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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 32, No 2, March/April 2021

AFRICA

105

recommendations regarding anticoagulant therapy initiation in

these patients are expert recommendations only. Therefore, patient

choice regarding this matter is an important consideration.

12,57

The CHA

2

DS

2

-VASc score seems to also be suitable to

assess the stroke risk in patients who present with AHRE.

21,25,58

A recent study, performed on over 21 000 non-anticoagulated

patients with CIEDs, showed that the annualised risk of systemic

embolism (SSE) was associated with increasing CHA

2

DS

2

-VASc

score and increasing AF duration.

In this study, in patients with a CHA

2

DS

2

-VASc score of 0 to

1, SSE rates were low, regardless of the duration of the device-

detected AF. However, the stroke risk increased, crossing an

actionable threshold, defined as > 1% per year, in patients with

CHA

2

DS

2

-VASc score of 2 with > 23.5 hours of AF, patients

with CHA

2

DS

2

-VASc score of 3–4 and > six minutes of AF, and

patients with a CHA

2

DS

2

-VASc score ≥ 5 even if they presented

with no AF.

58

More studies are necessary to assess if the usual

strategies for stroke risk stratification and bleeding risk apply to

these patients.

Both the ESC taskforce for the 2016 guidelines on the

management of AF and the EHRA consensus for device-

detected subclinical AT recommend using the CHA

2

DS

2

-VASc

score in order to initiate anticoagulation treatment, with similar

indications as in AF. Therefore, the ESC taskforce for the 2016

guidelines on the management of AF recommends initiating oral

anticoagulation when an AHRE is detected with a duration of

more than five to six minutes and an atrial rate of over 180 bpm

in male patients with a CHA

2

DS

2

-VASc score ≥ 1 or in female

patients ≥ 2.

57

The EHRA consensus for device-detected subclinical AT

proposes oral anticoagulation based on the same CHA

2

DS

2

-

VASc values in episodes that are ≥ 5.5 hours.

12

However, the same

consensus mentions that an AHRE episode of only minutes has

a similar stroke risk as one of > 5.5 hours. The question that

arises is whether continuous anticoagulation in these patients

is necessary. The 2019 American Heart Association/American

College of Cardiology/Heart Rhythm Society (AHA/ACC/

HRS)-focused update of the 2014 AHA/ACC/HRS guideline

for the management of patients with AF recommends further

evaluation in patients with AHRE to document clinically

relevant AF in order to guide the treatment

56

(Table 3).

Our approach

In CIED patients we interrogate the device at six weeks after

a successful implantation procedure to assess the functioning

parameters. Afterwards, we interrogate the devices once a year.

If an AHRE episode is observed, we ask for an expert opinion

(rhythmology specialist) to confirm that the recorded episode

is an AHRE instead of an inaccurately labelled (false-positive)

recording. Before considering anti-coagulation therapy, we try to

verify the presence of AF by one of the following: resting ECG,

Holter ECG recording, patient-operated devices or by reviewing

the EGM (if available) to determine if the AHRE was AF.

We sometimes use external ECG monitoring devices in CIED

patients where the data recorded by the device are uncertain.

After we confirm that the recorded episode is in fact AF,

we follow the recommendations of the EHRA consensus for

CIED-detected arrythmias and initiate lifelong anticoagulation

therapy if the episode was longer than 5.5 hours, based on the

patient’s CHA

2

DS

2

-VASc score (≥ 1 for male patients, ≥ 2 for

female patients).

12

In patients presenting with multiple short episodes of AHRE

(≥ five minutes) we follow the same indication, even though the

thromboembolic risk is not as high as in the previous group.

We therefore initiate anticoagulation therapy based on the

CHA

2

DS

2

-VASc score (≥ 1 for male patients, ≥ 2 for female

patients).

12

In patients with a single short episode of ≥ five minutes, we

follow individualised treatment and patient choice based on

the thromboembolic risk (CHA

2

DS

2

-VASc score) and bleeding

risk (HASBLED score). We follow the recommendations of the

same consensus and observe the AF burden of the patient on

multiple follow ups, usually every three to six months, before

initiating lifelong anticoagulation. We initiate anticoagulant

therapy in this group, only in patients with a high/very high risk

of stroke (CHA

2

DS

2

-VASc score > 4) and low bleeding risk,

in which a clear clinical benefit can be anticipated. We do not

usually initiate anticoagulant therapy in patients with AHRE

< five minutes, because of the lack of data in the literature

regarding this duration. Anticoagulant therapy is initiated in

these patients on a case-by-case basis.

12

Our strategy always takes

into consideration patient choice and wishes.

Conclusion

AHRE represent a complex arrhythmic entity that significantly

increases the thromboembolic risk. Further studies are necessary

to understand the underlying pathogenic mechanisms behind

AHRE and to guide the management of this arrythmia and its

complications.

References

1.

Benjamin EJ, Muntner P, Alonso A, Bittencourt MS, Callaway CW,

Carson AP,

et al.

; American Heart Association Council on Epidemiology

and Prevention Statistics Committee and Stroke Statistics subcommit-

tee. Heart Disease and Stroke Statistics – 2019 Update: a report from

the American Heart Association.

Circulation

2019;

139

(10): e56–e528.

2.

Stroke Risk in Atrial Fibrillation working group. Independent predic-

tors of stroke in patients with atrial fibrillation: a systematic review.

Neurology

2007;

69

(6): 546–554.

Table 3. Society guideline recommendations

Guideline

Subclinical

AF duration CHA

2

DS

2

-VASc score

Class of recommendation

Device-detected subclinical atrial tachyarrhythmias: definition, implications

and management; a European Heart Rhythm Association (EHRA) consen-

sus document

12

≥ 5.5 h*

≥ 5.5 h*

≥ 2

1 (men) or 2 (women)

Recommended/indicated

May be used or recommended

ESC 2016 guidelines for the management of atrial fibrillation

57

> 5–6 min ≥ 1 in male patients or 2 in female patients IA

*Data suggests risk is similarly increased by a mere five minutes. AF, atrial fibrillation.