Original Article
Preemptive Use of High-Dose Fluticasone for Virus-Induced Wheezing in Young Children
N Engl J Med 2009; 360:339-353January 22, 2009
- Abstract
Background
Although virus-induced wheezing is common in preschool-age children, optimal management remains elusive. We examined the efficacy and safety of preemptive treatment with high-dose fluticasone in reducing the severity of recurrent virus-induced wheezing in children.
Methods
We randomly assigned 129 children who were 1 to 6 years of age to receive 750 μg of fluticasone propionate (ex-valve [manufacturer-measured] dose) or placebo twice daily, beginning at the onset of an upper respiratory tract infection and continuing for a maximum of 10 days, over a period of 6 to 12 months. The primary outcome was rescue oral corticosteroid use. Secondary outcomes included symptoms, use of β2-agonists, acute care visits, hospitalizations, discontinuation of the study drug, change in growth and bone mineral density, basal cortisol level, and adverse events.
Results
Over a median period of 40 weeks, 8% of upper respiratory tract infections in the fluticasone group led to treatment with rescue systemic corticosteroids, as compared with 18% in the placebo group (odds ratio, 0.49; 95% confidence interval [CI], 0.30 to 0.83). Children who were treated with fluticasone, as compared with those who were given placebo, had smaller mean (±SD) gains from baseline in height (6.23±2.62 cm [unadjusted value]; z score, −0.19 ±0.42 vs. 6.56±2.90 cm [unadjusted value]; z score, 0.00±0.48; difference between groups in z score from baseline to end point, −0.24 [95% CI, −0.40 to −0.08]) and in weight (1.53±1.17 kg [unadjusted value]; z score, −0.15±0.48 vs. 2.17±1.79 kg [unadjusted value]; z score, 0.11±0.43; difference between groups in z score from baseline to end point, −0.26 [95% CI, −0.41 to −0.09]). There were no significant differences between the groups in basal cortisol level, bone mineral density, or adverse events.
Conclusions
In preschool-age children with moderate-to-severe virus-induced wheezing, preemptive treatment with high-dose fluticasone as compared with placebo reduced the use of rescue oral corticosteroids. Treatment with fluticasone was associated with a smaller gain in height and weight. Given the potential for overuse, this preventive approach should not be adopted in clinical practice until long-term adverse effects are clarified. (ClinicalTrials.gov number, NCT00238927.)
Media in This Article
Figure 1
Study Design and Schedule of Procedures.Figure 2
Screening, Randomization, Follow-up, and Analysis.Article Activity
- Article
Upper respiratory tract infections account for more than 80% of wheezing episodes in children.1,2 With more than 30 acute care visits per 1000 population, preschool-age children have a rate of acute care visits for asthma that is higher by a factor of three than that for school-age children and adults.3,4 Most children wheeze only when they have upper respiratory tract infections, are usually nonatopic, and outgrow symptoms by 6 years of age.5-7 Yet, since preschool-age children have 6 to 10 upper respiratory tract infections each year,8 recurrent virus-induced wheezing is associated with considerable distress and use of health care services. The optimal preventive management remains elusive, particularly for children with moderate-to-severe episodes.9-11
Randomized, placebo-controlled trials have examined five principal strategies for the secondary prevention of recurrent virus-induced wheezing.10 Oral corticosteroids at the onset of an upper respiratory tract infection, a treatment suggested by Brunette and colleagues,12 was not proved to be superior to placebo,13,14 and there has been concern about the safety profile.15 Preemptive use of leukotriene-receptor antagonists reduced symptoms and decreased the number of emergency room visits,16 and maintenance use reduced the rate of exacerbations17; however, neither preemptive nor maintenance use reduced rescue oral corticosteroid use in a diverse group of patients, including school-age children16 and children with persistent asthma.17 A Cochrane review18 examined the efficacy of inhaled corticosteroids. Maintenance therapy was no more effective than placebo,19-21 but preemptive high-dose therapy appeared to be promising, with a statistically nonsignificant but clinically important 20%22 to 50%23,24 reduction in the use of rescue oral corticosteroids. In this proof-of-concept trial, we hypothesized that high-dose inhaled fluticasone propionate initiated at the onset of an upper respiratory tract infection would be effective in decreasing the severity of episodes of virus-induced wheezing in preschool-age children.
Methods
Study Design and Patients
We conducted a parallel-group, randomized, placebo-controlled trial with triple blinding (parents, physicians and nurses, and biostatisticians) in five institutions in Quebec. The institutional review board at each site approved the study. Parents gave written informed consent for study participation. GlaxoSmithKline (Canada), one of the main sponsors of the study, and the public funding agencies had no input in the design and conduct of the study, the analysis of the data, or the preparation of the manuscript; the academic authors vouch for the accuracy and completeness of the reported data.
Children who were 1 to 6 years of age were eligible if they had had three or more wheezing episodes in their lifetime, seemingly triggered exclusively by upper respiratory tract infections; if they had no intercurrent symptoms; if they had received at least one course of rescue systemic corticosteroids — a marker of moderate exacerbation5 — in the previous 6 months (or two in the preceding 12 months); and if their parents were fluent in French or English. Hospital admission, a common marker of severe exacerbations, was not a prerequisite for enrollment. Exclusion criteria were prior intubation for a respiratory illness, neonatal respiratory conditions, other chronic diseases, suspected allergic rhinitis,25 and allergies to aeroallergens, documented by a positive skin test or elevated specific IgE levels.
The study design and schedule are shown in Figure 1Figure 1
Study Design and Schedule of Procedures.. After randomization, a medical visit was scheduled every 4 months to monitor symptoms, growth, and adverse events. At each visit, symptom control and adverse health events were documented, and the child was weighed and measured on an upright stadiometer (Health-o-Meter PRO Series, Sunbeam). Lumbar (L2 to L4) bone mineral content (in grams) and bone mineral density (in grams per square centimeter) were ascertained at baseline and at the end of the study period (or at the last visit, in the case of children whose parents withdrew them from the study) with the use of the Lunar DPX-IQ (GE Healthcare). Bone age was also measured at these two times. Scan quality and measurements were reviewed by an independent radiologist who was unaware of the treatment assignment. Basal serum cortisol level, sampled before 8 a.m. at baseline and at the end of the study, was measured with the Immulite assay (Diagnostic Products). Serum IgE levels, as well as varicella latex agglutination antibodies in susceptible children, were documented at the time of randomization to plan appropriate prophylaxis in case of exposure.Admission to an intensive care unit, chronic symptoms, poor control of exacerbations, use of the study drug for more than 15 days per month for 3 months, or perceived lack of efficacy led to discontinuation of the study drug. On the recommendation of an independent advisory board, the study period, which had been set at a mean (±SD) of 6±1 months, was extended to 12±2 months in November 2002 because of slow recruitment.
At the first sign of an upper respiratory tract infection (e.g., rhinorrhea, nasal congestion, sore throat, or earache), parents administered three inhalations of the study drug — 250 μg of fluticasone propionate (ex-valve [manufacturer-measured]) per inhalation — or placebo twice daily, until 48 hours had elapsed with no symptoms of cough or wheezing. If symptoms of cough, wheezing, or dyspnea developed, parents administered two to four inhalations of 100 μg of albuterol hydrofluoroalkane (Ventolin HFA, GlaxoSmithKline) every 4 hours as needed. If symptoms lasted longer than 10 days, the parents informed the research nurse, who made arrangements for a medical consultation. Both the study drug and albuterol inhalers were fitted with a dose counter (Doser CT, Meditrack) to allow for daily monitoring of the use of study inhalers without revealing the recorded doses.26 We reviewed the inhalation technique with the parents and provided an age-appropriate spacer with mask or mouthpiece for the children (AeroChamber, Trudell Medical International). Clearing of nasal passages with salty water was recommended to minimize postnasal drip. No additional asthma treatments were permitted, other than rescue systemic corticosteroids.
Outcomes
The primary outcome was the group rate of short courses of systemic corticosteroids, confirmed by hospital or pharmacy records or both. Secondary efficacy outcomes included upper respiratory tract infections with symptoms of cough, wheezing, or dyspnea; acute care visits and hospitalizations for wheezing; discontinuation of the study drug; duration and intensity of symptoms27; and use of rescue β2-agonists. The effect on parents was assessed for each upper respiratory tract infection with the use of three methods: a global assessment on a 7-point Likert scale (which was based on parents' responses at the end of the episode to the question, “Overall, how much did this asthma flare-up affect you?”; responses ranged from 1 [“not at all”] to 7 [“extremely”]); a record of the number of days of missed work (or usual activities); and the score on the Paediatric Asthma Caregiver's Quality of Life Questionnaire, developed by Juniper et al.28 (a 13-item questionnaire, in which the score for each item ranges from 1 to 7, with higher scores indicating better quality of life; a value of 0.5 on a 7-point Likert scale indicates a minimally important group difference28,29). For each information source (monthly contact, diary, dose counter, and questionnaires), only upper respiratory tract infections for which complete data were available were included in the analysis. Safety measures included the change from baseline in height, weight, and bone mineral density, reported as z scores adjusted for age and sex30,31; change in bone age32; adverse events; and basal cortisol level, with values below 138 nmol per liter (5.0 μg per deciliter) considered to be depressed.33
Randomization and Blinding
With the use of a central computerized procedure, we randomly assigned children to receive fluticasone or placebo, in permuted blocks of four, stratified according to center (of which there were five) and type of spacer (mouthpiece or mask); opaque sealed envelopes contained the assignment code. Parents were provided with a coded metered-dose inhaler containing 250 μg of hydrofluoroalkane (HFA)-propelled fluticasone propionate or with a coded metered-dose inhaler containing placebo, which looked identical in all respects to the fluticasone inhaler (GlaxoSmithKline). The randomization code was disclosed after the completion of preliminary analyses. At the end of follow-up, each child's parent, nurse, and physician were independently asked to guess the child's group assignment.
Statistical Analysis
We estimated that with 64 children per group, the study would have 80% power to show a 50% reduction in the rate of oral corticosteroid use in the fluticasone group, assuming a 12.5% rate of use in the placebo group, an intraclass correlation of 10% for clustering of upper respiratory tract infections within individual children, and an average of 10 infections per child, at a two-sided alpha level of 5%. We analyzed all randomly assigned children according to the intention-to-treat principle, with children included in the analysis until the end of the follow-up period, whether or not the study drug was discontinued; children whose parents withdrew them from the study were included in the analysis until the last contact, without imputation of values for missing data. An independent data and safety monitoring board, whose members were unaware of the group assignments, reviewed all serious adverse events to ascertain whether the event was potentially related to the study drug, to unblind the data, if necessary, or to recommend withdrawal of the child from the study. There were no interim analyses, nor was there an a priori stopping rule.
We examined the treatment effect using generalized linear regression models with binomial, Poisson (with overdispersion), or normal distribution, as applicable. Differences in event rates based on numbers of upper respiratory tract infections were adjusted for the clustering of upper respiratory tract infections in individual children, and an offset variable was used to account for variations in person-time, when applicable.34 Analyses of safety outcomes over the course of the study period were adjusted for baseline values and length of follow-up. For the primary outcome and safety end points, we repeated the analyses with adjustment for imbalances between the groups and for potential confounding variables (site, type of spacer, age, sex, race or ethnic group, birth weight, serum IgE level, presence or absence of eczema, presence or absence of a family history of asthma, presence or absence of exposure to tobacco in utero and in the household, status with respect to day-care attendance, age at first wheezing episode, number of times rescue systemic corticosteroids had been used in the previous 12 months, duration of viral prodrome, vaccination status, season in which the upper respiratory tract infection occurred, and duration of follow-up). In per-protocol analyses, we censored the data at the time of the discontinuation of the study drug.
The models were selected with the use of the stepwise selection method and Akaike's Information Criterion. The number needed to treat or harm was derived from the odds ratio with the use of Visual Rx (www.nntonline.net).35,36 Twenty-one analyses were fully prespecified, and the following seven analyses were post hoc: percentages of children with acute care visits, use of rescue corticosteroids, and hospitalization; bone age; severity of symptoms during episodes treated with or without systemic corticosteroids; correlation between cumulative dose and the primary and safety outcomes; and number needed to harm. Harm was defined as failure to thrive, which in turn was defined by a weight below the 3rd percentile (z score, less than −2) at the end of the study period or a decrease in weight by at least two major percentile lines on the Centers for Disease Control and Prevention growth charts (change in z score, less than −1.28).31,37
Continuous values are expressed as means ±SD or medians with interquartile ranges. All tests were two-sided, and estimates are shown with 95% confidence intervals. Analyses were performed with the use of SAS software, version 9.1 (SAS Institute). P values of less than 0.05 were considered to indicate statistical significance, with no correction for multiple testing.
Results
Children
From November 1999 through April 2005, we screened 2243 children; 1860 (83%) were ineligible (Figure 2Figure 2
Screening, Randomization, Follow-up, and Analysis.). Of the 383 provisionally eligible children, the parents of 199 (52%) declined participation, and 184 children were enrolled. The children whose parents declined participation were similar to those who were enrolled with respect to age, sex, and family income (with postal code used as a surrogate for family income). A total of 129 children were randomly assigned to a study group — 62 to the fluticasone group and 67 to the placebo group. The study drug was prematurely discontinued in 35 children (12 in the fluticasone group and 23 in the placebo group); 9 children (7 in the fluticasone group and 2 in the placebo group) were lost to follow-up, with no significant difference between the groups in overall withdrawals (P=0.54). The baseline characteristics of the two groups were similar, except that there were more boys, and the children were older at the time of the first wheezing episode, in the placebo group (Table 1Table 1
Characteristics of the Participants at Baseline.). There were no significant differences between the groups in the number of upper respiratory tract infections, the duration of treatment and follow-up periods, or the blinding of the treatment assignment, which was maintained in every case (Table E1 and Figure E1 in the Supplementary Appendix, available with the full text of this article at NEJM.org).Primary Outcome
Eight percent of upper respiratory tract infections in the fluticasone group led to treatment with rescue systemic corticosteroids, as compared with 18% of those in the placebo group (odds ratio, 0.49; 95% confidence interval [CI], 0.30 to 0.83) (Table 2Table 2
Primary and Secondary Efficacy Outcomes.). The odds ratio was similar with the per-protocol analysis, in which data were censored at the time of discontinuation of the study drug (odds ratio, 0.42; 95% CI, 0.25 to 0.73), and after adjustment for sex (odds ratio, 0.54; 95% CI, 0.32 to 0.91). As compared with children receiving placebo, significantly fewer children receiving fluticasone were treated with one or more bursts of systemic corticosteroids during the trial (39% vs. 64%; risk ratio with fluticasone, 0.60; 95% CI, 0.43 to 0.87) (Figure E1 in the Supplementary Appendix). A post hoc analysis confirmed that symptom scores (calculated on the basis of a 17-item diary in which each item is ranked on a 7-point Likert scale, with higher scores indicating greater intensity of symptoms) were higher for episodes in which children were treated with systemic corticosteroids than for those in which children were not treated with systemic corticosteroids (197 [interquartile range, 95 to 332] vs. 36 [interquartile range, 12 to 86], P<0.001]. The numbers needed to treat to prevent systemic corticosteroid use were 4 children (95% CI, 3 to 13) and 13 upper respiratory tract infections (95% CI, 9 to 39).Secondary Outcomes
The proportion of upper respiratory tract infections that were associated with symptoms of dyspnea, wheezing or cough, acute care visits, and hospital admissions for these symptoms did not differ significantly between the groups (Table 2). In 56% of acute care visits, no albuterol treatment was given; a post hoc analysis showed that children in the fluticasone group had fewer visits involving two or more albuterol treatments than did children in the placebo group (26% vs. 42%, P=0.03). Children treated with fluticasone had a shorter duration of symptoms and of use of β2-agonists during the course of the upper respiratory tract infections than those who were given placebo. These observations remained valid when the analysis was restricted to upper respiratory tract infections that were treated without systemic corticosteroids (rate ratio for symptoms, 0.85; 95% CI, 0.73 to 0.99; rate ratio for albuterol, 0.85; 95% CI, 0.72 to 1.00). The negative effect on the parents' lives, whether reported as a global assessment or as a quality-of-life score, was smaller with fluticasone than with placebo (mean global assessment, 3 vs. 3.5; mean quality of life score, 5.77 vs. 5.23). At the termination of the trial, physicians recommended rescue albuterol as the sole treatment during subsequent episodes in 75% and 60% of children in the fluticasone and placebo groups, respectively (P=0.07).
Safety Profile
The distribution of height and weight at baseline and at the end of the study period is shown in Table E2 in the Supplementary Appendix. The gain in height and weight was significantly lower in children treated with fluticasone than in children given placebo (Table 3Table 3
Secondary Outcomes Pertaining to the Safety Profile.), with a difference between the groups of 5 percentage points. Neither the per-protocol analyses nor the analyses adjusted for covariates (presence or absence of a family history of asthma and presence or absence of exposure to tobacco in the household) showed a significant difference between the groups in height (difference in the z-score change from baseline, –0.08; 95% CI, –0.25 to 0.08 in per-protocol analysis; –0.16; 95% CI, –0.31 to 0.00 in analysis adjusted for covariates). The observed difference in weight between the groups was similar in the per-protocol and intention-to-treat analyses. Figure E2 in the Supplementary Appendix shows the distribution of the change from baseline in height and weight. Post hoc analyses showed a significant correlation between the cumulative dose of fluticasone and the change in height (r=−0.21, P=0.02), but not in weight (r=−0.11, P=0.21). Two children in the fluticasone group and one in the placebo group met the definition of failure to thrive; the number needed to harm (54 children) was not significant (P=0.61).36 Owing to movement artifacts, only 59 children had valid bone mineral density measurements at both baseline and the end of the study period. There were no significant group differences in the change in lumbar bone mineral density, bone mineral content, or bone age; adjustment for covariates and per-protocol analyses did not alter these associations. Low values (less than –2 SD) for bone mineral density, bone mineral content, or basal cortisol level were infrequent in both groups, and all the children in whom low cortisol values were found had normal values when these tests were repeated or when corticotropin testing was performed.Adverse Events
Thirteen serious adverse events (four in the fluticasone group and nine in the placebo group) occurred in 13 children during the study period — namely, pneumonia (three events in the fluticasone group and two in the placebo group), seizure (one event in each group), admission to an intensive care unit (two in the placebo group), burn (one in the placebo group), respiratory syncytial virus infection (one in the placebo group), atelectasis (one in the placebo group), and Kawasaki's disease (one in the placebo group). None of the serious adverse events were considered by an independent physician masked to treatment assignment to be attributable to the study drug. The distribution of nonserious adverse events was similar between the groups (Table E3 in the Supplementary Appendix).
Discussion
In this proof-of-concept trial, high-dose fluticasone administered preemptively at the onset of upper respiratory tract infections reduced the frequency of clinician-initiated treatment with oral corticosteroids by 10 percentage points, a relative reduction of 50%. As compared with their counterparts who received placebo, children who were treated with fluticasone had symptoms that were milder and of shorter duration; they required fewer days of albuterol use, and their illness had a less negative effect on their parents' quality of life. There were no significant differences in the peak use of albuterol during upper respiratory tract infections, acute-care visits or hospitalizations for wheezing, or premature discontinuation of the study drug. The preemptive use of fluticasone was, however, associated with a reduced gain in height and weight. Because the adverse effects of preemptive treatment with fluticasone are still unknown, the potential risks associated with fluticasone treatment currently outweigh the identified benefit.
The duration of symptoms and of rescue β2-agonist use was reduced by 10 to 15% (representing 1 to 2 days) in the fluticasone group as compared with the placebo group. The magnitude of the effect did not vary significantly whether it was assessed by means of oral report, diary, or dose counter. Similar benefits were observed in the case of exacerbations that did not require treatment with systemic corticosteroids, confirming that the effect also applied to mild exacerbations. As compared with placebo, the use of fluticasone had a smaller overall negative effect on parents and on their quality of life, although the latter difference was small.
The smaller gain in height and weight in children treated with fluticasone as compared with those given placebo is cause for concern. The magnitude of the effect on height was similar to that observed with 1-year treatment with daily low-dose fluticasone (200 μg) in preschool-age children.38 The nonsignificant group difference observed after adjustment for covariates and in per-protocol analyses does not rule out a significant effect, particularly in view of the correlation between the cumulative dose and the change in height.39 To our knowledge, weight loss has not been previously reported in patients treated with inhaled corticosteroids40; in fact, the opposite would be expected through a systemic effect. The power of our study to detect a clinically important difference (0.5 SD) in bone mineral density at an alpha level of 0.05 was only 73%. Moreover, the basal cortisol level is a relatively insensitive measure of adrenal dysfunction, and measurements at baseline and at the end of the study period would fail to identify a transient adrenal suppression during or immediately after preemptive treatment.40 Whether trends toward more respiratory and gastrointestinal infections in the fluticasone-treated group are associated with the treatment or could be explained by small imbalances between the groups with respect to tobacco exposure and vaccination status is unclear.
The study results must be interpreted in light of the following limitations. First, we strived to enroll a homogeneous group of preschool-age children with a phenotype of virus-induced wheezing. Seventy-six percent of the children had normal serum IgE levels, a proportion similar to that previously reported among children with transient wheezing.6 Despite our best intentions, we inadvertently included nine children (7% of randomly assigned children) in whom persistent or atopic asthma symptoms developed during the study period. Second, we were unable to identify characteristics of patients that could modulate the risk–benefit ratio for preemptive treatment. Third, we tested parents' initiation of preemptive treatment with fluticasone as it would happen in real-life practice. Because of the perceived importance of treatment early in the course of an upper respiratory tract infection, the intervention was based on parental perception of the presence of an upper respiratory tract infection, rather than on objective documentation of infection or a specified minimal duration of symptoms.41 Although a viral cause has been confirmed in 74% of upper respiratory tract infections identified by parents,42 we cannot rule out possible misidentification of colds. Fourth, the subjectivity involved in physicians' prescribing of systemic corticosteroids would tend to underestimate any true association, thus reinforcing the significance of our findings. The higher severity of episodes treated with systemic corticosteroids as compared with those treated without systemic corticosteroids would support the appropriateness of corticosteroid prescriptions. Finally, we empirically used 1500 μg of fluticasone per day in this proof-of-concept study; the minimal dose and duration of treatment required to achieve similar outcomes remain to be clarified.
The findings of this trial apply to a small group of carefully screened young children with frequent wheezing episodes triggered by upper respiratory tract infections, no intercurrent symptoms or suspected allergy, and recent moderate or severe episodes. Only 17% of the children we screened met our selection criteria. Most participants (83%) were 1 to 3 years of age; in the preceding year they had received, on average, two courses of systemic corticosteroids, and half the children had been hospitalized. The findings should not be generalized to older children or to children with aeroallergen sensitization, owing to their specific exclusion from this study. In summary, preemptive fluticasone treatment, as compared with placebo, was associated with fewer wheezing episodes treated with systemic corticosteroids, but the smaller gain in height and weight and the potential unknown adverse effects are cause for concern and indicate that this management strategy should not yet be recommended for use in clinical practice.
Presented in part at the annual meeting of the Pediatric Academic Societies, Toronto, May 5–8, 2007, and at the annual meeting of the American Thoracic Society, San Francisco, May 18–22, 2007.
Supported by an unrestricted grant from GlaxoSmithKline (FAP30006) and by an additional grant from Réseau en Santé Respiratoire du Fonds de la Recherche en Santé du Québec; the Fonds de la Recherche en Santé du Québec also provided salary awards to Dr. Ducharme (National Scientist award) and Dr. Platt (Senior Scientist award).
Dr. Ducharme reports receiving research grants from GlaxoSmithKline, Merck, and Nycomed; Dr. Noya, grants from GlaxoSmithKline, AstraZeneca, Merck, and Nycomed; Dr. Leblond, lecture fees from Graceway Pharmaceuticals; and Dr. Platt, consulting fees from Novartis.
No other potential conflict of interest relevant to this article was reported.
We thank the parents of the children who were enrolled in this study; the research respiratory technicians and nurses for their 24-hour availability throughout the study, specifically Regina Pereira, Francine Proulx, Annie Roy, Jennifer Piette, Teena Marie Johns, Ann Kilculen, and Ainslie Rienke (McGill University Health Centre), Raymonde Fontaine (Hôpital Maisonneuve–Rosemont), Nathalie Bureau (Centre Hospitalier Universitaire Sainte-Justine), Marguerite Plante (Centre Hospitalier Universitaire de Sherbrooke), and Annie Gunner and Line Joncas (La Courte Échelle); Carol Fascia of the Immunology and Endocrinology Departments of the Montreal Children's Hospital for ensuring quality control of all cortisol and IgE assays; Diane Newby of the Virology and Microbiology Departments of the Montreal Children's Hospital for processing the varicella antibody; the staffs of Westmount Square Medical Imaging, Les Radiologistes St-Vincent, Centre Radiologique Sherbrooke, and Groupe Radiologie Ellendale, for their measurements of bone mineral density and bone age; Henri Bousquet of Trudell Medical Marketing for supplying the spacer free of charge; the members of the independent advisory board — Pierre Ernst, Marie-Claude Guertin, and Stan Shapiro — who carefully advised the study steering committee, and specifically Jacques Lacroix, pediatric intensivist, and Marie-Claude Guertin, Ph.D., biostatistician, who formed the data and safety monitoring committee (which was not involved in the planning or conduct of the study); Josee Dubois, radiologist, and Louise Gougeon, technician, of Centre Hospitalier Universitaire Sainte-Justine, for their review of all bone mineral density examinations; the project managers, Rick Jane, Rita Zakarian, and Dima Abou-Chakra; the data managers, Justin Grondine, Denis Lamontagne, and Linyan Meng; the medical technologist, Danielle McKenna; Mireille Tehbelian, Zachary Schwartz, Franco Di Salvio, Jean Potvin, Tania Khan, Jonathan Morin, and Stephanie Ducharme-Benard for data entry; Joanne Baird and Fleurette Grégoire for bibliographic assistance; Janine Dumont for assistance with the preparation of the manuscript; and Pierre Ernst, Jacques Lacroix, and Samy Suissa for their editorial comments.
Source Information
From the Applied Clinical Research Unit, Research Centre, Centre Hospitalier Universitaire Sainte-Justine, and the Department of Pediatrics, University of Montreal, Montreal (F.M.D., N.A., C.S., L.K.); the Department of Epidemiology, Biostatistics, and Occupational Health, McGill University, Montreal (R.W.P.); the Department of Pediatrics, Centre Hospitalier Universitaire de Sherbrooke, Sherbrooke (C.L.); the Department of Pediatrics, Research Institute of the Montreal Children's Hospital, McGill University Health Centre, Montreal (F.J.D.N., G.M.D.); Department of Pediatrics, Hôpital Maisonneuve–Rosemont, University of Montreal, Montreal (H.L.); and the Department of Pediatrics, Université Laval, Quebec (G.R.) — all in Quebec, Canada; and the Departments of Pediatrics and of Healthcare and Epidemiology, University of British Columbia, Vancouver, Canada (J.-P.C.).
Address reprint requests to Dr. Ducharme at the Department of Pediatrics, Centre Hospitalier Universitaire Sainte-Justine, Rm. 7939, University of Montreal, 3175 Côte Sainte-Catherine, Montreal, QC H3T 1C5, Canada, or at francine.m.ducharme@umontreal.ca.
- References
References
1
Wilson NM . Virus infections, wheeze and asthma. Paediatr Respir Rev 2003;4:184-192
CrossRef | Medline2
Johnston SL ,Pattemore PK ,Sanderson G , et al. Community study of role of viral infections in exacerbations of asthma in 9-11 year old children. BMJ 1995;310:1225-1229
CrossRef | Web of Science | Medline3
Lougheed MD ,Garvey N ,Chapman KR , et al. The Ontario Asthma Regional Variation Study: emergency department visit rates and the relation to hospitalization rates. Chest 2006;129:909-917
CrossRef | Web of Science | Medline4
Akinbami LJ ,Schoendorf KC . Trends in childhood asthma: prevalence, health care utilization, and mortality. Pediatrics 2002;110:315-322
CrossRef | Web of Science | Medline5
Global Initiative for Asthma (GINA). Global strategy for asthma management and prevention. 2007. (Accessed December 29, 2008, at http://www.ginasthma.org.)
6
Martinez FD ,Wright AL ,Taussig LM , et al. Asthma and wheezing in the first six years of life. N Engl J Med 1995;332:133-138
Full Text | Web of Science | Medline7
Castro-Rodriguez JA ,Holberg CJ ,Wright AL ,Martinez FD . A clinical index to define risk of asthma in young children with recurrent wheezing. Am J Respir Crit Care Med 2000;162:1403-1406
Web of Science | Medline8
Wald ER ,Guerra N ,Byers C . Frequency and severity of infections in day care: three-year follow-up. J Pediatr 1991;118:509-514
CrossRef | Web of Science | Medline9
Bacharier LB ,Phillips BR ,Bloomberg GR , et al. Severe intermittent wheezing in preschool children: a distinct phenotype. J Allergy Clin Immunol 2007;119:604-610
CrossRef | Web of Science | Medline10
Horner CC ,Bacharier LB . Management approaches to intermittent wheezing in young children. Curr Opin Allergy Clin Immunol 2007;7:180-184
CrossRef | Web of Science | Medline11
Bacharier LB ,Boner A ,Carlsen KH , et al. Diagnosis and treatment of asthma in childhood: a PRACTALL consensus report. Allergy 2008;63:5-34[Erratum, Allergy 2008;63:630.]
CrossRef | Web of Science | Medline12
Brunette MG ,Lands L ,Thibodeau L-P . Childhood asthma: prevention of attacks with short-term corticosteroid treatment of upper respiratory tract infection. Pediatrics 1988;81:624-629
Web of Science | Medline13
Stevens CA ,Wesseldine LJ ,Couriel JM ,Dyer AJ ,Osman LM ,Silverman M . Parental education and guided self-management of asthma and wheezing in the pre-school child: a randomised controlled trial. Thorax 2002;57:39-44
CrossRef | Web of Science | Medline14
Oommen A ,Lambert PC ,Grigg J . Efficacy of a short course of parent-initiated oral prednisolone for viral wheeze in children aged 1-5 years: a randomised controlled trial. Lancet 2003;362:1433-1438
CrossRef | Web of Science | Medline15
Vuillermin PJ ,Robertson CF ,South M . Parent-initiated oral corticosteroid therapy for intermittent wheezing illnesses in children: systematic review. J Paediatr Child Health 2007;43:438-442
CrossRef | Web of Science | Medline16
Robertson CF ,Price D ,Henry R , et al. Short-course montelukast for intermittent asthma in children: a randomized controlled trial. Am J Respir Crit Care Med 2007;175:323-329
CrossRef | Web of Science | Medline17
Bisgaard H ,Zielen S ,Garcia-Garcia ML , et al. Montelukast reduces asthma exacerbations in 2- to 5-year-old children with intermittent asthma. Am J Respir Crit Care Med 2005;171:315-322
CrossRef | Web of Science | Medline18
McKean M ,Ducharme F . Inhaled steroids for episodic viral wheeze of childhood. Cochrane Database Syst Rev 2000;2:CD001107-CD001107
Medline19
Wilson N ,Sloper K ,Silverman M . Effect of continuous treatment with topical corticosteroid on episodic viral wheeze in preschool children. Arch Dis Child 1995;72:317-320
CrossRef | Web of Science | Medline20
Doull IJ ,Lampe FC ,Smith S ,Schreiber J ,Freezer NJ ,Holgate ST . Effect of inhaled corticosteroids on episodes of wheezing associated with viral infection in school age children: randomised double blind placebo controlled trial. BMJ 1997;315:858-862
CrossRef | Web of Science | Medline21
Pao CS ,McKenzie SA . Randomized controlled trial of fluticasone in preschool children with intermittent wheeze. Am J Respir Crit Care Med 2002;166:945-949
CrossRef | Web of Science | Medline22
Svedmyr J ,Nyberg E ,Thunqvist P ,Asbrink-Nilsson E ,Hedlin G . Prophylactic intermittent treatment with inhaled corticosteroids of asthma exacerbations due to airway infections in toddlers. Acta Paediatr 1999;88:42-47
CrossRef | Web of Science | Medline23
Wilson NM ,Silverman M . Treatment of acute, episodic asthma in preschool children using intermittent high dose inhaled steroids at home. Arch Dis Child 1990;65:407-410
CrossRef | Web of Science | Medline24
Connett G ,Lenney W . Prevention of viral induced asthma attacks using inhaled budesonide. Arch Dis Child 1993;68:85-87
CrossRef | Web of Science | Medline25
Asher MI ,Keil U ,Anderson HR , et al. International Study of Asthma and Allergies in Childhood (ISAAC): rationale and methods. Eur Respir J 1995;8:483-491
CrossRef | Web of Science | Medline26
Bender B ,Wamboldt FS ,O'Connor SL , et al. Measurement of children's asthma medication adherence by self report, mother report, canister weight, and Doser CT. Ann Allergy Asthma Immunol 2000;85:416-421
CrossRef | Web of Science | Medline27
Ducharme FM, Mendelson MJ, Klassen TP, et al. The Preschool Asthma Diary (PAD): a validated instrument for day-to-day monitoring of asthma severity in young children. Pediatric Academic Societies, 2007:6310.6. (Accessed December 29, 2008, at http://www.abstracts2view.com/pasall.)
28
Juniper EF ,Guyatt GH ,Feeny DH ,Ferrie PJ ,Griffith LE ,Townsend M . Measuring quality of life in the parents of children with asthma. Qual Life Res 1996;5:27-34
CrossRef | Web of Science | Medline29
Juniper EF ,Guyatt GH ,Willan A ,Griffith LE . Determining a minimal important change in a disease-specific Quality of Life Questionnaire. J Clin Epidemiol 1994;47:81-87
CrossRef | Web of Science | Medline30
del Rio L ,Carrascosa A ,Pons F ,Gusinye M ,Yeste D ,Domenech FM . Bone mineral density of the lumbar spine in white Mediterranean Spanish children and adolescents: changes related to age, sex, and puberty. Pediatr Res 1994;35:362-366
Web of Science | Medline31
Kuczmarski RJ, Ogden CL, Grummer-Strawn LM, et al. CDC growth charts: United States. Advance data from vital and health statistics. No. 314. Hyattsville, MD: National Center for Health Statistics, 2000. (DHHS publication no. (PHS) 2000-1250 0-0431.)
32
Pyle SI, Waterhouse AM, Greulich WW. A radiographic standard of reference for the growing hand and wrist. Cleveland: Press of Case Western Reserve University, 1971.
33
Demers LM, Whitley RJ. Function of the adrenal cortex. In: Burtis CA, Ashwood ER, eds. Tietz textbook of clinical chemistry. 3rd ed. Philadelphia: W.B. Saunders, 1999:1530-69.
34
Suissa S . Statistical treatment of exacerbations in therapeutic trials of chronic obstructive pulmonary disease. Am J Respir Crit Care Med 2006;173:842-846
CrossRef | Web of Science | Medline35
Cates CJ . Simpson's paradox and calculation of number needed to treat from meta-analysis. BMC Med Res Methodol 2002;2:1-4
CrossRef | Medline36
Muthu V . The number needed to treat: problems describing non-significant results. Evid Based Ment Health 2003;6:72-73
CrossRef | Medline37
Bassali RW, Benjamin J. Failure to thrive. WebMD, April 25, 2006. (Accessed December 29, 2008, at http://www.emedicine.com/PED/topic738.htm.)
38
Guilbert TW ,Morgan WJ ,Zeiger RS , et al. Long-term inhaled corticosteroids in preschool children at high risk for asthma. N Engl J Med 2006;354:1985-1997
Full Text | Web of Science | Medline39
Malozowski S ,Purucker M . Growth as a biological marker of inhaled corticosteroid activity. Curr Ther Res Clin Exp 2001;62:796-802
CrossRef | Web of Science40
Lipworth BJ . Systemic adverse effects of inhaled corticosteroid therapy: a systematic review and meta-analysis. Arch Intern Med 1999;159:941-955
CrossRef | Web of Science | Medline41
Rubin DH ,Leventhal JM ,Krasilnikoff PA , et al. Relationship between infant feeding and infectious illness: a prospective study of infants during the first year of life. Pediatrics 1990;85:464-471
Web of Science | Medline42
Lambert SB ,Allen KM ,Carter RC ,Nolan TM . The cost of community-managed viral respiratory illnesses in a cohort of healthy preschool-aged children. Respir Res 2008;9:11-11
CrossRef | Web of Science | Medline
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CrossRef4
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CrossRef11
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CrossRef20
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CrossRef22
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CrossRef24
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