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Randomized comparison of second trimester pregnancy termination utilizing saline moistened or dry misoprostol
The aim of this randomized prospective study was to compare efficacy and side effects of saline moistened misoprostol with dry misoprostol, administered 800 mug intravaginally every 6 h up to a maximum of 3 doses in 24 h for second trimester pregnancy termination. A total of 81 women seeking termina...
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Published in: | Archives of gynecology and obstetrics 2007-11, Vol.276 (5), p.511-516 |
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creator | Yilmaz, Bulent Kelekci, Sefa Ertas, Ibrahim Egemen Ozel, Murat Sut, Necdet Mollamahmutoglu, Leyla Danisman, Nuri |
description | The aim of this randomized prospective study was to compare efficacy and side effects of saline moistened misoprostol with dry misoprostol, administered 800 mug intravaginally every 6 h up to a maximum of 3 doses in 24 h for second trimester pregnancy termination.
A total of 81 women seeking termination of second trimester pregnancy (55 fetal death, 17 fetal structural anomaly, 5 chromosomal abnormality, 4 other reasons) were randomly assigned to one of two treatment groups: (1) intravaginal non-moistened (dry) misoprostol in group A (n = 40) or (2) misoprostol moistened with 3 ml of saline in group B (n = 41).
All of the patients in either group aborted within 48 h (100% success rate). Delivery was achieved in a median (interquartile range) of 13 (40) h with the group A protocol and 12 (36) h with the group B protocol (P = 0.652). Delivery with first dose, delivery within 12 h and delivery within 24 h were similar (P > 0.05) in group B (34.1, 87.5 and 60%, respectively) and group A (25, 82.9, 46.3, respectively). Both treatment regimens were tolerable and with similar side effects.
Misoprostol moistened with saline was not more effective than dry misoprostol for second trimester pregnancy termination. |
doi_str_mv | 10.1007/s00404-007-0374-9 |
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A total of 81 women seeking termination of second trimester pregnancy (55 fetal death, 17 fetal structural anomaly, 5 chromosomal abnormality, 4 other reasons) were randomly assigned to one of two treatment groups: (1) intravaginal non-moistened (dry) misoprostol in group A (n = 40) or (2) misoprostol moistened with 3 ml of saline in group B (n = 41).
All of the patients in either group aborted within 48 h (100% success rate). Delivery was achieved in a median (interquartile range) of 13 (40) h with the group A protocol and 12 (36) h with the group B protocol (P = 0.652). Delivery with first dose, delivery within 12 h and delivery within 24 h were similar (P > 0.05) in group B (34.1, 87.5 and 60%, respectively) and group A (25, 82.9, 46.3, respectively). Both treatment regimens were tolerable and with similar side effects.
Misoprostol moistened with saline was not more effective than dry misoprostol for second trimester pregnancy termination.</description><identifier>ISSN: 0932-0067</identifier><identifier>EISSN: 1432-0711</identifier><identifier>DOI: 10.1007/s00404-007-0374-9</identifier><identifier>PMID: 17453221</identifier><language>eng</language><publisher>Germany: Springer Nature B.V</publisher><subject>Abortifacient Agents - administration & dosage ; Abortion, Therapeutic ; Administration, Intravaginal ; Adult ; Female ; Health risk assessment ; Humans ; Misoprostol - administration & dosage ; Pregnancy ; Pregnancy Trimester, Second ; Prospective Studies ; Sodium Chloride - administration & dosage ; Treatment Outcome</subject><ispartof>Archives of gynecology and obstetrics, 2007-11, Vol.276 (5), p.511-516</ispartof><rights>Springer-Verlag 2007.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c242t-6517ed0bb8c83e8b5f52d54947ff056f9e390145bdef6ea7f899f844a76b22bf3</citedby><cites>FETCH-LOGICAL-c242t-6517ed0bb8c83e8b5f52d54947ff056f9e390145bdef6ea7f899f844a76b22bf3</cites></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/17453221$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yilmaz, Bulent</creatorcontrib><creatorcontrib>Kelekci, Sefa</creatorcontrib><creatorcontrib>Ertas, Ibrahim Egemen</creatorcontrib><creatorcontrib>Ozel, Murat</creatorcontrib><creatorcontrib>Sut, Necdet</creatorcontrib><creatorcontrib>Mollamahmutoglu, Leyla</creatorcontrib><creatorcontrib>Danisman, Nuri</creatorcontrib><title>Randomized comparison of second trimester pregnancy termination utilizing saline moistened or dry misoprostol</title><title>Archives of gynecology and obstetrics</title><addtitle>Arch Gynecol Obstet</addtitle><description>The aim of this randomized prospective study was to compare efficacy and side effects of saline moistened misoprostol with dry misoprostol, administered 800 mug intravaginally every 6 h up to a maximum of 3 doses in 24 h for second trimester pregnancy termination.
A total of 81 women seeking termination of second trimester pregnancy (55 fetal death, 17 fetal structural anomaly, 5 chromosomal abnormality, 4 other reasons) were randomly assigned to one of two treatment groups: (1) intravaginal non-moistened (dry) misoprostol in group A (n = 40) or (2) misoprostol moistened with 3 ml of saline in group B (n = 41).
All of the patients in either group aborted within 48 h (100% success rate). Delivery was achieved in a median (interquartile range) of 13 (40) h with the group A protocol and 12 (36) h with the group B protocol (P = 0.652). Delivery with first dose, delivery within 12 h and delivery within 24 h were similar (P > 0.05) in group B (34.1, 87.5 and 60%, respectively) and group A (25, 82.9, 46.3, respectively). Both treatment regimens were tolerable and with similar side effects.
Misoprostol moistened with saline was not more effective than dry misoprostol for second trimester pregnancy termination.</description><subject>Abortifacient Agents - administration & dosage</subject><subject>Abortion, Therapeutic</subject><subject>Administration, Intravaginal</subject><subject>Adult</subject><subject>Female</subject><subject>Health risk assessment</subject><subject>Humans</subject><subject>Misoprostol - administration & dosage</subject><subject>Pregnancy</subject><subject>Pregnancy Trimester, Second</subject><subject>Prospective Studies</subject><subject>Sodium Chloride - administration & dosage</subject><subject>Treatment Outcome</subject><issn>0932-0067</issn><issn>1432-0711</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNpdkV1LBCEYhSWKdtv6Ad2EEHQ3pY6jzmVEX7AQRF2LM-riMqOTzlzs_vocdiHoyiM87_H1HACuMbrHCPGHhBBFtMiyQCWnRX0ClpiWpEAc41OwRPWsEeMLcJHSFiFMhGDnYIE5rUpC8BL0n8rr0Lu90bAN_aCiS8HDYGEybfAajtH1Jo0mwiGajVe-3cF8651Xo8vkNLrO7Z3fwKQ65w3sg8u4z34hQh13sM-OQwxpDN0lOLOqS-bqeK7A98vz19Nbsf54fX96XBctoWQsWIW50ahpRCtKI5rKVkRXtKbcWlQxW5uyRphWjTaWGcWtqGsrKFWcNYQ0tlyBu4NvfvdnyuvLvERruk55E6YkmSAcl5xn8PYfuA1T9Hk3SQjDIsdFWabwgWrzN1I0Vg45FRV3EiM5NyEPTchZzk3IOs_cHJ2npjf6b-IYffkLEFmGYA</recordid><startdate>200711</startdate><enddate>200711</enddate><creator>Yilmaz, Bulent</creator><creator>Kelekci, Sefa</creator><creator>Ertas, Ibrahim Egemen</creator><creator>Ozel, Murat</creator><creator>Sut, Necdet</creator><creator>Mollamahmutoglu, Leyla</creator><creator>Danisman, Nuri</creator><general>Springer Nature B.V</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>200711</creationdate><title>Randomized comparison of second trimester pregnancy termination utilizing saline moistened or dry misoprostol</title><author>Yilmaz, Bulent ; 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A total of 81 women seeking termination of second trimester pregnancy (55 fetal death, 17 fetal structural anomaly, 5 chromosomal abnormality, 4 other reasons) were randomly assigned to one of two treatment groups: (1) intravaginal non-moistened (dry) misoprostol in group A (n = 40) or (2) misoprostol moistened with 3 ml of saline in group B (n = 41).
All of the patients in either group aborted within 48 h (100% success rate). Delivery was achieved in a median (interquartile range) of 13 (40) h with the group A protocol and 12 (36) h with the group B protocol (P = 0.652). Delivery with first dose, delivery within 12 h and delivery within 24 h were similar (P > 0.05) in group B (34.1, 87.5 and 60%, respectively) and group A (25, 82.9, 46.3, respectively). Both treatment regimens were tolerable and with similar side effects.
Misoprostol moistened with saline was not more effective than dry misoprostol for second trimester pregnancy termination.</abstract><cop>Germany</cop><pub>Springer Nature B.V</pub><pmid>17453221</pmid><doi>10.1007/s00404-007-0374-9</doi><tpages>6</tpages></addata></record> |
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subjects | Abortifacient Agents - administration & dosage Abortion, Therapeutic Administration, Intravaginal Adult Female Health risk assessment Humans Misoprostol - administration & dosage Pregnancy Pregnancy Trimester, Second Prospective Studies Sodium Chloride - administration & dosage Treatment Outcome |
title | Randomized comparison of second trimester pregnancy termination utilizing saline moistened or dry misoprostol |
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