Stephanie Yerkovich

Stephanie Yerkovich
Stephanie Yerkovich is a Professor at the Menzies School of Health Research and the Queensland University of Technology. She received a Bachelor of Science (Hons) and a Ph.D. at the University of Western Australia and a Masters of Biostatistics at The University of Queensland. Her research includes multiple large, NHMRC- and MRFF-funded, multi-center, randomized controlled trials and observational studies, for which she provides statistical support. Her research themes have included both paediatric and adult respiratory disease and lung transplantation, and her current research interests are childhood chronic wet cough, particularly the spectrum between protracted bacterial bronchitis and bronchiectasis. She is interested in identifying biomarkers and novel gene expression pathways to define pheno-endotypes of childhood cough. Stephanie also chairs the Children’s Bronchiectasis, Education, Advocacy and Research Network (Child-BEAR-Net) international paediatric bronchiectasis registry.
Job Title
Principal Research Fellow
Faculty / Department / Division
Faculty of Health, School of Medicine
Institution / Organisation
Queensland University of Technology

20 November 2026, Friday

Time Session
14:00
15:00
Albert M. Li Chairperson Hong Kong
Siew Choo Su Chairperson Malaysia
  • Anne Chang Speaker Australia
    "Bronchiectasis exacerbations remain a significant cause of morbidity in children, associated with increased symptom burden, reduced quality of life, and recurrent health care utilisation and future lung function deterioration. Growing evidence indicates that exacerbation risk is shaped by a combination of clinical, microbiological, and radiological factors rather than by a single determinant. Previous exacerbation frequency, prior hospitalisation, younger age at presentation, chronic bacterial infection, and more extensive structural lung disease have all been associated with a higher likelihood of subsequent events. Although prediction is still imprecise at the individual level, these features may help define a higher-risk phenotype that can support closer surveillance and earlier intervention. Our recent work showed that the ‘daily wet-cough dominant’ and ‘Wheeze Dyspnoea’ phenotypes were associated with increased risk of hospitalisations post-recruitment. We have also identified six neutrophil-associated genes were associated with a future exacerbation, suggesting that peripheral blood gene expression may help identify children at risk of exacerbations. Prevention strategies are more established and include regular airway clearance, prompt treatment of wet cough episodes, vaccination, nutritional support, and individualized action plans. In selected children, long-term macrolide therapy may reduce exacerbation frequency, while careful follow-up and early intervention can limit progression. Overall, the current evidence supports a risk-stratified approach that combines clinical assessment with proactive management. We need future research that use validated paediatric prediction tools that integrate clinical, microbiologic, and imaging data to better guide prevention and treatment. "
  • Anna Marie Nathan Speaker Malaysia
    "Long Term prognosis of Chronic Suppurative Lung Disease Prof Dr Anna Marie Nathan Non-CF Bronchiectasis (NCFBE) and CSLD are the leading causes of BE in Asia. Recent interest has moved NCFBE out of the “orphan” disease category. Paediatric bronchiectasis is reversible with timely diagnosis and effective treatment (1). However, data on the ideal management of NCFBE remain limited, with a limited armamentarium of treatment options, especially in children, where randomised trials are severely lacking 1. We have published data on children with CSLD/BE 2. Seventy-eight per cent of children who performed spirometry had values <80% of the normal predicted value. Anthropometric measurements in children with NCFBE were static despite treatment. PC-QOL scores were low 2. A study from Thailand found that pulmonary exacerbation occurred in 80% of children, with a higher rate in non-infectious bronchiectasis than postinfectious bronchiectasis (90.9% vs 61.5%, p = 0.036). Hospitalisation was required for 77.1% of children, with a higher rate of non-infectious bronchiectasis than postinfectious bronchiectasis (86.3% vs 53.8%, p = 0.033) 3. Seventy-seven per cent of interviewed parents had abnormal DASS21 scores, with 54% being stressed and 51% being depressed. Parents of children diagnosed with CF had significantly lower DASS21 scores, hence indicating better mental health scores compared to non-CF CSLD 2. The presence of Pseudomonas aeruginosa (Pa) in the airways of patients with non-CF bronchiectasis has been associated with accelerated lung function decline and increased morbidity and mortality. Guidelines suggest inhaled antibiotics to promote eradication 1(1). We have found that eradication is associated with improved quality-of-life outcomes, with significant improvements in PC-QoL scores and cough scores after 3 months of treatment observed in patients who received both systemic and inhaled antibiotics (P = 0.002 and P = 0.003, respectively), but not in patients who received inhaled antibiotics alone (P = 0.09 and P = 0.89, respectively 4. In a study examining long-term outcomes of childhood bronchiectasis, young adults with bronchiectasis rarely attended adult respiratory clinics despite being symptomatic and having multiple emergency doctor visits5. This reflects inefficient transition programmes for our patients, which will translate to very poor adult outcomes. References 1.Chang, A. B., Fortescue, R., Grimwood, K., Alexopoulou, E., Bell, L., Boyd, J., Bush, A., Chalmers, J. D., Hill, A. T., Karadag, B., Midulla, F., McCallum, G. B., Powell, Z., Snijders, D., Song, W. J., Tonia, T., Wilson, C., Zacharasiewicz, A., & Kantar, A. (2021). European Respiratory Society guidelines for the management of children and adolescents with bronchiectasis. The European respiratory journal, 58(2), 2002990. https://doi.org/10.1183/13993003.02990-2020 2. Nathan, A. M., Muthusamy, A., Thavagnanam, S., Hashim, A., & de Bruyne, J. (2014). Chronic suppurative lung disease in a developing country: impact on child and parent. Pediatric pulmonology, 49(5), 435–440. https://doi.org/10.1002/ppul.23001 3.Sitthikarnkha P, Anekvorakul A, Niamsanit S, Techasatian L, Saengnipanthkul S, Uppala R. Clinical characteristics and outcome of non-cystic fibrosis bronchiectasis in children: A tertiary care perspective. SAGE Open Med. 2025 Feb 19;13:20503121251320849. doi: 10.1177/20503121251320849. PMID: 39980590; PMCID: PMC11840848 4. Goh WT, Hng SY, Azanan MS, Eg KP, Adam Q, Lee QY, et al. Utility of inhaled antibiotics in children with exacerbations of non-cystic fibrosis bronchiectasis: A pilot study. Pediatr Respirol Crit Care Med 2026;XX:XX-XX. 5. Sibanda D, Singleton R, Clark J, Desnoyers C, Hodges E, Day G, et al. Adult outcomes of childhood bronchiectasis. Int J Circumpolar Health 2020;79:1731059 "
  • Stephanie Yerkovich Speaker Australia
    Protracted bacterial bronchitis (PBB) is a common cause of chronic wet cough in children and an important contributor to respiratory morbidity. Increasing evidence suggests that PBB and bronchiectasis are not distinct disease entities but instead represent different stages along a spectrum. PBB and bronchiectasis share many clinical, microbiological and immunological features. Furthermore, persistent bacterial infection, neutrophilic airway inflammation and immune responses provide mechanistic links between PBB and bronchiectasis. Longitudinal follow-up studies have also demonstrated that recurrent PBB and persistent lower airway infection are associated with an increased risk of developing bronchiectasis, highlighting the importance of early recognition and effective management. Integrating advances in basic, translational, and clinical research, will improve the understanding of the PBB-bronchiectasis continuum. Identifying children at risk of developing bronchiectasis will allow targeted, implementable interventions to prevent irreversible lung disease and improve respiratory outcomes.
  • Q&A
Ballroom 2, Lower Ground Floor