INTRODUCTION
Bronchiolitis is the most common seasonal viral lower respiratory tract infection (LRTI) in infancy [1–Reference Grimprel3]. The leading aetiological agent of bronchiolitis is respiratory syncytial virus (RSV) that accounts for up to 80% of cases in infants during their first epidemic season [1–Reference Marguet5]. Although <2% of infants with bronchiolitis require hospital admission, RSV is responsible for up to 75% of the hospitalizations for severe bronchiolitis in infants aged <1 year [Reference Wainwright2, Reference Busch and Thomson4, Reference Calvo6].
There is substantial epidemiological evidence supporting the concept that severe RSV bronchiolitis resulting in hospitalization and occurring in the first months of life is associated with recurrent wheezing or asthma during childhood [Reference Jartti7–Reference Fjaerli9]. A recent literature review, which pooled data from epidemiological studies on the impact of severe RSV bronchiolitis on the subsequent respiratory morbidity, concluded that the history of severe bronchiolitis is strongly associated with the development of recurrent wheezing throughout childhood, and speculated on a complex relationship between viral LRTI in early life and the development of bronchial hyperreactivity [Reference Halfhide and Smyth10]. In the Tucson Children's Respiratory Study, early RSV LRTI was an independent risk factor of subsequent wheezing up to age 11 years but ceased to be so at age 13 years [Reference Stein11]. Sigurs and colleagues demonstrated an increased prevalence of asthma or recurrent wheezing and allergic sensitization in a cohort of infants hospitalized with RSV bronchiolitis during the first year of life compared to a matched control cohort at ages 3, 7 and 13 years [Reference Sigurs12–Reference Sigurs14]. Recently, the same group showed that severe RSV bronchiolitis, requiring hospitalization during the first year of life, is frequently followed by allergic asthma persisting into early adulthood [Reference Sigurs15], contrasting with previous data suggesting a shorter post-RSV bronchial hyperresponsiveness [Reference Stensballe16–Reference Thomsen18]. Conversely, asthma was associated with a threefold long-term increased susceptibility for severe RSV disease, suggesting that some host factors could be responsible for the severe response to RSV infection [Reference Stensballe16].
These data favour the hypothesis of a common genetic predisposition and/or common environmental exposures underlying the propensity of severe RSV infection and asthma rather than a causal effect of RSV [Reference Stensballe16, Reference Singh17]; RSV bronchiolitis might not be a trigger for subsequent asthma but simply a marker of the asthmatic genetic predisposition [Reference Thomsen18].
A number of recent studies have identified respiratory viruses other than RSV that might be involved in bronchiolitis, recurrent wheezing and asthma [Reference Singh17, Reference Lemanske19–Reference Greenough and Broughton25]. About 10–20% of bronchiolitis cases are due to rhinovirus (hRV), parainfluenza, influenza, adenovirus or human metapneumovirus (hMPV) [Reference Greenough and Broughton25]. Valkonen et al. [Reference Valkonen24] showed that infants hospitalized with non-RSV bronchiolitis have a substantially higher risk of developing recurrent wheezing during a 3-year period than those with RSV bronchiolitis. The Childhood Origins of Asthma (COAST) study also highlighted a close association between hRV infection and subsequent wheezing in a cohort of children at high risk of developing asthma or allergy [Reference Lemanske19]. Conversely, influenza virus infection was not associated with an excess of asthma episodes [Reference Fleming26]. The relationships between atopy, early viral respiratory infections, clinical bronchiolitis, and the development of asthma are rather complex, and further prospective studies are warranted to provide a better understanding of the underlying mechanisms [Reference Stein27].
Chronic respiratory morbidity is common after premature birth; in premature infants, the immaturity of the immune system confers an increased risk for severe respiratory viral infections and airway obstruction in the first 2 years of life [Reference Welliver28–Reference Broughton32]. Prematurity with respiratory morbidity, such as respiratory distress syndrome, can result in long-term lung damage and bronchial hyperreactivity, which predisposes to subsequent viral-induced wheezing later on in life [Reference Van33]. Romero et al. [Reference Romero34] showed that early RSV LRTIs in preterm infants were associated with an increased prevalence of serious early childhood wheezing by age 3 years. Moreover, it has been shown that RSV and hMPV LRTIs in preterm infants are associated with abnormal lung function and more wheezing at follow-up, persisting in adolescents and young adults, especially in those with a history of severe bronchopulmonary dysplasia (BPD) [Reference Broughton35, Reference Greenough36].
After the CASTOR study in which we showed that prematurity of <33 weeks gestational age (GA) was the only factor associated with a significantly increased risk of hospitalization for bronchiolitis in non-BPD infants during the infants' first RSV season, we performed this follow-up study of the same cohort, in order to evaluate the respiratory morbidity of these premature infants during the subsequent 12-month period. The aims of this follow-up study were first to describe the respiratory morbidity of the premature and full term infants, and second to identify the risk factors for respiratory morbidity during the 12-month period following the first RSV season.
METHODS
Design of the CASTOR study and its respiratory follow-up
This study was a follow-up study of the CASTOR study, and is referred to as the CASTOR follow-up study. The (original) CASTOR study was a multicentre, ambispective, longitudinal, non-interventional, epidemiological study conducted to compare hospitalization rates for RSV-confirmed bronchiolitis between preterm infants <33 weeks GA without BPD and matched full-term infants followed up during the 2008–2009 RSV season in France.
The rationale, design and outcomes of the CASTOR study have been presented in detail in a previous article [Reference Gouyon37]. In brief, 548 infants were recruited in nine regional neonatology networks (types 2 and 3 hospital centres) from 12 November 2008 to 31 January 2009. Each participating physician identified all the preterm infants <33 weeks GA without BPD born between 31 March and 2 October 2008 and matched each preterm to a full-term infant, according to chronological age ±1 month, gender and birth region; a total of 498 infants were matched (249 in each group). This cohort was followed during the 2008–2009 RSV season (Fig. 1); data on bronchiolitis hospitalizations from 29 September 2008 to inclusion (i.e. 12 November 2008) were collected retrospectively, and those regarding the hospitalizations from inclusion to the end of the study (i.e. 30 April 2009) were collected prospectively. Parents were telephoned every month; during the last call scheduled in the CASTOR study, they were asked whether they would participate in the CASTOR follow-up study during the next 12 months.
Fig. 1. Study design.
Study population of the CASTOR follow-up study
Eligible infants for the CASTOR follow-up study were those included in the CASTOR study, i.e. with chronological age <6 months upon CASTOR study enrolment, not having received specific RSV prophylaxis, and without documented immune deficiency or other serious or chronic illness that may have had an impact on their health status at the beginning of the 2008–2009 RSV season.
Infants with a GA <33 weeks without BPD (defined as oxygen dependence at 28 days of life) were eligible as preterm infants, and those with a GA between 39 and 41 weeks as full-term infants.
Data collection
During quarterly phone calls performed between June 2009 and June 2010, parents were asked whether their child had been hospitalized for bronchiolitis, wheezing, asthma or other respiratory morbidity, and whether the child had any wheezing episodes or any other episode of non-specified respiratory morbidity (NSRM, defined as any episode of respiratory morbidity reported by parents, excluding bronchiolitis, wheezing, asthma).
Data were collected for the period from 1 May 2009 to 30 April 2010. Parents were supplied with a diary to help them remember hospitalization episodes and identify the practitioners in charge of these hospitalizations. All these data were reported via a parents' questionnaire. Between phone calls, parents had a toll-free number at their disposal to report any hospital admission for bronchiolitis. Physicians in charge of hospitalizations had to complete a hospitalization form for each child that requested medical data related to any hospitalizations for bronchiolitis (RSV confirmed or not) or other respiratory problems occurring during the 12-month follow-up period starting 1 May 2009.
Statistical analysis
The statistical analyses were performed using SAS software, version 9.2 (SAS Institute Inc., USA). Quantitative variables were described by their frequency, mean plus or minus standard deviation, median, quartiles 1 and 3 and extreme values (minimum and maximum values), and qualitative variables by the frequency and percentage of each response choice with missing data being taken into account as a separate category in the calculation of the percentages. For comparison between preterm and full-term infants, t tests were used for continuous variables; χ 2 or Fisher's exact tests (depending on the standard conditions of application) were used for categorical variables; and Mann–Whitney-Wilcoxon tests were used for continuous variables when the assumptions of the t test were not satisfied (e.g. NSRM counts).
A logistic regression model was used to determine the risk factors for the presence of wheezing or recurrent wheezing episodes during the 12 months following the 2008–2009 RSV season; recurrent wheezing was defined as the occurrence of ⩾3 episodes of wheezing during the 12-month follow-up period.
The following covariates were first included in univariate logistic regression models: age groups at the beginning of the 2008–2009 RSV season (<60 days, 60–89 days, 90–119 days, 120–149 days, ⩾150 days); gender; geographical location (region); environmental risk factors (smoking status of the mother during pregnancy, smoking status of the parents since birth, breastfeeding, one or more sibling aged ⩾2 years, child care); gestational age (preterm infant, full-term infant); birth weight; multiple pregnancy; number of RSV-confirmed bronchiolitis hospitalizations during the first RSV season; number of bronchiolitis hospitalizations irrespective of aetiology during the first RSV season; severity of RSV-confirmed bronchiolitis hospitalizations during the first RSV season (admission to a neonatology unit for at least one bronchiolitis episode, admission to a paediatric intensive care unit for at least one bronchiolitis episode, need of oxygen therapy for at least one bronchiolitis episode, assisted ventilation for at least one bronchiolitis episode); and severity of bronchiolitis hospitalizations irrespective of aetiology during the first RSV season (admission to a neonatology unit for at least one bronchiolitis episode, admission to a paediatric intensive care unit for at least one bronchiolitis episode, need of oxygen therapy for at least one bronchiolitis episode, assisted ventilation for at least one bronchiolitis episode). Only the covariates significant at a threshold of P⩽0·25 were included in the subsequent logistic multivariate models. A backward selection was used in the final model to retain only those covariates significant at the threshold of P⩽0·05.
RESULTS
Of the 548 infants enrolled in the CASTOR study, 443 were followed in the CASTOR follow-up study from June 2009 to June 2010 (Fig. 2); 105 infants (50 full-term, 55 preterm) were not included in the follow-up study because parents did not sign the consent form. Followed-up infants had similar characteristics compared to those not enrolled in the follow-up, except for a younger mean age (12·5 months vs. 11·7 months, P < 0·001) in the non-followed-up group (Table 1). A total of 1985 parents' questionnaires were completed at quarterly phone calls.
Fig. 2. Disposition of infants.
Table 1. Comparison of socio-demographic characteristics of patients included and not included in the CASTOR follow-up study (N = 548)
* P value for between-group comparisons: t test for continuous variables, χ 2 test or Fisher's exact test for categorical variables.
† Age at the beginning of the CASTOR follow-up study, for the non-included population the date of inclusion is set at 24 June 2009.
Study population
At inclusion in the CASTOR follow-up study, the mean age of the infants was 12·5 ± 1·9 months (range 9·0–18·0 months) with the majority being boys (54%). Comparative characteristics of the preterm and full-term groups for the overall population are presented in Table 2.
Table 2. Characteristics of the overall CASTOR follow-up population (N = 443)
* Results are presented as mean±s.d. or n (%).
† P value for between-group comparisons: t test for continuous variables, χ 2 test or Fisher's exact test for categorical variables.
‡ From birth to going home.
§ Type 2: neonatal intermediate care units; type 3: neonatal intensive care units.
∥ Distinct hospital units dedicated to the postnatal management of preterm infants and/or newborns with an altered health status.
¶ From birth to date of inclusion in the CASTOR follow-up study.
# No details available as data recorded via parents' questionnaires.
Preterm infants had significantly lower birth weights and heights, and significantly more were from multiple pregnancies than full-term infants. All preterm infants and 3% of full-term infants were hospitalized in neonatology units at birth (Table 2). In the preterm group, 35% of infants (n = 85) required mechanical ventilation during the birth hospitalization (mean duration 1·7 ± 1·3 days) compared to none of the full-term infants (P = 0·215); 68% of the preterm infants (n = 164) had a non-invasive ventilation (mean duration 5·7 ± 6·1 days) in the postnatal period vs. only one full-term infant (P = 0·016). Regarding environmental risk factors for bronchiolitis, preterm infants were twice as often exposed to antenatal smoking and significantly less breastfed compared to full-terms; conversely, they were one-sixth as often kept in day care vs. full-term infants (Table 2). No significant difference between preterm and full-term infants was observed regarding the family history of allergy or respiratory problems (Table 2).
More preterm infants had been hospitalized for bronchiolitis (14%, n = 34, including 14 patients with RSV-confirmed bronchiolitis) from birth to date of inclusion (not limited to the first RSV season) in the follow-up study than full-term infants (2%, n = 4, including three patients with RSV-confirmed bronchiolitis) (P < 0·001) (Table 2).
Respiratory morbidities during the 12-month follow-up period
Wheezing and recurrent wheezing episodes
Seventy-four infants (23 full-term, 51 preterm) had at least one wheezing episode during the 12-month follow-up period following the first RSV season, 45 had one episode, 17 had two episodes, and 12 had ⩾3 wheezing episodes (Table 3).
Table 3. Disposition of respiratory morbidities during the 12 months following the 2008–2009 RSV season according to the history of bronchiolitis hospitalization irrespective of aetiology during the 2008–2009 RSV season (N = 443)
RSV, Respiratory syncytial virus; NSRM, non-specified respiratory morbidity.
Data are presented as n (%).
* All were for RSV bronchiolitis.
Preterm infants were more likely to have at least one wheezing episode than full-term infants: 51/242 (21%) versus 23/201 (11%) (P = 0·016 as shown in Table 3). Recurrent wheezing episodes (⩾3 wheezing episodes) concerned 4% of preterm infants (10/242) compared to only 1% of full-term infants (2/201) (P = 0·043).
According to the history of hospitalized bronchiolitis (irrespective of aetiology) during the first RSV season, 30% (11/37) of the previously hospitalized infants had at least one episode of wheezing during the follow-up period compared to only 15·5% (63/406) of the infants without a previous bronchiolitis hospitalization, irrespective of prematurity status (Table 3).
When considering the cases with a history of hospitalized RSV-confirmed bronchiolitis during the first RSV season, previously hospitalized infants irrespective of their prematurity status were more likely to have at least one wheezing episode than infants with no history of hospitalization [47% (8/17) vs. 15·5%, (66/426)] (Table 4).
Table 4. Disposition of respiratory morbidities during the 12 months following the 2008–2009 RSV season according to the history of RSV-confirmed bronchiolitis hospitalization during the 2008–2009 RSV season (N = 443)
RSV, Respiratory syncytial virus; NSRM, non-specified respiratory morbidity.
Data are presented as n (%).
* All were for RSV bronchiolitis.
NSRM
A total of 128 (28·9%) infants had at least one episode of NSRM (Table 5). Preterm infants were significantly (P = 0·034) more likely to have at least one episode of NSRM than full-terms, and had significantly (P = 0·042) more frequent NSRM episodes compared to full-term infants as shown in Table 5.
Table 5. Description of non-specified respiratory morbidity during the 12 months following the 2008–2009 RSV season in the overall CASTOR follow-up population (N = 443)
RSV, Respiratory syncytial virus; NSRM, non-specified respiratory morbidity.
Data are presented as n (%).
* χ 2 test.
† Mann–Whitney-Wilcoxon test.
According to the history of hospitalized bronchiolitis (irrespective of aetiology) during the first RSV season, previously hospitalized infants were more likely to have at least one episode of NSRM than those without a previous bronchiolitis hospitalization [54% (20/37) vs. 27% (108/406)], irrespective of prematurity status (Table 3). When analysing the impact of a RSV-confirmed bronchiolitis hospitalization during the first RSV season, previously hospitalized infants were more likely to have at least one episode of NSRM during the follow-up period than those with no history [71% (12/17) vs. 27% (116/426)], irrespective of their prematurity status (Table 4).
Hospitalizations for respiratory pathologies
Five infants (four preterm, one full-term) were hospitalized during the 12-month follow-up period. In the preterm group, the reasons for hospitalization were: RSV bronchiolitis (n = 1), wheezing (n = 2), and dyspnoea related to oesogastric reflux (n = 1); the full-term infant was hospitalized for a right basal pneumopathy.
All the hospitalizations for respiratory problems occurred in infants without a history of bronchiolitis hospitalization as shown in Table 3.
Predictive factors of wheezing and recurrent wheezing episodes during the 12-month follow-up period
The following factors were found to be linked to the occurrence of wheezing episodes at the threshold of P < 0·25 and were included in the multivariate logistic model: gender (P = 0·022), smoking status of the parents since birth to inclusion in the CASTOR study (P = 0·172), breastfeeding (P = 0·197), prematurity (P = 0·023), birth weight (P = 0·046), RSV-confirmed bronchiolitis hospitalization during the first RSV season (P = 0·002), and need of oxygen therapy for an RSV-confirmed bronchiolitis hospitalization during the first RSV season (P = 0·006). A backward selection was used to retain only those factors that were significant at the threshold of 5% in the final model. As shown in Table 6, three covariates were statistically significant in the final model, indicating that the probability of having wheezing episodes during the 12-month period following the first RSV season was significantly impacted by these three independent factors: male gender, birth weight <3330 g, and hospitalization for RSV-confirmed bronchiolitis during the first RSV season.
Table 6. Predictive factors of wheezing episodes that occurred during the 12 months following the 2008–2009 RSV season in the overall CASTOR follow-up population (N = 443)
RSV, Respiratory syncytial virus; OR, odds ratio; CI, confidence interval.
* Covariates included in the multivariate logistic regression model: gender, smoking status of the parents since birth to inclusion in the CASTOR study, breastfeeding, prematurity, birth weight, RSV-confirmed bronchiolitis hospitalization during the first RSV season, and need of oxygen therapy for an RSV-confirmed bronchiolitis hospitalization during the first RSV season.
† 820–<3330 g vs. 3330–4490 g.
‡ Hospitalization for RSV-confirmed bronchiolitis during the first RSV season.
Regarding recurrent wheezing episodes during the 12-month follow-up period, no independent predictive factors of such episodes were identified in the final multivariate model.
DISCUSSION
The main findings of the CASTOR follow-up study are: (i) preterm infants <33 weeks GA without BPD had a greater respiratory morbidity (wheezing episodes or NSRM episodes) than full-term infants; (ii) infants with a history of hospitalized bronchiolitis (RSV confirmed and all types) during their first RSV season were more likely to have at least one episode of wheezing or NSRM during the subsequent 12 months than infants without such a history; (iii) RSV-confirmed bronchiolitis hospitalization during their first RSV season, birth weight <3330 g and male gender emerged as independent risk factors for wheezing episodes during the subsequent 12 months.
The CASTOR follow-up study provides prospective data on the chronic respiratory morbidity in a large French cohort of 443 infants (out of which 242 preterm infants <33 weeks GA without BPD) followed up during the 12 months following their first RSV season. To our knowledge, only one previous prospective study evaluated post-RSV respiratory morbidity and that was in a smaller cohort of 126 preterm infants <32 weeks GA followed up to only age 1 year of [Reference Broughton32].
The main purpose of the CASTOR follow-up study was to collect data on the occurrence of wheezing and recurrent wheezing episodes during the 12 months following the 2008–2009 RSV season in infants from the CASTOR cohort. The comparison between the preterm group (<33 weeks GA) without BPD and the full-term group (39–41 weeks GA) highlighted the impact of premature birth (<33 weeks GA) on the increased incidence of wheezing episodes during the 12-month follow-up period after their first RSV season, even in the absence of an associated chronic lung disease.
Hoo et al. [Reference Hoo29] showed via paired measurements of maximal expiratory flow at functional residual capacity, obtained 3 weeks after birth in 24 preterm infants (mean GA 33·2 ± 2·2 weeks), and repeated at a mean corrected postnatal age of 57·0 ± 12·2 weeks, that preterm delivery (⩽36 weeks GA) was associated with altered airway development during early infancy even in the absence of neonatal respiratory disease. Friedrich et al. [Reference Friedrich30] previously showed persistently reduced expiratory flows in the presence of normal forced vital capacity and the absence of catch-up growth in airway function based on longitudinal measurements of forced expiratory flow obtained in the first and the second years of life for 26 preterms born on average at 32·7 (range 30–34) weeks' GA (n = 26) compared to 24 full-terms.
Our findings are in line with previous data on the relationship between early severe bronchiolitis and subsequent recurrent childhood wheezing, a long lasting reduction in pulmonary function, and asthma [Reference Jartti7, Reference Fjaerli9, Reference Sigurs13, Reference Singh17]. Despite the higher incidence of wheezing (including recurrent wheezing) episodes during the 12-month period following the first RSV season in the overall CASTOR follow-up population, i.e. 11/37 (30%) infants with a history of hospitalized bronchiolitis compared to 63/406 (15·5%) without such a history, we could not show a significant difference between these two groups given the small sample sizes.
Furthermore, infants with a history of early hospitalized RSV-confirmed bronchiolitis were more prone to at least one wheezing episode than those with no such history (47% vs. 15·5%), irrespective of their prematurity status, during the CASTOR follow-up period. Our results are consistent with previously published data [Reference Kneyber38, Reference Osundwa and Dawod39], but with lower incidences than those found by Sigurs et al. in 3-year-old children with RSV bronchiolitis during the first year of life (60% of infants with RSV history with any wheezing episodes vs. 32% of those with no history, P = 0·003) [Reference Sigurs12]; those authors confirmed the same tendency in this birth cohort up to the age of 7 years [Reference Sigurs13]. The ALSPAC Study Team showed a lower prevalence of any wheezing (28%) at 30–42 months after birth in the RSV subgroup (150 infants) of this large British birth cohort compared to our results (47%), despite a very close prevalence in controls (13% and 15·5%, respectively). A likely explanation for this observation is the increased loss of follow-up in the ALSPAC cohort infants with associated risk factors for RSV hospitalization, such as low birth weight, preterm delivery, housing and tobacco smoke exposure [Reference Henderson8]. Broughton et al. [Reference Broughton32] equally showed that early severe RSV disease in preterm infants had an impact on the subsequent respiratory morbidity and healthcare resources utilization, as preterm infants with a history of RSV infection had significantly more days of cough and wheeze at 1-year follow-up compared to those without LRTI or with RSV-negative LRTI [Reference Broughton32].
Our study confirms that early severe RSV bronchiolitis has a deleterious impact on clinical respiratory outcomes of infants followed-up during the 12 months subsequent to their first RSV season. Moreover, early severe viral LRTI in preterm infants has been shown to be associated with abnormal lung function at long-term follow-up [Reference Broughton35]. As suggested by Sigurs et al. based on the 18-year follow-up of a cohort of 138 children, out of which 46 had RSV bronchiolitis during their first year of life, the underlying mechanism of subsequent chronic respiratory morbidity could be the airways remodelling [Reference Sigurs15]. This hypothesis is supported by extensive experimental data showing that RSV infection induces cellular immune responses with subsequent production of inflammatory mediators that may cause tissue remodelling, with long-term effects on the lung structure and clinical outcomes [Reference Mohapatra and Boyapalle40, Reference Martin, Siddiqui and Hassan41].
Hospitalization for RSV bronchiolitis during the first RSV season was the most important risk factor for the development of subsequent wheezing episodes in the present study; infants with a history of early severe RSV bronchiolitis were 4·72 times as likely to develop wheezing episodes during the 12 months following their first RSV season than their non-hospitalized counterparts.
Our findings are equally supported by a recently published retrospective study based on a large (nearly 14 million members) US health plan database, showing that preterm infants with early severe RSV bronchiolitis were 2·52-fold (95% confidence interval 1·65–3·85, P < 0·001) as likely to develop early serious childhood wheezing by age 3 years [Reference Romero34].
The CASTOR follow-up study results should be interpreted in the light of several methodological limitations: (i) the study sample size was not determined by statistical considerations but only determined by the participation rate in the follow-up period, thereby imposing a cautious interpretation of the results; (ii) the main purpose of this study was to evaluate the relationship between bronchiolitis hospitalizations during the first RSV season and the occurrence of respiratory morbidities during the following 12 months in the overall follow-up population (larger sample size enabling more robust results); (iii) RSV testing in case of hospitalization for bronchiolitis was not required by the protocol (observational study) and therefore the incidence of RSV hospitalizations could have been underestimated, thus weakening the observed association between early severe RSV-confirmed bronchiolitis and subsequent wheezing. Moreover, while we found that a birth weight <3330 g was associated with a higher risk of respiratory morbidity after the first RSV season, this threshold was derived from a statistical approach, and further exploration is needed to strengthen this finding and assess its clinical relevance, in particular using the generally accepted clinical standards for low birth weight.
A potential underestimation of the incidence of wheezing/recurrent wheezing during the follow-up period in our study could have been also determined by: (i) the considerable number of infants who did not participate in the follow-up (19% of the overall CASTOR study population), especially as these infants were younger than those followed-up; (ii) the lack of diagnosis confirmation by a physician, with potential data loss (presence of wheezing/recurrent wheezing cases in infants diagnosed with other LRTI unknown diagnosis).
CONCLUSION
In conclusion, the present study demonstrated an increased incidence of respiratory morbidity during the 12 months subsequent to the first RSV season (2008–2009 RSV season) in preterm infants (<33 weeks GA) without associated BPD compared to full-term infants, as well as in infants with a history of early severe bronchiolitis (RSV confirmed and all types) hospitalization compared to those without such a history.
Three factors were predictive of wheezing episodes during the 12 months following the first RSV season, irrespective of prematurity status: early hospitalization for RSV-confirmed bronchiolitis, birth weight <3330 g, and male gender. The awareness of these risk factors could facilitate the identification of infants at high risk of respiratory morbidities, with the subsequent implementation of more rigorous prophylactic measures.
ACKNOWLEDGEMENTS
We are extremely grateful to the children and parents who contributed to this study. We thank all investigators and regional coordinators who participated in the study. We thank Brigitte Bourdillat for the manuscript editing. We acknowledge Muriel Viala-Danten, Fatoumata Fofana and Antoine Regnault from MAPI Consultancy for their contribution to the design of statistical analyses and the interpretation of study results. We also thank ProClinica for the logistic assistance in the phone call follow-up with the parents of enrolled children. This study was sponsored by AbbVie France.
DECLARATION OF INTEREST
B.F. has received honorarium for her scientific advice and expertise from AbbVie. J.B.G. has served as a consultant for AbbVie, Chiesi Laboratories, Orphan Europe Laboratories, and has received research funding from AbbVie, Chiesi Laboratories and Orphan Europe Laboratories. J.C.R. has served as a consultant for AbbVie. D.P. has received honoraria from pharmaceutical companies including AbbVie, GSK, Novartis, Sanofi Pasteur MSD and Wyeth for educational presentations and congress presentations. D.A. and T.M. are employees of AbbVie, and may own AbbVie stock. The design, study conduct, and financial support for the clinical trial was provided by AbbVie. AbbVie participated in the interpretation of data, review, and approval of the manuscript.
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