Skip to main content

Effect of intubation and mechanical ventilation on exhaled nitric oxide in preterm infants with and without bronchopulmonary dysplasia measured at a median postmenstrual age of 49 weeks



Exhaled nitric oxide (eNO) is a marker of established airway inflammation in adults and children, but conflicting results have been reported in preterm infants when postnatal eNO is measured during tidal breathing. This study investigated the extent to which intubation and mechanical ventilation (MV) affect eNO and NO production (V’ NO ) in preterm infants with and without bronchopulmonary dysplasia (BPD).

Patients and methods

A total of 176 very low birth weight (VLBW) infants (birth weight <1500 g), including 74 (42%) with and 102 (58%) without BPD, were examined at a median postmenstrual age of 49 weeks. Of the 176 infants, 84 (48%) did not require MV, 47 (27%) required MV for <7 days and 45 (26%) required MV for ≥7 days. Exhaled NO and tidal breathing parameters were measured in sleeping infants during tidal breathing, respiratory mechanics were assessed by occlusion tests, and arterialized capillary blood gas was analyzed.


eNO was significantly correlated with tidal breathing parameters, while V’ NO was correlated with growth parameters, including age and body length (p < 0.001 each). Infants who were intubated and received MV for <7 days had significantly lower eNO (p < 0.01) and V’ NO (p < 0.01) than non-ventilated infants. In contrast, eNO and V’ NO did not differ significantly in non-ventilated infants and those receiving MV for ≥7 days. Multivariate analysis showed that independent on the duration of MV eNO (p = 0.003) and V’ NO (p = 0.018) were significantly increased in BPD infants comparable with the effects of intubation and MV on eNO (p = 0.002) and V’ NO (p = 0.017).


Preterm infants with BPD show only weak postnatal increases in eNO and V’ NO , but these changes may be obscured by the distinct influences of breathing pattern and invasive respiratory support. This limits the diagnostic value of postnatal eNO measurements in the follow-up of BPD infants.


Chronic lung disease (CLD) of prematurity, also called bronchopulmonary dysplasia (BPD), is the most common long-term pulmonary disease after preterm birth and neonatal intensive care [1] with consequences for later lung function [24]. Although inconsistent findings have been reported, there is a consensus that prematurity per se may make a more important contribution to impaired lung function than BPD [57]. Moreover, in a recent study [8] we have shown that prematurity and neonatal lung disease, followed by mechanical ventilation (MV), are independently associated with impaired postnatal lung function.

Bronchial hyperreactivity is common in former preterm infants with BPD and is likely due to airway damage in early infancy caused by intubation and MV [9, 10]. Besides arresting lung maturation, lung inflammation is a major contributor to the pathogenesis of BPD. Since lung inflammation may be caused primarily by oxygen and/or MV, there is increased interest in postnatal measurements of exhaled nitric oxide (eNO), a marker of eosinophilic airway inflammation in adults and older children [11]. However, studies of postnatal eNO in BPD infants have yielded conflicting results, with some showing increased eNO in BPD infants [12, 13] and others showing no differences in infants with and without BPD [14, 15]. Moreover, unchanged or even decreased eNO has been observed when former BPD infants reached school age [1619].

A possible explanation for these conflicting results may be differences in patient populations, as well as differences in equipment and measuring conditions [20]. NO concentration in exhaled air is highly air flow-dependent and originates primarily in the nose and the paranasal sinuses, with some also originating in the lower part of the respiratory tract [21, 22]. Therefore, in adults and older children the measurement conditions have been standardized [23]. Online-measurements of eNO in spontaneously breathing newborns, however, can only be performed during tidal breathing, with a face mask that assesses mixed air from the nose and upper airway; hence such measurements in newborns may be affected by variations in breathing pattern and often an eNO plateau is missing in the exhaled air. We hypothesized that, in spontaneously breathing neonates, the different determinants of eNO may account for differences in eNO between BPD and non-BPD infants. This study was therefore designed to investigate the effects of breathing pattern and invasive respiratory support during the first days of life on differences in eNO between non-BPD and BPD infants at 46–54 postmenstrual weeks.



This retrospective study examined eNO concentrations in 176 very low birth weight (VLBW) infants, defined as birth weights <1500 g. Infants were assessed between June 2009 and June 2013 during lung function testing (LFT) as part of our routine follow-up care of preterm infants. At the time of measurement, the median age of the 176 infants was 49 postmenstrual weeks. Infants with congenital diaphragmatic hernia, congenital heart disease, neuromuscular disease, or thoracic wall deformities were excluded. Included infants were classified into three groups according to the degree of respiratory support during the first days of life in the same manner as in a former follow-up study [8]: 1) those without or with only a mild respiratory insufficiency who could be treated by non-invasive techniques (non-ventilated infants); 2) those requiring intubation and MV for <7 days; and 3) those requiring MV for ≥7 days. INSURE (INtubation, SURfactant, Extubation) [24] was not considered MV. Subjects were also classified as with or without BPD, with BPD defined as a requirement for supplemental oxygen at a postmenstrual age of 36 weeks.

All parents provided written informed consent before each LFT, and the Institutional Data Safety Committee approved this study.

eNO measurements

eNO was measured during routine LFT in clinically stable children who had no respiratory infections during the 3 weeks preceding the tests. Prior to testing, body weight was measured to the nearest 10 g (Seca, Hamburg, Germany) and body length (crown to heel) to the nearest 5 mm.

After a temperature stabilization period of at least 30 min, all devices were calibrated before measurement according to the manufacturers’ guidelines. Sleeping infants were measured in a supine position with the neck in a neutral position and supported by a neck roll. Sleep was induced 15–30 min before LFT by oral administration of chloral hydrate (50 mg∙kg-1), since sedation was necessary for more complex LFT [8]. A compliant silicon mask (Infant mask, size 1; Vital Signs Inc., Totowa, NJ, USA) was tightly placed over the nose and mouth of each subject.

An NO filter ensured that all infants inhaled NO-free air. eNO and tidal breathing were measured using the EXHALYZER D (EcoMedics AG, Duernten, Switzerland), which measures lung function in infants, and the fast chemiluminescence NO-analyzer CLD 88 (EcoMedics). Since eNO is strongly flow dependent, the EXHALYZER D also calculates NO production (V’ NO ) to consider different flow conditions [15]. eNO was measured during the third quartile of expiration, since it showed the lowest breath-to-breath variability [25, 26]. V’ NO was calculated by multiplying V’ by steady-state eNO (V’ NO = V’∙ eNO).

Simultaneously, the following tidal breathing parameters were recorded: tidal volume (VT), respiratory rate (RR), minute ventilation (V’E), expiratory time (te), the ratio of time to peak tidal expiratory flow to expiratory time (tptef/te), peak tidal inspiratory flow (PTIF), peak tidal expiratory flow (PTEF), mean tidal inspiratory flow (MTIF) and mean tidal expiratory flow (MTEF). Shortly afterwards, respiratory mechanics (respiratory compliance (Crs) and respiratory resistance (Rrs)) were measured by the single occlusion test using the same face mask and a balloon shutter to achieve brief airway occlusion at end-inspiration, as described [27]. Between 5 and 15 occlusions were performed and the mean of 5 valid measurements of Crs and Rrs reported. All measurements were performed using the MasterScreen™ BabyBody (CareFusion, Höchberg, Germany). All tidal breathing flow and volume parameters and Crs were divided by body weight on the day of measurement to reduce inter-subject variability.

An arterialized capillary blood gas sample was taken at the end of the LFT (ABL800 FLEX, Radiometer, Denmark). Heart rate and oxygen saturation were monitored continuously during the LFT by a pulse oximeter (N-200; Nellcor, Hayward, California, USA).

Statistical methods

Patient characteristics are reported as rates or as medians and interquartile ranges (IQR). Gender-specific birth weight z-scores were calculated using published national reference data [28]. Data were compared among the three ventilation groups by the chi-square test, Fisher’s exact test or the Kruskal-Wallis rank test, as appropriate. Lung function parameters of the three ventilation groups are reported as median (IQR) and the differences among the three groups were tested by the Kruskal-Wallis rank test with the Mann–Whitney test as post-hoc test. The effect of gender, antenatal steroids and surfactant treatment on eNO and V’ NO was tested using the Kruskal-Wallis test. The relationships of eNO and V’ NO with the anthropometric and lung function parameters were assessed by Spearman rank order correlation coefficients with Bonferroni correction for multiple correlations. The effect of BPD and mechanical ventilation on eNO and V’ NO and their interactions were investigated by two way analysis of variance (ANOVA), with anthropometric and tidal breathing parameters as covariates. All statistical analyses were performed using Statgraphics Centurion® software (Version 16.0, Statpoint Inc., Herndon, VA, USA), with a p-value < 0.05 considered statistically significant.


Patient characteristics

eNO and V’ NO were measured in 176 VLBW infants at a median (IQR) postmenstrual age of 49.0 (45.6 - 54.4) weeks. Of these infants, 74 (42%) formerly had BPD, and 92 (52%) had a severe respiratory insufficiency that required intubation and intermittent MV with a nasally inserted endotracheal tube for at least 24 h. Of the ventilated infants, 47 (27%) required MV for <7 days and 45 (26%) for ≥7 days. The median (IQR) duration of MV was 7 (1–14) days, and was significantly longer for BPD than for non-BPD infants (10 (3 – 27) days vs. 2.5 (1 – 7.5) days, p < 0.001).

Table 1 compares patient characteristics relative to the duration of MV. At the time of measurement, there were no statistically significant between-group differences in chronological age, postmenstrual age, body weight, and body length. Infants requiring MV were significantly (p < 0.001) more immature, had a lower birth weight and a higher incidence of surfactant administration. However, there were no statistically significant differences of birth weight z-scores between the ventilation groups. The incidence of BPD was higher in ventilated than in non-ventilated infants. Only the incidence of fetal lung maturation was similar in the ventilation groups.

Table 1 Patient characteristics in the neonatal period and at the time of measurement according to the duration of mechanical ventilation, presented as median and interquartile range (in brackets) or N (%)

Factors associated with eNO and V’NO

There were no statistically significant associations between eNO and V’ NO levels and gender, use of antenatal steroids, or surfactant treatment. Despite the strong correlation between eNO and V’ NO ( r = 0.778, p < 0.001), factors associated with them differed markedly. Table 2 shows the correlation of eNO and V’ NO with age, anthropometric parameters at birth and at the time of measurement and lung function parameters. After Bonferroni correction for multiple correlations, eNO showed statistically significant correlations only with tidal breathing parameters whereas V’ NO correlated significantly with growth parameters (age, postmenstrual age, body length), respiratory rate and duration of expiration. Gestational age, birth weight and birth weight z-scores failed to display a statistically significant correlation with eNO and V’ NO.

Table 2 Spearman rank order coefficients of eNO and V’ NO with patient characteristics at birth and at day of measurements and lung function parameters

The correlations between eNO and mean and peak (MTEF, PTEF) tidal expiratory flow were negative. Thus, as expiratory flow increased, the eNO concentration decreased. In contrast, eNO increased with increasing expiratory time.

NO production was positively correlated with age and anthropometric parameters, indicating that V’ NO increased with growth. There were no statistically significant correlations between V’ NO and tidal breathing parameters, except for a significant negative correlation between V’ NO and respiratory rate and a strong positive correlation with the expiratory time (both p < 0.001).

Effect of intubation and mechanical ventilation on eNO and V’NO

Table 3 shows the measured lung function parameters in the three patient groups classified by duration of MV. Of the tidal breathing parameters, only tidal volume showed a slight decrease (p = 0.034) and respiratory rate showed a slight increase in ventilated patients (p = 0.045). The compliance of the ventilated infants was also reduced, but differed significantly only between non-ventilated infants and infants mechanically ventilated for ≥7 days. There was no significant difference in respiratory resistance between the three patient groups. Blood gases, however, differed significantly among the three MV groups, with pO2 decreasing and pCO2 increasing significantly as the duration of MV increased (both p < 0.001).

Table 3 Lung function test results in VLBW infants according to the duration of mechanical ventilation

Intubation and mechanical ventilation had different effects on eNO and V’ NO . The largest differences were seen in infants ventilated <7 days, where eNO and V’ NO were significantly reduced (p < 0.01). In contrast, results were similar in long-term ventilated and non-ventilated infants.

Effects of BPD on eNO and V’NO

To consider the dependency of eNO and V’ NO on MV duration, the effect of BPD on both parameters was investigated by two way ANOVA, after adjustments for age, body length, expiratory time te and MTEF. As shown in Figure 1, both BPD and the duration of MV had significant effects on eNO, with a lesser effect on V’ NO . Despite different levels in all ventilation groups, mean eNO and V’ NO were higher in BPD than in non-BPD infants.

Figure 1
figure 1

Effect of BPD and the duration of mechanical ventilation on the exhaled NO (top) and the NO production (bottom). The p-values show the extent of statistical significance of the covariates mean tidal expiratory flow (pMTEF), expiratory time (pTE), age (pAge) and body length (pBL); those of the main effects by mechanical ventilation (pMV) and BPD (pBPD); and that of the interaction (pAB) of both factors. Statistically significant values are shown in bold.

Multivariate analysis showed that the tidal breathing parameters te and MTEF were significantly associated with eNO, whereas anthropometric measures were not. V’ NO was significantly affected only by chronological age . BPD and MV had no interactive effects on eNO and V’ NO (all p-values >0.1).


The results presented here demonstrate that, in very premature infants, BPD and intubation and MV due to severe respiratory insufficiency affect eNO and V’ NO independently and in different directions. The measured median (IQR) eNO in non-ventilated infants without BPD (10.0 (6.3 - 13.6) ppb) was slightly lower than reference values published by Fuchs et al. [29] (14 (10.7–17.4) ppb) using the same equipment measured in unsedated term-born healthy infants at 5 weeks of age. In our study, infants with previous BPD showed weak but statistically significant increases in eNO and V’ NO, whereas intubation and MV for <7 days decreased both parameters and did so to a greater degree. Thus, eNO may be lower in a short term ventilated BPD infant than in a non-ventilated infant without BPD. This hampers the clinical interpretation of postnatal eNO and V’ NO and can lead to conflicting results, as shown in recent studies measuring postnatal eNO in infants with and without chronic lung disease (CLD) or BPD.

Leipala et al. [13] examined infants with chronic lung disease (CLD) using tidal breathing measurements with a face mask at 36–45 weeks post-conception. They found higher peak nasal (p = 0.011) and facemask (p = 0.034) NO levels in CLD than in non-CLD infants, in agreement with our findings of weakly but significantly raised eNO in BPD infants. May et al. [12] found also elevated eNO in very premature intubated infants during MV on day 28 after birth, particularly in infants developing moderate or severe BPD [12]. However, Wiliams et al. [30] have shown that eNO during the first 4 weeks of life did not differ significantly in groups of infants with and without CLD, indicating that, in contrast to conventional LFT parameters (e.g. compliance, functional residual capacity), eNO measurements during the first weeks of life are not useful for predicting CLD and that eNO levels may be raised only in infants with established BPD and ongoing inflammation [30]. In contrast to the previous studies Roiha et al. [15], measuring eNO and V’no during tidal breathing in 39 unsedated pre-term infants with CLD (mean gestational age 27.3 weeks), found no statistically significant differences to term infants (39.9 weeks). Following adjustment of eNO and V’ NO for ventilatory parameters, V’ NO was slightly decreased in CLD infants (p = 0.024). In that study the median (range) duration of intubation and MV was 1 (0–63) days, indicating that most CLD infants received MV for only a short time. It remains unclear whether this may have influenced the results in the same way as in the present study.

It also remains unclear why eNO and V’ NO are reduced in short-term ventilated preterm infants. Nasal intubation and MV may induce ciliary dyskinesia, characterized by reduced eNO [22, 31, 32]. This would be on accordance with the findings of Baraldi et al. [19]. In this study eNO was reduced in school aged children who formerly had CLD [19]. They speculated that an impaired NO synthesis and/or diffusion in the airways could be a sequela of epithelial damage during the early phases of BPD. Filiponne et al. [16] have shown that children born prematurely with and without BPD have increase oxidative stress compared to children born at term despite normal eNO levels, pointing to other inflammatory pathways that cannot be picked up by eNO measurements. Ricciardlo et al. [33] investigated determinants of eNO in childhood atopic asthma. They found that neonatal respiratory distress has been associated with low eNO in children with atopic asthma [33]. The higher eNO and V’ NO in long-term (≥7 days) than in short-term (<7 days) ventilated infants may have been caused by established ongoing inflammation secondary to prolonged intubation and mechanical ventilation as well as exposure to supplemental oxygen [34].

We previously showed that, in preterm infants, intubation and MV were mainly associated with increased tissue and airway resistances, reduced effective lung volume and impaired blood gases [8]. However, we could not determine whether these changes were caused by intubation and MV or by the underlying respiratory disease. In the present study, we showed that intubation and MV due to neonatal lung diseases also affected eNO and V’ NO, although these effects depended on the duration of MV. Because infants with acute respiratory tract infection were excluded from the study, these effects on eNO were negligible [29]. Except for tidal breathing and anthropometric parameters, we could not find further associations with eNO and V’ NO levels, including data at birth. Unfortunately, in this study we had no verified access to data on maternal atopic disease [35], prenatal tobacco exposure [25, 26] or traffic-related air pollution [36, 37] and thus could not investigate the impact of these confounders on exhaled NO.

Ideally, eNO should be measured while the subject is breathing out at a constant expiratory flow rate to obtain an eNO plateau. Adults and older children exhale at a constant flow (V’) against a resistance, resulting in a plateau in the eNO signal [38]. However, this is not possible during postnatal tidal breathing. eNO measured during the third quartile of expiration should mimic the conditions of flow standardization in adults [25]. However, a higher respiratory rate and a shorter expiratory time increase the likelihood that an eNO plateau will not be achieved, a phenomenon known from capnographic measurements in small lungs [39], especially at appearance of air leaks [40]. The lack of a plateau in exhaled NO can lead to underestimations of eNO and V’ NO and may contribute to the negative correlations between these parameters and respiratory rate and the positive correlations with expiratory time.

Therefore, a numerical adjustment of the measured eNO and V’ NO is recommended in comparative studies [12] considering the differences in development and breathing pattern [41, 42]. Any such numerical adjustment, however, can only be useful if eNO and V’ NO are measured equally accurately across the range of respiratory rates of the sample. Using the measurement equipment available today, the reliability of eNO and V’ NO measurements in preterm infants is limited by the response time of the NO-analyzer. The strong decrease of V’ NO with increasing respiratory rate (Table 2) may be caused by this technical problem arising when the exhalation time is short. These limitations may also contribute to the conflicting results of the published studies.

This study has several strengths and limitations. The main strengths include the use of a large sample size classified by duration of MV and the use of the same investigator, equipment, and protocol for all patients, since measurements of lung function in infants of this age are highly dependent on device and protocol. The study limitations include its retrospective design and the lack of a control group of healthy infants [43]. Because this study was retrospective, important maternal (e.g., smoking, atopy, asthma, education), neonatal (e.g., birth characteristics, resuscitation management, postnatal steroids, infections) and environmental parameters (e.g., smoking exposure, air pollution) which may affect the postnatal lung development [44, 45] were unavailable. Further clinical data (e.g., the duration of non-invasive respiratory support or oxygen treatment) may help to understand the pathophysiology underlying this condition. Furthermore, the extreme skewness in the patient distribution (there were only 10 long-term ventilated infants without BPD) limits the number of parameters for multivariate modeling.


Online tidal breathing measurements of eNO and V’ NO via a face mask are a simple and noninvasive technique for assessing postnatal lung function. The inability to standardize measurement conditions during tidal breathing can result in a high dependency of measured parameters on breathing patterns. Although mean eNO and V’ NO are increased in BPD infants, these increases are only weak and may be obscured by other factors affecting eNO during tidal breathing. Thus the interpretation of individual measurements is difficult due to opposing influencing factors, making eNO and V’ NO unlikely to be helpful in following up BPD infants during the first months of life.



Bronchopulmonary dysplasia


Chronic lung disease


Respiratory compliance


Fractional exhaled nitric oxide.


Inter-quartile range


Lung function testing


Mean tidal expiratory flow


Mean tidal inspiratory flow


Mechanical ventilation


Postmenstrual age


Peak tidal expiratory flow


Peak tidal inspiratory flow


Respiratory rate


Respiratory resistance

R s :

Spearman rank order correlation coefficient


Tidal breathing


Expiratory time


Time to peak tidal expiratory flow related to the expiratory time


Air flow


Minute ventilation

V’ NO :

Nitric oxide production


Tidal volume.


  1. Jobe AH, Bancalari E: Bronchopulmonary dysplasia. Am J Respir Crit Care Med. 2001, 163: 1723-1729.

    Article  PubMed  CAS  Google Scholar 

  2. Fakhoury KF, Sellers C, Smith EO, Rama JA, Fan LL: Serial measurements of lung function in a cohort of young children with bronchopulmonary dysplasia. Pediatrics. 2010, 125: e1441-e1447.

    Article  PubMed  Google Scholar 

  3. Robin B, Kim YJ, Huth J, Klocksieben J, Torres M, Tepper RS, Castile RG, Solway J, Hershenson MB, Goldstein-Filbrun A: Pulmonary function in bronchopulmonary dysplasia. Pediatr Pulmonol. 2004, 37: 236-242.

    Article  PubMed  Google Scholar 

  4. Vrijlandt EJ, Boezen HM, Gerritsen J, Stremmelaar EF, Duiverman EJ: Respiratory health in prematurely born preschool children with and without bronchopulmonary dysplasia. J Pediatr. 2007, 150: 256-261.

    Article  PubMed  CAS  Google Scholar 

  5. Gappa M, Stocks J, Merkus P: Lung growth and development after preterm birth: further evidence. Am J Respir Crit Care Med. 2003, 168: 399-

    Article  PubMed  Google Scholar 

  6. Hoo AF, Dezateux C, Henschen M, Costeloe K, Stocks J: Development of airway function in infancy after preterm delivery. J Pediatr. 2002, 141: 652-658.

    Article  PubMed  Google Scholar 

  7. Kotecha SJ, Edwards MO, Watkins WJ, Henderson AJ, Paranjothy S, Dunstan FD, Kotecha S: Effect of preterm birth on later FEV1: a systematic review and meta-analysis. Thorax. 2013, 68: 760-766.

    Article  PubMed  Google Scholar 

  8. Schmalisch G, Wilitzki S, Roehr CC, Proquitte H, Bührer C: Differential effects of immaturity and neonatal lung disease on the lung function of very low birth weight infants at 48–52 postconceptional weeks. Pediatr Pulmonol. 2013, 48: 1214-1223.

    Article  PubMed  Google Scholar 

  9. Pelkonen AS, Hakulinen AL, Turpeinen M: Bronchial lability and responsiveness in school children born very preterm. Am J Respir Crit Care Med. 1997, 156: 1178-1184.

    Article  PubMed  CAS  Google Scholar 

  10. Smyth JA, Tabachnik E, Duncan WJ, Reilly BJ, Levison H: Pulmonary function and bronchial hyperreactivity in long-term survivors of bronchopulmonary dysplasia. Pediatrics. 1981, 68: 336-340.

    PubMed  CAS  Google Scholar 

  11. Gabriele C, Jaddoe VW, van Mastrigt E, Arends LR, Hofman A, Moll HA, de Jongste JC: Exhaled nitric oxide and the risk of wheezing in infancy: the generation R study. Eur Respir J. 2012, 39: 567-572.

    Article  PubMed  CAS  Google Scholar 

  12. May C, Williams O, Milner AD, Peacock J, Rafferty GF, Hannam S, Greenough A: Relation of exhaled nitric oxide levels to development of bronchopulmonary dysplasia. Arch Dis Child Fetal Neonatal Ed. 2009, 94: F205-F209.

    Article  PubMed  CAS  Google Scholar 

  13. Leipala JA, Williams O, Sreekumar S, Cheeseman P, Rafferty GF, Hannam S, Milner A, Greenough A: Exhaled nitric oxide levels in infants with chronic lung disease. Eur J Pediatr. 2004, 163: 555-558.

    PubMed  Google Scholar 

  14. Gabriele C, Nieuwhof EM, Van Der Wiel EC, Hofhuis W, Moll HA, Merkus PJ, de Jongste JC: Exhaled nitric oxide differentiates airway diseases in the first two years of life. Pediatr Res. 2006, 60: 461-465.

    Article  PubMed  CAS  Google Scholar 

  15. Roiha HL, Kuehni CE, Zanolari M, Zwahlen M, Baldwin DN, Casaulta C, Nelle M, Frey U: Alterations of exhaled nitric oxide in pre-term infants with chronic lung disease. Eur Respir J. 2007, 29: 251-258.

    Article  PubMed  CAS  Google Scholar 

  16. Filippone M, Bonetto G, Corradi M, Frigo AC, Baraldi E: Evidence of unexpected oxidative stress in airways of adolescents born very pre-term. Eur Respir J. 2012, 40: 1253-1259.

    Article  PubMed  Google Scholar 

  17. Cazzato S, Ridolfi L, Bernardi F, Faldella G, Bertelli L: Lung function outcome at school age in very low birth weight children. Pediatr Pulmonol. 2012, 48: 830-837.

    Article  PubMed  Google Scholar 

  18. Mieskonen ST, Malmberg LP, Kari MA, Pelkonen AS, Turpeinen MT, Hallman NM, Sovijarvi AR: Exhaled nitric oxide at school age in prematurely born infants with neonatal chronic lung disease. Pediatr Pulmonol. 2002, 33: 347-355.

    Article  PubMed  Google Scholar 

  19. Baraldi E, Bonetto G, Zacchello F, Filippone M: Low exhaled nitric oxide in school-age children with bronchopulmonary dysplasia and airflow limitation. Am J Respir Crit Care Med. 2005, 171: 68-72.

    Article  PubMed  Google Scholar 

  20. Manna A, Caffarelli C, Varini M, Povesi DC, Montella S, Maglione M, Sperli F, Santamaria F: Clinical application of exhaled nitric oxide measurement in pediatric lung diseases. Ital J Pediatr. 2012, 38: 74-

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  21. Chang CC, Liu TY, Hua YM, Lee CM, Yuh YS: Endogenous nitric oxide in the nasal airways of healthy term newborn infants in Taiwan. Pediatr Neonatol. 2008, 49: 166-170.

    Article  PubMed  Google Scholar 

  22. Sahin G, Klimek L, Mullol J, Hormann K, Walther LE, Pfaar O: Nitric oxide: a promising methodological approach in airway diseases. Int Arch Allergy Immunol. 2011, 156: 352-361.

    Article  PubMed  CAS  Google Scholar 

  23. Anonymous: ATS/ERS recommendations for standardized procedures for the online and offline measurement of exhaled lower respiratory nitric oxide and nasal nitric oxide, 2005. Am J Respir Crit Care Med. 2005, 171: 912-930.

    Article  Google Scholar 

  24. Bohlin K, Jonsson B, Gustafsson AS, Blennow M: Continuous positive airway pressure and surfactant. Neonatology. 2008, 93: 309-315.

    Article  PubMed  Google Scholar 

  25. Hall GL, Reinmann B, Wildhaber JH, Frey U: Tidal exhaled nitric oxide in healthy, unsedated newborn infants with prenatal tobacco exposure. J Appl Physiol. 2002, 92: 59-66.

    PubMed  CAS  Google Scholar 

  26. Latzin P, Kuehni CE, Baldwin DN, Roiha HL, Casaulta C, Frey U: Elevated exhaled nitric oxide in newborns of atopic mothers precedes respiratory symptoms. Am J Respir Crit Care Med. 2006, 174: 1292-1298.

    Article  PubMed  CAS  Google Scholar 

  27. Nguyen TT, Hoo AF, Lum S, Wade A, Thia LP, Stocks J: New reference equations to improve interpretation of infant lung function. Pediatr Pulmonol. 2012, 48: 370-380.

    Article  PubMed  Google Scholar 

  28. Voigt M, Schneider KT, Jährig K: Analysis of a 1992 birth sample in Germany. 1: new percentile values of the body weight of newborn infants. Geburtshilfe Frauenheilkd. 1996, 56: 550-558.

    Article  PubMed  CAS  Google Scholar 

  29. Fuchs O, Latzin P, Thamrin C, Stern G, Frischknecht P, Singer F, Kieninger E, Proietti E, Riedel T, Frey U: Normative data for lung function and exhaled nitric oxide in unsedated healthy infants. Eur Respir J. 2010, 37: 1208-1216.

    Article  PubMed  Google Scholar 

  30. Williams O, Dimitriou G, Hannam S, Rafferty GF, Greenough A: Lung function and exhaled nitric oxide levels in infants developing chronic lung disease. Pediatr Pulmonol. 2007, 42: 107-113.

    Article  PubMed  Google Scholar 

  31. Karadag B, James AJ, Gultekin E, Wilson NM, Bush A: Nasal and lower airway level of nitric oxide in children with primary ciliary dyskinesia. Eur Respir J. 1999, 13: 1402-1405.

    Article  PubMed  CAS  Google Scholar 

  32. Corbelli R, Hammer J: Measurement of nasal nitric oxide. Paediatr Respir Rev. 2007, 8: 269-272.

    Article  PubMed  Google Scholar 

  33. Ricciardolo FL, Silvestri M, Pistorio A, Strozzi MM, Tosca MA, Bellodi SC, Battistini E, Gardella C, Rossi GA: Determinants of exhaled nitric oxide levels (FeNO) in childhood atopic asthma: evidence for neonatal respiratory distress as a factor associated with low FeNO levels. J Asthma. 2010, 47: 810-816.

    Article  PubMed  CAS  Google Scholar 

  34. Speer CP: Inflammation and bronchopulmonary dysplasia: a continuing story. Semin Fetal Neonatal Med. 2006, 11: 354-362.

    Article  PubMed  Google Scholar 

  35. Frey U, Kuehni C, Roiha H, Cernelc M, Reinmann B, Wildhaber JH, Hall GL: Maternal atopic disease modifies effects of prenatal risk factors on exhaled nitric oxide in infants. Am J Respir Crit Care Med. 2004, 170: 260-265.

    Article  PubMed  Google Scholar 

  36. Latzin P, Frey U: Environmental exposure in relation to exhaled nitric oxide in newborns: is it all about timing?. Eur Respir J. 2008, 32: 252-254.

    Article  PubMed  CAS  Google Scholar 

  37. Eckel SP, Berhane K, Salam MT, Rappaport EB, Linn WS, Bastain TM, Zhang Y, Lurmann F, Avol EL, Gilliland FD: Residential traffic-related pollution exposures and exhaled nitric oxide in the children’s health study. Environ Health Perspect. 2011, 119: 1472-1477.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  38. Baraldi E, de Jongste JC: Measurement of exhaled nitric oxide in children, 2001. Eur Respir J. 2002, 20: 223-237.

    Article  PubMed  CAS  Google Scholar 

  39. Proquitte H, Krause S, Rüdiger M, Wauer RR, Schmalisch G: Current limitations of volumetric capnography in surfactant-depleted small lungs. Pediatr Crit Care Med. 2004, 5: 75-80.

    Article  PubMed  Google Scholar 

  40. Schmalisch G, Al-Gaaf S, Proquitte H, Roehr CC: Effect of endotracheal tube leak on capnographic measurements in a ventilated neonatal lung model. Physiol Meas. 2012, 33: 1-11.

    Article  Google Scholar 

  41. Latzin P, Roth S, Thamrin C, Hutten GJ, Pramana I, Kuehni CE, Casaulta C, Nelle M, Riedel T, Frey U: Lung volume, breathing pattern and ventilation inhomogeneity in preterm and term infants. PLoS One. 2009, 4: e4635-

    Article  PubMed  PubMed Central  Google Scholar 

  42. Schmalisch G, Wilitzki S, Wauer RR: Differences in tidal breathing between infants with chronic lung diseases and healthy controls. BMC Pediatr. 2005, 5: 36-

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  43. Lum S, Hoo AF, Hulskamp G, Wade A, Stocks J: Potential misinterpretation of infant lung function unless prospective healthy controls are studied. Pediatr Pulmonol. 2010, 45: 906-913.

    Article  PubMed  Google Scholar 

  44. Fawke J, Lum S, Kirkby J, Hennessy E, Marlow N, Rowell V, Thomas S, Stocks J: Lung function and respiratory symptoms at 11 years in children born extremely preterm: the EPICure study. Am J Respir Crit Care Med. 2010, 182: 237-245.

    Article  PubMed  PubMed Central  Google Scholar 

  45. Lum S, Kirkby J, Welsh L, Marlow N, Hennessy E, Stocks J: Nature and severity of lung function abnormalities in extremely pre-term children at 11 years of age. Eur Respir J. 2011, 37: 1199-1207.

    Article  PubMed  CAS  Google Scholar 

Download references


The authors would like to Jessica Blank and Regina Nagel for assisting with the data processing, and Dr. Scott Butler of English Manager Science Editing, Sydney, Australia, for linguistic revision.

Author information

Authors and Affiliations


Corresponding author

Correspondence to Gerd Schmalisch.

Additional information

Competing interests

None of the authors has a financial relationship with a commercial entity that has an interest in the subject of this manuscript.

Authors’ contribution

GS had primary responsibility for study design, data analysis and writing of the manuscript. SW carried out all lung function measurements and GS performed statistical analysis. HF and CB participated in the development of the study and contributed to the writing of the manuscript. All authors read and approved the final manuscript.

Authors’ original submitted files for images

Below are the links to the authors’ original submitted files for images.

Authors’ original file for figure 1

Rights and permissions

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Schmalisch, G., Wilitzki, S., Fischer, H.S. et al. Effect of intubation and mechanical ventilation on exhaled nitric oxide in preterm infants with and without bronchopulmonary dysplasia measured at a median postmenstrual age of 49 weeks. BMC Res Notes 7, 389 (2014).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: