[HTML][HTML] Inhaled zanamivir for the prevention of influenza in families

FG Hayden, LV Gubareva, AS Monto… - … England Journal of …, 2000 - Mass Medical Soc
FG Hayden, LV Gubareva, AS Monto, TC Klein, MJ Elliott, JM Hammond, SJ Sharp, MJ Ossi
New England Journal of Medicine, 2000Mass Medical Soc
Background As prophylaxis against influenza in families, amantadine and rimantadine have
had inconsistent effectiveness, partly because of the transmission of drug-resistant variants
from treated index patients. We performed a double-blind, placebo-controlled study of
inhaled zanamivir for the treatment and prevention of influenza in families. Methods We
enrolled families (with two to five members and at least one child who was five years of age
or older) before the 1998–1999 influenza season. If an influenza-like illness developed in …
Background
As prophylaxis against influenza in families, amantadine and rimantadine have had inconsistent effectiveness, partly because of the transmission of drug-resistant variants from treated index patients. We performed a double-blind, placebo-controlled study of inhaled zanamivir for the treatment and prevention of influenza in families.
Methods
We enrolled families (with two to five members and at least one child who was five years of age or older) before the 1998–1999 influenza season. If an influenza-like illness developed in one member, the family was randomly assigned to receive either inhaled zanamivir or placebo. The family member with the index illness was treated with either 10 mg of inhaled zanamivir (163 subjects) or placebo (158) twice a day for 5 days, and the other family members received either 10 mg of zanamivir (414 subjects) or placebo (423) once a day as prophylaxis for 10 days. The primary end point was the proportion of families in which at least one household contact had symptomatic, laboratory-confirmed influenza.
Results
The proportion of families with at least one initially healthy household contact in whom influenza developed was smaller in the zanamivir group than in the placebo group (4 percent vs. 19 percent, P<0.001); the difference represented a 79 percent reduction in the proportion of families with at least one affected contact. Zanamivir provided protection against both influenza A and influenza B. A neuraminidase-inhibition assay and sequencing of the neuraminidase and hemagglutinin genes revealed no zanamivir-resistant variants. Among the subjects with index cases of laboratory-confirmed influenza, the median duration of symptoms was 2.5 days shorter in the zanamivir group than in the placebo group (5.0 vs. 7.5 days, P=0.01). Zanamivir was well tolerated.
Conclusions
When combined with the treatment of index cases, prophylactic treatment of family members with once-daily inhaled zanamivir is well tolerated and prevents the development of influenza. In this study there was no evidence of the emergence of resistant influenza variants.
The New England Journal Of Medicine