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1.
J Assist Reprod Genet ; 39(8): 1693-1712, 2022 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-35870095

RESUMO

Since 2007, the Oncofertility Consortium Annual Conference has brought together a diverse network of individuals from a wide range of backgrounds and professional levels to disseminate emerging basic and clinical research findings in fertility preservation. This network also developed enduring educational materials to accelerate the pace and quality of field-wide scientific communication. Between 2007 and 2019, the Oncofertility Consortium Annual Conference was held as an in-person event in Chicago, IL. The conference attracted approximately 250 attendees each year representing 20 countries around the world. In 2020, however, the COVID-19 pandemic disrupted this paradigm and precluded an in-person meeting. Nevertheless, there remained an undeniable demand for the oncofertility community to convene. To maintain the momentum of the field, the Oncofertility Consortium hosted a day-long virtual meeting on March 5, 2021, with the theme of "Oncofertility Around the Globe" to highlight the diversity of clinical care and translational research that is ongoing around the world in this discipline. This virtual meeting was hosted using the vFairs ® conference platform and allowed over 700 people to participate, many of whom were first-time conference attendees. The agenda featured concurrent sessions from presenters in six continents which provided attendees a complete overview of the field and furthered our mission to create a global community of oncofertility practice. This paper provides a synopsis of talks delivered at this event and highlights the new advances and frontiers in the fields of oncofertility and fertility preservation around the globe from clinical practice and patient-centered efforts to translational research.


Assuntos
COVID-19 , Preservação da Fertilidade , Neoplasias , COVID-19/epidemiologia , Humanos , Pandemias
2.
Ann Pharm Fr ; 79(3): 266-274, 2021 May.
Artigo em Inglês | MEDLINE | ID: mdl-33091400

RESUMO

OBJECTIVE: The aim of this study is to validate a new HPLC-FIA method for routine analytical control of cyclosporine injectable preparations and to evaluate the routine analytical control with this technic. MATERIAL AND METHODS: Cyclosporine dosage was carried out by the HPLC-FIA method. The column was replaced by a PEEK (polyetheretherketone) loop tubing. The mobile phase consisted of ultrapure water. The injection volume was 1µL with a flow rate of 1mL/min. All determinations were performed at 35°C. The detection was carried out at 210nm. The accuracy profile method was used to validate the HPLC-FIA assay of cyclosporine. Routine control was applied for each cyclosporine preparation using the HPLC-FIA developed method. An acceptance limit of ±10% of the theoretical concentration has been set for the conformity of the preparation. RESULTS: The accuracy profile shows the validity of our method for the dosage of cyclosporine in the concentration range studied (0.5-2.5mg/mL) with good linearity (correlation coefficient>0.999), high precision (the relative standard deviation [RSD] values, for both repeatability and intermediate precision, were<3%) and acceptable trueness (the relative biases were found<2%). In our study, 220 injectable cyclosporine preparations were analyzed: 85% were compliant. All analyzes were conform after a second standardized homogenization of 10 shakes. CONCLUSIONS: The proposed HPLC-FIA method is a reliable, fast, simple, precise method that can be easily used for the routine quality control of cyclosporine injectable preparations.


Assuntos
Ciclosporina , Cromatografia Líquida de Alta Pressão , Controle de Qualidade , Reprodutibilidade dos Testes
3.
J Assist Reprod Genet ; 37(7): 1567-1577, 2020 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-32594284

RESUMO

PURPOSE: The state of limited resource settings that Coronavirus (COVID-19) pandemic has created globally should be taken seriously into account especially in healthcare sector. In oncofertility, patients should receive their fertility preservation treatments urgently even in limited resource settings before initiation of anticancer therapy. Therefore, it is very crucial to learn more about oncofertility practice in limited resource settings such as in developing countries that suffer often from shortage of healthcare services provided to young patients with cancer. METHODS: As an extrapolation during the global crisis of COVID-19 pandemic, we surveyed oncofertility centers from 14 developing countries (Egypt, Tunisia, Brazil, Peru, Panama, Mexico, Colombia, Guatemala, Argentina, Chile, Nigeria, South Africa, Saudi Arabia, and India). Survey questionnaire included questions on the availability and degree of utilization of fertility preservation options in case of childhood cancer, breast cancer, and blood cancer. RESULTS: All surveyed centers responded to all questions. Responses and their calculated oncofertility scores showed different domestic standards for oncofertility practice in case of childhood cancer, breast cancer, and blood cancer in the developing countries under limited resource settings. CONCLUSIONS: Medical practice in limited resource settings has become a critical topic especially after the global crisis of COVID-19 pandemic. Understanding the resources necessary to provide oncofertility treatments is important until the current COVID-19 pandemic resolves. Lessons learned will be valuable to future potential worldwide disruptions due to infectious diseases or other global crises.


Assuntos
Betacoronavirus/patogenicidade , Infecções por Coronavirus/prevenção & controle , Atenção à Saúde/normas , Preservação da Fertilidade/métodos , Neoplasias/terapia , Pandemias/prevenção & controle , Pneumonia Viral/prevenção & controle , Betacoronavirus/isolamento & purificação , COVID-19 , Infecções por Coronavirus/transmissão , Infecções por Coronavirus/virologia , Atenção à Saúde/economia , Países em Desenvolvimento , Feminino , Preservação da Fertilidade/economia , Preservação da Fertilidade/estatística & dados numéricos , Humanos , Neoplasias/virologia , Pneumonia Viral/transmissão , Pneumonia Viral/virologia , SARS-CoV-2 , Inquéritos e Questionários
5.
Ann Hum Biol ; 39(1): 76-9, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-22148899

RESUMO

BACKGROUND: Congenital bilateral absence of vas deferens (CBAVD) is responsible for 2-6% of male infertility. It occurs in 95% of men with cystic fibrosis. This malformation is present in patients with a sterile obstructive azoospermia but without clinical evidence of cystic fibrosis. Molecular study of the cystic fibrosis transmembrane conductance regulator (CFTR) gene responsible for cystic fibrosis could show the relationship between this disease and bilateral absence of vas deferens. PATIENTS AND METHODS: The study involved 20 male patients aged between 28-40 years, referred with suspected cystic fibrosis and in whom bilateral absence of vas deferens was confirmed by cyto-biochemical analyses and urogenital ultrasound. Molecular study of the CFTR gene was based on several techniques: DHPLC, DGGE and direct sequencing. RESULTS: Thirteen patients had CFTR mutations: F508del, G542X, W1282X, E1104X, 711+1G → T, V201M (TG) m and IVS8-5T. These mutations were associated with polymorphisms: M470V and D1270N. Seven cases presented only polymorphisms. CONCLUSION: The different mutations found in this study were associated with polymorphisms which decrease the severity of the disease and delay its onset. Thus, bilateral agenesis of the vas deferens is classed as a form of cystic fibrosis with only genital expression.


Assuntos
Regulador de Condutância Transmembrana em Fibrose Cística/genética , Doenças Urogenitais Masculinas/genética , Mutação/genética , Polimorfismo Genético , Adulto , África do Norte , Humanos , Masculino , Fenótipo , Ducto Deferente/anormalidades
6.
Artigo em Francês | MEDLINE | ID: mdl-1469235

RESUMO

The association of pelvic hydatid cyst with pregnancy is rare. We collected 4 cases between 1981-1990. Our incidence is of 1/30000 deliveries. The diagnosis was suggested in 3 cases by the patient's country of origin and previous history of extra-pelvic hydatid disease. It is confirmed by ultrasonography, which is still the first choice examination. During the 3 pregnancies managed to term, we did not find any modification in the cyst. One patient had vaginal delivery twice; however complications, sometimes fatal, are reported in the literature. The time for surgery and the mode of delivery are discussed because of the rarity of this association.


Assuntos
Equinococose/diagnóstico por imagem , Doenças dos Genitais Femininos/diagnóstico por imagem , Complicações Parasitárias na Gravidez/diagnóstico por imagem , Adulto , Anti-Helmínticos/uso terapêutico , Equinococose/tratamento farmacológico , Equinococose/epidemiologia , Feminino , Doenças dos Genitais Femininos/tratamento farmacológico , Doenças dos Genitais Femininos/epidemiologia , Humanos , Gravidez , Complicações Parasitárias na Gravidez/tratamento farmacológico , Complicações Parasitárias na Gravidez/epidemiologia , Resultado da Gravidez , Tunísia/epidemiologia , Ultrassonografia
7.
Artigo em Francês | MEDLINE | ID: mdl-1401770

RESUMO

We analyzed the relationship between the evolution of pregnancy and the amplitude of the lipid disorders in order to evaluate their chronologic transformations. This research concerned 83 pregnancies aged between 19-40 years during the 3 periods of gestation and 31 healthy control women in the same range of age. Our results showed an increased triglyceride in the 2nd period and an earlier decrease of both, cholesterol, phospholipid and apolipoproteins. These parameters showed a progressive increase of their blood concentrations during the 2nd and the 3rd period of pregnancy, in an other hand we evidenced a good correlation between gestational aged and these variations i.e.: triglyceride and mother's weight; this phenomenon could suggest an eventual role of the nutrition and the hygienic habitude in the lipid metabolism. The correlation between our observed lipid disorders and the mother's age or the parity were not significant.


Assuntos
Lipídeos/sangue , Gravidez/sangue , Apoproteínas/sangue , Colesterol/sangue , Estudos de Avaliação como Assunto , Feminino , Humanos , Metabolismo dos Lipídeos , Fosfolipídeos/sangue , Gravidez/metabolismo , Primeiro Trimestre da Gravidez , Segundo Trimestre da Gravidez , Terceiro Trimestre da Gravidez , Triglicerídeos/sangue
8.
Tunis Med ; 63(8-9): 475-7, 1985.
Artigo em Francês | MEDLINE | ID: mdl-4089991

RESUMO

PIP: A missing IUD string on examination is rare but poses problems of diagnosis and treatment. Sonography should be used to ascertain whether the IUD is in the uterus. If not, abdominal radiography should be used to determine whether the device has been expelled or has migrated. The diagnosis should be confirmed by hysteroscopy or laparoscopy. If the sonogram shows that the IUD is still in the uterus, hysteroscopy can be used to confirm the diagnosis and guide removal of the device. Blind removal may be traumatising and unsuccessful. General anesthesia was used during 7 removals of intrauterine IUDs with missing strings. 6 cases required more than 1 attempt. A Wolff type panoramic hysteroscope with CO2 was used. The IUD was removed with fine forceps. The patients were 30 years old on average and had 3 children. The average duration of IUD use was 5 years. 5 of the 7 were seen on the occasion of a voluntary or spontaneous abortion. The diagnosis of intrauterine IUD was made by sonography in 4 cases. In 5 cases, attempts at blind removal were made before hysteroscopy. 2 cases involved Lippes Loops and the rest were Copper Ts. The 2 devices are the only ones used in Tunisia. The predominance of Copper Ts may be explained by their reduced surface in comparison with Lippes Loops, which allow them to move more freely. Removal of an IUD under hysteroscopic control during induced abortion or curettage after spontaneous abortion allows repeated and possibly traumatizing attempts at removal to be avoided.^ieng


Assuntos
Dispositivos Intrauterinos/efeitos adversos , Adulto , Endoscopia , Feminino , Humanos
9.
Gynecol Obstet Fertil ; 40(7-8): 411-8, 2012.
Artigo em Francês | MEDLINE | ID: mdl-22521986

RESUMO

OBJECTIVE: To evaluate the results of controlled ovarian hyperstimulation (COH) for IVF in patients with low anti-Müllerian hormone (AMH) and normal basal follicle stimulating hormone (FSH) and Estradiol levels (≤50 pg/mL). PATIENTS AND METHODS: A retrospective cohort study including 704 patients for whom AMH and FSH levels (measured between days 3 and 5 of the menstrual cycle) were available, is performed in the IVF center at the Sèvres Hospital (France). Three groups are designed and analyzed: group 1 with AMH less or equal to 2 ng/mL and FSH less or equal to 10 mUI/mL (study group), Group 2 with AMH greater than 2 ng/mL and FSH less or equal to 10 mUI/mL (control group) and Group 3 with AMH less or equal to 2 ng/mL and FSH greater than 10 mUI/mL (group with decreased ovarian reserve). RESULTS: IVF outcome for patients from the study group is significantly worse than that of the second but not than that of the third group. In the first group, the number of retrieved oocytes, the number of total obtained embryos, the clinical pregnancy rate and the live birth rate are significantly lower than in the second group; moreover, there are more cancelled cycles because of poor response in the first group. There is no difference with the third group. DISCUSSION AND CONCLUSIONS: This study shows that women with a low baseline AMH have a similar response to COH to the poor responders patients with a decreased ovarian reserve revealed by an elevated FSH level. Thus, when a woman undergoing IVF cycle presents a low AMH, she might be considered as a poor responder patient regardless of the FSH level and, although the clinical pregnancy rate is not so disappointing (18%), the couple should be informed of a higher risk of cycle cancellation.


Assuntos
Hormônio Antimülleriano/sangue , Estradiol/sangue , Fertilização in vitro , Hormônio Foliculoestimulante/sangue , Indução da Ovulação , Adulto , Coeficiente de Natalidade , Feminino , Humanos , Recuperação de Oócitos , Gravidez , Taxa de Gravidez , Prognóstico , Estudos Retrospectivos
20.
Pathol Biol (Paris) ; 52(3): 138-47, 2004 Apr.
Artigo em Francês | MEDLINE | ID: mdl-15063933

RESUMO

Congenital heart block (CHB) associated with maternal anti-SSA/SSB antibodies: a report of four cases. CHB detected in utero is strongly associated with maternal antibodies to SSA (Ro) and SSB (La). Their pathogenic role in the development of CHB has been established in several studies. The mothers of affected infants frequently had autoimmune disease (systemic lupus erythematosus, Sjögren's syndrome) or were entirely asymptomatic. It is very difficult to identify pregnant asymptomatic mothers carrying anti-SSA/SSB antibodies. We report four cases of infants born to asymptomatic mothers with anti-SSA/SSB antibodies, three of them developed isolated congenital cardiac heart block and one with no evidence of CHB. All three CHB are detected during pregnancy between 16 and 24 weeks of gestation. All maternal sera contained antibodies to SSA alone or the both SSA and SSB. Three of four subsequent pregnancies were complicated by heart block. One child affected died in utero. While the two other newborns with CHB required pacemaker insertion during the first 3 months of life. Although the association of anti-SSA/SSB with CHB is widely accepted, the precise mechanism by which these antibodies cause cardiac conduction abnormalities remains to be defined. Antibodies to SSA/SSB have been proposed to be a serologic marker for neonatal lupus syndrome and CHB. Fetal and neonatal diseases are presumed to be due to the transplacental passage of these IgG autoantibodies from the mother into the fetal circulation. Since these antibodies may have a pathogenic role in CHB, screening of infants with isolated CHB or neonatal lupus and their mothers for the presence of anti-SSA and anti-SSB is strongly recommended.


Assuntos
Anticorpos Antinucleares/imunologia , Autoantígenos , Doenças Autoimunes/imunologia , Bloqueio Cardíaco/congênito , Imunidade Materno-Adquirida , Isoanticorpos/imunologia , Complicações na Gravidez/imunologia , RNA Citoplasmático Pequeno , Ribonucleoproteínas/imunologia , Adulto , Bradicardia/embriologia , Bradicardia/imunologia , Estimulação Cardíaca Artificial , Feminino , Morte Fetal/etiologia , Doenças Fetais/imunologia , Coração Fetal/imunologia , Coração Fetal/patologia , Bloqueio Cardíaco/imunologia , Bloqueio Cardíaco/terapia , Humanos , Recém-Nascido , Masculino , Gravidez , Antígeno SS-B
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