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1.
J Matern Fetal Neonatal Med ; 29(6): 954-61, 2016 Mar.
Article in English | MEDLINE | ID: mdl-25835381

ABSTRACT

OBJECTIVE: Lead (Pb), mercury (Hg) and cadmium (Cd) are environmental pollutants that are wide spread throughout the world. The present study aimed to investigate the level of exposure to Pb, Hg and Cd during the prenatal period, and the possible routes of maternal exposure to these toxic heavy metals. PARTICIPANTS: The study included 123 mothers and their newborns. Umbilical cord blood samples were collected immediately after delivery, and breast milk and newborn hair samples were collected between postpartum d 3 and 10. RESULTS: Among the 121 cord blood samples that were analyzed, Pb was present in 120 (99.2%) and the mean level was 1.66 ± 1.60 µg dL(-1) (range:

Subject(s)
Environmental Exposure , Fetal Blood/chemistry , Infant, Newborn/blood , Metals, Heavy/blood , Milk, Human/chemistry , Adult , Cross-Sectional Studies , Female , Hair/chemistry , Humans , Pregnancy , Risk Factors , Tobacco Smoke Pollution
2.
Turk J Pediatr ; 53(3): 261-8, 2011.
Article in English | MEDLINE | ID: mdl-21980806

ABSTRACT

Fetal malnutrition is an important risk factor for both early and late neonatal outcome and adult diseases. In this study, we aimed to investigate the incidence and characteristics of fetal malnutrition and its impacts on early neonatal morbidity and mortality in preterm infants by using the clinical assessment of nutritional status score (CANSCORE). Preterm infants whose gestational ages were between 28-34 weeks were included in the study. Detailed prenatal and natal history, anthropometric measurements, and intrauterine growth status were defined, and CANSCORE was applied to all infants. Infants were separated into two groups according to total score as malnourished (total score < 25) and well nourished (total score > or = 25). Early and late neonatal morbidities, which were observed during the clinical progress, were noted in all infants. A total of 93 preterm infants were enrolled in the study. The incidence of fetal malnutrition was 54.8% (n = 51) in all infants. The incidences of maternal hypertension and preeclampsia, oligohydramnios and disturbed umbilical artery Doppler flow in the prenatal period and the incidences of neonatal hypoglycemia, polycythemia, feeding intolerance, and necrotizing enterocolitis in the postnatal period were significantly higher in preterm infants with fetal malnutrition. Fetal malnutrition contributes significantly to many early and late neonatal morbidities in preterm infants, and it should be identified in every preterm infant in the first days of life for predicting neonatal outcome, even though they are appropriately grown.


Subject(s)
Fetal Nutrition Disorders/diagnosis , Infant, Premature, Diseases/diagnosis , Female , Humans , Infant, Newborn , Infant, Premature , Infant, Premature, Diseases/mortality , Male , Pregnancy , Pregnancy Complications , Prognosis
3.
Turk J Pediatr ; 53(4): 388-96, 2011.
Article in English | MEDLINE | ID: mdl-21980841

ABSTRACT

Bronchopulmonary dysplasia (BPD) survivors from the surfactant era were evaluated by echocardiography in a few studies and no significant differences were found between BPD and non-BPD children. In this study, we evaluated these children with myocardial performance index (MPI), which was obtained by tissue Doppler echocardiography (TDE) in addition to the conventional methods. Fifteen children with BPD who did not have any cardiopulmonary symptoms at the time of the study were examined. All children were studied with M-mode, two-dimensional and DE. Pulmonary artery systolic pressures (PAPs) were estimated from tricuspid regurgitant velocity, and MPI for both ventricles were obtained by TDE. Results were compared with those of term-born, age- and sex-matched control children. While the variables obtained by M-mode and DE did not differ between the groups, the right and left ventricular MPI were found to be significantly higher in the BPD group compared with the control group (mean right ventricular MPI 0.48 +/- 0.04 vs. 0.41 +/- 0.05; mean left ventricular MPI 0.47 +/- 0.05 vs. 0.39 +/- 0.06). In addition, mean PAPs values of the patients were found to be significantly higher than those of the controls (30.4 +/- 6.9 mmHg vs. 23.3 +/- 5.3 mmHg), and there was a positive correlation between PAPs and right ventricular MPI values in the BPD group (r = 0.5). While routine echocardiographic examinations revealed no difference between the groups, MPI measurements by TDE technique yielded significantly higher values in the BPD group. To this extent, our study is the first to show that survivors of BPD may, in fact, have a subclinical ventricular dysfunction.


Subject(s)
Bronchopulmonary Dysplasia/physiopathology , Cardiovascular Diseases/diagnostic imaging , Cardiovascular Diseases/physiopathology , Echocardiography, Doppler , Bronchopulmonary Dysplasia/diagnostic imaging , Child, Preschool , Female , Humans , Infant , Infant, Newborn , Male , Statistics, Nonparametric
4.
Turk J Pediatr ; 53(2): 169-72, 2011.
Article in English | MEDLINE | ID: mdl-21853654

ABSTRACT

Ponderal index (PI) is a weight-height related parameter that is mainly used to assess the pattern of fetal growth in small-for-gestational age infants. We aimed to use PI for large-for-gestational age (LGA) infants who were born to diabetic or non-diabetic mothers, in order to predict the fetal growth pattern. One hundred sixty-six LGA infants born at the Department of Obstetrics, Hacettepe University Hospital, Ankara, Turkey were included in the study. The PI was calculated by using the following formula: PI = weight (g) x 100/(height, cm)3. Sixty-seven (40%) of these infants were born to diabetic mothers. Maternal age, maternal weight and maternal weight gain during pregnancy were similar in the diabetic and non-diabetic groups. Mean birthweight, height and head circumference were similar in both groups, but median PI of infants of diabetic mothers was significantly higher than of infants of non-diabetic mothers (3.02 and 2.89, respectively, p < 0.05). Fetal growth was different between LGA infants of diabetic and non-diabetic mothers, and PI provided useful information on the proportionality of fetal growth in LGA infants.


Subject(s)
Birth Weight , Body Height , Diabetes, Gestational/diagnosis , Fetal Macrosomia/diagnosis , Neonatal Screening , Case-Control Studies , Diabetes, Gestational/etiology , Female , Fetal Macrosomia/etiology , Humans , Infant, Newborn , Male , Pregnancy , Reproducibility of Results
5.
Turk J Pediatr ; 53(2): 180-6, 2011.
Article in English | MEDLINE | ID: mdl-21853656

ABSTRACT

The aim of this study was to examine the diagnostic sensitivity and specificity of C-reactive protein (CRP) and procalcitonin (PCT) in neonates who were born after preterm premature rupture of membranes (PPROM) and compare these with interleukin-6 (IL-6). The study involved 74 preterm neonates who were born after PPROM. IL-6, CRP, complete blood count and leukocyte ratios, and PCT levels were measured in the 1st day of life, and CRP, PCT, and blood counts were repeated on the 3rd day of life. Seventy-four infants with PPROM were divided into two groups according to the development of sepsis and infection (Group 1: sepsis, n = 32; Group 2: no sepsis, n = 42). There were no significant differences between these groups with respect to gestational age, birthweight and duration of membrane rupture. There were significant differences between the two groups in the 1st day CRP (Group 1: 0.85 -/+ 1.36 mg/dl, Group 2: 0.23 +/- 0.25 mg/dl; p = 0.016), 1st day PCT (Group 1: 7.2 +/- 7.6 ng/ml, Group 2, 1.6 +/- 4.0 ng/ml; p < 0.001), and 3rd day PCT (Group 1: 9.01 +/-11.5 ng/ml, Group 2: 1.34 +/- 1.35 ng/ml; p = 0.001) and IL-6 (Group 1: 80.7 +/- 67.2 pg/ml, Group 2: 3.4 +/- 3.5 ng/ml; p < 0.001) levels. CRP levels were not significantly different between Group 1 (1.2 +/- 1.7 mg/dl) and Group 2 (0.58 +/- 1.1 mg/dl) on the 3rd day of life (p=0.059). CRP levels on the 1st day of life had a cut-off value of 0.72 mg/dl with a sensitivity and specificity of 56% and 58%, respectively. CRP levels on the 3rd day had a cut-off level of 0.78 mg/dl with 60% sensitivity and 63% specificity. PCT levels had a cut-off level of 1.74 ng/ml with 76% sensitivity and 85% specificity on the 1st day of life, and of 1.8 with 89% sensitivity and 86% specificity on the 3rd day of life. Statistical analysis revealed that the cut-off value of 7.6 pg/ml for IL-6 had a 93% sensitivity and 96.7% specificity. Interleukin (IL)-6 is the most reliable marker for the detection of early-onset sepsis in preterm neonates with PPROM. Early PCT levels seemed to be more sensitive than early CRP in this population.


Subject(s)
C-Reactive Protein/metabolism , Calcitonin/blood , Fetal Membranes, Premature Rupture/blood , Pregnancy Complications, Infectious/blood , Pregnancy Complications, Infectious/diagnosis , Protein Precursors/blood , Adult , Calcitonin Gene-Related Peptide , Cohort Studies , Female , Fetal Membranes, Premature Rupture/diagnosis , Humans , Infant, Newborn , Interleukin-6/blood , Male , Pregnancy , Sensitivity and Specificity
6.
J Pediatr ; 159(3): 398-403.e1, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21481414

ABSTRACT

OBJECTIVE: To evaluate the efficacy of inhaled salbutamol, a beta-2 adrenergic agonist, for the treatment of transient tachypnea of the newborn (TTN) and to determine whether inhaled salbutamol is safe in newborn infants. STUDY DESIGN: Inhaled salbutamol or normal saline solution was administered to 54 infants with gestational ages ranging from 34 to 39 weeks and TTN. The response to salbutamol therapy was evaluated by determining respiratory rate, clinical score of TTN, level of respiratory support, and fraction of inspired oxygen before and at 30 minutes and 1 and 4 hours after salbutamol nebulization. RESULTS: Among the 54 infants with TTN, 32 received salbutamol and 22 received normal saline solution. After one dose, the salbutamol group showed significant improvements in respiratory rate, clinical score of TTN, fraction of inspired oxygen, and level of respiratory support (P < .05). After treatment, the mean pH, partial pressure of arterial oxygen, and partial pressure of arterial carbon dioxide values were better in the salbutamol group when compared with the placebo group (P < .05). Duration of hospitalization in the neonatal intensive care unit was also shorter for the salbutamol group (P < .05). CONCLUSION: Inhaled salbutamol treatment was effective with respect to both clinical and laboratory findings of TTN and without adverse events.


Subject(s)
Adrenergic beta-2 Receptor Agonists/therapeutic use , Albuterol/therapeutic use , Respiration Disorders/drug therapy , Carbon Dioxide/blood , Double-Blind Method , Female , Humans , Hydrogen-Ion Concentration , Infant, Newborn , Length of Stay/statistics & numerical data , Male , Nebulizers and Vaporizers , Oxygen/blood , Oxygen Inhalation Therapy , Partial Pressure , Respiratory Rate , Severity of Illness Index
7.
J Matern Fetal Neonatal Med ; 24(5): 703-7, 2011 May.
Article in English | MEDLINE | ID: mdl-20836741

ABSTRACT

Adenosine is produced in the inflammed and damaged lung where it plays roles in the regulation of inflammation and tissue remodeling. Adenosine deaminase (ADA) is an enzyme responsible for the degradation of adenosine. Our aim was to compare the levels of ADA between infants with and without respiratory distress syndrome (RDS) and to determine the relationship between plasma ADA levels and bronchopulmonary dysplasia (BPD). One-hundred and twenty-five premature infants who were admitted to our neonatal intensive care unit were included in the study. Eighty-one of these infants with RDS were study group and the other 44 infants without RDS served as controls. Blood collection was made in the first day of life at the end of 24th-h and was used for laboratory testing. In the RDS group, mean ADA level was 25.5 (± 4.5) U/l, and in controls it was 26.3 (± 5.7) U/l. There was no statistically significant difference (p = 0.326) in these groups although there was a statistically difference of ADA levels between BPD (34.5 ± 5.2 U/l) and non-BPD (24.6 ± 4.1) patients (p = 0.001). There was also a positive relationship between ADA levels and severity of BPD (r = + 0.845, p = 0.01). Perinatal inflammation is the key mechanism of BPD. ADA level in early postnatal life is elevated in infants with BPD and may be related with perinatal inflammation.


Subject(s)
Adenosine Deaminase/blood , Bronchopulmonary Dysplasia/enzymology , Respiratory Distress Syndrome, Newborn/enzymology , Bronchopulmonary Dysplasia/immunology , Humans , Infant, Newborn , Infant, Premature , Lymphocytes/physiology , Respiratory Distress Syndrome, Newborn/immunology
9.
Turk J Pediatr ; 52(2): 145-9, 2010.
Article in English | MEDLINE | ID: mdl-20560249

ABSTRACT

Genetic polymorphisms in the gene that codes for endothelial nitric oxide synthase (eNOS) have been associated with less nitric oxide availability and with various cardiovascular diseases in humans. The objective of this study was to analyze the genotype distributions and allele frequencies for the Glu298Asp (G894T) and T(-786)C polymorphisms of the eNOS gene among neonates with respiratory distress in comparison to healthy control subjects. Fifty premature neonates with respiratory distress and 55 neonates without any respiratory problem were included in the study. Genomic DNA from all the neonates was analyzed by polymerase chain reaction. A polymerase chain reaction-restriction fragment length polymorphism analysis of eNOS gene polymorphisms was performed, and the results were compared. There were no significant differences between the groups regarding either genotype distributions or the allele frequencies for the Glu298Asp and T(-786)C polymorphisms. These results suggest that eNOS Glu298Asp and T(-786)C polymorphisms are not associated with development of respiratory distress.


Subject(s)
Nitric Oxide Synthase/genetics , Polymorphism, Single Nucleotide , Respiratory Distress Syndrome, Newborn/genetics , Case-Control Studies , Chi-Square Distribution , Female , Gene Frequency , Genetic Markers , Genetic Predisposition to Disease , Genotype , Humans , Infant, Newborn , Infant, Premature , Male , Mutation, Missense , Risk Factors , Statistics, Nonparametric
10.
Turk J Pediatr ; 52(2): 206-10, 2010.
Article in English | MEDLINE | ID: mdl-20560262

ABSTRACT

Pertussis, or whooping cough, a highly contagious disease caused by Bordetella pertussis, is making a comeback globally and nationally in spite of reasonable vaccination coverage. Worldwide, there have been increasing reports of Bordetella pertussis infection among adolescents and adults, but the peak incidence and highest mortality occur among infants. We report a 19-day-old female infant presenting with progressive respiratory failure. The mother was the only familial contact who complained of mild cough. However, occasional apneic episodes with cyanosis and peripheral lymphocytosis prompted us to examine the presence of Bordetella pertussis, which remains a significant cause of morbidity and mortality in unimmunized infants. Understanding the source of pertussis transmission to infants may provide new approaches to prevent pertussis in the most vulnerable infants. Various potential strategies have been reviewed or recommended in countries with the aim of better protecting infants against pertussis. Public health measures to prevent the disease could be strengthened and booster vaccinations against pertussis considered.


Subject(s)
Whooping Cough/transmission , Ampicillin/therapeutic use , Anti-Infective Agents/therapeutic use , Diagnosis, Differential , Drug Therapy, Combination , Enzyme-Linked Immunosorbent Assay , Erythromycin/therapeutic use , Female , Gentamicins/therapeutic use , Humans , Infant, Newborn , Mothers , Whooping Cough/diagnosis , Whooping Cough/drug therapy
11.
Pediatr Dev Pathol ; 13(2): 107-11, 2010.
Article in English | MEDLINE | ID: mdl-19968488

ABSTRACT

Low-molecular-weight heparin and aspirin are the most prescribed medical agents as anticoagulants in pregnancy. Our objective was to investigate the effects of antenatal use of low-molecular-weight heparin and aspirin on pulmonary vascular development in neonatal rabbits. Seven pregnant rabbits (42 newborn rabbits) were divided into 5 groups as follows: control group (group 1, n = 14), heparin treated (group 2, n = 8), heparin and aspirin treated (group 3, n = 7), only aspirin treated (group 4, n = 6), and high-dose heparin treated (group 5, n = 12). Pulmonary histologic evaluations were carried out for all groups. Angiogenesis was also tested by CD34 immunostained microvessel count (mvc). Pathologic examination of pulmonary vasculature revealed that pulmonary vascular thickening occurred at the level of alveoli in heparin-, heparin- and aspirin-, and high-dose-heparin-treated groups (groups 2, 3, and 5). The percentage of wall thickness was different in groups 2 (26%), 3 (28.2%), and 5 (30.8%) compared with group 1 (21.4%). Statistical differences were observed between group 1 vs 2, 3, and 5. Microvessel count was also different between groups 2 (mvc = 90.5), 3 (mvc = 90.2), and 5 (mvc = 96.3) vs group 1 (mvc = 86.7). The microvessel count was statistically different between groups that received low-dose heparin vs high-dose heparin. Antenatal administration of low-molecular-weight heparin showed an effect on pulmonary vascular development. This effect may be explained by the influence of heparin on angiogenesis through placental growth factors. Further experiments are needed to understand the pathophysiology of these findings, and clinical studies are needed to correlate of these results.


Subject(s)
Anticoagulants/adverse effects , Aspirin/adverse effects , Heparin, Low-Molecular-Weight/adverse effects , Lung/blood supply , Lung/drug effects , Prenatal Exposure Delayed Effects , Animals , Animals, Newborn , Blood Vessels/drug effects , Female , Neovascularization, Physiologic/drug effects , Pregnancy , Rabbits
13.
Turk J Pediatr ; 51(5): 515-8, 2009.
Article in English | MEDLINE | ID: mdl-20112613

ABSTRACT

Placental chorioangioma and thrombosis of an umbilical vein varix are rare etiologic factors of non-immune hydrops fetalis. Herein, we report a patient who had hydrops fetalis associated with placental chorioangioma and thrombosis of an umbilical vein varix. This is the first report of coexistence of non-immune hydrops fetalis with placental chorioangioma and thrombosis of an umbilical vein varix.


Subject(s)
Fetal Diseases/diagnostic imaging , Hemangioma/complications , Hydrops Fetalis/etiology , Placenta/pathology , Thrombosis/complications , Umbilical Veins/diagnostic imaging , Female , Hemangioma/pathology , Humans , Infant, Newborn , Infant, Premature , Pregnancy , Thrombosis/diagnostic imaging , Ultrasonography, Doppler, Color , Ultrasonography, Prenatal , Umbilical Veins/pathology , Varicose Veins/diagnostic imaging
14.
Am J Perinatol ; 26(2): 159-64, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19021100

ABSTRACT

The aim of the study was to investigate the effect of individual room care in the neonatal intensive care unit (NICU) on the factors that influence mother-preterm infant interaction. Mothers in group I had hospitalization with their preterm infants in an individual room in the NICU. Mothers in group II were not hospitalized but had opportunity to visit their babies and spend time with them whenever they wanted. On the postdischarge third month, mothers were assessed for parental stress, postpartum depression, and perception of vulnerability. Although the mean depression, stress, and vulnerability scores were higher in group II, there was no significant difference between the groups (P > 0.05). Postpartum depression rate was more than double in group II, but this difference was not statistically significant (P = 0.06). Individual room care in the NICU cannot prevent maternal stress, postpartum depression, and perception of vulnerability related to having a high-risk preterm infant by itself alone.


Subject(s)
Depression, Postpartum/psychology , Infant, Premature , Intensive Care Units, Neonatal/organization & administration , Mother-Child Relations , Patient-Centered Care , Adult , Female , Hospitalization , Humans , Infant, Newborn , Male , Premature Birth , Prospective Studies , Turkey
15.
Indian J Pediatr ; 75(10): 1015-7, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18810354

ABSTRACT

OBJECTIVE: The effects of meconium-stained amniotic fluid (MSAF) on cord blood vascular endothelial growth factor (VEGF) levels have not been explored. The aim of this study was to verify whether MSAF influences cord blood VEGF levels in healthy term neonates and we can use cord blood VEGF levels in infants with MSAF as an indicator of fetal distress. METHODS: Using an enzyme-linked immunosorbent assay double sandwich method, plasma VEGF levels were determined in 18 healthy term neonates with MSAF and in 16 healthy term neonates without MSAF. RESULTS: VEGF plasma levels were not significantly different between healthy term neonates with or without MSAF. CONCLUSION: Intrauterine meconium passage could not affect VEGF levels on cord blood in term newborn infants and VEGF level may not be used as an indicator of fetal distress in infants with MSAF.


Subject(s)
Amniotic Fluid , Fetal Blood/chemistry , Fetal Distress/diagnosis , Meconium , Vascular Endothelial Growth Factor A/blood , Asphyxia Neonatorum/diagnosis , Biomarkers/blood , Diagnosis, Differential , Humans , Hydrogen-Ion Concentration , Infant, Newborn
16.
Pediatr Nephrol ; 23(11): 2081-3, 2008 Nov.
Article in English | MEDLINE | ID: mdl-18536938

ABSTRACT

Cystatin C (CysC) is a low-molecular-mass protein (13,343 dalton, 120 amino acids) belonging to the cystatin superfamily of reversible inhibitors of cysteine proteases. CysC appears to be eliminated from the circulation almost exclusively by glomerular filtration, which makes it a promising endogenous marker of renal function. CysC has been demonstrated to reflect glomerular filtration rate better than other low-molecular-weight proteins, including creatinine (Cr). We established reference values for serum CysC and compared them with Cr in 108 preterm infants by particle-enhanced nephelometric immunoassay. On the first day, serum CysC values ranged from 1.25 to 2.84 mg/L, significantly decreasing after 3 days of life. Cr levels determined simultaneously on the first day ranged from 0.05 to 1.12 mg/dl and were also significantly different from day 3 levels. Both CysC and Cr levels were independent of gender, birth weight, hemoglobin levels, and hydration state. Cr correlated negatively with gestational age (r = -0.25, p = 0.009), but not CysC. A significant correlation was found between CysC and Cr on day 1 (r = 0.21, p = 0.031), but no correlation was found according to day 3 blood samples (r = 0.19, p = 0.053). CysC is regarded as an alternative for assessing renal function in preterm neonates, but its advantages over Cr are not yet proven.


Subject(s)
Biomarkers/blood , Chemistry, Clinical/standards , Creatinine/blood , Cystatin C/blood , Infant, Premature/blood , Kidney/physiology , Female , Humans , Infant, Newborn , Linear Models , Male , Reference Values , Sensitivity and Specificity
17.
J Matern Fetal Neonatal Med ; 21(2): 123-8, 2008 Feb.
Article in English | MEDLINE | ID: mdl-18240081

ABSTRACT

OBJECTIVE: Meconium-stained amniotic fluid (MSAF) is thought to be a sign of fetal hypoxia, which causes activation of coagulation and inhibition of fibrinolysis. Inflammation is also seen in MSAF. On the other hand, thrombin activatable fibrinolysis inhibitor (TAFI) is an inhibitor of fibrinolysis and a regulator of vascular inflammation. For this reason, in this study we aimed to evaluate the relation between hypoxia, fibrinolysis, and inflammation by determining the levels of TAFI activity (TAFIa) in MSAF where inflammation was also thought to have a role in the pathogenesis. METHODS: The MSAF group consisted of 22 neonates; 20 neonates served as the control group. Plasma TAFIa levels were evaluated in all neonates in the first six hours of life. RESULTS: TAFIa levels were significantly higher in the MSAF group when compared with the control group and the levels correlated negatively with cord blood pH levels. CONCLUSIONS: Increased TAFIa levels in neonates with MSAF might be due to hypoxia. Inflammation observed in MSAF may also play an additional role in increased TAFIa expression. Although no clinical complication that can be attributed to this increase was seen, one should be alert to the complications of depressed fibrinolysis that might be observed in these neonates.


Subject(s)
Amniotic Fluid , Carboxypeptidase B2/blood , Meconium , Female , Fetal Blood/chemistry , Gestational Age , Humans , Hydrogen-Ion Concentration , Hypoxia/blood , Infant, Newborn , Inflammation/blood , Male
18.
J Pediatr Endocrinol Metab ; 21(11): 1065-71, 2008 Nov.
Article in English | MEDLINE | ID: mdl-19189701

ABSTRACT

AIM: To evaluate associations between prenatal risk factors, neonatal characteristics and bone development. METHODS: Tibial speed of sound (SOS) of 317 neonates whose gestational ages ranged between 25 and 41 weeks and birth weight between 580 and 4,350 g was measured using quantitative ultrasound. RESULTS: Bone SOS values correlated significantly with gestational age and birth weight. Small for gestational age (SGA) infants had higher bone SOS values than appropriate for gestational age (AGA) infants. Infants born to multiple pregnancies had lower SOS values than singleton infants so two separate bone SOS curves were made: for singleton infants born AGA (n = 152), and for infants of multiple pregnancies born AGA (n = 104). Infants of preeclamptic mothers had significantly higher SOS values than the infants of mothers without preeclampsia. CONCLUSION: This is the first study reporting bone SOS values of Turkish neonates. Prenatal risk factors, such as preeclampsia, multiple pregnancy, and being SGA, affect the bone development of the fetus.


Subject(s)
Bone Development/physiology , Infant, Premature/physiology , Infant, Small for Gestational Age/physiology , Tibia/diagnostic imaging , Twins/physiology , Adult , Bone Density , Female , Gestational Age , Humans , Infant, Newborn , Male , Pre-Eclampsia , Pregnancy , Risk Factors , Tibia/growth & development , Ultrasonography , Young Adult
19.
Am J Hematol ; 83(1): 50-3, 2008 Jan.
Article in English | MEDLINE | ID: mdl-17654683

ABSTRACT

Intraalveolar fibrin deposition found in neonates with respiratory distress syndrome (RDS) is explained by the activation of the coagulation system and inefficient fibrinolysis. However, thrombin activatable fibrinolysis inhibitor activity (TAFIa), an inhibitor of fibrinolysis, and the ratio of D-dimer to thrombin-antithrombin complex (D-dimer/TAT), an index of fibrinolytic activity, have not been reported previously in neonatal RDS. Aim of this study is to evaluate the influence of plasma TAFIa levels on the fibrinolytic state in neonatal RDS. The RDS group (Group 1) consisted of 29 neonates, and 18 neonates served as the control group (Group 2). Plasma TAFIa levels and D-dimer/TAT ratios were evaluated in all neonates in the first 6 hr of life. Neonates in the RDS group were further divided into two subgroups; Group 1a consisted of 12 neonates with evidence of mild asphyxia (Apgar score at 5 min <7 and cord pH <7.26), and Group 1b consisted of 17 nonasphyxiated neonates. No significant difference was found in TAFIa levels and D-dimer/TAT ratios between Groups 1 and 2 [214% (56.2-361%) and 124.3 (4.4-3,921) in Group 1 and 201% (60.3-381%) and 147 (5.9-1,426) in Group 2]. There were negative correlations between cord pH and TAFIa levels in both groups. Increased TAFIa levels and decreased D-dimer/TAT ratios and platelet counts were detected in mildly asphyxiated neonates when compared with nonasphyxiated ones. TAFIa is not responsible for the hypofibrinolytic state reported in RDS. However, asphyxia influences TAFIa levels and increased TAFIa levels depress fibrinolysis.


Subject(s)
Antithrombins/metabolism , Carboxypeptidase B2/metabolism , Respiratory Distress Syndrome, Newborn/metabolism , Thrombin/metabolism , Dimerization , Enzyme Activation , Female , Humans , Hydrogen-Ion Concentration , Infant, Newborn , Male , Platelet Count , Time Factors
20.
Turk J Pediatr ; 49(3): 290-4, 2007.
Article in English | MEDLINE | ID: mdl-17990583

ABSTRACT

In this study, risk factors of developmental dysplasia of the hip (DDH) were evaluated. History, clinical examination and risk factors for DDH of the babies were recorded. The hips were evaluated with ultrasonography. Infantile hip ultrasonography is one of the best methods for screening of DDH. Ultrasonography is easy, repeatable and provides visualization of the cartilage part of the hip joint. Graf's method of infantile hip ultrasonography was used to evaluate the hip in this study. Both hips of 371 babies and 32 unilateral hips of 32 babies were included in the study. In 403 babies, 14 (3.4%) had DDH. There were 5 type IIB, 7 type IIC, 1 type D, and 1 type IV hips. Physiological immaturity was present in 81 hips (19% of babies). According to risk factor analysis, the only risk factor in unilateral analysis was presence of oligohydramnios (odd ratio-OR: 11.8, confidence interval-CI: 2.7-52.7). In correlation analysis, there was a correlation between female gender and swaddling. There was overall increase in DDH in female babies who were swaddled compared to those who were not. The results of this study showed that the most important risk factor was oligohydramnios for DDH. Swaddling and female gender increased the risk of the disease, but further studies in larger series are necessary for the confirmation of these results.


Subject(s)
Hip Dislocation, Congenital/diagnostic imaging , Oligohydramnios , Female , Hip Dislocation, Congenital/classification , Hip Dislocation, Congenital/etiology , Humans , Infant, Newborn , Male , Pregnancy , Risk Factors , Sex Distribution , Ultrasonography
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