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| Cases |
From the Tropical Diseases Unit (Boggild, Keystone) and the Division of Infectious Diseases (Boggild, Page, Keystone, Morris, Conrad, Liles), Toronto General Hospital, University Hospital Network and Mount Sinai Hospital; and the Department of Medicine (Page, Keystone, Morris, Conrad, Liles), University of Toronto, Toronto, Ont.
Correspondence to: Dr. Andrea K. Boggild, Tropical Diseases Unit, Toronto General Hospital, 200 Elizabeth St., North Wing, 13th Floor, Rm. 1350, Toronto ON M5G 2C4; fax 416 340-3260; andrea.boggild{at}utoronto.ca
A 68-year-old Canadian woman originally from the Democratic Republic of Congo returned to Canada after a 10-month stay in the Congo where she was visiting friends and relatives. She had taken no chemoprophylaxis for malaria and sought no pretravel advice. Three days after returning to Canada, she began to have fever, nausea and vomiting. She visited a walk-in clinic, but she was sent home with no specific therapy. Later that day, she presented to an emergency department, and she was again discharged home. Four days after the onset of symptoms, she was taken to the emergency department by her family, who found her to be lethargic, confused, feverish and incontinent. Thick and thin smears for malaria were performed. An infection of Plasmodium falciparum was detected, with 35% parasitemia (Figure 1). The patient was transferred to our hospital, where she was admitted to the intensive care unit. She was given quinine intravenously and 1 cycle of exchange transfusion. Although she had hypoglycemia (glucose in random samples 3.1 mmol/L), hyperbilirubinemia (total bilirubin 78 µmol/L), mild acute renal failure (creatinine 119 µmol/L) and thrombocytopenia (platelet count 16 x 109 cells/L), her symptoms responded well to quinine and a solution of 10% dextrose in water. Within 24 hours, she was coherent and afebrile.
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Repeat malaria smears performed 12, 24, and 48 hours after admission revealed parasitemia of 9.5%, 3% and < 1%, respectively. Intravenous quinine therapy was stopped and her treatment course was completed with quinine and doxycycline taken orally for 7 days total. She was discharged after 3 days in hospital. At this time, she had normoglycemia (glucose in random samples 4.2 mmol/L), mild anemia (hemoglobin 103 g/L) and thrombocytopenia (platelet count 76 x 109 cells/L). There was no parasitemia at discharge, and she was well 6 months after discharge.
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Discussion |
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Clinical presentation
Malaria is caused by protozoan parasite members of the genus Plasmodium and is transmitted via bites from infected Anopheles mosquitoes. Almost all deaths due to severe malaria are caused by infection with P. falciparum (Box 1).
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Fever is a common chief complaint of patients with malaria and occurs in 80%–90% of cases. 3–6 Other symptoms, such as malaise, coughing, vomiting, diarrhea, abdominal pain or headache, may be predominant. More than 90% of patients with malaria caused by P. falciparum show symptoms within 1 month of returning from travel. Almost all present for care within 2 months of the initial infection, although this may be delayed if the patient has taken chemoprophylaxis. 1,6,7
Malaria is endemic throughout the tropics and subtropics. The prevalence of malaria is high in sub-Saharan Africa and parts of Oceania, where the relative risks of malaria among travellers are 207.6 and 76.7, respectively. 7 Malaria can be prevented by a combination of mosquito-avoidance measures (e.g., mosquito netting, insect repellents, coils and sprays) and chemoprophylactic agents. No chemoprophylactic agent is 100% effective; thus, malaria should still be considered in febrile patients who have taken prophylaxis. Obtaining a detailed travel history, including destination, nature and duration of travel and adherence to preventive measures, in addition to a clinical history, is essential for diagnosing malaria.
About 400 cases of malaria occur each year in travellers returning to Canada. Most of these cases are caused by infection with P. falciparum, which can quickly lead to severe and potentially fatal disease in people who are not immune, including tourists, business travellers and people visiting friends and relatives. Although many people who grew up in countries where malaria is endemic believe themselves to be immune, 7,8 immunity begins to wane within 6 months of departure from the endemic area in the absence of re-exposure. 9–11 Thus, malaria should be included in the differential diagnosis of fever for people who were born in or previously lived in areas where malaria is endemic.
Malaria in children
Children born in countries where malaria is not endemic who travel to areas with malaria (e.g., their parents’ place of birth) represent a particularly vulnerable group of travellers. In this group of children, reported adherence to appropriate chemoprophylaxis is only 3%–15%. This may be, in part, attributed to the false assumption on the part of parents that their children are protected because of their ethnic background. 12,13 In many European countries, the greatest number of imported cases of malaria are among children. 12 Peak incidences of imported malaria in children visiting friends and relatives coincide with school holidays, mainly during the summer months and December and January. 12
Children are more likely than adults to present with non-specific symptoms, such as fever, lethargy and malaise, and gastrointestinal complaints, such as nausea, vomiting, abdominal pain and diarrhea. They are also more likely to have hepatosplenomegaly and jaundice. Children, especially those under 5 years of age, are more vulnerable to severe and cerebral manifestations of malaria. 4,6,12
Making the diagnosis
Of the imported cases of P. falciparum malaria in Canada, about 15 per year will have severe manifestations, leading to 1–2 deaths annually. 6 Inadequate or no chemoprophylaxis, the inability of health care providers to recognize the importance of fever in returned travellers, and the delayed initiation of treatment all contribute to the burden of severe imported malaria in Canada. 6,14 Exclusion of malaria requires 3 separate blood smears performed and promptly read at 12-hour intervals over a 24–48 hour period. 5,6 If a dipstick assay is used, it must be followed up with confirmatory blood smears, which allow for quantification of parasitemia and a determination of the species.
In this case, the patient made a complete recovery, despite having greater than 30% parasitemia and systemic involvement; this is an atypical result. A recent case series described 7 cases of fatal imported malaria in Canadian travellers or visitors to Canada. 14 None of these patients had the level of parasitemia observed in our patient. Although prompt initiation of parenteral antimalarial therapy can be life-saving for those with severe malaria, the fatality rate in this group remains between 10% and 30%, even if patients receive appropriate therapy. 4,6 Thus, recognition of malaria as a potential cause of illness in returned travellers, coupled with early diagnosis and initiation of treatment before the development of severe manifestations, provides the greatest likelihood of a successful clinical outcome. Uncomplicated malaria is easily treated with short courses of antimalarial drugs taken orally. Most patients who receive quick diagnosis and treatment recover uneventfully. Physicians should strongly consider seeking support from a consultant or an expert in infectious diseases for any patient in whom the diagnosis of malaria is confirmed (Box 2).
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Malaria continues to pose a diagnostic dilemma for physicians in countries where it is not endemic. 5,14,15 This case is a reminder to all front-line clinicians to suspect malaria in returning travellers who present with fever and to obtain a travel history, particularly if the patient’s primary complaint is fever.
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Footnotes |
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Competing interests: None declared.
The section Cases presents brief case reports that convey clear, practical lessons. Preference is given to common presentations of important rare conditions, and important unusual presentations of common problems. Articles start with a case presentation (500 words maximum) and a discussion of the underlying condition follows (1000 words maximum). Generally, up to 5 references are permitted and visual elements (e.g., tables of the differential diagnosis, clinical features or diagnostic approach) are encouraged. Written consent from patients for publication of their story is a necessity and should accompany submissions. See information for authors at www.cmaj.ca.
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