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I have no financial relationship(s) to disclose relevant to my presentation. [email protected] All Fluids are bad The Liver and abdominal hypertension Julia Wendon Consultant Intensivist and Hepatologist Institute of Liver Studies Kings College Hospital London

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All Fluids are bad The Liver and abdominal hypertension Julia Wendon Consultant Intensivist and Hepatologist Institute of Liver Studies Kings College Hospital London. I have no financial relationship(s) to disclose relevant to my presentation. [email protected]. - PowerPoint PPT Presentation

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Page 1: I have no financial relationship(s) to disclose relevant to my presentation

I have no financial relationship(s) to disclose relevant to my presentation.

[email protected]

All Fluids are bad The Liver and abdominal hypertension

Julia WendonConsultant Intensivist and Hepatologist

Institute of Liver Studies Kings College Hospital

London

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A bit is good – too much – well

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Potential Categorization of liver dysfunction in critical care /MOF

Primary liver InjuryAcute

Acute liver Injury

Acute Liver failure

Chronic

Decompensated CLD

Critically ill cirrhotics

Surgical

Hepatectomy

Trauma

Iatrogenic

Secondary liver Injury Sepsis / inflammation

Ischemia/Congestion

Systemic disease

DrugsTPNOther…..

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Fluids and liver disease

• 5% dextrose • 20-50% dextrose • N/ Saline / Hartmans / balanced crystalloids

• Colloids • 4.5% albumin 20% albumin • gelatins , starch

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Haemodynamics and issues • ALF

– Initially all volume deplete – difficult to say fluid is bad

– Risk of pancreatitis, gut oedema – Stiff liver, develop ascites easily

• Hepatic resection – Initially usually run dry – Risk of small for size syndrome – Portal inflow excessive to outflow– Adequate but not excess fluid required

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Haemodynamics of cirrhosis • Group 1

– Ascites, central hyovolaemia, total blood volume increased, usually diuresed ++ and low na and poor kidneys

• Group 2– RV volume / pressure overload, ascites and oedema,

cirrhotic cardiomyopathy, No PHT, usually high CI TPG• Group 3

– Portopulmonary syndrome with normal RA, initially maintained CI

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Situations for discussion • Acute liver failure

– Plasma exchange

• Ascites and drainage of said • Variceal haemorrhage • Hepatorenal failure

• Continuity between right heart, hepatic veins, liver and sinusoids and back to portal vein and hence guts – gut oedema, translocation

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IAP

CVPPcwP

PeeP

Compliance ↓

Echo findings also predictive of mortality post TIPS

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IAP and fluid responsiveness

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Problems related to hypotonic solutions

Replace with albumin 20% to prevent PICDAlso consider risk of variceal bleeding

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Consider IAP and renal perfusion pressure Options 1. Decrease IAP 2. Increase RPP 3. Improve central blood volume

RPP 61 to 67 mmHg

Potential risk of variceal bleed ???

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Pre paracentesis4-10 L +ive Pressors 0.45 µg/kg/min9 L ascitesDrained

Replaced 20% Albumin 1.2 L

PLR : no increase

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Terlipressin ± albumin Ortega et al Hepatology 2002;36:941

0.5 mg 4 hrly , albumin 1g/kg/body weight day 1 then 20 - 40 g/day

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Sanyal A Gatroenterology 2008 :134:1360

Albumin daily 1g/kg

Martin-Llahi M Gastroenterology 2008:134

Data also for norepinephrine and Ptx and NAC

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10 trials only type I and II Drug ± alb vs no intervention

Vasoconstrictors + Alb : Effect on mortality at 15 days but not at 30, 90 or 180 days RR 0.6 (0.37-0.97)

Terlipressin + Albumin vs Albumin : decreased mortality in type IRR 0.83 (0.65-1.05)

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MAP no relationship to changes in GFRMAP increased (>85)Reversal of RAA, NE levels

Creatinine is Dreadful measure Of renal function

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Airway Breathing Circulation

fluids - coagulation factors ??

others ?Na issues IAP – ascites &

endoscopyTerlipressin / somatostatin

Watch right sided pressures

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• 116 patients with cirrhosis and variceal bleed• Endoscopy and sclerotherapy• HVPG measured within first 24 hours: < or > 20

mmHg• If > 20 randomized to TIPS or medical Rx

Monescillo Hepatology 2004 ;40:793

Rx failureHVPG and CPscore

6 week survival

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alb

Given over 6 hours for 20% albumin and 18 hrs for HES 6%1.5 g/kg at day 1 and 1.0 g/kg at day 3

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1235 patients screened : 101 RV > 50 mmHgMPAP > 25 mmHg in 90%

PPS observed in 55%Remainder relate to increased MPAP in response to increased flowsCalculate transpulmonary gradient (MPAP-PAOP)

Poor correlation with MELD

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IAP 11.8±3.6

PDR 26.6 ± 13 vs 21.8± 7.8 (NS)

CVP 9.3±4.6 vs 15.7±4.7 (p<0.001)

Individual variation was however observed

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• SBP frequently associated with renal failure• Associated with decreased effective blood volume

and high mortality• 126 patients iv cefotaxime or iv cefotaxime plus

albumin (1.5g/kg) at day 0 and day 3 (1.0 g/kg)• 94% and 98 % had resolution of infection• Renal failure in 21 (33%) cef grp vs 6 (10%) in alb/cef

grp p=0.002• Mortality 18 (29%) vs 6 (10%) • At 3 months the mortality was 41% vs 22% p=0.03

Albumin and renal impairment in patients with cirrhosis and SBP Sort P et al N Engl J Med 1999 5; 341 (6):403

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cirrhosis

Budd chiari