periviability

周生能力
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  • 文章类型: Journal Article
    不能设置生存能力的任意胎龄限制,在临床实践中,重点应该放在生存间隔上-所谓的预后不确定性的“灰色地带”。对于此间隔内的情况,最适当的决策过程仍有争议,而生存能力已成为生物伦理学的最大挑战之一。由于社会经济原因,普遍公认的道德原则可能会有不同的解释,文化,和宗教方面。在长期生存能力的情况下,对于干预措施是否能使临床利益与伤害达到更大的平衡,存在相当大的不确定性.此外,胎儿或新生儿无法行使自主性,医生和父母将充当患者代理人。当父母和医生不同意婴儿的最佳利益时,没有家长式态度的对话至关重要,医生应该只提供,但不推荐,围产期干预措施。父母的选择,基于全面的信息,应在医学上可行和适当的范围内得到尊重。当父母和医生之间发生分歧时,如何达成共识?专业指南可以作为讨论的框架和起点。在现实中,然而,准则很少划出明确的界限,在许多情况下仍然含糊不清,措辞含糊不清。地方伦理委员会可以提供咨询,并在讨论期间担任主持人,但是伦理委员会没有决策优先权。咨询在生存讨论中扮演着最重要的角色,考虑到胎儿和母体的特殊特征,以及父母的价值观。应注意与咨询相关的几个警告:应尽量减少信息碎片或不一致,预后最好以积极的框架表示,应避免过度依赖统计。建议在出生前做出有关新生儿复苏的决定,而不是以新生儿出生时的外观为条件。不管做什么决定,重要的是要确保产前和产后的一致性。本文描述了个别医生,中心,各国在决定启动或放弃重症监护的方法上有所不同。不可能提供全球共识的观点,也不可能有统一的道德,道德,或实用的策略。然而,道德上合理的,优质护理包括产科和新生儿团队的早期参与,以实现连贯的,可理解的,非家长式,平衡的护理计划。最终,医生需要根据当地标准调整预期,当地结果数据,和当地新生儿支持的可用性。
    An arbitrary gestational age limit of viability cannot be set, and in clinical practice the focus should be on a periviability interval-the so-called \"gray zone\" of prognostic uncertainty. For cases within this interval, the most appropriate decision-making process remains debatable and periviability has emerged as one of the greatest challenges in bioethics. Universally recognized ethical principles may be interpreted differently due to socioeconomic, cultural, and religious aspects. In the case of periviability, there is considerable uncertainty over whether interventions result in a greater balance of clinical good over harm. Furthermore, the fetus or neonate is unable to exercise autonomy and the physicians and parents will act as patient surrogates. When parents and physicians disagree about the infant\'s best interest, a dialogue without paternalistic attitudes is essential, whereby physicians should only offer, but not recommend, perinatal interventions. Parental choice, based on thorough information, should be respected within the limits of what is medically feasible and appropriate. When disagreements between parents and physicians occur, how is consensus to be achieved? Professional guidelines can be helpful as a framework and starting point for discussion. In reality, however, guidelines only rarely draw categorical lines and in many cases remain vague and ambiguously worded. Local ethics committees can provide counseling and function as moderators during discussions, but ethics committees do not have decision precedence. Counseling assumes the most significant role in periviability discussions, taking into consideration the particular fetal and maternal characteristics, as well as parental values. Several caveats should be observed relative to counseling: message fragmentation or inconsistence should be minimized, prognosis should preferably be presented in a positive framing, and overreliance on statistics should be avoided. It is recommended that decisions regarding neonatal resuscitation in the periviability interval be made before birth and not conditional on the newborn\'s appearance at birth. Regardless of decision, it is important to assure pre- and postnatal coherence. The present article describes how individual physicians, centers, and countries differ in the approach to the decision to initiate or forgo intensive care in the periviability interval. It is impossible to provide a global consensus view and there can be no unifying ethical, moral, or practical strategy. Nevertheless, ethically justified, quality care comprises early involvement of the obstetric and neonatal team to enable a coherent, comprehensible, nonpaternalistic, and balanced plan of care. Ultimately, physicians will need to adjust the expectations to the local standards, local outcome data, and local neonatal support availability.
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  • 文章类型: Journal Article
    目的:本研究的目的是获得知识并确定在产科医生中关于生存咨询的挑战,以告知课程发展。
    方法:使用焦点组。向每组产科医生提出了一系列开放式问题;对回答进行音频记录和转录。两名编码人员使用主题分析对转录进行了分析。
    结果:召集了四个焦点小组。突出的主题包括:(1)产科医生关于新生儿结局的知识有限,(2)定期可行性咨询既是时间密集的,也是时间挑战的,(3)患者对信息的处理依赖于内容,分娩和患者准备情况,(4)产科医生倾向于倡导产妇安全,这可能与父母“做任何事情”的本能背道而驰。“最后一个主题是特别关注剖宫产的作用。
    结论:专注于改善产科医生围手术期咨询的课程应关注新生儿结局,剖宫产的作用,和利用共同决策。
    OBJECTIVE: The objective of this study was to gain knowledge and ascertain challenges about periviability counseling among obstetricians to inform curricular development.
    METHODS: Focus groups were utilized. A series of open-ended questions was posed to each group of obstetricians; responses were audio recorded and transcribed. Transcriptions were analyzed by two coders using thematic analysis.
    RESULTS: Four focus groups were convened. Prominent themes included: (1) Obstetrician knowledge about neonatal outcomes is limited, (2) Periviability counseling is both time intensive and time-challenged, (3) Patient processing of information relies on the content, delivery and patient readiness, and (4) Obstetrician bias is toward advocating for maternal safety, which may run counter to parental instinct to \"do everything.\" The last theme was specifically focused on the role of cesarean delivery.
    CONCLUSIONS: Curricula focused on improving obstetrician periviability counseling should focus on neonatal outcomes, the role of cesarean delivery, and utilization of shared decision-making.
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  • 文章类型: Editorial
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  • 文章类型: Journal Article
    背景:最近的ACOG实践公告没有提供关于少于24周具有严重特征的先兆子痫(带SF的PreE)的管理指南。历史上,由于围产期结局差和产妇发病率高,因此建议立即分娩.最近,新生儿复苏的进展导致围活产胎龄的存活率增加.
    方法:我们的目的是报告在<24周时采用SF对PreE进行预期管理后的围产期和产妇结局。
    方法:这是2017-2023年在IV级中心<24周时发生的带有SF的PreE回顾性病例系列。排除需要在诊断后24小时内分娩的个体。分析围产期和产妇结局。使用卡方检验将我们数据库中的分类变量与先前发布的数据进行了比较。
    结果:有41例患者被诊断为SF<24周的PreE。在24小时内排除交货后,对30人(73%)进行了评估。诊断时的中位胎龄为22周(IQR22-23周)。16%有辅助生殖技术,27%有慢性高血压,13%有孕前糖尿病,30%有先兆子痫,73%的BMI>30kg/m2。22周和23周的中位潜伏期为7天(IQR4-23)和8天(IQR4-13天)。新生儿生存率为44%(95%CI3-85%),SF在22周时发作为29%(95%CI1-56%)。有2例急性肾损伤(7%)和2例心包/胸腔积液(7%)。在我们目前的研究中,围产期<24周的总生存率为30%,而在以前的报告中为7%(p=0.02)。
    结论:对于在<24周时预期治疗患有SF的PreE的病例,我们的研究结果表明,与以前发表的数据相比,围产期生存率提高,孕产妇发病率降低.此信息可用于对SF<24周的PreE进行预期管理的咨询。
    BACKGROUND: The recent American College of Obstetricians and Gynecologists Practice Bulletin offers no guidance on the management of preeclampsia with severe features at <24 weeks of gestation. Historically, immediate delivery was recommended because of poor perinatal outcomes and high maternal morbidity. Recently, advances in neonatal resuscitation have led to increased survival at periviable gestational ages.
    OBJECTIVE: This study aimed to report perinatal and maternal outcomes after expectant management of preeclampsia with severe features at <24 weeks of gestation.
    METHODS: This was a retrospective case series of preeclampsia with severe features at <24 weeks of gestation at a level 4 center between 2017 and 2023. Individuals requiring delivery within 24 hours of diagnosis were excluded. Perinatal and maternal outcomes were analyzed. Categorical variables from our database were compared with previously published data using chi-square tests.
    RESULTS: A total of 41 individuals were diagnosed with preeclampsia with severe features at <24 weeks of gestation. After the exclusion of delivery within 24 hours, 30 individuals (73%) were evaluated. The median gestational age at diagnosis was 22 weeks (interquartile range, 22-23). Moreover, 16% of individuals had assisted reproductive technology, 27% of individuals had chronic hypertension, 13% of individuals had pregestational diabetes mellitus, 30% of individuals had previous preeclampsia, and 73% of individuals had a body mass index of >30 kg/m2. The median latency periods at 22 and 23 weeks of gestation were 7 days (interquartile range, 4-23) and 8 days (interquartile range, 4-13). In preeclampsia with severe features, neonatal survival rates were 44% (95% confidence interval, 3%-85%) at 22 weeks of gestation and 29% (95% confidence interval, 1%-56%) at 23 weeks of gestation. There were 2 cases of acute kidney injury (7%) and 2 cases of pericardial or pleural effusions (7%). Overall perinatal survival at <24 weeks of gestation was 30% in our current study vs 7% in previous reports (P=.02).
    CONCLUSIONS: For cases of expectant management of preeclampsia with severe features at <24 weeks of gestation, our findings showed an increased perinatal survival rate with decreased maternal morbidity compared with previously published data. This information may be used when counseling on expectant management of preeclampsia with severe features at <24 weeks of gestation.
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  • 文章类型: Journal Article
    背景:为达成共同决策而进行的妊娠咨询是具有挑战性的,当前,有限的证据阻碍了所提供信息的稳健性。
    目的:阐明对胎膜早破(PROM)在存活前或存活极限时进行预期处理后的产科和新生儿结局的发生率。
    方法:Medline,Embase,截至2023年9月,对Cinahl和WebofScience数据库进行了电子搜索。我们包括在生存能力之前和极限时进行的PROM单胎妊娠的前瞻性和回顾性研究(即,发生在妊娠14/0至24/6周之间)。纳入研究的质量评估使用纽卡斯尔-渥太华量表进行队列研究。我们使用比例的荟萃分析来组合数据和报告的汇总比例。鉴于临床异质性,使用随机效应模型计算合并数据分析.该研究在PROSPERO数据库(CRD42022368029)中注册。
    结果:合并终止妊娠(TOP)的比例为32.3%。排除TOP病例后,自然流产或胎儿死亡率为20.1%,而活产率为持续怀孕的65.9%。活产病例分娩时的平均胎龄为27.26周,胎膜早破与分娩之间的平均潜伏期为39.40天。剖宫产的合并比例为47.9%。47.1%的病例发生羊水过少。33.4%的病例发生绒毛膜羊膜炎;7%的病例发生子宫内膜炎,胎盘早剥9.2%,产后出血5.3%。1.2%的病例需要进行子宫切除术。在纳入的研究中,孕产妇败血症发生在1.5%的病例中,而没有孕产妇死亡报告。当关注新生儿结局时,活出生病例的平均出生体重为1022.85克。NICU入院率为86.3%,RDS并发66.5%;24.0%的病例诊断为肺发育不全或发育不良,40.9%的病例诊断为持续肺动脉高压。其他新生儿并发症包括11.1%的坏死性小肠结肠炎,ROP为27.1%,IVH在17.5%的存活新生儿中。新生儿败血症并发病例占30.2%,新生儿总死亡率为23.9%。在74.1%的可用病例中,2至4年的长期随访是正常的。
    结论:存活前或存活极限时的胎膜早破与产科和新生儿并发症的高负担相关,在近30%的病例中,2至4年的长期随访受损,因此对咨询和管理都是临床挑战。这些数据在首次接触此类患者时很有用,可以提供有关这种情况的短期和长期结果的最全面的情况,并帮助父母共同决策。
    Counseling of pregnancies complicated by pre- and periviable premature rupture of membranes to reach shared decision-making is challenging, and the current limited evidence hampers the robustness of the information provided. This study aimed to elucidate the rate of obstetrical and neonatal outcomes after expectant management for premature rupture of membranes occurring before or at the limit of viability.
    Medline, Embase, CINAHL, and Web of Science databases were searched electronically up to September 2023.
    Our study included both prospective and retrospective studies of singleton pregnancies with premature rupture of membranes before and at the limit of viability (ie, occurring between 14 0/7 and 24 6/7 weeks of gestation).
    Quality assessment of the included studies was performed using the Newcastle-Ottawa Scale for cohort studies. Moreover, our study used meta-analyses of proportions to combine data and reported pooled proportions. Given the clinical heterogeneity, a random-effects model was used to compute the pooled data analyses. This study was registered with the International Prospective Register of Systematic Reviews database (registration number: CRD42022368029).
    The pooled proportion of termination of pregnancy was 32.3%. After the exclusion of cases of termination of pregnancy, the rate of spontaneous miscarriage or fetal demise was 20.1%, whereas the rate of live birth was 65.9%. The mean gestational age at delivery among the live-born cases was 27.3 weeks, and the mean latency between premature rupture of membranes and delivery was 39.4 days. The pooled proportion of cesarean deliveries was 47.9% of the live-born cases. Oligohydramnios occurred in 47.1% of cases. Chorioamnionitis occurred in 33.4% of cases, endometritis in 7.0%, placental abruption in 9.2%, and postpartum hemorrhage in 5.3%. Hysterectomy was necessary in 1.2% of cases. Maternal sepsis occurred in 1.5% of cases, whereas no maternal death was reported in the included studies. When focusing on neonatal outcomes, the mean birthweight was 1022.8 g in live-born cases. The neonatal intensive care unit admission rate was 86.3%, respiratory distress syndrome was diagnosed in 66.5% of cases, pulmonary hypoplasia or dysplasia was diagnosed in 24.0% of cases, and persistent pulmonary hypertension was diagnosed in 40.9% of cases. Of the surviving neonates, the other neonatal complications included necrotizing enterocolitis in 11.1%, retinopathy of prematurity in 27.1%, and intraventricular hemorrhage in 17.5%. Neonatal sepsis occurred in 30.2% of cases, and the overall neonatal mortality was 23.9%. The long-term follow-up at 2 to 4 years was normal in 74.1% of the available cases.
    Premature rupture of membranes before or at the limit of viability was associated with a great burden of both obstetrical and neonatal complications, with an impaired long-term follow-up at 2 to 4 years in almost 30% of cases, representing a clinical challenge for both counseling and management. Our data are useful when initially approaching such patients to offer the most comprehensive possible scenario on short- and long-term outcomes of this condition and to help parents in shared decision-making. El resumen está disponible en Español al final del artículo.
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  • 文章类型: Journal Article
    背景:近年来,在许多机构中,围产期的生存能力已从妊娠24周转变为妊娠22周。监测这些胎儿是必不可少的,因为对于有生存能力极限的分娩风险的患者,可以进行产前复苏干预。然而,在非常早产的妊娠中尚未广泛研究使用生物物理谱进行胎儿监测,特别是在围活期(20周0天至23周6天)。
    目的:本研究旨在(1)探讨在30分钟内完成生物物理分析在极早产妊娠中是否可行,和(2)确定在20周0天至31周6天极早产妊娠中达到8分的平均观察时间。
    方法:这项研究前瞻性评估了在20周0天至23周6天(围活期或I组)接受常规超声检查的单胎妊娠的生物物理评分,24周0天至27周6天(II组),28周0天至31周6天(第III组)。将生物物理谱的结果和持续时间与接受指示胎儿监测的对照组(32周0天至35周6天)进行比较。对所有研究的怀孕进行生物物理分析,直到获得8分中的8分。当在怀孕期间获得>1个生物物理特征时,每个都进行了单独分析.排除有胎儿异常的妊娠或胎儿健康监测的产科/医学指征。使用方差分析和事后Tukey检验进行比较。
    结果:收集了123名参与者的数据,对第一组进行79、75和72项研究,II,III,分别。对照组包括42例患者,140项研究30分钟后,80%(63/79)的研究在周游组8分中有8分,而对照组为100%(140/140)(P<.001)。在周生组中,达到8分中8分的生物物理评分的平均值±标准偏差时间(以分钟为单位)为23.3±10.1,而对照组为9.4±6.5(P<.001)。将研究扩展到+2个标准偏差(43.6分钟)在周游组中导致97%(77/79)的扫描在没有不良结果的情况下8个中的8个评分。在其他群体中,在II组和III组中,97%(73/75)和100%(72/72)的生物物理评分在30分钟内达到8分,平均值±标准差时间分别为17.1±8.4分钟(第II组)和13.1±7.3分钟(第III组)。在I至III组的研究参与期间未出现不良结果。
    结论:在比标准的30分钟持续时间更长的观察时间内,在低风险的围活产妊娠(20周0天至23周6天)中,可以成功达到8分的生物物理评分。达到8分中的8分所需的时间随着妊娠的进行而减少。我们建议根据胎龄调整生物物理轮廓完成的观察时间。
    BACKGROUND: In recent years, perinatal viability has shifted from 24 to 22 weeks of gestation at many institutions after improvements in survival in neonates delivered at the limit of viability. Monitoring these fetuses is essential because antenatal interventions with resuscitation efforts are available for patients at risk of delivery at the limit of viability. However, fetal monitoring using biophysical profiles has not been extensively studied in very preterm pregnancies, particularly in the periviable period (20 weeks 0 days to 23 weeks 6 days).
    OBJECTIVE: This study aimed to (1) investigate whether the completion of biophysical profiles within 30 minutes is feasible in very preterm pregnancies, and (2) determine the average observation time required to achieve a score of 8 out of 8 in very preterm pregnancies from 20 weeks 0 days to 31 weeks 6 days.
    METHODS: This study prospectively evaluated biophysical scores in singleton pregnancies undergoing routine ultrasonography at or near viability from 20 weeks 0 days to 23 weeks 6 days (periviable or group I), 24 weeks 0 days to 27 weeks 6 days (group II), and 28 weeks 0 days to 31 weeks 6 days (group III). The results and duration of biophysical profiles were compared with those of a control group (32 weeks 0 days to 35 weeks 6 days) undergoing indicated fetal surveillance. Biophysical profiles were performed for all studied pregnancies until a score of 8 out of 8 was obtained. When >1 biophysical profile was obtained during pregnancy, each was analyzed individually. Pregnancies with fetal anomalies or obstetrical/medical indications for fetal well-being surveillance were excluded. Analysis of variance and post hoc Tukey tests were used for comparisons.
    RESULTS: Data were collected for 123 participants, yielding 79, 75, and 72 studies for groups I, II, and III, respectively. The control group included 42 patients, yielding 140 studies. At 30 minutes, 80% (63/79) of the studies in the periviable group had a score of 8 out of 8, as opposed to 100% (140/140) in the control group (P<.001). The mean±standard deviation time in minutes to achieve a biophysical score of 8 out of 8 was 23.3±10.1 in the periviable group, as opposed to 9.4±6.5 in controls (P<.001). Extending the study to +2 standard deviations (43.6 minutes) in the periviable group resulted in 97% (77/79) of the scans scoring 8 out of 8 in the absence of adverse outcomes. In the other groups, a biophysical score of 8 out of 8 within 30 minutes was obtained in 97% (73/75) and 100% (72/72) in groups II and III, respectively; the mean±standard deviation times were 17.1±8.4 minutes (group II) and 13.1±7.3 minutes (group III). No adverse outcomes developed during the study participation in groups I to III.
    CONCLUSIONS: Biophysical scores of 8 out of 8 can be successfully achieved in low-risk periviable pregnancies (20 weeks 0 days to 23 weeks 6 days) within an observation time longer than the standard 30-minute duration. The time required to reach a score of 8 out of 8 decreases as gestation progresses. We suggest adjusting the observation time for biophysical profile completion according to the gestational age.
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  • 文章类型: Journal Article
    存活前的早产胎膜破裂(PPROM)具有显着的围产期死亡率和发病率。临床管理和产前咨询是一项挑战,尤其是在双胎妊娠中,由于缺乏关于先前PPROM如何影响该人群的证据。这项研究的目的是描述双胎妊娠合并先前PPROM的妊娠结局,并评估可能预测围产期死亡率的潜在预后因素。评估了一项回顾性队列,包括在妊娠24+0周之前合并PPROM的双绒毛膜和单绒毛膜双胎妊娠。描述了预期妊娠的围产期结局。评估了预测围产期死亡率或达到围生性的因素(从23周0周开始定义)。在包括的45名患者中,7(15.6%)在诊断后的第一个24小时内自发分娩。两名患者(5.3%)要求选择性终止受影响的双胞胎。在选择期待管理的36例持续怀孕中,总生存率为35/72(48.6%).有25/36(69.4%)的患者在妊娠23+0周后分娩。当达到持久生存能力时,新生儿存活率增加至35/44(79.5%)。分娩时的妊娠年龄是围产期死亡的唯一独立危险因素。合并先前PPROM的双胎妊娠的总体生存率较差,但与单胎相似。无预后因素,除了实现持久生存能力,被确定为围产期死亡率的个体预测因子。
    Preterm prelabour rupture of membranes (PPROMs) before viability carries significant perinatal mortality and morbidity. Clinical management and prenatal counselling are a challenge, especially in twin pregnancies, due to scarce evidence on how previable PPROM affects this population. The aim of this study was to describe pregnancy outcomes of twin pregnancies complicated with previable PPROM and evaluate potential prognostic factors that may predict perinatal mortality. A retrospective cohort including dichorionic and monochorionic diamniotic twin pregnancies complicated with PPROM before 24 + 0 weeks of pregnancy was evaluated. Perinatal outcomes of pregnancies managed expectantly were described. Factors predicting perinatal mortality or reaching periviability (defined from 23 + 0 weeks onwards) were evaluated. Of the 45 patients included, 7 (15.6%) spontaneously delivered within the first 24 h after diagnosis. Two patients (5.3%) requested selective termination of the affected twin. In the 36 ongoing pregnancies that opted for expectant management, the overall survival rate was 35/72 (48.6%). There were 25/36 (69.4%) patients who delivered after 23 + 0 weeks of pregnancy. When periviability was achieved, neonatal survival increased up to 35/44 (79.5%). Gestational age at delivery was the only independent risk factor of perinatal mortality. The overall survival rate of twin pregnancies complicated with previable PPROM is poor but similar to singletons. No prognostic factors, apart from achieving periviability, were identified as individual predictors of perinatal mortality.
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  • 文章类型: Meta-Analysis
    目的:本研究旨在确定单胎妊娠妊娠24周后经阴道超声检测的宫颈环扎术是否能降低早产风险。
    方法:OvidMEDLINE,Scopus,并使用以下术语搜索了Cochrane中央对照试验登记册:“环扎,子宫颈,“\”子宫颈机能不全,\"\"产科外科手术,子宫颈,“”随机对照试验,“和”对照临床试验。
    方法:所有随机对照试验均可纳入,这些试验比较了在24+0/7周和29+6/7周之间经阴道超声检测的短宫颈长度≤25mm的单胎妊娠中没有环扎术的放置。
    方法:收集来自每个试验的个体患者水平数据。如果一项符合条件的试验包括在妊娠24+0/7周之前或之后检测到宫颈长度短的多胎妊娠和单胎妊娠的患者,仅包括在24+0/7周或之后出现的单身人士。主要结局为早产<37周妊娠。次要结局包括早产<34、<32和<28孕周,分娩时的胎龄,延迟,早产胎膜破裂,绒毛膜羊膜炎,和不良的新生儿结局。使用2阶段方法分析来自每个试验的个体患者水平数据。适当计算合并的相对风险或95%置信区间的平均差。
    结果:纳入了4项符合条件的随机对照试验的数据。在妊娠240/7至266/7周时,共有131例单胎出现,并进行了进一步分析;没有关于妊娠270/7周或更晚的环扎患者的数据。其中包括,环扎组66例(50.4%),无环扎组65例(49.6%)。在随机分配到环扎组的患者和随机分配到无环扎组的患者之间,早产<37周的发生率相似(27.3%vs38.5%;相对风险,0.78;95%置信区间,0.37-1.28)。次要结局包括早产<34、<32和<28孕周,分娩时的胎龄,从随机化到交付的时间间隔,早产胎膜破裂,和不良的新生儿结局,如低出生体重,出生体重很低,两组之间的围产期死亡相似。计划的亚组分析显示,根据宫颈长度测量(≤15mm或≤10mm),两组之间<妊娠37周的早产率无统计学差异。随机分组的孕龄(24+0/7至24+6/7周或25+0/7至26+6/7周),或早产史。
    结论:在妊娠24周后发现宫颈长度较短的单胎妊娠中,宫颈环扎术并没有降低或增加早产率。因为与环扎术相关的早产减少了22%,这是类似的风险降低量,通常与24周妊娠前超声指示的环扎术相关,有必要在该患者人群中进行进一步的随机对照试验.
    This study aimed to determine whether cervical cerclage for a transvaginal ultrasound-detected short cervical length after 24 weeks of gestation in singleton pregnancies reduces the risk for preterm birth.
    Ovid MEDLINE, Scopus, and the Cochrane Central Register of Controlled Trials were searched using the following terms: \"cerclage, cervical,\" \"uterine cervical incompetence,\" \"obstetrical surgical procedures,\" \"cervix uteri,\" \"randomized controlled trial,\" and \"controlled clinical trial.\"
    All randomized controlled trials comparing cerclage placement with no cerclage in singleton gestations with a transvaginal ultrasound-detected short cervical length ≤25 mm between 24+0/7 and 29+6/7 weeks of gestation were eligible for inclusion.
    Individual patient-level data from each trial were collected. If an eligible trial included patients with both multiple and singleton gestations with a short cervical length detected either before or after 24+0/7 weeks of gestation, only singletons who presented at or after 24+0/7 weeks were included. The primary outcome was preterm birth <37 weeks\' gestation. Secondary outcomes included preterm birth <34, <32, and <28 weeks\' gestation, gestational age at delivery, latency, preterm prelabor rupture of membranes, chorioamnionitis, and adverse neonatal outcomes. Individual patient-level data from each trial were analyzed using a 2-stage approach. Pooled relative risks or mean differences with 95% confidence intervals were calculated as appropriate.
    Data from the 4 eligible randomized controlled trials were included. A total of 131 singletons presented at 24+0/7 to 26+6/7 weeks of gestation and were further analyzed; there were no data on patients with a cerclage at 27+0/7 weeks\' gestation or later. Of those included, 66 (50.4%) were in the cerclage group and 65 (49.6%) were in the no cerclage group. The rate of preterm birth <37 weeks\' gestation was similar between patients who were randomized to the cerclage group and those who were randomized to the no cerclage group (27.3% vs 38.5%; relative risk, 0.78; 95% confidence interval, 0.37-1.28). Secondary outcomes including preterm birth <34, <32, and <28 weeks\' gestation, gestational age at delivery, time interval from randomization to delivery, preterm prelabor rupture of membranes, and adverse neonatal outcomes such as low birthweight, very low birthweight, and perinatal death were similar between the 2 groups. Planned subgroup analyses revealed no statistically significant differences in the rate of preterm birth <37 weeks\' gestation between the 2 groups when compared based on cervical length measurement (≤15 mm or ≤10 mm), gestational age at randomization (24+0/7 to 24+6/7 weeks or 25+0/7 to 26+6/7 weeks), or history of preterm birth.
    Cervical cerclage did not reduce or increase the rate of preterm birth among singleton pregnancies with a short cervical length detected after 24 weeks of gestation. Because there was a 22% nonsignificant decrease in preterm birth associated with cerclage, which is a similar amount of risk reduction often associated with ultrasound-indicated cerclage before 24 weeks\' gestation, further randomized controlled trials in this patient population are warranted.
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  • 文章类型: Journal Article
    Legal,机构,规范生殖保健的付款人政策缺乏与医学的共同语言,造成巨大的混乱和恐慌。本文严格审查了与堕胎护理有关的不清楚语言的含义和后果。使用基于案例的方法,我们强调了语言和术语可能影响护理质量和可及性的方式。我们还解决了对他们团队中的提供者和患者的影响,机构,state,和付款人景观。特别是,我们探讨堕胎的污名化既是一个词,也是一个过程,看护者作为看门人的角色,生存能力作为访问限制的含义,以及应得和价值的层次结构。认识到语言在这些讨论中的作用对于建立尊重以患者为中心的生殖决策的复杂性的系统至关重要。确保获得全面的生殖保健,包括堕胎,和中心患者自主权。医疗保健提供者在促进机构、state,和国家景观,在这些景观中,怀孕患者的自主权得到支持,并获得公正和公平的生殖保健。
    Legal, institutional, and payer policies regulating reproductive health care lack a shared language with medicine, resulting in great confusion and consternation. This paper critically examines the implications and ramifications of unclear language related to abortion care. Using a case-based approach, we highlight the ways in which language and terminology may affect the quality and accessibility of care. We also address repercussions for providers and patients within their team, institutional, state, and payer landscapes. In particular, we explore the stigmatization of abortion as both a word and a process, the role of caregivers as gatekeepers, the implications of viability as a limit for access, and the hierarchy of deservedness and value. Recognizing the role of language in these discussions is critical to building systems that honor the complexities of patient-centered reproductive decision-making, ensure access to comprehensive reproductive health care including abortion, and center patient autonomy. Healthcare providers are uniquely positioned to facilitate institutional, state, and national landscapes in which pregnant patients are supported in their autonomy and provided with just and equitable reproductive health care.
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