1 / 50

Cardiac Arrhythmia in Thalassaemia Limassol, 24 – 26 October 2012 Malcolm Walker

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

kory
Télécharger la présentation

Cardiac Arrhythmia in Thalassaemia Limassol, 24 – 26 October 2012 Malcolm Walker

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Cardiac Arrhythmia in Thalassaemia Limassol, 24 – 26 October 2012 Malcolm Walker University College and the Heart Hospitals, London Clinical Director Hatter Cardiovascular Institute

  2. Cardiac Arrhythmias in thalassaemia • Plan of talk • Historical aspects • Relationship to iron overload • Clinical Management: Principles & Investigation • Specific arrhythmia • Technology: Ablation & Devices

  3. Cardiac Arrhythmia in thalassaemia 1. Historical aspects

  4. History: incidence of arrhythmia & ECG changes thalassaemia, transfused but not chelated Adapted from Ehlers et al 1980

  5. Cardiac Arrhythmia in thalassaemia 2. Relationship to iron overload

  6. 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

  7. 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

  8. MIOT study group: gender differences Adapted from: Marsella et.al. Haematologica 2011; 96: 515

  9. MIOT study group: T2* and cardiac arrhythmia Adapted from: Marsella et.al. Haematologica 2011; 96: 515

  10. 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)

  11. 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)

  12. 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%

  13. AF in thalassaemia – UCH clinic % incidence 55 11 10 Heart iron load by current cMR T2*

  14. 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

  15. 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

  16. 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

  17. Cardiac Arrhythmia in thalassaemia 3. Clinical Management principles & investigation

  18. 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)

  19. 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

  20. 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

  21. Clinical aspects of arrhythmia in thalassaemia – the clinic ECG Supraventricular tachycardia SVT Atrial Fibrillation AF Ventricular ectopic VE

  22. 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

  23. 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

  24. 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

  25. 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

  26. 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

  27. 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

  28. 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

  29. Cardiac Arrhythmia in thalassaemia 4. Specific arrhythmia VT AF

  30. Specific arrhythmiaTachycardia – ventricular (VT) • Ventricular tachycardia (VT) or broad complex tachycardia

  31. 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

  32. 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

  33. Specific arrhythmiaAtrial Fibrillation AF • AF: the commonest arrhythmia • Paroxysmal • Persistent • Permanent

  34. 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.

  35. 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

  36. 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

  37. 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

  38. 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

  39. 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

  40. 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

  41. Catheter based ablation for AF

  42. Catheter based ablation for AF

  43. 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

  44. 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

  45. Bradycardia & heart block in thalassaemia • Complete heart block common in the past is rare today

  46. 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!

  47. “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/

  48. 4 chambers LA RA LV Lead Signal alteration RV

  49. cMR safe pacemakers

  50. 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

More Related