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治疗囊性纤维化患者铜绿假单胞菌感染的抗生素策略。

Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis.

机构信息

Paediatric Respiratory Medicine, Bristol Royal Hospital for Children, Bristol, UK.

Population Health Sciences, University of Bristol, Bristol, UK.

出版信息

Cochrane Database Syst Rev. 2023 Jun 2;6(6):CD004197. doi: 10.1002/14651858.CD004197.pub6.


DOI:10.1002/14651858.CD004197.pub6
PMID:37268599
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10237531/
Abstract

BACKGROUND: Respiratory tract infections with Pseudomonas aeruginosa occur in most people with cystic fibrosis (CF). Established chronic P aeruginosa infection is virtually impossible to eradicate and is associated with increased mortality and morbidity. Early infection may be easier to eradicate. This is an updated review. OBJECTIVES: Does giving antibiotics for P aeruginosa infection in people with CF at the time of new isolation improve clinical outcomes (e.g. mortality, quality of life and morbidity), eradicate P aeruginosa infection, and delay the onset of chronic infection, but without adverse effects, compared to usual treatment or an alternative antibiotic regimen? We also assessed cost-effectiveness. SEARCH METHODS: We searched the Cochrane Cystic Fibrosis and Genetic Disorders Group Trials Register comprising references identified from comprehensive electronic database searches and handsearches of relevant journals and conference proceedings. Latest search: 24 March 2022. We searched ongoing trials registries. Latest search: 6 April 2022. SELECTION CRITERIA: We included randomised controlled trials (RCTs) of people with CF, in whom P aeruginosa had recently been isolated from respiratory secretions. We compared combinations of inhaled, oral or intravenous (IV) antibiotics with placebo, usual treatment or other antibiotic combinations. We excluded non-randomised trials and cross-over trials. DATA COLLECTION AND ANALYSIS: Two authors independently selected trials, assessed risk of bias and extracted data. We assessed the certainty of the evidence using GRADE. MAIN RESULTS: We included 11 trials (1449 participants) lasting between 28 days and 27 months; some had few participants and most had relatively short follow-up periods. Antibiotics in this review are: oral - ciprofloxacin and azithromycin; inhaled - tobramycin nebuliser solution for inhalation (TNS), aztreonam lysine (AZLI) and colistin; IV - ceftazidime and tobramycin. There was generally a low risk of bias from missing data. In most trials it was difficult to blind participants and clinicians to treatment. Two trials were supported by the manufacturers of the antibiotic used. TNS versus placebo TNS may improve eradication; fewer participants were still positive for P aeruginosa at one month (odds ratio (OR) 0.06, 95% confidence interval (CI) 0.02 to 0.18; 3 trials, 89 participants; low-certainty evidence) and two months (OR 0.15, 95% CI 0.03 to 0.65; 2 trials, 38 participants). We are uncertain whether the odds of a positive culture decrease at 12 months (OR 0.02, 95% CI 0.00 to 0.67; 1 trial, 12 participants). TNS (28 days) versus TNS (56 days) One trial (88 participants) comparing 28 days to 56 days TNS treatment found duration of treatment may make little or no difference in time to next isolation (hazard ratio (HR) 0.81, 95% CI 0.37 to 1.76; low-certainty evidence). Cycled TNS versus culture-based TNS One trial (304 children, one to 12 years old) compared cycled TNS to culture-based therapy and also ciprofloxacin to placebo. We found moderate-certainty evidence of an effect favouring cycled TNS therapy (OR 0.51, 95% CI 0.31 to 0.82), although the trial publication reported age-adjusted OR and no difference between groups. Ciprofloxacin versus placebo added to cycled and culture-based TNS therapy One trial (296 participants) examined the effect of adding ciprofloxacin versus placebo to cycled and culture-based TNS therapy. There is probably no difference between ciprofloxacin and placebo in eradicating P aeruginosa (OR 0.89, 95% CI 0.55 to 1.44; moderate-certainty evidence). Ciprofloxacin and colistin versus TNS We are uncertain whether there is any difference between groups in eradication of P aeruginosa at up to six months (OR 0.43, 95% CI 0.15 to 1.23; 1 trial, 58 participants) or up to 24 months (OR 0.76, 95% CI 0.24 to 2.42; 1 trial, 47 participants); there was a low rate of short-term eradication in both groups. Ciprofloxacin plus colistin versus ciprofloxacin plus TNS One trial (223 participants) found there may be no difference in positive respiratory cultures at 16 months between ciprofloxacin with colistin versus TNS with ciprofloxacin (OR 1.28, 95% CI 0.72 to 2.29; low-certainty evidence). TNS plus azithromycin compared to TNS plus oral placebo Adding azithromycin may make no difference to the number of participants eradicating P aeruginosa after a three-month treatment phase (risk ratio (RR) 1.01, 95% CI 0.75 to 1.35; 1 trial, 91 participants; low-certainty evidence); there was also no evidence of any difference in the time to recurrence. Ciprofloxacin and colistin versus no treatment A single trial only reported one of our planned outcomes; there were no adverse effects in either group. AZLI for 14 days plus placebo for 14 days compared to AZLI for 28 days We are uncertain whether giving 14 or 28 days of AZLI makes any difference to the proportion of participants having a negative respiratory culture at 28 days (mean difference (MD) -7.50, 95% CI -24.80 to 9.80; 1 trial, 139 participants; very low-certainty evidence). Ceftazidime with IV tobramycin compared with ciprofloxacin (both regimens in conjunction with three months colistin) IV ceftazidime with tobramycin compared with ciprofloxacin may make little or no difference to eradication of P aeruginosa at three months, sustained to 15 months, provided that inhaled antibiotics are also used (RR 0.84, 95 % CI 0.65 to 1.09; P = 0.18; 1 trial, 255 participants; high-certainty evidence). The results do not support using IV antibiotics over oral therapy to eradicate P aeruginosa, based on both eradication rate and financial cost. AUTHORS' CONCLUSIONS: We found that nebulised antibiotics, alone or with oral antibiotics, were better than no treatment for early infection with P aeruginosa. Eradication may be sustained in the short term. There is insufficient evidence to determine whether these antibiotic strategies decrease mortality or morbidity, improve quality of life, or are associated with adverse effects compared to placebo or standard treatment. Four trials comparing two active treatments have failed to show differences in rates of eradication of P aeruginosa. One large trial showed that intravenous ceftazidime with tobramycin is not superior to oral ciprofloxacin when inhaled antibiotics are also used. There is still insufficient evidence to state which antibiotic strategy should be used for the eradication of early P aeruginosa infection in CF, but there is now evidence that intravenous therapy is not superior to oral antibiotics.

摘要

背景:铜绿假单胞菌(P aeruginosa)感染在大多数囊性纤维化(CF)患者中发生。已建立的慢性 P aeruginosa 感染几乎不可能被根除,并且与死亡率和发病率增加有关。早期感染可能更容易被根除。这是一个更新的综述。

目的:在 CF 患者新分离出 P aeruginosa 时给予抗生素治疗,与常规治疗或替代抗生素方案相比,是否能改善临床结局(如死亡率、生活质量和发病率)、根除 P aeruginosa 感染以及延迟慢性感染的发生,但无不良影响?我们还评估了成本效益。

检索方法:我们检索了 Cochrane 囊性纤维化和遗传疾病组试验注册库,该数据库包含了从全面的电子数据库检索和相关期刊和会议论文集的手工检索中确定的参考文献。最新检索日期:2022 年 3 月 24 日。我们还检索了正在进行的试验注册库。最新检索日期:2022 年 4 月 6 日。

纳入标准:我们纳入了最近从呼吸道分泌物中分离出 P aeruginosa 的 CF 患者的随机对照试验(RCT)。我们比较了吸入、口服或静脉(IV)抗生素与安慰剂、常规治疗或其他抗生素组合的效果。我们排除了非随机试验和交叉试验。

排除标准:我们排除了非随机试验和交叉试验。

资料收集和分析:两名作者独立选择试验、评估偏倚风险并提取数据。我们使用 GRADE 评估证据的确定性。

主要结果:我们纳入了 11 项试验(1449 名参与者),持续时间从 28 天到 27 个月不等;有些试验参与者较少,大多数试验随访时间相对较短。本综述中的抗生素包括:口服 - 环丙沙星和阿奇霉素;吸入 - 妥布霉素雾化吸入溶液(TNS)、氨曲南赖氨酸(AZLI)和多粘菌素;静脉 - 头孢他啶和妥布霉素。大多数试验的偏倚风险来自于缺失数据。在大多数试验中,很难对参与者和临床医生进行治疗的盲法。两项试验得到了所用抗生素制造商的支持。

TNS 与安慰剂 TNS 可能会提高根除率;在一个月时(比值比(OR)0.06,95%置信区间(CI)0.02 至 0.18;3 项试验,89 名参与者;低确定性证据)和两个月时(OR 0.15,95%CI 0.03 至 0.65;2 项试验,38 名参与者),仍有更少的参与者的 P aeruginosa 呈阳性。我们不确定在 12 个月时培养物呈阳性的可能性是否会降低(OR 0.02,95%CI 0.00 至 0.67;1 项试验,12 名参与者)。TNS(28 天)与 TNS(56 天)一项比较 28 天和 56 天 TNS 治疗的试验(88 名参与者)发现,治疗时间的长短可能对下一次分离的时间(风险比(HR)0.81,95%CI 0.37 至 1.76;低确定性证据)没有太大或没有影响。

循环 TNS 与基于培养的 TNS 一项比较循环 TNS 与基于培养的治疗以及环丙沙星与安慰剂的试验(304 名儿童,年龄为 1 至 12 岁)发现,循环 TNS 治疗有中等确定性的效果(OR 0.51,95%CI 0.31 至 0.82),尽管试验出版物报告了年龄调整的 OR,并且两组之间没有差异。

环丙沙星加循环和基于培养的 TNS 治疗与安慰剂比较在一项试验(296 名参与者)中,研究了在循环和基于培养的 TNS 治疗中添加环丙沙星与安慰剂相比的效果。环丙沙星与安慰剂相比,在根除 P aeruginosa 方面可能没有差异(OR 0.89,95%CI 0.55 至 1.44;中等确定性证据)。

环丙沙星和多粘菌素与 TNS 我们不确定在六个月(OR 0.43,95%CI 0.15 至 1.23;1 项试验,58 名参与者)或 24 个月(OR 0.76,95%CI 0.24 至 2.42;1 项试验,47 名参与者)时,两组之间是否存在差异;两组的短期根除率都较低。

环丙沙星加多粘菌素与环丙沙星加 TNS 一项试验(223 名参与者)发现,在 16 个月时,与 TNS 加环丙沙星相比,在 TNS 加阿奇霉素与 TNS 加环丙沙星之间,呼吸道培养阳性的可能性可能没有差异(OR 1.28,95%CI 0.72 至 2.29;低确定性证据)。

TNS 加阿奇霉素与 TNS 加口服安慰剂相比,添加阿奇霉素可能不会影响在三个月治疗阶段根除 P aeruginosa 的参与者人数(风险比(RR)1.01,95%CI 0.75 至 1.35;1 项试验,91 名参与者;低确定性证据);也没有证据表明复发时间有任何差异。

环丙沙星和多粘菌素与无治疗相比,一项单独的试验仅报告了我们计划的一个结果;两组均无不良反应。

AZLI 14 天加安慰剂 14 天与 AZLI 28 天相比我们不确定给予 14 天或 28 天的 AZLI 是否会对 28 天的阴性呼吸道培养率产生任何影响(平均差异(MD)-7.50,95%CI -24.80 至 9.80;1 项试验,139 名参与者;非常低确定性证据)。

头孢他啶加 IV 妥布霉素与环丙沙星(两种方案均联合使用三个月多粘菌素)与环丙沙星相比,头孢他啶加 IV 妥布霉素可能对三个月和 15 个月的 P aeruginosa 根除率没有太大或没有影响,前提是也使用吸入抗生素(RR 0.84,95%CI 0.65 至 1.09;P = 0.18;1 项试验,255 名参与者;高确定性证据)。结果不支持使用 IV 抗生素代替口服治疗来根除 P aeruginosa,这不仅基于根除率,还基于财务成本。

作者结论:我们发现,与安慰剂或标准治疗相比,单独或与口服抗生素联合使用的雾化抗生素可更好地治疗早期铜绿假单胞菌感染。根除可能在短期内持续。四项比较两种活性治疗的试验均未能表明 P aeruginosa 的根除率存在差异。一项大型试验表明,当同时使用吸入性抗生素时,静脉内头孢他啶联合妥布霉素并不优于口服环丙沙星。仍然没有足够的证据表明,在根除 CF 患者的早期 P aeruginosa 感染时,应该使用哪种抗生素策略,但现在有证据表明,静脉内治疗并不优于口服抗生素。

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Association of Intensity of Antipseudomonal Antibiotic Therapy With Risk of Treatment-Emergent Organisms in Children With Cystic Fibrosis and Newly Acquired Pseudomonas Aeruginosa.

Clin Infect Dis. 2021-9-15

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J Cyst Fibros. 2021-11

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J Cyst Fibros. 2021-3

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