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<title>Artikel in Fachzeitschriften</title>
<link>http://edoc.rki.de/176904/43</link>
<description/>
<pubDate>Fri, 21 Aug 2026 02:01:17 GMT</pubDate>
<dc:date>2026-08-21T02:01:17Z</dc:date>
<item>
<title>Over-The-Counter (OTC) Drug Consumption among Adults Living in Germany: Results from the German Health Interview and Examination Survey for Adults 2008-2011 (DEGS1)</title>
<link>http://edoc.rki.de/176904/13858</link>
<description>Over-The-Counter (OTC) Drug Consumption among Adults Living in Germany: Results from the German Health Interview and Examination Survey for Adults 2008-2011 (DEGS1)
Barrenberg, Eva; Knopf, Hildtraud; Garbe, Edeltraut
In order to assess the effects of prescription-only (Rx) to over-the-counter (OTC) drug switches and related policies, it is imperative to distinguish self-medication from OTC drug use. The objective of this study was to estimate the OTC drug use in the adult population in Germany, to identify its predictors and to highlight methodological differences when compared to the study of a self-medication prevalence. Seven-day prevalence of OTC drug use was calculated on the basis of information provided by 7091 participants of the German Health Interview and Examination Survey for Adults (DEGS1) conducted between 2008 to 2011. Logistic regression analysis was used to identify predictors of OTC drug use. Seven-day prevalence of OTC drug use was higher in women (47.16%) than in men (33.17%). Female gender, an age of more than 60 years, reduced health status, Rx drug use, and multi-morbidity were identified as predictors of OTC drug use. The levels of OTC drug use were higher than the self-medication prevalence found in the same data set probably because some OTC drugs are commonly prescribed by physicians. Drug utilization studies should, therefore, make a methodological distinction between self-medication and OTC drug use depending on whether the focus is on drug safety or the impact of regulatory decisions on the trade status
</description>
<pubDate>Wed, 11 Apr 2018 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://edoc.rki.de/176904/13858</guid>
<dc:date>2018-04-11T00:00:00Z</dc:date>
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<title>Metabolic interactions between Toxoplasma gondii an its host</title>
<link>http://edoc.rki.de/176904/13857</link>
<description>Metabolic interactions between Toxoplasma gondii an its host
Blume, Martin; Seeber, Frank
Toxoplasma gondii is an obligate intracellular parasite belonging to the phylum Apicomplexa that infects all warm-blooded animals, including humans. T. gondii can replicate in every nucleated host cell by orchestrating metabolic interactions to derive crucial nutrients. In this review, we summarize the current status of known metabolic interactions of T. gondii with its host cell and discuss open questions and promising experimental approaches that will allow further dissection of the host–parasite interface and discovery of ways to efficiently target both tachyzoite and bradyzoite forms of T. gondii, which are associated with acute and chronic infection, respectively
</description>
<pubDate>Tue, 30 Oct 2018 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://edoc.rki.de/176904/13857</guid>
<dc:date>2018-10-30T00:00:00Z</dc:date>
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<title>Upsurge in echovirus 30 detections in five EU/EEA countries, April to September, 2018</title>
<link>http://edoc.rki.de/176904/13856</link>
<description>Upsurge in echovirus 30 detections in five EU/EEA countries, April to September, 2018
Broberg, Eva K.; Simone, Benedetto; Jansa, Josep; Diederich, Sabine; Böttcher, Sindy; Keeren, Kathrin; EU/EEA Member State contributors
An upsurge in Echovirus 30 (E30) infections, associated with meningitis/meningoencephalitis, has been observed in Denmark, Germany, the Netherlands, Norway and Sweden in the period April to September 2018, compared with 2015–2017. In total, 658 E30 infections among 4,537 enterovirus infections were detected in 15 countries between January and September 2018 and affected mainly newborns and 26–45 year-olds. National public health institutes are reminded to remain vigilant and inform clinicians of the ongoing epidemic.
</description>
<pubDate>Thu, 01 Nov 2018 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://edoc.rki.de/176904/13856</guid>
<dc:date>2018-11-01T00:00:00Z</dc:date>
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<title>Prevalence and Clinical Correlates of Chronic Hepatitis E Infection in German Renal Transplant RecipientsWith Elevated Liver Enzymes</title>
<link>http://edoc.rki.de/176904/13855</link>
<description>Prevalence and Clinical Correlates of Chronic Hepatitis E Infection in German Renal Transplant RecipientsWith Elevated Liver Enzymes
Choi, Mira; Hofmann, Jörg; Köhler, Anja; Wang, Bo; Bock, Claus-Thomas; Schott, Eckart; Reinke, Petra; Nickel, Peter
Background&#13;
&#13;
Elevated liver enzymes are frequently observed in renal transplant recipients and warrant further exploration. In immunosuppressed patients, hepatitis E virus (HEV) infection may cause chronic hepatitis, cirrhosis, and extrahepatic manifestations such as renal injury.&#13;
Methods&#13;
&#13;
We performed a retrospective cross-sectional study investigating the prevalence, clinical correlates, and outcome of chronic HEV infection in a cohort of renal transplant recipients with elevated liver enzymes.&#13;
Results&#13;
&#13;
Over a period of 30 months, 140 of 1469 renal transplant recipients had elevated liver enzymes, of which serum samples from 98 patients were available to determine HEV status. Seventeen patients were detected with HEV infection, of which 16 developed chronic HEV infection, while 1 patient controlled viremia (prevalence of chronic infection of 16.3%, with a minimum prevalence of 1.1% in the whole cohort). Increased liver stiffness was indicated by an average FibroScan result of 11.2 kPa in these patients. All 16 patients with chronic HEV infection were treated with ribavirin for a mean duration of 3 months. Five patients developed a viral rebound and received a second treatment course, of which 2 controlled HEV replication. Six months after the end of therapy, HEV clearance was achieved in 81.3% of the patients. One patient developed ribavirin resistance. Hemolytic anemia after ribavirin treatment was frequent, requiring blood transfusion in 3 patients. Four patients developed de novo glomerulonephritis, of which 2 were possibly associated with HEV infection.&#13;
Conclusions&#13;
&#13;
This retrospective study showed that prevalence of chronic HEV infection was high in our renal transplant patient cohort and was associated with significant liver impairment and the occurrence of renal injury. Ribavirin treatment was effective and should be initiated early to avoid complications, but the risk of severe hemolytic anemia makes strict monitoring essential.&#13;
&#13;
Liver enzyme alteration without any preexisting liver disease is a frequent finding in renal transplant recipients.&#13;
Thorough diagnostic evaluation is required to rule out multiple infectious and noninfectious causes. Among the most important being bacterial, fungal, and viral infections, but implicated are also drug toxicity and malignancies. Hepatitis E virus (HEV) infection, particularly genotype 3, is well recognized in industrialized countries. In Germany, a seroprevalence of 16.8% has been reported among healthy adults. Usually, HEV infection is self-limiting, although an acute infection can lead to chronic HEV infection in immunocompromised patients with increased risk of developing significant chronic liver disease and cirrhosis. Moreover, HEV-infected patients may develop various extrahepatic complications including glomerular injury. In fact, histopathologic findings, such as membranoproliferative, membranous, or mesangioproliferative glomerulonephritis, in transplant patients have been described. Because glomerulonephritis is a major cause of long-term renal graft failure, HEV infection is a potential risk factor for renal graft survival.In renal transplant patients with persisting HEV infection resistant to reduction of immunosuppression, treatment with ribavirin for a period of 3 to 6 months has been reported to be effective. Ribavirin therapy usually leads to rapid normalization of liver enzyme levels, HEV clearance, and a sustained virologic response (SVR) in up to 78% of patients.&#13;
&#13;
Nevertheless, side effects are a limiting factor.&#13;
&#13;
Diagnosing HEV infection in immunosuppressed patients is not trivial. As serology is of limited value due to compromised humoral immune responses, a quantitative HEV reverse transcription polymerase chain reaction (RT-PCR) is required to exclude active infection.&#13;
&#13;
The HEV ribonucleinic acid (RNA) prevalence in patients with elevated liver enzymes has not been systematically addressed in kidney transplant recipients. Furthermore, additional data regarding clinical relevance and outcome of chronic HEV infection in renal transplant patients are warranted.&#13;
&#13;
This study is the first systematic cross-sectional screening for HEV infection in a large cohort of renal transplant recipients with elevated liver enzymes. Over a period of 30 months, all renal and combined renal and other organ transplant recipients were screened for abnormal liver enzymes, HEV RNA, and IgG/IgM antibodies. The clinical correlates of renal transplant recipients with chronic HEV infection were also established in detail
</description>
<pubDate>Thu, 01 Feb 2018 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://edoc.rki.de/176904/13855</guid>
<dc:date>2018-02-01T00:00:00Z</dc:date>
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