Department of Medical and Surgical Sciences, Alma Mater Studiorum University of Bologna, Bologna, Italy.
SSD Clinical Pharmacology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Mycoses. 2021 Nov;64(11):1317-1327. doi: 10.1111/myc.13362. Epub 2021 Aug 23.
Although echinocandins are recommended as first-line prophylaxis for high-risk orthotopic liver transplant (OLT) recipients, occurrence of breakthrough-invasive fungal infections (IFIs) remains a serious concern. We aim to assess the risk of breakthrough IFIs among OLT recipients exposed to prophylaxis with echinocandins compared to other antifungals.
Two authors independently searched PubMed-MEDLINE, Embase, study registries and reference lists from inception to March 2021, to retrieve randomised controlled trials (RCTs) or observational studies comparing efficacy and safety of echinocandins vs other antifungals for prophylaxis in OLT recipients. Data were independently extracted from two authors, and the quality of included studies was independently assessed according to ROB 2.0 tool for RCTs and ROBINS-I tool for observational studies. The primary outcome was occurrence of breakthrough IFI at the end of prophylaxis (EOP).
698 articles were screened, and ten studies (3 RCTs and 7 observational) were included. No difference between echinocandins and other antifungals in terms of breakthrough IFIs at the EOP emerged both from RCTs (odds ratio [OR] 0.85, 95% CI 0.24-2.99) and observational studies (OR 1.43, 95% CI 0.28-7.40). No difference emerged also for secondary outcomes. In the subgroup comparison between echinocandins and polyenes, a trend for higher risk of breakthrough IFI at the EOP (OR 4.82, 95% CI 0.97-24.03) was noted.
Echinocandins do not seem to be associated with increased risk of breakthrough IFIs in OLT recipients. However, the large diversity in the comparator group hinders a definitive interpretation. Further studies exploring the relationship between echinocandin use and breakthrough IFIs according to specific comparators are warranted.
虽然棘白菌素类药物被推荐作为高危原位肝移植(OLT)受者的一线预防药物,但突破性侵袭性真菌感染(IFI)的发生仍然是一个严重的问题。我们旨在评估与其他抗真菌药物相比,接受棘白菌素类药物预防的 OLT 受者发生突破性 IFI 的风险。
两名作者独立检索了从开始到 2021 年 3 月的 PubMed-MEDLINE、Embase、研究登记处和参考文献列表,以检索比较棘白菌素类药物与其他抗真菌药物预防 OLT 受者IFI 的疗效和安全性的随机对照试验(RCT)或观察性研究。数据由两名作者独立提取,根据 RCT 的 ROB 2.0 工具和观察性研究的 ROBINS-I 工具,独立评估纳入研究的质量。主要结局是预防结束时(EOP)突破性 IFI 的发生。
筛选出 698 篇文章,纳入 10 项研究(3 项 RCT 和 7 项观察性研究)。RCT 中(比值比[OR]0.85,95%CI0.24-2.99)和观察性研究中(OR1.43,95%CI0.28-7.40),棘白菌素类药物与其他抗真菌药物在 EOP 时突破性 IFI 方面均无差异。次要结局也无差异。在棘白菌素类药物与多烯类药物的亚组比较中,EOP 时突破性 IFI 的风险有增高趋势(OR4.82,95%CI0.97-24.03)。
棘白菌素类药物似乎不会增加 OLT 受者发生突破性 IFI 的风险。然而,由于比较组的多样性,很难做出明确的解释。需要进一步研究根据特定比较剂探索棘白菌素类药物使用与突破性 IFI 之间的关系。