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PORTAL HYPERTENSION

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PORTAL HYPERTENSION PRESENTER: KRITHIKA KRISHNAN MODERATOR : DR.R.PANDEY www.anaesthesia.co.in anaesthesia.co.in_at_gmail.com * * * * * * * HPS Presence of chronic ... – PowerPoint PPT presentation

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Title: PORTAL HYPERTENSION


1
PORTAL HYPERTENSION
  • PRESENTER KRITHIKA KRISHNAN
  • MODERATOR DR.R.PANDEY

www.anaesthesia.co.in anaesthesia.co.in_at_gmail.c
om
2
  • Mr. Anil Kumar Rai
  • 36yrs / male
  • Vendor
  • New Delhi
  • Presenting complaints
  • Vomiting of blood
  • Black tarry stools 1 month back
  • Loss of consciousness

3
History of presenting complaints
  • Vomiting of blood.
  • 2 episodes.
  • 50 ml each.
  • Dark colour mixed with fresh blood.
  • Not associated with cough.
  • Passage of black tarry stools.
  • 2 episodes.

4
  • H/O Loss of consciousness.
  • 1 episode.
  • Not associated with trauma.
  • Lasted for 30 seconds.
  • H/O abdominal distension.
  • 1 month.
  • Progressively increasing.
  • Uniform.
  • Not associated with abdominal pain.

5
  • H/O yellowish discolouration of the body and
    mucous membrane
  • 1 month.
  • Progressively deepening.
  • Not associated with clay stools or dark urine.
  • H/O fever 1 month
  • Low grade.
  • Intermittent.
  • Relieved with drugs.

6
  • H/O wakefulness in night and day time sleepiness.
  • 15 days back.
  • Improved with medications.
  • H/O loss of weight.
  • 15 kgs over past 2 years.
  • H/O loss of appetite.

7
  • No H/O.
  • Pedal edema.
  • Breathlessness on exertion.
  • Chest pain.
  • Palpitation.
  • Decreased urine output.
  • Bruising/ gum bleed .

8
  • Personal History
  • Consumes mixed diet.
  • Chronic alcoholic since 15 years of age, stopped
    one year back (8-10 pegs of country liquor/day).
  • H/O smoking since 15 years of age, stopped one
    year back about 15 pack- years.
  • No H/O drug abuse.

9
  • Treatment History
  • H/O upper GI endoscopy and sclerotherapy.
  • Repeated paracentesis for the ascites.
  • Antibiotics.
  • T. Aldactone 100mg OD.
  • T. Methyl cobalamine1500mg OD.
  • T. Thiamine 100mg OD.
  • Syrup. Lactulose 30ml TDS.

10
  • Past History
  • H/O similar episodes of hemetemesis present 2
    years
  • 4 such episodes.
  • UGI endoscopy done.diagnosed as oesophageal
    varices and sclerotherapy done.
  • Evaluated and diagnosed as cirrhosis with ESLD.
  • H/O spontaneous bacterial peritonitis.
  • 6 months back.
  • Treated with antibiotics.

11
  • No H/O any other systemic illness.
  • No H/O any surgery in the past.
  • Family History
  • No H/O any similar illness in the family.

12
General examination
  • 55 kg, 5 feet 7 inches.
  • Average built .
  • Pallor ve.
  • Icteric.
  • No clubbing.
  • No cyanosis.
  • No pedal edema.
  • No other sign of liver cell failure.
  • No significant lymphadenopathy.
  • Venous access - good

13
Vital Signs
  • Pulse rate
  • 72 beats/ min,
  • regular in rhythm,
  • normal in volume and character.
  • Blood pressure
  • 120/60 mm Hg
  • measured in right upper limb ,in the supine
    posture.
  • Jugular venous pulsations visible, pressure not
    elevated.
  • Temperature - 37ºC.

14
Airway Examination
  • MMP II.
  • Mouth opening and neck movements adequate.
  • No loose tooth/ artificial denture.
  • TMD gt3 fingers.

15
Systemic examination
  • Abdomen
  • On inspection
  • Distended uniformly.
  • All quadrants moving equally with respiration.
  • No dilated veins.
  • Needle prick scars made out in the flanks.
  • Umbilicus inverted.
  • Divarication of recti present.

16
  • On palpation
  • Soft.
  • No tenderness.
  • Spleen palpable below the left costal margin up
    to the umbilicus.
  • Liver not palpable.
  • On percussion
  • Shifting dullness present.
  • Liver span 7 cm.

17
  • Cardiovascular System
  • S1 S2 heard - normal, no murmurs.
  • Respiratory System
  • B/L vesicular breath sounds present, no added
    sounds.
  • Central Nervous System
  • Clinically normal.

18
Provisional diagnosis
  • Decompensated chronic liver disease with portal
    hypertension with ascites.

19
  • Investigation
  • Hemogram
  • Hb 9 g/dl
  • TLC 3700/cumm
  • DLC P 74, L 23, M 2
  • Platelet 71000/cumm
  • PT 12/16.2

20
  • Biochemistry
  • Blood sugar (R) 152 mg/dl
  • B.Urea 103 mg/dl
  • S. Creatinine 1.9 mg/dl
  • Na/K 141/4.1 meq/L
  • S.Bilirubin 3 mg/dl
  • 0.8mg/dl 2.2mg/dl
  • SGOT/PT 76/56
  • ALKPO4 222
  • T.Proteins/ Albumin/globulin 7.7/4.0/3.7

Unconjugated
Conjugated
21
  • CXR WNL
  • ECG WNL
  • Echo Normal study
  • USG abdomen Liver small in size with slightly
    coarse echotexture.
  • UGI endoscopy Grade III esophageal varices.
  • CECT atrophy of R lobe of liver , spleen
    enlarged with infarct.
  • HBsAg -ve.
  • Anti HCV antibodies ve.

22
Final diagnosis
  • Decompensated chronic liver disease, probably
    alcohol in etiology, with portal hypertension
    with ascites.

23
  • Portal hypertension(gt10mmHg) and its consequences
  • Gastroesophageal varices
  • Ascites
  • Hepatic encephalopathy
  • SBP
  • Hepatorenal syndrome
  • HCC

24
  • Laboratory findings (minimal or absent)
  • Anemia (a frequent finding)
  • Coagulation abnormalities
  • Increased AST, ALP, bilirubin, gamma globulins
  • Decreased albumin


25
  • Imaging
  • Spleen and hepatic enlargment
  • Barium / endoscopic studies- presence of varices
  • USG/ CT/ MRI for liver size, ascitis, hepatic
    nodules
  • Doppler- for assessing the patency of splenic,
    portal hepatic veins

26
  • Portal Hypertension
  • Hemorrhage from varices.
  • Splenomegaly with hypersplenism.
  • Ascites.
  • Acute and chronic hepatic encephalopathy.

27
  • Diagnosis
  • Fibreoptic esophagoscopy -for confirming varices.
  • MRI and contrast CT- tool for detecting the
    collateral circulation.
  • Percutaneous transhepatic catheterisation-Portal
    venous pressure.

28
  • Management of acute bleed
  • Prompt replacement of fluid loss
  • Replacement of clotting factors with fresh frozen
    plasma
  • Monitoring of CVP or cap.wedge pressure
  • Vasoconstrictors
  • Balloon tamponade
  • Endosopic variceal ligation
  • Sclerotherapy
  • Gastric devascularisation

29
  • Pathological feaures in advanced liver disease
  • 1.Hyperdynamic circulation
  • ? peripheral vascular resistance
  • ? cardiac output
  • Other CVS changes
  • Increased SV HR.
  • Normal filling pressures.
  • Decreased sensitivity to vasopressors.
  • Cardiomyopathy.

30
  • 2. Hypoxemia
  • Intrapulmonary shunting
  • Precapillary sphincter dilatation (HPS I).
  • AV shunting (HPS II).
  • V-Q abnormality in the lung.
  • Exacerbated in the upright position.
  • Pleural effusion.
  • Pulmonary infection.
  • Diaphragmatic dysfunction.
  • Dysfunction of HPV.
  • Rightward shift of O2 dissociation curve.

31
  • 3. Metabolic alkalosis
  • High aldosterone state.
  • 4. Coagulation abnormalities
  • Deficiency of plasma clotting factors.
  • ? platelet count.
  • ? platelet function.
  • Abnormal fibrinolytic factors.

32
  • 5. Hepatic blood flow
  • Summation of hepatic arterial portal venous
    blood flow
  • Effect of anesthetic drugs
  • Ventilation IPPV, CO2
  • Effect of surgery
  • 6. Ascites
  • 7. Renal impairment
  • 8. Hepatic encephalopathy

33
Ascites
  • Underfill hypothesis
  • Overflow hypothesis
  • Treatment
  • Spirnolactone
  • Paracentesis, large volume albumin
  • Frusemide
  • Peritoneovenous shunt

34
Hepatopulmonary syndrome
  • HPS
  • Presence of chronic disease
  • Absence of intrinsic cardiopulmonary disease
  • Pulmonary gas exchange abnormality
  • Intrapulmonary vascular dilatation
  • PPH
  • PAP gt25mmHg
  • PCWP lt15mmHg
  • PVR gt120 dynes/s/cm5

35
Hepatorenal syndrome
International ascites club criteria 1.
S.creatinine gt1.5mg/dl (133 µmol/l), GFR
lt40ml/min. 2. Absence of on going bact infection,
fluid loss, treatment with nephrotoxic drugs. 3.
No sustained improvement after diuretic
withdrawal and plasma volume expansion. 4.
Proteinuria lt 0.5g/dl. 5. No USG evidence of
parenchymal renal disease.
  • U. Na lt10
  • U.sediments N
  • U.osmolality exceeds pl osmolality by atleast
    100mosm/l
  • U/Pl cr. ratio gt301

36
Hepatic encephalopathy
CNS Asterixes EEG
Grade I Sleep inversion euphoria /- Triphasic
II Lethargy Triphasic
III Confusion Triphasic
IV Coma, initially responds to noxious stimulus - Delta activity
37
Precipitating factor
  • Hypoxia.
  • Hypovolemia.
  • Hypoglycemia.
  • Anemia.
  • Infection, pneumonia sepsis.
  • UGI bleed.
  • Increased protein intake.
  • Constipation.
  • Large volume parcentesis.
  • Diarrhea and vomiting.
  • Diuretic.
  • Sedatives.
  • Shunts.
  • Treatment
  • Avoid ppt factors.
  • Lactulose.
  • Neomycin . Metronidazole.
  • Liver transplantation.

38
  • Guidelines for anaesthetic management in patients
    with ESLD
  • Common operative procedures
  • Surgery for gastric/duodenal ulcer,
    cholecystectomy, colon carcinoma
  • Various orthopedic procedures
  • Portocaval shunts, Sclerotherapy, gastric
    devascularisation surgery

39
  • Preoperative instructions
  • NPO gt 8 hours.
  • High risk consent in the view of perioperative
    risk of renal and hepatic failure.
  • Hydration of the patient with IV fluids
    _at_100ml/hour.
  • CM S.electrolytes, PT and platelets.
  • Premedication with T.Lorazepam 4mg HS CM and
    T.Ranitidine 150mg HS CM.

40
  • Induction Mod RSI
  • Pre oxygenation for 3 minutes.
  • Titrated dose of propofol (Thio can also be
    used).
  • Intubate after giving scoline.
  • Maintenance -
  • Volatile agents Isoflurane, desflurane or
    sevoflurane.
  • NMB Non depolarizing agents - Altered Vdss.

41
  • Opioids
  • Fentanyl.
  • Morphine.
  • Pain Best controlled with epidural opioids if
    CNB is not contraindicated.

42
Drugs Effect of liver disease Effect of liver disease Effect of liver disease Effect of liver disease Dose adjustment
T1/2 Vd Cl Fp
Thiopentone U U U I May need to
Morphine U U U U Frequency
Fentanyl U U U None
Alfentanil I U D I
Midazolam I I D
Lorazepam I I D I None
Propofol U U U I None/
43
Risk assessment in patients with liver
diseaseChild Pugh score
C B A
gt3 2 - 3 lt2 Bilirubin
lt2.8 2.8 -3. 5 gt3.5 Albumin
Poorly controlled Well controlled None Ascites
Grade III-IV Grade I-II None Hepatic encepahalopathy
gt6/gt2.3 4 6/1.7-2.3 lt 4/lt1.7 PT/ INR
76 30 10 Surgical risk
44
  • MELD score
  • MELD 3.8 x loge(bil ) 11.2 x loge(INR) 9.6
    x loge(creatinine)
  • Causes of mortality in the periop period
  • Sepsis, pneumonia.
  • Renal failure.
  • Non mechanical bleeding.
  • Hepatic failure encephalopathy.

45
Liver transplantation
  • Indications
  • Children.
  • Adults.
  • Contraindications
  • Absolute.
  • Relative.

46
Preoperative preparation
  • Central nervous system status.
  • Encephalopathy grade.
  • ICP.
  • Coagulation status.
  • Renal failure.
  • Cardiopulmonary status.

47
Phases of OLT
  • Preanhepatic phase
  • Monitor placement to clamping.
  • Medications titrated.
  • Lorazepam, morphine, oxazepam.
  • Temperature monitoring and maintenance.
  • Invasive monitoring.
  • Defibrillator ready.
  • Rapid infusor.
  • Thromboelastography.
  • Periodic blood sampling.

48
  • Anhepatic phase
  • Occlusion of vascular supply to old liver to
    perfusion of new liver.
  • Metabolic acidosis/ alkalosis.
  • Hypocalcemia.
  • Hypokalemia.

49
  • Postanhepatic phase
  • After perfusion of the new liver.
  • Ventricular fibrillation - hyperkalemia.
  • Hypotension vasoactive amines.
  • Air embolism.
  • Paradox Hepatic congestion.

50
Jaundice
Hemolytic Hepatocellular cholestasis
Transaminase N N
S. Albumin N N
PT N N
Bilirubin Unconju Conju Conju
ALP N N
GGT N N
BUN N N N
ICG N Retention N/ Retention
51
Coagulation cascade
XII.XIIa
Intrinsic pathway
XIXIa
IX..IXa
IXaVIIIa
X..Xa
XaVa
II..IIa
IIa
52
TF
Extrinsic pathway
VII..VIIa TF
X.Xa
V..Va
II.IIa
I.Ia
53
ASRA guidelines
  • Recommendation with heparin
  • Sub cut heparin no CI
  • S.C gt 4 d platelet count
  • i.v heparin delay for 1 hr
  • indwelling catheter remove after 2- 4 hrs of
    last dose, next dose after atleast 1 hr.
  • syst heparinisation monitor neurologic status
    for 12 hr, dilute conc of LA
  • bloody tap no mandatory cancellation

54
  • Preoperative LMWH
  • LMWH thromboprophylaxis - needle placement 10-12
    hrs after LMWH dose
  • Acute coronary syndrome / thrombo -embolism
    therapy - 24 hrs after last LMWH dose
  • Post operative LMWH
  • Twice daily dosing
  • 1st dose LMWH 24 hrs postoperatively
  • Epidural catheter to be removed prior to LMWH
    initiation
  • LMWH dose 2 hours after catheter removal

55
  • Single daily dosing
  • Initiation of LMWH - 6-8 hrs postoperatively,
    then 24 hrs later
  • Indwelling catheters can be kept
  • Catheter removal 10-12 hrs after last LMWH dose
  • Subsequent LMWH dose 2 hours after catheter
    removal
  • If blood on needle/catheter placement - delay
    initiation of LMWH 24 hours postoperatively

56
  • Patients on chronic warfarin
  • Stop warfarin 4-5 days prior
  • Ensure PT/INR within normal limits
  • Patients given initial dose gt24 hrs prior to
    surgery or second dose administered
  • Check PT/INR prior to block
  • Low dose warfarin during epidural analgesia
  • PT/ INR checked daily before catheter removal
  • Catheter removal when INR lt1.5
  • Neurological testing for gt 24 hrs following
    catheter removal
  • INR gt 3 with epidural catheter in situ- with
    hold warfarin

57
  • Antiplatelets
  • Stop clopidrogel 7 days
  • Ticlopidine 14 days
  • eptifibatide, tirofiban 8hours
  • Abciximab 24- 48 hours
  • Avoid starting these with catheter in place
  • Start atleast 2 hrs of removal

58
THANK YOU
www.anaesthesia.co.in anaesthesia.co.in_at_gmail.c
om
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