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1.
Transplant Proc ; 48(8): 2615-2621, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27788791

ABSTRACT

BACKGROUND: Delayed graft function (DGF) is an early postoperative complication of kidney transplantation (KT) predisposing to acute rejection and lower graft survival. Intraoperative arterial hypotension and hypovolemia are associated with DGF. Central venous pressure (CVP) is used to estimate volemia but its reliability has been criticized. Pleth variability index (PVI) is a hemodynamic parameter predicting fluid responsiveness. The aim of this study was to examine the relationship between intraoperative PVI and CVP values and the occurrence of DGF. METHODS: This was a prospective, noninterventional, observational, single-center study. All consecutive patients with KT from deceased donors were included. Recipients received standard, CVP, and PVI monitoring. Intraoperative hemodynamic parameters were recorded from recipients at 5 time points during KT. RESULTS: Forty patients were enrolled. There was a poor correlation between PVI and CVP values (r2 = 0.003; P = .44). Immediate graft function and DGF patients had similar hemodynamic values during KT, with the exception of PVI values, which were significantly higher in the DGF group. In particular, a PVI >9% before unclamping of the renal artery was the only predictive parameter of DGF in our multivariate analysis (P = .02). CONCLUSIONS: This study suggests that PVI values >9% during KT are associated with the occurrence of DGF.


Subject(s)
Delayed Graft Function/etiology , Kidney Transplantation/adverse effects , Monitoring, Intraoperative/statistics & numerical data , Adult , Central Venous Pressure/physiology , Female , Hemodynamics/physiology , Humans , Male , Middle Aged , Monitoring, Intraoperative/methods , Monitoring, Physiologic/methods , Monitoring, Physiologic/statistics & numerical data , Plethysmography/methods , Plethysmography/statistics & numerical data , Prospective Studies , Reproducibility of Results , Risk Factors
2.
Klin Padiatr ; 228(4): 208-12, 2016 Jul.
Article in English | MEDLINE | ID: mdl-27362412

ABSTRACT

UNLABELLED: Background Nosocomial infections are a serious problem in the treatment of extremely low birth weight infants (ELBW, <1 000 g). In these patients, effective skin antisepsis is critical to prevent hospital-acquired infections and their sequelae. However, serious side effects of topical antiseptics have been repeatedly reported in extremely preterm infants and no agreement has been reached on the best product in this population. Therefore, we conducted a survey of the German NICUs aiming to investigate current practices and safety of topical antiseptics in ELBW neonates. METHODS: We sent anonymized questionnaires to 166 German NICUs with the highest level of care. RESULTS: Usable questionnaires were returned by 64 NICUs (39%). These NICUs had treated a total of 2130 patients with a birth weight<1 000 g in 2012. Octenidine without phenoxyethanol (OwPh) and Octenisept(®) were the predominantly used skin antiseptics for intensive-care procedures. At least one skin complication was reported by 27% (n=17) of the NICUs. In 9 cases Octenisept(®) was used, and in 6 cases octenidine was used. CONCLUSIONS: According to our knowledge, this is the first study surveying practices and safety of skin antisepsis in ELBWs in the German NICUs. Most German NICUs use octenidine, however, in different preparations. Skin complications including blistering, necrosis and scarring were seen with all octenidine products, a fact which has not been previously reported.


Subject(s)
Anti-Infective Agents, Local/adverse effects , Cross Infection/prevention & control , Drug Eruptions/etiology , Infant, Extremely Low Birth Weight , Infant, Premature, Diseases/chemically induced , Intensive Care Units, Neonatal , Female , Germany , Humans , Infant, Newborn , Male , Retrospective Studies , Surveys and Questionnaires
3.
Am J Transplant ; 16(5): 1612-9, 2016 05.
Article in English | MEDLINE | ID: mdl-26613381

ABSTRACT

Noninvasive methods to diagnose and differentiate acute cellular rejection from acute tubular necrosis or acute calcineurin inhibitor toxicity are still missing. Because T lymphocytes play a decisive role in early states of rejection, we investigated the suitability and feasibility of antibody-mediated contrast-enhanced ultrasound by using microbubbles targeted to CD3(+) , CD4(+) , or CD8(+) T cells in different models of renal disease. In an established rat renal transplantation model, CD3-mediated ultrasound allows the detection of acute rejection as early as on postoperative day 2. Ultrasound signal intensities increased with the severity of inflammation. Further, an early response to therapy could be monitored by using contrast-enhanced sonography. Notably, acute tubular necrosis occurring after ischemia-reperfusion injury as well as acute calcineurin inhibitor toxicity could easily be differentiated. Finally, the quantified ultrasound signal correlated significantly with the number of infiltrating T cells obtained by histology and with CD3 mRNA levels, as well as with chemokine CXCL9, CXCL11, and CCL19 mRNA but not with KIM-1 mRNA expression, thereby representing the severity of graft inflammation but not the degree of kidney injury. In summary, we demonstrate that antibody-mediated contrast-enhanced ultrasound targeting T lymphocytes could be a promising tool for an easy and reproducible assessment of acute rejection after renal transplantation.


Subject(s)
CD3 Complex/immunology , Graft Rejection/diagnosis , Kidney Transplantation/adverse effects , Molecular Imaging/methods , Reperfusion Injury/complications , T-Lymphocytes/immunology , Ultrasonography/methods , Acute Disease , Animals , Calcineurin Inhibitors/toxicity , Contrast Media/metabolism , Graft Rejection/diagnostic imaging , Graft Rejection/etiology , Isoantibodies/toxicity , Kidney Tubular Necrosis, Acute/diagnosis , Kidney Tubular Necrosis, Acute/diagnostic imaging , Kidney Tubular Necrosis, Acute/etiology , Male , Microbubbles , Rats , Rats, Inbred BN , Rats, Inbred Lew , Reperfusion Injury/surgery , Transplantation, Homologous
4.
Ultraschall Med ; 37(1): 82-91, 2016 Feb.
Article in English | MEDLINE | ID: mdl-25919412

ABSTRACT

PURPOSE: We propose CD3-antibody-mediated contrast-enhanced ultrasonography using human T-lymphocytes for image-based diagnosis of acute allograft rejection (AR) established in a rat renal transplantation model. MATERIALS AND METHODS: 15 minutes after tail vein injection of 30 × 10(6) human T-lymphocytes, contrast media/microbubbles conjugated with an anti-human CD3 antibody was applied to uni-nephrectomized 10-week-old allogeneically transplanted male rats (Lewis-Brown Norway (LBN) to Lewis, aTX) and ultrasound was performed to investigate the transplanted kidney as well as the native kidney. In vivo results were confirmed via immunohistochemical stainings of CD3 after post mortem dissection. Syngeneically transplanted rats (LBN to LBN, sTX), rats with ischemia/reperfusion injury (IRI, 45 min. warm ischemia), and rats subjected to acute cyclosporin A toxicity (CSA) (cyclosporine 50 mg/kg BW for 2 days i. p.) served as controls. RESULTS: Accumulation of human T-lymphocytes was clearly detected by antibody-mediated sonography und was significantly increased in allografts undergoing AR (5.41 ±â€Š1.32 A. U.) when compared to native control kidneys (0.70 ±â€Š0.08 A. U.). CD3 signal intensity was low in native kidneys, sTX (0.99 ±â€Š0.30 A. U.), CSA (0.10 ±â€Š0.02 A. U.) and kidneys with IRI (0.46 ±â€Š0.29 A. U.). Quantification of the ultrasound signal correlated significantly with the T-cell numbers obtained by immunohistochemical analysis (R2 = 0.57). CONCLUSION: Contrast-enhanced sonography using CD3-antibodies is an option for quick and highly specific assessment of AR in a rat model of renal transplantation.


Subject(s)
Antibodies/immunology , CD3 Complex/immunology , Disease Models, Animal , Graft Rejection/diagnostic imaging , Kidney Transplantation , Microbubbles , Molecular Imaging , T-Lymphocytes , Ultrasonography , Acute Disease , Animals , Graft Rejection/pathology , Kidney/diagnostic imaging , Kidney/pathology , Male , Rats , Rats, Inbred Lew , T-Lymphocytes/immunology , T-Lymphocytes/pathology
9.
Onkologie ; 23(5): 485-486, 2000 Oct.
Article in English | MEDLINE | ID: mdl-11441250
10.
Mol Biol Evol ; 16(6): 724-31, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10368951

ABSTRACT

Intra- and interspecific nucleotide variation for the major developmental gene runt in Drosophila was studied in D. melanogaster and D. simulans. The 1.5-kb protein-coding region and the 0.4-kb intron of the runt gene were sequenced for 11 alleles in each species. The D. melanogaster alleles originated from east Africa. Estimated parameters of intraspecific variation in D. melanogaster (exons: theta = 0.018, pi = 0.018; intron: theta = 0.014, pi = 0.014) and D. simulans (exons: theta = 0.007, pi = 0.005; intron: theta = 0.008, pi = 0.005) were below average for other X-linked genes, while divergence between species (exons: D = 0.094; intron: D = 0.069) fell within the normal range for both silent and replacement changes. This estimate for runt, along with published values for three other genes in regions of normal recombination, show east African D. melanogaster to be roughly twice as polymorphic as D. simulans. The majority of nucleotide variation, silent and replacement, in both species was found to be selectively neutral using various statistical tests (HKA, McDonald-Kreitman, Tajima, and Fu and Li tests). Monte Carlo simulations of the coalescent process significantly rejected a Wright-Fisher model with respect to an amino acid polymorphism and the distribution of polymorphic sites among the D. simulans lines. This indicated an old lineage and may reflect ancestral population substructuring in D. simulans.


Subject(s)
DNA-Binding Proteins/genetics , Drosophila melanogaster/genetics , Drosophila/genetics , Genes, Insect , Insect Proteins/genetics , Alleles , Animals , Base Sequence , DNA/genetics , Drosophila Proteins , Evolution, Molecular , Genetic Variation , Introns , Molecular Sequence Data , Nuclear Proteins , Polymorphism, Genetic , Sequence Homology, Nucleic Acid , Species Specificity , Transcription Factors
12.
J Clin Microbiol ; 37(3): 769-71, 1999 Mar.
Article in English | MEDLINE | ID: mdl-9986849

ABSTRACT

We report the case of a patient who developed a large brain abscess after neurosurgery. Cerebrospinal fluid from the abscess drainage yielded Abiotrophia adiacens-specific PCR products and microorganisms that were identified by conventional microbiological methods and by 16S ribosomal DNA analysis as Abiotrophia adiacens, which was formerly classified as a member of nutritionally variant streptococci.


Subject(s)
Astrocytoma/surgery , Brain Abscess/microbiology , Brain Neoplasms/surgery , Streptococcal Infections/diagnosis , Streptococcus/isolation & purification , Brain Neoplasms/cerebrospinal fluid , DNA, Ribosomal/genetics , Female , Humans , Middle Aged , Neurosurgical Procedures/adverse effects , Polymerase Chain Reaction , Postoperative Complications , RNA, Ribosomal, 16S/genetics , Streptococcal Infections/cerebrospinal fluid , Streptococcus/classification , Streptococcus/growth & development
13.
Mol Biol Evol ; 15(12): 1761-71, 1998 Dec.
Article in English | MEDLINE | ID: mdl-9866210

ABSTRACT

The acrosomal protein bindin attaches sperm to eggs during sea urchin fertilization. Complementary to ongoing functional biochemical studies, I take a comparative approach to explore the molecular evolution of bindin in a group of closely related free-spawning echinoid species. Two alleles of the mature bindin gene were sequenced for each of six species in the sea urchin family Strongylocentrotidae. The nucleotide sequences diverged by at least 1% per Myr at both silent and replacement sites. Two short sections flanking the conserved block show an excess of nonsynonymous substitutions. Each is homologous to a region that had been identified as a target of selection in other sea urchin comparisons. A large proportion of the bindin-coding sequence consists of a highly variable repeat region. Bindin sequences, even including the large intron, could not resolve the branching order among five of the species.


Subject(s)
Evolution, Molecular , Glycoproteins/genetics , Phylogeny , Sea Urchins/genetics , Spermatozoa/metabolism , Alleles , Amino Acid Sequence , Amino Acid Substitution , Animals , Base Sequence , Conserved Sequence , Female , Genetic Variation , Glycoproteins/chemistry , Male , Molecular Sequence Data , Point Mutation , Receptors, Cell Surface , Sea Urchins/classification , Sequence Alignment , Sequence Homology, Amino Acid , Sperm-Ovum Interactions/genetics
14.
Eur J Biochem ; 247(1): 209-16, 1997 Jul 01.
Article in English | MEDLINE | ID: mdl-9249028

ABSTRACT

Vibrio cholerae cytolysin (VCC) is produced by many non-choleratoxigenic strains of V. cholerae, and possibly represents a relevant pathogenicity determinant of these bacteria. The protein is secreted as a pro-toxin that is proteolytically cleaved to yield the active toxin with a molecular mass of approximately 63 kDa. We here describe a simple procedure for preparative isolation of mature VCC from bacterial culture supernatants, and present information on its mode of binding and pore formation in biological membranes. At low concentrations, toxin monomers interact with a high-affinity binding site on highly susceptible rabbit erythrocytes. This as yet unidentified binding site is absent on human erythrocytes, which are less susceptible to the toxin action. At higher concentrations, binding of the toxin occurs to both rabbit and human erythrocytes in a non-saturable manner. Cell-bound toxin monomers oligomerize to form supramolecular structures that are seen in the electron microscope as apparently hollow funnels, and oligomerization correlates functionally with the appearance of small transmembrane pores. Osmotic protection experiments indicate that the toxin channels are of finite size with a diameter of 1-2 nm. The mode of action of VCC closely resembles that of classical pore-forming toxins such as staphylococcal alpha-toxin and the aerolysin of Aeromonas hydrophila.


Subject(s)
Cytotoxins/metabolism , Vibrio cholerae/pathogenicity , Amino Acid Sequence , Animals , Binding Sites , Cytotoxins/chemistry , Cytotoxins/pharmacology , Erythrocyte Membrane/drug effects , Humans , Molecular Sequence Data , Molecular Weight , Rabbits
15.
Urology ; 49(4A Suppl): 66-76, 1997 Apr.
Article in English | MEDLINE | ID: mdl-9111616

ABSTRACT

OBJECTIVES: To identify complications of various forms of treatments for prostate cancer and their influence on patients' quality of life with the ultimate goal of suggesting a Quality of Life Questionnaire specific for prostate cancer for further validation. METHODS: The literature was screened for reports on the more common complications following various forms of therapy for prostate cancer. Frequencies were summarized. The scarce literature reporting on quality of life in prostate cancer was reviewed and conflicting data were discussed and reassessed. Suggested questionnaires used in other studies were critically scrutinized and the various questions recorded. RESULTS: Following radical surgery, impotence and incontinence were the most common complications reducing patients' quality of life. The literature was not uniform with regard to whether loss of sexual function was regarded as a worse complication than loss of urinary control. Following radiotherapy, intestinal problems and sexual dysfunction were the dominating side effects. Quality of life was best preserved in surveillance-only series. Following endocrine therapy, not only impotence and hot flushes were focused upon, but also mental dysfunction and intestinal dysfunction from nonsteroidal antiandrogens, additionally, the importance of effective palliation was highlighted. A Quality of Life Questionnaire should contain general domains relevant to cancer patients, cancer-specific questions, and prostate-cancer-specific questions. The latter group includes: worry for prostate cancer and its prognosis, bone/pelvic pain, lower urinary tract symptoms, urinary incontinence, urinary diversion, bowel function, sexual function, endocrine effects, and satisfaction with medical care for prostate cancer. CONCLUSIONS: A modern trial of prostate cancer treatment should be regarded as insufficient without including a validated Quality of Life Questionnaire.


Subject(s)
Prostatic Neoplasms/therapy , Quality of Life , Costs and Cost Analysis , Humans , Male , Neoplasm Staging , Prostatic Neoplasms/economics , Prostatic Neoplasms/pathology , Therapeutics/adverse effects
16.
Genetics ; 144(3): 1027-41, 1996 Nov.
Article in English | MEDLINE | ID: mdl-8913747

ABSTRACT

The nucleotide diversity across 1705 bp of the G6pd gene is studied in 50 Drosophila melanogaster and 12 D. simulans lines. Our earlier report contrasted intraspecific polymorphism and interspecific differences at silent and replacement sites in these species. This report expands the number of European and African lines and examines the pattern of polymorphism with respect to the common A/B allozymes. In D. melanogaster the silent nucleotide diversity varies 2.8-fold across localities. The B allele sequences are two-to fourfold more variable than the derived A allele, and differences between allozymes are twice as among B alleles. There is strong linkage disequilibrium across the G6pd region. In both species the level of silent polymorphism increases from the 5' to 3' ends, while there is no comparable pattern in level of silent site divergence or fixation. The neutral model is not rejected in either species. Using D. yakuba as an outgroup, the D. melanogaster lineage shows a twofold greater rate of silent fixation, but less than half the rate of amino acid replacement. Lineage-specific differences in mutation fixation are inconsistent with neutral expectations and suggest the interaction of species-specific population size differences with both weakly advantageous and deleterious selection.


Subject(s)
Drosophila melanogaster/enzymology , Drosophila/enzymology , Glucosephosphate Dehydrogenase/genetics , Polymorphism, Genetic , Animals , Base Sequence , DNA , Drosophila/genetics , Drosophila melanogaster/genetics , Linkage Disequilibrium , Molecular Sequence Data , Monte Carlo Method
17.
Eur J Biochem ; 236(1): 34-9, 1996 Feb 15.
Article in English | MEDLINE | ID: mdl-8617283

ABSTRACT

Streptolysin 0 (SLO) is the prototype of a family of cytolysins that consists of proteins which bind to cholesterol and form very large transmembrane pores. Structure/function studies on the pore-forming cytolysin SLO have been complicated by the proteolytic inactivation of a substantial portion of recombinant SLO (rSLO) expressed in Escherichia coli. To overcome this problem, translational fusions between the E. coli maltose-binding protein (MBP) gene and SLO were constructed, using the vectors pMAL-p2 and pMAL-c2. MBP-SLO fusion proteins were degraded if secreted into the E. coli periplasm, but intact, soluble MBP-SLO fusion proteins were produced at high levels in the cytoplasm. Active SLO with the expected N-terminus was separated from the MBP carrier by cleavage with factor Xa. Cleavage with plasmin or trypsin also yielded active, but slightly smaller forms of SLO. Surprisingly, uncleaved MBP-SLO was also hemolytic and cytotoxic to human fibroblasts and keratinocytes. The MBP-SLO fusion protein displayed equal activities to SLO. Sucrose density gradient analyses showed that the fusion protein assembled into polymers, and no difference in structure was discerned compared with polymers formed by native SLO. These studies show that the N-terminal 70 residues of mature (secreted) SLO are not required for pore formation and that the N-terminus of the molecule is probably not inserted into the bilayer. In addition, they provide a simple means for producing mutants for structure/function studies and highly purified SLO for use as a permeabilising reagent in cell biology research.


Subject(s)
ATP-Binding Cassette Transporters , Bacterial Proteins/biosynthesis , Escherichia coli Proteins , Hemolysis , Monosaccharide Transport Proteins , Streptococcus pyogenes/genetics , Streptolysins/biosynthesis , Bacterial Proteins/genetics , Bacterial Proteins/pharmacology , Base Sequence , Carrier Proteins/biosynthesis , Carrier Proteins/genetics , Cloning, Molecular , Erythrocytes/drug effects , Escherichia coli/genetics , Fluoresceins/metabolism , Humans , Liposomes/metabolism , Maltose-Binding Proteins , Molecular Sequence Data , Protein Conformation , Recombinant Fusion Proteins/biosynthesis , Recombinant Fusion Proteins/pharmacology , Sequence Analysis , Sequence Deletion , Streptolysins/genetics , Streptolysins/pharmacology , Structure-Activity Relationship
19.
Swiss Surg ; (6): 291-3, 1995.
Article in German | MEDLINE | ID: mdl-8581814

ABSTRACT

Malignant Fibrous Histiocytoma (MFH) is an unfrequent mesenchymal tumor first described by O'Brian in 1964 [1, 16]. The most common site of this malignancy is the limbs area and the retroperitoneum. Primary involvement of the kidney is extremely rare. Only thirteen cases are well documented in the literature. We report an additional case of such primary renal tumor.


Subject(s)
Histiocytoma, Benign Fibrous/diagnosis , Kidney Neoplasms/diagnosis , Aged , Histiocytoma, Benign Fibrous/pathology , Histiocytoma, Benign Fibrous/surgery , Humans , Kidney/pathology , Kidney Neoplasms/pathology , Kidney Neoplasms/surgery , Male , Neoplastic Cells, Circulating , Nephrectomy , Tomography, X-Ray Computed , Urography
20.
Swiss Surg ; (6): 285-9; discussion 289-90, 1995.
Article in German | MEDLINE | ID: mdl-8581813

ABSTRACT

During the last 20 years important improvements in diagnosis, staging and indications as well as in operative and conservative treatments of urological malignancies have been achieved. In consequence the prognoses of patients with these cancers have been improved. One remaining question concerns the impact of curative radical surgery on the individual's quality of life and life perspective. The purpose of this prospective study was to obtain relevant data upon which to develop tumor-specific modules according to the guidelines of the EORTC, so that this question can be studied. Between July, 1993 and July, 1994 data from 106 cancer patients with non metastatic urological malignancies (prostate, kidney and bladder) were gathered for analysis. Patients include 37 with prostatic cancer, who were treated by a radical prostatovesicalectomy. Fourty-two patients with renal cell carcinoma underwent radical nephrectomy. In 30 bladder cancer patients radical cystoprostatovesicalectomy with an ileum conduit was carried out. The first step was to describe the symptomatology in these patients by means of open interviews. In addition, one day postoperatively, the day before discharge and one year after surgery the patients completed self-administered symptomatic and psychological questionnaires. The symptomatic questionnaire contained 20 items, each with six response choices. For evaluating subjective well-being, we selected the "Basler Befindlichkeitsbogen" (Basler Psychological Balance), which has four dimensions: Vitality, vigilance, social extrovertivity and psychological balance. Descriptive and comparative analyses were performed with an SPSS programme. Comparing the preoperative and one year postoperative values, all patients groups showed a significant deterioration in the four dimensions of the psychological parameters. The data from the present study were the basis for the development of EORTC-specific tumor modules for urological cancer according to the guidelines of the EORTC.


Subject(s)
Postoperative Complications/psychology , Quality Assurance, Health Care , Quality of Life , Urogenital Neoplasms/surgery , Adaptation, Psychological , Aged , Cystectomy/psychology , Female , Follow-Up Studies , Humans , Male , Middle Aged , Nephrectomy/psychology , Prospective Studies , Prostatectomy/psychology , Sick Role , Urogenital Neoplasms/psychology
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