Volume 23, Issue 6 pp. 943-950

Evaluation of the coagulation and inflammatory responses in solid organ transplant recipients and donors

Josh Levitsky

Josh Levitsky

Northwestern University Feinberg School of Medicine, Chicago, IL

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Alison Freifeld

Alison Freifeld

University of Nebraska Medical Center, Omaha, NE, USA

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Elizabeth Lyden

Elizabeth Lyden

University of Nebraska Medical Center, Omaha, NE, USA

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Julie Stoner

Julie Stoner

University of Nebraska Medical Center, Omaha, NE, USA

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Diana Florescu

Diana Florescu

University of Nebraska Medical Center, Omaha, NE, USA

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Alan Langnas

Alan Langnas

University of Nebraska Medical Center, Omaha, NE, USA

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R. Brian Stevens

R. Brian Stevens

University of Nebraska Medical Center, Omaha, NE, USA

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Penny Hardiman

Penny Hardiman

University of Nebraska Medical Center, Omaha, NE, USA

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Lisa Hill

Lisa Hill

University of Nebraska Medical Center, Omaha, NE, USA

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Andre C. Kalil

Andre C. Kalil

University of Nebraska Medical Center, Omaha, NE, USA

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First published: 25 November 2009
Citations: 15
Andre Kalil, MD, University of Nebraska Medical Center, 985400 Nebraska Medical Center, Omaha, NE 68198, USA.
Tel.: +1 402 559 8650; fax: +1 402 559 5581;
e-mail: [email protected]

This study was supported by the Clinical Research Center at the University of Nebraska Medical Center

Abstract

Abstract: New strategies that modify the coagulation/inflammatory cascades may be applicable to solid organ transplant (SOT) recipients in the treatment of complications. However, data on kinetics of post-SOT cascades are needed before considering these strategies. Prospectively collected pre-transplant serum measurements of inflammatory (high-sensitive C-reactive protein, HS-CRP) and coagulation (d-Dimer, DD; protein C, PC) markers were compared to post-operative (day 1–90) values in deceased-donor liver (DDLT) and renal (DDRT) transplant recipients, living-related renal recipients (LRT) and donors (LRD). A total of 85 SOT were enrolled: 25 DDLT, 32 DDRT/LRT, 28 LRD. HS-CRP increased in all groups, mainly immediate post-SOT and in LRDs. DD had a similar pattern mainly in LRT and LRD. PC increased significantly over time in the DDLT group ( p < 0.01). Compared to those with no complications (infection, rejection or thrombosis), day 30 HS-CRP (p = 0.04) and DD (p = 0.06) were elevated in the DDRT/LRT group with complications; PC was decreased at day 7 (p = 0.04) and day 30 (p = 0.009) in DDLT and DDRT/LRT groups with complications, respectively. In conclusion, activation of the inflammatory/coagulation cascades occurs after SOT and is least pronounced in DDLT. This activation diminishes over time unless transplant complications occur. Our results support further research in approaches to altering these cascades in SOT recipients.

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