Randomised study of myringotomy, amoxycillin/clavulanate, or both for acute otitis media in infants
In a prospective study, 105 infants aged 3-12 months with acute otitis media were randomly assigned to one of three treatment groups: amoxycillin/clavulanate ('Augmentin') alone (36 patients), myringotomy plus placebo (35 patients), or augmentin plus myringotomy (34 patients). The last two...
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Veröffentlicht in: | The Lancet (British edition) 1989-07, Vol.2 (8655), p.141-143 |
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creator | ENGELHARD, D COHEN, D STRAUSS, N SACKS, T.G JORCZAK-SARNI, L SHAPIRO, M |
description | In a prospective study, 105 infants aged 3-12 months with acute otitis media were randomly assigned to one of three treatment groups: amoxycillin/clavulanate ('Augmentin') alone (36 patients), myringotomy plus placebo (35 patients), or augmentin plus myringotomy (34 patients). The last two groups were double-blinded. Bacterial pathogens, mainly Haemophilus influenzae (of which 20% were beta-lactamase producers) and Streptococcus pneumoniae, were isolated from 60% of the ear exudates and all isolates were sensitive to augmentin. Most of the infants improved clinically within 3-6 days irrespective of the treatment protocol. As judged by otoscopy, 60% of the patients receiving augmentin, with or without myringotomy, recovered completely compared with 23% of patients treated with myringotomy plus placebo. Treatment with augmentin was also more effective than myringotomy with regard to persistence of ear infection. In the myringotomy plus augmentin group closure of the incision and resolution of the discharge from the incision site was faster than in the myringotomy plus placebo group. The addition of myringotomy to augmentin did not seem to affect either the persistence of the infection after treatment or the residual middle ear effusion. |
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The last two groups were double-blinded. Bacterial pathogens, mainly Haemophilus influenzae (of which 20% were beta-lactamase producers) and Streptococcus pneumoniae, were isolated from 60% of the ear exudates and all isolates were sensitive to augmentin. Most of the infants improved clinically within 3-6 days irrespective of the treatment protocol. As judged by otoscopy, 60% of the patients receiving augmentin, with or without myringotomy, recovered completely compared with 23% of patients treated with myringotomy plus placebo. Treatment with augmentin was also more effective than myringotomy with regard to persistence of ear infection. In the myringotomy plus augmentin group closure of the incision and resolution of the discharge from the incision site was faster than in the myringotomy plus placebo group. The addition of myringotomy to augmentin did not seem to affect either the persistence of the infection after treatment or the residual middle ear effusion.</description><identifier>ISSN: 0140-6736</identifier><identifier>EISSN: 1474-547X</identifier><identifier>PMID: 2567903</identifier><identifier>CODEN: LANCAO</identifier><language>eng</language><publisher>London: Lancet</publisher><subject>Acute Disease ; Amoxicillin - administration & dosage ; Amoxicillin - therapeutic use ; Amoxicillin-Potassium Clavulanate Combination ; Bacterial Infections - drug therapy ; Biological and medical sciences ; Clavulanic Acids - administration & dosage ; Clavulanic Acids - therapeutic use ; Clinical Trials as Topic ; Combined Modality Therapy ; Diarrhea - chemically induced ; Double-Blind Method ; Drug Administration Schedule ; Ent. Stomatology ; Evaluation Studies as Topic ; Female ; Follow-Up Studies ; Humans ; Infant ; Male ; Medical sciences ; Otitis Media with Effusion - therapy ; Pharmacology. Drug treatments ; Prospective Studies ; Random Allocation ; Time Factors ; Tympanic Membrane - surgery</subject><ispartof>The Lancet (British edition), 1989-07, Vol.2 (8655), p.141-143</ispartof><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6733409$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2567903$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ENGELHARD, D</creatorcontrib><creatorcontrib>COHEN, D</creatorcontrib><creatorcontrib>STRAUSS, N</creatorcontrib><creatorcontrib>SACKS, T.G</creatorcontrib><creatorcontrib>JORCZAK-SARNI, L</creatorcontrib><creatorcontrib>SHAPIRO, M</creatorcontrib><title>Randomised study of myringotomy, amoxycillin/clavulanate, or both for acute otitis media in infants</title><title>The Lancet (British edition)</title><addtitle>Lancet</addtitle><description>In a prospective study, 105 infants aged 3-12 months with acute otitis media were randomly assigned to one of three treatment groups: amoxycillin/clavulanate ('Augmentin') alone (36 patients), myringotomy plus placebo (35 patients), or augmentin plus myringotomy (34 patients). The last two groups were double-blinded. Bacterial pathogens, mainly Haemophilus influenzae (of which 20% were beta-lactamase producers) and Streptococcus pneumoniae, were isolated from 60% of the ear exudates and all isolates were sensitive to augmentin. Most of the infants improved clinically within 3-6 days irrespective of the treatment protocol. As judged by otoscopy, 60% of the patients receiving augmentin, with or without myringotomy, recovered completely compared with 23% of patients treated with myringotomy plus placebo. Treatment with augmentin was also more effective than myringotomy with regard to persistence of ear infection. In the myringotomy plus augmentin group closure of the incision and resolution of the discharge from the incision site was faster than in the myringotomy plus placebo group. The addition of myringotomy to augmentin did not seem to affect either the persistence of the infection after treatment or the residual middle ear effusion.</description><subject>Acute Disease</subject><subject>Amoxicillin - administration & dosage</subject><subject>Amoxicillin - therapeutic use</subject><subject>Amoxicillin-Potassium Clavulanate Combination</subject><subject>Bacterial Infections - drug therapy</subject><subject>Biological and medical sciences</subject><subject>Clavulanic Acids - administration & dosage</subject><subject>Clavulanic Acids - therapeutic use</subject><subject>Clinical Trials as Topic</subject><subject>Combined Modality Therapy</subject><subject>Diarrhea - chemically induced</subject><subject>Double-Blind Method</subject><subject>Drug Administration Schedule</subject><subject>Ent. Stomatology</subject><subject>Evaluation Studies as Topic</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Infant</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Otitis Media with Effusion - therapy</subject><subject>Pharmacology. Drug treatments</subject><subject>Prospective Studies</subject><subject>Random Allocation</subject><subject>Time Factors</subject><subject>Tympanic Membrane - surgery</subject><issn>0140-6736</issn><issn>1474-547X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kFtLxDAQhYMo67r6E4Q8iE9bTJsmMY-yeIMFQRR8K9NcNNImtUnF_nsDFmFgBs7HcM45QOuyFnXBavF2iNakrEnBBeXH6CTGT0JIzQlboVXFuJCErpF6Bq9D76LROKZJzzhY3M-j8-8hhX7eYujDz6xc1zl_pTr4njrwkMwWhxG3IX1gmw9QUzI4JJdcxL3RDrDzeSz4FE_RkYUumrNlb9Dr3e3L7qHYP90_7m72xVBykQoJbVtVooWSAhOaacGYkBVntS2plga4tMxeM6W5ZsCqklitlaSEcAFES7pBl39_hzF8TSamJudSpsuGTZhikxMLJijJ4PkCTm022wyj62Gcm6WVrF8sOkQFnR3BKxf_sVworYmkv9UBbTM</recordid><startdate>19890715</startdate><enddate>19890715</enddate><creator>ENGELHARD, D</creator><creator>COHEN, D</creator><creator>STRAUSS, N</creator><creator>SACKS, T.G</creator><creator>JORCZAK-SARNI, L</creator><creator>SHAPIRO, M</creator><general>Lancet</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19890715</creationdate><title>Randomised study of myringotomy, amoxycillin/clavulanate, or both for acute otitis media in infants</title><author>ENGELHARD, D ; COHEN, D ; STRAUSS, N ; SACKS, T.G ; JORCZAK-SARNI, L ; SHAPIRO, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p167t-9abb227ba13a57d5d755792654f13d9ea69f5f85cd6d5a5210fddc930067a0d93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Acute Disease</topic><topic>Amoxicillin - administration & dosage</topic><topic>Amoxicillin - therapeutic use</topic><topic>Amoxicillin-Potassium Clavulanate Combination</topic><topic>Bacterial Infections - drug therapy</topic><topic>Biological and medical sciences</topic><topic>Clavulanic Acids - administration & dosage</topic><topic>Clavulanic Acids - therapeutic use</topic><topic>Clinical Trials as Topic</topic><topic>Combined Modality Therapy</topic><topic>Diarrhea - chemically induced</topic><topic>Double-Blind Method</topic><topic>Drug Administration Schedule</topic><topic>Ent. Stomatology</topic><topic>Evaluation Studies as Topic</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Infant</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Otitis Media with Effusion - therapy</topic><topic>Pharmacology. Drug treatments</topic><topic>Prospective Studies</topic><topic>Random Allocation</topic><topic>Time Factors</topic><topic>Tympanic Membrane - surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ENGELHARD, D</creatorcontrib><creatorcontrib>COHEN, D</creatorcontrib><creatorcontrib>STRAUSS, N</creatorcontrib><creatorcontrib>SACKS, T.G</creatorcontrib><creatorcontrib>JORCZAK-SARNI, L</creatorcontrib><creatorcontrib>SHAPIRO, M</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>The Lancet (British edition)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ENGELHARD, D</au><au>COHEN, D</au><au>STRAUSS, N</au><au>SACKS, T.G</au><au>JORCZAK-SARNI, L</au><au>SHAPIRO, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Randomised study of myringotomy, amoxycillin/clavulanate, or both for acute otitis media in infants</atitle><jtitle>The Lancet (British edition)</jtitle><addtitle>Lancet</addtitle><date>1989-07-15</date><risdate>1989</risdate><volume>2</volume><issue>8655</issue><spage>141</spage><epage>143</epage><pages>141-143</pages><issn>0140-6736</issn><eissn>1474-547X</eissn><coden>LANCAO</coden><abstract>In a prospective study, 105 infants aged 3-12 months with acute otitis media were randomly assigned to one of three treatment groups: amoxycillin/clavulanate ('Augmentin') alone (36 patients), myringotomy plus placebo (35 patients), or augmentin plus myringotomy (34 patients). The last two groups were double-blinded. Bacterial pathogens, mainly Haemophilus influenzae (of which 20% were beta-lactamase producers) and Streptococcus pneumoniae, were isolated from 60% of the ear exudates and all isolates were sensitive to augmentin. Most of the infants improved clinically within 3-6 days irrespective of the treatment protocol. As judged by otoscopy, 60% of the patients receiving augmentin, with or without myringotomy, recovered completely compared with 23% of patients treated with myringotomy plus placebo. Treatment with augmentin was also more effective than myringotomy with regard to persistence of ear infection. In the myringotomy plus augmentin group closure of the incision and resolution of the discharge from the incision site was faster than in the myringotomy plus placebo group. The addition of myringotomy to augmentin did not seem to affect either the persistence of the infection after treatment or the residual middle ear effusion.</abstract><cop>London</cop><pub>Lancet</pub><pmid>2567903</pmid><tpages>3</tpages></addata></record> |
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subjects | Acute Disease Amoxicillin - administration & dosage Amoxicillin - therapeutic use Amoxicillin-Potassium Clavulanate Combination Bacterial Infections - drug therapy Biological and medical sciences Clavulanic Acids - administration & dosage Clavulanic Acids - therapeutic use Clinical Trials as Topic Combined Modality Therapy Diarrhea - chemically induced Double-Blind Method Drug Administration Schedule Ent. Stomatology Evaluation Studies as Topic Female Follow-Up Studies Humans Infant Male Medical sciences Otitis Media with Effusion - therapy Pharmacology. Drug treatments Prospective Studies Random Allocation Time Factors Tympanic Membrane - surgery |
title | Randomised study of myringotomy, amoxycillin/clavulanate, or both for acute otitis media in infants |
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