27 research outputs found
Atypowe zapalenie płuc u dzieci i młodzieży
Podział zapaleń płuc na typowe i atypowe ma obecnie charakter głównie historyczny,
ze względu na poznanie i udokumentowanie wszystkich patogenów wywołujących zapalenie
„atypowe”. Poznano również dobrze przebieg tego rodzaju pozaszpitalnych zapaleń
płuc w których „atypowość” określano głównie w odniesieniu do klasycznego
przebiegu pneumokokowego zapalenia tkanki płucnej. W artykule opisano diagnostykę,
przebieg kliniczny oraz metody leczenia zapalenia płuc wywołane przez wszystkie
do tej pory zidentyfikowane patogeny „atypowe”. Szczególnie dokładnie potraktowano
zapalenie płuc wywołane przez najczęściej występujący czynnik etiologiczny atypowego
zapalenia płuc, jakim jest Mycoplasma pneumoniae. Szeroko omówiono również
zmiany kliniczne spowodowane przez legionellę oraz chlamydie.
Podkreślono ważną rolę antybiotyków makrolidowych w terapii tego rodzaju zapaleń płuc
Relations between Leu5-enkephalin- (LENK) and VIP-immunoreactive nerve fibres during human drug-resistant colitis. A case study
The double immunofluorescence technique was used to examine the distribution
and interrelationship between LENK- and VIP-immunoreactive nerve fibres
within the muscle layer and myenteric plexus of the large intestine in a young
female patient (aged 17 years) suffering from colitis ulcerosa activa (CUA). As
the CUA was found to be totally drug-resistant, a pancolotomy was performed
by means of the Soave technique. Varicose nerve fibres, immunoreactive either
to LENK or VIP, but not to both substances simultaneously, were found in all
fragments of the bowel studied. A striking feature was their distribution pattern
within the studied layers. In all cases LENK-IR fibres were closely accompanied
by VIP-IR terminals. The density of the examined fibres depended on the bowel
fragment studied, and was the greatest in the sigmoid colon, descending colon
and rectum, while the lowest number was found in the caecum. The results of
the present study may thus be indicative for the involvement of LENK- and VIPIR
nerve fibres in the control of bowel functions during CUA, possibly on the
basis of a "cross-talk" between terminals running in close vicinity to each other
The influence of experimental Bacteroides fragilis infection on substance P and somatostatin-immunoreactive neural elements in the porcine ascending colon - a preliminary report
The present study was aimed at disclosing the influence of Bacteroides fragilis
(one of the most important bacterial agents causing colitis in children) experimental
infection on the expression of substance P (SP) and somatostatin (SOM)
in neurons and nerve fibres within the porcine ascending colon. Distinct differences
in the distribution pattern of neural elements immunoreactive to the substances
studied were observed between the experimental (Inflam) and control
(Contr) pigs. In general, the number of SP-IR neurons and nerve terminals increased,
while the expression of SOM decreased after Bacteroides fragilis-induced
colitis (BFIC). However, distinct differences in the intensity of these alterations
were observed between particular compartments of the bowel segment
studied. Thus, the present results suggest that SP- and SOM-immunoreactive
(SOM-IR) elements of the enteric nervous system play a part in the control of
colonic activity during BFIC
The antioxidative-prooxidative balance in children with asthma treated with inhaled corticosteroids and long acting β2-agonists
The aim of study was to analyze the effect of treatment with inhaled corticosteroids and long acting ß2-agonists on antioxidative-prooxidative balance in children with asthma.
Material and methods: Twenty children with newly diagnosed asthma before treatment (group I), fourteen children with diagnosed asthma treated with inhaled corticosteroids and long acting β2-agonists and 57 healthy children were ioncluded in the study. In all cases plasma protein carbonyls and activity of erythrocyte SOD was assayed.
Results: Plasma protein carbonyls in both group I (1,01 nmol/g of protein, SD=0,30) and group II (0,94; SD=0,15) was significantly higher than in group III (0,85; SD=0,24) (I vs. III
Effect of education level on diabetes control and quality of life in insulin-treated type 2 diabetic patients
WSTĘP. Celem pracy była próba oceny wpływu edukacji
zdrowotnej prowadzonej przez doświadczoną,
merytorycznie przygotowaną pielęgniarkę diabetologiczną
na parametry wyrównania metabolicznego
i jakość życia oraz stopień kontroli własnego zdrowia
u chorych na cukrzycę typu 2 leczonych insuliną.
MATERIAŁ I METODY. Przebadano grupę 53 chorych
(32 kobiety i 21 mężczyzn) z cukrzycą typu 2 leczonych
insuliną. Średni czas trwania choroby wynosił
9,5 roku, czas leczenia insuliną 4 lata i 4 miesiące.
Średnia wieku badanych to 58,4 lat.
Jakość życia oraz stopień kontroli własnego zdrowia
pacjentów badano 2-krotnie: przed rozpoczęciem
edukacji diabetologicznej i po 3 miesiącach po jej
przeprowadzeniu. W pracy wykorzystano metodę
sondażu diagnostycznego wykonanego techniką
kwestionariuszową. Do oceny stopnia kontroli własnego
zdrowia przez pacjenta użyto: 1) kwestionariusza
wielowymiarowej Skali Umiejscowienia Kontroli
Zdrowia MHCL (wersja B) Wallstona, Wallstona,
DeVelisa w polskiej adaptacji Juczyńskiego, 2) Kwestionariusza Zachowań Zdrowotnych Komasińskiej-
Moller oraz 3) ankietę własną do oceny glikemii
i preferencji edukacyjnych. Do oceny poziomu jakości
życia użyto: Skali Satysfakcji z życia autorstwa
Diener, Larson, Emmons, Griffin w polskiej adaptacji
Juczyńskiego.
WYNIKI. Uzyskano znamienne różnice w zakresie
spadku i wzrostu glikemii na czczo oraz kontroli zdrowia,
a także jakości życia przed edukacją zdrowotną
i po jej przeprowadzeniu.
WNIOSKI. Prowadzenie edukacji w grupie chorych na
cukrzycę w ocenie pacjentów wpływa na wzrost poczucia
zadowolenia i satysfakcji z życia. Zaobserwowano
pozytywne zachowanie zdrowotne związane
z prowadzeniem samokontroli oraz zmniejszenie częstości
hiper- i hipoglikemii na czczo. (Diabet. Prakt.
2010; 11, 2: 46-53)BACKGROUND. The aim of the study was to evaluate
how health education by the experienced nurseeducator
affects quality of life and metabolic control
in patients with type 2 diabetes treated with insulin.
MATERIAL AND METHODS. The studied group
consisted of 53 insulin treated diabetic patients who
had never before undergone structured education. The mean diabetes duration in the group was ± 9.5
years and the mean duration of insulin treatment
± 4 years and 4 months. 32 women aged from 36 to
72 years and 21 men aged between 33 and 70 were
included in the study. Mean age in the control group
was ± 58.4 years.
The quality of life in the group was studied twice:
before the education and three months later.
A diagnostic poll method with the use of questionnaire
was used in the study. For patient’s estimation
of their own health authors used following tools:
1) A Multidimensional Health Scale of Control Location
(MHCL) Questionnaire, version of B. K.A. Wallston, B.S.
Wallston, R. DeVelisa - adapted by Z. Juczyński;
2) Health Behaviour Questionnaire by M. Komasińska-Moller; 3) author’s own questionnaire for educational
preferences and glycaemia estimation.
RESULTS. Significant differences were observed with
respect to fasting glycaemia, cooperation with the
doctor and the sense of inner control in the group of
patients who have undergone structural education.
CONCLUSIONS. Structural education has positive
influence on patients diabetes control as measured
by fasting glycaemia as well as on patients
cooperation and quality of life which in trun may affect
diabetes control. (Diabet. Prakt. 2010; 11, 2: 46-53
Polish statement on food allergy in children and adolescents
An adverse food reaction is defined as clinical symptoms occurring in children, adolescents or adults after ingestion of a food or chemical food additives. This reaction does not occur in healthy subjects. In certain individuals is
a manifestation of the body hypersensitivity, i.e. qualitatively altered response to the consumed food. The disease
symptoms observed after ingestion of the food can be triggered by two pathogenetic mechanisms; this allows
adverse food reactions to be divided into allergic and non-allergic food hypersensitivity (food intolerance). Food
allergy is defined as an abnormal immune response to ingested food (humoral, cellular or mixed). Non-immunological mechanisms (metabolic, pharmacological, microbiological or other) are responsible for clinical symptoms
after food ingestion which occur in non-allergic hypersensitivity (food intolerance).
Food allergy is considered a serious health problem in modern society. The prevalence of this disorder is varied
and depends, among other factors, on the study population, its age, dietary habits, ethnic differences, and the
degree of economic development of a given country. It is estimated that food allergy occurs most often among
the youngest children (about 6-8% in infancy); the prevalence is lower among adolescents (approximately 3-4%)
and adults (about 1-3%). The most common, age-dependent cause of hypersensitivity, expressed as sensitization or allergic disease (food
allergy), are food allergens (trophoallergens). These are glycoproteins of animal or plant origine contained in: cow's
milk, chicken egg, soybean, cereals, meat and fish, nuts, fruits, vegetables, molluscs, shellfish and other food products. Some of these allergens can cause cross-reactions, occurring as a result of concurrent hypersensitivity to food,
inhaled or contact allergens.
The development of an allergic process is a consequence of adverse health effects on the human body of different
factors: genetic, environmental and supportive. In people predisposed (genetically) to atopy or allergy, the development of food allergy is determined by four allergic-immunological mechanisms, which were classified and described
by Gell-Coombs. It is estimated that in approximately 48-50% of patients, allergic symptoms are caused only by
type I reaction, the IgEmediated (immediate) mechanism. In the remaining patients, symptoms of food hypersensitivity are the result of other pathogenetic mechanisms, non-IgE mediated (delayed, late) or mixed (IgE mediated,
non-IgE mediated). Clinical symptomatology of food allergy varies individually and depends on the type of food induced pathogenetic
mechanism responsible for their occurrence. They relate to the organ or system in which the allergic reaction has
occurred (the effector organ). Most commonly the symptoms involve many systems (gastrointestinal tract, skin,
respiratory system, other organs), and approximately 10% of patients have isolated symptoms. The time of symptoms onset after eating the causative food is varied and determined by the pathogenetic mechanism of the allergic immune reaction (immediate, delayed or late symptoms). In the youngest patients, the main cause of food reactions is allergy to cow’s milk. In developmental age, the clinical picture of food allergy can change, as reflected in the so-called allergic march, which is the result of anatomical and functional maturation of the effector organs, affected by various harmful allergens (ingested, inhaled, contact allergens and allergic cross-reactions). The diagnosis of food allergy is a complex, long-term and time-consuming process, involving analysis of the allergic history (personal and in the family), a thorough evaluation of clinical signs, as well as correctly planned allergic
and immune tests. The underlying cause of diagnostic difficulties in food allergy is the lack of a single universal laboratory test to identify both IgE-mediated and non-IgE mediated as well as mixed pathogenetic mechanisms of
allergic reactions triggered by harmful food allergens. In food allergy diagnostics is only possible to identify an
IgE-mediated allergic process (skin prick tests with food allergens, levels of specific IgE antibodies to food allergens). This allows one to confirm the diagnosis in patients whose symptoms are triggered in this pathogenetic
mechanism (about 50% of patients). The method allowing one to conclude on the presence or absence of food
hypersensitivity and its cause is a food challenge test (open, blinded, placebo-controlled). The occurrence of clinical symptoms after the administration of food allergen confirms the cause of food allergy (positive test) whereas
the time elapsing between the triggering dose ingestion and the occurrence of clinical symptoms indicate the pathogenetic mechanisms of food allergy (immediate, delayed, late). The mainstay of causal treatment is temporary removal of harmful food from the patient’s diet, with the introduction of substitute ingredients with the nutritional value equivalent to the eliminated food. The duration of dietary
treatment should be determined individually, and the measures of the effectiveness of the therapeutic elimination
diet should include the absence or relief of allergic symptoms as well as normal physical and psychomotor development of the treated child. A variant alternative for dietary treatment of food allergy is specific induction of food tolerance by intended contact of the patient with the native or thermally processed harmful allergen (oral immunotherapy). This method has
been used in the treatment of IgE-mediated allergy (to cow's milk protein, egg protein, peanut allergens).
The obtained effect of tolerance is usually temporary. In order to avoid unnecessary prolongation of treatment in a child treated with an elimination diet, it is recommended to perform a food challenge test at least once a year. This test allows one to assess the body's current ability to acquire immune or clinical tolerance. A negative result of the test makes it possible to return to a normal diet,
whereas a positive test is an indication for continued dietary treatment (persistent food allergy). Approximately 80% of children diagnosed with food allergy in infancy "grow out" of the disease before the age of
4-5 years. In children with non-IgE mediated food allergy the acquisition of food tolerance is faster and occurs in
a higher percentage of treated patients compared to children with IgE-mediated food allergy.
Pharmacological treatment is a necessary adjunct to dietary treatment in food allergy. It is used to control the rapidly increasing allergic symptoms (temporarily) or to achieve remission and to prevent relapses (long-term treatment).
Preventive measures (primary prevention of allergies) are recommended for children born in a "high risk" group for
the disease. These are comprehensive measures aimed at preventing sensitization of the body (an appropriate way
of feeding the child, avoiding exposure to some allergens and adverse environmental factors). First of all, the infants
should be breast-fed during the first 4-6 months of life, and solid foods (non milk products, including those containing gluten) should be introduced no earlier than 4 months of age, but no later than 6 months of age. An elimination diet is not recommended for pregnant women (prevention of intrauterine sensitization of the fetus and
unborn child). The merits of introducing an elimination diet in mothers of exclusively breast-fed infants, when the
child responds with allergic symptoms to the specific diet of the mother, are disputable. Secondary prevention focuses on preventing the recurrence of already diagnosed allergic disease; tertiary prevention is the fight against organ
disability resulting from the chronicity and recurrences of an allergic disease process. Food allergy can adversely affect the physical development and the psycho-emotional condition of a sick child, and
significantly interfere with his social contacts with peers. A long-term disease process, recurrence of clinical symptoms, and difficult course of elimination diet therapy are factors that impair the quality of life of a sick child and
his family. The economic costs generated by food allergies affect both the patient's family budget (in the household), and the overall financial resources allocated to health care (at the state level). The adverse socio-economic
effects of food allergy can be reduced by educational activities in the patient’s environment and dissemination of
knowledge about the disease in the society