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1.
Bioresour Technol ; 122: 70-7, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22595093

ABSTRACT

This study investigated nitrification performance and nitrifying community in one full-scale membrane bioreactor (MBR) treating TFT-LCD wastewater. For the A/O MBR system treating monoethanolamine (MEA) and dimethyl sulfoxide (DMSO), no nitrification was observed, due presumably to high organic loading, high colloidal COD, low DO, and low hydraulic retention time (HRT) conditions. By including additional A/O or O/A tanks, the A/O/A/O MBR and the O/A/O MBR were able to perform successful nitrification. The real-time PCR results for quantification of nitrifying populations showed a high correlation to nitrification performance, and can be a good indicator of stable nitrification. Terminal restriction fragment length polymorphism (T-RFLP) results of functional gene, amoA, suggest that Nitrosomonas oligotropha-like AOB seemed to be important to a good nitrification in the MBR system. In the MBR system, Nitrobacter- and Nitrospira-like NOB were both abundant, but the low nitrite environment is likely to promote the growth of Nitrospira-like NOB.


Subject(s)
Bacteria/metabolism , Bioreactors/microbiology , Liquid Crystals/microbiology , Membranes, Artificial , Nitrification , Transistors, Electronic/microbiology , Water Purification/instrumentation , Aerobiosis , Biodegradation, Environmental , Biological Oxygen Demand Analysis , Nitrates/analysis , Nitrogen/analysis , Oxidation-Reduction , Polymorphism, Restriction Fragment Length , Quaternary Ammonium Compounds/analysis , Real-Time Polymerase Chain Reaction , Sewage/microbiology , Waste Disposal, Fluid , Wastewater/microbiology
2.
J Eval Clin Pract ; 18(4): 919-22, 2012 Aug.
Article in English | MEDLINE | ID: mdl-21883713

ABSTRACT

OBJECTIVE: The National Health Insurance (NHI) in Taiwan raised the physician fee for myringotomy with ventilation tube insertion (VTI) from $61.5 to $117.6 in July 2004. This study aimed to evaluate if the increased payment affected the decision making of physicians. METHODS: This study is a retrospective analysis by using NHI databank in Taiwan. All children less than 12 years old who underwent VTI from 1 July 2003 to 30 June 2006 were included. Waiting time and case numbers before and after the increased VTI payment were compared. The waiting time between public and private hospitals was also examined. RESULTS: From the 7408 cases evaluated, there was no difference in waiting time before and after the raise of VTI payment, and no difference within each year group. The case number of VTI increased significantly after the increase in VTI payment (P < 0.05). The waiting time of VTI performed in private hospitals was shorter than that in public hospitals (P = 0.0001). CONCLUSION: The waiting time of VTI for children with otitis media with effusion (OME) has not been shortened after the increase in VTI payment. Waiting time in private hospitals is shorter than that in public hospitals. Increased payment for VTI has no effect on the physicians' decision making regarding to waiting time for children with OME in Taiwan.


Subject(s)
Decision Making , Fees, Medical , Middle Ear Ventilation/economics , Otitis Media with Effusion/surgery , Child , Databases, Factual , Hospitals, Public , Hospitals, Voluntary , Humans , Insurance, Health, Reimbursement , National Health Programs/economics , Retrospective Studies , Taiwan
3.
J Antimicrob Chemother ; 53(4): 600-3, 2004 Apr.
Article in English | MEDLINE | ID: mdl-14973155

ABSTRACT

OBJECTIVES: Tentative standards for testing MICs for Mycobacterium tuberculosis include agar dilution and the BACTEC method. However, the conventional agar dilution method requires 3-5 weeks to complete; whereas BACTEC, although a rapid test, involves the use of radioisotopes. In contrast, the MGIT 960 system uses a fluorescence quenching based oxygen sensor that can be read automatically. This system is not only robust, safe and simple, but has been validated for susceptibility tests of first-line antituberculous agents. METHODS: We evaluated 46 clinical strains of M. tuberculosis isolated from patients admitted to Kaohsiung Veterans General Hospital. Testing of MICs of ciprofloxacin and ethionamide was carried out by MGIT 960 and compared with the agar dilution method. RESULTS: Good agreement was found between MGIT 960 and agar dilution. The greatest concordance between the agar dilution and MGIT assay at +/-1 and +/-2 dilution was 80.4% and 97.8% for ciprofloxacin, and 82.6% and 93.5% for ethionamide, respectively. CONCLUSION: MGIT 960 was found to be comparable to the current NCCLS standard method, agar dilution, and has the advantage of being rapid (obtaining results within 5-17 days, average 8.9 days) and easy to achieve standardization.


Subject(s)
Antitubercular Agents/pharmacology , Ciprofloxacin/pharmacology , Ethionamide/pharmacology , Microbial Sensitivity Tests/methods , Mycobacterium tuberculosis/drug effects , Tuberculosis, Multidrug-Resistant/microbiology , Drug Resistance, Microbial/physiology , Humans , Mycobacterium tuberculosis/genetics , Mycobacterium tuberculosis/growth & development , Mycobacterium tuberculosis/isolation & purification
4.
Antimicrob Agents Chemother ; 47(11): 3672-3, 2003 Nov.
Article in English | MEDLINE | ID: mdl-14576145

ABSTRACT

A total of 76 clinical Mycobacterium tuberculosis isolates from Taiwan were tested for pyrazinamidase activity, pyrazinamide susceptibility, and pncA mutations. Frequency of resistance to PZA rose with increases in resistance to first-line drugs. Of 17 pyrazinamide-resistant strains, 7 (3 of which had not been previously described) possessed mutations in the pncA gene.


Subject(s)
Amidohydrolases/genetics , Antitubercular Agents/pharmacology , Mutation/genetics , Mycobacterium tuberculosis/drug effects , Mycobacterium tuberculosis/genetics , Pyrazinamide/pharmacology , Tuberculosis/microbiology , Amidohydrolases/metabolism , DNA, Bacterial/genetics , Drug Resistance, Bacterial/genetics , Drug Resistance, Multiple, Bacterial/genetics , Genotype , Reverse Transcriptase Polymerase Chain Reaction , Taiwan
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