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Epinephrine Improves the Efficacy of Nebulized Hypertonic Saline in Moderate Bronchiolitis: A Randomised Clinical Trial
There is no evidence that the epinephrine-3% hypertonic saline combination is more effective than 3% hypertonic saline alone for treating infants hospitalized with acute bronchiolitis. We evaluated the efficacy of nebulized epinephrine in 3% hypertonic saline. We performed a randomized, double-blind...
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Published in: | PloS one 2015-11, Vol.10 (11), p.e0142847-e0142847 |
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creator | Flores-González, J Carlos Matamala-Morillo, Miguel A Rodríguez-Campoy, Patricia Pérez-Guerrero, Juan J Serrano-Moyano, Belén Comino-Vazquez, Paloma Palma-Zambrano, Encarnación Bulo-Concellón, Rocio Santos-Sánchez, Vanessa Lechuga-Sancho, Alfonso M |
description | There is no evidence that the epinephrine-3% hypertonic saline combination is more effective than 3% hypertonic saline alone for treating infants hospitalized with acute bronchiolitis. We evaluated the efficacy of nebulized epinephrine in 3% hypertonic saline.
We performed a randomized, double-blind, placebo-controlled clinical trial in 208 infants hospitalized with acute moderate bronchiolitis. Infants were randomly assigned to receive nebulized 3% hypertonic saline with either 3 mL of epinephrine or 3 mL of placebo, administered every four hours. The primary outcome measure was the length of hospital stay.
A total of 185 infants were analyzed: 94 in the epinephrine plus 3% hypertonic saline group and 91 in the placebo plus 3% hypertonic saline group. Baseline demographic and clinical characteristics were similar in both groups. Length of hospital stay was significantly reduced in the epinephrine group as compared with the placebo group (3.94 ±1.88 days vs. 4.82 ±2.30 days, P = 0.011). Disease severity also decreased significantly earlier in the epinephrine group (P = 0.029 and P = 0.036 on days 3 and 5, respectively).
In our setting, nebulized epinephrine in 3% hypertonic saline significantly shortens hospital stay in hospitalized infants with acute moderate bronchiolitis compared to 3% hypertonic saline alone, and improves the clinical scores of severity from the third day of treatment, but not before.
EudraCT 2009-016042-57. |
doi_str_mv | 10.1371/journal.pone.0142847 |
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We performed a randomized, double-blind, placebo-controlled clinical trial in 208 infants hospitalized with acute moderate bronchiolitis. Infants were randomly assigned to receive nebulized 3% hypertonic saline with either 3 mL of epinephrine or 3 mL of placebo, administered every four hours. The primary outcome measure was the length of hospital stay.
A total of 185 infants were analyzed: 94 in the epinephrine plus 3% hypertonic saline group and 91 in the placebo plus 3% hypertonic saline group. Baseline demographic and clinical characteristics were similar in both groups. Length of hospital stay was significantly reduced in the epinephrine group as compared with the placebo group (3.94 ±1.88 days vs. 4.82 ±2.30 days, P = 0.011). Disease severity also decreased significantly earlier in the epinephrine group (P = 0.029 and P = 0.036 on days 3 and 5, respectively).
In our setting, nebulized epinephrine in 3% hypertonic saline significantly shortens hospital stay in hospitalized infants with acute moderate bronchiolitis compared to 3% hypertonic saline alone, and improves the clinical scores of severity from the third day of treatment, but not before.
EudraCT 2009-016042-57.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0142847</identifier><identifier>PMID: 26575036</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acute Disease ; Administration, Inhalation ; Bronchiolitis - drug therapy ; Bronchiolitis - pathology ; Bronchodilator Agents - administration & dosage ; Bronchopneumonia ; Clinical trials ; Demographics ; Disease ; Double-Blind Method ; Edema ; Epinephrine ; Epinephrine - administration & dosage ; Female ; Hospitals ; Humans ; Infant ; Infants ; Infections ; Length of Stay ; Male ; Maternal & child health ; Nebulizers and Vaporizers ; Osmosis ; Pediatrics ; Placebo Effect ; Randomization ; Respiratory Rate ; Respiratory therapy ; Rodents ; Saline Solution, Hypertonic - administration & dosage ; Severity of Illness Index ; Treatment Outcome</subject><ispartof>PloS one, 2015-11, Vol.10 (11), p.e0142847-e0142847</ispartof><rights>2015 Flores-González et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Flores-González et al 2015 Flores-González et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-df67aecfe2cf184f087bcc3ecf190a634ca4f7159a0586110deed848511cf2253</citedby><cites>FETCH-LOGICAL-c526t-df67aecfe2cf184f087bcc3ecf190a634ca4f7159a0586110deed848511cf2253</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1733924350/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1733924350?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26575036$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Esposito, Susanna</contributor><creatorcontrib>Flores-González, J Carlos</creatorcontrib><creatorcontrib>Matamala-Morillo, Miguel A</creatorcontrib><creatorcontrib>Rodríguez-Campoy, Patricia</creatorcontrib><creatorcontrib>Pérez-Guerrero, Juan J</creatorcontrib><creatorcontrib>Serrano-Moyano, Belén</creatorcontrib><creatorcontrib>Comino-Vazquez, Paloma</creatorcontrib><creatorcontrib>Palma-Zambrano, Encarnación</creatorcontrib><creatorcontrib>Bulo-Concellón, Rocio</creatorcontrib><creatorcontrib>Santos-Sánchez, Vanessa</creatorcontrib><creatorcontrib>Lechuga-Sancho, Alfonso M</creatorcontrib><creatorcontrib>Bronchiolitis of Cadiz Study group (BronCaS)</creatorcontrib><creatorcontrib>Bronchiolitis of Cadiz Study group (BronCaS)</creatorcontrib><title>Epinephrine Improves the Efficacy of Nebulized Hypertonic Saline in Moderate Bronchiolitis: A Randomised Clinical Trial</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>There is no evidence that the epinephrine-3% hypertonic saline combination is more effective than 3% hypertonic saline alone for treating infants hospitalized with acute bronchiolitis. We evaluated the efficacy of nebulized epinephrine in 3% hypertonic saline.
We performed a randomized, double-blind, placebo-controlled clinical trial in 208 infants hospitalized with acute moderate bronchiolitis. Infants were randomly assigned to receive nebulized 3% hypertonic saline with either 3 mL of epinephrine or 3 mL of placebo, administered every four hours. The primary outcome measure was the length of hospital stay.
A total of 185 infants were analyzed: 94 in the epinephrine plus 3% hypertonic saline group and 91 in the placebo plus 3% hypertonic saline group. Baseline demographic and clinical characteristics were similar in both groups. Length of hospital stay was significantly reduced in the epinephrine group as compared with the placebo group (3.94 ±1.88 days vs. 4.82 ±2.30 days, P = 0.011). Disease severity also decreased significantly earlier in the epinephrine group (P = 0.029 and P = 0.036 on days 3 and 5, respectively).
In our setting, nebulized epinephrine in 3% hypertonic saline significantly shortens hospital stay in hospitalized infants with acute moderate bronchiolitis compared to 3% hypertonic saline alone, and improves the clinical scores of severity from the third day of treatment, but not before.
EudraCT 2009-016042-57.</description><subject>Acute Disease</subject><subject>Administration, Inhalation</subject><subject>Bronchiolitis - drug therapy</subject><subject>Bronchiolitis - pathology</subject><subject>Bronchodilator Agents - administration & dosage</subject><subject>Bronchopneumonia</subject><subject>Clinical trials</subject><subject>Demographics</subject><subject>Disease</subject><subject>Double-Blind Method</subject><subject>Edema</subject><subject>Epinephrine</subject><subject>Epinephrine - administration & dosage</subject><subject>Female</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Infant</subject><subject>Infants</subject><subject>Infections</subject><subject>Length of Stay</subject><subject>Male</subject><subject>Maternal & child health</subject><subject>Nebulizers and Vaporizers</subject><subject>Osmosis</subject><subject>Pediatrics</subject><subject>Placebo Effect</subject><subject>Randomization</subject><subject>Respiratory Rate</subject><subject>Respiratory therapy</subject><subject>Rodents</subject><subject>Saline Solution, Hypertonic - 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We evaluated the efficacy of nebulized epinephrine in 3% hypertonic saline.
We performed a randomized, double-blind, placebo-controlled clinical trial in 208 infants hospitalized with acute moderate bronchiolitis. Infants were randomly assigned to receive nebulized 3% hypertonic saline with either 3 mL of epinephrine or 3 mL of placebo, administered every four hours. The primary outcome measure was the length of hospital stay.
A total of 185 infants were analyzed: 94 in the epinephrine plus 3% hypertonic saline group and 91 in the placebo plus 3% hypertonic saline group. Baseline demographic and clinical characteristics were similar in both groups. Length of hospital stay was significantly reduced in the epinephrine group as compared with the placebo group (3.94 ±1.88 days vs. 4.82 ±2.30 days, P = 0.011). Disease severity also decreased significantly earlier in the epinephrine group (P = 0.029 and P = 0.036 on days 3 and 5, respectively).
In our setting, nebulized epinephrine in 3% hypertonic saline significantly shortens hospital stay in hospitalized infants with acute moderate bronchiolitis compared to 3% hypertonic saline alone, and improves the clinical scores of severity from the third day of treatment, but not before.
EudraCT 2009-016042-57.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26575036</pmid><doi>10.1371/journal.pone.0142847</doi><oa>free_for_read</oa></addata></record> |
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subjects | Acute Disease Administration, Inhalation Bronchiolitis - drug therapy Bronchiolitis - pathology Bronchodilator Agents - administration & dosage Bronchopneumonia Clinical trials Demographics Disease Double-Blind Method Edema Epinephrine Epinephrine - administration & dosage Female Hospitals Humans Infant Infants Infections Length of Stay Male Maternal & child health Nebulizers and Vaporizers Osmosis Pediatrics Placebo Effect Randomization Respiratory Rate Respiratory therapy Rodents Saline Solution, Hypertonic - administration & dosage Severity of Illness Index Treatment Outcome |
title | Epinephrine Improves the Efficacy of Nebulized Hypertonic Saline in Moderate Bronchiolitis: A Randomised Clinical Trial |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T18%3A20%3A36IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Epinephrine%20Improves%20the%20Efficacy%20of%20Nebulized%20Hypertonic%20Saline%20in%20Moderate%20Bronchiolitis:%20A%20Randomised%20Clinical%20Trial&rft.jtitle=PloS%20one&rft.au=Flores-Gonz%C3%A1lez,%20J%20Carlos&rft.aucorp=Bronchiolitis%20of%20Cadiz%20Study%20group%20(BronCaS)&rft.date=2015-11-17&rft.volume=10&rft.issue=11&rft.spage=e0142847&rft.epage=e0142847&rft.pages=e0142847-e0142847&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0142847&rft_dat=%3Cproquest_plos_%3E1735906460%3C/proquest_plos_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c526t-df67aecfe2cf184f087bcc3ecf190a634ca4f7159a0586110deed848511cf2253%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1733924350&rft_id=info:pmid/26575036&rfr_iscdi=true |