Clinical Features of Imported Loiasis: A Case Series from the Hospital for Tropical Diseases, London

Makoto Saito Hospital for Tropical Diseases, London, United Kingdom; London School of Hygiene and Tropical Medicine, London, United Kingdom

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Margaret Armstrong Hospital for Tropical Diseases, London, United Kingdom; London School of Hygiene and Tropical Medicine, London, United Kingdom

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Samuel Boadi Hospital for Tropical Diseases, London, United Kingdom; London School of Hygiene and Tropical Medicine, London, United Kingdom

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Patricia Lowe Hospital for Tropical Diseases, London, United Kingdom; London School of Hygiene and Tropical Medicine, London, United Kingdom

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Peter L. Chiodini Hospital for Tropical Diseases, London, United Kingdom; London School of Hygiene and Tropical Medicine, London, United Kingdom

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Tom Doherty Hospital for Tropical Diseases, London, United Kingdom; London School of Hygiene and Tropical Medicine, London, United Kingdom

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We retrospectively analyzed the background, clinical features, and treatment response of 50 cases of imported loiasis who presented between 2000 and 2014 to the Hospital for Tropical Diseases (HTD), London, United Kingdom. Of them, 29 were migrants from, and 21 were visitors to, countries where the disease is endemic. Clinical features differed between these groups. Migrants experienced fewer Calabar swellings (odds ratio [OR] = 0.12), more eye worm (OR = 3.4), more microfilaremia (OR = 3.5), lower filarial antibody levels, and lower eosinophil counts (P < 0.05 for all tests). Among 46 patients who were started on treatment at HTD, 33 (72%) received diethylcarbamazine (DEC) monotherapy as first-line treatment, and among 26 patients who were followed up after treatment, seven (27%) needed a second course of treatment. There were 46 courses of treatment with DEC, and 20 (43%) of them had reactions. All patients with microfilaremia > 3,000 microfilariae/mL and all those with an elevated C-reactive protein (CRP) (≥ 5 mg/L) before treatment had reactions (P = 0.10 and P = 0.01, respectively). These data suggest that monotherapy with DEC may not be the optimal treatment for patients with loiasis, particularly for those with a high microfilarial load.

Author Notes

* Address correspondence to Makoto Saito, London School of Hygiene and Tropical Medicine, Keppel Street, London, WC1E 7HT, United Kingdom. E-mail: makosaitou-tky@umin.ac.jp

Financial support: Makoto Saito is supported by GlaxoSmithKline International Scholarship Charitable Trust Fund. Margaret Armstrong is supported by the Special Trustees of the Hospital for Tropical Diseases. Peter L. Chiodini is supported by the National Institute for Health Research University College London Hospitals Biomedical Research Centre.

Authors' addresses: Makoto Saito, London School of Hygiene and Tropical Medicine, London, United Kingdom, E-mail: makosaitou-tky@umin.ac.jp. Margaret Armstrong, Samuel Boadi, Patricia Lowe, Peter L. Chiodini, and Tom Doherty, Hospital for Tropical Diseases, London, United Kingdom, E-mails: margaret.armstrong@uclh.nhs.uk, samuel.boadi@uclh.nhs.uk, patricia.lowe@uclh.nhs.uk, peter.chiodini@uclh.nhs.uk, and tom.doherty1957@gmail.com.

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