4 research outputs found

    The problem of anemia in elderly patients

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    Introduction and purpose:  As healthcare develops, life expectancy increases. This makes anemia of the elderly an increasingly common problem. The appearance of this disease is influenced by many factors related to the aging process of the organism. The purpose of this study is to review information about the different mechanisms of anemia development in the elderly and to present the associated difficulties in medical practice. Description of the state of knowledge: Many different factors can affect the process of anemia. The causes of this disorder include chronic inflammatory diseases, cancer and nutritional deficiencies. Endocrine status is also important. The chronic inflammatory process may induce haemolysis and lead to the increased synthesis of hepcidin, which by blocking the activity of ferroportin leads to a decrease in the level of iron ions in the blood. Deficiency anemia often results from reduced appetite, inadequate quality of meals, chronic inflammation or taking medications without consulting a doctor. The consequence is a reduced level of iron and vitamin B12 and folic acid, which play a role in erythropoiesis. The hormones that play a significant role in the process of making red blood cells include erythropoietin, testosterone and thyroid hormones. Summary:  Anemia is a common problem among geriatric patients and one of the factors contributing to the increase in mortality in this age group. In medical care it is difficult to distinguish which symptoms are pathological and which are related to the natural aging process, overlapping symptoms of many diseases and related diagnostic problems. Diagnostics is a particular challenge due to the multi-morbidity, which is associated with taking many drugs with different mechanisms of action and side effects.  Keywords: anemia; aging; comorbidity; nutrient-deficiency anemia; inflammatio

    Pharmacotherapy of depression in palliative patients

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    Introduction: Depression often affects people suffering from serious illnesses, including oncological and palliative patients. It reduces their quality of life and worsens their prognosis. This is why it is so important to properly treat depression in palliative patients. Material and Methods: The information provided was collected as a result of analysis of various articles and textbooks on development, diagnosis and treatment, as well as prevention of depression in terminally ill patients using Google Scholar and PubMed databases. Results: The results show that the most common drug in therapy for palliative patients with depression are the sluggish serotonin reuptake inhibitors (SSRIs). SSRIs inhibit serotonin transporter reducing serotonin reuptake. This raises the level of neurotransmitter - serotonin - in the synaptic cleft. They are well tolerated and have fewer side effects than older antidepressants (tricyclic antidepressants and monoamine oxidase inhibitors). Tricyclic antidepressants may relieve neuropathic pain and they are also beneficial for patients with insomnia. Mirtazapine in addition to antidepressant effects also causes increasing appetite, reducing nausea and sedative effect. In cancer-diagnosed patients particular attention should be paid to side effects such as nausea and vomiting that may occur in patients undergoing radiotherapy and chemotherapy using SSRIs or TCAs. SSRI therapy have a good safety profile and also interacts less frequently, while atypical antipsychotics may reduce the discomforts of taking chemotherapy. An alternative method of treating depression is the use of psychostimulants such as methylphenidate. Another way to treat depression is psychotherapy. Conclusions: There are several options for treating depression in palliative patients. It is important to pay attention to the side effects of prescribed medicines. Nevertheless, the best results are obtained by combining pharmacotherapy with psychotherapy

    Relationship Between Anti-DFS70 Autoantibodies and Oxidative Stress

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    Background: The anti-DFS70 autoantibodies are one of the most commonly and widely described agent of unknown clinical significance, frequently detected in healthy individuals. It is not known whether the DFS70 autoantibodies are protective or pathogenic. One of the factors suspected of inducing the formation of anti-DFS70 antibodies is increased oxidative stress. We evaluated the coexistence of anti-DFS70 antibodies with selected markers of oxidative stress and investigated whether these antibodies could be considered as indirect markers of oxidative stress. Methods: The intensity of oxidative stress was measured in all samples via indices of free-radical damage to lipids and proteins such as total oxidant status (TOS), concentrations of lipid hydroperoxides (LPH), lipofuscin (LPS), and malondialdehyde (MDA). The parameters of the non-enzymatic antioxidant system, such as total antioxidant status (TAS) and uric acid concentration (UA), were also measured, as well as the activity of superoxide dismutase (SOD). Based on TOS and TAS values, the oxidative stress index (OSI) was calculated. All samples were also tested with indirect immunofluorescence assay (IFA) and 357 samples were selected for direct monospecific anti DFS70 enzyme-linked immunosorbent assay (ELISA) testing. Results:: The anti-DFS70 antibodies were confirmed by ELISA test in 21.29% of samples. Compared with anti-DFS70 negative samples we observed 23% lower concentration of LPH (P = .038) and 11% lower concentration of UA (P = .005). TOS was 20% lower (P = .014). The activity of SOD was up to 5% higher (P = .037). The Pearson correlation showed weak negative correlation for LPH, UA, and TOS and a weak positive correlation for SOD activity. Conclusion: In samples positive for the anti-DFS70 antibody a decreased level of oxidative stress was observed, especially in the case of samples with a high antibody titer. Anti-DFS70 antibodies can be considered as an indirect marker of reduced oxidative stress or a marker indicating the recent intensification of antioxidant processes
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