Using affinity analysis in diagnosing the needs of patients as regards e-Health.

INTRODUCTION: E-Health tools allow a medical facility to set a given patient's data in order using ICT techniques, and the patient to use those techniques when contacting a given organisation. MATERIAL AND METHODS: Secondary statistical data was used in the research. The study was carried out among primary health care patients. Mining for affinity rules was done in the R programme. The apriori and inspect functions from the arules package were used. Moreover, any redundant rules were removed from thoseobtained using the afero-mentioned method. Applying the general description of the affinity analysis method onto the survey described herein, it should be stressed that the aim of using affinity analysis was to discover the rules which contain the sub-transaction B={V_6=1} as a consequent. This was determined by the intention to discover associations regarding the knowledge about a uniform information system that the patients under study might have. RESULTS: In the discovered rules, the antecedent most often contained an indication of the need for introducing a uniform solution as regards telemedicine. Moreover, according to the opinions of 'conscious'patients, a uniform IT system should improve the work at primary health care institutions, introducing an on-line booking system for visits should improve the productivity and comfort of doctors, and an IT system should provide unambiguous identification of a patient. CONCLUSIONS: There is potential in using affinity analysis within e-Health. The example of affinity analysis described in his study led to the discovery of interesting and important (from the point of view of a medical facility) regularities regarding the knowledge and expectations of patients as regards e-Health.

An evaluation of the genetic conditioning of evoking pain.

INTRODUCTION AND OBJECTIVE: Pain is an integral element of the pathogenic process and sometimes determines its course. Disorders in pain sensation, as well as its lack, the pain threshold, and variability in sensation of the same pain stimuli as more or less intensive by different persons, may be genetically conditioned. The aim of the study is to examine genes in pathogenesis of chronic pain. MATERIAL AND METHODS: The study was conducted in a specially selected group of 31 persons: study group - 20 patients with chronic pain, and control group - 11 healthy individuals who did not experience pain. The control group of 11 healthy persons, compared with the study group, was the catalyst for determining the relative quantification (RQ) of gene expression. Biological material in the form of venous blood was collected from the study participants into the tubes containing anticoagulant EDTA KE/2.7 ml (ethylenediaminetetraacetic acid), preventing extracorporeal blood clotting. RESULTS: Analysis of expression of the examined genes showed over-expression of the DRD1 gene in patients experiencing chronic pain, which means that in these patients an increased number of dopamine D1 receptors encoded by this gene should be expected. The dopamine D1 receptor is a G-protein-coupled receptor which regulates (stimulates or inhibits) adenyl cyclase - the enzyme responsible for synthesis of cyclic AMP (cAMP). An increase in the concentration of cAMP in neurons enhances the sensation of pain. CONCLUSIONS: The genes (DRD1, COMT, OPRK1, HCN2) have a significant role in the pathogenesis of chronic pain in various diseases; they can also influence the perception of pain. Knowledge of these genes can contribute to the development of effective methods of combating pain.

The impact of selected factors on acceptance of illness and life satisfaction among female residents of rural areas treated for osteoporosis.

INTRODUCTION: Osteoporosis is a chronic condition with serious sequela, including primarily bone fractures, and impacts on almost all spheres of human life. It is important for patients undergoing treatment to accept their health status and feel satisfied with life. OBJECTIVE: The aim of the study was to determine the relationship between socio-demographic factors, duration of the illness, self-assessment of the patient's knowledge of osteoporosis, and also between illness management support and acceptance of the illness and life satisfaction among females with chronic osteoporosis, resident in rural areas. MATERIAL AND METHODS: The study, conducted from September 2016 - June 2017, involved 207 patients of the Clinic of Orthopaedics and Rehabilitation and the Clinic of Gynaecology at the Independent Public Teaching Hospital No. 4 in Lublin, eastern Poland. The study used the Acceptance of Illness Scale (AIS) and the Satisfaction With Life Scale (SWLS). Statistical analysis was performed with Student's t-test, analysis of variance (ANOVA), Tukey's range test, and chi-squared test. A p-value of <0.05 defined statistical significance of differences. The analysis was performed using commercial SPSS Statistics 19 software (IBM Corp., Armonk, NY, USA). RESULTS: The respondents showed average acceptance of their illness (22.2±6.9) and relatively low satisfaction with life (14.7±5.6). Older age, low level of education, poor living conditions, prolonged illness, and frequent ailments are all associated with lower acceptance of the illness and poorer life satisfaction. CONCLUSIONS: As part of their treatment, chronically ill patients should be provided with appropriate support, in particular from healthcare personnel, health education and improved living conditions.

Differences in the Perception of Social Support Among Rural Area Seniors-A Cross-Sectional Survey of Polish Population.

Introduction and objective: Social support constitutes an important determinant of an elderly person’s health and of functioning in his or her living environment. It depends on available support networks and the type of help received. Measurement of social support should encompass both its structure and the functions it fulfills, which enables detailed assessment of the phenomenon. The aim of the study was to compare the perception of social support among rural area seniors provided with institutional care with those living in a home setting. Material and method: Using the diagnostic survey method and the technique of the distribution of a direct questionnaire, 364 respondents from rural areas were examined: those living in an institutional environment (n = 190) and those living in their home (natural) environment (n = 174). The respondents were selected on the basis of a combined sampling method: proportionate, stratified, and systematic. Variables were measured with the following questionnaires: Courage Social Network Index (CSNI) and Social Support Scale (SSS). Results: The living environment has been proved to differentiate average values of support both in the structural and functional dimensions in a statistically significant way (p < 0.001). An untypical phenomenon was higher average values pertaining to emotional bonds, frequency of direct contacts, and help received in the group of respondents living in an institutional environment. Conclusions: The living environment and demographic variables affect the perception of social support among elderly people. Full-time institutional care of a senior citizen leads to the deterioration of social support; therefore, keeping an elderly person in a home environment should be one of the primary goals of the senior policy.

Attitudes of women after the age of 50 towards preventive screening.

INTRODUCTION: Prevention is one of the major branches of the health sector. The National Health Programme encompasses main risk factors, elimination of which may lead to a reduced incidence of illnesses in the society. At the same time, the criteria of selecting people eligible for preventive screening are established according to risk groups determined by sex, as well as age in the population of women. The perimenopausal and menopausal period contributes to occurrence of numerous systemic diseases and to an increased risk of illnesses, especially cancers. OBJECTIVE: The objective of the research was to evaluate the performance of preventive screening tests of women after 50 aimed at early detection of cervical and breast cancer. Furthermore, the research estimated frequency of pathological lesions detected and regularity of their monitoring. MATERIALS AND METHODS: The research covered 150 women after 50 years of age. The database was statistically examined with STATISTICA software. RESULTS: A low percentage of the respondents, in comparison to the risk increasing with age, had a Pap test (61.3%) and mammography (51.3%) in the last two years. In the case of women whose latest Pap test or mammography showed abnormalities and was the basis for diagnosing pathological lesions, 69.2% of them were under regular medical supervision if abnormalities were identified by a Pap test and 68.7% if lesions were detected in breast structure. CONCLUSIONS: In the examined group we observed a small percentage of women undergo Pap tests and mammography. Furthermore, medical recommendations regarding early detection of cancers are frequently ignored and disregarded by patients.

General self-efficacy level and health behaviours in women over the age of 45 years who have undergone osteoporosis treatment.

INTRODUCTION: Contemporary people do not follow the civilisation development in every life domain, their lifestyle is not always healthy. Self-efficacy is the factor that plays an important role in undertaking actions towards struggling with the disease. THE AIM OF THE STUDY: The aim of the study was to determine the relationship between the general self-efficacy level and health behaviours as well as chosen sociodemographic features in women over the age of 45 years who have undergone osteoporosis treatment. MATERIAL AND METHODS: The study comprised 151 women over the age of 45 years. The research was conducted in 2016 in health care centres in Lublin, a city in south-eastern Poland. The Generalised Self-Efficacy Scale (GSES) by R. Schwarzer, M. Jerusalem and Z. Juczynski and an original questionnaire were used as research tools. The obtained material was subjected to descriptive and statistical analysis. χ2 test, Kruskal-Wallis test, Mann-Whitney Test and Spearman's rank correlation coefficient were all applied. RESULTS: The analysis of obtained results showed that as much as 73.5% of the respondents showed very low and low generalised self-efficacy level. On the other hand, only 22.5% of the examined were characterised by high and very high generalised self-efficacy level. The longer the duration of osteoporosis treatment (rho = 0.251; p = 0.002) and the better the self-estimation of health status (rho = 0.473; p = 0.000), the higher the respondents' generalised self-efficacy level. The women's self-efficacy level declined with increasing ailments (rho = -0.190; p = 0.019). CONCLUSIONS: The generalized self-efficacy level and the health behaviours are not satisfactory.

Men's knowledge about osteoporosis and its risk factors.

INTRODUCTION: Until recently osteoporosis was seen mainly as a woman's problem. However, in the last ten years there has been rising awareness in society that osteoporosis constitutes an inseparable element of getting old for men as well. The aim of the research was to evaluate men's knowledge about osteoporosis and its risk factors contributing to the development of the disease. MATERIAL AND METHODS: The study included 205 men aged 20-60. The examined men were patients of selected healthcare centres in Lublin Voivodeship. The study was conducted between September 2014 and April 2015. The research was performed by means of the survey method, using a poll technique. Purposive sampling and an original questionnaire were used. Gathered material was subjected to descriptive and statistical analysis. The Mann-Whitney U test and Kruskal-Wallis test were applied. The statistical significance level was set at α = 0.05. IBM SPSS Statistics software was used to perform the statistical analysis. RESULTS: The respondents' level of knowledge about osteoporosis and its risk factors can be estimated as average. The polled men showed better knowledge on osteoporosis risk factors (M = 59.78) than general osteoporosis knowledge (M = 53.71). Significant differences were found between the respondents' education and their general osteoporosis knowledge as well as between the respondents' living conditions and their knowledge about osteoporosis risk factors. CONCLUSIONS: Because of the insufficient level of knowledge about osteoporosis and its risk factors in the male population it is advisable to launch prevention programmes aimed at men focusing on this issue.

Quality of life of patients with irritable bowel syndrome before and after education.

OBJECTIVES: The aim of the present study was to analyse the impact of education of patients with irritable bowel syndrome (IBS) on their quality of life. METHODS: The study was carried out at the Gastroenterology Outpatient Clinic of the Independent Public Clinical Hospital No. 4 in Lublin and Gastroenterology Outpatient Clinic of the Cardinal Stefan Wyszynski Regional Specialist Hospital in Lublin in the years 2010-2011. The quality of life was analysed using the Quality of Life Questionnaire (QOL-Q R. Schalock, K. Keith). The group of 83 patients with the diagnosis of irritable bowel syndrome, who gave their consent for inclusion in the study, was provided with information about the essence of the disease, disease-related diet and lifestyle, course of the disease, medications, and check-ups. RESULTS: Our patients educated by the physician, nurse and those provided with written information had substantially higher scores in multi-dimensional aspects of the quality of life after education. Six months after education patients with IBS showed a significantly higher quality of life in all aspects, i.e. Satisfaction, Competence/productivity, Empowerment/independence and Social inclusion/community integration. The understanding of the essence of their disease contributed to a decrease in anxiety associated with the neoplastic disease and worrying symptoms, which significantly reduced the incidence of complaints. CONCLUSIONS: 1. Quality of life of patients with irritable bowel syndrome is substantially reduced in all the examined spheres. 2. Education of patients with IBS resulted in enhanced quality of life and reduced disease-related complaints. 3. Education of patients with IBS plays a significant role in the entire therapeutic process.

Chosen risk factors for osteoporosis and the level of knowledge about the disease in peri- and postmenopausal women.

INTRODUCTION: Osteoporosis as a chronic disease, affecting especially women in postmenopausal age, is an important, social and economic health problem especially of women of today's world. The aim of the study was to assess the level of knowledge of women in the peri- and postmenopausal period about the prevention of osteoporosis and show the influence of chosen risk factors on the level of this knowledge. MATERIAL AND METHODS: A group of 300 women aged 45-65, being patients of healthcare centres in Chelm, Lublin and Zamosc (Lublin voivodeship, south-eastern Poland) were included in the study. The purposive sampling was used. Osteoporosis Knowledge Test (OKT) 2011 was the research tool. Gathered material was subjected to descriptive and statistical analysis. Tukey's test, t-student test and variance analysis (ANOVA) were all applied. An accepted p materiality level was < 0.05 and p < 0.01. RESULTS: Respondents presented the average level of knowledge about the role of physical activity in the prevention of osteoporosis (M = 13.93) and a low level of knowledge about well-balanced diet rich in calcium (M = 9.77). The knowledge about risk factors, screening and treatment remained on the average level (M = 8.00). An influence of socio-demographic factors on the level of knowledge was shown. Also some behaviours, associated with the lifestyle indeed influenced the level of this knowledge. CONCLUSIONS: Professional educational programs on osteoporosis should be implemented in the population of Polish peri- and postmenopausal women.

Knowledge of osteoporosis prophylaxis and health behaviours of the population of chosen countries of the world.

INTRODUCTION: Osteoporosis is recognized by the World Health Organization as a disease associated with the progress of civilization, also called the 'epidemic of the 21 st century'. OBJECTIVE: An attempt to portray the level of knowledge and health behaviours of societies of selected countries of the world in the prevention of osteoporosis, based on available studies. MATERIALS AND METHOD: Theoretical concepts and reviews of current published studies. RESULTS: Accessible study findings conducted worldwide are not exhaustive and often present the subject in a fragmentary way. Data presented in the presented article shows that knowledge of osteoporosis among the Polish population and the population of selected countries of the world appears insufficient in the issues associated with its prophylaxis and prevention; they also testify to a disregard and lack of application of the principles of a healthier lifestyle in daily life regarding this still little-known illness. Since the number of people threatened with osteoporosis, as well as the number of bone fractures, is constantly rising, versatile action should be undertaken aimed at preventing falling ill and progression of the disease. CONCLUSIONS: After reviewing the literature, it was realized that few researchers have been interested in the issue of osteoporosis. This fact is proved by an insufficient amount of publications dealing with the subject and the problem associated with osteoporosis from the point of view of the public. The findings of presented study show that most often the subject is not portrayed as a whole, but concerns only selected preventive behaviours or learning about some risk factors.

Analysis of the doctor-patient communication if breast cancer is diagnosed / Análisis de la comunicación médico-paciente en el diagnóstico de cáncer de mama / Análise da comunicação médico-paciente em caso de diagnóstico de câncer de mama

The aim of the paper is the recognition and evaluation of demand for medical information among patients suffering from breast cancer. The research was conducted among 120 women with diagnosed breast cancer in the Oncological Surgery Clinic of the Independent Public Research Hospital Nº 1 in Lublin, the Oncological Clinic of the Independent Public Research Hospital Nº 1 in Lublin and the Rehabilitation Centre with the Rehabilitation Clinic at the Lublin Oncology Centre. The research included women from the Club of Women after Mastectomy “Amazons”, the Club “Amazons” at the Complex of Specialist Clinics in Ostrowiec Swietokrzyski and the Club “Amazons” in Radom. Research showed that the demand for medical information among women with diagnosed breast cancer is very high. Respondents want to know all the information concerning the diagnosis, treatment and prognosis (93 percent). They also expect that the doctor will give them medical information concerning further consequences of cancer and its influence on future health and life (78 percent). Most of the respondents expect to receive information concerning medicaments which should be taken (77 percent) and the essence of the conducted treatment (93 percent). The research analysis showed that women with diagnosed breast cancer expect that the doctor will give them reliable and real medical information. Patients want the doctor to present them the probable course of the cancer (85 percent) and all the possible side effects connected with it (89 percent).

El objetivo de este trabajo es el reconocimiento y la evaluación de la demanda de información médica en pacientes con cáncer de mama. Se realizó la investigación con 120 mujeres diagnosticadas con cáncer de mama en la Clínica de Cirugía Oncológica y la Clínica Oncológica del Hospital de Investigación Público Independiente Nº 1 en Lublin, y el Centro de Rehabilitación con la Clínica de Rehabilitación del Centro Oncológico de Lublin. La investigación incluyó mujeres del Club “Amazons” de Mujeres que han sufrido Mastectomía, el Club “Amazons” del Complejo de Clínicas Especializadas en Ostrowiec Swietokrzyski y el Club “Amazons” en Radom. La investigación mostró que la demanda de información médica de mujeres con diagnóstico de cáncer de mama es muy alta. Aquellas que respondieron quieren saber todo acerca del diagnóstico, tratamiento y pronóstico (93 por ciento). También esperan que el médico les dé información médica respecto de posteriores consecuencias del cáncer y su influencia en su salud futura y su vida (78 por ciento). La mayoría de las que respondieron esperan recibir información sobre medicamentos que deberían tomar (77 por ciento) y lo esencial sobre el tratamiento realizado (93 por ciento). El análisis de la investigación muestra que las mujeres diagnosticadas con cáncer de mama esperan que el médico les dé información médica confiable y verdadera, les presente el curso probable del cáncer (85 por ciento) y todos los posibles efectos secundarios conectados (89 por ciento).

O objetivo deste artigo é o reconhecimento e a avaliação da demanda por informação médica entre pacientes que sofrem de câncer de mama. A investigação foi conduzida entre 120 mulheres diagnosticadas com câncer de mama na Oncological Surgery Clinic of the Independent Public Research Hospital Nº 1 de Lublin, a Oncological Clinic of the Independent Public Research Hospital Nº 1 de Lublin e a Rehabilitation Centre with the Rehabilitation Clinic do Lublin Oncology Centre. A pesquisa incluiu mulheres do Club of Women after Mastectomy “Amazons”, o Club “Amazons” do Complex of Specialist Clinic sem Ostrowiec Swietokrzyskie o Club “Amazons”em Radom. Pesquisa revelou que a demanda por informação médica entre mulheres com diagnóstico de câncer mamário é muito alta. As respondentes queriam saber todas as informações concernentes ao diagnóstico, tratamento e prognóstico (93 por cento). Elas também esperavam que o médico pudesse dar-lhes informação sobre consequências tardias do câncer e a influência sobre a sua saúde e vida futuras (78 por cento). A maioria dos respondentes tinham a expectativa de receber informação sobre medicamentos que deveriam tomar(77 por cento) e a essência do tratamento realizado(93 por cento). A análise da pesquisa demonstrou que as mulheres com diagnóstico de câncer de mama esperavam que o médico pudesse fornecer-lhes informação confiável e honesta. Pacientes queriam que o médico lhes apresentasse o provável curso do câncer (85 por cento) e todos os possíveis efeitos relacionados a ele (89 por cento).

Influence of sociodemographic factors on quality of life in women living in Lublin Province in Poland.

THE AIM OF THE STUDY: The aim of the study is to evaluate the impact of sociodemographic factors on the quality of life (QOL) in 45-65-year-old women. MATERIAL AND METHODS: The research by means of a survey method, postal questionnaire technique, comprised 2143 women - a representative sample of the female population living in Lublin Province. Three standardized questionnaires - WHOQOL-BREF, Women's Health Questionnaire and SF-36 - as well as an original questionnaire were used as research tools. In statistical analysis Student's t-test for two groups, an analysis of variance, Dunnett's T3 test for multiple comparisons, a one-way analysis of variance (one-way ANOVA) and a stepwise logistic regression analysis were used. RESULTS: In the population of peri- and postmenopausal women a significantly better quality of life in comparison with the rest of the studied women was established in women aged 45-49 years, respondents living permanently in urban areas as well as better educated women, those with full-time employment, especially those doing intellectual work, women remaining in a long-lasting relationship, and women assessing their financial situation and living conditions as well. Logistic regression analysis showed that the strong predictors of poor quality of life were as follows: self-assessment of living conditions as poor, self-assessment of financial situation as poor, permanent place of residence in the country, lower education level (incomplete primary education, primary education). CONCLUSIONS: The group of women with worse quality of life should become the main addressee of preventive programmes and health policy programmes designed for peri- and postmenopausal women.

The contemporary look at the problem of recognizing and diagnosing postmenopausal osteoporosis and eliminating the risk of a fall.

Osteoporosis constitutes a relevant health, social and economic problem of the contemporary world. As a chronic disease, often nicknamed the "silent thief", it is an object of the clinical research and a reason for many ambiguities. The most noticeable and basic symptom of osteoporosis is a low-energy fracture, which brings pain, physical disability, and a noticeable decrease in one's quality of life. Osteoporosis affects the entire population; however, women in the postmenopausal period and the elderly are mostly exposed to its progress. The risk of falling ill concerning women simply grows with the age and doubles with every decade after the age of 65. It is estimated that osteoporosis affects 200 million women worldwide, and about 20-25% of them will sustain an injury in the form of a bone fracture. In Poland, the problem of osteoporosis concerns 2.4 million women. The article attempts to show current views on examining and diagnosing postmenopausal osteoporosis and prevention of the fall risk. The BMD (bone mineral density) is considered the basis of osteoporosis diagnosis in postmenopausal women as well as an absolute 10-year risk of fractures and experienced osteoporotic fractures. All people at an increased fall risk should be provided with the multifactorial programme of fall prevention.

Psychosocial aspect of quality of life of Polish women with breast cancer.

INTRODUCTION AND OBJECTIVE: Breast cancer is one of the most frequently occurring malignant tumours among women in Poland. The highest incidence of the disease is registered among women aged 50 and more. Cancer imposes a considerable psychological strain on a woman. It causes a sense of uncertainty about one's health and further life, as well as frequent problems with accepting the image of one's own body. It often results in low self-esteem and a feeling of embarrassment, accompanied by symptoms of apathy and detachment. The aim of the study was to determine mental and social life quality of Polish women treated for breast cancer. MATERIALS AND METHODS: The research encompassed 107 women aged between 45 and 65 (SD=6.11) undergoing treatment for breast cancer. The WHOQOL-Bref scale was applied in the research. RESULTS: The social field was better evaluated in comparison with the mental sphere. There was a statistical correlation between place of residence and social sphere of quality of life (p=,036), with higher ratings assigned by respondents residing in rural areas (M=15.36) compared with residents of towns (M=14.15). CONCLUSIONS: Given the fact that respondents were coping with cancer or its consequences, paradoxically, perception of the overall quality of life and examined areas was generally good, especially among women with higher education, those who were single and those living in rural areas. Along with age, there decreases at the respondents the experienced quality of life, however a rise of evaluations of the mental sphere is accompanying the rise in the education level.

Quality of life in peri- and post-menopausal Polish women living in Lublin Province--differences between urban and rural dwellers.

INTRODUCTION AND OBJECTIVE: The quality of life in peri- and post-menopausal women constitutes a serious public health problem. The aim of this observational cross-sectional study was to reveal the influence of the permanent domicile on the quality of life of women in peri- and post-menopausal period, and to establish the influence of employment as a full-time agricultural worker on the quality of life in these women. MATERIALS AND METHODS: The research was carried out by means of a survey using the postal questionnaire technique. Three standardized questionnaires: WHOQOL-BREF, Women's Health Questionnaire (WHQ) and SF-36 were used as research tools. An original questionnaire was also used. The study comprised a representative sample of the female population aged 45-65 living in Lublin Province. The sample size was 2,143 women. RESULTS: The quality of the women's life was significantly affected by the place of permanent residence. The worst quality of life was found in permanent country dwellers. City and town inhabitants revealed a considerably higher level of quality of life. Permanent place of residence in the country was an independent predictor of a poorer quality of life. Employment as a full-time agricultural worker was an independent predictor of a worse quality of life in the SOM domain of WHQ, as well as RP, RF and RE domains of SF-36. On the other hand, employment as a full-time agricultural worker was an independent predictor of a better quality of life in the SLE domain of WHQ, and psychological domain of WHOQFL-BREF. CONCLUSIONS: Awareness of the dependence is necessary in order to effectively plan health education and physical and social health promotion campaigns. Country dwellers need special attention in the process of undertaking any preventive or curative steps.

[Pain in children in historical perspective]. / Ból u dzieci--spojrzenie historyczne.

Pain in children, especially in infancy, is frequently underestimated. Surprisingly, in ancient times, writers were more aware of the existence of pain in infancy and the need for its relief than in 20th century. They rated pain perception as being higher in infancy than in childhood. The study by McGraw (1941), although badly designed, convinced the vast majority of clinicians that infants do not feel pain and do not require analgesia. This theory, reinforced by the fear of using opioids in young children, dominated medical thinking for more than 30 years. Later studies on pain perception in foetuses, and careful analysis of infants' reactions to blood sampling, helped doctors to understand the necessity of adequate analgesia in young children. In this review, we present the approach to pain in children over centuries, from ancient times to the latest developments in this field.

[Social and healthy circumstances of women's decision about applying hormonal replacement therapy]. / Spoleczno-zdrowotne uwarunkowania decyzji kobiet o stosowaniu hormonalnej terapii zastepczej.

UNLABELLED: The aim of the study was to evaluate the frequency of hormonal replacement therapy (HRT) application among Polish women aged 40-65, patients of five selected health care institutions located in south-eastern Poland and to determine the most significant factors that influence women's decision to initiate HRT. The next purpose was to establish how the women learned about the possibility of receiving HRT. Women, who never decided to take sex hormones, were asked about the reasons of such decision. MATERIAL AND METHODS: The study comprised a group of 1033 women aged 40-65 years living in south-eastern Poland, the patients of various hospital wards and outpatient clinics. The study was conducted from January 2003 to December 2004 using categorized interview technique. The interview questionnaire was constructed by the authors. The statistical analysis was performed on the basis of the chi2 test of independence; log-linear analysis and Pareto's analysis were also used. RESULTS: Research result analysis proves that 30.5% of the examined women have used HRT currently or in the past. The sociodemographic and healthy variables that showed positive correlation with receiving hormonal treatment by midlife women were: age 51-65 years, the presence of climacteric ailments, the absence of monthly bleedings, possessing of permanent life partner and good self-estimation of one's financial status. It was not revealed that better educated women more frequently decide to take HRT. The main sources of women's knowledge about HRT were the mass media and health service employees. Among the reasons for not taking up hormonal treatment the most significant were: lack or small intensification of menopausal ailments as well as the fear of side effects of hormonal replacement therapy.

The type of relationship in marriages of patients with neurosis disorders.

Conjugal relationships are an integral part of spouses' bonds. The only pattern of relationships in the marriages of patients with neurosis disorders was a type based on a dependence mechanism, i.e. subordinating one partner to another, whereas in the control group the pattern is based on a sense of mutual confidence, self-control, and the need to understand oneself and other people as well.

Psychosocial functioning of the people with delusional disorders under forensic psychiatric observation in the ward of forensic psychiatry in 1998-2002.

In the literature on the subject frequency and kind of deeds committed by people with mental illness in relation to individual clinical diagnoses are analyzed mainly, whereas little attention is paid to the issue of their psychosocial functioning. Intellectual functioning of the people manifesting delusional disorders in the course of committing attributed deeds, was on an average level. The patients' social functioning was on a low level.

Frequency of self-monitoring and its effect on metabolic control in patients with type 2 diabetes.

The aim of the study was to investigate the frequency of self-monitoring of blood glucose in patients with type 2 diabetes and to determine its effect on metabolic control measured as glycosylated hemoglobin level. The study involved 218 patients with type 2 diabetes (68.8% of females and 31.19% of males) who reported to the Outpatient Department for Diabetes at the Institute of Agricultural Medicine in Lublin. All patients were asked to complete a questionnaire form containing questions concerning, among other things, demographic data, course of diabetes, method of treatment, ability to adjust insulin doses and frequency of self-monitoring of blood glucose level. The levels of glycosylated emoglobin were obtained based on medical records. The analysis of the data showed that 59.22% of patients tested their blood glucose levels at home > or = 1/day, 21.36% of them tested their blood glucose > or = 1/week, whereas 8.74% of patients tested glucose < or = 1/week. 10.68% of patients stated that they never racticed SMBG. Statistical differences were observed in the level of education. Among the group of patients who exercised self-monitoring the most dominant were those with secondary school or university level of education (60.66%), while among patients who did not maintain self-monitoring the greatest number had only elementary or vocational education (72.73) (p = 0.01). The greatest number of patients who most often maintained self-monitoring were office workers (52.46%), whereas among those who did not exercise self-monitoring, those employed in agriculture dominated (45.45%) (p < 0.01). Urban inhabitants exercised self-monitoring more frequently than urban inhabitants (p < 0.01). The frequency of self-monitoring did not affect glycemia control. Urban inhabitants with secondary school or university education level and those who perform office work are more keen on frequent home monitoring of glycemia. In patients with type 2 diabetes the intensity of self-monitoring does not exert any effect on diabetes control evaluated by means of glycosylated hemoglobin level.