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Frequency of Intake

Table 4 shows the results obtained after the simulation of the load of Listeria in each step of the food chain. The distribution found for the Ejqtosure Assessment of Listeria (C0-C4), i.e. LMh, represents the frequency of intake of contaminated liters at home. [Pg.1745]

As it can be observed in previous Tables 4 and 5, a correct pasteurization stage removes any initial load of LM content, so that only consequence type Ci can be expected with the load of LM through the milk chain and also the frequency of intake of contaminated milk being virtually zero. This is the normal situation one can expect. [Pg.1745]

The third sensitivity study assumes there is neither control of the pasteurization parameters nor analysis of LM content at cool storage nor inspection of LM content at retail. Tables 10 and 11 show the results found in this case. One can observe now the largest increase of LM content through the milk chain with consequences C3 to C4 possible only. Since it is assumed neither control in processing milk at the company nor inspection at retail, then, there are no consequences Ci orC2- For-trmately, consumer capacity to detect milk that smells awful reduces the frequency of intake of contaminated milk at home. [Pg.1746]

In this step, the assessor qiuuitifies tlie magnitude, frequency and duration of exposure for each patliway identified in Step 2. Tliis step is most often conducted in two stages estimation of exposure concentrations and calculation of intakes. The later estimation is considered in Step 4. In tliis part of step 3. the exposure assessor determines the concentration of chemicals tliat will be contacted over the exposure period. E.xposure concentrations are estimated using monitoring data and/or chemical transport and environmental fate models. Modeling may be used to estimate future chemical concentrations in media tliat are currently contaminated or tliat may become contaminated, and current concentrations in media and/or at locations for which tliere are no monitoring data. The bulk of the material in tliis chapter is concerned witli tliis step. [Pg.356]

DIARRHEA. When these dragp are used orally they occasionally result in excessive salivation, abdominal cramping, flatus, and sometimes diarrhea The patient is informed that these reactions will continue until tolerance develops, usually within a few weeks. Until tolerance develops, the nurse ensures that proper facilities, such as a bedside commode, bedpan, or bathroom, are readily available. The patient is encouraged to ambulate to assist the passing of flatus. If needed, a rectal tube may be used to assist in the passing of flatus. The nurse keeps a record of the fluid intake and output and tlie number, consistency, and frequency of stools if diarrhea is present. The primary health care provider is informed if diarrhea is excessive because this may be an indication of toxicity. [Pg.227]

SEOW A, SHI c Y, FRANKE A A, HANKIN J H, LEE H P and YU M c (1998) Isoflavonoid levels in spot urine are associated with frequency of dietary soy intake in a population-based sample of middle-aged and older Chinese in Singapore. Cancer Epidem Biomarkers Prev. 1 (2) 135-40. [Pg.219]

Ritenbaugh, C. et al.. New carotenoid values for foods improve relationship of food frequency questionnaire intake estimates to plasma values. Cancer Epidemiol. Biomarkers Prev., 5, 907, 1996. [Pg.140]

In Greece, a case-control study was conducted to investigate the incidence of liver cancer by estimating the consumption of six types of flavonoids with a semiquantitative questionnaire on the frequency of foods. The intake of flavones was inversely associated with hepatocellular carcinoma, irrespective of its etiology (viral or nonviral). With respect to cholangiocarcinoma, an inverse association with the consumption of flavan-3-ols, anthocyanidins, and total flavonoids studied was found. However, this last result should be viewed with caution because of the small sample size, due to the fact that this is a rare type of cancer (Lagiou and others 2008). [Pg.165]

An exposure assessment is the quantitative or qualitative evaluation of the amount of a substance that humans come into contact with and includes consideration of the intensity, frequency and duration of contact, the route of exposure (e.g., dermal, oral, or respiratory), rates (chemical intake or uptake rates), the resulting amount that actually crosses the boundary (a dose), and the amount absorbed (internal dose). Depending on the purpose of an exposure assessment, the numerical output may be an estimate of the intensity, rate, duration, and frequency of contact exposure or dose (the resulting amount that actually crosses the boundary). For risk assessments of chemical substances based on dose-response relationships, the output usually includes an estimate of dose (WHO/IPCS 1999). [Pg.315]

Detection times vary depending on analytical method used, drug metabolism, tolerance, patient s condition, fluid intake and method and frequency of ingestion. These are general guidelines only. [Pg.15]

No adverse effects in males at 30 mg/kg diet (1.06 mg/kg BW daily) and lower, or in females at 100 mg/kg diet (4.3 mg/kg BW daily) and lower. Lung histopathology observed in males at 100 mg/kg diet, and in both sexes at 300 mg/kg. At 300 mg/kg diet, clinical signs included reduced growth, reduced food and water intake, abnormal blood chemistry, and increased frequency of cataracts. No conclusive evidence of carcinogenicity (Anonymous 1988)... [Pg.1182]

The pharmacokinetics of a drug can also determine the frequency of monitoring. Many believe that TDM requires frequent blood drawings, primarily based on the experience with lithium. However, this drug is relatively unique in that its levels are determined by multiple independent factors. Thus, the plasma level of lithium is not solely a function of the dose and of renal status, but also of fluid and salt intake and output, which can vary independent of dose. [Pg.41]

Thus, the frequency of exposure is also an important factor because the concentration to which the organism, and more particularly the target site, is exposed can remain relatively constant or increase. As illustrated above, this is because repeated exposure may lead to accumulation of the chemical, depending on its half-life (see chap. 3), such that intake exceeds elimination. Thus the chemical can accumulate in the organism because of saturation of metabolism or elimination or because its physicochemical properties determine that the chemical becomes sequestered in tissues such as fat. Another factor in toxicity from chronic exposure can be the ability to repair damage or replace macro molecules and the speed with which this is done. If damage is not repaired or macro molecules are not replaced before the next exposure, then accumulation of damage or effect can also occur. [Pg.31]


See other pages where Frequency of Intake is mentioned: [Pg.15]    [Pg.15]    [Pg.15]    [Pg.108]    [Pg.345]    [Pg.432]    [Pg.361]    [Pg.326]    [Pg.208]    [Pg.208]    [Pg.15]    [Pg.15]    [Pg.15]    [Pg.108]    [Pg.345]    [Pg.432]    [Pg.361]    [Pg.326]    [Pg.208]    [Pg.208]    [Pg.280]    [Pg.141]    [Pg.597]    [Pg.345]    [Pg.69]    [Pg.815]    [Pg.225]    [Pg.12]    [Pg.165]    [Pg.214]    [Pg.681]    [Pg.1182]    [Pg.129]    [Pg.486]    [Pg.196]    [Pg.105]    [Pg.253]    [Pg.317]    [Pg.383]    [Pg.214]    [Pg.681]    [Pg.124]    [Pg.304]    [Pg.124]    [Pg.152]    [Pg.430]   


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