Evidence map›Paper›PMID 40439732›Full record

Trial reportEuropean journal of pediatrics2025

Less Invasive Surfactant Administration (LISA) versus Intubation Surfactant Extubation (InSurE) technique using higher volume surfactant in management of neonates with respiratory distress syndrome: an open-label randomized controlled trial.

Saamic Hooda, Jagjit Singh Dalal, Kapil Bhalla, N D Vaswani, Monika Dalal

Abstract readRandomized Controlled TrialComparative Study
PubMed Publisher
In one paragraph

Trial report in European journal of pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Saamic HoodaDepartment of Pediatrics, Pt B.D. Sharma Post Graduate Institute of Medical Sciences, Rohtak, Haryana, India.
Jagjit Singh DalalDepartment of Neonatology, Pt B. D. Sharma Post Graduate Institute of Medical Sciences, Rohtak, India. Jagjit.dr@gmail.com.ORCID http://orcid.org/0000-0002-3005-4531
Kapil BhallaDepartment of Pediatrics, Pt B.D. Sharma Post Graduate Institute of Medical Sciences, Rohtak, Haryana, India.
N D VaswaniDepartment of Pediatrics, Pt B.D. Sharma Post Graduate Institute of Medical Sciences, Rohtak, Haryana, India.
Monika DalalDepartment of Obstetrics and Gynaecology, Pt B. D. Sharma Post Graduate Institute of Medical Sciences, Rohtak, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Preterm neonates with respiratory distress syndrome (RDS) are commonly treated with surfactant by intubate surfactant extubate (InSurE) technique. Less invasive surfactant administration (LISA) is also being used as mode of surfactant delivery. The surfactant used in most of LISA technique is smaller volume poractant-alfa. We aim to compare InSurE versus LISA technique using more economical but higher volume (Bovine) surfactant and non-invasive positive pressure ventilation (NIPPV) as mode of support in low and middle income country settings. We randomised 100 preterm infants of 26-34 weeks of gestation with RDS within 6 h of birth to receive bovine lipid extract surfactant (100 mg/kg) by InSurE or LISA mode. NIPPV was used as primary mode of respiratory support. The primary objective was to compare the need of invasive mechanical ventilation (IMV) in first 72 h of life and secondary outcomes assessed were hemodynamically significant patent ductus arteriosus (hsPDA), intraventricular haemorrhage (IVH) (> grade II), bronchopulmonary dysplasia (BPD), episodes of bradycardia/desaturation, pulmonary haemorrhage and composite outcome of BPD/mortality. Out of the 100 neonates enrolled, 50 were randomized to the InSurE group and 50 to the LISA group. The mean gestational age and birth weight were 30.59 ± 2.19 weeks and 1.27 ± 0.41 kg in the InSurE group, and 30.53 ± 0.31 weeks and 1.26 ± 0.31 kg in the LISA group respectively. Insignificant statistical difference was seen in the need of IMV in first 72 h between LISA and InSurE (14/50 (28%) vs 15/50 (30%), p = 0.86). Additionally, there were no significant differences in the incidence of hsPDA, IVH (> grade 2), BPD, episodes of bradycardia/desaturation, pulmonary haemorrhage, and composite outcome of BPD/mortality.

conclusionLISA and InSurE are equally feasible strategies for surfactant administration in the treatment of neonatal RDS using NIPPV as primary respiratory support. Both groups had comparable outcomes using larger volume, cost effective bovine lipid extract surfactant with no added advantage of LISA as compared to InSurE technique.

trial registrationCTRI (CTRI/2021/08/035649) dated 13/08/21. WHAT IS KNOWN: • Most existing studies have employed more expensive, lower-volume surfactants for less invasive surfactant administration in neonates with nCPAP as primary mode of support. WHAT IS NEW: • LISA technique using more economical but higher volume (Bovine) surfactant (5 ml/kg) and Non-invasive positive pressure ventilation (NIPPV) as primary mode of respiratory support for RDS showed similar outcomes with no added advantage of LISA as compared to InSure Technique. LISA technique with higher volume and economical surfactant is well feasible using NIPPV as respiratory support.

Indexed as

Airway ExtubationBiological ProductsIntubation, IntratrachealPhospholipidsPulmonary SurfactantsRespiratory Distress Syndrome, NewbornFemaleHumansInfant, NewbornInfant, PrematureMalePositive-Pressure RespirationRespiration, ArtificialTreatment OutcomeBiological ProductsPhospholipidsporactant alfaPulmonary SurfactantsBovine lipid extract surfactantInSurELISANIPPVRespiratory distress syndrome

Identifiers

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.