Survival and Freedom From Reinterventions in Patients With Repaired Tetralogy of Fallot: Up to 42-Year Follow-Up of 917 Patients

. 2023 Oct 17 ; 12 (20) : e024771. [epub] 20231012

Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid37823375

Background To evaluate long-term outcome of tetralogy of Fallot repair analyzing an unbiased country-wide surgically treated population with tetralogy of Fallot. Methods and Results Retrospective analysis of consecutive patients aged <18 years who underwent tetralogy of Fallot repair at a single nationwide pediatric cardiac center. Death from any cause and need for surgical or catheter reintervention were the study end points. Cox regression analysis was used to identify related risk factors. A total of 917 patients (male, 56.3%) were analyzed. Staged repair was performed in 16.9%. Early mortality (24/917, 2.62% patients) was confined to the early surgical eras. Late mortality was 4.5% (40/893 patients). Survival probability was 95.1%, 93.8% and 91.9% at 10, 20 and 30 years after repair, respectively. Early surgical era (P=0.013) and surgical/catheter reinterventions (P<0.001) were multivariable predictors of late death. A total of 487 reinterventions were performed after initial repair in 253/917 patients (27.6%), with pulmonary artery revalvulation (196/917 patients, 21.4%) being most frequent. Probability of freedom from first reintervention was 89.0%, 73.3%, and 55.1% at 10, 20, and 30 years after primary repair, respectively. Transannular repair was associated with the need for pulmonary artery revalvulation (P<0.001). Patients who underwent staged repair were more likely to need reinterventions on pulmonary arteries (P<0.001). Conclusions In an unbiased nationwide cohort, tetralogy of Fallot repair carried a favorable survival of >90% at 30 years. Each reintervention significantly incrementally increased the risk of mortality. Type of initial repair predicted the need for specific surgical or catheter reinterventions.

Zobrazit více v PubMed

Ylitalo P, Nieminen H, Pitkanen OM, Jokinen E, Sairanen H. Need of transannular patch in tetralogy of Fallot surgery carries a higher risk of reoperation but has no impact on late survival: results of Fallot repair in Finland. Eur J Cardiothorac Surg. 2015;48:91–97. doi: 10.1093/ejcts/ezu401 PubMed DOI

Lindberg HL, Saatvedt K, Seem E, Hoel T, Birkeland S. Single‐center 50 years' experience with surgical management of tetralogy of Fallot. Eur J Cardiothorac Surg. 2011;40:518–542. PubMed

Padalino MA, Pradegan N, Azzolina D, Galletti L, Pace Napoleone C, Agati S, Palma G, Marianeschi SM, Seddio F, Cascarano MT, et al. The role of primary surgical repair technique on late outcomes of tetralogy of Fallot: a multicentre study. Eur J Cardiothorac Surg. 2020;57:565–573. doi: 10.1093/ejcts/ezz270 PubMed DOI

van den Bosch E, Bogers AJJC, Roos‐Hesselink JW, van Dijk APJ, van Wijngaarden MHEJ, Boersma E, Nijveld A, Luijten LWG, Tanke R, Koopman LP, et al. Long‐term follow‐up after transatrial‐transpulmonary repeť of tetralogy of Fallot: influence of timing on outcome. Eur J Cardiothorac Surg. 2020;57:635–643. doi: 10.1093/ejcts/ezz331 PubMed DOI PMC

van der Ven JPG, van den Bosch E, Bogers AJCC, Helbing WA. Current outcomes and treatment of tetralogy of Fallot. F1000Res. 2019;8:1–15. doi: 10.12688/f1000research.17174.1 PubMed DOI PMC

Smith CA, McCracken C, Thomas AS, Spector LG, St Louis JD, Oster ME, Moller JH, Kochilas L. Long‐term outcomes of tetralogy of Fallot: a study from the Pediatric Cardiac Care Consortium. JAMA Cardiol. 2019;4:34–41. doi: 10.1001/jamacardio.2018.4255 PubMed DOI PMC

Vida VL, Triglia LT, Zanotto L, Zanotto L, Bertelli F, Padalino M, Sarris G, Protopapas E, Prospero C, Pizarro C, et al. Late management of the aortic root after repair of tetralogy of Fallot: a European study. J Card Surg. 2020;35:40–47. doi: 10.1111/jocs.14316 PubMed DOI

Stulak JM, Dearani JA, Burkhart HM, Sundt JM, Connolly HM, Schaff HV. Does the dilated ascending aorta in an adult with congenital heart disease require intervention? J Thorac Cardiovasc Surg. 2010;140:552–557. doi: 10.1016/j.jtcvs.2010.08.052 PubMed DOI

Nagy CD, Alejo DE, Corretti MC, Ravekes WJ, Crosson JE, Spevak PJ, Ringel R, Carson KA, Khalil S, Dietz HC, et al. Tetralogy of Fallot and aortic root dilation: a log‐term outlook. Pediatr Cardiol. 2013;34:809–816. doi: 10.1007/s00246-012-0537-8 PubMed DOI

Georgiev S, Ewert P, Eicken A, Hager A, Hörer J, Cleziou J, Meierhofer C, Tanase D. Munich comparative study: prospective long‐term outcome of the transcatheter Melody valve versus surgical pulmonary bioprosthesis with up to 12 years of follow‐up. Circ Cardiovasc Interv. 2020;13:e008963. doi: 10.1161/CIRCINTERVENTIONS.119.008963 PubMed DOI

Therneau T (2023). A package for survival analysis in R . R package version 3.5‐5. Available at: https://CRAN.Rproject.org/package=survival. Accessed March 12, 2023.

Luijten LW, van den Bosch E, Duppen N, Tanke R, Roos‐Hesselink J, Nijveld A, van Dijk A, Bogers AJ, van Domburg R, Helbing WA. Long‐term outcomes of transatrial‐transpulmonary repair of tetralogy of Fallot. Eur J Cardiothorac Surg. 2015;47:527–534. doi: 10.1093/ejcts/ezu182 PubMed DOI

Ye XT, Buratto E, Konstantinov IE, d'Udeken Y. Does transatrial‐transpulmonary approach improve outcomes compared with transventricular approach in non‐neonatal patiets undergoing tetralogy of Fallot repair? Interact Cardiovasc Thorac Surg. 2019;29:960–966. doi: 10.1093/icvts/ivz204 PubMed DOI

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...