Beverley‐Ann Biggs · Wendy Page · Gail Williams · Donald P McManus · Darren Gray

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Clinical care of children and adolescents with COVID‐19: recommendations from the National COVID‐19 Clinical Evidence Taskforce

To the Editor: Fraile Navarro and colleagues1 recently published 20 recommendations for the treatment of coronavirus disease 2019 (COVID‐19) in children and adolescents from the National COVID‐19 Clinical Evidence Taskforce. For the paediatric inflammatory multisystem syndrome (PIMS‐TS) recommendations, the Taskforce convened an expert advisory group.1 In the absence of clinical trials, the panel considered peer‐reviewed guidelines and cohort studies to formulate consensus recommendations.1 However, they deferred providing any guidance to help clinicians prevent thromboembolism. We suggest the Taskforce consider the same approach for paediatric anticoagulation guidance. COVID‐19 is associated with marked coagulation activation and hypercoagulability in children.2,3 Life‐threatening pulmonary embolus requiring thrombolysis has been encountered in Australian adolescents hospitalised with COVID‐19. A retrospective cohort study published in 2021 found that 2.1% of children hospitalised with symptomatic COVID‐19 infection and 6.5% of those with PIMS‐TS developed thrombosis.4 Thrombosis occurred more frequently in children aged 12years and over who had central lines, PIMS‐TS, or an underlying oncological diagnosis. A D‐dimer of more than five times the upper limit of normal was significantly associated with thrombosis.4 The authors refer to “paediatric guidelines published in the US”, which are published on behalf of the Pediatric/Neonatal Hemostasis and Thrombosis Subcommittee of the International Society of Thrombosis and Haemostasis; these adapt current consensus prophylaxis guidelines to include COVID‐19‐specific features.5 In deferring making specific recommendations, the authors suggested using existing local thromboprophylaxis guidelines. The Royal Children’s Hospital, Melbourne and the Sydney Children’s Hospital, Randwick have both independently developed COVID‐19‐specific thromboprophylaxis guidelines (that are very closely aligned),6,7 as have many other centres globally because previous local thromboprophylaxis guidelines are inadequate for COVID‐19‐associated thrombotic coagulopathy. The Melbourne/Sydney guidelines advise baseline coagulation testing in hospitalised children with COVID‐19, incorporating D‐dimer to assist risk assessment, twice‐daily enoxaparin and anti‐Xa monitoring/dose titration.6,7 These could be provided as supplemental material in these living guidelines. The COVID‐19 anticoagulation in Children–Thromboprophylaxis (COVAC‐TP) trial — a phase 2 single‐arm study looking at 40 children who will receive monitored, low dose, twice‐daily enoxaparin (ClinicalTrials.gov Identifier NCT04354155) — will not change the level of evidence, so waiting for completion of this trial does not seem appropriate.

Gemma L Crighton · Anthea Greenway · Susan Russell

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Dermatology Letters 16 May 2022 Free

Mask exemptions for facial skin diseases: are they warranted?

To the editor: Clinicians are faced with requests for mask exemptions but guidance remains limited. In keeping with the Australasian College of Dermatologists’ guidelines,1 we believe skin problems are rarely severe enough to warrant exemption. The Department of Health and Human Services states people with “a serious skin condition of the face” are eligible for mask exemption,2 but this statement is open to interpretation. Mask exemptions for skin conditions are provided by numerous clinicians and not limited to dermatologists. Regardless of immunisation status, cases that may warrant exemption include severe dermatitis with crusting or weeping; severe infections such as impetigo or eczema herpeticum; bullous dermatoses, ectodermal dysplasias and other rare conditions featuring facial skin fragility; and post‐surgical procedures involving grafts or flaps where masks may impede healing. In addition, treatments for actinic damage such as 5‐fluorouracil, imiquimod or photodynamic therapy may cause severe inflammation.3 We suggest if exemptions are warranted, duration should be minimised, which may be before resolution of the dermatoses (eg, 2weeks followed by a review). This is essential given masks have been key in reducing severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) transmission.4 The development of an assessment pathway for facial dermatoses impeding mask use may be beneficial and should differentiate between health care workers, who wear fit‐tested masks, and the general public, guiding prompt treatment and follow‐up to facilitate a return to mask use. From our experience, facial masks may irritate the skin from pressure, sweating and humidity, and commonly aggravate underlying dermatoses, such as seborrheic dermatitis, acne or rosacea. Facial masks may rarely cause allergic contact dermatitis,5 and these cases should involve a contact dermatitis expert. Education regarding skin care is vital, in particular regular cleansing and reducing the number of products used which may aggravate acne. When utilising reusable masks, it is important to opt for an appropriate material such as light‐coloured cotton and maintain mask hygiene, which includes daily mask changes, regular washing, not sharing masks, and taking regular breaks from mask wearing. In summary, clinicians should remain vigilant when writing mask exemptions, aiming to minimise the duration by treating underlying skin problems and providing patient education.

Kajal Patel · Rosemary L Nixon

Mja2 51513

Effectiveness of COVID‐19 vaccines: findings from real‐world studies

To the Editor: We recently reviewed the first studies of the real‐world effectiveness of coronavirus disease 2019 (COVID‐19) vaccines.1 We found evidence of protection against serious illness and death but noted the difficulties in performing such studies in Australia. This was because of the (then) low national case numbers and lack of ready access to the necessary linked health data. Since then, the literature on vaccine effectiveness has expanded dramatically. By February 2022 the Johns Hopkins Bloomberg School of Public Health and partners had generated a database of 181 studies conducted in 26 countries.2 The most studied vaccines were Pfizer (117 studies), Moderna (47), AstraZeneca (43), Janssen (17) and Sinovac (8). Twenty‐three studies investigated booster doses, and seven studies mentioned analysis of the Omicron variant. Study outcomes included infections (117 studies), hospitalisations (69), deaths (30), and viral transmission (5). Study designs varied, with 32 mentioning cohort analysis and 16 mentioning test negative analysis in their titles. Most studies were performed in the United States (56 studies), followed by Israel (32), the United Kingdom (29), Qatar (9), Canada (8), Brazil (6) and Denmark (4). Not one of the listed studies was conducted in Australia. We should be asking why. Australia no longer lacks the case numbers to make estimates of vaccine effectiveness. We collect good data on vaccination status, infections (including viral variants), hospitalisations and deaths, plus the information needed to adjust for confounding of the associations between vaccine exposure and outcomes. However, authorities have not linked these datasets at individual level and made them available for detailed analysis. This situation should not continue. There are well established principles for protecting the privacy of individuals who are included in routinely collected data.3 The Commonwealth and state governments and relevant agencies seem unable or unwilling to link and properly analyse these data. Consequently, they should ensure that regularly updated comprehensively linked de‐identified datasets can be accessed by qualified researchers. Stephen Duckett has recently called for an Australian review of lessons from the COVID‐19 pandemic using a systems rather than a punitive lens.4 We agree. Better linkage, access and analysis of our health system data should be high on the list.

David A Henry · Mark A Jones · Paulina Stehlik · Paul P Glasziou

Mja2 51479

The COVID Positive Pathway: a collaboration between public health agencies, primary care, and metropolitan hospitals in Melbourne

About 80% of participants could be adequately supported by primary care and community organisations

Seok Ming Lim · Nicole L Allard · Janelle Devereux · Benjamin C Cowie · Michelle Tydeman · Alistair Miller · Khanh Ho · Brigitte Cleveland · Liz Singleton · Karen Aarons · Paul Eleftheriou · Thomas Chan · George Braitberg · Andrea Maier

Mja2 51449

COVID‐19 vaccination in children and adolescents aged 5 years and older undergoing treatment for cancer and non‐malignant haematological conditions: Australian and New Zealand Children’s Haematology/Oncology Group consensus statement

Recommendations are based on evidence-based knowledge of safety, immunogenicity and efficacy of the vaccines in the general population, plus emerging data regarding COVID-19 vaccination in immunocompromised individuals

Eliska Furlong · Rishi S Kotecha · Rachel Conyers · Tracey A O'Brien · Jordan R Hansford · Leanne Super · Peter Downie · David D Eisenstat · Gabrielle Haeusler · Brendan McMullan · Marianne B Phillips · Bhavna Padhye · Luciano Dalla‐Pozza · Frank Alvaro · Christopher J Fraser · Wayne Nicholls · Julia E Clark · Matthew O'Connor · Benjamin R Saxon · Heather Tapp · John Heath · Sarah E Hunter · Karen Tsui · Mark Winstanley · Amanda Lyver · Emma J Best · Ushma Wadia · Daniel Yeoh · Christopher C Blyth · Nicholas G Gottardo

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