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1.
J Travel Med ; 12(5): 248-53, 2005.
Article in English | MEDLINE | ID: mdl-16256047

ABSTRACT

BACKGROUND: Traveling to tropical regions is related to increased health risks. Travelers' diarrhea is the most frequent health problem, but the range of travel-related diseases also includes potential life-threatening diseases such as malaria. The actual risk of European travelers acquiring specific infectious diseases and other hazards in the tropics is to a large extent unknown and is therefore often adopted from that of the indigenous population. The objective of this study was to elucidate the risk for travel-related diseases, symptoms, and accidents in a population of Europeans who travel to popular tourist destinations. METHODS: From July 2003 to June 2004, 794 travelers consulting the travel clinic of the Berlin Institute of Tropical Medicine were recruited for a questionnaire-based observational study before traveling to Kenya, Tanzania, Senegal, the Gambia, India, Nepal, Thailand, or Brazil. RESULTS: Overall, illness was reported by 42.9% of travelers, with 10.2% reporting more than one adverse health event. Most frequently gastrointestinal symptoms were noted (34.6%), followed by respiratory symptoms (13.7%). More than 5% experienced an accident. Travel to the Indian subcontinent nearly doubled the risk of becoming ill; travel to Thailand significantly decreased the risk. Additional risk factors were a long duration of staying abroad, young age, and traveling under basic conditions. Of all travelers, 80% did not follow the traditionally recommended dietary restrictions. Among travelers visiting malaria-endemic areas, 20% did not carry any antimalarial drugs with them, not continuous chemoprophylaxis or standby medication. CONCLUSIONS: Because of the rising travel activity, especially to tropical countries, the importance of qualified pretravel advice consultation is increasing. To improve the travelers' health, attention needs to be paid to individual risk factors, the prevention and therapy of travelers' diarrhea, malaria prophylaxis, management of respiratory illness, and personal safety.


Subject(s)
Accidents/statistics & numerical data , Diarrhea/epidemiology , Health Knowledge, Attitudes, Practice , Malaria/epidemiology , Risk-Taking , Travel , Adult , Aged , Aged, 80 and over , Communicable Disease Control/methods , Communicable Diseases/epidemiology , Developing Countries , Diarrhea/prevention & control , Europe , Female , Health Education/methods , Health Services/statistics & numerical data , Humans , Malaria/prevention & control , Male , Middle Aged , Risk Factors , Surveys and Questionnaires
2.
J Infect Dis ; 190(9): 1541-6, 2004 Nov 01.
Article in English | MEDLINE | ID: mdl-15478057

ABSTRACT

BACKGROUND: Two single-point mutations of the Plasmodium falciparum cytochrome b gene (Tyr268Asn and Tyr268Ser) were recently reported in cases of atovaquone/proguanil (Malarone) treatment failure. However, little is known about the prevalence of codon-268 mutations and their quantitative association with treatment failure. METHODS: We set out to assess the prevalence of codon-268 mutations in P. falciparum isolates imported into Europe and to quantify their association with atovaquone/proguanil treatment failure. Isolates of P. falciparum collected by the European Network on Imported Infectious Disease Surveillance between April 2000 and August 2003 were analyzed for codon-268 mutations, by use of polymerase chain reaction-restriction fragment-length polymorphism. RESULTS: We successfully screened 504 samples for the presence of either Tyr268Ser or Tyr268Asn. One case of Ser268 and no cases of Asn268 were detected. Therefore, we can be 95% confident that the prevalence of Ser268 in the European patient pool does not exceed 0.96% and that Asn268 is less frequent than 0.77%. In 58 patients treated with atovaquone/proguanil, Tyr268Ser was present in 1 of 5 patients with treatment failure but in 0 of 53 successfully treated patients. CONCLUSIONS: Tyr268Ser seems to be a sufficient, but not a necessary, cause for atovaquone/proguanil treatment failure. The prevalence of both codon-268 mutations is currently unlikely to be >1% in the European patient pool.


Subject(s)
Antimalarials/pharmacology , Malaria, Falciparum/parasitology , Naphthoquinones/pharmacology , Plasmodium falciparum/drug effects , Plasmodium falciparum/genetics , Point Mutation , Proguanil/pharmacology , Adolescent , Adult , Aged , Amino Acid Substitution , Animals , Atovaquone , Codon , Cytochromes b/genetics , Cytochromes b/physiology , DNA, Protozoan/analysis , DNA, Protozoan/isolation & purification , Drug Combinations , Drug Resistance/genetics , Europe , Female , Genes, Protozoan , Humans , Malaria, Falciparum/drug therapy , Male , Middle Aged , Molecular Epidemiology , Mutation, Missense , Naphthoquinones/therapeutic use , Plasmodium falciparum/isolation & purification , Polymorphism, Restriction Fragment Length , Proguanil/therapeutic use , Protozoan Proteins/genetics , Protozoan Proteins/physiology , Treatment Failure
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