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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Il nuovo cimento della Società Italiana di Fisica 13 (1991), S. 1315-1319 
    ISSN: 0392-6737
    Keywords: Superconducting materials
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Summary We report here about measurements of resistancevs. temperature, alternating current (a.c.) susceptibility and X-ray diffraction performed on Ba2Sr2Ca2Cu3O x superconductor doped with various amounts of Pb. The results could be explained in terms of Pb contribution in increasing both the amount of the highestT C 0 phase and connectivity between superconductive regions. The Pb substitution on Bi sites is also discussed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Advances in contraception 11 (1995), S. 3-3 
    ISSN: 1573-7195
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Advances in contraception 11 (1995), S. 187-206 
    ISSN: 1573-7195
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Resumé La présente analyse concerne principalement la sécurité, l'utilité, les avantages et les inconvénients des interventions de stérilisation tubaire pratiquées durant la période puerpérale lorsque la femme est encore hospitalisée. Elle fait la synthèse des constatations de quatre études précédentes et évalue les résultats publiés plus récemment dans la littérature. Cette analyse conclut que la stérilisation tubaire pratiquée alors que la femme est encore sur la table d'accouchement, ou au début de la période puerpérale lorsqu'elle est encore hospitalisée, est une intervention plus aisée et plus sûre du point de vue médical, et qu'elle ne compromet pas la lactation. On a cependant été signalé des taux de grossesse en général plus élevés si la stérilisation est pratiquée au cours de la période puerpérale plutôt qu'après un intervalle, notamment lorsqu'on a recours à la technique de l'occlusion mécanique des trompes. La méthode de Pomeroy, éventuellement modifiée par à une minilaparotomy, est vivement recommandée. D'autre part, l'électrocoagulation par voie laparoscopique est associée à une grande utilité mais, potentiellement, à des risques accrus de complications et de difficultés d'inversion tubaire. La stérilisation tubaire peut être pratiquée facilement et sans danger dans des cas sélectionnés de césarienne. La stérilisation tubaire pratiquée durant la période puerpérale présente un certain nombre d'avantages comparée aux méthodes contraceptives post-partum agissant à court terme qui doivent être strictement observées. Toutefois, les candidates à la stérilisation tubaire doivent être attentivement triées et conseillées, car elles sont davantage susceptibles d'avoir des regrets après la stérilisation. Sont examinés aussi des questions non encore résolues de la stérilisation tubaire en période puerpérale et un certain nombre de problèmes d'ordre pratique à étudier avant de mettre en train un programme de stérilisation en période puerpérale dans une maternité.
    Abstract: Resumen Este examen se centra en la seguridad, eficacia, ventajas y desventajas de los procedimientos de esterilización tubárica realizados durante el período puerperal mientras la mujer continúa hospitalizada. Se resumen los resultados de cuatro trabajos anteriores y se evalúan los resultados difundidos en publicaciones más recientes. El examen llega a la conclusión de que la esterilización tubárica realizada cuando la mujer está todavía en la sala de partos o durante la primera etapa del puerperio, mientras continúa hospitalizada, es sencilla desde el punto de vista quirúrgico y segura desde el punto de vista médico, y no afecta adversamente la lactancia. Sin embargo, las tasas de embarazo notificadas son en general más altas en la esterilización tubárica puerperal que en la esterilización de intervalo, especialmente cuando se utiliza la técnica de oclusión tubárica mecánica. El método de Pomeroy, y sus modificaciones a través de la minilaparotomía, es muy recomendable. Por otra parte, la electrocoagulación mediante laparoscopía está asociada con una eficacia alta pero con un riesgo potencialmente mayor de complicaciones y dificultades en la inversión tubárica. Las esterilizaciones tubáricas pueden realizarse con facilidad y en condiciones de seguridad en las operaciones cesáreas en determinados casos. La esterilización tubárica realizada durante el puerperio tiene varias ventajas con respecto a los métodos anticonceptivos de acción breve, que requieren un cumplimiento estricto, para uso en el posparto. Sin embargo, las candidatas a la esterilización tubárica puerperal deben ser cuidadosamente examinadas y aconsejadas ya que es más probable que lamenten sur decisión después de la esterilización. Se discuten cuestiones no resueltas de la esterilización tubárica puerperal y varios problemas prácticos a los que se debe hacer frente antes de iniciar un programa de esterilización tubárica puerperal en un hospital/clínica de maternidad.
    Notes: Abstract This review focuses on the safety, efficacy, pros and cons of tubal sterilization procedures performed during the puerperium period while the woman is still in hospital. Findings from four previous reviews are synthesized, and the results published in more recent literature are evaluated. The review finds that tubal sterilization performed while the woman is still on the delivery table, or during a woman's early puerperium while she remains hospitalized, is operationally easy and medically safe, and does not adversely affect lactation. However, reported pregnancy rates are generally higher in puerperal tubal sterilization than in interval sterilization, especially when the mechanical tubal occlusion technique is used. The Pomeroy method, and its modifications via minilaparotomy, is highly recommendable. On the other hand, electrocoagulation via laparoscopy is associated with high efficacy, but a potentially increased risk of complications and difficulties in tubal reversal. Tubal sterilizations can be easily and safely performed at cesarean delivery in selected cases. Tubal sterilization performed during puerperium has a number of advantages over short-acting contraceptive methods, which require strict compliance, for postpartum use. However, candidates for puerperal tubal sterilization need to be carefully screened and counseled, since post-sterilization regret is more likely to occur. Unsettled issues for puerperal tubal sterilization and a number of practical problems that need to be addressed before initiation of a puerperal tubal sterilization program in a maternity clinic/hospital are discussed.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Advances in contraception 14 (1998), S. 185-192 
    ISSN: 1573-7195
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract This study was aimed to evaluate weight variation in 3183 women using the injectable contraceptive Cyclofem. All women were allocated to groups according to their weight at admission. The weight gain was inversely proportional to the weight at admission. The groups of women weighing less than 50 kg at admission, experienced a higher increase, 2.8% in four months, and they continued gaining weight, reaching 7.7% in 13 months. Women weighing more than 64 kg at admission did not present any weight change in 4 months and increased only 1.7% at 13 months. When women were classified as discontinuers due to weight increase, discontinuers due to other reasons, and continuers, at four months, the differences in the mean weight between the groups was statistically significant only in the groups weighing 55 kg or more at admission. At 13 months, the results were similar and the differences were statistically significant only in the groups weighing 55-59 kg and 60-64 kg. Discontinuation rates due to weight increase were proportional to the weight at admission. This rate was almost three times higher in the group of women weighing more than 64 kg at admission than in the group weighing less than 55 kg (p 〈 0.001). In conclusion, considering the data presented in this study, it is impossible to recommend health providers to inform women who choose Cyclofem as their contraceptive method, that this method may increase their weight throughout its use.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Advances in contraception 15 (1999), S. 275-281 
    ISSN: 1573-7195
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A modification of the TCu380A IUD to create the model TCu380S was introduced many years ago. The TCu380S utilizes copper sleeves that are flush in the plastic and are set at both ends of the horizontal arm. The objective of this study is to compare the clinical performance of the TCu380A and the TCu380S IUDs, especially regarding contraceptive performance and expulsion, in a cohort of women who had one of these two devices inserted at random. This paper presents the results up to 5 years of use. A total of 1568 women were enrolled: 806 women received a TCu380A and 762 women received a TCu380S IUD. The performance was evaluated by life-table analysis and significance between rates was tested by the method of log-rank. The cumulative pregnancy rate was low in users of both models of IUD but lower in users of the TCu380S model through the 5 years of use, without statistical significance. Expulsion was significantly higher in users of the TCu380S model during the five years of use. The other reasons for discontinuation were similar for both devices and did not show statistical significance. The continuation rate was significantly lower in users of the TCu380S model in the first and second years of use. Both devices presented a very low pregnancy rate and TCu380S presented a lower pregnancy rate than the TCu380A, although without statistical significance.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Advances in contraception 10 (1994), S. 257-264 
    ISSN: 1573-7195
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Resumé Pour évaluer dans quelle mesure les utilisatrices et non utilisatrices de contraceptifs oraux sont sensibilisées aux facteurs associés à des complications, cette étude a comparé la fréquence des facteurs et des maladies qui contribuent au risque que présente l'utilisation de ces contraceptifs. Dans l'Etat de Sao Paulo (Brésil), des données ont été recueillies auprès de 5317 utilisatrices et 8863 non utilisatrices, au moyen de questionnaires demandant des renseignements concernant les variables suivantes: utilisation de contraceptifs oraux, âge, poids, tabagisme, présence ou antécédents d'hypertension, diabète, cardiopathies, varices douloureuses et épilepsie. La moitié des utilisatrices présentaient certains facteurs de risque et 17,4% des facteurs de risque élevé de complications résultant de l'utilisation de contraceptifs oraux. Les facteurs de risque et les maladies dont la population semblait mal connaître l'effet d'augmentation des risques qu'entrîne l'ingestion de contraceptifs oraux étaient le tabagisme, l'hypertension et les varices douloureuses. Un faible pourcentage seulement de la population paraissait savoir que ces maladies et facteurs pouvaient accroître les risques de problèmes de santé durant l'utilisation des contraceptifs oraux. Les résultats suggèrent que les utilisatrices et les pourvoyeurs des services de contraception ne sont pas suffisamment informés des facteurs associés à un risque accru de problèmes de santé durant l'utilisation des contraceptifs oraux.
    Abstract: Resumen Este estudio comparó la frecuencia de factores y enfermedades que contribuyen al riesgo de los anticonceptivos orales (AO) entre usuarias y no usuarias corrientes de anticonceptivos orales a fin de evaluar el grado de conocimiento entre las usuarias de los factores asociados con complicaciones durante el uso de AO. Se recopilaron datos de 5317 usuarias y 8863 no usuarias corrientes del Estado de S@o Paulo, Brasil, utilizando cuestionarios en los que se solicitabe información acerca de las siguientes variables: uso de AO, edad, peso, fumadora/no fumadora y la presencia o historia de hipertensión, diabetes, cardiopatías, várices dolorosas y epilepsia. La mitad de las usuarias tenían algunos factores de riesgo y el 17,4% de ellas corrían un alto riesgo de complicaciones por el uso de anticonceptivos orales. Los factores de riesgo y enfermedades que parecían ser poco conocidos por la población como tendientes a aumentar el riesgo del uso de anticonceptivos orales eran el fumar, la hipertensión y las várices dolorosas. Sólo un pequeño porcentaje de la población parecía saber que estas enfermedades y factores podían aumentar el riesgo de problemas de salud durante el uso de anticonceptivos orales. Los resultados sugieren una falta de información de las usuarias y proveedores con respecto a factores que están asociados con un riesgo mayor de problemas de salud durante el uso de anticonceptivos orales.
    Notes: Abstract This study compared the frequency of factors and diseases that contribute to the risks of oral contraceptive use among current users and non-users of oral contraception in order to evaluate the users' awareness of factors associated with complications during oral contraceptive use. Data from 5317 current users and 8863 non-users in the state of São Paulo, Brazil, were collected using questionnaires requesting information on the following variables: use of oral contraceptives, age, weight, smoking status, and the presence or history of hypertension, diabetes, cardiopathies, painful varicose veins, and epilepsy. Half of the users had some risk factors, and 17.4% were at high risk of complications from oral contraceptive use. Risk factors and diseases which appeared to be poorly known by the population as increasing the risk of oral contraceptive use were smoking, hypertension and painful varicose veins. Only a small percentage of the population appeared to know that these diseases and factors could increase the risk of health problems during oral contraceptive use. The results suggest a lack of information among users and providers on factors which are associated with an increased risk of health problems during use of oral contraceptives.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1573-7195
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1573-7195
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1573-7195
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract This study evaluated endometrial histology in women using the once-a-month injectable contraceptive Cyclofem for one year or more. The study received IRB approval. Seventeen Cyclofem users accepted to be submitted to an endometrial biopsy. All the samples were collected with an endometrial suction curette (Z-Sampler, ZSI Gynecological Product, Chasworth, CA, USA) in an outpatient clinic, 27–33 days after the last injection. The material was fixed immediately in Bouin solution prior to wax embedding and screened as a routine histological examination by a senior pathologist. The pathologist did not know the bleeding status of each woman or the number of injections each woman had received before the biopsy. All women recorded bleeding and spotting for the last 60 days prior to the biopsy. The mean age of volunteers was 25.9 years (range 21–32) and the mean number of injections received was 24.8 (range 14–47). The results were: 4 out of 17 biopsies were found to be inadequate for diagnosis because they consisted of only blood and mucus. Two of these women were bleeding regularly and the other 2 had amenorrhea. Eight endometrial samples presented a proliferative pattern and, in this group, 3 women had amenorrhea and 5 were bleeding regularly. The other 5 biopsies were reported as secretory endometrium, and 4 of them showed pseudodecidual reaction compatible with the administration of progestin. All of these women were bleeding regularly. The results of the biopsies were not related to the number of injections received nor to the age of the women. In conclusion, long-term administration of the injectable contraceptive Cyclofem did not produce adverse alterations in the endometrium as hyperplasia.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1573-7195
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Resumé Cette étude avait pour objectif d'évaluer les résultats cliniques de la première année d'utilisation du DIU TCu200B dans une cohorte de femmes chez lesquelles le dispositif avait été réinséré immédiatement après le retrait à l'expiration de la durée de vie du précédent, en les comparant aux résultats dans un groupe de femmes l'utilisant pour la première fois et dans une cohorte de femmes ayant continué à utiliser ce DIU pendant plus de 60 mois. L'échantillon comprenait 1.066 utilisatrices, 339 dans chacun des deux premiers groupes, et 388 dans le troisième. Les analyses par les tables de survie ont servi à calculer les taux de poursuite et les taux bruts d'abandon en fonction des motifs. La signification des différences entre les groupes a été testée par les méthodes statistiques de rang. Les taux de grossesse ont été faibles, dans le groupe des réinsertions comme dans celui des premières insertions, et aucune grossesse n'est survenue dans le groupe ayant porté le dispositif au-delà de la cinquième année. On a constaté des taux d'expulsion et d'abandon du suivi significativement moins élevés chez les femmes ayant porté ce dispositif au-delà de la cinquième année. En outre, ce groupe a révélé un taux significativement plus fort de retraits à des fins d'investigation. Ces résultats montrent qu'il n'y a aucune raison de recommander le retrait ou le remplacement du DIU TCu200B avant la fin de la sixième année d'utilisation. Lorsqu'un nouveau dispositif doit être inséré à l'expiration de la durée de vie du précédent, il faut prescrire aux opérateurs de le faire immédiatement après le retrait, car cette pratique n'entraîne aucun risque supplémentaire, réduit le nombre des visites à la clinique et évite à la femme d'avoir recours à une méthode provisoire en attendant l'insertion d'un nouveau dispositif.
    Abstract: Resumen El objetivo del estudio fue evaluar el rendimiento clínico, durante et primer año, del DIU TCu200B en un grupo de mujeres en las que se había reinsertado el DIU inmediatamente después del retiro por expiración de la duración en comparación con un grupo de aceptadoras iniciales, y un grupo de mujeres que continuaron utilizando el dispositivo durante más de 60 meses. La muestra consistió en 1.066 usuarias, 339 en cada uno de los dos grupos y 388 en el tercero. Se utilizó el análisis de tablas de vida para calcular la tasa de continuación y la tasa bruta de abandono por razones. La significación estadística de las diferencias entre los grupos se sometió a prueba con el métodolog-rank. Las tasas de embarazo fueron bajas, tanto en el grupo de reinserciones como de primeras inserciones, y no se registró ningún embarazo en el grupo que utilizaba el dispositivo con posterioridad al quinto año. La tasa de expulsión y LFU fueron significativamente inferiores en el grupo de mujeres que utilizaban el dispositivo con posterioridad al quinto año. Además, este grupo señaló una tasa significativamente superior de retiro por elección del investigador. Estos resultados indican que no hay motivos para recomendar el retiro o reemplazo del TCu200B antes de concluir el sexto año de uso. Cuando se ha de insertar un nuevo DIU después del retiro por expiración de la duración, se debe indicar a los proveedores que lo coloquen inmediatamente después del retiro porque este procedimiento no presenta riesgos adicionales, reduce el número de visitas clínicas y evita a las mujeres el uso de un método transitorio mientras aguardan a la reinserción.
    Notes: Abstract The purpose of this study was to evaluate the first year clinical performance of the TCu200B IUD in a cohort of women who had the IUD re-inserted immediately after a removal for life-span expiration, compared with a group of initial acceptors, and a cohort of women who continued using the device for more than 60 months. The sample consisted of 1066 users, 339 in each of the two first groups and 388 in the third. Life-table analysis was used to calculate continuation and gross discontinuation rates by reason. Statistical significance of the differences between groups was tested by log-rank method. Pregnancy rates were low, both in the group of re-insertions and first insertions, and no pregnancies occurred in the group using the device beyond the fifth year. The expulsion rate and lost-to-follow-up (LFU) rate were significantly lower in the group of women who used the device beyond the fifth year. In addition, this group showed a significantly higher rate of removal for investigator's choice. These results show that there is no reason to recommend the removal and replacement of the TCu200B before the end of the sixth year of use. When a new IUD is to be inserted after removal for life-span expiration, providers should be instructed to insert it immediately after the removal, because this procedure does not pose additional risks, reduces the number of clinic visits, and relieves the women of the use of a temporary method while waiting for the re-insertion.
    Type of Medium: Electronic Resource
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