High flow therapy versus hypertonic saline in bronchiolitis: randomised controlled trial

Objective To demonstrate that heated humidified high-flow nasal cannula (HHHFNC) is superior to inhaled hypertonic saline solution (HSS) in improving respiratory distress in moderate bronchiolitis. In addition, it could improve comfort and reduce length of hospital stay (LOS) and admission to Paedia...

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Veröffentlicht in:Archives of disease in childhood 2014-06, Vol.99 (6), p.511-515
Hauptverfasser: Bueno Campaña, Mercedes, Olivares Ortiz, Jorge, Notario Muñoz, Cristina, Rupérez Lucas, Marta, Fernández Rincón, Adelaida, Patiño Hernández, Olga, Calvo Rey, Cristina
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container_end_page 515
container_issue 6
container_start_page 511
container_title Archives of disease in childhood
container_volume 99
creator Bueno Campaña, Mercedes
Olivares Ortiz, Jorge
Notario Muñoz, Cristina
Rupérez Lucas, Marta
Fernández Rincón, Adelaida
Patiño Hernández, Olga
Calvo Rey, Cristina
description Objective To demonstrate that heated humidified high-flow nasal cannula (HHHFNC) is superior to inhaled hypertonic saline solution (HSS) in improving respiratory distress in moderate bronchiolitis. In addition, it could improve comfort and reduce length of hospital stay (LOS) and admission to Paediatric Intensive Care Unit (PICU). Design Randomised Clinical Trial from 1 October 2010 to 31 December 2012. Setting Two urban secondary (no PICU available) paediatric hospitalisation units. Patients Hospitalised children aged up to 6 months with moderate acute bronchiolitis (Respiratory Distress Assessment Instrument, RDAI ≥4). Intervention Patients were randomised to HHHFNC or HSS. All of them received epinephrine as bronchodilator. Main outcomes Primary outcome was difference in mean Respiratory Assessment Change Score (RACS) between both groups measured in six previously defined consecutive moments. Secondary outcomes were difference in mean comfort scores in this period, LOS and rate of PICU admission. Results Seventy-five previously healthy patients were enrolled. Mean age was 2.4 months (95% CI 2.04 to 2.76). 43 were allocated to HSS group and 32 in HHHFNC. Data of 1 patient were lost, and 8 changed group over the study period. Intention-to-treat principle was applied. There were no significant differences in mean RACS and mean comfort scores between groups at the evaluation points. Median LOS or PICU admission rate were similar in both groups. No adverse events were observed. Conclusions HHHFNC was not superior to HSS in treatment of moderate acute bronchiolitis with respect to severity and comfort scores, LOS or PICU admission rate. Clinical Trial Registration ClinicalTrials.gov Identifier NCT01873144.
doi_str_mv 10.1136/archdischild-2013-305443
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In addition, it could improve comfort and reduce length of hospital stay (LOS) and admission to Paediatric Intensive Care Unit (PICU). Design Randomised Clinical Trial from 1 October 2010 to 31 December 2012. Setting Two urban secondary (no PICU available) paediatric hospitalisation units. Patients Hospitalised children aged up to 6 months with moderate acute bronchiolitis (Respiratory Distress Assessment Instrument, RDAI ≥4). Intervention Patients were randomised to HHHFNC or HSS. All of them received epinephrine as bronchodilator. Main outcomes Primary outcome was difference in mean Respiratory Assessment Change Score (RACS) between both groups measured in six previously defined consecutive moments. Secondary outcomes were difference in mean comfort scores in this period, LOS and rate of PICU admission. Results Seventy-five previously healthy patients were enrolled. Mean age was 2.4 months (95% CI 2.04 to 2.76). 43 were allocated to HSS group and 32 in HHHFNC. Data of 1 patient were lost, and 8 changed group over the study period. Intention-to-treat principle was applied. There were no significant differences in mean RACS and mean comfort scores between groups at the evaluation points. Median LOS or PICU admission rate were similar in both groups. No adverse events were observed. Conclusions HHHFNC was not superior to HSS in treatment of moderate acute bronchiolitis with respect to severity and comfort scores, LOS or PICU admission rate. Clinical Trial Registration ClinicalTrials.gov Identifier NCT01873144.</description><identifier>ISSN: 0003-9888</identifier><identifier>EISSN: 1468-2044</identifier><identifier>DOI: 10.1136/archdischild-2013-305443</identifier><identifier>PMID: 24521787</identifier><identifier>CODEN: ADCHAK</identifier><language>eng</language><publisher>London: BMJ Publishing Group</publisher><subject>Acute Disease ; Administration, Inhalation ; Admission Criteria ; Airway management ; Biological and medical sciences ; Bronchiolitis ; Bronchiolitis - drug therapy ; Bronchiolitis - therapy ; Care and treatment ; Chronic obstructive pulmonary disease, asthma ; Clinical trials ; Evaluation ; Female ; General aspects ; Hospitalization ; Humans ; Infant ; Infant, Newborn ; Intensive Care Units, Pediatric ; Length of Stay - statistics &amp; numerical data ; Male ; Medical sciences ; Miscellaneous ; Nurses ; Oxygen equipment (Medical care) ; Oxygen Inhalation Therapy - methods ; Oxygen therapy ; Patients ; Pediatrics ; Physiologic salines ; Pneumology ; Prevention and actions ; Protocol Analysis ; Public health. Hygiene ; Public health. Hygiene-occupational medicine ; Saline solution ; Saline Solution, Hypertonic - therapeutic use ; Severity of Illness Index ; Statistical analysis ; Treatment Outcome ; Ventilation ; Ventilators ; Young Children</subject><ispartof>Archives of disease in childhood, 2014-06, Vol.99 (6), p.511-515</ispartof><rights>Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>2015 INIST-CNRS</rights><rights>Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.</rights><rights>Copyright: 2014 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b505t-362a66b15420e3a298494c1e8d8d0d13b2f235214d18f2f175ed557eb8ae63dd3</citedby><cites>FETCH-LOGICAL-b505t-362a66b15420e3a298494c1e8d8d0d13b2f235214d18f2f175ed557eb8ae63dd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://adc.bmj.com/content/99/6/511.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://adc.bmj.com/content/99/6/511.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,780,784,3196,23571,27924,27925,77600,77631</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=28468925$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24521787$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bueno Campaña, Mercedes</creatorcontrib><creatorcontrib>Olivares Ortiz, Jorge</creatorcontrib><creatorcontrib>Notario Muñoz, Cristina</creatorcontrib><creatorcontrib>Rupérez Lucas, Marta</creatorcontrib><creatorcontrib>Fernández Rincón, Adelaida</creatorcontrib><creatorcontrib>Patiño Hernández, Olga</creatorcontrib><creatorcontrib>Calvo Rey, Cristina</creatorcontrib><title>High flow therapy versus hypertonic saline in bronchiolitis: randomised controlled trial</title><title>Archives of disease in childhood</title><addtitle>Arch Dis Child</addtitle><description>Objective To demonstrate that heated humidified high-flow nasal cannula (HHHFNC) is superior to inhaled hypertonic saline solution (HSS) in improving respiratory distress in moderate bronchiolitis. In addition, it could improve comfort and reduce length of hospital stay (LOS) and admission to Paediatric Intensive Care Unit (PICU). Design Randomised Clinical Trial from 1 October 2010 to 31 December 2012. Setting Two urban secondary (no PICU available) paediatric hospitalisation units. Patients Hospitalised children aged up to 6 months with moderate acute bronchiolitis (Respiratory Distress Assessment Instrument, RDAI ≥4). Intervention Patients were randomised to HHHFNC or HSS. All of them received epinephrine as bronchodilator. Main outcomes Primary outcome was difference in mean Respiratory Assessment Change Score (RACS) between both groups measured in six previously defined consecutive moments. Secondary outcomes were difference in mean comfort scores in this period, LOS and rate of PICU admission. Results Seventy-five previously healthy patients were enrolled. Mean age was 2.4 months (95% CI 2.04 to 2.76). 43 were allocated to HSS group and 32 in HHHFNC. Data of 1 patient were lost, and 8 changed group over the study period. Intention-to-treat principle was applied. There were no significant differences in mean RACS and mean comfort scores between groups at the evaluation points. Median LOS or PICU admission rate were similar in both groups. No adverse events were observed. Conclusions HHHFNC was not superior to HSS in treatment of moderate acute bronchiolitis with respect to severity and comfort scores, LOS or PICU admission rate. 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In addition, it could improve comfort and reduce length of hospital stay (LOS) and admission to Paediatric Intensive Care Unit (PICU). Design Randomised Clinical Trial from 1 October 2010 to 31 December 2012. Setting Two urban secondary (no PICU available) paediatric hospitalisation units. Patients Hospitalised children aged up to 6 months with moderate acute bronchiolitis (Respiratory Distress Assessment Instrument, RDAI ≥4). Intervention Patients were randomised to HHHFNC or HSS. All of them received epinephrine as bronchodilator. Main outcomes Primary outcome was difference in mean Respiratory Assessment Change Score (RACS) between both groups measured in six previously defined consecutive moments. Secondary outcomes were difference in mean comfort scores in this period, LOS and rate of PICU admission. Results Seventy-five previously healthy patients were enrolled. Mean age was 2.4 months (95% CI 2.04 to 2.76). 43 were allocated to HSS group and 32 in HHHFNC. Data of 1 patient were lost, and 8 changed group over the study period. Intention-to-treat principle was applied. There were no significant differences in mean RACS and mean comfort scores between groups at the evaluation points. Median LOS or PICU admission rate were similar in both groups. No adverse events were observed. Conclusions HHHFNC was not superior to HSS in treatment of moderate acute bronchiolitis with respect to severity and comfort scores, LOS or PICU admission rate. Clinical Trial Registration ClinicalTrials.gov Identifier NCT01873144.</abstract><cop>London</cop><pub>BMJ Publishing Group</pub><pmid>24521787</pmid><doi>10.1136/archdischild-2013-305443</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
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subjects Acute Disease
Administration, Inhalation
Admission Criteria
Airway management
Biological and medical sciences
Bronchiolitis
Bronchiolitis - drug therapy
Bronchiolitis - therapy
Care and treatment
Chronic obstructive pulmonary disease, asthma
Clinical trials
Evaluation
Female
General aspects
Hospitalization
Humans
Infant
Infant, Newborn
Intensive Care Units, Pediatric
Length of Stay - statistics & numerical data
Male
Medical sciences
Miscellaneous
Nurses
Oxygen equipment (Medical care)
Oxygen Inhalation Therapy - methods
Oxygen therapy
Patients
Pediatrics
Physiologic salines
Pneumology
Prevention and actions
Protocol Analysis
Public health. Hygiene
Public health. Hygiene-occupational medicine
Saline solution
Saline Solution, Hypertonic - therapeutic use
Severity of Illness Index
Statistical analysis
Treatment Outcome
Ventilation
Ventilators
Young Children
title High flow therapy versus hypertonic saline in bronchiolitis: randomised controlled trial
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