Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Wyszukujesz frazę "Kulak, E." wg kryterium: Autor


Wyświetlanie 1-7 z 7
Tytuł:
Knowledge of parents of children with autism from Poland, Belarus and France concerning their child’s condition
Wiedza rodziców dzieci z autyzmem z Polski, Białorusi i Francji na temat choroby dziecka
Autorzy:
Ślifirczyk, A.
Krajewska-Kułak, E.
Krukowska, M.
Maciorkowska, E.
Powiązania:
https://bibliotekanauki.pl/articles/2053512.pdf
Data publikacji:
2019
Wydawca:
Akademia Bialska Nauk Stosowanych im. Jana Pawła II w Białej Podlaskiej
Tematy:
autism
parents
knowledge
autyzm
rodzicie
wiedza
Opis:
Background. Autism is not only a problem for p eople with autism, but also for their entire families. Material and methods. 83 families were analysed, including 30 families from Poland, 25 families from Belarus and 28 families from France, an author’s questionnaire was used. Results. The majority of respondents were aware of the fact that autism can also be diagnosed in an adult person. Likewise, the notion of the autistic spectrum was known. While parents from Poland and France realised that a one-time diagnosis of the condition is insufficient, parents from Belarus more often chose the incorrect answer, and therefore they express the tendency to immediately start a therapy without additional consultations. All respondents from France chose the statement that treatment of autism should be started before the age of 3, which was confirmed by the majority of respondents from the other two countries. Polish parents barely considered the importance of preparation required to understand their child’s behaviour, whereas this aspect of the therapy was indicated by almost 90% of the respondents from the other two countries. Parents from Poland (69%) and Belarus (76%) were mostly convinced that autism cannot be cured completely. A different opinion was expressed by 42.9% of parents from France, who were convinced about it. The Poles most willingly used the Internet as a source of knowledge, while the French and Belarusians - a psychologist. A paediatrician was a preferred educator in Poland, in Belarus and France - a psychologist. Conclusions. The parents of autistic children, regardless of the country, showed a low level of knowledge about autism. The vast majority of respondents declared a desire to deepen their knowledge on autism, expressing their preference to have an individual conversation with an educator.
Wprowadzenie. Autyzm nie jest problemem jedynie osób z autyzmem, ale również całych ich rodzin. Materiał i metody. Analizie poddano 83 rodziny, w tym 30 rodzin z Polski, 25 rodzin z Białorusi oraz 28 rodzin z Francji i wykorzystano kwestionariusz autorski. Wyniki. Większość ankietowanych wiedziała, że autyzm można zdiagnozować także u osoby dorosłej, znane było także pojęcie spektrum autystycznego. O ile rodzice z Polski i Francji zdawali sobie sprawę, że jednorazowa diagnoza choroby jest niewystarczająca, to rodzice z Białorusi częściej wybierali błędną odpowiedź, a więc natychmiastowe rozpoczęcie terapii bez dodatkowych konsultacji. Wszyscy ankietowani z Francji wybierali stwierdzenie, iż leczenie autyzmu należy zacząć przed 3 rokiem życia, co potwierdziło większość ankietowanych z pozostałych dwóch krajów. Rodzice z Polski ledwie w połowie za ważne uznali przygotowanie rodziców do zrozumienia zachowań dziecka, podczas gdy ten aspekt terapii wskazało niemal 90% ankietowanych z dwóch pozostałych krajów. Rodzice z Polski (69%) i Białorusi (76%) byli w większości przekonani, iż autyzmu nie można wyleczyć całkowicie. Odmienną opinię wyraziło 42,9% przekonanych o tym rodziców z Francji. Polacy najchętniej jako źródło wiedzy wykorzystywali Internet, Francuzi i Białorusini - psychologa. Za edukatora w Polsce preferowano pediatrę, na Białorusi i we Francji - psychologa. Wnioski. Rodzice dzieci autystycznych, niezależnie od kraju, wykazywali niski poziom wiedzy na temat autyzmu. Zdecydowana większość respondentów deklarowała chęć pogłębienia wiedzy na temat autyzmu preferując w tym celu rozmowę indywidualną z edukatorem.
Źródło:
Health Problems of Civilization; 2019, 13, 2; 114-122
2353-6942
2354-0265
Pojawia się w:
Health Problems of Civilization
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Assessment of parents’ ways of coping with critical situations
Autorzy:
Ślifirczyk, A.
Krajewska-Kułak, E.
Brayer, A.
Sobolewski, M.
Maciorkowska, E.
Powiązania:
https://bibliotekanauki.pl/articles/1917663.pdf
Data publikacji:
2016
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
Autism
parents
Coping Inventory for Stress Situations
The General Self- Efficacy Scale
Opis:
Introduction: Stress experienced by parents of a disabled child can have a negative impact on family relationships. Purpose: Assessment of parents coping with critical situations. Materials and methods: We analyzed 83 families, including 30 families from Poland, 25 families from Belarus and 28 families from France and we used Coping Inventory for Stress Situations (CISS) and The General Self- Efficacy Scale (GSES). Results: After hearing the diagnosis most often parents felt shock (63.3% from Poland, 68% from Belarus and France 85.7%). Main parents' emotions induced by the disability was fatigue (76.7% from Poland, 44% from Belarus and 71.4% from France - p=0.028) and sadness (73.3% from Poland, 40% from Belarus and 28.6% from France - p=0.002). Most often in response to the annoying and stressful child’s behaviour parents tried to admonish (76.7% from Poland, 56% from Belarus and 75% from France) or shout at the child (66.7% from Poland, 24% from Belarus and 17.9% from France p <0.001). The least likely preferred style of coping with stress in all countries was the search for socializing. The highest rate of self-efficiency characterize parents from France, the lowest from Poland. Conclusions: The existence of factors which could significantly affect the level of burn-out syndrome in parents, such as the deterioration of the financial situation (mainly in Belarusian families), sadness, fatigue, insomnia (mainly in Polish families). Parents chose effective strategies of coping, and the predominant style was focused on the task. It has been shown that parents lack the ability to control negative emotions, which in particular affected Polish families (for example, domination of trials to admonish and explain, shouting at the child).
Źródło:
Progress in Health Sciences; 2016, 6(1); 116-122
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The quality of life in parents raising children with an autism spectrum disorder from Poland, Belarus and France
Autorzy:
Ślifirczyk, A.
Krajewska - Kułak, E.
Brayer, A.
Sobolewski, M.
Maciorkowska, E.
Powiązania:
https://bibliotekanauki.pl/articles/1917772.pdf
Data publikacji:
2016
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
autism spectrum disorder
children
parents
quality of life
Opis:
Purpose: To assess the health-related quality of life (HRQL) in parents of children with autism spectrum disorder (ASD). Materials and methods: The sample consisted of 83 families with children with ASD, including 30 families from Poland, 25 from Belarus, and 28 from France. Parental HRQL was surveyed with the World Health Organization Quality of Life–BREF (WHOQOL–BREF) and KINDLR questionnaires. Results: This study showed that Polish parents reported the lowest quality of life according to the WHOQOL–BREF. Parents from Belarus reported slightly worse HRQL than parents from France, though other aspects of quality of life (e.g, social sphere, somatic sphere) did not differ significantly between these parents. Parents from Poland also reported lower HQOL according to the KINDLR questionnaire, while parents from Belarus had a higher HQRL in the mental, physical, and self-esteem domains compared to parents from Poland and France. Conclusion: Parents from Poland with children with ASD reported lower HRQL both on the WHOQOL–BREF and KINDL R questionnaires compared to parents from Belarus and France.
Źródło:
Progress in Health Sciences; 2016, 6(1); 102-107
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The assessment of empathic understanding and control of emotions in parents of children with autism
Autorzy:
Ślifirczyk, A.
Krajewska-Kułak, E.
Brayer, A.
Sobolewski, M.
Maciorkowska, E.
Powiązania:
https://bibliotekanauki.pl/articles/1917777.pdf
Data publikacji:
2016
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
Autism
The Courtauld Emotional Control Scale
empathy
parents
Opis:
Introduction: Problems of families with autism are generally not visible or manifested, but without support, they become economically and educationally inefficient. Purpose: To assess the degree of empathic understanding of the child and the degree of emotional control by parents. Materials and methods: The study included 30 families from Poland, 25 from Belarus and 28 from France. We used Empathy Understanding Others questionnaire (KRE) and The Courtauld Emotional Control Scale (CECS). Results: The most common difficulty reported in the care of a child was gaining his/her independence (66.7% in Poland, 84% in Belarus, 78.6% in France). Parents from Poland more often (26.7%) than others (12% in Belarus, 3.6% in France) pointed out that the disability of a child caused that their friends turned their back to them. 40% of parents from Poland, 60% from Belarus and 57.1% from France claimed that the spouses accept the disability of the child. The disability induced in parents mainly fatigue (76.7% from Poland, 44% from Belarus, 71.4% from France). The level of empathy in Polish (64.2 ± 6.2) and French parents (64.8 ± 11.6) was almost identical, and the highest was among Belarusian parents (70.3 ± 8.3). Overall rate of CECS of the surveyed parents was at the average level (from Poland 47.4 ± 4.9; from Belarus 44.8 ± 6.1, from France 48.1 ± 6.0). Conclusions: Nurses evaluated their own preparation for educational activities usually very low. In the majority they would not want to take up the difficult role of educators of parents of autistic children. Due to a potential contact of a nurse with a child with autism and the child’s family, it is advisable to extend the knowledge of nurses in the care of a child with autism.
Źródło:
Progress in Health Sciences; 2016, 6(1); 108-115
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Factors determining the psychometric assessment of patients after hip replacement surgery
Czynniki warunkujące ocenę psychometryczną pacjentów po protezoplastyce stawu biodrowego
Autorzy:
Michalczuk, T.
Ślifirczyk, A.
Krajewska-Kułak, E.
Piszcz, P.
Gałecka, A.
Kowalenko, M.
Powiązania:
https://bibliotekanauki.pl/articles/2048811.pdf
Data publikacji:
2021
Wydawca:
Akademia Bialska Nauk Stosowanych im. Jana Pawła II w Białej Podlaskiej
Tematy:
psychometric assessment
patient
human disease
hip replacement
surgery
life quality
pain
hospitalization
Opis:
Background. The aim of this study was to investigate the influence of selected factors such as place of residence, education, age, duration of hospitalization and pain intensity before and after hip replacement surgery on the level of acceptance of the illness, on the subjective assessment of the patient’s state of health during surgery and on the level of pain and the ability to manage and reduce pain. Material and methods. The study included 181 patients diagnosed with hip joint degeneration and qualified for total hip replacement hospitalized in the Regional Specialist Hospital in Biała Podlaska, Poland. The study was conducted by means of a diagnostic survey with the use of a set of questionnaires: Acceptance of Illness Scale – AIS, WOMAC Scale, SF-36 Questionnaire, BPCQ Questionnaire. Results. More than half of the respondents (55.2%) were highly accepting of their condition. The level of acceptance was influenced by the place of residence, education, age, the intensity of pain after surgery and functional limitation. The overall assessment of the quality of life in the physical domain was – 62.9 points, with the worst scores for physical functioning and general health. Analysis with the WOMAC questionnaire showed that the majority of the subjects scored below 50 points on the functional limitation scale. All factors, except the level of pain before surgery, influenced the degree of functional limitation. Conclusions. Age, place of residence and education provided opportunities for pain control and the ability to reduce pain was perceived by those with longer hospital stays. Participants from cities had the highest quality of life. Education influenced the quality of life, which decreased with age and higher pain intensity. The better the quality of life, the higher the level of acceptance of illness, and vice versa.
Wprowadzenie. Celem niniejszej pracy było zbadanie wpływu wybranych czynników ta- kich jak: miejsce zamieszkania, wykształcenie, wiek, czas hospitalizacji oraz nasilenie bólu przed i po zabiegu operacyjnym protezoplastyki biodra na poziom akceptacji choroby, na su- biektywną ocenę stanu zdrowia operowanego pacjenta oraz na poziom bólowy i umiejętność panowania nad bólem i jego obniżeniem. Materiał i metody. Badaniem objętych zostało 181 pacjentów z rozpoznaniem zwyrodnienia stawu biodrowego i zakwalifikowanych do zabie- gu operacyjnego całkowitej alloplastyki biodra hospitalizowanych w Wojewódzkim Szpitalu Specjalistycznym w Białej Podlaskiej. Badanie przeprowadzono metodą sondażu diagno- stycznego z wykorzystaniem zestawu kwestionariuszy: Skali Akceptacji Choroby – AIS, Skali WOMAC, Kwestionariusza SF-36, Kwestionariusza BPCQ. Wyniki. Stwierdzono, że ponad połowa badanych (55,2%) w wysokim stopniu akceptowała swoje schorzenie. Na poziom akceptacji miały wpływ: miejsce zamieszkania, wykształcenie, wiek, natężenie bólu po zabiegu oraz ograniczenie sprawności funkcjonalnej. Ogólna ocena jakości życia w dziedzinie fizycznej wynosiła – 62,9 pkt., przy czym najgorzej wypadła ocena funkcjonowania fizycznego oraz zdrowia ogólnego. Analiza za pomocą kwestionariusza WOMAC wykazała, że większość badanych, w pomiarze stopnia ograniczenia sprawności funkcjonalnej, uzyskała poniżej 50 pkt. Wszystkie czynniki, poza poziomem bólu przed zabiegiem, wpływały na stopień ograniczenia sprawności. Wnioski. Wiek, miejsce zamieszkania oraz wykształcenie dały możliwości panowania nad bólem, a o możliwości jego zmniejszenia wiedziały osoby dłużej hospitalizowane. Najwyższą jakością życia charakteryzowały się osoby z dużych miast. Wykształcenie wpłynęło na jakość życia, która wraz z wiekiem i wyższym natężeniem bólu spadała. Im lepsza jakość życia, tym wyższy poziom akceptacji choroby i odwrotnie.
Źródło:
Health Problems of Civilization; 2021, 15, 2; 87-100
2353-6942
2354-0265
Pojawia się w:
Health Problems of Civilization
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Quality of life of patients with atrial fibrillation
Autorzy:
Ślifirczyk, A.
Michalczuk, T.
Piszcz, P.
Kierczuk, E.
Kowalenko, M.
Zalewski, R.
Krajewska-Kułak, E.
Powiązania:
https://bibliotekanauki.pl/articles/1918616.pdf
Data publikacji:
2018-06-18
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
Patient
quality of life
atrial fibrillation
treatment
Opis:
Introduction: Atrial fibrillation (AF) is one of the most frequent arrhythmias. In Poland, there is a risk of developing AF in about 400,000 people. Atrial fibrillation occurs most frequently as a result of disorders of physiological automatism and afterdepolarization and triggered activity. The treatment strategy of AF is based on pharmacological treatment and procedures such as ablation or cardioversion. The quality of life as defined by the WHO is an individual perception of one's well-being. On the other hand, the assessment of the quality of life in illness is modified regarding health problems. Purpose: The main goal of the study was to get to know the quality of life of people with atrial fibrillation. Materials and methods: The research was carried out using a diagnostic survey, based on a survey among 100 patients diagnosed with AF. The place of the research was the Regional Specialist Hospital in Biała Podlaska, in the Emergency Department. Results: Increased morbidity was observed among women and people over the age of 60. The majority of patients with AF declared the quality of life at the medium level. The respondents most often followed medical recommendations. The majority of respondents did not follow healthy lifestyle rules, because as many as 68% of respondents did not do any physical activity and a significant part of the respondents smoked cigarettes and had an inflated BMI. Conclusion: AF affects the quality life by causing sadness, irritation and insomnia.
Źródło:
Progress in Health Sciences; 2018, 8(1); 88-92
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Knowledge of risk factors of myocardial infarction in patients treated in the Interventional Cardiology Unit of the Regional Specialist Hospital in Biała Podlaska
Autorzy:
Ślifirczyk, A.
Michalczuk, T.
Piszcz, P.
Kowalenko, M.
Kierczuk, E.
Zalewski, R.
Krajewska – Kułak, E.
Powiązania:
https://bibliotekanauki.pl/articles/1918634.pdf
Data publikacji:
2018-06-18
Wydawca:
Uniwersytet Medyczny w Białymstoku
Tematy:
Myocardial infarction
risk factors
level of knowledge
Opis:
Purpose: To analyse knowledge of patients in the Interventional Cardiology Department in the field of theory of the disease entity, i.e. myocardial infarction and factors predisposing to its occurrence. Materials and methods: The study was carried out at the Interventional Cardiology Department of the Regional Specialist Hospital in BiałaPodlaska between 3.11.2017 and 20.12.2017. Sixty respondents were included, 62% women and 38% men. The largest group were patients between 46 and 60 years of age. The work involved an anonymous questionnaire, which contained 28 questions, including two open ones. Patients participated in the study were informed that the study was voluntary and the questionnaire was anonymous. Results: According to the respondents, the main cause of myocardial infarction is atherosclerosis (43.4%). The respondents indicate that cardiovascular diseases (including myocardial infarction) which are on the third place in Poland, right after cancer and injuries, cause death (63.3%). As the main factor that influences the occurrence of myocardial infarction is overweight and obesity (79.8%). More than half of the respondents assess their knowledge of myocardial infarction on average, while 18.3 % said that they have very good knowledge. Conclusions: Patients with myocardial infarction have quite a good knowledge about the risk factors for this disease. A large group of respondents tries to counteract the risk factors for myocardial infarction. A small part of the respondents undergoes regular blood tests (blood glucose level, total cholesterol and its fractions, measurement of blood pressure).
Źródło:
Progress in Health Sciences; 2018, 8(1); 93-101
2083-1617
Pojawia się w:
Progress in Health Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-7 z 7

    Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies