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Oseltamivir compared with the Chinese traditional therapy maxingshigan-yinqiaosan in the treatment of H1N1 influenza: a randomized trial.
Wang, Chen; Cao, Bin; Liu, Qing-Quan; Zou, Zhi-Qiang; Liang, Zong-An; Gu, Li; Dong, Jian-Ping; Liang, Li-Rong; Li, Xing-Wang; Hu, Ke; He, Xue-Song; Sun, Yan-Hua; An, Yu; Yang, Ting; Cao, Zhi-Xin; Guo, Yan-Mei; Wen, Xian-Min; Wang, Yu-Guang; Liu, Ya-Ling; Jiang, Liang-Duo.
Afiliación
  • Wang C; Beijing Chao-Yang Hospital, Beijing Institute of Respiratory Medicine, Capital Medical University, Beijing, China. cyh-birm@263.net
Ann Intern Med ; 155(4): 217-25, 2011 Aug 16.
Article en En | MEDLINE | ID: mdl-21844547
ABSTRACT

BACKGROUND:

Observational studies from Asia suggest that maxingshigan-yinqiaosan may be effective in the treatment of acute H1N1 influenza.

OBJECTIVE:

To compare the efficacy and safety of oseltamivir and maxingshigan-yinqiaosan in treating uncomplicated H1N1 influenza.

DESIGN:

Prospective, nonblinded, randomized, controlled trial. (ClinicalTrials.gov registration number NCT00935194)

SETTING:

Eleven hospitals from 4 provinces in China. PATIENTS 410 persons [corrected] aged 15 to 69 [corrected] years with laboratory-confirmed H1N1 influenza. INTERVENTION Oseltamivir, 75 mg twice daily; maxingshigan-yinqiaosan decoction (composed of 12 Chinese herbal medicines, including honey-fried Herba Ephedrae), 200 mL 4 times daily; oseltamivir plus maxingshigan-yinqiaosan; or no intervention (control). Interventions and control were given for 5 days. MEASUREMENTS Primary outcome was time to fever resolution. Secondary outcomes included symptom scores and viral shedding determined by using real-time reverse transcriptase polymerase chain reaction.

RESULTS:

Significant reductions in the estimated median time to fever resolution compared with the control group (26.0 hours [95% CI, 24.0 to 33.0 hours]) were seen with oseltamivir (34% [95% CI, 20% to 46%]; P < 0.001), maxingshigan-yinqiaosan (37% [CI, 23% to 49%]; P < 0.001), and oseltamivir plus maxingshigan-yinqiaosan (47% [CI, 35% to 56%]; P < 0.001). Time to fever resolution was reduced by 19% (CI, 0.3% to 34%; P = 0.05) with oseltamivir plus maxingshigan-yinqiaosan compared with oseltamivir. The interventions and control did not differ in terms of decrease in symptom scores (P = 0.38). Two patients who received maxingshigan-yinqiaosan reported nausea and vomiting.

LIMITATIONS:

Participants were young and had mild H1N1 influenza virus infection. Missing viral data precluded definitive conclusions about viral shedding.

CONCLUSION:

Oseltamivir and maxingshigan-yinqiaosan, alone and in combination, reduced time to fever resolution in patients with H1N1 influenza virus infection. These data suggest that maxingshigan-yinqiaosan may be used as an alternative treatment of H1N1 influenza virus infection. PRIMARY FUNDING SOURCE Beijing Science and Technology Project and Beijing Nova Program.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Antivirales / Medicamentos Herbarios Chinos / Gripe Humana / Subtipo H1N1 del Virus de la Influenza A / Oseltamivir Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Intern Med Año: 2011 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Antivirales / Medicamentos Herbarios Chinos / Gripe Humana / Subtipo H1N1 del Virus de la Influenza A / Oseltamivir Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Intern Med Año: 2011 Tipo del documento: Article País de afiliación: China