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      Humidity during high‐frequency oscillatory ventilation compared to intermittent positive pressure ventilation in extremely preterm neonates: An in vitro and in vivo observational study

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          Abstract

          Background

          Inappropriate humidification of inspired gas during mechanical ventilation can impair lung development in extremely low birthweight (ELBW) infants. Humidification depends on multiple factors, such as the heater‐humidifier device used, type of ventilation, and environmental factors. Few studies have examined inspired gas humidification in these infants, especially during high‐frequency oscillatory ventilation (HFOV). Our objective was to compare humidity during HFOV and intermittent positive pressure ventilation (IPPV), in vitro and in vivo.

          Methods

          In vitro and in vivo studies used the same ventilator during both HFOV and IPPV. The bench study used a neonatal test lung and two heater‐humidifiers with their specific circuits; the in vivo study prospectively included preterm infants born before 28 weeks of gestation.

          Results

          On bench testing, mean absolute (AH) and relative (RH) humidity values were significantly lower during HFOV than IPPV (RH = 79.4 ± 8.1% vs. 89.0 ± 6.2%, p < 0.001). Regardless of the ventilatory mode, mean RH significantly differed between the two heater‐humidifiers (89.6 ± 6.7% vs 78.7 ± 6.8%, p = 0.003). The in vivo study included 10 neonates (mean ± SD gestational age: 25.7 ± 0.9 weeks and birthweight: 624.4 ± 96.1 g). Mean RH during HFOV was significantly lower than during IPPV (74.6 ± 5.7% vs. 83.0 ± 6.7%, p = 0.004).

          Conclusion

          RH was significantly lower during HFOV than IPPV, both in vitro and in vivo. The type of heater‐humidifier also influenced humidification. More systematic measurements of humidity of inspired gas, especially during HFOV, should be considered to optimize humidification and consequently lung protection in ELBW infants.

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          Most cited references21

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          The acute respiratory distress syndrome.

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            Humidification during invasive and noninvasive mechanical ventilation: 2012.

            We searched the MEDLINE, CINAHL, and Cochrane Library databases for articles published between January 1990 and December 2011. The update of this clinical practice guideline is based on 184 clinical trials and systematic reviews, and 10 articles investigating humidification during invasive and noninvasive mechanical ventilation. The following recommendations are made following the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) scoring system: 1. Humidification is recommended on every patient receiving invasive mechanical ventilation. 2. Active humidification is suggested for noninvasive mechanical ventilation, as it may improve adherence and comfort. 3. When providing active humidification to patients who are invasively ventilated, it is suggested that the device provide a humidity level between 33 mg H(2)O/L and 44 mg H(2)O/L and gas temperature between 34°C and 41°C at the circuit Y-piece, with a relative humidity of 100%. 4. When providing passive humidification to patients undergoing invasive mechanical ventilation, it is suggested that the HME provide a minimum of 30 mg H(2)O/L. 5. Passive humidification is not recommended for noninvasive mechanical ventilation. 6. When providing humidification to patients with low tidal volumes, such as when lung-protective ventilation strategies are used, HMEs are not recommended because they contribute additional dead space, which can increase the ventilation requirement and P(aCO(2)). 7. It is suggested that HMEs are not used as a prevention strategy for ventilator-associated pneumonia.
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              Physiology and Pathophysiology of Human Airway Mucus.

              The mucus clearance system is the dominant mechanical host defense system of the human lung. Mucus is cleared from the lung by cilia and airflow, including both two-phase gas liquid pumping and cough-dependent mechanisms, and mucus transport rates are heavily dependent on mucus concentration. Importantly, mucus transport rates are accurately predicted by the gel-on-brush model of the mucociliary apparatus from the relative osmotic moduli of the mucus and periciliary-glycocalyceal (PCL-G) layers. The fluid available to hydrate mucus is generated by transepithelial fluid transport. Feedback interactions between mucus concentrations and cilia beating, via purinergic signaling, coordinate Na+ absorptive vs Cl- secretory rates to maintain mucus hydration in health. In disease, mucus becomes hyperconcentrated (dehydrated). Multiple mechanisms derange the ion transport pathways that normally hydrate mucus in muco-obstructive lung diseases, e.g., CF, COPD, NCFB, and PCD. A key step in muco-obstructive disease pathogenesis is the osmotic compression of the mucus layer onto the airway surface with the formation of adherent mucus plaques and plugs, particularly in distal airways. Mucus plaques create locally hypoxic conditions and produce airflow obstruction, inflammation, infection, and, ultimately, airway wall damage. Therapies to clear adherent mucus with hydrating and mucolytic agents are rational, and strategies to develop these agents are reviewed.
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                Author and article information

                Contributors
                claude.danan@chicreteil.fr
                Journal
                Pediatr Pulmonol
                Pediatr Pulmonol
                10.1002/(ISSN)1099-0496
                PPUL
                Pediatric Pulmonology
                John Wiley and Sons Inc. (Hoboken )
                8755-6863
                1099-0496
                19 September 2022
                January 2023
                : 58
                : 1 ( doiID: 10.1002/ppul.v58.1 )
                : 66-72
                Affiliations
                [ 1 ] Neonatal Intensive Care Unit Centre Hospitalier Intercommunal de Creteil Creteil France
                [ 2 ] EMR 7000 IMRB, CNRS, Universite Paris Est Creteil Creteil France
                [ 3 ] Clinical Research Center Centre Hospitalier Intercommunal de Creteil Creteil France
                [ 4 ] Pediatrics, Centre Hospitalier Intercommunal de Creteil Creteil France
                [ 5 ] Faculte de Sante Universite Paris Est Creteil Creteil France
                [ 6 ] GRC CARMAS, IMRB Universite Paris Est Creteil Creteil France
                Author notes
                [*] [* ] Correspondence Claude Danan, MD, Pédiatrie Néonatale, CHI Creteil, 40 Ave de Verdun, 94010 Creteil, France.

                Email: claude.danan@ 123456chicreteil.fr

                Author information
                http://orcid.org/0000-0001-9204-5713
                http://orcid.org/0000-0003-0547-4566
                Article
                PPUL26157
                10.1002/ppul.26157
                10086959
                36102687
                01d46653-7599-40a1-b5b3-2096cfc1adb5
                © 2022 The Authors. Pediatric Pulmonology published by Wiley Periodicals LLC.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 12 August 2022
                : 20 May 2022
                : 03 September 2022
                Page count
                Figures: 2, Tables: 2, Pages: 7, Words: 4002
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                January 2023
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.7 mode:remove_FC converted:11.04.2023

                Pediatrics
                elbw,hfov,humidification
                Pediatrics
                elbw, hfov, humidification

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