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Cardiac Arrhythmia in Thalassaemia Limassol, 24 – 26 October 2012 Malcolm Walker University College and the Heart Hospitals, London Clinical Director Hatter Cardiovascular Institute. Cardiac Arrhythmias in thalassaemia. Plan of talk Historical aspects Relationship to iron overload
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Cardiac Arrhythmia in Thalassaemia Limassol, 24 – 26 October 2012 Malcolm Walker University College and the Heart Hospitals, London Clinical Director Hatter Cardiovascular Institute
Cardiac Arrhythmias in thalassaemia • Plan of talk • Historical aspects • Relationship to iron overload • Clinical Management: Principles & Investigation • Specific arrhythmia • Technology: Ablation & Devices
Cardiac Arrhythmia in thalassaemia 1. Historical aspects
History: incidence of arrhythmia & ECG changes thalassaemia, transfused but not chelated Adapted from Ehlers et al 1980
Cardiac Arrhythmia in thalassaemia 2. Relationship to iron overload
Arrhythmia and myocardial iron assessed by cMR T2* • 652 patients with b-thalassaemia • Mean age 27 yr • Excluded those with heart failure (HF) at first scan
Arrhythmia and myocardial iron assessed by cMR T2* • Threshold for arrhythmia T2*<20ms • Types & frequency: • AF 78 (12%) • SVT 14 (2%) • VT 5 (<1%) • VF 1
MIOT study group: gender differences Adapted from: Marsella et.al. Haematologica 2011; 96: 515
MIOT study group: T2* and cardiac arrhythmia Adapted from: Marsella et.al. Haematologica 2011; 96: 515
Arrhythmia and myocardial iron assessed by cMR T2* Conclusions Incidence of arrhythmia very low in this Italian cohort 25 out of 776 patients (3.2%); compared to overall 15% incidence in 1 year (UK cohort; Kirk et al 2009) No statistical relationship with heart iron by T2* in Italian group; clear cut risk associated with T2* in UK cohort (Kirk et al 2009)
Arrhythmia and myocardial iron assessed by cMR T2* Reasons for differences between Italian and UK patients? Italian cohort more recent Overall lower T2*; very few patients with T2* < 20 ms More patients on combination Rx (DFO + DFP)
AF in thalassaemia major – UCH clinic • 80 consecutive clinic attenders 2011-2012 • Mean age 38 yr; 51% female • AF current 8.75% • History of AF or pAF 33.7% • DM 48.7% • Thyroid 22.0% • Hep C (ever) 15.0% • Heart failure in last 12 months 10.0%
AF in thalassaemia – UCH clinic % incidence 55 11 10 Heart iron load by current cMR T2*
AF in thalassaemia – UCH clinic Relationship between iron load & AF Reasons for differences between Italian and UK patients? T2* ms P < 0.05 Range 5 to 13 yr ago Walker et al unpublished observations
AF in thalassaemia – UCH clinic Relationship between iron load & AF Reasons for differences between Italian and UK patients? Atrial fibrillation (AF) occurs late in life and reflects past history, not current iron status T2* ms P < 0.05 Range 5 to 13 yr ago Walker et al unpublished observations
AF in thalassaemia – UCH clinic Risk factors for AF • Diabetes link • 71% of those in AF now have DM • 69% of those with a history or pAF have DM • LA size (by area by ECHO – cMR volumes awaited) • No clear correlation with AF • Current LV function (systolic, by EF) • No clear correlation with AF • Correlation with previous episode of LV dysfunction
Cardiac Arrhythmia in thalassaemia 3. Clinical Management principles & investigation
Clinical aspects of arrhythmia in thalassaemia • Symptoms • Palpitation • Breathlessness • Dizziness or near fainting • Collapse • There is a mismatch between symptoms & severity of arrhythmia • “Trivial” problems may cause immense anxiety • Potentially severe arrhythmia may cause only minor complaints (or no symptoms)
Clinical aspects of arrhythmia in thalassaemia • Symptoms • Palpitation • Breathlessness • Dizziness or near fainting • Collapse • Near fainting, loss of consciousness or collapse Always need to be taken very seriously
Clinical aspects of arrhythmia in thalassaemia • Management requires • Diagnosis of the arrhythmia causing the symptoms • ECG • Holter ambulatory monitor – 24 hr or longer • Techniques which may be useful • Implantable loop recorder – “Reveal” device • Analysis of repolarisation (QT and JT dispersion) • Electrophysiology study
Clinical aspects of arrhythmia in thalassaemia – the clinic ECG Supraventricular tachycardia SVT Atrial Fibrillation AF Ventricular ectopic VE
Clinical aspects of arrhythmia in thalassaemia • Management requires • Diagnosis of the arrhythmia causing the symptoms • ECG • Holter ambulatory monitor – 24 hr or longer • Event recorders • Techniques which may be useful • Implantable loop recorder – “Reveal” device
Clinical aspects of arrhythmia in thalassaemia – the Holter 24hr ECG Holter 24 hr ECG Patient aged 27 yr Symptom: palpitation + dizziness Shows Ventricular tachycardia VT
Holter ambulatory ECG screening • Holter screening failed to predict 2 patients • Significant arrhythmia detected in 15% patients (n=4) • Holter screening failed to predict 2 patients who went on to have significant arrhythmia • 30% of the patients with a normal Holter had symptoms • CONCLUSION • Routine screening of TM population with Holter not sensitive nor specific • Need to consider newer technologies – event recorders, ILR From Qureshi et al. Annals NY Acad Sci 2005
Clinical aspects of arrhythmia in thalassaemia • Management requires • Diagnosis of the arrhythmia causing the symptoms • ECG • Holter ambulatory monitor – 24 hr or longer • Event recorders • Techniques which may be useful • Implantable loop recorder – “Reveal” device
Clinical aspects of arrhythmia in thalassaemia • Management requires • Diagnosis However, making the ECG diagnosis is not enough on its own • Importance of the arrhythmia depends critically on knowledge of the underlying cardiac status • Ventricular function; structural heart defects • Iron burden (cMR T2*) • Pro-thrombotic tendency
Clinical aspects of arrhythmia in thalassaemia • Management requires • Precise diagnosis • Knowledge of underlying cardiac status • Ventricular function & cardiac structure by ECHO • Iron burden (T2*) by cMR An ECHO + cMR are URGENT when • Ventricular arrhythmia • Poorly tolerated AF • Symptoms include loss of consciousness/ collapse/ heart failure
Clinical aspects of arrhythmia in thalassaemia - conclusions • ECG • Necessary baseline at least every 12/12 • At every cardiovascular assessment • It tells us more about the heart than just arrhythmia • Holter 24hr ECG • Useful to investigate symptoms • Poor as a screening tool in asymptomatic well chelated TM patients with good LV function
Cardiac Arrhythmia in thalassaemia 4. Specific arrhythmia VT AF
Specific arrhythmiaTachycardia – ventricular (VT) • Ventricular tachycardia (VT) or broad complex tachycardia
Specific arrhythmiaTachycardia – ventricular (VT) • Ventricular tachycardia (VT) or broad complex tachycardia • This is a medical emergency • Input of emergency physicians/ cardiologists • Immediate cardioversion if in collapse or shock • It always complicates severe iron overload • It may respond to iv chelation with DFO • iv DFO must be started immediately • Combination treatment may be indicated
Specific arrhythmiaTachycardia – ventricular (VT) • Ventricular tachycardia (VT) or broad complex tachycardia • Once acute event controlled • Consider implantation of ICD • Poor LV function not improving with iv chelation • VT occurs without high iron overload – look for another cause! • ICD must be MRI compatible
Specific arrhythmiaAtrial Fibrillation AF • AF: the commonest arrhythmia • Paroxysmal • Persistent • Permanent
Specific arrhythmia: Atrial Fibrillation Risk to patient: Heart Failure • Cardiac decompensation/ overt heart failure • Most likely when AF first appears - when heart rate is high • Target treatment to: • Control rate • Restore normal sinus rhythm • Check, urgently if significant heart failure signs: • LV function by ECHO • Cardiac iron status by cMR T2* • Thyroid function etc.
Specific arrhythmia: Atrial Fibrillation Risk to patient: Stroke • Stroke risk depends critically on: • Prothrombotic status • Structural heart disease • Impaired LV • Higher risk if AF is persistent or permanent or frequent paroxysms of more than 12 hr duration • Restore normal sinus rhythm where possible • Anti-coagulation with warfarin (INR 2.5) or new agents • Check • Cardiac ECHO for LA size, LV function, valve disease
Specific arrhythmia AF – special circumstances • Complicating cardiac failure • Precipitating cardiac failure • In iron loaded TM with good LV function • In non iron loaded TM with good function
Specific arrhythmia AF – special circumstances • Complicating cardiac failure • Precipitating cardiac failure These are urgent situations requiring admission • Consider TOE guided DC Cardioversion • Itensify Rx: iv DFO: 24r x 7 days plus DFP (?) • Conventional long term management: aim to prevent further attacks • Betablockers • Amiodarone (short to medium term) • Anticoagulation
Specific arrhythmia AF – special circumstances • In iron loaded TM with good LV function • In non iron loaded TM with good function These are non-urgent situations requiring • Consider TOE guided DC Cardioversion after 4 weeks anticoagulation • Itensify chelation Rx: if iron overloaded • Conventional rate & rhythm control • Betablockers • Rate lowering calcium channel blockers • Anticoagulation with warfarin or new agents
Specific arrhythmia AF – long term prevention strategy • Long term prevention strategies of AF • Medication: generally poor at long term prevention • Effective drugs potentially too toxic (Amiodarone) • Less toxic drugs often less effective (Beta-block, Flecainide) Thalassaemia population may have an advantage, if AF complicates iron overload. Removing iron may effectively prevent AF for many years (?) • Consider ablation and other therapies
Catheter based ablation for AF Cardiac catheter based techniques Complex & time consuming (2 to 4hr) Often GA required Specialist EP cardiologists & service Success rates 70 to 80% Recurrence rates approx 15% at 1 year Risk of Stroke, cardiac perforation 1% to 2% Complications and success rates may be different for thalassaemia population
Catheter based ablation for AF • Rhythm control by ablation • General success rates 70% to 80% “cure” • 15% need second ablation • In TM population • Experience is young • Anecdotal evidence of much higher recurrence rates
AF: Interventional techniques to reduce stroke risk • Left atrial appendage occluder • Catheter based technique • Reduces risk of stroke • Structural defect closure • Patent foramen ovale (PFO) closure • If patient has strong pro-thrombotic tendency
Bradycardia & heart block in thalassaemia • Complete heart block common in the past is rare today
Bradycardia & heart block in thalassaemia • Complete heart block is rare • Mandates the use of a pacemaker • Historically this would prevent the use of cMR forever!
“Patients and the implanting community deserve nothing less than devices that are safe by design and not by chance.” – J. Rod Gimbel, MD, FACC Emanuel Kanal, MD, FACR For more information visit: http://www.medtronic.com/mrisurescan/
4 chambers LA RA LV Lead Signal alteration RV
Arrhythmia and thalassaemiaConclusions • Complex pathophysiology, which may be changing as TM population ages • Practical management issues largely revolve around intensified chelation, as this may control problem • Role of EP techniques needs to be fully defined • Devices need to be cMR compatible