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1.
Article in English | MEDLINE | ID: mdl-35564596

ABSTRACT

This exploratory study aimed to evaluate the effects of antenatal corticosteroids in singleton pregnancies of Asian women prior to elective cesarean section (CS) at early term on neonatal respiratory outcomes. METHODS: This is a pilot and pragmatic randomized trial conducted at a university hospital in Malaysia. Women with singleton pregnancies planned for elective CS between 37+0 and 38+6 weeks gestation were randomly allocated into the intervention group, where they received two doses of IM dexamethasone 12 mg of 12 h apart, 24 h prior to surgery OR into the standard care, control group, and both groups received the normal routine antenatal care. The primary outcome measures were neonatal respiratory illnesses, NICU admission and length of stay. RESULTS: A total of 189 patients were recruited, 93 women in the intervention group and 96 as controls. Between the steroid and control groups, the mean gestation at CS was similar, 266.1 ± 3.2 days (38 weeks) vs. 265.8 ± 4.0 days (37+6 weeks), p = 0.53. The mean birthweight of infants was 3.06 ± 0.41 kg vs. 3.04 ± 0.37 kg, p = 0.71. Infants with respiratory morbidities were primarily due to transient tachypnea of newborn (9.7% vs. 6.3%), and congenital pneumonia (1.1% vs. 3.1%) but none had respiratory distress syndrome. Only four infants required NICU admission (2.2% vs. 3.1%, p = 0.63). Their average length of stay was not statistically different; 3.5 ± 2.1 days vs. 5.7 ± 1.5 days, p = 0.27. CONCLUSIONS: Elective CS at early term before 39 weeks was associated with a modest overall incidence of neonatal respiratory illness (10.1%) in this Asian population. Antenatal dexamethasone did not diminish infants needing respiratory support, NICU admission and length of stay.


Subject(s)
Cesarean Section , Respiratory Distress Syndrome, Newborn , Adrenal Cortex Hormones/therapeutic use , Dexamethasone/therapeutic use , Female , Gestational Age , Humans , Infant , Infant, Newborn , Pregnancy , Respiratory Distress Syndrome, Newborn/epidemiology , Respiratory Distress Syndrome, Newborn/prevention & control
2.
Horm Mol Biol Clin Investig ; 39(2)2019 Jul 13.
Article in English | MEDLINE | ID: mdl-31301670

ABSTRACT

Beta-thalassemia major is a subtype component of hemoglobinopathies; autosomal recessive disorders complicated with anemia that affect at least 50,000 babies each year. It contributes to problems in reproductive entities such as infertility due to iron deposition in the endocrine organs, which leads to malfunction of the hypothalamus-pituitary axis. Due to this, there have been very few pregnancies discovered and reported with this type of condition as they usually required an ovulation-induction agent with assisted reproductive technique to achieved pregnancy. We report a successful spontaneous pregnancy in a woman with beta-thalassemia major who underwent splenectomy with lifelong transfusion-dependence complicated with myocardial siderosis and osteoporosis. The close monitoring and regular blood transfusion are a core of successful support to this type of pregnancy. The unintentional consumption of Fosamax, hydroxyurea and deferiprone (Ferriprox) up till 20 weeks of gestation did not show any adverse effects on fetal well-being. As expected, this pregnancy ended with the preterm delivery via cesarean section due to intrauterine growth restriction with oligohydramnios, and currently, this child is thriving. We concluded that pregnancy is not a contraindication in beta-thalassemia major; complex individual care is needed to achieve a safe outcome for the mother.


Subject(s)
Cardiomyopathies/etiology , Homozygote , Osteoporosis/etiology , Siderosis/etiology , beta-Globins/genetics , beta-Thalassemia/complications , Blood Transfusion , Cardiomyopathies/diagnosis , Cardiomyopathies/drug therapy , Deferiprone/administration & dosage , Deferiprone/therapeutic use , Female , Humans , Iron Chelating Agents/administration & dosage , Iron Chelating Agents/therapeutic use , Osteoporosis/drug therapy , Pregnancy , Pregnancy Complications , Pregnancy Outcome , Siderosis/diagnosis , Siderosis/drug therapy , Splenectomy/methods , Young Adult , beta-Thalassemia/diagnosis , beta-Thalassemia/etiology
3.
Horm Mol Biol Clin Investig ; 30(3)2016 Nov 15.
Article in English | MEDLINE | ID: mdl-27845881

ABSTRACT

Wernicke's encephalopathy (WE) is a rare life-threatening complication following severe hyperemesis gravidarum. Early recognition of this condition and prompt thiamine administration is the key to preventing devastating sequelae. We report a successful delivery of a small-for-gestational-age (SGA) baby by a patient with WE and thyrotoxicosis in pregnancy.


Subject(s)
Hyperemesis Gravidarum/complications , Thiamine/therapeutic use , Thyrotoxicosis/complications , Wernicke Encephalopathy/complications , Adult , Birth Weight , Female , Humans , Hyperemesis Gravidarum/therapy , Infant, Newborn , Live Birth , Male , Pregnancy , Thyrotoxicosis/therapy , Wernicke Encephalopathy/therapy
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