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1.
Acta Gastroenterol Belg ; 86(3): 486-489, 2023.
Article in English | MEDLINE | ID: mdl-37814565

ABSTRACT

Background: Faecal microbiota transplantation (FMT) has high efficacy against recurrent Clostridioides difficile infection (CDI). Despite the increasing use of this therapy, the delay between diagnosis and treatment is excessive. Furthermore, donor selection is an important and time-consuming process. Methods: We reviewed patients who underwent FMT for recurrent CDI at the CHU Charleroi Hospital between 2015 and 2022. The general context, type of administration, adverse events, and donor selection were reported. FMT was conducted using gastroduodenoscopy, colonoscopy, and enema with either fresh or frozen material. Results: Ten patients with multiple comorbidities were treated by FMT. Seven patients were cured after one procedure. One patient was successfully cured after a change to an unrelated donor, and preliminary efficacy was established. Conclusions: FMT is an effective treatment that should be considered during the earlier phases of treatment. Stool donors should be thoroughly screened for infectious diseases and other criteria related to microbiota composition.


Subject(s)
Clostridioides difficile , Clostridium Infections , Humans , Clostridium Infections/therapy , Fecal Microbiota Transplantation/methods , Feces , Recurrence , Treatment Outcome
2.
Arch Pediatr ; 28(4): 348-351, 2021 May.
Article in English | MEDLINE | ID: mdl-33858729

ABSTRACT

Moraxella osloensis has been reported in the literature as a human pathogen, particularly among immunocompromised adults. In contrast to the adult population, most pediatric cases are among patients with no underlying immunological defect; however, no patient underwent further investigation and no data about the long-term follow-up are available. We report the case of a 2-month-old previously healthy girl infected with Moraxella osloensis. Here, we review case reports and case series of children and adults with Moraxella osloensis infection and compare them with our experience. On the basis of our findings, we recommend further investigations (immunological or other underlying diseases) when a child is found to be infected with these bacteria.


Subject(s)
Moraxella/isolation & purification , Moraxellaceae Infections/diagnosis , Administration, Intravenous , Cefotaxime/administration & dosage , Cefotaxime/therapeutic use , Female , Fever/etiology , Humans , Infant , Moraxellaceae Infections/drug therapy , Treatment Outcome
3.
Pak J Pharm Sci ; 5(1): 101-9, 1992 Jan.
Article in English | MEDLINE | ID: mdl-16414708

ABSTRACT

Morphine in the urine of heroin addicts was identified by TLC using methanol, water, benzene and glacial acetic acid (80:15:15:5) and ethyl acetate, methanol and ammonium hydroxide (25:10:5) as solvent systems and potassium iodoplatinate and iodine as the developing reagents. Potassium iodate in alkaline medium gives a yellowish golden colour having maximum absorbance at 450 nm. By this reaction the minimum limit of identification and quantitative determination of morphine is 2 microg/ml. It provides a basis for the spectrophotometric determination of morphine in the urine of heroin addicts.

4.
Nucleic Acids Res ; 15(16): 6607-24, 1987 Aug 25.
Article in English | MEDLINE | ID: mdl-3628000

ABSTRACT

Five peaks of DNA glycosylase activity showing a preference for MNNG alkylated DNA have been identified from extracts of adapted M. luteus. They are numerically designated as GI to GV in order of their decreasing molecular weights. The first two of these peaks have been highly purified. GI, is a constitutive heat labile protein, 35% stimulated by the presence of 50 mM NaCl, acts exclusively on 3 MeA residues in alkylated DNA, 60-70% inhibited by the presence of 2 mM free 3MeA and has been designated as 3MeA DNA glycosylase enzyme. GII, which is an inducible protein, is heat stable, 28% inhibited by the presence of 50 mM NaCl, removes 3MeA, 3MeG, 7MeA & 7MeG with different efficiency, and has been designated as 3,7 methylpurine DNA glycosylase enzyme. The rate of release of 3 methylpurines is 30 times that of 7MeG. There is no activity of either enzyme on O2-MeC, O2-MeT, O4-MeT or O6-MeG. The apparent molecular weights of GI and GII proteins are 28 Kd and 22 Kd respectively.


Subject(s)
Bacterial Proteins/biosynthesis , DNA Glycosylases , DNA Repair , Micrococcus/enzymology , N-Glycosyl Hydrolases/biosynthesis , Bacterial Proteins/isolation & purification , Cations/pharmacology , Chromatography/methods , DNA Damage , DNA, Bacterial/drug effects , DNA, Bacterial/metabolism , Enzyme Induction/drug effects , Hot Temperature , Methylnitronitrosoguanidine/pharmacology , Micrococcus/drug effects , N-Glycosyl Hydrolases/classification , N-Glycosyl Hydrolases/isolation & purification , Sodium Chloride/pharmacology
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