JOURNAL OF THE
ROYAL MEDICAL SERVICES

Official Publication for the Jordanian Royal Medical Services


MALARIA INCIDENCE AMONG A GROUP JORDANIAN MILITARY TROOPS IN SIERRA LEONE - 2000


Sami Abu Rumman MD*, Yosef Wardat MD*, Mohamed Abu Rumman SN**, Munir Arabiat MD*, Mohamed Aljar MD^


ABSTRACT

Objective: To evaluate the efficacy of Mefloquine as a prophylactic treatment against malaria among Jordanian soldiers in Sierra Leone.

Methods: This is a retrospective study of 756 Jordanian soldiers among United Nation troops of Peace Keeping forces in Sierra Leone, during a period of 8 months extending from April until December 2000; they were given Mefloquine as a chemoprophylaxis upon United Nation recommendations in conjunction with Word Health Organization and Centers of Disease Control recommendations, other preventive measures were taken such as insect repellents and education.

Results: Out of the 756 soldiers of the battalion, only 39 [5.1%] had laboratory confirmed  malaria during this period, the patients who were diagnosed are admitted to the hospital with rapid improvement of their symptoms within 2 days of treatment, and by the 7th day all patients were free of any residual complaint.

Conclusion: Chemoprophylaxis with Mefloquine plus adequate preventive control measures against mosquito bites is not 100% effective to prevent falciparum malaria, but they reduce the incidence of the disease.

Key words: United Nation, Malaria, Mefloquine, Peas Keeping Forces.   

JRMS August 2008; 15(2): 38-40     
                                                                                                                                         
 
Introduction

Malaria in humans is caused by one of four protozoan species of the genus Plasmodium: P. falciparum, P. vivax, P. ovale, or P. malariae. All species are transmitted through the bite of an infected female Anopheles mosquito. Occasionally, transmission occurs by blood transfusion, organ transplantation, needle sharing, or congenitally from mother to fetus. Although malaria can be a fatal disease, in West Africa mainly in Sierra Leone.(1-3) Illness and death from malaria are largely preventable.(4,5)

 World wide it affects 270 million people each year, and has mortality rate of 1%. About 90% of Malaria cases and deaths are believed to occur in West Africa where is the incidence rate without prophylaxis estimated to be 1.4% per month.(6)  Travelers to this area have 1-4% chance to catch the disease.(7)  Malaria is found in all countries between the latitudes 30°S and 40°N and considered a primary disease of hot humid countries at altitudes less than 2200 m above mean sea level where conditions are ideal for prolific breeding of the mosquito, Anopheles.(4)

Travelers from temperate climate where infection with Plasmodium falciparum is endemic are at particular risk of morbidity and mortality, chemoprophylaxis with an antimalarial drug is generally recommended by World Health Organization and Centers for Disease Control.

United Nations recommendations obliged all military personal to take chemoprophylaxis in malarious areas to reduce the non-battle casualties, and to take Mefloquine as a chemoprophylactic agent in the following regimen:

-    The dosage is 250 mg (one tablet) once a week in the mission area.
-    The first dose should be taken 1 week before arrival to the malaria-risk area.
-    Dose should be taken once a week, at the same day of the week, while in the risk area.
-    Dose should be taken once a week for 4 weeks after leaving the risk area.
-    The drug to be taken on a full stomach with a full glass of liquid.


Methods

This is a retrospective study of 752 Jordanian military personal. The data was collected from the hospital medical records, the age range was 19-42 years and the mean age was 28 years.

All were participants among United Nations of peace keeping forces in Sierra Leone, who where given Mefloquine during a period of 8 months extending from April until December 2000, all personnel were enrolled in the study. Soldiers took the drug once weekly on Friday after lunch.

All our soldiers were young, healthy according to medical examination done prior to the mission.

The protective measures against the vector of malaria and insects were appliedthroughthefollowingmethods:                                                                                                                                                                  
-    Using the insect repellent on exposed parts of the body.
-    Weekly lecture by the medical staff about malaria and benefit of personal protective
-    Measures and Mefloquine against disease.
-    Medical staff was taking the drug in front of soldiers.
-    The officers checked their soldiers daily that they used the bed nets at night.
-    The soldiers are ordered to keep sleeves rolled down.     
-    Fumigation was done daily mainly in the evening when the mosquitoes were highly active.
-    The sources, which attracted insects, were sprayed weekly.
All suspected malaria cases were laboratory tested by thick smear and / or rapid test. All laboratories confirmed malaria cases were admitted and soon started proper anti malarial treatment.


Results

Out of the 756 soldiers of the battalion, only 39 [5.1%] had clinically manifested malaria during this period, the patients admitted to the hospital with rapid improvement of their symptoms within 2 days, and by the 7th day all patients were free of any residual symptom. The species was Plasmodium falciparum.

 Pallor, mild splenomegaly and tinge of jaundice were seen in a considerable number of patients, splenomegaly and hepatomegaly have persisted for the next 2-4 weeks of initiating treatment.

The evolution of symptoms in treated patients is illustrated in Table I.
.
Table I. Number of malaria cases with various presenting symptoms and the progressive disappearance of symptoms in the post-treatment period

Symptoms 

Day

0

Day 1

Day 2

Day 3

Day

 4

Day

5

Chills

35

6

0

0

0

0

Fever

38

2

0

0

0

0

Sweating

28

8

0

0

0

0

Bone aches

38

12

2

0

0

0

Cough

10

4

1

0

0

0


Both fever and bone aches were the most frequent presenting symptoms of the disease (38) followed in order of frequency by chills (35) and sweating (28).

As evidenced from this table the majority of patients felt well within 24 hours of starting treatment with dramatic improvement within the first 2 days and by the 7th day all patients were free of any residual symptoms.

Pallor, mild soft splenomegaly along with tinge of jaundice was seen in a considerable number of patients (38, 38 and 31 respectively). While tinge of jaundice has disappeared after initiating treatment, splenomegaly and hepatomegaly have persisted for the next 2-4 weeks with slow regression in some patients (Table II).

Table II. Number of malaria cases with various presenting signs and the progressive disappearance of signs in the post treatment days.

 Initial signs

Day 0

Day 1

Day 2

Day 3

Day 4

Day 5

Pallor

38

38

38

38

21

14

Splenomegaly

38

38

38

38

38

26

Hepatomegaly

17

17

17

12

10

9

Tinge of jaundice

31

28

4

0

0

0


Table III
shows that anemia has been corrected in 37 patients within 5 days after treatment; mild hyperbilirubinemia had disappeared within 48 hours of treatment. No side effects of anti malarial medications were reported.  

Table III. Frequency of relevant laboratory results and their evolution during and after treatment among 39 Falciparum malaria cases

Laboratory Results

Day 0

Day 1

Day 2

Day3

Day 4

Day 5

Anemia

38

38

38

38

16

1

Bilirubin>

1 mg/dl

37

35

18

0

0

0



Discussion

Mefloquine is an orally administered blood schizontide for prophylaxis against malaria and for treatment. Studies between 1977 and 1988 demonstrated efficacy of Mefloquine against multidrug resistant Plasmodium falciparum. Several studies suggested high protective efficacy of Mefloquine more than 91% of travelers to areas with resistant Plasmodium falciparum, it was also effective against Plasmodium vivax.(2,7,8,9)

 Centers for Disease Control advice all travelers to take Mefloquine for prophylaxis against malaria and reported that Mefloquine has rarely been reported to cause serious side effects, such as seizures, depression, and psychosis.(10) These serious side effects are more frequent with the higher doses used to treat malaria; few side effects occurred at the weekly prophylactic doses used to prevent malaria. The most common side effects reported by travelers taking Mefloquine include headache, nausea, dizziness, and difficulty in sleeping, anxiety, vivid dreams, and visual disturbances.(11)

 Higher incidence of  malaria cases in the Jordanian Hospital in Sierra Leone between January 2002 and July 2002 and United States troops deployed in Somalia between December 1992 and May 1993 and others was low compliance with personal protective measures and chemoprophylaxis.(7,12,13)

Mefloquine is eliminated slowly by the body and thus may stay in the body for a while even after the drug is discontinued. Therefore, side effects caused by Mefloquine may persist weeks to months after the drug has been stopped. The side effects of Mefloquine which occurred at the weekly prophylactic dose (250mg) rarely necessitate discontinuation and replacement of Mefloquine with other prophylactic treatment.  Most travelers taking Mefloquine do not have serious side effects necessitating stopping taking the drug.


Conclusion

Chemoprophylaxis with Mefloquine plus adequate preventive control measures against mosquito bites is not 100% effective to prevent falciparum malaria, but they reduce the incidence of the disease.


References

1. Centers for Disease Control and Prevention. Malaria information for travelers to countries in West Africa. Travelers Health; Regional Malaria Information file//C; My document/Destinations Malaria west Africa CDC Travelers Health. tm.

2.Parveen K, Michael C.
Clinical Medicine. Fourth edition; 1999: 77-80.

3.Goldman AB. BCh. Current Views on Malaria prophylaxis 12/11/ 2005. Avilabile from http://www.priory.com/ malaria.htm.

4.Filler S, CauserLM, Newman RD, et al.
Malaria surveillance USA 2001. MMWR Surveill Summ   2003; 52(5): 1-14. 
       
5.Huges C, Tucker R, Bannister B, Bradley DJ.
Malaria prophylaxis for long-term travelers. Communicable Disease and Public Health 2003; 6(3): 201-208.

6.Armengaud M. Arguments against Chemoprophylaxis in areas at low risk for chloroquine-resistant Pl. Falciparum. J Travel Med 1995; 2(1): 4-5.

7.Richie TL,Widjaja H, et al. Mefloquine compared with Doxacycline for the prophylaxis of malaria in Indonesian Soldiers, Ann Intern Med 1997; 126(12): 963-972.

8. Knobloch J. Long-Term Malaria Prophylaxis for Travelers. J Rravel Med 2004; 11(6): 374-378. 
 
9.Croft A Garner P. Mefloquine to prevent Malaria: A systematic review of trials, BMJ 1997; 315: 1412-1416.

10.Centers for Disease Control and Prevention. Information for the public: Prescription drugs for malaria, Available from www.CDC.cov

11. Kitchener ST, Nasveld PE, Gregory RM, Edstein MD. Mefloquine and doxycycline malaria prophylaxis in Australian soldiers in East Timor. MJA 2005; 182(4): 168-171.

12.Kwar GI, Maayah JF.
Malaria among Jordanian Medical Team on prophylactic Mefloquine in Sierra Leone.  JRMS 2004; 11(1): 10-12.

13.Wallace MR, Sharp TW, Smoak B. Malaria among United States troops in Somalia. Am J Med 1996; 100(1): 49- 55.

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