Hyperemesis Gravidarum and 75 Gram Oral Glucose Tolerance Test
Słowa kluczowe
Abstrakcyjny
Opis
This retrospective controlled study conducted by Obstetrics and Gynecology clinics of Kayseri Training and Research Hospital.Pregnant women who delivered at the Kayseri Education and Training Hospital of Medicine, in Turkey, between January 2010 and September 2016 were identified.This study was carried out with two groups. The study group consisted of women hospitalized for Hyperemesis gravidarum (HEG) during first trimester of their pregnancy, whereas the control group included all other women who delivered in the same period.Screening for GDM was performed twice during pregnancy. The first screening was performed during the first trimester using the random plasma glucose test with a cutoff value of 109 mg/dl. Screening for GDM was performed for all women during their first prenatal visit, regardless of the presence or absence of hyperemesis-associated symptoms.The second screening was performed during the second trimester, between 24 and 27 weeks, using a 75-g oral glucose tolerance test (OGTT), after pregnant women with HEG got rid of hyperemesis. GDM was diagnosed on the basis of the universal criteria established by the International Association of Diabetes and Pregnancy Study Group: a plasma glucose level that met or exceeded the fasting cutoff value 92 mg/dl, the first-hour cutoff value 180 mg/dl, or the second-hour cutoff value 153mg/dl.
To be considered for diagnosis of pre-gestational diabetes mellitus, women had to meet at least one of the following criteria: the fasting plasma glucose test with a cutoff value of 126 mg/dl or the random plasma glucose test with a cutoff value of 200 mg/dl or the second-hour cutoff value 153mg/dl after 75 gram OGGT (American Diabetes Association) The delivery midwifery and medical records were retrospectively evaluated. All of the patient's body mass index (BMI,calculated as weight in kilograms divided by the square of height in meters), urine ketone levels and ages were recorded separately both in the initial exam and during performing 75 gram OGTT.
Daktyle
| Ostatnia weryfikacja: | 03/31/2017 |
| Pierwsze przesłane: | 11/09/2016 |
| Szacowana liczba przesłanych rejestracji: | 11/09/2016 |
| Wysłany pierwszy: | 11/14/2016 |
| Ostatnia aktualizacja przesłana: | 04/11/2017 |
| Ostatnia opublikowana aktualizacja: | 04/12/2017 |
| Rzeczywista data rozpoczęcia badania: | 12/31/2015 |
| Szacowana data zakończenia podstawowej działalności: | 10/31/2016 |
| Szacowana data zakończenia badania: | 10/31/2016 |
Stan lub choroba
Faza
Grupy ramion
| Ramię | Interwencja / leczenie |
|---|---|
| hyperemesis gravidarum group The study group consisted of women hospitalized for hyperemesis during first trimester of their pregnancy | |
| the control group whereas the control group included all other women who delivered in the same period. |
Kryteria kwalifikacji
| Wiek kwalifikujący się do nauki | 18 Years Do 18 Years |
| Płeć kwalifikująca się do nauki | Female |
| Metoda próbkowania | Non-Probability Sample |
| Przyjmuje zdrowych wolontariuszy | tak |
| Kryteria | Inclusion Criteria: - between 18 and 35 years-old singleton pregnancies and performed 75 gram OGTT Exclusion Criteria: - Other causes lead to nausea and vomiting in pregnancy such as gastroenteritis, gastroparesis, hepatitis, intestinal obstruction, peptic ulcer, appendicitis, pyelonephritis, urolithiasis, ovarian torsion, diabetes mellitus, hyperthyroidism, hyperparathyroidism, migraine. - And also patients who have risks for GDM such as body mass index > 30, history of GDM in previous pregnancy and diabetes in the family were excluded. |
Wynik
Podstawowe miary wyników
1. To determine serum glucose levels in both groups during 75 gram oral glucose tolerance test screening [3 months]
