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Neonatal Med > Volume 25(3); 2018 > Article
Seo, Shim, and Chey: Clinical Outcomes of Minimally Invasive Surfactant Therapy via Tracheal Catheterization in Neonates with a Gestational Age of 30 Weeks or More Diagnosed with Respiratory Distress Syndrome

Abstract

Purpose

Minimally invasive surfactant therapy (MIST) is currently used as a method of surfactant replacement therapy (SRT) for the treatment of respiratory distress syndrome (RDS) in preterm infants with a gestational age of less than 30 weeks. However, few studies have been conducted on MIST in neonates with a gestational age of 30 weeks or more. In this study, we compared MIST with endotracheal intubation as a rescue SRT for spontaneously breathing neonates with a gestational age of 30 weeks or more who were diagnosed with RDS.

Methods

We investigated the clinical characteristics of spontaneously breathing neonates admitted to the neonatal intensive care unit of the Inje University Sanggye Paik Hospital from January 1, 2014 to December 31, 2016. These neonates were born at a gestational age of 30 weeks or more and were diagnosed with RDS. The neonates who were administered surfactant by MIST were categorized into the MIST group (n=16) and those who underwent endotracheal intubation were categorized into the control group (n=45). Thereafter, the clinical characteristics between the groups were compared.

Results

Compared to the control group, the MIST group was less likely to require mechanical ventilation within 72 hours (P<0.001). The frequency of bradycardia during SRT was also low in the MIST group (P=0.033).

Conclusion

MIST is considered relatively feasible and safe for treating RDS for reducing the need for mechanical ventilation and decreasing the occurrence of bradycardia during surfactant administration in neonates with a gestational age of 30 weeks or more.

INTRODUCTION

Respiratory distress syndrome (RDS) is one of the most common neonatal respiratory diseases, and it is an important cause of neonatal respiratory morbidity and mortality [1]. The treatment of neonatal RDS requires invasive or noninvasive ventilation with surfactant replacement therapy (SRT). It is now recognized that primary nasal continuous positive airway pressure (CPAP) is a reasonable alternative to early intubation and/or SRT in preterm infants with respiratory distress after birth [2,3]. Increased use of CPAP as a primary therapy for neonates with respiratory distress is accompanied by the dilemma regarding the exact time and method of starting SRT. To overcome this problem, Verder et al. [4,5] devised the INtubation-SURfactant-Extubation (INSURE) method, which has been reported to reduce the frequency and duration of invasive ventilation. However, the INSURE method is associated with problems such as the need for endotracheal intubation, positive pressure ventilation (PPV), and sedation [6-9]. Thus, many neonatologists are investigating minimally invasive surfactant therapy (MIST) to overcome these problems [10].
To date, there have been many studies on preterm infants with a gestational age of 24 to 29 weeks who were diagnosed with RDS and were administered surfactant by MIST [10]. However, few studies have reported on moderately preterm infants, late preterm infants, and term infants in whom RDS was treated via MIST. Accordingly, we aimed to compare the clinical outcomes of the MIST group (SRT by MIST) and control group (SRT by endotracheal intubation) to determine the optimal rescue SRT in the management of RDS for spontaneously breathing neonates with a gestational age of 30 weeks or more.

MATERIALS AND METHODS

This was a single-center, retrospective study conducted in the neonatal intensive care unit (NICU) of the Inje University Sanggye Paik Hospital from January 1, 2014 to December 31, 2016. The study protocol was reviewed and approved by the Institutional Review Board (IRB) of the hospital (approval number: SGPAIK 2017-08-008). The IRB waived the need for informed consent for this retrospective chart review.

1. Study population

Infants who were admitted to the NICU of Inje University Sanggye Paik Hospital at a gestational age of 30 weeks and over and who required respiratory support within 2 hours after birth were screened from January 1, 2014 to December 31, 2016. The study period was set since January 1, 2014, when MIST was introduced in this hospital. The MIST method includes tracheal catheterization, intrapharyngeal instillation, and aerosolization. Among the various MIST methods, our clinic uses the Cologne method [10]. This method uses a 4 to 5 FG (French Gauge) gastric tube as a conduit for insertion into the airway. The procedure involves checking the vocal cords using laryngoscopy, insertion of the gastric tube into the airway using Magill forceps, and administration of the surfactant [10]. The following infants were included in the study: (1) spontaneously breathing infants who were born at no less than 30 weeks of gestation and (2) infants diagnosed with RDS, who required a fraction of inspired oxygen of ≥0.35 and who were administered pulmonary surfactant within 48 hours. Infants who were transferred to other hospitals, those who required aggressive resuscitation such as endotracheal intubation in the delivery room, and those diagnosed with chromosomal abnormalities, or multiple congenital anomalies were excluded.
Infants who had received a pulmonary surfactant (200 mg/kg Curosurf®, Chiesi Pharmaceuticals, Parma, Italy) for the treatment of RDS were divided into two groups: the MIST group and the control group. The MIST group was defined as the group in which the surfactant was administered by MIST via a sterile 5-French, orogastric tube while receiving CPAP (peek end-expiratory pressure, 5 to 8 cm H2O) without endotracheal intubation. This protocol was based on the MIST procedure described by Gopel et al. [11]. The control group was defined as the group in which the surfactant was administered by the conventional endotracheal intubation procedure. Subsequently, each group was subdivided into two groups according to gestational age, with neonates with gestational age less than 35 weeks in one subgroup and those with age ≥35 weeks in the other group.
Prenatal parameters such as twin delivery, type of delivery, birth in our clinic, nulliparity, maternal age, maternal diabetes mellitus, maternal hypertension, use of antenatal steroids, premature rupture of membrane (PROM), and pathologic chorioamnionitis were reviewed. In addition, neonatal clinical characteristics such as gestational age, birth weight, small for gestational age (SGA, defined as birth weight below the 10th percentile for infants of the same gestational age), large for gestational age (LGA, defined as birth weight above the 90th percentile for infants of the same gestational age), sex, Apgar score (1- and 5-minute), meconium staining, and need for PPV support at birth were studied. Treatment data including time interval from birth to surfactant administration, failure to administer procedure on the first attempt, need for mechanical ventilation within 72 hours of birth or at any time, need for multiple doses of surfactant, bradycardia during surfactant administration, need for PPV during surfactant administration, duration of respiratory support, and duration of hospital stay were collected. Neonatal morbidities such as air-leak syndrome, pulmonary hemorrhage, patent ductus arteriosus (PDA), necrotizing enterocolitis (NEC), retinopathy of prematurity (ROP), intraventricular hemorrhage (IVH), hypoxic brain injury, bronchopulmonary dysplasia (BPD), use of antibiotic therapy for suspected infection, and culture proven sepsis were reviewed. Thereafter, we compared the results between groups through statistical analysis.

2. Primary and secondary outcomes

The primary outcomes of this study were need for mechanical ventilation within 72 hours of birth or at any time (failure of non-invasive respiratory support) and requirement of additional surfactant. Additional surfactant supplementation was considered in patients without clinical improvement even after SRT, consistent between the groups. The secondary outcomes were bradycardia during surfactant administration, air-leak syndrome, pulmonary hemorrhage, BPD, duration of mechanical ventilation, duration of CPAP, and duration of heated humidified high-flow nasal cannula. In addition, hospital days, PDA (requiring treatment), NEC (higher than stage 2), ROP, IVH (higher than stage 2), hypoxic brain injury, use of antibiotic therapy for suspected infection, and culture proven sepsis were investigated.

3. Definitions

The diagnosis of RDS was confirmed by a pediatric radiologist after observing reduced lung volumes, a reticulogranular pattern of lung consolidation, and air bronchograms [12]. Pulmonary hemorrhage was diagnosed on obtaining blood-tinge tracheal aspirate and the need for increasing fraction of inspired oxygen. BPD was defined according to the definition of the National Institutes of Health Consensus [13]. NEC was diagnosed as stage 2 or more, according to modified Bell’s staging [14]. International Classification of Retinopathy of Prematurity was used to classify ROP [15]. Grading of IVH was carried out as per the Papile grading system [16].

4. Statistical analysis

Continuous variables were analyzed using Student’s t-test or Mann-Whitney U-test. Chi-square test or Fisher’s exact test was used for categorical variables. In addition, multiple regression analysis was performed on related factors with a P-value below 0.05 in the univariate analysis. All analyses were considered statistically significant when the P-value was less than 0.05. Statistical analysis was carried out using the SPSS software version 19.0 for Windows (IBM Co., Armonk, NY, USA).

RESULTS

We investigated the perinatal characteristics and neonatal outcomes of 307 neonates who were born at no less than 30 weeks of gestation and had respiratory distress within 2 hours of birth from January 1, 2014 to December 31, 2016. Infants who died during hospitalization (n=3), infants who were transferred to other hospitals (n=2), neonates who required aggressive resuscitation such as tracheal intubation in the delivery room (n=2), and neonates already diagnosed with persistent pulmonary hypertension of the newborn or meconium aspiration syndrome at birth (n=3) were excluded from the study. Of the 297 newborns, those who were administered surfactant for the treatment of RDS (n=61) were divided into two groups: the gestational age group of 30 to 35 weeks (n=26) and the gestational age group of 35 weeks or more (n=35). Thereafter, each group was further divided into two groups, the MIST group and the control group (Figure 1).

1. Perinatal characteristics

Baseline demographic data analysis showed no significant difference between the MIST and control groups with respect to gestational age, birth weight, twin delivery, C-section, nulliparity, maternal age, maternal diabetes, maternal hypertension, antenatal steroid use, sex, LGA, SGA, 1- and 5-minute Apgar scores, PROM, pathologic chorioamnionitis, need for PPV at birth, and time interval from birth to surfactant administration. Of the total study population, the neonates who were born at our hospital were significantly more likely to receive MIST (P=0.036) (Table 1).

2. Neonatal outcomes

The MIST group was significantly less likely to receive mechanical ventilation within the hospitalization period than the control group was, in all study populations (P<0.001) (Table 2). Compared to neonates in the control group, those in the MIST group more frequently required additional administration of pulmonary surfactant (P=0.015) (Table 2, Figure 2A). The incience of bradycardia during pulmonary surfactant administration was significantly lower in the MIST group than in the control group (P=0.033) (Table 2, Figure 2B). In contrast, there were no significant differences in the occurrence of air-leak syndrome between the groups (Table 2). The duration of mechanical ventilation was significantly shorter in the MIST group than in the control group (Table 2, Figure 2C). For the subgroup with a gestational age of 35 weeks or more, the duration of hospital stay was significantly shorter in the MIST group than in the control group (P=0.035) (Table 2, Figure 2D).

3. Multiple logistic regression

To analyze independent factors, multiple logistic regression analysis was performed for each gestational age group for variables with P<0.05 in Tables 1, 2 (Table 3). Altogether, the MIST group was significantly less likely to receive mechanical ventilation during the hospitalization period than the control group was, independently (P<0.001; risk ratio [RR], 0.014; 95% confidence interval [CI], 0.002 to 0.125). The number of patients requiring more than secondary administration of pulmonary surfactant was significantly higher in the MIST group than in the control group (P=0.008; RR, 6.150; 95% CI, 1.455 to 26.001). Further, the incidence of bradycardia at the time of pulmonary SRT was significantly lower in the MIST group than in the control group (P=0.022; RR, 0.179; 95% CI, 0.036 to 0.879). During the clinical course, the duration of mechanical ventilation in the MIST group was found to have a statistically significant effect independently; however, there was no significant effect on the hospitalization period.

DISCUSSION

Surfactant application by MIST with tracheal catheterization is now recognized as one of the standard methods of SRT in preterm infants with a gestational age less than 30 weeks who are diagnosed with RDS, and it may improve their short-term and long-term outcomes. However, studies concerning the use of MIST in neonates with gestational ages of 30 weeks or more are insufficient, and the results are inconclusive [17]. Our study showed that MIST can safely be used and that it improves the short-term clinical outcomes in newborns with a gestational age of 30 weeks or more who are diagnosed with RDS.
Early noninvasive forms of ventilation such as CPAP have been applied as a primary strategy for the management of RDS in very-low-birth-weight infants with spontaneous breathing [18]. This is because the risk of airway and lung injury and respiratory tract infection, which is commonly associated with invasive mechanical ventilation, is relatively low in noninvasive ventilation [19]. However, if neonates who received only noninvasive ventilation without SRT at the time of birth show a clear sign of RDS later, the surfactant should be eventually administered through endotracheal intubation. To overcome this problem, Verder et al. [4] devised the INSURE method. However, this method also required endotracheal intubation; therefore, some physical concerns such as tracheal or laryngeal injury remained [20]. For this reason, some researchers modified the INSURE method to devise a new method, namely MIST [21]. The MIST procedure is commonly referred to as the less invasive surfactant administration (LISA). Thus, the European Consensus Guidelines, newly published in 2016 [2] added that INSURE should be considered in newborns with CPAP failure and that MIST can be substituted for INSURE in spontaneously breathing infants.
As observed in previous studies [10,11], the rate of application of mechanical ventilation was significantly reduced by the LISA method in this study; that is, it was lower in the MIST group than in the control group. Tomar et al. [22] published a study using a modified MIST method (Magill forceps are not used in this method, and the gastric tube is directly inserted into the airway by the practitioner). According to this study, in newborn infants with a gestational age of 24+0 to 33+6 weeks who were diagnosed with RDS, the durations of mechanical ventilation and CPAP support were significantly lower in the modified MIST group than in the INSURE group; however, there were no differences in the need for mechanical ventilation within the first 72 hours, and in the other neonatal morbidities and mortalities, between the groups.
In this study, the incidence of bradycardia during surfactant administration was significantly lower in the MIST group than in the control group in multiple regression analysis. In most cases, bradycardia results from vagal nerve reflex caused by uncomfortable stimulation of the pharynx and larynx during neonatal endotracheal intubation. This bradycardia is usually referred to as “stable bradycardia,” because it can be easily normalized by temporarily suspending intubation or by sufficient oxygenation [23]. MIST does not require endotracheal intubation; hence, it can be inferred that the occurrence of bradycardia, which is an adverse effect that can occur during endotracheal intubation, is reduced. Meanwhile, the American Academy of Pediatrics [24] recommends the use of premedication for endotracheal intubation in neonates, except in emergency situations. This premedication includes analgesics, sedatives, and muscle relaxants. Further, vagolytic agents can be used to prevent bradycardia that can occur during endotracheal intubation. However, according to a European survey published in 2017, 52% of neonatologists do not use premedication when administering MIST [25]. This is because spontaneous breathing plays a major role in the proper distribution of the pulmonary surfactant in the lungs in MIST, and the premedication can reduce the respiratory effort in premature infants in particular [26].
Meanwhile, Dargaville et al. [27] showed that the incidence of pneumothorax reduced from 8.0% to 2.4% after introducing MIST with a vascular catheter in neonates aged 29 to 32 weeks who were diagnosed with RDS. However, in our study, there was no significant difference in the occurrence of air-leak syndrome including pneumothorax between the two groups of neonates.
According to a recent analysis released in 2017 concerning the results of LISA treatment in premature infants, there was no significant difference between the LISA group and the control group with regard to the need for additional surfactant administration after primary pulmonary SRT [17]. Meanwhile, animal studies published in 2005 showed that the distribution of pulmonary surfactant was better in the noninvasive respiratory assist group than in the mechanical ventilation group, in spontaneously breathing rabbits [19]. However, in our study, compared to the control group, the need for additional administration of pulmonary surfactant was increased in the MIST group. These results may be attributable to the lack of experience of the operator with regard to MIST or the anxiety caused by it. Additional studies are warranted to explain the results that are different from those of the previous studies.
We subdivided each group into two more groups according to gestational age, with neonates with gestational age between 30 and 35 weeks in one group and those with age ≥35 weeks in the other group. The reasons for dividing the neonates into two groups based on the gestational age of 35 weeks as the cut off are as follows. Moderately premature infants, i.e., newborns with a gestational age of more than 30 weeks and less than 35 weeks, are known to contribute to increased neonatal morbidity. Although extremely preterm births are well known to have a higher risk of poor outcome, in practice, the number of moderately premature infant births is relatively higher, which may be perceived as a major health problem. According to a Swedish national population-based study published in 2011 [11], transient tachypnea of the newborn or RDS was observed in about one-third of moderate premature infants. Therefore, subgroup analysis was performed to determine whether morbidity was higher in moderately premature infants.
The limitations of this study may be that it was retrospective in nature, the number of subjects was small, randomization among the comparison groups was not possible, and the clinical severity of the two groups might have differed from the beginning. Another limitation was that the control group could not be subdivided into the INSURE group and the mechanical ventilation maintenance group, because the sample size of the INSURE group was too small. This was attributed to the cutbacks in the insurance amount for INSURE during the study period, and to the fact that INSURE was not performed as a routine procedure and was executed with early extubation after invasive ventilator application. Therefore, additional studies to address these limitations are warranted.
In conclusion, MIST is considered a relatively safe and effective procedure for treating RDS, and for reducing the need for mechanical ventilation and the occurrence of endotracheal intubation-induced bradycardia. For well-experienced practitioners, MIST may be an appropriate choice of treatment for RDS in neonates with a gestational age of 30 weeks or more.

ARTICLE INFORMATION

No potential conflict of interest relevant to this article was reported.

Figure 1.
Study population of this study and subgrouping by minimally invasive surfactant therapy (MIST) and control groups. Abbreviations: RDS, respiratory distress syndrome; SRT, surfactant replacement therapy; NICU, neonatal intensive care unit.
nm-2018-25-3-109f1.jpg
Figure 2.
Neonatal clinical outcomes: (A) need for >1 dose of surfactant, (B) events for bradycardia, (C) mean duration of mechanical ventilation, (D) mean duration of hospitalization. Values are expressed as mean. *Statistically significant (P<0.05). Abbreviations: GA, gestational age; MIST, minimally invasive surfactant therapy.
nm-2018-25-3-109f2.jpg
Table 1.
Baseline Demographic Data of Each Group
Baseline demographic Total (n=61) GA 30+o-34+6 (n=35) GA 35+0-41+6 (n=26)
MIST (n=16) Control (n=45) P- value MIST (n=10) Control (n=25) P- value MIST (n=6) Control (n=20) P- value
Gestational age (wk) 33.9±2.6 34.6±2.8 0.382 32.3±1.7 32.4±1.3 0.850 36.5±1.6 37.3±1.3 0.223
Birth weight (g) 2,272.2±757.6 2,331.7±736.7 0.784 1,885.0±511.7 1,777.0±368.5 0.489 2,917.5±671.6 3,025.0±417.8 0.636
Twin delivery 0 8 (18) 0.097 0 7 (28) 0.084 0 1 (5) 1.000
Cesarean section 13 (81) 36 (80) 1.000 9 (90) 18 (72) 0.390 4 (67) 18 (90) 0.218
Inborn 14 (88) 26 (58) 0.036 10 (100) 22 (23) 0.542 4 (67) 4 (20) 0.051
Nulliparous 10 (63) 20 (44) 0.902 6 (60) 12 (48) 0.711 4 (67) 8 (40) 0.365
Maternal age (yr) 33.5±3.7 33.0±3.7 0.656 33.1±4.1 31.7±3.6 0.331 34.2±3.3 34.7±3.1 0.741
Maternal DM 5 (31) 6 (13) 0.109 3 (30) 4 (16) 0.381 2 (33) 2 (10) 0.218
Maternal HTN 3 (19) 2 (4) 0.108 3 (30) 2 (8) 0.128 0 0 -
Antenatal steroids 7 (44) 14 (31) 0.835 7 (70) 14 (56) 0.704 0 0 -
Male sex 8 (50) 26 (58) 0.289 5 (50) 16 (64) 0.445 3 (50) 10 (51) 1.000
Large for gestational age 2 (13) 2 (4) 0.279 1 (10) 0 0.286 1 (17) 2 (10) 1.000
Apgar score-1 min 7.0±1.6 6.9±1.9 0.900 6.3±1.3 5.7±1.4 0.226 8.2±1.3 8.5±1.1 0.540
Apgar score-5 min 8.6±1.0 8.5±1.4 0.798 8.3±1.0 7.6±1.2 0.118 9.0±1.1 9.5±0.8 0.214
Meconium-stained fluid 0 1 (2) 1.000 0 0 - 0 1 (5) 1.000
PROM >18 hr 1 (6) 5 (11) 1.000 1 (10) 5 (20) 0.649 0 1 (5) 1.000
Pathologic chorioamnionitis 2 (13) 2 (4) 0.279 2 (20) 1 (4) 0.190 0 1 (5) 1.000
PPV at birth 4 (25) 9 (20) 0.800 4 (40) 8 (32) 0.849 0 1 (5) 0.577
Time interval from birth to surfactant administration (hr) 4.9±3.3 7.7±11.1 0.330 4.7±3.3 5.2±10.1 0.880 5.3±3.6 10.9 ±11.7 0.272

Values are expressed as mean±standard deviation or number (%). A P<0.05 represents statistically significant.

Abbreviations: GA, gestational age; MIST, minimally invasive surfactant therapy; DM, diabetes mellitus; HTN, hypertension; PROM, premature rupture of membrane; PPV, positive pressure ventilation.

Table 2.
Respiratory Outcomes and Relevant Morbidities
Variable Total (n=61) GA 30+0-34+6 (n=35) GA 35+0-41+6 (n=26)
MIST (n=16) Control (n=45) P- value MIST (n=10) Control (n=25) P- value MIST (n=6) Control (n=20) P- value
Failure of procedure on the 1st attempt 1 (6) 9 (20) 0.267 1 (10) 4 (16) 1.000 0 5 (25) 0.298
MV anytime 1 (6) 37 (82) <0.001 0 20 (80) <0.001 1 (17) 17 (85) 0.004
Need for >1 dose of surfactant 6 (38) 4 (9) 0.015 4 (40) 2 (8) 0.043 2 (33) 2 (10) 0.218
Bradycardia 2 (13) 20 (44) 0.033 1 (10) 9 (36) 0.218 1 (17) 11 (55) 0.170
Air-leak syndrome 4 (25) 8 (18) 0.715 2 (20) 2 (8) 0.561 2 (33) 6 (30) 1.000
Pulmonary hemorrhage 0 2 (4) 1.000 0 1 (4) 1.000 0 1 (5) 1.000
BPD 0 0 - 0 0 - 0 0 -
Duration of MV (d) 0.3±1.0 3.6±2.7 0.000 0.0±0.0 2.7±2.2 0.000 0.7±1.6 4.9±2.9 0.003
Duration of MV+CPAP (d) 3.5±1.7 4.7±3.1 0.134 3.6±1.4 3.6±2.6 1.000 3.3±2.3 6.2±3.2 0.054
Duration of MV+CPAP+HHHFNC (d) 7.4±4.1 7.6±3.9 0.846 8.3±4.9 7.1±4.1 0.472 5.8±1.9 8.2±3.6 0.143
Hospital stay (d) 23.6±14.8 29.7±17.2 0.217 30.5±14.7 39.6 ±16.8 0.144 12.2±4.1 17.3±5.9 0.035
PDA requiring treatment 10 (63) 24 (53) 0.781 6 (60) 15 (60) 1.000 4 (67) 9 (45) 0.645
NEC >stage 2 0 0 - 0 0 - 0 0 -
ROP 0 0 - 0 0 - 0 0 -
IVH >stage 2 0 1 (2) 1.000 0 1 (4) 1.000 0 0 -
HIE 1 (6) 10 (22) 0.259 1 (10) 4 (16) 1.000 0 6 (30) 0.280
Suspected sepsis 12 (75) 41 (91) 0.189 6 (60) 23 (92) 0.043 6 (100) 18 (90) 1.000
Culture proven sepsis 0 0 - 0 0 - 0 0 -

Values are expressed as number (%) or mean±standard deviation. A P<0.05 represents statistically significant.

Abbreviations: GA, gestational age; MIST, minimally invasive surfactant therapy; MV, mechanical ventilation; BPD, bronchopulmonary dysplasia; CPAP, continuous positive airway pressure; HHHFNC, heated humidified high flow nasal cannula; PDA, patent ductus arteriosus; NEC, necrotizing enterocolitis; ROP, retinopathy of prematurity; IVH, intraventricular hemorrhage; HIE, hypoxic ischemic encephalopathy.

Table 3.
Effect Estimate (RR) of MIST Group Over Non-MIST Group
Variable Total (n=61) GA 30+0-34+6 (n=35) GA 35+0-41+6 (n=26)
Effect estimate (RR) 95% CI P- value Effect estimate (RR) 95% CI P- value Effect estimate (RR) 95% CI P- value
MV anytime RR, 0.014 0.002 to 0.125 0.000 RR, 0.200 0.091 to 0.438 0.000 RR, 0.035 0.003 to 0.419 0.001
Need for >1 dose of surfactant RR, 6.150 1.455 to 26.001 0.008 RR, 7.667 1.123 to 52.321 0.023 RR, 4.500 0.479 to 42.248 0.165
Bradycardia RR, 0.179 0.036 to 0.879 0.022 RR, 0.198 0.021 to 1.822 0.124 RR, 0.164 0.016 to 1.666 0.099
Duration of MV (d) MD, 3.394 2.436 to 4.353 0.000 MD, 2.680 1.759 to 3.601 0.001 MD, 4.183 1.612 to 6.754 0.004
Hospital stay (d) MD, 6.042 -3.636 to 15.719 0.210 MD, 9.100 -3.282 to 21.482 0.136 MD, 5.083 -0.282 to 10.449 0.059
Antibiotics therapy for suspected infection RR, 0.293 0.064 to 1.349 0.101 RR, 0.130 0.019 to 0.890 0.023 RR, 0.900 0.778 to 1.042 0.420

A P<0.05 represents statistically significant.

Abbreviations: RR, relative risk ratio; MIST, minimally invasive surfactant therapy; GA, gestational age; CI, confidence interval; MV, mechanical ventilation; MD, mean difference.

REFERENCES

1. Speer CP. Neonatal respiratory distress syndrome: an inflammatory disease? Neonatology 2011;99:316–9.
crossref pmid
2. Sweet DG, Carnielli V, Greisen G, Hallman M, Ozek E, Plavka R, et al. European consensus guidelines on the management of respiratory distress syndrome: 2016 update. Neonatology 2017;111:107–25.
crossref pmid
3. Committee on Fetus and Newborn; American Academy of Pediatrics. Respiratory support in preterm infants at birth. Pediatrics 2014;133:171–4.
crossref pmid
4. Verder H, Robertson B, Greisen G, Ebbesen F, Albertsen P, Lundstrom K, et al. Surfactant therapy and nasal continuous positive airway pressure for newborns with respiratory distress syndrome. Danish-Swedish Multicenter Study Group. N Engl J Med 1994;331:1051–5.
crossref pmid
5. Verder H, Albertsen P, Ebbesen F, Greisen G, Robertson B, Bertelsen A, et al. Nasal continuous positive airway pressure and early surfactant therapy for respiratory distress syndrome in newborns of less than 30 weeks' gestation. Pediatrics 1999;103:E24.
crossref pmid
6. Venkatesh V, Ponnusamy V, Anandaraj J, Chaudhary R, Malviya M, Clarke P, et al. Endotracheal intubation in a neonatal population remains associated with a high risk of adverse events. Eur J Pediatr 2011;170:223–7.
crossref pmid
7. Nilsson R, Grossmann G, Robertson B. Bronchiolar epithelial lesions induced in the premature rabbit neonate by short periods of artificial ventilation. Acta Pathol Microbiol Scand A 1980;88:359–67.
crossref pmid
8. Kolatat T, Aunganon K, Yosthiem P. Airway complications in neonates who received mechanical ventilation. J Med Assoc Thai 2002;85 Suppl 2:S455–62.
pmid
9. Allen KA. Premedication for neonatal intubation: which medications are recommended and why. Adv Neonatal Care 2012;12:107–11.
crossref pmid pmc
10. Shim GH. Update of minimally invasive surfactant therapy. Korean J Pediatr 2017;60:273–81.
crossref pmid pmc
11. Gopel W, Kribs A, Ziegler A, Laux R, Hoehn T, Wieg C, et al. Avoidance of mechanical ventilation by surfactant treatment of spontaneously breathing preterm infants (AMV): an openlabel, randomised, controlled trial. Lancet 2011;378:1627–34.
crossref pmid
12. Gortner L, Bartmann P, Pohlandt F, Bernsau U, Porz F, Hellwege HH, et al. Early treatment of respiratory distress syndrome with bovine surfactant in very preterm infants: a multicenter controlled clinical trial. Pediatr Pulmonol 1992;14:4–9.
crossref pmid
13. Jobe AH, Bancalari E. Bronchopulmonary dysplasia. Am J Respir Crit Care Med 2001;163:1723–9.
crossref pmid
14. Kliegman RM, Walsh MC. Neonatal necrotizing enterocolitis: pathogenesis, classification, and spectrum of illness. Curr Probl Pediatr 1987;17:213–88.
crossref pmid
15. International Committee for the Classification of Retinopathy of Prematurity. The International Classification of Retinopathy of Prematurity revisited. Arch Ophthalmol 2005;123:991–9.
crossref pmid
16. Papile LA, Burstein J, Burstein R, Koffler H. Incidence and evolution of subependymal and intraventricular hemorrhage: a study of infants with birth weights less than 1,500 gm. J Pediatr 1978;92:529–34.
crossref pmid
17. Aldana-Aguirre JC, Pinto M, Featherstone RM, Kumar M. Less invasive surfactant administration versus intubation for surfactant delivery in preterm infants with respiratory distress syndrome: a systematic review and meta-analysis. Arch Dis Child Fetal Neonatal Ed 2017;102:F17–23.
crossref pmid
18. Lopez E, Gascoin G, Flamant C, Merhi M, Tourneux P, Baud O, et al. Exogenous surfactant therapy in 2013: what is next? Who, when and how should we treat newborn infants in the future? BMC Pediatr 2013;13:165.
crossref pmid pmc pdf
19. Bohlin K, Bouhafs RK, Jarstrand C, Curstedt T, Blennow M, Robertson B. Spontaneous breathing or mechanical ventilation alters lung compliance and tissue association of exogenous surfactant in preterm newborn rabbits. Pediatr Res 2005;57:624–30.
crossref pmid
20. Klebermass-Schrehof K, Wald M, Schwindt J, Grill A, Prusa AR, Haiden N, et al. Less invasive surfactant administration in extremely preterm infants: impact on mortality and morbidity. Neonatology 2013;103:252–8.
crossref pmid
21. Aguar M, Cernada M, Brugada M, Gimeno A, Gutierrez A, Vento M. Minimally invasive surfactant therapy with a gastric tube is as effective as the intubation, surfactant, and extubation technique in preterm babies. Acta Paediatr 2014;103:e229. –33.
crossref pmid
22. Tomar RS, Ghuliani R, Yadav D. Effect of surfactant therapy using orogastric tube for tracheal catheterization in preterm newborns with respiratory distress. Indian J Pediatr 2017;84:257–61.
crossref pmid pdf
23. Jones P, Dauger S, Peters MJ. Bradycardia during critical care intubation: mechanisms, significance and atropine. Arch Dis Child 2012;97:139–44.
crossref pmid
24. Kumar P, Denson SE, Mancuso TJ, Committee on Fetus and Newborn. Section on Anesthesiology and Pain Medicine. Premedication for nonemergency endotracheal intubation in the neonate. Pediatrics 2010;125:608–15.
crossref pmid
25. Klotz D, Porcaro U, Fleck T, Fuchs H. European perspective on less invasive surfactant administration-a survey. Eur J Pediatr 2017;176:147–54.
crossref pmid pdf
26. Kanmaz HG, Erdeve O, Canpolat FE, Mutlu B, Dilmen U. Surfactant administration via thin catheter during spontaneous breathing: randomized controlled trial. Pediatrics 2013;131:e502. –9.
crossref pmid
27. Dargaville PA, Ali SKM, Jackson HD, Williams C, De Paoli AG. Impact of minimally invasive surfactant therapy in preterm infants at 29-32 weeks gestation. Neonatology 2018;113:7–14.
crossref pmid


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