Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Language
Publication year range
1.
J Matern Fetal Neonatal Med ; 29(8): 1339-43, 2016.
Article in English | MEDLINE | ID: mdl-26037723

ABSTRACT

OBJECTIVE: To compare the incidence of postpartum maternal and neonatal complications and hospital readmission in patients discharged 24 versus 72 h after cesarean section. METHODS: Using randomization, 1495 patients were discharged after 24 h and 1503 patients were discharged after 72 h. All patients fulfilled the discharge criteria. Patients were assessed 6 weeks after delivery, any maternal or neonatal problems or hospital readmissions during this time interval were reported. RESULTS: There was no difference in maternal hospital readmission between the two groups, but there was a significantly higher neonatal readmission rate in the 24-h group mainly due to neonatal jaundice. As for the complications reported after 6 weeks, the only two significant outcomes were initiating breast feeding, being significantly higher in the 72-h group [OR and 95% CI 0.77 (0.66-0.89)] and the mood swings being significantly lower in the 72-h group [OR and 95% CI 2.28 (1.94-2.68)]. CONCLUSION: Our recommendation is still in favor of late discharge, after cesarean delivery. Bearing in mind, that an early 24-h discharge, after cesarean delivery is feasible, but with special care of the neonate, with early visit to the pediatrician and early establishment of effective lactation.


Subject(s)
Cesarean Section , Patient Discharge , Adult , Breast Feeding , Egypt/epidemiology , Female , Humans , Infant, Newborn , Jaundice, Neonatal/epidemiology , Mood Disorders/epidemiology , Patient Readmission/statistics & numerical data , Pregnancy , Prospective Studies , Time Factors
2.
Gynecol Endocrinol ; 30(6): 428-30, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24592983

ABSTRACT

This study aimed at evaluating possible associations of the single nucleotide polymorphism (SNP) in luteinizing hormone/choriogonadotropin receptor (LHCGR) gene G935A and polycystic ovary syndrome (PCOS) phenotype. The study included 100 PCOS female patients and 60 healthy female control subjects. The patients were recruited from the Gynecology out-patient clinic, Kasr Al-Aini Hospital, Cairo University. All candidates underwent full history taking and clinical examination with calculation of body mass index. Serum and EDTA samples were collected from each patient after a written consent. A hormonal profile was done for each patient as well as DNA analysis of the G935A polymorphism of LHCGR gene. In PCOS group, 26% were homozygous (AA), 27% were heterozygous (GA) and 47% were wild genotype (GG), while in controls 30% were heterozygous and 70% were wild genotype (OR: 2.25; CI: 1.16-4.386; p value: 0.012). The homozygous 935A individuals were at higher risk to develop PCOS than controls (OR: 1.80; CI: 1.54-2.09; p value < 0.001).We found a genetic variant, which is associated with PCOS in a sample of the Egyptian population. These results may provide an opportunity to test this SNP at the LHCGR gene in fertile or infertile women with family history to assess their risk of PCOS.


Subject(s)
Polycystic Ovary Syndrome/genetics , Polymorphism, Single Nucleotide , Receptors, LH/genetics , Adult , Alleles , Amino Acid Substitution , Body Mass Index , Case-Control Studies , Egypt , Female , Gene Frequency , Genetic Association Studies , Genetic Predisposition to Disease , Heterozygote , Homozygote , Hospitals, University , Humans , Obesity/complications , Outpatient Clinics, Hospital , Polycystic Ovary Syndrome/blood , Polycystic Ovary Syndrome/complications , Polycystic Ovary Syndrome/metabolism , Receptors, LH/metabolism , Young Adult
3.
J Matern Fetal Neonatal Med ; 27(3): 279-82, 2014 Feb.
Article in English | MEDLINE | ID: mdl-23772990

ABSTRACT

OBJECTIVE: To compare the incidence of congenital anomalies by ultrasound in intracytoplasmic sperm injection (ICSI) pregnancies and in spontaneous pregnancies with correlation to the neonatal outcome. METHODS: This is a prospective comparative study carried out in Kasr Al Aini Hospital Cairo University from January 2010 to December 2012, comparing 739 pregnant women conceived through ICSI and 843 pregnant women conceived spontaneously as regard to incidence of congenital anomalies, multiple pregnancy, preterm labor, cesarean section and neonatal outcome. RESULTS: The number of anomalies diagnosed by antenatal ultrasound in ICSI group was 14 (1.62%) while in spontaneous group was 13 (1.51%). The number of anomalies detected by postnatal examination in ICSI group was 20 (2.31%) while in spontaneous group was 16 (1.86%) (Odds ratio [OR] 1.438; 95% confidence interval [CI] 0.739-2.796). ICSI group was associated with higher incidence of twins 12.7% (p < 0.001), preterm labor 3.8% (p 0.022), preterm premature rupture of membranes 4.6% (p 0.001), cesarean section 74.1% (p < 0.001) and neonatal deaths 10.4% (p < 0.001). CONCLUSION: ICSI was associated with higher incidence of multiple pregnancy and cesarean section, with no difference in the incidence of congenital anomalies compared to spontaneous conception.


Subject(s)
Congenital Abnormalities/etiology , Sperm Injections, Intracytoplasmic/adverse effects , Cesarean Section/statistics & numerical data , Congenital Abnormalities/diagnostic imaging , Congenital Abnormalities/epidemiology , Egypt/epidemiology , Female , Follow-Up Studies , Humans , Incidence , Odds Ratio , Pregnancy , Pregnancy, Twin/statistics & numerical data , Prospective Studies , Ultrasonography, Prenatal
SELECTION OF CITATIONS
SEARCH DETAIL
...