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1.
Article in English | MEDLINE | ID: mdl-11315526

ABSTRACT

Faecal samples from suckling (n = 205) and weaned piglets (n = 82) with diarrhoea from 24 farms in Southern Germany were examined for shedding of important metazoic parasitic, viral and bacterial pathogens using culture, microscopic and electronmicroscopic methods. Escherichia coli isolates were tested further for the enterotoxin genes est-Ia and elt-I by colony blot hybridization. Isospora suis was diagnosed in 26.9% and Cryptosporidium parvum in 1.4% of the piglets investigated. The proportion of coronavirus-positive animals was 13.4% and 4% were positive for rotavirus. It was found that 17.6% of the animals were infected with enterotoxigenic E. coli (ETEC; 10.1% ETEC-ST-Ia and 8.6% ETEC-LT-I, respectively). The occurrence of the pathogens was significantly associated with the age of the animals examined (P < 0.001). Isospora suis was predominantly isolated from suckling piglets (in the second and third week of life), while in weaned piglets (fourth week of life) rotavirus and ETEC were most prevalent. On 22 of the 24 piglet production farms examined at least one of the investigated pathogens was detected. Coronavirus was diagnosed in 66.7%, I. suis in 62.5%, rotavirus in 20.8% and C. parvum in 8.3% of the farms. These results underline the fact that despite the hygienic, technical and immune preventive efforts during the last years, enteropathogens are still common in German piglet production units.


Subject(s)
Diarrhea/veterinary , Swine Diseases/epidemiology , Animals , Animals, Suckling , Coronavirus/isolation & purification , Cryptosporidium/isolation & purification , DNA Primers , Diarrhea/epidemiology , Diarrhea/microbiology , Escherichia coli/isolation & purification , Feces/microbiology , Feces/parasitology , Feces/virology , Female , Germany/epidemiology , Isospora/isolation & purification , Male , Polymerase Chain Reaction , Prevalence , Rotavirus/isolation & purification , Swine , Swine Diseases/microbiology , Weaning
2.
Eur J Gastroenterol Hepatol ; 12(5): 517-22, 2000 May.
Article in English | MEDLINE | ID: mdl-10833094

ABSTRACT

OBJECTIVE: The mortality of patients with liver cirrhosis admitted to an intensive care unit (ICU) has been found to be high. This study was performed to assess the physiological and laboratory parameters which are able to identify on ICU admission the cirrhotic patients who are most likely to die. DESIGN: Prospective clinical trial. METHODS: Two groups of patients were analysed. Group A consisted of 196 consecutive cirrhotic patients admitted to our medical ICU for various reasons. For the detection of independent outcome predictors, we used a multiple logistic regression model. Based on these variables, the 'intensive care cirrhosis outcome (ICCO) score' was calculated. The ability to discriminate between survivors and non-survivors was determined by receiver operating characteristic curves, and the area under the curve was calculated. Group B consisted of 70 consecutive cirrhotic patients for prospective validation of the ICCO score. RESULTS: Applying multiple logistic regression analysis, bilirubin, cholesterol, creatinine clearance and lactate were found to be independently associated with the hospital mortality. The ICCO score was 0.3707 + (0.0773 x bilirubin (mg/dl)) - (0.00849 x cholesterol (mg/dl)) -(0.0155 x creatinine clearance (ml/min)) + (0.1351 x lactate (mmol/l)), giving an area under a receiver operating characteristic curve of 0.9. Increasing score values were associated with an increase in mortality. All patients with an ICCO score > +2.6 died. CONCLUSIONS: Application of the ICCO score is rapid and available at the patient's bedside, and its application is simple and reproducible. In cirrhotic patients, the ICCO score has a high ability to discriminate between survivors and non-survivors. The ICCO score may facilitate estimation on ICU admission of the prognosis of critically ill cirrhotic patients.


Subject(s)
Liver Cirrhosis/mortality , Severity of Illness Index , Area Under Curve , Chi-Square Distribution , Critical Illness , Female , Humans , Intensive Care Units , Liver Function Tests , Logistic Models , Male , Middle Aged , Predictive Value of Tests , Prognosis , Prospective Studies , ROC Curve , Reproducibility of Results , Retrospective Studies , Statistics, Nonparametric
3.
Wien Klin Wochenschr ; 111(19): 810-4, 1999 Oct 15.
Article in English | MEDLINE | ID: mdl-10568012

ABSTRACT

BACKGROUND AND AIMS: We questioned whether heavy chronic alcohol abuse influences extrahepatic organ failure and ICU mortality in cirrhotic patients admitted to a medical intensive care unit. PATIENTS AND METHODS: Medical records of 208 consecutive cirrhotic critically ill patients were reviewed. Patients were classified into two groups. Group A comprised 144 patients with liver cirrhosis due to heavy chronic alcohol abuse and group B, 64 patients with liver cirrhosis due to non-alcoholic causes. The presence of extrahepatic organ failures in patients of both groups was assessed with parameters determined on the day of admission to the ICU. Furthermore, ICU mortality was determined. RESULTS: The occurrence of extrahepatic organ failure was similar in group A and group B (83% vs. 80%; p = NS). The rate of extrahepatic organ failure was 1.7 +/- 1.2 organs in group A, compared to 1.4 +/- 1 organs in group B (p = NS). ICU mortality was 53% in group A and 44% in group B (p = NS). An increase in the number of extrahepatic organ failures was associated with a concomitant increase in ICU mortality in both groups of patients. CONCLUSION: The occurrence of extrahepatic organ failure and ICU mortality was not different between patients with liver cirrhosis secondary to heavy chronic alcohol abuse and patients with liver cirrhosis due to nonalcoholic causes. Cirrhotic patients should be admitted to a medical intensive care unit for extended intensive care treatment prior to the occurrence of extrahepatic multiple organ failure, independent of the underlying aetiology.


Subject(s)
Alcoholism/mortality , Critical Care , Liver Cirrhosis, Alcoholic/mortality , Multiple Organ Failure/mortality , Adult , Aged , Austria , Cause of Death , Female , Humans , Male , Middle Aged , Retrospective Studies , Risk Factors
4.
Mater Med Pol ; 28(2): 42-8, 1996.
Article in English | MEDLINE | ID: mdl-9088126

ABSTRACT

Liver cells of rat's offspring were ultrastructurally examined after administering quinolinic acid to mothers intraperitoneally in a dose of 60 mmol or 100 mmol, once daily, throughout the entire gestation period. Liver tissue specimens were taken on day 5 after birth from experimental and control animals. Administration of quinolinic acid resulted in a marked proliferation of smooth elements of endoplasmic reticulum in liver cells of their offspring, which indicated microsomal enzymatic induction. Simultaneously, injuries of liver cells of varying intensity were observed, which were dose-dependent on quinolinic acid administration, the injured cells being more frequent at higher doses of the drug.


Subject(s)
Liver/ultrastructure , Prenatal Exposure Delayed Effects , Quinolinic Acid/pharmacology , Animals , Female , Liver/drug effects , Male , Pregnancy , Rats , Rats, Wistar
5.
Exp Toxicol Pathol ; 47(5): 375-9, 1995 Nov.
Article in English | MEDLINE | ID: mdl-8871070

ABSTRACT

Quinolinic acid was administered intraperitoneally in a dose of 30 or 60 mmol, once every 24 h for 8 days. Its result in the dose of 30 mmol was the proliferation of smooth elements of the endoplasmic reticulum. The use of quinolinic acid in a dose of 60 mmol was characterized by the presence of more profound damage of organelles, among them the distinct decrease of the rough elements of the endoplasmic reticulum and polyribosomal structures was seen, and moreover, wide areas devoid of organelles were observed.


Subject(s)
Liver/drug effects , Liver/ultrastructure , Quinolinic Acid/pharmacology , Animals , Dose-Response Relationship, Drug , Injections, Intraperitoneal , Male , Quinolinic Acid/administration & dosage , Rats , Rats, Wistar
7.
Phys Rev Lett ; 73(9): 1299-1302, 1994 Aug 29.
Article in English | MEDLINE | ID: mdl-10057675
8.
Mater Med Pol ; 21(4): 280-5, 1989.
Article in English | MEDLINE | ID: mdl-2518737

ABSTRACT

Rat kidney was studied histochemically and in electron microscope during administration of lithium carbonate for 14 days in doses of 4 mmol/l. Morphological examination demonstrated signs of damage exclusively to the epithelial cells in the proximal tubule. Histochemical examination demonstrated a major reduction of the reactions for succinate dehydrogenase and cytochrome oxidase. No difference was found in the intensity of the reaction for alkaline phosphatase and Ca-ATPase during lithium treatment as compared to controls. Additional observation demonstrated, only in histological examination, an increased number of cells of the macula densa.


Subject(s)
Kidney Tubules, Proximal/drug effects , Lithium/toxicity , Animals , Kidney Tubules, Proximal/ultrastructure , Lithium Carbonate , Male , Microscopy, Electron , Rats , Rats, Inbred Strains
17.
Acta Histochem ; 58(2): 210-8, 1977.
Article in English | MEDLINE | ID: mdl-197764

ABSTRACT

Six cases of C-cell carcinoma of thyroid gland were studied applying histologic and histochemical methods as well as electron microscopy technique. A histologic feature of the carcinoma pattern was the diversity of pictures. Amyloid was commonly found in the carcinoma stroma. In some cells glycogen was present. Histochemically the carcinoma cells were marked by a strong activity of oxidative enzymes (GDH, SDH, LDH and MAO) as well as hydrolitic one (G-6-P and non specific enterases). Serotonin was found in two cases. An ultrastructural feature of carcinoma cells was the presence of cytoplasmic electron-dense, specific "endocrine type" secretory granules.


Subject(s)
Thyroid Neoplasms/pathology , Amyloid/analysis , Esterases/analysis , Glucose-6-Phosphatase/analysis , Glycogen/analysis , Histocytochemistry , Humans , L-Lactate Dehydrogenase/analysis , Methods , Microscopy, Electron , Monoamine Oxidase/analysis , Quinone Reductases/analysis , Succinate Dehydrogenase/analysis , Thyroid Neoplasms/analysis , Thyroid Neoplasms/ultrastructure
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