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Number of benefit years for old-age pensions were replaced with the entire population at retirement age or older. Furthermore, only the number of beneficiaries of the survivors pension who are under the retirement age were taken into account when calculating the number of benefit years for the survivors pension. In the case of Spain, a comparable correction had to be made for the disability pension, as it can also be combined with an old-age pension. How to deal with partial benefits? Partial benefits are paid in the event of partial disablement from work, partial preretirement, and partial unemployment. Partial benefits need to be transformed into full benefit years for calculating the benefit dependency ratio. Benefits paid for partial disability can be expressed in full benefit years by multiplying the number of benefits paid and thus the number of beneficiaries ; by the average degree of disability. Someone who is considered to have lost 50 percent of his or her capacity to work is paid 50 percent of a full disability benefit. When such a benefit is paid throughout the year, this benefit is equal to half a benefit year. For all countries, the number of disability pensions paid in benefit years could be expressed by weighting the number of benefits by their respective rate, which reflects the degree of disability. Partial benefit in the case of part time unemployment can be weighted by the difference between the working hours when working full time and the working hours when working part time. This has been done for Belgium, Denmark, France, and Spain. In the Netherlands and Sweden, partial unemployment is already expressed in full-time equivalents in the national statistics. Part time pre-retirement is only possible in Denmark, Spain99, Sweden, and--since 1993--in Austria. The number of partial benefits is transformed into full benefit years by weighting them by the average rate of working time reduction of a full time job. How to deal with benefits that are only paid for part of the year? It may be the case that someone is unemployed for a few months and consequently he or she only receives an unemployment benefit for part of the year. This is also true for sickness and maternity benefits. In view of the methodology of using full-time equivalents, the benefits that are paid for only several months need to be expressed in full-time equivalents. Thus, persons who have received unemployment benefit at a 100 percent rate for only six months are, for example, counted as half a benefit year. Wherever possible, the number of days on which the benefit was paid were converted into benefit years by dividing them by the maximum number of days on which a benefit can be paid in a year. This maximum number of days is obtained by multiplying the number of payable days per week by 52 weeks. The number of days per week on which a benefit can be claimed differs between countries and schemes. For example, the Swedish unemployment benefit is payable five days a week, whereas a sickness or maternity benefit is payable seven days a week.
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Olerup O and Zetterquist H 1992 ; HLA-DR typing by PCR amplification with sequencespecific primers PCR-SSP ; in 2 hours: an alternative to serological DR typing in clinical practice including donor-recipient matching in cadaveric transplantation. Tissue Antigens 39: 225-35 and procrit.
Hematologic Toxicities 1. If ANC 1.0 x 109 L, or if Platelets 100 x 109 L, give 50% dose of Mechlorethamine and Procarbazine 2. If ANC 0.8 x 109 L, or if Platelets 75 x 109 L, HOLD dose for 1 week Renal failure Suggested action ; 1. If CrCl 12-48mL min, reduce Mechlorethamine to 75% dose 2. If CrCl 12mL min, reduce Mechlorethamine to 50% dose 3. Consider dose reduction of Procarbazine if renal function is reduced eg. reduced creatinine clearance serum creatinine ; Hepatic dysfunction Suggested action ; 1. If Bili 25-50mol L or AST 60-180IU L, reduce Vincristine to 50% dose 2. If Bili 50mol L or AST 180IU L, reduce Vincristine to 25% dose continued on page 47.
Meanwhile an epidemiological study lead from ARPA emphasized that 12 cases of Mesothelioma have been found in the last years in upward Susa valley, one of highest level of the Piedmont. Then there are all the effects due to the noise if this is not reduced to suitable levels, that are: troubles of the sleep, hypertension, effects on the mental health, besides the annoyance which is more or less known by everybody. However there is an extra series of auditory effects which might become important: changes in the electroencephalogram EGG ; , pot-seemed arterial, increase intercranial pressure, headache, cronassia reduction, aggressiveness, depression, conflicting syndromes, activation of the encephalic-hypofisis system, increase thyroidism and of adrenal activity. In addition there will be as well the risk of tumours and childlike leukaemia because of the presence of the new high voltage 380KV and 132KV electrical power lines for supplying the 25 KV aerial of the railway and prohibit.
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In many cancers, multi-agent chemotherapy constitutes the basis of the modern cancer treatment. Ovaries, which are endowed with an irreplaceable number of follicles, are extremely sensitive to cytotoxic drugs that induce an irreversible gonadal damage Oktay et al., 2001a ; . The end result of the chemotherapy-induced damage to steroid-producing cells of the ovary granulosa and theca cells ; , as well as to the oocyte, is premature ovarian failure leading to premature menopause and permanent infertility. Ultrastructurally it is associated with marked follicle loss Familiari et al., 1993 ; . Some chemotherapeutic agents are more commonly associated with gonadal damage; such as cyclophosphamide, chlorambucil, melphalan, busulfan, nitrogen mustard and procarbazine Warne et al., 1973; Koyama et al., 1977; Fisher et al., 1979; Viviani et al., 1985; Mackie et al., 1996; Teinturier et al., 1998; Legault and Bonny, 1999; Meirow et al., 1999; Blumenfeld et al., 2000; Kenney et al., 2001; Tauchmanova et al., 2002 ; . Among the moderately gonadotoxic agents are cisplatin and adriamycin Hortobagyi et al., 1986; Wallace et al., 1989a; Maneschi et al., 1994; Tangir et al., 2003 ; , while bleomycin, actinomycin D, vincristine, methotrexate and 5 uorouracil are associated with mild or no gonadotoxicity Van Thiel et al., 1970; Shamberger et al., 1981; Stillman et al., 1981; Sudman et al., 1992; Bines et al., 1996; Bower et al., 1998 ; Table I ; . Cyclophosphamide is the most commonly implicated agent in causing damage to oocytes and granulosa cells in a dosedependent manner Warne et al., 1973; Sanders et al., 1988; Montz et al., 1991; Meirow et al., 1999; Kenney et al., 2001 ; . In a recent mouse study, cyclophosphamide-induced follicular damage occurred in a dose-dependent manner, but destruction of primordial follicles was observed at all levels of the cyclophosphamide exposure, even at low cyclophosphamide doses of 20 mg kg Meirow et al., 1999 ; . Relative risk of premature ovarian failure was reported between 4 and 9.3 in patients receiving cyclophosphamide Byrne et al., 1992; Meirow and Nugent, 2001 ; . Sanders et al. 1988 ; reported that the probability of having ovarian failure in patients receiving high dose cyclophosphamide prior to haematopoietic stem cell transplantation HSCT ; was 0.35 by 7 years. Older women, with low primordial follicle pool, have higher risk to develop complete ovarian failure compared with young women with high primordial follicle number Schilsky et al, 1981; Richardson et al., 1987; Rivkees and Crawford, 1988; Sanders et al., 1988; Brice et al., 2002; Tauchmanova et al., 2002 ; . With advancing age, permanent gonadal damage can be induced with smaller doses of the implicated chemotherapeutic agent. Even though irregular menstrual pattern or amenorrhoea is highly likely to occur in a signicant number of patients during the chemotherapy, sometimes lasting for a considerable period after completion of the chemotherapy, many patients return to a prechemotherapy menstrual pattern Wallace et al., 1989a; Brewer et al., 1999; Low et al., 2000; Tangir et al., 2003 ; . Hormonal reversal of a hypergonadotrohpic hypogonadal state that commonly occurs during the courses of chemotherapy to a normagonadotrophic state may also be expected, especially in young patients Blumenfeld, 2001; Zanetta et al., 2001; Tauchmanova and prolixin.
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Cardiology consultation was sought in this case because of 2 mitigating factors: renal dysfunction and ischemic cardiomyopathy. Ischemic cardiomyopathy is defined as LV dysfunction secondary to coronary artery disease. This patient's LV ejection fraction was greatly diminished and the decompensation, catalyzed by the indomethacin, combined to decrease renal perfusion. The treatment goal in such a patient is to alleviate fluid congestion without worsening renal function and to increase cardiac output, which can improve renal function. At least 3 processes may lead to ADHF or CHF ; due to ischemic heart disease: myocardial infarction, which destroys myocytes, leading to scar tissue formation and impaired contractility; chronic myocardial dysfunction, including hibernation and stunning of myocytes; and myocardial dysfunction resulting from acute but reversible ischemia. Ischemia may also induce myocardial remodeling, leading to LV dysfunction.43, 44 In the current case, the patient presented with an already greatly diminished LV ejection fraction, which resulted in a low cardiac index and impaired renal function--the cardiorenal syndrome. Renal dysfunction may be a result of hypovolemia, vasoconstriction, low output, intrinsic renal disease, or medications Table 5, page 8 ; .45 Although some degree of renal dysfunction is extraordinarily common among patients with ADHF, 45 low cardiac output hypotension ; is rather uncommon, accounting for approximately 2% of all ADHF presentations.6 These are the most severely ill ADHF patients, with an in-hospital mortality rate that may exceed 20%.7, 9, 12, The cardiorenal syndrome can be broadly separated into patients with impaired renal perfusion and those with intrinsic renal abnormalities. Impaired perfusion may result from decreased cardiac output attributable to hypovolemia or poor preload. This is why it is necessary to ascertain a patient's fluid status. Renal dysfunction secondary to poor cardiac output may also result from excessively high SVR. Vasodilators are particularly important in such patients. Finally, as in the current case, impaired renal perfusion may be caused by pump failure. In such patients, inotropic therapy is required. The cardiorenal syndrome can also be caused by renal and or vascular abnormalities. For example, renal artery stenosis, especially in unstable hypertensive patients with a normal ejection fraction, may cause renal dysfunction. ACE inhibitors have the potential to decrease glomerular capillary pressure and, subsequently, the GFR. Drug therapy may also impair renal function. In the current case, an NSAID was suspected of precipitating decompensation. There are also patients with peripheral shunting. This is the population of patients with vasodilatory shock. Cardiac output is seemingly normal, but the SBP and SVR are very low. Such patients require pressors and 7.
Guardians before determining the applicant's eligibility. Applications must be submitted annually to determine continued medical and financial eligibility. Acceptance into the program at any time does not guarantee ongoing eligibility, nor does it mean that applicants are entitled to or will be granted benefits at a later time. Other Program Information Generally, a patient over 18 years of age may submit his or her own application. If the patient is an adult under the guardianship of another adult, or is a minor, the patient and his her guardian or parents must jointly submit an application. Applications are reviewed throughout the year. One application per patient, per year, will be accepted. In the event of a significant change in a patient's circumstances, a second application may be considered. Name Of Program NORD Sigma-Tau Matulane Patient Assistance Program Physician Requests Should be Directed To Matulane Patient Assistance Program c o NORD P.O. Box 8923 New Fairfield, CT 06812-8923 800 ; 999-NORD Product s ; Covered By Program Matulane procarbazine hydrochloride ; Eligibility All applicants must be medically eligible for Matulane by having a diagnosis of Stage III or IV Hodgkin's disease documented by the treating physician, or any other lymphomas where a physician feels a response is possible. All applicants must be a U.S. citizen or a permanent 28 and propantheline.
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A total of 46, 080 Lohmann Brown layers, 20 weeks of age, were used to examine the effect of yeast culture on layer performance and mortality. Birds were randomly assigned to 16 open-sided layer houses 2880 birds house ; equipped with wire-floored cages in a commercial layer farm in Indonesia. A corn-soybean meal-rice bran based diet supplemented with 0, 0.1, 0.2 or 0.3% of a commercial yeast culture product Diamond V XP Yeast Culture ; was fed to birds for 20 weeks. Each treatment consisted of 4 replicates 4 houses treatment ; . Feed and water were available for ad libitum consumption. Egg production and feed consumption were calculated on a weekly basis according to daily records. Mortality was checked daily, and weekly death loss was recorded for the whole trial period. Every 5th week of the experiment, twenty eggs were randomly taken from each replicate to measure egg quality including Haugh unit, shell weight, shell thickness and yolk color. The body weight was measured individually from 1% of sample population from each house at 20, 22, 26 and 30-weeks of age. Yeast culture tended to increase P 0.05 ; egg production % hen day and weekly egg production ; , more apparently from the beginning of the lay cycle up to peak production; 67.1, 13241; 72.2, and 73.1, 14488 for control, 0.1, 0.2 and 0.3% XP, respectively. Yeast culture improved P 0.05 ; feed conversion ratio feed egg ; significantly by up to 8.5% compared to control. Weekly mortality rate was reduced P 0.05 ; by all three levels of yeast culture; 0.18, 0.13, 0.12 and 0.11% for control, 0.1, 0.2 and 0.3% XP, respectively. Egg mass was increased numerically by yeast culture; 38.8, 41.7, 41.3 and 42.0g for control, 0.1, 0.2 and 0.3% XP, respectively. Yeast culture showed little effect on feed intake, body weight and egg quality parameters. The results of the study suggest that yeast culture can improve production efficiency of a layer business by increasing egg production and feed efficiency, and by decreasing mortality rate. Key Words: Yeast culture, Egg production, Mortality and propylthiouracil.
Sedative and hypotensive effects of the major tranquilizers. Unlike many of the phenothiazines, HALDOL haloperidol is relatively free of significant hypotensive or undue sedative effects; and reports of reactions such as hematologic changes, hepatic dysfunction and skin rash have been rare. It is not unlikely that patients in this age group will be ingesting medication for concomitant systemic disease e.g., oral diabetic agents, cardiovascular agents, diuretics, etc. ; . HALDOL haloperidol does not interact adversely with these drugs.
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CARNEY: Daniel Carney born c1814 in Yarmouth County, NS, died 24 Aug 1891, s o Daniel Carney and Hannah Ellis : came to NB by 1842 and settled in Bathurst, Gloucester County: m. 6 Oct 1842 at Bathurst, Ellen Gosnell born c1820 in County Cork, Ireland, probably near Skibbereen, d. 5 Apr 1861, d o Thomas Gosnell and Mary Wolfe: Children born at East Bathurst, NB: 1 ; Mary Gosnell Carney b. 5 Sep 1843, d. 12 Mar 1892 at Moncton, NB, m. 27 Aug 1872 at Bathurst, Charles Warren Edgett b. 7 Sep 1847 at Riverside, Albert County, NB, d. 2 Dec 1930 at Moncton, Westmorland County, s o John Abiel Edgett and Eleanor McCormick: had seven children: 2 ; John Carney born c1845, died 17 Dec 1887 at McIntosh's Cove, Caraquet, Gloucester County, NB, m. 24 Apr 1875 at Bathurst, Frances McEwen born 6 Dec 1860 at Bathurst, d o Robert McEwen and Eleanor Heskett: they had six children: 3 ; Thomas C. Carney b. c1847, d. 25 Sep 1897 unmarried probably at Spring Valley, MN: 4 ; Hannah E. Carney born c1850, died 24 May 1901 unmarried at Bathurst: 5 ; Daniel J. Carney b. c1852, d. unmarried 10 May 1919: 6 ; William Carney b. c1853, d. c1909 unmarried Bathurst. Source: MC1816 Carney family history, 32 pages on two sheets of microfiche kept in the MC1816 accession folder and protopic.
Is 5 times the mutation frequency induced by 600 R, the most effective acute dose of x-irradiation, and 13 times as effective as 600 R of chronic y irradiation 6 ; . Before these results were obtained, the most powerful chemical mutagen detected by using single doses in the mouse specific-locus test on spermatogonia was procarbazine 2 ; . The most effective injected dose for this compound was 600 mg kg, which produced 16 mutations in 45, 413 offspring. The induced mutation frequency from ENU at 250 mg kg is 15 times as high as that from procarbazine at 600 mg kg, even though the ENU dose is slightly less than the molar equivalent of the procarbazine dose. Even though the observed mutation frequency with ENU is extremely high, it is possible that we have not yet uncovered the dose level that gives the highest number of mutations per unit dose. The dose-response curve for x-rays goes through a maximum and then decreases. A dose of 1000 R, which gives a long sterile period as a result of spermatogonial killing, induces fewer mutations than does a dose of 600 R 5, 6 ; . The result is attributed to a lower mutational sensitivity of the spermatogonial cells that survive the 1000-R dose. Ehling and Neuhaiuser 2 ; reported a similar effect with procarbazine. A dose of 800 mg kg gave less than half as many mutations as did a dose of 600 mg kg. The length of the sterile period resulting from ENU at 250 mg kg is longer than that from procarbazine at 800 mg kg. So there is a possibility that the ENU dose is past the peak effect. The mechanism of the mutagenic action of ENU in the mouse is an intriguing subject which should stimulate further research. Our decision to test this compound grew out of our earlier work with diethylnitrosamine DEN ; . DEN had proved to be highly mutagenic in Drosophila 7, 8 ; which apparently has enzymes capable of activating it. In the mouse specific-locus test, however, DEN gave a total of only three mutations in 60, 179 offspring 9 ; , a rate almost identical with the control. The question arose as to whether the active metabolite of DEN was reaching the testis. ENU was then chosen for study because it also is highly mutagenic in Drosophila 8 ; and apparently needs no enzymic activation. Because many alkylating agents-for example, ethyl methanesulfonate-are not mutagenic in mouse spermatogonia, it is tempting to suppose that it is the site of alkylation that makes ENU mutagenic. Specifically, because the ratio of 06 to alkylation of guanine is higher with ENU than with many other alkylating agents 10 ; , it is tempting to invoke this property of ENU as the cause of its effective mutagenicity in the mouse. However, this hypothesis should be viewed with caution because of the results with isopropyl methanesulfonate which, like ENU, has a low Swain and procarbazine.
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