Clinical Controlled Study of Integrative Chinese and Western Medicine in Treating 49 Cases of SARS

来源 :Chinese Journal of Integrated Traditional and Western Medici | 被引量 : 0次 | 上传用户:xf6088
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Objective:To evaluate the efficacy of integrative Chinese and western medicine(ICWM)in treating severe acute respiratory syndrome(SARS)patients.Methods:Through parallel control design,49 SARS patients were observed.Used as control,there were in the western medicine(WM)group 29 pa-tients,who were treated with Ribavirin,Levofloxacin,Thymopentin,Azithromycin,methylprednisolone,etc.,on the basis of“Recommended Protocol for Infectious Atypical Pneumonia”(abbreviated as“Recom-mended Protocol”)issueed by Ministry of Health.As the treated group,there were in the ICWM 20 ca-ses.The protocol for treatment of SARS in“Special Science and Technological Action to Prevent andTreats SARS”(abbreviated as“Special S-T Action”),issued by Ministry of Science and Technology,to-gether with the same WM as those for the control group.Results:(1)Time from the disease onset to thesymptom improvement were 5.10±2.83 days and7.62±2.27 days ICWM and WM group respectively,P<0.05;(2)As to corticosteroid(CS)amount and days bef Objective: To evaluate the efficacy of integrative Chinese and western medicine (ICWM) in treating severe acute respiratory syndrome (SARS) patients. Methods: Through parallel control design, 49 SARS patients were observed. Used as control, there were in the western medicine ( WM) group 29 pa-tients, who were treated with Ribavirin, Levofloxacin, Thymopentin, Azithromycin, methylprednisolone, etc., on the basis of “Recommended Protocol for Infectious Atypical Pneumonia” (abbreviated as “Recom- mended Protocol”) issueed by Ministry of Health. As the treated group, there were in the ICWM 20 ca-ses.The protocol for treatment of SARS in “Special Science and Technological Action to Prevent andreats SARS” (abbreviated as “Special ST Action”), issued by Ministry of Science and Technology, to-gether with the same WM as those for the control group. Results: (1) Time from the disease onset to the progress of the study 5.10 ± 2.83 days and 7.62 ± 2.27 days ICWM and WM group respectively, P < 0.05; (2) As to corticoster oid (CS) amount and days bef
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