5 water cefazolin sodium in the treatment of purulent arthritis of the knee.docVIP

5 water cefazolin sodium in the treatment of purulent arthritis of the knee.doc

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5 water cefazolin sodium in the treatment of purulent arthritis of the knee

 PAGE \* MERGEFORMAT 5 5 water cefazolin sodium in the treatment of purulent arthritis of the knee [Abstract] Objective To evaluate the five water cefazolin sodium in the treatment of suppurative arthritis of the knee of the efficacy and safety. Methods Single-blind randomized controlled trial design, were randomly divided into 3 groups: Cefazolin Sodium Pentahydrate group of 48 cases, cefazolin sodium group of 40 patients, ceftriaxone group of 36 cases. Group 3 dosage, usage, course of treatment the same day, two times, each time intravenous infusion of 2g, course of treatment 10 ~ 14d. The results of the end of treatment, the five water cefazolin sodium, cefazolin sodium and ceftriaxone group were 95.8%, 87.5% and 66.6%; the incidence of adverse drug reactions were 4.2%, 5% and 5.56%. Conclusion 5 water cefazolin sodium in the treatment of suppurative arthritis of the knee, the exact efficacy and good safety. [Keywords:] 5 water cefazolin sodium; ceftriaxone; purulent arthritis of the knee Septic arthritis (septic arthritis, SA) refers to non-specific bacterial purulent infection within the joints, non-specific is defined in the TB bacteria, fungi and other pathogens than all the other [1]. SA can occur at any age, more common in children, if not treated in time can lead to disabling joint damage. Injection Cefazolin Sodium Pentahydrate in Shenzhen Pharmaceutical Co., Ltd. and China, nine new drugs and biological products of joint research, in the α -cefazolin sodium successful research based on the more stable generation cephalosporins. This study used five water injection cefazolin sodium, cefazolin sodium and ceftriaxone in the treatment of suppurative arthritis of the knee of the efficacy and safety of drugs designed to observe the stability and clinical efficacy, as well as the incidence of adverse drug reactions such as the relationship. 1 General Information 1.1 Case Selection Inclusion criteria aged 14 to 65 years of outpatient or hospitalizati

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