4.6 Article

Elderberry Extract Outpatient Influenza Treatment for Emergency Room Patients Ages 5 and Above: a Randomized, Double-Blind, Placebo-Controlled Trial

Journal

JOURNAL OF GENERAL INTERNAL MEDICINE
Volume 35, Issue 11, Pages 3271-3277

Publisher

SPRINGER
DOI: 10.1007/s11606-020-06170-w

Keywords

elderberry; Sambucus nigra; influenza; treatment

Funding

  1. Wendel Family Foundation
  2. Research Program Committee of the Cleveland Clinic
  3. Cleveland Clinic Children's
  4. PharmaCare

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Background Black elderberry, used medicinally for centuries, decreased influenza duration by 4 days in three previous peer-reviewed trials. US elderberry sales, possibly related to a high severity and high activity influenza season from January to March 2018, more than doubled from 2017 to 2018 to > $100 million. Objective To determine whether elderberry extract decreases influenza's duration and severity. Design FDA-approved, investigator-initiated, Investigational New Drug, double-blind, randomized, placebo-controlled trial. Conducted January 2018-April 2019 in three emergency rooms, two suburban and one urban, in the Midwestern Health System. Patients Eighty-seven consecutive, consenting patients, over age four, with < 48 h of at least 2 moderate-severity influenza symptoms and positive polymerase chain reaction influenza test. Intervention Patients from age 5 to 12 years received placebo or 15 ml (5.7 g) elderberry extract orally twice a day for 5 days; those > 12 years received 15 ml 4 times a day for 5 days. Patients were permitted to choose to also receive the standard dosage of oseltamivir. Measurements Primary: days until all symptoms were none or mild for 21.5 h. Secondary: days to complete symptom resolution for 24 h. Results The 87 participants were randomized to receive placebo (n = 44) or elderberry (n = 43). The average age was 25 +/- 20 years, and 56% were male. The average number of days to reach all symptoms none or mild for 21.5 h in the placebo group was 4.9 +/- 2.8 days compared to 5.3 +/- 3.6 in the elderberry group (p = 0.57). The average number of days to complete resolution was 8.7 +/- 3.8 and 8.6 +/- 3.9 in the placebo and elderberry group, respectively (p = 0.87). Limitations Small sample size, but powered > 0.90 to detect 2-day benefit of elderberry versus placebo. Conclusions We found no evidence that elderberry benefits the duration or severity of influenza. Post hoc analysis suggested primary outcomes with elderberry taken alone (without oseltamivir) were 2 days worse than with placebo taken alone. Our results contradict previous studies and demonstrate the need for further studies.

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