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Wyszukujesz frazę "congenital" wg kryterium: Temat


Wyświetlanie 1-3 z 3
Tytuł:
Non-invasive assessment of haemodynamic parameters in patients after Fontan procedure
Autorzy:
Gutknecht, P.
Kwiatkowska, J.
Wałdoch, A.
Siebert, K.
Siebert, J.
Powiązania:
https://bibliotekanauki.pl/articles/2085957.pdf
Data publikacji:
2020
Wydawca:
Instytut Medycyny Wsi
Tematy:
congenital heart disease
Fontan circulation
impedance cardiography
haemodynamics
Opis:
Introduction and objective. Single ventricle anomaly is one of the complex congenital heart defects. A dependable non-invasive method of evaluation of Fontan circulation haemodynamics for early diagnosing unstable patients is hardly available in routine clinical practice. The aim of the study is non-invasive evaluation of the haemodynamic parameters in patients after Fontan operation. Materials and method. The study involved 11 participants (age 24.4±4.3 years) with functionally univentricular hearts after Fontan operation. Evaluation of haemodynamic parameters was performed in supine and sitting positions using the impedance cardiography method. Results. In comparative analysis, heart rate (70.1 vs.78.3 1/min; p=0.001), diastolic blood pressure (73.9 vs. 76.7 mm Hg; p=0.026), mean arterial blood pressure (84.5 vs. 88.0 mm Hg; p=0.013), systemic vascular resistance (1284.8 vs. 1334.9 dyn*s*cm-5; p=0.024), systemic vascular resistance index (2178.7 vs. 2272.8 dyn*s*cm-5*m2; p=0.018), pre-ejection period (124.2 vs. 136.2 ms; p=0.009), systolic time ratio (0.43 vs. 0.53; p=0.0001), and Zo (26.2 vs. 28.7 Ω; p<0.00001), were significantly higher in the sitting position. Stroke volume (75.4 vs. 68.5 ml; p=0.013), stroke index (42.7 vs. 39.0 ml*m-2; p=0.014), thoracic fluid content (38.5 vs. 35.4 1*kΩ-1; p=<0.00001), thoracic fluid content index (22.8 vs. 21.0 1*kΩ-1*m-2; p=<0.00001), and left-ventricular ejection time 291.1 vs. 260.1 ms; p=<0.00001, were significantly higher in the supine position. Conclusions. In patients after Fontan procedure, impedance cardiography can be a useful tool the assessment of shortterm haemodynamic changes provoked by postural changes. Its clinical value in patients with congenital heart defects should be further investigated.
Źródło:
Annals of Agricultural and Environmental Medicine; 2020, 27, 3; 384-387
1232-1966
Pojawia się w:
Annals of Agricultural and Environmental Medicine
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Is congenital toxoplasmosis still an important clinical problem?
Autorzy:
Alghamdi, Ali Joman
Alabbas, Ali
Tadla, Monika
Agyemfra-Kumi, Catherine
Tarkowska, Agata
Furmaga-Jabłońska, Wanda
Powiązania:
https://bibliotekanauki.pl/articles/972434.pdf
Data publikacji:
2017
Wydawca:
Instytut Medycyny Wsi
Tematy:
congenital toxoplasmosis
risk factors
prophylaxy
undercooked meat
Toxoplasma gondii
Good hygiene
Spiromycin
Opis:
Introduction. Congenital toxoplasmosis is one of the most common intrauterine inherited diseases. The risk and severity of infection depends on the time of transmission during pregnancy. The earlier the infection, the lower the risk of transmission but with serious estimated outcomes and vice versa. Case report. A newborn with congenital toxoplasmosis was born to a mother who was seronegative at the beginning of pregnancy, and was not aware of toxoplasmosis risk factors during pregnancy. The newborn was born with features of small for gestational age and with intracranial calcification revealed in cranial ultrasonography, which emphasized the need for further investigations. Neonatal serological panel and cerebrospinal fluid analysis were both confirmative of congenital toxoplasmosis. Ophthalmological examination showed the typical whitish focus of retinochoroiditis which later led to a blindness in one eye. Additionally, hydrocephalus was progressing slowly until it became stable in 5 months. Objective. The aim of this study was to present the case of congenital toxoplasmosis in order to underline the lack of social awareness concerning risk factors in pregnant women. Thus, educational campaigns against the consumption of raw meat and unpasteurized milk while pregnant may prevent the recurrence of such cases. Moreover, proper washing of fruits and vegetables are advised in this respect.
Źródło:
Journal of Pre-Clinical and Clinical Research; 2017, 11, 2; 167-170
1898-2395
Pojawia się w:
Journal of Pre-Clinical and Clinical Research
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
A child with a rare genetic disease - Noonan syndrome
Autorzy:
Siwik, P.
Janas, A.
Powiązania:
https://bibliotekanauki.pl/articles/3700.pdf
Data publikacji:
2015
Wydawca:
Instytut Medycyny Wsi
Tematy:
child
human disease
rare disease
genetic disease
Noonan syndrome
autosomal dominant congenital disorder
surgical treatment
Opis:
Noonan syndrome is a congenital developmental disorder characterized by short stature, facial dysmorphia, congenital heart defects and skeletal anomalies, with as estimated incidence of between one per 1000 and one per 2500 live births. The aim of our study is to present a case of dental surgical treatment of a child with such disorder. It is widely reported that children with mental disabilities receive less dental and medical care than their nondisabled counterparts. Because of this problem, it seems justified to describe the procedures of treating such children with dental issues, basing on a case of a girl with Noonan Syndrome.
Źródło:
Journal of Pre-Clinical and Clinical Research; 2015, 09, 1
1898-2395
Pojawia się w:
Journal of Pre-Clinical and Clinical Research
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-3 z 3

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