Explained the whole clinical scenario. Overall underlying cardiac etiology/rhythm issues can not be ruled out, keeping in view the
profile Unlikely secondary to any significant cardiac etiology Multifactorial clinical scenario Reassuring no significant cardiovascular symptoms
Plan
Investigations Ordered: TTETOEHolterCTCAMyocardial Perfusion ScanExercise Stress EchoExercise Stress Test Then Other work up, functional testing/CTCA, if required Cardiac risk factors to be monitored Heart healthy lifestyle including diet and exercise
to lose weight Urgent ECG/ED visit, in case of significant symptoms/concern Lot of counseling has been done
Cardiology Follow Up: Next available appointment3 month6 month12 monthin a few weeksin a few monthsFace to FacePhone ReviewChart Review
Prior to Follow up GP to kindly complete: FBCChem20Fasting Lipid ProfileHbA1cTFTsLipoprotein (a) levelsCXROSA screeningMonitor renal function/potassium
Referral: HF nursing clinic referred for GDMTElectrophysiologist to consider AblationDCCV/Cardioversion
To Consider: Beta BlockerMetoprololAtenololBisoprololRAASiEntrestoRamiprilSGLT2iSpironolactone
Metoprolol: 12.5mg25mg50mg75mg100mgODBD
Atenolol: 25mg50mg100mgODBDAlternate Days
Bisoprolol: 1.25mg2.5mg3.75mg5mg7.5mg10mgOD PBS (Bisoprolol): Moderate-Severe HF (NYHA ≥ III) + Stable on RAASi
Sotalol: 40mg80mg120mg160mgBD(GP to kindly check QTc in 1wk)
Entresto: 24/26mg49/51mg97/103mgBD PBS (Entresto): symptomatic + NYHA ≥ II + on BB/ACEi or ARB + LVEF ≤ 40%
Perindopril: 2.5mg5mg10mgOD
Ramipril: 1.25mg2.5mg5mg10mgODBD
Dapagliflozin: 10mg OD PBS: stable + NYHA ≥ II + on BB/RAASi + LVEF ≤ 40% PBS: stable + NYHA ≥ II + on BB/RAASi + LVEF > 40%
+ Echo findings that would be expected to cause diastolic dysfunction (e.g. LV hypertrophy)
+ one of:
(i) diastolic dysfunction with high filling pressure on echocardiography, stress echocardiography
or cardiac catheterisation;
(ii) hospitalisation for heart failure in the 12 months prior to initiating treatment with
this drug;
(iii) requirement for intravenous diuretic therapy in the 12 months prior to initiating treatment with this
drug;
(iv) elevated N-terminal pro brain natriuretic peptide (NT-proBNP) levels in the absence of another cause