Myocardial function in patients with anomalous left coronary artery from the pulmonary artery syndrome: A long-term speckle tracking echocardiographic study
Autoři:
Alicja Dąbrowska-Kugacka aff001; Karolina Dorniak aff002; Jarosław Meyer-Szary aff003; Agnieszka Herrador Rey aff003; Ewa Lewicka aff001; Katarzyna Ostrowska aff004; Joanna Kwiatkowska aff003
Působiště autorů:
Department of Cardiology and Electrotherapy, Medical University of Gdansk, Gdansk, Poland
aff001; Department of Noninvasive Cardiac Diagnostics, Medical University of Gdansk, Gdansk, Poland
aff002; Department of Pediatric Cardiology and Congenital Heart Disease, Medical University of Gdansk, Gdansk, Poland
aff003; Department of Cardiology, Polish Mother’s Memorial Hospital–Research Institute, Lodz, Poland
aff004
Vyšlo v časopise:
PLoS ONE 14(10)
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pone.0223227
Souhrn
Background
Anomalous origin of the left coronary artery (LCA) from the pulmonary artery (ALCAPA) is a rare congenital heart disease. Retrograde flow from the right coronary artery (RCA) through natural collaterals to the low-pressure main pulmonary artery causes extensive ischemia. Limited data concerning the extent of permanent myocardial damage and functional recovery after surgical repair in the long-term follow-up is available.
Aim
Determination of the incidence of incipient myocardial dysfunction in ALCAPA patients in the long-term observation using tissue Doppler and speckle tracking echocardiography.
Methods and results
Eighteen ALCAPA patients after surgical repair (at median age of 7 months, range 3–167) underwent echocardiographic examination after (median) 17 years. All but 4 patients in NYHA class II presented well at follow-up. No narrowing in proximal LCA was detected in color Doppler. The initial (pre-surgical) left ventricular (LV) ejection fraction of 33±17% almost normalized to 55±6%, but was lower than in the age, sex and body surface area matched control group: 62±5% (p<0.001). At follow-up, LV global longitudinal strain (LS): -15.8±3.3% vs -21.9±1.7%; right ventricular LS: -20.6±3.9% vs -24.9±4.6%; left atrial LS: 27.7±4.3% vs 41.0±11.5%; right atrial LS: 26.8±7.4% vs 44.0±7.9% and early pulsed wave to tissue Doppler mitral filling ratio (E/E’): 8.1±2.6 vs 5.8±1.3 were impaired in the ALCAPA population in comparison to the control group (p<0.01 for all comparisons). LV radial and circumferential strain did not differ between groups. Mean LS in the ALCAPA patients in the RCA region was -19.0±4.4%, while in the LCA region -13.8±7.3% (p<0.00001).
Conclusions
Despite good clinical condition and normalized LV ejection fraction in ALCAPA patients after surgical repair in the long-term follow-up, the diastolic and longitudinal systolic function of all cardiac chambers remained impaired, especially in the LCA region. Lifelong surveillance of repaired ALCAPA patients is needed.
Klíčová slova:
Surgical and invasive medical procedures – Coronary heart disease – Ischemia – Stenosis – Echocardiography – Pulmonary arteries – Surgical repair – Papillary muscles
Zdroje
1. Farouk A, Zahka K, Siwik E, Golden A, Karimi M, Uddin M, et al. Anomalous origin of the left coronary artery from the right pulmonary artery. J Card Surg. 2009; 24: 49–54. doi: 10.1111/j.1540-8191.2008.00622.x 19120675
2. Lange R, Vogt M, Horer J, Hörer J, Cleuziou J, Menzel A, et al. Long-term results of repair of anomalous origin of the left coronary artery from the pulmonary artery. Ann Thorac Surg. 2007; 83: 1463–71. doi: 10.1016/j.athoracsur.2006.11.005 17383358
3. Alexi-Meskishvili V, Nasseri BA, Nordmeyer S, Schmitt B, Weng YG, Böttcher W, et al. Repair of anomalous origin of the left coronary artery from the pulmonary artery in infants and children. J Thorac Cardiovasc Surg. 2011; 142: 868–74. doi: 10.1016/j.jtcvs.2011.04.006 21665229
4. Hoashi T, Kagisaki K, Okuda N, Shiraishi I, Yagihara T, Ichikawa H. Indication of Takeuchi technique for patients with anomalous origin of the left coronary artery from the pulmonary artery. Circ J. 2013; 77: 1202–1207. doi: 10.1253/circj.cj-12-1321 23392121
5. Ling Y, Bhushan S, Fan Q and Tang M. Midterm outcome after surgical correction of anomalous left coronary artery from the pulmonary artery. Journal of Cardiothoracic Surgery. 2016, 11: 137. doi: 10.1186/s13019-016-0397-z
6. Naimo PS, Fricke TA, d’Udekem Y, Cochrane AD, Bullock A, Robertson T, et al. Surgical intervention for anomalous origin of left coronary artery from the pulmonary artery in children: A long-term follow-up. Ann Thorac Surg. 2016; 101: 1842–8. doi: 10.1016/j.athoracsur.2015.11.020 26897320
7. Kazmierczak PA, Ostrowska K, Dryzek P, Moll JA, Moll JJ. Repair of anomalous origin of the left coronary artery from the pulmonary artery in infants. Interact Cardiovasc Thor Surg. 2013; 16: 797–801.
8. Ben Ali W, Metton O, Roubertie F, Pouard P, Sidi D, Raisky O, et al. Anomalous origin of the left coronary artery from the pulmonary artery: late results with special attention to the mitral valve. Eur J Cardiothorac Surg. 2009; 36: 244–249. doi: 10.1016/j.ejcts.2009.03.014 19372048
9. Cabrera AG, Chen DW, Pignatelli RH, Khan MS, Jeewa A, Mery CM, et al. Outcomes of anomalous left coronary artery from pulmonary artery repair: beyond normal function. Ann Thorac Surg. 2015; 99: 1342–7. doi: 10.1016/j.athoracsur.2014.12.035 25725925
10. Browne LP, Kearney D, Taylor MD, Chung T, Slesnick TC, Nutting AC, et al. ALCAPA: the role of myocardial viability studies in determining prognosis. Pediatr Radiol. 2010; 40: 163–7. doi: 10.1007/s00247-009-1412-5 19795113
11. Schmitt B, Bauer S, Kutty S, Nordmeyer S, Nasseri B, Berger F, et al. Myocardial perfusion, scarring, and function in anomalous left coronary artery from the pulmonary artery syndrome: a long-term analysis using magnetic resonance imaging. Ann Thorac Surg. 2014; 98: 1425–36. doi: 10.1016/j.athoracsur.2014.05.031 25130077
12. Kanoh M, Inai K, Shinohara T, Tomimatsu H, Nakanishi T. Outcomes from anomalous origin of the left coronary artery from the pulmonary artery repair: long-term complications in relations to residual myocardial abnormalities. J Cardiol. 2017; 70: 498–503. doi: 10.1016/j.jjcc.2017.03.008 28427867
13. Zheng J, Ding W, Xiao Y, Jin M, Zhang G, Cheng P, et al. Anomalous origin of the left coronary artery from the pulmonary artery in children: 15 years experience. Pediatr Cardiol. 2011; 32: 24–31. doi: 10.1007/s00246-010-9798-2 20976445
14. Prakash A, Powell AJ, Krishnamurthy R, Geva T. Magnetic resonance imaging evaluation of myocardial perfusion and viability in congenital and acquired pediatric heart disease. Am J Cardiol. 2004; 93: 657–61. doi: 10.1016/j.amjcard.2003.11.045 14996605
15. Kwiatkowska J, Herrador Rey A, Meyer-Szary J, Dorniak K, Ostrowska K, Wałdoch A, Kozłowski D, Dabrowska-Kugacka A. Longterm outcome after surgical repair of anomalous origin of the left coronary artery from the pulmonary artery– 24 years of experience. Kardiol Pol Ahead of print / doi: 10.33963/KP.14816 31066728
16. Di Salvo G, Eyskens B, Claus P, D'hooge J, Bijnens B, Suys B, et al. Late post-repair ventricular function in patients with origin of the left main coronary artery from the pulmonary trunk. Am J Cardiol. 2004; 93: 506–8. doi: 10.1016/j.amjcard.2003.10.059 14969638
17. American Hospital Association; (2003-02-01). AHA: Advisory: HIPAA Updated Guidelines for Releasing Information on the Condition of Patients. American Hospital Association. Retrieved and archived on 2008-01-28
18. Lang RM, Badano LP, Mor-Avi V, Afilalo J, Armstrong A, Ernande L, et al. Recommendations for cardiac chamber quantification by echocardiography in adults: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. J Am Soc Echocardiogr. 2015; 28: 1–39. doi: 10.1016/j.echo.2014.10.003 25559473
19. Pettersen MD, Du W, Skeens ME, and Humes RA. Regression equations for calculation of z scores of cardiac structures in a large cohort of healthy infants, children, and adolescents: an echocardiographic study. J Am Soc Echocardiogr. 2008; 21: 922–934. doi: 10.1016/j.echo.2008.02.006 18406572
20. Nagueh SF, Smiseth OA, Appleton CP, Byrd BF 3rd, Dokainish H, Edvardsen T, et al. Recommendations for the evaluation of left ventricular diastolic function by echocardiography: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging European Heart Journal–Cardiovascular Imaging. 2016; 17: 1321–1360.
21. Marcus KA, Mavinkurve-Groothius A MC, Barends M, van Dijk A, Feuth T, de Korte C. Reference values for myocardial two-dimensional strain echocardiography in a healthy pediatric and young adult cohort. J Am Soc Echocardiogr. 2011; I6: 625–636.
22. Yingchoncharoen T, Agarwal S, Popovi ZB, Marwick TH. Normal ranges of left ventricular strain: a meta-analysis. J Am Soc Echocardiogr. 2013; 26: 185–91. doi: 10.1016/j.echo.2012.10.008 23218891
23. Castaldi B, Vida V, Reffo E, Padalino M, Daniels Q, Stellin G et al. Speckle tracking in ALCAPA patients after surgical repair as predictor of residual coronary disease. Pediatr Cardiol 2017; 38:794–800 doi: 10.1007/s00246-017-1583-z 28214964
24. Parizek P, Haman L, Harrer J, et al. Bland-White-Garland syndrome in adults: sudden cardiac death as a first symptom and long-term follow-up after successful resuscitation and surgery. Europace. 2010; 12:1338–1340. doi: 10.1093/europace/euq087 20348142
25. Maes A, Flameng W, Nuyts J, Borgers M, Shivalkar B, Ausma J, et al. Histological alterations in chronically hypoperfused myocardium: correlations with PET findings. Circulation. 1994; 90: 735–745. doi: 10.1161/01.cir.90.2.735 8044942
26. Gorcsan J, Tanaka H. Echocardiographic assessment of myocardial strain. J Am Coll Cardiol. 2011; 58: 1401–13. doi: 10.1016/j.jacc.2011.06.038 21939821
27. El-Menyar A, Galzerano D, Asaad N, Al-Mulla A, Arafa S, Al Suwaidi J. Detection of myocardial dysfunction in the presence of normal ejection fraction. J Cardiovasc Med. 2007; 8: 923–33.
28. Dandel M, Lehmkuhl H, Knosalla C, Suramelashvili N, Hetzer R. Strain and strain rate imaging by echocardiography—basic concepts and clinical applicability. Curr Cardiol Rev. 2009; 5: 133–48. doi: 10.2174/157340309788166642 20436854
29. Mertens L, Weidemann F, Sutherland GR. Left ventricular function before and after repair of an anomalous left coronary artery arising from the pulmonary trunk. Cardiol Young. 2001; 11: 79–83. 11233402
30. Di Salvo G, Siblini G, Issa Z, Mohammed H, Hazeem A, Pergola V, et al. Left ventricular mechanics in patients with abnormal origin of the left main coronary artery from the pulmonary trunk late after successful repair. Cardiology. 2017; 136: 71–76. doi: 10.1159/000447961 27562944
31. Secinaro A, Ntsinjana H, Tann O, Schuler PK, Muthurangu V, Hughes M, et al. Cardiovascular magnetic resonance findings in repaired anomalous left coronary artery to pulmonary artery connection (ALCAPA). J Cardiovasc Magn Reson. 2011; 16: 13–27.
32. Ginde S, Earing MG, Bartz PJ, Cava JR, Tweddell JS. Late complications after Takeuchi repair of anomalous left coronary artery from the pulmonary artery: case series and review of literature. Pediatr Cardiol. 2012; 33: 1115–23. doi: 10.1007/s00246-012-0260-5 22438016
Článok vyšiel v časopise
PLOS One
2019 Číslo 10
- Metamizol jako analgetikum první volby: kdy, pro koho, jak a proč?
- Nejasný stín na plicích – kazuistika
- Masturbační chování žen v ČR − dotazníková studie
- Úspěšná resuscitativní thorakotomie v přednemocniční neodkladné péči
- Fixní kombinace paracetamol/kodein nabízí synergické analgetické účinky
Najčítanejšie v tomto čísle
- Correction: Low dose naltrexone: Effects on medication in rheumatoid and seropositive arthritis. A nationwide register-based controlled quasi-experimental before-after study
- Combining CDK4/6 inhibitors ribociclib and palbociclib with cytotoxic agents does not enhance cytotoxicity
- Experimentally validated simulation of coronary stents considering different dogboning ratios and asymmetric stent positioning
- Prevalence of pectus excavatum (PE), pectus carinatum (PC), tracheal hypoplasia, thoracic spine deformities and lateral heart displacement in thoracic radiographs of screw-tailed brachycephalic dogs