Clinical articles

Current guidelines make no recommendations regarding the strategy for initiation of oral anticoagulant (OAC) therapy in patients who are hospitalised with newly diagnosed atrial fibrillation (AF). This was a single-centre, retrospective, observational study that included patients admitted in 2013 with newly diagnosed AF (ICD-10 I48). There were 234 patients hospitalised with newly documented AF. The mean CHA₂DS₂-VASc score was 3.8: 201 (86%) patients had a CHA₂DS₂-VASc score ≥2. Out of the 179 patients considered for anticoagulation, only 115 patients were intended to receive OAC therapy: 56 (49%) as an inpatient and 59 (51%) as an outpatient, either by anticoagulation clinic or primary care. In the outpatient group, only 41 patients (69%) were actually initiated on OAC, with a mean time delay of 10 and 93 days in anticoagulation clinic and primary care group, respectively. During mean follow-up of 194 days, there were two strokes in the outpatient group in patients intended to start anticoagulation but did not (2/59), while no episodes occurred in the inpatient group.

In summary, only 82% of patients with newly diagnosed AF and CHA₂DS₂-VASc score ≥2 were referred for initiation of OAC, and still fewer actually received such therapy. Outpatient anticoagulation is associated with poor uptake and significant delays.

Transradial access for coronary procedures is associated with less vascular access site complications. Occasionally, radial access fails and makes conversion to a transfemoral route inevitable. In this paper, which updates UK radial experience, we report the outcomes in a single UK centre in developing a transradial access programme.

We analysed 3,225 consecutive patients who underwent transradial coronary procedures over a five-year period. The primary outcome measure was rate of conversion from transradial to transfemoral access route. Of 3,225 radially approached cases, conversion from radial to femoral access route occurred in 148 patients (4.6%). With experience after the learning curve, the conversion rate fell to 2.0%.

In conclusion, after an initial learning curve, procedural success rate is high with low cross-over rate from radial to femoral entry site.

With the expansion of the heart failure services to meet the rise in demand, we established, in Sheffield, a new training post for the junior medical staff in their first year of training. This is a four-month post for the Foundation Year one (FY1) doctors in heart failure. The post differs from the classic FY1 posts in that it is based in the heart failure multi-disciplinary team (HF-MDT) rather than being ward-based. Thus, the trainee works under the supervision of a consultant cardiologist with an interest in heart failure, and works alongside a group of heart failure specialist nurses screening new admissions for heart failure, and offering advice and follow-up of patients with heart failure who are not under the care of the cardiologists. The trainee attends the heart failure diagnostic clinic along with the consultant cardiologist, and participates in the work of the HF-MDT ward round. These are the collective personal views of the first three trainees who have worked in this post in the year 2013–2014; with a footnote from their supervisor.

This case report invites discussion on the challenges of the management of extensive thromboembolism despite standard anticoagulation.

A previously healthy 49-year-old male had an acute pulmonary embolism (PE) and was managed with rivaroxaban anticoagulation and an inferior vena cava (IVC) filter implantation. This patient re-presented with occlusion of his IVC filter with extensive thrombus extending down to his femoral veins bilaterally.

We performed catheter-directed thrombolysis using the EKOSonic Endovascular system. The patient had invasive monitoring alongside use of peri-operative cardiac imaging (TOE). A valvuloplasty balloon was used to prevent upward migration of thrombus.

There is potential for the wider use of the EKOSonic Endovascular system and catheter-directed thrombolysis in centres where there is surgical support available, and in selected patients where there is extensive thrombotic burden with risk of recurrence or long-term complications.

Direct current cardioversion (DCCV) is a method to restore sinus rhythm in patients diagnosed with atrial fibrillation (AF). Despite having high initial efficacy, the long-term success rate of this procedure is lower. Consequently, the European Society of Cardiology (ESC) guidelines recommend indefinite anticoagulation in patients with a high risk of recurrence. We sought to establish whether these guidelines had been adhered to in a district general hospital.

Anticoagulation data were provided by GP practices for 208 patients who had undergone a DCCV for AF between 2008 and 2010. One hundred and sixty-five patients (79%) were prescribed warfarin. The remaining 43 patients were invited to a screening clinic with 21 subsequently attending (49%). Eleven of the patients were in AF (p=0.0002) and in five of the 11 patients this had not previously been documented (p=0.035). Nine of the 11 patients in AF (82%) met ESC criteria for anticoagulation with a mean CHA₂DS₂‑VASc score =2.18 ± 1.48.

Our findings suggest that nearly half of patients not on anticoagulation following DCCV have recurrence of AF warranting antithrombotic therapy. We propose similar screening is adopted in other centres in order to ensure that ESC guidelines are being met.

A 46-year-old man with cutaneous sarcoidosis and pulmonary involvement was referred to a cardiologist for possible pulmonary hypertension in view of increasing shortness of breath. Echocardiogram findings and electrocardiogram (ECG) changes prompted the need for coronary angiography, which was subsequently normal.

Cardiac sarcoidosis was one of the differential diagnoses. The patient was booked for a treadmill test. Unfortunately, in the interim, the patient had an episode of collapse while playing football. The local district hospital discharged the patient after finding normal computed tomography (CT) brain scan and negative troponin. He was re-admitted with a pre-syncopal episode and ambulatory ECG monitoring revealed non-sustained ventricular tachycardia. A cardiac magnetic resonance imaging (MRI) scan was arranged followed by insertion of an implantable cardioverter defibrillator (ICD).

This case report and literature review highlights the importance of cardiac screening in patients deemed ‘high risk’ for sudden cardiac death, and the need for immediate investigation and treatment. Current guidelines are yet to be universally accepted, so such cases are important in highlighting current methods of investigation and treatment.

Typical echocardiographic assessment of left ventricle (LV) size is based on single-dimensional measurements at mitral valve leaflet tips. In ischaemic and non-ischaemic cardiomyopathy (ICM and NICM) and aortic regurgitation (AR) where spherical remodelling is observed, this single-dimensional measurement at the LV base may underestimate LV volume. We hypothesised the maximum diameter would provide a closer approximation. A retrospective analysis of 1,680 consecutive cardiovascular magnetic resonance (CMR) examinations identified 82 patients with substantial LV dilation (LVEDVi >130 ml/m²) and 23 controls. LV end-diastolic and end-systolic diameters were measured using echocardiography and CMR at the standard level (EDD_MV and ESD_MV) and the maximum diameter (EDD_max and ESD_max). Indexed diameters were fitted to indexed volumes using cubic regressions. Maximum diameters had higher R² values in fitting LV volume, and improved categorisation of subjects with chamber enlargement without substantially increasing the false-positive rate. Standard measurements may underestimate LV volume in cases of spherical remodelling, use of the maximum dimension may be a straightforward approach to improve assessment of LV volume and remodelling.

Integration of healthcare services has been advocated to improve quality and cost-effectiveness. Different models of integrated care for cardiology have been suggested, but the cost-effectiveness of a consultant-run service has been questioned. We assessed the potential impact on secondary-care outpatient volumes of introducing a service run by GPs with a special interest, with support from consultant cardiologists. We retrospectively reviewed all cardiology outpatient attendances at the South London Healthcare NHS Trust for a period of three months in 2011. Using National Institute for Health and Care Excellence (NICE) guidelines and discussions between cardiologists and GPs, a novel outpatient referral triage protocol was drawn-up to decide the appropriate minimum level of care required for a range of cardiac conditions. Anonymised clinic letters were divided into new referrals and follow-ups, and were assessed to establish the diagnosis and clinical complexity. Implementing such an integrated community care service (ICC) would reduce new referrals to secondary care by 33%, and would enable transfer of 44% of patients currently followed up in secondary care to ICC. The study confirms that there is scope for significant transfer of care with the greatest gains in patients with valve disease, ischaemic heart disease and atrial fibrillation.

Venous thromboembolism (VTE) is a common cardiovascular disorder associated with considerable morbidity and mortality. The standard treatment for VTE comprises parenteral heparin overlapping with, and followed by, a vitamin K antagonist, which, although effective, has several limitations. Currently, many patients commence treatment for VTE in hospital and are discharged after 5–10 days to ongoing care in the community. With the introduction of non-vitamin K oral anticoagulants (NOACs), there is now the possibility for the complete management of patients with uncomplicated VTE to be undertaken by primary care, reducing the burden on hospitals and improving the patient experience. The NOAC rivaroxaban, a direct factor Xa inhibitor, has been widely approved for the treatment of VTE. This article offers guidance to general practitioners on the practical use of rivaroxaban for the treatment of patients with VTE, along with a discussion of its potential benefits compared with standard therapy.

Troponin testing is the cornerstone diagnostic test for evaluating acute coronary syndromes (ACS). Evidence suggests this test is increasingly being utilised in a less specific fashion. We sought to evaluate the appropriateness of bedside point-of-care (POC) troponin T (TnT) sampling in our hospital.

We examined the case records for 109 consecutive patients who underwent admission troponin testing. We reviewed the clinical presentation, baseline electrocardiogram (ECG) and final diagnoses.

Only 55% of patients presented with actual cardiac chest pain. A troponin-positive result was found in 19.2% of patients (n=21); however, only half of these had a final diagnosis of ACS. The troponin assay was negative in 80.8% of patients (n=88); under one-quarter of these (n=16) underwent further ischaemia assessment. Almost one-third of patients had neither chest pain nor ECG changes (n=35), but still underwent troponin testing. None had a final diagnosis of coronary artery disease.

Troponin assays are requested for patients with a relatively low suspicion of an ACS. A failure to undertake further ischaemia assessment suggests a lack of initial conviction of a cardiac diagnosis. True ACS was diagnosed in less than half of troponin-positive cases. These data support a need for more selective usage.