Vaginal cleansing before cesarean delivery to reduce postoperative infectious morbidity: a randomized, controlled trial

Objective The objective of the study was to determine whether vaginal preparation with povidone iodine before cesarean delivery decreased the risk of postoperative maternal morbidities. Study Design The design of the study was a randomized, controlled trial in women undergoing cesarean delivery with...

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Veröffentlicht in:American journal of obstetrics and gynecology 2010-03, Vol.202 (3), p.310.e1-310.e6
Hauptverfasser: Haas, David M., MD, MS, Pazouki, Fatemeh, MD, Smith, Ronda R, Fry, Amy M., MD, Podzielinski, Iwona, MD, Al-Darei, Sarah M., MD, Golichowski, Alan M., MD, PhD
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container_end_page 310.e6
container_issue 3
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container_title American journal of obstetrics and gynecology
container_volume 202
creator Haas, David M., MD, MS
Pazouki, Fatemeh, MD
Smith, Ronda R
Fry, Amy M., MD
Podzielinski, Iwona, MD
Al-Darei, Sarah M., MD
Golichowski, Alan M., MD, PhD
description Objective The objective of the study was to determine whether vaginal preparation with povidone iodine before cesarean delivery decreased the risk of postoperative maternal morbidities. Study Design The design of the study was a randomized, controlled trial in women undergoing cesarean delivery with subjects assigned to have a preoperative vaginal cleansing with povidone iodine or to a standard care group (no vaginal wash). The primary outcome was a composite of postoperative fever, endometritis, sepsis, readmission, wound infection, or complication. Results There were 155 vaginal cleansing subjects and 145 control subjects. Overall, 9.0% developed the composite outcome, with fewer women in the cleansing group (6.5%) compared with the control group (11.7%), although the difference was not statistically significant (relative risk, 0.55; 95% confidence interval, 0.26–1.11; P = .11). Length of surgery, being in labor, and having a dilated cervix were all associated with the composite morbidity outcome. Conclusion Vaginal cleansing with povidone iodine before cesarean delivery may decrease postoperative morbidities, although the reduction is not statistically significant.
doi_str_mv 10.1016/j.ajog.2010.01.005
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Study Design The design of the study was a randomized, controlled trial in women undergoing cesarean delivery with subjects assigned to have a preoperative vaginal cleansing with povidone iodine or to a standard care group (no vaginal wash). The primary outcome was a composite of postoperative fever, endometritis, sepsis, readmission, wound infection, or complication. Results There were 155 vaginal cleansing subjects and 145 control subjects. Overall, 9.0% developed the composite outcome, with fewer women in the cleansing group (6.5%) compared with the control group (11.7%), although the difference was not statistically significant (relative risk, 0.55; 95% confidence interval, 0.26–1.11; P = .11). Length of surgery, being in labor, and having a dilated cervix were all associated with the composite morbidity outcome. Conclusion Vaginal cleansing with povidone iodine before cesarean delivery may decrease postoperative morbidities, although the reduction is not statistically significant.</description><identifier>ISSN: 0002-9378</identifier><identifier>EISSN: 1097-6868</identifier><identifier>DOI: 10.1016/j.ajog.2010.01.005</identifier><identifier>PMID: 20207251</identifier><language>eng</language><publisher>United States: Mosby, Inc</publisher><subject><![CDATA[Adult ; Anti-Infective Agents, Local - administration & dosage ; cesarean delivery ; Cesarean Section ; Endometritis - prevention & control ; Female ; Fever - prevention & control ; Gravidity ; Humans ; Labor Stage, First ; Labor, Obstetric ; Obstetrics and Gynecology ; Parity ; Patient Readmission ; Postoperative Complications - prevention & control ; postoperative maternal morbidities ; povidone iodine ; Povidone-Iodine - administration & dosage ; Pregnancy ; Preoperative Care ; risk ; Sepsis - prevention & control ; Surgical Stapling ; Surgical Wound Infection - prevention & control ; Sutures ; Vagina - microbiology ; vaginal preparation]]></subject><ispartof>American journal of obstetrics and gynecology, 2010-03, Vol.202 (3), p.310.e1-310.e6</ispartof><rights>Mosby, Inc.</rights><rights>2010 Mosby, Inc.</rights><rights>Copyright 2010 Mosby, Inc. 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Study Design The design of the study was a randomized, controlled trial in women undergoing cesarean delivery with subjects assigned to have a preoperative vaginal cleansing with povidone iodine or to a standard care group (no vaginal wash). The primary outcome was a composite of postoperative fever, endometritis, sepsis, readmission, wound infection, or complication. Results There were 155 vaginal cleansing subjects and 145 control subjects. Overall, 9.0% developed the composite outcome, with fewer women in the cleansing group (6.5%) compared with the control group (11.7%), although the difference was not statistically significant (relative risk, 0.55; 95% confidence interval, 0.26–1.11; P = .11). Length of surgery, being in labor, and having a dilated cervix were all associated with the composite morbidity outcome. 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dosage</topic><topic>Pregnancy</topic><topic>Preoperative Care</topic><topic>risk</topic><topic>Sepsis - prevention &amp; control</topic><topic>Surgical Stapling</topic><topic>Surgical Wound Infection - prevention &amp; control</topic><topic>Sutures</topic><topic>Vagina - microbiology</topic><topic>vaginal preparation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Haas, David M., MD, MS</creatorcontrib><creatorcontrib>Pazouki, Fatemeh, MD</creatorcontrib><creatorcontrib>Smith, Ronda R</creatorcontrib><creatorcontrib>Fry, Amy M., MD</creatorcontrib><creatorcontrib>Podzielinski, Iwona, MD</creatorcontrib><creatorcontrib>Al-Darei, Sarah M., MD</creatorcontrib><creatorcontrib>Golichowski, Alan M., MD, PhD</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>Haas, David M., MD, MS</au><au>Pazouki, Fatemeh, MD</au><au>Smith, Ronda R</au><au>Fry, Amy M., MD</au><au>Podzielinski, Iwona, MD</au><au>Al-Darei, Sarah M., MD</au><au>Golichowski, Alan M., MD, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vaginal cleansing before cesarean delivery to reduce postoperative infectious morbidity: a randomized, controlled trial</atitle><jtitle>American journal of obstetrics and gynecology</jtitle><addtitle>Am J Obstet Gynecol</addtitle><date>2010-03-01</date><risdate>2010</risdate><volume>202</volume><issue>3</issue><spage>310.e1</spage><epage>310.e6</epage><pages>310.e1-310.e6</pages><issn>0002-9378</issn><eissn>1097-6868</eissn><abstract>Objective The objective of the study was to determine whether vaginal preparation with povidone iodine before cesarean delivery decreased the risk of postoperative maternal morbidities. Study Design The design of the study was a randomized, controlled trial in women undergoing cesarean delivery with subjects assigned to have a preoperative vaginal cleansing with povidone iodine or to a standard care group (no vaginal wash). The primary outcome was a composite of postoperative fever, endometritis, sepsis, readmission, wound infection, or complication. Results There were 155 vaginal cleansing subjects and 145 control subjects. Overall, 9.0% developed the composite outcome, with fewer women in the cleansing group (6.5%) compared with the control group (11.7%), although the difference was not statistically significant (relative risk, 0.55; 95% confidence interval, 0.26–1.11; P = .11). Length of surgery, being in labor, and having a dilated cervix were all associated with the composite morbidity outcome. Conclusion Vaginal cleansing with povidone iodine before cesarean delivery may decrease postoperative morbidities, although the reduction is not statistically significant.</abstract><cop>United States</cop><pub>Mosby, Inc</pub><pmid>20207251</pmid><doi>10.1016/j.ajog.2010.01.005</doi></addata></record>
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subjects Adult
Anti-Infective Agents, Local - administration & dosage
cesarean delivery
Cesarean Section
Endometritis - prevention & control
Female
Fever - prevention & control
Gravidity
Humans
Labor Stage, First
Labor, Obstetric
Obstetrics and Gynecology
Parity
Patient Readmission
Postoperative Complications - prevention & control
postoperative maternal morbidities
povidone iodine
Povidone-Iodine - administration & dosage
Pregnancy
Preoperative Care
risk
Sepsis - prevention & control
Surgical Stapling
Surgical Wound Infection - prevention & control
Sutures
Vagina - microbiology
vaginal preparation
title Vaginal cleansing before cesarean delivery to reduce postoperative infectious morbidity: a randomized, controlled trial
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