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ATRIAL FIBRILLATION


      Dr SYED RAZA
 MD,MRCP(UK),CCT(UK),MESC,Dip.Card(UK),FCCP

      Consultant Cardiologist
OBJECTIVES

•   Introduction
•   Classification
•   Burden of the problem
•   Diagnosis
•   Management
What is it ?

• Abnormal electrical wavelets originate from
  left atrium
• Propagating in different directions
• Disorganized atrial depolarisation without
  effective atrial contraction
DIAGNOSIS
• Pulse palpation
• 12 lead ECG
• Holter monitoring

• Others
• Echocardiogram, CXR
• TFT, Electrolytes, Clotting, LFT,CBC
ECG Diagnosis

• On ECG p waves are absent and RR interval is
  variable.
• f waves 350-600 beats /min.
• ventricular response is grossly irregular at
  100-160 beats /min.
• Rate : No. of R waves x 10 ( 6 sec strip)
Prevalance
•   2.2 Million people in the US
•   6.5 cases/1000 examinations
•   4% > 60yrs
•   8 % > 80 yrs
•   25% of individuals aged 40 yrs and older will
    develop AF in their life time.
Prevalence of AF in the Renfrew-
                                Paisley study




Cohort of men and women aged 45–64 years (n = 15,406)
              Reproduced with permission of the BMJ Publishing Group from Stewart S et al, Heart 2001: 86:516-21
Clinical events (outcomes) affected by
                   AF
Outcome Parameter       Relative change in AF
                        patients
1.Death                 1.Death rate is doubled
2.Stroke                2.Stroke risk increases 5
                        times
3.Hospitalisation       3.More frequent
4.Quality of life and   4.Can be markedly
exercise capacity       decreased
5.LV function           5.Tachycardiomyopathy/
                        heart failure
Classification of AF

Terminology            Clinical features
Initial event (first   Symptomatic                Rhythm/Rate
detected episode)      Asymptomatic
                       Onset unknown
Paroxysmal             Spontaneous termination    Rhythm
                       <7 days and most often     Control
                       <48 hours
Persistent             Not self-terminating       Rhythm or
                       Lasting >7 days or prior   Rate control
                       cardioversion
Permanent              Not terminated             Rate Control
(‘accepted’)           Terminated but relapsed
                                 No
                       cardioversion attempt
Etiologies of AF
                 CARDIAC
Hypertensive heart disease
Valvular heart disease
Ischaemic heart disease
Cardiomyopathy
Pericarditis
Congenital heart disease
Post Cardiac surgery
Etiologies of AF contd:
                 NON CARDIAC
1.   Pulmonary : Pneumonia, COPD,PE
2.   Hyperthyroidism
3.   Excess catecholamine /sympathetic activity
4.   Drugs and alcohol
5.   Significant electrolyte imbalance
LONE ATRIAL FIBRILLATION
•   Younger patients < 60
•   No underlying cause
•   Usually not much symptoms
•   Normal heart structure
•   No associated co-morbidities
Why AF management is
            important?

• extremely common
• Can lead to symptoms
• potentially serious consequences:
   – embolism
   – impaired cardiac output
   – increased mortality
Management of Acute AF (<48 hrs)
• Haemodynamically unstable :
  hypotension/heart failure/chest pain/syncope
  Use DC Cardioversion
  Haemodynamically stable :
  Rate control : If significant tachycardia
  Rhythm control : Flecainide, Propafenone (cl-
  I) Amiodarone, Sotalol (cl-III)
    Anticoagulant : LMWH
Treatment for permanent AF
• Heart Rate control

 minimise symptoms associated with
 excessive heart rates

 prevent tachycardia-associated
 cardiomyopathy

• Anticoagulation
Rhythm control as preferred
therapy
  – ? First episode afib
  – Reversible cause (alcohol)
  – Symptomatic patient despite rate control
  – Patient unable to take anticoagulant (falls, bleeding,
    noncompliance)
  – CHF precipitated or worsened by afib
  – ? Young afib patient (to avoid chronic electrical and
    anatomic remodeling that occurs with afib)
Rate control as preferred therapy


 –   Age > 65, less symptomatic, hypertension
 –   Recurrent afib
 –   Previous antiarrhythmic drug failure
 –   Unlikely to maintain sinus rhythm (enlarged LA)
Cardioversion
• Cardioversion is performed as part of a
  rhythm-control treatment strategy
• There are two types of cardioversion:
  electrical (ECV) and pharmacological (PCV)
• Cardioversion of AF is associated with
  increased risk of stroke in the absence of
  antithrombotic therapy.
AFFIRM : 5 Year Outcomes
  Survival           Rhythm Control        Rate Control
   1 year                96%                96%

   3 year                87%                89%

   5 year                76%                79%
                               p = 0.058

 NO Difference : death, disabling stroke, major bleed,
 or cardiac arrest
 Sinus rhythm maintained in only 63% of rhythm
 control group
NEJM 2002;347:1825
Rate Control Options

• Beta blocker
•   Calcium channel blocker
        • Verapamil, diltiazem


    . Digoxin


• AV junction ablation plus pacemaker
STROKE RISK
Without AF
< 60 yrs : 0.5%
> 80 yrs : 3 yrs

With AF
< 60 yrs : 3%
> 80 yrs : 30%
Lip Y, et al. Chest 2010, 137(2):263
How do we determine stroke risk ?


– 0 points – low risk (1.2-3.0 strokes per 100 patient years)
– 1-2 points – moderate risk (2.8-4.0 strokes per 100 patient years)
– > 3 points – high risk (5.9-18.2 strokes per 100 patient years)
Atrial fibrillation 2009
   Target INR 2-3
ACC AHA HRS Afib Focused Update
              (Dabigatran), March 2011
•   Non-inferior to warfarin re thromboembolism (afib)
•   Caution when CrCl < 30ml/min
•   Increased dabigatran levels with amiodarone, verapamil
•   Half life 12-17 hours
•   No reversal re hemorrhage
     – dialysis
•   Coagulation testing ??? aPTT, dilute thrombin time
Who should remain on warfarin?

• Patient already receiving warfarin and stable whose INR
  is easy to control
• If dabigatran, rivaroxaban, apixaban not available
• Cost
• If patient not likely to comply with twice daily dosing
  (Dabigatran, Apixaban)
• Chronic kidney disease (GFR < 30 ml/min)
Bleeding Risk
• Assessment of bleeding risk should be part of
  the clinical assessment of AF patients prior to
  starting anticoagulation
• Antithrombotic benefits and potential
  bleeding risks of long-term coagulation should
  be explained and discussed with the patient
• Aim for a target INR of between 2.0 and 3.0
• Forms of monitoring include point of care or
  near patient testing and patient self-
  monitoring
From Hart RG, et al. Stroke. 2005;36:1588
RF ABLATION THERAPY
Substrate for   Substrate for
Triggering events
                    initiation      perpetuation
When to consider ablation?

• Antiarrhythmic therapy ineffective
• Antiarrhythmic therapy not tolerated
• Symptomatic afib
Others in whom ablation may be a first strategy

• Patient very symptomatic in AF and refuses
  antiarrhythmic drug therapy
• Young patient whose only effective antiarrhythmic drug
  is amiodarone
• Patient with significant bradycardia for whom
  antiarrhythmic drug therapy will require pacemaker
Summary
• AF is the commonest arrhythmia
• High prevalence
• Stroke is one of the most dreadful
  complications .
• Different management strategies,

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Atrial fibrillation

  • 1. ATRIAL FIBRILLATION Dr SYED RAZA MD,MRCP(UK),CCT(UK),MESC,Dip.Card(UK),FCCP Consultant Cardiologist
  • 2.
  • 3. OBJECTIVES • Introduction • Classification • Burden of the problem • Diagnosis • Management
  • 4. What is it ? • Abnormal electrical wavelets originate from left atrium • Propagating in different directions • Disorganized atrial depolarisation without effective atrial contraction
  • 5.
  • 6. DIAGNOSIS • Pulse palpation • 12 lead ECG • Holter monitoring • Others • Echocardiogram, CXR • TFT, Electrolytes, Clotting, LFT,CBC
  • 7.
  • 8. ECG Diagnosis • On ECG p waves are absent and RR interval is variable. • f waves 350-600 beats /min. • ventricular response is grossly irregular at 100-160 beats /min. • Rate : No. of R waves x 10 ( 6 sec strip)
  • 9.
  • 10.
  • 11. Prevalance • 2.2 Million people in the US • 6.5 cases/1000 examinations • 4% > 60yrs • 8 % > 80 yrs • 25% of individuals aged 40 yrs and older will develop AF in their life time.
  • 12. Prevalence of AF in the Renfrew- Paisley study Cohort of men and women aged 45–64 years (n = 15,406) Reproduced with permission of the BMJ Publishing Group from Stewart S et al, Heart 2001: 86:516-21
  • 13. Clinical events (outcomes) affected by AF Outcome Parameter Relative change in AF patients 1.Death 1.Death rate is doubled 2.Stroke 2.Stroke risk increases 5 times 3.Hospitalisation 3.More frequent 4.Quality of life and 4.Can be markedly exercise capacity decreased 5.LV function 5.Tachycardiomyopathy/ heart failure
  • 14. Classification of AF Terminology Clinical features Initial event (first Symptomatic Rhythm/Rate detected episode) Asymptomatic Onset unknown Paroxysmal Spontaneous termination Rhythm <7 days and most often Control <48 hours Persistent Not self-terminating Rhythm or Lasting >7 days or prior Rate control cardioversion Permanent Not terminated Rate Control (‘accepted’) Terminated but relapsed No cardioversion attempt
  • 15.
  • 16. Etiologies of AF CARDIAC Hypertensive heart disease Valvular heart disease Ischaemic heart disease Cardiomyopathy Pericarditis Congenital heart disease Post Cardiac surgery
  • 17. Etiologies of AF contd: NON CARDIAC 1. Pulmonary : Pneumonia, COPD,PE 2. Hyperthyroidism 3. Excess catecholamine /sympathetic activity 4. Drugs and alcohol 5. Significant electrolyte imbalance
  • 18. LONE ATRIAL FIBRILLATION • Younger patients < 60 • No underlying cause • Usually not much symptoms • Normal heart structure • No associated co-morbidities
  • 19. Why AF management is important? • extremely common • Can lead to symptoms • potentially serious consequences: – embolism – impaired cardiac output – increased mortality
  • 20. Management of Acute AF (<48 hrs) • Haemodynamically unstable : hypotension/heart failure/chest pain/syncope Use DC Cardioversion Haemodynamically stable : Rate control : If significant tachycardia Rhythm control : Flecainide, Propafenone (cl- I) Amiodarone, Sotalol (cl-III) Anticoagulant : LMWH
  • 21. Treatment for permanent AF • Heart Rate control minimise symptoms associated with excessive heart rates prevent tachycardia-associated cardiomyopathy • Anticoagulation
  • 22. Rhythm control as preferred therapy – ? First episode afib – Reversible cause (alcohol) – Symptomatic patient despite rate control – Patient unable to take anticoagulant (falls, bleeding, noncompliance) – CHF precipitated or worsened by afib – ? Young afib patient (to avoid chronic electrical and anatomic remodeling that occurs with afib)
  • 23. Rate control as preferred therapy – Age > 65, less symptomatic, hypertension – Recurrent afib – Previous antiarrhythmic drug failure – Unlikely to maintain sinus rhythm (enlarged LA)
  • 24. Cardioversion • Cardioversion is performed as part of a rhythm-control treatment strategy • There are two types of cardioversion: electrical (ECV) and pharmacological (PCV) • Cardioversion of AF is associated with increased risk of stroke in the absence of antithrombotic therapy.
  • 25.
  • 26. AFFIRM : 5 Year Outcomes Survival Rhythm Control Rate Control 1 year 96% 96% 3 year 87% 89% 5 year 76% 79% p = 0.058 NO Difference : death, disabling stroke, major bleed, or cardiac arrest Sinus rhythm maintained in only 63% of rhythm control group NEJM 2002;347:1825
  • 27.
  • 28. Rate Control Options • Beta blocker • Calcium channel blocker • Verapamil, diltiazem . Digoxin • AV junction ablation plus pacemaker
  • 29. STROKE RISK Without AF < 60 yrs : 0.5% > 80 yrs : 3 yrs With AF < 60 yrs : 3% > 80 yrs : 30%
  • 30.
  • 31.
  • 32.
  • 33. Lip Y, et al. Chest 2010, 137(2):263
  • 34. How do we determine stroke risk ? – 0 points – low risk (1.2-3.0 strokes per 100 patient years) – 1-2 points – moderate risk (2.8-4.0 strokes per 100 patient years) – > 3 points – high risk (5.9-18.2 strokes per 100 patient years)
  • 35.
  • 36. Atrial fibrillation 2009 Target INR 2-3
  • 37. ACC AHA HRS Afib Focused Update (Dabigatran), March 2011 • Non-inferior to warfarin re thromboembolism (afib) • Caution when CrCl < 30ml/min • Increased dabigatran levels with amiodarone, verapamil • Half life 12-17 hours • No reversal re hemorrhage – dialysis • Coagulation testing ??? aPTT, dilute thrombin time
  • 38. Who should remain on warfarin? • Patient already receiving warfarin and stable whose INR is easy to control • If dabigatran, rivaroxaban, apixaban not available • Cost • If patient not likely to comply with twice daily dosing (Dabigatran, Apixaban) • Chronic kidney disease (GFR < 30 ml/min)
  • 39. Bleeding Risk • Assessment of bleeding risk should be part of the clinical assessment of AF patients prior to starting anticoagulation • Antithrombotic benefits and potential bleeding risks of long-term coagulation should be explained and discussed with the patient • Aim for a target INR of between 2.0 and 3.0 • Forms of monitoring include point of care or near patient testing and patient self- monitoring
  • 40. From Hart RG, et al. Stroke. 2005;36:1588
  • 42. Substrate for Substrate for Triggering events initiation perpetuation
  • 43. When to consider ablation? • Antiarrhythmic therapy ineffective • Antiarrhythmic therapy not tolerated • Symptomatic afib
  • 44.
  • 45.
  • 46. Others in whom ablation may be a first strategy • Patient very symptomatic in AF and refuses antiarrhythmic drug therapy • Young patient whose only effective antiarrhythmic drug is amiodarone • Patient with significant bradycardia for whom antiarrhythmic drug therapy will require pacemaker
  • 47. Summary • AF is the commonest arrhythmia • High prevalence • Stroke is one of the most dreadful complications . • Different management strategies,

Hinweis der Redaktion

  1. NOTES FOR PRESENTERS Refer to the full guideline – page 13, table 1.01. Renfrew-Paisley UK study, cohort of men and women aged 45-64 years (n = 15,406) there were 100 documented cases of AF. Prevalence of AF increased with age and more cases were detected in men.
  2. NOTES FOR PRESENTERS For more details, refer to the full guideline, pages 11 and 12, section 1.2 AF is considered recurrent when a patient develops two or more episodes. These episodes may be paroxysmal if they terminate spontaneously, defined by consensus as terminating within seven days, or persistent if the arrhythmia requires electrical or pharmacological cardioversion for termination. Successful termination of AF does not alter the classification of persistent AF in these patients. Longstanding AF (defined as over 1 year) not successfully terminated by cardioversion, or when cardioversion is not pursued, is classified as permanent. Without treatment, AF can result in some degree of disruption to the circulation of blood around the body. In some cases of AF, the degree of haemodynamic instability can represent a critical condition that requires immediate intervention. The next slide sets out why we need this guideline.
  3. NOTES FOR PRESENTERS There are many risk factors for developing AF. In the Framingham study, the development of AF was associated with increasing age, diabetes, hypertension and valve disease. It is also commonly associated with, and complicated by, congestive heart failure and strokes. Dietary and lifestyle factors have also been associated with AF, such as excessive alcohol and caffeine, as well as emotional and physical stress. Cardiac causes of AF Common cardiac causes: Ischaemic heart disease Rheumatic heart disease Hypertension Sick sinus syndrome Pre-excitation syndromes (e.g. Wolff-Parkinson-White syndrome) Less common cardiac causes: Cardiomyopathy or heart muscle disease Pericardial disease (including effusion and constrictive pericarditis) Atrial septal defect Atrial myxoma Non-cardiac causes of AF Acute infections, especially pneumonia Electrolyte depletion Lung carcinoma Other intrathoracic pathology (e.g. pleural effusion) Pulmonary embolism Thyrotoxicosis Refer to the full guideline – page 89, section 10 Post-op AF is associated with a greater risk of mortality and morbidity, and evidence is emerging that post-op AF predisposes people to a significantly increased risk of stroke and thromboembolism. The next slide highlights the classification of AF, which is based on the temporal pattern of the arrhythmia.
  4. NOTES FOR PRESENTERS In patients with permanent AF who need treatment for rate-control: - beta-blockers or rate-limiting calcium antagonists should be the preferred initial monotherapy in all patients In patients with permanent AF where monotherapy is inadequate: to control the heart rate during normal activities only, beta-blockers or rate-limiting calcium antagonists should be administered with digoxin to control the heart rate during both normal activities and exercise, rate-limiting calcium antagonists should be administered with digoxin
  5. NOTES FOR PRESENTERS For further details, refer to the NICE guideline – page 27. Patients undergoing PCV are usually admitted to hospital
  6. NOTES FOR PRESENTERS Refer to NICE guideline – pages 22 and 23 In order to provide adequate thromboprophylaxis with minimal risk of bleeding, current clinical practice aims for a target INR of between 2.0 and 3.0; INRs higher than 3.0 are associated with increases in bleeding, and INRs lower than 2.0 are associated with increases in stroke risk.