pregnancy termination

终止妊娠
  • 文章类型: Journal Article
    助产士为妇女提供生殖保健,包括终止妊娠期间(TOP)后12周(晚期TOP)。他们的专业知识,知识和以妇女为中心的护理方法使他们能够胜任这一角色。然而,医学,后期TOP的社交和情感复杂性会导致助产士严重困扰。使用综合审查方法来检查晚期TOP的助产护理研究,并确定助产士在这一角色中可用的支持策略和干预措施。搜索了五个数据库和参考文献清单,以查找2000年至2021年之间发表的相关研究。总共确定了2545条记录,包括24项研究。综合研究结果得出三个主题:积极方面,消极方面和照顾者需要照顾。助产士报告说,在TOP后期照顾女性时,工作满意度很高。学习新技能和克服挑战是他们工作的积极方面。然而,助产士感到没有准备好应对后期TOP护理的挑战性方面,如悲伤和心理负担的作用。有尊严地照顾婴儿既有积极的一面,也有消极的一面。助产士主要依靠亲密同事的帮助和汇报,因为他们感到管理层的支持不足,由同事判断,缺乏适当的支持来减少后期TOP护理的情绪影响。助产士需要支持,尽管目前的证据尚未确定最合适和有效的策略来支持他们发挥这一作用.
    Midwives provide reproductive healthcare to women, including during termination of pregnancy (TOP) after 12 weeks (late TOP). Their expertise, knowledge and woman-centred care approach sees them ideally placed for this role. However, the medical, social and emotional complexities of late TOP can cause midwives significant distress. An integrative review methodology was used to examine the research on midwifery care for late TOP and identify support strategies and interventions available to midwives in this role. Five databases and reference lists were searched for relevant studies published between 2000 and 2021. A total of 2545 records were identified and 24 research studies included. Synthesis of research findings resulted in three themes: Positive aspects, negative aspects and carers need care. Midwives reported a high level of job satisfaction when caring for women during late TOP. Learning new skills and overcoming challenges were positive aspects of their work. Yet, midwives felt unprepared to deal with challenging aspects of late TOP care such as the grief and the psychological burden of the role. Caring for the baby with dignity had both positive and negative aspects. Midwives relied predominantly on close colleagues for help and debriefing as they felt poorly supported by management, judged by co-workers and lacked appropriate support to reduce the emotional effects of late TOP care. Midwives need support, although current evidence has not identified the most appropriate and effective strategy to support them in this role.
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  • 文章类型: Systematic Review
    目的:剖宫产瘢痕妊娠(CSP)是一种可能危及生命的疾病,其患病率一直在稳步上升。鉴于危及生命的并发症的风险,通常建议终止妊娠。在某些情况下,患者拒绝终止可行的CSP,即使在咨询之后。最近的研究报告说,即使有可能的并发症和产妇发病率的高负担,许多CSP进展到生活,接近足月分娩。这项研究的目的是进一步证明可行的剖宫产瘢痕妊娠的自然史。
    方法:我们对报告胎儿心跳阳性的CSP期待管理的原始研究进行了系统评价。
    结果:选择后,28项研究包括在审查中,共有398例CSP,136例预期管理,117例胎儿心跳阳性。这项研究证实,大多数患者经历了活产,因为78%的选择进行期待管理的患者在足月或接近足月时经历过活产,79%的胎盘发育为病态贴壁,55%需要子宫切除术,40%有严重出血.
    结论:CSP的最佳治疗方案仍有待确定,需要更多的研究来进一步阐明这种罕见但正在上升的疾病。我们的研究提供了有关未经治疗的CSP的自然史的信息,并表明终止治疗可能不是患者的唯一选择。
    OBJECTIVE: Cesarean scar pregnancy (CSP) is a potentially life-threatening disease that has been steadily increasing in prevalence. Pregnancy termination is usually recommended given the risk of life-threatening complications. In some cases, patients refuse to terminate viable CSPs, even after counseling. Recent studies report that, even with a high burden of possible complications and maternal morbidity, many CSPs progress to live, close to term births. The aim of this study is to further demonstrate the natural history of viable cesarean scar pregnancies.
    METHODS: We conducted a systematic review of original studies reporting cases of expectant management of CSPs with positive fetal heartbeats.
    RESULTS: After selection, 28 studies were included in the review, with a total of 398 cases of CSP, 136 managed expectantly and 117 with positive fetal heartbeat managed expectantly. This study confirmed that the majority of patients experience live births, as 78% of patients selected for expectant management experienced live births at or close to term, with 79% developing morbidly adherent placenta, 55% requiring hysterectomy, and 40% having severe bleeding.
    CONCLUSIONS: The optimal management protocol for CSP is still to be defined and more studies are needed to further elucidate this rare but rising disease. Our study provides information on the natural history of untreated CSPs and suggests that termination may not be the only option offered to the patient.
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  • 文章类型: Journal Article
    UNASSIGNED: About 45.1% of all induced abortions are unsafe and 97% of these occur in low- and middle-income countries (LMICs). Women\'s abortion decisions may be complex and are influenced by various factors. We aimed to delineate women\'s abortion decision-making trajectories and their determinants in LMICs.
    UNASSIGNED: We searched Medline, EMBASE, PsychInfo, Global Health, Web of Science, Scopus, IBSS, CINAHL, WHO Global Index Medicus, the Cochrane Library, WHO website, ProQuest, and Google Scholar for primary studies and reports published between January 1, 2000, and February 16, 2021 (updated on June 06, 2022), on induced abortion decision-making trajectories and/or their determinants in LMICs. We excluded studies on spontaneous abortion. Two independent reviewers extracted and assessed quality of each paper. We used \"best fit\" framework synthesis to synthesise abortion decision-making trajectories and thematic synthesis to synthesise their determinants. We analysed quantitative findings using random effects model. The study protocol is registered with PROSPERO number CRD42021224719.
    UNASSIGNED: Of the 6960 articles identified, we included 79 in the systematic review and 14 in the meta-analysis. We identified nine abortion decision-making trajectories: pregnancy awareness, self-reflection, initial abortion decision, disclosure and seeking support, negotiations, final decision, access and information, abortion procedure, and post-abortion experience and care. Determinants of trajectories included three major themes of autonomy in decision-making, access and choice. A meta-analysis of data from 7737 women showed that the proportion of the overall women\'s involvement in abortion decision-making was 0.86 (95% CI:0.73-0.95, I2 = 99.5%) and overall partner involvement was 0.48 (95% CI:0.29-0.68, I2 = 99.6%).
    UNASSIGNED: Policies and strategies should address women\'s perceptions of safe abortion socially, legally, and economically, and where appropriate, involvement of male partners in abortion decision-making processes to facilitate safe abortion. Clinical heterogeneity, in which various studies defined \"the final decision-maker\" differentially, was a limitation of our study.
    UNASSIGNED: Nuffield Department of Population Health DPhil Scholarship for PL, University of Oxford, and the Medical Research Council Career Development Award for MN (Grant Ref: MR/P022030/1).
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  • 文章类型: Journal Article
    目的:本研究旨在对所进行的研究进行广泛的概述,并综合非药物干预措施对药物和手术流产中疼痛管理的效用的证据。
    背景:药物流产和手术流产的高质量护理需要有效控制疼痛。然而,女性报告对流产护理中疼痛管理的满意度较低.
    方法:采用范围审查设计。
    方法:没有设置日期限制。PubMed,科克伦图书馆,EMBASE,WebofScience,CINAHL,PsycINFO,ProQuest和Scopus于2021年4月进行了搜索。
    方法:使用Arksey和O\'Malley的框架。遵循系统评价和荟萃分析扩展-范围评价的首选报告项目。
    结果:共纳入15项研究。结果显示,支持干预措施,音乐疗法,穴位刺激和催眠镇痛是用于减少流产疼痛的非药物干预措施。
    结论:临床护士,护士管理者和政策制定者应充分重视人工流产中的疼痛管理,并可利用研究结果指导疼痛管理实践。
    OBJECTIVE: The study aimed to present a broad overview of the research conducted and to synthesize evidence of the utility of nonpharmacological interventions for pain management in medical and surgical abortions.
    BACKGROUND: High-quality care for medical and surgical abortion requires pain to be managed effectively. However, women reported low satisfaction with pain management in abortion care.
    METHODS: A scoping review design was employed.
    METHODS: No date limit was set. PubMed, Cochrane Library, EMBASE, Web of Science, CINAHL, PsycINFO, ProQuest and Scopus were searched in April 2021.
    METHODS: Arksey and O\'Malley\'s framework was used. The Preferred Reporting Items for Systematic reviews and Meta-analysis extension-Scoping Reviews was followed.
    RESULTS: Fifteen studies were included. The results revealed that support interventions, music therapy, acupoint stimulation and hypnotic analgesia were nonpharmacological interventions used to decrease abortion pain.
    CONCLUSIONS: Clinical nurses, nurse managers and policymakers should attach full importance to the pain management in abortion and may use the study findings to guide the pain management practice.
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  • 文章类型: Journal Article
    本系统评价的目的是评估在妊娠早期或中期药物终止妊娠之前用来曲唑预处理的疗效。
    我们搜索了来曲唑,femara,芳香化酶抑制剂,堕胎代理人,MEDLINE终止妊娠和引产,EMBASE,Cochrane数据库,GoogleScholar和PubMed从每个数据库开始到2015年9月,没有语言限制。对所有随机对照试验(RCT)进行了系统评价,其中妇女接受来曲唑和米索前列醇或安慰剂和米索前列醇终止妊娠。主要结果是完全流产率,定义为从子宫中完全排出受孕产物。使用95%置信区间的相对危险度报告数据。
    我们的系统评价确定了7项研究;4项RCTs被纳入评价。两项随机对照试验评估了妊娠直至9周的终止妊娠,而2人评估了妊娠9周的终止妊娠。对于每个胎龄组,一项试验支持提高完全流产率,而另一个没有区别,与安慰剂和米索前列醇相比,来曲唑和米索前列醇。在米索前列醇中加入来曲唑后,终止妊娠至妊娠9周的流产时间间隔没有改善。对于妊娠9周以上的终止妊娠,一项试验支持,一项试验驳斥了来曲唑和米索前列醇对流产时间间期缩短的影响.同样,对于每个胎龄组,一项研究支持降低,一项研究显示来曲唑和米索前列醇的扩张和刮治率(D&C)没有差异。两个治疗组之间的药物副作用相似。试验之间存在显著的异质性,因此,结果未进行荟萃分析.
    一些研究和试验报告了更好的结果(即,完全流产率,与安慰剂和米索前列醇相比,暴露于来曲唑和米索前列醇的女性的流产时间和D&C率),而其他试验表明没有差异。需要进一步研究探索来曲唑在药物流产前的预处理。
    本系统综述表明,在某些研究中,与单独使用米索前列醇相比,来曲唑和米索前列醇的组合可提高完全流产率,而在其他研究中却没有;还需要设计良好的RCT。
    The purpose of this systematic review was to evaluate the efficacy of pretreatment with letrozole prior to either a first- or second-trimester medical termination of pregnancy.
    We searched letrozole, femara, aromatase inhibitors, abortifacient agents, termination of pregnancy and labor induction in MEDLINE, EMBASE, Cochrane Database, Google Scholar and PubMed from inception of each database until September 2015 with no language limitation. A systematic review of all randomized controlled trials (RCTs) was performed where women received either letrozole and misoprostol or placebo and misoprostol for termination of pregnancy. The primary outcome was complete abortion rate, defined as complete evacuation of the products of conception from the uterus. Relative risk with 95% confidence intervals was used to report data.
    Our systematic review identified 7 studies; 4 RCTs were included in the review. Two RCTs evaluated terminations of pregnancy up to 9 weeks\' gestation, while 2 evaluated terminations over 9 weeks\' gestation. For each gestational age group, one trial supported an increase in complete abortion rate, while the other showed no difference, with letrozole and misoprostol compared with placebo and misoprostol. Time-to-abortion interval for terminations up to 9 weeks\' gestation was not improved with the addition of letrozole to misoprostol. For terminations over 9 weeks\' gestation, one trial supported and one trial refuted a decrease in time-to-abortion interval with letrozole and misoprostol. Similarly, for each gestational age group, one study supported a decrease and one study showed no difference in rate of dilation and curettage (D&C) with letrozole and misoprosol. Medication side effects were similar between both treatment groups. There was significant heterogeneity between the trials, and therefore, the results were not meta-analyzed.
    Some studies and trials report better outcomes (i.e., complete abortion rates, time-to-abortion and D&C rates) in women exposed to letrozole and misoprostol compared to placebo and misoprostol, while other trials demonstrate no difference. Further research exploring letrozole pretreatment prior to medical abortion is required.
    This systematic review demonstrated that a combination of letrozole and misoprostol increased the rate of complete abortion compared to misoprostol alone in some studies but not in others; additional well-designed RCT\'s are needed.
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  • 文章类型: Journal Article
    The availability and effectiveness of decision aids (DAs) on early abortion methods remain unknown, despite their potential for supporting women\'s decision making.
    To describe the availability, impact and quality of DAs on surgical and medical early abortion methods for women seeking induced abortion.
    For the systematic review, we searched MEDLINE, Cochrane Library, CINAHL, EMBASE and PsycINFO. For the environmental scan, we searched Google and App Stores and consulted key informants.
    For the systematic review, we included studies evaluating an early abortion method DA (any format and language) vs a comparison group on women\'s decision making. DAs must have met the Stacey et al (2014). Cochrane review definition of DAs. For the environmental scan, we included English DAs developed for the US context.
    We extracted study and DA characteristics, assessed study quality using the Effective Practice and Organization of Care risk of bias tool and assessed DA quality using International Patient Decision Aid Standards (IPDAS).
    The systematic review identified one study, which found that the DA group had higher knowledge and felt more informed. The evaluated DA met few IPDAS criteria. In contrast, the environmental scan identified 49 DAs created by non-specialists. On average, these met 28% of IPDAS criteria for Content, 22% for Development and 0% for Effectiveness.
    Research evaluating DAs on early abortion methods is lacking, and although many tools are accessible, they demonstrate suboptimal quality. Efforts to revise existing or develop new DAs, support patients to identify high-quality DAs and facilitate non-specialist developers\' adoption of best practices for DA development are needed.
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  • 文章类型: Journal Article
    OBJECTIVE: Termination of pregnancy (TOP) is one of the most performed interventions in women worldwide: approximately one in three women will have at least one TOP in their reproductive life. Intrauterine adhesions (IUAs) have been reported as a possible complication after TOP, but their prevalence has not been established, as women are not routinely evaluated. IUAs are associated with menstrual disturbances, infertility and obstetric complications.
    METHODS: We searched Ovid MEDLINE, Ovid EMBASE and CENTRAL from inception until November 2015 for studies evaluating women following TOP. We selected studies in which women were evaluated consecutively, independently of symptoms, by hysteroscopy or hysterosalpingography (HSG), for the presence of IUAs.
    RESULTS: After an extensive review of the literature, no studies were found that evaluated women after medical TOP and no randomised trials following surgical TOP. Only two prospective cohort studies were identified. In the first, IUAs were detected in 21.2% of women evaluated by hysteroscopy following first trimester surgical TOP; adhesions were moderate to severe in 48%. In the second, IUAs were detected in 16.2% of women evaluated by HSG after second trimester TOP by intra-amniotic prostaglandin induction followed by D&C; a pathologically wide internal cervical os was observed in 12%.
    CONCLUSIONS: This systematic review suggests a link between TOP and adhesion formation, but, according to the scientific literature and despite new diagnostic facilities, the relationship between the methods of TOP and IUA formation remains unclear. Nevertheless, the reported frequency is in accordance with that found in women following D&C for miscarriage. Further research is required.
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  • 文章类型: Journal Article
    OBJECTIVE: The aim of this systematic review and metaanalysis was to determine the efficacy and safety of cervical ripening agents in the second trimester of pregnancy in patients with previous cesarean delivery.
    METHODS: Data sources were PubMed, EMBASE, CINAHL, LILACS, Google Scholar, and clinicaltrials.gov (1983 through 2015). Eligibility criteria were cohort or cross-sectional studies that reported on efficacy and safety of cervical ripening agents in patients with previous cesarean delivery. Efficacy was determined based on the proportion of patients achieving vaginal delivery and vaginal delivery within 24 hours following administration of a cervical ripening agent. Safety was assessed by the risk of uterine rupture and complications such as retained placental products, blood transfusion requirement, and endometritis, when available, as secondary outcomes. Of the 176 studies identified, 38 met the inclusion criteria. Of these, 17 studies were descriptive and 21 studies compared the efficacy and safety of cervical ripening agents between patients with previous cesarean and those with no previous cesarean. From included studies, we abstracted data on cervical ripening agents and estimated the pooled risk differences and risk ratios with 95% confidence intervals. To account for between-study heterogeneity, we estimated risk ratios based on underlying random effects analyses. Publication bias was assessed via funnel plots and across-study heterogeneity was assessed based on the I(2) measure.
    RESULTS: The most commonly used agent was PGE1. In descriptive studies, PGE1 was associated with a vaginal delivery rate of 96.8%, of which 76.3% occurred within 24 hours, uterine rupture in 0.8%, retained placenta in 10.8%, and endometritis in 3.9% in patients with ≥1 cesarean. In comparative studies, the use of PGE1, PGE2, and mechanical methods (laminaria and dilation and curettage) were equally efficacious in achieving vaginal delivery between patients with and without prior cesarean (risk ratio, 0.99, and 95% confidence interval, 0.98-1.00; risk ratio, 1.00, and 95% confidence interval, 0.98-1.02; and risk ratio, 1.00, and 95% confidence interval, 0.98-1.01; respectively). In patients with history of ≥1 cesarean the use of PGE1 was associated with higher risk of uterine rupture (risk ratio, 6.57; 95% confidence interval, 2.21-19.52) and retained placenta (risk ratio, 1.21; 95% confidence interval, 1.03-1.43) compared to women without a prior cesarean. However, the risk of uterine rupture among women with history of only 1 cesarean (0.47%) was not statistically significant (risk ratio, 2.36; 95% confidence interval, 0.39-14.32), whereas among those with history of ≥2 cesareans (2.5%) was increased as compared to those with no previous cesarean (0.08%) (risk ratio, 17.55; 95% confidence interval, 3.00-102.8). Funnel plots did not demonstrate any clear evidence of publication bias. Across-study heterogeneity ranged from 0-81%.
    CONCLUSIONS: This systematic review and metaanalysis provides evidence that PGE1, PGE2, and mechanical methods are efficacious for achieving vaginal delivery in women with previous cesarean delivery. The use of prostaglandin PGE1 in the second trimester was not associated with significantly increased risk for uterine rupture among women with only 1 cesarean; however, this risk was substantially increased among women with ≥2 cesareans although the absolute risk appeared to be relatively small.
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  • 文章类型: Journal Article
    Aglepristone (RU 46534) is a competitive progesterone antagonist that is indicated for the treatment of various progesterone-dependent physiological or pathologic conditions. Aglepristone has proven to be an effective means of terminating pregnancy in most species. When used to induce parturition, aglepristone was effective in all cases in the bitch, cow, and goat, with no apparent adverse effects on neonatal health or milk production. When used to schedule an elective cesarean section, aglepristone treatment was deemed safe for dams and puppies, providing that the ovulation date had been accurately assessed at the time of breeding. Irrespective of the stage of pregnancy at injection, treatment with aglepristone has no apparent negative effects on subsequent fertility. Aglepristone is also a safe and relatively effective means of treating pyometra. However, given the high level of septic risk and the likelihood of rapid deterioration, such therapy is not recommended in emergency situations. Treatment of feline fibroadenomatosis using aglepristone has given promising results, but repeat treatment may be necessary in cats previously treated with long-acting progestagens. The use of aglepristone in other progesterone-dependent diseases has yet to be fully evaluated but may prove valuable, especially in the treatment of insulin-resistant diabetes mellitus, acromegaly, and the treatment of some vaginal tumors in the bitch.
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  • 文章类型: Journal Article
    With changing conditions affecting receipt of postabortion care, an updated estimate of the incidence of treatment for complications from unsafe pregnancy termination is needed to inform policies and programmes. National estimates of facility-based treatment for complications in 26 countries form the basis for estimating treatment rates in the developing world. An estimated seven million women were treated in the developing world for complications from unsafe pregnancy termination in 2012, a rate of 6.9 per 1000 women aged 15-44 years. Regionally, rates ranged from 5.3 in Latin America and the Caribbean to 8.2 in Asia. Results inform policies to improve women\'s health.
    CONCLUSIONS: An estimated 7 million women were treated in the developing world for complications of unsafe TOP in 2012.
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