A pilot randomised clinical trial of 670 nm red light for reducing retinopathy of prematurity.


Journal

Pediatric research
ISSN: 1530-0447
Titre abrégé: Pediatr Res
Pays: United States
ID NLM: 0100714

Informations de publication

Date de publication:
01 2020
Historique:
received: 11 03 2019
accepted: 10 07 2019
revised: 03 07 2019
pubmed: 21 8 2019
medline: 26 1 2021
entrez: 21 8 2019
Statut: ppublish

Résumé

Photobiomodulation by 670 nm red light in animal models reduced severity of ROP and improved survival. This pilot randomised controlled trial aimed to provide data on 670 nm red light exposure for prevention of ROP and survival for a larger randomised trial. Neonates <30 weeks gestation or <1150 g at birth were randomised to receive 670 nm for 15 min (9 J/cm placental pathology, growth, days of respiratory support and oxygen, bronchopulmonary dysplasia, patent ductus arteriosus, necrotising enterocolitis, sepsis, worst stage of ROP, need for laser treatment, and survival. Eighty-six neonates enrolled-45 no red light; 41 red light. There was no difference in severity of ROP (<27 weeks-p = 0.463; ≥27 weeks-p = 0.558) or requirement for laser treatment (<27 weeks-p = 1.00; ≥27 weeks-no laser treatment in either group). Survival in 670 nm red light treatment group was 100% (41/41) vs 89% (40/45) in untreated infants (p = 0.057). Randomisation to receive 670 nm red light within 24-48 h after birth is feasible. Although no improvement in ROP or survivability was observed, further testing into the dosage and delivery for this potential therapy are required.

Sections du résumé

BACKGROUND
Photobiomodulation by 670 nm red light in animal models reduced severity of ROP and improved survival. This pilot randomised controlled trial aimed to provide data on 670 nm red light exposure for prevention of ROP and survival for a larger randomised trial.
METHODS
Neonates <30 weeks gestation or <1150 g at birth were randomised to receive 670 nm for 15 min (9 J/cm
DATA COLLECTED
placental pathology, growth, days of respiratory support and oxygen, bronchopulmonary dysplasia, patent ductus arteriosus, necrotising enterocolitis, sepsis, worst stage of ROP, need for laser treatment, and survival.
RESULTS
Eighty-six neonates enrolled-45 no red light; 41 red light. There was no difference in severity of ROP (<27 weeks-p = 0.463; ≥27 weeks-p = 0.558) or requirement for laser treatment (<27 weeks-p = 1.00; ≥27 weeks-no laser treatment in either group). Survival in 670 nm red light treatment group was 100% (41/41) vs 89% (40/45) in untreated infants (p = 0.057).
CONCLUSION
Randomisation to receive 670 nm red light within 24-48 h after birth is feasible. Although no improvement in ROP or survivability was observed, further testing into the dosage and delivery for this potential therapy are required.

Identifiants

pubmed: 31430763
doi: 10.1038/s41390-019-0520-7
pii: 10.1038/s41390-019-0520-7
doi:

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

131-136

Références

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Auteurs

Alison L Kent (AL)

Division of Neonatology, Golisano Children's Hospital, University of Rochester, Rochester, NY, USA. alison_kent@urmc.rochester.edu.
Australian National University Medical School, Canberra, ACT, 2601, Australia. alison_kent@urmc.rochester.edu.

Mohamed E Abdel-Latif (ME)

Australian National University Medical School, Canberra, ACT, 2601, Australia.
Department of Neonatology, Centenary Hospital for Women and Children, Canberra Hospital, Woden, ACT, 2606, Australia.

Timothy Cochrane (T)

Australian National University Medical School, Canberra, ACT, 2601, Australia.
Department of Neonatology, Centenary Hospital for Women and Children, Canberra Hospital, Woden, ACT, 2606, Australia.

Margaret Broom (M)

Department of Neonatology, Centenary Hospital for Women and Children, Canberra Hospital, Woden, ACT, 2606, Australia.

Jane E Dahlstrom (JE)

Australian National University Medical School, Canberra, ACT, 2601, Australia.
Department of Anatomical Pathology, Canberra Hospital, Woden, ACT, 2606, Australia.
John Curtin School of Medical Research, College of Medicine Biology and Environment, ANU, Canberra, ACT, 2601, Australia.

Rohan W Essex (RW)

Australian National University Medical School, Canberra, ACT, 2601, Australia.
Department of Ophthalmology, Canberra Hospital, Woden, ACT, 2606, Australia.

Bruce Shadbolt (B)

Australian National University Medical School, Canberra, ACT, 2601, Australia.
Clinical Epidemiology, Canberra Hospital, Woden, ACT, 2606, Australia.

Riccardo Natoli (R)

Australian National University Medical School, Canberra, ACT, 2601, Australia.
John Curtin School of Medical Research, College of Medicine Biology and Environment, ANU, Canberra, ACT, 2601, Australia.

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