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Assessment of outcomes. Because of lack of detailed information no meta analysis could be performed to analyse the results related to several outcomes. [7] INPATIENT VERSUS OTHER SETTINGS FOR DETOXIFICATION FOR OPIOID DEPENDENCE Day E, Ison J, Strang J. Date first publication issue 2, 2005 Background There are a complex range of variables that can influence the course and subjective severity of opioid withdrawal. There is a growing evidence for the effectiveness of a range of medically-supported detoxification strategies, but little attention has been paid to the influence of the setting in which the process takes place. Objectives To evaluate the effectiveness of any inpatient opioid detoxification programme when compared with all other time-limited detoxification programmes on the level of completion of detoxification, the intensity and duration of withdrawal symptoms, the nature and incidence of adverse effects, the level of engagement in further treatment post-detoxification, and the rates of relapse post-detoxification. Search Strategy Cochrane Central Register of Controlled Trials CENTRAL - The Cochrane Library Issue 3, 2004 MEDLINE January 1966-March 2004 EMBASE January 1988-March 2004 PsycInfo January 1967-March 2004 CINAHL January 1982-March 2004 ; . In addition the Current Contents, Biological Abstracts, Science Citation Index and Social Sciences Index were searched. Selection criteria Randomised controlled clinical trials comparing inpatient opioid detoxification any drug or psychosocial therapy ; with other time-limited detoxification programmes including residential units that are not staffed 24 hours per day, day-care facilities where the patient is not resident for 24 hours per day, and outpatient or ambulatory programmes, and using any drug or psychosocial therapy ; . Main results Only one study met the inclusion criteria. This did not explicitly report the number of participants in each group that successfully completed the detoxification process, but the published data allowed us to deduce that 7 out of 10 70% ; in the inpatient detoxification group were opioidfree on discharge, compared with 11 out of 30 37% ; in the outpatient group. There was very limited data about the other outcomes of interest. Reviewers' conclusions This review demonstrates that there is no good available research to guide the clinician about the outcomes or cost-effectiveness of inpatient or outpatient approaches to opioid detoxification. OPIATE: MAINTENANCE TREATMENT [8] METHADONE MAINTENANCE VERSUS NO OPIOID REPLACEMENT THERAPY FOR OPIOID DEPENDENCE Mattick RP, Breen C, Kimber J, Davoli M. Date first publication issue 4, 2002; Date of the last substantial update issue 2, 2003 Background Methadone maintenance was the first widely used form of opioid replacement therapy developed to treat heroin dependence, and it remains the best-researched treatment for this problem. Despite the widespread use of methadone in maintenance treatment for opioid dependence in many countries, it is a controversial treatment whose effectiveness has been disputed. Objectives To evaluate the effects of methadone maintenance treatment MMT ; compared with treatments that did not involve opioid replacement therapy i.e., detoxification, offer of drug-free rehabilitation, placebo medication, wait-list controls ; for opioid dependence. Search Strategy All the following databases up to 2001 Cochrane Drugs and Alcohol Review Group Register, the Cochrane Controlled Trials Register, MEDLINE, EMBASE, Current Contents, Psychlit, CORK [ state.vt.su adap cork], Alcohol and Drug Council of Australia ADCA ; [ adca .au], Australian Drug Foundation ADF-VIC ; [ adf .au], Centre for Education and Information on Drugs and Alcohol CEIDA ; [ ceida .au], Australian Bibliographic Network ABN ; , and Library of Congress databases, available NIDA monographs and the College on Problems of Drug Dependence Inc. proceedings, the reference lists of all identified studies and, for instance, allegra or claritin.
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49% a statistically significant difference [t 1, 17.3 ; 2.5, p .05, two-tailed t test with Greenhouse-Geisser correction] Figure 3 ; , reflecting a large effect size of .97. Unmedicated adults with ADHD responded faster on 86 msec ; than control subjects no-signal trials 426 450 99 msec ; , but this was not a significant difference; [t 1, 24 ; 1, ns]. Unmedicated adults made significantly more discrimination errors on no-signal trials 2.5% ; compared with control subjects .4% ; U 34.5, p .05, nonparametric test for unequal variances ; . A pairwise t test two-tailed ; showed that adults with ADHD were significantly faster when medicated for SSRT 165 50 msec ; than when unmedicated Figure 3 ; 195 55 msec ; [t 1, 12 ; 4.2, p .05]; but this was not the case for no-signal RT medicated: 426 81 msec; unmedicated: 426 86 msec ; or for discrimination errors medicated: 1.6%; unmedicated: 2.5% ; [t 1, 12 ; 1.3, ns]. A split-half analysis of SSD after convergence on 50% P inhibit ; see Figure 2 ; taking the average of staircases 1 and 3 vs. average of staircases 2 and 4 ; showed highly significant correlations within all three groups medicated ADHD: r .94; unmedicated ADHD: r .90; control subjects: r .91; all p .0001 ; , indicating good internal consistency of average SSD estimation. High reliability of SSRT estimation with the current method was confirmed by comparison between the current control group and a different control group in a different study in which the same stop-signal test was used Turner et al 2002 ; mean age: 28 years, mean SSRT: 160 msec [c.f. 153 msec for current study] and amitriptyline.
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Sec. Mice of the second group yoked ; were placed individually in the paired shuttle boxes and exposed to the shocks over which behavioral control was not possible. For these animals, shock onset occurred at exactly the same time as it did for mice of the shocked group. However, shock offset occurred when their paired partners successfully escaped from the shock. Thus, both escapably and inescapably shocked mice received an identical amount of shock at exactly the same time, but only mice in the escapable condition could terminate shock by making the appropriate response. Mice in the third group served as the nonshocked condition sham ; . These animals were placed individually in the shuttle boxes for a period that matched the other two groups 60 min ; but shock was not delivered. Mice coming from a fourth group control ; were killed immediately upon removal from their home cage. Finally, since different results indicate that exposure to a novel environment elicits stress-like responses in mice Cabib et al., 1990; Prince and Anisman, 1990 ; , two other groups were exposed to the apparatus without shock delivery for 10 and 120 min before death to investigate possible time-dependent changes of DA metabolism in the NAS. Mice from a seventh group served as controls 0 min ; and were killed as previously described for the control group. Neurochemical analysis. All subjects were killed by decapitation followed by immediate head freezing. This method was preferred to microwave focusing since the latter procedure requires the animals to be restrained, a condition that produces stress responses Dunn and File, 1983; Puglisi-Allegra et al., 199 1 ; . Consequently, altered brain DA metabolism in control mice could not be ruled out, which may introduce an uncontrollable experimental variable. Moreover, immediate head freezing allows concentrations of 3-methoxytyramine 3-MT ; comparable or lower to those obtained by microwave irradiation Vulto et al., 1986; Green et al., 1988; Wood et al., 1988; Puglisi-Allegra and Cabib, 1990 ; to be obtained and both increase and decrease of the metabolite following treatments known to produce these effects to be evaluated Puglisi-Allegra and Cabib, 1990; Cabib and Puglisi-Allegra, 199 1; Puglisi-Allegra et al., 199 1 ; . Finally, it has been reported that in the NAS, acute restraint induces time-dependent variations of 3-MT concentrations in mice killed by this method, similar to the variations observed for extracellular DA detected through intracerebral microdialysis in restrained rats Puglisi-Allegra et al., 199 1 and amoxil and allegra.
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There is not much I can do in that village, " says Sister X, who assists self-help groups of people with HIV. "There, people with HIV AIDS have a difficult time getting organized, because local health centre staff don't welcome them. They miss a place to start from". "We have reflected on the factors involved in our psychological recovery after we had learned that we had HIV, " said a leader of a self-help group. "In each of our experiences, meeting a caring person is the key to our accepting our situation, and our moving on with our lives." When Ying was asked what role she thought Buddhism was playing in Phayao's response to HIV AIDS, she responded: "It is always on our minds.
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TABLE OF CONTENTS . 2 ACKNOWLEDGEMENTS. 4 SUMMARY . 5 1. INTRODUCTION . 8 2. TARGETS AND MODE OF ACTION OF CURRENT TB DRUGS. 8 3. WHY NEW DRUGS ARE NEEDED? . 9 4. THE NEW TB DRUG PIPELINE . 12 4.1 Novel chemical entities. 13 Diarylquinoline TMC207 Johnson & Johnson ; . 13 Nitroimidazole PA-824 Chiron Corp.-TB Alliance ; . 14 Nitroimidazole OPC-67683 Otsuka Pharmaceuticals, Japan ; . 15 Pyrrole LL- 3858 Lupin Limited, India ; . 16 Pleuromutilins GlaxoSmithKline-TB Alliance Partnership ; . 16 Dipiperidine SQ-609 Sequella Inc. ; . 16 ATP Synthase Inhibitor FAS20013 FASgene ; . 17 Translocase I Inhibitor Sequella Inc. ; . 17 InhA Inhibitors GlaxoSmithKline-TB Alliance ; . 17 Isocitrate Lyase Inhibitors GlaxoSmithKline-TB Alliance ; . 17 4.2 Compounds originating from existing families of drugs . 18 Using existing Fluoroquinolones for TB ? . New Quinolones . 22 Non-fluorinated quinolones. 23 Diamine SQ-109. 23 Macrolides. 23 Thiolactomycin analogs . 23 Nitrofuranylamides . 24 Nitroimidazole Analogs . 24 4.3 Summary of the drug pipeline. 25 5. EXPECTED TIMELINES TOWARDS APPROVAL FOR NEW CANDIDATE DRUGS . 27 6. CRUCIAL GAP: LACK OF EARLY STAGE DRUG DISCOVERY . 29 7. DISCUSSION AND CONCLUSIONS . 32 Pressing needs still remain. 32 Time to sow new seeds now as all the low-hanging fruit have been eaten . 36 APPENDIX A: PROMISES FROM THE BASIC RESEARCH FIELD . 38 Genes involved in energy metabolism and response to oxygen limitation . 39 Genes encoding enzymes of the glyoxylate shunt . 40 Genes involved in the response to nutrients limitation . 41 Genes involved in cell wall and membrane metabolism. 42 Genes involved in transcriptional regulation 43 Genes involved in promoting M. tuberculosis survival inside macrophages 44 Inhibition of phagosome maturation. 44 Resistance to nitric oxide stress . 45 APPENDIX B: UPDATE ON COMPOUNDS IN THE PIPELINE . 46 Malate Synthase Inhibitors GSK, Rockefeller University, Texas A&M ; . 46 Riminophenazines Institutes of Materia Medica BRTI ; . 46 Capuramycins Sankyo Sequella ; . 46 2.
Costochondritis 733.6 ; is an inflammation of the costochondral junction between the sternum breastbone ; and the ribs that can sometimes result from an injury or strain to the chest muscles. The etiology can also be unknown. Symptoms include a sharp anterior wall chest pain that can sometimes be similarly described in patients with coronary artery disease. This confusion of the symptoms of costochondritis with those of heart disease can sometimes result in patient admission. However, diagnostic studies such as chest radiograph, electrocardiogram, and blood chemistry e.g., troponin and creatine kinasemyocardial band are laboratory tests that can identify myocardial damage ; typically rule out the possibility of serious cardiac disorders in these cases. Costochondritis is a self-limiting condition. Medical treatment includes NSAIDs, and the pain usually resolves within a short time.
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Chair Ken Van Winkle Jr., Esq., Managing Partner Lewis & Roca Chair Elect Jeanne Pomatto, CEO Cranial Technologies VP Housing Stephen O. Evans, Trustee, Equity Residential Properties VP Endowment Eileen Rogers, President Allegrw Print & Imaging VP Development Karlene Keogh, President Arnold & Associates VP Programs Ser vices Steve Schramm, Mercer Human Resource Consulting Secretar y Barbara Pickrell, Community Volunteer Treasurer Rick Wardrip, Corporate Auditor SRP Members At Large Sally Ceccarelli-Wolf Arizona American Water Company Community Representative Candace Sherwood APS Community Representative Ramona Sullivan PacifiCare Community Representative Ex-Officio Bruce C. Ward President Alliance Residential Company Pamela A. Martin, Ph.D. President Executive Director Homeward Bound.
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179. Chen, H.W., Leonard, D.A., Fischer, R.T., Trzaskos, J.M. 532. Cmarik, J.L., Inskeep, P.B., Meredith, M.J., Meyer, D.J., Ketterer, B., Guengerich, F.P. 1254. Cook, C.S., Ames, G.B., Smith, M.E., Kowalski, K.G., Karim, A. 212. Covey, D.F., McMullan, P.C., Wixler, L.L., Cabell, M. 161. Crooks, P.A., Godin, C.S., Damani, L.A. 368. Damani, L.A., Shaker, M.S. 404. Damani, L.A., Shaker, M.S., Godin, C.S., Crooks, P.A., Ansher, S.S., Jadoby, W.B. 661. Daubner, S.C., Lauriano, C., Haycock, J.W., Fitzpatrick, P.F. 721. Davis, K.L., Dunn, M.W., Schwartzman, L.S. 1366. DeGeorge, G.L., Heck, D.E., Laskin, J.D. 1018. Delos, S., Iehle, C., Martin, P-M., Raynaud, J-P. 698. Ding, X., Coon, M.J. 699. Ding, X., Coon, M.J. 673. Dix, T.A., Fontana, R., Panthani, A., Marnett, L.J. 397. Eling, T.E., Curtis, J.F., Harman, L.S., Mason, R.P. 210. Elliott, W.J., Morrison, A.R., Sprecher, H., Needlemen, P. 766. Ericsson, J., Runquist, M., Thelin, A., Andersson, M., Chojnacki, T., Dallner, G. 828. Ericsson, J., Thelin, A., Chojnacki, T., Dallner, G. 806. Ericsson, J., Thelin, A., Chojnacki, T., Dallner, G. 1320. Faletto, M.B., Miller, W.H., Garvey, E.P., St.Clair, M.H., Daluge, S.M., Good, S.S. 68. Ferone, R., Singer, S.C., Hunt, D.F. 990. Fisher, C.W., Caudle, D.L., Martin-Wixtrom, C., Quattrochi, L.C., Tukey, R.H., Waterman, M.R., Estabrook, R.W. 28. Fong, K.-L.L., Hwang, B.Y.-H. 326. Foureman, G.L., Harris, C., Guengerich, F.P., Bend, J.R. 221. Gaines, D.W., Friedman, L., McCann, P.P. 789. Garver, W.S., Kemp, J.D., Kuehn, G.D. 485. George, R.J., Haycock, J.W., Johnston, J.P., Craviso, G.L., Waymire, J.C. 667. Gilmour, S.J., Bleecker, A.B., Zeevaart, J.A.D. 666. Gilmour, S.J., Zeevaart, J.A.D., Schwenen, L., Graebe, J.E. 203. Greenspan, M.D., Yudkovitz, J.B., Alberts, A.W., Argenbright, L.S., Arison, B.H., Smith, J.L. 934. Grem, J.L., McAtee, N., Steinberg, S.M., Hamilton, J.M., Murphy, R.F., Drake, J., Chisena, T., Balis, F., Cysyk, R., Arbuck, S.G., Sorensen, J.M., Chen, A.P., Goldstein, L., Jordan, E., Setser, A., Goldspiel, B., DeCarvalho, M., Allegra, C.J. 586. Gruys, K.J., Walker, M.C., Sikorski, J.A. 583. Guengerich, F.P., Kim, D.-H. 270. Guillemette, G., Balla, T., Baukal, A.J., Catt, K.J. 866. Guo, Z., Smith, T.J., Thomas, P.E., Yang, C.S. 540. Haaf, H., Metzler, M., Li, J.J. 273. Hanlon, M.H., Ferone, R., Mullin, R.J., Keith, B.R. 958. Hansbro, P.M., Foster, P.S., Hogan, S.P., Ozaki, Sl, Denborough, M.A. 1099. Hissong, B.D., Byrne, G.I., Padilla, M.L., Carlin, J.M.
And more identifiable as an injury. The forensic examiner can then photograph the area. The dye is not systematically absorbed and is thus completely safe. It can be used on pregnant females for the same reason. Colposcope - A special microscope may be used to visualize the hymen, the cervix, and the vaginal walls. It can have a binocular or monocular magnification system that is fixed or adjustable with capability to document through video or still photography. The colposcopic images can be digitally preserved for injury documentation and later reproduction for introducing the injuries into evidence.
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1-6-1 Okubo Kumamoto-shi 860-8568 Kumamoto JAPAN Phone: 81 ; 096 ; 344 1211 Fax: 81 ; 096 ; 345 1345 Email: : kaketsuken.or.jp index e Description KAKETSUKEN carries out research for the development if its knowledge in immunology, microbiology, and molecular biology and has capabilities in drug manufacturing and vaccine development. HISTORY KAKETSUKEN has its origin in the "Institute of Experimental Medicine" which was established on the premises of Kumamoto Medical College in 1926. KAKETSUKEN was founded to produce and supply vaccines, antiserums, and diagnostic antigens in 1945. R&D PRODUCTS KAKETSUKEN's technology has lead to the establishment of techniques for generic recombination a cell fusion process, and large-scale culture and refinement of cells. These technologies are now being applied to the production and development of preventive medicines and plasma protein products, and also to the fields of therapeutic medicines such as monoclonal antibody products and immunological-disorder therapeutics. KAKETSUKEN's other technology, such as sulfo human immunoglobulin and a gene-altered hepatitis B vaccine, have resulted in the development of new types of vaccines for humans, vector vaccines, and the application of human technology, including an HIV monoclonal antibody an anti-AIDS drug ; . BUSINESS STRATEGY KAKETSUKEN's research and development theme is to: "Make use of biological elements for the prevention and treatment of more diseases." To realize this theme, the company's technology is fostered through vaccines and blood plasma products, as well as peripheral technology from its completely equipped experimental facilities of the Good Laboratory Practice GLP ; , and experimental animal models. KAKETSUKEN are confident that their efforts will help improve preventive medicine as well as health and hygiene, which in turn will lead to solutions to various problems.
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