A MULTICENTER STUDY ON PANIPENEM/BETAMIPRON IN DERMATOLOGY
Panipenem/betamipron (PAPM/BP), a new carbapenem, was studied in dermatology. PAPM/BP was used clinically in the treatment of skin and skin structure infections in a multicenter trial. Fifty three patients were enrolled in the trial. Clinical evaluations were made in 50 patients. Most patients recei...
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| Veröffentlicht in: | Japanese journal of antibiotics 1992/02/25, Vol.45(2), pp.197-207 |
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| creator | ARATA, JIRO AKIYAMA, HISANORI KANZAKI, HIROKO TAKAHASHI, HISASHI TANAKA, YUI TAKAHAMA, HIDETO FUJIMURA, MAMI KUSHIBUCHI, SAYAKA ISHIBASHI, YASUMASA IHN, HIRONOBU ABE, MASAMIZU KOMINE, MAYUMI KUKITA, ATSUSHI HIRUMA, MASATARO MATSUI, RYOSUKE KANESHIGE, YOSHIAKI HARADA, SHOTARO MINAMI, HARUO TAMAKI, TAKESHI ANZAI, TAKASHI JITSUKAWA, KUMIKO SAITO, RYUZO URUSHIBATA, OSAMU ASASHIMA, HIROO YASUNO, YOICHI KISHIMOTO, SABURO KONISHI, KEISUKE TAKENAKA, HIDEYA OKA, FUMIKO UEDA, FUJIO ASADA, YASUO YAMAWAKI, MITSUO ISEI, TAIKI IMAMURA, SADAO TACHIBANA, TAKAO OOTANI, NORIO AKIOKA, NARIMI DOI, AKIRA MASUDA, RIE AKAI, YOKO HAYAKAWA, MINORU HAYASHI, MIZUYO TANABE, HIROSHI UEKI, HIROAKI INAGAKI, YASUNORI MIYOSHI, KAORU NAKATSUKASA, AKIHIRO UMEMURA, SHIGEO SUWAKI, MASAO AKAGI, OSAMU NAKAKITA, TAKASHI KODAMA, HAJIME YAMAMOTO, YASUO IKEDA, MASAMI HORI, YOSHIAKI NAGAE, SHONOSUKE |
| description | Panipenem/betamipron (PAPM/BP), a new carbapenem, was studied in dermatology. PAPM/BP was used clinically in the treatment of skin and skin structure infections in a multicenter trial. Fifty three patients were enrolled in the trial. Clinical evaluations were made in 50 patients. Most patients received intravenous infusion of PAPM/BP in a dose of 500 mg twice daily. Other dosages were used in some patients. The overall clinical efficacy rate was 78%. When 15 cases of secondary infections were excluded, the rate was 85.7%. Adverse responses were nausea and/or vomiting in 3 patients, redness with itching in 1 patient, headache or head heaviness in 2 patients and diarrhea in I patient. The patient with redness and itching had also nausea and vomiting. This occurred 1 hour after the start of the first infusion of this drug. After the discontinuation of the treatment the symptoms went away on the next day. Abnormalities in laboratory test results were observed in 7 out of 53 patients. One patient with liver cirrhosis and hepatocellular carcinoma developed anemia (RBC 372×104/mm3→275×104/mm3, Hb 11.9g/dl→8.8g/dl, 35.1%→26.0%). Other abnormalities were all mild. Penetration of the drug into skin tissues after intravenous infusion of 500mg of this drug in skin surgery patients was studied. Skin/serum concentration ratios ranged from 0.20 to 0.97. Skin concentrations were higher than the concentration of PAPM inhibiting 80% of clinical isolates over a period of 6 hours. In rats, skin concentrations were much lower than serum concentrations probably due to the difference in in vivo metabolism of PAPM. A few resistant strains of Staphylococcus aureus against PAPM and imipenem (IPM) were isolated. However, PAPM and IPM showed good antibacterial activities compared to other drugs tested. In conclusion, PAPM/BP is considered to be a useful drug in the treatment of skin and skin structure infections. |
| doi_str_mv | 10.11553/antibiotics1968b.45.197 |
| format | Article |
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PAPM/BP was used clinically in the treatment of skin and skin structure infections in a multicenter trial. Fifty three patients were enrolled in the trial. Clinical evaluations were made in 50 patients. Most patients received intravenous infusion of PAPM/BP in a dose of 500 mg twice daily. Other dosages were used in some patients. The overall clinical efficacy rate was 78%. When 15 cases of secondary infections were excluded, the rate was 85.7%. Adverse responses were nausea and/or vomiting in 3 patients, redness with itching in 1 patient, headache or head heaviness in 2 patients and diarrhea in I patient. The patient with redness and itching had also nausea and vomiting. This occurred 1 hour after the start of the first infusion of this drug. After the discontinuation of the treatment the symptoms went away on the next day. Abnormalities in laboratory test results were observed in 7 out of 53 patients. One patient with liver cirrhosis and hepatocellular carcinoma developed anemia (RBC 372×104/mm3→275×104/mm3, Hb 11.9g/dl→8.8g/dl, 35.1%→26.0%). Other abnormalities were all mild. Penetration of the drug into skin tissues after intravenous infusion of 500mg of this drug in skin surgery patients was studied. Skin/serum concentration ratios ranged from 0.20 to 0.97. Skin concentrations were higher than the concentration of PAPM inhibiting 80% of clinical isolates over a period of 6 hours. In rats, skin concentrations were much lower than serum concentrations probably due to the difference in in vivo metabolism of PAPM. A few resistant strains of Staphylococcus aureus against PAPM and imipenem (IPM) were isolated. However, PAPM and IPM showed good antibacterial activities compared to other drugs tested. In conclusion, PAPM/BP is considered to be a useful drug in the treatment of skin and skin structure infections.</description><identifier>ISSN: 0368-2781</identifier><identifier>EISSN: 2186-5477</identifier><identifier>DOI: 10.11553/antibiotics1968b.45.197</identifier><identifier>PMID: 1613973</identifier><language>jpn</language><publisher>Japan: Japan Antibiotics Research Association</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Animals ; Bacterial Infections - drug therapy ; Bacterial Infections - metabolism ; beta-Alanine - adverse effects ; beta-Alanine - analogs & derivatives ; beta-Alanine - pharmacokinetics ; beta-Alanine - therapeutic use ; Drug Therapy, Combination - adverse effects ; Drug Therapy, Combination - pharmacokinetics ; Drug Therapy, Combination - therapeutic use ; Female ; Humans ; Male ; Microbial Sensitivity Tests ; Middle Aged ; Nausea - chemically induced ; Rats ; Rats, Inbred Strains ; Skin - metabolism ; Skin Diseases, Infectious - drug therapy ; Skin Diseases, Infectious - metabolism ; Thienamycins - adverse effects ; Thienamycins - pharmacokinetics ; Thienamycins - therapeutic use ; Tissue Distribution ; Vomiting - chemically induced</subject><ispartof>The Japanese Journal of Antibiotics, 1992/02/25, Vol.45(2), pp.197-207</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>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1613973$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ARATA, JIRO</creatorcontrib><creatorcontrib>AKIYAMA, HISANORI</creatorcontrib><creatorcontrib>KANZAKI, HIROKO</creatorcontrib><creatorcontrib>TAKAHASHI, HISASHI</creatorcontrib><creatorcontrib>TANAKA, YUI</creatorcontrib><creatorcontrib>TAKAHAMA, HIDETO</creatorcontrib><creatorcontrib>FUJIMURA, MAMI</creatorcontrib><creatorcontrib>KUSHIBUCHI, SAYAKA</creatorcontrib><creatorcontrib>ISHIBASHI, YASUMASA</creatorcontrib><creatorcontrib>IHN, HIRONOBU</creatorcontrib><creatorcontrib>ABE, MASAMIZU</creatorcontrib><creatorcontrib>KOMINE, MAYUMI</creatorcontrib><creatorcontrib>KUKITA, ATSUSHI</creatorcontrib><creatorcontrib>HIRUMA, MASATARO</creatorcontrib><creatorcontrib>MATSUI, RYOSUKE</creatorcontrib><creatorcontrib>KANESHIGE, YOSHIAKI</creatorcontrib><creatorcontrib>HARADA, SHOTARO</creatorcontrib><creatorcontrib>MINAMI, HARUO</creatorcontrib><creatorcontrib>TAMAKI, TAKESHI</creatorcontrib><creatorcontrib>ANZAI, TAKASHI</creatorcontrib><creatorcontrib>JITSUKAWA, KUMIKO</creatorcontrib><creatorcontrib>SAITO, RYUZO</creatorcontrib><creatorcontrib>URUSHIBATA, OSAMU</creatorcontrib><creatorcontrib>ASASHIMA, HIROO</creatorcontrib><creatorcontrib>YASUNO, YOICHI</creatorcontrib><creatorcontrib>KISHIMOTO, SABURO</creatorcontrib><creatorcontrib>KONISHI, KEISUKE</creatorcontrib><creatorcontrib>TAKENAKA, HIDEYA</creatorcontrib><creatorcontrib>OKA, FUMIKO</creatorcontrib><creatorcontrib>UEDA, FUJIO</creatorcontrib><creatorcontrib>ASADA, YASUO</creatorcontrib><creatorcontrib>YAMAWAKI, MITSUO</creatorcontrib><creatorcontrib>ISEI, TAIKI</creatorcontrib><creatorcontrib>IMAMURA, SADAO</creatorcontrib><creatorcontrib>TACHIBANA, TAKAO</creatorcontrib><creatorcontrib>OOTANI, NORIO</creatorcontrib><creatorcontrib>AKIOKA, NARIMI</creatorcontrib><creatorcontrib>DOI, AKIRA</creatorcontrib><creatorcontrib>MASUDA, RIE</creatorcontrib><creatorcontrib>AKAI, YOKO</creatorcontrib><creatorcontrib>HAYAKAWA, MINORU</creatorcontrib><creatorcontrib>HAYASHI, MIZUYO</creatorcontrib><creatorcontrib>TANABE, HIROSHI</creatorcontrib><creatorcontrib>UEKI, HIROAKI</creatorcontrib><creatorcontrib>INAGAKI, YASUNORI</creatorcontrib><creatorcontrib>MIYOSHI, KAORU</creatorcontrib><creatorcontrib>NAKATSUKASA, AKIHIRO</creatorcontrib><creatorcontrib>UMEMURA, SHIGEO</creatorcontrib><creatorcontrib>SUWAKI, MASAO</creatorcontrib><creatorcontrib>AKAGI, OSAMU</creatorcontrib><creatorcontrib>NAKAKITA, TAKASHI</creatorcontrib><creatorcontrib>KODAMA, HAJIME</creatorcontrib><creatorcontrib>YAMAMOTO, YASUO</creatorcontrib><creatorcontrib>IKEDA, MASAMI</creatorcontrib><creatorcontrib>HORI, YOSHIAKI</creatorcontrib><creatorcontrib>NAGAE, SHONOSUKE</creatorcontrib><title>A MULTICENTER STUDY ON PANIPENEM/BETAMIPRON IN DERMATOLOGY</title><title>Japanese journal of antibiotics</title><addtitle>Jpn. J. Antibiotics</addtitle><description>Panipenem/betamipron (PAPM/BP), a new carbapenem, was studied in dermatology. PAPM/BP was used clinically in the treatment of skin and skin structure infections in a multicenter trial. Fifty three patients were enrolled in the trial. Clinical evaluations were made in 50 patients. Most patients received intravenous infusion of PAPM/BP in a dose of 500 mg twice daily. Other dosages were used in some patients. The overall clinical efficacy rate was 78%. When 15 cases of secondary infections were excluded, the rate was 85.7%. Adverse responses were nausea and/or vomiting in 3 patients, redness with itching in 1 patient, headache or head heaviness in 2 patients and diarrhea in I patient. The patient with redness and itching had also nausea and vomiting. This occurred 1 hour after the start of the first infusion of this drug. After the discontinuation of the treatment the symptoms went away on the next day. Abnormalities in laboratory test results were observed in 7 out of 53 patients. One patient with liver cirrhosis and hepatocellular carcinoma developed anemia (RBC 372×104/mm3→275×104/mm3, Hb 11.9g/dl→8.8g/dl, 35.1%→26.0%). Other abnormalities were all mild. Penetration of the drug into skin tissues after intravenous infusion of 500mg of this drug in skin surgery patients was studied. Skin/serum concentration ratios ranged from 0.20 to 0.97. Skin concentrations were higher than the concentration of PAPM inhibiting 80% of clinical isolates over a period of 6 hours. In rats, skin concentrations were much lower than serum concentrations probably due to the difference in in vivo metabolism of PAPM. A few resistant strains of Staphylococcus aureus against PAPM and imipenem (IPM) were isolated. However, PAPM and IPM showed good antibacterial activities compared to other drugs tested. In conclusion, PAPM/BP is considered to be a useful drug in the treatment of skin and skin structure infections.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Animals</subject><subject>Bacterial Infections - drug therapy</subject><subject>Bacterial Infections - metabolism</subject><subject>beta-Alanine - adverse effects</subject><subject>beta-Alanine - analogs & derivatives</subject><subject>beta-Alanine - pharmacokinetics</subject><subject>beta-Alanine - therapeutic use</subject><subject>Drug Therapy, Combination - adverse effects</subject><subject>Drug Therapy, Combination - pharmacokinetics</subject><subject>Drug Therapy, Combination - therapeutic use</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Microbial Sensitivity Tests</subject><subject>Middle Aged</subject><subject>Nausea - chemically induced</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Skin - metabolism</subject><subject>Skin Diseases, Infectious - drug therapy</subject><subject>Skin Diseases, Infectious - metabolism</subject><subject>Thienamycins - adverse effects</subject><subject>Thienamycins - pharmacokinetics</subject><subject>Thienamycins - therapeutic use</subject><subject>Tissue Distribution</subject><subject>Vomiting - chemically induced</subject><issn>0368-2781</issn><issn>2186-5477</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkM1OwkAURidGgwR5BJO-QGHu_I-7CoPW0EKwLFg1UzrVEkDS1oVv7xgICzf3Jvd8-ZJ7EAoAjwA4p2N77Oqi_urqbQtaqGLE-Ai0vEF9AkqEnEl5i_qYChUSqeAeDdu2LjAFqYhv6KEeCKBa0j56ioJkPc_iiUkzswres_V0EyzSYBml8dKkJhk_myxK4uXKH-M0mJpVEmWL-eJl84DuKrtv3fCyB2g9M9nkNfQwnkTzcAcE01AQK5lkgjirlRAlQGmZ5LoqsSIVFq6yXDHKNWwtpphYYJ4pRjghusSUDtDjuff0XRxcmZ-a-mCbn_zyg-dvZ75rO_vhrtw2XtDe5f9t5Yzn5G94ZdfQ9tM2uTvSXwTWYTg</recordid><startdate>199202</startdate><enddate>199202</enddate><creator>ARATA, JIRO</creator><creator>AKIYAMA, HISANORI</creator><creator>KANZAKI, HIROKO</creator><creator>TAKAHASHI, HISASHI</creator><creator>TANAKA, YUI</creator><creator>TAKAHAMA, HIDETO</creator><creator>FUJIMURA, MAMI</creator><creator>KUSHIBUCHI, SAYAKA</creator><creator>ISHIBASHI, YASUMASA</creator><creator>IHN, 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ISHIBASHI, YASUMASA ; IHN, HIRONOBU ; ABE, MASAMIZU ; KOMINE, MAYUMI ; KUKITA, ATSUSHI ; HIRUMA, MASATARO ; MATSUI, RYOSUKE ; KANESHIGE, YOSHIAKI ; HARADA, SHOTARO ; MINAMI, HARUO ; TAMAKI, TAKESHI ; ANZAI, TAKASHI ; JITSUKAWA, KUMIKO ; SAITO, RYUZO ; URUSHIBATA, OSAMU ; ASASHIMA, HIROO ; YASUNO, YOICHI ; KISHIMOTO, SABURO ; KONISHI, KEISUKE ; TAKENAKA, HIDEYA ; OKA, FUMIKO ; UEDA, FUJIO ; ASADA, YASUO ; YAMAWAKI, MITSUO ; ISEI, TAIKI ; IMAMURA, SADAO ; TACHIBANA, TAKAO ; OOTANI, NORIO ; AKIOKA, NARIMI ; DOI, AKIRA ; MASUDA, RIE ; AKAI, YOKO ; HAYAKAWA, MINORU ; HAYASHI, MIZUYO ; TANABE, HIROSHI ; UEKI, HIROAKI ; INAGAKI, YASUNORI ; MIYOSHI, KAORU ; NAKATSUKASA, AKIHIRO ; UMEMURA, SHIGEO ; SUWAKI, MASAO ; AKAGI, OSAMU ; NAKAKITA, TAKASHI ; KODAMA, HAJIME ; YAMAMOTO, YASUO ; IKEDA, MASAMI ; HORI, YOSHIAKI ; NAGAE, SHONOSUKE</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-j1203-62a747462ea9866d11da4759fd082f06efa5843591ca0302a149fd8425229d033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>jpn</language><creationdate>1992</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Animals</topic><topic>Bacterial Infections - drug therapy</topic><topic>Bacterial Infections - metabolism</topic><topic>beta-Alanine - adverse effects</topic><topic>beta-Alanine - analogs & derivatives</topic><topic>beta-Alanine - pharmacokinetics</topic><topic>beta-Alanine - therapeutic use</topic><topic>Drug Therapy, Combination - adverse effects</topic><topic>Drug Therapy, Combination - pharmacokinetics</topic><topic>Drug Therapy, Combination - therapeutic use</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Microbial Sensitivity Tests</topic><topic>Middle Aged</topic><topic>Nausea - chemically induced</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Skin - metabolism</topic><topic>Skin Diseases, Infectious - drug therapy</topic><topic>Skin Diseases, Infectious - metabolism</topic><topic>Thienamycins - adverse effects</topic><topic>Thienamycins - pharmacokinetics</topic><topic>Thienamycins - therapeutic use</topic><topic>Tissue Distribution</topic><topic>Vomiting - chemically induced</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ARATA, JIRO</creatorcontrib><creatorcontrib>AKIYAMA, HISANORI</creatorcontrib><creatorcontrib>KANZAKI, HIROKO</creatorcontrib><creatorcontrib>TAKAHASHI, HISASHI</creatorcontrib><creatorcontrib>TANAKA, YUI</creatorcontrib><creatorcontrib>TAKAHAMA, HIDETO</creatorcontrib><creatorcontrib>FUJIMURA, MAMI</creatorcontrib><creatorcontrib>KUSHIBUCHI, SAYAKA</creatorcontrib><creatorcontrib>ISHIBASHI, YASUMASA</creatorcontrib><creatorcontrib>IHN, HIRONOBU</creatorcontrib><creatorcontrib>ABE, MASAMIZU</creatorcontrib><creatorcontrib>KOMINE, MAYUMI</creatorcontrib><creatorcontrib>KUKITA, ATSUSHI</creatorcontrib><creatorcontrib>HIRUMA, MASATARO</creatorcontrib><creatorcontrib>MATSUI, RYOSUKE</creatorcontrib><creatorcontrib>KANESHIGE, YOSHIAKI</creatorcontrib><creatorcontrib>HARADA, SHOTARO</creatorcontrib><creatorcontrib>MINAMI, HARUO</creatorcontrib><creatorcontrib>TAMAKI, TAKESHI</creatorcontrib><creatorcontrib>ANZAI, TAKASHI</creatorcontrib><creatorcontrib>JITSUKAWA, KUMIKO</creatorcontrib><creatorcontrib>SAITO, RYUZO</creatorcontrib><creatorcontrib>URUSHIBATA, OSAMU</creatorcontrib><creatorcontrib>ASASHIMA, HIROO</creatorcontrib><creatorcontrib>YASUNO, YOICHI</creatorcontrib><creatorcontrib>KISHIMOTO, SABURO</creatorcontrib><creatorcontrib>KONISHI, KEISUKE</creatorcontrib><creatorcontrib>TAKENAKA, HIDEYA</creatorcontrib><creatorcontrib>OKA, FUMIKO</creatorcontrib><creatorcontrib>UEDA, FUJIO</creatorcontrib><creatorcontrib>ASADA, YASUO</creatorcontrib><creatorcontrib>YAMAWAKI, MITSUO</creatorcontrib><creatorcontrib>ISEI, TAIKI</creatorcontrib><creatorcontrib>IMAMURA, SADAO</creatorcontrib><creatorcontrib>TACHIBANA, TAKAO</creatorcontrib><creatorcontrib>OOTANI, NORIO</creatorcontrib><creatorcontrib>AKIOKA, NARIMI</creatorcontrib><creatorcontrib>DOI, AKIRA</creatorcontrib><creatorcontrib>MASUDA, RIE</creatorcontrib><creatorcontrib>AKAI, YOKO</creatorcontrib><creatorcontrib>HAYAKAWA, MINORU</creatorcontrib><creatorcontrib>HAYASHI, MIZUYO</creatorcontrib><creatorcontrib>TANABE, HIROSHI</creatorcontrib><creatorcontrib>UEKI, HIROAKI</creatorcontrib><creatorcontrib>INAGAKI, YASUNORI</creatorcontrib><creatorcontrib>MIYOSHI, KAORU</creatorcontrib><creatorcontrib>NAKATSUKASA, AKIHIRO</creatorcontrib><creatorcontrib>UMEMURA, SHIGEO</creatorcontrib><creatorcontrib>SUWAKI, MASAO</creatorcontrib><creatorcontrib>AKAGI, OSAMU</creatorcontrib><creatorcontrib>NAKAKITA, TAKASHI</creatorcontrib><creatorcontrib>KODAMA, HAJIME</creatorcontrib><creatorcontrib>YAMAMOTO, YASUO</creatorcontrib><creatorcontrib>IKEDA, MASAMI</creatorcontrib><creatorcontrib>HORI, YOSHIAKI</creatorcontrib><creatorcontrib>NAGAE, SHONOSUKE</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Japanese journal of antibiotics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ARATA, JIRO</au><au>AKIYAMA, HISANORI</au><au>KANZAKI, HIROKO</au><au>TAKAHASHI, HISASHI</au><au>TANAKA, YUI</au><au>TAKAHAMA, HIDETO</au><au>FUJIMURA, MAMI</au><au>KUSHIBUCHI, SAYAKA</au><au>ISHIBASHI, YASUMASA</au><au>IHN, HIRONOBU</au><au>ABE, MASAMIZU</au><au>KOMINE, MAYUMI</au><au>KUKITA, ATSUSHI</au><au>HIRUMA, MASATARO</au><au>MATSUI, RYOSUKE</au><au>KANESHIGE, YOSHIAKI</au><au>HARADA, SHOTARO</au><au>MINAMI, HARUO</au><au>TAMAKI, TAKESHI</au><au>ANZAI, TAKASHI</au><au>JITSUKAWA, KUMIKO</au><au>SAITO, RYUZO</au><au>URUSHIBATA, OSAMU</au><au>ASASHIMA, HIROO</au><au>YASUNO, YOICHI</au><au>KISHIMOTO, SABURO</au><au>KONISHI, KEISUKE</au><au>TAKENAKA, HIDEYA</au><au>OKA, FUMIKO</au><au>UEDA, FUJIO</au><au>ASADA, YASUO</au><au>YAMAWAKI, MITSUO</au><au>ISEI, TAIKI</au><au>IMAMURA, SADAO</au><au>TACHIBANA, TAKAO</au><au>OOTANI, NORIO</au><au>AKIOKA, NARIMI</au><au>DOI, AKIRA</au><au>MASUDA, RIE</au><au>AKAI, YOKO</au><au>HAYAKAWA, MINORU</au><au>HAYASHI, MIZUYO</au><au>TANABE, HIROSHI</au><au>UEKI, HIROAKI</au><au>INAGAKI, YASUNORI</au><au>MIYOSHI, KAORU</au><au>NAKATSUKASA, AKIHIRO</au><au>UMEMURA, SHIGEO</au><au>SUWAKI, MASAO</au><au>AKAGI, OSAMU</au><au>NAKAKITA, TAKASHI</au><au>KODAMA, HAJIME</au><au>YAMAMOTO, YASUO</au><au>IKEDA, MASAMI</au><au>HORI, YOSHIAKI</au><au>NAGAE, SHONOSUKE</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A MULTICENTER STUDY ON PANIPENEM/BETAMIPRON IN DERMATOLOGY</atitle><jtitle>Japanese journal of antibiotics</jtitle><addtitle>Jpn. J. Antibiotics</addtitle><date>1992-02</date><risdate>1992</risdate><volume>45</volume><issue>2</issue><spage>197</spage><epage>207</epage><pages>197-207</pages><issn>0368-2781</issn><eissn>2186-5477</eissn><abstract>Panipenem/betamipron (PAPM/BP), a new carbapenem, was studied in dermatology. PAPM/BP was used clinically in the treatment of skin and skin structure infections in a multicenter trial. Fifty three patients were enrolled in the trial. Clinical evaluations were made in 50 patients. Most patients received intravenous infusion of PAPM/BP in a dose of 500 mg twice daily. Other dosages were used in some patients. The overall clinical efficacy rate was 78%. When 15 cases of secondary infections were excluded, the rate was 85.7%. Adverse responses were nausea and/or vomiting in 3 patients, redness with itching in 1 patient, headache or head heaviness in 2 patients and diarrhea in I patient. The patient with redness and itching had also nausea and vomiting. This occurred 1 hour after the start of the first infusion of this drug. After the discontinuation of the treatment the symptoms went away on the next day. Abnormalities in laboratory test results were observed in 7 out of 53 patients. One patient with liver cirrhosis and hepatocellular carcinoma developed anemia (RBC 372×104/mm3→275×104/mm3, Hb 11.9g/dl→8.8g/dl, 35.1%→26.0%). Other abnormalities were all mild. Penetration of the drug into skin tissues after intravenous infusion of 500mg of this drug in skin surgery patients was studied. Skin/serum concentration ratios ranged from 0.20 to 0.97. Skin concentrations were higher than the concentration of PAPM inhibiting 80% of clinical isolates over a period of 6 hours. In rats, skin concentrations were much lower than serum concentrations probably due to the difference in in vivo metabolism of PAPM. A few resistant strains of Staphylococcus aureus against PAPM and imipenem (IPM) were isolated. However, PAPM and IPM showed good antibacterial activities compared to other drugs tested. In conclusion, PAPM/BP is considered to be a useful drug in the treatment of skin and skin structure infections.</abstract><cop>Japan</cop><pub>Japan Antibiotics Research Association</pub><pmid>1613973</pmid><doi>10.11553/antibiotics1968b.45.197</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0368-2781 |
| ispartof | The Japanese Journal of Antibiotics, 1992/02/25, Vol.45(2), pp.197-207 |
| issn | 0368-2781 2186-5477 |
| language | jpn |
| recordid | cdi_pubmed_primary_1613973 |
| source | MEDLINE; EZB-FREE-00999 freely available EZB journals |
| subjects | Adolescent Adult Aged Aged, 80 and over Animals Bacterial Infections - drug therapy Bacterial Infections - metabolism beta-Alanine - adverse effects beta-Alanine - analogs & derivatives beta-Alanine - pharmacokinetics beta-Alanine - therapeutic use Drug Therapy, Combination - adverse effects Drug Therapy, Combination - pharmacokinetics Drug Therapy, Combination - therapeutic use Female Humans Male Microbial Sensitivity Tests Middle Aged Nausea - chemically induced Rats Rats, Inbred Strains Skin - metabolism Skin Diseases, Infectious - drug therapy Skin Diseases, Infectious - metabolism Thienamycins - adverse effects Thienamycins - pharmacokinetics Thienamycins - therapeutic use Tissue Distribution Vomiting - chemically induced |
| title | A MULTICENTER STUDY ON PANIPENEM/BETAMIPRON IN DERMATOLOGY |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-31T00%3A29%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_jstag&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20MULTICENTER%20STUDY%20ON%20PANIPENEM/BETAMIPRON%20IN%20DERMATOLOGY&rft.jtitle=Japanese%20journal%20of%20antibiotics&rft.au=ARATA,%20JIRO&rft.date=1992-02&rft.volume=45&rft.issue=2&rft.spage=197&rft.epage=207&rft.pages=197-207&rft.issn=0368-2781&rft.eissn=2186-5477&rft_id=info:doi/10.11553/antibiotics1968b.45.197&rft_dat=%3Cpubmed_jstag%3E1613973%3C/pubmed_jstag%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/1613973&rfr_iscdi=true |