success rate

成功率
  • 文章类型: English Abstract
    BACKGROUND: Securing the airway in the emergency department (ED) is a high-stakes procedure; however, the primary success and complication rate are largely unknown in Germany. The aim of this study was a retrospective analysis of prospectively collected resuscitation room data for endotracheal intubation (ETI) regarding indications, performance and complications.
    METHODS: Between 1 January 2020 and 30 June 2023 all ETIs conducted in the ED (Kliniken Maria Hilf, Moenchengladbach, Germany) were analyzed following approval by the ethics committee (EK 23-369). Primary intubations performed by the anesthesiology department were excluded. The core medical team of the ED underwent a six-week training program including a two-week anesthesia rotation prior to performing ETI in the ED. There were standard operating procedures (SOP) for both rapid sequence induction (RSI) and airway exchange with a placed laryngeal tube (LT) utilizing video laryngoscopy (C-Mac, Storz), rocuronium for relaxation and primary intubation with an elastic bougie. The primary success rate, overall success rate and intubation-related complications were analyzed. Additionally, the factor of consultant ED staff and residents was evaluated with respect to the primary success rate.
    RESULTS: During the study period 499 patients were intubated by the core ED team and 28 patients underwent airway exchange from LT to ETI. Primary success could be achieved in 489/499 (98.0%) ETI and in 25/28 (89.3%) LT exchange patients. Surgically achieved securing of the airway was carried out in 5/527 (0.9%) patients in a cannot intubate situation and 11/527 (2.2%) patients suffered cardiac arrest minutes after the ETI. The overall first pass success rate of endotracheal tube placement was 514/527 (97.4%). The comparison of the primary success of consultants (168/175; 96.0%) vs. residents 320/325 (98.5%) yielded no significant differences (p = 0.08).
    CONCLUSIONS: In clinical acute and emergency medicine, a standardized approach utilizing video laryngoscopy and a bougie following a structured training concept, can achieve an above-average high primary success rate with simultaneous low severe complications in the high-risk collective of critically ill emergency patients in an intrahospital setting.
    UNASSIGNED: HINTERGRUND: Erfolgs- und Komplikationsraten endotrachealer Intubationen (ETI) in zentralen Notaufnahmen (ZNA) sind in Deutschland weitestgehend unbekannt. Ziel dieser Arbeit ist daher eine retrospektive Evaluation durchgeführter ETI in Bezug auf Indikationen, Performanz und Komplikationen.
    METHODS: Nach Freigabe der Ethikkommission (EK 23-369) erfolgte die Analyse aller ETI von PatientInnen (Kliniken Maria Hilf, Mönchengladbach), die im Zeitraum vom 01.01.2020 bis 30.06.2023 durch das ärztliche ZNA-Team durchgeführt wurden. Beim Polytrauma durchgeführte ETI durch die Klinik für Anästhesiologie wurden ausgeschlossen. Das ärztliche ZNA-Kernteam durchlief ein sechswöchiges Ausbildungskonzept inklusive zweiwöchigem Atemwegstraining im Zentral-OP. Für die Rapid Sequence Induction (RSI) und die Umintubation bei einliegendem Larynxtubus (LT) existieren Standard Operating Procedures (SOP) mit Videolaryngoskopie (C-MAC, Storz), Relaxierung und primärer Intubation mit elastischem Bougie. Primäre Erfolgsrate, Gesamterfolgsrate, intubationsassoziierte Komplikationen und der Einfluss einer „Facharztqualifikation“ sollten analysiert werden.
    UNASSIGNED: Bei 499 PatientInnen wurde die Indikation zur ETI, bei 28 PatientInnen zum Wechsel von LT auf ETI gestellt. Ein primärer Erfolg wurde bei 489/499 (98,0 %) bzw. 25/28 (89,3 %) detektiert, Gesamterfolgsrate 97,4 % (514/527). Ein chirurgischer Atemweg wurde bei 5/527 (0,9 %) PatientInnen bei „cannot intubate“ durchgeführt, 11/527 (2,2 %) PatientInnen erlitten in den Minuten nach der ETI einen Herz-Kreislauf-Stillstand. Ein Einfluss einer Facharztqualifikation auf den Primärerfolg konnte nicht festgestellt werden (168/175, 96,0 % (Facharzt) vs. 320/325 98,5 % (Nicht-Facharzt), p = 0,08).
    UNASSIGNED: In der klinischen Akut- und Notfallmedizin kann mit einer standardisierten Vorgehensweise nach strukturiertem Ausbildungskonzept eine im internationalen Vergleich überdurchschnittliche hohe primäre Erfolgsrate erzielt werden, bei Minimierung schwerwiegender Komplikationen in dem Hochrisikokollektiv kritisch kranker NotfallpatientInnen.
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  • 文章类型: Journal Article
    泪囊鼻腔吻合术(DCR)是一种绕过鼻泪管系统阻塞的手术。DCR可以分为两种主要技术:外部和内窥镜。本综述旨在评估外部DCR程序的成功率,无论是否使用支架。这项研究比较了多项研究中使用和不使用硅胶插管的原发性DCR的结果。审查的研究一致表明,硅胶插管显着提高DCR的成功率,成功率从80%到95%不等。所涉及的研究表明,硅胶插管在涉及远处和常见小管阻塞和复发性DCR手术的复杂病例中具有特定的优势。这篇综述强调,多项研究表明,当硅胶管用作支架时,外部泪囊鼻腔吻合术(DCR)的成功率更高。此外,外部DCR已被确定为医疗专业人员的首选程序。
    Dacryocystorhinostomy (DCR) is a procedure that bypasses an obstruction in the nasolacrimal duct system. DCR can be categorized into two primary techniques: external and endoscopic. This review aims to assess the success rate of external DCR procedures, both with and without the use of a stent. This study compared the outcomes of primary DCR with and without silicone intubation in multiple studies. The reviewed studies consistently showed that silicone intubation significantly improves the success rates of DCR, with success rates ranging from 80% to 95%. The involved studies suggest that silicone intubation offers specific advantages in complex cases involving distant and common canaliculus blockages and recurrent DCR surgeries. This review emphasizes that multiple studies have documented higher success rates of external dacryocystorhinostomy (DCR) when silicone tubes are utilized as stents. Furthermore, external DCR has been identified as the preferred procedure among medical professionals.
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  • 文章类型: Journal Article
    目的:目的是研究活动性中耳炎对慢性中耳炎(COM)和鼓膜穿孔患者鼓室成形术成功率的影响。
    PubMed,Embase和Cochrane图书馆。
    方法:纳入标准是对任何年龄的COM患者因COM引起鼓膜穿孔而进行鼓室成形术的闭合率的研究。排除标准是对同时进行乳突切除术的患者的研究,听骨链重建,输卵管成形术,腺样体切除术,翻修鼓室成形术,由于COM以外的其他条件而导致穿孔的患者,和给编辑的信,评论,会议摘要和案例报告。使用QUIPS工具对所包含的文章进行了严格评估。提取鼓膜闭合率数据,计算湿耳与干耳的闭合率的比值比(OR)和95%置信区间(CI).
    结果:搜索于2023年2月1日进行。在4671篇文章中,纳入了16项研究,并对其进行了严格评估。在这些观察性研究中(九项前瞻性研究,七个回顾性),共1509例患者(干耳组n=1003;湿耳组n=506),两项研究表明成功率有显著差异,一个赞成干燥的耳朵,一个赞成在手术时湿润的耳朵。所有其他研究均未显示统计学上的显着差异。总的来说,偏倚风险被认为是中等至高.
    结论:我们发现鼓室成形术期间活动性中耳炎对鼓膜闭合率无显著预后价值。因为总体偏倚风险被认为是中等到高的,无法得出强有力的结论。为了能够用更高水平的证据来回答这个问题,需要高质量的前瞻性或随机研究.
    OBJECTIVE: The aim is to investigate the influence of an active otitis media on the success rate of tympanoplasty in patients with a chronic otitis media (COM) and a tympanic membrane perforation.
    UNASSIGNED: PubMed, Embase and the Cochrane Library.
    METHODS: The inclusion criteria were studies on closure rates of tympanoplasty performed in COM patients of any age with a tympanic membrane perforation caused by COM. The exclusion criteria were studies on patients undergoing concomitant mastoidectomy, ossicular chain reconstruction, tuboplasty, adenoidectomy, revision tympanoplasty, patients with perforations due to other conditions than COM, and letters to editors, commentaries, conference abstracts and case reports. The included articles were critically appraised using the QUIPS tool. Data on tympanic membrane closure rate were extracted, odds ratio (OR) and 95% confidence intervals (CI) of the closure rate with a wet versus a dry ear were calculated.
    RESULTS: The search was performed on 1 February 2023. Of 4671 articles, 16 studies were included and critically appraised. Of these observational studies (nine prospective, seven retrospective), with a total of 1509 patients (dry ear group n = 1003; wet ear group n = 506), two studies stated a significant difference in success rate, one in favour of a dry ear and one in favour of a wet ear at time of surgery. All other studies did not show a statistically significant difference. Overall, the risk of bias was considered moderate to high.
    CONCLUSIONS: We found no significant prognostic value of having an active otitis media during tympanoplasty on tympanic membrane closure rates. Because the overall risk of bias was considered moderate to high, no strong conclusions can be made. To be able to answer this question with higher levels of evidence, high-quality prospective or randomized studies are needed.
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  • 文章类型: Journal Article
    我们调查了美国50个州的教育支出与教育成功之间的关系。我们的重点主要是使用州一级的教育支出数据,这些数据以一般和特定的方式出现。我们发现的结果可以总结如下。一,教育支出是激励人们接受高等教育的重要因素,也是确保完成学业的激励因素。两个,我们进一步强调支出的类型及其对教育成功的不同立场。虽然一般支出在这方面发挥着重要作用,发现特定的(特别是在资本项目上的支出)会逆转成功率。这表明,教育资本支出必然需要达到确定的阈值,以激发当前联系的积极检查。三,对总支出的影响程度低于使用一般支出时,这使得资本支出的影响更加突出。最后,我们还确定了黑带和非黑带州之间不同类别的支出的不对称影响。虽然这两个地区的支出模式都很重要,黑带地区的幅度更高,表明当支出改善时,该地区更容易受益。我们进一步提出重要的政策立场。
    We investigate the nexus between education spending and education success measured through attainment rate for 50 US states. Our emphasis is mainly to use state-level data on education spending which occur in general and specific terms. The outcome from our finding can be summarized as follows. One, education spending constitutes a significant factor that motivates people for higher education and it is a motivating factor that ensures completion. Two, we establish further emphasis with the types of spending and its differing stance on education success. While general spending plays important roles in this regard, specific (particularly spending on capital project) is found to reverse the success rate. This suggests that capital spending on education necessarily needs to reach a defined threshold to incite positive check in the current nexus. Three, the magnitude of impact for total spending is lower than when general spending is used, which make the impact of capital spending more conspicuous. Lastly, we also establish asymmetric impact of spending across differing categories between Black Belt and Non-Black Belt states. While the spending pattern is significant for both regions, the magnitude is higher for the Black Belt region indicating the tendency of the region to benefit more when spending improves. We further offer important policy stance.
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  • 文章类型: Journal Article
    目的:有几个因素可能会影响植入部位的准备,而植入物设计是最重要的因素;然而,很少有研究调查它的影响。该研究的目的是探索使用两种不同的钻孔方案使用不同设计的burs准备植入部位的比较功效,通过评估影像学和临床结果。
    方法:本随机对照临床试验的分配比例为1:1,由两名经验丰富的外科医生和研究人员在两个私人诊所进行。在对照组中,外科医生使用标准直钻遵循协议,而在测试组中,他们使用台阶钻。两组患者均接受相同类型的植入物和假体。主要结果是假体放置一年后的边缘骨吸收。
    结果:在研究中纳入并治疗了总共60名受试者(86个植入物)。在为期一年的随访中,筛选了54名受试者(74名植入物),和50在2年随访(69植入)。这项研究没有证据表明骨吸收有差异,随着时间的推移,两组之间。
    结论:临床参数和以患者为中心的结果均显示两种不同钻头形状的植入部位准备方案之间没有差异。
    OBJECTIVE: There are several factors that may influence implant site preparation with implant design being a paramount factor; however, few studies investigate its impact. The purpose of the study was to explore the comparative efficacy of using two different drilling protocols using burs with different design for preparing implant sites, by evaluating radiographic and clinical outcomes.
    METHODS: The present randomized controlled clinical trial with an allocation ratio of 1:1 was carried on in two private practice offices by two experienced surgeons and researchers. In the control group the surgeons followed the protocol with standard straight burs while in the test group they used step burs. In both groups the patients received the same type of implants and prosthesis. The primary outcome was the marginal bone resorption one year after the prosthetic placement.
    RESULTS: In the study were included and treated a total of 60 subjects (86 implants). At the one-year follow-up were screened 54 subjects (74 implants), and 50 at the 2-year follow-up (69 implants). This study showed no evidence of a difference in bone resorption, which increased significantly over time, between the two groups.
    CONCLUSIONS: Both clinical parameters and patientcentered outcomes revealed no difference between the two protocols of implant site preparation with two different drill shape.
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  • 文章类型: Journal Article
    背景:这项前瞻性临床研究评估了硅胶支架管(SST)对鼻内镜下泪囊鼻腔吻合术(EN-DCR)治疗原发性获得性鼻泪管阻塞成功率的影响。
    方法:患者在3个月的时间内随机分配接受有或没有SST插管的EN-DCR。使用标准化技术进行手术。在三个不同的时间点对患者进行评估:一天,术后12周和24周。比较结果以评估统计学差异。手术的成功取决于积极的冲洗程序,以及通过改善症状和高水平的患者满意度。
    结果:共有56例随机病例完成了24周的随访。1例患者因鼻泪管阻塞的恶性发生而退出。在24周的随访之后,没有发现在溢唇水平(p>.10)或通畅性(p>.16)方面的统计学显著差异。关于时间变化的比较没有显示出显著性水平(p>.28)。
    结论:本研究无法证实在EN-DCR中插入SST有统计学上显著的益处或缺点。
    BACKGROUND: This prospective clinical study evaluates the effect of a silicone stent tube (SST) on the success rate of endonasal-endoscopic dacryocystorhinostomy (EN-DCR) to treat primary acquired nasolacrimal duct obstruction.
    METHODS: Patients were randomly assigned to receive EN-DCR with or without SST intubation over a period of 3 months. The surgery was performed using standardized techniques. Patients were assessed at three different timepoints: one day, 12 weeks and 24 weeks after the surgery. The results were compared in order to evaluate statistical differences. Surgical success was determined by means of positive irrigation procedures, as well as by the improvement of symptoms and a high level of patient satisfaction.
    RESULTS: A total of 56 randomized cases completed 24 weeks of follow up. 1 Patient dropped out due to malignant genesis of the nasolacrimal duct obstruction. After 24 weeks of follow up no statistically significant differences in levels of epiphora (p > .10) or patency (p > .16) were revealed. Comparisons regarding changes in time did not show levels of significance (p > .28).
    CONCLUSIONS: This study could not confirm a statistically significant benefit or disadvantage for SST Insertion in EN-DCR.
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  • 文章类型: Journal Article
    目的:评估悬臂式氧化锆基树脂粘合固定局部义齿(RBFPDs)替代缺失后牙的寿命,以及接受氧化锆RBFPD的患者的生活质量和患者满意度。
    方法:进行了一项前瞻性单臂非受控临床试验,以使用悬臂式氧化锆RBFPD替换一个或多个缺失的前磨牙或磨牙,跨度为5至8mm。招募了36名具有40个假体的参与者,并进行了3年的临床评估。保持器设计包括0.8mm的最小厚度,至少200°圆周环绕与咬合杆,连接器尺寸为3×3毫米。患者报告的结果,包括患者满意度和口腔健康影响概况(OHIP),被评估。
    结果:参与者的平均年龄为45.8岁,72.5%是女性。后路氧化锆RBFPDs的成功率为76.2%,估计平均生存期为46.1个月。生存率为88.1%,估计平均成功持续时间为49.4个月。参与者对治疗非常满意,满意度平均得分为80.8±11.9。3年后,参与者的OHIP总分从52.3降至39.6,表明口腔健康相关生活质量显著改善(P=0.009)。
    结论:3年后,后悬臂式氧化锆RBFPD的生存率中等高,患者报告的结局良好.因此,它可以被推荐作为一种保守治疗选择,以取代缺失的后牙,前提是要考虑到保持器的设计因素。
    结论:用于后牙的悬臂式氧化锆RBFPDs可以作为一种保守治疗选择,既美观又具有生物相容性。与牙科植入物相比,它提供了更具成本效益的替代方案,对于大多数患者来说,这通常是非常昂贵的。这种方法有可能极大地改善患者报告的结果。
    OBJECTIVE: To evaluate the longevity of cantilevered zirconia-based resin-bonded fixed partial dentures (RBFPDs) in replacing missing posterior teeth, as well as the quality of life and patient satisfaction experienced by those receiving zirconia RBFPDs.
    METHODS: A prospective single-arm uncontrolled clinical trial was conducted to replace one or more missing premolars or molars with a span of 5 to 8 mm using cantilevered zirconia RBFPDs. Thirty-six participants with 40 prostheses were recruited and underwent a 3-year clinical evaluation. The retainer designs included a minimum thickness of 0.8 mm, a minimum of 200° circumferential wraparound with an occlusal bar, and a connector dimension of 3 × 3 mm. Patient-reported outcomes, including patient satisfaction and Oral Health Impact Profile (OHIP), were assessed.
    RESULTS: The average age of participants was 45.8 years, and 72.5 % were women. The success rate of the posterior zirconia RBFPDs was 76.2 %, with an estimated mean success duration of 46.1 months. The survival rate was 88.1 %, with an estimated mean survival duration of 49.4 months. Participants were highly satisfied with the treatment, achieving an average satisfaction score of 80.8 ± 11.9. Participants\' total OHIP scores decreased from 52.3 to 39.6 after 3 years, indicating a significant improvement in oral health-related quality of life (P = 0.009).
    CONCLUSIONS: After 3 years, a moderately high survival rate and favourable patient-reported outcomes of posterior cantilevered zirconia RBFPDs were achieved. Therefore, it can be recommended as a conservative treatment option to replace missing posterior teeth, provided that retainer design considerations are taken into account.
    CONCLUSIONS: Cantilevered zirconia RBFPDs for posterior teeth can serve as a conservative treatment option that is both aesthetically pleasing and biocompatible. It offers a more cost-effective alternative compared to dental implants, which are often prohibitively expensive for the majority of patients. This approach has the potential to greatly improve patient-reported outcomes.
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    文章类型: English Abstract
    Responsible for a significant morbidity and mortality, smoking remains a major public health issue. Smoking cessation clinics are an integral part of the fight against smoking. This retrospective study, carried out between January 2022 and January 2023 on 106 patients who attended the smoking cessation clinics in the Respiratory Department of the University Hospital of Liège, was designed to assess patient cessation rates at 6 months and 1 year, and to identify any factors predicting success or failure. Our data showed a cessation rate of 25 % at 6 months and 19 % at 1 year. Age was slightly more advanced in those who succeeded in smoking cessation at one year (p = 0.05). The obtained cessation rate strongly supports the utility of our smoking cessation clinic for patients wishing to quit smoking.
    Responsable d’une morbi-mortalité importante, le tabagisme reste un enjeu, non négligeable, de santé publique. Les consultations d’aide au sevrage font partie intégrante des moyens mis en œuvre pour lutter contre le tabagisme dans une optique de prévention. Cette étude rétrospective, menée entre janvier 2022 et janvier 2023, auprès de 106 patients ayant fréquenté les consultations de tabacologie du Service de Pneumologie du CHU de Liège, avait pour objectifs d’évaluer les taux de sevrage des patients à 6 mois et à 1 an et d’identifier d’éventuels facteurs prédictifs de succès, ou d’échec, au sein de l’échantillonnage étudié. L’analyse des données a démontré un taux de sevrage de 25 % à 6 mois et de 19 % à 1 an. L’analyse des facteurs démographiques montre une moyenne d’âge plus élevée chez les patients qui réussissent leur sevrage à 1 an (p = 0,05). Le taux de sevrage obtenu atteste de la pertinence et de la nécessité de notre accompagnement auprès des patients désireux de cesser de fumer.
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  • 文章类型: Journal Article
    有大量关于牙科贴面的公开文献;然而,牙齿预备的效果,老化,单板类型,而树脂粘固剂的失效类型对牙科贴面的实验室与临床情况尚不清楚。本叙述性综述的目的是确定与实验室测试中牙科贴面失败相关的主要因素,并了解这些因素如何转化为临床成功/失败。文章由主要作者在2024年1月使用关键词“牙齿贴面”进行识别和筛选,\"并发症\",“生存率”,\"失败\",和“成功率”使用PubMed/Medline,Scopus,谷歌学者,科学直接。纳入标准包括1999年1月至2024年1月发表的关于牙齿准备主题的文章,树脂水泥和单板的老化过程,半透明,厚度,单板的制造技术;遮阳,树脂水泥的厚度。排除标准包括讨论边际和内部匹配的文章,显微硬度,水吸附,溶解度,可抛光性,咬合贴面,保留,表面处理,和穿。本综述的结果表明,牙科贴面通常具有很高的存活率(超过10年>90%)。保存的釉质层的数量在贴面的存活率和成功率中起着至关重要的作用,和最少/没有准备的玻璃陶瓷贴面显示出最高的存活率。骨折是与存活率降低相关的主要失败机制,然后是脱粘和颜色变化。在存在功能异常活动的情况下,骨折增加。牙髓并发症较少与贴面修复相关。上颌和下颌牙齿之间没有观察到差异。临床意义:通过在胶结后立即评估咬合和使用高强度贴面材料可以减少骨折,低模量树脂水泥,和薄层高度抛光的贴面。脱粘失败可以用最少/无准备减少,当牙本质暴露时,应考虑立即密封牙本质。还可以通过防止血液污染来减少脱粘,唾液,手机油,或含氟抛光膏;通过适当的表面处理(对玻璃陶瓷进行20s的氢氟酸蚀刻,然后用硅烷蚀刻60s);并通过对薄单板使用光固化聚合。可以使用具有UDMA基树脂的树脂水泥保持长期颜色稳定性,玻璃陶瓷材料,和薄单板的光固化聚合。
    There is a vast amount of published literature concerning dental veneers; however, the effects of tooth preparation, aging, veneer type, and resin cement type on the failure of dental veneers in laboratory versus clinical scenarios are not clear. The purpose of the present narrative review was to determine the principal factors associated with failures of dental veneers in laboratory tests and to understand how these factors translate into clinical successes/failures. Articles were identified and screened by the lead author in January 2024 using the keywords \'\'dental veneer\", \"complication\", \"survival rate\", \"failure\", and \"success rate\" using PubMed/Medline, Scopus, Google Scholar, and Science Direct. The inclusion criteria included articles published between January 1999 and January 2024 on the topics of preparation of a tooth, aging processes of the resin cement and veneer, translucency, thickness, fabrication technique of the veneer; shade, and thickness of the resin cement. The exclusion criteria included articles that discussed marginal and internal fit, microhardness, water sorption, solubility, polishability, occlusal veneers, retention, surface treatments, and wear. The results of the present review indicated that dental veneers generally have a high survival rate (>90% for more than 10 years). The amount of preserved enamel layer plays a paramount role in the survival and success rates of veneers, and glass-ceramic veneers with minimal/no preparation showed the highest survival rates. Fracture was the primary failure mechanism associated with decreased survival rate, followed by debonding and color change. Fractures increased in the presence of parafunctional activities. Fewer endodontic complications were associated with veneer restorations. No difference was observed between the maxillary and mandibular teeth. Clinical significance: Fractures can be reduced by evaluation of occlusion immediately after cementation and through the use of high-strength veneer materials, resin cements with low moduli, and thin layers of highly polished veneers. Debonding failures can be reduced with minimal/no preparation, and immediate dentin sealing should be considered when dentin is exposed. Debonding can also be reduced by preventing contamination from blood, saliva, handpiece oil, or fluoride-containing polishing paste; through proper surface treatment (20 s of hydrofluoric acid etching for glass ceramic followed by silane for 60 s); and through use of light-cured polymerization for thin veneers. Long-term color stability may be maintained using resin cements with UDMA-based resin, glass ceramic materials, and light-cure polymerization with thin veneers.
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  • 文章类型: Journal Article
    目的:使用不同的甲氨蝶呤(MTX)方案治疗异位妊娠已经确立。本研究旨在评估单剂量和双剂量MTX方案治疗不明部位妊娠(PUL)的疗效。
    方法:这项回顾性研究是在妇科内分泌科进行的,大学医院,克拉科夫,波兰。2014年1月至2023年9月,血液动力学稳定的PUL女性入组。人口统计,比较单剂量MTX组和双剂量MTX组妇女的孕龄和治疗结局。主要结果是成功率,以未经手术干预治疗的妇女人数来衡量。次要结果是达到β-人绒毛膜促性腺激素(β-hCG)适当降低所需的MTX天数。
    结果:研究中纳入了211名妇女(平均年龄33±1.8岁),总体成功率为89.1%。发现单剂量和双剂量MTX方案具有可比的治疗成功率(93%和95%,分别)。与初始血清β-hCG较高的女性相比,初始血清β-hCG较低(<2000mIU/ml)的女性具有更高的治疗效果(96.5%vs71.4%)。无论协议类型如何。与使用双剂量MTX方案治疗的妇女相比,使用单剂量MTX方案治疗的妇女的住院时间缩短了1天。
    结论:单剂量和双剂量MTX方案具有相当的疗效和安全性,在初始β-hCG<2000mIU/ml的PUL女性中,应同样考虑。
    OBJECTIVE: The use of various methotrexate (MTX) protocols for the treatment of ectopic pregnancy is well established. This study aimed to evaluate the efficacy of single- and double-dose MTX protocols for the treatment of pregnancy of unknown location (PUL).
    METHODS: This retrospective study was conducted in the Department of Gynaecological Endocrinology, University Hospital, Krakow, Poland. Haemodynamically stable women with PUL were enrolled between January 2014 and September 2023. Demographics, gestational age and treatment outcomes were compared between women in the single-dose MTX group and women in the double-dose MTX group. The primary outcome was the success rate, measured as the number of women treated without surgical intervention. The secondary outcome was the number of days of MTX needed to achieve an appropriate decrease in beta-human chorionic gonadotrophin (β-hCG).
    RESULTS: Two hundred and eleven women (mean age 33 ± 1.8 years) with PUL were enrolled in the study, with an overall success rate of 89.1 %. Single- and double-dose MTX protocols were found to have comparable treatment success rates (93 % and 95 %, respectively). Women with lower initial serum β-hCG (<2000 mIU/ml) had higher treatment efficacy compared with women with higher initial serum β-hCG (96.5 % vs 71.4 %), regardless of protocol type. The length of hospital stay for the women treated with the single-dose MTX protocol was 1 day shorter compared with that for the women treated with the double-dose MTX protocol.
    CONCLUSIONS: Single- and double-dose MTX protocols have comparable efficacy and safety, and should be equally considered in women with PUL with initial β-hCG < 2000 mIU/ml.
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