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用于囊性纤维化的预防性抗葡萄球菌抗生素。

Prophylactic anti-staphylococcal antibiotics for cystic fibrosis.

作者信息

Rosenfeld Margaret, Rayner Oli, Smyth Alan R

机构信息

Department of Pediatrics, University of Washington School of Medicine, Seattle, Washington, USA.

University of Washington School of Public Health, Seattle, USA.

出版信息

Cochrane Database Syst Rev. 2020 Sep 30;9(9):CD001912. doi: 10.1002/14651858.CD001912.pub5.

Abstract

BACKGROUND

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.

OBJECTIVES

To assess continuous oral antibiotic prophylaxis to prevent the acquisition of Staphylococcus aureus versus no prophylaxis in people with cystic fibrosis, we tested the following hypotheses to investigate whether prophylaxis: 1. improves clinical status, lung function and survival; 2. leads to fewer isolates of Staphylococcus aureus; 3. causes adverse effects (e.g. diarrhoea, skin rash, candidiasis); 4. leads to fewer isolates of other common pathogens from respiratory secretions; 5. leads to the emergence of antibiotic resistance and colonisation of the respiratory tract with Pseudomonas aeruginosa.

SEARCH METHODS

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: 27 February 2020. Online trials registries were also searched. Most recent search of online trials registries: 15 September 2020.

SELECTION CRITERIA

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.

DATA COLLECTION AND ANALYSIS

The authors assessed studies for eligibility and methodological quality and extracted data. The quality of the evidence was assessed using the GRADE criteria. The review's primary outcomes of interest were lung function by spirometry (forced expiratory volume in one second (FEV)) and the number of people with one or more isolates of Staphylococcus aureus (sensitive strains).

MAIN RESULTS

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 quality was judged to be low for all outcomes assessed after being downgraded based on GRADE assessments. Downgrading decisions were due to limitations in study design (all outcomes), for imprecision and for inconsistency . Prophylactic anti-staphylococcal antibiotics probably make little or no difference to lung function measured as FEV % predicted after six years (mean difference (MD) -2.30, 95% confidence interval (CI) -13.59 to 8.99, one study, n = 119, low-quality evidence); but may reduce the number of children having one or more isolates of Staphylococcus aureus at two years (odds ratio (OR) 0.21, 95% CI 0.13 to 0.35, three studies, n = 315, low-quality evidence). At the same time point, there may be little or no effect on nutrition as reported using weight z score (MD 0.06, 95% CI -0.33 to 0.45, two studies, n = 140, low-quality evidence), additional courses of antibiotics (OR 0.18, 95% CI 0.01 to 3.60, one study, n = 119, low-quality evidence) or adverse effects (low-quality evidence). There was no difference in the number of isolates of Pseudomonas aeruginosa between groups at two years (OR 0.74, 95% CI 0.45 to 1.23, three studies, n = 312, 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 may lead 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.

摘要

背景

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。开具预防性抗生素以期预防此类感染及肺损伤。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。这是对之前发表的一篇综述的更新。

目的

为评估在囊性纤维化患者中持续口服抗生素预防与不进行预防相比对金黄色葡萄球菌感染的影响,我们检验了以下假设以研究预防性治疗是否:1. 改善临床状况、肺功能及生存率;2. 减少金黄色葡萄球菌分离株;3. 引起不良反应(如腹泻、皮疹、念珠菌病);4. 减少呼吸道分泌物中其他常见病原体的分离株;5. 导致抗生素耐药性的出现及呼吸道被铜绿假单胞菌定植。

检索方法

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、相关期刊手工检索以及会议论文摘要书籍确定的参考文献。我们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2020年2月27日。我们还检索了在线试验注册库。在线试验注册库的最新检索时间为2020年9月15日。

入选标准

将持续口服预防性抗生素(至少服用一年)与“按需”给予的间歇性抗生素进行比较的随机试验,纳入任何疾病严重程度的囊性纤维化患者。

数据收集与分析

作者评估研究的入选资格和方法学质量并提取数据。使用GRADE标准评估证据质量。该综述的主要关注结局为通过肺活量测定法测量的肺功能(一秒用力呼气量(FEV))以及有一株或多株金黄色葡萄球菌(敏感菌株)的人数。

主要结果

我们纳入了四项研究,共401名随机参与者,入组时年龄为零至七岁;一项研究正在进行中。与两项较新的研究相比,纳入的两项较早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结局数据不完整。尽管即便在此项研究中我们也不确定按方案分析对研究结果的影响,但我们仅将最新的这项研究视为总体上无偏倚。根据GRADE评估进行降级后,所有评估结局的证据质量均被判定为低质量。降级的决定是由于研究设计的局限性(所有结局)、不精确性和不一致性。预防性抗葡萄球菌抗生素对六年时以预测FEV%衡量的肺功能可能几乎没有影响(平均差(MD)-2.30,95%置信区间(CI)-13.59至8.99,一项研究,n = 119,低质量证据);但可能会减少两岁时出现一株或多株金黄色葡萄球菌的儿童数量(比值比(OR)0.21,95%CI为0.13至0.35,三项研究,n = 315,低质量证据)。在同一时间点,使用体重z评分报告的营养状况(MD 0.06,95%CI -0.33至0.45,两项研究,n = 140,低质量证据)、额外的抗生素疗程(OR 0.18,95%CI 0.01至3.60,一项研究,n = 119,低质量证据)或不良反应(低质量证据)可能几乎没有影响。两组在两岁时铜绿假单胞菌分离株数量没有差异(OR 0.74,95%CI 0.45至1.23,三项研究,n = 312,低质量证据),尽管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。由于所综述的研究持续时间为六年或更短,因此无法得出关于预防性治疗长期影响的结论。

作者结论

抗葡萄球菌抗生素预防性治疗在婴儿期早期开始并持续至六岁时,可能会减少出现金黄色葡萄球菌分离株的儿童数量。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预防性治疗后,更多囊性纤维化患儿出现铜绿假单胞菌这一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影响这一情况。

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本文引用的文献

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Prophylactic anti-staphylococcal antibiotics for cystic fibrosis.用于囊性纤维化的预防性抗葡萄球菌抗生素。
Cochrane Database Syst Rev. 2017 Apr 18;4(4):CD001912. doi: 10.1002/14651858.CD001912.pub4.
4
Prophylactic anti-staphylococcal antibiotics for cystic fibrosis.用于囊性纤维化的预防性抗葡萄球菌抗生素。
Cochrane Database Syst Rev. 2014 Nov 24(11):CD001912. doi: 10.1002/14651858.CD001912.pub3.
5
Prophylactic anti-staphylococcal antibiotics for cystic fibrosis.用于囊性纤维化的预防性抗葡萄球菌抗生素。
Cochrane Database Syst Rev. 2012 Dec 12;12:CD001912. doi: 10.1002/14651858.CD001912.pub2.
7
Infection, inflammation, and lung function decline in infants with cystic fibrosis.囊性纤维化患儿的感染、炎症与肺功能下降。
Am J Respir Crit Care Med. 2011 Jul 1;184(1):75-81. doi: 10.1164/rccm.201011-1892OC. Epub 2011 Apr 14.

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