1,927 results match your criteria: "Queensland Childrens Hospital[Affiliation]"

"You need to be supported": An integrative review of nurses' experiences after death in neonatal and paediatric intensive care.

Aust Crit Care

December 2024

End-of-Life Advisory Panel, Australian College of Critical Care Nurses, Banora Point, NSW, Australia; Paediatric Intensive Care Unit, Queensland Children's Hospital, South Brisbane, QLD, Australia.

Background: The death of a child can have a profound impact on critical care nurses, shaping their professional practice and personal lives in diverse, enduring ways. Whilst end-of-life care is recognised as a core component of critical care nursing practice and a research priority, evidence about nurses' experiences after death in neonatal and paediatric intensive care is poorly understood.

Research Question: What is the experience of the nurse after death of a patient in neonatal and/or paediatric intensive care?

Method: Following registration with Open Science Framework, an integrative review of the empirical literature was undertaken.

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Lung Point of Care Ultrasound (POCUS) strongly influences physiotherapy and respiratory therapy clinical decision-making in the intensive care unit (ICU). The uptake of Lung POCUS training by physiotherapists and respiratory therapists is low in some countries, often due to many barriers to its implementation. The safe and appropriate integration of Lung POCUS into physiotherapy and respiratory therapy clinical practice may be achieved by various means.

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Background: Rapid Response Systems are hospital-wide patient-focused systems aiming to improve recognition of acute deterioration in patients and trigger a rapid response aimed at preventing potentially avoidable adverse events such as cardiac arrest and death. In 1994, the Royal Children's Hospital in Brisbane, Australia, was one of the first institutions to adopt a paediatric rapid response system (RRS). The purpose of this study was to investigate the impacts of both introduction of a paediatric RRS and increasing RRS activations (MET dose) on hospital mortality.

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Compassionate access to virus-specific T cells for adoptive immunotherapy over 15 years.

Nat Commun

December 2024

Queensland Immunology Research Centre, Infection and Inflammation Program, QIMR Berghofer Medical Research Institute, Herston, Queensland, Australia.

Adoptive T-cell immunotherapy holds great promise for the treatment of viral complications in immunocompromised patients resistant to standard anti-viral strategies. We present a retrospective analysis of 78 patients from 19 hospitals across Australia and New Zealand, treated over the last 15 years with "off-the-shelf" allogeneic T cells directed to a combination of Epstein-Barr virus (EBV), cytomegalovirus (CMV), BK polyomavirus (BKV), John Cunningham virus (JCV) and/or adenovirus (AdV) under the Australian Therapeutic Goods Administration's Special Access Scheme. Most patients had severe post-transplant viral complications, including drug-resistant end-organ CMV disease, BKV-associated haemorrhagic cystitis and EBV-driven post-transplant lymphoproliferative disorder.

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Reporting Indigenous status, ethnicity, language and country of birth to build equity in international paediatric clinical trials with Australian sites: a scoping review.

Aust Health Rev

December 2024

School of Nursing, Midwifery and Social Work, Faculty of Health and Behavioural Sciences, The University of Queensland, St Lucia, Qld, Australia; and Queensland Children's Hospital, Children's Health Queensland Hospital and Health Service, South Brisbane, Qld, Australia.

Article Synopsis
  • The review emphasizes the need for equitable access to clinical trials for children from Indigenous and diverse backgrounds, which should be a priority in trial design.
  • A systematic search of clinical trials conducted in Australia between 2018 and 2022 revealed that over 58% did not report important demographic variables like Indigenous status or ethnicity, highlighting significant gaps in data collection.
  • The findings suggest implementing clear reporting standards and encouraging self-identification to improve demographic data collection, which is crucial for fostering health equity and safety in clinical trials involving children.
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Treatment regimens and glycaemic outcomes in more than 100 000 children with type 1 diabetes (2013-22): a longitudinal analysis of data from paediatric diabetes registries.

Lancet Diabetes Endocrinol

January 2025

Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden; Steno Diabetes Center Copenhagen, Herlev, Denmark; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.

Background: Advances in paediatric type 1 diabetes management and increased use of diabetes technology have led to improvements in glycaemia, reduced risk of severe hypoglycaemia, and improved quality of life. Since 1993, progressively lower HbA targets have been set. The aim of this study was to perform a longitudinal analysis of HbA, treatment regimens, and acute complications between 2013 and 2022 using data from eight national and one international paediatric diabetes registries.

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Objective: To stimulate discussion on how the RANZCP can contribute more constructively to the debate over Australia's immigration policies.

Conclusions: Updated in March 2024, RANZCP Position Statement 46, titled: 'The provision of mental health services for asylum seekers and refugees', continues the College's advocacy for a compassionate stance towards asylum seekers and refugees on the grounds of preventing or improving their mental health. College statements over the last decade have raised concerns about policies that are designed to deter boat arrivals; and recently, have endorsed the High Court's NZYQ decision to mandate community release of detained non-Australian citizens deemed to have failed 'the character test' under the .

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  • * Focus groups comprised of educators and practitioners shared insights on integrating VDS at different stages of dental training, using the Simodont® Dental Trainer system for curriculum design.
  • * Recommendations include introducing VDS for manual dexterity in the first year, cariology in the second, and crown preparation in the third, while allowing flexibility for each institution to customize the approach to suit their needs.
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Article Synopsis
  • - The study aimed to investigate parents' experiences with continuous glucose monitoring (CGM) for their young children who have early-stage type 1 diabetes enrolled in the ENDIA study.
  • - A total of nine parents participated in semi-structured phone interviews after a CGM monitoring period, highlighting three key themes: empowerment through information, acceptance of CGM use, and the benefits of involvement in research.
  • - Results showed that parents had a positive experience with their children's use of CGM, feeling supported and less uncertain about managing their child's diabetes with the valuable data provided by the monitoring.
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Background: Various mechanisms leading to early hyperlactataemia post-cardiac surgery have been postulated. Specifically, in the paediatric population, benign early hyperlactataemia may be associated with crystalloid priming in the cardiopulmonary bypass circuit. The aim of this study was to review paediatric patients who had crystalloid prime and assess their outcomes.

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The potential effects of climate change on non-cystic fibrosis bronchiectasis in children.

Paediatr Respir Rev

October 2024

Department of Respiratory and Sleep Medicine, Queensland Children's Hospital, Brisbane, Australia; Australian Centre for Health Services Innovation, Queensland University of Technology, Brisbane, Australia; Child Health Division, Menzies School of Health Research, Darwin, Australia.

Climate change may have devastating effects on the pathogenesis of non-cystic fibrosis bronchiectasis in children since it affects the biological cycle of the respiratory pathogens and alters the human respiratory defense mechanisms. Bronchiectasis in children has been identified as an emerging global epidemic that has attracted the attention of the medical community over recent years. Pediatric pulmonologists should be aware of the consequences of climate change on children with bronchiectasis and plan strategies to ameliorate these effects.

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Article Synopsis
  • Secondary deformities in the midface are common after cleft lip and palate repair, causing functional, aesthetic, and psychosocial issues.
  • Treatment options for patients with midfacial hypoplasia may include autologous and alloplastic maxillary augmentation, depending on individual deformity assessments.
  • A study using CT scans revealed significant variations in maxillary projection in cleft patients, emphasizing the need for precise evaluations to create tailored treatment plans for effective correction of nasomaxillary deformities.
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Outcomes after hospital discharge in children requiring post-cardiotomy extracorporeal membrane oxygenation: A binational retrospective cohort study.

J Thorac Cardiovasc Surg

November 2024

Faculty of Medicine, University of Queensland, Brisbane, Australia; Department of Cardiac Surgery, Queensland Children's Hospital, Brisbane, Australia. Electronic address:

Objectives: To describe longer-term survival and morbidity outcomes after hospital discharge in a binational cohort of children who required extracorporeal membrane oxygenation after cardiac surgery.

Methods: This was a retrospective cohort study from the Australia and New Zealand Congenital Outcomes Registry for Surgery database. All patients younger than 18 years of age (n = 12,290) undergoing pediatric cardiac surgical procedures between January 1, 2013, and December 31, 2021, who required post-cardiotomy extracorporeal membrane oxygenation in the same admission were included.

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Neurodevelopmental follow-up care pathways and processes for children with congenital heart disease in Australia.

Pediatr Res

November 2024

Australian Centre for Health Services Innovation and Centre for Healthcare Transformation, School of Public Health and Social Work, Faculty of Health, Queensland University of Technology, Brisbane, QLD, Australia.

Background: International consensus exists for neurodevelopmental follow-up care of children with congenital heart disease (CHD) to support timely intervention for developmental delays. Yet, documentation of how this care is implemented in Australia is lacking. This study aimed to identify, categorise, and understand care pathways and services supporting neurodevelopmental follow-up of Australian children with CHD.

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Background: Infectious syphilis among women of reproductive age continues to rise in many countries including Australia, with a resultant increase in congenital syphilis. In response, new guidelines for management of syphilis in pregnancy were published in Queensland, Australia in 2018.

Aims: This study evaluates the management of women diagnosed with syphilis in pregnancy in South-East Queensland (SEQ) after release of this guideline.

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Background: New paradigms of diagnosis and treatment have changed the neurodegenerative trajectory for individuals with spinal muscular atrophy (SMA). Registries are a critical tool to provide real-world data on treatment patterns, their effects and health care provision within this evolving paradigm of care. This study aimed to evaluate the phenotypic and genotypic landscape, treatment patterns and health impact of SMA in Australia through the national registry.

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Second Opinion Seeking in Paediatric Oncology: Motivations and Predictors.

Psychooncology

November 2024

School of Clinical Medicine, Discipline of Paediatrics and Child Health, UNSW Medicine & Health, UNSW Sydney, Sydney, Australia.

Introduction: This study investigated the prevalence, methods and factors leading carers of childhood cancer patients to seek second opinions.

Methods: A prospective, questionnaire-based study was conducted among families attending oncology clinics at Sydney Children's Hospital, Randwick. Participants were asked whether they had sought a second opinion for their child and if so, their motivations.

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  • A study reviewed medical records from eight hospitals in Australia and New Zealand examining how intravenous aciclovir is prescribed for suspected herpes simplex virus (HSV) disease in neonates and older children between January and December 2019.
  • Out of 1,426 patients, most received aciclovir for suspected cases without definitive HSV testing; notably, only a small fraction had confirmed diagnoses among older children, indicating potentially excessive and unjustified prescribing.
  • Among the patients, adverse effects included instances of nephrotoxicity and extravasation injuries, raising concerns about the safety and necessity of such treatments in the pediatric population.
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Background: Prompt antibiotic administration for febrile neutropenia (FN) is standard of care, and targets of time to antibiotics (TTA) <60 min are common. We sought to determine the effect of TTA ≥60 versus <60 min on adverse outcomes (intensive care unit (ICU) admission or death) in children with cancer and FN. Effect modification by a decision rule that predicts infection (AUS-rule) and bacteraemia were also investigated.

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  • Self-poisoning is the most common form of self-harm among young people in Australia, and rates have been increasing, especially during and after the COVID-19 pandemic.
  • A study analyzed data from poison information centers from 2018 to 2023, finding a significant rise in self-poisoning cases, particularly among females aged 5-19, with an overall increase of 29.6% during this period.
  • After pandemic restrictions lifted, there was an initial drop in self-poisoning cases, but they declined slowly overall, highlighting the need for ongoing monitoring and support for mental health among young people.
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Purpose: Heterozygous pathogenic variants in NTRK2 (HGNC: 8032) have been associated with global developmental delay. However, only scattered cases have been described in small or general studies. The aim of our work was to consolidate our understanding of NTRK2-related disorders and to delineate the clinical presentation.

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Perceptions of service providers on available care for paediatric feeding disorder: A survey study.

J Paediatr Child Health

January 2025

School of Health and Rehabilitation Sciences, The University of Queensland, Brisbane, Queensland, Australia.

Aim: This study aimed to describe current strengths and gaps in services for children with feeding needs in Southeast Queensland, Australia from the perspective of key professionals involved in service design and provision.

Methods: A web-based survey was distributed to health professionals involved in providing services to children with feeding needs, staff who triaged/managed referrals, and/or service team leaders in Southeast Queensland.

Results: There were 79 responses to the survey, with 61 of these responses included in the analysis.

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Purpose: Navigating the feeding journey of medically complex infants on long-term high flow nasal cannula support can be challenging for caregivers, especially given inconsistencies in clinical practice for oral feeding on high flow nasal cannula support. The aim of this study was to explore the perspectives of caregivers who have experienced this journey, to inform best practice care.

Method: This study used a generic qualitative inquiry approach.

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