Your browser doesn't support javascript.
loading
: 20 | 50 | 100
1 - 14 de 14
2.
Acta Anaesthesiol Scand ; 59(4): 414-26, 2015 Apr.
Article En | MEDLINE | ID: mdl-25789942

BACKGROUND: Intravenous ketamine has been used during general and regional anaesthesia for caesarean section. No systematic review and meta-analysis on the desired effects and adverse effects of ketamine administration during caesarean section have yet been performed. METHODS: After a systematic literature search a meta-analysis was conducted with the random effects model. Weighted mean difference (WMD) or risk ratio and 95% confidence intervals (CIs) were computed. RESULTS: Twelve randomised controlled double-blind trials comprising 953 patients were included: seven studies reported on spinal anaesthesia and five on general anaesthesia. Significant differences in the aforementioned outcome variables were found only in the spinal anaesthesia studies. In the spinal anaesthesia studies the time to the first analgesic request was significantly longer in ketamine-treated women, the WMD was 49.36 min (95% CI 43.31-55.41); visual analogue scale pain scores at rest 2 h after surgery were significantly lower. No differences were observed for maternal nausea, vomiting, pruritus, and psychomimetic effects. Only few data were found for neonatal outcomes. CONCLUSIONS: We conclude that ketamine enhances post-operative analgesia after caesarean section under spinal anaesthesia. There is a paucity of data for several maternal adverse effects as well as for neonatal well-being. Further studies are needed for general anaesthesia.


Anesthesia, General/methods , Anesthesia, Obstetrical/methods , Anesthesia, Spinal/methods , Anesthetics, Dissociative/administration & dosage , Cesarean Section/methods , Ketamine/administration & dosage , Adult , Anesthesia, General/adverse effects , Anesthesia, Obstetrical/adverse effects , Anesthesia, Spinal/adverse effects , Female , Humans , Pregnancy
3.
Acta Anaesthesiol Scand ; 58(9): 1075-85, 2014 Oct.
Article En | MEDLINE | ID: mdl-25069636

Tranexamic acid is effective in reducing blood loss during various types of surgery and after trauma. No compelling evidence has yet been presented for post-partum haemorrhage. A systematic literature search of relevant databases was performed to identify trials that assessed blood loss and transfusion incidence after tranexamic acid administration for post-partum haemorrhage. The random effects model was used for meta-analysis. Risk ratios (RRs) and weighted mean differences (WMDs) were calculated with 95% confidence intervals (CIs). Seven trials with a low risk of bias comparing tranexamic acid vs. placebo with a total of 1760 parturients were included in our systematic review and meta-analysis. Blood loss was significantly lower after tranexamic acid use (WMD -140.29 ml, 95% CI -189.64 to -90.93 ml; P<0.00001). Tranexamic acid reduced the risk for blood transfusions (RR 0.34, 95% CI 0.20-0.60, P=0.0001). The incidence of transfusions in the placebo group varied between 1.4% and 33%. When omitting the two trials with the highest incidence of transfusions, the RR was no longer significant. Additional uterotonics were necessary in the placebo groups; gastrointestinal adverse events were more common after tranexamic acid use. Only four cases of thrombosis were found, two each in the tranexamic acid and control groups. Tranexamic acid effectively reduced post-partum blood loss; the effect on the incidence of blood transfusions requires further studies. Only few trials observed adverse events including thromboembolic complications and seizures.


Antifibrinolytic Agents/therapeutic use , Postpartum Hemorrhage/drug therapy , Tranexamic Acid/therapeutic use , Blood Transfusion/statistics & numerical data , Female , Humans , Pregnancy
4.
Hautarzt ; 64(9): 685-94, 2013 Sep.
Article De | MEDLINE | ID: mdl-24022632

BACKGROUND: Phlebologic diseases have become extremely common and have major socio-economic impact. However, the percentage of dermatologists working in phlebology appears to be decreasing according to the data of the German Society of Phlebology (DGP). METHODS: To investigate the reasons for this development, we--on behalf of the DGP--sent a questionnaire to 120 German Departments of Dermatology in autumn 2012. RESULTS: In 76 returned questionnaires, the number of physicians with additional fellowship training in phlebology averaged 1.5; the average number of those who fulfill the criteria for training fellows in phlebology was 0.9. In 71.1 % of the departments there was a phlebologist. A special phlebologic outpatient clinic existed in 73.7 % of the departments. Sonography with Doppler (89.5 %) and duplex (86.8 %) was used as the most frequent diagnostic tool. For therapy, compression (94.7 %), sclerotherapy (liquid 78.9 %, foam 63.2 %, catheter 18.4 %), endoluminal thermic procedures (radio wave 28.9 %, laser 17.1 %) and surgery (especially crossectomy and stripping 67.1 %, phlebectomy of tributaries 75 %) were used. The average number of treatments was very heterogenous in the different departments. CONCLUSIONS: Phlebology definitely plays an important role in dermatology. Most departments fulfill the formal criteria for the license to conduct advanced training in phlebology. A wide spectrum of phlebological diagnostic and therapeutic procedures is available.


Dermatology/statistics & numerical data , Hospital Departments/statistics & numerical data , Practice Patterns, Physicians'/statistics & numerical data , Skin Diseases, Vascular/diagnosis , Skin Diseases, Vascular/therapy , Venous Insufficiency/diagnosis , Venous Insufficiency/therapy , Germany/epidemiology , Humans , Professional Competence/statistics & numerical data , Skin Diseases, Vascular/epidemiology , Surveys and Questionnaires , Venous Insufficiency/epidemiology
5.
Vet Microbiol ; 142(3-4): 293-302, 2010 May 19.
Article En | MEDLINE | ID: mdl-19913364

Enzootic pneumonia (EP) in pigs caused by Mycoplasma hyopneumoniae is a highly prevalent, chronic respiratory disease, which causes considerable economic losses in the swine industry. Most herds are vaccinated, but classical bacterin vaccines do not prevent colonization and it is not possible to detect flourishing M. hyopneumoniae infections in vaccinated herds since commonly used commercial ELISAs cannot differentiate infected from vaccinated animals. To solve this problem, new immunogenic proteins, up-regulated or solely expressed during infection, need to be identified. For this purpose a peptide-spot array was constructed which presents 105 potential linear B-cell epitopes identified by in silico analysis in 35 putative lipoproteins encoded on the genome of M. hyopneumoniae type strain 232. Subjecting this array to immunoblotting using porcine convalescent serum revealed a single strongly immunoreactive epitope on the Mhp366 protein which did not react with serum from bacterin-immunized pigs. In addition, it was not possible to detect Mhp366 in total cell lysates of in vitro grown M. hyopneumoniae strains, using a polyclonal rabbit serum raised against a recombinant GST-Mhp366 fusion protein. To investigate the possibility of using an Mhp366-based ELISA in the field for differentiating vaccinated herds with and without a flourishing infection it was shown that (i) homologues of the corresponding mhp366 gene were present in all 17 M. hyopneumoniae strains and porcine lung samples tested from different geographic origins and (ii) an ELISA based on epitope-specific synthetic peptides as solid phase antigen allowed a classification of field samples. Therefore, Mhp366 might be the first antigen identified which facilitates the detection of flourishing M. hyopneumoniae infections even in vaccinated herds.


Epitopes, B-Lymphocyte/isolation & purification , Lipoproteins/isolation & purification , Mycoplasma hyopneumoniae/immunology , Pneumonia of Swine, Mycoplasmal/microbiology , Protein Array Analysis/veterinary , Amino Acid Sequence , Animals , B-Lymphocytes/immunology , Enzyme-Linked Immunosorbent Assay/veterinary , Epitopes , Epitopes, B-Lymphocyte/chemistry , Epitopes, B-Lymphocyte/genetics , Epitopes, B-Lymphocyte/immunology , Immunoblotting/veterinary , Lipoproteins/chemistry , Lipoproteins/genetics , Lipoproteins/immunology , Pneumonia of Swine, Mycoplasmal/diagnosis , Pneumonia of Swine, Mycoplasmal/immunology , Rabbits , Recombinant Fusion Proteins/immunology , Sequence Alignment , Swine , Swine Diseases/diagnosis , Swine Diseases/immunology
6.
Clin Exp Allergy ; 33(7): 992-8, 2003 Jul.
Article En | MEDLINE | ID: mdl-12859458

BACKGROUND: The standard assay for the clinical detection of contact allergy against nickel is the patch test. For research purposes, the in vitro lymphocyte transformation test (LTT) is mostly applied. However, the in vivo application of allergens includes the potential of sensitization, whereas the LTT demands 6 days of cell culture and radioactive labelling procedures. OBJECTIVE: The purpose of this study was to validate an enzyme-linked immunospot (ELISpot) assay to specifically detect cellular response against nickel sulphate in correlation with patch test, anamnestic data, and LTT results. METHODS: In probands with positive (n=60) and negative patch test results (n=19), cytokine ELISpot and LTT were performed in parallel using various concentrations of nickel sulphate, various numbers of responding peripheral blood mononuclear cells (PBMC), and various durations of cell cultures. RESULTS: Concentrations of 50 and 75 microM nickel sulphate were found to be optimal to stimulate in the ELISpot 4x10(5) and in the LTT 2x10(5) PBMC, respectively. An increase in ELISpot sensitivity was reached by pre-incubation with nickel sulphate for 24 h prior to transfer to ELISpot plates. In nickel-sensitive probands, an average precursor cell frequency of 19x10(5), 1.7x10(5), and 0.7x10(5) could be defined for IFN-gamma, IL-2, and IL-4 producing PBMC, respectively. In non-sensitive probands IFN-gamma producing cells were detectable, but with significantly lower frequency (2x10(5); P=0.004). The prior performance of patch tests had no significant effect on cytokine production or lymphocyte proliferation. Overall, the parameters patch test, anamnestic nickel allergy, ELISpot, and LTT results were positively correlated (P<0.05). CONCLUSIONS: Based on these experiments, the quantitative in vitro detection of cell-mediated reactions towards nickel as well as other heavy metal ions should be possible utilizing the above-described ELISpot assay.


Dermatitis, Allergic Contact/diagnosis , Enzyme-Linked Immunosorbent Assay/methods , Nickel/adverse effects , Adolescent , Adult , Aged , Cytokines/metabolism , Enzyme-Linked Immunosorbent Assay/standards , Female , Humans , Lymphocyte Activation , Male , Middle Aged , Patch Tests
7.
Chemosphere ; 47(7): 777-88, 2002 May.
Article En | MEDLINE | ID: mdl-12079073

We investigated the integrity of fish assemblages of a small anthropogenically impacted urban stream system in south-western Germany. Heavy point and non-point pollution physiologically stresses the aquatic fauna while migration barriers and river morphological alterations negatively influence habitat availability. Investigations conducted in 1998 and 1999 revealed that the fish assemblage was altered and several site-specific fish species were missing while non-site-specific species were relatively common. Highest species diversity was recorded in a reach downstream of the main migration barrier, while upstream only a few species were present. In general, a shift to ubiquitous and limnophilic species as well as to less pollution sensitive species was observed. Adult fish dominated the population structure throughout the stream course. Recruitment was confined mainly to the less polluted headwater. In the present study we introduce an assessment system based on the similarity of the potential natural and the actually established fish assemblage as demanded by the Water Framework Directive of the European Union for the evaluation of the ecological status of a fish assemblage in a stream [EC of the European Parliament and of the Council of Europe establishing a framework for community action in the field of water policy. Brussels, 30 June, 2000. 1997/0067 (COD)]. Both, stream morphological quality and pollution data sampled within the two study years confirm the validity of the suggested assessment method.


Environmental Monitoring/methods , Fishes , Water Pollutants/adverse effects , Animals , Cities , Ecology , Germany , Population Dynamics , Sensitivity and Specificity
8.
Curr Eye Res ; 23(3): 206-14, 2001 Sep.
Article En | MEDLINE | ID: mdl-11803483

PURPOSE: Evaluation of effects of ascorbic acid on cell characteristics of dedifferentiated porcine retinal pigment epithelial (pRPE) cells. METHODS: pRPE cells were incubated in vitro with increasing concentrations of ascorbic acid (0.25-1.5 mMol). Cell proliferation was assayed by measuring the incorporation of 5-bromo-2'-deoxy-uridine (BrdU) into cellular DNA. Migration and contraction properties were studied on a cell permissive porous membrane and collagen gels, respectively. Phenotypic changes in response to ascorbic acid and its derivative ascorbic acid 2-phophate were evaluated by microscopy and indirect immunofluorescence. RESULTS: Ascorbic acid significantly inhibits cell proliferation, migration, and contraction in concentrations of 1 mMol or more. Under the influence of at least 1 mMol ascorbic acid dedifferentiated pRPE cells exhibited a pigmented status within 24 hours. Addition of 500 U/ml catalase prevented the antiproliferative effect of ascorbic acid and the formation of pigment. Concentrations of 0.5 mMol ascorbic acid as well as 1 mMol ascorbic acid 2-phosphate promoted differentiation of cell phenotype. Furthermore, ascorbic acid 2-phosphate supported the formation of in vivo-like epithelial structures. CONCLUSIONS: Ascorbic acid has an influence on vital cell characteristics such as proliferation, migration, contraction and differentiation of pRPE cells. As dedifferentiation of these cells is an integral part in the development of proliferative vitreoretinopathy (PVR), ascorbic acid should be taken into consideration as a supplement in the clinical management of this disease.


Ascorbic Acid/pharmacology , Pigment Epithelium of Eye/drug effects , Animals , Bromodeoxyuridine , Catalase/pharmacology , Cell Differentiation/drug effects , Cell Division/drug effects , Cell Movement/drug effects , Cell Separation , Cells, Cultured , Collagen/metabolism , DNA/biosynthesis , Fluorescent Antibody Technique, Indirect , Pigment Epithelium of Eye/cytology , Pigment Epithelium of Eye/metabolism , Platelet-Derived Growth Factor/pharmacology , Swine
9.
Histopathology ; 35(4): 373-9, 1999 Oct.
Article En | MEDLINE | ID: mdl-10564393

AIMS: Pleomorphic adenomas of the salivary glands are characterized by their high tissue diversity. Many studies have explored the derivation and differentiation of the neoplastic cells. We investigated the composition of the collagenous extracellular tumour matrix and could show a specific biochemical composition pattern in the different tumour areas. METHODS AND RESULTS: In epithelially differentiated acinar and ductal areas there was positive staining for basement membrane collagen type IV and no, or only scarce, staining for collagen types I, II, III, or VI. Solid areas mostly lacked any extracellular matrix. In areas with fibrous tissue-like appearance, the fibroblast-typical interstitial collagen types I, III and VI were seen. Chondroid areas showed abundantly the characteristic cartilage components, collagen type II and, pericellularly, type VI collagen. CONCLUSIONS: Our data show the presence of fibroblastic and chondrocytic cell differentiation in pleomorphic adenomas. Thus, they confirm that these neoplasms display, besides epithelial cell types, also real mesenchymal cell and tissue types. Differences in the abundance and the biochemical composition of the extracellular tumour matrix account largely for the morphological heterogeneity of pleomorphic adenomas of the salivary glands.


Adenoma/genetics , Adenoma/pathology , Collagen/genetics , Parotid Neoplasms/genetics , Parotid Neoplasms/pathology , Adenoma/metabolism , Collagen/classification , Collagen/metabolism , Extracellular Matrix/metabolism , Extracellular Matrix/pathology , Gene Expression , Humans , In Situ Hybridization , Parotid Neoplasms/metabolism , Phenotype , RNA, Messenger/genetics , RNA, Messenger/metabolism , RNA, Neoplasm/genetics , RNA, Neoplasm/metabolism
10.
Am J Obstet Gynecol ; 181(2): 283-7, 1999 Aug.
Article En | MEDLINE | ID: mdl-10454670

OBJECTIVE: The purpose of this study was to determine whether a wet mount preparation of endocervical secretions from obstetric patients can accurately rule out the presence of gonococci and Chlamydia trachomatis. STUDY DESIGN: Gravid patients were screened for gonococci and C trachomatis with a deoxyribonucleic acid probe and a wet mount preparation of endocervical secretions. The number of polymorphonuclear lymphocytes was counted and averaged per x400 high-power field. A count of <10 polymorphonuclear lymphocytes per high-power field was defined as predicting the absence of gonococci- and C trachomatis -induced cervicitis. A chi(2) analysis was used to compare the wet mount results to the deoxyribonucleic acid probe. RESULTS: Between January and March 1998, 341 patients were enrolled in the study. Wet mount results showed 32% (108/341) of patients had <10 polymorphonuclear lymphocytes per high-power field. The incidence of infection with gonococci and C trachomatis in this population, as determined by deoxyribonucleic acid probe, was 10 of 341 (2.9%) and 30 of 340 (8.8%), respectively. The sensitivity values for gonococci and C trachomatis were 90% and 87%, respectively. The negative predictive value of the wet mount for gonococci-induced cervicitis was 99%, and that for C trachomatis -induced cervicitis was 96%. CONCLUSION: In this population the wet mount accurately predicted the absence of gonococci- and C trachomatis -induced cervicitis. Use of this screening protocol in gravid patients has the potential to reduce the cost of screening for these 2 diseases.


Cervix Uteri/microbiology , Chlamydia trachomatis/isolation & purification , Neisseria gonorrhoeae/isolation & purification , Pregnancy Complications, Infectious/microbiology , Uterine Cervicitis/microbiology , Adult , Chlamydia Infections/microbiology , Chlamydia trachomatis/genetics , DNA, Bacterial/analysis , Female , Gonorrhea/microbiology , Humans , Leukocyte Count , Neisseria gonorrhoeae/genetics , Neutrophils , Pregnancy
11.
Biochemistry ; 35(1): 282-9, 1996 Jan 09.
Article En | MEDLINE | ID: mdl-8555186

Clostridium limosum ADP-ribosyltransferase modifies low molecular mass GTP-binding proteins of the Rho subtype family. Here we cloned and sequenced the gene of the transferase and expressed it in Escherichia coli. The gene encodes a protein of 250 amino acids (M(r) = 27,840), with a putative signal peptide of 45 amino acids, that shows about 60-65% identity with C3 transferases from Clostridium botulinum. The mature C. limosum transferase was expressed as a maltose-binding fusion protein in E. coli and purified to apparent homogeneity. To study the functional role of Glu174 of C. limosum transferase, which was recently photoaffinity-labeled with [carbonyl-14C]NAD [Jung, M., et al. (1993) J. Biol. Chem. 268, 23215-23218], two mutants E174D and E174Q were constructed by a polymerase chain reaction-based system. The E174D and E174Q mutants showed a dramatic decrease in kcat, but no major changes in Km,NAD. Furthermore, replacement of Glu174 by aspartic acid and glutamine largely reduced and completely blocked UV-induced incorporation of [carbonyl-14C]NAD into the transferase. The data indicate that Glu174 is an active site residue of C. limosum transferase.


ADP Ribose Transferases/chemistry , ADP Ribose Transferases/metabolism , Botulinum Toxins , Clostridium/enzymology , Glutamic Acid , Point Mutation , Amino Acid Sequence , Base Sequence , Binding Sites , Blotting, Southern , Cloning, Molecular , DNA Primers , DNA, Bacterial/analysis , DNA, Bacterial/metabolism , Escherichia coli , Kinetics , Molecular Sequence Data , Mutagenesis, Site-Directed , NAD+ Nucleosidase/metabolism , Recombinant Proteins/chemistry , Recombinant Proteins/metabolism , Restriction Mapping , Sequence Homology, Amino Acid
12.
Biochimie ; 77(5): 326-32, 1995.
Article En | MEDLINE | ID: mdl-8527485

Various C3-like ADP-ribosyltransferases like Clostridium botulinum exoenzyme C3, C limosum transferase, B cereus transferase and a transferase from Staphylococcus aureus (EDIN) selectively modify the low-molecular mass GTP-binding proteins RhoA,B,C. UV-irradiation of C limosum transferase in the presence of [carbonyl-14C]NAD resulted in radiolabeling of Glu-174. Concomitantly, ADP-ribosyltransferase and NAD glycohydrolase activities were inhibited. Site-directed mutagenesis of Glu-174 (E174D, E174Q) which resulted in more than 1000-fold reduction of enzyme activity, suggests that the glutamic acid residue is essentially involved in the catalytic action of C3-like transferases. These findings support the view that all bacterial ADP-ribosyltransferases share a similar active-site structure.


ADP Ribose Transferases/chemistry , ADP Ribose Transferases/metabolism , Adenosine Diphosphate Ribose/metabolism , Bacterial Toxins/metabolism , Botulinum Toxins , Clostridium botulinum/enzymology , Glutamic Acid , ADP Ribose Transferases/radiation effects , Affinity Labels , Amino Acid Sequence , Bacterial Toxins/chemistry , Binding Sites , Kinetics , Molecular Sequence Data , Sequence Homology, Amino Acid , Ultraviolet Rays
14.
J Microsc ; 162(Pt 1): 115-22, 1991 Apr.
Article En | MEDLINE | ID: mdl-1870107

Aluminium causes a variety of toxic effects in living organisms but very little is known about its uptake, pathways and locations of deposition. We have applied electron spectroscopic imaging (ESI) and electron energy-loss spectroscopy (EELS) to locate aluminium at the ultrastructural level in amphibian larvae from acidic ponds. It is found diffusely bound or precipitated in cell organelles. The spatial resolution of aluminium detection is high. The elemental composition of small areas can be demonstrated by EELS. Three different fixation procedures give similar results. The two- and three-window methods at the K- and L-edges are compared.


Aluminum/analysis , Triturus/metabolism , Water Pollution , Aluminum/pharmacokinetics , Animals , Fixatives , Fresh Water , Germany , Gills/chemistry , Gills/metabolism , Gills/ultrastructure , Image Processing, Computer-Assisted , Larva/metabolism , Larva/ultrastructure , Melanocytes/chemistry , Melanocytes/metabolism , Melanocytes/ultrastructure , Microscopy, Electron , Spectrum Analysis , Spine/chemistry , Spine/metabolism , Spine/ultrastructure
...