Metabolites of meperidine in the fetal and maternal serum
Although meperidine††Other names used for this compound are pethidine and Demerol (Winthrop Labs., Division of Sterling Drug, Inc., New York, New York). appears to be the safest obstetric analgesic agent, it has been associated with infant respiratory depression in certain situations. It would appea...
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Veröffentlicht in: | American journal of obstetrics and gynecology 1976-12, Vol.126 (8), p.997-1002 |
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container_title | American journal of obstetrics and gynecology |
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creator | Morrison, J.C. Whybrew, W.D. Rosser, S.I. Bucovaz, E.T. Wiser, W.L. Fish, S.A. |
description | Although meperidine††Other names used for this compound are pethidine and Demerol (Winthrop Labs., Division of Sterling Drug, Inc., New York, New York). appears to be the safest obstetric analgesic agent, it has been associated with infant respiratory depression in certain situations. It would appear that the incidence of fetal depression related to meperidine is dependent on the time of injection prior to delivery, the quantity of drug administered, and the rate of maternal metabolism of the analgesic. Previous work showed that meperidine is metabolized in the maternal system by one of three patterns. The present study demonstrates that the particular maternal serum pattern is characteristic for the individual, regardless of whether the patient is pregnant or not, and that the fetal depression, although usually mild, can be correlated with fetal pH data as well as Apgar scores. In addition, this study supports indirectly the contention that metabolites of meperidine rather than the parent compound cause fetal depression. It would appear, therefore, that in certain obstetric cases with a higher probability for infant depression, other analgesic agents might be considered, especially if the serum pattern indicates meperidine is being metabolized rapidly in the maternal system. |
doi_str_mv | 10.1016/0002-9378(76)90691-8 |
format | Article |
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It would appear that the incidence of fetal depression related to meperidine is dependent on the time of injection prior to delivery, the quantity of drug administered, and the rate of maternal metabolism of the analgesic. Previous work showed that meperidine is metabolized in the maternal system by one of three patterns. The present study demonstrates that the particular maternal serum pattern is characteristic for the individual, regardless of whether the patient is pregnant or not, and that the fetal depression, although usually mild, can be correlated with fetal pH data as well as Apgar scores. In addition, this study supports indirectly the contention that metabolites of meperidine rather than the parent compound cause fetal depression. It would appear, therefore, that in certain obstetric cases with a higher probability for infant depression, other analgesic agents might be considered, especially if the serum pattern indicates meperidine is being metabolized rapidly in the maternal system.</description><identifier>ISSN: 0002-9378</identifier><identifier>EISSN: 1097-6868</identifier><identifier>DOI: 10.1016/0002-9378(76)90691-8</identifier><identifier>PMID: 998689</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Apgar Score ; Depression, Chemical ; Female ; Fetal Blood - metabolism ; Humans ; Infant, Newborn ; Labor, Obstetric ; Maternal-Fetal Exchange ; Meperidine - blood ; Meperidine - metabolism ; Meperidine - pharmacology ; Postpartum Period ; Pregnancy ; Time Factors</subject><ispartof>American journal of obstetrics and gynecology, 1976-12, Vol.126 (8), p.997-1002</ispartof><rights>1976</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-2cad792b0efe4381b8fcddb6b7aa78258699d7ae02a3c86656e487f4f46912e63</citedby><cites>FETCH-LOGICAL-c381t-2cad792b0efe4381b8fcddb6b7aa78258699d7ae02a3c86656e487f4f46912e63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0002-9378(76)90691-8$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/998689$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Morrison, J.C.</creatorcontrib><creatorcontrib>Whybrew, W.D.</creatorcontrib><creatorcontrib>Rosser, S.I.</creatorcontrib><creatorcontrib>Bucovaz, E.T.</creatorcontrib><creatorcontrib>Wiser, W.L.</creatorcontrib><creatorcontrib>Fish, S.A.</creatorcontrib><title>Metabolites of meperidine in the fetal and maternal serum</title><title>American journal of obstetrics and gynecology</title><addtitle>Am J Obstet Gynecol</addtitle><description>Although meperidine††Other names used for this compound are pethidine and Demerol (Winthrop Labs., Division of Sterling Drug, Inc., New York, New York). appears to be the safest obstetric analgesic agent, it has been associated with infant respiratory depression in certain situations. It would appear that the incidence of fetal depression related to meperidine is dependent on the time of injection prior to delivery, the quantity of drug administered, and the rate of maternal metabolism of the analgesic. Previous work showed that meperidine is metabolized in the maternal system by one of three patterns. The present study demonstrates that the particular maternal serum pattern is characteristic for the individual, regardless of whether the patient is pregnant or not, and that the fetal depression, although usually mild, can be correlated with fetal pH data as well as Apgar scores. In addition, this study supports indirectly the contention that metabolites of meperidine rather than the parent compound cause fetal depression. It would appear, therefore, that in certain obstetric cases with a higher probability for infant depression, other analgesic agents might be considered, especially if the serum pattern indicates meperidine is being metabolized rapidly in the maternal system.</description><subject>Apgar Score</subject><subject>Depression, Chemical</subject><subject>Female</subject><subject>Fetal Blood - metabolism</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Labor, Obstetric</subject><subject>Maternal-Fetal Exchange</subject><subject>Meperidine - blood</subject><subject>Meperidine - metabolism</subject><subject>Meperidine - pharmacology</subject><subject>Postpartum Period</subject><subject>Pregnancy</subject><subject>Time Factors</subject><issn>0002-9378</issn><issn>1097-6868</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1976</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kElPwzAQhS3EVgr_oIecEBwCtpN6uSBVFZtUxAXOlmOPhVGWYidI_HscUvXIaTTzvnnSewgtCL4hmLBbjDHNZcHFFWfXEjNJcnGAZgRLnjPBxCGa7ZFTdBbj57hSSU_QsZQJkDMkX6DXVVf7HmLWuayBLQRvfQuZb7P-AzKXgDrTrc0a3UNo0xIhDM05OnK6jnCxm3P0_nD_tn7KN6-Pz-vVJjeFIH1OjbZc0gqDgzJdKuGMtRWruNZc0KVgUlquAVNdGMHYkkEpuCtdmfJQYMUcXU6-29B9DRB71fhooK51C90QlSgYEZwWCSwn0IQuxgBObYNvdPhRBKuxMDXGV2MbijP1V1j6nqPFzn-oGrD7p6mhJN9NMqSM3x6CisZDa8D6AKZXtvP_-_8CNEB5gQ</recordid><startdate>19761215</startdate><enddate>19761215</enddate><creator>Morrison, J.C.</creator><creator>Whybrew, W.D.</creator><creator>Rosser, S.I.</creator><creator>Bucovaz, E.T.</creator><creator>Wiser, W.L.</creator><creator>Fish, S.A.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19761215</creationdate><title>Metabolites of meperidine in the fetal and maternal serum</title><author>Morrison, J.C. ; Whybrew, W.D. ; Rosser, S.I. ; Bucovaz, E.T. ; Wiser, W.L. ; Fish, S.A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c381t-2cad792b0efe4381b8fcddb6b7aa78258699d7ae02a3c86656e487f4f46912e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1976</creationdate><topic>Apgar Score</topic><topic>Depression, Chemical</topic><topic>Female</topic><topic>Fetal Blood - metabolism</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Labor, Obstetric</topic><topic>Maternal-Fetal Exchange</topic><topic>Meperidine - blood</topic><topic>Meperidine - metabolism</topic><topic>Meperidine - pharmacology</topic><topic>Postpartum Period</topic><topic>Pregnancy</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Morrison, J.C.</creatorcontrib><creatorcontrib>Whybrew, W.D.</creatorcontrib><creatorcontrib>Rosser, S.I.</creatorcontrib><creatorcontrib>Bucovaz, E.T.</creatorcontrib><creatorcontrib>Wiser, W.L.</creatorcontrib><creatorcontrib>Fish, S.A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of obstetrics and gynecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morrison, J.C.</au><au>Whybrew, W.D.</au><au>Rosser, S.I.</au><au>Bucovaz, E.T.</au><au>Wiser, W.L.</au><au>Fish, S.A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolites of meperidine in the fetal and maternal serum</atitle><jtitle>American journal of obstetrics and gynecology</jtitle><addtitle>Am J Obstet Gynecol</addtitle><date>1976-12-15</date><risdate>1976</risdate><volume>126</volume><issue>8</issue><spage>997</spage><epage>1002</epage><pages>997-1002</pages><issn>0002-9378</issn><eissn>1097-6868</eissn><abstract>Although meperidine††Other names used for this compound are pethidine and Demerol (Winthrop Labs., Division of Sterling Drug, Inc., New York, New York). appears to be the safest obstetric analgesic agent, it has been associated with infant respiratory depression in certain situations. It would appear that the incidence of fetal depression related to meperidine is dependent on the time of injection prior to delivery, the quantity of drug administered, and the rate of maternal metabolism of the analgesic. Previous work showed that meperidine is metabolized in the maternal system by one of three patterns. The present study demonstrates that the particular maternal serum pattern is characteristic for the individual, regardless of whether the patient is pregnant or not, and that the fetal depression, although usually mild, can be correlated with fetal pH data as well as Apgar scores. In addition, this study supports indirectly the contention that metabolites of meperidine rather than the parent compound cause fetal depression. It would appear, therefore, that in certain obstetric cases with a higher probability for infant depression, other analgesic agents might be considered, especially if the serum pattern indicates meperidine is being metabolized rapidly in the maternal system.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>998689</pmid><doi>10.1016/0002-9378(76)90691-8</doi><tpages>6</tpages></addata></record> |
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subjects | Apgar Score Depression, Chemical Female Fetal Blood - metabolism Humans Infant, Newborn Labor, Obstetric Maternal-Fetal Exchange Meperidine - blood Meperidine - metabolism Meperidine - pharmacology Postpartum Period Pregnancy Time Factors |
title | Metabolites of meperidine in the fetal and maternal serum |
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