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Serial evaluation of bosentan monotherapy in a patient with Eisenmenger syndrome during an 11-year period: A case follow-up report

Cilt: 3 Sayı: 3 30 Eylül 2022
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Serial evaluation of bosentan monotherapy in a patient with Eisenmenger syndrome during an 11-year period: A case follow-up report

Öz

Eisenmenger syndrome is a rare disease primarily characterized by severe degrees of irreversible pulmonary arterial hypertension in the setting of congenital heart disease. In this report, we aim to report, on a yearly basis, the clinical, hemodynamic and echocardiographic parameters of a female patient with Eisenmenger syndrome who had been under bosentan treatment during an 11-year follow-up.

Anahtar Kelimeler

Kaynakça

  1. 1. Van Loon RLE, Hoendermis ES, Duffels MG, et al. Long-term effect of bosentan in adults versus children with pulmonary arterial hypertension associated with systemic-to-pulmonary shunt: does the beneficial effect persist?. Am Heart J 2007; 154: 776-82.
  2. 2. Beghetti M, Galiè N. Eisenmenger syndrome. J Am Coll Cardiol 2009; 53: 733–40.
  3. 3. Kaya MG, Lam YY, Erer B, et al. Long-term effect of bosentan therapy on cardiac function and symptomatic benefits in adult patients with Eisenmenger syndrome. J Card Fail 2012; 18: 379-84.
  4. 4. Galiè N, Humbert M, Vachiery JL, et al. 2015 ESC/ERS guidelines for the diagnosis and treatment of pulmonary hypertension: the joint task force for the diagnosis and treatment of pulmonary hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS): endorsed by: Association for European Pediatric and Congenital Cardiology (AEPC), International Society for Heart and Lung Transplantation (ISHLT). Eur Heart J 2016; 37: 67-119.
  5. 5. Baumgartner H, De Backer J, Babu-Narayan SV, et al. 2020 ESC Guidelines for the management of adult congenital heart disease: The Task Force for the management of adult congenital heart disease of the European Society of Cardiology (ESC). Endorsed by: Association for European Pediatric and Congenital Cardiology (AEPC), International Society for Adult Congenital Heart Disease (ISACHD). Eur Heart J 2021; 42: 563-645.
  6. 6. Hascoet S, Fournier E, Jaïs X, et al. Outcome of adults with Eisenmenger syndrome treated with drugs specific to pulmonary arterial hypertension: A French multicenter study. Arch Cardiovasc Dis 2017 110: 303-16.
  7. 7. LI Q, Kuang HY, Wu YH, et al. What is the position of pulmonary arterial hypertension-specific drug therapy in patients with Eisenmenger syndrome: A systematic review and meta-analysis. Medicine 2019, 98(20): e15632.

Ayrıntılar

Birincil Dil

İngilizce

Konular

Sağlık Kurumları Yönetimi

Bölüm

Olgu Sunumu

Yayımlanma Tarihi

30 Eylül 2022

Gönderilme Tarihi

7 Temmuz 2022

Kabul Tarihi

15 Eylül 2022

Yayımlandığı Sayı

Yıl 2022 Cilt: 3 Sayı: 3

Kaynak Göster

APA
Taylan, G., Gürlertop, Y., & Yalta, K. (2022). Serial evaluation of bosentan monotherapy in a patient with Eisenmenger syndrome during an 11-year period: A case follow-up report. Troia Medical Journal, 3(3), 117-119. https://doi.org/10.55665/troiamedj.1139311
AMA
1.Taylan G, Gürlertop Y, Yalta K. Serial evaluation of bosentan monotherapy in a patient with Eisenmenger syndrome during an 11-year period: A case follow-up report. Troia Med J. 2022;3(3):117-119. doi:10.55665/troiamedj.1139311
Chicago
Taylan, Gökay, Yekta Gürlertop, ve Kenan Yalta. 2022. “Serial evaluation of bosentan monotherapy in a patient with Eisenmenger syndrome during an 11-year period: A case follow-up report”. Troia Medical Journal 3 (3): 117-19. https://doi.org/10.55665/troiamedj.1139311.
EndNote
Taylan G, Gürlertop Y, Yalta K (01 Eylül 2022) Serial evaluation of bosentan monotherapy in a patient with Eisenmenger syndrome during an 11-year period: A case follow-up report. Troia Medical Journal 3 3 117–119.
IEEE
[1]G. Taylan, Y. Gürlertop, ve K. Yalta, “Serial evaluation of bosentan monotherapy in a patient with Eisenmenger syndrome during an 11-year period: A case follow-up report”, Troia Med J, c. 3, sy 3, ss. 117–119, Eyl. 2022, doi: 10.55665/troiamedj.1139311.
ISNAD
Taylan, Gökay - Gürlertop, Yekta - Yalta, Kenan. “Serial evaluation of bosentan monotherapy in a patient with Eisenmenger syndrome during an 11-year period: A case follow-up report”. Troia Medical Journal 3/3 (01 Eylül 2022): 117-119. https://doi.org/10.55665/troiamedj.1139311.
JAMA
1.Taylan G, Gürlertop Y, Yalta K. Serial evaluation of bosentan monotherapy in a patient with Eisenmenger syndrome during an 11-year period: A case follow-up report. Troia Med J. 2022;3:117–119.
MLA
Taylan, Gökay, vd. “Serial evaluation of bosentan monotherapy in a patient with Eisenmenger syndrome during an 11-year period: A case follow-up report”. Troia Medical Journal, c. 3, sy 3, Eylül 2022, ss. 117-9, doi:10.55665/troiamedj.1139311.
Vancouver
1.Gökay Taylan, Yekta Gürlertop, Kenan Yalta. Serial evaluation of bosentan monotherapy in a patient with Eisenmenger syndrome during an 11-year period: A case follow-up report. Troia Med J. 01 Eylül 2022;3(3):117-9. doi:10.55665/troiamedj.1139311