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地塞米松治疗儿童化脓性关节炎:一项随机双盲安慰剂对照研究的结果。

Dexamethasone therapy for septic arthritis in children: results of a randomized double-blind placebo-controlled study.

作者信息

Harel Liora, Prais Dario, Bar-On Elhanan, Livni Gilat, Hoffer Vered, Uziel Yosef, Amir Jacob

机构信息

Department of Pediatrics C, Schneider Children’s Medical Center of Israel, Petach Tikvah 49202, USA.

出版信息

J Pediatr Orthop. 2011 Mar;31(2):211-5. doi: 10.1097/BPO.0b013e3182092869.

Abstract

BACKGROUND

We evaluated the effect of adding dexamethasone to antibiotic therapy in the clinical course of septic arthritis in children.

METHODS

A randomized double-blind placebo-controlled trial was performed. The study group included 49 children with septicarthritis. In addition to antibiotic therapy given, patients were randomly assigned to receive intravenous dexamethasone 0.15 mg/kg every 6 hours for 4 days or placebo. The groups were compared for clinical and laboratory parameters, length of hospital stay, and late sequelae.

RESULTS

Mean age was 33±42 months (range: 6 to 161 mo). There was no significant difference between the dexamethasone and placebo groups in age, duration of symptoms, joint affected, or levels of acute phase reactants. Bacteria were isolated from joint fluid in 17 patients (35%) and from blood in 4 patients. Compared with the placebo group, patients treated with dexamethasone had a significantly shorter duration of fever (P=0.021; mean first day without fever 1.68 vs 2.83) and local inflammatory signs (P=0.021; mean first day without pain 7.18 vs 10.76), lower levels of acute phase reactants (P=0.003; mean last day of erythrocyte sedimentation rate>25 mm/h 3.76 vs 8.40), shorter duration of parenteral antibiotic treatment (P=0.007; mean of 9.91 d vs 12.60 d), and shorter hospital stay. No side effects of treatment were recorded in either group.

CONCLUSIONS

A 4-day course of dexamethasone given at the start of antibiotic treatment in children with septic arthritis, is safe, and leads to a significantly more rapid clinical improvement, shortening duration of hospitalization compared with those treated with antibiotics alone.

LEVEL OF EVIDENCE

I.

摘要

背景

我们评估了在儿童脓毒性关节炎临床病程中,抗生素治疗添加地塞米松的效果。

方法

进行了一项随机双盲安慰剂对照试验。研究组包括49例脓毒性关节炎患儿。除给予抗生素治疗外,患者被随机分配接受每6小时静脉注射地塞米松0.15mg/kg,共4天,或接受安慰剂治疗。比较两组的临床和实验室参数、住院时间及晚期后遗症。

结果

平均年龄为33±42个月(范围:6至161个月)。地塞米松组和安慰剂组在年龄、症状持续时间、受累关节或急性期反应物水平方面无显著差异。17例患者(35%)关节液中分离出细菌,4例患者血液中分离出细菌。与安慰剂组相比,接受地塞米松治疗的患者发热持续时间显著缩短(P=0.021;无发热的平均首日为1.68天对2.83天)和局部炎症体征显著缩短(P=0.021;无疼痛的平均首日为7.18天对10.76天),急性期反应物水平较低(P=0.003;红细胞沉降率>25mm/h的最后平均日为3.76天对8.40天),胃肠外抗生素治疗持续时间较短(P=0.007;平均为9.91天对12.60天),住院时间较短。两组均未记录到治疗的副作用。

结论

在儿童脓毒性关节炎抗生素治疗开始时给予4天地塞米松疗程是安全的,与单独使用抗生素治疗的患者相比,可显著加快临床改善,缩短住院时间。

证据级别

I级

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