Charles G Fahrenholtz, Laura S Bonanno, Jennifer B Martin
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This review will determine whether TXA administration to patients experiencing PPH leads to a reduction in blood loss, the requirement for transfusion of packed red blood cells and the need for emergency hysterectomies, in both developed and developing nations.</p><p><strong>Inclusion criteria: </strong>This review will consider studies that include women under 40 with a diagnosis of postpartum hemorrhage. Studies that evaluate intravenous administration of TXA within three hours of birth as adjuvant treatment of postpartum hemorrhage will be considered. The comparator will be groups that have not received TXA as part of the treatment for postpartum hemorrhage, with or without placebo.</p><p><strong>Methods: </strong>MEDLINE, Embase, CINAHL, CENTRAL, Scopus, Web of Science and ProQuest Nursing and Allied Health will be searched for eligible studies. The search for unpublished studies will include: ProQuest Dissertations and Theses (PQDT), ClinicalTrials.gov and New York Academy of Medicine Grey Literature Report. Retrieval of full-text studies, assessment of methodological quality and data extraction will be performed independently by two reviewers. Meta-analysis will be performed, if possible.</p>","PeriodicalId":73539,"journal":{"name":"JBI database of systematic reviews and implementation reports","volume":"17 8","pages":"1565-1572"},"PeriodicalIF":0.0000,"publicationDate":"2019-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.11124/JBISRIR-2017-003978","citationCount":"3","resultStr":"{\"title\":\"Tranexamic acid as adjuvant treatment for postpartum hemorrhage: a systematic review protocol.\",\"authors\":\"Charles G Fahrenholtz, Laura S Bonanno, Jennifer B Martin\",\"doi\":\"10.11124/JBISRIR-2017-003978\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>The objective of this review is to evaluate the effectiveness of intravenous administration of tranexamic acid (TXA) within three hours of birth in mothers with a diagnosis of postpartum hemorrhage (PPH).</p><p><strong>Introduction: </strong>Postpartum hemorrhage, that is, blood loss exceeding 500 mL for vaginal births or 1000 mL for cesarean sections within 24 hours of delivery, is the leading cause of maternal deaths worldwide. 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引用次数: 3
摘要
目的:本综述的目的是评估诊断为产后出血(PPH)的母亲在出生后3小时内静脉注射氨甲环酸(TXA)的有效性。产后出血,即阴道分娩时失血超过500毫升或剖宫产时在分娩24小时内失血超过1000毫升,是全世界孕产妇死亡的主要原因。世界卫生组织建议在婴儿出生后3小时内,除标准推荐治疗外,静脉注射TXA作为治疗PPH的辅助疗法。本综述将确定在发达国家和发展中国家,对PPH患者给予TXA是否会减少失血量、输血填充红细胞的需求和紧急子宫切除术的需要。纳入标准:本综述将纳入诊断为产后出血的40岁以下妇女的研究。将考虑在出生后3小时内静脉给予TXA作为产后出血辅助治疗的研究。比较者将是没有接受TXA作为产后出血治疗的一部分,有或没有安慰剂的组。方法:MEDLINE, Embase, CINAHL, CENTRAL, Scopus, Web of Science和ProQuest Nursing and Allied Health将检索符合条件的研究。搜索未发表的研究将包括:ProQuest学位论文和论文(PQDT), ClinicalTrials.gov和纽约医学研究院灰色文献报告。全文研究的检索、方法学质量评估和数据提取将由两名审稿人独立完成。如有可能,将进行meta分析。
Tranexamic acid as adjuvant treatment for postpartum hemorrhage: a systematic review protocol.
Objective: The objective of this review is to evaluate the effectiveness of intravenous administration of tranexamic acid (TXA) within three hours of birth in mothers with a diagnosis of postpartum hemorrhage (PPH).
Introduction: Postpartum hemorrhage, that is, blood loss exceeding 500 mL for vaginal births or 1000 mL for cesarean sections within 24 hours of delivery, is the leading cause of maternal deaths worldwide. The World Health Organization recommends intravenous TXA as an adjuvant therapy for the treatment of PPH, in addition to standard recommended treatments, within three hours of birth. This review will determine whether TXA administration to patients experiencing PPH leads to a reduction in blood loss, the requirement for transfusion of packed red blood cells and the need for emergency hysterectomies, in both developed and developing nations.
Inclusion criteria: This review will consider studies that include women under 40 with a diagnosis of postpartum hemorrhage. Studies that evaluate intravenous administration of TXA within three hours of birth as adjuvant treatment of postpartum hemorrhage will be considered. The comparator will be groups that have not received TXA as part of the treatment for postpartum hemorrhage, with or without placebo.
Methods: MEDLINE, Embase, CINAHL, CENTRAL, Scopus, Web of Science and ProQuest Nursing and Allied Health will be searched for eligible studies. The search for unpublished studies will include: ProQuest Dissertations and Theses (PQDT), ClinicalTrials.gov and New York Academy of Medicine Grey Literature Report. Retrieval of full-text studies, assessment of methodological quality and data extraction will be performed independently by two reviewers. Meta-analysis will be performed, if possible.