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"title": "Risk Factors for Cesarean Delivery following Labor Induction in Multiparous Women",
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"creatorType": "author",
"firstName": "Corine J",
"lastName": "Verhoeven"
},
{
"creatorType": "author",
"firstName": "Cedric T",
"lastName": "van Uytrecht"
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{
"creatorType": "author",
"firstName": "Martina M",
"lastName": "Porath"
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"creatorType": "author",
"firstName": "Ben Willem J",
"lastName": "Mol"
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"abstractNote": "Objective. To identify potential risk factors for cesarean delivery following labor induction in multiparous women at term. Methods. We conducted a retrospective case-control study. Cases were parous women in whom the induction of labor had resulted in a cesarean delivery. For each case, we used the data of two successful inductions as controls. Successful induction was defined as a vaginal delivery after the induction of labor. The study was limited to term singleton pregnancies with a child in cephalic position. Results. Between 1995 and 2010, labor was induced in 2548 parous women, of whom 80 had a cesarean delivery (3%). These 80 cases were compared to the data of 160 parous women with a successful induction of labor. In the multivariate analysis history of preterm delivery (odds ratio (OR) 5.3 (95% CI 1.1 to 25)), maternal height (OR 0.87 (95% CI 0.80 to 0.95)) and dilatation at the start of induction (OR 0.43 (95% CI 0.19 to 0.98)) were associated with failed induction. Conclusion. In multiparous women, the risk of cesarean delivery following labor induction increases with previous preterm delivery, short maternal height, and limited dilatation at the start of induction.",
"publicationTitle": "Journal of pregnancy",
"publisher": "",
"place": "",
"date": "2013",
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"pages": "820892",
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"title": "Future Research Needs for Strategies To Reduce Cesarean Birth in Low-Risk Women: Identification of Future Research Needs From Comparative Effectiveness Review No. 80",
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"firstName": "Rashonda M R M",
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"firstName": "J Nikki J N",
"lastName": "McKoy"
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"firstName": "Jeffrey C J C",
"lastName": "Andrews"
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{
"creatorType": "author",
"firstName": "Rebecca N R N",
"lastName": "Jerome"
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"creatorType": "author",
"firstName": "Frances E F E",
"lastName": "Likis"
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"firstName": "Tanya S T S",
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"firstName": "Stephaine H S H",
"lastName": "Walker"
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"firstName": "Katherine E K E",
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"abstractNote": "The objective of this Future Research Needs project is to identify top-priority research needs in the area of strategies to reduce cesarean birth in low-risk women. The research needs identified in this report include knowledge gaps related to the effectiveness of specific strategies for reducing use of cesarean birth compared with usual care, knowledge gaps about factors that drive patient and provider preferences and attitudes, and recommendations for methodologic improvements. This project builds on the evidence gaps and methodologic issues identified in the Comparative Effectiveness Review (CER) Strategies To Reduce Cesarean Birth in Low-Risk Women., In Phase 1, stakeholders participated in a teleconference and then a Web-based survey to build a comprehensive list of research questions and methodologic recommendations. In Phase 2, stakeholders participated in one conference call and completed three Web-based surveys to prioritize research questions and recommendations. We identified currently funded and recently completed research between February 2012 and June 2012. To identify currently funded or recently completed randomized controlled trials intended to reduce use of cesarean delivery, we conducted searches of U.S. government resources (i.e., ClinicalTrials.gov, NIH Reporter), international trial registries (e.g., Current Controlled Trials), and other potential funding sources such as relevant associations and organizations (e.g., American College of Nurse-Midwives, American Congress of Obstetricians and Gynecologists)., Thirteen stakeholders representing the perspective of patient advocacy groups, academic researchers, obstetrician-gynecologists, nursing and nurse-midwifery professional organizations, payers, and national foundations and societies agreed to participate in one or more of the stages of ranking and prioritization. The group included five Key Informants/Technical Expert Panel members from the draft CER. In Phase 1, stakeholders generated a “snowballed” list of 47 research questions and 17 methodologic recommendations. In Phase 2, stakeholders worked from the snowballed list to prioritize research needs. In Phase 3, the Evidence-based Practice Center investigators developed recommendations for optimal study design., Our multistep process for identifying, multiplying, and prioritizing research questions to advance research in the area of strategies to reduce cesarean birth in low-risk women resulted in an actionable list of research topics to fill specific knowledge gaps. The top-tier research questions reflect a focus on standardization strategies for induction and arrest of labor (three of the top five research questions), systems-level strategies (one of five), and novel staffing models (one of five). For strategies that standardize induction and definitions of arrest of labor, we recommend cluster randomized controlled trials with randomization of entire labor and delivery units. For trials of systems-level strategies and staffing models, we recommend multisite studies to improve power and generalizability. The top-tier methodologic improvements focused on improving the capture of short- and long-term birth outcomes.",
"series": "AHRQ Comparative Effectiveness Reviews",
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"date": "2012",
"publisher": "Agency for Healthcare Research and Quality (US)",
"place": "Rockville (MD)",
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"title": "The comparison of intraincisional injection tramadol, pethidine and bupivacaine on postcesarean section pain relief under spinal anesthesia",
"creators": [
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"creatorType": "author",
"firstName": "Mitra",
"lastName": "Jabalameli"
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{
"creatorType": "author",
"firstName": "Mohammadreza",
"lastName": "Safavi"
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{
"creatorType": "author",
"firstName": "Azim",
"lastName": "Honarmand"
},
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"lastName": "Moradi"
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"lastName": "Kashefi"
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"abstractNote": "BACKGROUND\n\nBupivacaine, tramadol, and pethidine has local anesthetic effect. The aim of this study was to compare effect of subcutaneous (SC) infiltration of tramadol, pethidine, and bupivacaine on postoperative pain relief after cesarean delivery.\n\n\nMATERIALS AND METHODS\n\n120 patient, scheduled for elective cesarean section under spinal anesthesia, were randomly allocated to 1 of the 4 groups according to the drugs used for postoperative analgesia: Group P (Pethidine) 50 mg ,Group T (Tramadol) 40 mg, Group B (Bupivacaine 0.25%) 0.7 mg/kg, and Group C (control) 20CC normal saline injection in incision site of surgery. Pain intensity (VAS = visual analogous scale) at rest and on coughing and opioid consumption were assessed on arrival in the recovery room, and then 15, 30, 60 minutes and 2, 6, 12, 24 hours after that.\n\n\nRESULTS\n\nVAS scores were significantly lower in groups T and P compared with groups B and C except for 24 hours (VAS rest) and 6 hours (VAS on coughing) postoperatively (P < 0.05). The number of patients requiring morphine were significantly different between the groups (105 doses vs. 87, 56, 46, doses for group C, B, T and P, respectively, P < 0.05) in all the times, except for 2 and 6 hours postoperatively.\n\n\nCONCLUSIONS\n\nThe administration of subcutaneous pethidine or tramadol after cesarean section improves analgesia and has a significant morphine-sparing effect compared with bupivacaine and control groups.",
"publicationTitle": "Advanced biomedical research",
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"title": "[Factors associated with the use of supplements among newborns in communal wards in Rio de Janeiro, 2009]",
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