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1.
Microbiol Insights ; 10: 1178636117691253, 2017.
Article in English | MEDLINE | ID: mdl-28469461

ABSTRACT

In Finland, all laboratories carrying out diagnostics of infectious diseases in humans are approved by the Regional State Administrative Agencies and are obligated to participate in External Quality Assurance rounds. Performance in these rounds is thought to reflect the quality of laboratory work. In the 6-year study period, 17 Finnish laboratories received 48 simulated faecal specimens for the culturing of diarrhoeal pathogens, yielding altogether 586 faecal culture External Quality Control specimens and 581 reports. The results were correct in 92% of all reports and in 67% of all specimens. False-negative Salmonella results were given for 2 of the 18 specimens, one with biochemically atypical Salmonella strain and the other with a low count of Salmonella cells. False-negative Shigella report was given for 6 of the 7 specimens in some participating laboratory. Detection of all common faecal pathogens is especially relevant to patient safety, public health, and epidemiological surveillance.

2.
Med Mycol ; 45(3): 201-9, 2007 May.
Article in English | MEDLINE | ID: mdl-17464841

ABSTRACT

A 5-year retrospective multicenter study was performed for microascaceous moulds (Microascaceae, Ascomycetes) in Finnish clinical specimens. The files from 1993-1997 of six clinical mycology laboratories in Finland were searched for reports of these fungi, mainly Scopulariopsis and Scedosporium anamorphs in keratinous specimens. From the 521 primary findings, 165 cases were selected for further study based on direct microscopy, colony numbers and accompanying fungi. The clinical records of 148 cases (141 Scopulariopsis, 7 Scedosporium) were studied. Of the nail infections from which Scopulariopsis was recovered, 39 cases were further separated which showed clinical or laboratory-based evidence of dermatophytosis. In the remaining 90 'non-dermatophyte' nail cases, Scopulariopsis spp. were the only documented fungal agents (c. 6 cases/million/year). The patients were mainly elderly, 66% of whom had problems involving their big toe nails. For 74% of them, the nail problem was mentioned as their reason for visiting the physician. However, only 18% had documented benefit from treatment. The Scopulariopsis nail infections seem to be treatment-resistant and the pathogenesis and etiological role of Scopulariopsis remain poorly understood.


Subject(s)
Ascomycota/isolation & purification , Dermatomycoses/microbiology , Nail Diseases/microbiology , Nails/microbiology , Skin/microbiology , Adolescent , Adult , Age Factors , Aged , Aged, 80 and over , Child , Dermatomycoses/drug therapy , Dermatomycoses/epidemiology , Dermatomycoses/pathology , Female , Finland/epidemiology , Humans , Incidence , Male , Middle Aged , Nail Diseases/drug therapy , Nail Diseases/epidemiology , Nails/pathology , Retrospective Studies , Skin/pathology , Treatment Outcome
3.
Eur J Pharm Sci ; 19(1): 31-6, 2003 May.
Article in English | MEDLINE | ID: mdl-12729859

ABSTRACT

We have evaluated the chemical and microbiological stability of sufentanil citrate, levobupivacaine hydrochloride and a mixture in a 0.9% sodium chloride infusion in order to provide background information on the storage of a sufentanil-levobupivacaine mixture in polypropylene (PP) syringes. Chemical assays were performed by HPLC on days 0, 1, 2, 3, 8, 14, 23, 28 and 30 after storage at 4, 21, and 36 degrees C. Microbiological stability was evaluated under aseptic conditions using a laminar air flow station, with a grade A environment and a B background. The samples taken for microbiological analysis were collected immediately after preparation of the solutions and then after 7, 14, 21 and 28 days storage. At 4 degrees C the sufentanil citrate solution was stable for 23 days. At 21 degrees C the sufentanil citrate solution maintained chemical stability for 3 days, but thereafter the concentration of sufentanil decreased 15% from day 3 to day 8. At 36 degrees C a similar decrease was noticed from day 1 to day 3. On the contrary, the levobupivacaine hydrochloride solution maintained chemical stability for 28 days at 4 and 21 degrees C and for 23 days at 36 degrees C. The sufentanil-levobupivacaine mixture maintained chemical stability for 28 days at 4, 21 and 36 degrees C. The sufentanil and levobupivacaine solutions and the mixture studied maintained microbiological stability for 28 days. According to the chemical and microbiological stability studies, the sufentanil-levobupivacaine mixture in PP syringes could be stored for 28 days at 4 and 21 degrees C.


Subject(s)
Anesthetics, Intravenous/chemistry , Bupivacaine/chemistry , Sufentanil/chemistry , Anesthetics, Intravenous/administration & dosage , Bupivacaine/administration & dosage , Bupivacaine/analogs & derivatives , Chromatography, High Pressure Liquid , Drug Combinations , Drug Contamination , Drug Incompatibility , Drug Stability , Drug Storage , Infusions, Intravenous , Injections, Epidural , Levobupivacaine , Pharmaceutical Solutions , Polypropylenes/chemistry , Sodium Chloride/chemistry , Sufentanil/administration & dosage , Syringes , Temperature , Time Factors
4.
Biol Pharm Bull ; 25(10): 1307-10, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12392084

ABSTRACT

The development of resistance to current antifungal therapeutics drives the search for effective new agents. The fact that some acetophenone-derived Mannich bases had shown antifungal activities in our previous studies led us to design and synthesize acetophenone-derived bis Mannich bases, B1-B5, bis(beta-aroylethyl)methylamine hydrochlorides, to evaluate their antifungal activity. These bis Mannich bases were then converted to the corresponding piperidinols, C1-C5, which are structural isomers of bis derivatives, 3-aroyl-4-aryl-1-methyl-4-piperidinol hydrochlorides, to see alterations in biological activity. A stability study of B1 and Cl was also carried out to estimate whether they alkylate the thiols. All compounds studied have shown antifungal activity, especially against dermatophytes (Trichophyton rubrum, Trichophyton mentagrophytes, Trichophyton tonsurans, and Microsporum canis), in the concentration range studied (2-128 microng/ml). The activity was especially apparent against T. tonsurans. All compounds had at least equal antifungal activity compared with the reference compound amphotericin-B against T. tonsurans. Bis Mannich bases were generally found to be more potent compounds than their structural isomer piperidinols. The results of our stability studies suggest that thiol alkylation may contribute to the antifungal activity of the Mannich bases synthesized. Even though all compounds showed antifungal activity against dermatophytes, bis Mannich bases B1, B2, B4, and B5 appear to have potential for developing novel antifungal agents against dermatophytes.


Subject(s)
Acetophenones/pharmacology , Antifungal Agents/pharmacology , Mannich Bases/pharmacology , Piperidones/pharmacology , Acetophenones/chemistry , Antifungal Agents/chemistry , Arthrodermataceae/drug effects , Arthrodermataceae/growth & development , Drug Evaluation, Preclinical/methods , Drug Stability , Mannich Bases/chemistry , Microbial Sensitivity Tests/statistics & numerical data , Piperidones/chemistry , Yeasts/drug effects , Yeasts/growth & development
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