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    <title>OAR@UM Collection:</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/40247</link>
    <description />
    <pubDate>Fri, 17 Apr 2026 20:52:34 GMT</pubDate>
    <dc:date>2026-04-17T20:52:34Z</dc:date>
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      <title>A study of the cost-effectiveness of colorectal cancer screening in the Maltese Islands.</title>
      <link>https://www.um.edu.mt/library/oar/handle/123456789/40354</link>
      <description>Title: A study of the cost-effectiveness of colorectal cancer screening in the Maltese Islands.
Abstract: This study purports to investigate the cost-effectiveness of a possible national colorectal&#xD;
cancer screening programme, the general public's awareness of the condition, its&#xD;
prevalence and risks, the possible rate of compliance and the reasons for non-compliance&#xD;
if ever such a programme were to take off. Screening would be offered to all those aged&#xD;
50 to 69, comprising 20.9% or 80,000 of the Maltese population. The initial screening&#xD;
test would be faecal occult blood testing every 2 years. The programme, administered by&#xD;
a newly set up screening centre would invite 10,000 every quarter. The compliance rate&#xD;
would be in the region of 50%. The invitation and test kit would be sent by post some&#xD;
time before the beginning of each quarter. Those with a positive initial screen (2%)&#xD;
would be recalled for assessment, resulting in 100 investigations every quarter.&#xD;
Deviation in the compliance rate would affect resources and costs. Colonoscopy and&#xD;
possible double-contrast barium enema (DCBE) would be used for further investigation -&#xD;
both procedures being carried out by highly skilled professionals to significantly reduce&#xD;
possible mortality from colonoscopy which has been quoted at 0.02%. All professionals&#xD;
involved would be co-ordinated by a programme manager and quality assurance would&#xD;
form an integral part of the whole programme. The total cost of the programme would&#xD;
reach LM230, 120 per year. Given an overall uptake rate of 50% and a test sensitivity of&#xD;
60%, 30% of all cancers in this age bracket (50-69 years) would be detected. These add&#xD;
up to 50 cancer cases and 230 new cases of adenomas. Added life expectancy for those&#xD;
with cancer would range between 2 and 1.35 years; so the cost per life year gained would&#xD;
fluctuate between LM2,301 and LM3,400. This is a small but significant benefit.
Description: M.SC. PUBLIC HEALTH</description>
      <pubDate>Mon, 01 Jan 2001 00:00:00 GMT</pubDate>
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      <dc:date>2001-01-01T00:00:00Z</dc:date>
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    <item>
      <title>The role of the mesolimbic dopamine system in interferon-α mediated anhedonia</title>
      <link>https://www.um.edu.mt/library/oar/handle/123456789/32266</link>
      <description>Title: The role of the mesolimbic dopamine system in interferon-α mediated anhedonia
Abstract: SAMMUT, S. The role of the mesolimbic dopamine system in Interferon-a&#xD;
mediated anhedonia&#xD;
&#xD;
Changes in sucrose intake were used as a measure of anhedonia. Non-drug&#xD;
manipulations confirmed that the differences observed in the sucrose concentration-intake&#xD;
curve between the single-bottle and three-bottle were not due to aversion or&#xD;
satiety but more likely attributable to an effort to regulate reward to an optimal level.&#xD;
In the single-bottle test increasing hours of deprivation prior to sucrose tests, nonspecifically&#xD;
altered sucrose intake, while increasing the response-force requirement to&#xD;
access the sucrose solutions decreased the consumption of the 1 % solution and&#xD;
increased the intake of the 32% solution, effectively shifting the bell-shaped response reward&#xD;
curve to the right. This effect was attributed to the motivational drive&#xD;
associated with the perceived reward value of the sucrose solution on offer.&#xD;
Sucrose intake is subject to modulation by several neurotransmitters including&#xD;
DAergic as evident by the effects of raclopride (RAC), a D2/D3/D4 receptor&#xD;
antagonist, glutamatergic (MK-801, non-competitive NMDA receptor antagonist) and&#xD;
GABAergic (muscimol and b acI of en , GABAA and GABAB receptor agonists&#xD;
respectively) systems which showed a similar intake pattern to those of increased&#xD;
response force requirement (i.e. decreased consumption at the 1 % sucrose solution&#xD;
and increased consumption at the 32% solution). Administration of chlordiazepoxide&#xD;
(CDP, a benzodiazepine anxiolytic) however, produced a non-specific increase at all&#xD;
concentrations of sucrose. These results indicate a close interaction between DA,&#xD;
GABA and glutamate in sucrose reward and anhedonia.&#xD;
&#xD;
rHIFN-α is a cytokine used in the treatment of various viral illnesses. A major&#xD;
limiting factor in the therapy is depression. Acute administration of rHIFN-α&#xD;
decreased sucrose intake in a three-bottle test at all concentrations of sucrose,&#xD;
although the effect was greater at 1 % solution. Chronic administration of rHIFN-α&#xD;
decreased sucrose intake at the 1 % and increased that at the 32%. The increase in&#xD;
consumption of the 32% solution was reversed by the chronic administration of a&#xD;
tricyclic and selective serotonin reuptake inhibitor antidepressant. rHIFN-α however&#xD;
failed to alter locomotor activity or amphetamine (AMP)-induced sensitisation.&#xD;
&#xD;
Using in vitro voltammetry in brain slices, it was shown that peripheral pretreatment&#xD;
with AMP led to increased levels of DA in the nucleus accumbens (NAcb)&#xD;
core relative to the rats that had been treated with vehicle. rHlFN- α, reduced evoked&#xD;
DA release in the NAcb core at all frequencies of stimulation. The administration of&#xD;
anti-human lFN-cx, antibody (mHlFNAb) reversed the decrease in sucrose intake at the&#xD;
32% solution produced by the acute administration of rHlFN-cx,. This strongly&#xD;
suggests that the behavioural effects produced by lFN- α, may be related to these&#xD;
central dopaminergic changes. These findings are discussed in relation to a&#xD;
behavioural model for rHINF-α,-induced depression and relative to furthering our&#xD;
understanding into the possible mechanisms through which rHIFN-α, may produce&#xD;
depression in patients and possible therapeutic strategies to alleviate such.
Description: PH.D.</description>
      <pubDate>Mon, 01 Jan 2001 00:00:00 GMT</pubDate>
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      <dc:date>2001-01-01T00:00:00Z</dc:date>
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