Walters Julia Ae, Tang Joanne Ngie Qing, Poole Phillippa, Wood-Baker Richard
School of Medicine, University of Tasmania, MSP, 17 Liverpool Street, PO Box 23, Hobart, Tasmania, Australia, 7001.
School of Medicine, University of Tasmania, Hobart, Australia.
Cochrane Database Syst Rev. 2017 Jan 24;1(1):CD001390. doi: 10.1002/14651858.CD001390.pub4.
People with chronic obstructive pulmonary disease (COPD) are at increased risk of pneumococcal disease, especially pneumonia, as well as acute exacerbations with associated morbidity and healthcare costs.
To determine the efficacy of injectable pneumococcal vaccination for preventing pneumonia in persons with COPD.
We searched the Cochrane Airways COPD Trials Register and the databases CENTRAL, MEDLINE and Embase, using prespecified terms. Searches are current to November 2016.
We included randomised controlled trials (RCT) comparing injectable pneumococcal polysaccharide vaccine (PPV) or pneumococcal conjugated vaccine (PCV) versus a control or alternative vaccine type in people with COPD.
We used standard Cochrane methodological procedures. For meta-analyses, we subgrouped studies by vaccine type.
For this update, we added five studies (606 participants), meaning that the review now includes a total of 12 RCTs involving 2171 participants with COPD. Average age of participants was 66 years, male participants accounted for 67% and mean forced expiratory volume in one second (FEV) was 1.2 L (five studies), 54% predicted (four studies). We assessed risks of selection, attrition and reporting bias as low, and risks of performance and detection bias as moderate.Compared with control, the vaccine group had a lower likelihood of developing community-acquired pneumonia (CAP) (odds ratio (OR) 0.62, 95% confidence interval (CI) 0.43 to 0.89; six studies, n = 1372; GRADE: moderate), but findings did not differ specifically for pneumococcal pneumonia (Peto OR 0.26, 95% CI 0.05 to 1.31; three studies, n = 1158; GRADE: low). The number needed to treat for an additional beneficial outcome (NNTB) (preventing one episode of CAP) was 21 (95% CI 15 to 74). Mortality from cardiorespiratory causes did not differ between vaccine and control groups (OR 1.07, 95% CI 0.69 to 1.66; three studies, n = 888; GRADE: moderate), nor did all-cause mortality differ (OR 1.00, 95% CI 0.72 to 1.40; five studies, n = 1053; GRADE: moderate). The likelihood of hospital admission for any cause, or for cardiorespiratory causes, did not differ between vaccine and control groups. Vaccination significantly reduced the likelihood of a COPD exacerbation (OR 0.60, 95% CI 0.39 to 0.93; four studies, n = 446; GRADE: moderate). The NNTB to prevent a patient from experiencing an acute exacerbation was 8 (95% CI 5 to 58). Only one study (n = 181) compared the efficacy of different vaccine types - 23-valent PPV versus 7-valent PCV - and reported no differences for CAP, all-cause mortality, hospital admission or likelihood of a COPD exacerbation, but investigators described a greater likelihood of some mild adverse effects of vaccination with PPV-23.
AUTHORS' CONCLUSIONS: Injectable polyvalent pneumococcal vaccination provides significant protection against community-acquired pneumonia, although no evidence indicates that vaccination reduced the risk of confirmed pneumococcal pneumonia, which was a relatively rare event. Vaccination reduced the likelihood of a COPD exacerbation, and moderate-quality evidence suggests the benefits of pneumococcal vaccination in people with COPD. Evidence was insufficient for comparison of different pneumococcal vaccine types.
慢性阻塞性肺疾病(COPD)患者发生肺炎球菌疾病的风险增加,尤其是肺炎,以及伴有相关发病率和医疗费用的急性加重。
确定注射用肺炎球菌疫苗预防COPD患者肺炎的疗效。
我们使用预先设定的检索词检索了Cochrane气道COPD试验注册库、CENTRAL、MEDLINE和Embase数据库。检索截至2016年11月。
我们纳入了比较注射用肺炎球菌多糖疫苗(PPV)或肺炎球菌结合疫苗(PCV)与对照或其他疫苗类型在COPD患者中的随机对照试验(RCT)。
我们采用标准的Cochrane方法学程序。对于荟萃分析,我们按疫苗类型对研究进行亚组分析。
在本次更新中,我们增加了5项研究(606名参与者),这意味着该综述现在总共包括12项RCT,涉及2171名COPD患者。参与者的平均年龄为66岁,男性参与者占67%,一秒用力呼气量(FEV)的平均值为1.2L(5项研究),预测值为54%(4项研究)。我们评估选择、失访和报告偏倚的风险较低,而实施和检测偏倚的风险为中等。与对照组相比,疫苗组发生社区获得性肺炎(CAP)的可能性较低(比值比(OR)0.62,95%置信区间(CI)0.43至0.89;6项研究,n = 1372;证据质量等级:中等),但肺炎球菌肺炎的结果无显著差异(Peto比值比0.26,95%CI 0.05至1.31;3项研究,n = 1158;证据质量等级:低)。为获得额外有益结果(预防一次CAP发作)所需治疗的人数(NNTB)为21(95%CI 15至74)。疫苗组和对照组之间心肺原因导致的死亡率无差异(OR 1.07,95%CI 0.69至1.66;3项研究,n = 888;证据质量等级:中等),全因死亡率也无差异(OR 1.00,95%CI 0.72至1.40;5项研究,n = 1053;证据质量等级:中等)。疫苗组和对照组之间因任何原因或心肺原因住院的可能性无差异。接种疫苗显著降低了COPD急性加重的可能性(OR 0.60,95%CI 0.39至0.93;4项研究,n = 446;证据质量等级:中等)。预防患者发生急性加重所需治疗的人数为8(95%CI 5至58)。只有一项研究(n = 181)比较了不同疫苗类型——23价PPV与7价PCV——的疗效,报告CAP、全因死亡率、住院或COPD急性加重可能性方面无差异,但研究者描述接种23价PPV出现一些轻度不良反应的可能性更大。
注射用多价肺炎球菌疫苗可显著预防社区获得性肺炎,尽管没有证据表明接种疫苗可降低确诊的肺炎球菌肺炎风险,而肺炎球菌肺炎是相对罕见的事件。接种疫苗降低了COPD急性加重的可能性,中等质量证据表明肺炎球菌疫苗对COPD患者有益。比较不同肺炎球菌疫苗类型的证据不足。