Elizabeth K. Powell MD , Guinevere A. Johnson MS-2 , William Teeter MD , Donna Mursch RN, BSN , Jeff Broski RN , Christopher Kolokythas RN, MS, CRNP, DNP , Katie B. Andersen RN, MS, CRNP , Shannon Gaasch RN, MS, CRNP , Deborah M. Stein MD , Thomas M. Scalea MD, MCCM , Samuel M. Galvagno Jr. DO, PhD
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The objective of this study was to assess the outcomes of patients with ALF who underwent MARS therapy at a single institution using institutionally developed indications based on current best evidence.</p></div><div><h3>Research Question</h3><p>Is MARS used for selected causes of ALF associated with better survivability than predicted by standardized mortality rates (SMRs)?</p></div><div><h3>Study Design and Methods</h3><p>This was a single-center, retrospective cohort study of the outcomes of patients with ALF who underwent MARS at the R. Adams Cowley Shock Trauma Center, University of Maryland Medical Center. All patients aged 18 years or older who were admitted to our institution and underwent MARS treatment between July 1, 2013, and February 9, 2021, were included in this study. Data relevant to the study were collected from electronic medical records and were stored in Research Electronic Data Capture tools. From these data, estimated mortality from Model for End-Stage Liver Disease scores were used to calculate SMR. The SMRs then were compared for different institutional indications for MARS. Additional descriptive statistics were applied.</p></div><div><h3>Results</h3><p>Sixty-one patients underwent MARS treatment during the study period. Overall survival in the cohort was 56%. The SMR was lower than expected for patients who underwent MARS who were transplant candidates (SMR, 0.78; 95% CI, 0.63-0.93). Although no significant differences were found before and after MARS treatment in median ammonia levels (58 Umol/L [interquartile range (IQR), 32-104 Umol/L] vs 39 Umol/L [IQR, 18-57 Umol/L]; <em>P</em> = .44) or norepinephrine doses (0.21 μg/kg/min [IQR, 0.08-0.4 μg/kg/min] vs 0.06 μg/kg/min [IQR, 0.04-0.14 μg/kg/min]; <em>P</em> = .46), significant decreases in median aspartate transferase (3,334 U/L [IQR, 1,174-11,151 U/L] vs 344 U/L [IQR, 196-978 U/L]; <em>P</em> < .001), alanine transaminase (1,410 U/L [IQR, 600-5,505 U/L] vs 347 U/L [IQR, 153-952 U/L]; <em>P</em> < .001), international normalized ratio (3.2 [IQR, 2-4.5] vs 1.5 [IQR, 1.3-1.9]; <em>P</em> < .001), and median lactic acid levels (7.7 mM [IQR, 4.8-13.2 mM] vs 2.4 mM [IQR, 1.7-3.1 mM]; <em>P</em> < .001) were seen.</p></div><div><h3>Interpretation</h3><p>We report our experience using MARS for institutionally developed indications in a level 1 trauma center and transplant center. These data add to a growing body of literature that support the use of MARS as an extracorporeal life support method for selected patients at centers experienced in the management of advanced liver disease.</p></div>","PeriodicalId":93934,"journal":{"name":"CHEST critical care","volume":"2 1","pages":"Article 100041"},"PeriodicalIF":0.0000,"publicationDate":"2023-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2949788423000412/pdfft?md5=67f4354cd80d5847617803051bd6fb88&pid=1-s2.0-S2949788423000412-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Actual vs Expected Survival With the Use of the Molecular Adsorbent Recirculating System for Acute Liver Failure\",\"authors\":\"Elizabeth K. Powell MD , Guinevere A. Johnson MS-2 , William Teeter MD , Donna Mursch RN, BSN , Jeff Broski RN , Christopher Kolokythas RN, MS, CRNP, DNP , Katie B. 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From these data, estimated mortality from Model for End-Stage Liver Disease scores were used to calculate SMR. The SMRs then were compared for different institutional indications for MARS. Additional descriptive statistics were applied.</p></div><div><h3>Results</h3><p>Sixty-one patients underwent MARS treatment during the study period. Overall survival in the cohort was 56%. The SMR was lower than expected for patients who underwent MARS who were transplant candidates (SMR, 0.78; 95% CI, 0.63-0.93). 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引用次数: 0
摘要
背景急性肝衰竭(ALF)的死亡率约为 50%。因此,显然有必要改进 ALF 的治疗方法。分子吸附再循环系统(MARS;Baxter)是一种体外肝脏支持系统,能解毒水溶性毒素和蛋白结合毒素。尽管一些研究显示 MARS 在 ALF 的治疗中具有疗效,但文献资料仍然有限。本研究的目的是评估在一家机构接受 MARS 治疗的 ALF 患者的预后,该机构根据当前最佳证据制定了适应症。研究问题与标准化死亡率 (SMR) 预测的相比,MARS 用于某些原因引起的 ALF 是否具有更好的存活率?本研究纳入了 2013 年 7 月 1 日至 2021 年 2 月 9 日期间入住本院并接受 MARS 治疗的所有 18 岁或以上患者。本研究的相关数据均从电子病历中收集,并存储在研究电子数据采集工具中。根据这些数据,利用终末期肝病模型评分估算出的死亡率来计算 SMR。然后比较不同机构 MARS 适应症的 SMR。结果61名患者在研究期间接受了MARS治疗。研究组的总生存率为 56%。接受 MARS 治疗的移植候选患者的 SMR 低于预期(SMR,0.78;95% CI,0.63-0.93)。虽然在 MARS 治疗前后,中位氨水平(58 Umol/L [四分位距(IQR),32-104 Umol/L] vs 39 Umol/L [四分位距(IQR),18-57 Umol/L];P = .44)或去甲肾上腺素剂量(0.21 μg/kg/min [IQR, 0.08-0.4 μg/kg/min] vs 0.06 μg/kg/min [IQR, 0.04-0.14 μg/kg/min];P = .46),天冬氨酸转移酶中位数显著下降(3 334 U/L [IQR, 1 174-11 151 U/L] vs 344 U/L [IQR, 196-978 U/L] ;P < .001)、丙氨酸转氨酶(1 410 U/L [IQR, 600-5 505 U/L] vs 347 U/L [IQR, 153-952 U/L]; P <.001)、国际标准化比率(3.2 [IQR, 2-4.5] vs 1.5 [IQR, 1.3-1.9]; P <.001)和中位乳酸水平(7.Interpretation 我们报告了在一级创伤中心和移植中心针对机构制定的适应症使用 MARS 的经验。越来越多的文献支持在具有晚期肝病治疗经验的中心将 MARS 作为一种体外生命支持方法用于选定的患者,这些数据是对这些文献的补充。
Actual vs Expected Survival With the Use of the Molecular Adsorbent Recirculating System for Acute Liver Failure
Background
Acute liver failure (ALF) has a mortality rate of approximately 50%. Thus, it is evident that improvements in treatment of ALF are necessary. The Molecular Adsorbent Recirculating System (MARS; Baxter), an extracorporeal liver support system that detoxifies water-soluble and protein-bound toxins, has been available at select centers worldwide for > 2 decades. Although some studies have shown the efficacy of MARS in the management of ALF, the literature remains limited. The objective of this study was to assess the outcomes of patients with ALF who underwent MARS therapy at a single institution using institutionally developed indications based on current best evidence.
Research Question
Is MARS used for selected causes of ALF associated with better survivability than predicted by standardized mortality rates (SMRs)?
Study Design and Methods
This was a single-center, retrospective cohort study of the outcomes of patients with ALF who underwent MARS at the R. Adams Cowley Shock Trauma Center, University of Maryland Medical Center. All patients aged 18 years or older who were admitted to our institution and underwent MARS treatment between July 1, 2013, and February 9, 2021, were included in this study. Data relevant to the study were collected from electronic medical records and were stored in Research Electronic Data Capture tools. From these data, estimated mortality from Model for End-Stage Liver Disease scores were used to calculate SMR. The SMRs then were compared for different institutional indications for MARS. Additional descriptive statistics were applied.
Results
Sixty-one patients underwent MARS treatment during the study period. Overall survival in the cohort was 56%. The SMR was lower than expected for patients who underwent MARS who were transplant candidates (SMR, 0.78; 95% CI, 0.63-0.93). Although no significant differences were found before and after MARS treatment in median ammonia levels (58 Umol/L [interquartile range (IQR), 32-104 Umol/L] vs 39 Umol/L [IQR, 18-57 Umol/L]; P = .44) or norepinephrine doses (0.21 μg/kg/min [IQR, 0.08-0.4 μg/kg/min] vs 0.06 μg/kg/min [IQR, 0.04-0.14 μg/kg/min]; P = .46), significant decreases in median aspartate transferase (3,334 U/L [IQR, 1,174-11,151 U/L] vs 344 U/L [IQR, 196-978 U/L]; P < .001), alanine transaminase (1,410 U/L [IQR, 600-5,505 U/L] vs 347 U/L [IQR, 153-952 U/L]; P < .001), international normalized ratio (3.2 [IQR, 2-4.5] vs 1.5 [IQR, 1.3-1.9]; P < .001), and median lactic acid levels (7.7 mM [IQR, 4.8-13.2 mM] vs 2.4 mM [IQR, 1.7-3.1 mM]; P < .001) were seen.
Interpretation
We report our experience using MARS for institutionally developed indications in a level 1 trauma center and transplant center. These data add to a growing body of literature that support the use of MARS as an extracorporeal life support method for selected patients at centers experienced in the management of advanced liver disease.