GLORIA

GEOMAR Library Ocean Research Information Access

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Alimentary pharmacology & therapeutics 21 (2005), S. 0 
    ISSN: 1365-2036
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background : Pyogenic liver abscess is a life-threatening disease. Accurate data on incidence and prognosis are important, but scarce.Aim : To examine changes in the incidence and 30-day mortality rate of patients with pyogenic liver abscess in Denmark.Methods : Using nationwide administrative registers, we identified all patients diagnosed with pyogenic liver abscess in Denmark, 1977–2002, and their dates of death. We computed annual standardized incidence and 30-day mortality rates, and used Poisson regression to adjust gender-specific mortality rates for year-by-year differences in age at diagnosis.Results : We identified 1448 patients with pyogenic liver abscess, of whom 54% were men. The crude incidence rate for the entire study period was 11.8 per 1 000 000 for men and 9.7 per 1 000 000 for women. Between 1977 and 2002, the incidence rate increased from 6 to 18 per 1 000 000 for men and from 8 to 12 per 1 000 000 for women. The cumulative 30-day mortality rate was 15% for men and 23% for women. The adjusted 30-day mortality rate decreased from 40% for men and 50% for women to around 10% for both genders.Conclusions : In this large nationwide study spanning a 26-year period, we found an increasing incidence rate and a decreasing mortality rate of pyogenic liver abscess. We believe that these changes are primarily explained by more sensitive diagnostic tools.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1365-2036
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background : Many cases of paracetamol poisoning are with suicidal intent, but the association between paracetamol poisoning and subsequent psychiatric disorder is unknown.Aim : To examine the association between poisoning with paracetamol or other weak analgesics and subsequent psychiatric disorder.Methods : The study was set in a nested case–control design and based on nationwide Danish registers. We identified all patients diagnosed with schizophrenia, affective disorder or eating disorder in 1994–1998 and matched population controls. We estimated the relative risk of these psychiatric disorders after admission for paracetamol or nonparacetamol poisoning, adjusting for income, employment and marital status.Results : We included 12 603 cases with psychiatric disorder, and 1.2% had a diagnosis of poisoning compared with 0.2% of the 252 060 matched population controls. Compared with those with no diagnoses of weak analgesic poisoning, the risk of schizophrenia increased 3.9-fold after paracetamol poisoning, and 2.0-fold after nonparacetamol poisoning. The risk of affective disorder increased 12.2-fold after paracetamol poisoning and 2.6-fold after nonparacetamol poisoning. The risk of eating disorder increased 5.0-fold after paracetamol poisoning, and 2.2-fold after nonparacetamol poisoning. The risk of a diagnosis of psychiatric disorder was very high immediately after poisoning and remained increased for more than 10 years.Conclusions : Paracetamol poisoning is a strong risk marker for psychiatric disorder, particularly affective disorders.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Theoretical Biology 101 (1983), S. 335-344 
    ISSN: 0022-5193
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Nuclear Physics 28 (1961), S. 689-690 
    ISSN: 0029-5582
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Nuclear Physics 28 (1961), S. 689-690 
    ISSN: 0029-5582
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Diabetologia 29 (1986), S. 812-816 
    ISSN: 1432-0428
    Keywords: Urea ; experimental diabetes ; nitrogen conversion ; hyperglucagonaemia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Diabetes was induced in Wistar rats by intravenous streptozotocin, 75 mg/kg. Four and 14 days after streptozotocin, fasting insulin decreased to about one-third, and fasting glucagon increased three-fold. The urea-N synthesis rate, stimulated by infusion of alanine, was measured at different amino acid concentrations 14 days after streptozotocin in 24 rats. The relationship was compatible with a barrier limited substrate inhibition kinetics. Data were examined accordingly by non-linear regression analysis. Among the estimated kinetic constants, only the 70% increase in Vmax was different from control values. In control rats the capacity of urea nitrogen synthesis, as measured within the amino acid concentration interval 7.3–11.6 mmol/1, was 10.2 ± 1.1 μmol · (min 100 g BW)−1 (mean ± SEM). The capacity was not different in 4 day diabetic rats, whereas it doubled in 14 day diabetic rats, 20.9 ± 1.7 μmol (min 100 g BW)−1. The alanine elimination rate was 35% higher in the 14 day diabetic rats compared both to 4 day diabetic and control rats. The increase of urea synthesis is suggested to be due to enzyme induction by glucagon. The net nitrogen balance was negative at amino acid concentrations up to 25 mmol/1, indicating that the urea synthesis was increased at the expense of amino nitrogen.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 7
    ISSN: 1432-0428
    Keywords: Experimental diabetes ; urea synthesis ; nitrogen-metabolism ; nitrogen-balance ; insulin therapy ; glucagon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In order to study the effect of hyperglucagonaemia on nitrogen metabolism in diabetes, zinc protamin glucagon 60 μg was injected subcutaneously 3 times daily for 4 weeks into streptozotocindiabetic rats (n=5), adequately treated with long acting insulin. This raised the plasma concentration of glucagon to 725±125 (mean±SEM), which is not different from that found in portal blood of uncontrolled diabetic rats: 400±75 ng/l. The controls were 5 diabetic rats treated with insulin alone and 5 non-diabetic rats. Compared with control rats the nitrogen balance was reduced (p〈0.05) and the nitrogen contents of carcass, heart, intestines, and kidneys were reduced by 15–30% (p〈0.05) in the glucagon treated rats. The hepatic capacity of urea synthesis and the alanine elimination rate were determined in the 3 above-mentioned groups, and confirmed in 3 identical groups followed for only 2 weeks; and in addition in a group of glucagon treated diabetic rats, where the long acting glucagon was substituted by neutral insulin the last two days before investigation. The capacity of urea-N synthesis and the alanine elimination rate were, respectively, in control rats: 9.6±0.8 and 5.9±0.3 μmol/(min 100 g body weight), in insulin treated diabetic rats: 8.5±0.7 and 5.4±0.6 μmol/(min 100g body weight), in glucagon treated rats: 6.3±0.4 (lower than controls, p〈0.05) and 10.4±0.4 (higher than controls, p〈0.05) (μmol/(min 100 g body weight), and in glucagon treated rats given neutral insulin: 20.7±1.6 and 10.9±0.3 μmol/(min 100 g body weight) (both higher than controls, p〈0.05). Hyperglucagonaemia in itself leads to loss of nitrogen from organs, probably by an increased hepatic conversion of amino-nitrogen to urea-nitrogen, as evidenced by the increased urea excretion. This proceeds despite an insulin induced decrease in the capacity of urea synthesis and may thus rather be attributed to changes in the affinity of urea synthesis for amino-nitrogen.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 8
    ISSN: 1432-0428
    Keywords: Experimental diabetes ; urea synthesis ; N-metabolism ; N-balance ; insulin therapy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Rats with experimental diabetes due to streptozotocin (75 mg/kg body weight) and free access to food were divided into two groups. One group (n=9) was optimally treated with insulin (glucosuria 〈4.0 mmol/24 h), using heat treated very long-acting ultralente insulin. The other group (n=10) was poorly treated with insulin (glucosuria 20–30 mmol/24 h). The nitrogen balance and energy balance of optimally treated diabetic rats was positive and not different from the control group (n=6). In the poorly treated diabetic rats the nitrogen balance was reduced whereas the energy balance was not different from that of control rats. After 4 weeks the fasting glucagon was: 50±21 ng/l (mean±SEM) in control rats, 62±18 ng/l in optimally treated diabetic rats and 249±58 ng/l in poorly treated diabetic rats (p〈0.01). The capacity of urea nitrogen synthesis determined during alanine loading was: 9.6±1.0 umol/(min 100 g body weight) in control rats, 10.6±1.7 umol/(min 100 g body weight) in optimally treated diabetic rats and 17.3±1.3 umol/(min 100 g body weight) in poorly treated diabetic rats (p〈0.01). Nitrogen contents of carcass, heart, intestines, liver, and kidneys as determined by Kjeldahl analyses were identical in control rats and optimally treated diabetic rats. In the poorly treated diabetic rats carcass-nitrogen and heart-nitrogen contents were reduced to 89% of the control value (p〈0.01), whereas the kidney-nitrogen content was increased to 112% of the control value (p〈0.01). Strict insulin therapy in experimental diabetes leads to a normalisation of nitrogen metabolism and hyperglucagonaemia, whereas less than optimally insulin treated rats show marked abnormalities in nitrogen metabolism as well as hyperglucagonaemia.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 9
    ISSN: 1432-0428
    Keywords: Experimental diabetes ; urea synthesis ; nitrogen metabolism ; nitrogen balance ; protein metabolism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Rats with experimental streptozotocin-induced diabetes (75 mg/kg) were divided into two groups. One group was free fed (n=8), the other group (n=7) pair fed to a group of control animals (n=8). The nitrogen and energy balances of the control rats were positive. In the free-fed diabetic rats the nitrogen balance was neutral and the energy balance higher than in controls. In the pair-fed diabetic rats the nitrogen balance was negative and the energy balance reduced. After 4 weeks the capacity of urea-nitrogen synthesis was: 8.1±0.6 μmol/(min 100 g body weight) (mean±SEM) in controls and 22.2±2.2 μmol/(min 100 g body weight) in both groups of diabetic rats. Initially, the whole body nitrogen content was 453±9 mmol. Four weeks later it was 536±19 mmol in controls, 410±21 mmol in the free-fed diabetic rats, and 315±6 mmol in the pair-fed diabetic rats. The largest changes occurred in the muscles, initially containing 278±6 mmol, 4 weeks later 328±8 mmol, compared to 234±19 in the free-fed diabetic rats and 166±18 mmol in the pair-fed diabetic rats. In conclusion uncontrolled diabetes is characterised by loss of nitrogen from muscles and most other organs. The losses from some organs are preventable by increased food intake. Irrespective of food intake the hepatic dynamics of amino nitrogen conversion is changed in a way that favours protein catabolism.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 40 (1984), S. 1255-1256 
    ISSN: 1420-9071
    Keywords: Rabbits ; renal failure, chronic ; liver function ; prothrombin index
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary In rabbits with chronic renal insufficiency the prothrombin index was increased by 25% and the alanine aminotransferase activity decreased by 20%; the results of other routine tests of hepatic function were not affected. The galactose elimination capacity was decreased by 12%, whereas the body clearance of antipyrine was unchanged. No change in hepatocytic structure was found.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...