CLINICAL EVALUATION OF CEFMENOXIME IN THE SEVERE INFECTIONS IN LEUKEMIA AND RELATED DISORDERS
Ninety nine patients with leukemia and/or related disorders were treated with cefmenoxime (CMX). Among them, 77 patients had severe infections, while other 22 patients did not suffer from infection, but it was expected that they would fall into serious conditions if they were infected. Sixty of the...
Gespeichert in:
Veröffentlicht in: | Japanese journal of antibiotics 1986/10/25, Vol.39(10), pp.2651-2660 |
---|---|
Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | jpn |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 2660 |
---|---|
container_issue | 10 |
container_start_page | 2651 |
container_title | Japanese journal of antibiotics |
container_volume | 39 |
creator | TSUDA, SHOICHIRO NISHIDA, KAZUHIRO MAEKAWA, TAIRA ABE, TATSUO TAKINO, TATSURO FUJII, HIROSHI TANIWAKI, MASAFUMI YASHIGE, HIROMI HORIIKE, SHIGEO YOKOTA, SYOHEI OH, ONGYOKU SONODA, YOSHIAKI |
description | Ninety nine patients with leukemia and/or related disorders were treated with cefmenoxime (CMX). Among them, 77 patients had severe infections, while other 22 patients did not suffer from infection, but it was expected that they would fall into serious conditions if they were infected. Sixty of the 77 patients who had severe infection were used in the evaluation of effectiveness. The remaining 17 patients were not evaluated because they were subjected to combined treatments of CMX and other therapeutic agents such as other antibiotics, rglobulin or interferon. Excellent responses were found in 26 (43. 3%) patients and good responses in 12 (20. 0%) patients. In total, the rate of effectiveness was 63. 3%. Nineteen of the 22 patients who were treated prophylactically with CMX were used in the evaluation of effectiveness, while 3 patients were excluded from the evaluation because peripheral neutrophils were counted to be more than 1, 000/mm3 before CMX was administrated, although these 3 patients were used in the final evaluation to examine side effects. In the prophylactic treatment, the rate of effectiveness was 89. 5%. The side effects were seen in 4 patients (4/82: 4. 9%). A different symptom was identified in each patient. These symptoms were skin rash, mild nausea, mild diarrhea and slight elevation of serum bilirubin. Prompt improvements of these symptoms occurred as soon as CMX administration was stopped. These results show that CMX is a therapeutically effective and safe antibiotics for the treatment of severe infections or for the prophylaxis of infections in patients associated with leukemia and/or related disorders. |
doi_str_mv | 10.11553/antibiotics1968b.39.2651 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_77254173</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>77254173</sourcerecordid><originalsourceid>FETCH-LOGICAL-j190t-fbb24d82972ec85934beec0bd0474d146dddd67b326a828b15afa355d69d61623</originalsourceid><addsrcrecordid>eNpdkU9rg0AQxZfSkoY0H6GwvfRm6u66fzyKbhqpUYgm9FJkVzetwSStmkO_fZWEHDqHGYb34w28AeAJ2TOEKCUv6tBVujp2VdEilwk9I-4MM4puwBgjwSzqcH4LxjZhwsJcoHswbdtK2wRxgXuLERgRhwnM8Rh8-FEYh74XQbnxorWXhUkMkzn05Xwp4-Q9XEoYxjBbSJjKjVwN21z6A5YOQiTXb3IZetCLA7iSkZfJAAZhmqwCuUofwN1W1a2ZXuYErOcy8xdWlLwOR60dcu3O2mqNnVJgl2NTCOoSRxtT2Lq0He6UyGFlX4xrgpkSWGhE1VYRSkvmlgwxTCbg-ez73Rx_Tqbt8n3VFqau1cEcT23OOaYO4qQHHy_gSe9NmX831V41v_klj16Pzvqu7dSnueqq6dOuTf4_-py4ObKHPjzgihVfqsnNgfwBT2l52w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>77254173</pqid></control><display><type>article</type><title>CLINICAL EVALUATION OF CEFMENOXIME IN THE SEVERE INFECTIONS IN LEUKEMIA AND RELATED DISORDERS</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>TSUDA, SHOICHIRO ; NISHIDA, KAZUHIRO ; MAEKAWA, TAIRA ; ABE, TATSUO ; TAKINO, TATSURO ; FUJII, HIROSHI ; TANIWAKI, MASAFUMI ; YASHIGE, HIROMI ; HORIIKE, SHIGEO ; YOKOTA, SYOHEI ; OH, ONGYOKU ; SONODA, YOSHIAKI</creator><creatorcontrib>TSUDA, SHOICHIRO ; NISHIDA, KAZUHIRO ; MAEKAWA, TAIRA ; ABE, TATSUO ; TAKINO, TATSURO ; FUJII, HIROSHI ; TANIWAKI, MASAFUMI ; YASHIGE, HIROMI ; HORIIKE, SHIGEO ; YOKOTA, SYOHEI ; OH, ONGYOKU ; SONODA, YOSHIAKI</creatorcontrib><description>Ninety nine patients with leukemia and/or related disorders were treated with cefmenoxime (CMX). Among them, 77 patients had severe infections, while other 22 patients did not suffer from infection, but it was expected that they would fall into serious conditions if they were infected. Sixty of the 77 patients who had severe infection were used in the evaluation of effectiveness. The remaining 17 patients were not evaluated because they were subjected to combined treatments of CMX and other therapeutic agents such as other antibiotics, rglobulin or interferon. Excellent responses were found in 26 (43. 3%) patients and good responses in 12 (20. 0%) patients. In total, the rate of effectiveness was 63. 3%. Nineteen of the 22 patients who were treated prophylactically with CMX were used in the evaluation of effectiveness, while 3 patients were excluded from the evaluation because peripheral neutrophils were counted to be more than 1, 000/mm3 before CMX was administrated, although these 3 patients were used in the final evaluation to examine side effects. In the prophylactic treatment, the rate of effectiveness was 89. 5%. The side effects were seen in 4 patients (4/82: 4. 9%). A different symptom was identified in each patient. These symptoms were skin rash, mild nausea, mild diarrhea and slight elevation of serum bilirubin. Prompt improvements of these symptoms occurred as soon as CMX administration was stopped. These results show that CMX is a therapeutically effective and safe antibiotics for the treatment of severe infections or for the prophylaxis of infections in patients associated with leukemia and/or related disorders.</description><identifier>ISSN: 0368-2781</identifier><identifier>EISSN: 2186-5477</identifier><identifier>DOI: 10.11553/antibiotics1968b.39.2651</identifier><identifier>PMID: 3468272</identifier><language>jpn</language><publisher>Japan: Japan Antibiotics Research Association</publisher><subject>Adolescent ; Adult ; Aged ; Bacterial Infections - drug therapy ; Bacterial Infections - etiology ; Cefmenoxime ; Cefotaxime - administration & dosage ; Cefotaxime - analogs & derivatives ; Cefotaxime - therapeutic use ; Female ; Humans ; Leukemia - complications ; Leukemia, Myeloid, Acute - complications ; Lymphoma - complications ; Male ; Middle Aged ; Sepsis - drug therapy</subject><ispartof>The Japanese Journal of Antibiotics, 1986/10/25, Vol.39(10), pp.2651-2660</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>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3468272$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>TSUDA, SHOICHIRO</creatorcontrib><creatorcontrib>NISHIDA, KAZUHIRO</creatorcontrib><creatorcontrib>MAEKAWA, TAIRA</creatorcontrib><creatorcontrib>ABE, TATSUO</creatorcontrib><creatorcontrib>TAKINO, TATSURO</creatorcontrib><creatorcontrib>FUJII, HIROSHI</creatorcontrib><creatorcontrib>TANIWAKI, MASAFUMI</creatorcontrib><creatorcontrib>YASHIGE, HIROMI</creatorcontrib><creatorcontrib>HORIIKE, SHIGEO</creatorcontrib><creatorcontrib>YOKOTA, SYOHEI</creatorcontrib><creatorcontrib>OH, ONGYOKU</creatorcontrib><creatorcontrib>SONODA, YOSHIAKI</creatorcontrib><title>CLINICAL EVALUATION OF CEFMENOXIME IN THE SEVERE INFECTIONS IN LEUKEMIA AND RELATED DISORDERS</title><title>Japanese journal of antibiotics</title><addtitle>Jpn. J. Antibiotics</addtitle><description>Ninety nine patients with leukemia and/or related disorders were treated with cefmenoxime (CMX). Among them, 77 patients had severe infections, while other 22 patients did not suffer from infection, but it was expected that they would fall into serious conditions if they were infected. Sixty of the 77 patients who had severe infection were used in the evaluation of effectiveness. The remaining 17 patients were not evaluated because they were subjected to combined treatments of CMX and other therapeutic agents such as other antibiotics, rglobulin or interferon. Excellent responses were found in 26 (43. 3%) patients and good responses in 12 (20. 0%) patients. In total, the rate of effectiveness was 63. 3%. Nineteen of the 22 patients who were treated prophylactically with CMX were used in the evaluation of effectiveness, while 3 patients were excluded from the evaluation because peripheral neutrophils were counted to be more than 1, 000/mm3 before CMX was administrated, although these 3 patients were used in the final evaluation to examine side effects. In the prophylactic treatment, the rate of effectiveness was 89. 5%. The side effects were seen in 4 patients (4/82: 4. 9%). A different symptom was identified in each patient. These symptoms were skin rash, mild nausea, mild diarrhea and slight elevation of serum bilirubin. Prompt improvements of these symptoms occurred as soon as CMX administration was stopped. These results show that CMX is a therapeutically effective and safe antibiotics for the treatment of severe infections or for the prophylaxis of infections in patients associated with leukemia and/or related disorders.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Bacterial Infections - drug therapy</subject><subject>Bacterial Infections - etiology</subject><subject>Cefmenoxime</subject><subject>Cefotaxime - administration & dosage</subject><subject>Cefotaxime - analogs & derivatives</subject><subject>Cefotaxime - therapeutic use</subject><subject>Female</subject><subject>Humans</subject><subject>Leukemia - complications</subject><subject>Leukemia, Myeloid, Acute - complications</subject><subject>Lymphoma - complications</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Sepsis - drug therapy</subject><issn>0368-2781</issn><issn>2186-5477</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU9rg0AQxZfSkoY0H6GwvfRm6u66fzyKbhqpUYgm9FJkVzetwSStmkO_fZWEHDqHGYb34w28AeAJ2TOEKCUv6tBVujp2VdEilwk9I-4MM4puwBgjwSzqcH4LxjZhwsJcoHswbdtK2wRxgXuLERgRhwnM8Rh8-FEYh74XQbnxorWXhUkMkzn05Xwp4-Q9XEoYxjBbSJjKjVwN21z6A5YOQiTXb3IZetCLA7iSkZfJAAZhmqwCuUofwN1W1a2ZXuYErOcy8xdWlLwOR60dcu3O2mqNnVJgl2NTCOoSRxtT2Lq0He6UyGFlX4xrgpkSWGhE1VYRSkvmlgwxTCbg-ez73Rx_Tqbt8n3VFqau1cEcT23OOaYO4qQHHy_gSe9NmX831V41v_klj16Pzvqu7dSnueqq6dOuTf4_-py4ObKHPjzgihVfqsnNgfwBT2l52w</recordid><startdate>198610</startdate><enddate>198610</enddate><creator>TSUDA, SHOICHIRO</creator><creator>NISHIDA, KAZUHIRO</creator><creator>MAEKAWA, TAIRA</creator><creator>ABE, TATSUO</creator><creator>TAKINO, TATSURO</creator><creator>FUJII, HIROSHI</creator><creator>TANIWAKI, MASAFUMI</creator><creator>YASHIGE, HIROMI</creator><creator>HORIIKE, SHIGEO</creator><creator>YOKOTA, SYOHEI</creator><creator>OH, ONGYOKU</creator><creator>SONODA, YOSHIAKI</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>198610</creationdate><title>CLINICAL EVALUATION OF CEFMENOXIME IN THE SEVERE INFECTIONS IN LEUKEMIA AND RELATED DISORDERS</title><author>TSUDA, SHOICHIRO ; NISHIDA, KAZUHIRO ; MAEKAWA, TAIRA ; ABE, TATSUO ; TAKINO, TATSURO ; FUJII, HIROSHI ; TANIWAKI, MASAFUMI ; YASHIGE, HIROMI ; HORIIKE, SHIGEO ; YOKOTA, SYOHEI ; OH, ONGYOKU ; SONODA, YOSHIAKI</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-j190t-fbb24d82972ec85934beec0bd0474d146dddd67b326a828b15afa355d69d61623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>jpn</language><creationdate>1986</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Bacterial Infections - drug therapy</topic><topic>Bacterial Infections - etiology</topic><topic>Cefmenoxime</topic><topic>Cefotaxime - administration & dosage</topic><topic>Cefotaxime - analogs & derivatives</topic><topic>Cefotaxime - therapeutic use</topic><topic>Female</topic><topic>Humans</topic><topic>Leukemia - complications</topic><topic>Leukemia, Myeloid, Acute - complications</topic><topic>Lymphoma - complications</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Sepsis - drug therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TSUDA, SHOICHIRO</creatorcontrib><creatorcontrib>NISHIDA, KAZUHIRO</creatorcontrib><creatorcontrib>MAEKAWA, TAIRA</creatorcontrib><creatorcontrib>ABE, TATSUO</creatorcontrib><creatorcontrib>TAKINO, TATSURO</creatorcontrib><creatorcontrib>FUJII, HIROSHI</creatorcontrib><creatorcontrib>TANIWAKI, MASAFUMI</creatorcontrib><creatorcontrib>YASHIGE, HIROMI</creatorcontrib><creatorcontrib>HORIIKE, SHIGEO</creatorcontrib><creatorcontrib>YOKOTA, SYOHEI</creatorcontrib><creatorcontrib>OH, ONGYOKU</creatorcontrib><creatorcontrib>SONODA, YOSHIAKI</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>TSUDA, SHOICHIRO</au><au>NISHIDA, KAZUHIRO</au><au>MAEKAWA, TAIRA</au><au>ABE, TATSUO</au><au>TAKINO, TATSURO</au><au>FUJII, HIROSHI</au><au>TANIWAKI, MASAFUMI</au><au>YASHIGE, HIROMI</au><au>HORIIKE, SHIGEO</au><au>YOKOTA, SYOHEI</au><au>OH, ONGYOKU</au><au>SONODA, YOSHIAKI</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CLINICAL EVALUATION OF CEFMENOXIME IN THE SEVERE INFECTIONS IN LEUKEMIA AND RELATED DISORDERS</atitle><jtitle>Japanese journal of antibiotics</jtitle><addtitle>Jpn. J. Antibiotics</addtitle><date>1986-10</date><risdate>1986</risdate><volume>39</volume><issue>10</issue><spage>2651</spage><epage>2660</epage><pages>2651-2660</pages><issn>0368-2781</issn><eissn>2186-5477</eissn><abstract>Ninety nine patients with leukemia and/or related disorders were treated with cefmenoxime (CMX). Among them, 77 patients had severe infections, while other 22 patients did not suffer from infection, but it was expected that they would fall into serious conditions if they were infected. Sixty of the 77 patients who had severe infection were used in the evaluation of effectiveness. The remaining 17 patients were not evaluated because they were subjected to combined treatments of CMX and other therapeutic agents such as other antibiotics, rglobulin or interferon. Excellent responses were found in 26 (43. 3%) patients and good responses in 12 (20. 0%) patients. In total, the rate of effectiveness was 63. 3%. Nineteen of the 22 patients who were treated prophylactically with CMX were used in the evaluation of effectiveness, while 3 patients were excluded from the evaluation because peripheral neutrophils were counted to be more than 1, 000/mm3 before CMX was administrated, although these 3 patients were used in the final evaluation to examine side effects. In the prophylactic treatment, the rate of effectiveness was 89. 5%. The side effects were seen in 4 patients (4/82: 4. 9%). A different symptom was identified in each patient. These symptoms were skin rash, mild nausea, mild diarrhea and slight elevation of serum bilirubin. Prompt improvements of these symptoms occurred as soon as CMX administration was stopped. These results show that CMX is a therapeutically effective and safe antibiotics for the treatment of severe infections or for the prophylaxis of infections in patients associated with leukemia and/or related disorders.</abstract><cop>Japan</cop><pub>Japan Antibiotics Research Association</pub><pmid>3468272</pmid><doi>10.11553/antibiotics1968b.39.2651</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0368-2781 |
ispartof | The Japanese Journal of Antibiotics, 1986/10/25, Vol.39(10), pp.2651-2660 |
issn | 0368-2781 2186-5477 |
language | jpn |
recordid | cdi_proquest_miscellaneous_77254173 |
source | MEDLINE; EZB-FREE-00999 freely available EZB journals |
subjects | Adolescent Adult Aged Bacterial Infections - drug therapy Bacterial Infections - etiology Cefmenoxime Cefotaxime - administration & dosage Cefotaxime - analogs & derivatives Cefotaxime - therapeutic use Female Humans Leukemia - complications Leukemia, Myeloid, Acute - complications Lymphoma - complications Male Middle Aged Sepsis - drug therapy |
title | CLINICAL EVALUATION OF CEFMENOXIME IN THE SEVERE INFECTIONS IN LEUKEMIA AND RELATED DISORDERS |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-15T00%3A49%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=CLINICAL%20EVALUATION%20OF%20CEFMENOXIME%20IN%20THE%20SEVERE%20INFECTIONS%20IN%20LEUKEMIA%20AND%20RELATED%20DISORDERS&rft.jtitle=Japanese%20journal%20of%20antibiotics&rft.au=TSUDA,%20SHOICHIRO&rft.date=1986-10&rft.volume=39&rft.issue=10&rft.spage=2651&rft.epage=2660&rft.pages=2651-2660&rft.issn=0368-2781&rft.eissn=2186-5477&rft_id=info:doi/10.11553/antibiotics1968b.39.2651&rft_dat=%3Cproquest_pubme%3E77254173%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=77254173&rft_id=info:pmid/3468272&rfr_iscdi=true |