Volume 35, Issue 5 pp. 828-833
Original Research
Open Access

Implementation of an integrated emergency department acute atrial fibrillation pathway safely reduces cardioversions and hospitalisations: A comparative pre–post study

Kaleb Addy MBChB

Kaleb Addy MBChB

House Officer

Department of General Medicine, Auckland City Hospital, Auckland, New Zealand

Department of Surgery and Critical Care, University of Otago, Christchurch, New Zealand

Dr Kaleb Addy completed the data collection for this study when he was a medical student at University of Otago, Christchurch, New Zealand.

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Laura R Joyce MBChB, FACEM, MMedEd, BMedSc (Hons)

Corresponding Author

Laura R Joyce MBChB, FACEM, MMedEd, BMedSc (Hons)

Emergency Medicine Specialist, Senior Lecturer

Department of Surgery and Critical Care, University of Otago, Christchurch, New Zealand

Emergency Department, Christchurch Hospital, Christchurch, New Zealand

Correspondence: Dr Laura R Joyce, Department of Surgery and Critical Care, University of Otago, 2 Riccarton Avenue, Christchurch 8011, New Zealand. Email: [email protected]

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Ibrahim S Al-Busaidi MBChB, BMedSc (Hons)

Ibrahim S Al-Busaidi MBChB, BMedSc (Hons)

Lecturer

Department of Primary Care and Clinical Simulation, University of Otago, Christchurch, New Zealand

Department of Medicine, Christchurch Hospital, Christchurch, New Zealand

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John W Pickering PhD

John W Pickering PhD

Research Professor

Emergency Department, Christchurch Hospital, Christchurch, New Zealand

Department of Medicine, University of Otago, Christchurch, New Zealand

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Richard Troughton MBChB, PhD

Richard Troughton MBChB, PhD

Professor, Cardiologist

Department of Medicine, University of Otago, Christchurch, New Zealand

Cardiology Department, Christchurch Hospital, Christchurch, New Zealand

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Martin Than MBBS

Martin Than MBBS

Professor, Emergency Medicine Specialist

Emergency Department, Christchurch Hospital, Christchurch, New Zealand

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First published: 11 May 2023
Citations: 4

Abstract

Objective

Atrial fibrillation/flutter (AF/AFL) accounts for high rates of ED presentations and hospital admissions. There is increasing evidence to suggest that delaying cardioversion for acute uncomplicated AF is safe, and that many patients will spontaneously revert to sinus rhythm (SR). We conducted a before-and-after evaluation of AF/AFL management after a change in ED pathway using a conservative ‘rate-and-wait’ approach, incorporating next working day outpatient clinic follow-up and delayed cardioversion if required.

Methods

We performed a before-and-after retrospective cohort study examining outcomes for patients who presented to the ED in Christchurch, New Zealand, with acute uncomplicated AF/AFL in the 1-year period before and after the implementation of a new conservative management pathway.

Results

A total of 360 patients were included in the study (182 ‘Pre-pathway’ vs 178 ‘Post-Pathway’). Compared to the pre-pathway cohort, those managed under the new pathway had an 81.2% reduction in ED cardioversions (n = 32 vs n = 6), and 50.7% reduction in all cardioversions (n = 65 vs n = 32). There was a 31.6% reduction in admissions from ED (n = 54 vs n = 79). ED length of stay (3.9 h vs 3.8 h, net difference −0.1 h, 95% confidence interval [CI] −0.6 to 0.3), 1-year ED AF representation (32.4% vs 26.4%, net difference −6.0% [95% CI −16.0% to 3.9%]), 1-year ED ischaemic stroke presentation (2.2% in both groups) and 7-day all-cause mortality rates (hazard ratio 1.05 [95% CI 0.6 to 1.9]) were all similar.

Conclusions

Using a conservative ‘rate-and-wait’ strategy with early follow-up for patients presenting to ED with AF/AFL can safely reduce unnecessary cardioversions and avoidable hospitalisations.

Key findings

  • A high proportion of patients presenting to ED with AF will spontaneously revert to sinus rhythm.
  • A conservative rate-control strategy for acute symptomatic AF that includes next working day outpatient review can safely reduce the burden of AF on the health system.
  • Delayed cardioversion, as part of a conservative management strategy for AF, has similar outcomes to early cardioversion in ED.

Introduction

Atrial fibrillation (AF) is the most common sustained abnormal cardiac rhythm in adults.1 Overall AF prevalence in New Zealand is estimated to be around 2–3%, which rises to at least 5% in those aged ≥65 years.2, 3 Stroke, heart failure and dementia, with reduced quality of life, are strongly associated with AF, as well as increased all-cause mortality.1, 4

AF accounts for 0.5% of all ED presentations, with up to 40% of these patients being admitted to hospital each year.5 There is wide variation in the ED management of acute AF internationally.6 Recent studies suggest that a high proportion (63–72%) of patients with acute uncomplicated AF/atrial flutter (AFL) spontaneously revert to sinus rhythm (SR), negating the need for ED cardioversion.7-9 Research also suggests that delayed cardioversion for AF is non-inferior to early cardioversion in achieving a return to SR after ED presentation.9 Furthermore, recent studies highlight that ED plays an important role in the initiation of anticoagulants in patients with increased stroke risk, compared to deferring to the patient's usual longitudinal care provider.10-15

In September 2015, Christchurch Hospital ED, New Zealand, adopted a multidisciplinary clinical AF and AFL (AF/AFL) pathway (thereafter termed AF pathway), with collaboration from medical specialists and nurses in emergency medicine and cardiology.8 This pathway involves a conservative ‘rate-and-wait’ approach for haemodynamically stable patients with acute uncomplicated AF/AFL, anticoagulant prescribing advice, and next working day AF-clinic follow-up incorporating delayed cardioversion when required. The pathway recommends metoprolol succinate or diltiazem as rate-control agents, with the majority of clinicians choosing to prescribe metoprolol succinate. Patients who convert to SR or achieve a heart rate of ≤110 beats per minute with relief of AF-related symptoms and remain haemodynamically stable are discharged home with a review scheduled for the next working day at the acute AF clinic. Here they are seen by a cardiology nurse, where an ECG is taken, and assessed by a cardiology registrar, with a consultant cardiologist available for further advise. A preliminary analysis of this pathway showed that over two-thirds (73%) of AF pathway patients spontaneously reverted to SR at ED discharge or by follow-up in clinic (97% attended within the next working/business day). The conservative strategy for acute uncomplicated AF/AFL within a treatment pathway safely prevented hospitalisations, unnecessary electrical cardioversions and ensured the delivery of longitudinal AF/AFL care.8 We aimed to evaluate the impact of this pathway on patient clinical outcomes and safety in an extended cohort.

Methods

Study design

This was a before-and-after study utilising a cross-sectional, retrospective cohort design, examining outcomes for patients who presented to Christchurch Hospital ED with acute uncomplicated AF or AFL in the year before and after the implementation of the pathway, between 28 September 2014 and 27 September 2015 (pre-pathway), and 28 September 2015 and 27 September 2016 (post-pathway). The University of Otago Ethics Committee (HD20/114) and the Canterbury District Health Board (RO#20325) approved the present study.

Acute AF management pre- and post-AF pathway implementation

Before the introduction of the Christchurch Hospital AF pathway in late 2015, electrical cardioversion played a major role in the management of patients with acute rapid AF, with direct current cardioversion being administered in ED or after admission to the cardiology ward. A prospective study of acute AF presentations at Christchurch Hospital prior to the introduction of the AF pathway found a significant proportion (27%) of patients had electrical cardioversion.16 The initiation of anticoagulation was done at the treating clinician's discretion. The pathway was developed based on increasing evidence suggesting that a ‘rate-and-wait’ approach is safe.7, 9 The pathway is designed for haemodynamically stable patients with confirmed rapid AF who do not have other diagnoses that require admission, such as sepsis or pulmonary oedema. The pathway gives rate control, with metoprolol succinate or diltiazem/digoxin, and guides the clinician to stratify stroke and bleeding risk and prescribe anticoagulation appropriately. This pathway was introduced prior to the funding of rivaroxaban.17, 18 Anticoagulation with dabigatran (or enoxaparin if estimated glomerular filtration rate is <30 mL/min) is recommended if the CHA2DS2VASc score ≥2.18

Patients are discharged under this pathway if they have achieved an adequate heart rate (<110 beats per minute) within 6 h, or have reverted to SR, and are clinically stable. Those discharged are provided with a prescription for rate control and anticoagulation, and are followed up the next working day in the outpatient AF clinic,8 based in the cardiology ward (Appendix S1).

Data collection

Presentations were identified using an inclusive keyword search strategy of ED triage documentation including ‘atrial fibrillation’, ‘AF’, ‘palpitations’ and ‘tachycardia’. Presentations were excluded if not in AF/AFL on arrival in ED, AF/AFL was not the primary presenting issue, they were not seen by an ED doctor, their ED assessment record was unable to be located or an earlier presentation by the same patient had already been included in the study. Information related to AF pathway patients who attended the acute AF clinic were obtained from a prospectively maintained database by clinic staff.

Demographic and presentation-related data were extracted from paper and electronic clinical records of identified patients. Co-morbidities, including a history of congestive heart failure, diabetes, stroke/transient ischaemic attack/thromboembolism and vascular disease were coded as present if these diagnoses were documented in the patient hospital record either at the index presentation or previously. A 12-lead ECG was used to determine admission and discharge rhythms. Cardioversion of AF/AFL to SR was deemed spontaneous if it occurred before or after the administration of only rate-control medications without active cardioversion (pharmacological or electrical cardioversion).

The primary outcome of the present study was rate of cardioversion for AF, comparing pre- and post-pathway implementation. Secondary outcomes included comparisons anticoagulation rates, rhythm at ED discharge, admission rate, ED and hospital length of stay (LOS), 7-day and 1-year ED representations and 7-day all-cause mortality. Mortality data were collected via the hospital medical records, linked to the national mortality database, with patients followed from the date of presentation of the first patient on 29 September 2014 until end of data collection on 7 February 2021.

Statistical analysis

Data were extracted into a custom Microsoft Excel spreadsheet, Version 2019 (Microsoft Corp., Redmond, WA, USA). Patient and AF-related data were summarised using frequencies and percentages for categorical variables and median and interquartile ranges for continuous variables. Differences in outcome measures between pre-pathway and post-pathway are presented and 95% confidence intervals (CI) calculated using bootstrapping or using a test of proportions (prop. test in base R). The hazard ratio (HR) for death between pre and post cohorts was obtained from a cox-regression model with age and sex as co-variates because they are known to be associated with mortality. All statistical analysis were carried out in R (version 4.1).19

Results

A total of 2673 presentations were identified of which 416 were not in AF/AFL on arrival in ED, 1455 AF/AFL was not the primary presenting issue, 206 were not seen by an ED doctor, 87 had missing ED assessment record and 149 were already included in the study. This left 360 presentations: 182 pre-pathway and 178 post-pathway (Table 1). Baseline characteristics of patients at ED presentation are displayed in Table 1.

TABLE 1. Baseline characteristics of pre- and post-pathway patients
Baseline characteristics Pre-pathway (n = 182) Post-pathway (n = 178)
Median age (IQR) 66 (56–76) 68 (58–79)
Female, n (%) 80 (44.0) 99 (55.6)
Ethnicity, n (%)
European 167 (91.8) 164 (92.1)
Māori 10 (5.5) 5 (2.8)
Pacific Peoples 0 (0.0) 5 (2.8)
Other ethnicities 5 (2.8) 4 (2.2)
Comorbidities, n (%)
Congestive heart failure 21 (11.8) 18 (10.3)
Diabetes 14 (7.8) 21 (12.0)
Stroke/TIA/thromboembolism 16 (8.9) 13 (7.5)
Vascular disease 49 (27.4) 29 (16.6)
CHA2DS2-VASc, n (%)
0 22 (12.1) 26 (14.6)
1 38 (20.9) 30 (16.9)
32 122 (67.0) 122 (68.5)
Patients indicated for anticoagulation, n (%) 109 (59.9) 107 (60.1)
Antiplatelet/anticoagulation use prior to ED visit, n (%)
Antiplatelet 62 (35.4) 55 (29.7)
Direct oral anticoagulation 36 (20.6) 27 (15.4)
Warfarin 20 (11.4) 16 (9.0)
  • Comorbidities as per CHA2DS2-VASc definitions.
  • As per 2020 ESC Guidelines (CHADS-VASc male ≥2, female ≥3).19
  • IQR, interquartile range; TIA, transient ischaemic attack.

The median ED LOS was similar for both groups (3.9 h vs 3.8 h, difference −0.1 h, 95% CI −0.6 to 0.3). Cardioversions in ED decreased by 81.3% (n = 32 vs n = 6), a −14.2% net difference (95% CI −20.9 to −7.5). There was a 13.1% net (30.1% relative) reduction in hospital admissions from ED in the post-pathway group (n = 54) compared to the pre-pathway group (n = 79, 95% CI −23.5 to −2.6%), although eight patients in the post-pathway group (4.5%) were subsequently admitted from AF clinic. The cumulative time spent in hospital was 813 h lower for the post-pathway group in the present study (95% CI −1731 to 107 h).

At discharge 23% of patients who were managed using the pathway had reversed spontaneously to SR. This increased to 64.5% (40/62) by the time patients had presented to the AF clinic. Eight (12.9%) AF clinic patients required admission (seven for cardioversion and one with acute coronary syndrome). The total number of cardioversions in the post-pathway group, accounting for those that occurred in ED, for patients admitted directly from ED, and those admitted from AF clinic (n = 32) was reduced by 50.7%, compared to the pre-pathway group (n = 65), with a net difference in cardioversion rates of 17.7% (95% CI −27.3 to −8.2%).

The rates of representation to ED with AF within 7 days (−0.5% difference, 95% CI −5.1 to 4.1%) and within 1-year (−6.0% difference, 95% CI −16.0 to 3.9%) were similar between both cohorts (Table 2). The rate of re-presenting to ED with an ischaemic stroke within 1-year was the same in both groups (1.1%: two patients). The 7-day all-cause mortality, with one patient in each group, was similar (0.1% difference, 95% CI −1.5 to 1.6%). Patients were followed for a median of 1839 days (range 7–2262) during which 30 in the pre-pathway and 23 in the post-pathway group died. The HR for death for the post-pathway group relative to pre-pathway group was 1.05 (95% CI 0.58–1.88).

TABLE 2. Treatment and outcomes for pre-pathway versus post-pathway patients
Treatment and outcomes Pre-pathway (n = 182) Post-pathway (n = 178) Difference (95% CI) P-value
Cardioversion, n (%)
ED 32 (17.6) 6 (3.4) −14.2% (−20.9 to −7.5%) <0.0001
Inpatient 33 (18.1) 26 (14.6) −3.5% (−11.7 to 4.7%) 0.45
Total cardioversions 65 (35.7) 32 (18.0) 17.7% (−27.3 to −8.2%) 0.0002
Anticoagulation prescribed in ED, n (%)
Dabigatran 7 (3.8) 16 (9.0) 5.2% (−0.5 to 10.7%) 0.08
Enoxaparin 5 (2.7) 1 (0.6) −2.1% (−5.4 to 1.0%) 0.23
Warfarin 0 (0.0) 1 (0.6) 0.6% (−1.1 to 2.2%) 0.99
Total 12 (6.6) 18 (10.1) 3.5% (−2.7 to 9.8%) 0.31
Rhythm at ED discharge, n (%)
AF/AFL 118 (67.0) 136 (76.8) 9.8% (−0.1 to 19.7%) 0.02
SR 58 (33.0) 41 (23.1) −9.9% (−19.7 to 0.1%) 0.08
Not recorded 6 1
AF clinic review (n = 62)
In sinus rhythm NA 40 (64.5)
Total patients in SR at ED discharge or AF clinic review, n (%) 58 (31.9) 71 (39.9) 8.0% (−2.4 to 18.5%) 0.14
Median ED LOS, h (IQR) 3.9 (2.9–5.3) 3.8 (2.9–5.3) −0.1 (−0.6 to 0.3) 0.88
Admitted to hospital (total), n (%) 79 (43.4) 62 (34.8) −8.6% (−19.1 to 2.0%) 0.12
Admitted to hospital from ED, n (%) 79 (43.4) 54 (30.3) −13.1% (−23.5 to −2.6%) 0.01
Admitted to hospital from AF clinic, n (%) NA 8 (4.5)
Median inpatient LOS, h (IQR) 26.2 (13.8–45.2) 19.9 (11.6–30.3) −6.3 (−10.9 to 1.3) 0.10
Total inpatient hours (95% CI) 2606 (1940–3326) 1793 (1055–2096) −813 (−1731 to 107)
Adverse events, n (%)
7-day ED-representation with AF 8 (4.4) 7 (3.9) −0.5% (−5.1 to 4.1%) 0.99
1-year ED-representation with AF 59 (32.4) 47 (26.4) −6.0% (−16.0 to 3.9%) 0.26
1-year all-cause ED-representations 84 (46.2) 85 (47.8) 1.6% (−9.3 to 12.5%) 0.84
7-day all-cause mortality 1 (0.5) 1 (0.6) 0.1% (−1.5 to 1.6%) 0.99
  • Tests are chi-squared for the difference in proportions, and Mann–Whitney U test for the difference in distributions (summarised with median and IQR). As the total patient hours are not individual patient numbers, a test is not appropriate.
  • Of the 26 inpatient cardioversions in the post-pathway group, seven were admitted from AF/AFL clinic.
  • CI, confidence interval; IQR, interquartile range; LOS, length of stay.

The proportion of patients indicated for anticoagulation as per 2020 ESC Guidelines were similar between the two groups (59.9 and 60.1%).17 The number of patients who are deemed ‘high risk’ for anticoagulation as per their HAS-BLED score were also similar between the two groups (6.0 vs 9.0%).20 Guideline-appropriate prescription of anticoagulants in ED (CHA2DS2VASc score Male ≥2, Female ≥3) showed an increase by 3.5% (12 vs 18%).

Discussion

In this pre-post-implementation study of the integrated acute AF pathway, we showed that using a ‘rate-and-wait’ strategy safely decreased hospital admissions, with most patients spontaneously reverting to SR within 24–48 h, meaning fewer patients required cardioversion.

After the implementation of this pathway, the overall utilisation of cardioversion reduced by 50.7% (net 17.7% reduction). Not only does this reduce patient exposure to cardioversion risk, but also sedation risk and other iatrogenic risks of longer hospital stays. Although retrospective, and therefore unable to imply causation, this confirms and supports the accumulating body of evidence in favour of delayed cardioversion as a safe and effective strategy of managing haemodynamically stable patients presenting to the ED with recent-onset symptomatic AF/AFL.7, 9

Similar to previous studies evaluating different AF treatment pathways in the ED, the utilisation of the AF pathway described in the present study reduced the rate of hospital admission by 30.1% (a net 13.1%).6, 21 Despite the significant reduction in hospitalisation, AF-related representation and all-cause mortality rates were similar between the two groups, positioning the AF pathway as a safe alternative to early cardioversion and/or inpatient management of acute uncomplicated symptomatic AF/AFL. Furthermore, implementation of this AF treatment strategy likely leads to significant savings by reducing the costs associated with unnecessary cardioversions, avoidable hospitalisations and their potential complications.5

Guideline-appropriate anticoagulation for patients with AF increased by a net 3.5% after implementation of this pathway from a low base. The poor rates of anticoagulation, both in the community and the ED, are a long-standing problem.17 However, a study examining a later cohort of patients managed under the AF pathway (May 2016 to April 2017, n = 143) demonstrated that 89% of those with a CHA2DS2-VASc score ≥2 had been prescribed anticoagulation by the time they were discharged from the AF clinic.8

Findings from the present study and previous analyses have resulted in changes to the design of this pathway.8 The pathway now contains more specific recommendations for anticoagulation on discharge, as well as recommending follow-up for all patients, no matter what their rhythm at discharge. Next-day follow-up on this pathway now occurs in a community clinic, with referral back to the cardiology service if required, aimed to improve access to follow-up and reduce ED re-presentations. There is work focused on determining whether particular factors may predict a failure to spontaneously revert to SR within a short timeframe in haemodynamically stable patients presenting to ED with uncomplicated acute AF, and therefore warranting active management with early cardioversion.22, 23

Limitations

Given the retrospective nature of the present study, there may be limitations related to coding and data collection. 35% of those patients discharged from ED under the AF pathway attended the AF clinic. It is not clear whether patients were not referred to clinic because they reverted to SR while in ED, or whether they were referred but did not attend. Patients who reverted to SR after ED discharge and were therefore asymptomatic may have chosen to follow-up with their general practitioner. It is noted that the AF cohort examined in the present study represents the first year of implementation of the AF pathway, and continued education has increased staff awareness of the referral process. A follow-up study of predictors of reversion to SR in a large cohort of patients (n = 734) managed under this pathway over 5 years (1 June 2016 to 31 May 2021) found only ~1% of patients did not attend the AF clinic, suggesting that AF clinic attendance rate has improved.23

As a retrospective observational study, we were unable to control for confounders over time, such as a change in the behaviours of individual clinicians working in the emergency medicine or cardiology services. Follow-up data may also be incomplete for patients who represented to an out-of-region ED hospital as the data collected only applied to Christchurch Hospital, although this is the only ED and only stroke-receiving hospital in the region, and therefore the majority of patients would continue to seek care at this hospital. Finally, our findings are based on a management pathway implemented at a single tertiary care hospital in New Zealand, which may limit the generalisability of findings to other care settings, including rural and centres lacking cardiology services.

Conclusions

To conclude, a conservative ‘rate-and-wait’ strategy with early outpatient follow-up for patients presenting to ED with acute symptomatic AF/AFL may reduce cardioversions and hospital admission, without significantly increasing ED LOS, ED representation rate, ischaemic stroke or mortality rates. Future research should focus on how these findings can be replicated in other settings, including rural centres without specialist cardiology services.

More individualised care can now be investigated to consider whether there are particular patient factors which predict spontaneous reversion to SR, and therefore a more nuanced pathway could be developed.

Acknowledgements

The Maurice and Phyllis Paykel Trust provided funding for KA to participate in a medical student summer studentship through University of Otago, for the collection of data for this project. Open access publishing facilitated by University of Otago, as part of the Wiley - University of Otago agreement via the Council of Australian University Librarians.

Competing interests

MT reports grants and speaker fees for clinical trials and education from Abbott, Alere, Beckman Radiometer, Roche and Siemens outside the submitted work.

    Data availability statement

    Data available on request from the authors

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