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Paeds Vivascardiology

Paeds Vivas · cardiology

Exercise evaluation and sports participation in heart disease — branching viva

Branching viva on exercise evaluation and sports participation in heart disease: the red-flag exertional history and family history that halt clearance, the Mitchell dynamic x static sport classification, the layered workup from history and examination through ECG, echocardiography and cardiopulmonary exercise testing, the three eligibility tiers applied across innocent murmurs and repaired lesions through bicuspid valve and repaired tetralogy to hypertrophic cardiomyopathy, channelopathy and anomalous coronary artery, and venue safety with a written emergency action plan and an accessible AED.

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Target exams

RACP DCEMRCPCH Clinical

Target exams

RACP DCEMRCPCH Clinical
Prompt
Outpatient clinic: a 15-year-old competitive cross-country runner is brought by her parents before the school athletics season. She collapsed during a race three days ago, mid-effort, with no prodrome, and recovered within a minute. Her father died suddenly at 41 with no cause identified. Her coach is pressuring for a clearance so she can run in the regional finals next week. Her resting 12-lead ECG shows a QTc of 470 milliseconds.

Branch 1 — The immediate decision (3 minutes)

Examiner: The coach wants this signed today. What do you do, and why? [2]

Candidate: I do not sign the clearance. Syncope that occurs DURING exertion, with no prodrome, combined with a family history of sudden unexplained death before 50, is a red-flag combination that halts clearance. Her rapid recovery does not make this benign — vasovagal syncope has a prodrome of warmth, nausea, and visual disturbance and occurs on standing or after effort, never mid-race. I would arrange a 12-lead ECG (already done, borderline), echocardiography, Holter monitoring, and an exercise stress test to look for exercise-provoked arrhythmia, because the resting ECG and echocardiogram may be normal in the child who collapses on the field. I would refer urgently to paediatric cardiology before any return to sport. [12] [13]

Branch 2 — The classification tool

Examiner: If the workup confirms a diagnosis and you must advise on sport, how do you decide what she may do? [1]

Candidate: I use the Mitchell classification of sport, which crosses dynamic intensity (percent maximal oxygen uptake) with static intensity (percent maximal voluntary contraction) into a three-by-three grid of nine cells, from billiards at the lowest-load corner to boxing, cycling, and rowing at the highest. I pair the cardiac lesion and its severity with the load of the intended sport, and I sort eligibility into three tiers — cleared, individualised, or disqualified — rather than applying a blanket ban. A low-risk lesion may enter almost any cell, a moderate lesion is matched to an acceptable cell, and a high-risk lesion is excluded from competitive sport regardless of cell. [1]

Branch 3 — The channelopathy angle

Examiner: Her QTc is 470. If genetics confirms long-QT type 1, what is her tier and what is the rationale? [8]

Candidate: Symptomatic long-QT syndrome is a channelopathy that disqualifies from competitive sport, because the risk of an arrhythmic event during adrenergic stress is substantially elevated. The QTc of 470 is borderline in a 15-year-old female, but the exertional syncope and the family history make this high-probability, and an exercise test showing failure of QT shortening, or a genetic confirmation of KCNQ1, would settle it. She remains encouraged toward leisure activity within limits, on beta-blocker therapy, with surveillance and cascade screening of relatives. I would emphasise that the resting ECG may be normal and exercise is the trigger — that is why the symptom drives the decision. [8] [10]

Branch 4 — The repaired-lesion contrast

Examiner: Contrast her with a 14-year-old who had a ventricular septal defect closed at age 4, with a clean current echo. Different tier? [4]

Candidate: Yes — that child is cleared. A repaired simple lesion with no residual shunt, normal function, and no pulmonary hypertension, plus a clean exertional history, places the athlete in the cleared tier for all sport. The contrast makes the principle explicit: clearance and individualisation are lesion-and-symptom matched, but a normal repaired lesion is not restricted, and unnecessary restriction is itself a harm because it removes the benefits of exercise and stigmatises the cardiac child. [4] [11]

Branch 5 — Venue safety

Examiner: The coach argues the school has no defibrillator. Why does that matter to your decision? [9]

Candidate: Every venue where children compete must have a written emergency action plan and an accessible automated external defibrillator, and trained staff to use it. Defibrillation within three to five minutes is the single biggest determinant of survival in athlete sudden cardiac arrest, and survival falls by roughly ten per cent for every minute of delay to shock in a shockable rhythm. No preparticipation screen is perfect, so the venue response is the secondary line of defence behind screening. I would not sign clearances for a venue that lacks an emergency action plan and an AED, and I would advocate for their provision as part of my role. [9] [13]

References

  1. [1]Levine BD, Baggish AL, Kovacs RJ, Link MS, Maron BJ Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 1: Classification of Sports: Dynamic, Static, and Impact. J Am Coll Cardiol, 2015.PMID 26542656
  2. [2]Maron BJ, Levine BD, Washington RL, Baggish AL, Kovacs RJ, Maron MS Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 2: Preparticipation Screening for Cardiovascular Disease in Competitive Athletes. J Am Coll Cardiol, 2015.PMID 26542659
  3. [3]Maron BJ, Udelson JE, Bonow RO, Nishimura RA, Ackerman MJ, et al. Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 3: Hypertrophic Cardiomyopathy, Arrhythmogenic Right Ventricular Cardiomyopathy, and Other Cardiomyopathies. J Am Coll Cardiol, 2015.PMID 26542657
  4. [4]Van Hare GF, Ackerman MJ, Evangelista JK, Kovacs RJ, Myerburg RJ Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 4: Congenital Heart Disease. J Am Coll Cardiol, 2015.PMID 26542660
  5. [6]Thompson PD, Myerburg RJ, Levine BD, Udelson JE, Kovacs RJ Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 8: Coronary Artery Disease. J Am Coll Cardiol, 2015.PMID 26542666
  6. [8]Ackerman MJ, Zipes DP, Kovacs RJ, Maron BJ Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 10: The Cardiac Channelopathies. J Am Coll Cardiol, 2015.PMID 26542662
  7. [9]Link MS, Myerburg RJ, Estes NAM 3rd Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 12: Emergency Action Plans, Resuscitation, Cardiopulmonary Resuscitation, and Automated External Defibrillators. J Am Coll Cardiol, 2015.PMID 26542665
  8. [10]Pelliccia A, Sharma S, Gati S, Bäck M, Börjesson M, et al. 2020 ESC Guidelines on sports cardiology and exercise in patients with cardiovascular disease. Eur Heart J, 2021.PMID 32860412
  9. [11]Longmuir PE, Brothers JA, de Ferranti SD, Hayman LL, McCrindle BW, et al. Promotion of physical activity for children and adults with congenital heart disease: a scientific statement from the American Heart Association. Circulation, 2013.PMID 23630128
  10. [12]Maron BJ, Thompson PD, Ackerman MJ, Balady G, Berger S, et al. Recommendations and considerations related to preparticipation screening for cardiovascular abnormalities in competitive athletes: 2007 update. Circulation, 2007.PMID 17353433
  11. [13]Corrado D, Basso C, Pavei A, Michieli P, Schiavon M, Thiene G Trends in sudden cardiovascular death in young competitive athletes after implementation of a preparticipation screening program. JAMA, 2006.PMID 17018804