| Literature DB >> 35820954 |
Sadie Bennett1, Martin Stout2, Thomas E Ingram3, Keith Pearce2, Timothy Griffiths4, Simon Duckett4, Grant Heatlie4, Patrick Thompson5, Judith Tweedie5, Jo Sopala6, Sarah Ritzmann7, Kelly Victor8, Judith Skipper9, Benoy N Shah10,11, Shaun Robinson12, Andrew Potter13, Daniel X Augustine14,15, Claire L Colebourn16.
Abstract
Transthoracic echocardiography (TTE) is widely utilised within many aspects of clinical practice, as such the demand placed on echocardiography services is ever increasing. In an attempt to provide incremental value for patients and standardise patient care, the British Society of Echocardiography in collaboration with the British Heart Valve Society have devised updated guidance for the indications and triaging of adult TTE requests for TTE services to implement into clinical practice.Entities:
Keywords: Echocardiography; Indications; Transthoracic echocardiography; Triage
Year: 2022 PMID: 35820954 PMCID: PMC9277869 DOI: 10.1186/s44156-022-00003-8
Source DB: PubMed Journal: Echo Res Pract ISSN: 2055-0464
Fig. 1Model for the effective triage of existing (long-standing) and new transthoracic echocardiography requests by appropriately trained clinical specialists only and in-sight of the patients medical records
Fig. 2Escalation or interaction of triage processes for more complex referrals
Appropriateness, timing and triage of the most common outpatient TTE referrals
• Assessment of an innocent murmur*diagnosed by a physician • Unchanged murmur in an asymptomatic individual with previous normal echocardiogram | • Murmur in the presence of cardiac or respiratory symptoms • Murmur in an asymptomatic individual in whom clinical features or other investigation suggest structural heart disease | • Murmur in the presence of class 3 or 4 heart failure symptoms or syncope |
• Radiographic cardiomegaly with no symptoms or signs of heart failure and in the absence of other clinical information • Assessment of patients with peripheral oedema but normal jugular venous pressure and no evidence of cardiac disease (e.g., asymptomatic with a normal 12 lead ECG) • Patients in AF with an uncontrolled ventricular rate (unless class 3 or 4 heart failure symptoms) | • Clinical signs of heart failure (e.g., peripheral oedema, bilateral pleural effusions) • Unexplained shortness of breath in the absence of clinical signs of heart failure if ECG/CXR abnormal • Persistent hypotension of unknown cause • Suspected cardiomyopathy based on abnormal examination, ECG, or family history in first degree relative • Assessment of neuromuscular diseases associated with cardiac manifestations, (e.g., muscular dystrophies, Friedreich's ataxia or mitochondrial myopathies) | • Class 3 or 4 heart failure symptoms • Raised NT-pro BNP* or previous history of myocardial infarction • Clinical suspicion of pericardial effusion • |
• Routine assessment of any patient with essential hypertension • Routine assessment of asymptomatic patients with an established genetic or infiltrative cause of LVH where there is no change in clinical status and where an echo has been performed within the last 12 months • Repeat assessment of LV function in asymptomatic patients • Repeat assessment for left ventricular mass regression (if clinical concern is present regarding hypertrophic cardiomyopathy then repeat assessment with cMRI is preferable) | • Suspected LV dysfunction • Evaluation of clinically suspected aortic co-arctation (e.g., hypertension in the young) • Elevated blood pressure with concerns for end organ damage • Patients with a suspected or established genetic or infiltrative cause of LVH (with support from appropriate specialist teams where relevant) | • Accelerated hypertension with breathlessness or other clinical concerns of acute LV dysfunction |
• Patients with terminal illness whose management would not be affected by identification of any TTE abnormalities • Patients in whom TTE will not affect the decision to commence anticoagulation (e.g., patients in AF with cerebrovascular event and no suspicion of structural heart disease) | • Embolic peripheral or neurological events suggesting intracardiac mass: ◦ Acute interruption of blood flow to major peripheral or visceral artery ◦ Unexplained stroke or TIA without evidence of prior cerebrovascular disease or without significant risk factors for other cause (consider saline-contrast echocardiography by TTE or TOE, this may only be appropriate in < 55 year old patients) • Cross-sectional imaging or clinical findings suggesting intra-cardiac mass (if possible left atrial appendage thrombus then TOE preferable) • Periodic repeat assessment following removal of cardiac mass/tumour (usually annual review will suffice after an initial post-op scan) • Known primary malignancies where echocardiographic surveillance for cardiac involvement forms part of the normal staging process (e.g., renal cell carcinoma) | • Embolic event in the presence of clinical or ECG suspicion of significant left ventricular impairment (e.g., anterior Q waves on 12 lead ECG or clinical examination findings suggestive of LV dysfunction) |
• Repeat assessment to evaluate the probability of PHT in the absence of a meaningful tricuspid regurgitation jet or other echo markers of PHT on echo within the last 12 months. If there is clinical concern regarding PHT then advice from a pulmonary hypertension specialist service is recommended • Lung disease with no clinical suspicion of cardiac involvement or PHT | • Lung disease combined with a clinical suspicion of RV failure (e.g., peripheral oedema, raised jugular venous pressure) • Following pulmonary embolism when clinical concern for right ventricular impairment and/or presence of developing PHT • Evaluation for suspected or established PHT • Evaluation of response to treatment of PHT and PE • To distinguish cardiac from non-cardiac causes of dyspnoea when the results of clinical and other diagnostic testing are ambiguous • Patients with unexplained persistent or positional oxygen desaturation (consider bubble-contrast echocardiography to evaluate for a right to left shunt) | • Not applicable |
• Patients requiring emergency cardioversion • Patients on long-term anti-coagulation at a therapeutic level with no clinical suspicion of structural heart disease • Patients on long-term anti-coagulation at a therapeutic level with structural heart disease but no recent clinical change | • To guide decision-making regarding DC cardioversion in a patient with no recent echo study (i.e. within the last 12 months) or in a patient with a recent echo study and a change in clinical cardiovascular status since it was performed • Patients requiring cardioversion with AF of greater than 48 h duration and not adequately anticoagulated (TOE required) • Repeat assessment of documented left atrial appendage thrombus (TOE required) Repeat assessment following an embolic event at previous cardioversion (TOE required) • Patients with AF of less than 48 h duration together with a clinical suspicion of structural heart disease and not adequately anticoagulated (TOE required) | • Not applicable |
• Palpitations without ECG proof of arrhythmia or clinical suspicion of structural heart disease on examination • Low-burden (< 5%) or isolated ventricular ectopy in absence of a clinical suspicion of structural heart disease • Classic neuro-cardiogenic syncope | • Clinical suspicion of structural heart disease in proven arrhythmia (e.g., AF or ventricular ectopy at greater than 10% frequency or ventricular ectopy occurring on exertion) • Routine assessment of ventricular function to assist with the calculation of risk of sudden cardiac death post-myocardial infarction or following documented ventricular tachycardia • Evaluation of cardiac structure and function to assist with future management (e.g., commencement of anti-arrhythmic medications) • Syncope in a patient with high-risk occupation (e.g., pilot, bus driver) • Assessment of patients without clinical suspicion of structural heart disease who have an arrhythmia commonly associated with structural heart disease (e.g., ventricular tachycardia) | • Syncope in a patient with clinically suspected structural of functional heart disease • Exertional syncope |
• Repeat assessment of small pericardial effusion (< 1 cm) with no hemodynamic compromise and without a change in clinical status • Follow-up studies in patients with terminal illness whose management would not be affected by echocardiographic abnormalities | • Clinically suspected pericarditis, pericardial effusion, or pericardial constriction • Periodic repeat assessment of moderate or large pericardial effusion • Repeat assessment of small pericardial effusion with change in clinical status | • Clinical suspicion of cardiac tamponade (especially if predisposing factors are present, e.g., known malignancy, suspected myo-pericarditis and recent cardiac surgery) |
• Patients with terminal illness whose management would not be affected by identification of any change in TTE appearance • Routine repeat assessment in clinically stable patients in whom no change in management is contemplated | • Repeat assessment in documented cardiomyopathy where the result may change management or following procedures that may improve ventricular function (e.g., cardioversion or coronary revascularisation) • Repeat assessment in documented cardiomyopathy where there has been a change in clinical status | • New onset class 3 or 4 heart failure symptoms |
• Patients with terminal illness whose management would not be affected by identification of any change in TTE appearance | • Assessment of suspected or proven genetic disorders in which aortic pathology may be a feature, (e.g., Marfan Syndrome) • Diagnosis and periodic assessment of aortic aneurysm, dilatation of the aorta and previous surgical repair of the aorta (an annual default interval between scans, but this timeline may be superseded following multi-disciplinary team review). Due to the limited ability of TTE to visualise the thoracic aorta the appropriate concomitant use of cross-sectional imaging is recommended | • Clinical suspicion of an acute aortic event (should not replace or delay cross-sectional imaging if more clinically appropriate) |
• Routine pre-operative assessment • Repeat assessment of previous echocardiogram in last 12 months with no intervening change in clinical status | • Murmur in an asymptomatic individual in whom clinical features suggest severe structural heart disease • Documented ischemic heart disease with reduced functional capacity (< 4 METs) • Murmur in the presence of cardiac or respiratory symptoms | • Not applicable |
AF (Atrial fibrillation), ECG (electro-cardiogram), NT-pro BNP (N-terminal pro hormone brain natriuretic peptide), CXR (chest x-ray), LV (left ventricular) TOE (trans-oesophageal echocardiogram), TTE (trans-thoracic echocardiogram), PHT (pulmonary hypertension), DC (direct current)
Appropriateness, timing and triage of the most common inpatient TTE referrals
| • Evaluation of cardiac chest pain with a normal ECG, no murmur and negative cardiac biomarkers | • Following confirmed acute myocardial infarction to assess for infarct size and complications | • Murmur following a recent acute myocardial infarction | • Chest pain with haemodynamic instability • Assessment of suspected type I aortic dissection often in conjunction with cross-sectional imaging |
| • Not applicable | • Not applicable | • Patients admitted for suspected heart failure commenced on inpatient treatment | • Cardiogenic shock as judged by an appropriately senior clinician • Return of circulation following cardiac arrest |
| • No murmur detected or documented malignant arrhythmias. Vaso-vagal or situational syncope | • Not applicable | • Murmur detected clinically • Arrhythmia-associated syncope • Significantly abnormal ECG e.g., LBBB, RBB or LVH | • Not applicable |
• Fast AF without hypotension or suspicion of structural heart disease • Symptomatic ectopics (defer to outpatient following Holter monitoring) | • Not applicable | • Arrythmia and hypotension • Ventricular tachycardia or ventricular fibrillation • Clinical suspicion of infective endocarditis with evidence of acute cardiac failure, valve decompensation, or abscess | • Not applicable |
• Asymptomatic patient post therapy for a CTPA confirmed PE and/or right heart strain (defer to 3 month OP TTE) • Pre-discharge to evaluate for features of persisting right heart strain in clinically stable patients (defer to 3 month OP echo) | • Re-evaluation for further therapy where CV compromise does not resolve with treatment | • To establish right heart function in clinically unstable patients to facilitate decision making regarding thrombolysis or alternative therapies | • Not applicable |
• Known ventricular or valvular dysfunction established on TTE within 12 months without a change in symptoms • AF without signs of congestive cardiac failure or murmur • Referral based on age or frailty only | • Not applicable | • Clinical suspicion of significant valvular or ventricular pathology which will alter the anaesthetic approach (e.g., LBBB, RBBB or significant LVH) | • Not applicable |
• Fever with no other positive Duke criteria • Repeat assessment in a clinically stable patient with known vegetations | • To characterise valve lesions and haemodynamic consequences where Duke’s criteria are positive • One week following a negative TTE study in cases of high clinical suspicion where a TOE is not possible • Detection of high-risk complications when suspected (e.g., fistula, abscess, mass lesions) • Persistent bacteraemia of unknown source, particularly in staphylococcal aureus infection • Baseline re-assessment prior to discharge following completion of treatment for endocarditis | • Not applicable | • Not applicable |
• Following routine elective coronary revascularisation in stable patients • Routine pre-discharge echo following valve replacement in asymptomatic patients. Obtain baseline haemodynamic data at 4–6 weeks post operation | • Routinely following AF ablation • Routinely following structural heart disease intervention e.g., PFO closure | • Concern regarding cardiac tamponade following any cardiac or thoracic cavity procedure • Concern regarding cardiac tamponade following structural heart disease procedure, coronary intervention or permanent/temporary pace-maker insertion or lead extraction | • Not applicable |
| • Patient not in AF with no murmurs or suspicion of regional wall motion abnormality | • Patient in AF • Audible murmur • Suspected regional wall motion abnormality from clinical assessment or ECG | • Not applicable | • Not applicable |
Shock: TTE is recommended as the primary assessment tool for the shock state following senior clinical assessment | |||
| • Prior to clinical assessment and initial management | • Not applicable | • Where initial clinical assessment and management has failed to provide reasonable clinical improvement | • Not applicable |
| • Not applicable | • Not applicable | • Where acute right heart dysfunction is clinically suspected (e.g., due to the use of high positive end expiratory pressure ventilation strategy or where ECG changes suggest right ventricular infarction) | • Not applicable |
| • Where clinical information is otherwise adequate to answer the clinical question | • Not applicable | • Following cardiac arrest and return of circulation • In cases of severe malnutrition • Where underlying cardiomyopathy is suspected | • Where there is difficulty in maintaining end organ perfusion despite senior assessment and therapy • Where a direct effect of pathology on ventricular function is suspected e.g., septic cardiomyopathy |
| • Prior to clinical assessment and initial management | • Not applicable | • To determine filling status in anuric state • To guide renal replacement therapy and fluid therapy planning | • Where despite evidence to the contrary hypovolaemia may be the cause of hypotension/perfusion e.g., following large volume resuscitation or where peripheral oedema is present |
| • Where the cause of interstitial fluid appearance on chest radiology is known for example in acute pneumonitis diagnosed on cCT imaging | • Not applicable | • Not applicable | • Where there is reasonable clinical suspicion that the cause of interstitial fluid seen on chest radiography or lung ultrasound is due to raised left ventricular end diastolic pressure |
| • Where history examination and current illness are not supportive of a diagnosis of valve dysfunction as a cause for haemodynamic compromise | • Not applicable | • Where the history and examination findings suggest that the clinical picture and/or organ failure may be due to critical or acute valve dysfunction, e.g., flail mitral valve | • Not applicable |
| • Small volume pericardial effusion is noted on cCT in the context of critical illness without haemodynamic effects | • Not applicable | • Where there is clinical suspicion of pyopericardium from clinical, microbiological and radiological information | • Where clinical findings suggest that known or suspected pericardial fluid is either contributing to haemodynamic compromise or causing acute cardiac tamponade |
| • Not applicable | • Assessment of cardiac function to facilitate organ donation • Guidance for positioning of extracorporeal support cannulae • Search for penetrating objects or assessment of cardiac structure following trauma to the thorax | • Not applicable | • Not applicable |
AF (atrial fibrillation), cCT (computed tomography), CTPA (computed tomography pulmonary artery), CXR (chest x-ray), DC (direct current), ECG (electro-cardiogram), LBBB (left bundle branch block), LVH (left ventricular hypertrophy), OP (out-patient), PFO (patent foramen ovale), PE (pulmonary embolus), PHT (pulmonary hypertension), RBBB (right bundle branch block), RV (right ventricle), TOE (trans-oesophageal echocardiogram), TTE (trans-thoracic echocardiogram)
Native valve follow-up: aortic stenosis and aortic regurgitation*
| Aortic stenosis | ||
|---|---|---|
• Vmax: 2.6–2.9 m/s: TTE every 3–5 years • Cardiologist review if symptomatic | • Vmax: 3.5–3.9 m/s: TTE every 12–18 months • Vmax: 3.0–3.4 m/s: TTE every 18–24 months • Valve area: 1.0–1.5cm2 • Cardiologist review | • Vmax: > 4 m/s • Aortic valve area: < 1 cm2 • TTE every 6 months • Cardiologist review |
• LVEF < 50% or reduced flow • Cardiology discussion advised if severe AS and reducing LVEF on sequential TTE’s, LVEF in range of 50–60% • Rapid progression of Vmax: > 0.3 m/s per year • Dilated aortic root (≥ 45 mm In Marfans syndrome; ≥ 50 mm in bicuspid aortic valve patients; ≥ 55 mm for all other patients | ||
• Development of symptoms: breathlessness, chest pain, pre-syncope, syncope • Bicuspid valve with no stenosis and mild regurgitation: TTE every 3–5 years • Bicuspid valve with thickening and mild stenosis: TTE every 2 years • Valve thickening and peak velocity ≤ 2.5 m/s: TTE every 5 years (no follow-up usually needed in > 80 years of age unless restricted cusp excursion) | ||
AR (aortic regurgitation), AS (aortic stenosis), cm2 (centimetres squared), LV (left ventricular), LVEF (left ventricular ejection fraction), m/s (meters per second), mm (millimetres), TTE (Transthoracic echocardiography), Vmax (maximum velocity)
*Adapted from Baumgartner et al. 2017 [13] and Chambers et al. 2017 [14]
Native valve follow-up: mitral stenosis and mitral regurgitation*
| Mitral stenosis | ||
|---|---|---|
• Valve area > 1.5 cm2 • TTE every 3–5 years | • Valve area: 1.0–1.5 cm2 • TTE every 1–2 years • Cardiologist review | • Valve area: < 1.0 cm2 • TTE every 6–12 months • Cardiologist review |
| N.B. Valve area < 1.5 cm2 = clinically significant mitral stenosis where valve intervention can be considered if patient is symptomatic or, asymptomatic with high risk of embolism/decompensation or, positive exercise stress echocardiography | ||
• PA systolic pressure > 50 mmHg • RV dysfunction • Dense spontaneous contrast in the LA | ||
• Development of symptoms • New AF • TIA or stroke | ||
AF (atrial fibrillation), AR (aortic regurgitation), AS (aortic stenosis), cm2 (centimetres squared), LA (left atrial), LV (left ventricular), LVEF (left ventricular ejection fraction), mm (millimetres), MR (mitral regurgitation), m/s (meters per second), PA: pulmonary artery, RV (right ventricular),TIA (transient ischemia attack), TTE (Transthoracic echocardiography), Vmax (maximum velocity)
*Adapted from Baumgartner et al. 2017 [13] and Chambers et al. 2017 [14]
Native valve follow-up: right heart valvular pathology (pulmonary/tricuspid regurgitation)*
| Pulmonary/tricuspid regurgitation | ||
|---|---|---|
| • No follow up usually needed if mild or moderate TR and normal valve and normal RV | • With abnormal valve or RV: • TTE every 2 years • Cardiologist review | • TTE every year • Cardiologist review |
• RV dysfunction • RV dilatation | ||
• Development of symptoms: breathlessness, chest pain, pre-syncope, syncope | ||
m/s (meters per second), RV (right ventricular), TTE (transthoracic echocardiography), TR (Tricuspid regurgitation), Vmax (maximum velocity)
*Adapted from Baumgartner et al. 2017 [13] and Chambers et al. 2017 [14]
Follow-up: prosthetic valve replacement, valve repair and aorta*
| Valve replacement/repair | |||
|---|---|---|---|
• Baseline (4–6 weeks post operatively) • If baseline TTE normal and no alerts (see below), no routine surveillance • If regurgitation review by native valve criteria; consider TOE | • Baseline (4–6 weeks post operatively) • MV/TV or AV < 60 years (unless alerts, see below): Annual TTE from 5 years post implant (for new valve with no durability data annual from implantation) • AV > 60 years and AV with proven longevity: Annual surveillance TTE from 10 years post implant (unless alerts, see below) If regurgitation review by native valve criteria | • Competent: Baseline (4–6 weeks post operatively), 1 year post op, then every 2–3 years • Incompetent: Individualised plan | |
• New or worsening prosthetic valve regurgitation • Gradient/effective orifice area outside of expected parameters • New LV dilatation or LV systolic dysfunction • Aortic root dilatation. Urgent if ≥ 45 mm in Marfans syndrome; ≥ 50 mm in bicuspid aortic valve; ≥ 55 mm for all other patients • Suggestion of infective endocarditis or previously medically treated prosthetic valve endocarditis • Worsening symptoms or other sonographer concerns | |||
• Ongoing assessment of the aortic root: individualised plan based on clinical, anatomical and surgical features • Reasonable default: 2 yearly cross sectional imaging | • If normal diameter by TTE, then TTE every 3–5 years • If aortic dilatation: individualised plan based on degree of dilatation and rate of progression on sequential TTE • If dilatation on TTE not reproducible with cCT/cMRI (> 2 mm difference): interval imaging with CR or MRI | ||
• Baseline (4–6 weeks post operatively) or as directed by operator, then annular surveillance. If stable then increase TTE surveillance to 2 years • If paravalvular/transvalvular regurgitation review by native valve criteria • If other native valve stenosis/regurgitation, review by native valve criteria • Complex cases with LV dysfunction or multi-native valve disease: individualised plan | • Competent: Baseline (4–6 weeks post operatively), then annually • Incompetent: individualised plan | ||
AV (aortic valve), cCT (cardiac computer tomography), cMRI (cardiac magnetic resonance), LV (left ventricular), mm (millimetres), MV (mitral valve), TAVI (transcatheter aortic valve implantation), TTE (transthoracic echocardiography), TV (tricuspid valve), TOE (trans-oesophageal echocardiography)
*Adapted from Chambers et al. 2019 [16] and Borger et al. 2018 [15]