Hawke Kate, van Driel Mieke L, Buffington Benjamin J, McGuire Treasure M, King David
Primary Care Clinical Unit, Faculty of Medicine, The University of Queensland, 288 Herston Road, Herston, Brisbane, Queensland, Australia, 4006.
Cochrane Database Syst Rev. 2018 Sep 9;9(9):CD005974. doi: 10.1002/14651858.CD005974.pub5.
Acute respiratory tract infections (ARTIs) are common and may lead to complications. Most children experience between three and six ARTIs annually. Although these infections are self-limiting, symptoms can be distressing. Many treatments are used to control symptoms and shorten illness duration. Most have minimal benefit and may lead to adverse effects. Oral homeopathic medicinal products could play a role in childhood ARTI management if evidence for effectiveness is established.
To assess the effectiveness and safety of oral homeopathic medicinal products compared with placebo or conventional therapy to prevent and treat acute respiratory tract infections in children.
We searched CENTRAL (2017, Issue 11) including the Cochrane Acute Respiratory Infections Specialised Register, MEDLINE (1946 to 27 November 2017), Embase (2010 to 27 November 2017), CINAHL (1981 to 27 November 2017), AMED (1985 to December 2014), CAMbase (searched 29 March 2018), British Homeopathic Library (searched 26 June 2013 - no longer operating). We also searched the WHO ICTRP and ClinicalTrials.gov trials registers (29 March 2018), checked references, and contacted study authors to identify additional studies.
Double-blind, randomised controlled trials (RCTs) or double-blind cluster-RCTs comparing oral homeopathy medicinal products with identical placebo or self-selected conventional treatments to prevent or treat ARTIs in children aged 0 to 16 years.
We used standard methodological procedures expected by Cochrane.
We included eight RCTs of 1562 children receiving oral homeopathic medicinal products or a control treatment (placebo or conventional treatment) for upper respiratory tract infections (URTIs). Four treatment studies examined the effect on URTI recovery, and four studies investigated the effect on preventing URTIs after one to three months of treatment, followed up for the remainder of the year. Two treatment and two prevention studies involved homeopaths individualising treatment. The other studies used predetermined, non-individualised treatments. All studies involved highly diluted homeopathic medicinal products.We found several limitations to the included studies, in particular methodological inconsistencies and high attrition rates, failure to conduct intention-to-treat analysis, selective reporting, and apparent protocol deviations. We assessed three studies as at high risk of bias in at least one domain, and many had additional domains with unclear risk of bias. Three studies received funding from homeopathy manufacturers; one support from a non-government organisation; two government support; one was cosponsored by a university; and one did not report funding support.Methodological inconsistencies and significant clinical and statistical heterogeneity precluded robust quantitative meta-analysis. Only four outcomes were common to more than one study and could be combined for analysis. Odds ratios (OR) were generally small with wide confidence intervals (CI), and the contributing studies found conflicting effects, so there was little certainty that the efficacy of the intervention could be ascertained. All studies assessed as at low risk of bias showed no benefit from oral homeopathic medicinal products; trials at uncertain and high risk of bias reported beneficial effects.We found low-quality evidence that non-individualised homeopathic medicinal products confer little preventive effect on ARTIs (OR 1.14, 95% CI 0.83 to 1.57). We found low-quality evidence from two individualised prevention studies that homeopathy has little impact on the need for antibiotic usage (N = 369) (OR 0.79, 95% CI 0.35 to 1.76). We also assessed adverse events, hospitalisation rates and length of stay, days off school (or work for parents), and quality of life, but were not able to pool data from any of these secondary outcomes.There is insufficient evidence from two pooled individualised treatment studies (N = 155) to determine the effect of homeopathy on short-term cure (OR 1.31 favouring placebo, 95% CI 0.09 to 19.54; very low-quality evidence) and long-term cure rates (OR 0.99, 95% CI 0.10 to 9.67; very low-quality evidence). Adverse events were reported inconsistently; however, serious events were not reported. One study found an increase in the occurrence of non-severe adverse events in the treatment group.
AUTHORS' CONCLUSIONS: Pooling of two prevention and two treatment studies did not show any benefit of homeopathic medicinal products compared to placebo on ARTI recurrence or cure rates in children. We found no evidence to support the efficacy of homeopathic medicinal products for ARTIs in children. Adverse events were poorly reported, so conclusions about safety could not be drawn.
急性呼吸道感染(ARTIs)很常见,且可能导致并发症。大多数儿童每年经历3至6次急性呼吸道感染。尽管这些感染是自限性的,但症状可能令人痛苦。许多治疗方法用于控制症状和缩短病程。大多数治疗方法益处甚微,且可能导致不良反应。如果能确立有效性证据,口服顺势疗法药品可能在儿童急性呼吸道感染的管理中发挥作用。
评估口服顺势疗法药品与安慰剂或传统疗法相比,在预防和治疗儿童急性呼吸道感染方面的有效性和安全性。
我们检索了CENTRAL(2017年第11期),包括Cochrane急性呼吸道感染专业注册库、MEDLINE(1946年至2017年11月27日)、Embase(2010年至2017年11月27日)、CINAHL(1981年至2017年11月27日)、AMED(1985年至2014年12月)、CAMbase(2018年3月29日检索)、英国家庭疗法图书馆(2013年6月26日检索 - 已不再运营)。我们还检索了世界卫生组织国际临床试验注册平台和ClinicalTrials.gov试验注册库(2018年3月29日),检查了参考文献,并联系研究作者以识别其他研究。
双盲、随机对照试验(RCTs)或双盲整群RCTs,比较口服顺势疗法药品与相同安慰剂或自选传统疗法,用于预防或治疗0至16岁儿童的急性呼吸道感染。
我们采用了Cochrane期望的标准方法程序。
我们纳入了8项RCT,共1562名接受口服顺势疗法药品或对照治疗(安慰剂或传统治疗)的儿童,用于治疗上呼吸道感染(URTIs)。4项治疗研究考察了对URTI恢复的影响,4项研究调查了治疗1至3个月后预防URTIs的效果,并在当年剩余时间进行随访。2项治疗和2项预防研究涉及顺势疗法医师进行个体化治疗。其他研究采用预先确定的、非个体化治疗。所有研究均涉及高度稀释的顺势疗法药品。我们发现纳入研究存在几个局限性,特别是方法学不一致和高失访率、未进行意向性分析、选择性报告以及明显的方案偏离。我们评估3项研究在至少一个领域存在高偏倚风险,许多研究在其他领域的偏倚风险不明确。3项研究接受了顺势疗法药品制造商的资助;1项得到非政府组织的支持;2项得到政府支持;1项由一所大学共同赞助;1项未报告资助支持情况。方法学不一致以及显著的临床和统计异质性妨碍了进行可靠的定量荟萃分析。只有4项结果在不止一项研究中常见,可合并进行分析。优势比(OR)通常较小,置信区间(CI)较宽,且参与研究的结果相互矛盾,因此几乎无法确定干预措施的疗效。所有评估为低偏倚风险的研究均显示口服顺势疗法药品无益处;偏倚风险不确定和高的试验报告了有益效果。我们发现低质量证据表明,非个体化顺势疗法药品对急性呼吸道感染几乎没有预防作用(OR 1.14,95%CI 0.83至1.57)。我们从两项个体化预防研究中发现低质量证据,表明顺势疗法对使用抗生素的必要性影响不大(N = 369)(OR 0.79,95%CI 0.35至1.76)。我们还评估了不良事件、住院率和住院时间、缺课天数(或家长误工天数)以及生活质量,但无法汇总这些次要结果中的任何数据。两项汇总的个体化治疗研究(N = 155)提供的证据不足,无法确定顺势疗法对短期治愈率(OR 1.31,支持安慰剂,95%CI 0.09至19.54;极低质量证据)和长期治愈率(OR 0.99,95%CI 0.10至9.67;极低质量证据)的影响。不良事件报告不一致;然而,未报告严重事件。一项研究发现治疗组非严重不良事件的发生率有所增加。
两项预防研究和两项治疗研究的汇总结果显示,与安慰剂相比,顺势疗法药品对儿童急性呼吸道感染的复发率或治愈率没有任何益处。我们没有发现证据支持顺势疗法药品对儿童急性呼吸道感染的疗效。不良事件报告不佳,因此无法得出关于安全性的结论。