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atrial fibrillation
1. MANAGEMENT OF AF WITH
SPECIAL REFERENCE TO ESC 2016
DR AURIOM KAR
2. CLASSIFICATION OF AF ACCORDING TO PATHOGENESIS
• The attempts of the guidelines to link distinct etiological factors with
specific pathophysiological mechanisms are somewhat speculative but
nonetheless interesting because this approach might suggest future line
of research to better understand the pathophysiology of AF.
• The hypothesis that there are different types of AF with distinct pathophysiological
bases is somewhat daring.
• Although the etiological factors can differ, the pathophysiological consequences
are probably similar, and there is no evidence for the hypothesized “distinct
pathophysiological mechanisms” and “different types of AF”, except in very
specific disease and clinical situations.
3.
4.
5.
6. NOAH – AFNET 6
• NOAH – AFNET 6 is a prospective, parallel-group, randomized,
open, double-blind, multi-center trial to evaluate the
potential benefit of oral anticoagulation therapy in patients
with AHRE, but without overt AF. The trial will test whether
treatment with edoxaban, a newly introduced non-vitamin K
antagonist oral anticoagulant (NOAC), is superior to current
therapy to prevent stroke, systemic embolism, or
cardiovascular death in this patient group.
• There is evidence that the stroke rate is increased in patients
with AHRE. A sizeable portion of these patients develop AF
over time. In these patients, AHRE can be considered as an
early manifestation of AF. There is uncertainty about the
optimal antithrombotic therapy in patients with AHRE.
Therefore, we conduct the NOAH – AFNET 6 trial.”
7.
8. COMMENTS
• The new guidelines classify AF episodes that are
cardioverted within 7 days as paroxysmal;
• in previous guidelines, all episodes requiring
cardioversion were considered persistent, even
those lasting less than 7 days. This criteria change
might be confusing and it remains to be seen
whether these definitions will also be adopted by the
guidelines of other scientific societies.
• . A new type of AF is introduced—long-standing
paroxysmal—but is insufficiently explained.
9.
10.
11.
12.
13. COMMENTS
• A CONTROVERSIAL ASPECT IS THE USE OF BIOMARKERS (HIGH-SENSITIVITY
TROPONIN AND N-TERMINAL PRO–B-TYPE NATRIURETIC PEPTIDE) TO STRATIFY
THROMBOEMBOLIC RISK, ALTHOUGH THE RECOMMENDATION IS IIB B.
• THE DIAGNOSTIC AND PROGNOSTIC USEFULNESS OF THESE BIOMARKERS HAS
BEEN SHOWN IN OTHER CARDIOVASCULAR DISEASES BUT CONFIRMATION IS
REQUIRED OF THEIR ADDITIONAL PROGNOSTIC VALUE IN CLINICAL RISK SCALES.
• THE STUDIES CONTRIBUTING TO THE INCLUSION OF THESE BIOMARKERS IN THE
GUIDELINES WERE PERFORMED IN PATIENTS ENROLLED IN LARGE TRIALS
COMPARING VITAMIN K ANTAGONISTS (VKAS) WITH NEW ORAL
ANTICOAGULANTS (NOACS).
• ACCORDINGLY, THE ROLE OF BIOMARKERS IS CONTROVERSIAL BECAUSE ALL
PATIENTS WERE ANTICOAGULATED.
• THEIR USE IN LOW-RISK PATIENTS HAS NOT BEEN VALIDATED AND THEIR ROLE
IN PATIENTS WITHOUT ANTICOAGULATION REMAINS TO BE STUDIED
14.
15.
16.
17.
18. COMMENTS
A list of modifiable risk factors for bleeding is
proposed but no bleeding risk scale is
explicitly recommended.
Another surprising change is the inclusion of
biomarkers that are not used in daily clinical
practice, such as GDF-15
29. REASON FOR CLOT FORMATION IN LAA
• INTENSE FIBROSIS AND INFLAMMATION
SEEEN IN LAA.
• PRESENCE OF PECTINATE MUSCLE-MORE
STASIS
30. PATIENTS IN WHOM LAA CLOSURE IS
CONSIDERED
• Thrombocytopenia or known coagulation defect associated
with bleeding
• Recurrent gastrointestinal bleeding
• Prior severe bleeding, including intracranial hemorrhage
• Combined use of dual antiplatelet and anticoagulant therapy
• Poor compliance with anticoagulant therapy
• High risk of the patient falling or prior falls resulting in injury
35. POST IMPLANTATION
NO ABSOLUTE C/I FOR OAC
• WARFARIN PLUS ASP FOR
45 DAYS
• ASPIRIN AND CLOPIDOGREL
FOR FOR 6 MONTH
• ASPIRIN INDEFINATELY
ABSOLUTE C/I OAC
• CLOP AND ASP FOR 6
MONTH
• ASP INDEFINATELY
39. ISCHEMIC STROKE IN PATIENT TAKING
WARFARIN
INR IN SUBTHERAPEUTIC LEVEL
• TEMPRARY INTERRUPTION
• RENEWED EFFORT TO KEEP
INR IN THERAPEUTIC LEVEL.
INR IN THERAPEUTIC LEVEL
• MOST OFTEN LACUNAR
RELATED TO SMALL VESSEL
ARTERY DISEASE RATHER
THAN OF CARDIOEMBOLIC .
• INCREASE WARF TO INR 2.5
TO 3.5 RATHER THAN
ADDING ANTIPLATELET
40. HEMMORHAGIC STROKE IN PATIENT
TAKING WARFARIN DUE TO AF
• For all patients who develop an ICH, all
anticoagulant and antiplatelet drugs should be
discontinued acutely, and anticoagulant
effects should be reversed immediately.
• Reversal of warfarin-induced anticoagulation.
• Resumption of anticoagulation.
51. COMMENTS
• A surprising recommendation is to use fresh
frozen plasma inpatients with a bleeding
event and anticoagulated with VKAs. Most
guidelines recommend the use of
prothrombin complex concentrate, given the
lack of efficacy of fresh frozen plasma and its
difficult administration (requiring thawing and
a large volume) and associated secondary
effects
60. Comments
The guidelines have removed the recommendation not to use digitalis
drugs as the only agents for heart rate control in patients with paroxysmal
AF.
This advice contrasts with North American guidelines, which only consider
BBs and CAs for long-term heart rate control and restrict the use of
digitalis to patients with heart failure
The guidelines barely consider combined heart rate and rhythm control,
Atrioventricular node ablation and pacemaker implantation is one way to
achieve heart rate control after drug therapy failure. However, the
guidelines have largely ignored the type of cardiac resynchronization
device, whether single-chamber, dual-chamber, or triple-chamber
61.
62.
63. WHY TO RESTORE SINUS RHYTHM
• TO REDUCE SYMPTOMS
• TO DECERASE STROKE RISK
• TO REDUCE MORTALITY
64.
65.
66. VERNAKALANT THE -NEW ENTRY
IN BROAD POPULATION OF PATIENTS WITH RECENT ONSET AF
,INCLUDING ELDERLY AND THOSE WITH STRUCTURAL HEART
DISEASE WITHOUT HF VERNALKALANT IS AN EFFECTIVE AND
SAFE FIRST CHOICE IN RAPID CONVERSION OF AF TO SR.
AS COMPARED TO AMIODARONE IT IS ASSPOCIATED WITH
1. HIGHER CONVERSION RATE
2. SMALLER INCREASE IN QTc
3. HIGHER RATE OF SYMPTOM RELIEF
4. MORE SIGNIFICANT IMPROVEMENT OF QOF
70. LONG TERM MAINTAINENCE OF
SINUS RHYTHM
• WHOM TO CONSIDER FOR LONG TERM
RHYTHM CONTROL THERAPHY?
• CHOICE OF DRUG?
• NEW ADDITION OF DRONEDARNE IN ESC
75. COMMENTS ON RHYTHM CONTROL
• THE FIRST MAJOR COMMENT OF THE GUIDELINES IN THIS AREA IS THAT
THE BENEFITS OF RHYTHM CONTROL THERAPY ARE LIMITED TO
SYMPTOM IMPROVEMENT.
• BECAUSE THERE ARE NO DATA ON REDUCED MORTALITY, THERE ARE NO
GUIDELINES FOR ASYMPTOMATIC PATIENTS.
• ABLATION, WHICH IS AWARDED A IIA RECOMMENDATION. THIS CLASS
OF RECOMMENDATION MIGHT BE A SOURCE OF CONTROVERSY DUE TO
THE CONSIDERABLE NUMBER OF RANDOMIZED STUDIES SHOWING THAT
ABLATION IS SUPERIOR TO ANTIARRHYTHMICS IN PATIENTS WITHOUT
PREVIOUS ANTIARRHYTHMIC THERAPY
• STOP-AF , CABANA. MANTRA PAF AND RAFFT 2: TRIALS
SHOW EFFECTIVENESS OF ABLATION OVER DRUGS IN AF
76. COMMENTS ON RHYTHM
CONTROL CONT..
• The guidelines fail to cite any study showing that ablation
boosts ventricular function recovery in patients with either
adequate or inadequate ventricular heart rate control.
• No convincing evidence is put forward showing that ablation
is superior to strict control of ventricular heart rate with node
ablation and subsequent resynchronization device
implantation.
• However, the guidelines do state that ablation is superior to
amiodarone in patients with ventricular dysfunction and an
implantable device.
77. COMBINATION OF RANOLAZINE AND
DRONADERONE
NO PLACE IN GUIDELINE
• HARMONY TRIAL
Neither placebo nor either drug alone significantly
reduced AFB.
Conversely, ranolazine 750 mg BID/dronedarone 225
mg BID reduced AFB by 59% vs placebo (p=0.008)
while ranolazine 750 mg BID/dronedarone 150 mg
BID reduced AFB by 43% (p=0.072). Both
combinations were well tolerated.
78.
79.
80. Types of hybrid therapies
• Antiarrythmic drugs with catheter ablation.
• Antiarrythmic drugs with pacemaker
• Cathether ablation with surgical af procedure
81. COMMENTS ON HYBRID
THERAPHY(2Ac)
• THE GUIDELINES MENTION THE POSSIBLE USE OF CAVOTRICUSPID
ISTHMUS ABLATION AND CONTINUED ANTIARRHYTHMIC DRUG
THERAPY—MAINLY WITH TYPE IC ANTIARRHYTHMIC DRUGS—IN
PATIENTS WITH AF AND ORGANIZED ATRIAL FLUTTER, BUT NO STRENGTH
OF RECOMMENDATION IS PROVIDED.
• IN THE EUROPEAN AND NORTH AMERICAN GUIDELINES FOR
SUPRAVENTRICULAR TACHYCARDIA TREATMENT, A STRONG
RECOMMENDATION (I AND IIA) IS AWARDED TO THIS APPROACH
• A PACEMAKER AND ANTIARRHYTHMIC DRUGS, LARGELY DUE TO THE
NEGATIVE CHRONOTROPIC EFFECTS OF THESE DRUGS. PACEMAKERS
PERMIT THE USE OF HIGHER DOSES OF THESE DRUGS.
• CATHETER ABLATION CAN SOMETIMES OBVIATE THE NEED FOR
ANTIARRHYTHMIC DRUGS AND PACEMAKERS. SOME OF THESE PATIENTS
HAVE REVERSE REMODELING OF THE SINUS NODE, WHICH CAN RETURN
TO NORMAL AFTER AF TERMINATION WITH ABLATION.
• HOWEVER, EARLY SINUS NODE DYSFUNCTION CAN BE UNMASKED
82. CATHETHER ABLATION WITH SURGICAL AF
PROCEDURE
ADVANTAGE
• INITIAL CATHETER ABLATION IS PREFERED FOR
PAROXYSMAL AF
• AF SURGERY IS BETTER AS FIRST OPTION FOR
PERSISTANT LONG ATANDING AF
• REQUIREMENT OF LESS RF ENERGY –SO LESS
COLLORARY DAMAGE TO SURROUNDING
STRUCTURE VIZ .ESOPHAGUS
• ENDOCARDIAL “TOUCH-UP” BY CATHETER
AFTER SURG
• REDUCED TIME IN LA SO LESS EMBOLISM AND
STROKE ,,LESS FLURO TIME.
• INTRAOPERATIVE VALIDATION OF THE
SURGICAL ABLATION MOST RELIABLE END
POINT FOR AN EFFECTIVE PVI IS THE
CONFIRMATION OF BIDIRECTIONAL
CONDUCTION BLOCK THROUGH THE BOX
LESION(INTRAOP REQ OF EP STUDY). TAILORED
DELIVERY OF RF APPLICATIONS, UNTIL SUCH
END-POINTS ARE MET, THEREBY REPRODUCING
THE EP CRITERIA FOR SUCCESS ALSO IN THE
SURGICAL SETTING.
DISADVANTAGE
• FALSE POSITIVES CONSIST IN EARLY
INDUCIBLE POSTOPERATIVE ATRIAL
ARRHYTHMIAS DETECTED BY EP MAY
BE DUE TO ATRIAL ODEMA DUE TO
SURG.
• ACUTE DEMONSTRATION OF A
BIDIRECTIONAL BLOCK COULD ONLY
BE TRANSIENT AND NOT CONFIRMED
BY DELAYED TESTING AT ONE
MONTH AFTER SURGERY.
• HEPARINIZATION FOLLOWING THE
TRANS-SEPTAL PUNCTURE WHICH
COULD INCREASE THE RISK OF
EPICARDIAL BLEEDING
• AVAILABILITY OF TWO SEPARATE TEAMS
(SURGEONS AND
ELECTROPHYSIOLOGISTS) DURING AN
OVERALL TIME-CONSUMING PROCEDURE
83. Hybrid Staged Operating Room and
Interventional Catheter Ablation
for Atrial Fibrillation (HISTORIC-AF)
CREATION OF CARDIAC LESION WITH
EPICARDIALY APPLIED RF ABLATION THROUGH
MIS APPROACH FOLLOWED BY DELAYED EP
ABLATION 1-2 MONTH AFTER SURGICAL
OPERATION
The hypothesis that there are different types of AF with distinct
pathophysiological bases is somewhat daring. Although the
etiological factors can differ, the pathophysiological consequences are
probably similar, and there is no evidence for the hypothesized
“distinct pathophysiological mechanisms” and “different types of AF”,
except in very specific disease and clinical situations.
ARTESIA-APIXABAN
NOAH FNET-ENDOXABAN
NOAH – AFNET 6 is a prospective, parallel-group, randomized, open, double-blind, multi-center trial to evaluate the potential benefit of oral anticoagulation therapy in patients with AHRE, but without overt AF. The trial will test whether treatment with edoxaban, a newly introduced non-vitamin K antagonist oral anticoagulant (NOAC), is superior to current therapy to prevent stroke, systemic embolism, or cardiovascular death in this patient group.
There is evidence that the stroke rate is increased in patients with AHRE. A sizeable portion of these patients develop AF over time. In these patients, AHRE can be considered as an early manifestation of AF. There is uncertainty about the optimal antithrombotic therapy in patients with AHRE. Therefore, we conduct the NOAH – AFNET 6 trial.”
Based on the presentation, duration, and spontaneous termination of AF episodes, five types of AF are traditionally distinguished: first diagnosed, paroxysmal, persistent, long-standing persistent, and permanent AF.
If patients suffer from both paroxysmal and persistent AF episodes, the more common type should be used for classification
PT WITH AF HAVE SIGNIFICANTLY POORER QUALITY OF LIFE THAN HEALTHY CONTROL EXPERIENCING VARIETY OF SYMPTOMS
LATHERGY
PALPITATIONS
DYSPNEA
CHEST TIGHTNESS
SLEEPING DIFF
PSHYCHOSOCHIAL DISTRESS
EHRA SYMP SCALE IS RECOMMENDED FOR SYM ASSESS MENT
The modified EHRA scale should be used to guide symptom orientated treatment decisions and for longitudinal patient profiling
The classification of AF based on etiology no longer seems to be relevant from the therapeutic perspective.
THE PREDICTIVE ABILITY OF CHADAVASC SCORE TO CATEGORISE LOW RISK PT WITH LOWER SCORE IS BETTER THAN CHADS2 SCORE.
Classification of CHADS2 vs CHADS2-VASc
In both scoring systems, a score of 0 is "low" risk of stroke, 1 is "moderate", and any score above 1 is a "high" risk. The CHADS2-VASc system, with having three more potential variables, inevitably classifies more patients into a high-risk group. As shown in the diagram below, CHADS2-VASc classifies the same patient group into a higher risk category compared to CHADS2.
SCORE 0- CHADS2 ANNUAL RISK OF STROKE IS 0.6%
SCORE 0 –CHADS VASC RISK 0.2%
CATHETHER ABLATION –NOT PROVEN TO REDUCE RISK OF CARDIOEMBOLIC STROKE
Some expert recommend procedure only for patients who can take warf for atleast 6 week
Based upon the results of PROTECT AF and PREVAIL, the WATCHMAN device was approved by the United States FDA in March 2015 for patients with nonvalvular AF for whom long-term anticoagulation is indicated, but who have a sensible reason to not take such therapy
STROKE REDUCTION WITH WARFARIN COMPARED WITH ASP IS MORE IN PT WITH COMPLETE STROKE AND ALMOST SAME IN PT WITH TIA.
START ASP TILL RESUMPTION OF OHA TO REDUCE THE RISK OF RECC STROKE
C/I FIBRINOLYSIS-INR>1.7 AND >4.5 HRS APTT OUTSIDE NORMAL RANGE FOR DABIGATRAN,LAST DOSE OF DABIGATRAN ADM WITHIN 48HRS
WARF CAN BE STARTED AFTER 24 HR
RECOMMENDED TO START NOAC AFTER 48 HRS AS THEY HAVE EARLY ONSET OF ANTICOAGULENT ACTION
OAC WITH LOW BLEEDING RISK BUT NO SPECIFIC AGENT IS ADVOCATED.
RIVAROXABAN APIXABAN AND ENDOXABAN –MOSTLY HEPATIC EXCREATION SO BIOACCCUMULATION IN HEPATIC FAILURE(ORAL ACTIVATED CHARCOAL FOR REVERSAL)
DABIGATRAN-80-85% RENAL.(HEMODIALYSIS REQUIRED TO REMOVE DRUG IN EXCESS)-----------IDARUCIZUMAB
THROMBIN CLOTTING TIME-DABIGATRAN(NORMAL VALUE RULES OUT DABIGATRAN EFFECT)
SPECIFIC ASSAYS FOR ANTI FACTOR Xa -
FOR PT WITH IMMENENT CAUSE OF DEATH FROM BLEEDING IN ADDITION TO TREATMENT WITH ANTIFIBRINOLYTIC AGENTS AND DRUG REMOVAL WITH ORAL CHARCOAL AND HEMODIALYSIS WE SUGGEST IDARICIZUMAB
FOR THOSE WHEN IDARICIZUMAB IS NOT AVAILABLE APCC IS GIVEN
WOULD NOT GIVE APCC AND IDARICIZUMAB TOGETHER –PROTHROMBOTIC RISK
WOEST TRIAL=OAC WITH CLOP VRS TRIPLE THERAPHY
ISAR TRIPLE=SHORTENING OF THE DURATION OF CLOP FROM 6 MONTH TO 6 WEEKS AFTER DES IN PT RECEIVING ASP AND OAC
NOVEL P2 Y12 INB NOT RECOMMENDED IN TRIPLE THERAPHY
RELY –COMB OF LOWER DOSE OF DABIGATRAN IF USED IN TRIPLE THERAPHY
ARISTOTLE TRIAL –IN CASE OF STRONG INDICATION FOR COMBINATION OF ASP APIXIBAN MAY BE SAFER THAN WARF
ENGAGE AF-
PIONEER AF
REDUAL PCI-DABIGATRAN
AUGUSTUS-APIXIBAN
VERNAKALANT NOT AVAILABLE IN USA
CRAFT TRIAL AND ACT 1 2 4 = COMPARED VERNAKALANT WITH PLACEBO
AVRO= COMPARED VERNAKALANT WITH AMIODARONE=SUPERIOR STUDY
C/I= SBP<1OO HF NYHA 3 AND 4 SEV AS ACS 30 DAYS BACK PROLINGED QT
If af >48 hrs –risk of stroke is high (6-7%) and prior a prior antocoagulation decreases the risk to <1%
DRUGS FOR PHARMACOLOGICAL CARDIOVERSION OF RECENT ONSET AF-AMIODARONE FLECAINIDE IBUTILIDE PROPAFENONE VERNAKALANT
MANTRA PAF TRIAL RAF BETTER THAN AAD
RAAFT2 TRIAL
1A –PAROXYSMAL AF
2Ab-PERSISTANT AND LONG STANDING PERSISTANT AF
The rationale of such strategy is based on the consideration that in presence of paroxysmal AF the majority of triggers are located within the four PVs while in presence of persistent AF surgical procedure in first instance allows for an extensive isolation of the PV and the posterior aspect of the left atrium, thereby excluding not only the ectopic foci within the PVs but also targeting the macro-reentrant circuits and the fragmented potentials usually located within this area.
from the EP standpoint, it is recommended to reduce RF energy delivery when treating the posterior left atrium as to minimize the potential collateral damage to the esophagus: such risk can be mitigated by the surgical box lesion which could also overcome such drawback of the transcatheter ablation
EP procedure, as a second step, can identify and treat any potential gap in the surgical ablation (endocardial “touch-up”) and and create additional ablation lines, if required, in a patient-tailored fashion.
f paroxysmal AF the majority of triggers are located within the four PVs while in presence of persistent AF surgical procedure in first instance allows for an extensive isolation of the PV and the posterior aspect of the left atrium, thereby excluding not only the ectopic foci within the PVs but also targeting the macro-reentrant circuits and the fragmented potentials usually located within this area