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Dive into the research topics where Carolyn Dakin is active.

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Featured researches published by Carolyn Dakin.


Journal of Paediatrics and Child Health | 2005

Sleep-related breathing disorder in Duchenne muscular dystrophy: Disease spectrum in the paediatric population

Sadasivam Suresh; Patricia Wales; Carolyn Dakin; M. Harris; David M. Cooper

Duchenne muscular dystrophy (DMD) is a progressive neuromuscular disease with death usually occurring because of respiratory failure. Signs of early respiratory insufficiency are usually first detectable in sleep.


Pediatrics | 2006

Breastfeeding does not increase the risk of asthma at 14 years.

Scott Burgess; Carolyn Dakin; Michael O'Callaghan

OBJECTIVES. There are conflicting data regarding the impact of breastfeeding on the development of asthma in late childhood. Our aim with this study was to investigate the relationship between breastfeeding and the prevalence of asthma in children at 14 years. METHODS. The Mater-University of Queensland Study of Pregnancy is a birth cohort of 7223 women and their infants recruited from a public antenatal clinic in Brisbane, Australia, between 1981 and 1984. Data regarding breastfeeding and the duration of breastfeeding were collected through the use of a questionnaire completed by the mother 6 months postdelivery, and the prevalence of asthma was determined through the use of a questionnaire completed by the mother 14 years postdelivery. RESULTS. Data regarding both breastfeeding and asthma were available for 4964 children. The prevalence of asthma in children at 14 years was 28.4%. Breastfeeding for ≥4 months was not found to have a significant effect on the prevalence of asthma in 14-year-olds. The unadjusted odds ratio of developing asthma at 14 years if the child was breastfed for ≥4 months was 1.03. The odds ratio of developing asthma did not change appreciably when allowance was made for potential confounding factors. CONCLUSION. Data from this study indicate that breastfeeding neither increases nor decreases the prevalence of asthma in children at 14 years.


Pediatric Pulmonology | 2009

Regional Ventilation Distribution in Non-Sedated Spontaneously Breathing Newborns and Adults Is Not Different

Andreas Schibler; M. Yuill; Chloe Parsley; T. Pham; Kristen Gilshenan; Carolyn Dakin

In adults, ventilation is preferentially distributed towards the dependent lung. A reversal of the adult pattern has been observed in infants using radionuclide ventilation scanning. But these results have been obtained in infants and children with lung disease. In this study we investigate whether healthy infants have a similar reverse pattern of ventilation distribution.


Pediatric Pulmonology | 2008

Safety of bronchoalveolar lavage in young children with cystic fibrosis

Claire Wainwright; Keith Grimwood; John B. Carlin; Suzanna Vidmar; Peter Cooper; P. Francis; Catherine A. Byrnes; B. Whitehead; A. J. Martin; If Robertson; David M. Cooper; Carolyn Dakin; Ian B. Masters; Rj Massie; P. Robinson; Sarath Ranganathan; David S. Armstrong; Lk Patterson; C. F. Robertson

Our aim was to determine the safety of BAL in young children <6 years with CF.


Journal of Cystic Fibrosis | 2015

Pseudomonas aeruginosa genotypes acquired by children with cystic fibrosis by age 5-years.

Timothy J. Kidd; Kay A. Ramsay; Suzanna Vidmar; John B. Carlin; Scott C. Bell; Claire Wainwright; Keith Grimwood; P. Francis; Carolyn Dakin; Joyce Cheney; Narelle George; Colin F. Robertson; Marj Moodie; Rosemary Carzino; Rob Carter; David S. Armstrong; Peter Cooper; Karen McKay; Anthony Martin; Bruce Whitehead; John Hunter; Catherine A. Byrnes; Harm A.W.M. Tiddens; Karla Graniel; Krista Gerbrands; Lauren S. Mott

BACKGROUND We describe Pseudomonas aeruginosa acquisitions in children with cystic fibrosis (CF) aged ≤5-years, eradication treatment efficacy, and genotypic relationships between upper and lower airway isolates and strains from non-CF sources. METHODS Of 168 CF children aged ≤5-years in a bronchoalveolar lavage (BAL)-directed therapy trial, 155 had detailed microbiological results. Overall, 201/271 (74%) P. aeruginosa isolates from BAL and oropharyngeal cultures were available for genotyping, including those collected before and after eradication therapy. RESULTS Eighty-two (53%) subjects acquired P. aeruginosa, of which most were unique strains. Initial eradication success rate was 90%, but 36 (44%) reacquired P. aeruginosa, with genotypic substitutions more common in BAL (12/14) than oropharyngeal (3/11) cultures. Moreover, oropharyngeal cultures did not predict BAL genotypes reliably. CONCLUSIONS CF children acquire environmental P. aeruginosa strains frequently. However, discordance between BAL and oropharyngeal strains raises questions over upper airway reservoirs and how to best determine eradication in non-expectorating children.


European Respiratory Journal | 2011

Regional ventilation distribution in the first 6 months of life

T. Pham; M. Yuill; Carolyn Dakin; Andreas Schibler

Electrical impedance tomography (EIT) has been used to study regional ventilation distribution in neonatal and paediatric lung disease; however, little information has been obtained in healthy newborns and infants. Data on regional ventilation distribution and regional filling characteristics were obtained using EIT in the neonatal period, at 3 and 6 months of age, in spontaneously breathing infants during non-rapid eye movement sleep. Regional ventilation distribution was described using regional end-expiratory and end-inspiratory impedance amplitudes, and geometric centre of ventilation. Regional filling characteristics were described with the phase lag or lead of the regional impedance change in comparison to global impedance change. 32 infants were measured in the supine position. Regional impedance amplitudes increased with age but regional ventilation distribution remained unchanged in all infants at any age, with the dependent (posterior) lung always better ventilated. Regional filling characteristics showed that the dependent lung filled during inspiration before the nondependent lung during all follow-up measurements. Regional ventilation distribution and regional filling characteristics remained unchanged over the first 6 months of life, and the results obtained on regional ventilation distribution are very similar to those in adult subjects.


Acta Paediatrica | 2006

Screening of obstructive and central apnoea/hypopnoea in children using variability: a preliminary study.

Jong Yong A. Foo; Andrew P. Bradley; Stephen J. Wilson; Gordon R. Williams; Carolyn Dakin; David M. Cooper

AIM Polysomnography (PSG) is the current standard protocol for sleep disordered breathing (SDB) investigation in children. Presently, there are limited reliable screening tests for both central (CE) and obstructive (OE) respiratory events. This study compared three indices, derived from pulse oximetry and electrocardiogram (ECG), with the PSG gold standard. These indices were heart rate (HR) variability, arterial blood oxygen de-saturation (SaO2) and pulse transit time (PTT). METHODS 15 children (12 male) from routine PSG studies were recruited (aged 3-14 years). The characteristics of the three indices were based on known criteria for respiratory events (RPE). Their estimation singly and in combination was evaluated with simultaneous scored PSG recordings. RESULTS 215 RPE and 215 tidal breathing events were analysed. For OE, the obtained sensitivity was HR (0.703), SaO2 (0.047), PTT (0.750), considering all three indices (0) and either of the indices (0.828) while specificity was (0.891), (0.938), (0.922), (0.953) and (0.859) respectively. For CE, the sensitivity was HR (0.715), SaO2 (0.278), PTT (0.662), considering all indices (0.040) and either of the indices (0.868) while specificity was (0.815), (0.954), (0.901), (0.960) and (0.762) accordingly. CONCLUSIONS Preliminary findings herein suggest that the later combination of these non-invasive indices to be a promising screening method of SDB in children.


Physiological Measurement | 2005

Variability in time delay between two models of pulse oximeters for deriving the photoplethysmographic signals

Jong Yong A. Foo; Stephen J. Wilson; Carolyn Dakin; M. Harris; David A. Cooper

Pulse oximetry is commonly used as an arterial blood oxygen saturation (SaO2) measure. However, its other serial output, the photoplethysmography (PPG) signal, is not as well studied. Raw PPG signals can be used to estimate cardiovascular measures like pulse transit time (PTT) and possibly heart rate (HR). These timing-related measurements are heavily dependent on the minimal variability in phase delay of the PPG signals. Masimo SET Rad-9 and Novametrix Oxypleth oximeters were investigated for their PPG phase characteristics on nine healthy adults. To facilitate comparison, PPG signals were acquired from fingers on the same hand in a random fashion. Results showed that mean PTT variations acquired from the Masimo oximeter (37.89 ms) were much greater than the Novametrix (5.66 ms). Documented evidence suggests that 1 ms variation in PTT is equivalent to 1 mmHg change in blood pressure. Moreover, the PTT trend derived from the Masimo oximeter can be mistaken as obstructive sleep apnoeas based on the known criteria. HR comparison was evaluated against estimates attained from an electrocardiogram (ECG). Novametrix differed from ECG by 0.71+/-0.58% (p<0.05) while Masimo differed by 4.51+/-3.66% (p>0.05). Modern oximeters can be attractive for their improved SaO2 measurement. However, using raw PPG signals obtained directly from these oximeters for timing-related measurements warrants further investigations.


Archives of Disease in Childhood | 2015

Nocturnal oxygen saturation profiles of healthy term infants

Philip I. Terrill; Carolyn Dakin; Ian P. Hughes; Maggie Yuill; Chloe Parsley

Objective Pulse oximetry is used extensively in hospital and home settings to measure arterial oxygen saturation (SpO2). Interpretation of the trend and range of SpO2 values observed in infants is currently limited by a lack of reference ranges using current devices, and may be augmented by development of cumulative frequency (CF) reference-curves. This study aims to provide reference oxygen saturation values from a prospective longitudinal cohort of healthy infants. Design Prospective longitudinal cohort study. Setting Sleep-laboratory. Patients 34 healthy term infants were enrolled, and studied at 2 weeks, 3, 6, 12 and 24 months of age (N=30, 25, 27, 26, 20, respectively). Interventions Full overnight polysomnography, including 2 s averaging pulse oximetry (Masimo Radical). Main outcome measurements Summary SpO2 statistics (mean, median, 5th and 10th percentiles) and SpO2 CF plots were calculated for each recording. CF reference-curves were then generated for each study age. Analyses were repeated with sleep-state stratifications and inclusion of manual artefact removal. Results Median nocturnal SpO2 values ranged between 98% and 99% over the first 2 years of life and the CF reference-curves shift right by 1% between 2 weeks and 3 months. CF reference-curves did not change with manual artefact removal during sleep and did not vary between rapid eye movement (REM) and non-REM sleep. Manual artefact removal did significantly change summary statistics and CF reference-curves during wake. Conclusions SpO2 CF curves provide an intuitive visual tool for evaluating whether an individuals nocturnal SpO2 distribution falls within the range of healthy age-matched infants, thereby complementing summary statistics in the interpretation of extended oximetry recordings in infants.


Journal of Paediatrics and Child Health | 2006

Successful management of lymphangiomatosis and chylothorax in a 7‐month‐old infant

Scott Burgess; Margaret Harris; Carolyn Dakin; Peter Borzi; Christopher Ryan; David A. Cooper

Abstract:  A 7‐month old infant presented with an effusion and multiple lesions in his spleen. A diagnosis of lymphangiomatosis was made based on chylous effusion and an MRI demonstrating numerous enhancing lesions within the spleen on T2‐weighed images. Conservative measures, including the withdrawal of feeds and octreotide, did not significantly reduce the rate of chyle production and increasing requirement for respiratory support. Resection of the patient’s spleen and partial pleurectomy were associated with a dramatic improvement in his condition. At 27 months the patient was well with no evidence of further lymphangiomas or a recurrence of his chylothoraces.

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David M. Cooper

Boston Children's Hospital

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Helen Heussler

University of Queensland

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Ross Norris

University of Queensland

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Sadasivam Suresh

Boston Children's Hospital

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B. G. Charles

University of Queensland

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David Pache

University of Queensland

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