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1.
J Gynecol Obstet Hum Reprod ; 51(1): 102237, 2022 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-34614436

RESUMO

INTRODUCTION: To create a scoring system by including all of the factors that are recommended for an ideal ET and to investigate its correlation with the Β-HCG results. MATERIALS AND METHODS: This study was conducted as a retrospective trial between January 2009 and December 2018. Women who had a single ET between the specified dates were included in the study. The embryo grade, ET day, distance between the fundus to embryo transfer site measured via ultrasonography, endometrial thickness on ET day, and presence of mucus and blood in the catheter after transfer were the variables evaluated. Each one of the five variables that constituted the scoring system were rated separately. RESULTS: Overall, 1652 patients participated in this research. Antral follicle count (13,3 ± 8 vs. 14,6 ± 8,2, p: 0,001), endometrial thickness on the ET day (9.9 ± 2 vs.10.3 ± 2, p = 0.006) and number of mature oocytes (8.6 ± 6 vs. 9 ± 5.1, p: 0.003) were significantly higher in patients with positive Β-HCG values. The total score in the Β-HCG positive group was 9.8 ± 1.4 versus 8.9 ± 1.4 in the Β-HCG negative group (p < 0.001). The best ETSS cut-off value for predicting Β-HCG positivity was 9.5, with 82% sensitivity and 67% specificity (AUC:0.808). CONCLUSION: Our scoring system is an important step toward standardization, as it offers a new, practical, cost-free, and applicable scoring system based on pre- and post-ET measurements and laboratory data.


Assuntos
Transferência Embrionária/classificação , Projetos de Pesquisa/normas , Adulto , Distribuição de Qui-Quadrado , Estudos de Coortes , Transferência Embrionária/métodos , Feminino , Fertilização in vitro/classificação , Fertilização in vitro/métodos , Humanos , Estudos Retrospectivos , Estatísticas não Paramétricas
2.
Braz. J. Pharm. Sci. (Online) ; 58: e20151, 2022. tab, graf
Artigo em Inglês | LILACS | ID: biblio-1403754

RESUMO

Abstract This was a forthcoming study of those patients, who undergo in-vitro fertilization (IVF) and freeze-all embryo, who acquiesce for the study. The number of participated patients (n=350) in this study, underwent for IVF. The blood sample was collected from patients to evaluate the level of serum progesterone in vacuum vials on the day of ovulation trigger. After 36 hrs of ovulation trigger, ovum picked up was done. Quantitative methods were used to estimate the level of serum progesterone through the electrochemiluminescence immunoassay and correlation of serum progesterone with embryo transfer (ET) outcomes. Main outcome of this current study was to evaluate the value of mean serum progesterone level i.e.0.868± 0.712 ng/ml and 0.88±0.723 ng/ml was found in case of pregnancy positive and negative respectively, at p=0.216 value. In antagonist (n=40) and agonist (n=310) cases, it was 8(20%) and 37(11.94%) PL occurrence was noted at p=0.143 respectively. An overall value of the premature lutenization (PL) occurrences was 13.63% and 15.25% observed in both positive and negative cases of pregnancy at p=0.216 respectively. This study concluded that 12.66% of PL occurrences were recorded in the case of IVF. Study results proved, there were no significant effect of PL on pregnancy outcomes.


Assuntos
Humanos , Feminino , Adulto , Progesterona/agonistas , Endométrio , Histologia/classificação , Métodos , Ovulação/genética , Óvulo , Pacientes/classificação , Imunoensaio , Fertilização in vitro/classificação , Transferência Embrionária/instrumentação , Estruturas Embrionárias
3.
Fed Regist ; 81(3): 378-80, 2016 Jan 06.
Artigo em Inglês | MEDLINE | ID: mdl-26742184

RESUMO

The Food and Drug Administration (FDA) is classifying the intravaginal culture system into class II (special controls). The special controls that will apply to the device are identified in this order and will be part of the codified language for the intravaginal culture system's classification. The Agency is classifying the device into class II (special controls) in order to provide a reasonable assurance of safety and effectiveness of the device.


Assuntos
Técnicas de Cultura/classificação , Técnicas de Cultura/instrumentação , Aprovação de Equipamentos/legislação & jurisprudência , Fertilização in vitro/classificação , Fertilização in vitro/instrumentação , Embrião de Mamíferos , Feminino , Células Germinativas , Humanos , Estados Unidos , United States Food and Drug Administration , Vagina
4.
Fed Regist ; 69(248): 77623-4, 2004 Dec 28.
Artigo em Inglês | MEDLINE | ID: mdl-15624253

RESUMO

The Food and Drug Administration (FDA) is classifying the assisted reproduction laser system into class II (special controls). The special control that will apply to the device is the guidance document entitled "Class II Special Controls Guidance Document: Assisted Reproduction Laser Systems." The agency is classifying this device into class II (special controls) in order to provide a reasonable assurance of safety and effectiveness of the device. Elsewhere in this issue of the Federal Register, FDA is publishing a notice of availability of the guidance document that is the special control for this device.


Assuntos
Fertilização in vitro/instrumentação , Lasers/classificação , Técnicas de Reprodução Assistida/instrumentação , Desenho de Equipamento , Segurança de Equipamentos/classificação , Feminino , Fertilização in vitro/classificação , Humanos , Técnicas de Reprodução Assistida/classificação , Estados Unidos , United States Food and Drug Administration
5.
Scand J Public Health ; 32(3): 203-9, 2004.
Artigo em Inglês | MEDLINE | ID: mdl-15204181

RESUMO

AIMS: The purpose of this study was to describe equity in the use of in vitro fertilization (IVF; including micro-injections and frozen-embryo transfers), and compare its use with that of other assisted reproduction technologies (other ARTs; including ovulation inductions with or without inseminations). METHODS: The women who received IVF (n=9, 175) and other ARTs (n=10,254) between 1996 and 1998 were identified from the reimbursement records of the Social Insurance Institution (SII) covering all Finns. Population controls, matched by age and municipality, were selected for IVF women (n=9,175). Information concerning background characteristics came from the Central Population Register and the SII's reimbursement files. The sector (public vs. private) was defined using prescribing physicians' codes. IVF use was studied by the proportions of women treated and the frequency of treatment. RESULTS: The age-standardized IVF incidence per thousand 20-to-49-year-old women was 8.8 in urban and 7.3 in rural areas, but the use of other ARTs did not vary correspondingly (9.2, 9.3). The regional incidence of IVF and other ARTs varied considerably. In the private sector, women in the highest socioeconomic position were over-represented (29% private, 18% public, 16% controls). During the mean 1.5 years of the study period, the IVF women had somewhat more treatment cycles in the private than in the public sector (mean 3.3, 2.7), and those in the highest socioeconomic position had more cycles than others (3.5, 3.2); the frequency was not age-dependent. In the public sector the number of cycles did not differ by socioeconomic group (mean 2.7-2.8 per woman), and women aged 25 to 39 had more cycles than others. CONCLUSION: There were socioeconomic differences in use of IVF services, but they were small because of the equitable use of public services.


Assuntos
Fertilização in vitro/estatística & dados numéricos , Classe Social , Justiça Social , Adulto , Fatores Etários , Feminino , Fertilização in vitro/classificação , Finlândia , Humanos , Incidência , Estado Civil , Pessoa de Meia-Idade , Setor Privado/ética , Setor Privado/estatística & dados numéricos , Setor Público/ética , Setor Público/estatística & dados numéricos , Técnicas de Reprodução Assistida/classificação , Técnicas de Reprodução Assistida/estatística & dados numéricos , População Rural , População Urbana
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