Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request

The surgical treatment of anomalous origin of one pulmonary artery from the ascending aorta.

Item request has been placed! ×
Item request cannot be made. ×
loading   Processing Request
اقرأ على الانترنت اقرأ أكثر حفظ في قائمتي
  • معلومة اضافية
    • المصدر:
      Publisher: BioMed Central Country of Publication: England NLM ID: 101265113 Publication Model: Electronic Cited Medium: Internet ISSN: 1749-8090 (Electronic) Linking ISSN: 17498090 NLM ISO Abbreviation: J Cardiothorac Surg Subsets: MEDLINE
    • بيانات النشر:
      Original Publication: [London] : BioMed Central, 2006-
    • الموضوع:
      Aorta/*surgery ; Cardiovascular Abnormalities/*surgery ; Heart Defects, Congenital/*surgery ; Pulmonary Artery/*surgery; Adolescent ; Anastomosis, Surgical ; Aorta/abnormalities ; Aorta/transplantation ; Cardiovascular Surgical Procedures ; Child ; Child, Preschool ; Female ; Humans ; Infant ; Infant, Newborn ; Male ; Pericardium/transplantation ; Pulmonary Artery/abnormalities ; Pulmonary Artery/transplantation ; Retrospective Studies ; Surgical Flaps ; Treatment Outcome ; Young Adult
    • نبذة مختصرة :
      Objective: This study sought to summarize the clinical experience of surgical treatment of anomalous origin of pulmonary arteries from the ascending aorta (AOPA) in Fuwai hospital.
      Methods: Fifty-two patients (28 males, 17.2 ± 27.2 months old and 8.7 ± 10.2 Kg weight) who have AOPA undertook surgical treatment between 1998 and 2017 were reviewed in this study, 47 out of 52 are anomalous origin of the right pulmonary artery (AORPA), among the rest of the patients are anomalous origin of left pulmonary artery (AOLPA). 27 out of 52 associate with simple cardiac abnormalities, 20 out of 52 associate with complex cardiac malformations, the remaining 5 patients without cardiac abnormalities. Among all patients who underwent surgical treatment, the direct end-to-side anastomosis strategy was applied in 26 patients, autologous pericardial-homograft patch and aortic flap were employed in 20 patients, and synthetic graft was used in 6 patients.
      Results: No patient died during the perioperative period. 50 out of 52 patients were followed-up for 100.1 ± 70.9 months. The rate of pulmonary arterial free restenosis for 2 years, 5 years, and 10 years is 98.0, 96.0 and 92.0%, respectively.
      Conclusions: The correct diagnosis and appropriate surgical treatment for AOPA could obtain excellent early and medium-term result.
    • References:
      Eur J Cardiothorac Surg. 2002 Jul;22(1):148-50. (PMID: 12103393)
      Circulation. 1961 Sep;24:662-8. (PMID: 13684281)
      J Card Surg. 2004 Mar-Apr;19(2):103-12. (PMID: 15016045)
      Eur J Cardiothorac Surg. 2004 Oct;26(4):762-6. (PMID: 15450569)
      Ann Thorac Surg. 2008 Apr;85(4):1407-11. (PMID: 18355536)
      Thorac Cardiovasc Surg. 2008 Oct;56(7):432-4. (PMID: 18810705)
      Pediatr Cardiol. 2010 Oct;31(7):944-51. (PMID: 20490479)
      Int J Cardiol. 2015 Apr 1;184:750-4. (PMID: 25827936)
      J Cardiothorac Surg. 2015 Jul 11;10:97. (PMID: 26162911)
      Am J Cardiol. 1988 Apr 1;61(10):850-6. (PMID: 3354450)
      Ann Surg. 1987 Jul;206(1):102-13. (PMID: 3606229)
      J Thorac Cardiovasc Surg. 1979 Jul;78(1):21-7. (PMID: 449383)
      Br Heart J. 1978 Jun;40(6):681-9. (PMID: 656242)
      Ann Thorac Surg. 1995 Sep;60(3):681-2; discussion 682-3. (PMID: 7677500)
      Am J Cardiol. 1995 Jun 15;75(17):1294-5. (PMID: 7778565)
      Cardiol Young. 1998 Oct;8(4):449-54. (PMID: 9855098)
    • Contributed Indexing:
      Keywords: Anomalous origin of pulmonary artery; Congenital heart disease; Pulmonary hypertension
    • الموضوع:
      Date Created: 20190429 Date Completed: 20190701 Latest Revision: 20200225
    • الموضوع:
      20240628
    • الرقم المعرف:
      PMC6487052
    • الرقم المعرف:
      10.1186/s13019-019-0904-0
    • الرقم المعرف:
      31029153