Department of Respiratory and Sleep Medicine, Austin Health, Heidelberg, Victoria, Australia.
Respiratory Research@Alfred, Central Clinical School, Monash University, Melbourne, Victoria, Australia.
Ann Am Thorac Soc. 2022 May;19(5):833-844. doi: 10.1513/AnnalsATS.202102-172OC.
Idiopathic pulmonary fibrosis (IPF) is a fibrosing interstitial pneumonia with impaired survival. Previous guidelines recommend antacid medication to improve respiratory outcomes in patients with IPF. This systematic review was undertaken during the development of an American Thoracic Society, European Respiratory Society, Japanese Respiratory Society, and Asociación Latinoamericana del Tórax guideline. The clinical question was, "Should patients with IPF who have documented abnormal gastroesophageal reflux (GER) with or without symptoms of GER disease ) be treated with antacid medication or ) undergo antireflux surgery to improve respiratory outcomes?" Medline, Embase, the Cochrane Central Register of Controlled Trials, and the gray literature were searched through June 30, 2020. Studies that enrolled patients with IPF and ) compared antacid medication to placebo or no medication or ) compared antireflux surgery to no surgery were selected. Meta-analyses were performed when possible. Outcomes included disease progression, mortality, exacerbations, hospitalizations, lung function, respiratory symptoms, GER severity, and adverse effects/complications. For antacid medication, when two studies were aggregated, there was no statistically significant effect on disease progression, defined as a 10% or more decline in FVC, more than 50-m decline in 6-minute walking distance, or death (risk ratio [RR], 0.88; 95% confidence interval [CI], 0.76-1.03). A separate study that could not be included in the meta-analysis found no statistically significant effect on disease progression when defined as a 5% or more decline in FVC or death (RR, 1.10; 95% CI, 1.00-1.21) and an increase in disease progression when defined as a 10% or more decline in FVC or death (RR, 1.28; 95% CI, 1.08-1.51). For antireflux surgery, there was also no statistically significant effect on disease progression (RR, 0.29; 95% CI, 0.06-1.26). Neither antacid medications nor antireflux surgery was associated with improvements in the other outcomes. There is insufficient evidence to conclude that antacid medication or antireflux surgery improves respiratory outcomes in patients with IPF, most of whom had not had abnormal GER confirmed. Well-designed and adequately powered prospective studies with objective evaluation for GER are critical to elucidate the role of antacid medication and antireflux surgery for respiratory outcomes in patients with IPF.
特发性肺纤维化 (IPF) 是一种伴有生存受损的纤维性间质性肺炎。先前的指南建议使用抗酸药物来改善 IPF 患者的呼吸结局。本系统评价是在美国胸科学会、欧洲呼吸学会、日本呼吸学会和拉丁美洲胸科学会指南制定过程中进行的。临床问题是,“是否应该对有或无胃食管反流病 (GERD) 症状的 IPF 患者进行抗酸药物治疗或抗反流手术以改善呼吸结局?”通过 2020 年 6 月 30 日检索了 Medline、Embase、Cochrane 中央对照试验注册库和灰色文献。选择了纳入 IPF 患者并比较抗酸药物与安慰剂或无药物治疗或抗反流手术与无手术的研究。当可能时进行了荟萃分析。结果包括疾病进展、死亡率、恶化、住院、肺功能、呼吸症状、GER 严重程度和不良反应/并发症。对于抗酸药物,当汇总两项研究时,在疾病进展(定义为 FVC 下降 10%或更多、6 分钟步行距离下降 50m 或以上或死亡)方面无统计学意义的效果(风险比 [RR],0.88;95%置信区间 [CI],0.76-1.03)。另一项无法纳入荟萃分析的单独研究发现,当疾病进展定义为 FVC 下降 5%或更多或死亡时(RR,1.10;95%CI,1.00-1.21)以及 FVC 下降 10%或更多或死亡时(RR,1.28;95%CI,1.08-1.51),疾病进展增加时,无统计学意义的效果。对于抗反流手术,疾病进展也无统计学意义(RR,0.29;95%CI,0.06-1.26)。抗酸药物和抗反流手术都不能改善其他结果。没有足够的证据表明抗酸药物或抗反流手术可以改善 IPF 患者的呼吸结局,其中大多数患者的异常 GER 并未得到证实。具有客观 GER 评估的精心设计和充分有效的前瞻性研究对于阐明抗酸药物和抗反流手术对 IPF 患者呼吸结局的作用至关重要。
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