Respiratory symptoms in preterm infants: burden of disease in the first year of life
European Journal of Medical Research volume 16, Article number: 223 (2011)
While respiratory symptoms in the first year of life are relatively well described for term infants, data for preterm infants are scarce. We aimed to describe the burden of respiratory disease in a group of preterm infants with and without bronchopulmonary dysplasia (BPD) and to assess the association of respiratory symptoms with perinatal, genetic and environmental risk factors.
Single centre birth cohort study: prospective recording of perinatal risk factors and retrospective assessment of respiratory symptoms during the first year of life by standardised questionnaires. Main outcome measures: Cough and wheeze (common symptoms), re-hospitalisation and need for inhalation therapy (severe outcomes). Patients: 126 preterms (median gestational age 28.7 weeks; 78 with, 48 without BPD) hospitalised at the University Children's Hospital of Bern, Switzerland 1999-2006.
Cough occurred in 80%, wheeze in 44%, rehospitalisation in 25% and long term inhalation therapy in wheezers in 13% of the preterm infants. Using logistic regression, the main risk factor for common symptoms was frequent contact with other children. Severe outcomes were associated with maximal peak inspiratory pressure, arterial cord blood pH, APGAR and CRIB-Score.
Cough in preterm infants is as common as in term infants, whereas wheeze, inhalation therapy and re-hospitalisations occur more often. Severe outcomes are associated with perinatal risk factors. Preterm infants who did not qualify for BPD according to latest guidelines also showed a significant burden of respiratory disease in the first year of life.
Respiratory problems are major consequences of prematurity, however the heterogeneity of respiratory sequelae and varying definitions have made a systematic assessment difficult. Northway et al. were the first to describe them as "bronchopulmonary dysplasia" (BPD) . The definition of BPD has been revised several times as with advances in perinatal treatment the clinical and pathomorphological patterns have changed. The most recent consensus definition of 2001 groups severity of "new BPD" into mild, moderate and severe according to gestational age and duration of supplementary oxygen . Recently a large American cohort study used this definition to assess its usefulness for predicting respiratory morbidity in the first year of life . The authors found a high sensitivity using this BPD classification, but specificity was poor: 30% of preterm infants had severe respiratory problems without qualifying for BPD. Since information on additional risk factors is lacking, it remains unclear whether the identification of risk factors could help improving prediction of respiratory morbidity after preterm birth.
Incidence and severity of respiratory symptoms in the first year of life are relatively well described in term born infants. One study reported persistent cough to occur in 56% and wheeze in 45% of termborn infants in the USA . Another study, conducted in Australia, found 77% of the infants coughing and 27% wheezing during the first year of life . In a recent prospective study from our group assessing respiratory morbidity in a birth cohort of term-born infants, any cough occurred in 93% and wheeze in 21% of the infants during the first year of life . Frequency of symptoms was associated with male sex, higher birthweight, pre- and postnatal smoke exposure and day care or older siblings. Only 3 of all 195 infants (1.5%) had to be hospitalised for respiratory problems in their first year of life .
In contrast to term infants, few data are available on respiratory morbidity in preterm infants. There are studies on outcome and associated risk factors from the pre-surfactant era , but data including children with the "new" form of BPD are scarce. Most of these studies focused on severe outcomes  and only few have determined risk factors  for pulmonary sequelae for which preterm infants show a predisposition [9–11].
The aim of the present study was to describe frequency and spectrum of respiratory symptoms during the first year of life in a contemporary population of preterm infants with and without BPD and to identify environmental and perinatal risk factors associated with common and severe respiratory symptoms.
Preterm infants (gestational age < 37 wks), born between July 1999 and June 2005 and hospitalised at the University Hospital of Bern, Switzerland, were prospectively recruited during a consultation of a paediatric pulmonologist before discharge. Perinatal data were routinely recorded using the institutional neonatology database (NEODAT 4.10, Tubingen, Germany). After the first year of life, a standardised questionnaire was sent to the parents to assess respiratory morbidity during the first year after discharge and ongoing environmental exposures.
We approached preterm infants independent of their birthweight with 168 being recruited for the study. More parents of infants with lower birthweight agreed to participate resulting in a study population of 123 (72%), 67 (40%) and 3 (2%) preterms with birthweights below 1500 g, below 1000 g and below 500 g, respectively.
Based on the ATS definition of BPD, we categorised preterm infants into healthy, mild, moderate and severe BPD, respectively . BPD was defined as supplemental oxygen requirement for at least 28 days. Time point of assessment for BPD severity was at 36 weeks post-menstrual age (PMA) or at discharge (whichever occurred first) in infants born at less than 32 weeks of gestation, and at day 56 of life in infants born with at least 32 weeks of gestation. Mild BPD was defined as breathing room air, moderate BPD as requiring less than 30% supplemental oxygen and severe BPD as the need for more than 30% of oxygen. The standardised internal hospital guidelines were applied to determine the exact amount of oxygen needed (aiming for 92% or more oxygen saturation allowing dips to 86%) and BPD classification was verified in each case by review of the medical records. The ethics committee of the canton of Bern approved the study protocol and written informed consent was obtained from the parents.
Assessment of Perinatal Data
Definition of Respiratory Morbidity (Outcomes)
Respiratory morbidity was assessed by a standardised questionnaire using modified questions from the International Study on Asthma and Allergies in Childhood (ISAAC) [12, 13] to the parents. The main outcomes were categorised into common and severe: Cough with cold ("did your child cough during times with a cold?") and wheeze were considered as common respiratory symptoms, whereas re-hospitalisation for pulmonary reasons (excluding readmissions for diagnostic purposes) or long-term inhalation therapy (longer than four weeks) in wheezing infants were defined as severe outcomes [3, 14]. In addition the subjective burden of disease and the need for consultations at any healthcare institution were assessed by the questionnaire.
Definition of Risk Factors
Potential risk factors were grouped into 3 categories:
Perinatal risk factors: Factors that have previously been described as either influencing the outcome of preterm infants or having an effect on the occurrence of BPD such as gestational age, sex, birthweight, maternal chorioamnionitis (histopathologically confirmed), PDA (patent ductus arteriosus) when of hemodynamic relevance in echocardiography, peak inspiratory pressure (PIP) during mechanical ventilation and antenatal steroids [15–18].
Factors of postnatal adaptation: Perinatal parameters reflecting the adaptation and initial condition of the newborn, such as APGAR score, arterial cordblood pH-value  and CRIB score.
Environmental and sociodemographic exposures: Known risk factors for respiratory symptoms in term infants including day care or older siblings, history of parental atopic disease and smoke exposure [6, 20].
We used descriptive statistics to illustrate the occurrence and parental perception of respiratory morbidity. Second, to identify possible risk factors, we grouped all outcome parameters into binary categories and calculated the association between outcomes and risk factors using logistic regression analysis. All listed risk factors were entered into the model one by one as explanatory factors; continuous variables were centred. Results are given as odds ratios with confidence intervals and exact p-values. Due to the small sample size and a strong co-linearity between many of the parameters, only univariable analysis was performed. Sensitivity analysis stratifying for gestational age, sex, birthweight and age at reply of questionnaire confirmed the main results. Data analyses were performed using STATA® version 8.2 for Windows (STATA Corporation, College Station, TX, USA).
We primarily recruited 168 infants and received 126 (75%) completed questionnaires back. Median gestational age was 28.7 weeks (range 23.9-36.1), median birthweight was 1070 g (range 420-2980), 71 (56%) infants were male and 55 (44%) female; 78 (62%) fulfilled the criteria of new BPD and 48 (38%) were classified as having no BPD.
Of all questionnaires, 65% were filled in by the parents when their child was 1-3 years, 35% when the child was older. A sensitivity analysis showed no differences between those two groups. Descriptive data of the study group are given in Table 1.
Burden of Respiratory Morbidity
The occurrence of common respiratory symptoms (e.g. cough and wheeze) and severe outcomes (e.g. rehospitalisation and long term inhalation therapy) is shown in Table 2 burden of disease is illustrated in Figure 1. Common respiratory symptoms occurred with high frequency: 80% (95%-CI 71-86%) of the infants had cough and 44% (95%-CI 36-54%) wheeze.
Severe outcomes were less frequent: re-hospitalisation occurred in 25% (95%-CI 17-33%) of all children, and long term inhalation because of wheezing in 13% (95%-CI 7-20%) of the infants. Parental statement of re-hospitalisation was very consistent with medical records.
While frequency of common symptoms did not differ between children with and without BPD, there was a trend towards more inhalation therapy in the BPD group.
Of the patients included 9 (7%) had RSV vaccination; 8 (6%) children suffered from severe RSV infection they needed to be hospitalised for, two of those had been vaccinated before.
Parental Perception of Respiratory Morbidity
In 53 families (45%) parents considered their infant to cough as much as a healthy term infant, 34 (29%) believed their infant to cough more often and 30 (26%) less often than healthy infants.
Slightly more than half of the parents (n = 65, 55%) reported that they consulted the community paediatrician in an emergency situation during the first year of life, 43 (73%) of those once or twice and 16 (27%) more often, up to a maximum of 10 times.
Determinants of Respiratory Outcome
Table 3 shows associations between analysed risk factors and respiratory morbidity.
Common respiratory symptoms were mainly associated with environmental exposures. Children who were exposed to other children had a four-fold risk of having common symptoms (OR 4.7; 95%-CI 1.8-12.6, p = 0.002). While there was no difference between the outcomes cough and wheeze for most of the risk factors, maternal smoking during pregnancy was associated mainly with wheeze (OR 4.7; 95%-CI 1.2-18.1, p = 0.024) and contact with other children mainly with cough in the first year of life (OR 4.1; 95%-Cl 1.6-10.5, p = 0.004).
Contrary to those for common symptoms, risk factors for severe outcomes were mainly parameters representing perinatal adaptation. A significant association with both re-hospitalisation and inhalation therapy was found for high peak inspiratory pressure, low arterial cord blood pH, low APGAR-score and low CRIB-score, as shown in Table 3. Low arterial cord blood pH (< 7.15) was associated with a 4.4-fold (95%-CI 1.4-13.6, p = 0.011) increased likelihood of severe symptoms.
No association was found between any of the investigated outcomes and need for intubation, surfactant therapy, parental educational status or parental smoking in the first year.
In our cohort of preterm infants with and without BPD, respiratory symptoms were frequent during infancy: cough with cold was reported for 80% and wheeze for 45% of infants, respectively. More severe symptoms were less common, with re-hospitalisation for respiratory reasons occurring in 25% of infants and 13% of infants needing long-term inhalation therapy of more than four weeks because of wheezing.
Risk factors differed between common and severe symptoms. While common symptoms were associated with environmental factors such as contact to other children, severe symptoms were associated with risk factors reflecting perinatal adaptation, such as APGAR-score, CRIB-score and cord blood pH.
Data on prevalence of cough and wheeze in preterm infants from the post-surfactant era are rare: Greenough et al. reported that 51% of preterm infants born at less than 29 weeks of gestation suffered from cough and 42% from wheeze during the first year of life . Vrijland et al. described cough to occur in 97% and wheeze in 39% of preterm infants . In an important study from the presurfactant era 53 to 65% of the infants had cough or wheeze during the first 6 months of life . Our results are well in line with these reports. Interestingly, despite differences in data assessment, age range, observational periods and countries, the high prevalence of wheeze and even higher prevalence of cough seems to be a consistent finding among studies.
Re-hospitalisation rates of preterm infants in the first 1-2 years are reported in the literature to occur in 14%  to 38%  of preterm infants with and without BPD, well comparable to our results and known to be dependent on gestational age and differences in patient management .
To our knowledge there are no data available comparing respiratory morbidity between term- and preterm-born infants from the same area and time period. We have recently reported on respiratory morbidity and risk factors in a large unselected prospective cohort of term-born infants with weekly assessment of respiratory symptoms . Recruitment area and time period were the same as in the present study. In these healthy term-born infants, the overall prevalence of cough was comparable (93%, compared to 79% in preterm children), whereas wheeze occurred less often in term children (21%) than in preterm children (44%). This is quite remarkable, considering that the method of data collection used for term infants (weekly phone calls) is expected to be more sensitive than the method used for preterm children (retrospective questionnaire) . Hospitalisation due to respiratory reasons in the first year of life was reported for 25% of preterm, but only for 1.5% of term-born infants .
Common symptoms were mainly associated with environmental exposures, in accordance with findings by Greenough et al. who reported that male sex, duration of oxygen therapy, older siblings and socioeconomic status were associated with respiratory symptoms in the first year of life in preterms born before 29 weeks of gestation . Our results show that this holds also for preterms born after 29 weeks of gestation. In contrast, severe respiratory symptoms were stronger associated with parameters reflecting perinatal adaptation. APGAR- and CRIB score have been described to predict outcome of preterm infants  and it has been shown that higher PIP is associated with decreased survival rates .
Surprisingly, BPD was not correlated with severe respiratory morbidity in the present study, although a trend was found for severe outcomes. The association with BPD severity and long-term respiratory morbidity has remained controversial and comparison of these studies is difficult due to varying BPD definitions [25–28]. Ehrenkranz et al. found a reasonable association between severe outcomes and the "new BPD" classification . One possible explanation might be differing neonatal treatment strategies between Europe and the USA. Premature infants in our cohort had shorter mechanical ventilation and early nasal CPAP therapy. In contrast, different guidelines lead to intubation and longer duration of mechanical ventilation in the USA .
Gestational age was not associated with respiratory symptoms. These results are again different than American results  but in line with the London cohort . This might reflect the different picture of "new" BPD, which is indeed known not to be exclusively dependent on gestational age .
While risk factors for common respiratory symptoms were similar for premature and term neonates, severe outcomes in preterms were related to perinatal factors. Furthermore, other factors found to be associated with respiratory morbidity in the term-born cohort, such as sex, birthweight and maternal atopy were not associated with respiratory symptoms in preterms. We assume that the influence of these factors is masked by stronger effects induced by prematurity and the related developmental changes of the immune system as well as of lung and airway growth. It is e.g. known that boys have smaller airways at birth and thus more respiratory problems than girls , but this gender difference is less prominent in premature infants  and likely to be overruled by other factors.
One third of the parents may overestimate the common respiratory morbidity of their preterm born children when comparing to term infants and consult their Paediatrician early. Thus parental counselling at discharge related to common in respect to severe respiratory morbidity may help to improve the burden of the health care system.
There are limitations of our study. It is a retrospective survey, with questionnaires sent to the parents at different ages of their children. This may lead to recall bias, however similar results after stratification by age at reply of questionnaires makes this unlikely. Furthermore it has been shown that questions on respiratory symptoms have a good repeatability, supporting validity of our findings [13, 33]. Another possible bias is the fact that we only included children who underwent infant lung function which makes generalisation of the results more difficult. Due to rather low numbers we were not able to perform multivariable analyses. The relatively small sample size might also explain why parameters like gestational age or chorioamnionitis were only weakly associated with respiratory morbidity . In addition, causal pathways are difficult to model in the analysis, because many of the examined parameters may function either as independent risk factor or alternatively be a consequence of another risk factor, therefore lying in the causal pathway. For instance high peak inspiratory pressure can injure the premature lung by itself, on the other hand, ventilation with high pressures could have been made necessary because of an injured premature lung. All these factors are important to bear in mind when interpreting the results. To validate our findings and clearly disentangle all these interactions, larger studies should be conducted in future.
From a clinical point of view, the identification of risk factors may help to promote further individualized treatment and prevent long-term sequelae in preterm infants. The risk factors for respiratory diseases during infancy should be considered as an important part of planning discharge and follow-up of high-risk premature infants. For instance, in line with other, mainly European studies, we can support the hypothesis that gentle breathing support results in less frequent BPD rates as well as in less respiratory symptoms even in very young preterm infants .
From a public health point of view, prenatal birth is the commencement of a relevant burden of disease for patients, parents  and the health care system. This includes doctor visits apart from routine checkups, re-hospitalisations as well as psychological and financial burden of long-term medication. This burden is strongly dependent on the correct identification of those infants subject to appropriate treatment. In Switzerland, decisions on medication and reimbursement of health care costs are strongly influenced by the current BPD definition. For instance, vaccination against respiratory syncytial virus is only recommended and paid in preterm infants with severe BPD, it can be considered for patients with moderate BPD and is not recommended for patients with mild BPD. However, our data and other studies show that prematurity rather than BPD definitions and other risk factors define respiratory morbidity in these preterm infants in the first year of life. Due to these aspects current health care policies need urgent reconsideration.
The results of this study indicate that premature infants are subject to a high incidence of respiratory morbidity even after hospital discharge imposing a relevant burden of disease for patients, parents and the health care system. By describing respiratory morbidity in the first year of life in these preterm infants and assessing associated risk factors, our study will contribute to the identification of patients with the highest risk for later respiratory morbidity. Growing knowledge on the pathophysiology as well as changes in perinatal management will however lead to continuous changes of this picture. As more patients with the "new" form of BPD will reach older age, larger studies with longer follow-up times and measurement of subtle lung function indices will be needed to assess the long-term outcome of these children.
Northway WH Jr, Rosan RC, Porter DY: Pulmonary disease following respirator therapy of hyaline-membrane disease. Bronchopulmonary dysplasia. N Engl J Med 1967,276(7):357–68. 10.1056/NEJM196702162760701
Jobe AH, Bancalari E: Bronchopulmonary dysplasia. Am J Respir Crit Care Med 2001,163(7):1723–9.
Ehrenkranz RA, Walsh MC, Vohr BR, Jobe AH, Wright LL, Fanaroff AA, et al.: Validation of the National Institutes of Health consensus definition of bronchopulmonary dysplasia. Pediatrics 2005,116(6):1353–60. 10.1542/peds.2005-0249
Belanger K, Beckett W, Triche E, Bracken MB, Holford T, Ren P, et al.: Symptoms of wheeze and persistent cough in the first year of life: associations with indoor allergens, air contaminants, and maternal history of asthma. Am J Epidemiol 2003,158(3):195–202. 10.1093/aje/kwg148
Kusel MM, de Klerk NH, Holt PG, Kebadze T, Johnston SL, Sly PD: Role of respiratory viruses in acute upper and lower respiratory tract illness in the first year of life: a birth cohort study. Pediatr Infect Dis J 2006,25(8):680–6. 10.1097/01.inf.0000226912.88900.a3
Latzin P, Frey U, Roiha HL, Baldwin DN, Regamey N, Strippoli MP, et al.: Prospectively assessed incidence, severity, and determinants of respiratory symptoms in the first year of life. Pediatr Pulmonol 2007,42(1):41–50. 10.1002/ppul.20542
Gross SJ, Iannuzzi DM, Kveselis DA, Anbar RD: Effect of preterm birth on pulmonary function at school age: a prospective controlled study. J Pediatr 1998,133(2):188–92. 10.1016/S0022-3476(98)70219-7
Greenough A, Limb E, Marston L, Marlow N, Calvert S, Peacock J: Risk factors for respiratory morbidity in infancy after very premature birth. Arch Dis Child Fetal Neonatal Ed 2005,90(4):F320–3. 10.1136/adc.2004.062018
Bush A: COPD: a pediatric disease. Copd 2008,5(1):53–67. 10.1080/15412550701815965
Greenough A: Long-term pulmonary outcome in the preterm infant. Neonatology 2008,93(4):324–7. 10.1159/000121459
Aukland SM, Rosendahl K, Owens CM, Fosse KR, Eide GE, Halvorsen T: Neonatal bronchopulmonary dysplasia predicts abnormal pulmonary HRCT scans in long-term survivors of extreme preterm birth. Thorax 2009,64(5):405–10. 10.1136/thx.2008.103739
Asher MI, Keil U, Anderson HR, Beasley R, Crane J, Martinez F, et al.: International Study of Asthma and Allergies in Childhood (ISAAC): rationale and methods. Eur Respir J 1995,8(3):483–91. 10.1183/09031936.95.08030483
Strippoli MP, Silverman M, Michel G, Kuehni CE: A parent-completed respiratory questionnaire for 1-year-old children: repeatability. Arch Dis Child 2007,92(10):861–5. 10.1136/adc.2007.117978
McLeod A, Ross P, Mitchell S, Tay D, Hunter L, Hall A, et al.: Respiratory health in a total very low birthweight cohort and their classroom controls. Arch Dis Child 1996,74(3):188–94. 10.1136/adc.74.3.188
Watterberg KL, Demers LM, Scott SM, Murphy S: Chorioamnionitis and early lung inflammation in infants in whom bronchopulmonary dysplasia develops. Pediatrics 1996,97(2):210–5.
Rojas MA, Gonzalez A, Bancalari E, Claure N, Poole C, Silva-Neto G: Changing trends in the epidemiology and pathogenesis of neonatal chronic lung disease. J Pediatr 1995,126(4):605–10. 10.1016/S0022-3476(95)70362-4
Gray PH, Grice JF, Lee MS, Ritchie BH, Williams G: Prediction of outcome of preterm infants with severe bronchopulmonary dysplasia. J Paediatr Child Health 1993,29(2):107–12.
Cunha GS, Mezzacappa-Filho F, Ribeiro JD: Risk factors for bronchopulmonary dysplasia in very low birth weight newborns treated with mechanical ventilation in the first week of life. J Trop Pediatr 2005,51(6):334–40. 10.1093/tropej/fmi051
Forsblad K, Kallen K, Marsal K, Hellstrom-Westas L: Apgar score predicts short-term outcome in infants born at 25 gestational weeks. Acta Paediatr 2007,96(2):166–71. 10.1111/j.1651-2227.2007.00099.x
DiFranza JR, Aligne CA, Weitzman M: Prenatal and postnatal environmental tobacco smoke exposure and children's health. Pediatrics 2004,113(4 Suppl):1007–15.
Vrijlandt EJLE, Boezen HM, Gerritsen J, Stremmelaar FF, Duiverman EJ: Respiratory health in prematurely born preschool children with and without bronchopulmonary dysplasia. Journal of Pediatrics 2007,150(3):256–261. 10.1016/j.jpeds.2006.12.007
Greenough A, Maconochie I, Yuksel B: Recurrent respiratory symptoms in the first year of life following preterm delivery. J Perinat Med 1990,18(6):489–94. 10.1515/jpme.19126.96.36.1999
Resch B, Pasnocht A, Gusenleitner W, Muller W: Rehospitalisations for respiratory disease and respiratory syncytial virus infection in preterm infants of 29–36 weeks gestational age. J Infect 2005,50(5):397–403. 10.1016/j.jinf.2004.06.015
Blondel B, Truffert P, Lamarche-Vadel A, Dehan M, Larroque B: [Use of medical services by very preterm children during the first year of life in the Epipage cohort]. Arch Pediatr 2003,10(11):960–8. 10.1016/j.arcped.2003.09.009
Greenough A: Measuring respiratory outcome. Semin Neonatol 2000,5(2):119–26. 10.1053/siny.1999.0006
Greenough A, Cox S, Alexander J, Lenney W, Turnbull F, Burgess S, et al.: Health care utilisation of infants with chronic lung disease, related to hospitalisation for RSV infection. Arch Dis Child 2001,85(6):463–8. 10.1136/adc.85.6.463
Gregoire MC, Lefebvre F, Glorieux J: Health and developmental outcomes at 18 months in very preterm infants with bronchopulmonary dysplasia. Pediatrics 1998,101(5):856–60. 10.1542/peds.101.5.856
Furman L, Baley J, Borawski-Clark E, Aucott S, Hack M: Hospitalization as a measure of morbidity among very low birth weight infants with chronic lung disease. J Pediatr 1996,128(4):447–52. 10.1016/S0022-3476(96)70353-0
Vanpee M, Walfridsson-Schultz U, Katz-Salamon M, Zupancic JA, Pursley D, Jonsson B: Resuscitation and ventilation strategies for extremely preterm infants: a comparison study between two neonatal centers in Boston and Stockholm. Acta Paediatr 2007,96(1):10–6; discussion 8–9. 10.1111/j.1651-2227.2007.00063.x
Kumar R, Yu Y, Story RE, Pongracic JA, Gupta R, Pearson C, et al.: Prematurity, chorioamnionitis, and the development of recurrent wheezing: a prospective birth cohort study. J Allergy Clin Immunol 2008,121(4):878–84 e6. 10.1016/j.jaci.2008.01.030
Hibbert M, Lannigan A, Raven J, Landau L, Phelan P: Gender differences in lung growth. Pediatr Pulmonol 1995,19(2):129–34. 10.1002/ppul.1950190208
Stocks J, Henschen M, Hoo AF, Costeloe K, Dezateux C: Influence of ethnicity and gender on airway function in preterm infants. Am J Respir Crit Care Med 1997,156(6):1855–62.
Kuehni CE, Brooke AM, Silverman M: Prevalence of wheeze during childhood: retrospective and prospective assessment. Eur Respir J 2000,16(1):81–5. 10.1034/j.1399-3003.2000.16a14.x
Ramanathan R: Optimal ventilatory strategies and surfactant to protect the preterm lungs. Neonatology 2008,93(4):302–8. 10.1159/000121456
McLean A, Townsend A, Clark J, Sawyer MG, Baghurst P, Haslam R, et al.: Quality of life of mothers and families caring for preterm infants requiring home oxygen therapy: a brief report. J Paediatr Child Health 2000,36(5):440–4. 10.1046/j.1440-1754.2000.00561.x
O Ahrens, MD, NEODAT administrator at the division of neonatology at the University Children's hospital of Bern.
About this article
Cite this article
Pramana, I., Latzin, P., Schlapbach, L. et al. Respiratory symptoms in preterm infants: burden of disease in the first year of life. Eur J Med Res 16, 223 (2011). https://doi.org/10.1186/2047-783X-16-5-223
- premature birth
- risk factors
- bronchopulmonary dysplasia