Introduction:We evaluated the heterogeneity of outcomes among heart failure patients with ventricular recovery. Methods:The BEST trial studied patients with left ventricular ejection fraction (LVEF) ≤35%. Serial LVEF assessment were performed at baseline, 3 months, and 12 months. Heart failure with better ejection fraction (HFbEF) was defined as an LVEF > 40% at any point. Results:Of the patients who survived to one year, 399 (21.3%) had HFbEF. Among subjects with HFbEF, 173 (43.4%) had "Extended"-recovery, 161 (40.4%) had "Late"-recovery and 65 (16.3%) patients had "Transient"-recovery. Subjects with HFbEF had an improved event-free survival from death or first HF-hospitalization compared to subjects without recovery (HR 0.50, 95%CI, 0.39-0.64, p<0.001). Compared to "Transient"-recovery, "Late"-and "Extended"-recovery were associated with an improved event-free survival from all-cause death and HF-hospitalization (HR 0.55, 95%CI, 0.34 -0.90, p=0.016). Discussion:Our study shows patients with HFbEF to be a heterogeneous population with differing prognoses.

Mucormycosis is an invasive fungal infection due to molds in the order Mucorales. These opportunistic pathogens found in soil or decaying organic matter mostly affect immunocompromised hosts. Rhino-orbital-cerebral, pulmonary, gastrointestinal, cutaneous, and disseminated patterns are possible. We describe a case of angioinvasive colonic mucormycosis in a patient with recent diabetic ketoacidosis and undiagnosed colon adenocarcinoma. The diagnosis was made on histopathology after the patient developed intestinal ischemia and underwent hemicolectomy. This case highlights the potentially diverse manifestations of Mucorales infections, typical and atypical risk factors, and the index of suspicion necessary for early diagnosis and outcome optimization.

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histologically validated to provide information on the microstructure of the myocardium. [1][2][3] There is a standard helical myocyte arrangement in the situs solitus (SS) heart, as viewed from the apex; left-handed in the epicardium, circumferential in the mesocardium and right-handed in the endocardium. This generates the opposing basal clockwise rotation and apical anticlockwise rotation necessary for torsion. 4 However in situs inversus totalis (SIT) there is mirror image arrangement of the visceral organs. There are no histological studies assessing how myocardial microstructure is affected in SIT. DT-CMR offers a unique opportunity to evaluate the microstructural abnormalities in SIT. Methods 12 SIT patients and 12 matched healthy volunteers were scanned in a 3T Siemens Skyra scanner. DT-CMR was performed at peak systole in the short axis at base, mid and apex. 2 people had whole heart tractography. A STEAM sequence with bmain=600 s/mm 2 and bref=150 s/mm 2 was used, as previously described.3 Strain and torsion assessment was performed using DENSE5. Results Patients were age and sex-matched (SIT 39.5 and SS 34.5 years, 3/12 male). Myocyte organisation at base, mid and apex was significantly different in SIT hearts compared to the SS hearts. Figure 1 shows example tractography. In SS, the endocardial positive helix angle (HA) progressed to a negative HA in the epicardium. In SIT hearts this pattern was inverted at the base and approached normal at the apex, with a midventricular transition zone.Mid-ventricular peak radial and circumferential strain were reduced in SIT (0.4±0.16 vs 0.56±0.16, p=0.02, and À0.16 ±0.02 vs À0.18±0.01 p=0.04 respectively). Peak absolute torsion was reduced in SIT 3.6°[3.6°] vs 8.0° [3.5°]. Conclusion This is the first human DT-CMR study of SIT hearts. We demonstrate that the SIT heart has an inverted myocyte orientation at the base that approaches normal towards the apex. Peak absolute torsion is reduced. Peak radial and circumferential strain are also reduced at the midventricle. The deranged microstructure in SIT has functional effects, the long-term outcomes of which require further study. Background Cancer survivorship is an international priority and mortality from cardiac damage is one of the greatest concerns. Anthracycline chemotherapy is cardiotoxic but remains highly effective against cancer. Methods This translational project involved the development of a pre-clinical rat model of progressive anthracycline-induced cardiotoxicity (1.25mg/m 2 doxorubicin weekly for 8 doses) and a concurrent clinical study of 30 cancer patients receiving 6 cycles of curative anthracycline therapy (doxorubicin 50mg/ m 2 ). A bespoke cardiac magnetic resonance imaging (CMR) protocol was developed which included longitudinal T1 REFERENCES1. Reese TG, Weisskoff RM, Smith RN, et al. Imaging myocardial fibre architecture inAbstract 18 Figure 1 Tractography of a SIT and SS heart.