Sheikh A, Hurwitz B, Cave J
Department of General Practice and Primary Health Care, Imperial College School of Medicine at St. Mary's, Norfolk Place, London, UK, W2 1PG.
Cochrane Database Syst Rev. 2000(2):CD001211. doi: 10.1002/14651858.CD001211.
There are concerns regarding whether antibiotic therapy confers significant benefit in the treatment of acute bacterial conjunctivitis.
The aim of this review is to assess the benefit and harm of antibiotic therapy in the management of acute bacterial conjunctivitis.
We searched the Cochrane Eyes and Vision Group specialised register, the Cochrane Controlled Trials Register - Central, MEDLINE and the reference lists of identified trial reports. We used the Science Citation Index to look for articles that cited the relevant studies, and we contacted investigators and pharmaceutical companies for information about additional trials. The most recent searches were carried out in September 1998.
We included double masked randomised controlled trials in which any form of antibiotic treatment had been compared with placebo in the management of acute bacterial conjunctivitis. This included topical, systemic and combination (for example, antibiotics and steroids) antibiotic usage.
One reviewer extracted data and the accuracy was checked by a second reviewer. Relative risks were summarised. We tested for heterogeneity between studies.
Six published trials were identified of which three fulfilled the eligibility criteria for inclusion in this review. One trial was single masked and therefore excluded. A second report, when translated, was found to have no placebo group and was therefore excluded. One trial is currently 'awaiting assessment'. This has been published in abstract form and has yet to be fully reported. All the trials thus far identified appear to have been conducted on a selected specialist care patient population. The trials were heterogeneous in terms of their inclusion and exclusion criteria, the nature of the intervention, and the outcome measures assessed. Meta-analysis indicates that acute bacterial conjunctivitis is frequently a self-limiting condition, as clinical remission (cure or significant improvement) occurred by days two to five in 64% (95% confidence interval (CI) 57% to 71%) of those treated with placebo. Treatment with antibiotics was, however, associated with significantly better rates of clinical remission (days two to five: relative risk (RR) 1.31 95% CI 1.11 to 1.55, NNT=5) with a suggestion that this benefit was maintained for late clinical remission (days six to 10: RR 1.27 95% CI 1.00 to 1.61, NNT=5). Antibiotic treatment was associated with rates of microbiological remission (pathogen eradication or reduction). No serious outcomes were reported in either the active or placebo arms of these trials, indicating that important sight-threatening complications are an infrequent occurrence.
REVIEWER'S CONCLUSIONS: Acute bacterial conjunctivitis is frequently a self-limiting condition but the use of antibiotics is associated with significantly improved rates of early clinical remission and early and late microbiological remission. Since trials to-date have been conducted in selected specialist care patient populations these results may not necessarily be generalisable to a primary care based population. A trial based in primary care designed to assess the cost-effectiveness of commonly prescribed antibiotic(s) versus placebo in acute bacterial conjunctivitis is warranted.
抗生素疗法在治疗急性细菌性结膜炎时是否能带来显著益处备受关注。
本综述旨在评估抗生素疗法在急性细菌性结膜炎治疗中的利弊。
我们检索了Cochrane眼科与视力组专业注册库、Cochrane对照试验注册库 - 中心库、MEDLINE以及已识别试验报告的参考文献列表。我们利用科学引文索引查找引用相关研究的文章,并联系研究者和制药公司获取其他试验的信息。最近一次检索于1998年9月进行。
我们纳入了双盲随机对照试验,这些试验将急性细菌性结膜炎治疗中任何形式的抗生素治疗与安慰剂进行了比较。这包括局部、全身以及联合(如抗生素与类固醇)使用抗生素。
由一名审阅者提取数据,另一名审阅者检查其准确性。总结相对风险。我们对各研究之间的异质性进行了检验。
共识别出6项已发表的试验,其中3项符合纳入本综述的资格标准。一项试验为单盲试验,因此被排除。另一篇报告经翻译后发现没有安慰剂组,所以也被排除。一项试验目前“等待评估”。该试验已以摘要形式发表,但尚未完整报告。目前已识别的所有试验似乎都是在特定的专科护理患者群体中进行的。这些试验在纳入和排除标准、干预性质以及评估的结局指标方面存在异质性。荟萃分析表明,急性细菌性结膜炎通常是一种自限性疾病,因为在接受安慰剂治疗的患者中,64%(95%置信区间(CI)57%至71%)在第2至5天出现临床缓解(治愈或显著改善)。然而,使用抗生素治疗的临床缓解率显著更高(第2至5天:相对风险(RR)1.31,95%CI 1.11至1.55,需治疗人数(NNT)=5),提示这种益处持续至晚期临床缓解(第6至10天:RR 1.27,95%CI 1.00至1.61,NNT=5)。抗生素治疗与微生物学缓解率(病原体根除或减少)相关。这些试验的活性组或安慰剂组均未报告严重不良事件,表明严重威胁视力的并发症很少发生。
急性细菌性结膜炎通常是一种自限性疾病,但使用抗生素与早期临床缓解率以及早期和晚期微生物学缓解率的显著提高相关。由于迄今为止的试验是在特定的专科护理患者群体中进行的,这些结果不一定能推广到基于初级保健的人群。有必要开展一项基于初级保健的试验,以评估常用处方抗生素与安慰剂在急性细菌性结膜炎治疗中的成本效益。