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Measurement of Nasal Nitric Oxide by Hand-held and Stationary Devices

Overview
Publisher Wiley
Specialty General Medicine
Date 2011 Mar 19
PMID 21413977
Citations 13
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Abstract

Background: Nasal nitric oxide (nNO) is assessed by nasal aspiration/insufflation via one nostril or by nasal silent exhalation through a facemask and is also measured during humming, a manoeuvre that results in increased nNO in the presence of a patent osteomeatal complex. Humming nNO peak is absent in primary ciliary dyskinesia (PCD) and in cystic fibrosis (CF). Hand-held devices are used successfully for exhaled or nNO analysis. No study compared nNO during silent and humming exhalation using hand-held and stationary analysers.

Methods: Thirty-eight subjects (14 PCD; 11 CF; 13 healthy individuals) measured nNO with a stationary and a hand-held analyser during silent and humming exhalations.

Results: No difference between nNO obtained from stationary or hand-held analyser during silent and humming exhalation was found (P > 0·05). Patients with PCD exhibited lower silent and humming nNO than CF or controls (P < 0·001). During both silent and humming exhalation, there was a significant correlation between nNO from the two analyzers both in the whole study population and within each group (r ≥ 0·7, P < 0·01). Bland-Altman plots confirmed this agreement. Using the hand-held device during humming, nNO values of 50, 81 and 21 ppb had sensitivity and specificity > 90% for discriminating PCD or CF from healthy subjects, and patients with PCD from patients with CF, respectively.

Conclusions: The hand-held device is as effective as the stationary analyzer for assessing nNO during silent and humming exhalation. Its wider use might result in an increased number of subjects suspected to have PCD.

Citing Articles

Fractional Exhaled Nitric Oxide (FeNO) in Patients with Stable Chronic Obstructive Pulmonary Disease: Short-Term Variability and Potential Clinical Implications.

Ambrosino P, Fuschillo S, Accardo M, Mosella M, Molino A, Spedicato G J Pers Med. 2022; 12(11).

PMID: 36422082 PMC: 9699194. DOI: 10.3390/jpm12111906.


An international survey on nasal nitric oxide measurement practices for the diagnosis of primary ciliary dyskinesia.

Beydon N, Ferkol T, Harris A, Colas M, Davis S, Haarman E ERJ Open Res. 2022; 8(2).

PMID: 35386825 PMC: 8977594. DOI: 10.1183/23120541.00708-2021.


Severe pulmonary disease in an adult primary ciliary dyskinesia population in Brazil.

Olm M, Marson F, Athanazio R, Nakagawa N, Macchione M, Loges N Sci Rep. 2019; 9(1):8693.

PMID: 31213628 PMC: 6582273. DOI: 10.1038/s41598-019-45017-1.


Primary Ciliary Dyskinesia: An Update on Clinical Aspects, Genetics, Diagnosis, and Future Treatment Strategies.

Mirra V, Werner C, Santamaria F Front Pediatr. 2017; 5:135.

PMID: 28649564 PMC: 5465251. DOI: 10.3389/fped.2017.00135.


Accuracy of Nasal Nitric Oxide Measurement as a Diagnostic Test for Primary Ciliary Dyskinesia. A Systematic Review and Meta-analysis.

Shapiro A, Josephson M, Rosenfeld M, Yilmaz O, Davis S, Polineni D Ann Am Thorac Soc. 2017; 14(7):1184-1196.

PMID: 28481653 PMC: 6137897. DOI: 10.1513/AnnalsATS.201701-062SR.