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21 results on '"Akiba, Miki"'

5. One-year change in the health status predicts the subsequent hospitalization and mortality in patients waitlisted for lung transplantation in Japan

Author

Ikeda, Masaki, Wakatsuki, Yusuke, Oga, Toru, Tokuno, Junko, Sugimoto, Seiichiro, Ishihara, Megumi, Okada, Yoshinori, Akiba, Miki, Kayawake, Hidenao, Tanaka, Satona, Yamada, Yoshito, Yutaka, Yojiro, Ohsumi, Akihiro, Nakajima, Daisuke, Hamaji, Masatsugu, Kimura, Jumpei, Chen-Yoshikawa, Toyofumi F., and Date, Hiroshi

Published
2023
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15. Efficacy of carboplatin with an MEP (mitoxantrone, etoposide and prednisone) regimen for relapsed and CHOP-resistant diffuse large B-cell lymphomas

Author

Murohashi, Ikuo, Kashimura, Takuya, Tominaga, Kazunori, Wakao, Daisuke, Takahashi, Takashi, Akiba, Miki, Kishimoto, Kuniya, Yoshida, Katsuhiko, Yagasaki, Fumiharu, Itoh, Yoshihiro, Sakata, Tohru, Kawai, Nobutaka, Itoh, Katsurou, Suzuki, Toshiya, Matsuda, Akira, Hirashima, Kunitake, and Bessho, Masami

Published
2002
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17. Improvement of native pulmonary alveolar proteinosis after contralateral single living‐donor lobar lung transplantation: A case report.

Author

Kobayashi, Kazuma, Ohkouchi, Shinya, Sasahara, Yoji, Ebina, Masahito, Nakata, Koh, Saito, Ryoko, Akiba, Miki, Sado, Tetsu, Oishi, Hisashi, Watanabe, Tatsuaki, Kurosawa, Hajime, and Okada, Yoshinori

Subjects
PULMONARY alveolar proteinosis, LUNG transplantation, BONE marrow transplantation, GRAFT versus host disease, RARE diseases
Abstract

PAP is a rare disease characterized by the accumulation of surfactant materials in the alveolar spaces due to the imbalance of surfactant homeostasis (production and clearance). We herein report a case of an 8‐year‐old girl who developed PAP after BMT from her mother for the treatment of DBA. The anemia was improved by BMT; however, respiratory dysfunction due to graft‐versus‐host disease gradually progressed. She eventually underwent right single LDLLT from her mother when she was 14 years old. A pathological examination of the excised lung confirmed the finding of diffuse bronchiolitis obliterans and unexpectedly revealed widespread alveolar proteinosis. Interestingly, the GGO of her native left lung on chest X‐ray was improved after LDLLT. We present the very unique clinical course of this patient and discuss the mechanisms underlying the development of PAP after BMT and its improvement after LDLLT from the same donor. [ABSTRACT FROM AUTHOR]

Published
2020
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18. Lung transplantation for lymphangioleiomyomatosis in Japan

Author

Ando, Katsutoshi, Okada, Yoshinori, Akiba, Miki, Kondo, Takashi, Kawamura, Tomohiro, Okumura, Meinoshin, Chen, Fengshi, Date, Hiroshi, Shiraishi, Takeshi, Iwasaki, Akinori, Yamasaki, Naoya, Nagayasu, Takeshi, Chida, Masayuki, Inoue, Yoshikazu, Hirai, Toyohiro, Seyama, Kuniaki, Mishima, Michiaki, Nishimura, Masaharu, Nakata, Koh, Tatsumi, Koichiro, Akashiba, Tsuneto, Betsuyaku, Tomoko, Nagase, Takahide, Tamaoki, Jun, Kubo, Keishi, Taniguchi, Hiroyuki, Chin, Kazuo, Urade, Yoshihiro, Nakanishi, Norifumi, Nakano, Yasutaka, Kimura, Hiroshi, Yokoyama, Akihito, Hoshino, Tomoaki, and Watanabe, Kentaro

Subjects
surgical procedures, operative
Abstract

Background: Lung transplantation has been established as the definitive treatment option for patients with advanced lymphangioleiomyomatosis (LAM). However, the prognosis after registration and the circumstances of lung transplantation with sirolimus therapy have never been reported. Methods: In this national survey, we analyzed data from 98 LAM patients registered for lung transplantation in the Japan Organ Transplantation Network. Results: Transplantation was performed in 57 patients as of March 2014. Survival rate was 86.7% at 1 year, 82.5% at 3 years, 73.7% at 5 years, and 73.7% at 10 years. Of the 98 patients, 21 had an inactive status and received sirolimus more frequently than those with an active history (67% vs. 5%, p

Published
2016

19. Successful bilateral lung transplantation after 16 h of lung preservation with EP-TU solution: report of a case.

Author

Oishi, Hisashi, Okada, Yoshinori, Sado, Tetsu, Noda, Masafumi, Hoshikawa, Yasushi, Endo, Chiaki, Sakurada, Akira, Maeda, Sumiko, Kondo, Takashi, Saiki, Yoshikatsu, Akiba, Miki, and Hoshi, Kunihiko

Subjects
LUNG transplantation, PRESERVATION of organs, tissues, etc., IDIOPATHIC pulmonary fibrosis, HEMODIAFILTRATION, REPERFUSION injury, ISCHEMIA
Abstract

We report a case of bilateral lung transplantation (BLT) after preservation of the donor graft for 16 h 5 min with EP-TU, an extracellular phosphate-buffered lung preservation solution. The recipient was a 26-year-old woman with idiopathic pulmonary arterial hypertension and the graft ischemic time was prolonged significantly because of the time required to induce peripheral veno-arterial extracorporeal membrane oxygenation (V-A ECMO) under local anesthesia, and address the severe intrathoracic and pericardial adhesions from past surgery for partial anomalous pulmonary venous return, with concurrent annular plication of the tricuspid valve. After the operation, ECMO and continuous hemodiafiltration were started preemptively to protect the grafts against excessive edema. Postoperative chest X-ray showed diffuse bilateral infiltrates, which improved within a few days and she was weaned off ECMO on day 9. Successful BLT after a graft ischemic time of over 16 h has rarely been described in clinical lung transplantation. [ABSTRACT FROM AUTHOR]

Published
2015
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20. Lung Transplant for Pulmonary Arterial Hypertension After Arterial Switch Operation.

Author

Watanabe, Tatsuaki, Adachi, Osamu, Suzuki, Yasuto, Notsuda, Hirotsugu, Niikawa, Hiromichi, Matsuda, Yasushi, Noda, Masafumi, Sado, Tetsu, Hoshikawa, Yasushi, Akiba, Miki, Tatebe, Shunsuke, Saiki, Yoshikatsu, and Okada, Yoshinori

Abstract

Pulmonary arterial hypertension after arterial switch operation for transposition of the great arteries is an infrequent but life-threatening complication. We report successful lung transplantation in a case of pulmonary hypertension after arterial switch operation. Cardiopulmonary bypass outflow was established through the right subclavian and femoral arteries because of the previous arterial switch operation. Abnormal anatomy and severe pleural and pericardial adhesions as a result of previous operations resulted in prolonged graft ischemic and operation times. Despite delayed left heart adaptation and primary graft dysfunction requiring prolonged extracorporeal membrane oxygenation, the recipient was eventually discharged without activity limitations. [ABSTRACT FROM AUTHOR]

Published
2015
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