Volume 29, Issue 4 pp. 782-786
Hepatology

Efficacy of continuous plasma diafiltration therapy in critical patients with acute liver failure

Takuya Komura

Takuya Komura

Intensive Care Unit, Kanazawa University Hospital, Kanazawa, Japan

Disease Control and Homeostasis, Kanazawa University, Kanazawa, Japan

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Takumi Taniguchi

Takumi Taniguchi

Intensive Care Unit, Kanazawa University Hospital, Kanazawa, Japan

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Yoshio Sakai

Yoshio Sakai

Disease Control and Homeostasis, Kanazawa University, Kanazawa, Japan

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Tatsuya Yamashita

Tatsuya Yamashita

Disease Control and Homeostasis, Kanazawa University, Kanazawa, Japan

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Eishiro Mizukoshi

Eishiro Mizukoshi

Disease Control and Homeostasis, Kanazawa University, Kanazawa, Japan

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Toru Noda

Toru Noda

Intensive Care Unit, Kanazawa University Hospital, Kanazawa, Japan

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Masaki Okajima

Masaki Okajima

Intensive Care Unit, Kanazawa University Hospital, Kanazawa, Japan

Disease Control and Homeostasis, Kanazawa University, Kanazawa, Japan

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Shuichi Kaneko

Corresponding Author

Shuichi Kaneko

Disease Control and Homeostasis, Kanazawa University, Kanazawa, Japan

Correspondence

Dr Shuichi Kaneko, Disease Control and Homeostasis, Graduate School of Medical Science, Kanazawa University, Kanazawa 920-8641, Japan. Email: [email protected]

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First published: 13 November 2013
Citations: 13
Disclosures: The authors have no financial conflicts of interest.

Abstract

Background and Aims

Acute liver failure (ALF) is a critical illness with high mortality. Plasma diafiltration (PDF) is a blood purification therapy that is useful for ALF patients, but it is difficult to use when those patients have multiple organ failure or unstable hemodynamics. In these patients, symptoms are also likely to exacerbate immediately after PDF therapy. We developed continuous PDF (CPDF) as a new concept in PDF therapy, and assessed its efficacy and safety in ALF patients.

Methods

Ten ALF patients (gender: M/F 6/4, Age: 47 ± 14) were employed CPDF therapy. The primary outcomes were altered liver function, measured by the model for end-stage liver disease (MELD) score, and total bilirubin and prothrombin time international normalized ratios (PT-INR), 5 days after CPDF therapy. Secondary outcomes included sequential organ failure assessment (SOFA) scores, 5 days after CPDF therapy, and the survival rate 14 days after this therapy.

Results

The MELD score (34.5–28.0; P = 0.005), total bilirubin (10.9–7.25 mg/dL; P = 0.048), PT-INR (1.89–1.31; P = 0.084), and SOFA score (10.0–7.5; P < 0.039) were improved 5 days after CPDF therapy. Nine patients were alive, and one patient died because of acute pancreatitis, complicated by ALF. There were no major adverse events related to this therapy under hemodynamic stability.

Conclusion

In the present study, CPDF therapy safely supported liver function and generally improved the condition of critically ill patients with ALF.

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