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1.
Open Forum Infect Dis ; 11(5): ofae263, 2024 May.
Article in English | MEDLINE | ID: mdl-38798896

ABSTRACT

Data on posaconazole serum levels of patients on prophylaxis with delayed-release tablets or oral suspension during intensive chemotherapy for acute myeloid leukemia and myelodysplastic syndrome are scarce. In this analysis, the proportion of patients with acute myeloid leukemia/myelodysplastic syndrome achieving posaconazole target concentrations with delayed-release tablets was higher than with oral suspension.

2.
Comp Immunol Microbiol Infect Dis ; 86: 101816, 2022 Jul.
Article in English | MEDLINE | ID: mdl-35472655

ABSTRACT

Cystic echinococcosis (CE) is a disease caused by Echinococcus granulosus sensu lato (s.l.), an ubiquitous worldwide zoonotic agent affecting humans and animals. Diagnosis of CE in humans is usually performed by imagine techniques along with immunoassays. The aim of our study was to evaluate and compare four commercial diagnostic kits, based on the detection of IgG antibodies against E. granulosus and E. multilocularis. The study was performed on a total of 259 sera: the positive (n = 74) and the negative (n = 185) group. The following analytic and diagnostic performances of the four kits were evaluated: operator skills, specificity, sensitivity, repeatability, reproducibility, accuracy, positive and negative predictive values. Based on the parameters evaluated, all four tests demonstrated excellent quality and proved to be reliable diagnostic tools to support the clinical evaluation of human patients suspected of having CE. The four commercial assays, in our hands, presented altogether, a range of performances from good to excellent, being immunoblotting (IB) the most reliable, used as gold standard, followed by the immunochromatographic test (ICT) and finally the two enzyme linked immunosorbent assay (ELISAs).


Subject(s)
Echinococcosis , Echinococcus granulosus , Animals , Echinococcosis/diagnosis , Echinococcosis/veterinary , Enzyme-Linked Immunosorbent Assay/methods , Enzyme-Linked Immunosorbent Assay/veterinary , Humans , Immunoblotting/veterinary , Reproducibility of Results
3.
Emerg Infect Dis ; 18(1): 98-101, 2012 Jan.
Article in English | MEDLINE | ID: mdl-22261201

ABSTRACT

We report 5 cases of disseminated infection caused by Blastoschizomyces capitatus yeast in central Switzerland. The emergence of this yeast in an area in which it is not known to be endemic should alert clinicians caring for immunocompromised patients outside the Mediterranean region to consider infections caused by unfamiliar fungal pathogens.


Subject(s)
Ascomycota/isolation & purification , Communicable Diseases, Emerging/epidemiology , Mycoses/epidemiology , Mycoses/microbiology , Aged , Antifungal Agents/therapeutic use , Communicable Diseases, Emerging/drug therapy , Fatal Outcome , Female , Humans , Immunocompromised Host , Male , Microbial Sensitivity Tests , Middle Aged , Mycoses/drug therapy , Switzerland/epidemiology
4.
Cornea ; 28(9): 1067-9, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19724200

ABSTRACT

PURPOSE: The purpose of this study was to report the first case of fungal keratitis resulting from Thielavia sp. METHODS: We conducted a retrospective chart review. RESULTS: A 10-year old girl presented 2 weeks after ocular plant injury with pain and corneal stromal infiltration with central ulceration and ill-defined margins. Cultures of corneal scrapings and biopsy sequence analysis of the ribosomal internal transcribed spacer region isolated Thielavia subthermophila Mouchacca. Clinically, the organism appeared to respond to topical amphotericin B and oral voriconazole. Best-corrected visual acuity at last follow-up visit counted 0.5. CONCLUSIONS: A rare case of Thielavia sp. keratitis was successfully treated with topical amphotericin B and oral voriconazole. Newly developed molecular diagnostic tools contribute to the recognition of a widening spectrum of emerging fungal pathogens capable of causing serious ocular infections.


Subject(s)
Corneal Ulcer/microbiology , Eye Infections, Fungal/microbiology , Mycoses/microbiology , Sordariales/isolation & purification , Amphotericin B/therapeutic use , Antifungal Agents/therapeutic use , Child , Corneal Ulcer/diagnosis , Corneal Ulcer/drug therapy , Drug Therapy, Combination , Eye Infections, Fungal/diagnosis , Eye Infections, Fungal/drug therapy , Female , Humans , Mycoses/diagnosis , Mycoses/drug therapy , Pyrimidines/therapeutic use , Retrospective Studies , Triazoles/therapeutic use , Voriconazole
5.
J Clin Microbiol ; 43(8): 4112-20, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16081958

ABSTRACT

Here we describe a new panel of short tandem repeats (STRs) for a novel exact typing assay that can be used to discriminate between Aspergillus fumigatus isolates. A total of nine STR markers were selected from available genomic A. fumigatus sequences and were divided into three multicolor multiplex PCRs. Each multiplex reaction amplified three di-, tri-, or tetranucleotide repeats, respectively. All nine STR markers were used to analyze 100 presumably unrelated A. fumigatus isolates. For each marker, between 11 and 37 alleles were found in this population. One isolate proved to be a mixture of at least two different isolates. With the remaining 99 isolates, 96 different fingerprinting profiles were obtained. The Simpson's diversity index for the individual markers ranged from 0.77 to 0.97. The diversity index for the multiplex combination of di-, tri-, and tetranucleotide repeats ranged from 0.9784 to 0.9968. The combination of all nine markers yielded a Simpson's diversity index of 0.9994, indicative of the high discriminatory power of these new loci. In theory, this panel of markers is able to discriminate between no less than 27 x 10(9) different genotypes. The multicolor multiplex approach allows large numbers of markers to be tested in a short period of time. The exact nature of the assay combines high reproducibility with the easy exchange of results and makes it a very suitable tool for large-scale epidemiological studies.


Subject(s)
Aspergillus fumigatus/genetics , DNA Fingerprinting/methods , Tandem Repeat Sequences , Base Sequence , Humans , Molecular Sequence Data , Polymerase Chain Reaction
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