Imtiaz Sooliman – Don’t rush the roll out, cautions doctor Imtiaz

Imtiaz Sooliman
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The potential for a COVID-19 vaccine to become effective in the future is uncertain due to the lack of exact timeline and potential risks. The vaccine is still under experimental phase and may not be registered for use in the United States or South Africa. The speakers emphasize the importance of treating patients with COVID-19 rather than just vaccinating them and stress the need for more healthcare workers to prevent third pandemics. They also discuss the importance of upgrading healthcare workers and increasing oxygen supplies to manage the crisis and emphasize the need for a parallel vaccination campaign.

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			From the beginning, it was when
covid 19 hit the country,
		
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			everybody was starting to panic,
and the solution, everybody said,
		
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			lies in the vaccine. The problem
is that we know the that the virus
		
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			that's so aggressive that has
killed so many people worldwide,
		
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			that is still very active all over
the world, and the numbers haven't
		
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			really come down relatively it
means it at some point, this is
		
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			the type of virus that's going to
mutate. And when you're pushing
		
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			for a vaccine very early in the in
the history of the virus, it's
		
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			possible that you're going to get
the wrong vaccine. And that's
		
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			exactly what happened in the
restaurant case. It may not be
		
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			wrong for some other parts of the
world, but for South Africa,
		
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			because we got a mutant sprint.
And in fact, new researchers just
		
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			come out that in the first part of
last year, there were 42 different
		
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			variants, of which 16 were not
recorded. And of the 16, the new
		
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			one is, you know, the fo, 1b 501,
y, v2, is one of those variants.
		
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			So we Yes, it's understandable way
people responded. There was panic,
		
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			especially with the healthcare
workers. I mean, what kind of
		
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			safeguard do they have? They're
losing colleagues, they're losing
		
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			family members, and you understand
the difficulty that they're facing
		
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			because they are in the front
line, but we had to be prudent,
		
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			because if you take all the
precautions, you know, and all and
		
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			still being worried about getting
the vaccine, which is important,
		
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			and you make all the arrangements,
you spend, all the money, you
		
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			create, all the hope the vaccine
comes. And we can see how people
		
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			were dejected. The medical
fraternity. Were very dejected
		
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			when this is any kind of vaccine
was not known or not seen to be
		
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			positive support or works against
the salary constraint.
		
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			Fortunately, there was a
replacement. Professor, Glenda
		
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			Gray was very good in getting the
Johnson and Johnson one. But this
		
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			one also, although it's 57 is a
good start, it's much more than
		
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			22% it gives the medical
fraternity more hope, you know.
		
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			And I'm very happy for them,
because, you know, they've all
		
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			been racing to the to the sites,
to the 18 sites in the country, to
		
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			get vaccinated. But I say we need
to be cautious, because this
		
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			vaccine is under study at the
moment. It's not a vaccine that
		
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			has been released after studies
have been done. Those 80,000
		
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			people taking the vaccine are part
of the study. They're not a result
		
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			of people getting the vaccine
after the study was done. So it's
		
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			a vaccine. It's still in the in
the study stages, but given the
		
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			circumstances, because people say,
Okay, it's it has been safe, and
		
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			yes, from the last few days, the
reports coming from the medical
		
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			fraternity, you get a bit of a
fever, some body ache, you know,
		
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			and maybe someone, some of them,
got a rash or two, but nothing
		
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			unmanageable, and within two or
three days, they've recovered. So
		
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			the safety aspect is there? What
we don't know is, how long will
		
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			the vaccine last for? In terms of
antibodies, for how many months
		
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			will it cause, you know,
		
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			immunization? Secondly, will it
work if new strains come? We don't
		
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			know that. And strangers keeps and
the strains keep changing, so we
		
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			don't know that. And also, the
vaccine is still not registered in
		
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			its own country, in a for, for for
use, for in the general public, in
		
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			America, it's still under
experimental phase. And in South
		
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			Africa too, it's not recommended
or not registered for use in the
		
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			general public. It's an
experimental phase. So all those,
		
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			all those who have registered or
taken the vaccine, have to be part
		
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			of this two year trial for the
vaccine itself. And what is the
		
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			risk to that? According to you?
		
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			Well, to me, I the part time
worried about is. And, you know,
		
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			I'm, I'm hopeful that people will
be and I mean, medical
		
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			professionals will be rational,
because if everybody takes that
		
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			vaccine, they need to understand
that although they are vaccinated,
		
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			they may not be immunized. Mm, so,
in other words, we have, we
		
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			vaccinated so many people, but I'm
so confident that you can walk
		
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			into a ward and say, discovered 19
patients here, and I'm not I'm not
		
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			worried. I'm vaccinated and I'm
immunized. The danger of that is
		
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			you can get infection even though
you've been vaccinated. And worse
		
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			than that, you can carry, carry it
onto your family. You can pass it
		
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			on to your family. You can be a
carrier, because though you're
		
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			vaccinated and you don't have the
right amount of antibodies and the
		
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			right response to the vaccine, it
can be a problem. So we can
		
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			actually create a false sense of
security,
		
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			which can be a very big danger.
It's been a huge danger. Look,
		
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			already the government is some
places are shutting down field
		
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			hospitals, but I'll be honest, I
was in a favor of field hospitals.
		
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			From the beginning, my idea was,
or my thought was, let's upgrade
		
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			existing hospitals. Then you got
them post covid 19 for anything
		
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			else. Now you decommission field
hospitals and all that money is
		
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			gone. It got no value. And we set
the example. We took a hospital in
		
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			Mitchell plain.
		
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			Nine, and we converted the whole
Ward into a dedicated covid 19
		
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			facility at for a cost of 10
million Rand. But it's therefore
		
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			always now for somebody else did
something similar in settlers, and
		
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			we did something similar in Bucha
hospital. So we we keep harping on
		
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			the vaccination, but if the
strains keep changing, we still
		
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			know we have made no progress in
terms of dealing with the virus,
		
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			where we should be focusing, with
life saving with a definite end
		
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			result, put oxygen points in all
the hospital, put stuff. I mean,
		
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			up till now, nobody has addressed
the issue of putting more staff to
		
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			back up the healthcare workers in
hospital. We've already shot short
		
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			staffed even before the pandemic
came. And the pandemic, I mean, it
		
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			exhausted the healthcare
personnel. And in the second wave,
		
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			how many passed on? Many passed on
an exhaustion is one of the main
		
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			criteria for that. So we need to
spend a lot of money putting
		
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			healthcare workers in and putting
oxygen points and oxygen machines
		
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			to be on standby in case the third
wave hits us. What do you suggest
		
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			we do then to go about this in in
a better way,
		
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			uh, treating this
		
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			more to our advantage. Look, it's
a given if, if the third wave
		
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			comes, we will know what this
virus does in the second wave. Of
		
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			course, it required far more
oxygen than the first wave because
		
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			of the strain it the type of
condition it caused people needed
		
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			much more oxygen than the first
wave. So let's be prudent. Let's
		
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			hope it doesn't happen. Let's hope
it doesn't require that amount of
		
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			oxygen. But we know what it has
done, so the rational thing to be
		
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			to do, because a lot of people
died outside hospital. They died
		
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			in their cars, they died in
accused and they died in the
		
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			emergency because there was not
enough oxygen points, and it was
		
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			not enough oxygen. So we can't
save everybody. Let's be just we
		
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			can't save everybody. But if you
put more oxygen points, increase
		
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			the bulk oxygen supply, put in
more stuff to manage the people,
		
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			we can do a huge difference. You
know, if the same type of wave
		
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			comes the third time around. The
second important point is to make
		
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			sure ask the public, at their own
cost, who can afford it by pulse
		
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			oximeters, one per house or one
per two houses, because a lot of
		
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			the patients who came to hospital,
the oxygen saturation was already
		
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			40% and they were smiling, and
they didn't know they were ill,
		
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			and they just dropped dead at the
hospital because they look so
		
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			well, so people having pulse
oximeters at home just randomly.
		
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			Even if there's nothing wrong, you
just test yourself and test your
		
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			own family. That could be life
saving again. The other thing that
		
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			could be life saving is putting
oxygen machines in ambulances,
		
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			because ambulances are the first
port of call. They fetch the
		
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			patients from the home and many
ambulances were driving in
		
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			circles, round and round and round
until a point became available at
		
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			the hospital, whether private or
public, whilst having oxygen
		
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			machines and oxygen in ambulance,
that patient could be kept alive
		
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			for six, 810, hours until the
hospital the ambulance can find a
		
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			hospital that can take the
Patient. Now, all these
		
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			arrangements should be put in
place without relying on the
		
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			vaccination. The vaccination is a
parallel program. Yes, if the 57%
		
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			works and it works against the
South African strain, and
		
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			antibodies develop, and antibodies
last six, 810, months, it's
		
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			fantastic. It's a great
achievement. Run parallel what the
		
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			preparation of the patients, but
at the same time also reset other
		
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			vaccines. They said, You know,
some other vaccines are far more
		
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			efficient, but they haven't been
tested in HIV patients, or other
		
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			type, you know, or some similar
kind of studies in the South
		
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			Africa situation. But we can then
use those vaccines in non HIV
		
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			patients, in patients where, if it
works against the South African
		
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			strain. The trial is done. Let's
use it in non HIV patients,
		
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			because then you have a basket of
vaccines modified to work in
		
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			different conditions, in different
patients with different
		
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			comorbidities, or no
comorbidities. On condition, they
		
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			work against the South African
strain. You run a parallel program
		
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			for