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1.
J Obstet Gynaecol Res ; 49(1): 122-127, 2023 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-36183741

RESUMO

AIM: To evaluate the success of local methotrexate (MTX) treatment, the side-effect profile and its fertility effect in patients diagnosed with cesarean scar pregnancy. MATERIALS: This retrospective cohort study included 56 cesarean scar pregnancy patients who applied to Erciyes University Faculty of Medicine, Department of Obstetrics and Gynecology between January 2012 and January 2022 and were treated with ultrasound-guided local MTX. The results of 56 patients with cesarean scar pregnancy who underwent transvaginal ultrasound-guided single-dose local MTX treatment were evaluated. First, the contents of the sac were aspirated, and then 50 mg of MTX was injected into the gestational sac. RESULTS: The median gestational age at diagnosis was 7 weeks 2 days. The mean beta human chorionic gonadotrophin level was 31 345 ± 37 838 (range: 113-233 835 mIU/mL). Fifty-four patients were successfully treated with local MTX therapy. The interval between the first MTX injection and the normalization of beta human chorionic gonadotrophin was 55.2 ± 41.0 days. None of our patients required surgical treatment. Beta human chorionic gonadotrophin values did not decrease in one patient and she was treated with systemic MTX. Local MTX therapy could not be applied to one patient for technical reasons. Only one patient needed blood transfusion after local MTX. Thirteen patients become pregnant after treatment (76%). No systemic side effects related to MTX were observed in any of the patients. CONCLUSION: Transvaginal ultrasound-guided single-dose local MTX treatment is an effective, safe, and fertility-preserving treatment method for cesarean scar pregnancy.


Assuntos
Abortivos não Esteroides , Gravidez Ectópica , Feminino , Humanos , Gravidez , Abortivos não Esteroides/uso terapêutico , Cesárea/efeitos adversos , Gonadotropina Coriônica Humana Subunidade beta , Cicatriz/tratamento farmacológico , Cicatriz/etiologia , Metotrexato/uso terapêutico , Gravidez Ectópica/terapia , Estudos Retrospectivos , Resultado do Tratamento
2.
J Obstet Gynaecol ; 41(8): 1246-1251, 2021 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-33629621

RESUMO

This study aimed to evaluate the efficacy and adverse effects of dienogest for the treatment of endometriomas. Dienogest (2 mg/day) was administered to patients with endometrioma continuously through the 6-month study period. The patients were prospectively examined on the efficacy and side effects at baseline, at third months, and sixth months of the treatment. Twenty-four out of 30 patients were able to complete the study. The mean volume of the endometrioma decreased significantly from 112.63 ± 161.31 cm³ at baseline to 65.47 ± 95.69 cm³ at a 6-month follow-up (-41%) (p = .005). The VAS score for pelvic pain decreased significantly from 7.50 to 3.00 (p < .001) at the sixth months of treatment. The most common side effects were menstrual irregularities. Laboratory parameters did not change during the study. Dienogest considered being effective for 6 months of use in decreasing the size of endometrioma, reducing endometriosis-associated pain with a favourable safety and tolerability profile.Impact statementWhat is already known on this subject? Laparoscopic excisional surgery for endometrioma is currently the most valid approach in the treatment of endometriomas. However, there are concerns about ovarian reserve damage during surgery.What do the results of this study add? Dienogest considered being effective in decreasing the size of endometrioma, reducing endometriosis-associated pain with a favourable safety and tolerability profile. Long-term use of dienogest in younger patients with endometriomas who are yet to give birth may reduce the possibility of surgery by reducing the size of the endometriomas and may preserve ovarian reserve.What are the implications of these findings for clinical practice and/or further research? Dienogest may reduce the incidence of infectious complications such as pelvic abscess after oocyte retrieval and the surgical procedures in infertile patients with endometrioma.


Assuntos
Anticoncepcionais Orais Hormonais/administração & dosagem , Endometriose/tratamento farmacológico , Endométrio/patologia , Nandrolona/análogos & derivados , Dor Pélvica/tratamento farmacológico , Doenças Uterinas/tratamento farmacológico , Adulto , Anticoncepcionais Orais Hormonais/efeitos adversos , Endometriose/complicações , Endometriose/patologia , Feminino , Humanos , Distúrbios Menstruais/induzido quimicamente , Nandrolona/administração & dosagem , Nandrolona/efeitos adversos , Tamanho do Órgão/efeitos dos fármacos , Medição da Dor , Dor Pélvica/etiologia , Dor Pélvica/patologia , Estudos Prospectivos , Resultado do Tratamento , Doenças Uterinas/complicações , Doenças Uterinas/patologia
3.
J Obstet Gynaecol Res ; 44(10): 1985-1994, 2018 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-30117221

RESUMO

AIM: The aims of this study were to present the results of using infragluteal folds as a skin graft donor site in cases of Mullerian agenesis undergoing full-thickness skin graft vaginoplasty and to evaluate the outcomes of the surgical technique. METHODS: Demographics and clinical parameters of 24 consecutive Mullerian agenesis patients refusing any dilatational procedure and undergoing neovaginal construction using infragluteal folds skin grafts from May 2004 to July 2015 were analyzed. RESULTS: The mean age of the patients was 21.5 ± 5.7 years. Five patients had nonfunctional rudimentary uterus, one patient had unilateral ovarian agenesis, one patient had unilateral renal agenesis, and one had undergone a previous vaginoplasty. There were no serious complications needing surgical or medical intervention. The depth of the neovagina in patients with a follow-up period of more than 6 months (n = 17) varied from 7 to 12 cm. Of these patients, the sexually active ones (n = 8) did not complain of dyspareunia or vaginal dryness during sexual intercourse. The resulting scars were satisfactory and acceptable for all patients. CONCLUSION: It has been our practice to use infragluteal folds as a skin graft donor site for full-thickness skin graft vaginoplasty. We believe that the results of this study demonstrate that this area is versatile and an excellent alternative to the groins and lower abdomen. Further clinical and histomorphological investigations are necessary for strong statements and results.


Assuntos
Transtornos 46, XX do Desenvolvimento Sexual/cirurgia , Anormalidades Congênitas/cirurgia , Procedimentos Cirúrgicos em Ginecologia/métodos , Ductos Paramesonéfricos/anormalidades , Procedimentos de Cirurgia Plástica/métodos , Transplante de Pele/métodos , Anormalidades Urogenitais/cirurgia , Vagina/cirurgia , Transtornos 46, XX do Desenvolvimento Sexual/patologia , Adolescente , Adulto , Anormalidades Congênitas/patologia , Feminino , Humanos , Ductos Paramesonéfricos/patologia , Ductos Paramesonéfricos/cirurgia , Vagina/anormalidades , Adulto Jovem
4.
Eur J Obstet Gynecol Reprod Biol ; 206: 131-135, 2016 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-27693933

RESUMO

OBJECTIVE: The aim of this study was to compare the use of systemic and local methotrexate in the treatment of cesarean scar pregnancy. STUDY DESIGN: In this retrospective cohort study, we collected the data of 44 patients with cesarean scar pregnancy. The patients were grouped according to treatment modality: Group 1, local methotrexate injection (n=17) and Group 2, systemic methotrexate (n=27). The groups were compared with respect to side effects, recovery time, reproductive outcome, and treatment cost. RESULTS: The mean gestational age at diagnosis (6.4±0.93 vs. 5.4±0.80 weeks, p=0.001), pretreatment serum ß-human chorionic gonadotrophin level [27,970 (11,010-39,421) vs. 7606 (4725-16,996) mIU/mL, p=0.001], and lesion size (2.74±1.36 and 1.28±0.55cm, p=0.001) were higher in Group 1. All patients were cured by primary therapy without additional surgery. The mean times for ß-human chorionic gonadotrophin normalization, the uterine-mass disappearance, were significantly shorter in Group 1 than in Group 2 (6.17±1.55 vs. 8.11±2.0 weeks, p=0.001 and 10.47±4.14 vs. 13.40±4.44 weeks, p=0.002, respectively). The cost of treatment was similar between groups (281.133±112.123$ vs. 551.134±131.792$, p=0.76). The total pregnancy rates were not different between groups (5/16, 31.4% vs. 6/11, 54.6%, p=0.301). One recurrent cesarean scar pregnancy occurred after systemic methotrexate. Oral ulcers, the most common side effect, were seen in seven patients in Group 2. CONCLUSION: Even though treatment success and reproductive outcomes are similar, local methotrexate is superior to systemic methotrexate with regard to recovery time, side effects, and treatment costs, even in patients with unfavorable pretreatment prognostic predictors.


Assuntos
Abortivos não Esteroides/administração & dosagem , Cesárea/efeitos adversos , Cicatriz/etiologia , Metotrexato/administração & dosagem , Gravidez Ectópica/tratamento farmacológico , Abortivos não Esteroides/uso terapêutico , Adulto , Bases de Dados Factuais , Feminino , Humanos , Metotrexato/uso terapêutico , Gravidez , Estudos Retrospectivos , Resultado do Tratamento
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