Suppr超能文献

在 UNOS 数据库中,儿科慢加急性肝衰竭患者的候补名单死亡率更高。

Higher Waitlist Mortality in Pediatric Acute-on-chronic Liver Failure in the UNOS Database.

机构信息

Baylor College of Medicine.

Texas Children's Hospital, Houston, TX.

出版信息

J Pediatr Gastroenterol Nutr. 2021 Jan 1;72(1):80-87. doi: 10.1097/MPG.0000000000002891.

Abstract

OBJECTIVES

Acute-on-chronic liver failure (ACLF), whereas increasingly well-defined in adults, has been poorly characterized in pediatric patients other than having a poor prognosis. This study aimed to identify ACLF and evaluate prognosis in the American pediatric population.

METHODS

Modified ACLF definitions (p-CLIF) were applied to 11,300 children listed for liver transplantation from March 2002 through 2017 in the Organ Procurement and Transplantation Network (OPTN) database.

RESULTS

Pediatric ACLF patients have greater mortality within 90 days from listing (46.6% by p-CLIF) than other types of failure (<30%), including acute liver failure, as well as greater mortality within the first 30 and 90 days after transplantation than all other types of liver failure, but do not have increased mortality rates relative to other groups between 90 and 365 days from transplant. Although some ACLF listings also received 1B status, ACLF mortality at 90 days was greater than the general 1B population (50 vs 29.4%). Model for End-Stage Liver Disease/Pediatric End-Stage Liver Disease scores of ACLF patients are lower than 1B listings, and do not predict waitlist or posttransplant death. Greater number of organ failures does correlate with increased mortality. Biliary atresia is the leading etiology of pediatric chronic liver disease, accounting for over 30% of chronic and 45% of ACLF listings, yet is protective against mortality (hazard ratio [HR] = 0.142 for ACLF). Receiving exception approval is independently but similarly protective in ACLF (HR = 0.145).

CONCLUSIONS

These findings pose a challenge for allocation decisions but indicate greater attention to ACLF is needed, as scoring systems may not capture these children's risk of early death, which appears to currently be mitigated by exceptions. Multicenter, clinical, preferably prospective study of ACLF is necessary to determine how to prioritize ACLF relative to other liver failure types to address its relatively higher early mortality.

摘要

目的

急性肝衰竭(ACLF)在成人中的定义越来越明确,但在儿科患者中的特征较差,除了预后不良外。本研究旨在确定美国儿科人群中的 ACLF 并评估其预后。

方法

应用改良 ACLF 定义(p-CLIF)对 2002 年 3 月至 2017 年期间在美国器官获取和移植网络(OPTN)数据库中列出的 11300 名接受肝移植的儿童进行分析。

结果

与其他类型的衰竭(<30%)相比,包括急性肝衰竭,p-CLIF 定义的儿科 ACLF 患者在列入名单后 90 天内的死亡率更高(46.6%),以及在移植后 30 天和 90 天内的死亡率更高,比所有其他类型的肝衰竭都高,但在移植后 90 天至 365 天期间,与其他组相比,死亡率没有增加。尽管一些 ACLF 患者也被列为 1B 状态,但 ACLF 在 90 天的死亡率高于一般的 1B 人群(50%比 29.4%)。ACLF 患者的终末期肝病模型/小儿终末期肝病评分低于 1B 患者,不能预测等待名单或移植后死亡。器官衰竭的数量越多,死亡率越高。胆道闭锁是小儿慢性肝病的主要病因,占慢性肝病的 30%以上,占 ACLF 患者的 45%,但可降低死亡率(ACLF 的风险比[HR]为 0.142)。获得例外批准在 ACLF 中是独立但相似的保护因素(HR 为 0.145)。

结论

这些发现对分配决策提出了挑战,但表明需要对 ACLF 给予更多关注,因为评分系统可能无法捕捉到这些儿童的早期死亡风险,而例外情况似乎目前可以减轻这种风险。需要进行多中心、临床、最好是前瞻性的 ACLF 研究,以确定如何将 ACLF 相对于其他类型的肝衰竭进行优先级排序,以解决其相对较高的早期死亡率。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验