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CLINICAL REVIEW:
David G Lalloo and David R Hill
Preventing malaria in travellers
BMJ 2008; 336: 1362-1366 [Full text]
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[Read Rapid Response] Preventing malaria in travellers, the HIV patient.
Ahmed H. Omar, Anne E. McCarthy, Associate Professor of Medicine   (15 June 2008)

Preventing malaria in travellers, the HIV patient. 15 June 2008
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Ahmed H. Omar,
Honorary Research Assistant
Ottawa General Hospital Campus, ON, K1H 8L6, Canada,
Anne E. McCarthy, Associate Professor of Medicine

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Re: Preventing malaria in travellers, the HIV patient.

We read with interest the review by Lalloo and Hill (1), but we were surprised to see no mention of an important risk group, the HIV positive traveller. The advent of highly active antiretroviral therapy (HAART) has markedly improved the health and quality of life for these individuals, allowing them to live full and active lives, this includes travel to malaria endemic areas (2). The counselling of these patients requires an accurate risk assessment taking into account the level of immune compromise and the risks involved in travelling to tropical countries (3, 4).
HIV-infected adults are more prone to acquiring malaria and are at an increased risk of severe malaria and death. Therefore, prevention of malaria is even more important in these individuals.
Patients’ awareness of malaria risk is crucial. A 2006 survey in our department of 124 HIV-infected patients, showed that 46% of patients (N=19/41) with recent travel had visited a country with a malaria risk (5). Interestingly, of 21 patients born in malaria endemic countries, nine (43%) stated that their birth country was not at risk of malaria, a lack of awareness which may prevent seeking appropriate precautions prior to travel. Consistent with these findings, a survey of 130 HIV patients living in Toronto who travelled internationally showed that more than 50% visited malaria areas, but only 7% had taken chemoprophylaxis (6). These results suggest that a significant number of HIV patients travel to malaria endemic areas, but a portion of them may not be taking adequate chemoprophylaxis.
An important issue is the possible toxic interaction of antimalarials with antiretroviral drugs. This is more complicated if their regimen includes a protease inhibitor, shown to be the case in approximately 60% to 70% of HIV patients in Ottawa and Toronto-based centres (5, 6).
Special consideration needs to be made for patients going to areas of Chloroquine Resistant Plasmodium Falciparum Malaria (CRPF). The current first-line drugs recommended by the Public Health Agency of Canada for CRPF malaria include Doxycycline, Mefloquine and Atovaquone/Proguanil (Malarone) (7). There remains a paucity of data about the safe use of these drugs with HIV therapy. A study conducted at our institution demonstrated a concerning 40% decrease in Ritonavir levels when co-administered with Mefloquine (8). Doxycycline is often utilised in this travelling population, but must be continued for four weeks after leaving the malaria-endemic areas.
Malarone is well tolerated and only requires continuation for 7 days after malaria exposure, thus having a potential to limit pill burden in this population. Currently there is a lack of data on the safety and potential interactions of Malarone with protease inhibitors (9). Future research is important to establish its safety in this context.
Patient counselling is imperative in this setting and until more data is available, the choice of malaria chemoprophylaxis for HIV positive travellers on HAART remains limited and will need careful selection.

Dr. Ahmed H. Omar, Honorary Research Assistant.
Dr. Anne E. McCarthy, Associate Professor of Medicine.
Division of Infectious Diseases, the Ottawa Hospital General campus, Ottawa, Canada.
E-mail correspondence: ahomar@toh.on.ca or amccarthy@ottawahospital.on.ca

References:
1. Lalloo DG, Hill DR. Preventing malaria in travellers. BMJ 2008;336:1362-1366 (14 June), doi:10.1136/bmj.a153.
2. Castelli F, Patroni A. The human immunodeficiency virus–infected traveller.Clin Infect Dis 2000; 31:1403–1408.
3. Malaria and HIV interactions and their implications for public health policy. Geneva, Switzerland, WHO. Technical Consultation. 2004.
4. McCarthy AE, Mileno MD. Prevention and treatment of travel-related infections in compromised hosts.Curr Opin Infect Dis. 2006 Oct;19(5):450-5.
5. Béïque L, Denommé N, la Porte C, Thibert J, McCarthy AE: Travel Survey among Canadian HIV-Infected patients PO01.05 10th Conference of the International Society of Travel Medicine (CISTM10). Vancouver May 20-24, 2007.
6. Salit IE, Sano M, Boggild AK, Kain KC. Travel patterns and risk behaviour of HIV-positive people travelling internationally. CMAJ 2005;172(7):884-8.
7. Health Canada. Canadian recommendations for the prevention and treatment of malaria among international travelers. CCDR 2004;30S1: 1-62.
8. Khaliq Y, Gallicano K, Tisdale C, et al. Pharmacokinetic interaction between mefloquine and ritonavir in healthy volunteers. Br J Clin Pharm 2001;6: 591-600.
9. Khoo S, Back D, Winstanley P. The potential for interactions between antimalarial and antiretroviral drugs. AIDS 2005; 19: 995-1005.

Competing interests: None declared