LV Dysplasia in the Absence of Complex Congenital Heart Disease: A New Entity?

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ABSTRACTS S12 Abstracts Heart, Lung and Circulation 2008;17S:S1–S209 23 Impact of Coronary Sinus Flow on Lesion Morphology during RF Ablations Sujitha Thavapalachandran , M.A. Tony Barry, Toon-Wei Lim, Karen Byth, David Ross, Pramesh Kovoor, Aravinda Thiagalingam Westmead Hospital, Sydney, NSW, Australia Introduction: It is recognised that ablation of the mitral isthmus line is difficult and we hypothesised that this may be a result of flow within the coronary sinus (CS). We tested this hypothesis using a novel ablation modelling system with high spatial (<100 m) and temporal resolution (<1 s) utilising thermochromic liquid crystals. Methods: The phantom was constructed from a sheet of thermochromic liquid crystal (TLC) sandwiched vertically between blocks of agar. A catheter was placed on the edge of the TLC, and 37 C saline pumped across the blocks to mimic blood flow. Gel and saline were adjusted to mimic myocardial and blood impedance. TLC operating colour range was 50–78 C. The CS was modelled as a 5 mm diam- eter vessel located 4 mm below the endothelial surface. Ablations were performed with and without flow (i.e. flow of 100 ml/s or 0 mls/s through the CS) with 10 ablations in each group. All ablations were performed using a Thermo- cool catheter (50 W, 50 C, 120 s, 15 mL/min irrigant flow). Results: All ablation lesions performed without flow within the CS were transmural. In contrast, no ablations performed during flow within the CS were transmural (mean distance from CS = 0.74 ± 0.02 mm; p < 0.01). Conclusion: Flow within the CS appeared to have a sig- nificant contribution to the lesion morphology. These results suggest that abolishing flow within the CS during mitral isthmus line ablation may allow transmural abla- tion lesions to be created without the need for ablation within the CS. doi:10.1016/j.hlc.2008.05.024 MYOCARDIAL 24 The Clinical Spectrum of Clozapine-induced Myocarditis Kathlyn Ronaldson 1,, John McNeil 1 , Andrew Taylor 2 , Paul Fitzgerald 2 , Duncan Topliss 2 1 Monash University, Melbourne, VIC, Australia; 2 Alfred Hos- pital, Melbourne, VIC, Australia Background: Serious adverse effects, including myocardi- tis, limit the use of clozapine, an exceptionally effective treatment for schizophrenia. To date, no systematic studies have been conducted of the clinical history of clozapine- related myocarditis. Context: In Australia, clozapine is typically initiated while the patient is hospitalised and compliance with weekly blood monitoring is ensured by a clozapine coordinator. Cardiac monitoring guidelines are also followed. Purpose: To identify trends in a case series with signifi- cance for monitoring and diagnosis of clozapine-related myocarditis. Method: Daily data on medication, symptoms and vital signs, together with all pathology results were docu- mented from the commencement of clozapine for each potential case of myocarditis. Cases were reviewed by the study Steering Group for compliance with the case defini- tion. Results: Of 48 potential cases reviewed, 31 met the case definition. Onset for 29 cases was in the third week of cloza- pine. Two patients died. The clinical course of myocarditis generally involved sequential rises in C-reactive protein (CRP), then troponin I/T and finally eosinophils. However, only 61% of cases had rises in eosinophils above the nor- mal range. The peak in eosinophils was delayed 0–7 (mean 3.5) days after the troponin I/T maximum. Conclusion: Patients initiated on clozapine should be monitored intensively in the third week for signs of the development of myocarditis. Eosinophilia should not be relied on as a diagnostic feature, but if CRP is raised, troponin I/T and ECG should be monitored over the fol- lowing days. doi:10.1016/j.hlc.2008.05.025 25 LV Dysplasia in the Absence of Complex Congenital Heart Disease: A New Entity? Tanya Wood , James Challen, Wendy Strugnell, Mark Hansen, Richard Slaughter Queensland Institute of Technology, Brisbane, Australia Introduction: Abnormalities of ventricular development are common in complex congenital heart disease (CHD) but may also occur in its absence. Cardiac magnetic resonance imaging (CMRI) is an ideal modality for demon- strating the spectrum of abnormalities that may occur. Method: We report findings in nine patients with abnormal ventricular morphology which could not be categorised according to previously described diagnostic

Transcript of LV Dysplasia in the Absence of Complex Congenital Heart Disease: A New Entity?

Page 1: LV Dysplasia in the Absence of Complex Congenital Heart Disease: A New Entity?

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S12 Abstracts Heart, Lung and Circulation2008;17S:S1–S209

23Impact of Coronary Sinus Flow on Lesion Morphologyduring RF Ablations

Sujitha Thavapalachandran ∗, M.A. Tony Barry, Toon-WeiLim, Karen Byth, David Ross, Pramesh Kovoor, AravindaThiagalingam

Westmead Hospital, Sydney, NSW, Australia

Introduction: It is recognised that ablation of the mitralisthmus line is difficult and we hypothesised that this maybe a result of flow within the coronary sinus (CS). We testedthis hypothesis using a novel ablation modelling systemwith high spatial (<100 �m) and temporal resolution (<1 s)utilising thermochromic liquid crystals.Methods: The phantom was constructed from a sheet ofthermochromic liquid crystal (TLC) sandwiched verticallybetween blocks of agar. A catheter was placed on the edgeof the TLC, and 37 ◦C saline pumped across the blocks tomimic blood flow. Gel and saline were adjusted to mimicmyocardial and blood impedance. TLC operating colourrange was 50–78 ◦C. The CS was modelled as a 5 mm diam-eter vessel located 4 mm below the endothelial surface.Ablations were performed with and without flow (i.e. flowof 100 ml/s or 0 mls/s through the CS) with 10 ablations ineach group. All ablations were performed using a Thermo-cool catheter (50 W, 50 ◦C, 120 s, 15 mL/min irrigant flow).Results: All ablation lesions performed without flow

MYOCARDIAL

24The Clinical Spectrum of Clozapine-induced Myocarditis

Kathlyn Ronaldson 1,∗, John McNeil 1, Andrew Taylor 2,Paul Fitzgerald 2, Duncan Topliss 2

1 Monash University, Melbourne, VIC, Australia; 2 Alfred Hos-pital, Melbourne, VIC, Australia

Background: Serious adverse effects, including myocardi-tis, limit the use of clozapine, an exceptionally effectivetreatment for schizophrenia. To date, no systematic studieshave been conducted of the clinical history of clozapine-related myocarditis.Context: In Australia, clozapine is typically initiated whilethe patient is hospitalised and compliance with weeklyblood monitoring is ensured by a clozapine coordinator.Cardiac monitoring guidelines are also followed.Purpose: To identify trends in a case series with signifi-cance for monitoring and diagnosis of clozapine-relatedmyocarditis.Method: Daily data on medication, symptoms and vitalsigns, together with all pathology results were docu-mented from the commencement of clozapine for eachpotential case of myocarditis. Cases were reviewed by thestudy Steering Group for compliance with the case defini-tion.

within the CS were transmural. In contrast, no ablationsperformed during flow within the CS were transmural(mean distance from CS = 0.74 ± 0.02 mm; p < 0.01).

Conclusion: Flow within the CS appeared to have a sig-nificant contribution to the lesion morphology. Theseresults suggest that abolishing flow within the CS duringmitral isthmus line ablation may allow transmural abla-tion lesions to be created without the need for ablationwithin the CS.

doi:10.1016/j.hlc.2008.05.024

Results: Of 48 potential cases reviewed, 31 met the casedefinition. Onset for 29 cases was in the third week of cloza-pine. Two patients died. The clinical course of myocarditisgenerally involved sequential rises in C-reactive protein(CRP), then troponin I/T and finally eosinophils. However,only 61% of cases had rises in eosinophils above the nor-mal range. The peak in eosinophils was delayed 0–7 (mean3.5) days after the troponin I/T maximum.Conclusion: Patients initiated on clozapine should bemonitored intensively in the third week for signs of thedevelopment of myocarditis. Eosinophilia should not berelied on as a diagnostic feature, but if CRP is raised,troponin I/T and ECG should be monitored over the fol-lowing days.

doi:10.1016/j.hlc.2008.05.025

25LV Dysplasia in the Absence of Complex Congenital HeartDisease: A New Entity?

Tanya Wood ∗, James Challen, Wendy Strugnell, MarkHansen, Richard Slaughter

Queensland Institute of Technology, Brisbane, Australia

Introduction: Abnormalities of ventricular developmentare common in complex congenital heart disease (CHD)but may also occur in its absence. Cardiac magneticresonance imaging (CMRI) is an ideal modality for demon-strating the spectrum of abnormalities that may occur.Method: We report findings in nine patients withabnormal ventricular morphology which could not becategorised according to previously described diagnostic

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criteria. All patients were referred for CMRI assessment offunction and viability. Steady-state free precession (SSFP)imaging was used for functional assessment. Standardparameters of function were calculated and indexed tobody surface area (BSA). Delayed enhancement imagingwas performed in short axis, four chamber and verti-cal long axis planes, 8–15 min after IV administration of0.2 mmol/kg of gadolinium-DTPA.Results: LV function was normal in five patients. Threepatients had indexed end-diastolic volumes (EDVi),masses (EDMi) and ejection fractions (EF) higher than thenormal range. One patient had higher than normal EDViand EDMi with normal EF. One patient had reduced EF.No patients had delayed enhancement.Morphological abnormalities included focal wall thinning,scalloping, clefts and pseudoaneurysm formation in theabsence of scarring. Abnormal trabecular development,muscle bands and papillary muscle abnormalities werealso.These features did not fulfil recognised diagnostic criteriafor previously described entities including isolated ven-tricular non-compaction. In four cases these abnormalitieswere associated with aortic coarctation, three of which alsohad bicuspid aortic valves.Conclusion: We describe a spectrum of morphologicalabnormalities within the ventricular wall that have notbeen previously described and are probably congenital inop

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Results: TM patients had a higher heart rate and a lowerbody surface area (BSA) than controls (p < 0.05 for both).SE, S′, EDE and E′ were all lower in TM (by 13%, 10%, 19%and 10%, respectively, p ≤ 0.005 for all). After adjustmentfor heart rate and BSA, TM remained an independentpredictor of a lower EDE (p = 0.001), SE (p < 0.05) and E′(p < 0.03), but not a lower S′. In TM subjects, the 5-yearaverage ferritin was an inverse correlate of SE (r = −0.42,p = 0.001) and S′ (r = −0.39, p = 0.002) but was not related toEDE or E′.Conclusion: In TM EDE is reduced proportionally morethan E′, SAE and S′, but neither EDE nor E′ appear to beaffected by iron overload. In contrast, both S′ and SAEhave modest inverse relationships with the extent of ironoverload.

doi:10.1016/j.hlc.2008.05.027

27Insights into Mitral Annular Early Diastolic Motion bySimultaneous Assessment of the Extent, Peak Velocity (E′)and Duration of Excursion

Bon Chou ∗, Lesley Donelan, Philip M. Mottram, StuartMoir, John S. Gelman, Roger E. Peverill

Monash Cardiovascular Research Centre, Monash Heart &Southern Health, Monash University Department of Medicine(MMC), Clayton, Victoria, Australia

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rigin. The clinical implications of these abnormalities arerobably mild and long-term outcomes are unknown.

oi:10.1016/j.hlc.2008.05.026

6ong Axis Left Ventricular Systolic and Diastolic Excur-ion in Thalassaemia Major—Divergent Relations withron Overload

on Chou 1,∗, Lesley Donelan 1, Don K. Bowden 2, Roger. Peverill 1

Monash Cardiovascular Research Centre, Monash Heart &outhern Health, Monash University Department of MedicineMMC), Clayton, Victoria, Australia; 2 Medical Therapy Unit,outhern Health, Clayton, Victoria, Australia

ackground: Thalassaemia major (TM) patients are sus-eptible to cardiac dysfunction due to iron overload andven TM patients with a normal ejection fraction haveeduced left ventricular (LV) long axis systolic (S′) andarly diastolic (E′) peak velocities. We investigated theossibility that measurement of the extent of mitral annu-

ar excursion during systole (SE) and early diastole (EDE)ould provide further insights into the subclinical LV dys-

unction found in TM.ethods: 58 TM patients (age 30 ± 7 years, 24 men) with

reserved LV ejection fraction were compared to 58 sexnd aged matched controls. TDI was performed at the lat-ral mitral annulus for measurement of SE, S′, EDE, and′. The average 5-year ferritin level was calculated in TMatients.

ackground: The peak velocity of early diastolic mitralnnular motion (E′) using tissue Doppler imaging (TDI) isn routine use as a surrogate of left ventricular (LV) relax-tion. We hypothesized that simultaneous assessment ofxcursion and timing would provide further insight intoV long axis function and its determinants. We investi-ated the relationship of early diastolic mitral annularxcursion (EDE), duration (EDdur) and E′ and also theelationship of these three TDI variables with age, LV

ass index (LVMI), heart rate (HR) and blood pressureBP).

ethods: Echocardiography was performed in 76 healthyubjects (age 30 ± 7 years, 38 men). LVMI was calculatedrom M-mode measurements. TDI signals were recordedt the septal border of the mitral annulus. EDE was mea-ured from the integral of the early diastolic TDI signal.nivariate and multivariate linear regression analysesere performed and only statistically significant (p < 0.05)

orrelations are shown.esults: E′ was positively correlated with EDE (r = 0.68)nd inversely correlated with EDdur (r = −0.28), whereasDE was positively correlated with EDdur (r = 0.23). EDEnd E′ were both inversely correlated with age (r = −0.35nd −0.50, respectively). The only correlate of HR wasDE (r = −0.25), the only correlate of diastolic BP was′ (r = −0.36) and the only correlate of LVMI was EDdur

r = 0.39). On multivariate analysis, E′ was independentlyorrelated with age (β = − 0.22), diastolic BP (β = − 0.19)nd EDE (β = 0.57).onclusion: E′ only provides a partial perspective on earlyiastolic mitral annular motion and its determinants in