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Journal of Arrhythmia logoLink to Journal of Arrhythmia
. 2021 Dec 28;38(1):31–49. doi: 10.1002/joa3.12669

2021 Asia Pacific Heart Rhythm Society (APHRS) practice guidance on atrial fibrillation screening

Ngai‐Yin Chan 1,, Jessica Orchard 2,3, Michael‐Joseph Agbayani 4,5, Dean Boddington 6, Tze‐Fan Chao 7,8, Sofian Johar 9,10,11, Bobby John 12,13, Boyoung Joung 14, Saravanan Krishinan 15, Rungroj Krittayaphong 16, Sayaka Kurokawa 17, Chu‐Pak Lau 18, Toon Wei Lim 19, Pham Tran Linh 20, Vien Hoang Long 20, Ajay Naik 21, Yasuo Okumura 17, Tetsuo Sasano 22, Bernard Yan 23, Sunu Budhi Raharjo 24, Dicky Armein Hanafy 24, Yoga Yuniadi 24, Nwe Nwe 25, Zahid Aslam Awan 26, He Huang 27, Ben Freedman 3,28
PMCID: PMC8851593  PMID: 35222749

Abstract

In this paper, the Asia Pacific Heart Rhythm Society (APHRS) sought to provide practice guidance on AF screening based on recent evidence, with specific considerations relevant to the Asia‐Pacific region. A key recommendation is opportunistic screening for people aged ≥65 years (all countries), with systematic screening to be considered for people aged ≥75 years or who have additional risk factors (all countries).

graphic file with name JOA3-38-31-g002.jpg

Keywords: atrial fibrillation, prevention, screening, stroke

1. INTRODUCTION

Atrial fibrillation (AF) is the most common sustained arrhythmia, and the global prevalence is estimated to be 46.3 million. 1  With an aging population worldwide and increased detection, the prevalence of AF has been increasing. Notably, the prevalence has increased by 20‐fold over a period of 11 years in China and is projected to double in the European Union by 2060. 2 , 3 Despite the fact that 70% of AF‐related stroke can be prevented by oral anticoagulation (OAC) therapy, 4 over 70% of AF‐related strokes or transient ischemic attacks occur in nonanticoagulated patients in Hong Kong. 5

Ischemic stroke rates in Asia vary widely. 6 In Japanese AF patients, the annual incidence has been reported at 1.3%, 7 while a rate of 10.4% was reported in hospitalized Chinese AF patients in Hong Kong. 8 Higher rates of 13% have been reported in Southeast Asia and the Far East. 9

AF screening is recommended by a number of guidelines, but not all. Remarkable controversy exists as to the optimal approach for AF screening which is evident in the recommendations of different international guidelines. In the European Society of Cardiology (ESC) guidelines, for primary stroke prevention, it is a class I recommendation to perform opportunistic AF screening by pulse taking or electrocardiogram (ECG) rhythm strip in patients aged ≥65 years and a class IIa recommendation for systematic ECG screening in individuals aged ≥75 years. 10 In the American College of Cardiology (ACC) guidelines, no recommendation has been put forward for AF screening. 11 , 12  The United States Preventive Services Task Force (USPSTF) concluded that there was inadequate evidence to assess whether AF screening with electrocardiography identifies older adults with previously undiagnosed AF more effectively than usual care. 13 In Australia, the Heart Foundation and Cardiac Society of Australia and New Zealand (CSANZ) included a recommendation for opportunistic screening in people aged ≥65 years and a practice point that a single‐lead ECG rhythm strip might be preferred. 14 In the Asia Pacific region, there is no specific guidance on screening, although Asia Pacific Heart Rhythm Society (APHRS) supported the consensus document of the European Heart Rhythm Association (EHRA) in 2018 which recommended opportunistic screening. 15

Importantly, there is huge heterogeneity in AF epidemiology, ethnicity, socioeconomic status, access to technologies, and healthcare system among different countries in the Asia Pacific region. To embrace the heterogeneity in the Asia Pacific region, three levels of recommendations according to the applicability to different countries are created in this APHRS AF Screening Practice Guidance (Table 1). To further address this heterogeneity, a special section on AF screening in APHRS countries is included in the Online Appendix. This Online Appendix includes information on the healthcare system, AF epidemiology, current status, and challenges in AF screening and future perspectives in different countries in the Asia Pacific region. Furthermore, since chronic rheumatic heart disease (RHD) remains prevalent in some Asia Pacific countries, special emphasis is placed in this condition in the preparation of this APHRS AF Screening Practice Guidance (Figure 1).

TABLE 1.

Levels of recommendation for AF screening

Level 1 Recommended in all countries
Level 2 Recommended in most countries
Level 3 Recommended in some countries

FIGURE 1.

FIGURE 1

Summary of key practice recommendations for atrial fibrillation screening

2. EPIDEMIOLOGY OF ATRIAL FIBRILLATION

2.1. Prevalence and incidence of AF

The reported prevalence of AF in Asia Pacific countries varies from 0.49% to 5.4% (Table 2). The prevalence of AF in those aged >70 or 80 years was 4.6%–8.2%. The prevalence of AF progressively increased more than twofold for the last 10 years 16 , 17 and is significantly greater in men than in women for all years (Figure 2A). AF prevalence in Thailand has been reported to be 1.9% for those aged ≥65 years, and 2.2% in rural areas for those aged ≥60 years. 18 AF prevalence in Korea is expected to be 5.8% in 2060, and 4.0% in Taiwan by 2050. 16 Although the prevalence of AF is increasing steeply in Asia, it remains lower than in many Western countries. The prevalence increased over the study period, mainly among those >70 years (Figure 2B).

TABLE 2.

Prevalence of AF in the Asia Pacific region

Country/

region

Year(s) data‐obtained Sample size (n) Study population Age Prevalence (%) total (men, women) Study
Australia June 2014 6,140,651 Seven international epidemiology studies ≥55 5.4 (6.0, 4.8) Ball et al. (2015) 124
China 2014–2015 726,451 Nationally representative cross‐sectional study.

≥40

≥70

2.3 (1.9, 2.7)

4.6 (ND, ND)

Wang et al. (2008) 125
China 2015–2017 12,013 Population‐based study, the Guangzhou Heart Study

≥35

≥80

1.5 (2.0, 1.2)

5.0 (ND, ND)

Deng et al. (2018) 126
Hong Kong 2014–2015 13,122 Territory‐wide, community‐based screening program

≥15

≥80

1.8 (1.6, 2.0)

5.0 (3.9, 6.1)

Chan et al.

(2017) 82

India 2016–2017 2100 Indian adults living in the rural region of Anand district, Gujarat, India. ≥40 1.6 (2.3, 1.0) Soni et al. (1995) 127
Indonesia 1990 2073 Random selection of people from three districts in Jakarta 25–64 0.2 Boedhi‐Darmojo R 128
Iran 2001 463 Two general practitioners serving the National Iranian Oil Company‡ 50–79 2.8 (1.3, 4.3) Habibzadeh et al. (2004) 129
Japan 2012

630,138

123,425

Iwate Prefecture

≥40

≥80–89

1.3 (1.9, 0.5)

4.7 (6.0, 3.8)

Tamaki et al. (2017) 130
Japan 2013–2014 108,951 Data from the periodic health examinations, Tochigi Prefecture, Japan

≥40

≥80

0.9 (1.5, 0.4)

4.5 (5.5, 3.4)

Yonezawa et al. (2009) 131
Malaysia 2007–2014 10,805 18 urban, 22 rural communities across Malaysia ≥30 0.5 Lim et al. (2016) 132
Singapore Prospective 1,839 Community‐based study, health screening project

≥55

≥80

1.5 (2.6, 0.6)

5.8

Yap et al. (2008) 133
South Korea 2013 819,948 Korean National Health Insurance Data Sample Cohort ≥15 1.4 (0.7, 0.7) Lee et al. (2018) 20
South Korea 2015

41,701,269

1,371,423

Korean National Health Insurance Service database

≥20

≥80

1.5 (1.6, 1.4)

8.2 (ND, ND)

Kim et al. (2018) 17
Taiwan 2011 289,559 Taiwan National Health Insurance Research Database

≥20

≥80~90

1.1 (0.6, 0.4)

5.9 (ND, ND)

Chao et al. (2018) 16
Thailand Prospective 1,277 Cross section of Maerim District, Chiang Mai ≥65 1.9 Phrommintikul et al. (2016) 18
Thailand Prospective 13,864 Communities in Phetchaburi and Lopburi provinces ≥65 2.8 Suwanwela et al (2020) 114

FIGURE 2.

FIGURE 2

Annual prevalence of atrial fibrillation between 2006 and 2015 stratified according to gender (A) and age (B). *P value for increasing trends <0.001. †P value for decreasing trends <0.001. AF, atrial fibrillation. Source: Kim DH, et al. 2018, 17 reproduced with permission

In terms of incidence, annual trends in Asia were more stable. The 10‐year overall incidence was 1.51–1.77 per 1000 person‐years 16 , 17 and was higher for men than women. 17

The proportion of patients with high stroke risk (CHA2DS2‐VASc score ≥2) increased progressively, and was more than 80%. 16 , 17  The proportion of patients with high bleeding risk (HAS‐BLED score ≥3) increased to about 60%. 16 , 17

2.2. Healthcare burden of AF

The hospitalization and healthcare burden of AF increased in many Asian countries over the past decade. 16 , 17 , 19 Hospitalizations for AF increased by 420% from 2006 to 2015 in Korea. Most admissions occurred in patients aged ≥70 years, and the most frequent coexisting conditions were hypertension, heart failure, and chronic obstructive pulmonary disease (COPD). Hospitalizations due to major bleeding and AF rate control increased, whereas those due to ischemic stroke and myocardial infarction decreased. 17 , 20  The risks of ischemic stroke, heart failure, and mortality were higher compared with patients without AF in the initial period (approximately 6 months) after AF was first diagnosed. 16

In Korea, the total cost of care related to AF was equivalent to 0.78% of the Korean National Health Insurance Service total expenditure. In comparison, in the United States, the national incremental AF cost was estimated as $6–26 billion, and in the United Kingdom, the direct cost of AF in 2000 was £459 million which was the equivalent of 1% of the national healthcare budget. 21 , 22 , 23

2.3. AF prognosis

Over the last 5 decades, AF‐associated mortality decreased by 25% in the Framingham Heart Study. 24 Among AF patients, annual event rates for all‐cause mortality, ischemic stroke, intracranial bleeding, heart failure admission, and myocardial infarction significantly declined for a decade. AF‐associated mortality decreased by 20% over a decade from 5.0%/year in 2006 to 4.0%/year in 2015 in Korea. 17 , 25 Improvement in survival might be related to a 52% reduction of heart failure and a 9% reduction of ischemic stroke. 17 , 25 Better treatment of risk factors like hypertension might be playing a role.

2.4. Epidemiology of AF in rheumatic heart disease

The prevalence of RHD has declined in the developed world since the industrial revolution. However, RHD is still a common health burden in some Asian and African countries. In 2015, 73% of global RHD cases were located in India, China, Pakistan, Indonesia, and the Democratic Republic of the Congo, 26 demonstrating that RHD continues to be a significant health problem for developing countries. Lower socioeconomic status and overcrowding are associated with higher prevalence of RHD, particularly for children living in households of >8. 27 , 28 Prevalence in the Indian population has been reported as 6 per 1000. RHD also remains a substantial problem for first nations people, such as Indigenous Australians (prevalence up to 15 per 1000 in the Top End of the Northern Territory) 29 and Māori and Pacific Islanders. 30 , 31

It is estimated that 15.6 million people suffer from RHD and 3–7.5% of all strokes in developing countries are directly related to RHD. 32 , 33 , 34 Estimates of the prevalence of AF in the rheumatic population vary widely because of differing periods of study, diagnostic methods employed, and in different countries. An Indian study found that those with tricuspid regurgitation had the highest prevalence of AF (34.9%) as compared with mitral stenosis (31.7%) and mitral regurgitation (25.3%). 35

Native valvular AF is mainly due to rheumatic mitral stenosis. Mechanical outflow obstruction because of mitral stenosis results in higher left atrial (LA) pressure that in turn causes LA enlargement which is associated with AF. The Canadian Registry of AF (CARAF) found that a larger baseline LA dimension is associated with progression to chronic AF. In addition, patients with no or paroxysmal AF recurrence had no change in LA dimension over a 4‐year period. 36

Age is also a major determinant of AF in mitral stenosis. Rates of persistent AF are <20% in cohorts with a mean age <35 years, while rates of persistent AF range between 30% and 60% for cohorts with age >45 years. 37 In a global hospital‐based RHD registry, the REMEDY study, that included some African countries, Yemen and India, AF was found in 21.8% of 3343 RHD subjects. 38 In the Asia Pacific region, AF prevalence was reported to be between 10% and 36% of patients with rheumatic mitral stenosis who underwent percutaneous mitral commissurotomy. 39 , 40 , 41

2.5. Key points

  1. The prevalence of AF is increasing steeply in Asia but remains lower than in many Western populations. The prevalence increased mainly among elderly populations.

  2. The hospitalization and healthcare burden of AF increased in many Asian countries over the past decade.

  3. RHD is still a common health burden in some Asian and African countries, and in first nations people.

3. PRIMARY STROKE PREVENTION BY ATRIAL FIBRILLATION SCREENING

3.1. Primary stroke prevention by AF screening

3.1.1. International recommendations on screening

At present, none of the US ACC/AHA AF guidelines have clear recommendations for AF screening, 11 , 12 although the AHA/American Stroke Association guideline states that “active screening” for AF in primary care “can be useful.” 42  The USPSTF 13 concluded that while systematic ECG screening can detect previously unknown cases of AF, it has not been shown to detect more cases than screening based on routine pulse palpation followed by ECG assessment if the pulse is irregular. Based on a comprehensive literature review published in 2018, 43 the task force concluded that there was insufficient evidence that systematic screening for AF with ECG in asymptomatic older adults led to better health outcomes than usual care or waiting until after symptoms have developed (“I” recommendation). The 2021 draft Evidence Review for the USPSTF still has an “I” recommendation for AF screening. 44  To generate this evidence would require large randomized controlled trials of screening for AF with stroke as an outcome as recommended by the AF‐SCREEN International Collaboration. 45  There are numerous such trials underway:

  • the Screening for Atrial Fibrillation with ECG to Reduce stroke (SAFER) study in the United Kingdom (ISRCTN16939438);

  • the US Heartline study (NCT04276441); and

  • the US ReducinG stroke by screening for UndiAgnosed atRial fibrillation in elderly inDividuals (GUARD‐AF) study (NCT04126486).

Two landmark randomized trials have recently published their results: the Danish LOOP study 46 and the STROKESTOP study. 47  The LOOP study included 6000 participants aged 70–90 years (without AF), who were randomly assigned in a 1:3 ratio to receive implantable loop recorder (ILR) monitoring or usual care. After a median follow‐up of just over 5 years, AF (>6 min) was detected in 32% of participants in the ILR group versus 12% in the usual care group. In total, 4.5% in the ILR group experienced a stroke or systemic arterial embolism versus 5.6% in the usual care group (HR 0.80, p = .11). 48 In summary, this large, well‐executed study showed a nonsignificant relative risk reduction in stroke/systemic arterial embolism in the ILR group, compared with control, over 5 years. 49 In addition, it demonstrates the higher detection rate of intensive monitoring, as almost a third of participants in the ILR group had AF detected.

The STROKESTOP study is the largest randomized trial of AF screening using a handheld ECG. Almost 30,000 people aged 75–76 years were randomly assigned to receive an invitation for AF screening or registry follow‐up (without screening or contact). 50  Just over 50% of those invited for screening participated, and screened themselves with a thumb ECG twice daily for 14 days. This resulted in a small increase in AF in the invited‐to‐screen group (12.1%–14%). While the study was well‐conducted, the main limitation is that the 49% of people who did not take up the invitation for screening were different to the group who participated: those who did not participate had a lower socioeconomic profile, higher stroke risk, and higher baseline AF prevalence. 51  This issue will be clarified by the study design of SAFER, although the study will not report for another 5 years. The economic analysis of STROKESTOP is awaited.

The 2020 ESC guidelines recommend opportunistic screening by pulse pulsation or ECG rhythm strip in patients ≥65 years (Class I). 10  The ESC guidelines now state that a 30 second rhythm strip showing AF is diagnostic if read by someone who is expert in ECG interpretation. This is also the basis of the 2018 recommendation in the Australian Heart Foundation guideline, which also recommends use of a single‐lead ECG rhythm strip. In the 2017 EHRA consensus statement on AF screening in 2017, 15 which is endorsed by the APHRS, the same recommendation was made. Most recently, the Canadian Cardiovascular Society (CCS) has also recommended opportunistic screening for people aged ≥65 years using pulse check or rhythm‐based devices. 52 Primary systematic ECG screening may be considered in patients ≥75 years or in those at high stroke risk (Class IIa). This APHRS practice guideline endorses all of these recommendations (Table 3).

TABLE 3.

Recommendations on primary stroke prevention by AF screening

Consensus Statement/recommendation Level
1. Opportunistic screening for AF is recommended for people aged ≥65 years by pulse palpation followed by an ECG confirmation. Alternatively, a 30 second rhythm strip could be used as the primary method of screening 1
2. Systematic screening may be considered to detect AF in people aged ≥75 years or those with at high stroke risk 2
3. Consideration of healthcare and social economic issues, patients’ concerns and proper management of screen‐detected AF is important 1
4. An ECG (12‐lead or single‐lead ≥30 s) showing AF analyzed by a physician with expertise in ECG rhythm interpretation is required to establish a definitive diagnosis of AF 1

3.1.2. Opportunistic versus systematic screening

AF screening can either be opportunistic or systematic. Opportunistic screening is where a health professional checks for AF during a routine consultation or attendance (e.g., during a routine visit to a family physician). Systematic screening is where all people in a particular age group are invited to attend a location (e.g., pharmacy) for screening.

However, in reality, there may not be a substantial difference in the proportion of people screened under a systematic or opportunistic program. 53  The two largest studies of systematic AF screening achieved an uptake of around 50%, 47 , 54 which is similar to what may be achievable in an opportunistic program in primary care. Importantly, whichever method is adopted, a clear pathway to treatment is required for those diagnosed, the benefits must outweigh the harms of screening in the given population, and cost‐effectiveness is an important consideration. 55 A summary of the rationale for screening is provided in Table 4.

TABLE 4.

Rationale for AF screening

1. AF is highly prevalent and often without symptoms, and increases the risk of stroke
2. Strokes in AF is more severe than strokes without AF
3. Thrombolysis in AF‐related stroke is less effective
4. In‐hospital mortality for patients with AF‐related stroke is double that for stroke patients without AF
5. Strokes with AF have higher permanent disability
6. About one in five of patients with stroke have AF discovered for the first time
7. Preventive therapy such as oral anticoagulation can reduce stroke risk in AF in patients at risk
8. Careful management, and rhythm and rate therapy may also reduce heart failure, adverse atrial remodeling, tachycardiomyopathy, and other AF‐related mortality and morbidity

Hypothesis: If persons with undiagnosed AF can be detected earlier, some strokes can be prevented and other adverse consequences of AF can be reduced.

3.1.3. Recommendations

Recommendations are summarized in Table 3.

3.2. Primary stroke prevention by AF screening in CIED patients

Atrial tachyarrhythmias including AF episodes, are often incidentally detected by the atrial lead in cardiac implantable electronic devices (CIEDs). These are recorded as atrial high‐rate episodes (AHREs). CIEDs include bradycardia pacemakers, implantable cardioverter defibrillators (ICDs), and cardiac resynchronization therapy devices (CRTs). AHREs in devices implanted for a clinical reason are not really screening, as the intent of the device implantation was not to screen for AF. Therefore, AF detected in this way is more akin to clinically detected AF than screen‐detected AF. Patients with AHREs are often asymptomatic, and AHREs occur more frequently in patients with the following risk factors: older age, male gender, heart failure, sinus node disease, a high percentage of right ventricular pacing, and an enlarged left atrial volume.

The reported incidence of AHREs is relatively high, although it depends on the definition used. The 2017 EHRA consensus statement defines an AHRE as an atrial rate >190 bpm recorded from an implanted atrial lead in a CIED. 55 Studies from Asia 56 , 57  show a high prevalence of AHREs in pacemaker recipients (44%–48%) that were associated with a prior history of AF. Patients with AHREs had a 2–3.7 times higher risk of major cardiovascular events compared to those without. These data are similar to other international cohorts.

In patients without a prior history of AF, an AHRE lasting ≥5 min confirmed by device atrial electrograms, is termed subclinical AF (SCAF). For the purpose of this guidance, SCAF is defined as validated AHREs of at least 5–6 min in duration independent of prior AF. The presence of SCAF increases the likelihood of future clinical (ECG‐documented) AF and increases the risk of stroke and thromboembolism. In the Registry of Atrial Tachycardiac and Atrial Fibrillation Episodes (RATE), 58 54.1% of those with pacemakers and 72.4% of those with ICDs had SCAF. Data from Asymptomatic Atrial Fibrillation and Stroke Evaluation in Pacemaker Patients and the Atrial Fibrillation Reduction Atrial Pacing Trial (ASSERT) 59  showed that the presence of SCAF at 3 months increased the risk of ECG‐documented AF by 5.6 times. However, 75% of these patients did not have clinical AF detected during the follow‐up period. Importantly, SCAF increased the annual risk of stroke and thromboembolism from 0.69% to 1.78%. 59  The risk is higher for those with an underlying stroke risk (CHADS2 score ≥2) and a significant SCAF duration/burden (with >5.5 h /day burden often defined as significant). 55 , 60 , 61 However, the stroke/systemic thromboembolism risk is still lower for SCAF than for ECG‐detected AF, 62 , 63 and OAC may not reduce the risk or the net clinical gain may not be in favor of OAC therapy. 64 Importantly, the temporal relationship between SCAF and stroke/systemic thromboembolism in both the Prospective Study of the Clinical Significance of Atrial Arrhythmias Detected by Implanted Device Diagnostics (TRENDS) 60 and ASSERT 59 is not well established, suggesting that SCAF may be a risk marker rather than an immediate cause of stroke/thromboembolism.

3.2.1. Key points

  1. AHREs are commonly detected in CIEDs, and when lasting for ≥5 min are termed SCAF.

  2. Use of bipolar atrial sensing, and appropriate device programming to optimize SCAF detection are important.

  3. Validation by device stored atrial electrograms is essential especially for shorter durations of SCAF.

  4. The risk of clinical AF is higher in those with SCAF than those without. The risk is increased by progression of SCAF over time.

  5. Risk of stroke/systemic thromboembolism is increased by longer episodes of SCAF, and strongly influenced by the underlying stroke/systemic thromboembolism risk.

  6. The role of OAC remains unconfirmed without the documentation of clinical AF or a high risk of stroke/systemic thromboembolism.

3.2.2. Practical management of SCAF

Four recent major international guidelines have commented on the management of SCAF detected by CIEDs. 11 , 55 , 65 , 66  The 2017 ESC consensus document 55 on device‐detected SCAF, endorsed by the APHRS, forms the basis of the current guidance. In a patient with prior AF, the occurrence of SCAF should only serve as a reminder to consider OAC, which should have been initiated before based on their CHA2DS2‐VASc score.

The fundamental question is whether SCAF detected by a CIED alone represents clinical AF and be managed as such. The risks of future ECG‐documented AF and stroke/systemic thromboembolism are higher in those with SCAF detected than for those without, but the stroke/systemic thromboembolism risks are substantially lower than clinical AF. There is also evidence of progression of SCAF duration and burden over time. Transition to clinical AF, a higher risk of stroke/systemic thromboembolism and heart failure are also observed in patients with SCAF. 67 , 68

3.2.3. Key points

  1. When SCAF is detected, it is recommended to document AF on an ECG including the use of ambulatory recording. When present, the strategy becomes standard AF management, and OAC will be recommended according to the balance between clinical bleeding risk and stroke risk.

  2. For patients with prior stroke/systemic thromboembolism or transient ischemic attack (TIA), it is recommended that if SCAF is documented, OAC would be required. The same will probably apply to a patient with significant mitral stenosis even if no ECG documented AF is yet available.

  3. For patients without prior stroke/systemic thromboembolism or TIA, and without ECG documented AF, there is no evidence that OAC has any benefit (and may be harmful). If AF burden is ≤5.5 h/day (TRENDS) or the longest AF episode is <24 h (ASSERT), it is recommended to continue to monitor SCAF progression over time and to document AF with ECG. If thresholds for AF burden/episode duration are exceeded, then OAC is considered in patients with high stroke/systemic thromboembolism risk such as when CHA2DS2‐VASc score ≥2 for men and ≥3 for women, as suggested in the 2019 AHA consensus statement. 66 For intermediate risk individuals, a monitoring strategy is recommended for SCAF progression and clinical AF occurrence.

  4. A clinical guidance flow chart is shown (Figure 3).

FIGURE 3.

FIGURE 3

Management of subclinical atrial fibrillation (SCAF) in patients with either pacemakers, implantable cardioverter defibrillators, or cardiac resynchronization therapy devices without prior documented AF. Level of recommendations for use of oral anticoagulation (OAC) is included. *CHA2DS2‐VASc score ≥2 in men and ≥3 in women. Initiation of OAC, including nonvitamin K antagonist oral anticoagulant will also depend on bleeding risk and local health authority recommendation. AHRE =Atrial high‐rate episode; S/TE =Stroke and thromboembolism

3.2.4. Recommendations

Recommendations are summarized in Table 5.

TABLE 5.

Recommendation on management of subclinical atrial fibrillation (SCAF)

Consensus Statements/recommendations Level
1. It is important to consider bipolar atrial sensing and device programming to optimize SCAF detection 1
2. Validation of SCAF by stored AEGMs is recommended if available 1
3. Progression of SCAF burden/episode duration should be monitored 2
4. SCAF burden >5.5h/day or a SCAF episode ≥24h are considered significant. For significant SCAF, clinical AF documentation with ECG, including the use of ambulatory external recordings is recommended 2
5. OAC is recommended in a person with prior stroke/systemic thromboembolism or significant mitral stenosis when SCAF is detected 1
6. No OAC will be necessary if CHA2DS2‐VASc score =0 in men and =1 in women 1
7. In the absence of stroke/systemic thromboembolism, if CHA2DS2‐VASc score =1 in men or =2 in women, observation for SCAF progression and clinical AF documentation with ECG, including the use of ambulatory external recordings, is recommended 2
8. In the absence of stroke/systemic thromboembolism and ECG documented AF, significant SCAF detection in patients with CHA2DS2‐VASc score ≥2 for men and ≥3 for women, OAC can be considered 2
9. Bleeding risk and patient preference should be considered when OAC is recommended 1

Abbreviations: AEGM, atrial electrogram; AF, atrial fibrillation; OAC, oral anticoagulation.

3.3. Primary stroke prevention by AF screening in chronic rheumatic heart disease

AF in the rheumatic population results in greater morbidity and mortality compared with the nonrheumatic population. Silent AF poses a particular risk for thromboembolic events, with one study showing >20% of patients with RHD presenting with ischemic stroke for the first time were in sinus rhythm. Therefore, they are likely to have had periods of AF that predisposed them to embolic events.

Evidence is lacking regarding predictors of AF in native RHD. Current studies show:

  • Patients aged >50 years at presentation have been found to have a high prevalence of AF (33%–57%). 35 , 56 , 57 , 58 , 59 , 60 , 61

  • Left atrial diameter >4.0 cm on echocardiogram has shown to be an important predictor of AF. 62 , 63

  • Mitral valve calcification is found in 35% of patients with mitral valve disease and has been found to be a significant predictor of AF. 64 , 65 It is an important marker for embolic events and may well be a manifestation of the length of time the disease process has been established. 65 , 66

  • The severity of mitral valve stenosis is correlated with AF, with a mitral valve area <1.0 cm2 linked to increased risk of AF. 67 , 68

AF in RHD patients poses a significant risk for comorbidities that affect not only the individual but also poses a burden on healthcare system. Therefore, AF screening to prevent stroke is recommended for higher risk groups of RHD patients (Table 6).

TABLE 6.

Screening for AF in patients with RHD

Screening for AF is recommended for patients with RHD in the following higher risk groups: Level
  • Patients aged >50 years

1
  • LA dimension >4.0cm on echocardiogram

2
  • Mitral valve area <1.0cm2

2
  • Mitral valve calcification

2
  • Mitral valve gradient >10 mmHg

2
  • NYHA Class II or higher

1

Abbreviation: NYHA, New York Heart Association.

4. WHAT METHODS AND TOOLS SHALL WE USE TO SCREEN FOR ATRIAL FIBRILLATION?

Pulse palpation is a simple and time‐honored method for AF screening. In the 2020 ESC guidelines, pulse palpation is a Class I recommendation for opportunistic AF screening in people ≥65 years of age. 10  The recommendation originates from the SAFE study which concluded that opportunistic screening with pulse palpation detected more patients with newly diagnosed AF than routine practice and was more cost‐effective than systematic screening. 69 Pulse palpation has been shown to be a rather sensitive but less specific method for AF screening. 70 , 71  More importantly, the compliance rate of physicians to opportunistic screening by pulse palpation is poor. Opportunistic AF screening in primary care varied from 5% to 42% in a healthcare survey involving 1000 physicians across 20 countries. 72 In some countries screening was done by an ECG, although in most we presume it was done by pulse palpation.

With technological advancement, many smartphone‐based, smartwatch‐based, handheld and other devices have been introduced for AF screening (Table 7). A single‐lead ECG showing AF of duration ≥30 s is now accepted as being diagnostic. 10  This has important implication for using ECG devices over other non‐ECG devices in AF screening in that a confirmatory ECG is not required, as is the case for pulse‐taking or pulse‐based devices. The accuracy of ECG devices for detecting AF and other arrhythmias has been validated in a number of studies. 73 , 74 , 75 , 76 , 77  Moreover, the requirement for a single‐lead ECG obtainable from a handheld device instead of a 12‐lead ECG may improve applicability to more countries. Automatic ECG diagnostic algorithms for AF are available in these devices with varying sensitivity and specificity.

TABLE 7.

Diagnostic performance of different methods and tools for atrial fibrillation screening

Methods/Tools Authors Sensitivity (%) Specificity (%) PPV (%) NPV (%) Reference standard for comparison Remarks
Pulse palpation Taggar et al 70 92 (85–96) 82 (76–88) N/A N/A 12‐lead ECG
Cooke et al 71 94 (84–97) 72 (69–75) N/A N/A 12‐lead ECG
Handheld or wearable single‐lead ECG device
AliveCor (Kardia) Heart Monitor Chan NY et al 74 75 (70–80) 98 (98–98.4) 65 (59–71) 99.5 (99.4–99.6) Single‐lead ECG interpretation by cardiologists 7% of ECGs were uninterpretable by cardiologists and were excluded from analysis
Zenicor II Svennberg et al 75 98 (96–100) 88.2 (88–88.4) 2.8 (2.5–3.1) 100 Single‐lead ECG interpretation by specially trained nurses and physicians 1% of ECGs were of poor quality and were excluded from analysis
Mydiagnostick Tieleman et al 76 100 (93–100) 96 (91–98) 90 (82–98) 100 12‐lead ECG
Vaes et al 79 94 (87–98) 93 (85–97) 94 (89–99) 93 (88–98) 12‐lead ECG
Omron HCG−801 Monitor Kearley et al 77 99 (93–100) 76 (73–79) 26 (21–32) 99.9 (99–100) 12‐lead ECG
Apple Watch AliveCor Kardia Band Bumgarner et al 92 93 (86–98) 84 (73–95) 90 (83–97) 88 (78–98) 12‐lead ECG 34% of ECGs were uninterpretable by Kardia Band algorithm and were excluded from analysis
Modified blood pressure monitor
Microlife WatchBP Home A Chan PH et al 85 83 (68–98) 99 (98–99) 43 (29–57) 99.8 (99.6–100) 12‐lead ECG
Microlife BPA 200 plus Marazzi et al 83 92 (87–97) 95 (93–97) 83 (76–90) 98 (97–99) 12‐lead ECG
Omron M6 Marazzi et al 83 100 94 (92–97) 82 (75–88) 100 12‐lead ECG
Omron M6 Comfort Wiesel et al 95 30 (15–49) 97 (93–99) 69 (44–94) 88 (83–93) 12‐lead ECG
Plethysmographic device
iPhone photo‐plethysmography McManus et al 87 97 (94–100) 94 (89–98) 92 (87–97) 97 (95–100) 12‐lead ECG or 3‐lead telemetry
Cardiio Rhythm Chan PH et al 86 93 (77–99) 98 (97–99) 53 (38–67) 99.8 (99–100) Single‐lead ECG interpretation by cardiologists
Cardiio Rhythm facial photo‐plethysmography Yan et al 88 95 (87–98) 96 (91–98) 92 (84–96) 97 (93–99) 12‐lead ECG
Samsung Gear Fit 2 smartwatch (1‐minute pulse plethysmography analysis) Dörr et al 89 94 (90–96) 98 (96–99) 98 (95–99) 95 (91–97) Single‐lead ECG interpretation by cardiologists 22% of PPG signals were of insufficient quality for algorithmic diagnosis and were excluded for analysis
CART CardioTracker Kwon et al 90 99 94 96 99 Simultaneous single‐lead ECG interpreted by cardiologists

Numbers in parentheses represent 95% confidence intervals

Abbreviations: ECG, electrocardiogram; N/A, not applicable; NPV, negative predictive value; PPV, positive predictive value.

Single‐lead ECG can be performed by handheld or wearable devices. The AliveCor (Kardia) Heart Monitor is a handheld device which works with a smartphone application to produce a lead I ECG. It was used in a community‐based AF screening program involving 11,574 citizens in Hong Kong. 74  The automatic diagnostic algorithm for AF was shown to be highly specific (98%) and fairly sensitive (75%). In another study in pharmacies, the sensitivity and specificity were 98.5% and 91.4%, respectively, which may be related to changes in the algorithm over time. 78 In contrast, in the STROKESTOP study, the Zenicor handheld device was used to produce a lead I ECG and the automatic diagnostic algorithm achieved a sensitivity of 98% and specificity of 88% for AF. 75 Other examples of handheld single‐lead ECG devices include Mydiagnostick 76 , 79 and Omron Monitor. 77 A 6‐lead smartphone‐based handheld ECG device, with three conducting surfaces (AliveCor Kardia 6L), has recently become available. 80 , 81  The diagnostic accuracy for AF may be significantly improved, although the inconvenience of requiring electrical contact with the left leg may make it less feasible for screening and the current algorithm uses only a single lead.

Hypertension and AF are common comorbidities 82 and modified blood pressure monitors have been used in AF screening. 83 , 84 , 85 One of these modified blood pressure monitors (Microlife WatchBP Home A) was studied for AF screening in 5,969 patients in a primary healthcare setting in Hong Kong. 85 In this device, an irregularity index represented by the ratio of the standard deviation of successive R‐R intervals to the mean R‐R intervals is calculated and AF is diagnosed if a certain cut‐off is exceeded. The sensitivity and specificity of the algorithm was reported to be 83% and 99%, respectively.

Smartphone‐based and smartwatch‐based photoplethysmographic (PPG) waveform analysis has been introduced for AF screening. 86 , 87 , 88 , 89 A smartphone camera‐based pulse PPG waveform measurement algorithm (Cardiio Rhythm) was studied for AF screening in 1,013 patients with hypertension, diabetes, and/or aged ≥65 years in a primary healthcare setting in Hong Kong. 86 PPG waveforms can be acquired when a patient's finger is placed over the camera of the smartphone and illuminated by the LED flash. The reflected light captured by the camera changes according to the arterial blood volume pulsations. AF is diagnosed by a lack of repeating patterns in the PPG waveforms. A high sensitivity of 93% and high specificity of 98% were achieved with this algorithm. More recently, facial pulsatile PPG signals (Cardiio Rhythm) were tested for contact‐free AF screening in 217 patients admitted to a cardiology ward. 88  The patients faced the front camera of a smartphone and the camera detected subtle beat‐to‐beat variations of skin color by the changes in the amount of reflected light according to the arterial blood volume pulsations. Similar to pulse PPG, AF was diagnosed by a lack of repeating patterns in the facial PPG waveforms. Again, a high sensitivity of 95% and high specificity of 96% were observed in this study. In addition, a smartwatch‐based algorithm using PPG signals was used for AF screening in 672 hospitalized patients. 89  The performance of this device, however, was limited by suboptimal quality in 22% of PPG signals. Ring‐type wearable devices with deep learning analysis of PPG signals have also been used to detect AF with high accuracy. 90 , 91

The AliveCor ECG technology was incorporated in Apple Watch via the Kardia band and tested in patients before and after electrical cardioversion for AF. 92  Notably, 34% of ECGs were classified as uninterpretable by the Kardia band algorithm and were excluded from analysis. For the remaining ECGs, the sensitivity and specificity of the diagnostic algorithm for AF were 93% and 84%, respectively. Apple now has its own inbuilt smartwatch ECG and algorithm but is not available in every country, and there are several other smartwatch ECGs with algorithms now in the market. A similar issue of nondiagnostic watch traces and greater false positives may occur given the demographic of those using smartwatches and the inability of the algorithm to diagnose at higher heart rates. These devices can be used in individual patients to screen for AF, as event monitors, or to screen for AF using the PPG function of the smartwatch to alert the user to possible AF.

As well as the remarkable disparity in disease epidemiology, ethnicity, and socioeconomic status among different countries in the Asia Pacific region, access to technology is also largely unequal. Therefore, the adoption of methods and tools for AF screening in patients or citizens without prior history of stroke should be individualized (Table 8).

TABLE 8.

Recommendations for different methods and tools for AF screening in patients without prior history of stroke

The following methods are recommended for AF screening in patients without a prior history of stroke: Level
  • Pulse palpation

1*
  • Modified blood pressure monitors

2*
  • Smartphone‐based single‐lead or multi‐lead ECG devices

3
  • Smartphone‐based photoplethysmographic devices

3*
*

Where an ECG confirmation is required for a pulse‐based screening method, a handheld single‐lead ECG may be a practical alternative to a 12‐lead ECG.

4.1. Key points

  1. Pulse palpation is a simple, time‐honored and guideline‐recommended method for AF screening. It has been shown to be rather sensitive but less specific. However, the compliance rate of physicians with opportunistic screening by pulse palpation is poor.

  2. Different tools, namely handheld or wearable single‐lead ECG devices, modified blood pressure monitors and plethysmographic devices, have been used in different settings for AF screening with differing sensitivity and specificity.

  3. A single‐lead ECG showing AF of duration ≥30 s is currently accepted as being diagnostic and this provides an important advantage of ECG devices over non‐ECG devices in AF screening.

  4. The use of tools for AF screening in the Asia Pacific region should be individualized since there is remarkable disparity in disease epidemiology, ethnicity, socioeconomic status, and access to technology.

4.2. Recommendations

Recommendations are shown in Table 8.

5. SCREENING FOR ATRIAL FIBRILLATION FOLLOWING A STROKE

5.1. Background

Studies show that up to one third of all ischemic stroke patients had underlying AF. 93 In addition, patients with AF‐related strokes suffer more severe neurological syndromes. 94 , 95 A possible explanation is that AF‐related stroke is more likely due to large vessel occlusion by virtue of comparatively larger thrombus with resultant larger volumes of infarcted brain parenchyma. 95  The consequence of a more severe stroke syndrome is a heightened risk for hemorrhagic transformation. 96  This inherent risk for hemorrhage has therapeutic implications for the timing of commencement of OACs.

AF prevalence poststroke has not been extensively investigated in the Asia Pacific region. A global survey of AF suggested a discrepancy in prevalence between Western stroke populations (33%–35%) and Asian populations (22% in East Asia and Pacific region). 93 A substantially lower rate was demonstrated in the large China National Stroke Registry of 20 000 stroke patients, with a reported rate of AF of only 5.5%. 97  Therefore, a different approach to screening for AF poststroke in the Asia Pacific region may be justified given the different epidemiological profile, especially considering the heterogeneous healthcare systems and resources.

5.2. Screening tools for detection of AF poststroke

There are no randomized trials showing that AF screening improves outcomes following a stroke. However, the fact that prior stroke is a powerful predictor of future stroke in those with clinical AF suggests that a strategy of searching for AF is reasonable and is supported by current guidelines with the initiation of OAC if AF is detected. 10 , 98  The optimal timing and duration of monitoring for AF is unclear and will be dependent on the patient population and availability of testing and healthcare resources. 99

Although the diagnostic yield for the detection of AF increases with the duration of monitoring, 100 a single timepoint 12‐lead ECG detects previously unknown AF in 4%–8% presenting with stroke. 100 , 101  More prolonged monitoring, whether by handheld ECG, 102 inpatient telemetry, 24–72‐h Holter monitors, repeated assessment by ambulatory monitoring, 103 prolonged external monitors, 104 or the use of implantable loop recorders, 105 is associated with increased detection of AF but with marked heterogeneity of detection rates. A systematic review and meta‐analysis showed an AF detection rate of 7.7% on presentation, increasing to 23.7% with sequential monitoring. 100  More recently, a study has been published supporting the use of handheld ECG devices in the stroke unit to screen for AF poststroke, 106 , 107 which may be of particular relevance to the Asia Pacific region and could be used in places without telemetry.

Widespread prolonged poststroke screening may be difficult in many countries in the Asia Pacific region. However, the diagnostic yield of a screening program can be increased by selective screening of those most at risk of AF. 99 Following stroke, age is the only consistent clinical predictor of AF. 108 However, ECG abnormalities such as a prolonged PR interval, 108 frequency of premature atrial contractions on a Holter, 104 elevated levels of natriuretic peptides, 109 evidence of atrial myopathy 110 or the presence of co‐existing acute and chronic infarction on brain imaging 111  may all help in selecting patients more at risk of AF. Risk factors such as heart failure, obesity, hypertension, alcohol intake, and physical inactivity increase the risk of AF and may be used to risk‐stratify patients. 112

5.3. Screening for AF poststroke in the Asia Pacific Region

Registry data showed that AF detection rate poststroke was much lower in the Asia Pacific region compared with that of Western countries. 97  This may reflect low rates of AF screening. Although the choice of method and duration of screening for AF will be different in each country, influenced by cultural, socioeconomic, and healthcare system factors (Table 9), it is suggested that all countries adopt a clearly defined recommendation for screening based on availability of resources.

TABLE 9.

Recommendations for different methods and tools for AF screening in patients with prior history of stroke

Screening for AF poststroke is recommended using the following methods in the acute phase and nonacute phase: Level
Acute phase Pulse palpation 1
12 lead ECG 1
Inpatient Holter monitor or telemetry 2
Nonacute phase Serial ECG 2
Ambulatory monitoring 2
Smartphone or smartwatch‐based ECG 3
Serial multi‐day recording devices 3
Implantable loop recorder 3

Pulse palpation and 12‐lead ECGs are recommended in all countries. Early telemetry, either inpatient or 24–72‐h Holter monitoring, is recommended for the majority of countries within the Asia Pacific region. As an alternative, nurse‐led handheld ECG would be relatively easy to implement. 16 In the nonacute phase, repeat testing with serial handheld ECGs and/or outpatient ambulatory monitoring should be considered where possible, either for all patients or in high‐risk patients. More invasive and prolonged screening using serial multi‐day recording devices or implantable loop recorders can be considered in high‐risk patients in some countries with sufficient resources.

5.4. Key points

  1. The prevalence of AF after stroke appears to be lower in the Asia Pacific region compared with that of Western countries. This may be a result of a lower rate of AF screening.

  2. Various approaches with differing screening tools and duration of monitoring for AF have been studied. The method of choice will be different in each country in the Asia Pacific region and depends on a combination of cultural, socioeconomic, and healthcare system factors.

5.5. Recommendations

Recommendations are shown in Table 9.

6. SETTING AND SOCIOECONOMIC CONSIDERATIONS

AF screening can be undertaken in a range of settings (Table 10). For example, in Pakistan, AF screening by pulse palpation has been included as part of a diabetes screening program. In Taiwan, AF screening has been successfully performed in pharmacies using an oscillometric device during the blood pressure measurements for patients refilling prescriptions for long‐term medications. In India, village health workers were able to successfully implement a screening program with the advantage of having an immediate diagnostic ECG available. 113 A recent study in Thailand used local primary care nurses and village health volunteers to screen people aged ≥65 years for AF using a blood pressure device with AF algorithm. Those requiring follow‐up were given appointments at a hospital in their province. However, there were challenges in this model as only 58% of those requiring follow‐up actually attended the appointment, which was up to 3 months after their screening. 114 Another model using handheld ECG performed opportunistic single‐timepoint screening in patients attending several outpatient clinics in Hong Kong. 115  They found an incidence of 2.3% for screen‐detected AF, and importantly demonstrated a similar stroke risk to those with known AF attending the same clinics when AF was untreated by OAC.

TABLE 10.

Settings for opportunistic and systematic AF screening

Opportunistic
A. Visits to medical‐related facilities
1. Family practice/primary care
2. Pharmacy
3. Vaccination center
4. Rehabilitation center
5. Health/insurance attendance
6. Regular complications evaluation service such as in a diabetic clinic
B. Visits to nonmedical facilities
1. Elderly centers
2. Recreational centers
C. Created opportunities
Health promotion/awareness program
Systematic
A. Population based
B. Community based
C. Workplace based

As may be expected, there are large regional variations throughout the Asia Pacific region, both in terms of AF screening and the availability of further diagnosis and medical management. Overall, it is suggested that the clinic or primary care setting is often the preferred setting for an opportunistic single‐timepoint program as it often has nursing support and a clear pathway to treatment. 45 , 116 , 117 However, in some countries, primary care centers are unable to prescribe OAC, as in community centers in China. 118  This results in suboptimal anticoagulation and emphasizes the need for a clear pathway to treatment.

Different settings may be preferred for continuous or intermittent programs, which would require a different workflow. For example, one study in India adopted a model where a health worker from each village in a rural area used a smartphone single‐lead ECG to screen participants for AF three times on three separate days. 113 If an ECG‐based method is used, one advantage is that the trace can be sent elsewhere for interpretation in a “hub and spoke” model. 119

Whatever the setting, a clear pathway to management must exist, including diagnosis, evaluation, OAC prescription, and other pharmacological management (Figure 4). 45 , 120 Practically, this is easier to facilitate in some settings than others.

FIGURE 4.

FIGURE 4

Requirements for AF screening pathway to treatment. *Hindricks et al (2020) 10

6.1. Key points

  1. Opportunistic AF screening can be implemented in medical‐related facilities, nonmedical facilities, or during ad hoc occasions like health promotion and disease awareness programs.

  2. Systematic AF screening can be population based, community based, or workplace based.

  3. Whichever setting for AF screening is used, a clear pathway to management must exist.

  4. In general, the primary care clinic setting is the preferred approach for an opportunistic screening program since there is often existing nursing support and a clear pathway to treatment.

6.2. Recommendations

Table 11 presents the recommendations for AF screening.

TABLE 11.

Recommendations for AF screening

Recommendation Explanation Level
An ECG is required for diagnosis Whichever method of screening is used, an ECG (single lead or 12 lead) is required for diagnosis. 10 1
The ECG should be interpreted by someone with expertise The ECG should be interpreted by someone with appropriate expertise (this could be done by someone located elsewhere if the ECG is transmitted electronically). 1
For those diagnosed with AF, an evaluation including 12‐lead ECG, echocardiogram and assessment using the 4S‐AF scheme is recommended Once diagnosed, the patient should be evaluated, including a 12‐lead ECG, echocardiogram and assessed using the 4S‐AF scheme (stroke risk, symptom severity, severity of AF burden, and substrate severity). 10  The 12‐lead ECG used for evaluation is recommended to add extra leads for the diagnostic workup. In addition, for patients with paroxysmal AF where AF is documented on a single‐lead ECG but the 12‐lead ECG shows sinus rhythm, a comparison can be made between the p‐waves and regularity of the rhythm on the single‐lead ECG and lead I of the 12‐lead ECG. 134 2
OAC prescription should be available if required If the diagnosis is confirmed and stroke risk score is sufficiently high, there should be a clinician medically available to prescribe OAC treatment. 1

7. HEALTH ECONOMICS AND AFFORDABILITY OF SCREENING

It is acknowledged that there is a wide variability of health resources available in different countries in the Asia Pacific region. The affordability of the screening process is quite cheap, for example, screening by pulse palpation, PPG, or single‐lead ECG by a health worker. However, there are more substantial costs involved for the pathway to treatment for those with an abnormal result, including evaluation and treatment for those diagnosed, which may be more difficult to afford for some populations.

Numerous studies have shown AF screening to be cost effective or even cost saving. 121 , 122 Importantly, these studies show that increasing the proportion screened prevents many more strokes with minimal change to the incremental cost‐effectiveness ratio. 78 , 121 However, these analyses are heavily dependent on the features of each country's health system. For example, these models often assume relatively high OAC treatment rates, which is probably not the case in low‐ and middle‐income countries. 118 , 123  Nonvitamin K antagonist OACs (NOACs) were added to the World Health Organization essential medicines list in 2019, which may assist with ensuring access in future.

8. CONCLUSIONS

Similar to other parts of the world, the prevalence of AF is increasing in the Asia Pacific region and there is a consequent rise in AF‐related hospitalization and burden to the healthcare system. Chronic rheumatic heart disease, an important underlying cause for AF, remains a common condition in some Asia Pacific countries. In this practice guidance, the heterogeneity in different Asia Pacific countries is acknowledged and three levels of recommendations are made according to the applicability to different countries.

In patients with cardiac implantable electronic devices, SCAF is common and the risk of developing clinical AF is higher when it is present. Furthermore, the risk of stroke is increased with longer episodes of SCAF and in patients with higher CHA2DS2‐VASc score. However, the role of OACs in the management of SCAF when clinical AF is not documented remains controversial.

In patients with chronic rheumatic heart disease, AF screening is recommended for patients with high‐risk features like age above 50 years, LA dimension greater than 4 cm, mitral valve area less than 1 cm2, mitral valve calcification, mitral valve gradient over 10 mmHg, and NYHA Class II or above.

Opportunistic screening for AF in patients aged 65 years or above by pulse palpation is affordable and recommended in all Asia Pacific countries while systematic screening for individuals aged 75 years or above and with high risk for stroke or thromboembolic events may only be applicable in countries with adequate healthcare resources. Various tools including modified blood pressure monitors, smartphone‐based single‐lead or multi‐lead ECG devices, and smartphone‐based PPG devices may be applicable to different Asia Pacific countries for AF screening depending on available healthcare resources and access to technologies, however, an ECG rhythm strip read by a health professional with appropriate expertise is always required to make the diagnosis.

In patients with ischemic stroke, AF screening by pulse palpation and 12‐lead ECG is recommended in all Asia Pacific countries in the acute setting. Inpatient monitoring with Holter or telemetry is recommended in most countries. After the acute phase, serial or ambulatory ECG monitoring are recommended in most countries while smartphone or smartwatch‐based ECG, serial multi‐day recordings, and implantable loop recorder would only be applicable in some countries.

AF screening has been studied under various settings but the crucial component in each program is a clear pathway to management including diagnosis, evaluation, and treatment. Although many studies have shown that AF screening is cost‐effective, high treatment rates with OAC for stroke prevention were often assumed. In Asia Pacific countries with limitations in health resources, the situation may be different. With the wide variability in AF epidemiology, ethnicity, socioeconomic development, and health care systems, the most appropriate model for AF screening in different Asia Pacific countries should be tailored to the country and healthcare setting.

CONFLICT OF INTEREST

All other authors declared no conflict of interest related to this paper.

Supporting information

Supplementary Material

ACKNOWLEDGMENTS

No specific funding for this paper. Jessica Orchard reports investigator‐initiated research grants from Pfizer/BMS to her institution. Dr Orchard was supported by a Postdoctoral Fellowship (Award Reference No. 104809) from the National Heart Foundation of Australia. Toon Wei Lim has received research funding from Bayer and Panasonic, and speaker's fees from Bayer, Medtronic, Biotronik, and Abbott. Sofian Johar reports being on the speaker’s bureau of Medtronic. Boyoung Joung reports grants from Medtronic, Abbott, Boston Scientific, and Samjin, and speaker’s fee from Bayer, BMS/Pfizer, Medtronic, and Daiichi‐Sankyo. Yasuo Okumura has received research funding from Bayer Healthcare, Daiichi‐Sankyo, Bristol‐Meyers Squibb, Nippon Boehringer Ingelheim, Pfizer, TORAY, and Boston Scientific Japan and has accepted remuneration from Bayer Healthcare, Daiichi‐Sankyo, and Bristol‐Myers Squibb. Ben Freedman reports grants to the Institution, speaker’s fees and nonfinancial support from BMS/Pfizer Alliance, speaker’s fees and nonfinancial support from Daiichi Sankyo, nonfinancial support from AliveCor, and speaker’s fees and nonfinancial support from Omron outside the submitted work.

Chan N‐Y, Orchard J, Agbayani M‐J, Boddington D, Chao T‐F, Johar S, et al. 2021 Asia Pacific Heart Rhythm Society (APHRS) practice guidance on atrial fibrillation screening. J Arrhythmia. 2022;38:31–49. 10.1002/joa3.12669

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