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1.
Bone Joint J ; 96-B(11 Supple A): 87-92, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25381416

ABSTRACT

A retrospective review was performed of patients undergoing primary cementless total knee replacement (TKR) using porous tantalum performed by a group of surgical trainees. Clinical and radiological follow-up involved 79 females and 26 males encompassing 115 knees. The mean age was 66.9 years (36 to 85). Mean follow-up was 7 years (2 to 11). Tibial and patellar components were porous tantalum monoblock implants, and femoral components were posterior stabilised (PS) in design with cobalt-chromium fibre mesh. Radiological assessments were made for implant positioning, alignment, radiolucencies, lysis, and loosening. There was 95.7% survival of implants. There was no radiological evidence of loosening and no osteolysis found. No revisions were performed for aseptic loosening. Average tibial component alignment was 1.4° of varus (4°of valgus to 9° varus), and 6.2° (3° anterior to 15° posterior) of posterior slope. Mean femoral component alignment was 6.6° (1° to 11°) of valgus. Mean tibiofemoral alignment was 5.6° of valgus (7° varus to 16° valgus). Patellar tilt was a mean of 2.4° lateral (5° medial to 28° lateral). Patient satisfaction with improvement in pain was 91%. Cementless TKR incorporating porous tantalum yielded good clinical and radiological outcomes at a mean of follow-up of seven-years.


Subject(s)
Arthroplasty, Replacement, Knee/methods , Knee Joint/surgery , Knee Prosthesis , Osteoarthritis, Knee/surgery , Adult , Aged , Aged, 80 and over , Female , Follow-Up Studies , Humans , Knee Joint/physiopathology , Male , Middle Aged , Osteoarthritis, Knee/diagnostic imaging , Osteoarthritis, Knee/physiopathology , Patient Satisfaction , Prosthesis Design , Radiography , Range of Motion, Articular , Retrospective Studies , Tantalum , Treatment Outcome
2.
Int J Tuberc Lung Dis ; 17(3): 354-6, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23228433

ABSTRACT

We assessed the association between diabetes mellitus and drug-resistant tuberculosis (TB). Among new patients, diabetes was significantly associated with any resistance to isoniazid excluding multidrug-resistant TB (MDR-TB; adjusted OR [aOR] 1.88, 95%CI 1.07-3.31), but not with MDR-TB (aOR 0.95, 95%CI 0.34-2.68). Among previously treated patients, diabetes was also significantly associated with INH resistance (aOR 6.76, 95%CI 1.53-29.98) but not with MDR-TB (aOR 1.52, 95%CI 0.59-3.95). We concluded that diabetes was associated with INH resistance and speculated that the sample size of retreatment cases was insufficient to confirm the association between diabetes and MDR-TB.


Subject(s)
Antitubercular Agents/therapeutic use , Diabetes Mellitus, Type 1/epidemiology , Diabetes Mellitus, Type 2/epidemiology , Isoniazid/therapeutic use , Tuberculosis, Multidrug-Resistant/epidemiology , Tuberculosis, Pulmonary/epidemiology , Adolescent , Adult , Aged , Child , Child, Preschool , Cross-Sectional Studies , Diabetes Mellitus, Type 1/diagnosis , Diabetes Mellitus, Type 2/diagnosis , Female , Humans , Infant , Infant, Newborn , Logistic Models , Male , Middle Aged , Odds Ratio , Risk Assessment , Risk Factors , Taiwan/epidemiology , Tuberculosis, Multidrug-Resistant/diagnosis , Tuberculosis, Multidrug-Resistant/drug therapy , Tuberculosis, Pulmonary/diagnosis , Tuberculosis, Pulmonary/drug therapy , Young Adult
3.
Int J Tuberc Lung Dis ; 14(7): 924-6, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20550780

ABSTRACT

Taiwan initiated a multidrug-resistant tuberculosis (MDR-TB) programme in May 2007. Seventy-seven MDR-TB patients were enrolled from May 2007 to February 2009 in Eastern Taiwan. Isolates of 73 (94%) patients were available for genotyping using spoligotyping and MIRU-VNTR (mycobacterial interspersed repetitive unit-variable number of tandem repeats). Spoligotyping results indicated the Beijing strain as the predominant genotype (n = 48, 66%). Of the 73 isolates, 28 (38.4%) had a unique pattern and 45 (61.6%) were clustered pattern strains. Epidemiological links could be established in 21 (46.7%) of the 45 patients with a clustered pattern strain. The proportion of MDR-TB patients with a clustered pattern strain in Eastern Taiwan was high.


Subject(s)
Molecular Epidemiology/methods , Mycobacterium tuberculosis/genetics , Tuberculosis, Multidrug-Resistant/genetics , Adult , Aged , Bacterial Typing Techniques/methods , Female , Genotype , Humans , Male , Middle Aged , Mycobacterium tuberculosis/isolation & purification , Taiwan/epidemiology , Tuberculosis, Multidrug-Resistant/microbiology , Tuberculosis, Multidrug-Resistant/transmission , Young Adult
4.
Eye (Lond) ; 23(7): 1582-8, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19407845

ABSTRACT

AIMS: To compare intraocular pressure (IOP) readings between Tono-Pen tonometry and GAT, between noncontact tonometry (NCT) and GAT, and between dynamic contour tonometry (DCT) and Goldmann applanation tonometry (GAT). The correlation between IOP reading and possible confounder was identified. METHODS: This observational cross-sectional study enrolled sixty-two healthy subjects. All IOP and ocular pulse amplitude (OPA) measurements were taken by a single ophthalmologist; mean keratometric power (MK), central corneal thickness (CCT), and lens thickness (LT) were measured by a single experienced technician. RESULTS: Stepwise multiple regression analysis indicated that GAT (P=0.017) and DCT (P=0.002) readings correlated positively with MK; GAT, NCT, and Tono-Pen readings correlated positively with CCT (P<0.05); NCT (P=0.035), and DCT (P=0.016) readings correlated negatively with LT; GAT (P=0.006) and Tono-Pen (P=0.009) readings correlated positively with OPA. CONCLUSIONS: The K, CCT, LT, and OPA are confounders in tonometry readings.


Subject(s)
Intraocular Pressure/physiology , Tonometry, Ocular/methods , Adult , Aged , Cornea/physiology , Cross-Sectional Studies , Female , Humans , Male , Middle Aged , Regression Analysis , Tonometry, Ocular/instrumentation , Young Adult
5.
J Antibiot (Tokyo) ; 49(3): 253-9, 1996 Mar.
Article in English | MEDLINE | ID: mdl-8626240

ABSTRACT

Quinoxapeptin A and B are novel chromodepsipeptides which were isolated from a nocardioform actinomycete with indeterminant morphology. Quinoxapeptins A and B are potent inhibitors of HIV-1 and HIV-2 reverse transcriptase and almost equally active against two single mutants forms as well as a double mutant form of HIV-1 reverse transcriptase. Quinoxapeptin A and B are specific inhibitors of HIV-1 and HIV-2 reverse transcriptase because they did not inhibit human DNA polymerase alpha, beta, gamma and delta. Quinoxapeptin A and B are structurally similar to luzopeptin A which was also active against HIV-1 and HIV-2 reverse transcriptase.


Subject(s)
HIV-1/enzymology , HIV-2/enzymology , Peptides, Cyclic/metabolism , Peptides, Cyclic/pharmacology , Quinoxalines/metabolism , Quinoxalines/pharmacology , RNA-Directed DNA Polymerase/metabolism , Reverse Transcriptase Inhibitors/metabolism , Reverse Transcriptase Inhibitors/pharmacology , Actinomycetales/classification , Actinomycetales/metabolism , HIV Reverse Transcriptase , HIV-1/genetics , Humans , Hydroxyquinolines/chemistry , Hydroxyquinolines/pharmacology , In Vitro Techniques , Kinetics , Molecular Structure , Mutation , Nucleic Acid Synthesis Inhibitors , Peptides, Cyclic/chemistry , Quinoxalines/chemistry , RNA-Directed DNA Polymerase/genetics , Reverse Transcriptase Inhibitors/chemistry
6.
Mol Pharmacol ; 35(1): 48-58, 1989 Jan.
Article in English | MEDLINE | ID: mdl-2536468

ABSTRACT

(trans)-2-(3-Methoxy-5-methylsulfonyl-4-propoxyphenyl)-5-(3,4,5- trimethoxyphenyl)tetrahydrofuran (L-659,989) is a potent and orally active platelet-activating factor (PAF)-specific and competitive receptor antagonist. The 2,5-tritium-labeled L-659,989 ([3H]L-659,989) specifically binds to rabbit platelet membranes with an equilibrium dissociation constant (KD) of 1.60 +/- 0.20 nM in 10 mM MgCl2. Several selected PAF analogs and PAF receptor antagonists show equilibrium inhibition constants roughly similar to those found in the specific [3H]PAF binding assay. Other pharmacological agents with no PAF antagonistic activities do not inhibit the specific binding of [3H]L-659,989. K+ and divalent cations such as Mg2+, Ca2+, and Mn2+ potentiate the specific [3H]L-659,989 binding. Na+ and Li+ also enhance but GTP shows no effect on the specific binding of [3H]L-659,989. However, Ni2+ inhibits the specific binding. Scatchard analysis demonstrates that the potentiating effect of these cations is due to an increase in the detectable receptor number for L-659,989. In 10 mM MgCl2 [3H]L-659,989 shows higher receptor number than [3H]PAF. Under various ionic conditions with or without GTP, in which [3H] L-659,989 binding remains approximately the same, C16-PAF shows different potencies in competing against the specific [3H] L-659,989 binding. These results demonstrate the existence of multiple conformational states of the PAF-specific receptor. The variation in the detectable receptor number under different conditions is due to the coexistence of the high and low affinity states and the fact that the low affinity state(s) of the receptor with KD value(s) possibly in the micromolar range cannot be detected in the Scatchard analysis with the radioligand at nanomolar concentrations. In the presence of 150 mM NaCl and 1 mM GTP, receptors exist in a single conformational state with an equilibrium dissociation constant (KB) of 0.931 microM for PAF.


Subject(s)
Blood Platelets/analysis , Furans/metabolism , Platelet Membrane Glycoproteins , Receptors, Cell Surface/analysis , Receptors, G-Protein-Coupled , Animals , Binding Sites , Binding, Competitive , Guanosine Triphosphate/pharmacology , In Vitro Techniques , Magnesium/pharmacology , Platelet Activating Factor/metabolism , Protein Conformation , Rabbits , Receptors, Cell Surface/drug effects , Receptors, Cell Surface/physiology , Sodium/pharmacology
7.
Appl Environ Microbiol ; 53(8): 1798-802, 1987 Aug.
Article in English | MEDLINE | ID: mdl-16347405

ABSTRACT

The influence of pH on the type and concentration of metabolites produced from pyruvate by Lactobacillus plantarum ATCC 8014 was examined in pH-controlled fermentors at pH values of 4.5 to 6.5. Specific growth rates, cell dry weights, and diacetyl concentrations were highest at pH 5.5, with values of 0.78 h, 190 mg/liter, and 1.2 mM, respectively. While the conversion efficiency (millimoles of acetoin formed per millimoles of pyruvate utilized) was highest (94.6%) at pH 4.5, acetoin levels were similar (20 mM) between pH 4.5 and 5.5. Feeding stationary-phase cells exogenous pyruvate increased acetoin levels to 78 mM.

8.
Antonie Van Leeuwenhoek ; 53(3): 191-6, 1987.
Article in English | MEDLINE | ID: mdl-3662489

ABSTRACT

A novel approach to determine the tetracycline susceptibility of Chlamydia trachomatis directly from specimens without cell culture propagation and adaptation has been explored. Out of a total of 1290 genital specimens from a sexually transmitted disease clinic, 211 (16.4%) were positive for C. trachomatis. A tetracycline concentration of 0.032 microgram/ml completely inhibited the appearance of inclusions in all of the 211 positive specimens. Of the positive specimens, 120 (56.9%) and 18 (8.5%) respectively showed the presence of 1 to 9 and 100 or more inclusions per microtiter well in antibiotic free medium. Other antibiotics are being tested in the same manner.


Subject(s)
Chlamydia trachomatis/drug effects , Tetracycline/pharmacology , Chlamydia trachomatis/isolation & purification , Genitalia/microbiology , Humans , Microbial Sensitivity Tests , Tetracycline Resistance
12.
Bull World Health Organ ; 49(5): 507-16, 1973.
Article in English | MEDLINE | ID: mdl-4547302

ABSTRACT

In this investigation a simple urine test for phenotyping isoniazid inactivators is evaluated. In the new method, isoniazid is artificially acetylated in urine and determined by the same colour reaction as that used for acetylisoniazid. Comparative studies showed that the test is reliable and can be performed with accuracy and ease even in poorly equipped laboratories. In contrast to other urine tests, it does not require an expensive spectrophotometer, tedious hydrolysis processing of the samples, or standard curves. The results can be read on a plain colorimeter, or even without any instrument.


Subject(s)
Isoniazid/urine , Pharmacogenetics , Phenotype , Tuberculosis/drug therapy , Acetates/urine , Humans , Isoniazid/analogs & derivatives , Isoniazid/therapeutic use , Methods , Tuberculosis/urine
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