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1.
J Hosp Infect ; 112: 108-113, 2021 Jun.
Article in English | MEDLINE | ID: mdl-33864891

ABSTRACT

BACKGROUND: The presence of coronaviruses on surfaces in the patient environment is a potential source of indirect transmission. Manual cleaning and disinfection measures do not always achieve sufficient removal of surface contamination. This increases the importance of automated solutions in the context of final disinfection of rooms in the hospital setting. Ozone is a highly effective disinfectant which, combined with high humidity, is an effective agent against respiratory viruses. Current devices allow continuous nebulization for high room humidity as well as ozone production without any consumables. AIM: In the following study, the effectiveness of a fully automatic room decontamination system based on ozone was tested against bacteriophage Φ6 (phi 6) and bovine coronavirus L9, as surrogate viruses for the pandemic coronavirus SARS-CoV-2. METHODS: For this purpose, various surfaces (ceramic tile, stainless steel surface and furniture board) were soiled with the surrogate viruses and placed at two different levels in a gas-tight test room. After using the automatic decontamination device according to the manufacturer's instructions, the surrogate viruses were recovered from the surfaces and examined by quantitative cultures. Then, reduction factors were calculated. FINDINGS: The ozone-based room decontamination device achieved virucidal efficacy (reduction factor >4 log10) against both surrogate organisms regardless of the different surfaces and positions confirming a high activity under the used conditions. CONCLUSION: Ozone is highly active against SARS-CoV-2 surrogate organisms. Further investigations are necessary for a safe application and efficacy in practice as well as integration into routine processes.


Subject(s)
Automation/instrumentation , COVID-19/prevention & control , Disinfectants/pharmacology , Disinfection/instrumentation , Disinfection/methods , Ozone/pharmacology , Animals , Bacteriophages/drug effects , COVID-19/transmission , Cattle , Coronavirus, Bovine/drug effects , Cross Infection/prevention & control , Cross Infection/virology , Decontamination/instrumentation , Decontamination/methods , Equipment and Supplies, Hospital/virology , Hospitals , Humans , SARS-CoV-2/drug effects
2.
Infection ; 40(4): 451-4, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22086667

ABSTRACT

An acute infection with hepatitis E virus (HEV) genotype 3 subtype c was diagnosed in a patient with chronic lymphatic B-cell leukemia 6 weeks after the infusion of donor lymphocytes. Despite intensive care the patient died 39 days after admission due to pericardial effusion that was related to acute liver failure. We suggest that diagnostic procedures for detection of HEV infection should be seriously considered for the immunocompromised patient with elevated liver enzymes in the absence of a travel history to HEV endemic countries.


Subject(s)
Hepatitis E/mortality , Leukemia, Lymphocytic, Chronic, B-Cell/therapy , Lymphocyte Transfusion , Acute Disease , Fatal Outcome , Germany , Hepatitis E/drug therapy , Hepatitis E/etiology , Humans , Lymphocyte Transfusion/adverse effects , Male , Middle Aged
3.
Clin Infect Dis ; 50(8): 1112-9, 2010 Apr 15.
Article in English | MEDLINE | ID: mdl-20205588

ABSTRACT

BACKGROUND: This article describes multiple transmissions of rabies via transplanted solid organ from a single infected donor. The empirical Milwaukee treatment regimen was used in the recipients. METHODS: Symptomatic patients were treated by deep sedation (ketamine, midazolam, and phenobarbital), ribavirin, interferon, and active and passive vaccination. Viral loads and antibodies were continuously monitored. RESULTS: Recipients of both cornea and liver transplants developed no symptoms. The recipient of the liver transplant had been vaccinated approximately 20 years before transplantation. Two recipients of kidney and lung transplants developed rabies and died within days of symptomatic disease. Another kidney recipient was treated 7 weeks before he died. The cerebrospinal fluid viral load remained at constant low levels (<10,000 copies/mL) for approximately 5 weeks; it increased suddenly by almost 5 orders of magnitude thereafter. After death, no virus was found in peripheral compartments (nerve tissue, heart, liver, or the small intestine) in this patient, in contrast to in patients in the same cohort who died early. CONCLUSIONS: Our report includes, to our knowledge, the longest documented treatment course of symptomatic rabies and the first time that the virus concentration was measured over time and in different body compartments. The postmortem virus concentration in the periphery was low, but there was no evidence of a reduction of virus in the brain.


Subject(s)
Antibodies, Viral/administration & dosage , Antiviral Agents/therapeutic use , Hypnotics and Sedatives/therapeutic use , Organ Transplantation/adverse effects , Rabies Vaccines/administration & dosage , Rabies virus/isolation & purification , Rabies/drug therapy , Adult , Aged , Antibodies, Viral/blood , Female , Humans , Male , Middle Aged , Rabies Vaccines/immunology , Treatment Outcome , Viral Load
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