Marta Szymankiewicz

Poznan University of Medical Sciences, Posen, Greater Poland Voivodeship, Poland

Are you Marta Szymankiewicz?

Claim your profile

Publications (51)82.11 Total impact

  • D Szpecht · M Szymankiewicz · A Seremak-Mrozikiewicz · J Gadzinowski ·
    [Show abstract] [Hide abstract]
    ABSTRACT: Intraventricular hemorrhage (IVH) affects 15-20% of babies born before 32 weeks of pregnancy. Besides gestational age (below 32 weeks) there are a number of IVH risk factors. Increasing attention is being paid to genetic factors in the development of IVH. The authors discuss genetic factors (mutations of coagulation factors, gene polymorphisms in pro-inflammatory cytokines, mutation of type IV collagen gene, polymorphisms of genes responsible for the regulation of systemic blood pressure and cerebral blood flows) whose involvement in IVH pathogenesis has been confirmed in the highest number of reports and for which being a carrier plays an important role in their pathophysiology. The role of genetic factors in IVH remains unclear. Further analysis of the role of genetic factors in the pathophysiology of IVH will make it possible to determine the group of newborns who are specifically at risk of developing IVH in the perinatal period.
    04/2015; 53(1):1-7. DOI:10.5114/fn.2015.49968
  • Teresa Mendaluk · Agata Mościcka · Bartłomiej Mroziński · Marta Szymankiewicz ·
    [Show abstract] [Hide abstract]
    ABSTRACT: We report a case of a female neonate with an incomplete (Class II) pentalogy of Cantrell (PC) presenting: omphalocoele, thoracoabdominal type of partial ectopia cordis with ventricular septal defect and valvular pulmonary stenosis. The patient underwent a successful complete operation. We discuss associated anomalies that might occur with PC and the general overall prognosis for patients with PC. This report describes a very rare case of a patient with PC and coexisting partial ectopia cordis who survived.
    Pediatria polska 02/2015; 90(3). DOI:10.1016/j.pepo.2015.02.002
  • Source
    [Show abstract] [Hide abstract]
    ABSTRACT: The study aimed at investigating the impact of late prematurity (LPT) on neonatal outcome in twins and neonatal morbidity and mortality within LPT with regard to the completed weeks of gestation. The study was conducted in six tertiary obstetric departments from different provinces of Poland (Warsaw, Lublin, Poznan, Wroclaw, Bytom). It included 465 twin deliveries in the above centers in 2012. A comparative analysis of maternal factors, the course of pregnancy and delivery and neonatal outcome between LPT (34 + 0-36 + 6 weeks of gestation) and term groups (completed 37 weeks) was performed. The neonatal outcome included short-term morbidities. The analysis of neonatal complication rates according to completed gestational weeks was carried out. Out of 465 twin deliveries 213 (44.8%) were LPT and 156 (33.55%) were term. There were no neonatal deaths among LPT and term twins. One-third of LPT newborns suffered from respiratory disorders or required antibiotics, 40% had jaundice requiring phototherapy, and 30% were admitted to NICU. The analysis of neonatal morbidity with regard to each gestational week at delivery showed that most analyzed complications occurred less frequently with the advancing gestational age, especially respiratory disorders and NICU admissions. The only two factors with significant influence on neonatal morbidity rate were neonatal birth weight (OR = 0.43, 95% CI = 0.2-0.9, p = .02) and gestational age at delivery (OR = 0.62, 95% CI = 0.5-0.8, p < .01). LPT have a higher risk of neonatal morbidity than term twins. Gestational age and neonatal birth weight seem to play a crucial role in neonatal outcome in twins.
    Twin Research and Human Genetics 08/2014; 17(5):1-7. DOI:10.1017/thg.2014.48 · 2.30 Impact Factor
  • [Show abstract] [Hide abstract]
    ABSTRACT: Abstract Adrenal diseases in pregnant women are diagnosed relatively rarely. The main cause of hypercortisolemia during pregnancy is Cushing's syndrome related to adrenal adenoma. It is important to diagnose Cushing's syndrome in pregnant women because it can lead to significant maternal and foetal complications and morbidity. However, due to physiological endocrine changes and symptoms in pregnant women the diagnosis of this disorder can be a challenge. One current case describes a 38-year-old pregnant woman with hypertension, oedema and an adrenal tumour. At the beginning, Conn syndrome was suspected, but after careful analysis Cushing's syndrome (with an adenoma of the right adrenal gland) was diagnosed. After delivery and 5 weeks of pharmacological treatment the patient underwent right side adrenalectomy by laparoscopy.
    Gynecological Endocrinology 01/2014; 30(5). DOI:10.3109/09513590.2013.879857 · 1.33 Impact Factor
  • Source
    [Show abstract] [Hide abstract]
    ABSTRACT: The incidence of multiple pregnancies has increased dramatically over the last few years in developed countries, largely attributed to delayed childbearing and the increasing use of assisted reproduction technologies and ovulation inducing hormones. Relatively few countries have population-based statistics covering birth statistics. Of those that do, the numbers of quintuplet pregnancies rose sharply in the nineties while, at the same time, their delivery rates decreased greatly because of the use of fetal reduction. Fetal reduction is not possible or legal in some countries, Poland being one of them, and therefore obstetricians are faced with the challenges of quintuplet deliveries. Conservative treatment and management is difficult, and outcomes often vary greatly. Despite this, expert care provided at tertiary care centers can positively influence outcomes. The objective of this article is to present different care options and their consequences in two illustrative cases, as well as to establish a set of obstetric care and management goals that would allow prolongation of the gestation time. Quintuplet pregnancy is rare but poses relevant clinical problems to both the obstetrician and the neonatologist. It should be managed with close cooperation between all concerned. Due to the extreme and invariable risk of premature delivery associated with quintuplet pregnancies, we recommend early diagnosis, adequate prenatal care at one tertiary medical center, routine hospitalization and bed rest, repeated ante partum ultrasound surveillance with tests of fetal well-being, tocolytic therapy at first signs of the risk of premature labor, and specialized neonatology care after delivery.
    Twin Research and Human Genetics 12/2011; 14(6):580-5. DOI:10.1375/twin.14.6.580 · 2.30 Impact Factor
  • Source
    [Show abstract] [Hide abstract]
    ABSTRACT: The aim of the study was to evaluate the pentoxifylline administration on the foetal-placental circulation and neonatal outcome in women with threatened preterm labour. Pentoxifylline was given as a supplement to standard tocolytic therapy in a group of 43 patients (pentoxifylline group) as an intravenous infusion and oral supplementation in a total dosage of 800 mg/day. The drug was administered within 3 weeks after admission. No pentoxifylline was given in the control group (53 patients). Doppler velocimetry of pulsatility indices (PI) of the umbilical (UA) and middle cerebral (MCA) arteries as well as cerebro-placental ratio (CPR) were calculated. Also, the neonatal outcome was estimated in both groups. From the second week of therapy with pentoxifylline, the PI decreased in umbilical artery and increased in the MCA, whereas in the control group, there were no changes. The value of PIUA, evaluated after the third week of pentoxifylline administration, was statistically significantly lower when compared to data obtained on admission (mean: 0.99 ± 0.22 versus 0.82 ± 0.12; p =0.016). Pentoxifylline significantly increased CPR values calculated after third week of drug administration, which were statistically significantly higher in the pentoxifylline group when compared with respective data in the control group (mean: 2.30 versus 1.61; p = 0.001). The risk of severe neonatal complications was significantly lower in the pentoxifylline group (p = 0.026). Pentoxifylline changed foetal-placental blood circulation in patients with threatened preterm labour and improved neonatal outcome.
    Basic & Clinical Pharmacology & Toxicology 10/2011; 110(4):342-6. DOI:10.1111/j.1742-7843.2011.00809.x · 2.38 Impact Factor
  • [Show abstract] [Hide abstract]
    ABSTRACT: A systemic fetal inflammatory response, reflected by histological funisitis is associated with pulmonary morbidity and increased mortality after premature birth. The receptor for advanced glycation end products (RAGE) is a membrane-bound multiligand receptor with a key role in inflammation. Soluble RAGE (sRAGE) is created by alternative mRNA splicing or shedding of the receptor's extracellular domain and can inhibit RAGE-activation. To assess the association of funisitis with airway and systemic concentrations of sRAGE in very premature infants. Forty-two ventilated infants (gestational age: 27.4 +/- 1.8weeks, birth weight: 1017 +/- 229 g [mean +/- SD]) were studied. sRAGE concentrations were measured in tracheobronchial aspirate fluid (TAF) on days of life 1, 3, 5, 7 and 10 and in umbilical cord serum of 28 infants by ELISA. The secretory component for IgA (SC) served as reference protein in TAF. Placental tissue, membranes and umbilical cords were examined microscopically to distinguish three groups: chorioamnionitis (n=9), funisitis (n=17) and controls (n=16). The funisitis group had lower sRAGE concentrations than both other groups in cord blood serum (median: 0.52 ng/ml [25th-75th centile: 0.32-0.91]; control, 1.72 [1.02-2.69]; chorioamnionitis, 1.44 [0.92-1.63], p<0.01) and TAF on day 1 (290 ng/ngSC [140-400]; control, 2750 [1470-28920]; chorioamnionitis, 2150 [1220-7140], p<0.01). sRAGE in TAF remained lower in the funisitis than in the chorioamnionitis group on days 3 and 10, p<0.01 respectively. Decreased sRAGE in airways and circulation after funisitis may contribute to an imbalance between pro- and anti-inflammatory factors priming very premature infants for pulmonary injury and increasing the risk of adverse outcome.
    Early human development 09/2010; 86(9):593-8. DOI:10.1016/j.earlhumdev.2010.07.013 · 1.79 Impact Factor

  • Klinische Pädiatrie 06/2010; 222:S5-S5. · 1.06 Impact Factor

  • Klinische Pädiatrie 06/2010; 222. DOI:10.1055/s-0030-1261292 · 1.06 Impact Factor
  • [Show abstract] [Hide abstract]
    ABSTRACT: A systemic fetal inflammatory response, reflected by chorioamnionitis with funisitis, is a risk factor for bronchopulmonary dysplasia. Clara cell secretory protein (CC10), a product of pulmonary Clara cells, has anti-inflammatory properties. Local down-regulation of CC10 has been associated with inflammatory lung disease. Increased serum levels of CC10 can indicate injury to alveolar-capillary integrity. We hypothesized that extremely premature infants with a systemic fetal inflammatory response would have decreased concentrations of CC10 in tracheobronchial aspirates and that CC10 concentrations in umbilical cord serum of these infants would be increased, reflecting alveolar epithelial damage. We measured CC10 concentrations in tracheobronchial aspirates of 42 ventilated extremely premature infants during their first week of life and in umbilical cord serum of 24 of them by ELISA. Standardized histological examination of the placenta, membranes and umbilical cord was used to identify infants with funisitis. Seventeen infants with funisitis had lower CC10 concentrations in tracheobronchial aspirates on days 1 (p < 0.01) and 3 (p < 0.05) than the remaining 25. Exogenous surfactant treatment was associated with higher CC10 concentrations on day 1 (p < 0.05). Initial leukocyte count correlated inversely with CC10 in tracheobronchial aspirates on days 1-5. Umbilical cord serum concentrations of CC10 did not differ between the infants with funisitis and the controls. Reduced anti-inflammatory CC10 concentrations in airways of extremely premature infants with a fetal inflammatory response might make their lungs susceptible for further postnatal injuries. Umbilical cord serum CC10 is not an indicator for a fetal systemic inflammatory reaction.
    Neonatology 10/2009; 97(3):228-34. DOI:10.1159/000253152 · 2.65 Impact Factor
  • [Show abstract] [Hide abstract]
    ABSTRACT: A systemic inflammatory response of the fetus, reflected by histologic funisitis, is a risk factor for bronchopulmonary dysplasia (BPD). Impaired pulmonary angiogenesis accompanied by simplification and rarification of alveoli is a histologic hallmark of BPD. Angiopoietin-1 mediates vascular development, maturation, and stabilization. Endostatin mainly acts as an angiostatic factor. We hypothesized that funisitis was associated with changes of endostatin and angiopoietin-1 concentrations in the airways and that an imbalance between the factors might be associated with BPD or death. We measured concentrations of angiopoietin-1 and endostatin by enzyme-linked immunosorbent assay in tracheobronchial aspirate fluid samples of 42 ventilated preterm infants during postnatal days 1 through 15. The secretory component for IgA served as reference protein. A standardized histologic examination was used to distinguish three groups: chorioamnionitis, funisitis, and controls without inflammation. Concentrations of the mediators steadily decreased. Funisitis was associated with lower concentrations of both proteins, which might impair their physiologic activities in pulmonary angiogenesis. An increase of the ratio angiopoietin-1/endostatin until day 7 of life indicated a shift of the mediators potentially favoring angiogenesis. However, infants, who developed BPD or died, had a decreased ratio on days 1, 3, and 15, suggesting an imbalance toward inhibition of pulmonary angiogenesis.
    Pediatric Research 04/2009; 65(4):468-73. DOI:10.1203/PDR.0b013e3181991f35 · 2.31 Impact Factor
  • [Show abstract] [Hide abstract]
    ABSTRACT: Macrophage migration inhibitory factor is a proinflammatory mediator of innate immunity, enhances cell growth, and plays a role in preterm delivery. We speculated that funisitis, reflecting fetal systemic inflammation, would be associated with higher concentrations of macrophage migration inhibitory factor in airways of extremely premature infants. We measured macrophage migration inhibitory factor by enzyme linked immunosorbent assay in tracheobronchial aspirate fluid of 35 ventilated infants less than 30 weeks' gestational age, throughout the first week of life. Three groups were distinguished histologically: chorioamnionitis, funisitis, and control. Unexpectedly, funisitis was associated with significantly decreased macrophage migration inhibitory factor in tracheobronchial aspirate fluid on day 1 (P < .01) and levels remained lower than in the chorioamnionitis group thereafter. For the 35 patients in total, macrophage migration inhibitory factor steadily declined. Decreased macrophage migration inhibitory factor concentrations in airways of extremely premature infants with systemic fetal inflammation early in life might predispose them to pulmonary infection and interfere with maturation of the lung, contributing to adverse pulmonary outcome.
    American journal of obstetrics and gynecology 01/2008; 198(1):64.e1-6. DOI:10.1016/j.ajog.2007.06.010 · 4.70 Impact Factor
  • M Szymankiewicz · M Matuszczak-Wleklak · A Siwinska · G Breborowicz ·

    Ultraschall in der Medizin 01/2008; 29. DOI:10.1055/s-2008-1080813 · 4.92 Impact Factor
  • N Kawczynska-Leda · M Szymankiewicz · J Gadzinowski · G Breborowicz ·

    Ultraschall in der Medizin 01/2008; 29. DOI:10.1055/s-2008-1080806 · 4.92 Impact Factor
  • W Thomas · S Seidenspinner · BW Kramer · N Kawczynska-Leda · M Szymankiewicz ·

    Zeitschrift für Geburtshilfe und Neonatologie 01/2007; 211. DOI:10.1055/s-2007-1002941 · 0.48 Impact Factor

  • Zeitschrift für Geburtshilfe und Neonatologie 01/2007; 211(S 1). DOI:10.1055/s-2007-983054 · 0.48 Impact Factor

  • Choroby układu krążenia a ciąża, Edited by Grzegorz H. Bręborowicz, Andrzej Tykarski, 01/2007: pages 237-243; Poznań, 2007.
  • [Show abstract] [Hide abstract]
    ABSTRACT: Perinatal asphyxia has a high impact on neonatal mortality, morbidity, and neurological outcome. The hypoxic effects on brain, kidney and gastrointestinal system are well recognized in newborns. While it is known that hypoxia also effects cardiac function, there are few studies of quantitative myocardial injury in premature infants who suffered hypoxia. To investigate usefulness of cardiac troponin (cTnT) and creatinine kinase MB (CK-MB) in the diagnosis of myocardial injury due to birth hypoxia and to correlate these markers with cardiac functions as measured by echocardiogram. We studied 43 preterm infants: 21 with birth asphyxia and 22 controls. Echocardiographic studies and quantitative determination of cTnT and CK-MB in blood serum was performed between the 12(th) and the 24(th) h of life. cTnT and CK-MB levels were higher in asphyxiated infants compared to controls (0.287 +/- 0.190 vs. 0.112 +/- 0.099 ng/mL, P < 0.001) and (18.35 +/-14.81 vs. 11.09 +/- 5.17 ng/L, P < 0.05). Among controls, we observed an elevated value of cTnT in those with respiratory distress syndrome (RDS). We found a decrease in fractional shortening (P < 0.05) and an increase in tricuspid insufficiency (P < 0.01) in asphyxiated newborns. cTnT and CK-MB levels are strong indicators of myocardial injury due to perinatal hypoxia. The cTnT level was most strongly related to RDS.
    Journal of Perinatal Medicine 02/2006; 34(3):220-5. DOI:10.1515/JPM.2006.040 · 1.36 Impact Factor
  • Source
    [Show abstract] [Hide abstract]
    ABSTRACT: In the last years several reports on exploiting cardiac troponin T in the retrospective diagnosis of perinatal asphyxia have been published. Application of these method in neonates still stays open. Aim of the study was to evaluate usefulness of cTnT determination in the diagnosis of hypoxic myocardial injury in full-term infants.
    Pediatric Research 08/2005; 58(2). DOI:10.1203/00006450-200508000-00160 · 2.31 Impact Factor
  • Source
    [Show abstract] [Hide abstract]
    ABSTRACT: In the last years several reports on exploiting cardiac troponin T in the retrospective diagnosis of perinatal asphyxia have been published. Application of these method in neonates still stays open. Aim of the study was to evaluate usefulness of cTnT determination in the diagnosis of hypoxic myocardial injury in full-term infants.Material and method: 105 neonates >37 weeks of gestation were enrolled into the study. We separated study group of 45 asphyxiated neonates (umbilical pH<7,10, BE<-12mmol/1), with mean gestational age 38,7±1,3 weeks and birth weight 3246,4±587,0 g and control group (60 non-asphyxiated infants) with mean gestational age 38,6±1,5 weeks and birth weight 3374,8±496,9g. Quantitative determinations of cTnT in blood serum were performed between 12th and 24th hour of life using Elecsys cTnT STAT Immunoassay, that contains specific monoclonal antibodies against human cTnT.Results: cTnT levels were higher in the asphyxiated infants comparing to controls (0,21+/-103ng/ml and 0,054+/-0,039ng/ml, respectively) (p<0,00001). ROC curve proved that cTnT had high value in the diagnosis of posthypoxic myocardial injury in newborn. Discriminate value of cTnT was 0,060ng/ml (sensitivity 71,1%, specificity 66,7%, positive predictive value 61,5%). cTnT levels correlated with pH and BE in umbilical blood (p<0,00001 and p<0,00001, respectively), Apgar score in the 1min and 5 min (p<0,0002 and p<0,0002, respectively), abnormal fetal heart pattern on cardiotocography (p<0,01).Conclusions: cTnT determination is useful method of myocardial injury diagnosis in full-term infants after perinatal asphyxia. Serum blood levels of cTnT indicate, that cardiac dysfunction in neonates who suffered intrauterine hypoxia is more frequent than would be diagnosed based solely on clinical symptoms.
    Pediatric Research 08/2005; 58(2). DOI:10.1203/00006450-200508000-00161 · 2.31 Impact Factor