Clinical management of ir patients in gonda
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Transcript of Clinical management of ir patients in gonda
Clinical ManagementIR patients in the GOU
Justin McWilliams, M.D.
Assistant Professor of Radiology
UCLA
Intro to IR
General principles
IR procedures relevant to GOU Description of procedure Post-procedure management Complications
Case scenarios
Outline
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Interventional Radiology
What do we do?
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Interventional Radiology
What do we do?
“Minimally invasive procedures with imaging guidance”
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Interventional Radiology
What do we do?
“Minimally invasive procedures with imaging guidance”
Whaaa?
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• Close things down• Tumor embolization• Bleeding• Fibroids• Varicose veins• Varicoceles
Interventional Radiology
Open things up Thrombolysis TIPS Angioplasty and stenting Dialysis access
management
Put things in Venous access G and GJ tubes IVC filters Vertebroplasty Nerve blocks
Take things out Abscess drainage Nephrostomy Biliary drainage Foreign body retrieval
Diagnose things Angiography Cholangiography Needle biopsy Venous sampling
(and tumor ablation)
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Interventional RadiologyWhat is most relevant to GOU?
Embolization proceduresTACEUFE
Ablation proceduresRFAMWA
TACE and RFARationale and technique
Liver cancer treatments OLT
Treatment of choice for HCC, especially in cirrhotics Milan criteria: one lesion up to 5 cm, or up to 3 lesions, each up to 3 cm. No
vascular invasion or mets 5-year survival ~70%
Resection Treatment of choice for HCC in non-cirrhotics Any size lesion if limited to one lobe, PV invasion OK 5-year survival ~50%
RFA Treatment of choice in non-operative candidates with limited disease Effective in lesions up to 3-5 cm, up to 3 or 4 lesions 5-year survival ~40%
TACE Treatment of choice in non-operative candidates with intermediate stage HCC
(large or numerous tumors) Give chemotherapy-eluting particles directly into arteries feeding the tumor 5-year survival ~20%
Nexavar Treatment of choice in advanced HCC (extrahepatic spread or vascular
invasion) Tyrosine kinase inhibitor with proven survival benefit in RCT Median survival 10 months (vs 7 months with placebo)
Transarterial chemoembolizationRationale
HCC takes its blood supply almost exclusively from the hepatic artery
Surrounding normal liver has dual blood supply (with portal vein)
Chemotherapy + embolic agent administered into hepatic artery should selectively kill tumor while sparing normal liver
1. Conscious sedation2. Common femoral artery access3. Catheter to select hepatic artery4. Microcatheter to superselect tumor-bearing
artery5. Embolize to near-stasis or stasis
• Conventional TACE: Chemotherapy (doxorubicin, cisplatin, mitomycin C) with Lipiodol, followed by Gelfoam or Embospheres
• DEB-TACE: Doxorubicin-eluting LC beads
• Chemo elutes more slowly than with Lipiodol
• Reduced liver toxicity
• Less side effects
6. Arterial closure7. Overnight admission
TACETechnique
RCT of TACE vs. symptomatic treatment for unresectable HCC
Llovet: 112 patients
Lo: 80 patients
TACELlovet and Lo, 2002
3-year survival:29% with TACE17% with supportive care
3-year survival:26% with TACE3% with supportive care
“TACE is first-line non-curative therapy for non-surgical patients with large or multifocal HCC who do not have vascular invasion or extrahepatic spread (level I evidence).”
TACEConsensus statement
American Association for Study of Liver Diseases (AASLD) and European Association for the Study of the Liver (EASL).
RF current induces thermal coagulation necrosis around an electrode
• Complete ablation rates >80% for small to medium HCC
• Local recurrence uncommon (1-12%)
Disadvantages• Relies on thermal conduction
(limited ablation size) Best for tumors <3 cm
Increasing technical failure and local recurrence for tumors >3 cm
• Heat sink effect• Slow
McWilliams J, et al. Percutaneous ablation of hepatocellular carcinoma: current status. J Vasc Interv Radiol 2010;21:S204-S213.Hinshaw J. The role of image-guided tumor ablation in the management of liver cancer. Cancer News review article.
Radiofrequency ablationRationale
1. General anesthesia (usually)2. Ultrasound used to guide 1-3 needles into
tumor3. CT to confirm and/or adjust position4. Ablation performed (3-5 cm burn possible)5. Adjust needle position and repeat as
necessary6. Needle removal with tract cauterization7. Contrast CT to confirm adequate treatment8. MRI after anesthesia wears off9. Discharge same day (ideally)
RFATechnique
“Local ablation is safe and effective therapy for patients who cannot undergo resection, or as a bridge to transplantation.”
Percutaneous ablationConsensus statement
American Association for Study of Liver Diseases (AASLD) and European Association for the Study of the Liver (EASL).
Post-embo and post-ablation managementGeneral principles
Occurs in 80-90% of patients who undergo embolization (TACE, UFE, etc)
Within 24 hours of embolization, tissue and cell death begins, and breakdown products are released into the circulation
• Pain – At site of embolization, may be severe
• Nausea/vomiting – About 1/3 of patients
• Fever – 15-30% of patients, up to 104 degrees
• Leukocytosis – 15-30% of patients, can exceed WBC 20k
• Fatigue – Most patients, can last for weeks
Some or all of these symptoms may not manifest until after patient discharge
Post-ablation syndrome consists of the same symptoms, but is less frequent (<1/3 of patients)
Most symptoms resolve by 72 hours (except fatigue, and sometimes pain)
General PrinciplesPost-embolization syndrome (PES)
Can occur during the procedure, but often does not occur until post-procedure
Referred visceral pain from the liver is often found in the right shoulder
Opioid analgesia is treatment of choice for severe pain
• Dilaudid or morphine
• PCA is often best method of delivery
NSAIDs can be useful for minor pain, but generally avoid in liver patients
Tylenol is OK but limit to 1.5 grams/day in liver patients
General PrinciplesPain
Often multifactorial
• PES
• Chemotherapy
• Opioid use
Zofran works great (4 mg q4 or 8 mg q8)
Can add dexamethasone in non-diabetics (12 mg on day of treatment)
Compazine or droperidol for breakthrough nausea
General PrinciplesNausea
15-30% of patients develop fever after intervention
• Usually at 24-48 hours
• May be up to 104, but usually <102
Leukocytosis is normal
• Can exceed 20k
Low grade or moderate fever in first few days after treatment should not warrant fever work-up
Differentiating infection vs. PES is difficult
• Gas in embolized area on CT is normal, not abscess
• Fevers beyond 48 hours may require work-up
• Abscess usually occurs at 2-4 weeks
General PrinciplesFever
Extremely common after embolization, and to a lesser extent, ablation
Peaks several days after treatment
Can last for days or weeks
Risk factors
• Baseline fatigue
• High dose of chemo used
General PrinciplesFatigue
Post-embo and post-ablation managementThe specifics
Fluids/Diet
Activity
Pain control
Nausea control
Antibiotics
Puncture site
Labs
TACEPost-procedure management
Fluids/Diet• IV hydration NS ~250 cc/hr x 5 hours
• Advance diet as tolerated (do not start with Salisbury steak)
Activity
Pain control
Nausea control
Antibiotics
Puncture site
Labs
TACEPost-procedure management
Fluids/Diet
Activity• Bed rest at least 2 hours (closure device)
• Bed rest at least 6 hours (manual compression)
• Bed rest overnight (higher risk patients)
Pain control
Nausea control
Antibiotics
Puncture site
Labs
TACEPost-procedure management
Fluids/Diet
Activity
Pain control
• PCA (almost everyone)
• If pain stays controlled, switch to PO Vicodin/Percocet/Oxycodone the next AM
Nausea control
Antibiotics
Puncture site
Labs
TACEPost-procedure management
Fluids/Diet
Activity
Pain control
Nausea control• Dexamethasone 6 hours post-procedure (if non-diabetic)
• Zofran (4 mg q4 hours, or 8 mg q8 hours)
• If ineffective, can use Phenergan or Droperidol or Reglan
Antibiotics
Puncture site
Labs
TACEPost-procedure management
Fluids/Diet
Activity
Pain control
Nausea control
Antibiotics• No data prove their necessity or effectiveness post-TACE
• Used empirically by some operators, especially in higher risk patients
• Cipro +/- Flagyl x 7 days
Puncture site
Labs
TACEPost-procedure management
Fluids/Diet
Activity
Pain control
Nausea control
Antibiotics
Puncture site
• First 2 hours post-procedure are critical
• Groin checks and vitals q15 min x 4, then q30 min x 2
• The most dangerous bleeds are not externally obvious
Labs
TACEPost-procedure management
Fluids/Diet
Activity
Pain control
Nausea control
Antibiotics
Puncture site
Labs• AST and ALT
• Total bilirubin
• Creatinine
• Sodium
TACEPost-procedure management
Liver failure
Bleeding
Nontarget embolization
Acute renal failure
Infection/abscess
TACEComplications
Liver failure• Risk factors: Child B/C, total bili >3.0, albumin <2.0, ECOG >2
• Mechanism: TACE-related injury to “normal” liver parenchyma (poor reserve in cirrhotic livers)
• Incidence: 13% of TACE patients suffer some degree of liver failure.
• Diagnosis: Elevated bilirubin/INR, jaundice, itchiness, dark urine, light stool
• Avoidance strategy: Superselective embo
• Treatment: Supportive care
• Outcome: Most recover. 30-day TACE-related mortality from liver failure is 2%
TACEComplications
Bleeding (puncture site)• Risk factors: Low platelets, high INR, obesity, closure device failure, uncooperative patient
• Mechanism: Platelet plug does not form or dislodges
• Incidence: Minor groin hematoma <10%. Major intramuscular or retroperitoneal bleed is rare but devastating.
• Diagnosis: Groin swelling/pain (not if retroperitoneal), tachycardia, hypotension, orthostasis, pallor, dizziness, lightheadedness, weakness
• Avoidance strategy: Careful access and closure, bed rest with leg straight
• Treatment: Pressure. IVF. Stat type/cross and transfuse. Stat CT. Consider angio.
• Outcome: Depends on blood loss.
TACEComplications
Bleeding (variceal)• Risk factors: Presence of varices, previous variceal bleed, low platelets, high INR
• Mechanism: Increased portal HTN in setting of periprocedural liver insult (varices)
• Incidence: <1%, anecdotal
• Diagnosis: Hematemesis, shock
• Avoidance strategy: Pre-TACE banding? Superselective TACE
• Treatment: IVF. Type/cross and transfuse. Immediate endoscopy with banding. Consider emergent TIPS if no other options.
• Outcome: High mortality rate.
TACEComplications
Nontarget embolization• Risk factors: Lobar (nonselective) treatment
• Mechanism: Embolic material passes into gallbladder, stomach or intestine
• Incidence: <<10%
• Diagnosis: Ulceration, perforation, pain, bleeding
• Avoidance strategy: Superselective embo
• Treatment: NPO. Hydration. PPI. Prolonged observation. Consider surgery if bowel necrosis.
• Outcome: Most recover with supportive care alone.
TACEComplications
Acute renal failure• Risk factors: High baseline creatinine (CRI), diabetes, dehydration
• Mechanism: Nephrotoxic contrast, nephrotoxic chemotherapy, tumor lysis syndrome
• Incidence: <1-8%
• Diagnosis: Rising creatinine, peaking 2-3 days after insult; oliguria
• Avoidance strategy: IV hydration. Minimize contrast. Bicarbonate/Mucomyst.
• Treatment: IV hydration. Temporary dialysis if necessary.
• Outcome: 1/3 require permanent dialysis. 2/3 recover.
TACEComplications
Fluids/Diet
Activity
Pain control
Nausea control
Antibiotics
Puncture site
Labs
RFA/MWAPost-procedure management
Fluids/Diet
• IVF (gentle)
• Advance as tolerated (most had general anesthesia)
Activity
Pain control
Nausea control
Antibiotics
Puncture site
Labs
RFA/MWAPost-procedure management
Fluids/Diet
Activity• Ad lib
Pain control
Nausea control
Antibiotics
Puncture site
Labs
RFA/MWAPost-procedure management
Fluids/Diet
Activity
Pain control
• Usually PO narcotics suffice (Vicodin, Percocet)
• PCA or IV morphine/dilaudid if pain is severe
Nausea control
Antibiotics
Puncture site
Labs
RFA/MWAPost-procedure management
Fluids/Diet
Activity
Pain control
Nausea control
• Rarely needed
• Zofran
Antibiotics
Puncture site
Labs
RFA/MWAPost-procedure management
Fluids/Diet
Activity
Pain control
Nausea control
Antibiotics
• Little evidene to support its use in routine ablation
• Cipro +/- Flagyl if chance of biliary/bowel injury or high risk patient
Puncture site
Labs
RFA/MWAPost-procedure management
Fluids/Diet
Activity
Pain control
Nausea control
Antibiotics
Puncture site
• Usually nothing to see
• Rare skin burns
Labs
RFA/MWAPost-procedure management
Fluids/Diet
Activity
Pain control
Nausea control
Antibiotics
Puncture site
Labs
• Hemoglobin, Total Bilirubin, AST/ALT, sodium
RFA/MWAPost-procedure management
Hemorrhage
Liver failure
Nontarget ablation
Infection
Tumor seeding
RFA/MWAComplications
Hemorrhage• Risk factors: Low platelets, high INR, multiple needle placements, ascites
• Mechanism: Arterial injury by needle, or persistent oozing from liver puncture
• Incidence: ~1% clinically significant hemorrhage rate
• Diagnosis: Hypotension, tachycardia, pallor, pain, dizziness, orthostasis
• Avoidance strategy: Tract cauterization, FFP/platelet support
• Treatment: IVF resuscitation. Transfuse. Stat CTA (look for active extravasation). Hepatic angiography and embolization.
• Outcome: Depends on blood loss.
RFA/MWAComplications
Liver failure• Risk factors: Child B/C, total bili >3.0, albumin <2.0, ECOG >2, large ablation zone,
multiple ablations
• Mechanism: Ablation of “normal” liver parenchyma (poor reserve in cirrhotic livers)
• Incidence: 12% risk of death from liver failure in ablation of Child C patients; <1% risk for Child A or B
• Diagnosis: Elevated bilirubin/INR, jaundice, itchiness, dark urine, light stool
• Avoidance strategy: Staged ablation
• Treatment: Supportive care
• Outcome: Recovery is less likely than in TACE as liver is permanently damaged with ablation
RFA/MWAComplications
Nontarget ablation• Risk factors: Target tumor near stomach, bowel, bile ducts, gallbladder
• Mechanism: Nontarget tissues lie within ablation zone
• Incidence: 2%
• Diagnosis: Bowel or gallbladder perforation, bile leak or obstruction
• Avoidance strategy: Hydrodissection, positioning
• Treatment: Surgery or supportive care
• Outcome: Mortality is high for bowel injury in this population
RFA/MWAComplications
Infection/abscess• Risk factors: Hepatojejunostomy, biliary drainage tube
• Mechanism: Colonized biliary system seeds the necrotic treated ablation zone
• Incidence: <5% with normal sphincter of Oddi; 30-80% if compromised
• Diagnosis: Pain, fever
• Avoidance strategy: Periprocedural antibiotics, bowel prep
• Treatment: Antibiotics and drainage
• Outcome: Most recover
RFA/MWAComplications
Tumor seeding• Risk factors: Multiple needle insertions, concomitant biopsy
• Mechanism: Tumor cells on needle seed tract as needle is removed
• Incidence: <1%
• Diagnosis: Imaging
• Avoidance strategy: Tract ablation/cauterization with needle removal
• Treatment: Ablation or surgery
• Outcome: Most are detected on follow up and treated
RFA/MWAComplications
TG
39 y/o female
Fibrolamellar HCC diagnosed in 2001
Left lobe resection of 9 x 11 cm mass in 2001
Recurrence 2007 with partial right lobe resection
Presents with multifocal recurrence 2/2010
Not a surgical or transplant candidate
Presented at tumor board and referred for locoregional therapy
CT 4/9/2010: At least 10 hypervascular liver
masses
100 mg doxorubicin on LC beads
TACE 5/3/2010
2 weeks later, returns with fevers, RUQ pain
Percutaneous biloma drainage
CT 5/19/2010: near- complete tumor necrosis
CT 8/6/2010: Biloma resolved, but
intrahepatic recurrence and new lung nodule.
To study drug
Prolonged catheter drainage
Four
39 year old female
Fibrolamellar hepatocellular carcinoma
Status post left lobectomy and partial right lobectomy
No longer a surgical candidate OLT? RFA? TACE? Chemotherapy?
OLT Treatment of choice for HCC, especially in cirrhotics Milan criteria: one lesion up to 5 cm in size, or up to 3 lesions, each
up to 3 cm in size. No vascular invasion and no mets.
RFA Place ablation needle into lesion (under CT/US guidance) and cook it Effective in lesions up to 3 cm (sometimes larger), up to 3 or 4 lesions Damage to adjacent bile ducts or bowel can be a concern
TACE CFA access, catheterize hepatic artery and subselect tumor feeders Give chemotherapy-eluting particles
Block blood flow
Release tumoricidal chemotherapy
Targeted chemotherapy Nexavar (tyrosine kinase inhibitor) – extends survival in advanced HCC Avastin (monoclonal VEGF inhibitor) – promising but unproven
Liver cancer treatments
OLT Too many lesions to qualify (outside Milan criteria)
Can consider Milan exception if we can decrease her disease burden
RFA Too many lesions to effectively treat, and marginal location increases
risk for bowel/stomach injury
TACE Suitable
Targeted chemotherapy Suitable, if TACE fails
Liver cancer treatments
Status post 100 mg doxorubicin on 100-300 and 300-500 micron LC beads
Discharged home the next day, doing well
2 weeks later, having persistent high fevers to 103 and night sweats
Abscess?
Biloma?
Necrotic tumor?
10F drain placed under ultrasound
One week later Output 150-200 cc/day
Biloma with continued leak Drain upsized to 12 French Contrast injection – no obvious communication Improved with 6 weeks of drainage