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Of Supportive Care, Pain & Palliative Medicine, City of Hope National Medical Center, Duarte, CA; and 2Department of Family and Preventive Medicine, University of California, San Diego, La Jolla, CA. A growing body of literature suggests that many cancer survivors associate positive personal changes, or posttraumatic growth PTG ; , with their illness experience. However, relatively little is known about the correlates of PTG. We present cross-sectional data obtained from a sample of women N 1470 ; diagnosed with early-stage breast cancer to a ; describe the extent of PTG reported by this sample, and b ; shed light on the demographic and medical predictors of PTG. Women were a mean of 6.76 years from diagnosis at the time of assessment. Participants reported a moderate level of PTG Mean PTG score 61; total possible 105 ; . PTG was significantly higher in participants who were: a ; younger, b ; less educated, c ; non-Caucasian, d ; diagnosed with Stage II disease, and e ; received chemotherapy. PTG was unrelated to time since diagnosis, marital status, type of surgery, or whether patient had radiation treatment. In the multivariate analysis, ethnicity and education retained significance as unique predictors of PTG, however, medical and demographic variables accounted for only a small proportion of the variance in the total PTG score R2 .04 ; . Findings suggest that demographic variables may be correlated with PTG and future research should consider potential mediating variables. CORRESPONDING AUTHOR: Andrea A. Thornton, PhD, Supportive Care, Pain, & Palliative Medicine, City of Hope National Medical Center, 1500 E. Duarte Rd, Duarte, CA, USA, 91010-3000; athornton coh.
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OBJECTIVE: Hospital discharge within 48 hours following vaginal delivery has become common practice throughout North America. In 1996 the Canadian Paediatric Society CPS ; and the Society of Obstetricians and Gynaecologists of Canada SOGC ; recommended that infants with length of stay LOS ; less than 48 hours be seen in follow-up within 48 hours after discharge and that all infants be seen in follow-up within the first week following discharge. The Objectives were 1 ; to determine if the above guidelines were being followed; and 2 ; to identify any factors associated with differences in follow-up rates. METHODS: During 1998-1999, we surveyed the first 1250 eligible, consenting mothers following uncomplicated vaginal delivery from 5 Ontario sites. Self-administered questionnaires were completed by mothers prior to discharge, then a telephone questionnaire was administered at 4 weeks post-discharge. RESULTS: 1250 women were recruited and 875 70% ; completed the post-discharge questionnaire. Characteristics of study respondents were: maternal age 30.2 5.2 years, first liveborn infant 42.7%, mother with a partner 94.2%, English as first language 84.6%, mother completed post-secondary education 66.4%, annual household income $20, 000 14.4%, $80, 000 20.8%, BW 3540 451 grams, GA 39.7 1.4 weeks, breastfeeding at discharge 89.3%. 85.3% of infants had LOS 48 hours after delivery. Among infants with LOS 48 hours, 47.4% were seen by a health care professional physician, public health nurse, clinic nurse etc. ; , and 29.4% by a physician within 48 hours of discharge. For infants with any LOS, 91.0% were seen by a health care professional, and 80.2% by a physician within 7 days of discharge. The proportion of infants with visits to emergency departments was 8.0% and walk-in clinics 7.2%. The readmission rate was 4.0%. Statistically significant factors associated with a visit to a health care professional within the first week of discharge were OR, 95% CI, p-value ; : annual household income $40, 000 1.7, 1.0-2.8, p 0.04 ; , breastfeeding 1.9, 1.1-3.6, p 0.023 ; , and LOS 48 hours 2.8, 1.6-4.8, p 0.001 ; . CONCLUSION: Guidelines from the CPS and SOGC for follow-up within the first week of discharge were being followed by the majority of respondents. Appropriately, breastfeeding and LOS 48 hours were significantly associated with compliance with follow-up guidelines. The association of higher annual household incomes with timely follow-up suggest that health services may be more utilized by socially less disadvantaged respondents. Supported by a grant from Canadian Health Services Research Foundation and ketoconazole.
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| Values, in nmol min g , are medians 25th75th percentiles ; . The colorectal group is based on the pooled data of the 3 colorectal groups controls, CD, and UC ; from Table 1. The values of CO2 production for fatty acids and glucose correspond to the oxidation of [1-C] and [6-C] substrate carbons, respectively, whereas the values of ATP production were calculated on the assumption that fatty acids were completely oxidized. Values not sharing the same superscript letter within a column are significantly different at P 0.05. * P values for ATP production are the same as for CO2 production and lansoprazole.
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Koljonen m, hakala ks, ahtola-stil t, laitinen l, kostiainen r, kotiaho t, kaukonen am, hirvonen j drug discovery and development technology center ddtc ; , faculty of pharmacy , university of helsinki, finland and macrodantin.
57 ; Abstract: A ring binder having actuating lever with cushion member includes a substantially rigid curved upper plate supporting a pair of hinged leaves. A plurality of ring members are secured to the hinged leaves for engaging corresponding holes in sheets of material retained by the ring binder. An actuating lever is located at each end of the curved upper plate for actuating the hinged leaves to open and close the ring members. Each actuating lever includes a tab having a pair of spaced-apart apertures therein. A cushion member is located on the tab, which includes an inner cushion part and an outer cushion part which are interconnected by a pair of connecting parts which extend through the spaced-apart apertures in the tab to securely attach the cushion member to the tab. The cushion member is engaged by the fingers of a user to pivot the actuating lever in order to move the ring members between the open position and the closed position. The cushion member is a soft pad of resilient material such as rubber or soft plastic. The cushion member provides improved tactile characteristics to the actuating lever, making the actuating lever comfortable to use. The cushion member also minimizes the feedback of undesirable shock forces produced by the snap action of the rings when opening and closing the rings. Drawing: 04 Sheets ; Total Pages: 20.
Address for reprints: Atsushi Kanno, M.D., Department of Internal Medicine, Tohoku Koseinenkin Hospital, 12-1 Fukumuro, 1 cho-me, Miyagino-ku, Sendai 983-8512, Japan.
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Community of science and technology with the Academy's purposes of further knowledge and advising the federal government. NRC is part of the National Academies, which also comprise the National Academy of Sciences, National Academy of Engineering and Institute of Medicine. In their 2001 report, Informing America's Policy on Illegal Drugs: What We Don't Know Keeps Hurting Us, the NRC reports that there is little research to support the current drug enforcement policy.26 In 1999, only $1 was spent on researching enforcement policies for every $107 spent on enforcement itself. Despite there being data systems and research infrastructure within law enforcement and the public health sector, NRC reported that there was little research either on the monitoring of drug use or its treatment and prevention. As a result, there was insufficient knowledge of current drug control efforts and a lack of understanding whether spending is minimizing drug use. NRC further noted that existing research appears to indicate that there is "little apparent relationship between severity of sanctions prescribed for drug use and prevalence or frequency of use, and that perceived legal risk explains very little in the variance of individual drug use."27 This finding suggests that drug users do not appear to be affected by enforcement penalties, thereby showing that spending may not be allocated most efficiently. NRC concluded that there is no empirical basis for the current national drug control policy and its emphasis on criminal justice responses to drug use, stating, "it is unconscionable for this country to continue to carry out a public policy of this magnitude and cost without any way of knowing whether and to what extent it is having the desired effect, because .
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Yawu Liu, Jari O. Karonen, Juho Nuutinen, Mervi Knnen, Esko Vanninen, Jyrki T. Kuikka, Ritva L. Vanninen Department of Clinical Radiology, Kuopio University Hospital; Kuopio University, Kuopio, Finland Background and purpose: The crossed cerebellar diaschisis CCD ; refers to a matched hypoperfusion and hypometabolism in cerebellum due to remote effect of contralateral supratentorial lesion. The purpose of our study was to evaluate whether hemispheric ischemic lesions could cause apparent diffusion coefficient ADC ; change in the cerebellum. Methods: Twenty-two stroke patients underwent diffusion-weighted MRI DWI ; and SPECT within first 48 hours and at day 8 after onset of stroke. SPECT interhemispheric asymmetry indexes AIs ; were calculated for medial, intermediate, and lateral zones in cerebellum. ADC of cerebellar white matter, cortex of medial, intermediate, and lateral zones were bilaterally measured from patients and 15 age-matched healthy volunteers. Results: The ADC values within the first 48 hours and on day 8 were or tended to be significantly higher in patients than controls on both sides 0.087 ; with one exception in the gray matter of the intermediate zone within 48 hours. Within the first 48 hours but not on day 8, the ADC ratio ipsi contra ; of cerebellar white matter was significantly associated with the AIs of intermediate and lateral zones 0.027 the ADC ratio ipsi contra ; and AI of the intermediate zone was significantly associated with each other p 0.044 ; . The ADC ratio ipsi contra ; of cerebellar white matter within the first 48 hours significantly associated with NIHSS within 48 hours, on day 8, and at 3-month 0.028 ; . Conclusion: The ADC changes in cerebellum represent a complex physiological and pathological phenomenon in patients with supratentorial ischemic infarction. ADC measurements may afford additional information in investigating the CCD.
FDA Patent Exclusivity Drug Chemical Approval Expiration Expiration Eloxatin Oxaliplatin 2002 2013 2007 Enbrel Etanercept N A N Enbrel Etanercept N A N Enfamil N A N Epivir Lamivudine 1995-1998 2009-2018 2002-2005 Epogen Epoetin Alfa N A N Eprex Procrit Epoetin Alfa N A N Ethyol Amifostine 1995 2012-2017 2002-2006 Euphylong Theophylline 1982 None None Evista Raloxifene 1997 2003-2015 2002 Exelon Rivastigmine 2000 Fabrazyme Agalsidase Beta N A N 2010 None Famvir Famcyclovir 1994-1996 Faslodex Fulvestrant 2002 2004 2007 Femara Letrozole 1997 Ferro Ferrous Fumarate N A N Flixonase Flonase Fluticasone 1994 2003 2005 Flixotide Flovent Fluticasone 1993-1997 2003 None Tamsulosin 1997 2004-2009 2002 Flomax Floxin Levaquin Ofloxacin 1990-1997 2003-2012 None 2006 None Foradil Formoterol 2001 Fortum Fortaz Ceftazidime 1985-1989 None None Fosamax Alendronate 1995 2007-2015 2002-2003 Fraction V Albumin N A N Fragmin Dalteparin 1994-1998 None 2002-2003 Fraxiparene Nadroparin N A N Frova Frovatriptan Succinate 2001 2012-2015 2006 Furtulon Doxifluridine N A 2007-2016 2004 Gabitril Tiagibine Hydrochloride 1997-1999 2008-2012 2002 Gamimune Immunoglobulin N A N Gemzar Gemcitabine 1996 2010-2012 None Gengraf Cyclosporine 2000 None None Genotropin Somatropin 1995-1998 2013-2018 2003-2008 Geodon Ziprasidone 2001 2007-2019 2006 Glivec Gleevec Imatinib 2001 Glucobay Precose Acarbose 1995-1997 2007 None Glucophage Metformin 1995-1998 None 2002-2004 Glucophage XR Metformin 1998 None 2003 Glucotrol Glucotrol XL Glipizide 1984-1999 None None Glucovacne Glyburide + Metformin 2000 2019 2003 Gonal-F Follitropin Alfa 1997-2001 None None Growth Hormone Sales N A N Hepatitis Vaccines N A N Hepatitis Vaccines N A N Herceptin Anti-HER Monoclonal Antibody N A N Herceptin Transtuzumab N A N HRT Products N A N Humalog Lispro Insulin 1996-1999 2013-2014 2003 Humatrope Somatropin 1987-1999 None None Humulin Insulin 1994 None None Hycamtin Topotecan 1996 2010 None Imigran Imitrex Sumatriptan 1992-1997 2006-2013 None Diptheria + Tetanus Toxoid + Pertussis Vaccine N A N Infanrix Influenza Vaccine N A N Inhibace Cilazapril Not Approved Insuman Insulin N A N Intal Sodium Cromoglycate Not Approved Integrilin Eptifibatide 1999 2014-2016 2003-2005 Integrilin Eptifibatide 1998 2014-2015 2003-2004 Intron Recombinant Interferon Alfa-2b N A N A Invanz Ertapenem 2001 2013-2017 2006 Major Drug Database. Updates available at : geocities pchang 99 drugdatabase.
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The fda warned that health care providers, caregivers, patients, and their families should also be alert for certain behaviors associated with antidepressants, such as anxiety, agitation, panic attacks, insomnia, irritability, hostility, impulsivity, severe restlessness, and mood disorders marked by agitation, excitability, or elation hypomania and mania.
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Changed several times. The clinical records are insufficient to resolve these conflicts between the parties' accounts. Clearly, however, if Mr A gave varying information this should have been recorded, discussed, and checked; whether or not his responses were clear and coherent, the medication chart should have been completed and countersigned with Mr A' s allergy status specifically recorded. Had these steps been taken, it is probable that Dr B and Mr C would have identified a conflict in the information they had received. Furthermore, had the request for Mr A's previous medical records been pursued, or PMS Alpha accessed and checked, Dr B and Mr C would more likely than not have realised that there was also a conflict between the information Mr A had given them, and what had previously been entered on his medical file. Dr Hughes commented that the availability of Mr A's previous notes may not have "materially changed what happened". I agree this is possible - the "[District Health Board's] Medical Warning" and front-sheet are undated and therefore I cannot be certain that "Maxolon" had been recorded on them before 30 January 2002. However, as the second public hospital notes of 22 June 2001 contained information confirming that Maxolon caused Mr A to become agitated, and his AMRs had been entered on PMS in October 2001, I consider it likely that in January 2002 the warning label would have included reference to Maxolon. Accordingly, had Dr B or seen this information, they would have recognised that Maxolon presented difficulties for this patient and that the possibility of prescribing or administering it should be discussed with him. Of particular concern in respect of these issues are Dr B's concession that she was unaware how to access information regarding a patient's AMRs on the computer system, the DHB's advice that Mr C received no training on the system at all, and Dr D's statement that the previous records were delivered to the ED "sometime after midnight". The Director of Emergency Medicine suggested that Mr A's advice to Dr B regarding Stemetil, Mr C's tick in the "allergies" box on the triage sheet, and "AMR" on the patient label were sufficient to allow Dr B to have taken Mr A "at his word". He stated that "it is only reasonable to expect the doctor or the nurse to have gone to the patient management system for further information if they thought the patient was either giving incomplete information or unable to give information at all". The difficulties with this argument are that neither Mr C nor Dr B appears to have noticed or fully recognised the significance of "AMR" on Mr A's pre-printed patient label; Dr B's verbatim note of Mr A's advice gave an insufficiently clear clinical picture of his actual AMR status; and Dr B and Mr C failed to recognise that their patient had given different information to each of them about his AMRs. Moreover, the requirement to check Mr A's previous records was one of the three minimum steps required to establish Mr A's allergy status, and was not subject to conditions or qualification. I accept that communication between Mr A and those caring for him in the early hours of 30 January 2002 was difficult, and that because he gave conflicting information to his providers, a degree of confusion arose. I acknowledge that Dr B and Mr C acted in good faith when providing services to Mr A, and agree with the comment that Mr A had a degree of responsibility to provide reasonable information to his providers, to assist them to make.
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