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2.
Eur J Obstet Gynecol Reprod Biol ; 183: 159-63, 2014 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-25461371

RESUMEN

OBJECTIVE: To evaluate modified anterior abdominal wall cervicopexy (AWC) as a less invasive (via 3-cm minilaparotomy) and more augmented (via securing posterior vaginal wall to uterosacral ligaments) technique. METHODS: Case series of 30 women with Stages III and IV apical uterine prolapse assessed by the pelvic organ prolapse quantification system. RESULTS: The modified AWC procedure was performed successfully for 17 cases with Stage III uterovaginal prolapse and 13 cases with Stage IV uterovaginal prolapse. The procedure was conducted safely with no operative or postoperative complications, apart from two cases with postoperative urinary retention. Operative time ranged from 45 to 70min. Follow-up was available for 1-3 years. Overall, 27 cases were satisfied with the procedure, and three cases developed recurrence after caesarean section due to cutting the supporting sutures. CONCLUSIONS: The modified AWC procedure is less invasive, simple and effective for Stages III and IV uterine prolapse.


Asunto(s)
Cuello del Útero/cirugía , Procedimientos Quirúrgicos Ginecológicos/métodos , Procedimientos Quirúrgicos Mínimamente Invasivos/métodos , Prolapso Uterino/cirugía , Adulto , Femenino , Estudios de Seguimiento , Humanos , Tempo Operativo , Complicaciones Posoperatorias , Resultado del Tratamiento , Retención Urinaria/etiología , Prolapso Uterino/diagnóstico
3.
Int J Gynaecol Obstet ; 110(2): 130-2, 2010 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-20493488

RESUMEN

OBJECTIVE: To study the operative and postoperative outcomes of anterior abdominal wall cervicopexy (AWC) for treatment of stage III and stage IV uterine prolapse. METHODS: AWC was performed by anchoring the supravaginal cervix to the anterior abdominal wall. This was done following obliteration of the pouch of Douglas via laparotomy. RESULTS: Among 37 patients, AWC was performed in 21 women with stage III and 16 women with stage IV uterine prolapse. Overcorrection was observed in 3 women. Postoperatively, 2 women experienced febrile morbidity and 5 had urinary retention. Thirteen women complained of urinary frequency, but all reported improvement at 3-month follow up. Among 24 women who became pregnant, 14 delivered vaginally, 5 delivered by cesarean, and 5 had an ongoing pregnancy. Four recurrences occurred: 2 stage II and 2 stage III prolapses. Three of these women had delivered by cesarean, while the fourth recurrence occurred after the patient's third vaginal birth. CONCLUSIONS: AWC is a simple and effective procedure to treat stage III and stage IV uterine prolapse. However, some surgical modifications and more studies are required to ascertain its validity.


Asunto(s)
Cuello del Útero/cirugía , Procedimientos Quirúrgicos Ginecológicos/métodos , Índice de Embarazo , Prolapso Uterino/cirugía , Adolescente , Adulto , Cesárea , Femenino , Estudios de Seguimiento , Procedimientos Quirúrgicos Ginecológicos/efectos adversos , Humanos , Embarazo , Técnicas de Sutura , Retención Urinaria/etiología , Adulto Joven
4.
Int J Gynaecol Obstet ; 103(3): 222-6, 2008 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-18805523

RESUMEN

OBJECTIVE: To assess the safety and short-term efficacy of bilateral uterine artery ligation (UAL) via minilaparotomy for the management of heavy menstrual bleeding (HMB). METHODS: A prospective study of 30 women with HMB who underwent UAL. The primary outcome was cumulative treatment failure 12 months after the procedure. Treatment failure was defined as the need for hysterectomy during the follow-up period. RESULTS: At 12 months, 6 women had undergone hysterectomy for bleeding, for a cumulative failure rate of 20% (95% CI, 9%-38%). The number of bleeding days was significantly reduced by 11.9+/-1.5 days (P<0.001) and hemoglobin level significantly increased by 1.3+/-0.15 g/dL (P<0.001). Of the 30 women, 24 (80%) were satisfied with the results. No major complications were reported during the procedure or median follow-up period of 13.2 months. CONCLUSION: Bilateral UAL is a safe and effective minimally invasive procedure that can provide an alternative treatment for HMB.


Asunto(s)
Histerectomía , Laparotomía/métodos , Menorragia/cirugía , Útero/irrigación sanguínea , Adulto , Amoxicilina/administración & dosificación , Amoxicilina/uso terapéutico , Analgésicos no Narcóticos/administración & dosificación , Analgésicos no Narcóticos/uso terapéutico , Profilaxis Antibiótica , Femenino , Estudios de Seguimiento , Humanos , Ibuprofeno/administración & dosificación , Ibuprofeno/uso terapéutico , Estimación de Kaplan-Meier , Ligadura/métodos , Meperidina/administración & dosificación , Meperidina/uso terapéutico , Persona de Mediana Edad , Satisfacción del Paciente , Modelos de Riesgos Proporcionales , Estudios Prospectivos , Insuficiencia del Tratamiento , Útero/cirugía
5.
Am J Obstet Gynecol ; 199(2): 117.e1-6, 2008 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-18674655

RESUMEN

OBJECTIVE: The purpose of this study was to screen a panel of targeted adenoviruses as vectors for endometriosis gene therapy. STUDY DESIGN: Endometriotic cells were obtained from subjects with ovarian endometriomas. Liver tissues were taken from donors during hepatic transplantation surgery. Human endometriotic cells and liver tissues were transfected by targeted adenoviruses expressing luciferase reporter gene. Luciferase activity that was mediated by each virus was expressed as a percentage of adenovirus serotype 5 (Ad5-CMV-luc) activity. The 2-tailed Studentt test was used to compare the adenovirus data. RESULTS: In endometriotic cells, the adenovirus-RGD (Ad-RGD-luc), adenovirus under secretory leukocyte protease inhibitor promoter (Ad-SLPI-luc), and adenovirus under heparanase promoter (Ad-heparanase-luc) showed significantly higher activity, compared with the adenovirus serotype 5. In liver tissues, adenovirus-survivin (Ad-survivin-luc) and Ad-heparanase-luc had significantly lower activity, compared with adenovirus serotype 5. CONCLUSION: Ad-heparanase-luc showed "endometriosis on, liver off" phenotype and is a promising vector for endometriosis gene therapy.


Asunto(s)
Adenoviridae/genética , Endometriosis/terapia , Marcación de Gen/métodos , Terapia Genética/métodos , Proteínas de la Cápside , Células Cultivadas , Endometrio/citología , Femenino , Vectores Genéticos , Glucuronidasa/metabolismo , Humanos , Hígado/enzimología , Luciferasas/metabolismo , Activación Transcripcional/fisiología , Transducción Genética/métodos , Transfección
6.
Eur J Obstet Gynecol Reprod Biol ; 137(2): 240-6, 2008 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-17582674

RESUMEN

OBJECTIVE: To test the ability of a group of serum cytokines, either individually or in combination, to serve as biomarkers for the nonsurgical diagnosis of endometriosis. STUDY DESIGN: Subjects were allocated to two groups according to their laparoscopic diagnosis. The first group consisted of patients with endometriosis and the second group was made up of infertile women with no pelvic pathology (controls). Blood samples were collected preoperatively and stored. Cytokines were measured in the serum of all participants using the Bio-Plex Protein Array System. Nonparametric statistics and the Mann-Whitney test were used to compare groups. Subjects were seen at the Gynecologic endoscopy unit. RESULTS: Three cytokines were significantly higher in the serum of subjects with endometriosis than in the control group: interleukin-6 (IL-6) [4.41 pg/ml (range: 1.47-15.01) versus 0.97 pg/ml (range: 0.29-2.98), respectively; p<0.001], monocyte chemotactic protein-1 (MCP-1) [37.91 pg/ml (range: 24.54-94.74) versus 22.13 pg/ml (range: 13.85-39.45), respectively; p<0.001], and interferon-gamma (INF-gamma) [19.01 pg/ml (range: 1.19-73.52) versus 0.30 pg/ml (range: 0.00-13.05), respectively; p<0.001]. There was no statistically significant difference between subjects with endometriosis and controls in the serum concentration of vascular endothelial growth factor (VEGF), tumor necrosis factor-alpha (TNF-alpha), or granulocyte macrophage colony stimulating factor (GM-CSF). Interleukin-2 (IL-2), interleukin-8 (IL-8), and interleukin-15 (IL-15) were undetectable in the serum of both groups. None of the measured cytokines showed significant correlation with the cycle phase or stage of endometriosis. In a multivariate analysis, serum interleukin-6 provided a sensitivity of 71% and a specificity of 66% to discriminate between endometriosis patients and controls at a cutoff point of 1.9 pg/ml. Adding monocyte chemotactic protein-1 and interferon-gamma to interleukin-6 did not increase the discriminative ability over that achieved by measuring serum interleukin-6 alone. CONCLUSIONS: Serum of subjects with endometriosis contains significantly higher levels of interleukin-6, monocyte chemotactic protein-1, and interferon-gamma than control women. Serum interleukin-6 measurements discriminate between women with endometriosis and controls. Interleukin-6 provides a promising serum marker for the nonsurgical prediction of endometriosis.


Asunto(s)
Quimiocina CCL2/sangre , Endometriosis/sangre , Endometriosis/diagnóstico , Interferón gamma/sangre , Interleucina-6/sangre , Adulto , Biomarcadores/sangre , Estudios de Casos y Controles , Femenino , Factor Estimulante de Colonias de Granulocitos y Macrófagos/sangre , Humanos , Interleucina-15/sangre , Interleucina-2/sangre , Interleucina-8/sangre , Análisis Multivariante , Valor Predictivo de las Pruebas , Sensibilidad y Especificidad , Factor de Necrosis Tumoral alfa/sangre , Factor A de Crecimiento Endotelial Vascular/sangre
7.
Afr J Reprod Health ; 9(1): 24-31, 2005 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-16104652

RESUMEN

Uniplant is a single 35mm contraceptive implant releasing nomegestrol acetate with an effective life span of one year. This study was undertaken to evaluate the possible effects of three-year use of uniplant on some liver enzymes (SGPT, SGOT and GGT) in Egyptian women and to evaluate whether the past asymptomatic hepatitis B virus infection would predispose to any changes in these enzymes. This is an uncontrolled prospective study including 187 women of reproductive age who desired contraception for three years (three segments each year). They were apparently healthy on clinical assessment with no history of jaundice or liver diseases. They also had normal levels of liver function enzymes (SGPT, SGOT & GGT). Fasting blood samples were drawn at admission for assessing the levels of these liver enzymes and to detect anti-HBS antibodies as a marker of past asymptomatic hepatitis B virus infection (HBV) and HBS antigen to diagnose the chronic carrier state. The liver enzymes were measured at 6th. 12th, 18th, 24th, 30th and 36th month of use, and 3-6 months after implant removal. Out of 187 subjects enrolled 159, 83 and 33 women completed one, two and three years of Uniplant use respectively. The mean levels of SGPT, SGOT and GGT showed slight but significant elevations at the end of the first and second years of use compared to the pre-insertion levels. By the end of the third year, the elevated mean values of all enzymes gradually decreased to approach the pre-insertion levels without any significant differences. The percentage of anti-HBS antibodies positive titre due to past asymptomatic infection was 23.3% (n = 41) while HBsAg positive antigenaemia (i.e., carrier state) was 3.4%, (n = 5). In both groups of women--anti-HBS antibodies positive (n = 41) without antigenaemia and anti-HBS antibodies negative (n = 129)--the changes in the mean levels of all enzymes during uniplant use were closely similar without any statistical significance. These results demonstrated that: (1) uniplant induced slight but significant elevations in the mean levels of SGPT, SGOT and GGT these elevations were within the normal ranges, completely reversible and of doubtful clinical significance. (2) The non-carrier women who had been exposed to past asymptomatic HBV infection showed no significant effects on the studied liver enzymes compared to the normal women during long-term use of Uniplant.


Asunto(s)
Preparaciones de Acción Retardada/efectos adversos , Implantes de Medicamentos/efectos adversos , Virus de la Hepatitis B/aislamiento & purificación , Hepatitis B/diagnóstico , Adolescente , Adulto , Estudios de Cohortes , Preparaciones de Acción Retardada/administración & dosificación , Países en Desarrollo , Remoción de Dispositivos , Progresión de la Enfermedad , Egipto , Femenino , Estudios de Seguimiento , Humanos , Dispositivos Intrauterinos , Pruebas de Función Hepática , Persona de Mediana Edad , Medición de Riesgo , Índice de Severidad de la Enfermedad , Factores de Tiempo
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