Feasibility of nasal NO screening in healthy newborns.

chemoluminescence electrochemical sensor nasal nitric oxide newborns primary ciliary dyskinesia screening

Journal

Pediatric pulmonology
ISSN: 1099-0496
Titre abrégé: Pediatr Pulmonol
Pays: United States
ID NLM: 8510590

Informations de publication

Date de publication:
01 2022
Historique:
revised: 10 09 2021
received: 20 10 2020
accepted: 20 09 2021
pubmed: 28 9 2021
medline: 4 1 2022
entrez: 27 9 2021
Statut: ppublish

Résumé

Nasal nitric oxide (nNO) measurement is recommended as a first line screening test for primary ciliary dyskinesia (PCD). While reliable velum- and non-velum-closure techniques exist for preschool children and older individuals, no data are available for neonates. To determine feasibility of nNO screening and nNO concentration in healthy newborns in the first week of life. Nasal NO was analyzed in tidal breathing during natural sleep using a CLD-88 sp NO analyzer (chemoluminescence sensor) and a NIOX MINO (electrochemical sensor). Test success and nNO concentration were determined and compared between the two devices. Nasal NO was measured in 62 healthy neonates within the first week of life. Feasibility of nNO measurement was 100% for at least one nostril and 85.5% for both nostrils using the chemoluminescence device, but significantly lower with the electrochemical device (85.5% and 53.2%; p < .001). Median nNO concentration was 38 ppb (interquartile range, 27-55; range, 9-100) with the ECOMEDICS device and 23 (15-33, 8-59) with the NIOX MINO (p < .001), with a trend towards higher values for older subjects. None of the subjects exceeded nNO levels of 100 ppb. Measurement of nNO using a chemoluminescence device is highly feasible in newborns during natural sleep. However, nNO levels are considerably lower compared to the published data for older individuals and in the range of a PCD reference group of infants between 4 and 8 weeks of age, potentially resulting in a great overlap with subjects with PCD in this age group. Therefore, screening for PCD using nasal NO might not be useful in the first week of life. Upon clinical suspicion, other diagnostic tests such as high-speed video analysis of the cilia should be applied.

Sections du résumé

BACKGROUND
Nasal nitric oxide (nNO) measurement is recommended as a first line screening test for primary ciliary dyskinesia (PCD). While reliable velum- and non-velum-closure techniques exist for preschool children and older individuals, no data are available for neonates.
AIMS
To determine feasibility of nNO screening and nNO concentration in healthy newborns in the first week of life.
METHODS
Nasal NO was analyzed in tidal breathing during natural sleep using a CLD-88 sp NO analyzer (chemoluminescence sensor) and a NIOX MINO (electrochemical sensor). Test success and nNO concentration were determined and compared between the two devices.
RESULTS
Nasal NO was measured in 62 healthy neonates within the first week of life. Feasibility of nNO measurement was 100% for at least one nostril and 85.5% for both nostrils using the chemoluminescence device, but significantly lower with the electrochemical device (85.5% and 53.2%; p < .001). Median nNO concentration was 38 ppb (interquartile range, 27-55; range, 9-100) with the ECOMEDICS device and 23 (15-33, 8-59) with the NIOX MINO (p < .001), with a trend towards higher values for older subjects. None of the subjects exceeded nNO levels of 100 ppb.
CONCLUSION
Measurement of nNO using a chemoluminescence device is highly feasible in newborns during natural sleep. However, nNO levels are considerably lower compared to the published data for older individuals and in the range of a PCD reference group of infants between 4 and 8 weeks of age, potentially resulting in a great overlap with subjects with PCD in this age group. Therefore, screening for PCD using nasal NO might not be useful in the first week of life. Upon clinical suspicion, other diagnostic tests such as high-speed video analysis of the cilia should be applied.

Identifiants

pubmed: 34570949
doi: 10.1002/ppul.25702
pmc: PMC9292553
doi:

Substances chimiques

Nitric Oxide 31C4KY9ESH

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

231-238

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2021 The Authors. Pediatric Pulmonology published by Wiley Periodicals LLC.

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Auteurs

Flurina Buechel (F)

Division of Respiratory Medicine & Children's Research Centre, University Children's Hospital Zurich.

Jakob Usemann (J)

Division of Respiratory Medicine & Children's Research Centre, University Children's Hospital Zurich.
University Children's Hospital Basel, Basel, Switzerland.

A Aline (A)

Division of Respiratory Medicine & Children's Research Centre, University Children's Hospital Zurich.

Peter Salfeld (P)

Kantonsspital Muensterlingen, Münsterlingen, Switzerland.

Alexander Moeller (A)

Division of Respiratory Medicine & Children's Research Centre, University Children's Hospital Zurich.

Andreas Jung (A)

Division of Respiratory Medicine & Children's Research Centre, University Children's Hospital Zurich.

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Classifications MeSH