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Table 2. Mean scores and standard deviation ; for all categories, analysis by study group Category Diary items Latency WASO WMINS TST SQUAL EASE SQF SQL Rested Enough 42.46 28.54 ; 1.62 0.88 ; 44.71 55.95 ; 426.70 112.89 ; 48.13 20.44 ; 45.62 28.11 ; 43.23 25.64 ; 52.21 21.76 ; 65.11 19.97 ; 53.85 20.80 ; 13.85 10.81 ; 1.33 0.92 ; 16.79 19.97 ; 410.14 35.49 ; 29.96 18.33 ; 22.41 17.67 ; 22.04 17.67 ; 35.33 19.41 ; 39.02 17.92 ; 36.43 16.00 ; 136.06 94.74 ; 197.78 95.54 ; 267.56 109.42 ; 355.56 156.81 ; 130.44 95.75 ; 1087.39 385.45 ; 18.86 9.69 ; 1.53 1.22 ; 29.82 54.16 ; 411.82 57.34 ; 33.62 21.25 ; 25.38 11.19 ; 29.63 19.79 ; 38.16 19.14 ; 44.04 21.69 ; 45.45 20.73 ; 133.90 96.55 ; 209.10 93.38 ; 271.90 172.60 ; 246.00 137.61 ; 144.90 147.28 ; 1005.80 538.27 ; 15.69 8.36 ; 1.54 1.05 ; 10.32 11.43 ; 433.19 46.81 ; 30.32 11.32 ; 22.38 15.29 ; 18.78 16.84 ; 39.24 16.95 ; 42.56 20.63 ; 44.38 19.97 ; 132.70 78.36 ; 214.30 104.36 ; 268.40 170.12 ; 297.00 147.88 ; 159.30 135.61 ; 1071.70 573.76 ; A Depressed n 18 ; B Control n 18 ; C Relative of Dep n 10 ; D Relative of Con n 10 ; Sig. 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THALLIUM SCTNTICRAPHY. * John H. wartheimer, M.D., Melvin Schwartz, M.D., Anthony P. Goldman, M.D., S. Yazdanfar, M.D. # P. Todd Makler, M.D., Fred IC. Uakhjavan, M.D., Albert Einstein Medical Center, Philadelphia, PA. PTCA of the lschamia-roIatd vessel In unstable angina and multLveael coronary disease has been proposed as an alternative to coronary bypass surgery. We so treated 19 patients with multivessel disease 14-7 vessel, S--S vessel ; and evaluated regional perfusion by follow--up exercise thallium sclnt.igraphy ETS ; . The ages ranged from 34-78 mean 55 ; yrs. The responsible vessel was determined by the EC in 12 pta 9 unstable angina, 3 post non--Q wave MX ; , by exercise thallium defect In 7 pta, arid by coronary anglography in 5 pta 1 subtot.alty occluded Iresponsiblej and 1 totally occluded vessel ; . PTCA was initially successful in all 19 pta. The mean reduction in stenosis was 98% 80-99 ; to 157. 0--SO ; and the mean reduction in Iranatenotic gradient was 53 mmHg 30-90 ; to 8.5 mmHg 0-20 ; . At follow up a mean of 54 3-165 ; days post-PTCA, by ETS the zone of the PTCA vessel showed no exercise-induced ischemia In 17 of pta. There were 6 normal SCanS, and 11 with Ischemia 8 ; , scar 2 ; , or both 1 ; in a remote zone. Two pta had exercise-induced Ischemia In the distribution of the responsible vessel, I per!scar. The other had documented restenosis and repeat PTCA. Clinical follow up was available in 13 pta; 11 were Class I and 2 Class TI. Thus El's confirms that PTCA of the responsible vessel is efficacious and a reasonable clinical approach and montelukast. Table 5. Chemotherapeutic Options in Prostate Cancer: Summary and naprelan and ponstel, for example, high blood pressure. This presentation contains forward-looking statements regarding the company's business and the therapeutic and commercial potential of its technologies and products in development. Any statement describing the company's goals, expectations, intentions or beliefs is a forward-looking statement and should be considered an at-risk statement. Such statements are subject to certain risks and uncertainties, particularly those risks or uncertainties inherent in the process of developing technology and in the process of discovering, developing and commercializing drugs that can be proven to be safe and effective for use as human therapeutics, and in the endeavor of building a business around such products and services. Actual results could differ materially from those discussed in this presentation. Factors that could cause or contribute to such differences include, but are not limited to, those discussed in the Metabolic Pharmaceuticals Ltd Annual Report for the year ended June 30, 2005, copies of which are available from the company or at metabolic .au. Possible side effects this medication may cause stomach upset, diarrhea, loss of appetite, nausea, vomiting, and headache and nimotop. While this outcomes were further transmiss pohstel contacts. P2.17.02 THE SAFETY OF TERMINATION OF PREGNANCY BY MANUAL VACUUM ASPIRATION MVA ; Dr. Odongo Odiyo, MB. Ch.B, M.Med Obs Gyn ; Nbi, Cert. Rep. Health Research, Dr. Juma E. A., MB. Ch.B. Introduction. The main objective of this Programme is to provide a safe means for termination of unwanted pregnancy and to increase contraceptive acceptance and use among clients. This would in turn reduce the rate of unwanted pregnancies and thus reduce maternal mortality caused by unsafe abortions, which stand at between 30% and 50% of the current Kenyan National Maternal Mortality rate. Between September 1996 and October 1999, 613 clients seeking menstrual regulation were treated using MVA at the Nakuru Reproductive Health Centre. Methods: Retrospective study of demographic and relevant medical data of clients who came for MVA, carried out as an outpatient procedure between September 1996 and October 1999. Results: A total of 613 clients' records were analysed. The mean age was 26.0 years. Most of the clients were nulliparous 33.0% ; . The median gestation was 8 weeks. 53.0% of the clients were single while 43.4% were married. 67.7% of them had secondary level education. Those who had used contraceptives were 294 48.0% ; . 317 51.7% ; had not used any contraceptives. Of those who used contraceptives, 52.7% used oral contraceptives, 13.6% Intra-Uterine Contraceptive Devices, 11.9% Injectables, 1% Norplant, 6.5% used safe days and 3.7% used condoms. Only 31.0% stopped the use of contraceptives due to side effects. 27.1% of the clients went home on a contraceptive method after the procedure. This figure is a lot higher in reality as a number of clients did not have their contraceptive choice recorded on the MVA card. Conclusion: We have found this method an effective and safe means of termination of pregnancy as an out patient procedure, for the needy patient. It is also clear that with post MVA counselling, a good number of clients accept the use of contraceptives. This Programme needs to be expanded to include other medical personnel in the use of MVA and post-MVA management. This will be an effective way of reducing unwanted pregnancies, and maternal deaths caused by unsafe abortions. P2.17.03 UTERINE HEALING AFTER MYOMECTOMY: A SONOGRAPHIC STUDY A. M. Darwish, and A. A. Youssef, Dept. OB GYN, Assiut University, 7111 Assiut, Egypt Objectives: To study the pattern of healing of the uterine scars after abdominal myomectomy and to evaluate the different preoperative and intraoperative factors affecting the process of healing. Patients and methods: Forty-nine patients diagnosed to have one or more leiomyomata and desiring further fertility were submitted to abdominal myomectomy operation. Preoperative assessment included ultrasonographic measurement of the uterine volume, number and site of the leiomyomata. Detailed operative notes were reported for every case. Transvaginal ultrasonography was done for all cases on the second day, second week and one month postoperatively to assess the uterine scar and uterine volume. Results: In all cases, the shape of the uterine scar appeared as a heterogenous echogenic area. Hematoma of the scar was diagnosed as a hypoechoic measurable area which was seen in 41 83% ; , 33 67% ; and 10 20% ; of the patients on 2nd day, 2nd weeks and 1 month postoperatively respectively. Follow-up of the 10 patients with persistent hematoma revealed complete resolution at 3 months postopertively. The use of torniquet was highly significantly related to the formation of the hematoma at the site of the scar. Other preoperative and operative factors showed insignificant impact on the hematoma formation. There was significant reduction of the uterine volume with better remodeling on follow-up. Conclusions: Healing of the myomectomy scar is completed within 3 months postoperatively. The use of torniquet is associated with hematoma formation with subsequent weak scar and hence better to be avoided. Online PharmacyGive the total number of subjects involved in the study sufficient to allow dropouts and variability of effects ; . The age of subjects appropriate to problem under study should also be provided. Mention the sex of subjects, including reasons for limitations, if any. State the selected health disease states with diagnostic criteria and confirmatory tests ; , socio-economic and cultural factors, geographical areas, criteria for exclusion, withdrawal of subjects, compatibility of study group, etc! FOOTNOTES A ; S. Olivier was supported by a TELEVIE grant from The Belgian National Fund for Scientific Research FNRS ; . M.P. Merville, A. Chariot and N. Franchimont are Research Associates at the F.N.R.S. Belgium ; . We thank TELEVIE F.N.R.S. ; , the F.I.R.S. CHU Lige ; , the Centre AntiCancreux University of Lige ; and the Belgian Federation against cancer for their financial support. B ; Address for reprint requests : Vincent Bours Laboratory of Medical Chemistry and Human Genetics CHU B35, University of Lige, Sart Tilman, 4000, Lige BELGIUM Tel : + 32 Fax : + 32 Email : vbours ulg.ac.be C ; 1The two senior authors share equal responsibility. But one very important fact: both drugs may only be given by a pediatric. Validation of countries by clorazepate the central tapazole ed patients ponstel home. I always followed up a pill with a yummy treat, so after a while, he didn't mind taking his meds anymore, for example, side effects of ponstel. The tablet according to claim 5, comprising 15 to 30 percent by weight of at least one filler.
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