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The safety of combined triple drug therapy with ivermectin, diethylcarbamazine and albendazole in the neglected tropical diseases co-endemic setting of Fiji: A cluster randomised trial

Author

Listed:
  • Myra Hardy
  • Josaia Samuela
  • Mike Kama
  • Meciusela Tuicakau
  • Lucia Romani
  • Margot J Whitfeld
  • Christopher L King
  • Gary J Weil
  • Anneke C Grobler
  • Leanne J Robinson
  • John M Kaldor
  • Andrew C Steer

Abstract

Lymphatic filariasis has remained endemic in Fiji despite repeated mass drug administration using the well-established and safe combination of diethylcarbamazine and albendazole (DA) since 2002. In certain settings the addition of ivermectin to this combination (IDA) remains a safe strategy and is more efficacious. However, the safety has yet to be described in scabies and soil-transmitted helminth endemic settings like Fiji. Villages of Rotuma and Gau islands were randomised to either DA or IDA. Residents received weight-based treatment unblinded with standard exclusions. Participants were actively found and asked by a nurse about their health daily for the first two days and then asked to seek review for the next five days if unwell. Anyone with severe symptoms were reviewed by a doctor and any serious adverse event was reported to the Medical Monitor and Data Safety Monitoring Board. Of 3612 enrolled and eligible participants, 1216 were randomised to DA and 2396 to IDA. Age and sex in both groups were representative of the population. Over 99% (3598) of participants completed 7 days follow-up. Adverse events were reported by 600 participants (16.7%), distributed equally between treatment groups, with most graded as mild (93.2%). There were three serious adverse events, all judged not attributable to treatment by an independent medical monitor. Fatigue was the most common symptom reported by 8.5%, with headache, dizziness, nausea and arthralgia being the next four most common symptoms. Adverse events were more likely in participants with microfilaremia (43.2% versus 15.7%), but adverse event frequency was not related to the presence of scabies or soil-transmitted helminth infection. IDA has comparable safety to DA with the same frequency of adverse events experienced following community mass drug administration. The presence of co-endemic infections did not increase adverse events. IDA can be used in community programs where preventative chemotherapy is needed for control of lymphatic filariasis and other neglected tropical diseases.Author summary: Lymphatic filariasis is a parasitic infection that is spread between humans by mosquitos. The adult worms can live up to 6 years in humans causing chronic irreversible damage to lymphatic vessels resulting in permanent limb swelling known as elephantiasis. The filariasis worm is susceptible to three different drugs: ivermectin, diethylcarbamazine and albendazole. They have been used in two drug combinations globally in communities at risk of filariasis infection, including Fiji, for over a decade. In an attempt to improve efficacy of the treatment with the ultimate goal of eliminating the infection, the three drugs are now being used in the one administration. In this study, the safety of the triple combination in Fiji was proven to be as safe as the standard two drug treatment. Two other common infections that will be affected by the new treatment, scabies and intestinal worms, did not impact on the frequency of adverse events. The use of the triple combination in Fiji has the potential to improve the control of common neglected diseases without excess side effects.

Suggested Citation

  • Myra Hardy & Josaia Samuela & Mike Kama & Meciusela Tuicakau & Lucia Romani & Margot J Whitfeld & Christopher L King & Gary J Weil & Anneke C Grobler & Leanne J Robinson & John M Kaldor & Andrew C Ste, 2020. "The safety of combined triple drug therapy with ivermectin, diethylcarbamazine and albendazole in the neglected tropical diseases co-endemic setting of Fiji: A cluster randomised trial," PLOS Neglected Tropical Diseases, Public Library of Science, vol. 14(3), pages 1-17, March.
  • Handle: RePEc:plo:pntd00:0008106
    DOI: 10.1371/journal.pntd.0008106
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