Long-term outcomes of percutaneous closure of patent ductus arteriosus associated with unilateral absence of a pulmonary artery

被引:3
作者
Wang, Zhiyuan [1 ]
Guo, Baojing [1 ]
Wang, Xiaofang [1 ]
Xiao, Yanyan [1 ]
LV, Zhenyu [1 ]
Liang, Yongmei [1 ]
Jin, Mei [1 ]
机构
[1] Capital Med Univ, Beijing Anzhen Hosp, Beijing Pediat Heart Ctr, Dept Pediat,Heart Ctr, Beijing, Peoples R China
关键词
absence of pulmonary artery; outcome; patent ductus arteriosus; pulmonary hypertension; transcatheter closure; HYPERTENSION; HEMOPTYSIS; AGENESIS; REPAIR;
D O I
10.1111/jocs.15495
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: This study aimed to evaluate the long-term outcomes of patients with patent ductus arteriosus (PDA) associated with unilateral absence of a pulmonary artery (UAPA). Methods: Patients diagnosed with PDA associated with UAPA between January 2005 and June 2019 were retrospectively enrolled in this study. Demographic and clinical characteristics, treatments, and follow-up information were evaluated. Results: A total of 11 patients were diagnosed with PDA associated with UAPA. Percutaneous closure was successfully conducted in nine patients. The mean diameters of the PDA measured by aortogram and occluders were 5.3 +/- 1.8 mm and 11.5 +/- 3.9 mm, respectively. The median pulmonary systemic flow ratio (Qp:Qs) in five patients was 1.41, and the median total lung resistance was 12 Wood Units. The mean systolic pulmonary artery (PA) pressure was 68.3 +/- 19.1 mmHg. In five patients with pre- and postprocedure catheter data, the systolic pulmonary arterial pressure decreased significantly after closure (from 77.0 +/- 20.2 to 58.8 +/- 17.5 mmHg; p = .024), as did the mean pulmonary arterial pressure (from 58.2 +/- 14.6 to 39.0 +/- 14.1 mmHg; p = .18). The PA pressure and heart size gradually decreased to normal levels in eight patients. and their quality of life was significantly improved. The ratio of lung to systemic circulation pressure was less than 0.75. Conclusions: In appropriate patients with PDA associated with UAPA. transcatheter closure of PDA has the potential to improve PA hypertension. A ratio of lung to systemic circulation pressure less than 0.75 may be an important reference index for predicting whether PA pressure can be reduced to a normal level after occlusion.
引用
收藏
页码:2029 / 2034
页数:6
相关论文
共 18 条
[1]   Absent pulmonary artery in one adult and five pediatric patients: Imaging, embryology, and therapeutic implications [J].
Apostolopoulou, SC ;
Kelekis, NL ;
Brountzos, EN ;
Rammos, S ;
Kelekis, DA .
AMERICAN JOURNAL OF ROENTGENOLOGY, 2002, 179 (05) :1253-1260
[2]   PNEUMONECTOMY FOR UNREMITTING HEMOPTYSIS IN UNILATERAL ABSENCE OF PULMONARY-ARTERY [J].
BEKOE, S ;
PELLEGRINI, RV ;
DIMARCO, RF ;
GRANT, KJ ;
WOELFEL, GF .
ANNALS OF THORACIC SURGERY, 1993, 55 (06) :1553-1554
[3]   Palliative surgical treatment of congenital heart defects associated with unilateral absence of the pulmonary artery [J].
Bockeria, Leo A. ;
Podzolkov, Vladimir P. ;
Makhachev, Osman A. ;
Alekyan, Bagrat G. ;
Khiriev, Titalav Kh. ;
Zelenikin, Mikhail A. ;
Shatalov, Konstantin V. ;
Zaets, Sergey B. .
INTERACTIVE CARDIOVASCULAR AND THORACIC SURGERY, 2013, 16 (03) :286-292
[4]   eComment: Congenital isolated unilateral absence of pulmonary artery and variants of collateral blood supply of the ipsilateral lung [J].
Bockeria, Leo A. ;
Makhachev, Osman A. ;
Khiriev, Titalav Kh. ;
Abramyan, Mikhail A. .
INTERACTIVE CARDIOVASCULAR AND THORACIC SURGERY, 2011, 12 (03) :509-510
[5]   THE VARIED MANIFESTATION OF PULMONARY-ARTERY AGENESIS IN ADULTHOOD [J].
BOUROS, D ;
PARE, P ;
PANAGOU, P ;
TSINTIRIS, K ;
SIAFAKAS, N .
CHEST, 1995, 108 (03) :670-676
[6]   Therapy for pulmonary arterial hypertension due to congenital heart disease and Down's syndrome [J].
D'Alto, Michele ;
Romeo, Emanuele ;
Argiento, Paola ;
D'Andrea, Antonello ;
Sarubbi, Berardo ;
Correra, Anna ;
Scognamiglio, Giancarlo ;
Papa, Silvia ;
Bossone, Eduardo ;
Calabro, Raffaele ;
Vizza, Carmine D. ;
Russo, Maria G. .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2013, 164 (03) :323-326
[7]   Definition and Management of Segmental Pulmonary Hypertension [J].
Dimopoulos, Konstantinos ;
Diller, Gerhard-Paul ;
Opotowsky, Alexander R. ;
D'Alto, Michele ;
Gu, Hong ;
Giannakoulas, George ;
Budts, Werner ;
Broberg, Craig S. ;
Veldtman, Gruschen ;
Swan, Lorna ;
Beghetti, Maurice ;
Gatzoulis, Michael A. .
JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2018, 7 (14)
[8]   Successful one-stage repair of unilateral agenesis of pulmonary artery [J].
Hamdan, MA ;
Al Meshham, Y ;
Najm, HK .
PEDIATRIC CARDIOLOGY, 2005, 26 (05) :724-726
[9]   Age-Related Clinical Characteristics of Isolated Congenital Unilateral Absence of a Pulmonary Artery [J].
Koga, Hiroshi ;
Hidaka, Tomoko ;
Miyako, Kenichi ;
Suga, Naohiro ;
Takahashi, Noboru .
PEDIATRIC CARDIOLOGY, 2010, 31 (08) :1186-1190
[10]   Unilateral absence of pulmonary artery: Pathophysiology, symptoms, diagnosis and current treatment [J].
Kruzliak, Peter ;
Syamasundar, Rao P. ;
Novak, Miroslav ;
Pechanova, Olga ;
Kovacova, Gabriela .
ARCHIVES OF CARDIOVASCULAR DISEASES, 2013, 106 (8-9) :448-454