Background: Imported malaria is quite common in the United States. Increasi
ng antimalarial drug resistance and changes in travel patterns may have imp
ortant implications for the prevention, clinical presentation, and manageme
nt of this disease.
Methods: Medical records were reviewed for 121 patients with microscopicall
y confirmed malaria diagnosed at 2 university-affiliated hospitals in San F
rancisco, Calif, between 1988 and 1997.
Results: Among 57 travelers from the United States, only 13 (23%) had been
compliant with an appropriate chemoprophylactic regimen. No patients develo
ped falciparum malaria after consistent chemoprophylactic therapy with mefl
oquine hydrochloride. However, 12 (19%) of US residents with imported malar
ia developed Plasmodium vivax or Plasmodium ovale infections despite an app
ropriate chemoprophylactic regimen, generally with a late onset suggestive
of relapsing disease. Clinical presentations were similar between foreign r
esidents and American travelers and between patients with falciparum and no
nfalciparum infections; 98% of patients had a history of fever. Sixteen per
cent of patients had received previous evaluations during which the diagnos
is of malaria was not considered. In 9% of patients, there were errors in t
reatment. Only I patient developed severe malaria.
Conclusions: Our results suggest that a standard chemoprophylactic regimen
is highly effective in preventing falciparum malaria, but that many America
n travelers do not receive it. Also, relapsing P vivax or P ovale infection
despite appropriate chemoprophylactic therapy was not uncommon among our c
ases. The presentation of imported malaria is nonspecific, highlighting the
need to consider the diagnosis in any febrile patient who has been in a ma
laria-endemic area. Although errors in diagnosis and treatment were quite c
ommon in our study population, patient outcomes were good once the appropri
ate therapy was initiated.