Outcomes in Patients After Repaired Tetralogy of Fallot at Maharaj Nakorn Chiang Mai Hospital

Authors

  • Silvilairat S Department of Pediatrics, Faculty of Medicine
  • Tanetsakulwatana N Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand
  • Kamsap N Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand
  • Jewreungwinyu T Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand
  • Watthanayanont N Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand
  • Chanyutthana S Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand
  • Sethasathien S Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand

Keywords:

Tetralogy of Fallot, total correction, RV to PA conduit, outcome, mortality

Abstract

Background: Total correction has been performed in patients with tetralogy of Fallot (TOF) to prevent early death from systemic hypoxemia. However, short- and long-term complications are the major concerns in Thai patients due to insufficient data and loss of follow-up.

Objectives: The aim of this study was to identify the survival rate and predictors for the mortality of patients with TOF after total correction.

Methods: We included all patients with TOF who had undergone total correction between 1993 and 2020. Medical records were reviewed for patient demographics, operative details and complications. Patients who were diagnosed with double outlet right ventricle (TOF type), lost follow-up or missing data were excluded.

Results: A total of 638 patients were included (57.5% male patients, 15.2% TOF with pulmonary atresia, 10.2% genetic abnormalities, 7.2% right ventricle to pulmonary artery conduit). The median age at total correction of TOF was 4.4 years ( IQR; 2.9-7.4 years).  Early and late events developed in 109 (17.1%) and 320 patients (50.2%). The 25-year survival rate was 90%. The crude mortality rate was 7.1%. Multivariate cox regression analysis demonstrated genetic abnormality (HR 3.18 [95%CI 1.61-6.29], p=0.001) and RV to PA conduit utilization (HR 3.29 [95%CI 1.53-7.10], p=0.002) were the predictors for mortality.

Conclusions:The survival rate was 90% after repaired TOF. The presence of genetic abnormality and RV to PA conduit operation were the predictors of the mortality.

References

Forman J, Beech R, Slugantz L, Donnellan A. A review of tetralogy of Fallot and postoperative management. Crit Care Nurs Clin North Am. 2019;31:315-28.

Parker SE, Mai CT, Canfield MA, Rickard R, Wang Y, Meyer RE, et al. Updated national birth prevalence estimates for selected birth defects in the United States, 2004-2006. Birth Defects Res A Clin Mol Teratol. 2010;88:1008-16.

Mosca RS. Tetralogy of Fallot: Total correction. Operative Techniques in Thoracic and Cardiovascular Surgery. 2002;7:22-8.

Mouws E, de Groot NMS, van de Woestijne PC, de Jong PL, Helbing WA, van Beynum IM, et al. Tetralogy of Fallot in the current era. Semin Thorac Cardiovasc Surg. 2019;31:496-504.

Bacha E. Valve-sparing or valve reconstruction options in tetralogy of Fallot surgery. Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu. 2017;20:79-83.

Smith CA, McCracken C, Thomas AS, Spector LG, St Louis JD, Oster ME, et al. Long-term outcomes of tetralogy of Fallot: A study from the pediatric cardiac care consortium. JAMA Cardiol. 2019;4:34-41.

Boonnoom R SR, Pongprot Y, Makonkawkeyoon K. Earthy Postoperative Outcomes of tetralogy of Fallot in pediatric patients at Chiang Mai University Hospital: A ten-year experience. Thai Journal of Pediatrics. 2015;54:144-51.

Dennis M, Moore B, Kotchetkova I, Pressley L, Cordina R, Celermajer DS. Adults with repaired tetralogy: Low mortality but high morbidity up to middle age. Open Heart. 2017; 4:e000564.

Park CS, Lee JR, Lim HG, Kim WH, Kim YJ. The long-term result of total repair for tetralogy of Fallot. Eur J Cardiothorac Surg. 2010;38:311-7.

Blais S, Marelli A, Vanasse A, Dahdah N, Dancea A, Drolet C, et al. The 30-year outcomes of tetralogy of Fallot according to native anatomy and genetic conditions. Can J Cardiol. 2021;37:877-886.

Kirsch RE, Glatz AC, Gaynor JW, Nicolson SC, Spray TL, Wernovsky G, et al. Results of elective repair at 6 months or younger in 277 patients with tetralogy of Fallot: a 14-year experience at a single center. J Thorac Cardiovasc Surg. 2014;147:713-7.

Cheung EW, Wong WH, Cheung YF. Meta-analysis of pulmonary valve replacement after operative repair of tetralogy of Fallot. Am J Cardiol. 2010;106:552-7.

Dluzniewska N, Podolec P, Olszowska M, Werynski P, Suder B, Kopec G, et al. Quality of life in adults with repaired tetralogy of Fallot. Kardiochir Torakochirurgia Pol. 2018;15:107-13.

Possner M, Tseng SY, Alahdab F, Bokma JP, Lubert AM, Khairy P, et al. Risk factors for mortality and ventricular tachycardia in patients with repaired tetralogy of Fallot: A systematic review and meta-analysis. Can J Cardiol. 2020;36:1815-25.

Dluzniewska N, Podolec P, Skubera M, Smas-Suska M, Pajak J, Urbanczyk-Zawadzka M, et al. Long-term follow-up in adults after tetralogy of Fallot repair. Cardiovasc Ultrasound. 2018;16:28.

Hickey EJ, Veldtman G, Bradley TJ, Gengsakul A, Manlhiot C, Williams WG, et al. Late risk of outcomes for adults with repaired tetralogy of Fallot from an inception cohort spanning four decades. Eur J Cardiothorac Surg. 2009; 35:156-64.

Dorobantu DM, Stoicescu C, Tulloh RM, Stoica SC. Surgical repair of tetralogy of Fallot with absent pulmonary valve: Favorable long-term results. Semin Thorac Cardiovasc Surg. 2019;31:847-9.

Hock J, Schwall L, Pujol C, Hager A, Oberhoffer R, Ewert P, et al. Tetralogy of Fallot or pulmonary atresia with ventricular septal defect after the age of 40 years: A single center study. J Clin Med. 2020;9:1533.

Grigaliūnas G, Gumbienė L, Valevičienė N, Matačiūnas M, Tarutis V, Marinskis G, et al. Late arrhythmia in patients with repaired tetralogy of Fallot: who is at risk? Seminars in Cardiovascular Medicine. 2015;21:1-8.

Sirapoom Niamsanit YW, Chusak Kuptarnond, Sompop Prathanee. Long term outcome after total correction of tetralogy of Fallot in Srinagarind hospital. Thai Journal of Pediatrics. 2019;58:166-74.

Azari A, Moravvej Z, Fazlinezhad A, Bigdelu L. Congenital coronary artery anomaly simulating a ventricular septal defect. Asian Cardiovasc Thorac Ann. 2015;23:1062-4.

Sakornpant P, Kojaranjit V. Practice of congenital cardiac surgery in Thailand: Analysis of performance and outcome. The Society of Thoracic Surgeons of Thailand; 2014. Table 1.2, Frequency of procedure and mortality risk in all age group (n=12,482 missing 4.7%) Mortality category 2; p.98.

Lertsakulpiriya K, Vijarnsorn C, Chanthong P, Chungsomprasong P, Kanjanauthai S, Durongpisitkul K, et al. Current era outcomes of pulmonary atresia with ventricular septal defect: A single center cohort in Thailand. Sci Rep. 2020;10:5165.

Kalfa DM, Loundou A, Nouaille de Gorce Y, Fraisse A, Metras DR, Mace L, et al. Pulmonary position cryopreserved homograft in non-Ross patients: how to improve the results? Eur J Cardiothorac Surg. 2012;42:981-7.

Kim H, Sung SC, Kim SH, Chang YH, Lee HD, Park JA, et al. Early and late outcomes of total repair of tetralogy of Fallot: Risk factors for late right ventricular dilatation. Interact Cardiovasc Thorac Surg. 2013;17:956-62.

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Published

2021-10-01

How to Cite

1.
S S, N T, N K, T J, N W, S C, S S. Outcomes in Patients After Repaired Tetralogy of Fallot at Maharaj Nakorn Chiang Mai Hospital. BSCM [Internet]. 2021 Oct. 1 [cited 2024 Apr. 27];60(4):463-74. Available from: https://he01.tci-thaijo.org/index.php/CMMJ-MedCMJ/article/view/248442

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