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Dive into the research topics where Philip Pattemore is active.

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Featured researches published by Philip Pattemore.


Pediatrics | 2011

Cord-Blood 25-Hydroxyvitamin D Levels and Risk of Respiratory Infection, Wheezing, and Asthma

Carlos A. Camargo; Tristram Ingham; Kristin Wickens; Ravi Thadhani; Karen M. Silvers; Michael Epton; George I. Town; Philip Pattemore; Janice A. Espinola; Julian Crane

OBJECTIVE: Higher maternal intake of vitamin D during pregnancy is associated with a lower risk of wheezing in offspring. The relationship between cord-blood levels of 25-hydroxyvitamin D (25[OH]D) and childhood wheezing is unknown. We hypothesized that cord-blood levels would be inversely associated with risk of respiratory infection, wheezing, and asthma. PATIENTS AND METHODS: Cord blood from 922 newborns was tested for 25(OH)D. Parents were asked if their child had a history of respiratory infection at 3 months of age or a history of wheezing at 15 months of age and then annually thereafter. Incident asthma was defined as doctor-diagnosed asthma by the time the child was 5 years old and reported inhaler use or wheezing since the age of 4 years. RESULTS: The median cord-blood level of 25(OH)D was 44 nmol/L (interquartile range: 29–78). Follow-up was 89% at the age of 5 years. Adjusting for the season of birth, 25(OH)D had an inverse association with risk of respiratory infection by 3 months of age (odds ratio: 1.00 [reference] for ≥75 nmol/L, 1.39 for 25–74 nmol/L, and 2.16 [95% confidence interval: 1.35–3.46] for <25 nmol/L). Likewise, cord-blood 25(OH)D levels were inversely associated with risk of wheezing by 15 months, 3 years, and 5 years of age (all P < .05). Additional adjustment for more than 12 potential confounders did not materially change these results. In contrast, we found no association between 25(OH)D levels and incident asthma by the age of 5 years. CONCLUSIONS: Cord-blood levels of 25(OH)D had inverse associations with risk of respiratory infection and childhood wheezing but no association with incident asthma.


Clinical & Experimental Allergy | 2008

The association of early life exposure to antibiotics and the development of asthma, eczema and atopy in a birth cohort: confounding or causality?

Kristin Wickens; Tristram Ingham; Michael Epton; Philip Pattemore; Ian Town; David Fishwick; Julian Crane

Background In general, studies reporting positive associations between antibiotic exposure and respiratory and allergic disease have been unable to determine the nature of this association.


The Journal of Pediatrics | 2012

Breastfeeding Protects against Current Asthma up to 6 Years of Age

Karen M. Silvers; Chris Frampton; Kristin Wickens; Philip Pattemore; Tristram Ingham; David Fishwick; Julian Crane; G. Ian Town; Michael Epton

OBJECTIVE To investigate the effects of breastfeeding on wheezing and current asthma in children 2 to 6 years of age. STUDY DESIGN Infants (n=1105) were enrolled in a prospective birth cohort in New Zealand. Detailed information about infant feeding was collected using questionnaires administered at birth and at 3, 6, and 15 months. From this, durations of exclusive and any breastfeeding were calculated. Information about wheezing and current asthma was collected at 2, 3, 4, 5, and 6 years. Logistic regression was used to model associations between breastfeeding and outcomes with and without adjustment for confounders. RESULTS After adjustment for confounders, each month of exclusive breastfeeding was associated with significant reductions in current asthma from 2 to 6 years (all, P<.03). Current asthma at 2, 3, and 4 years was also reduced by each month of any breastfeeding (all, P<.005). In atopic children, exclusive breastfeeding for ≥ 3 months reduced current asthma at ages 4, 5, and 6 by 62%, 55%, and 59%, respectively. CONCLUSION Breastfeeding, particularly exclusive breastfeeding, protects against current asthma up to 6 years. Although exclusive breastfeeding reduced risk of current asthma in all children to age 6, the degree of protection beyond 3 years was more pronounced in atopic children.


Clinical & Experimental Allergy | 2011

The effects of early and late paracetamol exposure on asthma and atopy: a birth cohort.

Kristin Wickens; Richard Beasley; Ian Town; Michael Epton; Philip Pattemore; Tristram Ingham; Julian Crane

Cite this as: K. Wickens, R. Beasley, I. Town, M. Epton, P. Pattemore, T. Ingham, J. Crane and the New Zealand Asthma and Allergy Cohort Study Group, Clinical & Experimental Allergy, 2011 (41) 399–406.


Clinical & Experimental Allergy | 1993

Viruses as precipitants of asthma symptoms III. Rhinoviruses: molecular biology and prospects for future intervention

Sebastian L. Johnston; Philip G. Bardin; Philip Pattemore

In the first twoarticlesin this series [1,2], we examined the epidemiological evidence for an association between respiratory viral infections and asthma exacerbations, and the physiological and experimental evidence for the proposed cellular and biochemical mechanisms involved in this association. As mentioned in Part I, most previous studies have indicated that rhinoviruses are the most common viruses associated with wheezing illness (except in infancy), and are also among the viruses with the greatest propensity to trigger wheezing or asthma attacks. Our own studies among children with recurrent wheeze and/or cough suggested that rhinoviruses may be found in as many as half of all such episodes of respiratory illness—six times as common as the next most common virus [3]. This last article in the series will review recent developments in the molecular biology of rhinoviruses and their receptors, and will examine the potential for preventing or ameliorating attacks precipitated by viral infections.


Journal of Paediatrics and Child Health | 2002

Cost-effectiveness of palivizumab in New Zealand

Alison Vogel; Mj McKinlay; T Ashton; Lennon; Jane E. Harding; Ralph Pinnock; David Graham; Keith Grimwood; Philip Pattemore; M Schousboe

Objective:  To establish the preterm infant hospitalization risks from respiratory syncytial virus (RSV) in New Zealand and the net cost per hospitalization averted by palivizumab.


Maternal and Child Nutrition | 2009

Breastfeeding protects against adverse respiratory outcomes at 15 months of age.

Karen M. Silvers; Chris Frampton; Kristin Wickens; Michael Epton; Philip Pattemore; Tristram Ingham; David Fishwick; Julian Crane; G. Ian Town

The relationship between breastfeeding, respiratory and other allergic disorders has been controversial. Our aim was to investigate the relationships between breastfeeding, respiratory outcomes, eczema and atopy at 15 months of age in a prospective birth cohort in New Zealand. A total of 1105 children were enrolled at birth, and 1011 (91.2%) were followed up at 15 months. Logistic regression was used to model associations between breastfeeding duration and respiratory outcomes, eczema and atopy after adjusting for relevant confounding variables: ethnicity, socio-economic status, parity, body mass index, smoking in pregnancy, gender and respiratory infections in the first 3 months of life. Breastfeeding was associated with a significant reduction in the risk of adverse respiratory outcomes at 15 months. After adjustment for confounders, each month of exclusive breastfeeding reduced the risk of doctor-diagnosed asthma by 20% (odds ratio 0.80, 95% confidence interval 0.71 to 0.90), wheezing by 12% (0.88, 0.82 to 0.94) and inhaler use by 14% (0.86, 0.78 to 0.93). Associations for both exclusive and additional breastfeeding durations, and respiratory outcomes remained independently significant when modelled simultaneously. Although independently associated with all respiratory outcomes, adjusting for parental history of allergic disease or maternal history of asthma did not alter our findings. Breastfeeding was not associated with eczema or atopy at 15 months. In conclusion, there was a significant protective effect of breastfeeding on infant wheezing and other adverse respiratory outcomes that may be early indicators of asthma in New Zealand children.


Chest | 2010

Beginning School With Asthma Independently Predicts Low Achievement in a Prospective Cohort of Children

Kathleen A. Liberty; Philip Pattemore; Jim Reid; Michael Tarren-Sweeney

BACKGROUND Concerns about the achievement of children with asthma and respiratory conditions are especially important in New Zealand, which has one of the worlds highest rates of childhood asthma. The present study evaluated whether entering school with asthma was associated with low achievement after the first year. METHODS A child cohort was recruited to a prospective study at time of first enrollment into randomly selected schools in Christchurch. Parent interviews covered demographics and respiratory status. Physician reports were sought for children with asthma, and all respiratory information was clinically reviewed. The childrens achievement in reading and math was individually assessed at school entry and reassessed after 12 months. Schools reported absences. Intelligence subtests were administered. RESULTS Two hundred ninety-eight children were recruited, including 55 (18.5%) with current asthma. At 1-year follow-up, retention was 93.7%. Children who entered school with asthma were more likely to be ≥ 6 months behind other participants in reading words (P = .023) and books (P = .026), but not in math (P = .167) at the end of the first year of school. Achievement was not related to asthma severity. Entering school with asthma reliably predicted low reading achievement independent of other known covariates of low achievement (high absenteeism, minority status, male gender, single-parent family, poor academic skills at school entry, and low socioeconomic status). CONCLUSIONS Entering school with asthma was a significant predictor of low achievement in reading at 12-month follow-up, independent of asthma severity, high absenteeism, or other covariates of low achievement.


European Respiratory Journal | 2008

Pseudomonas aeruginosa transmission is infrequent in New Zealand cystic fibrosis clinics

Jan Schmid; L.J. Ling; J.L.S. Leung; Ningxin Zhang; John Kolbe; A.W. Wesley; G.D. Mills; P.J. Brown; D.T. Jones; R.T.R. Laing; Philip Pattemore; D.R. Taylor; Keith Grimwood

Pseudomonas aeruginosa is an important pathogen in cystic fibrosis (CF). Although most patients harbour unique P. aeruginosa isolates, some clinics report patients sharing common strains. The overall importance of person-to-person transmission in P. aeruginosa acquisition and whether routine patient segregation is necessary remains uncertain. The present authors therefore investigated the extent of P. aeruginosa transmission in New Zealand CF clinics. New Zealand’s seven major CF centres were assessed, combining epidemiological data with computer-assisted SalI DNA fingerprinting of 496 isolates from 102 patients. One cluster of related isolates was significantly more prevalent in the largest clinic than expected by chance. The seven patients with isolates belonging to this cluster had more contact with each other than the remaining patients attending this centre. No other convincing evidence of transmission was found in any of the other smaller clinics. Three P. aeruginosa strains believed to be transmissible between patients in Australian and British CF clinics are present in New Zealand, but there was no definite evidence they had spread. Pseudomonas aeruginosa transmission is currently infrequent in New Zealand cystic fibrosis clinics. This situation could change rapidly and ongoing surveillance is required. The current results confirm that computer-assisted SalI DNA fingerprinting is ideally suited for such surveillance.


Pediatric Allergy and Immunology | 2012

Asthma, atopy and exhaled nitric oxide in a cohort of 6-yr-old New Zealand children

Julian Crane; Philippa Lampshire; Kristin Wickens; Michael Epton; Robert Siebers; Tristram Ingham; Philip Pattemore; Ian Town

To cite this article: Crane J, Lampshire P, Wickens K, Epton M, Siebers R, Ingham T, Pattemore P, Town GI and The Year Six New Zealand Asthma and Allergy Cohort Study Group (NZAACS6). Asthma, atopy and exhaled nitric oxide in a cohort of 6‐yr‐old New Zealand children. Pediatric Allergy Immunology 2012: 23: 59–64.

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