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[08/04/2005]
Sao Tome and Principe | |
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Dr Francis Louis, Yaounde, Cameroon
Acknowledgments : Dr Vilfrido Gil, Centre National des Grandes
Endémies, Sao Tomé - Dr Lucie Brunet, Service d'Action Culturelle,
Sao Tomé - Dr Conceiçao Ferreira, Centre National des Grandes
Endémies, Sao Tomé
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General Statistics
Area: 1,001 km² (Sao Tome: 836 km² ; Principe:
119 km²) Population: 134,785 inhabitants (1998
estimation) Capital: Sao Tome Currency: Dobra Official Language: Portuguese Surrounding regions: Sao Tome and Principe are two
islands, in the Gulf Of Guinea situated off the coast of Cameroon,
Equatorial Guinea and Gabon. 
Out of 192 countries, Sao Tome and Principe ranks 108th for life
expectancy, 80th for infant mortality, 176th for GNP, 163rd for
daily calorie intake, 147th for literacy, 130th for the percentage
of children in full-time education (source: Atlas Encyclopédique
Mondial, Nathan Ed., Paris 1996, pp.118-119). Sao Tome and Principe rest on the equator and so the climate is
hot and humid. There is however a relative dry season in July and
August, whilst the average temperature oscillates between 20 °C
(July - August) and 30 °C (January to April).
| Epidemiological facies
The oldest facts on malaria in Sao Tome and Principe are no more
than twenty years old. According to Gérard Martet et al., "Malaria has existed for a
very long time on the archipelago. It is characterized by a
permanent transmission with seasonal outbreaks that correspond with
the end of the rainy season and the start of the dry one
(April-May) Another slightly smaller peak occurs from
November–December. Transmission decreases with altitude: above 300m
of altitude the bio-ecology of the main vector (Anopheles
gambiae) and the drop in the density of the human population
cause the transmission to decline" (1). From the 10th to the17th May 1990, a number of tests were run in
Sao Tome on 780 children aged from 2 to 9 years old: the prevalence
rate of splenomegalies was at 24% and that of hematozoon carriers
41%; this means that Sao Tome can be classified as a meso-endemic
zone Of the 318 positive slides, Plasmodium
falciparum was present in 87.4% of
cases, Plasmodium ovale in
11%, Plasmodium malariae in
1.3% and Plasmodium vivax only
once (0.3%)(1). These figures were not confirmed in 1996 by L.F.
Loureiro et al.: who listed 87.2% of infections
from Plasmodium falciparum
only, 4.5% from Plasmodium
malariae, 3.5% from Plasmodium
vivax and 4.5% of mixed
infection. Plasmodium ovale was not
found (3). According to the “Direction du Plan du Ministère de la Santé”,
malaria is the leading cause or morbidity: in effect, 12,413 cases
of malaria were reported in 1991, 15,112 in 1992 and 12,514 in
1993, far greater than diarrhea and acute respiratory infections
(5). In 1988, 67,162 cases were reported, an incidence rate of 60%
(1). Malaria represents 25% of all reported deaths (5).
| Vectors
According to Jacques Brunhes et al., only four species of anopheles
were identified: Anopheles funestus, Anopheles gambiae,
Anopheles paludis and Anopheles pharoensis
(Les anophèles de la région afro-tropicale, logiciel ORSTOM Ed.,
1998).
| Chemoresistance
1. Resistance to chloroquine: in vivo: - The first case of chloroquine failure was reported in 1984
(CEITA J.G.V., in Proceedings of the Conference on Malaria in
Africa. Practical Considerations on Malaria Vaccines and Clinical
Trials, ed. Buck, A 142-156, Washington DC, U.S.A.I.D.). - In 1990, a WHO test over 7 days on 58 children showed a
chloroquine-resistance rate of 23% (RI: 9% ; RII: 14%) (1). - The National Anti-Malaria Program for Sao Tome and Principe
showed chloroquine to be 75% to 90% effective in vivo (simplified
WHO test) in 1995, 75% to 87.5% effective in 1996 and 75% effective
in 1997, without however giving any further precision as to the
group tested (V. Gil, comm. pers.) in vitro: Three studies have been published: in 1990, out of 10 strains
successfully tested, 9 were chloroquine resistant and one of these
at a very high level (1). In 1992-1993, 14 out of 29 isolates
(48.3%) were chloroquine resistant (8). In 1994, more than 90% of
the 53 isolates tested were chloroquine-resistant (3). 2. Resistance to other antimalarial drugs: No resistance to quinine, mefloquine or halofantrine has yet
been proved.(1, 3, 8). Sao Tome and Principe’s National Anti-Malaria Program showed the
sulfadoxine-pyrimethamine combination to be 90% to 99% effective in
vivo (Simplified WHO test) in the years 1995, 1996 and 1997,
without stating any more information concerning the test group (V.
Gil, comm. pers.). 3. Recommendations of the National Anti Malaria Program
: Since 25th february 2005, the NAMP recommends the
artesunate + amodiaquine association as first line treatment and
the coartem as second line treatment.
| The National Anti Malaria Program
According to J.L. Baptista et al., a mass chemoprophylaxis
campaign based upon free handouts of chloroquine was started in
1947. During the 80’s, anti-malaria action consisting in the use of
insect sprays and the screening and treating of patients, lead to a
significant drop in malaria caused morbidity and also the loss of
malaria immunity by the population. It is believed that clinical
cases totally disappeared between 1980 and 1983, which lead to the
termination of anti-malaria actions in 1984 , and consequently an
epidemic revival in 1985-1986 (8). Today, an active Anti Malaria program exists thanks to the
‘Centre National des Grandes Endémies’. The program employs 21
people and is well equipped. The action plan is built upon the
correct treatment of cases, the distribution of treated mosquito
nets (less than 1% of the population used them in 1996; 27,000 were
installed in 1998), and a chemoprophylaxis for pregnant women and
non immune people (V. Gil, comm. pers.).
| Research institutions
There is no malaria research in Sao Tome and Principe. The only
research undertaken is in conjunction with foreign teams.
| Advice to Travelers
According to the B.E.H. « Bulletin épidémiologique hebdomadaire
» n°24-25 of 14th june 2005, Sao Tome and Principe is classified
under chemoresistance group III which implies that travelers to the
region should take Mefloquine (Lariam®) or Atovaquone-Proguanil
combined treatment. Individual measures of protection against insect bites should
also be taken
| Bibliography
(only the first author is mentioned) 1. MARTET G. et Coll. - Le paludisme en République de Sao tomé
et Principe. Evaluation épidémiologique et chimiorésistance
de Plasmodium falciparum.
Bull. Soc. Path. Exot. 1991 ; 84: 273-280. 2. CAMBOURNAC F.J. - Contribution to the history of malaria
epidemiology and control in Portugal and some other places.
Parassitologia 1994 ; 36: 215-222. 3. LOUREIRO L.F. et Coll. - Malaria in Sao Tomé and Principe:
prevalence and drug-susceptibility. Ann. Trop. Med. Parasitol. 1996
; 90: 223-224. 4. RIPERT C. et Coll. - Epidémiologie de certaines endémies
parasitaires dans la ville de Guadalupe (République de Sao Tomé et
Principe). II. Autres endémies parasitaires. Bull. Soc. Path. Exot.
1996 ; 89: 259-261. 5. COCHET P., LOUIS F.J. - Sao Tomé e Principe, à la dérive du
continent africain. Med. Trop. 1996 ; 56: 21-24. 6. BAPTISTA J.L. - The history of malaria in Sao Tomé.
Considerations on an epidemic. Acta Med. Port. 1996 ; 9:
259-265. 7. BAPTISTA J.L. et Coll. - Variations dans les taux de lipides
plasmatiques en fonction de l'infection
à Plasmodium falciparum à Sao
Tomé. Parasite 1996 ; 4: 335-340. 8. BAPTISTA J.L. et Coll.
- Plasmodium falciparum
chloroquine and quinine sensitivity in asymptomatic and symptomatic
children in Sao Tomé Island. Trop. Med. Int. Health 1997 ; 2:
582-588. 9. BAPTISTA J.L. et Coll. - Cytokine levels during mild and
cerebral falciparum malaria in children living in a mesoendemic
area. Trop. Med. Int. Health 1997 ; 2: 673-679. 10. SNOUNOU G. et Coll. - Non immune patients in the Democratic
Republic of Sao Tomé e Principe reveal a high level of transmission
of Plasmodium ovale
and Plasmodium vivax despite
low frequency in immune patients. Acta Trop. 1998 ; 70:
197-203. 11. KASSANKOGNO Y. - Aperçu sur le programme de lutte contre le
paludisme africain pour la période 1996-1997. Malaria and
Infectious Diseases in Africa 1999 ; n°9bis: 52-61
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