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Harper grein:
Transitions can occur at dramatically different paces in different
places. Omrans classic model was developed based on findings in
the U.S. and Western Europe; he estimated that it took about 200
years, from start to finish, though other authors have argued that it
actually began even earlier
Demographic Transistion - 4 stig yfir 1200 r.
More people live to longer age, they get sick later but the time they
are sick is longer than it would have been before. Makes up the
difference, longer life in sickness according to this theory, taking
into account social and economic differences. Failure of success:
people live longer do to medical interventions (not quit true) but its
not possible to cure the people.
It is presumed the life expectancy from 1990 to 2010 have been
expanded by four years. For each of those years healthy years
increased by 0,8. People lived four years longer but not with full
health (Fyrir hvert r jukust 0,8 r af healthy life af essu fjrum
rum. Lifir fjgur r lengur en ert ekki me fulla heilsu ll fjgur rin
heldur 0,8 fyrir hvert r).
Compression of Morbidity
The same factors that lead to extension of life are the same factors
that lead to compression of morbidity. These factors that lead to
longer life lead to life with better health. The time when we are sick
is minimized but when we get sick we die very soon thereafter.
Dynamic Equilibrium
risk individuals so they dont profit from any intervention. The idea
is to alter the risk factors for everybody, produce a population shift,
with physical activity and diet. There is a big impact and fewer at
high risk although there is not that much of a change for the
community as a whole.
For example the drug Statins (cholesterol lowering drug), it is known
that they benefit and can provide better longevity. Why than not
proscribe Statins to everybody? That is because of the side effects
of the drug, they can be minimal but can also be very severe. There
is a risk for everybody. If you are at high risk for a disease then the
benefit is more than the harm of taking the drug. For those at low
risk, there is little benefit but the risk for harm of the side effects is
more.
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medical harm. That still leaves 40% of things that are not
predictable so what should be done with that big problem and
the public grossly underestimates the problem.
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could may occur, before the drugs go into sale to the public. This
came to be known as the Cochrane collaboration: systematic
reviews, meta-analysis and more research on treatment and drugs
so doctors can use the database and learn how the product has
worked before they decide to use it. It summarizes the idea that you
have low quality evidence and high quality evidence. The lowest is
clinical observation and expert opinion and the highest in the
hierarchy is systematic reviews and meta-analyses. Sadly this is not
that perfect because of the self-serving bias from industry gifts and
so on that effects their decision.
Cochranes hierarchy of evidence: The questions are, Can it
work? Does it do more good than harm in ideal circumstances. Does
it work in practice? Does it do more good than harm under usual
circumstances. Is it worth it? Is the drug to expensive.
The human genome project
To identify and map all of the genes of the human genome.
Personalised medicine: to replace the one size fits all approach of
conventional medicine to deliver the right drug to the right patient
at the right time. The target continues to be to develop drugs that
are specifically targeted to every single persons genome. With new
technology, people could offer their complete genomic information
and then reference against the population and then prevent,
diagnose and treat diseases. Doing this it would change health-care
as we know it today, but it didnt quit work as they expected. Within
personalised medicine the myth is that biological is the fundamental
importance, start with biology and it is the ultimate cause. The most
logical cause is the environment and its shape and other is the
behavior. Complex interaction between genes, behavior and
environment. Though specific genes are in a disease, other factors
have an impact. The solution is to collect data. Data can be
collected in population, in subgroups and then individualized. The
main goal is to use genetic information for screening and testing.
Collecting data was thought to be a solution Big Data collect
more and more data about the problem and be able to solve it with
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the information. With the data they are able to conduct huge
epidemiologic studies with all the geno-information. The
personalized medicine movement is that the government pays for
this which is very costly. The problem is that health is random, there
are chance factors going on at every level all the way in the process,
from the subcellular to biographical. The magnitude of these
chances are major and not minor. Chance explained 65% in the
variation in cancer risk, the environment and behavior explained 2530% and genes only explained 5-10% of the variance. This tells us
that most cancers are due to chance random mutation and other
factors in the genetic process determining whether cancer
immerges.
Inverse care law
screened for other things as well. Test results can give wrong
predictions of disease.
Issues: Presumed benefit of treatment is an assumption. People
think, if i have a disease i want to know about it and get it treated.
Nna er bi a identifya snemma, mun a contributea til length of
life or quality of life. People presume it will. a sem gerist
venjulega er a flk greinie sig sjlft og presentar a vi lkninn.
Ef ert me einkenni, ertu me einkenni og ess vegna meikar
sense a lta skoa a.
Ef ert me sjkdm, og veist af honum snemma er the treatment
only modestly effective. Er a gott a f treatment einhvern tma
og borga fyrir a ea f ekki treatment og pay some small price for
that later in life.
Ef biomedical healthcare er eins gott og haldi er, afhverju er veri
a screena snemma ef inngripin eru svona g late diagnosis.
Me t.d. krabbamein, er mguleiki a lkna a ef a er greint
snemma en ekki ef a er seint. a er rttltingin sem er oft
notu.
a eru einhverjar lkur a the condition is so slow progressing a
a mun ekki hafa mikil hrif fyrr en mun seinna t.d. eins og
ristilkrabbamein. En san eins og rannskn sndi me
brjstamyndatku til a ath brjstakrabbamein hj konum, a a
finna early stages tti a hafa hrif late stages en a virist ekki
gera a raun. Niursturnar voru r a screening minnkai
aeins ltillega the rate at which women present with advanced
cancer.
Negative side effects: anxiety over abnormal results & years of
uncertainty surrounding treatment outcomes.
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