Atrial Fibrillation (AF) is the most common sustained cardiac arrhythmia, affecting 1-2 million people in the UK. AF is characterised by uncoordinated electrical activation and ineffective contraction of the upper cardiac chambers. AF can occur in temporary episodes, as in paroxysmal AF, or can be sustained continuously beyond 7 days' duration, as in persistent AF. The most significant potential complication of AF is stroke caused by a blood clot (thromboembolic stroke). If untreated, the risk of stroke in AF can be increased as much as five-fold, depending on the presence of other risk factors. The mechanism of thromboembolic stroke in AF patients is complicated and understanding of factors involved remains incomplete. AF has been shown to disrupt normal bodily mechanisms for controlling bleeding and clotting (haemostasis) and normal blood flow inside the cardiac chambers. In disrupting these mechanisms, AF can be said to create a 'prothrombotic' state or environment within the blood and heart (a tendency to form clots) which can lead to blood clot formation and subsequently to stroke. There is research evidence that AF-related stroke risk is not fixed and changes over time. This dynamic risk may be related to the episodic nature of AF, with stroke risk changing during an episode of AF and for a period of weeks after the episode terminates. Analytic studies have shown that the risk of stroke is highest in the days after an AF episode has occurred, peaking at 5 days and returning to baseline by 30 days. Other studies have shown that the duration of the AF episode can also influence the risk of stroke following each episode, with longer episodes being higher risk. This dynamic risk likely relates to changes in the activation of the body's blood-clotting system and changes in blood flow within the heart. Current clinical guidelines recommend that patients with AF and risk factors for stroke are treated with daily, uninterrupted anticoagulation (blood-thinning medication) to reduce the risk of stroke. These guidelines do not take into account the temporal pattern of AF or the frequency or duration of AF episodes. An emerging approach to anticoagulation in AF is pill-in-pocket oral anticoagulation (PIPOAC). In this approach, AF patients only take their anticoagulation in response to episodes of AF, and for a period of time after normal heart rhythm is restored. This approach may suit AF patients who have lower risk, lower frequency AF and who wish to reduce their exposure to anticoagulation medication. It may also suit AF patients who have higher bleeding risk related to anticoagulation. The RESPOND-AF study proposes a novel approach to delivering PIPOAC. It is a pilot study of this novel approach recruiting 50 participants. This includes participants having continuous heart rhythm monitoring using the Medtronic LINQ II implantable cardiac monitor. The LINQ II continuously monitors for evidence of AF. If AF is detected a transmission is uploaded to the Medtronic Carelink cloud portal. Traditionally, healthcare professionals need to sign in to this portal to check for any transmissions. For the purposes of PIPOAC this traditional approach would be too slow and create a burdensome workload for clinicians. Due to the properties of blood clot formation in AF, it is important to initiate oral anticoagulation within 48 hours of AF episode onset to disrupt the clot-formation process. For the purposes of this study, the investigators have developed a custom-designed software which continuously screens for transmissions of AF on the Carelink cloud portal. When an AF episode has been detected by the LINQ II monitor, the software will send an SMS smartphone alert to the patient informing them of the AF episode and instructing them to commence their oral anticoagulation as soon as possible. This approach, if shown to be safe and effective and acceptable to patients, could open the path to wider use of Pill-in-pocket oral anticoagulation. This novel treatment can reduce the need for anticoagulation, meaning fewer bleeding complications. Pill-in-pocket oral anticoagulation empowers patients by offering a new treatment choice beyond current limited options.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
50
Participants will stop their oral anticoagulation after a 30-day period free of AF episodes. After this, they will only take their anticoagulation in response to an episode of AF detected by their implantable cardiac monitor. The participants will receive an automated smartphone alert instructing them to commence their anticoagulation as soon as AF is detected.
Oxford University Hospitals NHS Trust, John Radcliffe Hospital
Oxford, Oxfordshire, United Kingdom
RECRUITINGTo investigate the reduction in oral anticoagulation (OAC) utilisation during follow-up.
Calculate the proportion of time off anticoagulation OAC
Time frame: During follow-up (minimum 13 months)
Thromboembolic events (Ischaemic stroke, transient ischaemic attack (TIA) and systemic embolism)
Calculate the rate of ischaemic stroke, TIA and systemic embolism in patients on as-required OAC
Time frame: During follow-up (minimum 13 months)
Major bleeding
Calculate the rate of major bleeding in patients on as-required OAC
Time frame: During follow-up (minimum 13 months)
Minor bleeding
Calculate the rate of minor bleeding in patients on as-required OAC
Time frame: During follow-up (minimum 13 months)
Any stroke (ischaemic, haemorrhagic or undetermined)
Calculate the stroke rate (ischaemic, haemorrhagic or undetermined)
Time frame: During follow-up (minimum 13 months)
All-cause mortality
Calculate the rate of all-cause mortality in patients on as-required OAC
Time frame: During follow-up (minimum 13 months)
Protocol adherence
Calculate the number of daily transmissions and percentage of patients that restarts OAC within 24 hours of the smartphone-alert.
Time frame: During follow-up (minimum 13 months)
To assess response time from AF episode onset to patient starting as-required OAC
Time from AF episode onset to detection, time to alerts being sent and acknowledged and OAC
Time frame: During follow-up (minimum 13 months)
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