DAR ES SALAAM, Oct. 1 (Xinhuanet)
-- Starting on Oct. 1, some of the HIV-positive people in
Tanzania are to get free-of-charge anti-retroviral drugs
(ARVs) to prolong their lives as the country starts its
special assistance program.
As many as 3,360 adults and 940 children are among the first
beneficiaries of this program.
The Tanzanian government has promised to distribute free ARVs
to no less than 30,000 people in fiscal year 2004-2005 while the
number of HIV/AIDS patients receiving free ARVs will increase
to 220,000 between 2005 and 2006.
The government has worked out a four-year national care and treatment
program in that HIV/AIDS prevalence rate now stands at 10 percent
in Tanzania, with 140,000 sufferers dying from the disease annually,
out of almost two million people living with thevirus.
Mother-to-child infection is high in the country.
Tanzania is among the poorest countries in the world. Most people
in the rural areas each live with less than a US dollar a day
whereas a monthly dose of anti-HIV/AIDS drugs costs more than
30 dollars.
The free drugs, purchased by the government at a cost of 26 billion
Tanzanian shillings (26 million dollars), will first be distributed
through 32 local hospitals and the services will be extended to
91 hospitals and health centers throughout the country.
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NEWS
Glaxo seeks dismissal
of hearing into its Aids drugs prices
September 23, 2004
By
Vernon Wessels
Johannesburg
- GlaxoSmithKline, the world's largest maker of HIV treatments,
has asked South African competition authorities to drop an "unfounded"
probe into the price of its Aids drugs.
The Los Angeles-based
Aids Healthcare Foundation has asked the competition tribunal
to rule whether Glaxo's antiretroviral drugs are excessively priced.
The group, which distributes free medicines in South Africa, may
sue Glaxo if the tribunal rules against the UK-based company.
"Glaxo
doesn't believe that the foundation's claim has any merit,"
the company said. It asked the tribunal to end the probe "on
the basis that the complaint requested by the foundation is unfounded".
The tribunal
can fine a company as much as 10 percent of local revenue for
breaches of competition law. Last year the competition commission,
which investigates complaints before referring them to the tribunal,
found Glaxo abused its market dominance.
Glaxo reached
a settlement with the commission by allowing other producers to
make its Aids drugs at a reduced cost.
"It's
very ironic that the foundation has filed this complaint against
Glaxo, since in June 2003 we signed an agreement with them to
supply the Ithembalabantu clinic in Umlazi with Glaxo's antiretrovirals
at not-for-profit prices," said Michael Spector, the general
manager of Glaxo's South African unit.
The foundation
operates Ithembalabantu, the isiZulu word for people's hope, as
a free Aids treatment clinic in the KwaZulu Natal township of
Umlazi with the Network of Aids Communities of SA, a local non-governmental
organisation.
"Like most bullies, Glaxo was full of bluster when it vowed
repeatedly that it would appeal the very filing of our tribunal
complaint," Michael Weinstein, the president of the foundation,
said. "Glaxo hides behind a wall of lawyers and legal arguments,
attempting to assert technicalities as to why the tribunal should
not hear this case."
The organisation
was in the process of drafting an answering affidavit to Glaxo,
said Musa Ntsibande, a director of Strauss Daly, the foundation's
legal representatives, in a telephone interview. "After that
we will apply for a hearing date with the tribunal."
Glaxo has
agreed to allow drug manufacturers, such as Aspen Pharmacare,
Thembalami Pharmaceuticals and Feza Pharmaceuticals, to distribute
its medicines in Africa.
The foundation
and the Treatment Action Campaign (TAC), an Aids advocacy group,
filed the complaint with the competition commission in January
2003.
The foundation
rejected the settlement Glaxo struck with the commission and the
TAC because it had not been included in the process and the agreement
"didn't go far enough", Ntsibande said.
Statistics
SA estimated in July that 3.83 million of the country's 46.6 million
people were infected with Aids.
The
UN put the number higher in a report it issued in the same month,
estimating that 5.3 million South Africans had Aids.
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 |
| Web
Issue 2110 |
October
08 2004 |
Geldof defends Blair plan for African debt
MICHAEL
SETTLE, Chief UK Political Correspondent
BOB Geldof last night rallied behind the proposals of
Tony Blair and Gordon Brown to cut Third World debt after Europe's
aid chief denounced Britain's efforts as similar to the accounting
malpractices of Enron.
The plain-speaking anti-poverty campaigner
accused Poul Nielson, the outgoing EU humanitarian aid commissioner,
of "talking through his arse", adding: "He shouldn't have his
job if he doesn't want to help."
Mr Nielson incurred the wrath of the Band
Aid organiser after he claimed the government's plans to relieve
poorer nations of their debt would force future generations to
pay the price of glory for today's politicians.
"Everybody is worried, for very good reasons,
about the debt burden of developing countries, so to introduce
a new dimension of debt … only to impose on our children in the
donor countries the burden of actually paying what we now take
the glory for doing – that I don't like," Mr Nielson told MEPs
in Brussels.
"This should be about solidarity, not about borrowing from our
children," argued the EU's outgoing aid chief.
His criticism centred on the chancellor's brainchild, the International
Finance Facility (IFF), which aims to double to £600m a year the
aid to the world's poorest countries. The plan involves issuing
bonds in the markets using donor countries' long-term funding
commitments as collateral.
Britain, which will use its presidency
of the G8 and the EU next year to make reducing poverty and debt
a global priority, believes the IFF is essential to meet the United
Nations' so-called "millennium development goals" of reducing
poverty by half, cutting infant mortality by two-thirds and ensuring
every child has primary schooling.
Yet Mr Nielson said the IFF plan "smells
too much of innovative Enron accounting". Accountancy malpractices
led to the fall of the US energy giant.
During the British-sponsored Commission
for Africa summit in Ethiopia, Geldof rounded on Mr Nielson, telling
reporters: "It's rich of the EU aid commissioner. He should look
to his own books. They're wholly woeful in what they do. I don't
think the debt relief issue is economic sophistry if that's what
he's suggesting. I think the IFF is elegant, timely, simple, necessary."
Mr Blair and Meles Zenawi, his Ethopian counterpart, sitting
next to the Irish rock singer, also brushed aside the EU commissioner's
criticism – albeit in more diplomatic language.
"Obviously, we support the IFF and do not think it is an accounting
gimmick," said Mr Zenawi.
The prime minister added: "There will be
particular aspects (of our plans) people have difficulty with
… Let's have a debate and see if we can persuade people."
Also at the press conference, in Addis
Ababa, Mr Blair pressed the international community to raise £122m
to help people caught up in violence in the crisis-hit Darfur
region of Sudan.
He said Britain planned to train 20,000
African peacekeepers over the next five years to boost the continent's
ability to respond to conflicts like the one in Darfur, where
the Janjaweed, the pro-Sudanese government Arab militia, have
been raiding African villages, killing tens of thousands of locals
and forcing more than a million to flee their homes.
The commission's report on what Africa
needs to do to develop its infrastructure and to avoid war and
famine in the future will be published next spring in time for
the UK's presidency of the G8 and EU.
"Next year will be the year of decision
for Africa and the international community," said the prime minister.
"The time for excuses will be over."
In the past 50 years, 186 coups and 26
major wars have killed more than seven million people and cost
Africa more than £200bn. Half a dozen African nations are still
troubled by serious conflicts.
HIV and Aids complicate efforts to promote
economic growth and development on the continent. More than 26
million Africans are infected with HIV and an estimated 15 million
have died from Aids.
"The problems are multiple. We know them
all," said Mr Blair.
"The difference is that this time we have to put together a plan
that is comprehensive in its scope and has at its core a real
partnership between Africa and the developed world."
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BMI
valuable tool for assessing when to start ARVs in resource limited
settings
Michael
Carter, Wednesday, September 29, 2004
Body mass index (BMI)
at the time of HIV diagnosis can predict survival according to
a study conducted in The Gambia and published in the October 1st
edition of the Journal of Acquired Immune Deficiency Syndromes.
The study found that patients with a BMI below 16 have a similar
prognosis to those with CD4 cell counts below 200 cells/mm3.
The investigators believe that BMI could be a low cost, low technology
means of assessing when an individual needs to start antiretroviral
therapy.
Although viral load measurements and CD4 cell counts are basic
diagnostic tools and play a key role in the initiation and monitoring
of highly active antiretroviral therapy (HAART) in rich countries,
many resource-limited countries lack the funds or technology to
use these tests. Investigators from the London School of Hygiene
and Tropical Medicine wished to see if BMI at the time of initial
HIV diagnosis provided a robust, affordable, and easily used monitoring
tool, capable of determining the prognosis of HIV-positive individuals.
Between 1992 and 2001 a total of 1657 individuals in The Gambia
had their BMI assessed within three months of their initial HIV
diagnosis. CD4 cell count was also measured and patients had their
Karnofsky score assessed. The Karnofsky score is a measure of
how well a patient is doing, on a scale from 0 to 100, where 100
is when the patient has no complaints or evidence of disease,
50 is when the patient requires considerable assistance and frequent
medical care, and 0 is when the patient is dead.
At the time of HIV diagnosis, individuals had a median BMI of
18.8 kg/m2, the median CD4 cell count was 250 cells/mm3
and the median Karnofsky score was 80. A total of 11% of patients
were assessed as having wasting at baseline, and at this point
16% were also diagnosed with tuberculosis.
Investigators found a significant relationship between CD4 cell
count and BMI at baseline. The median BMI for patients with a
CD4 cell count below 200 cells/mm3 was 17.9 kg/m2.
Patients with a CD4 cell count between 200 – 500 cells/mm3
had a BMI of 19.5 kg/m2 and individuals with a CD4
cell count above 500 cells/mm3 had a BMI above 20 kg/m2
(p < 0.001).
Karnofsky score was also significantly related to BMI (p = 0.05).
BMI at the time of HIV diagnosis was able to predict survival
time. A total of 849 patients (51%) died during follow-up with
individuals with a low BMI at diagnosis having the greatest risk
of death. The overall mortality rate was 229 per 1000 patient
years of follow-up and median survival was 2.8 years. However,
median survival for patients with a BMI below 16 was only 0.8
years compared to 8.9 years for individuals with a BMI above 22
at baseline (p < 0.0001).
Patients with a BMI below 18 at diagnosis were 3.4 times more
likely to die than individuals with a BMI above 18 kg/m2,
i.e. the hazard ratio (HR) was 3.4. The HR of death for individuals
with a BMI below 16 was 6.4 kg/m2 compared to patients
with a BMI above 22 kg/m2. The investigators note that
this “is similar to the HR of those with a CD4 cell count below
200 cells/mm3 compared with those with a CD4 cell count
above 500 cells/mm3 (HR 6.8).”
Even after adjusting for type of HIV (HIV-1, HIV-2 and dual infection),
CD4 cell count at baseline, age, sex, infection with tuberculosis,
and the receipt of Pneumocystis pneumonia (PCP) prophylaxis,
a BMI below 16 kg/m2 still involved a HR of death of
2.5.
Even if a patient had a high BMI at baseline, they still had a
significantly increased risk of death if it fell during follow-up.
A total of 166 patients had a BMI above 18 kg/m2 at
diagnosis. Of these 109 died during follow-up. Median survival
for these patients, once their BMI dropped below 18 kg/m2,
was 0.8 years, and their mortality rate was 571 per 1000 patient-years.
This compared to a mortality rate of 112 per 1000 patient years
for patients whose BMI remained above 18 kg/m2.
“Our data show that baseline BMI recorded within three months
of the diagnosis of HIV infection is a strong and independent
predictor of mortality in this West African cohort. The magnitude
of this predictive effect, and the sensitivity and specificity
were similar to those of the CD4 cell count on mortality”, write
the investigators. They add that they found a persistent and strong
“independent association between BMI and mortality; indeed the
increased risk of a BMI <18 is comparable to the increased
risk with a CD4 cell count <200.”
The investigators believe that their findings have important implications
for antiretroviral access programmes in resource limited countries,
and conclude “BMI at diagnosis is a low-technology, affordable,
prognostic indicator, independent of age, sex, CD4 cell count,
or HIV type.”
Reference
van der Sande MAB et al. Body mass index at the time of HIV
diagnosis: a strong and independent predictor of survival.
J Acquir Immune Defic Syndr 37: 1288–1294, 2004.