BACTERIOLOGICAL AND CLINICAL EVALUATION OF PIPERACILLIN IN THE FIELD OF OBSTETRICS AND GYNECOLOGY
In vitro activity of piperacillin (PIPC) against 150 recent clinical isolates from obstetric and gynecologic infections was performed in comparison with sulbenicillin (SBPC), cefmetazole (CMZ), cefotiam (CTM) and cefsulodin (CFS). At 6.25μglml PIPC inhibited 93% of S. epidermidis, 86% of S. faecalis...
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Veröffentlicht in: | Japanese journal of antibiotics 1982/10/25, Vol.35(10), pp.2323-2329 |
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container_title | Japanese journal of antibiotics |
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creator | NINOMIYA, KEIU MAKINO, SHIGENORI HASEGAWA, YUKIO YOSHIMOTO, TOSHIKO MASUDA, KAORUKO HAMAYA, KEIKO |
description | In vitro activity of piperacillin (PIPC) against 150 recent clinical isolates from obstetric and gynecologic infections was performed in comparison with sulbenicillin (SBPC), cefmetazole (CMZ), cefotiam (CTM) and cefsulodin (CFS). At 6.25μglml PIPC inhibited 93% of S. epidermidis, 86% of S. faecalis, 67% of E. coli and 80% of Klebsiella. At 0.2μg/ml PIPC inhibited 100% of Peptococcus, 73% of Peptostreptococcus and 100%, of B. melaninogenicus group. At 3.13μg/mi PIPC inhibited 71% of B. fragilis 9 strains, B. distasonis 3 strains, B. thetaiotaomicron 1 strain, B. ovatus 1 strain.PIPC was constantly more active than SBPC, and it was especially more active against S. faecalis, Peptococcus, Peptostreptococcus and B. melaninogenicus group than other antibiotics. These findings show that PIPC is a broad spectrum penicillin against both Gram-positive and Gram-negative organisms including anaerobic organisms. PIPC was administered to 5 patients intravenously and all cases proved to be effective. No side effects and no abnormalities in laboratory findings were observed. These results suggest that PIPC may be highly effective in the treatment of bacterial infections. |
doi_str_mv | 10.11553/antibiotics1968b.35.2323 |
format | Article |
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At 6.25μglml PIPC inhibited 93% of S. epidermidis, 86% of S. faecalis, 67% of E. coli and 80% of Klebsiella. At 0.2μg/ml PIPC inhibited 100% of Peptococcus, 73% of Peptostreptococcus and 100%, of B. melaninogenicus group. At 3.13μg/mi PIPC inhibited 71% of B. fragilis 9 strains, B. distasonis 3 strains, B. thetaiotaomicron 1 strain, B. ovatus 1 strain.PIPC was constantly more active than SBPC, and it was especially more active against S. faecalis, Peptococcus, Peptostreptococcus and B. melaninogenicus group than other antibiotics. These findings show that PIPC is a broad spectrum penicillin against both Gram-positive and Gram-negative organisms including anaerobic organisms. PIPC was administered to 5 patients intravenously and all cases proved to be effective. No side effects and no abnormalities in laboratory findings were observed. These results suggest that PIPC may be highly effective in the treatment of bacterial infections.</description><identifier>ISSN: 0368-2781</identifier><identifier>EISSN: 2186-5477</identifier><identifier>DOI: 10.11553/antibiotics1968b.35.2323</identifier><identifier>PMID: 6223149</identifier><language>jpn</language><publisher>Japan: Japan Antibiotics Research Association</publisher><subject>Adult ; Bacterial Infections - drug therapy ; Escherichia coli - drug effects ; Female ; Genital Diseases, Female - drug therapy ; Humans ; Pelvic Inflammatory Disease - drug therapy ; Penicillin Resistance ; Penicillins - pharmacology ; Penicillins - therapeutic use ; Piperacillin ; Pseudomonas - drug effects</subject><ispartof>The Japanese Journal of Antibiotics, 1982/10/25, Vol.35(10), pp.2323-2329</ispartof><rights>Japan Antibiotics Research Association</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27911,27912</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6223149$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>NINOMIYA, KEIU</creatorcontrib><creatorcontrib>MAKINO, SHIGENORI</creatorcontrib><creatorcontrib>HASEGAWA, YUKIO</creatorcontrib><creatorcontrib>YOSHIMOTO, TOSHIKO</creatorcontrib><creatorcontrib>MASUDA, KAORUKO</creatorcontrib><creatorcontrib>HAMAYA, KEIKO</creatorcontrib><title>BACTERIOLOGICAL AND CLINICAL EVALUATION OF PIPERACILLIN IN THE FIELD OF OBSTETRICS AND GYNECOLOGY</title><title>Japanese journal of antibiotics</title><addtitle>Jpn. J. Antibiotics</addtitle><description>In vitro activity of piperacillin (PIPC) against 150 recent clinical isolates from obstetric and gynecologic infections was performed in comparison with sulbenicillin (SBPC), cefmetazole (CMZ), cefotiam (CTM) and cefsulodin (CFS). At 6.25μglml PIPC inhibited 93% of S. epidermidis, 86% of S. faecalis, 67% of E. coli and 80% of Klebsiella. At 0.2μg/ml PIPC inhibited 100% of Peptococcus, 73% of Peptostreptococcus and 100%, of B. melaninogenicus group. At 3.13μg/mi PIPC inhibited 71% of B. fragilis 9 strains, B. distasonis 3 strains, B. thetaiotaomicron 1 strain, B. ovatus 1 strain.PIPC was constantly more active than SBPC, and it was especially more active against S. faecalis, Peptococcus, Peptostreptococcus and B. melaninogenicus group than other antibiotics. These findings show that PIPC is a broad spectrum penicillin against both Gram-positive and Gram-negative organisms including anaerobic organisms. PIPC was administered to 5 patients intravenously and all cases proved to be effective. No side effects and no abnormalities in laboratory findings were observed. These results suggest that PIPC may be highly effective in the treatment of bacterial infections.</description><subject>Adult</subject><subject>Bacterial Infections - drug therapy</subject><subject>Escherichia coli - drug effects</subject><subject>Female</subject><subject>Genital Diseases, Female - drug therapy</subject><subject>Humans</subject><subject>Pelvic Inflammatory Disease - drug therapy</subject><subject>Penicillin Resistance</subject><subject>Penicillins - pharmacology</subject><subject>Penicillins - therapeutic use</subject><subject>Piperacillin</subject><subject>Pseudomonas - drug effects</subject><issn>0368-2781</issn><issn>2186-5477</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1982</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkVtrg0AQhZfSkoY0P6FgX_pmuhfdy6OxJhFEQ2IKeZJd3bYGc6lrHvrvq4nkoTDMMHyHM3AGgBcEJwi5LnmTh6ZU5bEpc4ME5WpC3AkmmNyBIUac2q7D2D0YQkK5jRlHj2BsTKkgQYzj1mIABhRjghwxBHLq-WmwCpMomYe-F1le_G75URhfluDDizZeGiaxlcysZbgMVp4fRi222koXgTULg-i9g8l0nQbpKvTXF4v5Ng78znT7BB4-ZWX0uJ8jsJkFqb-w-4v2DgnY2AQjR1LiSqEVU1wJSvOCIyqwVA7BBeNUQCG4I_MC54wL7ehcEA05LBzYSkbg9ep7qo8_Z22abF-aXFeVPOjj2WQcEkwZ74TPvfCs9rrITnW5l_Vv1mfS8ujKd6aRX_rGZd0mXunsf_wZcTMEu9494SbLv2Wd6QP5A21eeiU</recordid><startdate>198210</startdate><enddate>198210</enddate><creator>NINOMIYA, KEIU</creator><creator>MAKINO, SHIGENORI</creator><creator>HASEGAWA, YUKIO</creator><creator>YOSHIMOTO, TOSHIKO</creator><creator>MASUDA, KAORUKO</creator><creator>HAMAYA, KEIKO</creator><general>Japan Antibiotics Research Association</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>198210</creationdate><title>BACTERIOLOGICAL AND CLINICAL EVALUATION OF PIPERACILLIN IN THE FIELD OF OBSTETRICS AND GYNECOLOGY</title><author>NINOMIYA, KEIU ; MAKINO, SHIGENORI ; HASEGAWA, YUKIO ; YOSHIMOTO, TOSHIKO ; MASUDA, KAORUKO ; HAMAYA, KEIKO</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-j190t-3214a635a9eb7b8b966cd81692ab432d786909984acd2c789e4ec93e080d40b43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>jpn</language><creationdate>1982</creationdate><topic>Adult</topic><topic>Bacterial Infections - drug therapy</topic><topic>Escherichia coli - drug effects</topic><topic>Female</topic><topic>Genital Diseases, Female - drug therapy</topic><topic>Humans</topic><topic>Pelvic Inflammatory Disease - drug therapy</topic><topic>Penicillin Resistance</topic><topic>Penicillins - pharmacology</topic><topic>Penicillins - therapeutic use</topic><topic>Piperacillin</topic><topic>Pseudomonas - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>NINOMIYA, KEIU</creatorcontrib><creatorcontrib>MAKINO, SHIGENORI</creatorcontrib><creatorcontrib>HASEGAWA, YUKIO</creatorcontrib><creatorcontrib>YOSHIMOTO, TOSHIKO</creatorcontrib><creatorcontrib>MASUDA, KAORUKO</creatorcontrib><creatorcontrib>HAMAYA, KEIKO</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Japanese journal of antibiotics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>NINOMIYA, KEIU</au><au>MAKINO, SHIGENORI</au><au>HASEGAWA, YUKIO</au><au>YOSHIMOTO, TOSHIKO</au><au>MASUDA, KAORUKO</au><au>HAMAYA, KEIKO</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>BACTERIOLOGICAL AND CLINICAL EVALUATION OF PIPERACILLIN IN THE FIELD OF OBSTETRICS AND GYNECOLOGY</atitle><jtitle>Japanese journal of antibiotics</jtitle><addtitle>Jpn. J. Antibiotics</addtitle><date>1982-10</date><risdate>1982</risdate><volume>35</volume><issue>10</issue><spage>2323</spage><epage>2329</epage><pages>2323-2329</pages><issn>0368-2781</issn><eissn>2186-5477</eissn><abstract>In vitro activity of piperacillin (PIPC) against 150 recent clinical isolates from obstetric and gynecologic infections was performed in comparison with sulbenicillin (SBPC), cefmetazole (CMZ), cefotiam (CTM) and cefsulodin (CFS). At 6.25μglml PIPC inhibited 93% of S. epidermidis, 86% of S. faecalis, 67% of E. coli and 80% of Klebsiella. At 0.2μg/ml PIPC inhibited 100% of Peptococcus, 73% of Peptostreptococcus and 100%, of B. melaninogenicus group. At 3.13μg/mi PIPC inhibited 71% of B. fragilis 9 strains, B. distasonis 3 strains, B. thetaiotaomicron 1 strain, B. ovatus 1 strain.PIPC was constantly more active than SBPC, and it was especially more active against S. faecalis, Peptococcus, Peptostreptococcus and B. melaninogenicus group than other antibiotics. These findings show that PIPC is a broad spectrum penicillin against both Gram-positive and Gram-negative organisms including anaerobic organisms. PIPC was administered to 5 patients intravenously and all cases proved to be effective. No side effects and no abnormalities in laboratory findings were observed. These results suggest that PIPC may be highly effective in the treatment of bacterial infections.</abstract><cop>Japan</cop><pub>Japan Antibiotics Research Association</pub><pmid>6223149</pmid><doi>10.11553/antibiotics1968b.35.2323</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Bacterial Infections - drug therapy Escherichia coli - drug effects Female Genital Diseases, Female - drug therapy Humans Pelvic Inflammatory Disease - drug therapy Penicillin Resistance Penicillins - pharmacology Penicillins - therapeutic use Piperacillin Pseudomonas - drug effects |
title | BACTERIOLOGICAL AND CLINICAL EVALUATION OF PIPERACILLIN IN THE FIELD OF OBSTETRICS AND GYNECOLOGY |
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