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1.
Public Health ; 180: 141-148, 2020 Mar.
Article in English | MEDLINE | ID: mdl-31918048

ABSTRACT

OBJECTIVES: Germany has a mandatory surveillance system for acute hepatitis B (AHB) with the Protection against Infection Act as the legal basis in place since 2001. An amendment was introduced in 2013. We aimed at evaluating the surveillance systems' performance regarding timeliness, data quality, and simplicity from 2005 to 2014 and at assessing the effect of the amendment on timeliness of AHB surveillance. STUDY DESIGN: This study is a trend analysis of surveillance data. METHODS: Aspects of simplicity versus complexity of the surveillance system were assessed by describing data flow, levels of reporting, and data management procedures. Data quality, in terms of data completeness, was evaluated by quantitative indicators, and timeliness was measured in days between different levels of the surveillance system, notification delay, and reporting delay. Trends over time in data quality were analyzed by logistic regression, while negative binomial regression was used to test for trend over time regarding mean notification and reporting delay. RESULTS: Between January 2005 and December 2014, a total of 22,549 AHB infections were reported at the national level. The data flow of the German AHB surveillance system showed structural characteristics of a complex system. Over the 10-year period, completeness of reporting sex, age, probable route of transmission, and hepatitis B virus (HBV) vaccination were 99%, 100%, 25%, and 73%, respectively. However, data quality decreased over the evaluation period. Although notification delay improved over time (incident rate ratio [IRR] = 0.95, 95% confidence interval [CI] = 0.95-0.96; P < 0.05), reporting delay improved only since the amendment (IRR = 0.76, 95% CI = 0.70-0.82; P < 0.05). In total, mean notification and reporting delay were 3.0 days and 14.3 days, respectively. CONCLUSIONS: The German AHB surveillance system is operating in a timely manner. Although timeliness improved over the evaluation period and the amendment to the Protection against Infection Act succeeded in reducing reporting time, data quality in terms of completeness of information decreased considerably. As improved data completeness is required to adequately design prevention activities, reasons for this decrease should further be explored.


Subject(s)
Hepatitis B/epidemiology , Population Surveillance/methods , Data Accuracy , Disease Notification/statistics & numerical data , Germany/epidemiology , Humans , Time Factors
2.
Pneumologie ; 70(4): 250-76, 2016 Apr.
Article in English | MEDLINE | ID: mdl-27064418

ABSTRACT

Non-tuberculous mycobacterioses comprise a group of diseases caused by mycobacteria which do not belong to the Mycobacterium (M.) tuberculosis-complex and are not ascribed to M. leprae. These mycobacteria are characterized by a broad variety as to environmental distribution and adaptation. Some of the species may cause specific diseases, especially in patients with underlying immunosuppressive diseases, chronic pulmonary diseases or genetic predisposition, respectively. Worldwide, a rising prevalence and significance of non-tuberculous mycobacterioses is recognized. The present recommendations summarise current aspects of epidemiology, pathogenesis, clinical aspects, diagnostics - especially microbiological methods including susceptibility testing -, and specific treatment for the most relevant species. Diagnosis and treatment of non-tuberculous mycobacterioses during childhood and in HIV-infected individuals are described in separate chapters.


Subject(s)
Diagnostic Techniques, Respiratory System/standards , Infectious Disease Medicine/standards , Mycobacterium Infections, Nontuberculous/diagnosis , Mycobacterium Infections, Nontuberculous/therapy , Practice Guidelines as Topic , Pulmonary Medicine/standards , Evidence-Based Medicine , Germany , Humans , Mycobacterium Infections, Nontuberculous/microbiology , Treatment Outcome
3.
Zentralbl Chir ; 127(10): 850-4, 2002 Oct.
Article in German | MEDLINE | ID: mdl-12410450

ABSTRACT

UNLABELLED: At our institution we have used fresh-frozen allografts for the reconstruction of the anterior and posterior cruciate ligament since 1993. METHOD: In this retrospective study we evaluated the clinical outcome of 325 fresh-frozen allografts (bone-patellar-tendon-bone allografts and Achilles-bone-tendon allografts) for primary and revision ACL-reconstruction. Patients (average age 38 years) were operated between 5/1993 and 2/1998 and mean follow-up was 38 (range 24 to 71) months. Clinical evaluation consisted of a case history, an examination, IKDC, Cincinnati knee score (CKS), KT-1000 testing and standardized X-rays. RESULTS: Overall subjective rating according to the CKS was more than 82 points for both groups. Objective results according to the IKDC were normal or nearly normal in 75.6 % of primary- and 67.0 % of revision-ACL reconstructions. The stability measured with the KT-1000 showed an average maximum side to side difference of 2.1 mm for primary ACL reconstruction and 2.3 mm for revisioners. The total failure-rate (= rerupture-rate + laxity-failures) was 13.7 % for primary and 15.0 % for revision ACL reconstructions. CONCLUSION: Given the increased failure-rate, autograft tissue remains our graft of first choice for primary ACL-reconstruction. We advise to reserve allografts for revision procedures where suitable autogenous tissues have been previously compromised, where a contraindication for autogenous tissue harvest exists or for multiple ligament surgery. No specific complications were observed with the use of allograft tissue.


Subject(s)
Anterior Cruciate Ligament Injuries , Bone Transplantation/methods , Knee Injuries/surgery , Postoperative Complications/surgery , Tendon Transfer/methods , Adolescent , Adult , Aged , Anterior Cruciate Ligament/surgery , Female , Follow-Up Studies , Humans , Male , Middle Aged , Postoperative Complications/etiology , Recurrence , Reoperation , Retrospective Studies , Transplantation, Homologous
4.
J Immunol ; 166(4): 2801-7, 2001 Feb 15.
Article in English | MEDLINE | ID: mdl-11160347

ABSTRACT

The acute-phase reactant rabbit serum amyloid A 3 (SAA3) was identified as the major difference product in Ag-induced arthritis in the rabbit, a model resembling in many aspects the clinical characteristics of rheumatoid arthritis (RA) in humans. In Ag-induced arthritis, up-regulated SAA3 transcription in vivo was detected in cells infiltrating into the inflamed joint, in the area where pannus formation starts and, most notably, also in chondrocytes. The proinflammatory cytokine IL-1beta induced SAA3 transcription in primary rabbit chondrocytes in vitro. Furthermore, rSAA3 protein induced transcription of matrix metalloproteinases in rabbit chondrocytes in vitro. In the human experimental system, IL-1beta induced transcription of acute-phase SAA (A-SSA; encoded by SAA1/SAA2) in primary chondrocytes. Similar to the rabbit system, recombinant human A-SAA protein was able to induce matrix metalloproteinases' transcription in chondrocytes. Further, immunohistochemistry demonstrated that A-SAA was highly expressed in human RA synovium. A new finding of our study is that A-SSA expression was also detected in cartilage in osteoarthritis. Our data, together with previous findings of SAA expression in RA synovium, suggest that A-SAA may play a role in cartilage destruction in arthritis.


Subject(s)
Arthritis, Rheumatoid/enzymology , Matrix Metalloproteinases/metabolism , Serum Amyloid A Protein/biosynthesis , Transcription, Genetic , Up-Regulation , Amino Acid Sequence , Animals , Arthritis, Rheumatoid/immunology , Arthritis, Rheumatoid/metabolism , Arthritis, Rheumatoid/pathology , Cartilage, Articular/metabolism , Cell Movement/genetics , Chondrocytes/enzymology , Chondrocytes/metabolism , Chondrocytes/pathology , Disease Models, Animal , Female , Gene Expression Regulation , Humans , Interleukin-1/pharmacology , Matrix Metalloproteinases/biosynthesis , Matrix Metalloproteinases/genetics , Molecular Sequence Data , RNA, Messenger/biosynthesis , Rabbits , Recombinant Proteins/biosynthesis , Recombinant Proteins/isolation & purification , Recombinant Proteins/pharmacology , Serum Amyloid A Protein/genetics , Serum Amyloid A Protein/isolation & purification , Serum Amyloid A Protein/physiology , Synovial Membrane/enzymology , Synovial Membrane/immunology , Synovial Membrane/metabolism , Synovial Membrane/pathology , Transcription, Genetic/immunology , Tumor Necrosis Factor-alpha/pharmacology , Up-Regulation/genetics , Up-Regulation/immunology
5.
Aliment Pharmacol Ther ; 13(11): 1531-4, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10571612

ABSTRACT

OBJECTIVES: To compare testing for Helicobacter pylori IgG antibodies using a dried plasma collection card device with specimens obtained by venepuncture. METHODS: Eighty-four patients underwent testing for H. pylori IgG antibodies by venepuncture and by fingerstick using a single drop of blood placed on each of two dried plasma collection card devices. The correlation of venepuncture results to dried plasma card results was assessed. RESULTS: There was a high degree of correlation of EIA results between venepuncture and dried plasma card specimens (r=0.98). The qualitative result of the first dried plasma card and venepuncture specimen testing differed in 7 of 84 patients and for the second dried plasma card differed in 7 of 82 patients. The first dried plasma card was 93% sensitive and 100% specific and the second was 93% sensitive and 98% specific as compared to the venepuncture result. There was a high degree of correlation between the first and second dried plasma cards (r=0.996). CONCLUSIONS: The dried plasma collection card has adequate sensitivity and excellent specificity as compared to venepuncture specimens and is a feasible alternative for H. pylori IgG antibody testing.


Subject(s)
Helicobacter Infections/blood , Helicobacter Infections/diagnosis , Helicobacter pylori , Plasma/chemistry , Antibodies, Bacterial/analysis , Blood Specimen Collection , Enzyme-Linked Immunosorbent Assay , Female , Humans , Immunoglobulin G/analysis , Male , Middle Aged , Reproducibility of Results , Smoking
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