Ultrasound indications for chronic pain management: an update on the most recent evidence.

Purpose Of Review: The ability of ultrasound to provide detailed anatomic visualization while avoiding radiation exposure continues to make it an appealing tool for many practitioners of chronic pain management. This review will present the most recent evidence regarding the use of ultrasound-guidance for the performance of interventional procedures in the treatment of chronic pain.

Recent Findings: For a variety of different procedures, studies continue to compare ultrasound-guided techniques to commonly used fluoroscopic or landmark-based techniques.

Amide derivatives with H1-antihistaminic effect.

The synthesis and the structure-activity correlation of a series of N-aminoalkylacetamides as H1-antihistaminic agents have been carried out. The compounds were tested in vitro by measurement of the inhibition of histamine-induced contractions on isolated guinea pig ileum; the results are expressed as pA2.

In vivo inhibition of nitric oxide synthase by bisisothiouronium and bisguanidinium salts.

The ability of two S,S'-(alkane-1,omega-diyl) bisisothiouronium dibromides, three N,N'-(alkane-1, omega-diyl) bis guanidinium dinitrates and N,N'-bis (3-guanidinopropyl)piperazine dinitrate to inhibit constitutive (i.e. endothelial and neuronal forms) and inducible forms of nitric oxide synthases has been evaluated in vivo.

Sequence-selective binding to DNA of bis(amidinophenoxy)alkanes related to propamidine and pentamidine.

The DNA sequences targeted by a complete homologous series of aromatic diamidines have been determined at single-nucleotide resolution via protection from cutting by the endonucleases DNase I, DNase II and micrococcal nuclease. Propamidine, pentamidine and to a lesser extent hexamidine bind selectively to nucleotide sequences composed of at least four consecutive A-T base pairs. In contrast, the binding to DNA of butamidine, heptamidine, octamidine and nonamidine is poorly sequence-selective.

Synthesis and pharmacological activities of some 2,3,4,5-tetrahydro[1,5]benzo[f]thiazepines.

In search of new biological active agents in the series of [1,5]benzothiazepines, some 2,3,4,5-tetrahydro-N-(5-morpholinopentanoyl)-[1,5]benzo[f] thiazepines were synthesized and examined in vitro for their calcium antagonist activity compared to the Diltiazem one.

Amoebicidal efficiencies of various diamidines against two strains of Acanthamoeba polyphaga.

The first medical cure of Acanthamoeba keratitis was obtained by use of propamidine isethionate. Since then, it has been the basic drug recommended for use in treatment. Because some Acanthamoeba strains have been reported to be resistant to propamidine and propamidine was found to be only weakly cysticidal, superior homologs such as butamidine, pentamidine, hexamidine, heptamidine, octamidine, and nonamidine were tested for their amoebicidal effects on two Acanthamoeba strains isolated from patients with keratitis.

[In vitro changes induced by phenylmercury nitrate on fungi causing keratitis. Scanning electron microscopy study].

Antifungal activity of phenylmercury nitrate was studied on fungi from keratitis. Important deterioration and bursting were observed with 2 mg/100 ml phenylmercury nitrate concentration on Aspergillus flavus, Scedosporium and Candida albicans spores.

Successful treatment of Acanthamoeba keratitis by hexamidine.

Acanthamoeba keratitis remains very difficult to treat because of the lack of antiamoebic agents completely effective against cysts. Currently, the recommended treatment includes the use of topical neomycin sulfate, various imidazoles, and propamidine isethionate (Brolene) 0.1% eye drops, a compound of the diamidine family.

[The efficacy of water ozonation on the inactivation of oocysts of Cryptosporidium].

Cryptosporidium oocysts are currently found in surface waters. Their incomplete removal by sand filtration and their high resistance to chlorinated disinfectants make possible waterborne cryptosporidiosis outbreaks after drinking treated water. Because ozone is an alternative to chlorine for final drinking water disinfection the aim of our study was to determine the ozonation conditions able to eliminate the infectivity of oocysts.

Parasitic hazard with sewage sludge applied to land.

A modification of the FAUST technique allowed a highly regular recovery of Taenia saginata eggs from sewage sludge, as well as their quantification. Despite the low viability (8%) noted, the viable T. saginata egg level remains high (20.

[Possibility of the survival of free-living amoebae which cause keratitis in decontamination solutions used for the maintenance of contact lenses].

Because Acanthamoeba keratitis associated with contact lenses were described, several solutions used in stationary eye wash stations were contaminated by free-living amoebae. 0.9% sodium chloride rinsing solutions allowed cyst and trophozoite growth and only one solution for decontamination using hydrogen peroxide led to rapid elimination of cysts and trophozoites.

Light-dependent effects of alpha-terthienyl in eggs, larvae, and pupae of mosquitoAedes aegypti.

Alpha-terthienyl is toxic toAedes aegypti larvae in the dark, but its activity is much enhanced in the presence of ultraviolet light. The development of first-instar larvae treated with alpha-terthienyl and ultraviolet light was followed until the emergence of adults. The LC50 value for first instars was about 0.

[Comparative in vitro activity of chlorine and bromine on the cysts of free-living amoebae].

A continuous flow type apparatus is used for investigation of the chlorine and bromide activity in vitro on the cysts of two free-living amoeba strains : Naegleria gruberi and Acanthamoeba polyphaga. The Naegleria cysts are sensitive more to chlorine than to bromine ; those of Acanthamoeba are perfectly resistant to these disinfectants in the limit of the available concentrations in swimming-pools. The sensibility to these disinfectants stays the same at 25 degrees C and 35 degrees C.

[Effect of acetylcholine on the heart ventricle of the goldfish Carassius auratus, Teleosts, Cyprinidae. Modification of the response as a function of temperature].

Acetylcholine (Ach) is more efficient on the red fish heart at 14 degrees C than at 5 degrees C or 8 degrees C. It does not probably exist a cholinesterasic system and high concentrations of Ach are to be used to obtain significant variations of the heart frequency. Ach does not appear as a physiological mediator and temperature seems to be an essential factor in heart regulation and modulation of the pharmacological effects of eventual mediators.