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1.
J Obstet Gynaecol Res ; 39(5): 1045-51, 2013 May.
Article in English | MEDLINE | ID: mdl-23379512

ABSTRACT

AIM: The aim of this study was to evaluate the efficacy of 3D power Doppler angiography (3D-PDA) for distinguishing between benign endometrial lesions and endometrial carcinoma in patients with postmenopausal bleeding (PMB). MATERIAL AND METHODS: One-hundred and fifty women with PMB and an endometrial thickness (ET) of ≥4 mm on 2D sonography were assessed by 3D-PDA before endometrial sampling to obtain definitive histological diagnosis of endometrial pathology. Endometrial volume (EV), vascularity index (VI), flow index (FI) and vascularity-flow index (VFI) were calculated by computer-aided analysis. RESULTS: Of the 150 women, 114 (76%) had benign endometrial lesions and 36 (24%) had endometrial carcinoma. Patients with endometrial carcinoma had significantly thicker endometrium (15.8 ± 7.7 vs 9.9 ± 5.9 mm; P < 0.001), larger EV (9.1 ± 4.7 vs 2.6 ± 3.5 mL, P < 0.001) and higher 3D-PDA indices (P < 0.001) than patients with benign endometrial lesions. The best variable for distinguishing between benign and malignant endometrium was VI, with an area under the receiver operating characteristic curve (AUC) of 0.86. In contrast, the ET had an AUC of only 0.62. The best-fit logistic regression model for the diagnosis malignancy contained only VI as an independent factor (P = 0.002). CONCLUSION: 3D-PDA measurements may be useful for distinguishing between benign endometrial lesions and endometrial carcinoma in patients with postmenopausal bleeding.


Subject(s)
Carcinoma/diagnostic imaging , Endometrial Neoplasms/diagnostic imaging , Endometrium/diagnostic imaging , Uterine Hemorrhage/etiology , Aged , Carcinoma/physiopathology , Endometrial Neoplasms/physiopathology , Endometrium/physiopathology , Female , Humans , Imaging, Three-Dimensional , Middle Aged , Postmenopause , Sensitivity and Specificity , Ultrasonography, Doppler , Uterine Diseases/diagnostic imaging , Uterine Diseases/physiopathology
2.
J Obstet Gynaecol Res ; 38(5): 787-92, 2012 May.
Article in English | MEDLINE | ID: mdl-22414094

ABSTRACT

AIM: The aim of this study was to evaluate the role of blunt suture needles for episiotomy repair at uncomplicated vaginal deliveries in reducing glove perforation rate. METHODS: This was a prospective randomized controlled trial wherein 300 nulliparous women with uncomplicated vaginal deliveries were randomized to episiotomy repair with either blunt or sharp suture needles. Patient demographics and clinical variables were collected. Postoperatively, the surgeons were surveyed regarding ease of using the needle, and glove perforation was determined by three tests: air insufflation, water filling and water load. RESULTS: A total of 41 perforations occurred in the 39 episiotomy repairs with glove perforations (13%). There was a significantly higher number of glove perforations using the sharp suture needles (28/150; 18.7%) than with the blunt suture needles (11/150; 7.3%) (P = 0.005). Glove perforation of the non-dominant hand occurred in 90% of the cases. Using a blunt suture needle took significantly more time (P < 0.001) to complete the repair than using a sharp needle. Surgeons reported that blunt needles were more difficult to use than sharp needles (P < 0.001). CONCLUSION: Blunt suture needles for episiotomy repair were shown to have a significantly lower instance of glove perforation but required more time and are perceived to be more difficult to complete the repair as compared to sharp needles.


Subject(s)
Delivery, Obstetric , Episiotomy/instrumentation , Gloves, Surgical , Needles , Suture Techniques/instrumentation , Female , Humans , Pregnancy , Prospective Studies , Treatment Outcome
3.
J Obstet Gynaecol Res ; 38(2): 383-9, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22229712

ABSTRACT

AIM: The aim of this study was to evaluate the effectiveness of meperidine, administered during the first stage of labor in patients with uterine dystocia, on the duration of labor and neonatal acid-base status at birth. MATERIAL AND METHODS: We randomly assigned 240 nulliparous women with a singleton pregnancy at term who were diagnosed with uterine dystocia in labor at 4-6-cm cervical dilatation to receive either a single dose of 50 mg meperidine in 10 mL of saline (slow intravenous injection over 2 min) or 10 mL of isotonic saline (control group). The primary outcome measures were duration of labor (from the time of beginning of the intervention to the time of the expulsion of the fetal head) and umbilical cord arterial acid-base status. RESULTS: The evidence revealed no statistically significant difference between the two groups in length of labor (188.2 ± 92.3 min in the meperidine group compared to 205.4 ± 96.1 min in the placebo group, P = 0.159). The pH of the umbilical cord arterial samples was lower in the meperidine group than in the control group, although the difference was not statistically significant (P = 0.089). CONCLUSION: Because of the absence of any beneficial effect of meperidine on uterine dystocia, its use in labor should be limited to pain relief in the absence of epidural analgesia.


Subject(s)
Acid-Base Equilibrium/drug effects , Analgesics, Opioid/therapeutic use , Dystocia/drug therapy , Labor, Obstetric/drug effects , Meperidine/therapeutic use , Adolescent , Adult , Double-Blind Method , Female , Humans , Hydrogen-Ion Concentration , Infant, Newborn , Pregnancy , Prospective Studies , Time Factors
4.
Int J Gynaecol Obstet ; 113(2): 137-40, 2011 May.
Article in English | MEDLINE | ID: mdl-21334621

ABSTRACT

OBJECTIVE: To evaluate the effect of antichlamydial treatment and Chlamydia pneumoniae seroconversion on the incidence of pre-eclampsia among Egyptian primigravidae. METHODS: The present prospective study included 600 healthy normotensive primigravidae who attended an outpatient clinic at 10-16weeks of pregnancy. A single venous blood sample was collected to test for C. pneumonia-specific immunoglobulin G (IgG) antibodies using an enzyme-linked immunosorbent assay. Seropositive women were randomly allocated to receive or not receive antichlamydial treatment before 20weeks of pregnancy. Seronegative participants had another test at delivery for the presence of C. pneumonia-specific IgG to determine seroconversion. All participants were followed up for up to 8weeks postpartum and observed for the development of pre-eclampsia. RESULTS: The rate of pre-eclampsia among seropositive participants differed significantly depending on whether the women received treatment or not (6.5% and 19.1%, respectively; P=0.014). No statistically significant difference in the rate of pre-eclampsia was detected between seronegative participants who underwent seroconversion and those who did not. CONCLUSION: The present results indirectly support the hypothesis that infectious agents (in particular C. pneumoniae) have a role in the development of pre-eclampsia. The findings also indicate that antichlamydial treatment might help to reduce the incidence of pre-eclampsia.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Chlamydophila Infections/complications , Chlamydophila pneumoniae/isolation & purification , Pre-Eclampsia/epidemiology , Chlamydophila Infections/diagnosis , Chlamydophila Infections/drug therapy , Chlamydophila pneumoniae/immunology , Egypt/epidemiology , Enzyme-Linked Immunosorbent Assay , Female , Follow-Up Studies , Humans , Immunoglobulin G/blood , Mass Screening/methods , Pre-Eclampsia/etiology , Pregnancy , Prenatal Care/methods , Prospective Studies , Serologic Tests/methods
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