Vascular Access for Haemodialysis. Mike Stephens

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Transcription:

Vascular Access for Haemodialysis Mike Stephens

Overview Learning Objectives History and development of vascular access Standards in vascular access surgery Types of vascular access Complications

Objectives of the Session Understand the different types of vascular access available for haemodialysis patients Know how to assess a patient for vascular access surgery Know how to consent a patient for vascular access procedures

Development of Vascular Access Surgery 1657 Sir Christopher Wren invented an instrument for IV injections 1665 Lower reported the first transfusion between dogs 1667 Jean Denys performed the first successful transfusion into humans 1818 James Blundell performed the first trabsfusion of human blood 1901 Karl Landsteiner discovered ABO blood groups 1914 Richard Lewisohn introduced sodium citrate as anticoagulant 1937 Landsteiner and Weiner discovered the Rh factor 1913 Abel, Rowntree and Turner created an artificial kidney 1943 Kolff developed the first practical model for humans 1955 Kolff revised model (including 7 beer cans and a fruit juice can) 1960 Scribner, Dillard, Quinton devised a Teflon-Silastic AV shunt 1966 Brescia, Cimino, Appel and Hurwich described a subcutaneous AVF 1973 Indwelling right atrial catheter developed for TPN 1979 Hickman and colleagues reported their modification 1984 Bothe and colleagues described their Port-a-Cath

promptly jumped down from the table, and apparently oblivious of its hurts, soon began to fondle its master.. Lower, 1665

Development of Vascular Access Surgery 1657 Sir Christopher Wren invented an instrument for IV injections 1665 Lower reported the first transfusion between dogs 1667 Jean Denys performed the first successful transfusion into humans 1818 James Blundell performed the first trabsfusion of human blood 1901 Karl Landsteiner discovered ABO blood groups 1914 Richard Lewisohn introduced sodium citrate as anticoagulant 1937 Landsteiner and Weiner discovered the Rh factor 1913 Abel, Rowntree and Turner created an artificial kidney 1943 Kolff developed the first practical model for humans 1955 Kolff revised model (including 7 beer cans and a fruit juice can) 1960 Scribner, Dillard, Quinton devised a Teflon-Silastic AV shunt 1966 Brescia, Cimino, Appel and Hurwich described a subcutaneous AVF 1973 Indwelling right atrial catheter developed for TPN 1979 Hickman and colleagues reported their modification 1984 Bothe and colleagues described their Port-a-Cath

Development of Vascular Access Surgery 1657 Sir Christopher Wren invented an instrument for IV injections 1665 Lower reported the first transfusion between dogs 1667 Jean Denys performed the first successful transfusion into humans 1818 James Blundell performed the first trabsfusion of human blood 1901 Karl Landsteiner discovered ABO blood groups 1914 Richard Lewisohn introduced sodium citrate as anticoagulant 1937 Landsteiner and Weiner discovered the Rh factor 1913 Abel, Rowntree and Turner created an artificial kidney 1943 Kolff developed the first practical model for humans 1955 Kolff revised model (including 7 beer cans and a fruit juice can) 1960 Scribner, Dillard, Quinton devised a Teflon-Silastic AV shunt 1966 Brescia, Cimino, Appel and Hurwich described a subcutaneous AVF 1973 Indwelling right atrial catheter developed for TPN 1979 Hickman and colleagues reported their modification 1984 Bothe and colleagues described their Port-a-Cath

The Ideal Vascular Access Provide safe and effective therapy by enabling the removal and return of blood via an extracorporeal circuit Easy to use Reliable Minimal risk to the individual

Options

Options Arteriovenous fistula Arteriovenous graft Tunnelled venous catheter Non-tunnelled venous catheter

UK Renal Association Guidelines 65% of incident HD patients should commence dialysis with an AV fistula 85% of prevalent HD patients should receive dialysis via a functioning fistula Clinical Practice Guidelines 2011

Incident patients Cardiff % 100 90 80 70 60 50 40 30 20 10 0 2010/11 2011/12 Audit Target 65% 2012/13 2013/14

Prevalent patients Cardiff % 100 90 80 70 60 50 40 30 20 10 0 2010/11 2011/12 Audit Target 85% 2012/13 2013/14

When to start planning for Vascular Access

When to start planning for Vascular Access When patients enter CKD stage 4 Exact timing of placement will depend on rate of decline, co-morbidities, transplant options and type of access planned

CKD patient with declining egfr<20 (<25 with DM) or likely to require dialysis in the next 6 months Needle fistula Discharge Referral to Access Coordinator Crash Lander Prevalent dialysis patient with fistula problem Transplant assessment required Transplant assessment not required Double OPA with prior duplex Date for surgery Pre-op assessment One stop access clinic Date for surgery Pre-op assessment Surgery 1 week post-op OPD review 4 weeks post-op Doppler Fistulogram USS Mature Not Maturing Review by access surgeon Fistulogram Re-do surgery

Vascular Access Clinic

Vascular Access Clinic General Health (DM/CVD/PVD) Medication history (anticoagulants/antiplatelets) Occupation Dominant Arm Superficial veins Allen s test Doppler Ultrasound Scan Date for Surgery Pre-operative Assessment

Options for AV fistulae

Options for AV fistulae Snuff-box fistula Radiocephalic fistula (wrist or forearm) Brachiocubital fistula Brachiocephalic fistula Brachiobasilic fistula Saphenous vein fistula

AV graft options Forearm straight graft Forearm loop graft Brachio-axillary graft Femoro-saphenous loop graft Femero-femoral loop graft Axillo-axillary graft

Assessing maturation Clinical Doppler Ultrasound Flow >600ml/min Cannulation segment >10cm long or two 4cm segments Outflow vein diameter >6mm Cannulation segment <6mm from skin surface

Complications of Vascular Access

Thrombosis 1 year patency AVFs approx. 65% Many factors small vessels dehydration hypotension venous outflow obstruction Primary patency at 2 years:- AVF 43% AVG 31% Secondary patency at 2 years:- AVF 64% AVG 60%

High Output Heart Failure Rapid flow changes immediately after construction RC AVF 250ml/min BC AVF 600ml/min Heart Failure relatively uncommon (surprisingly) Probably need 25%-50% cardiac output through fistula to result in failure Revision possible

Venous Hypertension Rapid if central stenosis May be due to retrograde flow Treatment depends on exact cause May get better May need to ligate fistula Consider venogram

Aneurysms Pseudo-aneurysms Needling sites Infection True aneurysms If skin threatened may bleed Management depends on size/symptoms/skin

Ischaemic Steal Syndrome Prevalence 10-20% (symptomatic), 4% requiring intervention More likely and more rapid with AVG Diagnosis clinical plus Doppler assessment Difficult to predict Operative treatments:- Ligation Banding DRIL RUDI

Neuropathy Carpal tunnel syndrome-like symptoms Ischaemic Monomelic Neuropathy (Vascular Access Neuropathic Syndrome)

Summary Vascular Access takes careful planning High failure rates but successful outcomes achievable Complications are common but usually manageable