Smyth Alan R, Rosenfeld Margaret
Division of Child Health, Obstetrics & Gynaecology (COG), School of Medicine, University of Nottingham, Queens Medical Centre, Derby Road, Nottingham, UK, NG7 2UH.
Pediatric Clinical Research Center, Seattle Children's Hospital, A-5937 - Pulmonary, 4800 Sand Point Way NE, Seattle, Washington, USA, WA 98105.
Cochrane Database Syst Rev. 2017 Apr 18;4(4):CD001912. doi: 10.1002/14651858.CD001912.pub4.
Staphylococcus aureus causes pulmonary infection in young children with cystic fibrosis. Prophylactic antibiotics are prescribed hoping to prevent such infection and lung damage. Antibiotics have adverse effects and long-term use might lead to infection with Pseudomonas aeruginosa. This is an update of a previously published review.
To assess continuous oral antibiotic prophylaxis to prevent the acquisition of Staphylococcus aureus versus no prophylaxis in people with cystic fibrosis, we tested these hypotheses. Prophylaxis:1. improves clinical status, lung function and survival;2. causes adverse effects (e.g. diarrhoea, skin rash, candidiasis);3. leads to fewer isolates of common pathogens from respiratory secretions;4. leads to the emergence of antibiotic resistance and colonisation of the respiratory tract with Pseudomonas aeruginosa.
We searched the Cochrane Cystic Fibrosis and Genetic Disorders Group Trials Register, comprising references identified from comprehensive electronic database searches, handsearches of relevant journals and abstract books of conference proceedings. Companies manufacturing anti-staphylococcal antibiotics were contacted.Most recent search of the Group's Register: 29 September 2016.
Randomised trials of continuous oral prophylactic antibiotics (given for at least one year) compared to intermittent antibiotics given 'as required', in people with cystic fibrosis of any disease severity.
The authors assessed studies for eligibility and methodological quality and extracted data.
We included four studies, with a total of 401 randomised participants aged zero to seven years on enrolment; one study is ongoing. The two older included studies generally had a higher risk of bias across all domains, but in particular due to a lack of blinding and incomplete outcome data, than the two more recent studies. We only regarded the most recent study as being generally free of bias, although even here we were not certain of the effect of the per protocol analysis on the study results. Evidence was downgraded based on GRADE assessments and outcome results ranged from moderate to low quality. Downgrading decisions were due to limitations in study design (all outcomes); for imprecision (number of people needing additional antibiotics); and for inconsistency (weight z score).Fewer children receiving anti-staphylococcal antibiotic prophylaxis had one or more isolates of Staphylococcus aureus (low quality evidence). There was no significant difference between groups in infant or conventional lung function (moderate quality evidence). We found no significant effect on nutrition (low quality evidence), hospital admissions, additional courses of antibiotics (low quality evidence) or adverse effects (moderate quality evidence). There was no significant difference in the number of isolates of Pseudomonas aeruginosa between groups (low quality evidence), though there was a trend towards a lower cumulative isolation rate of Pseudomonas aeruginosa in the prophylaxis group at two and three years and towards a higher rate from four to six years. As the studies reviewed lasted six years or less, conclusions cannot be drawn about the long-term effects of prophylaxis.
AUTHORS' CONCLUSIONS: Anti-staphylococcal antibiotic prophylaxis leads to fewer children having isolates of Staphylococcus aureus, when commenced early in infancy and continued up to six years of age. The clinical importance of this finding is uncertain. Further research may establish whether the trend towards more children with CF with Pseudomonas aeruginosa, after four to six years of prophylaxis, is a chance finding and whether choice of antibiotic or duration of treatment might influence this.
金黄色葡萄球菌可导致患有囊性纤维化的幼儿发生肺部感染。人们会开具预防性抗生素以预防此类感染和肺部损伤。抗生素存在不良反应,长期使用可能导致铜绿假单胞菌感染。这是对先前发表的一篇综述的更新。
为评估持续口服抗生素预防措施与不进行预防措施相比,对囊性纤维化患者预防金黄色葡萄球菌感染的效果,我们检验了以下假设。预防措施:1. 改善临床状况、肺功能并提高生存率;2. 引起不良反应(如腹泻、皮疹、念珠菌病);3. 减少呼吸道分泌物中常见病原体的分离株;4. 导致抗生素耐药性的出现以及呼吸道被铜绿假单胞菌定植。
我们检索了Cochrane囊性纤维化和遗传疾病小组试验注册库,其中包括通过全面电子数据库检索、对相关期刊的手工检索以及会议论文摘要集识别出的参考文献。我们还联系了生产抗葡萄球菌抗生素的公司。该小组注册库的最新检索时间为2016年9月29日。
针对任何疾病严重程度的囊性纤维化患者,比较持续口服预防性抗生素(至少服用一年)与按需服用的间歇性抗生素的随机试验。
作者评估了研究的 eligibility 和方法学质量,并提取了数据。
我们纳入了四项研究,共有401名年龄在零至七岁的随机参与者入组;一项研究正在进行中。与两项较新的研究相比,两项较早纳入的研究在所有领域的偏倚风险通常更高,尤其是由于缺乏盲法和不完整的结局数据。我们仅认为最新的研究总体上无偏倚,尽管即便在此研究中,我们也不确定符合方案分析对研究结果的影响。根据GRADE评估,证据质量被下调,结局结果的质量从中等到低不等。下调决策是由于研究设计的局限性(所有结局);不精确性(需要额外抗生素治疗的人数);以及不一致性(体重Z评分)。接受抗葡萄球菌抗生素预防的儿童中,分离出一株或多株金黄色葡萄球菌的人数较少(低质量证据)。两组在婴儿期或常规肺功能方面无显著差异(中等质量证据)。我们发现对营养、住院次数、额外抗生素疗程(低质量证据)或不良反应(中等质量证据)均无显著影响。两组之间铜绿假单胞菌的分离株数量无显著差异(低质量证据),不过在两年和三年时,预防组铜绿假单胞菌的累积分离率有降低趋势,而在四年至六年时有升高趋势。由于所审查的研究持续时间不超过六年,因此无法得出关于预防措施长期效果的结论。
在婴儿期早期开始并持续至六岁时,抗葡萄球菌抗生素预防措施可使分离出金黄色葡萄球菌的儿童数量减少。这一发现的临床重要性尚不确定。进一步的研究可能会确定,在进行四年至六年的预防后,更多囊性纤维化儿童感染铜绿假单胞菌的趋势是否为偶然现象,以及抗生素的选择或治疗持续时间是否会对此产生影响。