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Effects of inhaled hypertonic (7%) saline on lung function test in preschool children with cystic fibrosis: results of a crossover, randomized clinical trial
This crossover, randomized, double-blind study (conducted over a 32-week period) was performed to determine, in clinically stable Cystic fibrosis (CF) preschool children: the effects of 7% inhaled hypertonic saline on spirometry and interrupter resistance technique (Rint), and the possible side effe...
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Published in: | Italian journal of pediatrics 2017-07, Vol.43 (1), p.60-60, Article 60 |
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creator | Nenna, Raffaella Midulla, Fabio Lambiase, Caterina De Castro, Giovanna Zicari, Anna Maria Indinnimeo, Luciana Cimino, Giuseppe Troiani, Patrizia Quattrucci, Serena Tancredi, Giancarlo |
description | This crossover, randomized, double-blind study (conducted over a 32-week period) was performed to determine, in clinically stable Cystic fibrosis (CF) preschool children: the effects of 7% inhaled hypertonic saline on spirometry and interrupter resistance technique (Rint), and the possible side effects.
Twelve CF children (6M, mean age ± SD: 5.7 ± 0.8 yrs) were enrolled and randomly assigned to receive hypertonic saline (HS-4 ml 7% sodium chloride), or normal saline (NS-0.9% sodium chloride) twice a day. After a 16 weeks period, therapy was exchanged to allow all the patients enrolled in the study to carry out both treatments. Monitoring visits, spirometry (COSMED Quark PFT4 ergo) and Rint were scheduled at 0,4,16,20,32 weeks. At T0, spirometric measurements and Rint were performed immediately before and 30 min after the inhalation therapy. Salbutamol (400 mcg) was administered before the drug at each visit.
After a 16-weeks treatment with HS an improvement of FVC (p = 0.02) and a favorable trend of FEV1 were registered. A worsening of FEV
(p |
doi_str_mv | 10.1186/s13052-017-0376-6 |
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Twelve CF children (6M, mean age ± SD: 5.7 ± 0.8 yrs) were enrolled and randomly assigned to receive hypertonic saline (HS-4 ml 7% sodium chloride), or normal saline (NS-0.9% sodium chloride) twice a day. After a 16 weeks period, therapy was exchanged to allow all the patients enrolled in the study to carry out both treatments. Monitoring visits, spirometry (COSMED Quark PFT4 ergo) and Rint were scheduled at 0,4,16,20,32 weeks. At T0, spirometric measurements and Rint were performed immediately before and 30 min after the inhalation therapy. Salbutamol (400 mcg) was administered before the drug at each visit.
After a 16-weeks treatment with HS an improvement of FVC (p = 0.02) and a favorable trend of FEV1 were registered. A worsening of FEV
(p < 0.0001) and of FEF25-75 (p = 0.019) were found in NS group. No differences were found in expiratory and inspiratory Rint in both groups. No serious adverse events occurred.
Seven percent hypertonic saline therapy proved to be a useful and safe treatment in young CF children with clinically stable conditions.
ISRCTN12345678 .</description><identifier>ISSN: 1824-7288</identifier><identifier>ISSN: 1720-8424</identifier><identifier>EISSN: 1824-7288</identifier><identifier>DOI: 10.1186/s13052-017-0376-6</identifier><identifier>PMID: 28709466</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Administration, Inhalation ; Age ; Airway management ; Albuterol - administration & dosage ; Anti-Asthmatic Agents - administration & dosage ; Child, Preschool ; Children ; Children & youth ; Chloride ; Clinical trials ; Cross-Over Studies ; Cystic fibrosis ; Cystic Fibrosis - physiopathology ; Cystic Fibrosis - therapy ; Double-Blind Method ; Female ; Humans ; Hypertonic saline ; Inhalation ; Male ; Mutation ; Pediatrics ; Respiratory Function Tests ; Saline Solution, Hypertonic - administration & dosage ; Sodium ; Studies ; Therapy</subject><ispartof>Italian journal of pediatrics, 2017-07, Vol.43 (1), p.60-60, Article 60</ispartof><rights>Copyright BioMed Central 2017</rights><rights>The Author(s). 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c560t-54bc4b77ad7863e573fe7fbcc4e41e3ce1698f69ee53b4406a4ff113ae37436d3</citedby><cites>FETCH-LOGICAL-c560t-54bc4b77ad7863e573fe7fbcc4e41e3ce1698f69ee53b4406a4ff113ae37436d3</cites><orcidid>0000-0001-8880-3462</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5512793/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1925960771?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28709466$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nenna, Raffaella</creatorcontrib><creatorcontrib>Midulla, Fabio</creatorcontrib><creatorcontrib>Lambiase, Caterina</creatorcontrib><creatorcontrib>De Castro, Giovanna</creatorcontrib><creatorcontrib>Zicari, Anna Maria</creatorcontrib><creatorcontrib>Indinnimeo, Luciana</creatorcontrib><creatorcontrib>Cimino, Giuseppe</creatorcontrib><creatorcontrib>Troiani, Patrizia</creatorcontrib><creatorcontrib>Quattrucci, Serena</creatorcontrib><creatorcontrib>Tancredi, Giancarlo</creatorcontrib><title>Effects of inhaled hypertonic (7%) saline on lung function test in preschool children with cystic fibrosis: results of a crossover, randomized clinical trial</title><title>Italian journal of pediatrics</title><addtitle>Ital J Pediatr</addtitle><description>This crossover, randomized, double-blind study (conducted over a 32-week period) was performed to determine, in clinically stable Cystic fibrosis (CF) preschool children: the effects of 7% inhaled hypertonic saline on spirometry and interrupter resistance technique (Rint), and the possible side effects.
Twelve CF children (6M, mean age ± SD: 5.7 ± 0.8 yrs) were enrolled and randomly assigned to receive hypertonic saline (HS-4 ml 7% sodium chloride), or normal saline (NS-0.9% sodium chloride) twice a day. After a 16 weeks period, therapy was exchanged to allow all the patients enrolled in the study to carry out both treatments. Monitoring visits, spirometry (COSMED Quark PFT4 ergo) and Rint were scheduled at 0,4,16,20,32 weeks. At T0, spirometric measurements and Rint were performed immediately before and 30 min after the inhalation therapy. Salbutamol (400 mcg) was administered before the drug at each visit.
After a 16-weeks treatment with HS an improvement of FVC (p = 0.02) and a favorable trend of FEV1 were registered. A worsening of FEV
(p < 0.0001) and of FEF25-75 (p = 0.019) were found in NS group. No differences were found in expiratory and inspiratory Rint in both groups. No serious adverse events occurred.
Seven percent hypertonic saline therapy proved to be a useful and safe treatment in young CF children with clinically stable conditions.
ISRCTN12345678 .</description><subject>Administration, Inhalation</subject><subject>Age</subject><subject>Airway management</subject><subject>Albuterol - administration & dosage</subject><subject>Anti-Asthmatic Agents - administration & dosage</subject><subject>Child, Preschool</subject><subject>Children</subject><subject>Children & youth</subject><subject>Chloride</subject><subject>Clinical trials</subject><subject>Cross-Over Studies</subject><subject>Cystic fibrosis</subject><subject>Cystic Fibrosis - physiopathology</subject><subject>Cystic Fibrosis - therapy</subject><subject>Double-Blind Method</subject><subject>Female</subject><subject>Humans</subject><subject>Hypertonic saline</subject><subject>Inhalation</subject><subject>Male</subject><subject>Mutation</subject><subject>Pediatrics</subject><subject>Respiratory Function Tests</subject><subject>Saline Solution, Hypertonic - administration & dosage</subject><subject>Sodium</subject><subject>Studies</subject><subject>Therapy</subject><issn>1824-7288</issn><issn>1720-8424</issn><issn>1824-7288</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkt9qFDEUxgdRbF19AG8kIEIFR5NJJpn0QiilaqHgjV6HTOZkJ0s2WZOZyvoufVeznVpar_LvO78v5_BV1WuCPxLS8U-ZUNw2NSaixlTwmj-pjknXsFo0Xff0wf6oepHzBmPatJw8r46aTmDJOD-ubi6sBTNlFC1yYdQeBjTud5CmGJxBJ-Lde5S1dwFQDMjPYY3sHMzkymmCPJUitEuQzRijR2Z0fkgQ0G83jcjs81QY1vUpZpdPUdHNfvHSyJTLHK8hfUBJhyFu3Z_ibYqVM9qjKTntX1bPrPYZXt2tq-rnl4sf59_qq-9fL8_PrmrTcjzVLesN64XQg-g4hVZQC8L2xjBgBKgBwmVnuQRoac8Y5ppZSwjVQAWjfKCr6nLhDlFv1C65rU57FbVTtxcxrZVOpRcPyuAeA9DiM_RMWCZZazpJG0u7xhjaFdbnhbWb-y0MBsKUtH8EffwS3KjW8Vq1LWmEpAVwcgdI8ddcZqy2LhvwXgeIc1ZENphIJkubq-rtf9JNnFMoozqoWsmxEKSoyKK6HXkCe_8ZgtUhSGoJkipBUocgKV5q3jzs4r7iX3LoX847xs0</recordid><startdate>20170715</startdate><enddate>20170715</enddate><creator>Nenna, Raffaella</creator><creator>Midulla, Fabio</creator><creator>Lambiase, Caterina</creator><creator>De Castro, Giovanna</creator><creator>Zicari, Anna Maria</creator><creator>Indinnimeo, Luciana</creator><creator>Cimino, Giuseppe</creator><creator>Troiani, Patrizia</creator><creator>Quattrucci, Serena</creator><creator>Tancredi, Giancarlo</creator><general>BioMed Central</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-8880-3462</orcidid></search><sort><creationdate>20170715</creationdate><title>Effects of inhaled hypertonic (7%) saline on lung function test in preschool children with cystic fibrosis: results of a crossover, randomized clinical trial</title><author>Nenna, Raffaella ; Midulla, Fabio ; Lambiase, Caterina ; De Castro, Giovanna ; Zicari, Anna Maria ; Indinnimeo, Luciana ; Cimino, Giuseppe ; Troiani, Patrizia ; Quattrucci, Serena ; Tancredi, Giancarlo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c560t-54bc4b77ad7863e573fe7fbcc4e41e3ce1698f69ee53b4406a4ff113ae37436d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Administration, Inhalation</topic><topic>Age</topic><topic>Airway management</topic><topic>Albuterol - administration & dosage</topic><topic>Anti-Asthmatic Agents - administration & dosage</topic><topic>Child, Preschool</topic><topic>Children</topic><topic>Children & youth</topic><topic>Chloride</topic><topic>Clinical trials</topic><topic>Cross-Over Studies</topic><topic>Cystic fibrosis</topic><topic>Cystic Fibrosis - physiopathology</topic><topic>Cystic Fibrosis - therapy</topic><topic>Double-Blind Method</topic><topic>Female</topic><topic>Humans</topic><topic>Hypertonic saline</topic><topic>Inhalation</topic><topic>Male</topic><topic>Mutation</topic><topic>Pediatrics</topic><topic>Respiratory Function Tests</topic><topic>Saline Solution, Hypertonic - administration & dosage</topic><topic>Sodium</topic><topic>Studies</topic><topic>Therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nenna, Raffaella</creatorcontrib><creatorcontrib>Midulla, Fabio</creatorcontrib><creatorcontrib>Lambiase, Caterina</creatorcontrib><creatorcontrib>De Castro, Giovanna</creatorcontrib><creatorcontrib>Zicari, Anna Maria</creatorcontrib><creatorcontrib>Indinnimeo, Luciana</creatorcontrib><creatorcontrib>Cimino, Giuseppe</creatorcontrib><creatorcontrib>Troiani, Patrizia</creatorcontrib><creatorcontrib>Quattrucci, Serena</creatorcontrib><creatorcontrib>Tancredi, Giancarlo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Italian journal of pediatrics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nenna, Raffaella</au><au>Midulla, Fabio</au><au>Lambiase, Caterina</au><au>De Castro, Giovanna</au><au>Zicari, Anna Maria</au><au>Indinnimeo, Luciana</au><au>Cimino, Giuseppe</au><au>Troiani, Patrizia</au><au>Quattrucci, Serena</au><au>Tancredi, Giancarlo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of inhaled hypertonic (7%) saline on lung function test in preschool children with cystic fibrosis: results of a crossover, randomized clinical trial</atitle><jtitle>Italian journal of pediatrics</jtitle><addtitle>Ital J Pediatr</addtitle><date>2017-07-15</date><risdate>2017</risdate><volume>43</volume><issue>1</issue><spage>60</spage><epage>60</epage><pages>60-60</pages><artnum>60</artnum><issn>1824-7288</issn><issn>1720-8424</issn><eissn>1824-7288</eissn><abstract>This crossover, randomized, double-blind study (conducted over a 32-week period) was performed to determine, in clinically stable Cystic fibrosis (CF) preschool children: the effects of 7% inhaled hypertonic saline on spirometry and interrupter resistance technique (Rint), and the possible side effects.
Twelve CF children (6M, mean age ± SD: 5.7 ± 0.8 yrs) were enrolled and randomly assigned to receive hypertonic saline (HS-4 ml 7% sodium chloride), or normal saline (NS-0.9% sodium chloride) twice a day. After a 16 weeks period, therapy was exchanged to allow all the patients enrolled in the study to carry out both treatments. Monitoring visits, spirometry (COSMED Quark PFT4 ergo) and Rint were scheduled at 0,4,16,20,32 weeks. At T0, spirometric measurements and Rint were performed immediately before and 30 min after the inhalation therapy. Salbutamol (400 mcg) was administered before the drug at each visit.
After a 16-weeks treatment with HS an improvement of FVC (p = 0.02) and a favorable trend of FEV1 were registered. A worsening of FEV
(p < 0.0001) and of FEF25-75 (p = 0.019) were found in NS group. No differences were found in expiratory and inspiratory Rint in both groups. No serious adverse events occurred.
Seven percent hypertonic saline therapy proved to be a useful and safe treatment in young CF children with clinically stable conditions.
ISRCTN12345678 .</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>28709466</pmid><doi>10.1186/s13052-017-0376-6</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-8880-3462</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Inhalation Age Airway management Albuterol - administration & dosage Anti-Asthmatic Agents - administration & dosage Child, Preschool Children Children & youth Chloride Clinical trials Cross-Over Studies Cystic fibrosis Cystic Fibrosis - physiopathology Cystic Fibrosis - therapy Double-Blind Method Female Humans Hypertonic saline Inhalation Male Mutation Pediatrics Respiratory Function Tests Saline Solution, Hypertonic - administration & dosage Sodium Studies Therapy |
title | Effects of inhaled hypertonic (7%) saline on lung function test in preschool children with cystic fibrosis: results of a crossover, randomized clinical trial |
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