
Overview
Background
Conjoint Professor Paul Robinson is the Deputy Director of the Children’s Health Environment Program within the Child Health Research Centre (CHRC), and Senior Staff Specialist in Respiratory and Sleep Medicine at the Queensland Children’s Hospital. His research program performs translational research outlining the role of peripheral airway function tests in early lung disease detection and ongoing monitoring of established disease.
He has led the development and standardisation of novel measures of lung function across the entire age range from infancy onwards, facilitating the development of commercial equipment available for widespread use. His research focuses on defining the clinical utility of two specific peripheral airway function tests (Multiple breath washout, MBW, and oscillometry) in important obstructive lung diseases (e.g., asthma, cystic fibrosis, and post bone marrow transplant pulmonary graft vs host disease) and in understanding the impacts of environmental exposures. Structure-function relationships have been explored using state-of-the-art imaging techniques, with the aim of also developing new strategies to reduce any radiation exposure associated with these to advance incorporation into clinical care (e.g., ultra-low dose CT).
These novel lung function tools not only in the hospital setting but also in the school and home setting, enabling the successful development of a parent-supervised remote monitoring strategy for asthma which has been shown to reflect clinically meaningful outcomes missed by conventional approaches. In collaboration with industry, this strategy is now being employed in a series of research projects.
Involvement in longitudinal birth cohorts has outlined the early lung function trajectories in health, and the identification of risk factors affecting normal lung development and contributing to the early development of asthma. Studies investigating environmental health have highlighted the adverse effects of ultrafine particle air pollution.
Professor Robinson’s standing as an international expert, both in terms of clinical and research experience, has led to broader leadership roles across national and international levels.
Availability
- Professor Paul Robinson is:
- Available for supervision
Fields of research
Research interests
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Asthma
Understanding mechanisms that underlie risks for developing asthma in susceptible children. Improving diagnosis of early asthma and monitoring of disease once established to prevent exacerbations and reduce risk of poor asthma outcomes.
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Cystic Fibrosis
Understanding the mechanisms underlying the development of lung disease early in life and why and how this progresses. Optimising the detection of early lung disease to facilitate earlier effective intervention to improve outcomes.
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Pulmonary Graft vs. Host Disease
Understanding the mechanisms underlying the development of respiratory complications following Haematopoietic Stem Cell Transplantation and why and how this progresses. Optimising the detection of early Pulmonary Graft-vs-Host disease to facilitate earlier intervention and improved outcomes.
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Impact of environmental exposures in early life
Improving methods of assessing environmental exposures and their effects across the lifespan and understanding how these increase long-tern risk of chronic disease in the lungs and other organ systems
Research impacts
Professor Robinson’s research program has informed a paradigm shift in management of chronic respiratory disease to ignore the reassurance of “normal” conventional lung function (spirometry) and target early lung disease detection arising in the peripheral airways and intervention through proactive (not reactive symptom-driven) strategies for 3 important obstructive lung conditions: (1) cystic fibrosis (CF); (2) asthma; and (3) post haemopoietic stem cell transplant (HSCT) pulmonary graft-vs-host disease (pGVHD).
Impact is evidenced by >150 published manuscripts of which >80 manuscripts are specific to this research program focus. A lead role on seminal consensus standards have resulted in a >4-times increase in MBW publications since their publication and widespread availability of robust commercial equipment (based on consensus recommendations adopted by all 4 global manufacturers). MBW has been formally as a primary outcome measure for CF intervention studies by independent institutions and integration into >30 international multicentre clinical trials. MBW has played a central role in registration of effective CFTR modulator therapy for young children, with significant projected survival benefits. Advances in oscillometry, including novel remote monitoring approaches targeting enhanced detection of disease exacerbation and prevention, have provided a platform for the first consensus clinical applications document for oscillometry.
Works
Search Professor Paul Robinson’s works on UQ eSpace
2018
Journal Article
Variability of lung clearance index in clinically stable cystic fibrosis lung disease in school age children
Svedberg, Marcus, Gustafsson, Per M., Robinson, Paul D., Rosberg, Monica and Lindblad, Anders (2018). Variability of lung clearance index in clinically stable cystic fibrosis lung disease in school age children. Journal of Cystic Fibrosis, 17 (2), 236-241. doi: 10.1016/j.jcf.2017.08.004
2017
Journal Article
The effect of inert gas choice on multiple breath washout in healthy infants: differences in lung function outcomes and breathing pattern
Gustafsson, Per M., Bengtsson, Lovisa, Lindblad, Anders and Robinson, Paul D. (2017). The effect of inert gas choice on multiple breath washout in healthy infants: differences in lung function outcomes and breathing pattern. Journal of Applied Physiology, 123 (6), 1545-1554. doi: 10.1152/japplphysiol.00524.2017
2017
Conference Publication
DEVELOPMENT OF AN IN-VITRO MUCUS MODEL TO EVALUATE THE EFFECT OF MAGNESIUM ON CURRENT MUCOLYTIC THERAPIES FOR CYSTIC FIBROSIS TREATMENT
Mamlouk, Mariam, Young, Paul, Traini, Daniela, Ghadiri, Maliheh, Ong, Hui Xin and Robinson, Paul (2017). DEVELOPMENT OF AN IN-VITRO MUCUS MODEL TO EVALUATE THE EFFECT OF MAGNESIUM ON CURRENT MUCOLYTIC THERAPIES FOR CYSTIC FIBROSIS TREATMENT. HOBOKEN: WILEY.
2017
Journal Article
In vitro and in vivo functional residual capacity comparisons between multiple-breath nitrogen washout devices
Tonga, Katrina O., Robinson, Paul D., Farah, Claude S., King, Greg G. and Thamrin, Cindy (2017). In vitro and in vivo functional residual capacity comparisons between multiple-breath nitrogen washout devices. ERJ Open Research, 3 (4) 00011-2017, 1-8. doi: 10.1183/23120541.00011-2017
2017
Journal Article
Automated quality control of forced oscillation measurements: respiratory artifact detection with advanced feature extraction
Pham, Thuy T., Leong, Philip H. W., Robinson, Paul D., Gutzler, Thomas, Jee, Adelle S., King, Gregory G. and Thamrin, Cindy (2017). Automated quality control of forced oscillation measurements: respiratory artifact detection with advanced feature extraction. Journal of Applied Physiology, 123 (4), 781-789. doi: 10.1152/japplphysiol.00726.2016
2017
Journal Article
Exercise capacity is not decreased in children who have undergone lung resection early in life for congenital thoracic malformations compared to healthy age-matched children
Dunn, Ashlee, Pearce, Kasey, Callister, Robin, Collison, Adam, Morten, Matthew, Mandaliya, Payal, Platt, Lauren, Dascombe, Ben, Kumar, Rajendra, Selvadurai, Hiran, Robinson, Paul D. and Mattes, Joerg (2017). Exercise capacity is not decreased in children who have undergone lung resection early in life for congenital thoracic malformations compared to healthy age-matched children. Pediatric Pulmonology, 52 (10), 1340-1348. doi: 10.1002/ppul.23772
2017
Journal Article
Question 11: how should Allergic Bronchopulmonary Aspergillosis [ABPA] be managed in Cystic Fibrosis?
Ohn, Mon, Robinson, Paul, Selvadurai, Hiran and Fitzgerald, Dominic A. (2017). Question 11: how should Allergic Bronchopulmonary Aspergillosis [ABPA] be managed in Cystic Fibrosis?. Paediatric Respiratory Reviews, 24, 35-38. doi: 10.1016/j.prrv.2016.10.001
2017
Journal Article
Respiratory artefact removal in forced oscillation measurements: a machine learning approach
Pham, Thuy T., Thamrin, Cindy, Robinson, Paul D., McEwan, Alistair L. and Leong, Philip H. W. (2017). Respiratory artefact removal in forced oscillation measurements: a machine learning approach. IEEE Transactions on Biomedical Engineering, 64 (8) 7453188, 1679-1687. doi: 10.1109/TBME.2016.2554599
2017
Journal Article
Determinants of peripheral airway function in adults with and without asthma
Robinson, Paul D., King, Gregory G., Sears, Malcolm R., Hong, Chuen Y. and Hancox, Robert J. (2017). Determinants of peripheral airway function in adults with and without asthma. Respirology, 22 (6), 1110-1117. doi: 10.1111/resp.13045
2017
Conference Publication
LONG-TERM MORBIDITY OF RESPIRATORY VIRAL INFECTIONS DURING CHEMOTHERAPY IN CHILDREN WITH LEUKAEMIA - PILOT STUDY
Lin, Beryl, Kennedy, Brendan, McBride, Jamie, Dalla-Pozza, Luciano, Trahair, Toby, McCowage, Geoff, Coward, Emma, Plush, Leanne, Robinson, Paul, Hardaker, Kate, Widger, John, Jaffe, Adam and Selvadurai, Hiran (2017). LONG-TERM MORBIDITY OF RESPIRATORY VIRAL INFECTIONS DURING CHEMOTHERAPY IN CHILDREN WITH LEUKAEMIA - PILOT STUDY. HOBOKEN: WILEY.
2017
Conference Publication
CHANGES IN PERIPHERAL AIRWAY FUNCTION AT 12 MONTHS POST ALLOGENEIC HAEMATOPOIETIC STEM CELL TRANSPLANTATION (ALLO-HSCT)
Htun, Christopher, Schoeffel, Robin, Lahzami, Samir, Philips, Craig, Pope, Alun, Robinson, Paul, Greenwood, Matthew and King, Gregory (2017). CHANGES IN PERIPHERAL AIRWAY FUNCTION AT 12 MONTHS POST ALLOGENEIC HAEMATOPOIETIC STEM CELL TRANSPLANTATION (ALLO-HSCT). HOBOKEN: WILEY.
2017
Conference Publication
CHANGES IN PERIPHERAL AIRWAY FUNCTION AT 12 MONTHS POST ALLOGENEIC HAEMATOPOIETIC STEM CELL TRANSPLANTATION (ALLO-HSCT)
Htun, Christopher, Schoeffel, Robin, Lahzami, Samir, Philips, Craig, Pope, Alun, Robinson, Paul, Greenwood, Matthew and King, Gregory (2017). CHANGES IN PERIPHERAL AIRWAY FUNCTION AT 12 MONTHS POST ALLOGENEIC HAEMATOPOIETIC STEM CELL TRANSPLANTATION (ALLO-HSCT). HOBOKEN: WILEY.
2017
Journal Article
Is twice the duration of washout sufficient time between multiple breath nitrogen washout tests?
Hardaker, Kate M., Gustafsson, Per, Cooper, Peter, Fitzgerald, Dominic, Selvadurai, Hiran and Robinson, Paul D. (2017). Is twice the duration of washout sufficient time between multiple breath nitrogen washout tests?. European Respiratory Journal, 49 (2) 1501832, 1501832. doi: 10.1183/13993003.01832-2015
2017
Conference Publication
Long-Term Morbidity Of Respiratory Viral Infections During Chemotherapy In Children With Leukaemia: A Historical Prospective Cohort Study
Lin, B., Kennedy, B., McBride, J., Dalla-Pozza, L., Trahair, T., McCowage, G., Coward, E., Plush, L., Robinson, P. D., Hardaker, K., Widger, J., Jaffe, A. and Selvadurai, H. (2017). Long-Term Morbidity Of Respiratory Viral Infections During Chemotherapy In Children With Leukaemia: A Historical Prospective Cohort Study. International Conference of the American-Thoracic-Society (ATS), Washington Dc, May 19-24, 2017. NEW YORK: AMER THORACIC SOC.
2017
Conference Publication
Asthma Control During Pregnancy, 17Q21 Variants and Childhood-Onset Asthma
Morten, Matthew, Collison, Adam, Murphy, Vanessa, Barker, Daniel, Meredith, Joseph, Powell, Heather, Robinson, Paul, Sly, Peter, Gibson, Peter and Mattes, Joerg (2017). Asthma Control During Pregnancy, 17Q21 Variants and Childhood-Onset Asthma. The Australia & New Zealand Society of Respiratory Science and The Thoracic Society of Australia and New Zealand (ANZSRS/TSANZ) Annual Scientific Meeting, Canberra, Australia, 24–28 March 2017. Richmond, VIC Australia: Wiley.
2016
Journal Article
Feasibility of squeezing multiple breath washout testing into busy clinical laboratories
Robinson, Paul D. (2016). Feasibility of squeezing multiple breath washout testing into busy clinical laboratories. Pediatric Pulmonology, 51 (12), 1271-1273. doi: 10.1002/ppul.23560
2016
Journal Article
Specific airway resistance in preschool children: Why not panting after all?
Ioan, Iulia, Silvia, Demoulin-Alexikova, Coutier, Laurianne, Bonabel, Claude, Kirkby, Jane, Nielsen, Kim G., Tomalak, Waldemar, Thompson, Bruce, Schweitzer, Cyril, Robinson, Paul D. and Marchal, François (2016). Specific airway resistance in preschool children: Why not panting after all?. European Respiratory Journal, 48 (6), 1804-1807. doi: 10.1183/13993003.01302-2016
2016
Journal Article
Real-life effectiveness of omalizumab in severe allergic asthma above the recommended dosing range criteria
Hew, M., Gillman, A., Sutherland, M., Wark, P., Bowden, J., Guo, M., Reddel, H. K., Jenkins, C., Marks, G. B., Thien, F., Rimmer, J., Katsoulotos, G. P., Cook, M., Yang, I., Katelaris, C., Bowler, S., Langton, D., Wright, C., Bint, M., Yozghatlian, V., Burgess, S., Sivakumaran, P., Yan, K. Y., Kritikos, V., Peters, M., Baraket, M., Aminazad, A., Robinson, P., Jaffe, A. ... Gibson, P. G. (2016). Real-life effectiveness of omalizumab in severe allergic asthma above the recommended dosing range criteria. Clinical and Experimental Allergy, 46 (11), 1407-1415. doi: 10.1111/cea.12774
2016
Journal Article
Novel methodology to perform sulfur hexafluoride (SF6)-based multiplebreath wash-in and washout in infants using current commercially available equipment
Gustafsson, P. M., Robinson, P. D., Lindblad, A. and Oberli, D. (2016). Novel methodology to perform sulfur hexafluoride (SF6)-based multiplebreath wash-in and washout in infants using current commercially available equipment. Journal of Applied Physiology, 121 (5), 1087-1097. doi: 10.1152/japplphysiol.00115.2016
2016
Journal Article
Question 7: for an infant with an equivocal sweat chloride following newborn screening, how likely is a diagnosis of cystic fibrosis?
Groves, Tyler, Robinson, Paul and Fitzgerald, Dominic A. (2016). Question 7: for an infant with an equivocal sweat chloride following newborn screening, how likely is a diagnosis of cystic fibrosis?. Paediatric Respiratory Reviews, 20, 48-50. doi: 10.1016/j.prrv.2015.11.007
Funding
Current funding
Past funding
Supervision
Availability
- Professor Paul Robinson is:
- Available for supervision
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Available projects
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Remote monitoring of Paediatric Asthma to Improve Asthma Diagnosis and Control
Childhood asthma mortality remains substantial, and rates of hospitalisation are increasing globally in young children. This is driven by poor asthma control (which affects 50% of asthmatics) and ongoing exacerbations (which affects 25%). Of the 40,000 admissions each year, 80% are preventable! Current symptom-based management approaches fail – limited by poor perception/reporting by children and parents - and conventional spirometry/peak flow is insensitive or too challenging for this setting. In addition, the preschool age range is a critical period in asthma pathogenesis: symptoms emerge, airway structure changes, and a window for intervention exists before permanent lung function deficit is established by early school age. Preschool symptom-based diagnostic and/or predictive tools (for later asthma) perform poorly and ignore lung function due to spirometry’s limitations. Improved ability to differentiate early asthma phenotypes is a priority of international societies.
This research program consists of a series of projects to analyse existing, and collect new, data to define the clinical utility of a unique remote home-based monitoring strategy focused on the day-to-day variability of a novel and sensitive lung function test. Studies will investigate its ability to correctly identify evolving asthma, detect loss of asthma control and provide an early signal of an impending asthma exacerbation to improve long term asthma outcomes.
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Improving detection of Pulmonary Graft-vs-Host Disease to facilitate earlier intervention
Chronic Graft-vs-Host Disease affects 60% of Haematopoeitic Stem Cell Transplant (HSCT) survivors by 6 years after their transplant, affecting multiple organs including skin, liver, gastrointestinal tract and lungs. Gold standard for pulmonary GVHD diagnosis is abnormal spirometry and subsequent CT-based imaging. Pulmonary GVHD is estimated to affect 20% of all subjects post HSCT yet this incidence is a gross underestimate due to the insensitivity of spirometry to detect peripheral lung changes. This leads to late diagnosis, poor response to treatment, and poor prognosis (5-year mortality is 85%). Better tools to detect and monitor pulmonary GVHD are urgently required.
This research program builds on previous work highlighting the potential utility of novel peripheral airway function test in this setting. It will analyse both local data and pooled international data across 12 international centres (including both paediatric and adult data) to define the utility of these tools to provide an earlier diagnosis of pulmonary GVHD to facilitate earlier invention and improve outcomes. It will also explore novel applications of these tests to enhance detection further in the initial period post HSCT to predict and detect those at risk.
-
Remote monitoring of Paediatric Asthma to Improve Asthma Diagnosis and Control
Childhood asthma mortality remains substantial, and rates of hospitalisation are increasing globally in young children. This is driven by poor asthma control (which affects 50% of asthmatics) and ongoing exacerbations (which affects 25%). Of the 40,000 admissions each year, 80% are preventable! Current symptom-based management approaches fail – limited by poor perception/reporting by children and parents - and conventional spirometry/peak flow is insensitive or too challenging for this setting. In addition, the preschool age range is a critical period in asthma pathogenesis: symptoms emerge, airway structure changes, and a window for intervention exists before permanent lung function deficit is established by early school age. Preschool symptom-based diagnostic and/or predictive tools (for later asthma) perform poorly and ignore lung function due to spirometry’s limitations. Improved ability to differentiate early asthma phenotypes is a priority of international societies. This research program consists of a series of projects to analyse existing, and collect new, data to define the clinical utility of a unique remote home-based monitoring strategy focused on the day-to-day variability of a novel and sensitive lung function test. Studies will investigate its ability to correctly identify evolving asthma, detect loss of asthma control and provide an early signal of an impending asthma exacerbation to improve long term asthma outcomes.
This program of research includes projects suitable for PhD, honours or masters students.
For more information, contact Professor Paul Robinson at paul.robinson@uq.edu.au.
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Assessing the impact of a Complex Asthma model of care to service all eligible Queensland children
A significant driver of the huge healthcare burden of asthma is children with difficult-to-treat or severe asthma (5-10% of childhood asthma, termed collectively as “Complex Asthma”). A recent survey of Australian and New Zealand paediatric tertiary services has highlighted the lack of a standardised approach to services and issues adequately identifying these children affected to ensure access to recommended models of care. At Queensland Children’s hospital (QCH) we have established a unique multidisciplinary team (MDT) service, involving nine different medical teams: Respiratory, Allergy & Immunology, Psychology, Psychiatry, Adolescent Medicine, Speech Pathology, Physiotherapy, ENT and Social work. The research program will focus on evaluating the effectiveness of this approach through i) the creation of a complex asthma database to assess health outcomes, describe key factors predicting those outcomes and enable a cost-effectiveness analysis, ii) the evaluation of currently employed screening questionnaires to correctly identify important co-morbidities, and iii) using the established Project ECHO platform at QCH, the creation of a community of practice and an education module to educate and empower non-tertiary community-based services to better identify and contribute to ongoing management the impact of which will be formally assessed. This work coincides with the establishment of a national Australian and New Zealand Paediatric Severe Asthma Registry (led by QCH staff) which will enable benchmarking of outcomes to data collected at other tertiary centres.
This program of research includes projects suitable for PhD, honours or masters students
For more information, contact Professor Paul Robinson at paul.robinson@uq.edu.au
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Improving detection of Pulmonary Graft-vs-Host Disease to facilitate earlier intervention
Chronic Graft-vs-Host Disease affects 60% of Haematopoietic Stem Cell Transplant (HSCT) survivors by 6 years after their transplant, affecting multiple organs including skin, liver, gastrointestinal tract and lungs. Gold standard for pulmonary GVHD diagnosis is abnormal spirometry and subsequent CT-based imaging. Pulmonary GVHD is estimated to affect 20% of all subjects post HSCT yet this incidence is a gross underestimate due to the insensitivity of spirometry to detect peripheral lung changes. This leads to late diagnosis, poor response to treatment, and poor prognosis (5-year mortality is 85%). Better tools to detect and monitor pulmonary GVHD are urgently required.
This research program builds on previous work highlighting the potential utility of novel peripheral airway function test in this setting. It will analyse both local data and pooled international data across 12 international centres (including both paediatric and adult data) to define the utility of these tools to provide an earlier diagnosis of pulmonary GVHD to facilitate earlier invention and improve outcomes. It will also explore novel applications of these tests in a new prospective cohort to enhance detection further in the initial period post HSCT to predict and detect those at risk.
This program of research includes projects suitable for PhD, honours or masters students.
For more information, contact Professor Paul Robinson at paul.robinson@uq.edu.au.
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Defining early lung function and respiratory health trajectories in First Nations infants
Disparities in health for indigenous communities are a global issue. The Strong Families Study is a First Nations peoples co-designed cohort to support improved perinatal and early childhood outcomes. It is the largest birth cohort study of its kind to date and the first inclusive of mothers, partners, and their children. This research program will focus on identifying important events happening within the first year of life that determine respiratory health and lung function trajectories in recruited infants. The projects will focus on pre-natal and post-natal factors determining i) baseline offspring lung function at 6 weeks, ii) lung function trajectories determined by respiratory function tested at 6 weeks and 12 months and iii) respiratory health defined by episodes of wheeze and bronchiolitis within the first 12 months of life. Relationships observed within this cohort will be compared to those within other important birth cohorts both nationally (Barwon Infant Study) and internationally (Drakenstein study, South Africa).
This program of research includes projects suitable for PhD, honours or masters students. Experience working with first nations communities, with children and in lung function techniques is desirable.
For more information, contact Professor Paul Robinson at paul.robinson@uq.edu.au.
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