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1.
J Obstet Gynaecol ; 40(2): 200-204, 2020 Feb.
Article in English | MEDLINE | ID: mdl-31347423

ABSTRACT

This study aimed to investigate if the pregnancy associated plasma Protein-A (PAPP-A) multiples of median (MoM) levels could be used as a marker for the early prediction of RDS. The present study was designed with data gathered from 1773 patients who were referred to our institution for first trimester fetal chromosomal anomaly screening. First trimester PAPP-A MoM values and postnatal RDS occurrences in these pregnancies were retrospectively analysed. Of the 1773 neonates that were included in the study, 28 were delivered at or beyond 37 weeks, and 42 were delivered less than 37 weeks of gestation. In the group of neonates at or beyond 37 weeks, the cut-off value for RDS prediction was determined as 1.02. For this cut-off value, sensitivity was 72.41% and specificity was 91.84%. The area under curve (AUC) was determined to be statistically significant (p < .01). In conclusion, it was determined that in neonates that were delivered at or beyond 37 weeks of gestation, RDS occurrence could be predicted at a significant rate by utilising PAPP-A MoM values.IMPACT STATEMENTWhat is already known on this subject? Respiratory distress syndrome (RDS) is one of the major global healthcare problems, and continues to effect newborns despite the improvements in diagnosis and treatments of the disease. Studies have shown that pregnancy associated plasma protein-A (PAPP-A) has a critical role in cellular proliferation and differentiation, and it is closely associated with many physiological and pathological processes via regulation of local insulin like growth factor (IGF) concentrations. In majority of the past studies in the literature regarding PAPP-A values in pregnancies, the association between low values of PAPP-A MoM and maternal-fetal complications were investigated.What do the results of this study add? This study retrospectively examines the PAPP-A MoM levels and the occurence of RDS. In neonates that were delivered at or beyond 37 weeks of gestation, RDS occurrence could be predicted at a significant rate by utilising PAPP-A MoM values which was measured at the first trimester fetal anomaly screening test.What are the implications of these findings for clinical practice and/or further research? In the light of these findings, in order to reduce RDS related neonatal morbidity and mortality, pregnancies with PAPP-A MoM values greater than 1.02 at the first trimester fetal anomaly screening should be more closely followed up and a higher rate of suspicion should be kept for RDS occurrence.


Subject(s)
Maternal Serum Screening Tests/statistics & numerical data , Pregnancy Trimester, First/blood , Pregnancy-Associated Plasma Protein-A/analysis , Respiratory Distress Syndrome, Newborn/epidemiology , Term Birth , Adult , Area Under Curve , Biomarkers/blood , Female , Humans , Incidence , Infant, Newborn , Predictive Value of Tests , Pregnancy , Reference Values , Retrospective Studies , Sensitivity and Specificity
2.
Ginekol Pol ; 87(5): 399-404, 2016.
Article in English | MEDLINE | ID: mdl-27304659

ABSTRACT

OBJECTIVES: To compare the 'strictly' active management protocol in women with low risk of postpartum hemorrhage using the expectant management protocol with respect to changes in hematologic parameters, uterotonics, blood transfusions, or additional interventions. MATERIAL AND METHODS: A randomized controlled prospective trial in which 934 singleton parturients enrolled; 654 were randomly assigned to the active and mixed management groups. The primary outcome parameter was the reduction in hemoglobin concentrations due to delivery, and the secondary outcome parameters were changes in hemoglobin of more than 3 g/dL (ΔHb ≥ 3 g/dL), durations of the third stage of labor, need for additional uterotonic agents, blood transfusions, manual removal of the placenta, and surgical evacuation of retained products of conception. RESULTS: The mean postpartum hemoglobin concentration was significantly higher (P = 0.04) in the active management group with a significantly lower reduction (P = 0.03). Falls of hemoglobin levels of more than 3 g/dL (ΔHb ≥ 3g/dL) were less common in the active management group though not significantly (P = 0.32). The mean duration of the third stage of labor was significantly (P < 0.001) shorter in the active management group. There was no significant difference between the two groups with regard to the need for additional uterotonic agents, uterine atony, blood transfusion, manual removal of the placenta, surgical evacuation of retained products of conception, and prolonged third stage of labor. CONCLUSIONS: Although active management of the third stage of labor was associated with higher postpartum hemoglobin levels, it did not influence the risk of 'severe postpartum hemorrhage' in women with low risk of postpartum hemorrhage.


Subject(s)
Clinical Protocols/standards , Delivery, Obstetric , Monitoring, Physiologic/methods , Postpartum Hemorrhage , Adult , Blood Transfusion/statistics & numerical data , Delivery, Obstetric/adverse effects , Delivery, Obstetric/methods , Female , Hemoglobins/analysis , Humans , Labor Stage, Third , Oxytocics/therapeutic use , Parturition , Postpartum Hemorrhage/diagnosis , Postpartum Hemorrhage/prevention & control , Pregnancy , Pregnancy Outcome , Risk Adjustment/methods , Risk Factors , Time Factors
3.
J Pediatr Surg ; 50(7): 1205-9, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25783344

ABSTRACT

PURPOSE: The purpose of the study is to evaluate the effect of vardenafil on the histopathology and biochemical parameters in reducing damage in experimental ovarian ischemia and ischemia/reperfusion injury in a rat model and to compare the effect of two different doses of vardenafil. METHODS: Forty-two rats with experimental ovarian torsion. Group-I: sham; Group-II: ovarian ischemia; Group-III: 2 hours of ischemia followed by a 2-hour reperfusion. Group-IV: two hours before the sham operation, rats received 1mg/kg vardenafil; Group V and VI: A 2-hour period of ovarian ischemia was applied, in which rats were treated with intraperitoneal vardenafil 1 and 2mg/kg dose, after 1.5 hours of ovarian ischemia. After 2 hours of reperfusion, the ovaries on the right side were removed for examination. The ovarian ischemia/reperfusion injury was evaluated by calculating total antioxidant status, total oxidant status and oxidative stress index; and histopathologic examination of all ovarian rat tissue. RESULTS: The histologic findings in vardenafil treatment groups were statistically significant decreased edema and follicle degeneration, with vascular congestion, hemorrhage and follicle degeneration being dose-dependent. There were no statistically significant changes in the biochemical parameters. CONCLUSIONS: According to histopathological examination, low and high dose vardenafil is effective in attenuating ischemia-reperfusion induced ovary injury.


Subject(s)
Ovarian Diseases/drug therapy , Ovary/blood supply , Reperfusion Injury/drug therapy , Torsion Abnormality/complications , Vardenafil Dihydrochloride/administration & dosage , Vasodilator Agents/administration & dosage , Animals , Antioxidants/therapeutic use , Female , Ischemia/pathology , Ovarian Diseases/pathology , Oxidative Stress/drug effects , Rats , Rats, Wistar , Reperfusion Injury/pathology
4.
J Matern Fetal Neonatal Med ; 28(14): 1716-9, 2015.
Article in English | MEDLINE | ID: mdl-25231598

ABSTRACT

OBJECTIVE: The aim of the present study was to evaluate the utility of ductus venosus (DV) and hepatic artery (HA) doppler in pregnant women who have high risk for aneuploidy in first trimester combined screening. METHODS: This prospective study was performed between February 2011 and February-2012, at a tertiary referral hospital. Singleton pregnancies with high risk for aneuploidy in combined screening test and normal nuchal translucency (NT) measurements were included in the study group. Measurements of DV Pulsatility Index of Veins (PIV) and HA Pulsatility Index (PI) were compared between the study group and controls. RESULTS: Within the study period, 104 women with singleton pregnancies were evaluated for DV and HA measurements and among these, 64 women met the inclusion criteria. A control group that comprised 40 women with similar gestational age, normal NT measurements and low-risk in first trimester combined tests was generated. DV-PIV measurements were significantly higher (p = 0.03), whereas HA-PI measurements were similar (p > 0.05) in women who had high-risk for aneuploidy in first trimester combined test. CONCLUSION: We concluded that the addition of DV-PIV and HA-PI measurements to the first trimester combined screening might increase the accuracy for Down syndrome detection.


Subject(s)
Down Syndrome/diagnostic imaging , Hepatic Artery/diagnostic imaging , Pregnancy Trimester, First , Ultrasonography, Doppler , Ultrasonography, Prenatal/methods , Umbilical Veins/diagnostic imaging , Adult , Case-Control Studies , Female , Hepatic Artery/embryology , Hepatic Artery/physiology , Humans , Pregnancy , Prospective Studies , Pulsatile Flow , Umbilical Veins/embryology , Umbilical Veins/physiology
5.
Int J Gynaecol Obstet ; 126(2): 123-5, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24792406

ABSTRACT

OBJECTIVE: To investigate the effects of long-lasting maternal fasting on fetal biometry, amniotic fluid volume, fetal Doppler parameters, and neonatal outcomes. METHODS: The present study, conducted at Solhan State Hospital, Bingol, Turkey, between July and August 2013 recruited 82 healthy and otherwise normal pregnant women with a gestational age of 29 weeks or more who were fasting for at least 20 days. The control group comprised 87 healthy non-fasting women matched for maternal age, parity, gestational age. Fetal parameters were measured at the beginning and the end of the fasting month. Perinatal outcomes were compared between the groups. RESULTS: There were no significant differences between the groups in fetal biometry, fetal Doppler parameters, or neonatal outcomes. In the fasting group, however, there was a significantly greater decrease in amniotic fluid index during the fasting period (P<0.001). The number of women who initially had a normal amniotic fluid measurement and subsequently developed oligohydramnios was also significantly higher in the religious fasting group (P<0.05). CONCLUSION: Fetal development, Doppler parameters, and neonatal outcomes were not significantly affected in healthy fasting women; however, there was a significant association between fasting and amniotic fluid index. These findings mandate more frequent follow-up visits for this group of women.


Subject(s)
Amniotic Fluid/diagnostic imaging , Fasting/adverse effects , Oligohydramnios/etiology , Ultrasonography, Prenatal , Adult , Amniotic Fluid/physiology , Fasting/physiology , Female , Gestational Age , Humans , Infant, Newborn , Islam , Oligohydramnios/diagnostic imaging , Pregnancy
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