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1.
Gynecol Oncol ; 116(1): 28-32, 2010 Jan.
Article in English | MEDLINE | ID: mdl-19875161

ABSTRACT

OBJECTIVE: To compare the incidence of pelvic lymph node metastases in early stage cervical cancer patients undergoing sentinel lymph node biopsy (SLN) to a matched cohort undergoing pelvic lymphadenectomy. METHODS: All patient data were entered prospectively into an ongoing cervical cancer database. Since April 2004, 87 patients with FIGO stage IA/B1 cervical cancer underwent SLN detection with identification of bilateral SLN. This cohort (cases) was compared to a matched group of patients who underwent complete pelvic lymphadenectomy (controls). The groups were matched 3:1 for tumour size (+/-5 mm), histology, depth of invasion (+/-2 mm), and presence of capillary lymphatic space invasion (CLS). Descriptive statistics were calculated for all variables of interest. The association between cases and controls and lymph node metastases was carried out using a conditional logistic regression analysis. RESULTS: 81 women in the SLN cohort were matched with 1 control, 72 cases with 2 controls, and 65 cases with 3 controls. Among cases, 14 (17%) had pelvic lymph nodes metastases vs. 15 (7%) in the controls (p=0.0059, odds ratio= 2.8, 95% CI=1.3-5.9). Among the 14 cases of SLN metastases, 11 were detected by frozen section and 3 were detected on final paraffin sectioning. All were detected by H and E stains. The size of the SLN metastases ranged from less than 1 mm to 8 mm. CONCLUSIONS: Sentinel lymph node biopsy in early cervical cancer is a more sensitive procedure in detecting pelvic lymph node metastases compared to complete lymphadenectomy.


Subject(s)
Lymph Nodes/pathology , Lymph Nodes/surgery , Uterine Cervical Neoplasms/pathology , Uterine Cervical Neoplasms/surgery , Adult , Case-Control Studies , Cohort Studies , Female , Humans , Lymph Node Excision , Lymphatic Metastasis , Neoplasm Staging/standards , Sentinel Lymph Node Biopsy
2.
Eur J Clin Microbiol Infect Dis ; 25(7): 443-8, 2006 Jul.
Article in English | MEDLINE | ID: mdl-16802129

ABSTRACT

A high prevalence of maternal group B Streptococcus (GBS) carriage and an extremely low incidence of invasive neonatal disease have been reported from southern Israel. In order to obtain insight into this discrepancy, this study was performed to determine the population structure of GBS from asymptomatic pregnant women living in this area. Seventy-two strains from maternal GBS carriers were characterized using multilocus sequence typing (MLST). Epidemiologic characteristics of the carriers and their newborns, including demographic variables, obstetric status, and general health parameters, were collected by means of a postpartum interview and a review of the relevant medical records. The MLST analysis grouped the bacteria into six different lineages (clonal complexes). Lineage ST-2 was prevalent among Bedouin-Arabs (p=0.01) and lineage ST-22 among Jews (p=0.001). Lineage ST-17 was prevalent among carriers who emigrated after 1997 from western nations of the former USSR (p<0.001). Lineage ST-22 was associated with carriage of surface-protein C (p=0.01) and lineage ST-17 with surface-protein R (p<0.01). Lineage ST-2 was prevalent among consumers of antibiotics (p=0.02) and was associated with erythromycin-resistant strains (p<0.001). Each subgroup of the southern Israeli maternal population has a different distribution of GBS clones. The clones prevalent among the Bedouin-Arabs and the Jews are known to be of low virulence. Lineage ST-17, which is associated with invasive disease, is prevalent among women who emigrated from western Soviet nations. Therefore, a different policy of GBS prophylaxis, resembling the one executed in endemic areas, should be considered in this population.


Subject(s)
Carrier State/epidemiology , Streptococcal Infections/epidemiology , Streptococcus agalactiae/classification , Arabs/ethnology , Carrier State/microbiology , DNA, Bacterial/analysis , Female , Humans , Infant, Newborn , Israel/epidemiology , Jews/ethnology , Phylogeny , Pregnancy , Sequence Analysis, DNA , Serotyping , Streptococcal Infections/microbiology , Streptococcus agalactiae/genetics , USSR/ethnology
3.
Arch Mal Coeur Vaiss ; 96(4): 305-10, 2003 Apr.
Article in French | MEDLINE | ID: mdl-12741306

ABSTRACT

The diagnosis of unstable angina (troponine undetectable) is often difficult in the absence of electrocardiographic changes after suggestive chest pains. The object of this study was to analyse the kinetics of Brain Natiuretic Peptide (BNP) during acute coronary syndromes (ACS) without ST elevation. Plasma BNP was measured every 6 hours for 48 hours in 65 patients admitted for suspicion of ACS without ST elevation and without clinical, radiological or echocardiographic signs of left ventricular dysfunction. The results of BNP measurements were masked until the final diagnosis was established on the usual investigations (ECG changes, troponine I values, myocardial scintigraphy, coronary angiography). These investigations identified 3 groups of patients: non-Q wave infarction (group A: 19 patients), unstable angina (group B: 21 patients) and non-coronary chest pain (group C: 25 patients). The peak BNP was significantly higher in groups A (210 +/- 172 pg/ml) and B (152 +/- 159 pg/ml) than in group C (16 +/- 14 pg/ml). However, the BNP was normal or only slightly increased (< 50 pg/ml) in 25% of cases of ACS. Analysis of the kinetics of BNP was much more discriminating: early increase after the pain, peak between the 14th and 24th hours (19th hour on average), followed by a progressive decrease. The kinetics were identical in Groups A and B, contrasting with the flat profile of the curve in group C. A change of > 20 pg/ml in BNP was a better criterion of ACS with a diagnostic accuracy > 90% than increased troponine (group A) or undetectable troponine (group B). The authors conclude that BNP kinetics is a new and reliable diagnostic marker of unstable angina when the usual criteria of ACS are not present (notably a normal ECG and undetectable troponine).


Subject(s)
Angina, Unstable/diagnosis , Natriuretic Peptide, Brain/blood , Aged , Biomarkers/blood , Chest Pain/etiology , Coronary Disease/classification , Coronary Disease/diagnosis , Female , Humans , Kinetics , Male , Middle Aged , Reference Values , Reproducibility of Results , Time Factors
4.
J Matern Fetal Neonatal Med ; 13(1): 45-9, 2003 Jan.
Article in English | MEDLINE | ID: mdl-12710856

ABSTRACT

OBJECTIVE: To determine the incidence, obstetric risk factors and pregnancy outcome of placental abruption at term. METHODS: A comparison of all singleton term deliveries (> or = 37 weeks' gestation) complicated with placental abruption to singleton term deliveries without placental abruption. Multivariate analysis was performed to investigate independent risk factors for placental abruption. RESULTS: Placental abruption complicated 0.3% of all term deliveries (n = 72,995). A multiple logistic regression model with backward elimination found the following factors to be independently associated with the occurrence of placental abruption in term pregnancies: pregnancy-induced hypertension (PIH), intrauterine growth restriction (IUGR), non-vertex presentation, hydramnios and advanced maternal age. Perinatal mortality was significantly higher in pregnancies complicated with placental abruption (OR = 30.0, 95% CI 19.7-45.6; p < 0.001). In order to assess whether the increased risk for perinatal mortality was due to the placental abruption or to its significant association with other risk factors, a multivariate analysis was constructed with perinatal mortality as the outcome variable. Placental abruption (OR = 50.5, 95% CI 32.2-79.1), cord prolapse, small for gestational age and congenital malformations were found to be independent risk factors for perinatal mortality. CONCLUSION: Abruption of the placenta at term was found to be significantly associated with PIH, non-vertex presentation, IUGR, hydramnios and advanced maternal age. Owing to the independent association found between placental abruption and perinatal mortality, these conditions should be carefully evaluated in order to reduce the occurrence of placental abruption.


Subject(s)
Abruptio Placentae/etiology , Abruptio Placentae/physiopathology , Labor, Obstetric , Pregnancy Complications , Abruptio Placentae/epidemiology , Adult , Female , Fetal Growth Retardation/complications , Humans , Hypertension/complications , Labor Presentation , Maternal Age , Multivariate Analysis , Polyhydramnios/complications , Pregnancy , Pregnancy Complications, Cardiovascular , Pregnancy Outcome , Pregnancy, High-Risk , Risk Factors
5.
Arch Mal Coeur Vaiss ; 94(9): 1017-20, 2001 Sep.
Article in French | MEDLINE | ID: mdl-11603065

ABSTRACT

The generalisation of the use of transthoracic echocardiography in the investigation of pulmonary embolism leads to the diagnosis of mobile right heart thrombus in about 5% of cases. A review of the literature shows that this association is mainly observed in clinically severe pulmonary embolism. The presence of a mobile right heart thrombus is associated with a poor prognosis and emergency treatment is based on thrombolytic therapy or surgical embolectomy. In minimal or infraclinical pulmonary embolism, the finding of a mobile right heart thrombus is rare and there is no consensus about its treatment. The authors report the case of a 61 year old man admitted to hospital for bilateral deep vein thrombosis with no symptoms of pulmonary embolism in whom investigations revealed a mobile right heart thrombus with minimal pulmonary embolism. The outcome was favourable with progressive resolution of the right heart thrombus with oral anticoagulation after three weeks of heparin therapy.


Subject(s)
Coronary Thrombosis/complications , Pulmonary Embolism/etiology , Anticoagulants/therapeutic use , Coronary Thrombosis/pathology , Heparin/therapeutic use , Humans , Male , Middle Aged , Prognosis , Pulmonary Embolism/pathology , Severity of Illness Index , Treatment Outcome , Venous Thrombosis/complications
6.
J Matern Fetal Med ; 10(6): 393-7, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11798449

ABSTRACT

OBJECTIVES: To assess the perinatal outcome of teenage pregnancy in a large cohort and to determine risk factors for low birth weight (LBW) in teenage pregnancy. STUDY DESIGN: All singleton first deliveries to mothers of age 16-24 years between 1990 and 1997 were included. The deliveries were subdivided into three maternal age groups (16-17 and 18-19 compared to 20-24 years) and parameters of perinatal outcomes were compared. To adjust for potential confounding effects on the association between young maternal age and birth weight, logistic regression analysis was performed for LBW with maternal ethnicity, pregnancy-induced hypertension, lack of prenatal care and malformations of the newborn. RESULTS: Among a total of 11 496 patients, 600 (5.2%) were 16-17 years old, 2097 (18.2%) were 18-19 years old and the remaining 8799 (76.6%) were 20-24 years old. Bedouin ethnicity and lack of prenatal care were common in the youngest mothers. Rates of preterm delivery were 14.2%, 9.8% and 8.8% in the three age groups, respectively (p < 0.05). Rates of malformations, small for gestational age, LBW and very LBW were also significantly higher in the youngest mothers. Rates of pregnancy-induced hypertension, operative delivery and Cesarean delivery were not significantly different among the three age groups. A multivariate analysis on LBW was performed to assess the unique contribution of young maternal age, adjusted for potential confounders. Adjusted ORs for LBW were 1.25 (95% CI 1.00-1.56) for maternal age < 18 years, 1.80 (95% CI 1.54-2.03) for Bedouin ethnicity, 2.57 (95% CI 2.14-3.07) for pregnancy-induced hypertension, 1.55 (95% CI 1.30-1.84) for lack of prenatal care and 4.09 (95% CI 3.2-5.2) for malformations. CONCLUSIONS: Teenage pregnancy was found to be associated with adverse outcome such as LBW, preterm delivery, small for gestational age and malformations. The risk for LBW was affected mainly by demographic factors (maternal ethnicity, lack of prenatal care) and medical factors (pregnancy-induced hypertension, malformations).


Subject(s)
Pregnancy Complications/epidemiology , Pregnancy Complications/etiology , Pregnancy in Adolescence/statistics & numerical data , Adolescent , Adult , Age Distribution , Age Factors , Arabs/statistics & numerical data , Child , Female , Humans , Infant, Low Birth Weight , Infant, Newborn , Infant, Premature , Israel/ethnology , Jews/statistics & numerical data , Logistic Models , Pregnancy , Pregnancy Complications/ethnology , Pregnancy Outcome/ethnology , Pregnancy in Adolescence/ethnology , Prenatal Care/statistics & numerical data , Risk Factors
7.
J Reprod Med ; 46(11): 1017-20, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11762146

ABSTRACT

BACKGROUND: Transverse vaginal incision during cesarean section, also known as anterior vaginotomy, is a recognized entity, mostly made unintentionally. CASES: At our institution, four patients underwent a transverse vaginal incision during cesarean section over an eight-year period. In three of them, excessive bleeding required blood transfusion. In one case, only hypogastric artery ligation resulted in bleeding control. None of the patients had subsequent vaginal deliveries. CONCLUSION: The exact incidence of anterior vaginotomy is difficult to evaluate. Accidental vaginal incision occurs mostly following a prolonged second stage of labor but is possible during the first stage. Risk factors include prolonged second stage of labor and an emergency setup. Reported complications resulting from anterior vaginotomy include excessive hemorrhage, with a possible need for hysterectomy, difficult approximation, and bladder or ureter injury. Massive bleeding and multiple blood transfusions occurred in our series as well. Fetal outcome and future obstetric behavior do not seem to be compromised. A high index of suspicion is essential when trying to avoid accidental anterior vaginotomy. Meticulous hemostasis, a search for bladder injury and anatomic closure are mandatory when managing this complication.


Subject(s)
Accidents , Cesarean Section/adverse effects , Colpotomy , Medical Errors/adverse effects , Vagina/injuries , Adult , Female , Humans , Pregnancy
8.
J Reprod Med ; 45(7): 588-90, 2000 Jul.
Article in English | MEDLINE | ID: mdl-10948473

ABSTRACT

BACKGROUND: Hypophosphatasia is a rare autosomal recessive metabolic disorder characterized by low serum and tissue alkaline phosphatase activity, increased urinary excretion of phosphoethanolamine and ricketslike changes in the bone. CASE: We present a case of prenatal diagnosis of congenital hypophosphatasia in a consanguineous Bedouin couple. The case was diagnosed at 24.5 weeks of gestation. Sonographic evaluation revealed a fetus with short and deformed bones and a hypoechogenic skull. Based on the sonographic findings and the obstetric history of the couple, hypophosphatasia was diagnosed. The parents opted for pregnancy termination. Feticide was accomplished uneventfully. Laboratory findings confirmed the diagnosis. CONCLUSION: This couple was prone to this metabolic disorder due to their consanguineous marriage and previous affected fetus. Early-first-trimester prenatal diagnosis by first-trimester chorionic villus sampling or second-trimester measuring of alkaline phosphatase activity in the amniotic fluid is required to exclude this lethal disease in subsequent pregnancies.


Subject(s)
Fetal Diseases/diagnosis , Hypophosphatemia, Familial/diagnosis , Prenatal Diagnosis , Ultrasonography, Prenatal , Abnormalities, Multiple/diagnostic imaging , Adult , Female , Fetal Diseases/diagnostic imaging , Humans , Hypophosphatemia, Familial/diagnostic imaging , Pregnancy , Pregnancy Trimester, First
9.
Rev Prat ; 50(1): 30-5, 2000 Jan 01.
Article in French | MEDLINE | ID: mdl-10731824

ABSTRACT

Acute cardiogenic pulmonary oedema is a medical emergency. It generally result from an acute left ventricular insufficiency, itself resulting from systolic or diastolic dysfunction (alteration in relaxation or distensibility). Clinical presentation may be atypical, especially in the elderly. Treatment is based on oxygen, diuretics and nitrates. In severe cases, mechanical ventilation may be required.


Subject(s)
Pulmonary Edema/therapy , Ventricular Dysfunction, Left/complications , Aged , Diagnosis, Differential , Diuretics/therapeutic use , Emergency Medical Services , Humans , Oxygen/therapeutic use , Pulmonary Edema/diagnosis , Pulmonary Edema/etiology , Respiration, Artificial
10.
Harefuah ; 135(5-6): 175-80, 256, 1998 Sep.
Article in Hebrew | MEDLINE | ID: mdl-9885628

ABSTRACT

From 1989 to 1996, 139 cases of invasive Hemophilus influenzae B (Hib) infections were identified in children in the Negev, 110 of which occurred before introduction of the conjugate vaccine (1989-92). At that time there were 60.5 cases of Hib per 100,000 in the Negev among children under 5 years of age. During 1995-1996, when Hib conjugate vaccine was part of the regular immunization program, Hib decreased to 6.5 cases per 100,000 in that age group. The effectiveness of PRP-OMP vaccine was 96.5% among Jews and 89% among Bedouins, and the efficacy of the immunization program was 99.99%. This degree of success exceeded all expectations based on the literature. During the whole study period, Hib infections were more frequent among Bedouins than Jews. There was no significant difference in the occurrence of Hib among Jews in the Negev before and after the vaccine was introduced. Hib among Bedouins in the Negev was significantly more frequent than in the Israeli population as a whole before the vaccine was introduced. That gap narrowed after the vaccine was introduced because of the decrease in morbidity among the 2 groups.


Subject(s)
Haemophilus Infections/epidemiology , Haemophilus Vaccines , Vaccines, Conjugate , Arabs/statistics & numerical data , Child, Preschool , Haemophilus Infections/prevention & control , Haemophilus influenzae , Humans , Incidence , Infant , Israel/epidemiology , Jews/statistics & numerical data , Time Factors
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