Journals / Türk Göğüs Kalp Damar Cerrahisi Dergisi / 2013 / Cilt: 21 - Sayı: 4

An evaluation of efficacy and utility of palliative pulmonary balloon valvuloplasty in symptomatic infants with tetralogy of Fallot

Semptomatik Fallot tetralojili infantlarda palyatif pulmoner balon valvüloplasti uygulamasının etkinliğinin ve yararlılığının değerlendirilmesi

Pages
885–891
Publication Date
2022-09-02
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Conclusion: The PPBV is an effective, beneficial and safe procedure in TOF patients eliminating hypoxia, maintaining pulmonary vascular bed and delaying the surgery time for total repair.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Background: In this study, we aimed to evaluate the results, efficacy and utility of palliative pulmonary balloon valvuloplasty (PPBV) procedure performed on tetralogy of Fallot (TOF) patients.
📊
Key Findings & Data:Methods: Study population included 40 TOF patients aged under one year who underwent PPBV between July 2005 and November 2011.
💡
Conclusion & Impact:Conclusion: The PPBV is an effective, beneficial and safe procedure in TOF patients eliminating hypoxia, maintaining pulmonary vascular bed and delaying the surgery time for total repair.
🔬Design:Research Article
📍Scope:2005 Verileri
⚙️Variables:Domain Parameters

Abstract

Background: In this study, we aimed to evaluate the results, efficacy and utility of palliative pulmonary balloon valvuloplasty (PPBV) procedure performed on tetralogy of Fallot (TOF) patients. Methods: Study population included 40 TOF patients aged under one year who underwent PPBV between July 2005 and November 2011. The indications for PPBV were defined as a pulse oxymetric oxygen saturation of <70% or echocardiographic McGoon index <1.7. Results: The mean oxygen saturation increased from 66.1% to 83.5% following the procedure, which was statistically significant (p<0.0001). After PPBV, 13 patients had total repair directly without any other procedure. Five patients underwent a Blalock- Taussig (BT) shunt operation, while one had a Brock operation. During follow-up, 19 patients had a second cardiac catheterization. Patients who had a second cardiac catheterization had a statistically significant difference in terms of the McGoon index, the pulmonary annulus diameters and Z-scores, the right pulmonary artery diameters and Z-scores and the left pulmonary artery diameters and Z-scores. After the second cardiac catheterization, 17 more patients underwent total repair surgery. A total of 30 patients were able to undergo total repair surgery without any additional palliative method (transcatheter or surgical). The median time to delayed total repair was 12.5 months (range: 2-25 months). No procedure-related mortality was observed. Conclusion: The PPBV is an effective, beneficial and safe procedure in TOF patients eliminating hypoxia, maintaining pulmonary vascular bed and delaying the surgery time for total repair.

Özet

Amaç: Bu çalışmada palyatif pulmoner balon valvüloplasti(PPBV) yapılan Fallot tetralojili (FT) hastalarda işlemin sonuç-ları, etkinliği ve yararlılığı araştırıldı.Ça­lış­ma pla­nı: Çalışmaya Temmuz 2005 - Kasım 2011 tarihleriarasında kliniğimizde bir yaş altında PPBV uygulanmış FT’li 40 hasta dahil edildi. Palyatif pulmoner balon valvüloplasti endikasyonu; oksijen satürasyonunun <%70 veya ekokardiyografikolarak McGoon indeksinin <1.7 olması olarak tanımlandı.Bul­gu­lar: İşlem sonrası ortalama oksijen satürasyonu ista- tistiksel olarak anlamlı bir şekilde %66.1’den %83.5’e çıktı (p<0.0001). Palyatif pulmoner balon valvüloplasti sonrası 13 has-taya herhangi başka bir işlem yapılmadan doğrudan tam düzelt- me ameliyatı yapıldı. Toplam beş hastaya Blalock-Taussig (BT) şant, bir hastaya Brock ameliyatı uygulandı. İzlemde 19 hastaya ikinci kez kalp kateterizasyonu uygulandı. İkinci kez kalp katete-rizasyonu yapılmış hastalarda McGoon indeksi, pulmoner anülüsçapı ve Z değerleri, sağ pulmoner arter çapı ve Z değerleri ve solpulmoner arter çapı ve Z değerleri artışı yönünden istatistikselolarak anlamlı bir fark saptandı. İkinci kalp kateterizasyonu sonrası 17 hasta daha tam düzeltme ameliyatı oldu. Toplam 30 hastaya ilave başka bir palyatif yöntem (transkateter veya cerra-hi) gerekmeksizin tam düzeltme ameliyatı yapıldı. Tam düzeltmeameliyatı medyan 12.5 ay (dağılım 2-23 ay) geciktirilmiş oldu. İşleme bağlı mortalite gözlenmedi.So­nuç: Palyatif pulmoner balon valvüloplasti, FT’li hastalardahipoksiyi gidermesi, pulmoner damar yatağını geliştirmesi vetam düzeltme ameliyatı zamanının geciktirilmesi açısındanetkin, yararlı ve güvenli bir yöntemdir.

🔖

Cite This Article

DEMİR, F., DEDEOĞLU, R., SARITAŞ, T., EROL, N., OZDEMIR, H. I., YÜCEL, İ. K., ÇELEBİ, A., AYDEMİR, N. A., ERDEM, A. (2022). An evaluation of efficacy and utility of palliative pulmonary balloon valvuloplasty in symptomatic infants with tetralogy of Fallot. Türk Göğüs Kalp Damar Cerrahisi Dergisi, Cilt: 21 - Sayı: 4, 885–891. https://ajindex.com/articles/424584

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (13)

  1. Kouchoukos NT, Blackstone EH, Doty DB, Hanley FL, Karp RB, editors. Tetralogy of Fallot with pulmoner stenosis. In: Kirklin/ Barratt-Boyes cardiac surgery. 3th ed. New York: Churchill Livingstone; 2003. p. 946-1012
  2. Seddio F, Migliazza L, Borghi A, Crupi G. Previous palliation in patients with tetralogy of Fallot does not influence the outcome of later repair. J Cardiovasc Med (Hagerstown) 2007;8:119-22
  3. Vobecky SJ, Williams WG, Trusler GA, Coles JG, Rebeyka IM, Smallhorn J, et al. Survival analysis of infants under age 18 months presenting with tetralogy of Fallot. Ann Thorac Surg 1993;56:944-9
  4. Tamesberger MI, Lechner E, Mair R, Hofer A, Sames-Dolzer E, Tulzer G. Early primary repair of tetralogy of fallot in neonates and infants less than four months of age. Ann Thorac Surg 2008;86:1928-35
  5. Seipelt RG, Vazquez-Jimenez JF, Sachweh JS, Seghaye MC, Messmer BJ. Antegrade palliation for diminutive pulmonary arteries in Tetralogy of Fallot. Eur J Cardiothorac Surg 2002;21:721-4
  6. Qureshi SA, Kirk CR, Lamb RK, Arnold R, Wilkinson JL. Balloon dilatation of the pulmonary valve in the first year of life in patients with tetralogy of Fallot: a preliminary study. Br Heart J 1988;60:232-5
  7. Heusch A, Tannous A, Krogmann ON, Bourgeois M. Balloon valvoplasty in infants with tetralogy of Fallot: effects on oxygen saturation and growth of the pulmonary arteries. Cardiol Young 1999;9:17-23
  8. Godart F, Rey C, Prat A, Muilwijk C, Francart C, Vaksmann G,et al. Early and late results and the effects on pulmonary arteries of balloon dilatation of the right ventricular outflow tract in tetralogy of Fallot. Eur Heart J 1998;19:595-600
  9. Sluysmans T, Neven B, Rubay J, Lintermans J, Ovaert C, Mucumbitsi J, et al. Early balloon dilatation of the pulmonary valve in infants with tetralogy of Fallot. Risks and benefits. Circulation 1995;91:1506-11
  10. McGoon DC, Baird DK, Davis GD. Surgical management of large bronchial collateral arteries with pulmonary stenosis or atresia. Circulation 1975;52:109-18
  11. Kouchoukos NT, Blackstone EH, Doty DB, Hanley FL, Karp RB, editors. Anatomy, dimensions, and terminology. In: Kirklin/Barratt-Boyes cardiac surgery. 3rd ed. New York: Churchill Livingstone; 2003. p. 3-65
  12. Shimazaki Y, Blackstone EH, Kirklin JW, Jonas RA, Mandell V, Colvin EV. The dimensions of the right ventricular outflow tract and pulmonary arteries in tetralogy of Fallot and pulmonary stenosis. J Thorac Cardiovasc Surg 1992;103:692-705
  13. Sharland G