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James D. Fortenberry MD, FCCM, FAAP Associate Professor of Pediatrics

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Presentation on theme: "James D. Fortenberry MD, FCCM, FAAP Associate Professor of Pediatrics"— Presentation transcript:

1 Plasma Exchange and Plasmapheresis in Septic Shock and Acute Kidney Injury
James D. Fortenberry MD, FCCM, FAAP Associate Professor of Pediatrics Emory University School of Medicine Director, Critical Care Medicine and Pediatric ECMO/Advanced Technologies Children’s Healthcare of Atlanta at Egleston

2

3 The Problem of Sepsis in Children
42,000 pediatric sepsis cases/year Annual cost > $2 billion Increased mortality 5.49.5/100,000 10.3% hospitalized pediatric sepsis mortality rate overall in US = the potential target

4 Overwhelming Sepsis: Desperate Times…
Diseases desperate grown By desperate appliance are relieved, Or not at all. -Claudius, King of Denmark In Hamlet Act IV Scene 3 W. Shakespeare

5 Desperate but Reasonable?

6 Potential “Desperate Devices” For Extracorporeal Use In Sepsis
Continuous renal replacement therapies (CRRT) Extracorporeal membrane oxygenation (ECMO) Extracorporeal liver support devices Plasma Exchange/Plasmapheresis

7 Extracorporeal Therapies in Septic Shock
Potential benefits Immunohomeostasis: pro/anti-inflammatory mediators Control of fluid overload Mechanical support of organ perfusion during acute episode Improved coagulation response with decreased organ thrombosis

8 Mechanisms of Sepsis and Multiple Organ Failure
Death still related to development of MOF Net effect: conversion of anticoagulant/profibrinolytic state procoagulant/antifibrinolytic state Microvascular coagulation Thrombotic microangiopathy (TMA) Link with sepsis: Platelet/vWf microthrombipredispose to MOF

9 Thrombotic Thrombocytopenic Purpura (TTP): A TMA Syndrome
Critical defect: ADAMTS-13 deficiency (< 10% of normal) Ultra-large vWf multimer-platelet thrombi Microthrombotic multi-organ vascular injury AKI central injury

10 ADAMTS-13 ADAMTS-13 = A Disintegrin And Metalloprotease with ThromboSpondin type 1 motif “The molecule formerly known as vWf-CP” = a “good” molecule Cleaves vWf multimers, reduces thrombogenic potential

11 Homeostasis Platelet vWF ADAMTS 13 (vWF-CP) tPA PGI Endothelium

12 TTP Platelet vWF vWF Shear stress

13 TTP X Platelet Platelet Endothelium ADAMTS 13 (vWF-CP) vWF
ADAMTS 13 (vWF-CP Ab) Platelet

14 vWF vWF Platelet Fibrin Platelet vWF Fibrin

15 Benefits of Plasma Exchange in TTP
Has resulted in remarkable improvement in outcome 80-90% mortality  10% Replenishes ADAMTS-13 Removes ADAMTS-13 inhibitors Removes thrombogenic ULvWf multimers -Rock, NEJM 1991

16 ADAMTS-13 Deficiency Is Also Seen in Adult Sepsis
-Martin et al., Crit Care Med 2007

17 Decreased Sepsis Survival with Decreased ADAMTS-13
Above median Below median -Martin et al., Crit Care Med 2007

18 ADAMTS-13 Deficiency Correlates with Organ Failure

19 ADAMTS-13 Deficiency Seen in Pediatric Sepsis
-Nguyen, Hematologica 2006

20 Thrombocytopenia and MOF
New-onset thrombocytopenia is independent risk factor for MOF (Carcillo 2001) OR 11.9 Thrombocytopenia with MOF increased death (OR 6.3) vs. MOF alone

21 Thrombocytopenia-Associated Multiple Organ Failure (TAMOF)
Recently described entity (Nguyen, Carcillo 2001) Children MOF>2 organs Platelet count < 100K Similarities to TTP Primarily secondary to sepsis High mortality Deficient ADAMTS-13 Increased ADAMTS-13 antibodies Increased ul-vWf multimers

22 Thrombotic Microangiopathy: TAMOF
IL- 8 TNF- IL- 6+R ADAMTS13 Ab IL-6 X ADAMTS13 (vWF-CP) Endothelium PAI-1 vWF TFPI Plasm in Plasminogen Platelet TF Shear stress x

23 Could plasma exchange be beneficial in severe sepsis and MOF/AKI?

24 Peak Concentration Model of Sepsis

25 Controlled Trials: Plasma Therapies and Sepsis
Study Design Children Included? Technique Condition Treated Mortality Tx group Mortality Control Difference RC81 Yes Plasma Exchange Meningococ-cemia 1/13 6/10 0.025 RC82 Leukaplasmapheresis 3/13 7/9 0.02 RC68 No Plasma exchange and CVVH Septic shock 1/7 8/21 0.25 RC83 Plasmapheresis/CVVH Surgical sepsis 11/19 13/24 0.94 PC70 Plasmapheresis versus plasma infusion TMA/sepsis 0/14 7/22 0.05 PRCT63 Plasmapheresis Sepsis 6/14 8/16 0.73 PRCT69 Plasmapheresis/exchange 18/52 28/52

26 Plasmapheresis in Severe Sepsis and Septic Shock
PRCT, Russian adult ICU 106 sepsis patients randomized to: Standard therapy Addition of plasmapheresis (1/2 FFP, 1/2 albumin) Decreased mortality with plasma exchange * - Busund et al., Intensive Care Medicine 2002;28:1410

27 TAMOF In Children: CHP Trial
10 children with TAMOF Decreased ADAMTS-13 (mean 33.3% of normal) Randomized trial: stopped after 10 patients: 28-day survival 1/5 standard therapy 5/5 plasma exchange (p < .05) -Nguyen, Carcillo et al., CCM 2008

28 Children’s of Pittsburgh- Pediatric TAMOF Trial
-Nguyen, Carcillo et al., CCM 2008

29 Plasma Exchange Replenishes ADAMTS-13
-Nguyen, Carcillo et al., CCM 2008

30 Plasma Therapies Plasmapheresis: plasma removed  replaced with 5% albumin Plasma exchange: plasma removed  replaced with donor plasma centrifugation filtration

31 Plasma Therapy: Centrifugation
COBE Spectra Apheresis System

32 Plasma Therapy: Filtration
B Braun Diapact

33 Why Not Plasma Infusion Alone?
Restores procoagulant factors Restores anticoagulant factors (protein C, AT III, TFP-I) Restores prostacyclin Restores tPA Restores ADAMTS-13 Requires additional volume Plasma Exchange Restores factor homeostasis as per plasma infusion In addition: Removes ADAMTS-13 inhibitors Removes ultra-large vWF multimers Removes tissue factor Removes excess PAI-1 Maintains fluid balance during procedure

34 - Darmon et al., Crit Care Med, 2006
Course of Organ Dysfunction and TMA: Plasma Infusion vs. Plasma Exchange 36 adult TMA patients Decreased mortality with plasma exchange Plasma infusion group received larger volume of plasma Plasma infusion group had larger weight gain * - Darmon et al., Crit Care Med, 2006

35 Pediatric Patients Receiving CVVH Fluid Overload Increases Mortality
- Foland, Fortenberry et al., CCM 2004

36 Plasma Exchange vs. Infusion: Weight Gain
- Darmon et al., Crit Care Med, 2006

37 TAMOF in Children: Further Studies
10 institution pediatric multicenter TAMOF study network Registry of TAMOF patients Biochemical measurements Plasma exchange in 6 centers Obtaining data to inform development of randomized trial

38 Children’s TAMOF Network
Actively participating centers: Children’s of Atlanta at Egleston: coordinating center Children’s of Atlanta at Scottish Rite Children’s of Pittsburgh Cook Children’s-Fort Worth Vanderbilt Children’s Cincinnati Children’s Columbus Children’s LSU-Shreveport Children’s Arkansas Children’s University of Michigan-Mott Children’s

39 Children’s TAMOF Network Preliminary Data
53 TAMOF patients registered to date-21 data complete Median age 12 years Median OFI: 4 Similar PRISM, PELOD at admission

40 Conclusions Sepsis/MOF (including AKI): coagulopathy/thrombosis a major contributor ADAMTS-13 deficiency may be a key component Plasma exchange a promising therapy Needs further study

41 I hope I haven’t led you astray

42 TAMOF Network Preliminary Data
Dying with standard therapy Surviving with plasma exchange PELOD Score


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