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呼吸道感染的延迟抗生素处方

Delayed antibiotic prescriptions for respiratory infections.

作者信息

Spurling Geoffrey Kp, Del Mar Chris B, Dooley Liz, Foxlee Ruth, Farley Rebecca

机构信息

Discipline of General Practice, School of Medicine, The University of Queensland, Herston, Brisbane, Queensland, Australia, 4029.

出版信息

Cochrane Database Syst Rev. 2017 Sep 7;9(9):CD004417. doi: 10.1002/14651858.CD004417.pub5.

Abstract

BACKGROUND

Concerns exist regarding antibiotic prescribing for respiratory tract infections (RTIs) owing to adverse reactions, cost, and antibacterial resistance. One proposed strategy to reduce antibiotic prescribing is to provide prescriptions, but to advise delay in antibiotic use with the expectation that symptoms will resolve first. This is an update of a Cochrane Review originally published in 2007, and updated in 2010 and 2013.

OBJECTIVES

To evaluate the effects on clinical outcomes, antibiotic use, antibiotic resistance, and patient satisfaction of advising a delayed prescription of antibiotics in respiratory tract infections.

SEARCH METHODS

For this 2017 update we searched the Cochrane Central Register of Controlled Trials (CENTRAL) (the Cochrane Library, Issue 4, 2017), which includes the Cochrane Acute Respiratory Infection Group's Specialised Register; Ovid MEDLINE (2013 to 25 May 2017); Ovid Embase (2013 to 2017 Week 21); EBSCO CINAHL Plus (1984 to 25 May 2017); Web of Science (2013 to 25 May 2017); WHO International Clinical Trials Registry Platform (1 September 2017); and ClinicalTrials.gov (1 September 2017).

SELECTION CRITERIA

Randomised controlled trials involving participants of all ages defined as having an RTI, where delayed antibiotics were compared to immediate antibiotics or no antibiotics. We defined a delayed antibiotic as advice to delay the filling of an antibiotic prescription by at least 48 hours. We considered all RTIs regardless of whether antibiotics were recommended or not.

DATA COLLECTION AND ANALYSIS

We used standard Cochrane methodological procedures. Three review authors independently extracted and collated data. We assessed the risk of bias of all included trials. We contacted trial authors to obtain missing information.

MAIN RESULTS

For this 2017 update we added one new trial involving 405 participants with uncomplicated acute respiratory infection. Overall, this review included 11 studies with a total of 3555 participants. These 11 studies involved acute respiratory infections including acute otitis media (three studies), streptococcal pharyngitis (three studies), cough (two studies), sore throat (one study), common cold (one study), and a variety of RTIs (one study). Five studies involved only children, two only adults, and four included both adults and children. Six studies were conducted in a primary care setting, three in paediatric clinics, and two in emergency departments.Studies were well reported, and appeared to be of moderate quality. Randomisation was not adequately described in two trials. Four trials blinded the outcomes assessor, and three included blinding of participants and doctors. We conducted meta-analysis for antibiotic use and patient satisfaction.We found no differences among delayed, immediate, and no prescribed antibiotics for clinical outcomes in the three studies that recruited participants with cough. For the outcome of fever with sore throat, three of the five studies favoured immediate antibiotics, and two found no difference. For the outcome of pain related to sore throat, two studies favoured immediate antibiotics, and three found no difference. One study compared delayed antibiotics with no antibiotic for sore throat, and found no difference in clinical outcomes.Three studies included participants with acute otitis media. Of the two studies with an immediate antibiotic arm, one study found no difference for fever, and the other study favoured immediate antibiotics for pain and malaise severity on Day 3. One study including participants with acute otitis media compared delayed antibiotics with no antibiotics and found no difference for pain and fever on Day 3.Two studies recruited participants with common cold. Neither study found differences for clinical outcomes between delayed and immediate antibiotic groups. One study favoured delayed antibiotics over no antibiotics for pain, fever, and cough duration (moderate quality evidence for all clinical outcomes - GRADE assessment).There were either no differences for adverse effects or results favoured delayed antibiotics over immediate antibiotics (low quality evidence - to GRADE assessment) with no significant differences in complication rates. Delayed antibiotics resulted in a significant reduction in antibiotic use compared to immediate antibiotics prescription (odds ratio (OR) 0.04, 95% confidence interval (CI) 0.03 to 0.05). However, a delayed antibiotic was more likely to result in reported antibiotic use than no antibiotics (OR 2.55, 95% CI 1.59 to 4.08) (moderate quality evidence - GRADE assessment).Patient satisfaction favoured delayed over no antibiotics (OR 1.49, 95% CI 1.08 to 2.06). There was no significant difference in patient satisfaction between delayed antibiotics and immediate antibiotics (OR 0.65, 95% CI 0.39 to 1.10) (moderate quality evidence - GRADE assessment).None of the included studies evaluated antibiotic resistance.

AUTHORS' CONCLUSIONS: For many clinical outcomes, there were no differences between prescribing strategies. Symptoms for acute otitis media and sore throat were modestly improved by immediate antibiotics compared with delayed antibiotics. There were no differences in complication rates. Delaying prescribing did not result in significantly different levels of patient satisfaction compared with immediate provision of antibiotics (86% versus 91%) (moderate quality evidence). However, delay was favoured over no antibiotics (87% versus 82%). Delayed antibiotics achieved lower rates of antibiotic use compared to immediate antibiotics (31% versus 93%) (moderate quality evidence). The strategy of no antibiotics further reduced antibiotic use compared to delaying prescription for antibiotics (14% versus 28%). Delayed antibiotics for people with acute respiratory infection reduced antibiotic use compared to immediate antibiotics, but was not shown to be different to no antibiotics in terms of symptom control and disease complications. Where clinicians feel it is safe not to prescribe antibiotics immediately for people with respiratory infections, no antibiotics with advice to return if symptoms do not resolve is likely to result in the least antibiotic use while maintaining similar patient satisfaction and clinical outcomes to delaying prescription of antibiotics. Where clinicians are not confident in using a no antibiotic strategy, a delayed antibiotics strategy may be an acceptable compromise in place of immediate prescribing to significantly reduce unnecessary antibiotic use for RTIs, and thereby reduce antibiotic resistance, while maintaining patient safety and satisfaction levels.Editorial note: As a living systematic review, this review is continually updated, incorporating relevant new evidence as it becomes available. Please refer to the Cochrane Database of Systematic Reviews for the current status of this review.

摘要

背景

由于不良反应、成本和抗菌药物耐药性等问题,呼吸道感染(RTIs)的抗生素处方备受关注。一种减少抗生素处方的建议策略是开具处方,但建议延迟使用抗生素,期望症状先自行缓解。这是对一篇Cochrane系统评价的更新,该评价最初发表于2007年,并于2010年和2013年进行了更新。

目的

评估在呼吸道感染中建议延迟开具抗生素处方对临床结局、抗生素使用、抗生素耐药性和患者满意度的影响。

检索方法

对于本次2017年更新,我们检索了Cochrane对照试验中心注册库(CENTRAL)(Cochrane图书馆,2017年第4期),其中包括Cochrane急性呼吸道感染小组的专业注册库;Ovid MEDLINE(2013年至2017年5月25日);Ovid Embase(2013年至2017年第21周);EBSCO CINAHL Plus(1984年至2017年5月25日);Web of Science(2013年至2017年5月25日);世界卫生组织国际临床试验注册平台(2017年9月1日);以及ClinicalTrials.gov(2017年9月1日)。

入选标准

随机对照试验,参与者为所有年龄段且被定义为患有RTIs,将延迟使用抗生素与立即使用抗生素或不使用抗生素进行比较。我们将延迟使用抗生素定义为建议将抗生素处方的取药时间至少推迟48小时。我们考虑所有的RTIs,无论是否推荐使用抗生素。

数据收集与分析

我们采用了标准的Cochrane方法学程序。三位综述作者独立提取和整理数据。我们评估了所有纳入试验的偏倚风险。我们联系试验作者以获取缺失信息。

主要结果

对于本次2017年更新,我们增加了一项新试验,涉及405例无并发症的急性呼吸道感染参与者。总体而言,本综述包括11项研究,共3555名参与者。这11项研究涉及急性呼吸道感染,包括急性中耳炎(3项研究)、链球菌性咽炎(3项研究)、咳嗽(2项研究)、咽痛(1项研究)、普通感冒(1项研究)以及多种RTIs(1项研究)。5项研究仅涉及儿童,2项仅涉及成人,4项包括成人和儿童。6项研究在初级保健机构进行,3项在儿科诊所进行,2项在急诊科进行。研究报告良好,质量似乎为中等。两项试验未充分描述随机化情况。4项试验对结局评估者进行了盲法处理,3项试验对参与者和医生进行了盲法处理。我们对抗生素使用和患者满意度进行了荟萃分析。我们发现,在招募咳嗽参与者的三项研究中,延迟、立即和未开具抗生素在临床结局方面没有差异。对于咽痛伴发热的结局,五项研究中的三项支持立即使用抗生素,两项未发现差异。对于与咽痛相关的疼痛结局,两项研究支持立即使用抗生素,三项未发现差异。一项研究比较了延迟使用抗生素与不使用抗生素治疗咽痛的情况,发现临床结局没有差异。三项研究纳入了急性中耳炎参与者。在有立即使用抗生素组的两项研究中,一项研究发现发热无差异,另一项研究支持立即使用抗生素治疗第3天的疼痛和不适严重程度。一项纳入急性中耳炎参与者的研究比较了延迟使用抗生素与不使用抗生素的情况,发现第3天的疼痛和发热无差异。两项研究招募了普通感冒参与者。两项研究均未发现延迟和立即使用抗生素组在临床结局上有差异。一项研究支持延迟使用抗生素优于不使用抗生素治疗疼痛、发热和咳嗽持续时间(所有临床结局的中等质量证据 - GRADE评估)。不良反应方面要么没有差异,要么结果支持延迟使用抗生素优于立即使用抗生素(低质量证据 - GRADE评估),并发症发生率无显著差异。与立即开具抗生素处方相比,延迟使用抗生素导致抗生素使用显著减少(比值比(OR)0.04,95%置信区间(CI)0.03至0.05)。然而,延迟使用抗生素比不使用抗生素更有可能导致报告使用抗生素(OR 2.55,95%CI 1.59至4.08)(中等质量证据 - GRADE评估)。患者满意度支持延迟使用抗生素优于不使用抗生素(OR 1.49,95%CI 1.08至2.06)。延迟使用抗生素与立即使用抗生素在患者满意度方面没有显著差异(OR 0.65,95%CI 0.39至1.10)(中等质量证据 - GRADE评估)。纳入的研究均未评估抗生素耐药性。

作者结论

对于许多临床结局,处方策略之间没有差异。与延迟使用抗生素相比,立即使用抗生素可适度改善急性中耳炎和咽痛的症状。并发症发生率没有差异。与立即提供抗生素相比,延迟开处方在患者满意度水平上没有显著差异(86%对91%)(中等质量证据)。然而,延迟开处方优于不使用抗生素(87%对82%)。与立即使用抗生素相比,延迟使用抗生素的抗生素使用率较低(31%对93%)(中等质量证据)。不使用抗生素的策略与延迟开具抗生素处方相比,进一步降低了抗生素使用率(14%对28%)。与立即使用抗生素相比,为急性呼吸道感染患者延迟使用抗生素可减少抗生素使用,但在症状控制和疾病并发症方面与不使用抗生素没有差异。如果临床医生认为对于呼吸道感染患者不立即开具抗生素是安全的,那么不使用抗生素并建议如果症状未缓解则复诊,可能会导致抗生素使用最少,同时在患者满意度和临床结局方面与延迟开具抗生素处方相似。如果临床医生对不使用抗生素的策略没有信心,延迟使用抗生素策略可能是一个可接受的折衷方案,以代替立即开处方,从而显著减少RTIs的不必要抗生素使用,进而降低抗生素耐药性,同时保持患者安全和满意度水平。编辑说明:作为一项动态系统评价,本评价会持续更新,纳入新的相关证据。有关本评价的当前状态,请参考Cochrane系统评价数据库。

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