• 【TCu 380A宫内节育器和无框宫内节育器“ FlexiGard”:来自国际多中心试验的三年期中期数据。开发计划署,人口基金和卫生组织关于人类生殖的研究,开发和研究培训特别方案,世界银行:宫内节育器研究】 复制标题 收藏 收藏
    DOI:10.1016/s0010-7824(95)00140-9 复制DOI
    作者列表:
    BACKGROUND & AIMS: The TCu 380A and FlexiGard IUDs were compared in a randomized multicenter trial including 28 institutes in 13 countries. There were 53 insertion failures with the FlexiGard and one with the TCu 380A. There were 2184 successful insertions of the TCu380A and 2102 of the FlexiGard device. The three-year pregnancy rates for the TCu 380A and FlexiGard were similar (1.6 and 1.9 per 100 women, respectively) but the FlexiGard three-year expulsion rate (7.4 per 100 women) was significantly higher than that of the TCu 380A (4.4 per 100 women). The insertion technique for the FlexiGard needs to be improved in order to lower the expulsion rate.

    背景与目标: 在包括13个国家的28个研究所的随机多中心试验中,对TCu 380A和FlexiGard宫内节育器进行了比较。 FlexiGard发生53次插入故障,而TCu 380A发生1次插入故障。 TCu380A成功插入2184次,FlexiGard设备成功插入2102次。 TCu 380A和FlexiGard的三年妊娠率相似(分别为每100名女性1.6和1.9),但FlexiGard三年驱逐率(每100名妇女7.4)显着高于TCu 380A(4.4名妇女)。 100名女性)。需要改进FlexiGard的插入技术,以降低驱逐率。

  • 2 Contraindications to IUD and IUS use. 复制标题 收藏 收藏

    【IUD和IUS使用的禁忌症。】 复制标题 收藏 收藏
    DOI:10.1016/j.contraception.2007.01.004 复制DOI
    作者列表:Nelson AL
    BACKGROUND & AIMS: :Contraindications to IUD or IUS use can be found on product labeling, in the guidelines of various specialty groups and in recommendations from peer-reviewed articles. Overly restrictive contraindications block access to this top-tier method for many women who would be candidates based on current scientific evidence. Assuming that a condition should be listed as a contraindication only if the risk of IUD/IUS use by a woman with that condition exceeds her risk with pregnancy, the list of contraindications is reduced to pregnancy, active uterine infection, malignancy in the uterus or cervix, an inability to place or retain the device, unexplained abnormal bleeding and adverse reaction to product ingredients.
    背景与目标: :在产品标签上,各种专业团体的指南中以及在经过同行评审的文章中的建议中,都可以找到宫内节育器或宫内节育器的禁忌症。过于严格的禁忌症阻碍了许多将根据当前科学证据成为候选人的妇女使用这种顶级方法。假设仅当患有该疾病的妇女使用IUD / IUS的风险超过其怀孕风险时,才应将该疾病列为禁忌证,禁忌证的清单将减少为怀孕,活动性子宫感染,子宫或子宫颈恶性肿瘤。 ,无法放置或保留设备,无法解释的异常出血以及对产品成分的不良反应。
  • 【取出宫内节育器后开始受孕的时间:使用时间,宫内节育器类型,盆腔炎和年龄的重要性。】 复制标题 收藏 收藏
    DOI:10.1016/0020-7292(86)90100-1 复制DOI
    作者列表:Andolsek L,Teeter RA,Kozuh-Novak M,Wheeler R,Fortney JA,Rosenberg MJ
    BACKGROUND & AIMS: :Some investigations of IUD use have demonstrated impaired ability to become pregnant after removal, while others have not. None of these studies, however, have adequately considered such potentially influencing variables as age and a history of pelvic inflammatory disease (PID). To study the effect of length of IUD use, IUD type and the modifying influences of age and PID history on time required to conceive, we followed women trying to become pregnant after removal of their IUD. Five hundred forty women in Ljubljana, Yugoslavia who were first fitted with an IUD between 1964 and 1972 and had their IUD removed in order to become pregnant were followed through 1980. We found no relationship between the duration of IUD use or type of IUD used, but increasing age and a history of PID each decreased the monthly probability of conception. These findings, along with other recent work, indicate that IUDs are a safe and efficacious contraceptive for women at low risk for sexually transmitted diseases. :Previous investigations of IUD use have demonstrated impaired ability to become pregnant after removal, while other studies have not. None of these studies, however, have adequately considered such potentially influencing variables as age and a history of pelvic inflammatory disease (PID). This investigation uses regression analysis to assess the influence of various factors individually on time to conceive. 540 women in Ljubljana, Yugoslavia, who were 1st fitted with an IUD between 1964 and 1972 and had their IUD removed to become pregnant, were followed through 1980. The COX regression model is used to assess simultaneously the influences of length of IUD use, device type (Lippes Loop), age at removal, parity, previous PID history, and duration of marriage on time to conception, thus controlling for the interrelationships between variables. This technique estimates the probability of conceiving at different times. Results indicate that duration of IUD use did not affect the time to conception. In addition, IUD type, duration of marriage or parity did not affect the time required to conceive. These findings demonstrate that the use of IUDs does not, in and of itself, lead to problems with subsequent fertility. However, these results underscore the importance of limiting IUDs to women who are not at high risk of sexually transmitted diseases.
    背景与目标: :一些对宫内节育器使用的调查显示,取出宫内避孕器后怀孕的能力受损,而其他人则没有。然而,这些研究都没有充分考虑诸如年龄和盆腔炎史(PID)之类的潜在影响因素。为了研究宫内节育器使用时间,宫内节育器类型以及年龄和PID史对怀孕时间的影响,我们追踪了那些试图在取出宫内节育器后怀孕的妇女。在南斯拉夫的卢布尔雅那有540名妇女在1964年至1972年之间首次装有宫内节育器,并为了怀孕而拔掉宫内节育器,直到1980年。我们发现宫内节育器的使用时间或宫内节育器的类型之间没有关系,但是年龄的增长和PID的病史都降低了每月受孕的可能性。这些发现以及最近的其他工作表明,宫内节育器对于性传播疾病风险低的妇女是一种安全有效的避孕药具。
    :以前的宫内节育器使用研究表明,取出后怀孕的能力受损,而其他研究则没有。然而,这些研究都没有充分考虑诸如年龄和盆腔炎史(PID)之类的潜在影响因素。这项研究使用回归分析来评估各个因素对受孕时间的影响。在1964年至1972年之间,对南斯拉夫卢布尔雅那的540名妇女进行了第一次子宫内节育器的配戴,并在1980年之前将其取出。妇女使用COX回归模型同时评估了宫内节育器使用时间,装置的影响。类型(“ Lippes循环”),移除时的年龄,奇偶校验,以前的PID历史记录以及准时结婚的持续时间,从而控制变量之间的相互关系。该技术估计在不同时间受孕的可能性。结果表明,宫内节育器的使用时间不影响受孕时间。此外,宫内节育器的类型,婚姻的持续时间或同等的年龄并没有影响怀孕的时间。这些发现表明,宫内节育器的使用本身并不会导致随后的生育问题。但是,这些结果强调了将宫内节育器仅限于没有性传播疾病高风险的妇女的重要性。
  • 4 IUD use and the risk of endometrial cancer. 复制标题 收藏 收藏

    【使用宫内节育器和子宫内膜癌的风险。】 复制标题 收藏 收藏
    DOI:10.1016/s0301-2115(02)00153-7 复制DOI
    作者列表:Benshushan A,Paltiel O,Rojansky N,Brzezinski A,Laufer N
    BACKGROUND & AIMS: OBJECTIVE:Although the intrauterine device (IUD) is one of the most widely used forms of contraception throughout the world, its potential long-term effects on the uterus have not been thoroughly evaluated. This paper reports the long-term results of IUD use on the incidence of endometrial cancer. STUDY DESIGN:The data is part of a nationwide case-control, pilot study that was undertaken in order to evaluate the possible influence of ovulation induction drugs on the risk of endometrial cancer. The study included 128 living women 35-64 years old, with a histologically confirmed diagnosis of endometrial carcinoma. The controls were 255 women from the same dialing areas selected by random digit dialing. A multivariate logistic model, controlling for age, was used to assess the independent effects of factors found to be significantly associated with endometrial cancer on univariate analysis. RESULTS:The following parameters were found to be independently associated with endometrial cancer controlling for age: nulliparity OR=2.7 (95% CI 1.1-6.5, P=0.03); history of infertility OR=1.8 (95% CI 1.0-3.3, P=0.05); BMI>/=27 OR=2.3 (95% CI 1.4-3.8, P=0.001). The use of oral contraceptives and IUD were found to be protective; OR=0.29 and 0.37, respectively, (95% CI 0.14-0.61, P=0.001, 0.19-0.70, and 0.003, respectively). CONCLUSIONS:IUD use may have a protective effect on endometrial cancer risk. The protective effect of IUD may be either, through the intense inflammatory response that leads to other lisosomal and inflammatory actions, which may include cells responsible for early elimination of hyperplastic endometrial epithelial cells or, the more complete shedding of the endometrium associated with IUD use may decrease hyperplasia of the endometrium, a known risk factor for endometrial carcinoma.
    背景与目标: 目的:尽管宫内节育器(IUD)是世界范围内使用最广泛的避孕方法之一,但尚未全面评估其对子宫的潜在长期影响。本文报道了宫内节育器使用对子宫内膜癌发生率的长期结果。
    研究设计:数据是一项全国病例对照研究的一部分,该研究旨在评估排卵诱导药物对子宫内膜癌风险的可能影响。该研究包括128名35-64岁的活着的妇女,这些妇女在组织学上被确诊为子宫内膜癌。对照是来自通过随机数字拨号选择的相同拨号区域的255名女性。使用控制年龄的多元逻辑模型评估单因素分析中与子宫内膜癌显着相关的因素的独立影响。
    结果:发现以下参数与控制年龄的子宫内膜癌独立相关:无效性OR = 2.7(95%CI 1.1-6.5,P = 0.03);不孕史OR = 1.8(95%CI 1.0-3.3,P = 0.05); BMI> / = 27 OR = 2.3(95%CI 1.4-3.8,P = 0.001)。口服避孕药和宫内节育器被发现具有保护作用。 OR分别为0.29和0.37(95%CI为0.14-0.61,P = 0.001、0.19-0.70和0.003)。
    结论:IUD的使用可能对子宫内膜癌的风险具有保护作用。宫内节育器的保护作用可能是通过导致其他溶酶体和炎性作用的强烈炎症反应而引起,其中可能包括负责尽早消除增生性子宫内膜上皮细胞的细胞,或者与宫内节育器使用相关的子宫内膜脱落更为彻底。减少子宫内膜增生,子宫内膜癌是子宫内膜癌的已知危险因素。
  • 【[由宫内节育器形成的膀胱结石。罕见的情况]。】 复制标题 收藏 收藏
    DOI: 复制DOI
    作者列表:Hermida Pérez JA,del Corral Suárez T,Cerdeiras Martínez G,Agüero Gómez JL,Machado V
    BACKGROUND & AIMS: OBJECTIVE:To describe an uncommon case of bladder calculus arising from an intrauterine device (IUD).

    METHODS/RESULTS:A female patient with an IUD for the past 10 years consulted for frequent episodes of cystitis. Patient evaluation demonstrated a bladder calculus that warranted surgery. Treatment was by cystolithotomy, which disclosed a 6 cm calculus attached to the IUD.

    CONCLUSION:Bladder calculus arising from an IUD is rare. The case described herein was successfully managed by cystolithotomy.

    背景与目标: 目的:描述子宫内节育器(IUD)引起的膀胱结石的罕见病例。

    方法/结果:一名患有宫内节育器的女性患者在过去的十年中,膀胱炎频繁发作。患者评估显示,需要进行手术的膀胱结石。膀胱切开术治疗了结石,发现结石附着在IUD上有一个6厘米的结石。

    结论:IUD引起的膀胱结石很少见。本文描述的病例已通过膀胱切开术成功治疗。

  • 【产后宫内节育器干预对咨询和选择的影响:来自斯里兰卡的整群随机阶梯楔入试验的证据。】 复制标题 收藏 收藏
    DOI:10.1186/s13063-019-3473-6 复制DOI
    作者列表:Karra M,Pearson E,Pradhan E,de Silva R,Samarasekera A,Canning D,Shah I,Weerasekera D,Senanayake H
    BACKGROUND & AIMS: BACKGROUND:The International Federation of Gynaecology and Obstetrics (FIGO), in collaboration with the Sri Lankan College of Obstetrics and Gynaecologists (SLCOG), launched an initiative in 2014 to institutionalize immediate postpartum IUD (PPIUD) services as a routine part of antenatal counseling and delivery room services in Sri Lanka. In this study, we evaluate the effect of the FIGO-SLCOG PPIUD intervention in six hospitals by means of a cluster-randomized stepped-wedge trial. METHODS/DESIGN:Six hospitals were randomized into two groups of three using matched pairs. Following a 3-month baseline period, the intervention was administered to the first group, while the second group received the intervention after 9 months of baseline data collection. We collected data from 39,084 women who delivered in these hospitals between September 2015 and January 2017. We conduct an intent-to-treat (ITT) analysis to determine the impact of the intervention on PPIUD counseling and choice of PPIUD, as measured by consent to receive a PPIUD, as well as PPIUD uptake (insertion following delivery). We also investigate how factors related to counseling, such as counseling timing and quality, are linked to choice of PPIUD. RESULTS:We find that the intervention increased rates of counseling, from an average counseling rate of 12% in all hospitals prior to the intervention to an average rate of 51% in all hospitals after the rollout of the intervention (0.307; 95% CI 0.148-0.465). In contrast, we find the impact of the intervention on choice of PPIUD to be less robust and mixed, with 4.1% of women choosing PPIUD prior to the intervention compared to 9.8% of women choosing PPIUD after the rollout of the intervention (0.027; 95% CI 0.000-0.054). CONCLUSIONS:This study demonstrates that incorporating PPIUD services into postpartum care is feasible and potentially effective. Taking the evidence on both counseling and choice of PPIUD together, we find that the intervention had a generally positive impact on receipt of PPIUD counseling and, to a lesser degree, on choice of the PPIUD. Nevertheless, it is clear that the intervention's effectiveness can be improved to be able to meet the demand for postpartum family planning of women. TRIAL REGISTRATION:ClinicalTrials.gov, NCT02718222 . Registered on 11 March 2016 (retrospectively registered).
    背景与目标: 背景:国际妇产科联合会(FIGO)与斯里兰卡妇产科学院(SLCOG)合作,于2014年发起一项倡议,以将产后即刻宫内节育器(PPIUD)服务制度化,作为产前咨询和治疗的常规组成部分。斯里兰卡的孕妇送餐服务。在这项研究中,我们通过聚类随机逐步楔入试验评估了FIGO-SLCOG PPIUD干预在六家医院中的效果。
    方法/设计:使用配对对将六家医院随机分为两组,每组三个。在三个月的基线期之后,对第一组进行干预,而第二组在收集基线数据9个月后接受干预。我们收集了2015年9月至2017年1月之间在这些医院分娩的39,084名妇女的数据。我们进行了意向性治疗(ITT)分析,以确定干预对PPIUD咨询和选择PPIUD的影响,通过同意接收PPIUD以及PPIUD摄取量(分娩后插入)。我们还将调查与咨询相关的因素,例如咨询时间和质量,如何与PPIUD的选择相关联。
    结果:我们发现,干预可以提高咨询率,从干预前所有医院的平均咨询率达到12%,到实施干预后所有医院的平均咨询率达到51%(0.307; 95%CI 0.148 -0.465)。相比之下,我们发现干预措施对PPIUD选择的影响较小,且混合性较差,干预前选择PPIUD的女性为4.1%,而干预措施实施后选择PPIUD的女性为9.8%(0.027; 95)。 %CI 0.000-0.054)。
    结论:这项研究表明,将PPIUD服务纳入产后护理是可行且潜在有效的。结合咨询和选择PPIUD的证据,我们发现该干预措施对接收PPIUD咨询具有普遍的积极影响,并且在较小程度上对PPIUD的选择产生了积极影响。然而,很明显,可以提高干预措施的有效性,从而能够满足妇女产后计划生育的需求。
    试验注册:ClinicalTrials.gov,NCT02718222。 2016年3月11日注册(追溯注册)。
  • 【铜T IUD引起的部分子宫穿孔(2型):超声检查的诊断和处理。】 复制标题 收藏 收藏
    DOI:10.7863/jum.1985.4.7.381 复制DOI
    作者列表:Abramovici H,Sorokin Y,Bornstein J,Auslander R
    BACKGROUND & AIMS: :The case reported in this paper demonstrates the difficulties in establishing the diagnosis of type 2 uterine perforation incident to the use of an IUD. A type 2 perforation is considered to have occurred when the IUD is entirely within the myometrium, no part of the IUD can be detected in the uterine cavity, and no part can be visually detected in the peritoneal cavity. The patient, a 28-year old gravida 3, para 2, had an IUD inserted 18 months prior to admittance, 7 weeks after her 2nd delivery. 1 year later she became pregnant. During a therapeutic abortion, the IUD string was removed without the device, which was considered to be outside and behind the uterus. Ultrasonography revealed that the IUD was inside the posterior uterine wall, parallel to the endometrial mucosal lining, with no connection to the uterine cavity. Other diagnostic methods used in this case included plain abdominal films, hysterography, and hysteroscopy; however, neither these methods nor uterine palpation suggested that there was an IUD in the uterus. The original diagnosis was later confirmed by intraoperative radiography, and the IUD was removed through a small incision on the posterior uterine wall. This case demonstrates the useful role of ultrasonography in the work-up of a woman with a missing IUD. It is suggested that ultrasonography be used following difficult IUD insertions or postpartum insertions, since most perforations occur in such cases. Partial and complete uterine perforation is considered more likely when the IUD is inserted during the 1st 3 months postpartum.
    背景与目标: :本文报道的病例证明了在确定因使用宫内节育器而引起的2型子宫穿孔的诊断方面存在困难。当宫内节育器完全位于子宫肌层内,子宫腔内无法检测到宫内节育器且在腹膜腔内无法视觉检测到IUD时,则认为发生了2型穿孔。该患者是一名28岁孕妇gravida 3,第2段,在入院前18个月(第二次分娩后7周)插入了宫内节育器。一年后,她怀孕了。在治疗性流产过程中,未放置器械的情况下取出了宫内节育器串,该装置被认为位于子宫的外面和后面。超声检查显示宫内节育器位于子宫后壁内,与子宫内膜粘膜内层平行,与子宫腔无任何连接。在这种情况下使用的其他诊断方法包括腹部平片,宫腔造影和宫腔镜检查;然而,这些方法和子宫触诊均未提示子宫内有宫内节育器。最初的诊断随后通过术中X线检查得以证实,并通过子宫后壁的小切口移除了宫内节育器。该病例证明了超声检查在宫内节育器缺失的妇女的检查中的有用作用。建议在困难的宫内节育器插入或产后插入后使用超声检查,因为大多数穿孔发生在这种情况下。在产后前三个月内插入宫内节育器时,子宫部分穿孔和完全子宫穿孔的可能性更高。
  • 【释放左炔诺孕酮的宫内节育器的母乳喂养妇女的牛奶和血浆中的左炔诺孕酮。】 复制标题 收藏 收藏
    DOI:10.1016/0010-7824(82)90017-8 复制DOI
    作者列表:Heikkilä M,Haukkamaa M,Luukkainen T
    BACKGROUND & AIMS: A levonorgestrel-releasing intrauterine contraceptive device was used by 10 breast-feeding women beginning 6 weeks after delivery. Two models of IUD were used. One released 10 microgram (5 patients), the other 30 microgram (5 patients) of levonorgestrel per day. Plasma and milk samples were collected 8 times over a 3-month period and the concentrations of levonorgestrel determined by radioimmunoassay. An improved and sensitive method for the determination of levonorgestrel in milk was developed. A column chromatographic purification of a milk extract before radioimmunoassay made possible the use of large milk samples in order to improve the sensitivity. The plasma concentrations during the follow-up period were 207 +/- 64 pg/ml (mean + SD) in the 10 microgram and 235 +/- 87 pg/ml in the 30 microgram/day releasing IUD groups. The milk levonorgestrel concentrations were 56 +/- 35 and 57 +/- 34 pg/ml, respectively. The plasma to milk ratio of levonorgestrel was initially 10025. There were no significant differences in the milk and plasma concentrations between the study groups. The total amount of levonorgestrel excreted per day in 600 ml breast milk is approximately 0.1 per cent of a daily dose of 30 microgram.

    背景与目标: 分娩后6周开始,有10名母乳喂养妇女使用了释放左炔诺孕酮的宫内节育器。使用了两种宫内节育器模型。一位每天释放10微克(5位患者),另一位每天释放30微克(5位患者)左炔诺孕酮。在3个月的时间内收集了8次血浆和牛奶样品,并通过放射免疫法测定了左炔诺孕酮的浓度。建立了一种测定牛奶中左炔诺孕酮的改进,灵敏的方法。放射免疫分析之前,对牛奶提取物进行柱色谱纯化,可以使用大牛奶样品,以提高灵敏度。在随访期间,释放IUD组的血浆浓度在10微克中为207 /-64 pg / ml(平均SD),在30微克/天中为235 /-87 pg / ml。牛奶左炔诺孕酮浓度分别为56 /-35和57 /-34 pg / ml。左炔诺孕酮的血浆/牛奶比率最初为10025。研究组之间的牛奶和血浆浓度没有显着差异。每天从600毫升母乳中排出的左炔诺孕酮总量约为每日30微克剂量的0.1%。

  • 【使用铜制宫内节育器前后妇女的血清催乳素水平。】 复制标题 收藏 收藏
    DOI: 复制DOI
    作者列表:Raikar RS,Mehta S,Joshi J,Virkar KD,Sheth AR
    BACKGROUND & AIMS: -2
    背景与目标: -2
  • 【剖宫产分娩的妇女在宫内节育器插入前使用米索前列醇的益处:一项随机对照试验。】 复制标题 收藏 收藏
    DOI:10.1080/13625187.2018.1428297 复制DOI
    作者列表:Maged AM,Youssef G,Eldaly A,Omran E,El Naggar M,Abdel Hak A,Kotb A,Ogila AI
    BACKGROUND & AIMS: OBJECTIVE:The aim of the study was to evaluate the value of vaginal misoprostol 6 h prior to intrauterine device (IUD) insertion in women with previous Caesarean delivery. METHODS:A double-blind randomised controlled trial was conducted in 120 women who were eligible for IUD insertion. Participants were randomly divided to receive either 600 μg vaginal misoprostol or placebo 6 h before IUD insertion. The primary outcome measure was the pain score during the procedure. Secondary outcome measures were failure of insertion, insertion difficulty score, complications of IUD insertion and side effects related to misoprostol. RESULTS:Pain and insertion difficulty scores were significantly lower in the misoprostol group compared with the placebo group (5.7 ± 1.4 vs. 6.5 ± 0.9 and 4.1 ± 1.1 vs. 5.4 ± 2.2, respectively; p < .001). More women experienced nausea, vomiting (5 vs. 0; p = .06) and cramps (10 vs. 0; p < .001) in the misoprostol group than in the placebo group, respectively. CONCLUSIONS:The use of misoprostol before IUD insertion is associated with less painful and easier placement.
    背景与目标: 目的:本研究的目的是评估子宫剖宫产妇女在宫内节育器(IUD)插入前6小时阴道米索前列醇的价值。
    方法:对120名符合IUD置入条件的妇女进行了双盲随机对照试验。参加者随机分为两组,分别在放置宫内节育器前6小时接种600μg阴道米索前列醇或安慰剂。主要结果指标是手术过程中的疼痛评分。次要结果指标是插入失败,插入难度评分,宫内节育器插入并发症以及米索前列醇相关的副作用。
    结果:与安慰剂组相比,米索前列醇组的疼痛和插入困难评分显着降低(分别为5.7 vs±1.4 vs. 6.5±0.9和4.1±1.1 vs. 5.4±2.2; p <0.001)。米索前列醇组比安慰剂组分别有更多的女性出现恶心,呕吐(5比0; p = 0.06)和抽筋(10比0; p <0.001)和抽筋。
    结论:在宫内节育器插入前使用米索前列醇可减轻疼痛并易于放置。
  • 【铜宫内节育器和脂环对人宫颈粘液中精子迁移的影响。】 复制标题 收藏 收藏
    DOI:10.1016/0010-7824(75)90108-0 复制DOI
    作者列表:Hefnawi F,Kandil O,Askalani H,Serour G
    BACKGROUND & AIMS: :30 women (24-34 years; parity 3-6) randomly selected from the family planning clinic at Al-Azhar University Hospital, Cairo, were divided into 3 groups: 1) 10 normal fertile; 2) 10 women fitted with T-Cu-200 for 2-20 months; and 3) 10 women fitted with Lippes loop for 2-8 years. On the 13th-15th day of the cycle cervical mucus was sample and tested for sperm penetration, motility, turbidity, Spinnbarkeit, and ferning. Sperm penetration tests used the sperm migration meter of Kremer and turbidity and clarity were assessed by the naked eye. Sperm penetration and motility were greatly impaired with Cu-device users, while with Lippes loop the findings approached that of the normal control women. Turbidity results were significant (p less than .01) for Cu-device users. Diminished Spinnbarkeit and positive ferning were also observed in the presence of the Cu device. The impaired sperm penetration and immobilization with the use of the Cu-devices as opposed to Lippes loop suggests a local lethal effect of the increased copper on cervical mucus rather than a local foreign body reaction.
    背景与目标: 从开罗Al-Azhar大学医院的计划生育诊所随机抽取30名妇女(24-34岁; 3-6岁),分为3组:1)10名正常可育; 2)正常生育。 2)10名装有T-Cu-200的妇女使用2-20个月; 3)10位装有Lippes环的女性,佩戴时间为2-8年。在周期的第13-15天对宫颈粘液进行取样并测试精子的渗透,运动性,浊度,Spinnbarkeit和精子。精子渗透测试使用Kremer精子迁移仪,用肉眼评估浊度和透明度。使用铜器的使用者会极大地损害精子的渗透和运动能力,而使用Lippes loop时,其结果接近于正常对照女性。铜装置用户的浊度结果显着(p小于0.01)。在铜装置的存在下,也观察到了纺锤形变小和正转角。与Lippes环相反,使用Cu装置导致精子穿透和固定受损,这表明增加的铜对子宫颈粘液的局部致死作用,而不是局部的异物反应。
  • 【低度子宫间质肉瘤和鳞状细胞癌伴宫内节育器:附2例报告。】 复制标题 收藏 收藏
    DOI: 复制DOI
    作者列表:Valente PT,Ahmad MM
    BACKGROUND & AIMS: BACKGROUND:Although intrauterine device (IUD) usage has not been linked to uterine cancer and has even been considered protective against neoplasia, sporadic cases of IUD-associated uterine malignancies have been reported. CASES:One cystic low grade stromal sarcoma of the uterus occurred in a 7-year IUD user, and 1 invasive endometrial squamous cell carcinoma following 25 years of IUD retention occurred in another. The latter case was notable for extensive in situ squamous cell carcinoma involving the entire uterine cavity and extending to the ectocervix and into both fallopian tubes. In situ hybridization for high-risk HPV DNA was negative. These findings raise the possibility of a non-HPV-related pathway for the squamous cell carcinoma case due possibly to prolonged chronic irritation and pyometra. CONCLUSION:The association of low grade stromal sarcoma with the IUD in the first case is extremely rare and most likely coincidental. The squamous carcinoma case, however, may have arisen via a non-HPV-related pathway, possibly related to IUD-induced chronic irritation and pyometra.
    背景与目标: 背景:尽管子宫内节育器(IUD)的使用并未与子宫癌相关,甚至被认为可以预防肿瘤,但已有零星的宫内节育器相关子宫恶性病例报道。
    病例:7年的宫内节育器使用者发生了1例子宫囊性低度间质性肉瘤,而宫内节育器保留25年后发生了1例浸润性子宫内膜鳞状细胞癌。后一种情况是广泛的原位鳞状细胞癌,累及整个子宫腔,并延伸至子宫颈并进入两个输卵管。高危HPV DNA的原位杂交为阴性。这些发现增加了鳞状细胞癌病例与人乳头瘤病毒无关的途径的可能性,这可能是由于长期的慢性刺激和脓毒症所致。
    结论:在首例情况下,低度间质肉瘤与宫内节育器的关联非常罕见,并且很可能是偶然的。但是,鳞状细胞癌病例可能是通过非HPV相关途径引起的,可能与IUD引起的慢性刺激和脓毒症有关。
  • 【ACOG指南的使用:计划生育提供者对宫内节育器和植入物使用的禁忌症。】 复制标题 收藏 收藏
    DOI:10.1007/s10995-017-2320-1 复制DOI
    作者列表:Philliber AE,Hirsch H,Brindis CD,Turner R,Philliber S
    BACKGROUND & AIMS: :Objectives The uptake and actual use of the current guidelines from the American College of Obstetrics and Gynecology (ACOG) is unknown. Methods Family planning providers across Colorado and Iowa were surveyed as part of statewide initiatives to reduce unintended pregnancy in 2010 and 2012, both before and after the release of the guidelines. These initiatives focused on the promotion of intrauterine devices (IUDs) and implants. These surveys included questions on providers' views regarding the suitability and safety of the copper T IUD, hormonal IUD, and single rod implant for various subgroups of clients. The results are contrasted with guidelines provided in July of 2011 by ACOG. This strategy provides both baseline and follow-up models about the methods promoted in these guidelines. Results Findings show that there is some improvement in beliefs that IUDs are suitable and safe for women who are post-partum, post-abortion, have had an ectopic pregnancy, are nulliparous, teenagers, or have a history of STIs. However, these clinicians' views are not entirely in alignment with ACOG recommendations in their beliefs that these methods should not be used immediately post-partum or post-abortion. Notable percentages of these clinicians were hesitant to recommend these effective methods for other groups of patients, approved for use by ACOG. Conclusions While the cost of these methods is a barrier to adoption, these data suggest that there are continuing provider barriers to their use as well. The paper concludes with suggestions for further training for family planning providers.
    背景与目标: :目的尚不清楚美国妇产科学院(ACOG)对当前指南的采用和实际使用。方法科罗拉多州和爱荷华州的计划生育提供者在该指南发布之前和之后,都作为一项全州性计划的一部分进行了调查,以减少2010年和2012年的意外怀孕。这些举措集中于促进宫内节育器(IUD)和植入物。这些调查包括服务提供商关于铜T IUD,激素IUD和单杆植入物针对不同亚组客户的适用性和安全性的观点。该结果与ACOG在2011年7月提供的指南进行了对比。该策略提供了有关本指南中提倡的方法的基准模型和后续模型。结果发现表明,对宫内节育器适用于产后,流产,异位妊娠,未生育,青少年或有性传播感染史的妇女的看法已有一定改善。但是,这些临床医生的观点并不完全符合ACOG的建议,因为他们认为这些方法不应在产后或流产后立即使用。这些临床医生中有显着百分比的人不愿向ACOG批准使用的其他患者推荐这些有效方法。结论虽然这些方法的成本是采用的障碍,但这些数据表明,提供商在使用它们方面也存在持续的障碍。本文最后提出了对计划生育提供者进行进一步培训的建议。
  • 【在300名IUD佩戴者的宫颈阴道涂片中发现了放线菌样生物的流行。】 复制标题 收藏 收藏
    DOI: 复制DOI
    作者列表:Jones MC,Buschmann BO,Dowling EA,Pollock HM
    BACKGROUND & AIMS: :The association of Actinomyces with IUD wearers has been widely documented and the possibility of the recognition of actinomycetes-like organisms in routine Papanicolaou-stained cervicovaginal smears has been reported. We conducted a retrospective study of IUD wearers to determine the prevalence and significance of actinomycetes-like organisms found in such smears. Three hundred smears from current IUD wearers were rescreened for actinomycetes-like organisms. Of this group, 200 patients were from a public health family planning clinic, and 100 were private patients. The incidence for the public health group was 25.5% and for the private patient group, 8%. A case history of actinomycosis is included. Findings such as other infectious agents, abnormal cytology and symptoms are also discussed. Although the presence of Actinomyces probably represents an opportunistic infection, the threat of pelvic actinomycosis with serious complications poses a management problem to the clinician when Actinomyces is reported in a routine Papanicolaou smear. Our findings lead us to question the practicality of the earlier recommendations of IUD removal and antibiotic therapy. :300 Papanicolaou smears from current IUD wearers were rescreened to determine the prevalence of actinomycetes. Of the 300 patients, 59 showed actinomycetes-like organisms in cervicovaginal smears. Of the 59 positive cases, 51 (of 200, 25%) were from public health clinics and 8 (of 100, 8%) were from private patients. Of 21 patients complaining of irregular bleeding, only 4 had positive actinomycete cultures. In cases positive for the organisms there was no correlation of prevalence found with the phase of the menstrual cycle or with menstruation itself. A case history of actinomycosis is included. Although the presence of Actinomyces probably represents an opportunitistic pathogenic infection, management of this infection is important to eradicate the threat of pelvic actinomycosis. In the case history described, however, antibiotic therapy failed, and a complete abdominal hysterectomy was performed.
    背景与目标: :放线菌与IUD配戴者的关联已被广泛记录,并且已报道了在常规巴氏染色的宫颈阴道涂片中识别放线菌样生物的可能性。我们进行了一项对IUD佩戴者的回顾性研究,以确定在这些涂片中发现的放线菌样生物的患病率和意义。从目前的宫内节育器佩戴者进行了300次涂片检查,重新筛选了放线菌样生物。在这一组中,有200名患者来自公共卫生计划生育诊所,还有100名私人患者。公共卫生组的发生率为25.5%,私人患者组的发生率为8%。包括放线菌病的病史。还讨论了其他发现因素,细胞学异常和症状等发现。尽管放线菌的存在可能代表了机会性感染,但是当在常规的Papanicolaou涂片中报告有放线菌时,带有严重并发症的盆腔放线菌病的威胁给临床医生带来了管理上的问题。我们的发现使我们对子宫内节育器切除和抗生素治疗的早期建议的实用性提出质疑。
    从目前的宫内节育器佩戴者中进行了300次Papanicolaou涂片检查,以确定放线菌的患病率。在300例患者中,有59例在宫颈阴道涂片中显示了放线菌样生物。在59例阳性病例中,有51例(占200%,占25%)来自公共卫生诊所,而8例(占100%,占8%)来自私人患者。在21位抱怨不规则出血的患者中,只有4位放线菌培养阳性。在对生物体呈阳性的病例中,发现患病率与月经周期阶段或月经本身没有相关性。包括放线菌病的病史。尽管放线菌的存在可能代表机会病原性感染,但这种感染的管理对于根除盆腔放线菌病的威胁很重要。然而,在所描述的病例史中,抗生素治疗失败,并进行了完整的腹部子宫切除术。
  • 【NOVA T 380铜制宫内节育器的五年临床经验。】 复制标题 收藏 收藏
    DOI:10.1016/s0010-7824(02)00385-2 复制DOI
    作者列表:Batár I,Kuukankorpi A,Siljander M,Elomaa K,Rauramo I
    BACKGROUND & AIMS: :In an open, single-group, phase III clinical trial of 5 years, the clinical performance of NOVA T 380 was investigated in three centers. The device having a higher copper surface of 380 mm(2) is a modification of NOVA T. A total of 400 voluntary women were enrolled in the study. The mean age was 31.4 years (SD 5.5) with the minimum of 18 and the maximum of 44 years. At the end of the study, 211 women had passed the 60-month visit. Cumulative discontinuation rates at the end of the first and the fifth year calculated by Kaplan-Meier estimates, were respectively as follows: pregnancy 0.5 and 1.9, expulsion 1.3 and 4.1, bleeding 4.4 and 14.0, pain 1.3 and 4.2, removal for other medical reason 1.4 and 6.4, planning pregnancy 0.8 and 13.5, and removal for other personal reason 2.4 and 11.9 per 100 users. Neither ectopic pregnancies nor episodes of pelvic inflammatory diseases (PIDs) occurred. One perforation was recorded; the calculated rate is 0.3 per 100 women (first year). The continuation rate was 88.3 and 52.5 at 1 and 5 years, respectively. In conclusion, the 5-year performance of NOVA T 380 was good compared to other "high-loaded" copper devices. Safety was acceptable over the entire study period.
    背景与目标: :在一项为期5年的开放性,单组,III期临床试验中,在三个中心对NOVA T 380的临床性能进行了研究。该设备具有380 mm(2)的较高铜表面,是NOVA T的改进形式。共有400名志愿妇女参加了这项研究。平均年龄为31.4岁(SD 5.5),最小18岁,最大44岁。研究结束时,有211名妇女通过了60个月的访问。由Kaplan-Meier估算得出的第一年和第五年末的累积停药率分别为:妊娠0.5和1.9,驱逐1.3和4.1,出血4.4和14.0,疼痛1.3和4.2,由于其他医疗原因而去除1.4和6.4,计划怀孕0.8和13.5,并出于其他个人原因删除每100个用户2.4和11.9。既未发生异位妊娠,也未发生盆腔炎。记录了一个穿孔;计算的比率是每100名妇女(第一年)0.3。 1年和5年的持续率分别为88.3和52.5。总之,与其他“高负载”铜制设备相比,NOVA T 380的5年性能很好。在整个研究期间,安全性是可以接受的。

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