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Dive into the research topics where Lianne S. Kopel is active.

Publication


Featured researches published by Lianne S. Kopel.


Pediatric Allergy and Immunology | 2013

Exposures to Molds in School Classrooms of Children with Asthma

Sachin N. Baxi; Michael L. Muilenberg; Christine A. Rogers; William J. Sheehan; Jonathan M. Gaffin; Perdita Permaul; Lianne S. Kopel; Peggy S. Lai; Jeffrey P. Lane; Ann Bailey; Carter R. Petty; Chunxia Fu; Diane R. Gold; Wanda Phipatanakul

Students spend a large portion of their day in classrooms which may be a source of mold exposure. We examined the diversity and concentrations of molds in inner‐city schools and described differences between classrooms within the same school.


Pediatric Pulmonology | 2015

Perceived neighborhood safety and asthma morbidity in the school inner-city asthma study.

Lianne S. Kopel; Jonathan M. Gaffin; Al Ozonoff; Devika R. Rao; William J. Sheehan; James Friedlander; Perdita Permaul; Sachin N. Baxi; Chunxia Fu; S.V. Subramanian; Diane R. Gold; Wanda Phipatanakul

The aim of this study was to investigate whether neighborhood safety as perceived by primary caregivers is associated with asthma morbidity outcomes among inner‐city school children with asthma.


Paediatric Respiratory Reviews | 2014

Social disadvantage and asthma control in children.

Lianne S. Kopel; Wanda Phipatanakul; Jonathan M. Gaffin

This review discusses various aspects of social disadvantage and their association with poor asthma control, including socioeconomic status, exposure to psychosocial stress and violence, minority affiliation, environmental concerns such as allergens and pollution, and poverty in rural settings. Each of these elements has been linked with worsened asthma outcomes in children. Known and hypothesized mechanisms behind these associations are described in an effort to further understand the complex entity of poorly controlled asthma among socially deprived children. Intervention studies to improve asthma outcomes in these vulnerable populations are also described.


Pediatric and Developmental Pathology | 2013

Impact of Cilia Ultrastructural Examination on the Diagnosis of Primary Ciliary Dyskinesia

Tregony Simoneau; Stephanie O. Zandieh; Devika R. Rao; Phuong Vo; Kara E. Palm; Michael McCown; Lianne S. Kopel; Allan Dias; Alicia Casey; Antonio R. Perez-Atayde; Zhaohui Zhong; Dionne A. Graham; Sara O. Vargas

Ultrastructural examination of cilia is the “gold standard” for diagnosing primary ciliary dyskinesia. There is little evidence suggesting the most effective method of procuring a ciliary biopsy and scant benchmark data on rates of conclusive biopsies or on the diagnostic impact of such biopsies. To critically assess rates of inconclusive, positive, and negative ciliary biopsies and to identify clinical factors associated with conclusive results, we reviewed ciliary biopsies submitted for electron microscopy from 2006 to 2011, noting whether specimens were adequate for analysis and whether the ciliary structure was normal. The biopsy site, method used, procedurists specialty, and clinical diagnoses were determined. Biopsy findings were categorized by diagnostic impact. Over 5 years, 187 patients had 211 biopsies. Conclusive results were obtained on 133/211 biopsies (63%); the remainder were insufficient. The rate of inconclusive biopsies did not vary significantly (P > 0.05; Fishers exact) among sampling methods. Abnormal results were identified in 8/133 (6.0%) of the adequate specimens. Forceps compared to brush biopsies (abnormal in 4/12 versus 4/121 of the adequate specimens, P = 0.002), along with multiple biopsy samples (taken on same or different days) compared with a single biopsy sample (abnormal in 3/12 versus 1/110 of the adequate specimens, P = 0.01), were more likely to yield an abnormal result. Only 63% of pediatric ciliary biopsies provide adequate morphology for analysis, the large majority of these samples showing normal ciliary anatomy. The method of obtaining biopsies did not significantly affect result conclusiveness. Understanding the diagnostic impact of ultrastructural analysis is important as new diagnostic algorithms are developed for primary ciliary dyskinesia.


Annals of Allergy Asthma & Immunology | 2015

Association between allergic sensitization and exhaled nitric oxide in children in the School Inner-City Asthma Study

Devika R. Rao; Joanne E. Sordillo; Lianne S. Kopel; Jonathan M. Gaffin; William J. Sheehan; Elaine Hoffman; Al Ozonoff; Diane R. Gold; Wanda Phipatanakul

Fractional exhaled nitric oxide (FeNO) is increased in children with asthma and is thought to reflect eosinophilic lung inflammation.1, 2 It is not known whether sensitization to one particular allergen is more strongly associated with worsened lung inflammation over any other particular allergen. Our aim was to determine whether children with asthma and allergic sensitization have higher levels of lung inflammation as measured by FeNO compared to children without allergic sensitization, and whether sensitization to one specific allergen was most predictive of elevated FeNO in a school-based setting. We studied 128 children consecutively enrolled in the School Inner-City Asthma Study (SICAS) from 2008–2012 for whom we obtained skin prick testing for indoor allergens, outdoor allergens and FeNO (NIOX TM System, Aerocrine, Sweden). Further details regarding SICAS methods have been previously reported3. The FeNO was obtained at the same time as the skin prick testing utilizing standard methods3, and a wheal size of >3 mm compared with a saline control was used to define a positive sensitization test. FeNO was collected according to standard ATS procedures.4 The primary outcome was FeNO, and the logarithmic value of FeNO was used to obtain an approximately normal distribution. We performed an independent t-test of the mean FeNO (log transformed) between sensitized and unsensitized children, and the Mann-Whitney U test was used to compare untransformed FeNO levels in sensitized vs. unsensitized children. Univariate regression was utilized to determine the relationship between sensitization to allergens and FeNO (log transformed). In the multiple regression model, we adjusted for age, gender, inhaled corticosteroid use and multiple sensitizations, all variables that were significantly associated with model outcome. Analyses were conducted using SPSS version 19 (SPSS, Chicago, IL) and SAS v9.2 (Cary, NC: SAS Institute Inc, 2011). The mean FeNO level was 24.75 ppb, and the median was 15 ppb (range, 5–143) for the 128 children studied (eTable 1). Only 6% of children were white, while 40.6% and 28.1% of children were black and Hispanic respectively. The mean age at the time of FeNO measurement was 8.8 years. Over 70% of SICAS children were sensitized to more than one allergen, and over 60% were sensitized to more than two allergens. The most common allergens to which children were sensitized were cat (40.6%), dust mite (35%), tree pollen (32%), mouse (37.5%), cockroach (24.2%), grass (25%), rat (25.8%) and ragweed (20.3%). We found that log-transformed FeNO significantly increased as the number of positive skin prick tests per child increased. Mean FeNO levels (ppb) were significantly different between those children with no sensitization and those children with 1–3, 4–5 and ≥ 6 positive skin prick tests. In comparing FeNO levels between children with and without sensitization to specific indoor allergens, we found that for cat, mouse, dust mite, rat and cockroach, the FeNO levels were significantly higher in children who were sensitized to that specific allergen compared to those who were not. Sensitization to cat, rat, mouse, tree pollen, dust mite, and cockroach were significant predictors of increased FeNO in the univariate model (Table 1). When adjusted for age, gender, inhaled corticosteroid use, asthma control and multiple sensitizations (more than one positive skin prick test), sensitization to cat and rat allergen were significant predictors of increased FeNO with p values of <0.01 and 0.016 respectively. Table 1 Predictors of FeNO, Multivariate regression; Outcome is the natural log of FeNO Our study focused on the relationship between allergic sensitization and FeNO levels, an objective measure of lung inflammation in children with asthma. The children enrolled in SICAS were highly allergic, with over 70% being sensitized to more than one allergen. This high degree of allergic sensitization translated to higher FeNO levels in comparison to unsensitized children. The mean FeNO for our cohort was above 20 ppb (24.75 ppb), indicating that significant eosinophilic airway inflammation is likely present.5 In attempting to identify which allergens contribute most to elevated FeNO levels, we found sensitization to cat and rat, and also multiple sensitizations to be significant independent predictors of increased FeNO after adjusting for age, gender and ICS use. To our knowledge, no other studies have shown sensitization to rat allergen to be a significant independent predictor of increased FeNO levels, adjusting for other factors. There may be unique characteristics of this allergen that correlate with allergic airway inflammation. In our multiple regression model, sensitization to six or more allergens carried the strongest beta-coefficient of 0.608. This is in contrast to some studies that have demonstrated that sensitization to specific allergens such as dust mite are major determinants of increased FeNO in children.6 Our study highlights the importance of rat allergen sensitization as well and the dose-response relationship of polysensitization and airway inflammation. Other studies have demonstrated that sensitization to multiple specific allergens is associated with elevated FeNO levels7–9, and our study adds to this body of literature by confirming this relationship in a population that is more diverse compared to other communities that have been studied. Our results are therefore generalizable to other diverse, urban populations with a high proportion of non-white ethnicities. The clinical implications of our results are important. A study from the National Cooperative Inner City Asthma Study showed that children with asthma who were both exposed and sensitized to rat allergen had higher rates of hospitalization and unscheduled doctor visits.10 Our study adds to these findings by showing that sensitization to rat allergy also predicts airway inflammation. Finding that rat and multiple sensitization predicts high FeNO levels is important as FeNO levels have been shown to be predictive of asthma exacerbations.11 We acknowledge that we are limited by sample size in that limited resources allowed us to obtain FeNO in a subset of children. We found that in our school-based cohort of ethnically diverse, highly allergic children, that FeNO levels were predicted by cat and rat sensitization, and most strongly by having multiple sensitizations. Future studies should be aimed at reducing cat and rat allergen exposure and assessing the effect on asthma morbidity as well as markers of airway inflammation


Clinical Pediatrics | 2018

Bronchodilator Use for Acute Chest Syndrome Among Large Pediatric Hospitals in North America

Lianne S. Kopel; Elizabeth S. Klings; Michael C. Monuteaux; Jonathan M. Gaffin; Matthew M. Heeney; Wanda Phipatanakul

The utility of bronchodilators to treat acute chest syndrome (ACS) in patients with sickle cell disease is unknown. Our objectives were to examine the variability in bronchodilator use for ACS among pediatric hospitals contributing to a large database and to examine the relationship between bronchodilator use and length of stay (LOS) and mortality. Between 2005 and 2011, bronchodilators were used during 6812/11 328 hospitalizations (60.1%) and use varied from 0.0% to 97.0% (median = 46.0%, interquartile range = 37.0% to 74.0%). Median LOS was 4 days, and interquartile range was 2 to 6 days. Bronchodilator use was associated with a 13.2% increase in LOS (95% confidence interval = 9.2% to 17.3%, P < .001). However, in the subgroup with asthma, bronchodilator use was associated with a 17.9% decrease in LOS (95% confidence interval = 1.7% to 31.4%, P = .03). There is wide variability in bronchodilator use for ACS, and it has variable association with LOS, depending on comorbid asthma. Prospective trials are needed to evaluate bronchodilators for ACS.


Pediatrics | 2014

Add-on Omalizumab in Children With Severe Allergic Asthma: A 1-Year Real Life Survey

Lianne S. Kopel; Wanda Phipatanakul

A Deschildre, C Marguet, J Salleron. Eur Respir J. 2013;42(5):1224–1233 The goal of this study was to report the real-life efficacy and safety of add-on treatment with omalizumab in a large group of children with severe allergic asthma. The primary aim of this observational study was to evaluate the effect of omalizumab on asthma control. Secondary aims were to evaluate outcomes, including asthma exacerbations, health care utilization, inhaled corticosteroid (ICS)-sparing effect, pulmonary function test results, and safety. A total of 104 children …


The Journal of Allergy and Clinical Immunology: In Practice | 2012

Food allergy and increased asthma morbidity in a School-based Inner-City Asthma Study.

James Friedlander; William J. Sheehan; Sachin N. Baxi; Lianne S. Kopel; Jonathan M. Gaffin; Al Ozonoff; Chunxia Fu; Diane R. Gold; Wanda Phipatanakul


Allergy | 2014

Allergens on desktop surfaces in preschools and elementary schools of urban children with asthma.

Watcharoot Kanchongkittiphon; William J. Sheehan; James Friedlander; Martin D. Chapman; Eva-Maria King; Karine Martirosyan; Sachin N. Baxi; Perdita Permaul; Jonathan M. Gaffin; Lianne S. Kopel; Ann Bailey; Chunxia Fu; Carter R. Petty; Diane R. Gold; Wanda Phipatanakul


The Journal of Allergy and Clinical Immunology: In Practice | 2017

Caregiver stress among inner-city school children with asthma

Lianne S. Kopel; Carter R. Petty; Jonathan M. Gaffin; William J. Sheehan; Sachin N. Baxi; Watcharoot Kanchongkittiphon; Chunxia Fu; Diane R. Gold; Wanda Phipatanakul

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Chunxia Fu

Brigham and Women's Hospital

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Carter R. Petty

Boston Children's Hospital

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Devika R. Rao

Boston Children's Hospital

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