“Muscle Bridge” as a Possible Risk Factor for Sudden Cardiac Death in a Child with Hypertrophic Cardiomyopathy: Case Study
https://doi.org/10.15690/vsp.v24i3.2908
Abstract
Background. Hypertrophic cardiomyopathy (HCM) is one of the most common causes of sudden cardiac death (SCD) in young adults under the age of 35. SCD may be the first and only clinical manifestation of the disease in children. Case presentation. Female patient with HCM and low risk of cardiac events suffered the first episode of SCD associated with physical activity at the age of 12 years 4 months. Acute myocardial ischemia was suspected due to abnormal coronary arteries, “muscle bridge”, that was the trigger of malignant ventricular arrhythmias leading to cardiac arrest. Implantable cardioverter defibrillator (ICD) was installed for secondary SCD prevention. However, the disease has progressed, and the child suffered two more episodes due to ventricular fibrillation, managed by ICD and resuscitation measures. Drug therapy and ICD regimens were adjusted. Myocardial revascularization was not performed due to high surgical risk. Conclusion. Difficulties in management of patient with HCM complicated with acute myocardial ischemia due to congenital coronary arteries anomaly are presented. Myocardial ischemia is not considered as “large” risk factor for SCD in children (according to traditional evaluation). However, it can be a trigger for life-threatening ventricular arrhythmias and negatively affect HCM prognosis as it has been shown in our observation.
About the Authors
Larisa A. BalykovaRussian Federation
Saransk
Disclosure of interest:
None
Irina V. Leontyeva
Russian Federation
Moscow
Disclosure of interest:
None
Irina M. Miklashevich
Russian Federation
Moscow
Disclosure of interest:
None
Sergey A. Thermosesov
Russian Federation
Moscow
Disclosure of interest:
None
Anna V. Krasnopolskaya
Russian Federation
Saransk
Disclosure of interest:
None
Marina V. Shirmankina
Russian Federation
Saransk
Disclosure of interest:
None
Natalya V. Shchekina
Russian Federation
Saransk
Disclosure of interest:
None
Yuliya S. Isaeva
Russian Federation
Moscow
Disclosure of interest:
None
Pavel A. Shkurin
Russian Federation
Saransk
Disclosure of interest:
None
References
1. Arghami A, Dearani JA, Said SM, et al. Hypertrophic cardiomyopathy in children. Ann Cardiothorac Surg. 2017;6(4): 376-385. doi: https://doi.org/10.21037/acs.2017.07.04
2. Ommen SR, Mital S, Burke MA, et al. 2020 AHA/ACC Guideline for the diagnosis and treatment of patients with hypertrophic cardiomyopathy: executive summary: A report of the American College of Cardiology / American Heart Association Joint Committee on Clinical Practice Guidelines. Circulation. 2020;142(25):e533-e5357. doi: https://doi.org/10.1161/cir.0000000000000938
3. Tsatsopoulou A, Protonotarios I, Xylouri Z, et al. Cardiomyopathies in children: An overview. Hellenic J Cardiol. 2023;72:43-56. doi: https://doi.org/10.1016/j.hjc.2023.02.007
4. Colan SD, Lipshultz SE, Lowe AM, et al. Epidemiology and cause-specific outcome of hypertrophic cardiomyopathy in children: findings from the Pediatric Cardiomyopathy Registry. Circulation. 2007;115(6):773-781. doi: https://doi.org/10.1161/CIRCULATIONAHA.106.621185
5. Möbius-Winkler MN, Laufs U, Lenk K. The Diagnosis and Treatment of Hypertrophic Cardiomyopathy. Dtsch Arztebl Int. 2024;121(24):805-811. doi: https://doi.org/10.3238/arztebl.m2024.0196
6. Lipshultz SE, Law YM, Asante-Korang A, et al. Cardiomyopathy in children: classification and diagnosis: a scientific statement from the American Heart Association. Circulation. 2019;140(1):e9-e68. doi: https://doi.org/10.1161/CIR.0000000000000682
7. Monda E, Palmiero G, Lioncino M, et al. Multimodality imaging in cardiomyopathies with hypertrophic phenotypes. J Clin Med. 2022;11(3):868. doi: https://doi.org/10.3390/jcm11030868
8. Leontyeva IV. Sudden cardiac death in children with hypertrophic cardiomyopathy: approaches to prevention. Rossiyskiy Vestnik Perinatologii i Pediatrii = Russian Bulletin of Perinatology and Pediatrics. 2024;69(3):6-18. (In Russ). doi: https://doi.org/10.21508/1027-4065-2024-69-3-6-18
9. Deraz SE, Esmat OD, El-Hmid RGA, Amin SA. Evaluation of diastolic dysfunction in children with hypertrophic cardiomyopathy and its relationship with development of myocardial fibrosis. Egypt Heart J. 2023;75(1):54. doi: https://doi.org/10.1186/s43044-023-00382-1
10. Alexander PMA, Nugent AW, Daubeney PEF, et al. Longterm outcomes of hypertrophic cardiomyopathy diagnosed during childhood: results from a national population-based study. Circulation. 2018;138(1):29-36. doi: https://doi.org/10.1161/CIRCULATIONAHA.117.028895
11. Mascia G, Crotti L, Groppelli A, et al. Syncope in hypertrophic cardiomyopathy (part I): An updated systematic review and metaanalysis. Int J Cardiol. 2022;357:88-94. doi: https://doi.org/10.1016/j.ijcard.2022.03.028
12. Norrish G, Field E, Mcleod K, et al. Clinical presentation and survival of childhood hypertrophic cardiomyopathy: a retrospective study in United Kingdom. Eur Heart J. 2019;40(12):986-993. doi: https://doi.org/10.1093/eurheartj/ehy798
13. Cai ML, Zhong GQ. Hypertrophic Obstructive Cardiomyopathy with SAM Phenomenon: A Case Report and Literature Review. Cardiol Cardiovasc Med. 2022;6:515-522. doi: https://doi.org/10.26502/fccm.92920293
14. Kotkar KD, Said SM, Dearani JA, Schaff HV. Hypertrophic obstructive cardiomyopathy: the Mayo Clinic experience. Ann Cardiothorac Surg. 2017;6(4):329-336. doi: https://doi.org/10.21037/acs.2017.07.03
15. Miron A, Lafreniere-Roula M, Steve Fan CP, et al. A validated model for sudden cardiac death risk prediction in pediatric hypertrophic cardiomyopathy. Circulation. 2020;142(3):217-229. doi: https://doi.org/10.1161/CIRCULATIONAHA.120.047235
16. Maurizi N, Passantino S, Spaziani G, et al. Long-term Outcomes of Pediatric-Onset Hypertrophic Cardiomyopathy and Age-Specific Risk Factors for Lethal Arrhythmic Events. JAMA Cardiol. 2018;3(6): 520-525. doi: https://doi.org/10.1001/jamacardio.2018.0789
17. Norrish G, Cantarutti N, Pissaridou E, et al. Risk factors for sudden cardiac death in childhood hypertrophic cardiomyopathy: A systematic review and meta-analysis. Eur J Prev Cardiol. 2017;24(11): 1220-1230. doi: https://doi.org/10.1177/2047487317702519
18. Hong Y, Su WW, Li X. Risk factors of sudden cardiac death in hypertrophic cardiomyopathy. Curr Opin Cardiol. 2022;37(1):15-21. doi: https://doi.org/10.1097/HCO.0000000000000939
19. Petryka-Mazurkiewicz J, Ziolkowska L, Kowalczyk-Domagala M, et al. LGE for Risk Stratification in Primary Prevention in Children With HCM. JACC Cardiovasc Imaging. 2020;13(12):2684-2686. doi: https://doi.org/10.1016/j.jcmg.2020.06.009
20. Sedaghat-Hamedani F, Kayvanpour E, Tugrul OF, et al. Clinical outcomes associated with sarcomere mutations in hypertrophic cardiomyopathy: a meta-analysis on 7675 individuals. Clin Res Cardiol. 2018;107(1):30-41. doi: https://doi.org/10.1007/s00392-017-1155-5
21. Arbelo E, Protonotarios A, Gimeno JR, et al. ESC Scientific Document Group2023 ESC Guidelines for the management of cardiomyopathies. Eur Heart J. 2023;44(37):3503-3626. doi: https://doi.org/10.1093/eurheartj/ehad
22. Maron BJ, Desai MY, Nishimura RA, et al. Diagnosis and Evaluation of Hypertrophic Cardiomyopathy: JACC State-of-the-Art Review. J Am Coll Cardiol. 2022;79(4):372-389. doi: https://doi.org/10.1016/j.jacc.2021.12.002
23. Bohm P, Barra S, Weizman O, et al. Sudden Cardiac Arrest During Sports in Children and Adolescents. Circulation. 2024;149(10): 794-796. doi: https://doi.org/10.1161/CIRCULATIONAHA.123.064739
24. Shafqat A, Shaik A, Koritala S, et al. Contemporary review on pediatric hypertrophic cardiomyopathy: insights into detection and management. Front Cardiovasc Med. 2024;10:1277041. doi: https://doi.org/10.3389/fcvm.2023.1277041
25. Xia K, Sun D, Wang R, Zhang Y. Factors associated with the risk of cardiac death in children with hypertrophic cardiomyopathy: a systematic review and meta-analysis. Heart Lung. 2022;52: 26-36. doi: https://doi.org/10.1016/j.hrtlng.2021.11.006
26. Marston NA, Han L, Olivotto I, et al. Clinical characteristics and outcomes in childhood-onset hypertrophic cardiomyopathy. Eur Heart J. 2021;42(20):1988-1996. doi: https://doi.org/10.1093/eurheartj/ehab14
27. Norrish G, Qu C, Field E, et al External validation of the HCM Risk-Kids model for predicting sudden cardiac death in childhood hypertrophic cardiomyopathy. Eur J Prev Cardiol. 2022;29(4): 678-686. doi: https://doi.org/10.1093/eurjpc/zwab181
28. Joseph A, Hernandez NB, Davies R, Tan W. Managing Myocardial Bridge and Right Ventricular Outflow Tract Obstruction in an Adolescent With Hypertrophic Cardiomyopathy. World J Pediatr Congenit Heart Surg. 2023;14(4):530-532. doi: https://doi.org/10.1177/21501351231166661
29. Yildiz O, Altin FH, Tosun O, et al. Myocardial bridging in a child with hypertrophic obstructive cardiomyopathy. World J Pediatr Congenit Heart Surg. 2014;5(4):611-614. doi: https://doi.org/10.1177/2150135114536901
30. Mohiddin SA, Begley D, Shih J, Fananapazir L. Myocardial bridging does not predict sudden death in children with hypertrophic cardiomyopathy but is associated with more severe cardiac disease. J Am Coll Cardiol. 2000;36(7):2270-2278. doi: https://doi.org/10.1016/s0735-1097(00)00987-6
31. Lysenko AV, Salagaev GI, Lednev PV, Belov YuV. Surgical treatment of obstructive hypertrophic cardiomyopathy combined with muscle bridging of the left anterior descending artery. Pirogov Russian Journal of Surgery. 2022;(1):81-83. (In Russ). doi: https://doi.org/10.17116/hirurgia201911152
32. Kurath-Koller S, Sallmon H, Scherr D, et al. Wearable cardioverter-defibrillator as bridging to ICD in pediatric hypertrophic cardiomyopathy with myocardial bridging — a case report. BMC Pediatr. 2020;20(1):207. doi: https://doi.org/10.1186/s12887-020-02113-w
33. Coleman JA, Ashkir Z, Raman B, Bueno-Orovio A. Mechanisms and prognostic impact of myocardial ischaemia in hypertrophic cardiomyopathy. Int J Cardiovasc Imaging. 2023;39(10): 1979-1996. doi: https://doi.org/10.1007/s10554-023-02894-y
34. Östman-Smith I. What Aspects of Phenotype Determine Risk for Sudden Cardiac Death in Pediatric Hypertrophic Cardiomyopathy? J Cardiovasc Dev Dis. 2022;9(5):124. doi: https://doi.org/10.3390/jcdd9050124
Review
For citations:
Balykova L.A., Leontyeva I.V., Miklashevich I.M., Thermosesov S.A., Krasnopolskaya A.V., Shirmankina M.V., Shchekina N.V., Isaeva Yu.S., Shkurin P.A. “Muscle Bridge” as a Possible Risk Factor for Sudden Cardiac Death in a Child with Hypertrophic Cardiomyopathy: Case Study. Current Pediatrics. 2025;24(3):193-202. (In Russ.) https://doi.org/10.15690/vsp.v24i3.2908