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Preventing the spread of the HIV infection
and controlling mother-to-child transmission in a co-operation project between
Bologna and the district of Tharaka (Kenya) At this
time, the community of Materi (Tharaka) has the availability of services of a dispensary
and a maternity hospital managed by nursing personnel, which is capable of
performing approximately 700 births per year. The
epidemiological statistics relating to the spread of the HIV infection among
pregnant women correspond to those identified in the current maternity
hospital, such as 23%. It is expected that, with the foreseen opening of the
local Hospital, the number of births will increase significantly to a likely
figure of approximately 1.000 per year. The entire
population of 110.000 people living in the Tharaka district, who will be
reached by the healthcare information/mobilisation programmes trough the
involvement of the mobile clinic healthcare team, can be considered as
beneficiaries of the specific co-operation project. The direct
beneficiaries of the PMTC program will be considered the expectant mothers, the
mothers and their respective children, who will join the programme of
prevention, diagnosis and treatment of HIV infection. Strategy to
prevent mother-to-child transmission of HIV (as recommended by WHO) Primary
prevention of HIV infection among parents Prevention
of unwanted pregnancies in women known to be infected with HIV Prevention
of HIV transmission from HIV-infected women to their infants Main project objectives To improve
the healthcare conditions of the population of the Tharaka district, by
preventing the spread of HIV infection To reduce
mother-to-child transmission of HIV infection To ensure
the survival of the mother and baby pair for as long as possible, to safeguard
the family unit Expected results Reduction
of the risk of infection among pregnant mothers Reduction
in the rate of mother-to-child transmission of HIV infection Increased
survival and quality of life of infected mothers, as far as possible Improved
professional autonomy of local medical and health care personnel involved in
prevention, diagnostic and treatment of HIV infection and related diseases Knowledge
and awareness of the population of the real problems associated with HIV disease,
and concurrent reduction of precoceived ideas in relation to it. Materials and methods Prevention phase: throughout the region, to raise
the level of awareness about HIV infection among young people in schools,
military barracks, the countryside and the villages (Healthcare Mobilisation
Programme, carried out with a specifically addressed mobile unit), to promote a
change in the behaviour of the people in order to avoid HIV infection. To do
this, it will be necessary to undertake a mapping of the territory to: - Identify
relevant villages - Identify
existing infrastructures and their features - Identify
the population profile of the village - Acquire
knowledge of the local behavioral uses - Take a census of the population to
identify the extent of the diffusion iof the disease - Take a census of pregnant women, and
pregnancies expected in the short- and mid-term future Diagnostic phase: identification and recognition
of the disease (VCT) Treatment phase: PMTC program The care of
HIV-infected women during antenatal period, labor and delivery and the
post-partum will include: - Intensive
counseling and voluntary testing (VCT) -
Screening/obstetric interventions -
Laboratory investigations - Specific
(antiretroviral) treatment - Prophylactic
measures The local
personnel (medical doctors, nurses, obstetrics, laboratory technicians, and so
on), will be trained by the resident hospital medical team. Antenatal care VCT
recommended to all pregnant women Every
HIV-infected pregnant woman will receive a specific information and couseling
proggram focusing on: - the rate of mother-to-child
transmission of HIV, and the strategy to reduce the risk - the potential effects of
antiretroviral treatment during the course of the pregnancy - the necessity of periodic
monitoring up to the moment of childbirth - the need to resort to a scheduled
Caesarean section to further reduce risk of vertical transmission - the necessity to avoid breastfeeding Monitoring
every two or three months of at least the following parameters: - Clinical assessment (total body
weight, blood pressure, nutritional state, current stage of advancement and
course of the pregnancy, physical symptoms, eventual opportunistic infections) - Laboratory assessment (complete
blood cells count, evalutation of CD4+ lymphocyte count whenever possible,
glycemia, hepatic and renal function,
urinalysis) - Antiretroviral treatment during
pregnancy (performed as recommended by the
up-to-date international guidelines on anti-retroviral therapy): Symptomatic
HIV infection (stage IV, CDC): Zidovudine + lamivudine
+ nevirapine to be initiated as soon as possible,
regardless of the total lymphocyte count, to be continued up to birth, and to
be maintained after completion of the pregnancy (together with eventual
specific treatment of opportunistic infections and/or STIs) Asymptomatic
HIV infection (stage I, II, III, CDC): - T CD4+ lymphocyte count <200/ml: see
case 1 - Total lymphocyte <1200/ml: see case 1 - Total lymphocyte >1200/ml (or CD4+
>200/mmc) Zidovudine + lamivudine, or zidovudine
alone Administered from the 14th
week of pregnancy, and to be continued up to the birth. Treatment interruption has
to be taken into account when the pregnancy reaches term.
Antiretroviral
drug dosage and mode of administration Zidovudine:
250 mg BID, for women
with a body weight <60 Kg 300
mg BID, for women with a body weight
>60 Kg Lamivudine:
150 mg BID (or 300 mg
QD), regardless of body weight Zidovudine 300 mg + 150 mg BID (COMBIVIR®)
plus
lamivudine (only for women
with a body weight >60 Kg) Nevirapine:
200 mg QD for the first
14 days, then 200 mg BID, regardless of body weight Intrapartum
care - Whenever
possible, perform a scheduled Caesarean section at 38th or 39
th week of pregnancy -
Administer i.v. zidovudine at 2 mg/kg, staring three hours before delivery, and
continuing infusion over one hour, followed by continuous i.v. infusion of 1
mg/Kg/hour up to the birth Postpartum
care - For all
new-born babies: prophylactic treatment with zidovudine oral solution,
beginning 8-12 hours following birth, at the dosage of 2 mg/Kg every 6 hours
during the first 6 weeks of life, or 1.5 mg/kg i.v. zidovudine every 6 hours
for the new-born babies unable to tolerate oral administration. At the end of
the prophylactic treatment, an evaluation of serum hemoglobin levels should be
obtained. - In
accordance with internationally recognized guidelines, babies born to
HIV-infected mothers will be weaned with artificial milk up to the age of
one-and-a-half years. Should the
woman is already in an advanced state of pregnancy when first coming under our
observation, or should she refused antiretroviral treatment during pregnancy,
prophylactic therapy based on zidovudine alone is recommended, regardless of
the clinical and immune conditions of the mother. The following schedule should be
therefore followed: Mother: zidovudine: 250 or 300 mg BID to start as
soon as possible after the 14th week of pregnancy, plus i.v.
zidovudine at 2 mg/kg to start three hours before delivery, and subsequent
infusion over 1 hour followed by continuous infusion of 1 mg/Kg/h up to the
birth Newborn baby: zidovudine at 2 mg/kg as oral
solution every 6 hours for 6 weeks, beginning 8-12 hours after birth or 1.5
mg/kg i.v. zidovudine every 6 hours for the new-born babies unable to tolerate
oral administration. In the
event that the HIV-infected woman is already in labour when first coming under
our observation, or she refused anti-retroviral therapy and prophylactic
treatment with zidovudine during pregnancy, prophylactic treatment with the
non-nucleoside analogue nevirapine is recommended, according to the subsequent
schedule: Mother: nevirapine at 200 mg (single dose) to the
mother, soon before delivery New-born baby: nevirapine at 2 mg/kg within the
first 72 hours of birth Careful
clinical and haematologic monitoring should be performed to the mother and and
her baby, at least every three months, to assess their general conditions, the
rate of mother-to-child transmission of HIV infection (with serial serological
controls interesting the child after 6, 12 and 18 months of life), and the
efficacy, tolerability and eventual need of change of antiretroviral regimen
for the mother, due to resistance, toxicity, poor adherence, or reduced
tolerability rate. Francesco
Chiodo, Marina Tadolini, Roberto Manfredi Department
of Clinical and Experimental Medicine, Division of Infectious Diseases,
University of Bologna “Alma Mater Studiorum”, Policlinico S. Orsola-Malpighi,
Bologna | |||||||||||||||||||||||