Bilateral lung transplant with pulmonary artery reconstruction using donor aorta for pulmonary hypertension with a giant pulmonary arterial aneurysm

Author:

Watanabe Tatsuaki1ORCID,Matsuo Satoshi2,Watanabe Yui1,Hirama Takashi13,Matsuda Yasushi14,Noda Masafumi1,Niikawa Hiromichi1,Oishi Hisashi1ORCID,Suzuki Yamato1,Ejima Yutaka5,Toyama Hiroaki5,Saiki Yoshikatsu2,Okada Yoshinori13

Affiliation:

1. Department of Thoracic Surgery, Institute of Development, Ageing and Cancer, Tohoku University , Sendai, Japan

2. Division of Cardiovascular Surgery, Tohoku University Graduate School of Medicine , Sendai, Japan

3. Division of Organ Transplantation, Tohoku University Hospital , Sendai, Japan

4. Department of Thoracic Surgery, Fujita Health University , Toyoake, Japan

5. Department of Anesthesiology and Perioperative Medicine, Tohoku University Graduate School of Medicine , Sendai, Japan

Abstract

Abstract OBJECTIVES Standard bilateral lung transplantation (BLT) is not feasible for patients with pulmonary arterial hypertension (PAH) complicated with a giant pulmonary arterial aneurysm (PAA). This study aimed to describe the outcomes of BLT with pulmonary artery reconstruction (PAR) using donor aorta for such patients. METHODS This is a retrospective single-centre study reviewing PAH patients with a PAA who received BLT with PAR using donor aorta from January 2010 through December 2020. We compared the characteristics and short- and long-term outcomes of recipients receiving PAR (PAR group) with those who had no PAA and received standard BLT (non-PAR group). RESULTS Nineteen adult PAH patients underwent cadaveric lung transplantation during the study period. Among them, 5 patients with a giant PAA (median pulmonary artery trunk diameter, 69.9 mm) underwent BLT with PAR using donor aorta and the others received standard BLT. Although the operation time tended to be longer in the PAR group compared with the non-PAR group (1239 vs 958 mins, P = 0.087), 90-day mortality (PAR group: 0% vs non-PAR group: 14.3%, P > 0.99), and 5-year survival rate (PAR group: 100% vs non-PAR group: 85.7%, P = 0.74) was comparable between the groups. No dilatation, constriction or infection of the aortic grafts were recorded during the study period with a median follow-up time of 94 months in the PAR group. CONCLUSIONS Lung transplantation with PAR using donor aorta is a valid surgical option for PAH patients complicated with a giant PAA.

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Pulmonary and Respiratory Medicine,General Medicine,Surgery

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