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Long-term management of a child with aortopulmonary septal defect and Eisenmenger syndrome: a 6-year follow-up case study.

Long-term management of a child with aortopulmonary septal defect and Eisenmenger syndrome: a 6-year follow-up case study.

期刊: Folia medica 日期: 2026-03-19 PMID: 42677704 DOI: 10.3897/folmed.68.e149000 浏览: 6
作者: Milanova-Ilieva D, Ketev K, Karavelikova I, Chochkova-Bukova L, Levunlieva E, Kaneva-Nencheva A
D, M.I., K, K., I, K., L, C.B., E, L., & A, K.N. (2026). Long-term management of a child with aortopulmonary septal defect and Eisenmenger syndrome: a 6-year follow-up case study.. Folia medica. https://doi.org/10.3897/folmed.68.e149000
D MI, K K, I K, L CB, E L, A KN. Long-term management of a child with aortopulmonary septal defect and Eisenmenger syndrome: a 6-year follow-up case study.. Folia medica. 2026; doi: 10.3897/folmed.68.e149000
D MI, K K, I K, et al. Long-term management of a child with aortopulmonary septal defect and Eisenmenger syndrome: a 6-year follow-up case study.[J]. Folia medica. 2026. DOI: 10.3897/folmed.68.e149000.
@article{d2026,
  author = {Milanova-Ilieva D and Ketev K and Karavelikova I and Chochkova-Bukova L and Levunlieva E and Kaneva-Nencheva A},
  title = {Long-term management of a child with aortopulmonary septal defect and Eisenmenger syndrome: a 6-year follow-up case study.},
  journal = {Folia medica},
  year = {2026},
  doi = {10.3897/folmed.68.e149000},
  note = {PMID: 42677704},
}
TY  - JOUR
AU  - Milanova-Ilieva D
AU  - Ketev K
AU  - Karavelikova I
AU  - Chochkova-Bukova L
AU  - Levunlieva E
AU  - Kaneva-Nencheva A
TI  - Long-term management of a child with aortopulmonary septal defect and Eisenmenger syndrome: a 6-year follow-up case study.
T2  - Folia medica
PY  - 2026
DO  - 10.3897/folmed.68.e149000
AN  - PMID:42677704
ER  - 

摘要

We report the case of a boy diagnosed at age 9 with a large aortopulmonary septal defect and Eisenmenger syndrome, highlighting the challenges of late diagnosis and management of fixed pulmonary hypertension. Over the course of six years (2018-2024), the patient underwent several follow-ups, including invasive hemodynamic assessments and echocardiography, revealing progressive pulmonary vascular disease. Despite the administration of medical therapy with sildenafil, bosentan, and antiplatelets, the patient's condition remained unfavorable due to fixed pulmonary vascular obstructive disease. This case underscores the importance of early diagnosis and the complexities of managing advanced pulmonary hypertension in congenital heart defects.

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