BibTex RIS Kaynak Göster

Treatment Strategies of Pulmonary Arterial Hypertension Associated with Congenital Heart Defects with Shunt: A Group of Important Intensive Care Patient in Cardiology and Cardiovascular Surgery

Yıl 2013, Cilt: 16 Sayı: 3, 173 - 176, 01.03.2012
https://doi.org/10.5578/kkd.6837

Öz

Kaynakça

  • D’Alonzo GE, Barst RJ, Ayres SM, Bergofsky EH, Brundage BH, Detre KM, et al. Survival in patients with primary pulmonary hyper- tension. Results from a national prospective registry. Ann Intern Med 1991;115:343-9.
  • Korurek M, Yildiz M, Yüksel A, Şahin A. Simulation of Eisenmen- ger syndrome with ventricular septal defect using equivalent elect- ronic system. Cardiol Young 2012;22:301-6.
  • Yıldız M, Yüksel A, Korürek M, Aykan AÇ, Şahin Yıldız B, Şa- hin A, et al. Classifi cation of Aatrial septal defect and ventricular septal defect with documented hemodynamic parameters via vardiac catheterization by genetic algorithms and multi-layered artifi cial neural network. Kosuyolu Kalp Derg 2012;15:45-50.
  • Engelfriet PM, Duffels MGJ, Moller T, Boersma E, Tijssen JGP, Thaulow E, et al. Pulmonary arterial hypertension in adults born with a heart septal defect: the Euro Heart Survey on adult conge- nital heart disease. Heart 2007;93:682-7.
  • Daliento L, Somerville J, Presbitero P, Menti L, Brach-Prever S, Rizzoli G, et al. Eisenmenger syndrome. Factors relating to dete- rioration and death. Eur Heart J 1998;19:1845-55.
  • Beghetti M, Galie N. Eisenmenger syndrome: a clinical perspecti- ve in a new therapeutic era of pulmonary arterial hypertension. J Am Coll Cardiol 2009;53:733-40.
  • Broberg CS, Ujita M, Prasad S, Li W, Rubens M, Bax BE, et al. Pulmonary arterial thrombosis in Eisenmenger syndrome is as- sociated with biventricular dysfunction and decreased pulmonary fl ow velocity. J Am Coll Cardiol 2007;50:634-42.
  • Hoeper MM, Barst RJ, Bourge RC, Feldman J, Frost AE, Galié N, et al. Imatinib mesylate as add-on therapy for pulmonary arterial hypertension: results of the randomized IMPRES study. Circulati- on 2013;127:1128-38.
  • Xiong CM, Lu XL, Shan GL, Wu BX, Zhu XY, Wu GH, et al. Oral sil- denafi l therapy for Chinese patients with pulmonary arterial hyper- tension: a multicenter study. J Clin Pharmacol 2012;52:425-31.
  • Gatzoulis MA, Alonso-Gonzalez R, Beghetti M. Pulmonary arterial hypertension in paediatric and adult patients with congenital heart disease. Eur Respir Rev 2009;18:154-61.
  • Galiè N, Beghetti M, Gatzoulis MA, Granton J, Berger RM, La- uer A, et al.; Bosentan Randomized Trial of Endothelin Antago- nist Therapy-5 (BREATHE-5) Investigators. Bosentan therapy in patients with Eisenmenger syndrome: a multicenter, double-blind, randomized, placebo-controlled study. Circulation 2006;114:48- 54.
  • Cacoub P, Dorent R, Nataf P, Carayon A. Endothelin-1 in pulmo- nary hypertension. N Engl J Med 1993;329:1967-8.
  • Gatzoulis MA, Beghetti M, Galiè N, Granton J, Berger RM, Lauer A, et al.; BREATHE-5 Investigators. Longer-term bosentan the- rapy improves functional capacity in Eisenmenger syndrome: re- sults of the BREATHE-5 open-label extension study. Int J Cardiol 2008;127:27-32.
  • Zuckerman WA, Leaderer D, Rowan CA, Mituniewicz JD, Rosenz- weig EB. Ambrisentan for pulmonary arterial hypertension due to congenital heart disease. Am J Cardiol 2011;107:1381-5.
  • Prasad S, Wilkinson J, Gatzoulis MA. Sildenafi l in primary pulmo- nary hypertension. N Engl J Med 2000;343:1342.
  • Humpl T, Reyes JT, Holtby H, Stephens D, Adatia I. Benefi cial effect of oral sildenafi l therapy on childhood pulmonary arterial hypertension: twelve-month clinical trial of a single-drug, open-la- bel, pilot study. Circulation 2005;111:3274-80.
  • Chau EM, Fan KY, Chow WH. Effects of chronic sildenafi l in pa- tients with Eisenmenger syndrome versus idiopathic pulmonary arterial hypertension. Int J Cardiol 2007;120:301-5.
  • Mukhopadhyay S, Sharma M, Ramakrishnan S, Yusuf J, Gupta MD, Bhamri N, et al. Phosphodiesterase- 5 inhibitor in Eisen- menger syndrome: a preliminary observational study. Circulation 2006;114:1807-10.
  • Rosenzweig EB, Kerstein D, Barst RJ. Long-term prostacyclin for pulmonary hypertension with associated congenital heart defects. Circulation 1999;99:1858-65.
  • Thomas IC, Glassner-Kolmin C, Gomberg-Maitland M. Long-term effects of continuous prostacyclin therapy in adults with pulmonary hypertension associated with congenital heart disease. Int J Car- diol 2013;168:4117-21.
  • D’Alto M, Romeo E, Argiento P, Sarubbi B, Santoro G, Grimaldi N, et al. Bosentan-sildenafi l association in patients with congenital heart disease-related pulmonary arterial hypertension and Eisen- menger physiology. Int J Cardiol 2012;155:378-82.
  • Iversen K, Jensen AS, Jensen TV, Vejlstrup NG, Sondergaard L. Combination therapy with bosentan and sildenafi l in Eisenmenger syndrome: a randomized, placebo-controlled, double-blinded trial. Eur Heart J 2010;31:1124-31.
  • Dimopoulos K, Inuzuka R, Goletto S, Giannakoulas G, Swan L, Wort SJ, et al. Improved survival among patients with Eisenmen- ger syndrome receiving advanced therapy for pulmonary arterial hypertension. Circulation 2010;121:20-5.
  • Gatzoulis MA, Alonso-Gonzalez R, Beghetti M. Pulmonary arterial hypertension in paediatric and adult patients with congenital heart disease. Eur Respir Rev 2009;18:154-61.

Doğumsal Kardiyak Şantlarla Bağlantılı Pulmoner Arteriyel Hipertansiyonda Tedavi Yaklaşımları: Kardiyoloji ve Kalp-Damar Cerrahisinde Önemli Bir Yoğun Bakım Hasta Grubu

Yıl 2013, Cilt: 16 Sayı: 3, 173 - 176, 01.03.2012
https://doi.org/10.5578/kkd.6837

Öz

hipertansiyonda kombinasyon tedavisiyle ilgili yapılan ça- lışmalardan elde edilen veriler çelişkilidir. Bazı çalışmalar- da bosentan tedavisine sildenafi l eklenmesi hemodinamik özellikleri ve egzersiz kapasitesini artırırken; bazı çalışma- larda kombinasyon tedavisi etkisiz bulunmuştur(23). Fakat yine de doğumsal kalp hastalığıyla ilişkili pulmoner arte- riyel hipertansiyon hastalarının, pulmoner arteriyel hiper- tansiyon spesifi k tedaviden fayda gördüğü gösterilmiştir. Ortalama dört yıl takip edilen toplam 229 Eisenmenger sendromlu hastada yapılan retrospektif bir çalışmada pul- moner arteriyel hipertansiyon spesifi k tedavi gören grupta, tedavi almayan gruba göre daha düşük ölüm oranı saptan- mıştır(24)

Kaynakça

  • D’Alonzo GE, Barst RJ, Ayres SM, Bergofsky EH, Brundage BH, Detre KM, et al. Survival in patients with primary pulmonary hyper- tension. Results from a national prospective registry. Ann Intern Med 1991;115:343-9.
  • Korurek M, Yildiz M, Yüksel A, Şahin A. Simulation of Eisenmen- ger syndrome with ventricular septal defect using equivalent elect- ronic system. Cardiol Young 2012;22:301-6.
  • Yıldız M, Yüksel A, Korürek M, Aykan AÇ, Şahin Yıldız B, Şa- hin A, et al. Classifi cation of Aatrial septal defect and ventricular septal defect with documented hemodynamic parameters via vardiac catheterization by genetic algorithms and multi-layered artifi cial neural network. Kosuyolu Kalp Derg 2012;15:45-50.
  • Engelfriet PM, Duffels MGJ, Moller T, Boersma E, Tijssen JGP, Thaulow E, et al. Pulmonary arterial hypertension in adults born with a heart septal defect: the Euro Heart Survey on adult conge- nital heart disease. Heart 2007;93:682-7.
  • Daliento L, Somerville J, Presbitero P, Menti L, Brach-Prever S, Rizzoli G, et al. Eisenmenger syndrome. Factors relating to dete- rioration and death. Eur Heart J 1998;19:1845-55.
  • Beghetti M, Galie N. Eisenmenger syndrome: a clinical perspecti- ve in a new therapeutic era of pulmonary arterial hypertension. J Am Coll Cardiol 2009;53:733-40.
  • Broberg CS, Ujita M, Prasad S, Li W, Rubens M, Bax BE, et al. Pulmonary arterial thrombosis in Eisenmenger syndrome is as- sociated with biventricular dysfunction and decreased pulmonary fl ow velocity. J Am Coll Cardiol 2007;50:634-42.
  • Hoeper MM, Barst RJ, Bourge RC, Feldman J, Frost AE, Galié N, et al. Imatinib mesylate as add-on therapy for pulmonary arterial hypertension: results of the randomized IMPRES study. Circulati- on 2013;127:1128-38.
  • Xiong CM, Lu XL, Shan GL, Wu BX, Zhu XY, Wu GH, et al. Oral sil- denafi l therapy for Chinese patients with pulmonary arterial hyper- tension: a multicenter study. J Clin Pharmacol 2012;52:425-31.
  • Gatzoulis MA, Alonso-Gonzalez R, Beghetti M. Pulmonary arterial hypertension in paediatric and adult patients with congenital heart disease. Eur Respir Rev 2009;18:154-61.
  • Galiè N, Beghetti M, Gatzoulis MA, Granton J, Berger RM, La- uer A, et al.; Bosentan Randomized Trial of Endothelin Antago- nist Therapy-5 (BREATHE-5) Investigators. Bosentan therapy in patients with Eisenmenger syndrome: a multicenter, double-blind, randomized, placebo-controlled study. Circulation 2006;114:48- 54.
  • Cacoub P, Dorent R, Nataf P, Carayon A. Endothelin-1 in pulmo- nary hypertension. N Engl J Med 1993;329:1967-8.
  • Gatzoulis MA, Beghetti M, Galiè N, Granton J, Berger RM, Lauer A, et al.; BREATHE-5 Investigators. Longer-term bosentan the- rapy improves functional capacity in Eisenmenger syndrome: re- sults of the BREATHE-5 open-label extension study. Int J Cardiol 2008;127:27-32.
  • Zuckerman WA, Leaderer D, Rowan CA, Mituniewicz JD, Rosenz- weig EB. Ambrisentan for pulmonary arterial hypertension due to congenital heart disease. Am J Cardiol 2011;107:1381-5.
  • Prasad S, Wilkinson J, Gatzoulis MA. Sildenafi l in primary pulmo- nary hypertension. N Engl J Med 2000;343:1342.
  • Humpl T, Reyes JT, Holtby H, Stephens D, Adatia I. Benefi cial effect of oral sildenafi l therapy on childhood pulmonary arterial hypertension: twelve-month clinical trial of a single-drug, open-la- bel, pilot study. Circulation 2005;111:3274-80.
  • Chau EM, Fan KY, Chow WH. Effects of chronic sildenafi l in pa- tients with Eisenmenger syndrome versus idiopathic pulmonary arterial hypertension. Int J Cardiol 2007;120:301-5.
  • Mukhopadhyay S, Sharma M, Ramakrishnan S, Yusuf J, Gupta MD, Bhamri N, et al. Phosphodiesterase- 5 inhibitor in Eisen- menger syndrome: a preliminary observational study. Circulation 2006;114:1807-10.
  • Rosenzweig EB, Kerstein D, Barst RJ. Long-term prostacyclin for pulmonary hypertension with associated congenital heart defects. Circulation 1999;99:1858-65.
  • Thomas IC, Glassner-Kolmin C, Gomberg-Maitland M. Long-term effects of continuous prostacyclin therapy in adults with pulmonary hypertension associated with congenital heart disease. Int J Car- diol 2013;168:4117-21.
  • D’Alto M, Romeo E, Argiento P, Sarubbi B, Santoro G, Grimaldi N, et al. Bosentan-sildenafi l association in patients with congenital heart disease-related pulmonary arterial hypertension and Eisen- menger physiology. Int J Cardiol 2012;155:378-82.
  • Iversen K, Jensen AS, Jensen TV, Vejlstrup NG, Sondergaard L. Combination therapy with bosentan and sildenafi l in Eisenmenger syndrome: a randomized, placebo-controlled, double-blinded trial. Eur Heart J 2010;31:1124-31.
  • Dimopoulos K, Inuzuka R, Goletto S, Giannakoulas G, Swan L, Wort SJ, et al. Improved survival among patients with Eisenmen- ger syndrome receiving advanced therapy for pulmonary arterial hypertension. Circulation 2010;121:20-5.
  • Gatzoulis MA, Alonso-Gonzalez R, Beghetti M. Pulmonary arterial hypertension in paediatric and adult patients with congenital heart disease. Eur Respir Rev 2009;18:154-61.
Toplam 24 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Bölüm Makaleler
Yazarlar

Mustafa Yıldız Bu kişi benim

Hasan Sunar Bu kişi benim

Ali Metin Esen Bu kişi benim

Yayımlanma Tarihi 1 Mart 2012
Yayımlandığı Sayı Yıl 2013 Cilt: 16 Sayı: 3

Kaynak Göster

APA Yıldız, M. ., Sunar, H. ., & Esen, A. M. . (2012). Doğumsal Kardiyak Şantlarla Bağlantılı Pulmoner Arteriyel Hipertansiyonda Tedavi Yaklaşımları: Kardiyoloji ve Kalp-Damar Cerrahisinde Önemli Bir Yoğun Bakım Hasta Grubu. Koşuyolu Kalp Dergisi, 16(3), 173-176. https://doi.org/10.5578/kkd.6837
AMA Yıldız M, Sunar H, Esen AM. Doğumsal Kardiyak Şantlarla Bağlantılı Pulmoner Arteriyel Hipertansiyonda Tedavi Yaklaşımları: Kardiyoloji ve Kalp-Damar Cerrahisinde Önemli Bir Yoğun Bakım Hasta Grubu. Koşuyolu Kalp Dergisi. Mart 2012;16(3):173-176. doi:10.5578/kkd.6837
Chicago Yıldız, Mustafa, Hasan Sunar, ve Ali Metin Esen. “Doğumsal Kardiyak Şantlarla Bağlantılı Pulmoner Arteriyel Hipertansiyonda Tedavi Yaklaşımları: Kardiyoloji Ve Kalp-Damar Cerrahisinde Önemli Bir Yoğun Bakım Hasta Grubu”. Koşuyolu Kalp Dergisi 16, sy. 3 (Mart 2012): 173-76. https://doi.org/10.5578/kkd.6837.
EndNote Yıldız M, Sunar H, Esen AM (01 Mart 2012) Doğumsal Kardiyak Şantlarla Bağlantılı Pulmoner Arteriyel Hipertansiyonda Tedavi Yaklaşımları: Kardiyoloji ve Kalp-Damar Cerrahisinde Önemli Bir Yoğun Bakım Hasta Grubu. Koşuyolu Kalp Dergisi 16 3 173–176.
IEEE M. . Yıldız, H. . Sunar, ve A. M. . Esen, “Doğumsal Kardiyak Şantlarla Bağlantılı Pulmoner Arteriyel Hipertansiyonda Tedavi Yaklaşımları: Kardiyoloji ve Kalp-Damar Cerrahisinde Önemli Bir Yoğun Bakım Hasta Grubu”, Koşuyolu Kalp Dergisi, c. 16, sy. 3, ss. 173–176, 2012, doi: 10.5578/kkd.6837.
ISNAD Yıldız, Mustafa vd. “Doğumsal Kardiyak Şantlarla Bağlantılı Pulmoner Arteriyel Hipertansiyonda Tedavi Yaklaşımları: Kardiyoloji Ve Kalp-Damar Cerrahisinde Önemli Bir Yoğun Bakım Hasta Grubu”. Koşuyolu Kalp Dergisi 16/3 (Mart 2012), 173-176. https://doi.org/10.5578/kkd.6837.
JAMA Yıldız M, Sunar H, Esen AM. Doğumsal Kardiyak Şantlarla Bağlantılı Pulmoner Arteriyel Hipertansiyonda Tedavi Yaklaşımları: Kardiyoloji ve Kalp-Damar Cerrahisinde Önemli Bir Yoğun Bakım Hasta Grubu. Koşuyolu Kalp Dergisi. 2012;16:173–176.
MLA Yıldız, Mustafa vd. “Doğumsal Kardiyak Şantlarla Bağlantılı Pulmoner Arteriyel Hipertansiyonda Tedavi Yaklaşımları: Kardiyoloji Ve Kalp-Damar Cerrahisinde Önemli Bir Yoğun Bakım Hasta Grubu”. Koşuyolu Kalp Dergisi, c. 16, sy. 3, 2012, ss. 173-6, doi:10.5578/kkd.6837.
Vancouver Yıldız M, Sunar H, Esen AM. Doğumsal Kardiyak Şantlarla Bağlantılı Pulmoner Arteriyel Hipertansiyonda Tedavi Yaklaşımları: Kardiyoloji ve Kalp-Damar Cerrahisinde Önemli Bir Yoğun Bakım Hasta Grubu. Koşuyolu Kalp Dergisi. 2012;16(3):173-6.