Malaria in Pregnancy 4
Malaria in Pregnancy 4
Malaria in Pregnancy 4
Pregnancy
50
40
30
20
10
0
a
ia
ire
st
a
i
aw
nd
a-
a-
er
an
oa
Za
bi
bi
al
ig
ga
nz
M
am
am
N
U
y
Ta
or
G
Iv
Asymptomatic Infection
Placental Sequestration
Altered Placental Integrity
Clinical Illness
Severe Disease
Primigravid
All parities
ae in
in Unstable
Effects Stable
malaria
malaria
areas
areas
• High fever + +++
• Placental +++ +
infection ++ ++
• Puerperal sepsis
• Complicated +++
( +++ =Very Common, ++ =Common, + =Infrequent, -- =Rare)
30
1-999 1000-9,999 >10,000
25
% parasitemic
20
15
10
5 772
402 479
0
First Pregnancies Second Pregnancies Three or more
pregnancies
25
20
With placental
15 parasites
10 Without placental
parasites
5
0
First Second Three or more
Pregnancy Pregnancy pregnancies
25
20
15
10
231 159 197 772
5 402 479
0
G1 G2 G3 G1 G2 G3
HIV (+) HIV (-)
Summary RR = 1.63 (1.41-1.89), p <0.001
Total n = 2263
Source: van Eijk AM et al 2001. Malaria During Pregnancy 12
Components of
Malaria Control During
Pregnancy
1.Quality focused antenatal care and health
education
2.Intermittent preventive treatment (IPT)
3.Use of insecticide-treated nets (ITNs)
4.Case management of malaria disease
90
80
Percenta
70
60
50
40
ge
30
20
10
0
Burkina
Benin
ue
Niger
Togo
Faso
Mali
Cameroon
Guinea
Nigeria
Chad
CAR
Mozambiq
Eritrea
Senegal
Zimbabwe
Tanzania
Cote
d’Ivoire
Malawi
Zambia
Botswana
Kenya
Uganda
Ghana
Namibia
Last
month
10 16 20 30
Birth
Conception Weeks of gestation
Source: WHO 2002. Malaria During Pregnancy 20
Fetal Growth Velocity
Quickening Last
month
10 16 20 30
Birth
Conception Weeks of gestation
Source: WHO 2002. Malaria During Pregnancy 21
Rationale for the Timing
of the SP Doses
Fetal growth velocity
Rx Rx
Quickening Last
month
10 16 20 30
Birth
Conception Weeks of gestation
Source: WHO 2002. Malaria During Pregnancy 22
Key Issues About Timing of
Doses
• SP should be avoided during the first 16
weeks of pregnancy which is the period of
initial development of the fetus
• It is best to clear the placenta of parasites
during the period of maximum fetal growth
• IPT allows the mother to recover from
anemia by clearing peripheral
parasitaemia
30 control
25 bednets
20
15
10
5
0
<3
>4
<3
>4
<3
>4
G
Gravidity G
During Pregnancy
• Tetracycline
– Cause abnormalities of skeletal and
muscular growth, tooth development,
lens/cornea
• Doxycycline
– Risk of cosmetic staining of primary teeth
is undetermined
– Excreted into breast milk
• Primaquine
– Harmful to newborns who are relatively
Malaria During Pregnancy 32
Glucose-6-Phosphatase-Dehydrogenase
A Partnership for Malaria
Control
During Pregnancy
• WHO Programs
– Making Pregnancy Safer
– Roll Back Malaria
• Partnership between both
programs and national
reproductive health
programs essential
• Partnership of programs
and individual involvement
necessary to reach Abuja
Malaria During Pregnancy 33
Country Activities at Different
Levels
District Teams
Program Leaders Operationalize
Develop policies, guidelines and
standards, and support
guidelines, advocacy, IEC, National Program Leadership Level supervision,
PST/IST, support drug supply
supervision, M&E logistics,
District Level and sensitization
of public,
Facility Level promotion of ITNs,
M&E
Community
Facilities Level
Integrated health ed.,
community mobilization,
promotion of ITNs, Communities
provision of IPT, CHWs and TBAs
treatment of complications sensitize about
such as anemia, data malaria control,
collection and feedback referrals, followup