CC BY-NC-ND 4.0 · Am J Perinatol 2024; 41(02): 211-227
DOI: 10.1055/a-2001-9139
Clinical Opinion

Less Invasive Surfactant Administration: A Viewpoint

1   Department of Pediatrics, University of Toledo, Toledo, Ohio
,
Munmun Rawat
2   Department of Pediatrics, University at Buffalo, Buffalo, New York
› Institutsangaben
 

Abstract

The standard of care in treating respiratory distress syndrome in preterm infants is respiratory support with nasal continuous positive airway pressure or a combination of continuous positive airway pressure and exogenous surfactant replacement. Endotracheal intubation, the conventional method for surfactant administration, is an invasive procedure associated with procedural and mechanical ventilation complications. The INSURE (intubation, surfactant administration, and extubation soon after) technique is an accepted method aimed at reducing the short-term complications and long-term morbidities related to mechanical ventilation but does not eliminate risks associated with endotracheal intubation and mechanical ventilation. Alternative methods of surfactant delivery that can overcome the problems associated with the INSURE technique are surfactant through a laryngeal mask, surfactant through a thin intratracheal catheter, and aerosolized surfactant delivered using nebulizers. The three alternative methods of surfactant delivery studied in the last two decades have advantages and limitations. More than a dozen randomized controlled trials have aimed to study the benefits of the three alternative techniques of surfactant delivery compared with INSURE as the control arm, with promising results in terms of reduction in mortality, need for mechanical ventilation, and bronchopulmonary dysplasia. The need to find a less invasive surfactant administration technique is a clinically relevant problem. Before broader adoption in routine clinical practice, the most beneficial technique among the three alternative strategies should be identified. This review aims to summarize the current evidence for using the three alternative techniques of surfactant administration in neonates, compare the three techniques, highlight the knowledge gaps, and suggest future directions.

Key Points

  • The need to find a less invasive alternative method of surfactant delivery is a clinically relevant problem.

  • Clinical trials that have studied alternative surfactant delivery methods have shown promising results but are inconclusive for broader adoption into clinical practice.

  • Future studies should explore novel clinical trial methodologies and select clinically significant long term outcomes for comparison.


#

Respiratory distress syndrome (RDS) is a disorder affecting preterm infants due to pulmonary surfactant deficiency. This condition's standard treatment is respiratory support with nasal continuous positive airway pressure (nCPAP) or a combination of CPAP and exogenous surfactant replacement.[1] Surfactant is conventionally administered through the endotracheal tube.[2] [3]

Endotracheal intubation for surfactant administration is an invasive procedure associated with procedural and mechanical ventilation complications.[4] The availability of health care personnel skilled in the neonatal airway is a limiting factor that makes early surfactant administration difficult in resource-limited settings. Elective neonatal endotracheal intubation for surfactant administration may require premedication, like sedatives and vagolytics.[5] Despite using premedication, the infant may poorly tolerate the procedure of direct laryngoscopy with complications of autonomic disturbances manifesting as apnea, bradycardia, hypoxemia, and systemic or intracranial hypertension.[6]

Even a short period of mechanical ventilation (<24 hours) of the developing lung (late canalicular and saccular stages) can result in volutrauma due to overdistension of the lung, barotrauma due to excessive pressure, atelectotrauma due to cyclical recruitment and de-recruitment, biotrauma due to inflammation and oxidative stress, and rheotrauma due to inappropriate airway flow.[7] [8] The long-term morbidities associated with mechanical ventilation include bronchopulmonary dysplasia and poor neurodevelopmental outcomes.[9] INSURE (intubation, surfactant administration, and extubation soon after) is an accepted method aimed at reducing the short-term complications and long-term morbidities related to mechanical ventilation, especially in extreme (<28.0 weeks of gestational age [GA]) and very (<32.0 weeks of GA) preterm infants.[10] The INSURE technique still carries several risks associated with endotracheal intubation and mechanical ventilation.

In this review, we aim to summarize the current evidence from randomized controlled trials (RCTs) and meta-analysis for using the alternative techniques of surfactant administration in neonates, compare the three well-studied techniques, highlight the knowledge gaps, and suggest future directions.

Alternative Surfactant Delivery Methods

The search for alternative methods that are less invasive than the INSURE technique began in the early 2000s. Three important alternative methods can overcome the problems associated with the INSURE technique. These are (1) surfactant through a laryngeal mask, (2) surfactant through a thin intratracheal catheter, and (3) aerosolized surfactant using nebulizers.


#

Laryngeal Mask-Assisted Surfactant Delivery

The success of surfactant delivery feasibility through supraglottic airway devices in preterm infants was first reported in 2004 ([Fig. 1]).[11] Following this, eight RCTs were conducted to compare the efficacy of surfactant administration through laryngeal mask or supraglottic airway (SALSA) against nCPAP without surfactant[12] [13] or INSURE technique surfactant delivery ([Table 1]).[14] [15] [16] [17] [18] [19]

Table 1

Clinical trials for laryngeal mask-assisted surfactant delivery

Citation

Design

Population

Intervention/

comparison

Analysis/

sample

size

Primary outcome

Results

Conclusion/comments

Attridge et al [13] (2013)

Single-center, prospective, unblinded RCT at the University of Virginia, United States

Inclusion:

1. X-ray and clinical RDS

2. BW >1,200 g

3. <72 h old

4. On nCPAP for at least 30 min with FiO2 -0.30–0.60

Exclusion:

1. Pneumothorax

2. Prior surfactant or intubation

3. Congenital

anomaly

Calfactant (3 mL/kg.

) administered through LMA in 2–4 aliquots via a catheter with the tip midway down the airway lumen.

nCPAP (comparison)

Priori SS: 183

Enrolled: 26

ITT analysis

13 (LMA) group vs. 13 (nCPAP group)

Need for mechanical ventilation

CPAP vs. LMA: 23 vs. 8% (p = 0.59)

Underpowered

No significant difference detected in the primary outcome

Sadeghnia et al[14] (2014)

Dual center RCT at the Shahid Beheshti and Al-Zahra Hospitals, Iran.

Randomization and Allocation: not reported

Inclusion:

1.BW ≥ 2 kg with RDS symptoms at birth or within 48 h

2. On bubble CPAP needing

FiO2 ≥0.3 for >

30 min

Exclusion:

1. Airway abnormalities 2.Cardiothoracic

or craniofacial malformations, 3.Perinatal asphyxia

4. Air-leak syndromes

Beractant (100 mg/kg) was administered through i-gel (intervention) and by INSURE

(comparison)

Priori SS: not reported.

35 (i-gel) vs.

35 (Insure)

a/A PO2 before and after surfactant

i-gel vs. INSURE: Before surfactant mean (SD)-0.18 (0.03) vs. 0.19 (0.04; p = 0.39)

After surfactant: 0.48 (0.08) vs. 0.43 (0.08)

( p  = 0.014)

Surfactant administration using i-gel resulted in better oxygenation than the INSURE technique

Pinheiro et al[15] (2016)

Single-center RCT at Albany Medical Center, United States.

Randomization: 1:1 ratio within two GA blocks (<33 and ≥ 33 wk) using a computerized algorithm.

Allocation

concealed by clerical staff in serially numbered opaque

envelopes.

Inclusion:

1. GA 290/7–366/7 wk

2. Diagnosis of RDS 4. 48 h of age

3. On nCPAP ≥5 cm H2O (with or without NIPPV) 4.FiO2 0.30–0.60 to maintain SpO2

88 to 95%

Exclusion:

1. Prior intubation or surfactant therapy

2. BW < 1 kg

3. Major malformations

4. Apgar's score ≤ 3 at 5 min

5.Pneumothorax

6. Severe RDS indicated by FiO2 0.40–0.60

Calfactant 3 mL/kg/ dose

administered through size 1 LMA classic using a 5 Fr catheter or ETT

Premedication: Atropine (0.01 mg/kg) in the LMA group

Atropine (0.01 mg/kg) and morphine (0.1 mg/kg) in INSURE group.

Priori SS: 78 (39 in each group)

30 (LMA) vs. 31 (INSURE)

Need for MV

LMA vs. INSURE: 30 vs. 77% ( p ≤ 0.001)

Surfactant therapy through an LMA decreased the need for MV in newborns with moderate RDS

compared with INSURE with sedation

Barbosa et al[16] (2017)

Prospective, unblinded single-center RCT at Maternidade Unimed-BH in Belo Horizonte, Brazil.

Randomization: By table of random numbers.

Inclusion:

1. GA at birth 28–35 wk

2.BW ≥1 kg

3. < 8 h of age

4. On nCPAP

5.SA score > 4 or respiratory frequency >60 bpm or FiO2 ≥ 0.40

6. Clinical and X-ray diagnosis of RDS

Exclusion:

1. GA > 35 wk

2. Major congenital anomalies

3. Prior intubation

4.Apgar's score <3 at 5 min

5.Chorioamnionitis and/or ROM >18 h

Poractant 200 mg/kg administered within 8 h of age through size 1 proseal LMA using 6 Fr catheter

ETT surfactant followed by mechanical ventilation (comparison)

Premedication- Remifentanil and midazolam bolus for ETT group.

Priori SS: 30

Enrolled and analyzed: 48

26 (LMA) vs. 22 (ETT)

SS reduced after an interim analysis showed equivalence

Reduction of oxygen need to FiO2 ≤ 0.30 at 3 h after surfactant

LMA vs. ETT: 77 vs. 77% (p = 0.977)

LMA surfactant had equivalent supplemental oxygen need at 3 h compared with ETT surfactant

Roberts et al[12] (2018)

Multicenter, prospective RCT

All the centers were in the United States

Randomization:

Computer-generated

random numbers stratified by study site and

GA at the time of enrollment (280/7–316/7 wk and 320/7–356/7 wk) using random blocks of 2, 4, and 6.

Allocation:

sequentially numbered, opaque, sealed

envelopes.

Inclusion:

1.GA 280/7–356/7 wk

2. BW ≥1,250 g 3. Age ≤36 h 4.On noninvasive respiratory support (CPAP, NIPPV, or BiPAP)

5. Need for FiO2 0.30–0.40 for ≥30 min

6. CXR and clinical RDS.

Exclusion:

1. Prior MV or surfactant administration

2. Major congenital anomalies

3. Airway abnormality

4. Respiratory

distress because of non-RDS etiology

5. Apgar's score <5 at 5 min.

Poractant alfa 200 mg/kg was administered

via size 1 LMA Unique

CPAP (comparison)

Priori SS estimate:

144 (72 per group)

Enrolled and analyzed: 103

Enrollment was terminated after four years due to difficulty in recruitment

50 (LMA group) vs. 53 (CPAP group)

Need for invasive MV in the first 7 d of life

LMA vs. CPAP: 38 vs. 64% (p = 0.006)

Surfactant via LMA decreased the rate of invasive MV compared with CPAP alone in preterm infants with moderate RDS

Gharehbaghi et al [17] (2018)

Single center RCT at Al-Zahra hospital, Tabriz. Iran

Randomization and Allocation:

Computer-generated numbers in sealed opaque envelopes.

Inclusion:

1.GA 33–37 wk and

BW ≥ 1,800 g

2. Clinical and X-ray signs of RDS

Exclusion:

1. Apgar's score <4 at 5 min

2. Major congenital anomalies

3. Pneumonia

4. Pneumothorax

Beractant 100 mg/kg was given via size 1 LMA

Or ETT

After surfactant therapy, LMA and ETT were removed and infants were placed on CPAP

Premedication:

INSURE group only—Fentanyl (1–2 µg/kg)

Priori SS estimate: not reported

Enrolled and analyzed: 50

25 (LMA) vs. 25 (INSURE)

Reduction in patient's FiO2 requirement following surfactant administration

LMA vs. INSURE: FiO2 before and after surfactant in mean (SD) = 0.60 (0.12) vs. 0.57 (0.12) and 0.42 (0.15) vs. 0.36 (0.10; (p < 0.001)

Surfactant via LMA is a safe and effective alternative to surfactant therapy via ETT

Amini et al [18] (2019)

Single-center prospective, open-label RCT conducted at Tehran University of Medical Sciences, Tehran, Iran.

Randomization:

Computer-generated random numbers

Allocation concealment: consecutive opaque envelopes

Inclusion:

1.GA <37 wk

2.BW ≥1,200 g

3. Diagnosis of RDS in < 2 h of life 4.Need for CPAP ≥5 cm H2O with FiO2 0.30–0.60

Exclusion:

1.Prior intubation 2.Major malformations 3. mean BP < 40 mm Hg

4.Apgar's score ≤3 at 5 min

5. FiO2 need > 0.60

6. Pneumothorax 7. Apnea requiring assisted ventilation.

Poractant α 2.5 mL/kg/dose was given via size 1 LMA or via ETT by INSURE

Premedication: INSURE group only—morphine (0.1 mg/kg)

Priori SS estimate: not reported

Enrolled and analyzed: 60 (30 in each group)

30 (LMA) vs. 30 (INSURE)

Need for RDS-related MV

LMA vs. INSURE: 23.3 vs. 20% (p = 0.75)

Early surfactant via LMA and ETT is equally effective with no significant differences in the adverse outcomes

Gallup et al[19] (2022)

Single-center RCT conducted at Albany Medical Center, United States.

Randomization and allocation:

Computer-based stratified block randomization

1:1 allocation for the first half of the study, followed by 2:1

Concealment: opaque sealed envelopes

Inclusion:

1. GA 270/7-366/7 wk and BW >800 g

2. RDS needing CPAP >5 cm H20, or NIPPV and FiO2 0.30–0.60 for >2 hours within 48 hours of birth.

Exclusion:

1. Pneumothorax

2. Prior intubation

3. Major malformations

4. Apgar's score <3 at 5 min of life or encephalopathy

Calfactant

3 mL/kg (105 mg/kg phospholipid) was given via size 1 LMA Unique or via ETT by INSURE

Premedication:

LMA group: atropine (0.01 mg/kg) only

ETT group:

Atropine and remifentanil (2 µg/kg)

Priori SS estimate:

130 (65 in each group)

Randomized and analyzed:

93

51 (LMA group) vs. 42 (ETT group)

Failure of surfactant therapy defined as

1. Need for invasive mechanical ventilation (or)

2. Need for >2 doses of surfactant therapy

3. Need for FiO2 >0.60

4. Need for the second dose of surfactant within 8 hours

LMA vs. INSURE: 20 vs. 29% (p = 0.311)

Surfactant therapy via LMA is noninferior to INSURE technique

Abbreviations: a/A PO2, arterial-to-alveolar oxygen tension ratio; BW, birth weight; BP, blood pressure; BW, birth weight; CPAP, continuous positive airway pressure; ETT, endotracheal tube; FiO2, fraction of inspired oxygen; GA, gestational age; INSURE, intubation, surfactant administration, and extubation soon after; LMA, laryngeal mask airway; MV, mechanical ventilation; nCPAP, nasal continuous positive airway pressure; NIPPV, nasal intermittent positive pressure ventilation; RCT, randomized controlled trial; RDS, respiratory distress syndrome; SA, Silverman-Andersen score; SD, standard deviation; SS, sample size.


Zoom Image
Fig. 1 Surfactant delivery through LMA with the use of a syringe and 5 Fr catheter inserted into the LMA. (Image courtesy: Dr. Satyan Lakshminrusimha, modified with permission).

The critical limitation of these trials is that they either did not report the prior sample size estimate or did not recruit enough participants to meet the calculated sample size. Six out of eight clinical trials were single-center trials which reduces the external validity of the results. Single-center trials tend to show larger treatment effects than multicenter RCTs.[20] The primary outcomes studied in most trials were the need for invasive mechanical ventilation (from 1 hour to 7 days) or improvement in oxygenation. However, the need for invasive mechanical ventilation cannot be automatically construed as a failure of surfactant therapy because preterm diseases like a hemodynamically significant patent ductus arteriosus, congenital pneumonia, early pulmonary hypertension, perinatal asphyxia, and apnea of prematurity can lead to invasive mechanical ventilation or contribute to the outcome in varying proportions.

A meta-analysis including five of seven RCTs found that surfactant administration through laryngeal mask airway (LMA) reduces the need for invasive mechanical ventilation compared with nCPAP alone without any surfactant or surfactant delivery by INSURE.[21] The meta-analysis showed that surfactant delivery via LMA is associated with a reduction in oxygen requirement compared with nCPAP alone and increased oxygen requirement compared with INSURE in 1 to 6 hours after treatment. However, this meta-analysis did not find evidence supporting SALSA for reducing mortality or short-term morbidities like pneumothorax, bronchopulmonary dysplasia, intraventricular hemorrhage, and length of hospital stay. None of the trials investigated long-term neurodevelopmental outcomes. The heterogeneity in the type of surfactant used, the type of LMA device, and the premedication use in the control arm (INSURE group) of these trials provides low-quality evidence, which limits our ability to make meaningful conclusions regarding its routine use in clinical practice


#

Thin Intratracheal Catheter-Assisted Surfactant Delivery

Kribs et al in 2007 demonstrated the feasibility and safety of the surfactant administration by intratracheal catheter in extremely preterm infants up to the limits of viability (23 weeks GA).[22] In this study, a 0.04 Charrière catheter was clamped with Magill forceps at an angle of 120 degree and inserted into the trachea using a laryngoscope to deliver the liquid surfactant (see [Fig. 2]). Eight RCTs compared surfactant administration using a thin catheter, also known as less invasive surfactant administration (LISA) or minimally invasive surfactant therapy (MIST), with the standard delivery method through an endotracheal tube ([Table 2]).[23] [24] [25] [26] [27] [28] [29] [30] One RCT compared surfactant delivery by a thin catheter technique with the continuation of CPAP alone without surfactant.[31]

Table 2

Clinical trials for thin intratracheal catheter-assisted surfactant delivery

Citation

Design

Population

Intervention/

comparison

Analysis/

sample

size

Primary outcome

Results

Conclusion

Göpel et al[23] (2011)

Multicenter unblinded RCT at 12 NICUs (level 3) in

Germany

Randomization: RITA (v1.2) 1:1 ratio with variable block sizes

Allocation: sequentially

numbered, sealed, opaque envelopes stratified by center

and multiple birth statuses

Inclusion:

1. GA 26–286/7 wk

2. BW < 1.5 kg

Exclusion:

1. Lethal malformations

2. Surfactant without intubation before enrollment

Enrolled all infants, irrespective of their respiratory

status

Infants on CPAP with a FiO2 > 0.30

received surfactant (100 mg/kg) using 2.5–5 Fr catheter placed in the trachea using Magill forceps and laryngoscope

Standard treatment included Surfactant via ETT followed by MV

Sedation and analgesia

were used at the discretion of each neonatologist.

Atropine (5 μg/kg) was optional

Priori SS estimate: 105 in each group

Enrolled and analyzed: 220

108 (Thin catheter group) vs. 112 (standard treatment group)

Need for MV or pCO2 >65 mm Hg or FiO2 > 0.60, or both, for more than 2 h between 25 and 72 h of age

Thin catheter vs. Standard treatment:

28 vs. 46%

(p = 0·008)

Surfactant via thin catheter reduces the need for MV

Kanmaz et al [25] (2013)

Single-center RCT conducted

in the NICU of Zekai Tahir Burak

Maternity Teaching Hospital, Turkey

Randomization and Allocation:

Sequentially numbered sealed opaque

envelopes stratified by GA

Inclusion

GA <32 wk with RDS by clinical, chest X-ray and blood gas parameters on nCPAP with ≥ 0.4 FiO2 in the first 2 h of life

Exclusion

1. Major

congenital anomalies

2. Need for PPV or intubation

in the delivery room

3. Infants not resuscitated by trial

investigators

A 5F catheter was inserted beyond the vocal cords and porcine surfactant

100 mg/kg was administered in the intervention group

INSURE group (comparison)

No premedication

Priori SS estimate:

100 in each group

Enrolled and analyzed:

200

100 (thin catheter group) vs. 100 (INSURE group)

Need for invasive MV in the first 72 h of life

Thin catheter vs. INSURE:

30 vs. 45%

(p = 0.02)

Surfactant via thin catheter reduces the need and duration of MV in very low birth weight infants

Mirnia et al[24] (2013)

Multicenter RCT conducted in the NICU of three university hospitals in Tabriz, Isfahan

and Mashhad, Iran

Inclusion

GA 27–32 wk

on nCPAP needed FiO2 >30% for establishing

SpO2 >85% and needed surfactant

Exclusion

1. 5 min Apgar score < 6

2. Congenital malformations and congenital heart disease

5F feeding

tube was guided through 1–2 cm below the vocal cords and

poractant α 200 mg/kg was given over 1–3 min

INSURE group: Same dose of surfactant through ETT

Premedication: Atropine 5 µg/kg before intubation

Priori SS estimate – not reported

Enrolled and analyzed – 136

66 (thin endotracheal catheter (TEC) group) V. 70 (INSURE group)

Primary outcome not identified

Need for MV at 72 h

Mortality

BPD

TEC vs. INSURE:

19 vs. 22%

(p = 0.6)

9.3 vs. 15.7% (p = 0.01)

7.5% vs. 7.1%

(p = 0.9)

TEC was effective in treating RDS

Mortality was significantly decreased in the TEC group

Bao et al[27] (2015)

Single-center RCT in the Women's Hospital NICUs, Zhejiang University, China

Inclusion

1. GA 28–32 wk

2. Signs of RDS needing nCPAP ≥7 cm H2O and FiO2 ≥0.3 (280/7–296/7 wk gestation) or ≥0.35

(300/7–326/7 wk) to maintain SpO2 at 85–95%

Exclusion

1. Prior intubation

2. Congenital anomalies affecting respiratory

function.

16G, 130 mm Angiocath,

BD, Sandy, Utah, United States, was marked at 1.5 cm(28–29 wk) or 2 cm (30–32 wk) and using direct laryngoscopy

the catheter was inserted beyond the vocal cords surfactant was given at a standard

dose over 3–5 min. Infants were continued

on nCPAP throughout the procedure.

INSURE group - Surfactant via ETT

Priori SS estimate - 60 infants in each group.

Enrolled and analyzed:

90

47(LISA group) vs. 43 (INSURE group)

Need for intubation and MV within 72 h.

LISA vs. INSURE:

17 vs. 23.3%

(p = 0.44)

LISA in spontaneously breathing infants on nCPAP is an alternative for surfactant therapy avoiding

Mohammadi Zadeh et al[28] (2015)

RCT at 2 NICUs in the tertiary care hospitals affiliated with Isfahan University of Medical Sciences, Isfahan, Iran.

Randomization and Allocation:

Using cards provided in consecutively numbered, opaque, and sealed envelopes

Inclusion

GA < 34 wk and

BW 1–1.8 kg with signs of RDS within the first h of life and need for surfactant after 30 min of nCPAP

Exclusion

1. Maternal chorioamnionitis

2. Apgar's score ≤ 4 at 5 min

3. Congenital anomalies

4. Invasive MV at birth

5. Need for MV for more than a few minutes after Surfactant

4F feeding tube marked 1.5 cm above the tip was inserted using Magill forceps and laryngoscope, and poractant alfa was injected into the trachea over 1–3 min.

nCPAP was continued during and after the procedure

In the ETT group, the same dose of surfactant was administered using INSURE technique.

Premedication: intravenous atropine (0.025 mg/kg)

Priori SS estimate: 34

Enrolled and analyzed: 38

19 (CATH group) 19 vs. (ET group)

Need for MV within 72 h of birth.

CATH vs. INSURE:

10.5 vs. 15.8% (p = 0.99)

Surfactant administration via a thin intratracheal catheter has similar feasibility, efficacy, and safety as INSURE technique

Kribs et al[26] (2015)

Multicenter, randomized clinical parallel-group study conducted

at 13 level III NICUs in Germany

Randomization and Allocation:

1:1 ratio with variable block sizes using

serially numbered opaque, sealed envelopes

Inclusion

1. GA

230/7–266/7 wk

2. Spontaneous breathing, age 10 to 120 min

Exclusion

1. Prenatally diagnosed severe underlying disease

2. Primary cardiopulmonary failure

3. Enrolled in any other interventional trial

A laryngoscope and a Magill forceps were used to

intubate a 4F catheter up to the 1.5 cm mark. After removing

the laryngoscope

100 mg/kg of poractant alfa was instilled over 30 to 120 seconds. CPAP was continued after the intervention.

In the control group, infants were intubated, MV was initiated, and surfactant was given via ET.

MV was

weaned as soon as possible according to the center's standard practice.

Priori SS estimate:

87 infants in each group

Enrolled and analyzed: 211

107 (LISA group) vs. 104 (ETT group)

Survival without BPD

Death

LISA vs. ETT:

67.3 vs. 58.7%

(p = 0.20)

9.3 vs. 11.5%

(p = 0.59)

Surfactant via LISA technique was not superior to surfactant via ETT, followed by MV concerning survival without BPD in extremely preterm infants (23–26 wk).

Halim et al[29] (2019)

Single-center RCT in the NICU of Pakistan Institute of Medical Sciences, Islamabad, Pakistan

Randomization and Allocation:

Random numbers using a web-based randomization tool

Inclusion

1. GA ≤34 wk

2. Clinical and radiological evidence of RDS treated with CPAP

Exclusion

1. Major congenital malformations

2. Intubation at birth

6F nasogastric tube was inserted 1–2 cm past the vocal cords under direct visualization using a laryngoscope.100 mg/kg of beractant was administered while CPAP was continued.

INSURE Surfactant

(Comparison)

Premedication:

not reported

Priori SS estimate:

43 infants in each group

Enrolled and analyzed:

100

50 (LISA group) vs. 50 (INSURE group)

Need for invasive mechanical ventilation

LISA vs. INSURE:

30 vs. 60%

(p = 0.003)

LISA technique was more effective than INSURE in preventing the need for invasive mechanical ventilation

Han et al[30] (2020)

Multicenter RCT at eight level III

NICUs in Beijing, Tianjin, and Hebei province, China

Randomization and Allocation:

Sequentially numbered opaque sealed envelopes were used for the 1:1 assignment

Inclusion

1. GA < 316/7 wk

2. On NCPAP

3. Signs of

respiratory distress with

FiO2 >0.4 for SpO2 >85%

4. Surfactant need

within 6 h of life

Exclusion

1. Delivery room

intubation

2. Major

congenital malformations

3. Death or transfer

4. Enrolled in other studies

5 Repeat dose of

surfactant via ETT in first 72 h

5F gastric tube was inserted 1 cm past the vocal cords using a 10 cm ophthalmic forceps and laryngoscope.70–100 mg/kg of calf pulmonary surfactant was administered while continuing CPAP.

INSURE Surfactant

(comparison)

Premedication: none

Priori SS estimate:

130 infants in each group

Enrolled and analyzed:

298

151 (MISA group) vs. 147 (EISA group)

Development of bronchopulmonary dysplasia (MV or CPAP or FiO2 > 0.3 at 36 wk CGA)

MISA V. EISA:

19.2 vs. 25.9%

(p = 0.17)

Minimally invasive surfactant administration was not superior to endotracheal surfactant delivery concerning a reduction in BPD

Dargaville et al[31] (2021)

Multicenter RCT at 33 tertiary-level NICUs in 11 countries

Randomization and Allocation:

Permuted block randomization with stratification using a computer-generated code linked to a corresponding opaque sealed envelope

1:1 group assignment

Blinding: A screen was used to blind clinicians and parents

Inclusion:

1.GA 250/7–286/7 wk

2. Inborn at a study center and admitted to the NICU

3. On CPAP/ NIPPV without prior intubation with a CPAP level of 5–8 cm H2O and requiring FIO2 of ≥0.30 within the first 6 h of life

Exclusion:

1. Serious congenital anomaly

2. Imminent need for intubation

A 16-gauge vascular catheter, or a proprietary catheter (LISAcath), was inserted via direct laryngoscopy into the trachea to instill surfactant (200 mg/kg of poractant alfa). CPAP was applied throughout the procedure

Control (sham treatment):

Transient repositioning with CPAP

Premedication:

Atropine, 25% sucrose (optional)

Priori SS estimate: 606

Enrolled and analyzed: 485

241 (MIST group) vs. 244 (control group)

Composite of death prior to 36 wk PMA or BPD assessed at 36 wk (oxygen requirement)

MIST vs. CPAP

43.6 vs. 49.6%

(RR, 0.87; 95% CI, 0.74–1.03, p = 0.1)

MIST technique of surfactant delivery

did not cause a statistically significant reduction in the composite outcome of death or bronchopulmonary dysplasia.

Abbreviations: BW, birth weight; BPD, bronchopulmonary dysplasia; CI, confidence interval; CPAP, continuous positive airway pressure; EISA, endotracheal intubation surfactant administration; ETT, endotracheal tube; FiO2, fraction of inspired oxygen; GA, gestational age; INSURE, intubate-surfactant-extubate; LISA, less invasive surfactant administration; MISA, minimally invasive surfactant administration; MIST, minimally invasive surfactant therapy; MV, mechanical ventilation; NICU, neonatal intensive care unit; NIPPV, nasal intermittent positive pressure ventilation; PMA, postmenstrual age; PPV, positive pressure ventilation; RCT, randomized controlled trial; RDS, respiratory distress syndrome; RITA, randomization in treatment arms; RR, relative risk; SS, sample size; TEC, thin endotracheal catheter.


Zoom Image
Fig. 2 Surfactant delivery through a intratracheal 4 Fr catheter inserted with the help of magill forceps and laryngoscope (Image courtesy: Dr. Satyan Lakshminrusimha, modified with permission).

Six out of the nine RCTs were multicenter trials. Two studies included only very preterm infants, and three included only extremely preterm infants. Two studies included a combination of both. Six trials studied the LISA technique using a porcine surfactant, and three RCTs used a bovine surfactant. Seven trials used either a feeding tube or a vascular catheter for surfactant administration. Three trials used Magill forceps, and one used ophthalmic forceps to guide the catheter through the vocal cords. Two RCTs used a narrow-bore vascular catheter (16-gauge Angiocath, Becton Dickinson, Sandy, UT), of which one trial also used a proprietary semirigid catheter called LISAcath (Chiesi Farmaceutici SpA, Parma, Italy) for endotracheal instillation of surfactant. These catheters can be inserted endotracheally using a laryngoscope without Magill forceps by the Hobart method.[32] Three studies used atropine as premedication for the procedure. One study did not use any premedication. Other studies did not report premedication use specifically.

All the clinical trials that studied the LISA technique have reported the prior sample size estimation except one study. Six studies enrolled enough participants to meet the sample size. Two studies did not fulfill the sample size requirement. Six of the nine clinical trials evaluated the need for invasive mechanical ventilation as the primary outcome. Five of them specifically looked at the need for invasive mechanical ventilation within 72 hours. Three studies had bronchopulmonary dysplasia at 36 weeks as their primary outcome. Of the three studies, one evaluated death or bronchopulmonary dysplasia (BPD) at 36 weeks as a composite outcome, and another studied survival without BPD and death as two different outcomes.

Subsequently, a meta-analysis of six out of nine trials showed that in preterm infants receiving nCPAP as the respiratory support, the intratracheal catheter technique for surfactant delivery compared with endotracheal intubation was beneficial in terms of reduction in the composite outcome of death or BPD at 36 weeks, BPD at 36 weeks among survivors, and the need for mechanical ventilation with a trend toward lower rates of air leaks.[33]


#

Noninvasive Surfactant Delivery by Aerosolization

Early attempts to study surfactant delivery by aerosolization through a jet nebulizer in an RCT showed no difference in the arterial/alveolar PO2 and the need for mechanical ventilation.[34] The authors of this study felt that the failure of effective aerosolized surfactant delivery could be the reason for their negative results. Finer et al showed the feasibility and safety of aerosolized delivery of Aerosurf, a peptide-containing synthetic surfactant by nCPAP, to preterm infants at risk for RDS using a clinically approved vibrating membrane nebulizer called Aeroneb Pro.[35] Following this, an RCT using aerosolized surfactant (poractant alfa) through a new-generation vibrating membrane nebulizer called eFlow neonatal showed that early postnatal administration of nebulized surfactant might reduce the need for intubation in preterm infants with mild RDS ([Table 3]).[36]

Table 3

Clinical trials for surfactant delivery by aerosolization

Citation

Design

Population

Intervention/comparison

Analysis/sample size

Outcomes

Results

Conclusion

Berggren et al[34] (2000)

Multicenter RCT was conducted at six NICUs in Sweden

Randomization and Allocation: Randomized using sealed envelopes

Inclusion

1. GA <36 wk

2. Age 2–36 h

3. Clinically and radiologically diagnosed progressive RDS

4. Arterial/alveolar oxygen tension ratio 0.15–0.22

5. FiO2 > 0.4 needed to maintain SaO2 85–95%.

6. No evident lung or cardiovascular malformation

Exclusion

Not fulfilling the inclusion criteria

A jet nebulizer (Aiolos Karlstad, Sweden) was used to generate surfactant aerosol and was administered via the CPAP equipment into the nostril. Dose - 480 mg dry weight of poractant α

CPAP alone with no aerosols (control group)

Priori SS estimate – not reported

Enrolled–34 infants

Analyzed–32 infants

16 (nebulized surfactant group) vs. 16 (CPAP group)

Need for MV

Nebulized surfactant group vs. CPAP group

37.5 vs. 31.3%

No beneficial effects of aerosolized surfactant were demonstrated in this trial with a small sample size

Minocchieri et al[36] (2019)

Single-center blinded RCT conducted in tertiary NICU in Western Australia

Randomization and Allocation:

Computer-generated block stratified randomization was used with opaque sealed sequentially numbered envelopes.

Stratification was based on GA: 290/7–316/7 wk and 320/7–336/7 wk

Inclusion

1. GA 290/7–336/7 wk

2. Age < 4 h

3. Clinical signs of mild-to-moderate RDS requiring CPAP 5–8 cm H2O

4. FiO2 requirement 0.22–0.30 to maintain SpO2 86–94%

Exclusion

1.Prior intubation or surfactant

2. Known pneumothorax

3. Cardiorespiratory instability

4. Cardiothoracic malformation

5. Chromosomal aberrations.

A customized vibrating membrane nebulizer (eFlow neonatal nebulizer system, PARI Pharma, Starnberg) was used to administer poractant alfa 200 mg/kg body weight.

Control – nasal bubble CPAP alone without surfactant.

Priori SS estimate–70 (35 patients/group)

Randomized and analyzed: 64

32 in Nebulized surfactant group vs. 32 in CPAP group

Intention to treat analysis

Need for intubation within the first 72 h*

Nebulized surfactant vs. CPAP alone

34.4 vs. 68.8%

(RR [95% CI]: 0.526 [0.292–0.950])

Nebulized surfactant in the first 4 h of life reduced the need for intubation within the first 72 h in the study population

Cummings et al[37] (2020)

Multicenter RCT conducted in 22 level three or four NICUs in the United States

Randomization and Allocation:

Moses-Oakford algorithm was used to generate sequential randomization codes. Two different codes were used to recruit two cohorts.

Inclusion

Cohort 1

1. Nonintubated and not received prior surfactant.

2. Age >1 h but <12 h of life

3. Suspected or confirmed RDS requiring nCPAP, HFNC, or NIV.

Cohort 2

1. Age <24 h

2. Received liquid surfactant by 1 h of age

3. Extubated to nasal respiratory support

Exclusion

1. Congenital anomaly

2. Hypotension with metabolic acidosis (base deficit > 10 meq/L)

3. Hypoxemia (SpO2 <88%) or hypercapnia (paCO2 ≥ 60 mm Hg)

4. Grade 3 or 4 IVH or acute hypoxic-ischemic encephalopathy

The aerosol group received 6 mL/kg

body weight of 35 mg/mL calfactant suspension, 210 mg

phospholipids/kg body weight,

through a modified Solarys nebulizer.

Usual care group – determined as appropriate by the physician

Priori SS estimate = 458 (229 patients per group)

Randomized and analyzed = 457

230 in the aerosol group vs. 227 in the usual care group

Intention to treat analysis

Need for endotracheal intubation and liquid surfactant administration within the first 4 d

Aerosol group vs. usual care group 26 vs. 50%

(p < 0.001)

Aerosolized calfactant administration reduces the need for intubation and liquid surfactant instillation in infants with mild-to-moderate RDS during the first 4 d of life

Sood et al[38] (2021)

Single-center Phase II RCT at a level III NICU in the United States

and

Computer-generated stratified block randomization assigned patients to 4 groups at a 1:1:1:1 ratio

Inclusion:

1. GA 240/7–366/7 with RDS

2. On noninvasive respiratory support with FiO2 ≥25%, PEEP ≥4 cm H2O or flow rate ≥2 LPM for ≤8 h in the 1st 24 h of life

Exclusion:

1. Unstable infants requiring immediate intubation

2. Pneumothorax 3. Prior receipt of surfactant

4. Serious congenital malformations 5. Death anticipated within 3 d.

Nebulized beractant was administered through two types of nebulizers (MiniHeart Lo-Flo jet nebulizer (WestMed) or the AeroNeb Solo (Aerogen) vibrating mesh nebulizer) attached to the inspiratory limb of the noninvasive respiratory support in four fixed doses

Dose Schedule I: Survanta dose 100 mg/kg; dilution 12.5 mg /

mL

Dose Schedule II: Survanta dose 100 mg/kg; dilution 8.3 mg/mL

Dose Schedule III: Survanta dose 200 mg/kg; dilution 12.5 mg/

mL

Dose Schedule IV: Survanta dose 200 mg/kg; dilution 8.3 mg/

mL

Priori SS estimate: 30 in each dosing schedule

Randomized

and analyzed:

149

Four primary outcomes:

1. Safety

A. Surfactant reflux

2. Feasibility

3. Impact of different dosing schedules

4. Efficacy

defined as the need for intubation within 72 h of aerosolized surfactant

Dose I vs. Dose II vs. Dose III vs. Dose IV:

8 vs. 21% vs. 11 vs. 13%

(p < 0.05)

Data for primary outcomes 2 and 3 compared between three GA strata

Study was not powered for efficacy.

Efficacy was compared with historical controls

Aerosolized surfactant therapy is feasible without any serious adverse outcomes. Short-term efficacy was better than historical controls

Dani et al[39] (2022)

Multicenter, open-label,

RCT was conducted in 34 centers in six European countries.

Randomization and Allocation:

Computer-based balanced block randomization scheme

Inclusion

1.GA 280/7–326/7

2. mild to moderate RDS

3. On nCPAP 5–8 cm H2O with

FiO2 0.25–0.40

Exclusion:

1. Intubation

within 1 h after birth

2. Surfactant use before study

entry

3. RDS not secondary to surfactant deficiency

4. Severe asphyxia

5. Major congenital abnormalities 6.PROM (>21 d) 7. Air leak

8. IVH ≥ grade III

9. Hemodynamic instability

A vibrating membrane

nebulizer (investigational eFlow Neos, PARI

Pharma GmbH) was connected close to the patient between the nasal prongs

and the connection of the ventilator circuit to deliver poractant α in two doses - 200 mg/kg (group 1)

and 400 mg/kg (group 2)

Group 3: CPAP only without surfactant

Priori SS estimate:

252 (84 infants in each group)

Randomized and analyzed:

126

42 (group 1) vs. 41 (group 2) vs. 43 (group 3)

Respiratory failure within 72 h

Group 1 vs. Group 3:

57 vs. 58% (p = 0.926)

Group 2 vs. group 3:

49 vs. 58% (p = 0.39)

Nebulized surfactant did not decrease the likelihood of respiratory failure within the first 72 h of life

compared with CPAP alone

Abbreviations: CI, confidence interval; FiO2, fraction of inspired oxygen; GA, gestational age; HFNC, high-flow nasal cannula; IVH, intraventricular hemorrhage; MV, mechanical ventilation; nCPAP, nasal continuous positive airway pressure; NICU, neonatal intensive care unit; NIV, noninvasive ventilation; PEEP, positive end-expiratory pressure; PROM, prolonged rupture of membranes; RCT, randomized controlled trial; RDS, respiratory distress syndrome; RR, relative risk; SS, sample size.


Among the two strata of preterm infants (29.0–31.6 and 32.0–33.6 weeks of GA) studied in this trial, the nebulized surfactant aided the successful establishment of noninvasive support in the 32.0 to 33.6 weeks of group alone. This study's results were limited by the single-center enrollment and small sample size (n = 32/group). A recently published multicenter pragmatic RCT including 457 infants (23–41 weeks of GA) used a modified Solarys nebulizer to deliver aerosolized surfactant into the mouth ([Fig. 3]).[37] The study has reported an approximately 50% reduction in the need for subsequent intubation for liquid surfactant administration. This difference was not consistent among infants born at various GA strata, especially extreme preterm infants. A single-center phase 2 trial investigated four dosing schedules of beractant α delivered using two nebulizers, compared the data between three gestational strata, and found that aerosolized surfactant therapy is feasible without serious adverse outcomes.[38]

Zoom Image
Fig. 3 Aerosolized surfactant delivered with the help of a modified Solarys nebulizer resembling a pacifier (Image courtesy: Dr. Satyan Lakshminrusimha, modified with permission).

A multicenter RCT enrolled spontaneously breathing preterm infants (28.0–32.6 weeks of GA) with mild-to-moderate RDS to investigate the safety, tolerability, and efficacy of nebulized poractant alfa, a porcine surfactant in comparison with nCPAP alone.[39] After the interim evaluation of the first 120 randomized neonates, the trial was terminated prematurely because the nebulized surfactant was found to have negligible efficacy in the study population. The authors analyzed the randomized infants and found that the nebulized surfactant did not reduce the likelihood of intubation within 72 hours of life compared with CPAP alone. Although the trial was conceptualized based on robust preclinical data, it could not be translated to clinical efficacy. The authors speculate that significant surfactant aerosol loss due to a leak at the nasal interface leading to decreased deposition in the lungs could be a reason for the loss of efficacy.


#

Comparison of Three Alternative Methods with INSURE

Three alternative methods of surfactant delivery studied in the last two decades have both advantages and limitations when compared with each other ([Table 4]). A recent network meta-analysis compared their efficacy with INSURE.[40] Sixteen RCTs and 20 observational studies with a large sample size (n = 13,234) were included in the analysis. The primary outcomes analyzed were mortality (n = 12,155), the need for mechanical ventilation (n = 5,961), and BPD(n = 10,993). The sample's median GA and birth weights were 29 weeks 6 days (interquartile range [IQR]: 28 weeks 1 days–31 weeks) and 1,289 g (IQR: 1,040.8–1,622.5). Compared with the INSURE method, surfactant delivery via a thin catheter alone and not SALSA or nebulization showed a significant decrease in mortality, need for mechanical ventilation (MV), and BPD. The significance of the difference in mortality and BPD seen with the thin catheter method was lost when RCTs alone were included for analysis. The main limitations of this study are the pooling of the results from RCTs and observational studies, the exclusion of three RCTs involving SALSA as the intervention,[17] [18] [19] two RCTs studying thin catheter technique,[29] [31] and one RCT comparing nebulized surfactant with usual care,[37] and lack of adequate representation of extremely preterm infants (<28 weeks) in the sample.

Table 4

Comparison of alternative methods of surfactant delivery

Alternative methods of surfactant delivery

Laryngeal mask

Thin catheter

Aerosolization

Advantages

1. Avoids complications due to direct laryngoscope

2. Availability of the device in the NICU

3. Familiarity with the use of the device among NICU providers.

4. Ability to treat apnea/hypoxemia (potential complication of surfactant administration) with PPV - potential complication of surfactant administration

1. Can be used in the extremely preterm infants

2. Avoids PPV for surfactant administration

3. Reduces the need for intubation and mechanical ventilation in preterm infants

4. Some evidence for a reduction in BPD/mortality

1. Truly a noninvasive strategy for surfactant delivery

2. Allows concurrent use of CPAP

3. Avoids direct laryngoscopy and PPV

4. Some evidence for the reduced need for intubation and mechanical ventilation

5. No premedication is required

Disadvantages

1. Interruption of CPAP during the procedure

2. Need for PPV to disperse the surfactant through the lungs.

3. Cannot be used in extremely preterm infants

4. Lack of evidence for a reduction in BPD

1. Need direct laryngoscopy with the associated risks

2. Need availability and use of Magill forceps

3. Need training and providers with advanced skills.

4. May need premedication

4. Lack of evidence regarding the long-term neurodevelopmental outcome

1. Optimal dose of surfactant for the nebulization route is unknown

2. Deposition of a significant fraction of the aerosolized dose in the upper airways

3. Lack of an effective nebulizer to aerosolize surfactant

4. Lack of evidence for use in severe RDS

5. Data on the effect on BPD and NDO is unavailable

Abbreviations: BPD, bronchopulmonary dysplasia; CPAP, continuous positive airway pressure; NDO, neurodevelopmental outcome; NICU, neonatal intensive care unit; PPV, positive pressure ventilation; RDS, respiratory distress syndrome.



#

Conclusion

The need to find a LISA technique is a clinically relevant problem. The three alternative methods, namely surfactant delivery through (1) laryngeal mask, (2) thin intratracheal catheter, and (3) aerosolization, have shown promising results in clinical trials. Before broader adoption in routine clinical practice, we must identify the most beneficial technique among the three alternative strategies. There is no RCT comparing these three techniques. An essential challenge of conducting well-designed RCT is the recruitment of participants. A multicenter RCT with a multiarm, multistage (MAMS) design will be one way to move forward. MAMS trial design provides the benefit of a smaller sample size, shorter duration, lower cost, and a shared control arm.[41]

The recent RCTs, which have studied outcomes like death and BPD rather than the need for invasive mechanical ventilation, have shown that equipoise still exists between the alternative methods of surfactant delivery and nCPAP alone. So, future trials should have four arms comparing the three surfactant delivery methods simultaneously with a control arm of nCPAP without surfactant. Those trials should study the composite outcome of death or respiratory morbidity as the primary outcome and report the adverse effects of each modality of surfactant delivery, other short-term morbidities, and long-term neurodevelopmental outcomes. Such trials can be resource intensive during the initial phases, but they might have the potential to provide definitive data to make recommendations for standardized surfactant delivery techniques.


#
#

Conflict of Interest

None declared.

Acknowledgment

We thank Dr. Satyan Lakshminrusimha, MD (Professor and Chair of Pediatrics, UC Davis), and Ms. Sylvia Gugino, MA (Senior Research Support Specialist, University at Buffalo), for helping with the figures.

  • References

  • 1 Polin RA, Carlo WA. Committee on Fetus and Newborn, American Academy of Pediatrics. Surfactant replacement therapy for preterm and term neonates with respiratory distress. Pediatrics 2014; 133 (01) 156-163
  • 2 Kendig JW, Notter RH, Cox C. et al. A comparison of surfactant as immediate prophylaxis and as rescue therapy in newborns of less than 30 weeks' gestation. N Engl J Med 1991; 324 (13) 865-871
  • 3 Kendig JW, Ryan RM, Sinkin RA. et al. Comparison of two strategies for surfactant prophylaxis in very premature infants: a multicenter randomized trial. Pediatrics 1998; 101 (06) 1006-1012
  • 4 Foglia EE, Ades A, Sawyer T. et al; NEAR4NEOS Investigators. Neonatal intubation practice and outcomes: an international registry study. Pediatrics 2019; 143 (01) e20180902
  • 5 Barrington K. Premedication for endotracheal intubation in the newborn infant. Paediatr Child Health 2011; 16 (03) 159-171
  • 6 Maheshwari R, Tracy M, Badawi N, Hinder M. Neonatal endotracheal intubation: how to make it more baby friendly. J Paediatr Child Health 2016; 52 (05) 480-486
  • 7 Donn SM, Sinha SK. Minimising ventilator induced lung injury in preterm infants. Arch Dis Child Fetal Neonatal Ed 2006; 91 (03) F226-F230
  • 8 Mokres LM, Parai K, Hilgendorff A. et al. Prolonged mechanical ventilation with air induces apoptosis and causes failure of alveolar septation and angiogenesis in lungs of newborn mice. Am J Physiol Lung Cell Mol Physiol 2010; 298 (01) L23-L35
  • 9 Jobe AH. The new bronchopulmonary dysplasia. Curr Opin Pediatr 2011; 23 (02) 167-172
  • 10 Verder H, Robertson B, Greisen G. et al; Danish-Swedish Multicenter Study Group. Surfactant therapy and nasal continuous positive airway pressure for newborns with respiratory distress syndrome. N Engl J Med 1994; 331 (16) 1051-1055
  • 11 Brimacombe J, Gandini D, Keller C. The laryngeal mask airway for administration of surfactant in two neonates with respiratory distress syndrome. Paediatr Anaesth 2004; 14 (02) 188-190
  • 12 Roberts KD, Brown R, Lampland AL. et al. Laryngeal mask airway for surfactant administration in neonates: a randomized, controlled trial. J Pediatr 2018; 193: 40-46.e1
  • 13 Attridge JT, Stewart C, Stukenborg GJ, Kattwinkel J. Administration of rescue surfactant by laryngeal mask airway: lessons from a pilot trial. Am J Perinatol 2013; 30 (03) 201-206
  • 14 Sadeghnia A, Tanhaei M, Mohammadizadeh M, Nemati M. A comparison of surfactant administration through i-gel and ET-tube in the treatment of respiratory distress syndrome in newborns weighing more than 2000 grams. Adv Biomed Res 2014; 3: 160
  • 15 Pinheiro JM, Santana-Rivas Q, Pezzano C. Randomized trial of laryngeal mask airway versus endotracheal intubation for surfactant delivery. J Perinatol 2016; 36 (03) 196-201
  • 16 Barbosa RF, Simões E Silva AC, Silva YP. A randomized controlled trial of the laryngeal mask airway for surfactant administration in neonates. J Pediatr (Rio J) 2017; 93 (04) 343-350
  • 17 Gharehbaghi M, Yalda JM, Radfar R. Comparing the efficacy of surfactant administration by laryngeal mask airway and endotracheal intubation in neonatal respiratory distress syndrome. Crescent J Med Biol Sci 2018; 5 (03) 222-227
  • 18 Amini E, Sheikh M, Shariat M, Dalili H, Azadi N, Nourollahi S. Surfactant administration in preterm neonates using laryngeal mask airway: a randomized clinical trial. Acta Med Iran 2019; 57 (06) 348
  • 19 Gallup JA, Ndakor SM, Pezzano C, Pinheiro JMB. Randomized trial of surfactant therapy via laryngeal mask airway versus brief tracheal intubation in neonates born preterm. J Pediatr 2022; (e-pub ahead of print). DOI: 10.1016/j.jpeds.2022.10.009.
  • 20 Dechartres A, Boutron I, Trinquart L, Charles P, Ravaud P. Single-center trials show larger treatment effects than multicenter trials: evidence from a meta-epidemiologic study. Ann Intern Med 2011; 155 (01) 39-51
  • 21 Calevo MG, Veronese N, Cavallin F, Paola C, Micaglio M, Trevisanuto D. Supraglottic airway devices for surfactant treatment: systematic review and meta-analysis. J Perinatol 2019; 39 (02) 173-183
  • 22 Kribs A, Pillekamp F, Hünseler C, Vierzig A, Roth B. Early administration of surfactant in spontaneous breathing with nCPAP: feasibility and outcome in extremely premature infants (postmenstrual age </=27 weeks). Paediatr Anaesth 2007; 17 (04) 364-369
  • 23 Göpel W, Kribs A, Ziegler A. et al; German Neonatal Network. Avoidance of mechanical ventilation by surfactant treatment of spontaneously breathing preterm infants (AMV): an open-label, randomised, controlled trial. Lancet 2011; 378 (9803): 1627-1634
  • 24 Mirnia K, Heidarzadeh M, Hosseini Mb, Sadeghnia A, Balila M, Ghojazadeh M. Comparison outcome of surfactant administration via tracheal catheterization during spontaneous breathing with insure. Med J Islamic World Acad Sci 2013; 21 (04) 143-148
  • 25 Kanmaz HG, Erdeve O, Canpolat FE, Mutlu B, Dilmen U. Surfactant administration via thin catheter during spontaneous breathing: randomized controlled trial. Pediatrics 2013; 131 (02) e502-e509
  • 26 Kribs A, Roll C, Göpel W. et al; NINSAPP Trial Investigators. Nonintubated surfactant application vs conventional therapy in extremely preterm infants: a randomized clinical trial. JAMA Pediatr 2015; 169 (08) 723-730
  • 27 Bao Y, Zhang G, Wu M, Ma L, Zhu J. A pilot study of less invasive surfactant administration in very preterm infants in a Chinese tertiary center. BMC Pediatr 2015; 15: 21
  • 28 Mohammadizadeh M, Ardestani AG, Sadeghnia AR. Early administration of surfactant via a thin intratracheal catheter in preterm infants with respiratory distress syndrome: feasibility and outcome. J Res Pharm Pract 2015; 4 (01) 31-36
  • 29 Halim A, Shirazi H, Riaz S, Gul SS, Ali W. Less invasive surfactant administration in preterm infants with respiratory distress syndrome. J Coll Physicians Surg Pak 2019; 29 (03) 226-330
  • 30 Han T, Liu H, Zhang H. et al. Minimally Invasive surfactant administration for the treatment of neonatal respiratory distress syndrome: a multicenter randomized study in China. Front Pediatr 2020; 8: 182
  • 31 Dargaville PA, Kamlin COF, Orsini F. et al; OPTIMIST-A Trial Investigators. Effect of minimally invasive surfactant therapy vs sham treatment on death or bronchopulmonary dysplasia in preterm infants with respiratory distress syndrome: the OPTIMIST-a randomized clinical trial. JAMA 2021; 326 (24) 2478-2487
  • 32 Dargaville PA, Kamlin COF, De Paoli AG. et al. The OPTIMIST-a trial: evaluation of minimally-invasive surfactant therapy in preterm infants 25-28 weeks gestation. BMC Pediatr 2014; 14 (01) 213
  • 33 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 (01) F17-F23
  • 34 Berggren E, Liljedahl M, Winbladh B. et al. Pilot study of nebulized surfactant therapy for neonatal respiratory distress syndrome. Acta Paediatr 2000; 89 (04) 460-464
  • 35 Finer NN, Merritt TA, Bernstein G, Job L, Mazela J, Segal R. An open label, pilot study of Aerosurf® combined with nCPAP to prevent RDS in preterm neonates. J Aerosol Med Pulm Drug Deliv 2010; 23 (05) 303-309
  • 36 Minocchieri S, Berry CA, Pillow JJ. CureNeb Study Team. Nebulised surfactant to reduce severity of respiratory distress: a blinded, parallel, randomised controlled trial. Arch Dis Child Fetal Neonatal Ed 2019; 104 (03) F313-F319
  • 37 Cummings JJ, Gerday E, Minton S. et al; AERO-02 STUDY INVESTIGATORS. Aerosolized calfactant for newborns with respiratory distress: a randomized trial. Pediatrics 2020; 146 (05) e20193967
  • 38 Sood BG, Thomas R, Delaney-Black V, Xin Y, Sharma A, Chen X. Aerosolized Beractant in neonatal respiratory distress syndrome: a randomized fixed-dose parallel-arm phase II trial. Pulm Pharmacol Ther 2021; 66: 101986
  • 39 Dani C, Talosi G, Piccinno A. et al; CURONEB Study Group. A randomized, controlled trial to investigate the efficacy of nebulized poractant alfa in premature babies with respiratory distress syndrome. J Pediatr 2022; 246: 40-47.e5
  • 40 Bellos I, Fitrou G, Panza R, Pandita A. Comparative efficacy of methods for surfactant administration: a network meta-analysis. Arch Dis Child Fetal Neonatal Ed 2021; 106 (05) 474-487
  • 41 Millen GC, Yap C. Adaptive trial designs: what are multiarm, multistage trials?. Arch Dis Child Educ Pract Ed 2020; 105 (06) 376-378

Address for correspondence

Srinivasan Mani
Department of Pediatrics, The University of Toledo, ProMedica Russell J. Ebeid Children's Hospital
2142 North Cove Boulevard, Toledo, OH 43606

Publikationsverlauf

Eingereicht: 05. September 2022

Angenommen: 12. Dezember 2022

Accepted Manuscript online:
20. Dezember 2022

Artikel online veröffentlicht:
15. Februar 2023

© 2023. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

Thieme Medical Publishers, Inc.
333 Seventh Avenue, 18th Floor, New York, NY 10001, USA

  • References

  • 1 Polin RA, Carlo WA. Committee on Fetus and Newborn, American Academy of Pediatrics. Surfactant replacement therapy for preterm and term neonates with respiratory distress. Pediatrics 2014; 133 (01) 156-163
  • 2 Kendig JW, Notter RH, Cox C. et al. A comparison of surfactant as immediate prophylaxis and as rescue therapy in newborns of less than 30 weeks' gestation. N Engl J Med 1991; 324 (13) 865-871
  • 3 Kendig JW, Ryan RM, Sinkin RA. et al. Comparison of two strategies for surfactant prophylaxis in very premature infants: a multicenter randomized trial. Pediatrics 1998; 101 (06) 1006-1012
  • 4 Foglia EE, Ades A, Sawyer T. et al; NEAR4NEOS Investigators. Neonatal intubation practice and outcomes: an international registry study. Pediatrics 2019; 143 (01) e20180902
  • 5 Barrington K. Premedication for endotracheal intubation in the newborn infant. Paediatr Child Health 2011; 16 (03) 159-171
  • 6 Maheshwari R, Tracy M, Badawi N, Hinder M. Neonatal endotracheal intubation: how to make it more baby friendly. J Paediatr Child Health 2016; 52 (05) 480-486
  • 7 Donn SM, Sinha SK. Minimising ventilator induced lung injury in preterm infants. Arch Dis Child Fetal Neonatal Ed 2006; 91 (03) F226-F230
  • 8 Mokres LM, Parai K, Hilgendorff A. et al. Prolonged mechanical ventilation with air induces apoptosis and causes failure of alveolar septation and angiogenesis in lungs of newborn mice. Am J Physiol Lung Cell Mol Physiol 2010; 298 (01) L23-L35
  • 9 Jobe AH. The new bronchopulmonary dysplasia. Curr Opin Pediatr 2011; 23 (02) 167-172
  • 10 Verder H, Robertson B, Greisen G. et al; Danish-Swedish Multicenter Study Group. Surfactant therapy and nasal continuous positive airway pressure for newborns with respiratory distress syndrome. N Engl J Med 1994; 331 (16) 1051-1055
  • 11 Brimacombe J, Gandini D, Keller C. The laryngeal mask airway for administration of surfactant in two neonates with respiratory distress syndrome. Paediatr Anaesth 2004; 14 (02) 188-190
  • 12 Roberts KD, Brown R, Lampland AL. et al. Laryngeal mask airway for surfactant administration in neonates: a randomized, controlled trial. J Pediatr 2018; 193: 40-46.e1
  • 13 Attridge JT, Stewart C, Stukenborg GJ, Kattwinkel J. Administration of rescue surfactant by laryngeal mask airway: lessons from a pilot trial. Am J Perinatol 2013; 30 (03) 201-206
  • 14 Sadeghnia A, Tanhaei M, Mohammadizadeh M, Nemati M. A comparison of surfactant administration through i-gel and ET-tube in the treatment of respiratory distress syndrome in newborns weighing more than 2000 grams. Adv Biomed Res 2014; 3: 160
  • 15 Pinheiro JM, Santana-Rivas Q, Pezzano C. Randomized trial of laryngeal mask airway versus endotracheal intubation for surfactant delivery. J Perinatol 2016; 36 (03) 196-201
  • 16 Barbosa RF, Simões E Silva AC, Silva YP. A randomized controlled trial of the laryngeal mask airway for surfactant administration in neonates. J Pediatr (Rio J) 2017; 93 (04) 343-350
  • 17 Gharehbaghi M, Yalda JM, Radfar R. Comparing the efficacy of surfactant administration by laryngeal mask airway and endotracheal intubation in neonatal respiratory distress syndrome. Crescent J Med Biol Sci 2018; 5 (03) 222-227
  • 18 Amini E, Sheikh M, Shariat M, Dalili H, Azadi N, Nourollahi S. Surfactant administration in preterm neonates using laryngeal mask airway: a randomized clinical trial. Acta Med Iran 2019; 57 (06) 348
  • 19 Gallup JA, Ndakor SM, Pezzano C, Pinheiro JMB. Randomized trial of surfactant therapy via laryngeal mask airway versus brief tracheal intubation in neonates born preterm. J Pediatr 2022; (e-pub ahead of print). DOI: 10.1016/j.jpeds.2022.10.009.
  • 20 Dechartres A, Boutron I, Trinquart L, Charles P, Ravaud P. Single-center trials show larger treatment effects than multicenter trials: evidence from a meta-epidemiologic study. Ann Intern Med 2011; 155 (01) 39-51
  • 21 Calevo MG, Veronese N, Cavallin F, Paola C, Micaglio M, Trevisanuto D. Supraglottic airway devices for surfactant treatment: systematic review and meta-analysis. J Perinatol 2019; 39 (02) 173-183
  • 22 Kribs A, Pillekamp F, Hünseler C, Vierzig A, Roth B. Early administration of surfactant in spontaneous breathing with nCPAP: feasibility and outcome in extremely premature infants (postmenstrual age </=27 weeks). Paediatr Anaesth 2007; 17 (04) 364-369
  • 23 Göpel W, Kribs A, Ziegler A. et al; German Neonatal Network. Avoidance of mechanical ventilation by surfactant treatment of spontaneously breathing preterm infants (AMV): an open-label, randomised, controlled trial. Lancet 2011; 378 (9803): 1627-1634
  • 24 Mirnia K, Heidarzadeh M, Hosseini Mb, Sadeghnia A, Balila M, Ghojazadeh M. Comparison outcome of surfactant administration via tracheal catheterization during spontaneous breathing with insure. Med J Islamic World Acad Sci 2013; 21 (04) 143-148
  • 25 Kanmaz HG, Erdeve O, Canpolat FE, Mutlu B, Dilmen U. Surfactant administration via thin catheter during spontaneous breathing: randomized controlled trial. Pediatrics 2013; 131 (02) e502-e509
  • 26 Kribs A, Roll C, Göpel W. et al; NINSAPP Trial Investigators. Nonintubated surfactant application vs conventional therapy in extremely preterm infants: a randomized clinical trial. JAMA Pediatr 2015; 169 (08) 723-730
  • 27 Bao Y, Zhang G, Wu M, Ma L, Zhu J. A pilot study of less invasive surfactant administration in very preterm infants in a Chinese tertiary center. BMC Pediatr 2015; 15: 21
  • 28 Mohammadizadeh M, Ardestani AG, Sadeghnia AR. Early administration of surfactant via a thin intratracheal catheter in preterm infants with respiratory distress syndrome: feasibility and outcome. J Res Pharm Pract 2015; 4 (01) 31-36
  • 29 Halim A, Shirazi H, Riaz S, Gul SS, Ali W. Less invasive surfactant administration in preterm infants with respiratory distress syndrome. J Coll Physicians Surg Pak 2019; 29 (03) 226-330
  • 30 Han T, Liu H, Zhang H. et al. Minimally Invasive surfactant administration for the treatment of neonatal respiratory distress syndrome: a multicenter randomized study in China. Front Pediatr 2020; 8: 182
  • 31 Dargaville PA, Kamlin COF, Orsini F. et al; OPTIMIST-A Trial Investigators. Effect of minimally invasive surfactant therapy vs sham treatment on death or bronchopulmonary dysplasia in preterm infants with respiratory distress syndrome: the OPTIMIST-a randomized clinical trial. JAMA 2021; 326 (24) 2478-2487
  • 32 Dargaville PA, Kamlin COF, De Paoli AG. et al. The OPTIMIST-a trial: evaluation of minimally-invasive surfactant therapy in preterm infants 25-28 weeks gestation. BMC Pediatr 2014; 14 (01) 213
  • 33 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 (01) F17-F23
  • 34 Berggren E, Liljedahl M, Winbladh B. et al. Pilot study of nebulized surfactant therapy for neonatal respiratory distress syndrome. Acta Paediatr 2000; 89 (04) 460-464
  • 35 Finer NN, Merritt TA, Bernstein G, Job L, Mazela J, Segal R. An open label, pilot study of Aerosurf® combined with nCPAP to prevent RDS in preterm neonates. J Aerosol Med Pulm Drug Deliv 2010; 23 (05) 303-309
  • 36 Minocchieri S, Berry CA, Pillow JJ. CureNeb Study Team. Nebulised surfactant to reduce severity of respiratory distress: a blinded, parallel, randomised controlled trial. Arch Dis Child Fetal Neonatal Ed 2019; 104 (03) F313-F319
  • 37 Cummings JJ, Gerday E, Minton S. et al; AERO-02 STUDY INVESTIGATORS. Aerosolized calfactant for newborns with respiratory distress: a randomized trial. Pediatrics 2020; 146 (05) e20193967
  • 38 Sood BG, Thomas R, Delaney-Black V, Xin Y, Sharma A, Chen X. Aerosolized Beractant in neonatal respiratory distress syndrome: a randomized fixed-dose parallel-arm phase II trial. Pulm Pharmacol Ther 2021; 66: 101986
  • 39 Dani C, Talosi G, Piccinno A. et al; CURONEB Study Group. A randomized, controlled trial to investigate the efficacy of nebulized poractant alfa in premature babies with respiratory distress syndrome. J Pediatr 2022; 246: 40-47.e5
  • 40 Bellos I, Fitrou G, Panza R, Pandita A. Comparative efficacy of methods for surfactant administration: a network meta-analysis. Arch Dis Child Fetal Neonatal Ed 2021; 106 (05) 474-487
  • 41 Millen GC, Yap C. Adaptive trial designs: what are multiarm, multistage trials?. Arch Dis Child Educ Pract Ed 2020; 105 (06) 376-378

Zoom Image
Fig. 1 Surfactant delivery through LMA with the use of a syringe and 5 Fr catheter inserted into the LMA. (Image courtesy: Dr. Satyan Lakshminrusimha, modified with permission).
Zoom Image
Fig. 2 Surfactant delivery through a intratracheal 4 Fr catheter inserted with the help of magill forceps and laryngoscope (Image courtesy: Dr. Satyan Lakshminrusimha, modified with permission).
Zoom Image
Fig. 3 Aerosolized surfactant delivered with the help of a modified Solarys nebulizer resembling a pacifier (Image courtesy: Dr. Satyan Lakshminrusimha, modified with permission).